terms of the existence of or arrangement of branches in the polymer structure.. Recently, there have been many materials used for denture base such as polymethyl methacrylate (PMMA) resin, modified PMMA resin and nylon. The material most often use
of JR-spectroscopy, Fourier Transform infrared Spectroscopy (FT-IR), still holds some secrets for the chemist who is trained lo work with conventional grating.
Jan 13, 2010 - B3LYP/6-311++G(d,p). (Theoretical). (FT-IR Gas phase). (FT-IR Solid phase). Wavenumber / cm-1. Absorbance. Figure 3. Comparison of observed and computed FT-IR spectrum of 4- methoxy-2-methylbenzoic acid. 27 components of the 3D matrix
Oct 4, 2016 - FTIR Spectroscopy - A Potential Tool to Identify Metabolic Changes in Dementia. Patients. .... Spectroscopy has recently appeared as one of the major tools for .... tra were acquired with a Perkin-Elmer Spectrum BX FT-IRTM.
Xiaomei Cai,a Tingping Lei,*bc Daoheng Sund and Liwei Linde. Poly(vinylidene ... assigned the FTIR bands at around 840 and 510 cm. Ð1 to the b and/or g.
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Jan 22, 2013 - Received: 12 December 2012; in revised form: 12 January 2013 / Accepted: 16 January 2013 /. Published: 22 ... In general, the quantity of cellulose in cotton fibers increases rapidly, thus it ..... Hsieh et al. reported a steady increa
Aug 23, 2010 - Abstract: A series of asymmetrically substituted free-base di- and tetra-phenylporphyrins and the associated Zn-phenylporphyrins were synthesized and studied by X-ray diffraction,. NMR, infrared, electronic absorption spectra, as well
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Methamphetamine Using Fourier Transform Infrared (FTIR). Spectroscopy ... Controlled Substances Act regulated the production of methamphetamine .
Feb 11, 2016 - Agilent 4500 Portable FTIR Systems for Detection of Counterfeit. Pharmaceuticals. Authors. Alan Rein and Frank Higgins. Agilent Technologies ...
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Applications of Micro-Fourier Transform Infrared Spectroscopy (FTIR) in the Geological Sciences—A Review Yanyan Chen 1, *, Caineng Zou 1 , Maria Mastalerz 2 , Suyun Hu 1 , Carley Gasaway 3 and Xiaowan Tao 1 Received: 29 May 2015; Accepted: 23 November 2015; Published: 18 December 2015 Academic Editor: Nick Hadjiliadis 1 2 3
Abstract: Fourier transform infrared spectroscopy (FTIR) can provide crucial information on the molecular structure of organic and inorganic components and has been used extensively for chemical characterization of geological samples in the past few decades. In this paper, recent applications of FTIR in the geological sciences are reviewed. Particularly, its use in the characterization of geochemistry and thermal maturation of organic matter in coal and shale is addressed. These investigations demonstrate that the employment of high-resolution micro-FTIR imaging enables visualization and mapping of the distributions of organic matter and minerals on a micrometer scale in geological samples, and promotes an advanced understanding of heterogeneity of organic rich coal and shale. Additionally, micro-FTIR is particularly suitable for in situ, non-destructive characterization of minute microfossils, small fluid and melt inclusions within crystals, and volatiles in glasses and minerals. This technique can also assist in the chemotaxonomic classification of macrofossils such as plant fossils. These features, barely accessible with other analytical techniques, may provide fundamental information on paleoclimate, depositional environment, and the evolution of geological (e.g., volcanic and magmatic) systems. Keywords: micro-FTIR; coal; shale; fluid inclusion; chemical mapping; geological sciences
1. Introduction Fourier transform infrared spectroscopy (FTIR) can provide fundamental information on the molecular structure of organic and inorganic components, and is one of the most versatile analytical techniques for the non-destructive, chemical characterization of geological samples, such as coal, shale, fluid and melt inclusions, silicate glass, minerals, and microfossils, e.g., [1–6]. The underlying mechanism of the FTIR technique is associated with transitions between quantized vibrational energy states . In FTIR analysis, absorption of IR radiation occurs when a photon transfers to a molecule and excites it to a higher energy state . The excited states result in the vibrations of molecular bonds (i.e., stretching, bending, twisting, rocking, wagging, and out-of-plane deformation) occurring at varying wavenumbers (or frequencies) in the IR region of the light spectrum. The wavenumber of each IR absorbance peak is determined by the intrinsic physicochemical properties of the corresponding molecule, and is thus diagnostic, like a fingerprint of that particular functional group (e.g., C–H, O–H, C=O, etc.). A detailed introduction of the fundamental mechanism of this
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technique can be found in Griffiths and de Haseth  and Smith . Molecules with dipole moments are IR detectable, and the majority of inorganic and organic compounds in the environment are IR active . Much of the FTIR-related literature in geological sciences focuses on the mid-infrared (MIR) region of light (approximately 4000 to 400 cm´1 ). The absorbances of molecular vibrations under IR radiation are proportional to the abundance of the functional groups. The absorbance of each vibrational band is often measured by the maximum height or the integrated area between the peak and a baseline. Several algorithms are available to define a baseline. The most widely used baseline is a linear line that is tangent to the minima on each side of the peak . This type of baseline is easy to define and highly reproducible between operators . Alternatively, baselines have been defined with a flexicurve or French curve [10,11], the combinations of Gaussians , and using spectra of analyzed samples of the same composition except that the molecules of interest are absent . The concentration of the compound of interest can be determined from the IR absorbance using the Beer-Lambert Law (or simply Beer’s Law): A “ ´log10
I “ e¨ l¨ c I0
where A is the absorbance (dimensionless), and I and I0 denote the intensities of transmitted light and incident light. Parameters e (in L¨ mol´1 ¨ cm´1 ), l (in cm), and c (in mol¨ cm´1 ) stand for the molar absorptivity, sample thickness, and molar concentration, respectively. The modified Beer-Lambert Law [14,15] is used more often in the geological sciences: w“
A¨ M e¨ l¨ ρ
with w as the wt. % of the species of interest within the sample, M as the molar mass (in g¨ mol´1 ), and ρ as the density (in g¨ mol´1 ). Equation (2) requires the absorbance of the species, sample density, thickness, and the molar absorptivity of a sample to determine the concentration of the species in the sample. The modified Beer’s Law can be directly applied to samples containing simple components such as volatiles in glasses or inclusions which mainly consist of H and C species. However, proper mathematical algorithms are required for the multicomponent quantification of more complex samples like coal and shale, principally owing to the overlap of the characteristics peaks of many components. This issue will be elaborated in Section 2.3. 1.1. Conventional FTIR Techniques for Bulk Sample Characterization Most commonly used FTIR techniques for bulk sample analysis are transmission FTIR (e.g., potassium bromide (KBr)-pellet FTIR), attenuated total reflection (ATR)-FTIR, and diffuse reflection infrared Fourier Transform (DRIFT) spectroscopy (Figure 1a–c). Transmission FTIR is a fast and relatively cost-efficient technique which has been used extensively in chemistry, geology, and other scientific fields [1,2,16]. In this approach, the sample pellet is placed in the path of the IR beam and the resulting transmitted IR signal is recorded by the detector (Figure 1a). A KBr pellet is prepared by applying sufficiently high pressure to a homogenous mixture of KBr and the pulverized sample until the pellet turns transparent. KBr is used as the background matrix because it is IR transparent. The major challenge is to estimate the right proportion of the sample material in the pellet so that the resulting peak absorbances are not too weak nor too intense (preferably between 0.2 to 0.7 absorbance units). The linearity of Beer’s Law holds well when the absorbance is <0.7 . Additionally, the analytical sample must be translucent enough (usually KBr pellets must be no more than 0.5–1 mm thick) to allow abundant light to pass through and reach the detector . ATR-FTIR spectra provide chemical information on functional groups distributed near the surface of an internal reflection element [7,18,19]. Unlike transmission FTIR, IR radiation is not transmitted through the
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sample in ATR-FTIR, and consequently, the sample does not need to be prepared as a thin pellet. Moreover, the incorporation of the ATR crystal allows IR spectra with improved signal-to-noise ratios to be obtained with FTIR . An additional advantage of ATR-FTIR is the relative ease of collecting quality data in the presence of water, which enables the examination of aqueous species sorption at crystal interfaces [20,21]. However, it is noteworthy that band intensities of ATR-FTIR spectra differ from those of transmission FTIR spectra owing to the interaction between IR beams and the ATRInt.crystal . This effect needs to be corrected by multiplying the spectrum with a J. Mol. Sci. 2015, 16, page–page linear function . Diffuse reflection infrared Fourier Transform (DRIFT) spectroscopy requires [20,21]. However, it is noteworthy that band intensities of ATR-FTIR spectra differ from those of simpler sample preparation compared with transmission FTIR. In DRIFT, the IR beam penetrates transmission FTIR spectra owing to the interaction between IR beams and the ATR crystal . This the analytical sample certainbydepth, andtheisspectrum then re-emitted from the sample and focused by a effect needs totobeacorrected multiplying with a linear function . Diffuse reflection Fourier Transform (DRIFT) spectroscopy simpler sample is preparation mirror onto infrared the detector (Figure 1c). The resultingrequires DRIFT spectrum similar compared to that obtained by transmission FTIR. In DRIFT, the IR beam penetrates the analytical sample to a certain depth, transmissionwith FTIR technique , although the former is more dependent on physical characteristics and is then re-emitted from the sample and focused by a mirror onto the detector (Figure 1c). The of samples like absorptivity andisreflectance DRIFT quantitative analysis requires the use of resulting DRIFT spectrum similar to that . obtained by transmission FTIR technique , although the former(KM) is more function, dependent onwhich physicalprovides characteristics samples like absorptivity reflectance and sample the Kubelka-Munk a of correlation between and reflectance . DRIFT quantitative analysis requires the use of the Kubelka-Munk (KM) function, which concentration . provides a correlation between reflectance and sample concentration .
Figure 1. Simplified schematics of common Fourier transform infrared spectroscopy (FTIR) analysis
Figure 1. Simplified schematics of common Fourier transform infrared spectroscopy (FTIR) analysis modes including: (a) transmission FTIR; (b) attenuated total reflectance (ATR)-FTIR. Note that the modes including: (a) depth transmission FTIR; attenuated totalofreflectance (ATR)-FTIR. Note that the penetration is dependent on the(b) physical characteristics internal reflection element (IRE) material is anddependent the angle of incidence (c) diffuse reflectance infrared transform (DRIFT) penetration depth on the ; physical characteristics of Fourier internal reflection element (IRE) micro-FTIR. The penetration depth for reflectance micro-FTIR is usually material andspectroscopy; the angle(d) ofreflectance incidence ; (c) diffuse reflectance infrared Fourier transform (DRIFT) less than 10 μm. Modified after figure 1 in Parikh and Chorover  with copyright permission from spectroscopy;Taylor (d) reflectance micro-FTIR. The penetration depth for reflectance micro-FTIR is usually & Francis. less than 10 µm. Modified after figure 1 in Parikh and Chorover  with copyright permission from Although widely used in the determination of chemical structure in a variety of materials, these Taylor & Francis.
conventional FTIR techniques are limited to the investigation of bulk sample rather than individual components occurring at fine scales [6,25]. This characteristic largely restricts the extensive application of conventional FTIR in techniques to homogeneousof geological samples, since theinresults on bulkof materials, Although widely used the determination chemical structure a variety sample are weighted averages that fail to capture the wealth of information expressed by the these conventional FTIR techniques are limited to the investigation of bulk sample rather than heterogeneity at high spatial resolution .
individual components occurring at fine scales [6,25]. This characteristic largely restricts the extensive 1.2. Micro-FTIR for in Situ High Resolution Characterization application of conventional FTIR techniques to homogeneous geological samples, since the results on the development of mercury-cadmium telluride (MCT) detector technology, the micro-FTIR bulk sample areSince weighted averages that fail to capture the wealth of information expressed by the technique has become increasingly popular in characterizing samples that are too small to be heterogeneity at high spatial resolution . chemically analyzed by conventional FTIR techniques. This modern technique can collect IR signals at high spatial resolution (the beam size can be as small as 5 μm), and has great potential for the
1.2. Micro-FTIR for in SituofHigh Resolution Characterization characterization compositionally complex samples. More importantly, micro-FTIR enables in situ, non-destructive analysis without the demand for sample purification and concentration, a process
Since the development of mercury-cadmium telluride (MCT) detector technology, the micro-FTIR technique has become increasingly popular in characterizing samples that are too small to be chemically analyzed by conventional FTIR 3techniques. This modern technique can collect IR signals at high spatial resolution (the beam size can be as small as 5 µm), and has great potential for the characterization of compositionally complex samples. More importantly, micro-FTIR enables 30225
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in situ, non-destructive analysis without the demand for sample purification and concentration, a process which is necessary in conventional FTIR analysis and very likely leads to specimen loss and alteration of chemical properties. Micro-FTIR characterization can be conducted either in transmitted or reflected light mode. The principle of transmitted light mode is similar to that presented in Figure 1a. Transmission micro-FTIR can provide high-quality spectra and has often been used in coal structure characterization . Nonetheless, sample preparation is critical to benefit from the potential advantages of transmission micro-FTIR. The analytical samples need to be thin enough to transmit light (Figure 1d), which is of great technical difficulty for some geological samples, e.g., coal and shale. In reflectance micro-FTIR, IR radiation reflects from a polished and smooth solid sample surface, and the resulting signal is processed with an appropriate mathematical transformation (e.g., Kramers-Kronig transformation) to achieve similar spectra as transmission micro-FTIR spectra. The Kramers-Kronig transformation corrects for transflectance and shifts bands to the positions comparable to those in the KBr pellet spectra [28,29]. In reflectance micro-FTIR analysis, samples are usually prepared as thick blocks with well-polished, smooth surfaces, in the same manner as for the standard organic petrology techniques . Although care is necessary, sample preparation in reflectance micro-FTIR is much easier and more time efficient compared with that for transmission micro-FTIR as only one side of the sample has to be prepared and the thickness of the sample is not critical. This easier sample preparation promotes the increasing use of reflectance micro-FTIR in geology and other sciences recently [26,31–45]. The beam size of micro-FTIR typically ranges from 20–100 µm when using a conventional IR source, and can be reduced down to 3–5 µm using a synchrotron radiation source . The coupling of micro-FTIR and visible light microscopy opens the possibility of visualization and mapping of functional group abundances and molecular arrangements in samples across 2D regions [36,40] or even 3D cubes . In micro-FTIR mapping mode, the infrared spectrum at each sampling point is measured and integrated, and parameters like peak areas in defined spectral regions are then used to map the distributions of target functional groups . The acquisition time of micro-FTIR mapping depends largely on experimental settings, including the total number of sampling spots and scan numbers for each sampling spot, and may vary from hours to days. Recently, FTIR imaging performed with bi-dimensional arrays (e.g., focal plane array detectors, FPA) has become increasingly attractive for the speed at which data can be collected. In FPA imaging mode, the whole image is obtained in a single data collection by the use of multichannel detection, and a typical FPA-micro-FTIR image can be completed in a few minutes . FPA’s fast data-collecting speed facilitates an even more exciting application, namely 3D FPA-micro-FTIR imaging. Operating like conventional X-ray CT microtomography, this approach rotates the sample through the IR beam and collects frequency attenuation images at different sample positions. The individual images are then processed to reconstruct a 3D rendering of the object, portraying the abundance and spatial distribution of IR-active chemicals within the sample . In this paper, we will (i) present recent advances in the application of micro-FTIR techniques in a broad range of geological materials including natural and experimental glasses, minerals, inclusions and microfossils; and (ii) address in particular the chemical characterization of microscopic heterogeneity in coal and shale by using micro-FTIR and mapping techniques. The employment of reflectance-micro-FTIR mapping in geological samples, particularly shale, is still scarce in terms of fine-scale chemical characterization. This review underscores the great potential of non-destructive micro-FTIR technique in the high-resolution characterization of chemical heterogeneity in coal, shale, and other geological materials. 2. Application of FTIR to the Chemical Characterization of Coal and Shale Organic matter (OM) contained in coal and shale is often heterogeneous, or comprised of numerous microscopically distinctive components. These components are usually on the micrometer
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scale and are referred to as macerals by coal and organic petrologists . Chemically similar macerals can be generally grouped into the same type of kerogen, i.e., macromolecular geopolymers which are technically defined as insoluble OM in commonly used organic solvents . As a result of their microscopic sizes, the chemical characterization of individual macerals requires analytical tools that capture information at the micrometer scale to be used. This section will discuss the application of micro-FTIR for geochemical characterization and maturation of OM in coal (Section 2.1) and Int. 2.2), J. Mol. Sci. 16, page–page shale (Section as2015, well as FTIR quantification of organic and inorganic compositions in shale (Section 2.3). 2.1. Coal
of their microscopic sizes, the chemical characterization of individual macerals requires analytical tools that capture information at the micrometer scale to be used. This section will discuss the application of micro-FTIR for geochemical characterization and maturation of OM in coal (Section 2.1) and shale (Section 2.2), as well as FTIR quantification of organic and inorganic compositions in shale highly heterogeneous, organic-rich sedimentary rock, consists largely of helophytic (Section 2.3).
Coal, a and aquatic plant debris and derivatives ( and references therein). Coal macerals originating from 2.1. Coal various parental materials exhibit extraordinarily complex chemical properties, including a large Coal, a highly heterogeneous, organic-rich sedimentary rock, consists largely of helophytic variety and abundance of functional groups. Owing to the remarkably intricate chemical structure of and aquatic plant debris and derivatives ( and references therein). Coal macerals originating from coal, investigating coal with FTIRexhibit initially encountered challenges, with major various parental materials extraordinarily complexgreat chemical properties, including a largecontroversies variety and abundance of functional groups. Owing to remarkably intricate chemical structure of functional being associated with the correct assignments ofthediagnostic bands to particular coal, investigating coal with FTIR initially encountered great challenges, with major controversies groups [50–53]. Recently, FTIR has received renewed interest among those studying coal following being associated with the correct assignments of diagnostic bands to particular functional groups [50–53]. improvements in accessories and renewed spectral processing techniques . IR absorption of Recently, FTIR has received interest among those studying coal following improvements frequencies in processing techniques groups . IR absorption fundamental fundamentalaccessories organic and andspectral inorganic functional in coalfrequencies are listedof in Table 1 organic [50–52,54,55], and and inorganic functional groups in coal are listed in Table 1 [50–52,54,55], and typical micro-FTIR typical micro-FTIR spectra of coal macerals are shown in Figure 2. spectra of coal macerals are shown in Figure 2.
Figure 2. Micro-FTIR spectra of liptinite, vitrinite, and inertinite. Liptinite shows the strongest
Figure 2. Micro-FTIR spectra signal of liptinite, vitrinite, and inertinite. Liptinite shows and the most intense oxygenated group stretching at ~1710 cm−1, butthe strongest aliphatic CHx stretching −1, aromatic CHx stretching, and out-of-plane lowest intensities for C=C ring stretching ~1600 cmoxygenated aliphatic CHthe signal and the most atintense group stretching at ~1710 cm´1 , x stretching deformation. Dashed lines represent the linear baselines applied during FTIR analysis. Note but the lowest intensities for C=C ring stretching at ~1600 cm´1 , the aromatic CHx stretching, and integrated areas of oxygenated and aromatic peak can be obtained by Fourier self-deconvolution  out-of-plane ordeformation. Dashed lines represent the linear baselines applied during the FTIR curve-fitting of peaks in the ~1560–1800 cm−1 region . Note υ—stretching vibration; δ—deformation vibration γ—deformation vibration out of plane; analysis. Note integrated areasin plane; of oxygenated and aromatic peak subscript can beal—aliphatic; obtained by Fourier subscript ar—aromatic. The spectra of liptinite and inertinite have been moved up the´1 axis to self-deconvolution  or curve-fitting of peaks in the ~1560–1800 cm vertical region . Note avoid overlaps. Modified after figure 6 in Chen et al.  with copyright permission from Elsevier. υ—stretching vibration; δ—deformation vibration in plane; γ—deformation vibration out of plane; subscript al—aliphatic; subscript ar—aromatic. The spectra of liptinite and inertinite have been moved up the vertical axis to avoid overlaps. Modified after figure 6 in Chen et al.  with copyright 5 permission from Elsevier.
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Table 1. Band assignments for the infrared spectra of coals [50–52,54,55]. Organic Functional Groups Wavenumber (cm´1 )
Inorganic Functional Groups
Wavenumber (cm´1 )
OH stretch intermolecular bonding
3698, 3652,1095, 1034, 908, 689, 528, 338
Kaolinite, Al2 (Si2 O5 )(OH)4
1464, 705, 245
1450, 882, 729
Dolomite, CaMg(CO3 )2
Aliphatic CH, CH2 , and CH3
1431, 869, 307
3550, 3400,1615, 1155, 1132, 1106, 660
Gypsum, CaSO4 ¨ 2H2 O
C=O, ester with electron withdrawing group attached to single bonded oxygen
CH2 and CH3 bend, possibility of some aromatic ring modes
C-O stretch and O–H bend in phenoxy structures, ethers
Aliphatic ethers, alcohols
Aromatic C–H out-of-plane bending modes
Isolated aromatic H
1,4-substituted aromatic groups
Isolated H and/or 2 neighboring H
1,2-substituted, i.e., 4 neighboring H
where A = Al, Fe, Li, Ca, Mg, or Ni, D = Al, Fe, Li, Mg, Cr, or Cu, T = Al, Si, and Z = O, OH. Data adopted from http://www.mindat.org/min-11119.html; § : where A = Al, Fe, Li, Mg, Mn, or Ni, while T = Al, Fe, Si, and Z = O, OH. Data adopted from http://www.mindat.org/min-1016.html.
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2.1.1. Geochemistry of Coal Macerals Investigated by Micro-FTIR Advanced insights into the geochemical properties of coal macerals are necessary for effective coal processing and utilization. Consequently, geochemical characterization of macerals has been the subject of numerous studies in recent years [18,19,26,32–35,37,38,40,56]. Purification and concentration by manual picking or physical separation is a crucial practice prior to collecting IR spectra when using conventional FTIR techniques on macerals . Although useful information can be derived from the investigation of individual maceral concentrates, the physical separation process tends to cause specimen loss and introduce unexpected experimental errors . In addition to the impossibility of obtaining clean concentrates, chemical properties of coal macerals can also be altered during the separation processes, especially when a strong acid or base is applied . Moreover, the chemical and physical properties of macerals vary substantially, sometimes even within the same maceral group [32,33]. Because of this internal variability, bulk sample analysis often does not provide data that are insightful enough to understand coal utilization processes, and thus micro-techniques capable of high resolution measurements requiring minimal sample preparation have become indispensable for coal characterization. Increasing attempts have been made to characterize individual coal macerals with micro-FTIR given its capability of portraying chemical information non-destructively at high spatial resolution. Commonly studied macerals are vitrinites, including macerals collinite and telinite [32–35,58], sporinite [59–61], resinite [37,38], cutinite [31,37,58], barkinite [41,60], alginite [31,58], fusinite and semifusinite , and funginite . Although the coal samples may vary in ages and depositional environments, several common conclusions can be drawn from these investigations regarding functional group chemistry of liptinite, vitrinite, and inertinite maceral groups. Firstly, liptinite (e.g., sporinite, resinite, cutinite, alginite) contains the highest concentrations of aliphatic moieties and the lowest aromatic moieties compared to other maceral groups at similar maturities, whereas inertinite consists of the most aromatic and the least aliphatic moieties, with vitrinite displaying intermediate values for both proxies [26,37,38,58,61]. Secondly, vitrinite and inertinite have significantly lower CH2 /CH3 ratios compared to liptinite, indicating that vitrinite and inertinite generally comprise shorter and more branched aliphatic chains containing higher terminal CH3 relative to methylene CH2 [31,62]. Finally, coal macerals are highly heterogeneous, and notable differences were observed even within the same particle of individual coal macerals [26,32,33,37,38]. This heterogeneity may be attributed to differences in depositional environments, digenetic processes, or botanical precursors . Recent studies on vitrinite [26,59], sporinite, resinite, and funginite , and barkinite  have demonstrated the great potential for chemical imaging of coal macerals with the micro-FTIR mapping technique. Micro-FTIR mapping enables the visualization of chemistry of coal macerals across a certain microscopic region on a sample surface, and can be performed either in line or area modes. Line mapping contrasts the chemical properties along a certain intersection on a sample surface, and has been used to investigate coal samples containing vitrinite, resinite, exsudatinite, and funginite . The intensity of aliphatic CHx stretching has been observed to increase with a closer proximity to resinite (Figure 3c) and exsudatinite (Figure 3d), whereas it decreased towards funginite (Figure 3e). Area mapping is used more frequently in coal studies since it captures chemical properties and abundance of functional groups across the whole sampling region. A representative micro-FTIR mapping area study has been performed to investigate the chemical heterogeneity of a microscopic area featuring sporinite and funginite distributed among vitrinite, as is shown in Figure 4 (). Micro-FTIR mapping displays the spectral absorbance of characteristic wavenumbers in color-coded images, in which red color denotes high signal intensity and blue color denotes low signal intensity. As demonstrated in Figure 4, sporinite features the most intense aliphatic CHx peak at 3000–2800 cm´1 (red regions in Figure 4c), while funginite contains the strongest aromatic moieties (the red region in Figure 4d, showing the highest ratio between the 3100–3000 cm´1 peak and 30229
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Int. J. Mol. Sci. 2015, 16, page–page 3000–2800 cm´1 peak). Similar
observations are made using micro-FTIR mapping and single-spot micro-FTIR analysis provided that mapping is essentially the IRofspectra provided that micro-FTIR mappingmicro-FTIR is essentially an integration of thean IRintegration spectra of aofseries single of a seriesspots. of single sampling spots. sampling
Figure Figure 3. 3. Chemical Chemicalmapping mapping ofof vitrinite, vitrinite, resinite, resinite, funginite, funginite, and and exsudatinite exsudatinite in in coal coal samples. samples. (a) Photomicrograph of the sample in reflected light showing the location of transect A (a) Photomicrograph of the sample in reflected light showing the location of transect A indicated indicated by by yellow dots. The sampling points are evenly distributed along the transect. The sampling area at point yellow dots. The sampling points are evenly distributed along the transect. The sampling area at A1 contains pure resinite, and points A2 andA2 A3and represent pure vitrinite (Vit). The sampling area at point A1 contains pure resinite, and points A3 represent pure vitrinite (Vit). The sampling point A4 covers half resinite and half vitrinite; (b) FTIR spectra of resinite, vitrinite, and a resinite-vitrinite area at point A4 covers half resinite and half vitrinite; (b) FTIR spectra of resinite, vitrinite, and a mixture. The blue-filled areasThe show how the absorbance in panel (c) are defined. integrated resinite-vitrinite mixture. blue-filled areas showplotted how the absorbance plotted (c) in the panel (c) are −1 area of aliphatic x stretching at 3000–2800 cm as a function of distance A1. The ´1 aspoint defined. (c) the CH integrated area of aliphatic CHx stretching at 3000–2800 cmfrom a function of aliphatic character is strongest in resinite (point A1), decreases toward vitrinite (points A2 and A3) distance from point A1. The aliphatic character is strongest in resinite (point A1), decreases toward and increases in the to point A4 that a mixed from both vitrinite and resinite; vitrinite (points A2 approach and A3) and increases in receives the approach to signal point A4 that receives a mixed signal (d) Photomicrograph of the sample in reflected light showing the location of transect B (yellow dots) from both vitrinite and resinite; (d) Photomicrograph of the sample in reflected light showing the through maceral; points B1 and B5 are in the points location aoffunginite transect (Fu) B (yellow dots) through a funginite (Fu)adjacent maceral;vitrinite; points B1 andB2 B5and are B4 in are the on the exterior funginite rim;and point B3 is exsudatinite (Ex) impregnation; (e)the Anexsudatinite alternative adjacent vitrinite; points B2 B4 are onon thethe exterior funginite rim; point B3 is on x stretching bands at 3000– way showing the (e) variation in FTIR-spectral absorbance aliphaticin CH (Ex) of impregnation; An alternative way of showing theofvariation FTIR-spectral absorbance of −1 across transect B (shown in d) through ´1 2800 cm funginite into adjacent vitrinite. Units in panels c aliphatic CHx stretching bands at 3000–2800 cm across transect B (shown in d) through funginite and are arbitrary absorbance (AU). Modified after figures 4 and units 8 in Chen al.  with into eadjacent vitrinite. Units in units panels c and e are arbitrary absorbance (AU). et Modified after copyright permission from and Sons.permission from John Wiley and Sons. figures 4 and 8 in Chen et al.John Wiley with copyright
More importantly, the non-destructive nature of micro-FTIR mapping enables the interactions More importantly, the non-destructive nature of micro-FTIR mapping enables the interactions between macerals to be observed in situ, which has previously eluded coal geologists [63,64]. The between macerals to be observed in situ, which has previously eluded coal geologists [63,64]. The chemical mapping of a coal surface containing several resinite grains dispersed in vitrinite matrix chemical mapping of a coal surface containing several resinite grains dispersed in vitrinite matrix indicated that aliphatic CHx stretching intensity was higher for the vitrinite immediately adjacent to indicated that aliphatic CHx stretching intensity was higher for the vitrinite immediately adjacent to resinite than those more distant (figure 5 in Chen et al. ). This suggests that chemical components resinite than those more distant (figure 5 in Chen et al. ). This suggests that chemical components (such as aliphatic moieties) from resinite can diffuse into adjoining vitrinite. Contrary to this, (such as aliphatic moieties) from resinite can diffuse into adjoining vitrinite. Contrary to this, funginite did not appear to influence the chemistry of adjacent vitrinite, which was attributed to the funginite did not appear to influence the chemistry of adjacent vitrinite, which was attributed to highly aromatic structure of this type of funginite . the highly aromatic structure of this type of funginite .
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Figure 4. Chemical Chemicalmaps mapsofof a microscopic distinct sporinite (Sp), funginite (Fu), and Figure 4. a microscopic fieldfield withwith distinct sporinite (Sp), funginite (Fu), and vitrinite vitrinite (V). (a) Photomicrograph in reflected light showing mapping sequence, indicated by yellow (V). (a) Photomicrograph in reflected light showing mapping sequence, indicated by yellow dots; dots; (b) Representative FTIR spectra of sporinite, vitrinite, and funginite. The blue-filled areas (b) Representative FTIR spectra of sporinite, vitrinite, and funginite. The blue-filled areas represent represent the the absorbance absorbance values values that that are are mapped mapped in in panel panel (c); (c);the theratios ratiosof ofredred-over overblue-filled blue-filledareas areasare are mapped mapped −1 x groups (3000–2800 cm in panel (d); (c) Chemical mapping of integrated peak of aliphatic CH in panel (d); (c) Chemical mapping of integrated peak of aliphatic CHx groups (3000–2800 cm´1 −1 −1 and 3000–2800 3000–2800 cm cm´1 region); of the the ratio ratio of of the the integrated integratedareas areasbetween between3100–3000 3100–3000cm cm ´1 and region); (d) (d) Map Map of (i.e., (i.e., aa proxy proxy of of aromaticity); aromaticity); Units Units in in panels panels cc and and d d are are arbitrary arbitrary absorbance absorbance units. units. Modified Modified after after figure 8 in Chen et al.  with copyright permission from Elsevier. figure 8 in Chen et al.  with copyright permission from Elsevier.
2.1.2. 2.1.2. Maceral Maceral Coalification Coalification Thermal maturation coalification) advances as aasresult of increasing temperature and Thermal maturationofofcoal coal(or(or coalification) advances a result of increasing temperature burial depth in sedimentary basins . A A variety of ofmicrobiological, and burial depth in sedimentary basins . variety microbiological,chemical, chemical, and and physical physical processes contribute to this intricate system. Detailed descriptions of the processes leading to coalification processes contribute to this intricate system. Detailed descriptions of the processes leading can be found in Stach . Improved knowledge of these physicochemical processes and controlling to coalification can be found in Stach . Improved knowledge of these physicochemical mechanisms of great significance utilization and effective hydrocarbons-from-coal processes andis controlling mechanismsforis coal of great significance for coal utilization and effective exploration and development. hydrocarbons-from-coal exploration and development. Coal and coal macerals change their properties with increasing coalification; therefore determining Coal and coal macerals change their properties with increasing coalification; therefore the coalification level (termed coal rank) is of primary importance for coal scientists. Coal geologists determining the coalification level (termed coal rank) is of primary importance for coal scientists. Coal document and compare the chemistry of coals with varying thermal maturities not only in order to geologists document and compare the chemistry of coals with varying thermal maturities not only better understand their complex maturation processes but also to make recommendations about their in order to better understand their complex maturation processes but also to make recommendations utilization. A large body of related work has been conducted in the past few decades on thermal about their utilization. A large body of related work has been conducted in the past few decades maturities of coal macerals [26,28,33,40,66]. Coal samples with a wide range of coal ranks have been on thermal maturities of coal macerals [26,28,33,40,66]. Coal samples with a wide range of coal collected and analyzed by FTIR in combination with other independent methods, such as optical ranks have been collected and analyzed by FTIR in combination with other independent methods, microscopy, electron microprobe, X-ray diffraction, SEM, etc. The microanalysis of macerals [26,28] such as optical microscopy, electron microprobe, X-ray diffraction, SEM, etc. The microanalysis of (Figure 5) distinctly demonstrates that the abundance of functional groups and concentrations of macerals [26,28] (Figure 5) distinctly demonstrates that the abundance of functional groups and elements like C, O, and H in coal macerals evolve in a consistent pattern in response to coalification. concentrations of elements like C, O, and H in coal macerals evolve in a consistent pattern in The percentage of C increases with thermal maturity, mainly in the form of condensed aromatic response to coalification. The percentage of C increases with thermal maturity, mainly in the form moieties, as reflected by the FTIR spectra. On the contrary, the IR absorbance of O/H-containing of condensed aromatic moieties, as reflected by the FTIR spectra. On the contrary, the IR absorbance functional groups (e.g., CHx, O–H, C=O, etc.) drops with increasing maturation, which is in agreement of O/H-containing functional groups (e.g., CHx , O–H, C=O, etc.) drops with increasing maturation, with the decrease in the concentrations of H and O. which is in agreement with the decrease in the concentrations of H and O.
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Figure 5. Micro-FTIR spectra of vitrinite in coals of different ranks. Adjacent pie diagrams represent Figure 5. Micro-FTIR spectra of vitrinite in coals of different ranks. Adjacent pie diagrams represent elemental composition of these macerals measured by an electron microprobe. The hydrogen content elemental composition of these macerals measured by an electron microprobe. The hydrogen content is calculated by difference . Red dashed lines represent the linear baselines applied to the FTIR is calculated by difference . Red dashed lines represent the linear baselines applied to the FTIR spectra. Modified after figure 2 in Chen et al.  with copyright permission from Elsevier and spectra. Modified after figure 2 in Chen et al.  with copyright permission from Elsevier and Mastalerz and Bustin  with copyright permission from Elsevier. The elemental analysis results for Mastalerz and Bustin  with copyright permission from Elsevier. The elemental analysis results low-volatile coal sample are not available. for low-volatile coal sample are not available.
Artificially maturated coal samples or individual coal macerals have been used in some Artificially maturated coal samples individual coalthermal macerals have been used in[53,67]. some laboratories to trace the chemical evolutionoracross increased maturation gradients laboratories trace thematuration chemical evolution across maturation Most of thesetoartificial experiments are increased conductedthermal in muffle ovens, or gradients inert and [53,67]. ductile Most of these artificial maturation experiments are conducted in muffle ovens, or inertThe andthermal ductile gold tubes, and the starting materials are commonly coal or macerals of low maturities. gold tubes, and the starting materials are commonly coal or macerals of low maturities. The maturity of a coal sample increases as the heating temperature and dwell time increase. This way maturity a coal sample increases as the heating temperature and dwell timeartificially increase. athermal series of samplesofwith varying ranks can be synthesized. The major advantage of using This way a series of samples with varying ranks can be synthesized. The major advantage matured samples is that rock properties other than thermal maturity (e.g., mineralogical compositions, of using artificially is that rockamong properties other suite thanofthermal maturity (e.g., rock fabric, and grainmatured contact) samples remain comparable the whole samples. Controversy mineralogical compositions, rock fabric, andartificial grain contact) remain comparable among whole still remains because short-term and intense heating in a laboratory setting is verythe different suite of samples. Controversy still remains because short-term and intense artificial heating in a from thermal maturation in nature, which is an extraordinarily long-term and gentle heating process . laboratory setting is veryand different from results thermalhave maturation in nature, which is an extraordinarily Nevertheless, insightful interesting been achieved with this approach in the past long-term and gentle heating process . Nevertheless, insightful and interesting results have few decades. Mursito et al.  have observed a significant loss in O and an increase in C with thermal been achieved with this approach in the past few decades. Mursito et al.  have observed maturation, which caused a rise in carbon aromaticity and, thus, the sample’s hydrophobicity. Morgaa significant loss in O and an increase in C with thermal maturation, which causedinaUpper rise inSilesian carbon  has characterized a change in internal structure of semifusinite and fusinite aromaticity and, thus, the sample’s hydrophobicity. Morga  has characterized a change in coals (Poland) before and after heat-treatment (400–1200 °C). The results indicated that semifusinite internal structure of semifusinite and fusinite in Upper Silesian coals (Poland) before and after and fusinite experienced an increase in aromaticity and condensation of the molecular structure, ˝ C). The results indicated that semifusinite and fusinite experienced an heat-treatment (400–1200by which was accompanied a significant increase in reflectance under heating. An alternative artificial practice can be conducted by coupling micro-FTIR with a diamond anvil compression cell (DAC). Although the credibility of the results can be partially hampered by the small sample size used that may be unrepresentative of the whole sample, micro-FTIR-DAC is 30232 10
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increase in aromaticity and condensation of the molecular structure, which was accompanied by a significant increase in reflectance under heating. An alternative artificial practice can be conducted by coupling micro-FTIR with a diamond anvil compression cell (DAC). Although the credibility of the results can be partially hampered by the small sample size used that may be unrepresentative of the whole sample, micro-FTIR-DAC is capable of performing real-time monitoring of changes in chemistry in response to maturation, which makes the dynamic recording and analysis of geological processes possible. By using micro-FTIR-DAC, Ruau et al.  have been able to observe a progression of aromatization in vitrinite’s molecular structures through increasing coalification. In addition, they suggested that there was a functional rearrangement within the C=O groups during maturation. Micro-FTIR-DAC is particularly suitable for experiments requiring high temperature and pressure, which are unlikely to be achieved by a conventional artificial-maturation apparatus. When performed in mapping mode, micro-FTIR-DAC provides a new approach for the study of non-ambient chemical reaction dynamics, which we will describe in detail in Section 3.3. Investigations by FTIR on OM transformations during thermal maturations have shown that with increasing thermal maturation: (i) OM expresses rising aromaticity and condensation of aromatic rings but decreasing aliphatic chain length [31–33]; (ii) the absorbance of oxygenated groups increases initially but decreases prominently later, which is likely the result of decarboxylation/dehydroxylation during coalification [47,66]; (iii) the ratio of CHal /(CHal + C=C), a proxy of hydrocarbon-generating potential, rises in low-rank coal, but decreases in higher-rank coal . These micro-FTIR studies and findings on coal improve our understanding of the fundamental processes occurring during maturation, as well as reaction mechanisms taking place during OM maturation and oil generation, which is of major importance in the development of models for petroleum exploration. 2.2. Shale Shale is commonly composed of clay minerals, quartz, and fragments of other minerals (e.g., calcite and feldspar). It can contain variable amounts of OM. Shale has been attracting attention as worldwide shale gas and oil become more important resources. Shale rich in OM shares many petrologic and geochemical properties with coal. However, the characterization of shale is more challenging, because (i) multiple types of OM (primarily type I/II kerogen) are finely dispersed within the mineral matrix; and (ii) the coexistence of OM and various minerals creates highly heterogeneous shale compositions and severely complicates analyses. Compared to the IR spectrum of coal, shale’s spectrum typically displays much weaker vibrational bands of aliphatic C–H at 3000–2800 cm´1 , but features strong IR absorbance from minerals at 1500–400 cm´1 (Figure 6), which can mask aromatic and aliphatic peaks occurring in the same wavenumber range. The inorganic vibration bands may overlap the same group of minerals (e.g., calcite and dolomite) in the MIR spectral range, complicating FTIR qualification and quantification of mineral-abundant shale. 2.2.1. Geochemistry of Organic Matter and Minerals in Shale Prior to conventional FTIR analysis of OM in shale, pure kerogen has to be extracted and separated from bulk shale samples by repeatedly applying organic solvents, hydrochloric and hydrofluoric acids [70,71]. Micro-FTIR can be used directly on individual components of polished shale samples, including kerogen, removing the need to separate kerogen, greatly easing the sample preparation. In addition, kerogen-mineral interactions in shale can be documented in situ by micro-FTIR. Alstadt et al.  have studied the molecular properties of light and dark colored laminae of selected Green River oil shale (the Piceance Basin, CO, USA) with a step-scan photoacoustic FTIR. Their results revealed that mineral components significantly interacted with the kerogen molecules at molecular level, and the interaction acted differently between light and dark colored layers in the oil
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shale. The successful application of micro-FTIR to finely laminated shale also implies that this form of analysis will be useful in interpreting paleoclimate changes and cycles represented by differences in mineralogical composition of successive laminae over depth . Int. J. Mol. Sci. 2015, 16, page–page
Figure 6. Comparison between the spectra of shale (red) and coal (green). Dashed lines are the linear
Figure 6. Comparison between the spectra of shale (red) and coal (green). Dashed lines are the linear baselines applied to the FTIR spectra. Note that the IR spectrum of shale contains strong absorbance baselines applied to the FTIR spectra. Note that the IR spectrum of shale contains strong absorbance of of minerals occurring at 1500–400 cm−1, but low band intensity from organic matter at 3000–2800 cm−1. minerals occurring at 1500–400 cm´1 , but low band intensity from organic matter at 3000–2800 cm´1 .
The hydrocarbon-generating potential of source rocks can be assessed by tracking physical and chemical changes in the molecular structureof of source kerogenrocks through thermal maturation A routine The hydrocarbon-generating potential can be assessed by . tracking physical approach to address this issue is the artificial maturation of immature, extracted kerogen, as . and chemical changes in the molecular structure of kerogen through thermal maturation described in Section 2.1.2. Micro-FTIR mapping of kerogen in shale provides a simplified approach A routine approach to address this issue is the artificial maturation of immature, extracted kerogen, to address this matter. Chemical maps of the New Albany Shale (Illinois Basin, IN, USA) samples of as described in Section 2.1.2. Micro-FTIR mapping of kerogen in shale provides a simplified approach varying thermal maturities are displayed in Figure 7 (data from Chen et al. ). In response to to address this thermal matter. stress, Chemical maps of the New Albany Shale (Illinois Basin, IN, USA)that samples increasing convertible carbon  gradually transforms into hydrocarbons can of varying thermal maturities are displayed in Figure 7 (data from Chen et al. ). In response later be expelled from the rock, and as a consequence the intensity of aliphatic groups decrease, as to increasing thermal stress, convertible carbonIR  gradually into hydrocarbons that can evidenced by the low intensity of aliphatic absorbance in transforms highly mature samples (Figure 7d,e). later Although be expelled from the rock, a consequence thecontent intensity aliphatic groups decrease, largely controlled byand totalas organic carbon (TOC) and of original OM arrangement, the as abundance and spatial distribution of OM in shale can also be affected by OM migration and evidenced by the low intensity of aliphatic IR absorbance in highly mature samples (Figure 7d,e). expulsion of hydrocarbons thattotal shrink the volume of original kerogen [75,76]. Although largely controlled by organic carbon (TOC) content and original OM arrangement, Micro-FTIR has also proved to be useful in paleoenvironment and and the abundance and spatial distribution of OM in shale can also be affected reconstruction by OM migration hydrocarbon-generation model development. Transmission micro-FTIR studies on G. prisca alginite expulsion of hydrocarbons that shrink the volume of original kerogen [75,76]. varieties (Upper Ordovician Yeoman Formation, Saskatchewan, Canada) indicated that thick-walled Micro-FTIR has also proved to be useful in paleoenvironment reconstruction and alginite varieties (disseminated B) and stromatolitic G. prisca contained stronger OH and aromatic hydrocarbon-generation development. Transmission micro-FTIR studies G.ofprisca alginite CHx absorbances thanmodel thin-walled alginite varieties (disseminated A) at the same on level thermal varieties (Upper Formation, Saskatchewan, Canada) indicated thick-walled maturity .Ordovician This may beYeoman attributed to the formation of phenolic-rich biopolymers in that the cell walls alginite varieties (disseminated B) and stromatolitic G. prisca contained stronger OH and aromatic in response to a fluctuation in oxygen or salinity levels in the paleoenvironment . The subtle CHx changes absorbances thin-walled alginite varietieshave (disseminated A) ata fundamental the same level of thermal in algathan cell wall composition and structure in turn imparted control on the onset and amount of petroleum generation in response to thermal maturation in(Figure 8).walls maturity . This may be attributed to the formation of phenolic-rich biopolymers the cell Specifically, A generates hydrocarbons during diagenesis, which is supported by the in response to a disseminated fluctuation in oxygen or salinity levels in the paleoenvironment . The subtle reduction in aliphatic CH x absorption of the alginites with increasing thermal maturity (Figure 8). changes in alga cell wall composition and structure have in turn imparted a fundamental control In contrast, the disseminated B variety progressively transforms from an alkyl long chain structure on the onset and amount of petroleum generation in response to thermal maturation (Figure 8). into a more cyclic bitumen maceral before peak generation, evidenced by the increased aliphatics Specifically, disseminated A generates hydrocarbons during diagenesis, which is supported by the with maturity in combination with other semi-quantitative FTIR data .
reduction in aliphatic CHx absorption of the alginites with increasing thermal maturity (Figure 8). In contrast, the disseminated B variety progressively transforms from an alkyl long chain structure into 12 30234
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a more cyclic bitumen maceral before peak generation, evidenced by the increased aliphatics with maturity in combination with other semi-quantitative FTIR data . Int. J. Mol. Sci. 2015, 16, page–page
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Figure 7. (a) A representative FTIR spectrum of the studied shale samples. The blue-filled areas
Figure 7. (a)represent A representative spectrum of in the studied The blue-filled areas the absorbance FTIR values that are mapped panels b1, c1, shale d1 and samples. e1. Micro-FTIR chemical of organic matter in (b) earlyare mature shale MM4; chemistry represent themaps absorbance values that mapped in b0:photomicrograph; panels b1, c1, d1b1:micro-FTIR and e1. Micro-FTIR chemical map of integrated peak area of aliphatic CHx groups; (c) mature shale NA2; c0: photomicrograph; maps of organic matter in (b) early mature shale MM4; b0:photomicrograph; b1:micro-FTIR chemistry c1:micro-FTIR chemistry map of integrated peak area of aliphatic CHx groups; (d) late mature shale Figure 7.peak (a) A area representative FTIR spectrum of the studied shale samples. The blue-filled areas map of integrated of aliphatic CHxchemistry groups; (c)ofmature NA2; c0: photomicrograph; IL5; d0: photomicrograph; d1: micro-FTIR map integratedshale peak area of aliphatic CHx represent the absorbance values that are mapped in panels b1, c1, d1 and e1. Micro-FTIR chemical groups; and (e) postmature shale IL1; e0: photomicrograph; e1: micro-FTIR chemistry map c1:micro-FTIR chemistry map of integrated peak area of aliphatic CHx groups; (d) lateofmature shale maps of organic matter in (b) early mature shale MM4; b0:photomicrograph; b1:micro-FTIR chemistry integrated peak area of aliphatic CHx groups. Min, med, and max values stand for the minimum, IL5; d0: photomicrograph; d1: area micro-FTIR map of integrated area of aliphatic CHx map of integrated peak of aliphatic chemistry CHx groups; (c) mature shale NA2; c0:peak photomicrograph; median, and maximum values of integrated peak areas of aliphatic CHx groups in 3000–2800 cm−1. groups; (d) late mature shale chemistry map ofIL1; integrated peak area of aliphatic CHxe1: groups; andc1:micro-FTIR (e) postmature shale e0: photomicrograph; micro-FTIR chemistry map of Modified after figure 4 in Chen et al.  with copyright permission from John Wiley and Sons. IL5; d0: photomicrograph; d1: micro-FTIR chemistry map of integrated peak area of aliphatic CHx integrated peak area of aliphatic CHx groups. Min, med, and max values stand for the minimum, groups; and (e) postmature shale IL1; e0: photomicrograph; e1: micro-FTIR chemistry map of median, andintegrated maximum of integrated peak areas in 3000–2800 cm´1 . x groups peakvalues area of aliphatic CHx groups. Min, med, of andaliphatic max valuesCH stand for the minimum, −1. median, and maximum values of integrated peak areas of aliphatic CH x groups in 3000–2800 Modified after figure 4 in Chen et al.  with copyright permission from John Wiley cm and Sons. Modified after figure 4 in Chen et al.  with copyright permission from John Wiley and Sons.
Figure 8. Model of petroleum generation for Yeoman Formation (Saskatchewan, Canada) G. prisca alginite . Thin-walled G. prisca disseminated A contribute to pre-catagenic petroleum products. In contrast, thick-walled disseminated B alginite and stromatolitic G. prisca undergo a structural transformation into a bitumen-like maceral with increasing thermal maturity. Adjacent photomicrographs are those of G. prisca disseminated A and stromatolitic G. prisca alginite. Modified after figure 10 in Figure 8. Model of petroleum generation for Yeoman Formation (Saskatchewan, Canada) G. prisca Stasiuk et al.  with copyright permission from Elsevier. Figure 8. Model of Thin-walled petroleum generation forAYeoman Formation alginite . G. prisca disseminated contribute to pre-catagenic(Saskatchewan, petroleum products. Canada) G. In contrast, thick-walled disseminated B alginite and stromatolitic G. prisca undergo a structural petroleum prisca alginite . Thin-walled G. prisca disseminated A contribute to pre-catagenic 2.2.2. FTIR Spectral Data as a Proxy for Porosity and Permeability transformation into a bitumen-like maceral with increasing thermal maturity. Adjacent photomicrographs products. InPorosity contrast, thick-walled B alginiteevaluation and stromatolitic G. prisca undergo a and are disseminated among most significant criteriaafter for shale are those of G.permeability prisca disseminated A andthe stromatolitic G. prisca alginite. Modified figurereservoirs, 10 in structuraland transformation into a bitumen-like maceral with increasing thermal maturity. substantial efforts have recently been devoted to develop effective and fast approaches for theirAdjacent Stasiuk et al.  with copyright permission from Elsevier.
photomicrographs are those of G. prisca disseminated A and stromatolitic G. prisca alginite. Modified 13 Permeability 2.2.2. FTIR Spectral Data as a Proxy for Porosity and after figure 10 in Stasiuk et al.  with copyright permission from Elsevier. Porosity and permeability are among the most significant evaluation criteria for shale reservoirs, and substantial efforts have recently been devoted to develop effective and fast approaches for their
2.2.2. FTIR Spectral Data as a Proxy for Porosity and Permeability 13
Porosity and permeability are among the most significant evaluation criteria for shale reservoirs, and substantial efforts have recently been devoted to develop effective and fast approaches for their characterization and quantification [78,79]. Tools commonly used for the investigation of porosity and permeability include high-resolution microscopic techniques which directly view pore 30235
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geometry and morphology at fine scales, and probe-based porosimetric techniques measuring the porosity and permeability indirectly. Chen et al.  have developed an approach to relate shale chemical maps obtained via micro-FTIR to shale porosity and permeability, based on the observations that porosity in OM typically accounts for a large portion of total porosity in shale [80,81]. Then better interconnectivity of porous organic domains must be accompanied by the increased interconnectivity of pores in OM, and thus the permeability of shale. Indeed, positive correlations between the interconnectivity of OM domains, porosity, and Swanson permeability were observed by Chen et al. , indicating that interconnectivity of OM domains might be a useful proxy for shale permeability. Micro-FTIR, accompanied by porosimetric techniques, can improve our understanding of porosity networks in shale . 2.3. Quantification of Organic Matter and Minerals in Coal and Shale “In the case of nearly all branches of science a great advance was made when accurate quantitative methods were used instead of merely qualitative.” (Sorby, 1908 ). Abundant publications have highlighted the importance of fast and accurate quantification of organic and mineralogical components in coal , shale [84–87] and other sedimentary rocks [55,88,89] using FTIR techniques. Quantitative information about the compositions of rock and other geological samples can be obtained with FTIR tools since OM and minerals display most of their characteristic vibration modes in the IR spectral region . The critical importance of sample preparation has been emphasized in several previous studies on transmission-FTIR quantification [55,83,84]. The absorbance is strongly related to a mineral’s grain size . A large mineral grain size (>2.5 µm) may induce the dispersion of the IR beam . Careful grinding is therefore required for transmission FTIR quantification. Appropriate algorithms are also important in assuring credible FTIR quantification results, particularly for compositionally complex samples like coal and shale. The determination of the composition of a multicomponent sample from its FTIR spectrum is complicated by the overlap of IR bands and the nearly identical FTIR spectra of many components [55,85,88]. The measured absorbance is thus the sum of the absorbances of all the components (not only the component of interest) in the sample, and as a result the Beer’s Law cannot be directly applied to coal and shale. Proper algorithms are required to enable multicomponent FTIR quantification. A common procedure for multicomponent quantification is so-called “sequential subtraction” [83–88]. A library of the spectra of mineral and OM standards is used to sequentially subtract from the spectra of the coal/shale. The subtraction coefficient, which results in the complete elimination of the typical peaks of the particular component being subtracted, provides a measure of the weight fraction of that component present in the coal/shale . Evident double peaks at 3000–2800 cm´1 from aliphatic C–H stretching are usually used for the quantification of OM. Characteristic bands of mineral components can be found in Table 1. Although sequential subtraction is straightforward and was used in a large body of FTIR quantification studies, the accuracy of the results generated in this way largely relies on subjective decisions about the subtracted spectrum, and analytical errors can become critical when determining low concentrations of certain components [83,87]. Least squares (LS) curve fitting has recently become an alternative computational tool for FTIR quantification. These results are more reproducible and objective compared to manual subtraction [50,55,74,90–92]. For instance, the LS regression of the spectra of 49 synthetic mineral mixtures predicted an average absolute difference between the known and derived mineral concentration of ˘2.6 wt. % . It is important that all of the components existing in the sample should be included in the LS regression model, otherwise the calculation is invalid. This shortcoming limits the application of LS in very complicated mixtures with unknown components. The feasibility of partial least squares (PLS) regression to DRIFTS and ATR-FTIR quantification of mineral mixtures has also been investigated, and shows considerable potential for accurate and precise mineralogical analysis [93,94]. PLS regression can be used to quantify complicated samples. However, the calculations tend to be rather slow. In addition, PLS
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requires a large number of mixture spectra to yield precise results, usually 3–5 times as many mixtures as constituents . A non-negative least squares (NNLS)-FTIR quantitative study of an artificial mixture of multiple natural minerals, and shale samples from the Western Sedimentary Basin (Alberta, Canada) was recently presented by Chen et al. . Limited errors below ˘4 wt. % compared to the known mineral composition suggest that NNLS-FTIR is capable of rapid and accurate quantification of mineral fractions, kerogen in synthetic mixtures, and kerogen in natural shale. Using the same strategy, the micro-FTIR technique was tested for its applicability of in situ, high-resolution quantification of shale composition. Measured IR spectra agree more closely with a model prediction derived from NNLS-micro-FTIR than with a model prediction derived from NNLS-bulk FTIR, partially because analyses conducted by micro-FTIR avoid the necessity to crush and grind samples. The capability of performing high-spatial resolution quantification renders micro-FTIR as a particularly suitable tool for the quantitative portrayal of heterogeneities in coal and shale at small scales . 2.4. Limitations of Micro-FTIR in Coal and Shale Studies Micro-FTIR possesses a few advantages over conventional transmission FTIR methods: (i) it alleviates the difficulties associated with sample preparation by using bulk samples instead of isolated macerals; and (ii) it analyzes samples non-destructively with intact inter-maceral or OM-mineral associations. These valuable attributes make this technique especially attractive in the analysis of microscopic heterogeneities in coal and shale in relation to their mineralogy and OM types. There are, however, some inherent limitations associated with the application of this technique to coal and shale studies. One of these limitations is that micro-FTIR cannot reliably identify components smaller than 15 micrometers owing to the relative large aperture size of micro-FTIR with a conventional light source . An additional drawback on OM characterization is the difficulty in identifying OM in highly mature shale, because aliphatic moieties in immobile OM (i.e., kerogen, pyrobitumen) are chemically depleted during thermal maturation. Therefore, alternative approaches, for example using imaging processing software, have to be employed to discriminate between highly mature OM and minerals occurring on the surface via their contrasting color and reflectance intensity . Another constraint comes from the fact that micro-FTIR, with a conventional IR source, only maps the chemical properties across a 2D surface, which may pose challenges to the translation of 2D chemical data to real 3D reservoir attributes. Two options may solve this problem: (i) the employment of multi-channel FPA-micro-FTIR 3D mapping ; or (ii) the integration of multiple micro-FTIR maps performed on surfaces perpendicular to each other following a Cartesian coordinate system. A few noteworthy limitations also affect micro-FTIR quantification: (i) the great difficulty in obtaining pure mineral standards and homogeneous organic macerals that have unadulterated FTIR spectra ; (ii) the quantification errors of minor concentrations of certain minerals (e.g., phosphates and pyrite); and (iii) the inability to compare and calibrate micro-FTIR quantitative results with other independent analyses, primarily because quantitative information on the micrometer scale cannot currently be assessed with other techniques. 3. Other Geological Application of Micro-FTIR 3.1. Application to the Analysis of Volatiles in Glasses and Minerals Volatiles (primarily H2 O and CO2 ) drive volcanic eruptions . Dissolved volatiles can strongly affect the physical properties and geochemical signatures of silicate melts and magmatic rocks [96,97]. Therefore, the characterization of volatiles is critical in order to improve the understanding of volcanic and magmatic processes. Methods commonly used for volatile analysis in volcanic rocks and minerals include Karl Fischer titration , FTIR [99,100], Raman spectroscopy [101,102], secondary ion mass spectrometry (SIMS) , and electron backscatter methods [104,105]. Among these
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approaches, FTIR is relatively simple, highly sensitive, and can provide quantitative measurements of different volatile species at high spatial resolution [10,106]. The use of synchrotron radiation micro-FTIR permits a spatial resolution of about 3–5 µm with the detection limits at the ppm level . Sample preparation is an important step in guaranteeing satisfactory measurements using transmission FTIR. A doubly-polished wafer with parallel sides has to be prepared for the analysis . The thickness of the wafer needs to be estimated prior to sample preparation. Optimal results are achieved when the maximum absorbance in the spectral range being used for quantitative analysis does not exceed 0.7 . For example, a graph, such as figure 5 in von Aulock et al.  for rhyolitic glasses, can be used to estimate the optimum thickness for a volcanic glass sample. Additionally, appropriate adhesive for mounting the sample should be carefully selected based on their specific properties. Sample preparation can be tedious and challenging for fractured samples, fragile samples, such as pumices, and very small samples, such as inclusions within crystals. The contents of H2 O and CO2 can be quantitatively determined from IR spectra using the modified Beer’s Law (Equation (2)), which requires absorbance, density, thickness, and the molar absorptivity. The peak heights at ~3550 cm´1 and ~1630 cm´1 are commonly used to calculate the concentrations of total H2 O (H2 Ot ) and molecular H2 O (H2 Om ) , and the contents of CO2 and CO3 2´ can be determined from the peak heights of the bands at ~2350 cm´1 and ~1430 cm´1 [109,110]. The choice of baseline needs to be carefully considered as it may introduce large errors in absorbance measurements. The molar absorptivity (e) is chemical-composition specific, and should theoretically be determined for every sample. However, literature values (see Table 1 in von Aulock et al. ) for similar chemical compositions offer sufficient accuracy in most cases. The density of natural glasses that are thin and heterogeneous can be calculated using the models developed by Lange and Carmichael  and Ochs and Lange . The thickness (l) measurements are challenging, especially for thin and fragile samples. The most common way to determine sample thickness is directly using micrometers or digital displacement gauges, however, these can damage the samples if not performed carefully. Tamic et al. , Wysoczanski and Tani , and Nichols and Wysoczanski  used a new strategy to indirectly determine thicknesses by counting the interference fringes across a region of the reflectance FTIR spectra. Other tools for thickness measurements include calibrated microscope stages and optical profilometers. A good introduction to the approaches for thickness measurements is presented in von Aulock et al. . Great efforts have recently been dedicated to developing reflectance micro-FTIR to analyze volatiles [42,44,45,108]. This modern FTIR technique requires only one exposed and polished surface, easing sample preparation. Reflectance micro-FTIR provides a means to analyze volatile abundances in fragile samples (e.g., cracked, vesicular glasses) and unusually H-rich samples that are otherwise impossible to analyze or prepare for analysis with transmission micro-FTIR techniques [42,43]. In addition, different depths within a single sample can be analyzed using sequential polishing procedures . The application of the reflectance micro-FTIR also avoids the difficulties associated with thickness measurements. Using reflectance micro-FTIR, King and Larsen  have successfully retrieved linear functions relating H2 Ot contents with the Kramas-Kronig absorbance at 3550 cm´1 for basaltic, andesitic, phonolitic, and rhyolitic glasses. ATR micro-FTIR is an alternative FTIR-based technique that requires samples to be polished on only one side. Lowenstern and Pitcher  have determined H2 O contents in hydrous glasses using ATR micro-FTIR, and the derived concentration values were comparable with those obtained by transmission micro-FTIR. ATR micro-FTIR yields higher sensitivity for a given optical aperture size than reflectance micro-FTIR [5,108]. However, ATR micro-FTIR can damage fragile samples through direct contact of the ATR accessory with the sample’s surface . An increasing amount of publications have demonstrated the capabilities of micro-FTIR techniques in the high-resolution characterization of volatiles in natural, e.g., [10,116,117] and experimental glasses, e.g., . The distribution and diffusion of H2 O in the samples can facilitate the
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identification of the exsolution and re-dissolution of H2 O in the melt [96,114,116], and provide better constraints on volcanic temperatures and timescales [5,99]. H2 O distribution profiles created using micro-FTIR also assist in the recording and quantification of bubble evolution in the melt [43,97,118], which is a fundamental research topic in volcanology. Such studies are particularly important in understanding magmatic processes, and constructing and developing eruption mechanisms . Recent advances in FTIR techniques allow H2 O to be analyzed in nominally anhydrous minerals (NAMs) [4,119]. NAMs can accommodate H2 O in the form of protons in defects in the mineral structure . The study of H2 O in NAMs is vital for constraining the H budget of Earth’s mantle, past and present mantle geodynamics, and the origin of volatiles in terrestrial planets [96,120]. Micro-FTIR maps displaying volatile distributions across minerals are of great interest to Earth scientists, as they may improve our understanding of crystallization processes . Della Ventura et al.  observed an interesting compositional zonation of CO2 and CO3 2´ contents in vishnevite from Latium, Italy, which may be induced by a major change in the physical conditions of the environment, such as temperature, during the mineral crystallization. The crystallographic orientations of the hydrous species in NAMs can be acquired using polarized FTIR [4,122]. 3.2. Application to the Characterization of Fluid and Melt Inclusions Crystals may contain small impurities of variable shape, referred to as inclusions , which are frequently grouped by the proportion of vapor, liquid or solid phase present in them at room temperature. Droplets consisting of liquid/vapor/daughter crystals are referred to as fluid inclusions, and melt inclusions are parcels of glass/vesicles/daughter crystals that were trapped within crystals as they grow in the magma [46,124]. Inclusions are a record of the geological environment in which the melt and/or fluids were trapped, and are thus of continuing interest to geologists [107–109,112,114,124]. Advances in analytical techniques have created an evolution in scientific methods used to characterize inclusions. Initially, bulk extraction was used, which is destructive, time consuming, and limited to the larger inclusions . Recently, non-destructive micro-Raman spectroscopy has been developed to measure H2 O in inclusions, e.g., [101,125]. Nonetheless, this technique requires calibrations, which largely depend on sample composition and analytical parameters that are currently laboratory dependent . In recent years there has been an increased availability of synchrotron radiation, which enables the application of synchrotron-based FTIR imaging techniques to related studies, e.g., [107,126]. To achieve a good chemistry image of melt and fluid inclusions with transmission micro-FTIR, the host crystal has to be doubly polished in a careful manner so that the inclusion is completely exposed on both sides of the crystal slice [44,107,127]. That way, the IR beam interacts solely with the inclusion. The occurrence of H2 O was successfully FTIR-mapped in fluid and melt inclusions hosted in crystals from Stromboli (Sicily, Italy), the Alban Hills volcano (Rome, Italy), and Franklin Furnace (Franklin, NJ, USA) (see figure 5 in Della Ventura ). The same technique was applied to study the distribution of volatile CO2 and H2 O in an olivine-hosted melt inclusion hosted in a rock erupted at Procida Island, Southern Italy (figure 6 in Mormone et al. ). Reflectance micro-FTIR requires only one surface to be exposed and polished, which is particularly suitable for the analysis of small inclusions in fragile samples [44,103]. Yasuda  has developed a method to measure H2 O contents of silicate glasses by reflectance micro-FTIR. The method was calibrated using 32 synthesized glasses ranging from basalt to rhyolite in composition and a range of H2 O contents. To apply the technique to melt inclusions he developed a method to correct for contamination from the host crystal calculating the overlapping volume of the host crystal using the reflectance spectra between 800 and 1300 cm´1 . H2 O contents of melt inclusions have also been determined using ATR micro-FTIR , which provides higher signal-to-noise ratios than reflectance micro-FTIR, and is thus well suited for imaging of volatiles in very small melt inclusions (<15 µm).
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In addition to investigating inorganic H2 O and CO2 in inclusions, the measurement and imaging of CH4 and other hydrocarbons can also be performed by micro-FTIR [128,129]. Barrès et al.  initiated the micro-FTIR analysis of hydrocarbon-bearing inclusions. This study demonstrated that micro-FTIR can distinguish various individual hydrocarbon fluid inclusions within a single sample, and this can be used to study the crude chemical evolution of hydrocarbons during the geological history of the sample . However, because of IR source constraints, the quality of spectra was only sufficient for fluid inclusions with diameters larger than 30 µm to be successfully analyzed . Applying sophisticated synchrotron-radiation micro-FTIR, Bourdet et al.  was able to map compositional variability within hydrocarbon inclusions in quartz using a beam size of ~3 µm. IR spectra of individual inclusions (figure 8 in Bourdet et al. ) were used to quantify methane concentrations, CH Int. J. Mol. Sci. 2015, 16, page–page 2 /CH 3 ratios and H2 O–Hydrocarbon ratios. Applyingtosophisticated synchrotron-radiation micro-FTIR, Bourdet et al.  was able to map 3.3. Application High-Temperature Studies compositional variability within hydrocarbon inclusions in quartz using a beam size of ~3 μm. IR
FTIR, together with inclusions a diamond or 8 sapphire heating (FTIR-DAC), has spectra of individual (figure in Bourdet cell et al. and )awere used tostage quantify methane CH2/CH ratios and Hmonitoring 2O–Hydrocarbon recentlyconcentrations, been employed in 3 real-time of ratios. geochemical reactions taking place at high temperatures [132–138]. A few investigations have applied FTIR-DAC to processes in which 3.3. Application to High-Temperature Studies the dehydration of H2 O was involved [134,136,138]. In these studies FTIR spectra of the FTIR, were together with a at diamond or of sapphire and a heatingand stage has mineral sample collected a series presetcell temperatures, the(FTIR-DAC), extent to which the recently been employed in real-time monitoring of geochemical reactions taking place at high absorbance of a vibrational band associated with H2 O (e.g., O–H peak) changes with temperature temperatures [132–138]. A few investigations have applied FTIR-DAC to processes in which the can be dehydration observed of [134,136]. Dehydration ratios can be easily calculated by processing these H2O was involved [134,136,138]. In these studies FTIR spectra of the mineral sample temperature-dependent spectra, and plotted asand a the function temperature to of retrieve the kinetic were collected at a series of preset temperatures, extent toof which the absorbance a vibrational information of mineral dehydration. For example, Prasad et al.  recorded the dehydration band associated with H2O (e.g., O–H peak) changes with temperature can be observed [134,136]. ratiosstilbite can be easily calculated processing these spectra, FTIR-DAC and behaviorDehydration of a natural sample from by Poona (India) bytemperature-dependent employing transmission plotted as a function of temperature to retrieve the kinetic information of mineral dehydration. For with the sample in a KBr pellet (Figure 9). Based on their FTIR spectra, the relative absorbance of example, Prasad et al.  recorded the dehydration behavior of a natural stilbite sample from Poona H2 O (i.e., absorbance ratios of O–H band at an elevated temperature (i.e., 425–770 K) over that at (India) by employing transmission FTIR-DAC with the sample in a KBr pellet (Figure 9). Based on 300 K) was calculated plotted versus temperature, as shown inofFigure 10.at The dehydration their FTIR spectra, and the relative absorbance of H2O (i.e., absorbance ratios O–H band an elevated rate of stilbite can thus be easily derived from the tangential slops at various temperatures. temperature (i.e., 425–770 K) over that at 300 K) was calculated and plotted versus temperature, as Kinetic shownon in geochemical Figure 10. The dehydration rate also of stilbite can thus beusing easily micro-FTIR derived from mapping/imaging. the tangential information processes can be achieved slops atetvarious Kinetic information geochemical processesthe candehydration also be achieved Della Ventura al. temperatures. creatively applied micro-FTIRonimaging to monitor of a single using micro-FTIR mapping/imaging. Ventura6etin al. ).  creatively appliedindicated micro-FTIRthat imaging crystal of leucite at high temperatures Della (see figure The images increasing to monitor the dehydration of a single crystal of leucite at high temperatures (see figure 6 in ). temperature and time yielded clear dehydration. The images indicated that increasing temperature and time yielded clear dehydration.
Figure 9. Left: Micro-IR spectra of stilbite collected at different temperatures (300, 425, 475, 575 and
Figure 9. Left: Micro-IR spectra of stilbite collected at different temperatures (300, 425, 475, 575 and 770 K) in the 4000–400 cm−1 wavenumber range. Modified after figure 2 in Prasad et al.  with ´1 770 K) in the 4000–400 cm wavenumber range. Modified after figure 2 in Prasad et al.  with copyright permission from Mineralogical Society of America; Right: absorbance of H2O (represented copyright from Mineralogical Society of America; Right: H2 O (represented by permission O–H bending, purple-filled area) with increasing temperature fromabsorbance 425 to 770 Kof normalized to by O–H that bending, purple-filled area) increasing from 425 to 770 Kspectra normalized at 300 K. The normalized H2Owith absorbances weretemperature derived from corresponding FTIR on the to that and show dehydration with increasingwere temperature. at 300 K.left The normalized H2 O absorbances derived from corresponding FTIR spectra on the left and show dehydration with increasing temperature. 3.4. Application to Microfossil Characterization and Chemotaxonomy
Increasing efforts have been made to employ micro-FTIR techniques to the study of microfossils, given the high sensitivity of this technique and the very low amount of specimen that it requires 30240 (typically 1–2 mg). Dutta et al. [139–141] used micro-FTIR to characterize well-preserved microfossils from Silurian and younger sedimentary sequences in the U.S., Turkey, Germany, and Sweden. The spectroscopic investigation indicated that the macromolecular structure of these microfossils consisted of both aliphatic and aromatic moieties (Figure 10). Tasmanites, Leiosphaeridia, and a plant
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3.4. Application to Microfossil Characterization and Chemotaxonomy Increasing efforts have been made to employ micro-FTIR techniques to the study of microfossils, given the high sensitivity of this technique and the very low amount of specimen that it requires (typically 1–2 mg). Dutta et al. [139–141] used micro-FTIR to characterize well-preserved microfossils from Silurian and younger sedimentary sequences in the U.S., Turkey, Germany, and Sweden. The spectroscopic investigation indicated that the macromolecular structure of these microfossils consisted of both aliphatic and aromatic moieties (Figure 10). Tasmanites, Leiosphaeridia, and a J. Mol. Sci. 2015, 16, page–page plant cuticle Int. had long-chain aliphatics and tended to be oil-prone, whereas the aliphatic chains in zoomorphs (i.e., chitinozoans, and arthropod cuticles) short and more cuticle had long-chain scolecodonts, aliphatics and tended to be oil-prone, whereaswere the aliphatic chains in gas-prone in response tozoomorphs thermal(i.e., stress. Megaspores exhibited moderate aliphatic and absorbance, and chitinozoans, scolecodonts, and arthropod cuticles) were short andaromatic more gas-prone in response to thermal stress. Megaspores exhibited moderate aliphatic and aromatic absorbance, and had both oil and gas generating potential . had both oil and gas generating potential .
Figure 10. Left: Micro-FTIR spectra of prasinophycean algae (a) Tasmanites sp. from the Silurian, Oklahoma (USA) and (b) Leiosphaeridia sp. from the Late Silurian, Hazro (Turkey); (c)sp. a megaspore Figure 10. Left: Micro-FTIR spectra of prasinophycean algae (a)area Tasmanites from the Silurian, Zonalessporites sp. from the Pennsylvanian, Saarland (Germany); (d) a plant cuticle from the Late Oklahoma (USA) and (b) Leiosphaeridia sp. from the Late Silurian, Hazro area (Turkey); (c) a Cretaceous-Early Paleocene (western Germany); and (e) zoomorph Chitinozoa from the Silurian, megaspore Zonalessporites sp.Dashed from lines the Pennsylvanian, (Germany); (d) a plant Gotland (Sweden). indicate the linear Saarland baselines applied to the spectra. Right: cuticle from the Late Cretaceous-Early Paleocene (western Germany); and (e) 1–5 zoomorph from the Photomicrography of corresponding microfossils. Modified after figures in Dutta et al.Chitinozoa  with copyright permissionDashed from Elsevier. Silurian, Gotland (Sweden). lines indicate the linear baselines applied to the spectra. Right: Photomicrography of corresponding microfossils. Modified after figures 1–5 in Dutta et al.  with 19 copyright permission from Elsevier.
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Microbial Microbial fossils fossils with with well-preserved well-preserved morphological morphological structures structures can can provide provide direct direct evidence evidence for for the existence of life in old (e.g., the Precambrian) geological strata . However, degraded microbial the existence of life in old (e.g., the Precambrian) geological strata . However, degraded fossils often resemble anotherone in shape taxonomy istaxonomy usually not microbial fossils oftenone resemble anotherand in size, shapeand andmorphological size, and morphological is enough to determine the precise phylogenetic positions. High spatial resolution and non-destructive usually not enough to determine the precise phylogenetic positions. High spatial resolution and analyses make micro-FTIR particularly useful particularly in distinguishing theinphylogenetic position of microbial non-destructive analyses make micro-FTIR useful distinguishing the phylogenetic fossils. Igisu et al.  applied to well-preserved from ~850 Ma from and position of microbial fossils. Igisu etmicro-FTIR al.  applied micro-FTIR to microfossils well-preserved microfossils ~1900 Ma stromatolites, and demonstrated that CH /CH absorbance ratios were a good proxy for 3 2 CH3/CH2 absorbance ratios were a good ~850 Ma and ~1900 Ma stromatolites, and demonstrated that the chemical composition precursor membrane lipidsmembrane and a useful indicator Archaea, proxy for the chemical of composition of precursor lipids and toa distinguish useful indicator to Bacteria, andArchaea, possiblyBacteria, Eucarya and (Figure 11). Eucarya (Figure 11). distinguish possibly
Figure 11. Relationship between R3/2 (aliphatic CH3/CH2 absorbance ratios) and ratio of CH3/CH2 for Figure 11. Relationship between R3/2 (aliphatic CH3 /CH2 absorbance ratios) and ratio of CH3 /CH2 n-alkane standard samples (n-C5 to n-C40). The CH3/CH2 ratio can be converted to carbon number of for n-alkane standard samples (n-C5 to n-C40 ). The CH3 /CH2 ratio can be converted to carbon the n-alkane. Modified after figure 6 in Igisu et al.  with copyright permission from Elsevier. number of the n-alkane. Modified after figure 6 in Igisu et al.  with copyright permission from Using this equation, R3/2 values of Eucarya, Bacterial and Archaeal lipids are estimated to be 0.19–0.22, Elsevier. Using this equation, R3/2 values of Eucarya, Bacterial and Archaeal lipids are estimated to 0.32–0.37, and 1.16, respectively . The carbon number of Eucarya lipids (C25–C29) and bacterial be 0.19–0.22, 0.32–0.37, and 1.16, respectively . The carbon number of Eucarya lipids (C25 –C29 ) lipids (C16–C18) are from Han and Calvin  and Ladygina et al. . and bacterial lipids (C16 –C18 ) are from Han and Calvin  and Ladygina et al. .
The research of Igisu et al.  focused on demonstrating the feasibility of micro-FTIR mapping The research of Igisu et al.  focused on demonstrating feasibility of micro-FTIR mapping in distinguishing microfossils morphologically. They mappedthetwo morphotypes of phosphatized in distinguishing microfossils morphologically. They mapped two morphotypes of phosphatized embryo-like microfossils, together with algal fossils from the Doushantuo group, China. Displaying embryo-like microfossils, together with algal fossils from the Doushantuo group, China. the distribution of aliphatic and aromatic functional groups inside the embryo-like fossils, Displaying micro-FTIR the distribution of aliphatic and aromatic groups inside the embryo-like fossils, micro-FTIR maps differentiated microfossils that arefunctional morphologically within the same taxon (see figure 15 in maps differentiated microfossils that are morphologically within the same taxon (see figure 15 Igisu et al. ). The chemical characterization of microfossils together with a morphological analysis in Igisu et al. ). The chemical characterization of microfossils together with a morphological may provide new biological information on embryo-like fossils. analysis may provide new biological information on embryo-like Additionally, FTIR data provide insightful chemical criteria forfossils. plant fossil taxonomic classification FTIR databyprovide chemical criteriataxonomic for plant criteria fossil taxonomic whenAdditionally, it is complemented known insightful morphologically-derived [146–149]. classification when it is complemented by known morphologically-derived taxonomic Zodrow et al.  investigated well-preserved cuticles isolated from Geinitz leaf compressions with criteria [146–149]. Zodrow et al.  investigated well-preserved cuticles isolated from Geinitz FTIR. The similarities between spectra in the three cuticular morphotypes supported their leaf compressions FTIR. The similarities between spectra inmethods, the threelike cuticular morphotypes classification into awith single cordaite-leaf taxon. The use of statistical principle component supported their classification into a single cordaite-leaf taxon. The use of statistical methods, analysis (PCA), may aid in fossil-leaf chemotaxonomy when paired with FTIR techniques. like For principle component analysis (PCA), may aid in fossil-leaf chemotaxonomy when paired with FTIR instance, D’Angelo et al.  introduced a new strategy for studying Carboniferous compression techniques. For instance, et analysis al.  introduced new strategy for studying Carboniferous foliage by coupling FTIRD’Angelo and PCA in order toa gain insight into the types and relative compression foliage by coupling FTIR and PCA analysis in order to gain insight into the types and proportions of structural groups in pinnules of the same segment. The results displayed a non-uniformity relative proportionsofof structural groups pinnules of the same The results displayed in the fossilization Carboniferous foliageinwithin a plant fossil for segment. a given geological setting, which asuggests non-uniformity in the fossilization of Carboniferous foliage within a plant fossil for a given variable physicochemical potentials driving OM transformation. These findings geological setting, which suggests variable physicochemical potentials transformation. demonstrate that FTIR-assisted chemotaxonomy can be a valuable tool todriving further OM distinguish between These findings demonstrate that FTIR-assisted chemotaxonomy can be a valuable tool to further plant-fossil groups. distinguish between plant-fossil groups. 30242 20
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4. Conclusions Micro-FTIR provides insightful data on the chemical structure at the molecular scale, and is a very promising technique for the characterization of microscopic heterogeneity of geological samples like coal and shale. The chemical varieties within macerals can be well-documented and imaged with this non-destructive technique. More importantly, micro-FTIR provides a suitable and a straightforward way of tracing OM transformation across maturation by mapping shale samples of varying maturities. In addition, FTIR provides a fast, convenient, and accurate quantitative approach to investigate shale compositions that is complementary to XRD. The non-destructive character of micro-FTIR enables chemical investigations of geological samples that are micrometer in size, such as fluid and melt inclusions hosted in minerals, and microfossils not easy to classify with other methods. Moreover, the possibility of real-time monitoring of chemical evolution in response to thermal stress by micro-FTIR provides a new opportunity to study problems associated with chemical reaction rates under non-ambient conditions. Thermal treatment, dehydration processes, and many other geochemical processes can benefit from this convenient, in situ technique. In addition, FTIR data can provide insightful chemical information for the taxonomic classification of plant fossils (and likely other macrofossils). Acknowledgments: This work was supported by PetroChina Science and Technology Major Project “The formation and distribution of deep gigantic hydrocarbon fields” (Grant2014E-3201), the National Key Basic Research and Development Program, China (Grant 2014CB239000), and the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under Award Number DE-SC0006978 (formerly DE-FG02-11ER16246). The manuscript greatly benefited from constructive comments of three reviewers. Conflicts of Interest: The authors declare no conflict of interest.
References 1. 2.
6. 7. 8. 9. 10. 11. 12.
Iglesias, M.J.; Jiménez, A.; Laggoun-Défarge, F.; Suárez-Ruiz, I. FTIR study of pure vitrains and associated coals. Energy Fuels 1995, 9, 458–466. [CrossRef] Lis, G.P.; Mastalerz, M.; Schimmelmann, A.; Lewan, M.D.; Stankiewicz, B.A. FTIR absorption indices for thermal maturity in comparison with vitrinite reflectance R0 in type-II kerogens from Devonian black shales. Org. Geochem. 2005, 36, 1533–1552. [CrossRef] Behrens, H.; Romano, C.; Nowak, M.; Holtz, F.; Dingwell, D.B. Near-infrared spectroscopic determination of water species in glasses of the system MAlSi3 O8 (M = Li, Na, K): An interlaboratory study. Chem. Geol. 1996, 128, 41–64. [CrossRef] Rossman, G.R. Analytical methods for measuring water in nominally anhydrous minerals. Rev. Mineral. Geochem. 2006, 62, 1–28. [CrossRef] Von Aulock, F.W.; Kennedy, B.M.; Schipper, C.I.; Castro, J.M.; Martin, D.E.; Watkins, J.M.; Wallace, P.J.; Puskar, L.; Bégué, F.; Nochols, A.R.L.; et al. Advances in Fourier transform infrared spectroscopy of natural glasses: From sample prepration to data analysis. Lithos 2014, 206–207, 52–64. [CrossRef] D’Angelo, J.A.; Zodrow, E.L. Chemometric study of functional groups in different layers of Trigonocarpus grandis ovules (Pennsylvanian seed fern, Canada). Org. Geochem. 2011, 42, 1039–1054. [CrossRef] Griffiths, P.R.; de Haseth, J.A. Fourier Transform Infrared Spectrometry, 2nd ed.; John Wiley & Sons, Inc.: New York, NY, USA, 2007. Parikh, S.J.; Chorover, J. FTIR spectroscopic study of biogenic Mn-oxide formation by Pseudomonas putida GB-1. Geomicrobiol. J. 2005, 22, 207–218. [CrossRef] Smith, B.C. Fundamentals of Fourier Infrared Spectroscopy, 2nd ed.; CRC Press, Taylor & Francis Group: Boca Raton, FL, USA, 2011. Zhang, Y.; Xu, Z.; Behrens, H. Hydrous species geospeedmeter in rhyolite: Improved calibration and application. Geochim. Cosmochim. Acta 2000, 64, 3347–3355. [CrossRef] Di Matteo, V.; Carroll, M.R.; Behrens, H.; Vetere, F.; Brooker, R.A. Water solubility in trachytic melts. Chem. Geol. 2004, 213, 187–196. [CrossRef] Ohlhorst, S.; Behrens, H.; Holtz, F. Compositional dependence of molar absorptivities of near-infrared OH- and H2 O bands in rhyolitic to basaltic glasses. Chem. Geol. 2001, 174, 5–20. [CrossRef]
Int. J. Mol. Sci. 2015, 16, 30223–30250
13. 14. 15. 16. 17. 18.
22. 23. 24.
25. 26. 27.
28. 29. 30. 31. 32. 33.
Dixon, J.E.; Stopler, E.; Delaney, J.R. Infrared spectropic measurements of CO2 and H2 O IN Juan de Fuca Ridge basaltic glasses. Earth Planet. Sci. Lett. 1988, 90, 87–104. [CrossRef] Stopler, E.M. The speciation of water in silicate melts. Geochim. Cosmochim. Acta 1982, 46, 2609–2620. Stopler, E.M. Water in silicate glasses: An infrared spectroscopic study. Contrib. Mineral. Petrol. 1982, 81, 1–17. Ibarra, J.V.; Muñoz, E.; Moliner, R. FTIR study of the evolution of coal structure during the coalification process. Org. Geochem. 1996, 24, 725–735. [CrossRef] Schrader, B. Infrared and Raman Spectroscopy: Methods and Applications; VCH Verlagsgesellschaft mbH: Weinheim, Germany, 1995. Li, Z.; Fredericks, P.M.; Rintoul, L.; Ward, C.R. Application of attenuated total reflectance micro- Fourier transform infrared (ATR-FTIR) spectroscopy ot the study of coal macerals: Examples from the Bowen Basin, Australia. Int. J. Coal Geol. 2007, 70, 87–94. [CrossRef] Li, Z.; Fredericks, P.M.; Ward, C.R.; Rintoul, L. Chemical functionalities of high and low sulfur Australian coals: A case study using micro attenuated total reflectance–Fourier transform infrared (ATR-FTIR) spectrometry. Org. Geochem. 2010, 41, 554–558. [CrossRef] Borer, P.; Hug, S.J.; Sulzberger, B.; Kraemer, S.M.; Kretzschmar, R. ATR-FTIR spectroscopic study of the adsorption of desferrioxamine B and aerobactin to the surface of lepidocrocite (γ-FeOOH). Geochim. Cosmochim. Acta 2009, 73, 4661–4672. [CrossRef] Goyne, K.W.; Chorover, J.; Kubicki, J.D.; Zimmerman, A.R.; Brantley, S.L. Sorption of the antibiotic ofloxacin to mesoporous and nonporous alumina and silica. J. Colloid Interface Sci. 2005, 283, 160–170. [CrossRef] [PubMed] Harrick, N.J. Internal Reflection Spectroscopy; Wiley-Interscience: New York, NY, USA, 1967. Griffiths, P.R.; de Haseth, J.A. Fourier Transform Infrared Spectrometry-Application to Chemical Systems; Wiley-Interscience: New York, NY, USA, 1986. Greene, E.F.; Tauch, S.; Webb, E.; Amarasiriwardena, D. Application of diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) for the identification of potential diagensis and crystallinity changes in teeth. Microchem. J. 2004, 76, 141–149. [CrossRef] Supaluknari, S.; Larkins, F.P. An FTIR study of Australian coals: Characterization of oxygen functional groups. Fuel Process. Technol. 1988, 19, 123–140. [CrossRef] Chen, Y.; Mastalerz, M.; Schimmelmann, A. Characterization of chemical functional groups in macerals across different coal ranks via micro-FTIR spectroscopy. Int. J. Coal Geol. 2012, 104, 22–33. [CrossRef] Landais, P.; Rochdi, A.; Largeau, C.; Derenne, S. Chemical characterization of torbanites by transmission micro-FTIR spectroscopy: Origin and extent of compositional heterogeneities. Geochim. Cosmochim. Acta 1993, 57, 2529–2539. [CrossRef] Kramers, H.A. La diffusion de la lumiere par les atomes. Atti Congr. Int. Fis. 1927, 2, 545–557. Kronig, R. On the theory of the dispersion of X-rays. J. Opt. Soc. Am. 1926, 12, 547–557. [CrossRef] International Committee for Coal Petrology (ICCP). International Handbook of Coal Petrography, 2nd ed.; Centre National de la Recherche Scientifique: Paris, France, 1963. Lin, R.; Ritz, G.P. Studying individual macerals using i.r. microspectroscopy, and implications on oil versus gas/condensate proneness and “low-rank” generation. Org. Geochem. 1993, 20, 695–706. [CrossRef] Mastalerz, M.; Bustin, R.M. Electron microprobe and micro-FTIR analyses applied to maceral chemistry. Int. J. Coal Geol. 1993, 24, 333–345. [CrossRef] Mastalerz, M.; Bustin, R.M. Variation in maceral chemistry within and between coals of varying rank: An electronic microprobe and micro-Fourier transform infra-red investigation. J. Microsc. 1993, 171, 153–166. [CrossRef] Mastalerz, M.; Bustin, R.M. Application of reflectance micro-Fourier transform infrared spectrometry in studying coal macerals: Comparison with other Fourier transform infrared techniques. Fuel 1995, 74, 536–542. [CrossRef] Mastalerz, M.; Bustin, R.M. Application of reflectance micro-Fourier Transform infrared analysis to the study of coal macerals: An example from the Late Jurassic to Early Cretaceous coals of the Mist Mountain Formation, British Columbia, Canada. Int. J. Coal Geol. 1996, 32, 55–67. [CrossRef] Garcia, D.; Black, J. Fourier transform infrared micro spectroscopy mapping. Applications to the vinyl siding industry. J. Vinyl Addit. Technol. 1997, 3, 200–204. [CrossRef]
Int. J. Mol. Sci. 2015, 16, 30223–30250
37. 38. 39.
40. 41. 42. 43. 44. 45. 46.
51. 52. 53. 54. 55.
Guo, Y.; Bustin, R.M. Micro-FTIR spectroscopy of liptinite macerals in coal. Int. J. Coal Geol. 1998, 36, 259–275. [CrossRef] Chen, Y.; Caro, L.; Mastalerz, M.; Schimmelmann, A.; Blandón, A. Mapping the chemistry of resinite, funginite, and associated vitrinite in coal with micro-FTIR. J. Microsc. 2013, 249, 69–81. [CrossRef] [PubMed] Martin, M.C.; Dabat-Blondeau, C.; Unger, M.; Sedlmair, J.; Parkinson, D.Y.; Bechtel, H.A.; Illman, B.; Castro, J.M.; Keiluweit, M.; Buschke, D.; et al. 3D spectral imaging with synchrotron Fourier transform infrared spectro-microtomography. Nat. Methods 2013, 10, 861–864. [CrossRef] [PubMed] Chen, Y.; Mastalerz, M.; Schimmelmann, A. Heterogeneity of shale documented by micro-FTIR and image analysis. J. Microsc. 2014. [CrossRef] [PubMed] Mastalerz, M.; Hower, J.C.; Chen, Y. Microanalysis of barkinite from Chinese coals of high volatile bituminous rank. Int. J. Coal Geol. 2015, 141, 103–108. [CrossRef] King, P.L.; Dalby, K.D.; Lui, D.K.; Griffin, T. A new reflectance IR spectroscopy method for analyzing H2 O in rhyolitic to basaltic glasses. Geochim. Cosmochim. Acta 2005, 69 (Suppl. S1), A744. Mongrain, J.; Larsen, J.F.; King, P.L. Rapid water exsolution, degasing, and bubble collapse observed experimentaly in K-phonolite melts. J. Volcanol. Geotherm. Res. 2008, 173, 178–184. [CrossRef] King, P.L.; Larsen, J.F. A micro-reflectance IR spectroscopy method for analyzing volatile species in basaltic, andesitic, phonolitic, and rhyolitic glasses. Am. Mineral. 2013, 98, 1162–1171. [CrossRef] Yasuda, A. A new technique using FT-IR micro-reflectance spectroscopy for measurement of water concentrations in melt inclusions. Earth Planets Space 2014, 66, 34–44. [CrossRef] Della Ventura, G.; Bellatreccia, F.; Marcelli, A.; Cestelli Guidi, M.; Piccinini, M.; Cavallo, A.; Piochi, M. Application of micro-FTIR imaging in the Earth Sciences. Anal. Bioanal. Chem. 2010, 297, 2039–2049. [CrossRef] [PubMed] Stach, E. The macerals of coal. In Stach's Textbook of Coal Petrology; Stach, E., Mackowsky, M., Teichmüller, M., Taylor, G.H., Chandra, D., Teichmüller, R., Eds.; Gebrüder Borntraeger: Berlin-Stuttgart, Germany, 1982; pp. 87–140. Tissot, B.; Welte, D.H. Petroleum Formation and Occurrence; Springer-Verlag: Berlin, Germany, 1978; p. 538. O’keefe, J.M.K.; Bechtel, A.; Christanis, K.; Dai, S.; DiMichele, W.A.; Eble, C.F.; Esterle, J.S.; Mastalerz, M.; Raymond, A.L.; Valentim, B.V.; et al. On the fundamental difference between coal rank and coal type. Int. J. Coal Geol. 2013, 118, 58–87. [CrossRef] Painter, P.C.; Starsinic, M.; Coleman, M.M. Determination of functional groups in coal by Fourier transform interferometry. In Fourier Transform Infrared Spectroscopy; Ferraro, J.R., Basile, L.J., Eds.; Academic Press: New York, NY, USA, 1985; pp. 169–240. Wang, S.; Griffiths, P.R. Resolution enhancement of diffuse reflectance I.R. spectra of coals by Fourier self-deconvolution. 1. C–H stretching and bending modes. Fuel 1985, 64, 229–236. [CrossRef] Solomon, P.R.; Carangelo, R.M. FTIR analysis of coal. 2. Aliphatic and aromatic hydrogen concentration. Fuel 1988, 67, 949–959. [CrossRef] Fredericks, P.M. Infrared Spectroscopy. In Spectroscopic Analysis of Coal Liquids; Kershaw, J.R., Ed.; Elsevier: New York, NY, USA, 1989; p. 395. Estep, P.A.; Kovach, J.J.; Karr, C., Jr. Quantitative infrared multicomponent analysis of minerals occurring in coal. Pet. Sci. Eng. 2008, 60, 1–17. Matteson, A.; Herron, M.M. Quantitative Mineral Analysis by Fourier Trannsform Infrared Spectroscopy. Paper No. 9308. In Pooceedings of the Society of Core Analysts Conference, Houston, TX, USA, 9–11 August 1993; pp. 1–15. Morga, R. Chemical structure of semifusinite and fusinite of steam and coking coal from the Upper Silesian Coal Basin (Poland) and its changes during heating as inferred from micro-FTIR analysis. Int. J. Coal Geol. 2010, 84, 1–15. [CrossRef] Kruge, M.A.; Landais, P.; Bensley, D.F.; Stankiewicz, B.A.; Elie, M.; Ruau, O. Speration and artificial maturation of macerals from type II kerogen. Energy Fuels 1997, 11, 503–514. [CrossRef] Pradier, B.; Landais, P.; Rochdi, A.; Davis, A. Chemical basis of fluorescence alteration of crude oils and kerogens—II. Fluorescence and infrared micro-spectrometric analysis of vitrinite and liptinite. Org. Geochem. 1992, 18, 241–248. [CrossRef] Hacura, A.; Wrzalik, R.; Matuszewska, A. Application of reflectance micro-infrared spectroscopy in coal structure studies. Anal. Bioanal. Chem. 2003, 375, 324–326. [PubMed]
Int. J. Mol. Sci. 2015, 16, 30223–30250
60. 61. 62. 63. 64. 65. 66. 67. 68.
69. 70. 71.
72. 73. 74.
Sun, X. The investigation of chemical structure of coal macerals via transmitted-light FT-IR microspectroscopy. Spectrochim. Acta Part A 2005, 62, 557–564. Stankiewicz, B.A.; Kruge, M.A.; Mastalerz, M. A geochemical study of macerals from a Miocene lignite and an Eocene bituminous coal, Indonesia. Org. Geochem. 1996, 24, 531–545. [CrossRef] Killops, S.; Killops, V. Introduction to Organic Geochemistry, 2nd ed.; Blackwell Science Ltd.: Malden, MA, USA, 2005. Hutton, A.C.; Cook, A.C. Influence of alginite on the reflectance of vitrinite from Joadja, NSW, and some other coals and oil shales containing alginite. Fuel 1980, 59, 711–714. [CrossRef] Suárez-Ruiz, I.; Jiménez, A.; Iglesias, M.J.; Laggoun-Defarge, F.; Prado, J.G. Influence of resinite on huminite properties. Energy Fuels 1994, 8, 1417–1424. [CrossRef] Seewald, J.S. Organic-inorganic interactions in petroleum-producing sedimentary basins. Nature 2003, 426, 327–333. [CrossRef] [PubMed] Drobniak, A.; Mastalerz, M. Chemical evolution of Miocene wood: Example from the Belchatow brown coal deposit, central Poland. Int. J. Coal Geol. 2006, 66, 157–178. [CrossRef] Mursito, A.R.; Hirajima, T.; Sasaki, Keiko. Upgrading and dewatering of raw tropical peat by hydrothermal treatment. Fuel 2010, 89, 635–641. [CrossRef] Schimmelmann, A.; Mastalerz, M.; Gao, L.; Sauer, P.E.; Topalov, K. Dike intrusions into bituminous coal, Illinois Basin: H, C, N, O isotopic responses to rapid and brief heating. Geochim. Cosmochim. Acta 2009, 73, 6264–6281. [CrossRef] Ruau, O.; Landais, P.; Michels, R.; Langlois, E. Evaluation of organic matter reactivity during pyrolysis by micro-FTIR technqiues. Prepr. Am. Chem. Soc. 1997, 42, 164–167. Robl, T.L.; Davis, B.H. Comparison of the HF-HCl and HF-BF3 maceration techniques and the chemistry of resultant organic concentrates. Org. Geochem. 1993, 20, 249–255. [CrossRef] Schimmelmann, A.; Lewan, M.D.; Wintsch, R.P. D/H isotope ratios of kerogen, bitumen, oil, and water in hydrous pyrolysis of source rocks containing kerogen types I, II, IIS, and III. Geochim. Cosmochim. Acta 1999, 63, 3751–3766. [CrossRef] Alstadt, K.N.; Katti, D.R.; Katti, K.S. An in situ FTIR step-scan photoacoustic investigation of kerogen and mienrals in oil shale. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 2011, 89, 105–113. [CrossRef] [PubMed] Chen, Y.; Furmann, A.; Mastalerz, M.; Schimmelmann, A. Quantitative analysis of shale with KBr-FTIR and novel micro-FTIR. Fuel 2014b, 116, 538–549. [CrossRef] Jarvie, D.M. Total organic carbon (TOC) analysis. In Source and Migration Processes and Evalutaion Techniques: AAPG Treatise of Petroleum Geology, Handbook of Petroleum Geology; Merrill, R.K., Ed.; American Association pf Petroleum Geoologist: Tulsa, OH, USA, 1991; pp. 113–118. Jarvie, D.M.; Hill, R.J.; Ruble, T.E.; Pollastro, R.M. Unconventional shale-gas systems: The Mississippian Barnett Shale of north-central Texas as one model for thermogenic shale-gas assessment. AAPG Bull. 2007, 91, 475–499. [CrossRef] Loucks, R.G.; Reed, R.M.; Ruppel, S.C.; Jarvie, D.M. Morphology, genesis, and distriubtion of nanometer-scale pores in siliceous mudstons of the Mississippian Barnett Shale. J. Sediment. Res. 2009, 79, 848–861. [CrossRef] Stasiuk, L.D.; Kybett, B.D.; Bend, S.L. Reflected light microscopy and micro-FTIR of Upper Ordovician Gloeocapsomorpha prisca alginite in relation to paleoenvironment and petroleum generation, Saskatchewan, Canada. Org. Geochem. 1993, 20, 707–719. [CrossRef] Suarez-Rivera, R.; Deenadayalu, C.; Chertov, M.; Hartanto, R.N.; Gathogo, P.; Kunjir, R. Improving Horizontal Completions on Heterogeneous Tight Shales. In Proceedings of the Canadian Unconventional Resources Conference, Clagary, AB, Canda, 15–17 November 2011. Suarez-Rivera, R.; Chertov, M.; Dean, W.; Sidney, G.; John, K. Understanding Permeability Measruments in Tight Shales Promotes Enhanced Determination of Reservoir Quality. In Proceedings of the SPE Canadian Unconventional Resources Conderence, Clagary, AB, Canda, 30 October–1 November 2012. Ross, D.J.K.; Bustin, R.M. The importance of shale composition and pore structure upon gas storage potential of shale gas reservoirs. Mar. Petr. Geol. 2009, 26, 916–927. [CrossRef] Mastalerz, M.; He, L.; Melnichenko, Y.B.; Rupp, J.A. Porosity of coal and shale: Insights from gas adsorption and SANS/USANS techniques. Energy Fuels 2012, 26, 5109–5120. [CrossRef]
Int. J. Mol. Sci. 2015, 16, 30223–30250
Sorby, H.C. On the application of quantitative methods to the study of the structure and history of rocks. Q. J. Geol. Soc. Lond. 1908, 64, 171–232. [CrossRef] 83. Painter, P.C.; Coleman, M.M.; Jenkins, R.G.; Whang, P.W.; Walker, P.L. Fourier Transform Infrared study of mineral matter in coal. A novel method for quantitative mineralogical analysis. Fuel 1978, 57, 337–344. [CrossRef] 84. Cronauer, D.C.; Snyder, R.W.; Painter, P.C. Characterization of oil shale by FTIR spectroscopy. Abstr. Pap. Am. Chem. Soc. 1982, 27, 122–130. 85. Brown, J.M.; Elliott, J.J. Quantitative analysis of minerals in oil shales by Fourier transform infrared spectroscopy. Am. Chem. Soc. Div. Petr. Chem. 1987, 32, 65–70. 86. Charsky, A.; Herron, M.M. Quantitative Analysis of Kerogen Content and Mineralogy in Shale Cuttings by Diffuse Reflectance Infrared Fourier Transform Spectroscopy. In Proceedings of the International Symposium of the Society of Core Analysts, Aberdeen, UK, 27–30 August 2012. 87. Solomon, P.R.; Miknis, F.P. Use of Fourier transform infrared spectroscopy for determining oil shale properties. Fuel 1980, 59, 893–896. [CrossRef] 88. Bertaux, J.; Fröhich, F.; Ildefonse, P. Multicomponent analysis of FTIR spectra: Quantification of amorphous and crystallized mineral phases in synthetic and natural sediments. J. Sediment. Res. 1998, 68, 440–447. [CrossRef] 89. Ballard, B.D. Quantitative mineralogy of reservoir rocks using Fourier transform infrared spectroscopy. In Proceedings of the Annual Technical Conference and Exhibition, Anaheim, CA, USA, 11–14 November 2007. 90. Antoon, M.K.; Koenig, J.H.; Koenig, J.L. Least-squres curve-fitting of Fourier transform infrared spectra with appplications to polymer systems. Appl. Spectrosc. 1977, 31, 518–524. [CrossRef] 91. Saarinen, P.; Kauppinen, J. Multicomponent analysis of FT-IR spectra. Appl. Spectrosc. 1991, 45, 953–963. [CrossRef] 92. Herron, M.M.; Matteson, A.; Gustavson, G. Dual Range FT-IR Mineralogy and the Analysis of Sedimentary Formation. In Proceedings of the International Symposium of the Society of Core Analysts, Calgary, Canada, 7–10 September 1997; pp. 1–12. 93. Breen, C.; Clegg, F.; Herron, M.M.; Hild, G.P.; Hillier, S.; Hughes, T.L.; Jones, T.G.J.; Matteson, A.; Yarwood, J. Bulk mineralogical characterization of oilfield reservoir rocks and sandstones using Diffuse Reflectance Infrared Fourier Transform Spectroscopy and Partial Least Squares analysis. Pet. Sci. Eng. 2008, 60, 1–17. [CrossRef] 94. Washburn, K.E.; Birdwell, J.E. Multivariate analysis of ATR-FTIR spectra for assessment of oil shale organic geochemical properties. Org. Geochem. 2013, 63, 1–7. [CrossRef] 95. Sparks, R.S.J. The dynamics of buble formation and growth in magmas: A review and analysis. J. Volcanol. Geotherm. Res. 1978, 3, 1–37. [CrossRef] 96. Johnson, E.A. Water in nominally anhydrous crustal minerals: Speciation, concentration, and geological significance. Rev. Mineral. Geochem. 2006, 62, 117–154. [CrossRef] 97. McIntosh, I.M.; Llewellin, E.W.; Humphreys, M.C.S.; Nichols, A.R.L.; Burgisser, A.; Schipper, C.I.; Larsen, J.F. Distribution of dissolved water in magmatic glass records growth and resorption of bubbles. Earth Planet. Sci. Lett. 2014, 401, 1–11. [CrossRef] 98. Turek, A.; Riddle, C.; Cozens, B.; Tetley, N. Determination of chemical water in rock analysis by Karl Fischer titration. Chem. Geol. 1976, 17, 261–267. [CrossRef] 99. von Aulock, F.W.; Nichols, A.R.L.; Kenndy, B.M.; Oze, C. Timescales of texture development in a cooling lava dome. Geochim. Cosmochim. Acta 2013, 114, 72–80. [CrossRef] 100. Ryan, A.G.; Russell, J.K.; Nichols, A.R.L.; Hess, K.-U.; Porritt, L.A. Experiments and models on H2 O retrograde solubility in volcanic systems. Am. Mineral. 2015, 100, 774–786. [CrossRef] 101. Behrens, H.; Roux, J.; Neuville, D.R.; Siemann, M. Quantification of dissolved H2 O in silicate glasses using confocal microRaman spectroscopy. Chem. Geol. 2006, 229, 96–112. [CrossRef] 102. Di Muro, A.; Villemant, B.; Montagnac, G.; Scaillet, B.; Reynard, B. Quantification of water content and speciation in natural silicic glasses (phonolite, dacite, rhyolite) by confocal microRaman spectdrometry. Geochim. Cosmochim. Acta 2006, 70, 2868–2884. [CrossRef]
Int. J. Mol. Sci. 2015, 16, 30223–30250
103. Hervig, R.L.; Mazdab, F.K.; Moore, G.; McMillan, P.F. Analyzing hydrogen (H2 O) in silicate glass by secondary ion mass spectrometry and reflectance Fourier transform infrared spectroscopy. In Melt Inclusions in Volcanic Systems: Methods, Applications and Problems; de Vivo, B., Bodnar, R.J., Eds.; Elsevier: New York, NY, USA, 2003; pp. 83–103. 104. Humphreys, M.C.S.; Menand, T.; Blundy, J.D.; Klimm, K. Magma ascent rates in explosive eruptions: Constraints from H2 O diffusion in melt inclusions. Earth Planet. Sci. Lett. 2008, 270, 25–40. [CrossRef] 105. Berlo, K.; Tuffen, H.; Smith, V.; Castro, J.M.; Pyle, D.; Mather, T.; Geraki, K. Element variations in rhyolitic magma resulting from gas transport. Geochim. Cosmochim. Acta 2013, 121, 436–451. [CrossRef] 106. Ihinger, P.D.; Hervig, R.L.; McMillan, P.F. Analytical methods for volatiles in glasses. Rev. Mineral. 1994, 30, 67–121. 107. Nieuwoudt, M.K.; Simpson, M.P.; Tobin, M.; Puskar, L. Synchrotron FTIR microscopy of synthetic and natural CO2 -H2 O fluid inclusions. Vib. Spectrosc. 2014, 75, 136–148. [CrossRef] 108. Lowenstern, J.B.; Pitcher, B.W. Analysis of H2 O in silicate glass using attenuated total reflectance (ATR) micro-FTIR spectroscopy. Am. Mineral. 2013, 98, 1660–1668. [CrossRef] 109. Dixon, J.E.; Pan, V. Determination of the molar absorptivity of dissolved carbonate in basaltic glass. Am. Mineral. 1995, 80, 1339–1342. 110. Mormone, A.; Piochi, M.; Bellatreccia, F.; de Astis, G.; Moretti, R.; Della Ventura, G.; Cavallo, A.; Mangiacapra, A. A CO2 -rich magma source beneath the Phlegraean Volcanic District (Southern Italy): Evidence from a melt inclusion study. Chem. Geol. 2011, 287, 66–80. [CrossRef] 111. Lange, R.A.; Carmichael, I.S. Densities of Na2 O-K2 O-MgO-FeO-Fe2 O3 -Al2 O3 -TiO2 -SiO2 liquids: New measurements and derived partial molar properties. Geochim. Cosmochim. Acta 1987, 51, 2931–2946. [CrossRef] 112. Ochs, F.A., III; Lange, R.A. The density of hydrous magmatic liquids. Science 1999, 283, 1314–1317. [CrossRef] [PubMed] 113. Tamic, N.; Behrens, H.; Holtz, F. The solubility of H2 O and CO2 in rhyolitic melts in equilibrium with a mixed CO2 -H2 O fluid phase. Chem. Geol. 2001, 174, 333–347. [CrossRef] 114. Wysoczanski, R.; Tani, K. Spectroscopic FTIR imaging of water species in silicic volcanic glasses and melt inclusions: An example from the Izu-Bonin arc. J. Volcanol. Geotherm. Res. 2006, 156, 302–314. [CrossRef] 115. Nichols, A.R.L.; Wysoczanski, R.J. Using micro-FTIR spectroscopy to measure volatile contents in small and unexposed inclusions hosted in olivine crystals. Chem. Geol. 2007, 242, 371–384. [CrossRef] 116. Castro, J.M.; Manga, M.; Martin, M.C. Vesiculation rates of obsidian domes inferred from H2 O concentration profiles. Geophys. Res. Lett. 2005, 32, 1–5. [CrossRef] 117. Castro, J.M.; Dingwell, D.B. Rapid ascent of rhyolitic magma at Chaitén volcano, Chile. Nature 2009, 461, 780–784. [CrossRef] [PubMed] 118. Watkins, J.M.; Manga, M.; DePaolo, D.J. Bubble geobarometry: A record of pressure changes, degassing, and regassing at Mono Craters, California. Geology 2012, 40, 699–702. [CrossRef] 119. Della Ventura, G.; Marcelli, A.; Bellatreccia, F. SR-FTIR microscopy and FTIR imaging in the Earth sciences. Rev. Mineral. Geochem. 2014, 78, 447–479. [CrossRef] 120. Peslier, A.H. A review of water contents of nominally anhydrous natural minerals in the mantlels of Earth, Mars, and the Moon. J. Volcanol. Geotherm. Res. 2010, 197, 239–258. [CrossRef] 121. Della Ventura, G.; Bellatreccia, F.; Parodi, G.C.; Cámara, F.; Piccinini, M. Single-crystal FTIR and X-ray study of vishnevite, ideally [Na2 (SO4 )][Na2 (H2 O)2 ](Si6 Al6 O24 ). Am. Mineral. 2007, 92, 713–721. [CrossRef] 122. Bellatreccia, F.; Della Ventura, G.; Ottolini, L.; Libowitzky, E.; Beran, A. The quantitative analysis of OH in vesuviantie: A polirized FTIR and SIMS study. Phys. Chem. Miner. 2005, 32, 65–76. [CrossRef] 123. Roedder, E. Fluid Inclusions; Mineralogical Society of America: Chantilly, VA, USA, 1984; p. 644. 124. Danyushevsky, L.V.; McNeill, A.W.; Sobolev, A.V. Experimental and petrological studies of melt inclusions in phenocrysts from mantle-derived magmas: An overview of techniques, advantages and complications. Chem. Geol. 2002, 183, 5–24. [CrossRef] 125. Thomas, R.; Kamenetsky, V.S.; Davidson, P. Laser Raman spectroscopic measurements of water in unexposed glass inclusions. Am. Mineral. 2006, 91, 467–470. [CrossRef] 126. Guilhaumou, N.; Sautter, V.; Dumas, P. Synchrotron FTIR microanalysis of volatiles in melt inclusions and exsolved particles in ultramafic deep-seated garnets. Chem. Geol. 2005, 223, 82–92. [CrossRef]
Int. J. Mol. Sci. 2015, 16, 30223–30250
127. Mercier, M.; Di Muro, A.; Métrich, N.; Giordano, D.; Belhadj, O.; Mandeville, C.W. Spectroscopic analysis (FTIR, Raman) of water in mafic and intermediate glasses and glass inclusions. Geochim. Cosmochim. Acta 2010, 74, 5641–5656. [CrossRef] 128. Pironon, J.; Barres, O. Semi-quantitative FT-IR microanalysis limits: Evidence from synthetic hydrocarbon fluid inclusions in sylvite. Geochim. Cosmochim. Acta 1990, 54, 509–518. [CrossRef] 129. Pironon, J.; Barres, O. FT-IR microanalysis of hydrocarbon fluid inclusions. Chem. Geol. 1990, 84, 224–226. [CrossRef] 130. Barrès, O.; Burneau, A.; Dubessy, J.; Pagel, M. Application of micro-FT-IR spectroscopy to individual hydrocarbon fluid inclusion analysis. Appl. Spectrosc. 1987, 41, 1000–1008. [CrossRef] 131. Bourdet, J.; Burruss, R.C.; Chou, I-M.; Kempton, R.; Liu, K.; Hung, N.V. Evidence for a palaeo-oil column and alteration of residual oil in a gas-condensate field: Integrated oil inclusion and experimental results. Geochim. Cosmochim. Acta 2014, 142, 362–385. [CrossRef] 132. Nowak, M.; Behrens, H. Water in rhyolitic magmas: Getting a grip on a slippery problem. Earth Planet. Sci. Lett. 2001, 184, 515–522. [CrossRef] 133. Behrens, H.; Nowak, M. Quantification of H2 O speciation in silicate glasses and melts by IR spectroscopyin situ versus quench techniques. Phase Transit. 2003, 76, 45–61. [CrossRef] 134. Prasad, R.S.R.; Prasad, K.S.; Murthy, S.R. Dehydration of natural stilbite: An in situ FTIR study. Am. Mineral. 2005, 90, 1636–1640. [CrossRef] 135. Kolesov, B.A.; Geiger, C.A. Behavior of H2 O molecules in the channels of natrolite and scolecite: A Raman and IR spectroscopic investigation of hydrous microporous silicates. Am. Mineral. 2006, 91, 1039–1048. [CrossRef] 136. Prasad, R.S.R.; Prasad, K.S.; Chaitanya, V.K.; Babu, E.V.S.S.K.; Sreedhar, B.; Murthy, S.R. In situ FTIR study on the dehydration of natural geothite. J. Asian Earth Sci. 2006, 27, 503–511. [CrossRef] 137. Prasad, R.S.R.; Prasad, K.S. Dehydration and rehydration of mesolite: An in situ FTIR study. Microporous Mesoporous Mater. 2007, 100, 287–294. [CrossRef] 138. Tokiwai, K.; Nakashima, S. Integral molar absorptivities of OH in muscovite at 20 to 650 ˝ C by in situ high-temperature IR microspectroscopy. Am. Mineral. 2010, 95, 1052–1059. [CrossRef] 139. Dutta, S.; Hartkopf-Fröder, C.; Witte, K.; Brocke, R.; Mann, U. Molecular characterization of fossil palynomorphs by transmission micro-FTIR spectroscopy: Implications for hydrocarbon source evaluation. Int. J. Coal Geol. 2013, 115, 13–23. [CrossRef] 140. Dutta, S.; Brocke, R.; Hartkopf-Fröder, C.; Littke, R.; Wilkes, H.; Mann, U. Highly aromatic character of biogeomacromolecules in Chitinozoa: A spectroscopic and pyrolytic study. Org. Geochem. 2007, 38, 1625–1642. [CrossRef] 141. Dutta, S.; Hartkopf-Fröder, C.; Mann, U.; Wilkes, H.; Brocke, R.; Bertram, N. Macromolecular composition of Palaeozoic scolecodonts: Insights into the molecular taphonomy of zoomorphs. Lethaia 2009, 43, 334–343. [CrossRef] 142. Igisu, M.; Ueno, Y.; Shimojima, M.; Nakashima, S.; Awramik, S.M.; Ohta, H.; Maruyama, S. Micro-FTIR spectroscopic signatures of Bacterial lipids in Proterozoic microfossils. Precambrian Res. 2009, 173, 19–26. [CrossRef] 143. Han, J.; Calvin, M. Hydrocarbon distribution of algae and bacteria, and microbiological activity in sediments. Proc. Natl. Acad. Sci. USA 1983, 64, 436–443. [CrossRef] 144. Ladygina, N.; Dedyukhina, E.G.; Vainshtein, M.B. A review on microbial synthesis of hydrocarbons. Process Biochem. 2006, 41, 1001–1014. [CrossRef] 145. Igisu, M.; Komiya, T.; Kawashima, M.; Nakashima, S.; Ueno, Y.; Han, J.; Shu, D.; Li, Y.; Guo, J.; Maruyama, S.; Takai, K. FTIR microspectroscopy of Ediacaran phosphatized microfossils from the Doushantuo Formation, Weng’an, South China. Gondwana Res. 2014, 25, 1120–1138. [CrossRef] ˚ 146. Zodrow, E.L.; Mastalerz, M.; Orem, W.H.; Šimunek, Z.; Bashforth, A.R. Functional groups and elemental analyses of cuticular morphotypes of Cordaites principalies (Germar) Geinitz, Carboniferous Martitimes Basin, Canada. Int. J. Coal Geol. 2000, 45, 1–19. [CrossRef] 147. Zodrow, E.L.; D'Angelo, J.A.; Mastalerz, M.; Keefe, D. Compression-cuticle relationship of seed ferns: Insights from liquid-solid states FTIR (Late Palaeozoic-Early Mesozoic, Canada-Spain-Argentina). Int. J. Coal Geol. 2009, 779, 61–73. [CrossRef]