The dataset covers X-ray diffraction (XRD) applied for mineral determination in shales from the Utica, Excello, Niobrara, and Monterey formations. The XRD was performed prior to modified Rock-Eval pyrolysis, reflectance, organic petrology, and Fourier-transform infrared spectroscopy (FTIR) being employed to analyze geochemical properties; gas adsorption (CO2 and N2) was used to characterize pore structures.

Here the spatial variation in Raman estimates of thermal maturity within individual organic domains from several shale geologic reference materials originating from the Boquillas, Marcellus, Niobrara, and Woodford Formations are assessed from the respective Raman response. We show that for all four shales the thermal maturity parameters extracted from Raman spectra by iterative peak fitting can vary widely across distances of ≤5 µm within the same organic domain.

Raman spectroscopy was studied as a thermal maturity probe in a series of Upper Devonian Ohio Shale samples from the Appalachian Basin spanning from immature to dry gas conditions. Raman spectroscopy also was applied to samples spanning a similar thermal range created from 72-hour hydrous pyrolysis (HP) experiments of the Ohio Shale at temperatures from 300 to 360°C and isothermal HP experiments lasting up to 100 days of similar Devonian-Mississippian New Albany Shale. Raman spectra were treated by an automated evaluation software based on iterative and simultaneous modeling of signal and baseline functions to decrease subjectivity. Spectra show robust correlation to measured solid bitumen reflectance (BRo) values and were therefore used to construct logarithmic regression relationships for calculation of BRo equivalent values. Raman spectra show considerable differences between natural samples and HP. residues with similar measured BRo values, indicating as-yet undetermined differences in carbon chemistry. We speculate this result may be due to differences in the sampling interactions of Raman vs. reflectance measurements, and the incomplete nature of maturation reactions in the time-limited hydrous pyrolysis residues. Samples used in this study are similar in organic assemblage (dominantly solid bitumen) to other commonly exploited North American shale petroleum systems, i.e., Bakken, Barnett, Duvernay, Fayetteville and Woodford shales. Therefore, results presented herein may be broadly applicable to other important shale plays. However, caution is suggested and Raman spectroscopy as a thermal probe may need individual calibration in each shale play due to differences in solid bitumen carbon chemistry. Samples were collected and tested between 2013 and 2018, in studies preformed by Ryder et al., 2013; Hackley and Lewan, 2018; Hackley et al., 2017; Yang et al., 2017; Hackley and Lundsdorf, 2018.

Raman spectroscopy was studied as a thermal maturity probe in a series of Upper Devonian Ohio Shale samples from the Appalachian Basin spanning from immature to dry gas conditions. Raman spectroscopy also was applied to samples spanning a similar thermal range created from 72-hour hydrous pyrolysis (HP) experiments of the Ohio Shale at temperatures from 300 to 360°C and isothermal HP experiments lasting up to 100 days of similar Devonian-Mississippian New Albany Shale. Raman spectra were treated by an automated evaluation software based on iterative and simultaneous modeling of signal and baseline functions to decrease subjectivity. Spectra show robust correlation to measured solid bitumen reflectance (BRo) values and were therefore used to construct logarithmic regression relationships for calculation of BRo equivalent values. Raman spectra show considerable differences between natural samples and HP. residues with similar measured BRo values, indicating as-yet undetermined differences in carbon chemistry. We speculate this result may be due to differences in the sampling interactions of Raman vs. reflectance measurements, and the incomplete nature of maturation reactions in the time-limited hydrous pyrolysis residues. Samples used in this study are similar in organic assemblage (dominantly solid bitumen) to other commonly exploited North American shale petroleum systems, i.e., Bakken, Barnett, Duvernay, Fayetteville and Woodford shales. Therefore, results presented herein may be broadly applicable to other important shale plays. However, caution is suggested and Raman spectroscopy as a thermal probe may need individual calibration in each shale play due to differences in solid bitumen carbon chemistry. Samples were collected and tested between 2013 and 2018, in studies preformed by Ryder et al., 2013; Hackley and Lewan, 2018; Hackley et al., 2017; Yang et al., 2017; Hackley and Lundsdorf, 2018.

This data release is a compilation of published and unpublished thermal maturity and source rock geochemical data (Rock-Eval, pyrolysis) from subsurface wells in the Permian Basin, west Texas and southeast New Mexico. These data include 67 newly collected samples and analyses from Delaware Basin wells (identified as Cicero_2022), as well as 1028 previously unpublished USGS analyses from the entire province (identified as LIMS). Data were also synthesized from publicly available sources, such as theses and dissertations, state agencies and databases, as well as from the body of published literature.

This data release is a compilation of published and unpublished thermal maturity and source rock geochemical data (Rock-Eval, pyrolysis) from subsurface wells in the Permian Basin, west Texas and southeast New Mexico. These data include 67 newly collected samples and analyses from Delaware Basin wells (identified as Cicero_2022), as well as 1028 previously unpublished USGS analyses from the entire province (identified as LIMS). Data were also synthesized from publicly available sources, such as theses and dissertations, state agencies and databases, as well as from the body of published literature.

Solid organic matter (OM) in sedimentary rocks produces petroleum and solid bitumen when it undergoes thermal maturation. The solid OM is a ‘geomacromolecule’, usually representing a mixture of various organisms with distinct biogenic origins, and can have high heterogeneity in composition. Programmed pyrolysis is a common conventional method to reveal bulk geochemical characteristics of the dominant OM while detailed organic petrography is required to reveal information about the biogenic origin of contributing macerals. Despite advantages of programmed pyrolysis, it cannot provide information about the heterogeneity of chemical compositions present in the individual OM types. Therefore, other analytical techniques such as Raman spectroscopy are necessary. In this study, we compared geochemical characteristics and Raman spectra of two sets of naturally and artificially matured Bakken source rock samples. A continuous Raman spectral map on solid bitumen particles was created from the artificially matured hydrous pyrolysis residues, in particular, to show the systematic chemical modifications in microscale. Spectroscopy data was plotted for both sets against thermal maturity to compare maturation rate/path for these two separate groups. The outcome showed that artificial maturation through hydrous pyrolysis does not follow the same trend as naturally-matured samples although having similar solid bitumen reflectance values (%SBRo). Furthermore, Raman spectroscopy of solid bitumen from artificially matured samples indicated the heterogeneity of OM decreases as maturity increases. This represents an alteration in chemical structure towards more uniform compounds at higher maturity. This study may signify the potential of Raman spectroscopy as an alternative to the conventional (pseudo) Van Krevelen diagram, by revealing the underlying chemical changes. Finally, observation by Raman spectroscopy of chemical alteration of OM during artificial maturation may assist in the proposal of improved pyrolysis protocols to better resemble natural geologic processes.