Characterization of oil shale, isolated kerogen, and postpyrolysis residues using advanced 13C solid-state nuclear magnetic resonance spectroscopy

被引:34
|
作者
Cao, Xiaoyan [1 ]
Birdwell, Justin E. [2 ]
Chappell, Mark A. [3 ]
Li, Yuan [1 ]
Pignatello, Joseph J. [4 ]
Mao, Jingdong [1 ]
机构
[1] Old Dominion Univ, Dept Chem & Biochem, Norfolk, VA 23529 USA
[2] US Geol Survey, Denver Fed Ctr, Denver, CO 80225 USA
[3] USA, Environm Lab, Corps Engineers, Vicksburg, MS USA
[4] Connecticut Agr Expt Stn, Dept Environm Sci, New Haven, CT 06504 USA
基金
美国国家科学基金会;
关键词
NMR-SPECTROSCOPY; THERMAL MATURATION; HUMIC SUBSTANCES; MAS NMR; PYROLYSIS; CARBON; DEGRADATION;
D O I
10.1306/09101211189
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
Characterization of oil shale kerogen and organic residues remaining in postpyrolysis spent shale is critical to the understanding of the oil generation process and approaches to dealing with issues related to spent shale. The chemical structure of organic matter in raw oil shale and spent shale samples was examined in this study using advanced solid-state C-13 nuclear magnetic resonance (NMR) spectroscopy. Oil shale was collected from Mahogany zone outcrops in the Piceance Basin. Five samples were analyzed: (1) raw oil shale, (2) isolated kerogen, (3) oil shale extracted with chloroform, (4) oil shale retorted in an open system at 500 degrees C to mimic surface retorting, and (5) oil shale retorted in a closed system at 360 degrees C to simulate in-situ retorting. The NMR methods applied included quantitative direct polarization with magic-angle spinning at 13 kHz, cross polarization with total sideband suppression, dipolar dephasing, CHn selection, C-13 chemical shift anisotropy filtering, and H-1-C-13 long-range recoupled dipolar dephasing. The NMR results showed that, relative to the raw oil shale, (1) bitumen extraction and kerogen isolation by demineralization removed some oxygen-containing and alkyl moieties; (2) unpyrolyzed samples had low aromatic condensation; (3) oil shale pyrolysis removed aliphatic moieties, leaving behind residues enriched in aromatic carbon; and (4) oil shale retorted in an open system at 500 degrees C contained larger aromatic clusters and more protonated aromatic moieties than oil shale retorted in a closed system at 360 degrees C, which contained more total aromatic carbon with a wide range of cluster sizes.
引用
收藏
页码:421 / 436
页数:16
相关论文
共 50 条
  • [31] Chlorination of Hydrogenated Silicon Nanosheets Revealed by Solid-State Nuclear Magnetic Resonance Spectroscopy
    Dorn, Rick W.
    Ryan, Bradley J.
    Lamahewage, Sujeewa N. S.
    V. Dodson, Mark
    Essner, Jeremy B.
    Biswas, Rana
    Panthani, Matthew G.
    Rossini, Aaron J.
    CHEMISTRY OF MATERIALS, 2023, 35 (02) : 539 - 548
  • [32] A study on molecular structural evolution of type II kerogen in a gold tube thermal system: Insights from solid-state 13C NMR
    Zhang, Deping
    Cao, Huairen
    Lei, Yan
    Wu, Hao
    Wang, Xiaoyu
    Guo, Xuelian
    Yan, Jianping
    Wang, Shuhua
    Shi, Tianchi
    Li, Haolin
    Zou, Yan-rong
    Peng, Ping'an
    FUEL, 2023, 331
  • [33] Metabolism of lactate in cultured GABAergic neurons studied by 13C nuclear magnetic resonance spectroscopy
    Waagepetersen, HS
    Bakken, IJ
    Larsson, OM
    Sonnewald, U
    Schousboe, A
    JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1998, 18 (01) : 109 - 117
  • [34] Quantitative Identification of Metastable Magnesium Carbonate Minerals by Solid-State 13C NMR Spectroscopy
    Moore, Jeremy K.
    Surface, J. Andrew
    Brenner, Allison
    Skemer, Philip
    Conradi, Mark S.
    Hayes, Sophia E.
    ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2015, 49 (01) : 657 - 664
  • [35] Analyzing the effects of thermal stress on insulator papers by solid-state 13C NMR spectroscopy
    Jusner, Paul
    Bacher, Markus
    Simon, Jonas
    Bausch, Florian
    Khaliliyan, Hajar
    Schiehser, Sonja
    Sumerskii, Ivan
    Schwaiger, Elisabeth
    Potthast, Antje
    Rosenau, Thomas
    CELLULOSE, 2022, 29 (02) : 1081 - 1095
  • [36] Photocatalytic degradation of highly refractive phenolic polymer Mechanistic insights as revealed by Electron Spin Resonance (ESR) and solid-state 13C NMR spectroscopy
    Sundarapandiyan, Sundaramoorthy
    Renitha, Thankaswamy Shiny
    Sridevi, Janardhanam
    Saravanan, Palanivel
    Chandrasekaran, Bangaru
    Raju, Guntamadugu Bhaskar
    CHEMICAL ENGINEERING JOURNAL, 2017, 313 : 1112 - 1121
  • [37] The identification of synthetic cannabinoids surface coated on herbal substrates using solid-state nuclear magnetic resonance spectroscopy
    Burns, N. K.
    Theakstone, A. G.
    Zhu, H.
    O'Dell, L. A.
    Pearson, J. R.
    Ashton, T. D.
    Pfeffer, F. M.
    Conlan, X. A.
    ANALYTICA CHIMICA ACTA, 2020, 1104 : 105 - 109
  • [38] 13C-13C spin-coupling constants in crystalline 13C-labeled saccharides: conformational effects interrogated by solid-state 13C NMR spectroscopy
    Zhang, Wenhui
    Yoon, Mi-Kyung
    Meredith, Reagan J.
    Zajicek, Jaroslav
    Oliver, Allen G.
    Hadad, Matthew
    Frey, Michael H.
    Carmichael, Ian
    Serianni, Anthony S.
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2019, 21 (42) : 23576 - 23588
  • [39] Corrected solid-state 13C nuclear magnetic resonance peak assignment and side-group quantification of hydroxypropyl methylcellulose acetyl succinate pharmaceutical excipients
    Zheng, Zhaoxi
    Su, Yongchao
    Schmidt-Rohr, Klaus
    MAGNETIC RESONANCE IN CHEMISTRY, 2023, 61 (11) : 595 - 605
  • [40] 13C-13C Homonuclear Recoupling in Solid-State Nuclear Magnetic Resonance at a Moderately High Magic-Angle-Spinning Frequency
    Mithu, Venus Singh
    Bakthavatsalam, Subha
    Madhu, Perunthiruthy K.
    PLOS ONE, 2013, 8 (01):