Characterization of kerogen using solid-state nuclear magnetic resonance spectroscopy: A review

被引:50
作者
Cao, Xiaoyan [1 ]
Yang, John [2 ]
Mao, Jingdong [1 ]
机构
[1] Old Dominion Univ, Dept Chem & Biochem, Norfolk, VA 23529 USA
[2] Lincoln Univ Missouri, Dept Agr & Environm Sci, Jefferson City, MO 65102 USA
基金
美国国家科学基金会;
关键词
Kerogen; Oil shale; NMR; Quantification; Spectral editing; Aromatic cluster size; AMPLITUDE CROSS-POLARIZATION; PARTICLE-SIZE FRACTIONS; C-13; NMR-SPECTROSCOPY; OIL-SHALE KEROGEN; QUANTITATIVE RELIABILITY; MOLECULAR-STRUCTURE; THERMAL MATURATION; HUMIC SUBSTANCES; ORGANIC-MATTER; CPMAS NMR;
D O I
10.1016/j.coal.2011.12.001
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Heterogeneity, complexity, and insolubility of kerogen have presented a big challenge in its characterization. Among the various analytical methods applied to kerogen characterization, solid-state nuclear magnetic resonance (NMR) spectroscopy becomes increasingly the method of choice due to its capacity to provide comprehensive structural information nondestructively. This review first summarized the structural studies of oil shale and kerogen using solid-state NMR spectroscopy, including the applications in the comparative studies of kerogen and its source rocks (oil shale), evaluation of oil shale resource, determination of kerogen types, and assessment of thermal maturity. Then conventional solid-state NMR techniques used in the literature and limitations of C-13 cross polarization/magic angle spinning (C-13 CP/MAS) technique were critically reviewed. Finally, advanced C-13 NMR techniques were presented and their applications discussed. The conventional technique used for kerogen study was primarily C-13 CP/MAS, which was sometimes combined with dipolar dephasing. The drawbacks of C-13 CP/MAS technique include sidebands, baseline distortions, and poor quantification. The problems with deconvolution as an attempt to resolve overlapping peaks were also discussed. Possible solutions to these problems were provided. Recently, significant advances have been made in solid state NMR toward more structural details, as well as more reliable quantification. These advanced NMR techniques include spectral editing techniques, two dimensional H-1-C-13 heteronuclear correlation spectroscopy, H-1 spin diffusion, etc. Their applications allow for identification and quantification of specific functional groups, detection of connectivities and proximities of specific functional groups, examinations of domains and heterogeneities as well as estimation of aromatic cluster size for systematic characterization of kerogen. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:83 / 90
页数:8
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