Organic structural properties of kerogen as predictors of source rock type and hydrocarbon potential

被引:31
作者
Longbottom, Todd L. [1 ]
Hockaday, William C. [1 ]
Boling, Kenneth S. [1 ,2 ]
Li, Gaoyuan [3 ]
Letourmy, Yohan [1 ]
Dong, Hailiang [3 ,4 ]
Dworkin, Stephen I. [1 ]
机构
[1] Baylor Univ, Dept Geosci, Waco, TX 76706 USA
[2] Univ Tennessee, Dept Earth & Planetary Sci, Knoxville, TN 37916 USA
[3] China Univ Geosci, State Key Lab Biogeol & Environm Geol, Beijing 100083, Peoples R China
[4] Miami Univ, Dept Geol & Environm Earth Sci, Oxford, OH 45056 USA
关键词
Kerogen; C-13; NMR; Pyrolysis; Cretaceous source rock; Coal; NUCLEAR-MAGNETIC-RESONANCE; C-13; NMR-SPECTRA; DETERMINING QUANTITATION; MOLECULAR-STRUCTURE; EVAL PYROLYSIS; OIL SHALES; MAS NMR; MATTER; SPECTROSCOPY; YIELDS;
D O I
10.1016/j.fuel.2016.07.066
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
This study improves upon previously identified correlations between the chemical structure of kerogen and potential hydrocarbon (oil and gas) yields assayed by Rock-Eval pyrolysis. We propose a quantitative structure-catagenesis relationship that predicts the hydrocarbon generation potential of source rocks and of lacustrine, marine, and terrestrial origin (types I, II, and humic coals). We used one-dimensional solid-state C-13 Nuclear Magnetic Resonance (C-13 NMR) spectroscopy with H-1 spectral editing to determine the abundance of carbon functional groups, including non-protonated and mobile groups. An NMR-based van Krevelen analysis readily separated the kerogen types. Single regression matrices of NMR-based structure parameters against Rock-Eval hydrocarbon yield revealed distinct dynamics of the kerogen types upon pyrolysis. Multiple regression showed that alkyl, oxygen-substituted alkyl, and carbonyl groups were strong contributors to hydrocarbon production, while oxygen-substituted aromatic carbons were strongly counterproductive. Catagenetic relationships established for kerogen provide insight into kerogen structure evolution upon pyrolysis, and can more closely constrain the mechanisms of hydrocarbon generation for use in sedimentary basin modeling. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:792 / 798
页数:7
相关论文
共 50 条
[1]  
[Anonymous], 1984, PETROLEUM FORMATION
[2]  
[Anonymous], 1961, COAL TYPOLOGY CHEM P
[3]   Precursor biostructures in kerogen matrix revealed by oxidative degradation:: oxidation of kerogen from Estonian kukersite [J].
Bajc, S ;
Amblès, A ;
Largeau, C ;
Derenne, S ;
Vitorovic, D .
ORGANIC GEOCHEMISTRY, 2001, 32 (06) :773-784
[4]   Cycling and composition of organic matter in terrestrial and marine ecosystems [J].
Baldock, JA ;
Masiello, CA ;
Gélinas, Y ;
Hedges, JI .
MARINE CHEMISTRY, 2004, 92 (1-4) :39-64
[5]  
Barwise A., 1984, Organic geochemistry, V6, P343, DOI [DOI 10.1016/0146-6380, DOI 10.1016/0146-6380(84)90056-1]
[6]   Hydropyrolysis of algae, bacteria, archaea and lake sediments; insights into the origin of nitrogen compounds in petroleum [J].
Bennett, B ;
Lager, A ;
Russell, CA ;
Love, GD ;
Larter, SR .
ORGANIC GEOCHEMISTRY, 2004, 35 (11-12) :1427-1439
[7]   Elucidation of the Alum Shale kerogen structure using a multi-disciplinary approach [J].
Bharati, S ;
Patience, RL ;
Larter, SR ;
Standen, G ;
Poplett, IJF .
ORGANIC GEOCHEMISTRY, 1995, 23 (11-12) :1043-1058
[8]   Origin of organic matter in the Eagle Ford Formation [J].
Boling, Kenneth S. ;
Dworkin, Stephen I. .
INTERPRETATION-A JOURNAL OF SUBSURFACE CHARACTERIZATION, 2015, 3 (01) :SH27-SH39
[9]   MOLECULAR CHARACTERIZATION OF KEROGEN FROM THE KIMMERIDGE CLAY FORMATION BY MILD SELECTIVE CHEMICAL DEGRADATION AND SOLID-STATE C-13-NMR [J].
BOUCHER, RJ ;
STANDEN, G ;
PATIENCE, RL ;
EGLINTON, G .
ORGANIC GEOCHEMISTRY, 1990, 16 (4-6) :951-958
[10]   OXYGEN GROUPS AND OIL SUPPRESSION DURING COAL PYROLYSIS [J].
BOUDOU, JP ;
ESPITALIE, J ;
BIMER, J ;
SALBUT, PD .
ENERGY & FUELS, 1994, 8 (04) :972-977