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Abstract

AAPG Bulletin, V. 97, No. 3 (March 2013), P. 421436.

Copyright copy2013. The American Association of Petroleum Geologists. All rights reserved.

DOI:10.1306/09101211189

Characterization of Previous HitoilNext Hit Previous HitshaleNext Hit, isolated kerogen, and postpyrolysis residues using advanced 13C solid-state nuclear magnetic resonance spectroscopy

Xiaoyan Cao,1 Justin E. Birdwell,2 Mark A. Chappell,3 Yuan Li,4 Joseph J. Pignatello,5 Jingdong Mao6

1Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, Virginia; [email protected]
2U.S. Geological Survey, Denver Federal Center, Denver, Colorado; [email protected]
3Environmental Laboratory, U.S. Army Corps of Engineers, Vicksburg, Mississippi; [email protected]
4Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, Virginia; [email protected]
5Department of Environmental Sciences, The Connecticut Agricultural Experiment Station, New Haven, Connecticut; [email protected]
6Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, Virginia; [email protected]

ABSTRACT

Characterization of Previous HitoilNext Hit Previous HitshaleNext Hit kerogen and organic residues remaining in postpyrolysis spent Previous HitshaleNext Hit is critical to the understanding of the Previous HitoilNext Hit generation process and approaches to dealing with issues related to spent Previous HitshaleNext Hit. The chemical structure of organic matter in raw Previous HitoilNext Hit Previous HitshaleNext Hit and spent Previous HitshaleNext Hit samples was examined in this study using advanced solid-state 13C nuclear magnetic resonance (NMR) spectroscopy. Previous HitOilNext Hit Previous HitshaleNext Hit was collected from Mahogany zone outcrops in the Piceance Basin. Five samples were analyzed: (1) raw Previous HitoilNext Hit Previous HitshaleNext Hit, (2) isolated kerogen, (3) Previous HitoilNext Hit Previous HitshaleNext Hit extracted with chloroform, (4) Previous HitoilNext Hit Previous HitshaleNext Hit retorted in an open system at 500degC to mimic surface retorting, and (5) Previous HitoilNext Hit Previous HitshaleNext Hit retorted in a closed system at 360degC 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, 13C chemical shift anisotropy filtering, and 1H-13C long-range recoupled dipolar dephasing. The NMR results showed that, relative to the raw Previous HitoilNext Hit Previous HitshaleNext Hit, (1) bitumen extraction and kerogen isolation by demineralization removed some oxygen-containing and alkyl moieties; (2) unpyrolyzed samples had low aromatic condensation; (3) Previous HitoilNext Hit Previous HitshaleNext Hit pyrolysis removed aliphatic moieties, leaving behind residues enriched in aromatic carbon; and (4) Previous HitoilNext Hit Previous HitshaleNext Hit retorted in an open system at 500degC contained larger aromatic clusters and more protonated aromatic moieties than Previous HitoilNext Hit Previous HitshaleNext Hit retorted in a closed system at 360degC, which contained more total aromatic carbon with a wide range of cluster sizes.

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