A NOVEL APPROACH TO CATALYTIC DESULFURIZATION OF COAL
Abstract
The nonionic superbase P(MeNCH{sub 2}CH{sub 2}){sub 3}N (A) efficiently desulfurizes trisulfides to disulfides and monosulfides, disulfides to monosulfides, and propylene sulfide to propene. S=P(MeNCH{sub 2}CH{sub 2}){sub 3}N (B) was formed as the sulfur acceptor. P(NMe{sub 2}){sub 3} was a much poorer desulfurizing agent than A under the same reaction conditions. Thiocyanates and triphenylphosphine sulfide were also desulfurized with A, but N-(phenylthio)phthalimide formed [A-SP]{sup +} phthalimide in quantitative yield.
- Authors:
- Publication Date:
- Research Org.:
- Federal Energy Technology Center Morgantown (FETC-MGN), Morgantown, WV (United States); Federal Energy Technology Center Pittsburgh (FETC-PGH), Pittsburgh, PA (United States)
- Sponsoring Org.:
- US Department of Energy (US)
- OSTI Identifier:
- 757297
- Report Number(s):
- DE-FG22-95PC95208-06
TRN: AH200031%%33
- DOE Contract Number:
- FG22-95PC95208
- Resource Type:
- Technical Report
- Resource Relation:
- Other Information: PBD: 31 Aug 1998
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 01 COAL, LIGNITE, AND PEAT; COAL; DESULFURIZATION; DISULFIDES; PROPYLENE; SULFIDES; SULFUR COMPOUNDS; REMOVAL; THIOCYANATES; CHEMICAL REACTION KINETICS
Citation Formats
Verkade, John G. A NOVEL APPROACH TO CATALYTIC DESULFURIZATION OF COAL. United States: N. p., 1998.
Web. doi:10.2172/757297.
Verkade, John G. A NOVEL APPROACH TO CATALYTIC DESULFURIZATION OF COAL. United States. https://doi.org/10.2172/757297
Verkade, John G. 1998.
"A NOVEL APPROACH TO CATALYTIC DESULFURIZATION OF COAL". United States. https://doi.org/10.2172/757297. https://www.osti.gov/servlets/purl/757297.
@article{osti_757297,
title = {A NOVEL APPROACH TO CATALYTIC DESULFURIZATION OF COAL},
author = {Verkade, John G},
abstractNote = {The nonionic superbase P(MeNCH{sub 2}CH{sub 2}){sub 3}N (A) efficiently desulfurizes trisulfides to disulfides and monosulfides, disulfides to monosulfides, and propylene sulfide to propene. S=P(MeNCH{sub 2}CH{sub 2}){sub 3}N (B) was formed as the sulfur acceptor. P(NMe{sub 2}){sub 3} was a much poorer desulfurizing agent than A under the same reaction conditions. Thiocyanates and triphenylphosphine sulfide were also desulfurized with A, but N-(phenylthio)phthalimide formed [A-SP]{sup +} phthalimide in quantitative yield.},
doi = {10.2172/757297},
url = {https://www.osti.gov/biblio/757297},
journal = {},
number = ,
volume = ,
place = {United States},
year = {Mon Aug 31 00:00:00 EDT 1998},
month = {Mon Aug 31 00:00:00 EDT 1998}
}
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