Muthu Kumaran Gnanamani

Dr. Muthu Kumaran Gnanamani

Clean Fuels and Chemicals group, Center for Applied Energy Research, University of Kentucky, 2540 Research Park Dr Lexington, KY 40511, USA
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Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 January 2016 in ACS Catalysis
Verified
Journal Article
Closed access
Muthu Kumaran GnanamaniMuthu Kumaran Gnanamani
Muthu Kumaran Gnanamani
Gary JacobsGary Jacobs
Gary Jacobs
HHHussein H. Hamdeh
Hussein H. Hamdeh
WSWilson D. Shafer
Wilson D. Shafer
FLFang Liu
Fang Liu
BDBurtron Davis
Burtron Davis

1 November 2020 in Applied Catalysis A: General
Verified
Journal Article
Closed access
MMMichela Martinelli
Michela Martinelli
Muthu Kumaran GnanamaniMuthu Kumaran Gnanamani
Muthu Kumaran Gnanamani
SLSteve LeViness
Steve LeViness
Gary JacobsGary Jacobs
Gary Jacobs
Wilson ShaferWilson Shafer
Wilson Shafer

1 October 2013 in Catalysis Today
Verified
Journal Article
Closed access
Muthu Kumaran GnanamaniMuthu Kumaran Gnanamani
Muthu Kumaran Gnanamani
Gary JacobsGary Jacobs
Gary Jacobs
WSWilson D. Shafer
Wilson D. Shafer
BDBurtron H. Davis
Burtron H. Davis

17 October 2011 in ACS Catalysis
Verified
Journal Article
Closed access
JMJanet Chakkamadathil Mohandas
Janet Chakkamadathil Mohandas
Muthu Kumaran GnanamaniMuthu Kumaran Gnanamani
Muthu Kumaran Gnanamani
Gary JacobsGary Jacobs
Gary Jacobs
WMWenping Ma
Wenping Ma
YJYaying Ji
Yaying Ji
BDBurtron Davis
Burtron Davis

14 March 2019 in Catalysts
Verified
Journal Article
Open access
PDF file
Wilson ShaferWilson Shafer
Wilson Shafer
Muthu Kumaran GnanamaniMuthu Kumaran Gnanamani
Muthu Kumaran Gnanamani
UGUschi M. Graham
Uschi M. Graham
JYJia Yang
Jia Yang
CMCornelius Masuku
Cornelius Masuku
BDBurtron Davis
Burtron Davis
The bulk of the products that were synthesized from Fischer–Tropsch synthesis (FTS) is a wide range (C1–C70+) of hydrocarbons, primarily straight-chained paraffins. Additional hydrocarbon products, which can also be a majority, are linear olefins, specifically: 1-olefin, trans-2-olefin, and cis-2-olefin. Minor hydrocarbon products can include isomerized hydrocarbons, predominantly methyl-branched paraffin, cyclic hydrocarbons mainly derived from high-temperature FTS and internal olefins. Combined, these products provide 80–95% of the total products (excluding CO2) generated from syngas. A vast number of different oxygenated species, such as aldehydes, ketones, acids, and alcohols, are also embedded in this product range. These materials can be used to probe the FTS mechanism or to produce alternative chemicals. The purpose of this article is to compare the product selectivity over several FTS catalysts. Discussions center on typical product selectivity of commonly used catalysts, as well as some uncommon formulations that display selectivity anomalies. Reaction tests were conducted while using an isothermal continuously stirred tank reactor. Carbon mole percentages of CO that are converted to specific materials for Co, Fe, and Ru catalysts vary, but they depend on support type (especially with cobalt and ruthenium) and promoters (especially with iron). All three active metals produced linear alcohols as the major oxygenated product. In addition, only iron produced significant selectivities to acids, aldehydes, and ketones. Iron catalysts consistently produced the most isomerized products of the catalysts that were tested. Not only does product selectivity provide a fingerprint of the catalyst formulation, but it also points to a viable proposed mechanistic route.

1 June 2011 in Catalysis Communications
Verified
Journal Article
Closed access
Muthu Kumaran GnanamaniMuthu Kumaran Gnanamani
Muthu Kumaran Gnanamani
WSWilson D. Shafer
Wilson D. Shafer
DSDennis E. Sparks
Dennis E. Sparks
BDBurtron H. Davis
Burtron H. Davis