V
Vasant R. Choudhary
Researcher at National Chemical Laboratory
Publications - 386
Citations - 13683
Vasant R. Choudhary is an academic researcher from National Chemical Laboratory. The author has contributed to research in topics: Catalysis & Methane. The author has an hindex of 63, co-authored 386 publications receiving 12994 citations. Previous affiliations of Vasant R. Choudhary include Council of Scientific and Industrial Research.
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Catalysts for combustion of methane and lower alkanes
TL;DR: In this paper, a review of the use of catalysts for methane combustion in high temperature natural gas-turbines can be found, where a large amount of work has been undertaken to develop catalysts both for controlling methane emission as well as for generating power.
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Energy‐Efficient Syngas Production through Catalytic Oxy‐Methane Reforming Reactions
TL;DR: The catalytic oxy reforming of methane, which is an energy-efficient process that can produce syngas at extremely high space-time yields, is discussed in this Review.
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Acidity/basicity of rare-earth oxides and their catalytic activity in oxidative coupling of methane to C2-hydrocarbons
Vasant R. Choudhary,V.H. Rane +1 more
TL;DR: In this paper, the authors compared rare earth metal oxides for their acid and base strength distribution and their catalytic activity/selectivity in oxidative coupling of methane to C2-hydrocarbons at 973-1123 K (space velocity = 108,000 cm 3 · g −1 h −1 and CH 4 /O 2 = 4 and 8).
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Low-Temperature Nonoxidative Activation of Methane over H-Galloaluminosilicate (MFI) Zeolite
TL;DR: Methane can be highly activated, yielding high rates of conversion to higher hydrocarbons and aromatics by its reaction over H-galloaluminosilicate ZSM-5 type (MFI) zeolite in the presence of alkenes or higher alkanes.
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Role of chloride or bromide anions and protons for promoting the selective oxidation of H2 by O2 to H2O2 over supported Pd catalysts in an aqueous medium
TL;DR: In this article, the influence of protons and halide anions in the aqueous reaction medium on H 2 O 2 formation in the direct oxidation of H 2 to H 2O 2 (at 27 °C) over different supported Pd catalysts (i.e., Pd supported on carbon, alumina, gallia, silica, zirconia, or ceria) in their reduced form, and also on the activity of the catalysts for the destruction of H2 O 2 by its decomposition and/or hydrogenation reactions