2005
DOI: 10.1016/s0255-2701(04)00143-6
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The dehydrogenation of methanol to methyl formatePart I: Kinetic studies using copper-based catalysts

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Cited by 16 publications
(20 citation statements)
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“…Kinetics of the dehydrogenation of methanol to MF has been examined for a commercial copper-chromite catalyst. Following is the rate expression obtained by Huang et al [62,68]:…”
Section: Methanol Dehydration To Dmementioning
confidence: 99%
“…Kinetics of the dehydrogenation of methanol to MF has been examined for a commercial copper-chromite catalyst. Following is the rate expression obtained by Huang et al [62,68]:…”
Section: Methanol Dehydration To Dmementioning
confidence: 99%
“…40 and 41) can occur in the PROX system. CO + ½ O2 → CO2 ∆H 0 = -282.98 kJ/mol (40) H2 + ½ O2 → H2O ∆H0 = -241.82 kJ/mol (41) CO is a typical by-product in the production of hydrogen by reforming of alcohols or hydrocarbons and must be reduced down to ppm levels in order to be used as feed for proton-exchange membrane fuel cells. Up to date, several options for CO removal have been studied and the selective oxidation (CO-PROX) is considered one of the most H2 + CO + O2 (air) → CO2 + H2 (42) Many industrial applications using H2 as a feedstock require a H2 stream containing a little CO.…”
Section: Preferential Oxidation Of Comentioning
confidence: 99%
“…Many research projects sanctioned [12,[26][27][28][29], several Ph.D. theses approved [30][31][32][33][34], a number of patents granted [35][36][37][38][39] and numerous studies [14,15,17,19,[40][41][42] have been conducted on innovative preparation methods and utilizations of the copper chromite catalysts. However, preparation methods and utilizations of such catalysts have hardly been reviewed so far.…”
Section: Introductionmentioning
confidence: 99%
“…Methanol can be produced indirectly from the gasification of biomass through the process listed earlier and serves as a reactant to form many other high valued products such as acetic acid [46,47], acetic anhydride [47], BTX [48], chloromethanes [49], dimethyl oxalate [50], dimethyl carbonate [51], ethanol (and other higher alcohols [52]), ethylene [53] , ethylene glycol [54], formaldehyde [55,56], methyl acetate [57], methyl chloride [58], methyl formate [59][60][61], methyl esters [62,63], methyl glycolate [211,64], MTBE [65][66][67][68], methylamines [69][70][71], olefins, [72][73][74], propylene [75] and vinyl acetate [76]. Methanol can be the reactant to form many higher alcohols but one common practice is methanol coupling to form ethanol.…”
Section: Synthesis Of High-value Compounds Via Post-conversion Of Metmentioning
confidence: 99%