2004
DOI: 10.1016/j.apcata.2003.08.024
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Direct insertion of methane into C3–C4 paraffins over zeolite catalysts: a start to the development of new one-step catalytic processes for the gas-to-liquid transformation

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Cited by 40 publications
(30 citation statements)
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“…It seems that the alkanes (propane or ethane) could be more easily activated to give surface intermediate species, and then more methane could be activated to produce aromatics. Indeed, Echevsky et al [21] had reported similar results for the reaction of methane with isobutane over a 2% Ga/HZSM-5 catalyst. Nevertheless, the present results contradict with the work of Brandford et al [22].…”
Section: Influence Of Co 2 and Ch 4 Additive On The Catalytic Activitsupporting
confidence: 50%
“…It seems that the alkanes (propane or ethane) could be more easily activated to give surface intermediate species, and then more methane could be activated to produce aromatics. Indeed, Echevsky et al [21] had reported similar results for the reaction of methane with isobutane over a 2% Ga/HZSM-5 catalyst. Nevertheless, the present results contradict with the work of Brandford et al [22].…”
Section: Influence Of Co 2 and Ch 4 Additive On The Catalytic Activitsupporting
confidence: 50%
“…In the presence of alkenes or higher alkanes over Ga promoted ZSM-5 catalyst, they obtained a higher rate of methane conversion to higher hydrocarbons at 673-873 K. The similar results were reported by the other researchers afterwards [2][3][4][5][6][7][8][9][10]. The direct formation of benzene from methane at £823 K is thermodynamically unfavorable.…”
Section: Introductionsupporting
confidence: 89%
“…Aromatic compounds such as benzene, toluene, xylene and trimethylbenzene are important raw materials in the chemical industry; they are collected as by-products of coal coking or derived from processes of catalytic reforming and gasoline cracking. There are various routes for the conversion of natural gas into aromatic hydrocarbons, e.g., the direct aromatization route [2][3][4], syngas route [5][6][7], chloride route [8][9][10][11][12], and bromide route [13][14][15]. Recently, we reported a new route: first CH 3 Br is formed from CH 4 using HBr/H 2 O as mediator in the presence of oxygen, and then CH 3 Br is catalytically transformed into hydrocarbons or compounds of high carbon number [16][17][18][19][20].…”
Section: Introductionmentioning
confidence: 99%