4.8 Article

Heterogeneous Mn-Based Catalysts for the Aerobic Conversion of Methane-to-Methyl Trifluoroacetate

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ACS CATALYSIS
卷 13, 期 6, 页码 3896-3901

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AMER CHEMICAL SOC
DOI: 10.1021/acscatal.2c062923896

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heterogeneous catalysis; methane partial oxidation; product protection; methyl trifluoroacetate; supported manganese catalysts

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Methane conversion strategies with in situ esterification achieve higher yields but operate under unfavorable conditions. Limited research has been done on heterogeneous catalysts for methane-to-methyl-ester conversion and on the activity of manganese for methane conversion. This study demonstrates the activity of silica-, titania-, and zirconia-supported manganese catalysts for methane-to-methyl-ester conversion and shows that silica-supported catalyst exhibits high overall activity.
Methane conversion strategies that protect meth-anol via in situ esterification achieve higher yields compared to direct methane conversion without product protection; however, most of these high-yield systems operate under unfavorable conditions. To date, there is very limited work in developing heterogeneous catalysts for methane-to-methyl-ester conversion, and studies demonstrating the activity of manganese for methane conversion are limited. We have prepared a series of silica-, titania-, and zirconia-supported manganese catalysts and measured the activity of these catalysts for the aerobic conversion of methane to methyl trifluoroacetate in diluted trifluoroacetate acid. The silica-supported catalyst exhibits high overall activity, but significant amounts of homogeneously active manganese are observed. Titania-and zirconia-supported manganese catalysts catalyze the reaction heterogeneously with activities up to 613 mu mol gcat-1 h-1 and show nondetectable leaching. Manganese oxide is poorly dispersed on titania and zirconia, whereas high dispersion is realized on silica. This work demonstrates a facilely synthesized supported manganese catalyst that converts methane heterogeneously in satisfactory yields under improved conditions in a diluted acid, compared to those of conventional methane-to-methyl-ester systems.

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