کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
69172 | 48532 | 2006 | 5 صفحه PDF | دانلود رایگان |

H3PMo12O40 (PMo) catalyst was immobilized on the aminated polystyrene (PS) support as a charge compensating component, by taking advantage of the overall negative charge of [PMo12O40]3−. It was revealed that PMo catalyst was finely and molecularly dispersed on the PS support via chemical immobilization. The supported H3PMo12O40–polystyrene (PMo–PS) catalyst was applied to the vapor-phase oxidation of methacrolein into methacrylic acid, a typical surface-type reaction. The PMo–PS catalyst exhibited higher conversion of methacrolein and higher selectivity for methacrylic acid than the unsupported PMo catalyst. It is concluded that [PMo12O40]3− species were chemically and finely immobilized on the PS support as charge matching species, and thus, the PMo–PS catalyst showed an excellent oxidation activity in the model surface-type reaction.
H3PMo12O40 (PMo) catalyst was immobilized on the aminated polystyrene (PS) support as a charge compensating component, by taking advantage of the overall negative charge of [PMo12O40]3−. The supported H3PMo12O40–polystyrene catalyst exhibited higher catalytic performance than the unsupported catalyst in the vapor-phase oxidation of methacrolein into methacrylic acid. Figure optionsDownload as PowerPoint slide
Journal: Journal of Molecular Catalysis A: Chemical - Volume 248, Issues 1–2, 3 April 2006, Pages 21–25