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Effect of different acidity modifications on the activity and selectivity on H-ZSM5 zeolites in n-butene isomerization

机译:不同酸度修饰对正丁烯异构化过程中H-ZSM5沸石活性和选择性的影响

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摘要

H-ZSM-5 was modified by silylation [tetraethylorthosilicate (TEOS) and triaminopropyltriethoxysilane], alkali (NaOH), acid (HCl) and ammoniumhexafluorosilicate (AHFS) treatments. The parent and modified zeolite forms were tested in n-butene isomerization. Modifications affected total acidities, the strength of the acid sites, pore sizes and surface areas of the H-ZSM-5 differently. The modifications decreased the conversion obtained by the parent catalyst. TEOS and alkali modifications did not promote formation of isobutene. Pre-alkali treatment before acid treatment increased selectivity to isobutene from 56.0 to 66.7 %, while conversion changed a little, it dropped from 52 to 50 %. AHFS modification provided the highest enhancement in selectivity to isobutene (87.5 %) for which n-butene conversion was dropped by about 10 % compared to H-ZSM-5. This was attributed to a slight modification of the pore size and to the reduction in strong and weak acid sites and generation of new Lewis acid sites.
机译:通过甲硅烷基化[原硅酸四乙酯(TEOS)和三氨基丙基三乙氧基硅烷],碱(NaOH),酸(HCl)和六氟硅酸铵(AHFS)处理对H-ZSM-5进行改性。在正丁烯异构化中测试了母体和改性沸石的形式。修饰对H-ZSM-5的总酸度,酸位点强度,孔径和表面积的影响不同。改性降低了由母体催化剂获得的转化率。 TEOS和碱改性不会促进异丁烯的形成。酸处理前的碱前处理将对异丁烯的选择性从56.0增至66.7%,而转化率则有所变化,从52%降至50%。 AHFS改性对异丁烯的选择性提高了最高(87.5%),与H-ZSM-5相比,正丁烯的转化率下降了约10%。这归因于孔径的轻微改变以及强酸和弱酸位点的减少以及新路易斯酸位点的产生。

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