TiO2SiO2未经H2SO4修饰和经H2SO4修饰后的理化性质及酸催化活性

Q4 Chemical Engineering 分子催化 Pub Date : 1994-10-13 DOI:10.1016/0304-5102(94)00117-0
Jong Rack Sohn , Hyang Ja Jang , Man Young Park , Eun Hee Park , Sang Eun Park
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引用次数: 25

摘要

以四氯化钛与水玻璃的混合溶液为原料,采用共沉淀法制备了一系列TiO2SiO2催化剂。用0.5 M H2SO4对部分样品进行改性,作为改性催化剂。SiO2中加入TiO2后,其酸性和酸强度增加,硅醇基OH和SiO拉伸带随TiO2含量的增加而向较低频率偏移。2-丙醇脱水和异丙烯脱烷基的催化活性随酸度的增加而增加,且能带向低频移动。改性催化剂的催化活性高于未改性催化剂,改性对2-丙醇脱水催化活性的影响大于对异丙烯脱烷基催化活性的影响。改性对催化剂活性的影响随着TiO2含量的增加而增强。实际上,92-TiO2SiO2/SO2−4对2-丙醇脱水的催化活性增量最大,10-TiO2SiO2/SO2−4的催化活性增量最小。
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Physicochemical properties of TiO2SiO2 unmodified and modified with H2SO4 and activity for acid catalysis

A series of TiO2SiO2 catalysts were prepared by coprecipitation from the mixed solution of titanium tetrachloride and sodium silicate. Some of the sample were modified with 0.5 M H2SO4 and used as modified catalysts. The addition of TiO2 to SiO2 caused the increase of acidity and acid strength, and the shifts of OH and SiO stretching bands of silanol group to lower frequencies in proportion to the TiO2 content. Catalytic activities for 2-propanol dehydration and cumene dealkylation increased in relation to the increase of acidity and the band shifts to lower frequencies. The catalytic activities of modified catalysts were higher than those of unmodified catalysts, and the effect of modification on catalytic activity was higher for 2-propanol dehydration than for cumene dealkylation. The effect of modification on catalytic activity increased with increasing TiO2 content of the catalysts. Actually, 92-TiO2SiO2/SO2−4 had the highest increment in catalytic activity and 10-TiO2SiO2/SO2−4 had the lowest increment for the 2-propanol dehydration.

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来源期刊
分子催化
分子催化 Chemical Engineering-Catalysis
CiteScore
1.50
自引率
0.00%
发文量
2959
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Author index Subject index Hydrolysis of sucrose by dealuminated Y-zeolites Synthesis and application of organophilic polystyrene-montmorillonite supported onium salts in organic reactions Effect of the reduction temperature on the selectivity of the high temperature reaction of acetone and hydrogen over alumina and titania supported nickel and cobalt catalysts
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