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机构地区:[1]复旦大学化学系
出 处:《高等学校化学学报》1995年第12期1926-1929,共4页Chemical Journal of Chinese Universities
基 金:国家自然科学基金
摘 要:氯丙烯在不同催化剂表面上吸附的TPD结果表明:在TS-1上有三重脱附峰,而在TiO2/Silicalite上仅有单峰。H_2O_2或分子O_2在催化剂表面吸附后,在脱附物种中可用质谱检测到原子O(16)物种;说明H_O_2或分子O_2在样品表面存在解离吸附;并发现解离分子O_2的活性很低。TS-1能同时吸附氯丙烯和H_2O_2,而在SiO_2/Silicalite表面的吸附却与吸附顺序有关。环氧化活性顺序如下:TS-1(TPAOH)>TS-1(TPABr+NaOH)>TiO_2/Silicalite。TS-1沸石的高氧化活性可能与H_2O_2吸附后表面原子O(16)的形成有关。In the TPSR-TPD curves of allyl chloride, there are multiple desorption peaks (amount to triplet)on TS-1 zeolites,however there is only a single desorption peak on TiO2/silicalite. After the adsorption of H2O2 or molecular O2 separately,O(16)atoms are discovered in the desorbed species by MS. It is found that the activity of the samples dissociating molecular O2 into atomic O(16)is low. TS-1 zeolites can simultaneously adsorb H2O2 and allyl chloride, but the adsorption of both of them on TiO2/silicalite surface is relevant to adsorptive sequence, The order of epoxidation activity is as follows:TS-1(TPAOH)>TS-1 (TPABr+NaOH)>TiO2/silicalite, It is postulated that the higher oxidation activity of Ti-Si zeolites is related to the formation of surface O(16)atoms adsorbed on the zeolites after the adsorption of H2O2.
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