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Preparation and characterization of H_4SiW_(12)O_(40)@MIL-100(Fe) and its catalytic performance for synthesis of 4,4'-MDA 被引量:3
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作者 Yunhuan Kong Xiaomeng Cheng +2 位作者 Hualiang An Xinqiang Zhao Yanji Wang 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2018年第2期330-336,共7页
The catalytic performance of co mmonly used heteropolyacids (H3PW12O40, H4SiW12O40 and H3PMO12O40 synthesis of 4,4'-methylenedianiline (4,4'-MDA) from aniline and formaldehyde was evaluated and the result showed ... The catalytic performance of co mmonly used heteropolyacids (H3PW12O40, H4SiW12O40 and H3PMO12O40 synthesis of 4,4'-methylenedianiline (4,4'-MDA) from aniline and formaldehyde was evaluated and the result showed that H4SiW12O40 with moderate acid strength exhibited the best catalytic performance. Then HaSiW12O40@MIL-100(Fe) was prepared by encapsulating H4SiW12O40 within the pores of MIL-100(Fe) to facilitate its recovery and reuse. The prepared H4SiW12O40@MIL-100(Fe) was characterized by means of FT-IR, N2 adsorption-desorption, XRD, TG and then the catalytic performance was evaluated. The result showed that H4SiW12O40 was highly dispersed in the pores of MIL-100(Fe), and both the Keggin structure of HaSiW12O40 and the crystal skeleton structure of MIL-100(Fe) could be effectively/preserved. Furthermore, H4SiW12O40@ MIL-100(Fe) showed excellent catalytic performance under the following reaction conditions: a molar ratio of aniline to formaldehyde = 5, a mass ratio of catalyst to formaldehyde = 1.2, a reaction temperature of 120 ℃ and a reaction time of 6 h. Under the above reaction conditions, the conversion of aniline was 41.1%, and the yield and selectivity of 4,4'-MDA were 81,6% and 79.2%, respectively. Unfortunately, an appreciable loss in the catalytic activity of the recovered H4SiW12O40@MIL-100(Fe) was observed because of the blocking of the pores and the change of the acidity resulted from the adsorption of alkaline organics such as aniline and 4,4'-MDA. The adsorbed alkaline organics could be cleaned up when the recovered catalyst was washed by methanol and DMF. Then the catalyst was effectively reused up to three cycles without much loss in its activity. 展开更多
关键词 h4SiW12 O40@MIL- 100 Fe catalyst activation 4 4'-Methylenedianilinc synthesis Mukiphase reaction Stability
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外给电子体对BCM系列催化剂的影响 被引量:7
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作者 徐秀东 谭忠 +1 位作者 周奇龙 张锐 《石油化工》 CAS CSCD 北大核心 2020年第7期639-643,共5页
以二异丁基二甲氧基硅烷(Donor B)、环己基甲基二甲氧基硅烷、二环戊基二甲氧基硅烷(Donor D)、二异丙基二甲氧基硅烷(Donor P)和二苯基二甲氧基硅烷(DDS)为外给电子体,研究了它们对BCM-100H和BCM-200催化性能的影响,并与NG催化剂进行... 以二异丁基二甲氧基硅烷(Donor B)、环己基甲基二甲氧基硅烷、二环戊基二甲氧基硅烷(Donor D)、二异丙基二甲氧基硅烷(Donor P)和二苯基二甲氧基硅烷(DDS)为外给电子体,研究了它们对BCM-100H和BCM-200催化性能的影响,并与NG催化剂进行了对比。实验结果表明,无论采用哪种外给电子体,BCM-200的活性和立体定向性能最高,但氢调敏感性最低。BCM-200和NG催化剂采用Donor D时活性最高,BCM-100H采用Donor P时活性最高。当用Donor D时,三种催化剂的立体定向性能最高;当用Donor B和DDS时,三种催化剂的氢调敏感性最高。BCM-200制备的聚丙烯的堆密度及细粉含量最低,流动性最好。BCM-100H采用Donor P制备的聚丙烯的堆密度和细粉含量最低。BCM-200更适合开发有大分子牌号的聚丙烯树脂。当用Donor D时,三种催化剂制备的聚丙烯颗粒的MW均最大。 展开更多
关键词 外给电子体 聚丙烯 bcm-100h bcm-200 流动性 催化活性
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高流动高刚性抗冲共聚聚丙烯的工业化开发 被引量:14
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作者 王旭 《合成树脂及塑料》 CAS 北大核心 2018年第5期54-57,69,共5页
在Horizone工艺装置使用BCM-100H型催化剂成功开发高熔体流动速率高刚性抗冲共聚聚丙烯KH39M。讨论了KH39M生产的技术路线、操作条件、产品指标控制和试生产情况,对KH39M的力学性能、共聚单体含量、粉料粒径等进行了分析。结果表明:首... 在Horizone工艺装置使用BCM-100H型催化剂成功开发高熔体流动速率高刚性抗冲共聚聚丙烯KH39M。讨论了KH39M生产的技术路线、操作条件、产品指标控制和试生产情况,对KH39M的力学性能、共聚单体含量、粉料粒径等进行了分析。结果表明:首次生产的KH39M弯曲模量达1 590 MPa,简支梁缺口冲击强度达7.6 k J/m^2,下游用户测试结果表明,KH39M性能与进口同类产品相当。 展开更多
关键词 聚丙烯 ZIEGLER-NATTA催化剂 高流动 高刚性 bcm-100h型催化剂
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