曹平,杨先贵,辛阳,王公应.碳酸二甲酯和乙酸苯酯合成碳酸二苯酯的研究--焙烧温度对MoO3催化剂性能的影响[J].分子催化,2011,(6):520-526
碳酸二甲酯和乙酸苯酯合成碳酸二苯酯的研究--焙烧温度对MoO3催化剂性能的影响
Effect of Calcination Temperature on Properties of MoO3 Catalyst for Transesterification of Dimethyl Carbonate and Phenyl Acetate to Diphenyl Carbonate
投稿时间:2011-11-29  修订日期:2011-12-30
DOI:
中文关键词:  焙烧温度  MoO3  碳酸二甲酯  乙酸苯酯  碳酸二苯酯  机理
英文关键词:calcination temperature  molybdenum trioxide  dimethyl carbonate  phenyl acetate  diphenyl carbonate  mechanism
基金项目:国家“十一五”科技支撑计划(2006BAE02B03)资助项目;江苏省常州市工业科技攻关计划(CE2008091)资助项目;重庆市教育委员会科学技术研究项目(KJ110815);重庆理工大学科研启动基金项目(2010ZD29)
作者单位E-mail
曹平 重庆理工大学 c.p-9@163.com 
杨先贵 中科院成都有机化学有限公司 yangxg@cioc.ac.cn 
辛阳 常州化学研究所 xinyang2002@foxmail.com 
王公应* 中科院成都有机化学有限公司 gywang@cioc.ac.cn 
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中文摘要:
      用焙烧法制备了碳酸二甲酯(DMC)与乙酸苯酯(PA)酯交换合成碳酸二苯酯(DPC)反应的正交晶系MoO3催化剂,并用N2吸附-脱附法(BET)、X射线衍射(XRD)、扫描电镜(SEM)等表征手段,考察了焙烧温度对催化剂结构和催化性能的影响。结果表明,随着焙烧温度的升高,催化剂的比表面积逐渐减小,正交晶系MoO3的(110)、(021)晶面强度逐渐减弱,(020)、(040)、(060)晶面强度增强,(021)和/或(110)晶面有利于酯交换反应。过高的焙烧温度,使得正交晶系MoO3晶体结构发生变化,催化剂活性降低。另外,本文通过改变物料投加顺序,就MoO3催化DMC和PA合成DPC反应机理进行了探索。
英文摘要:
      Molybdenum trioxide catalyst for the transesterification of phenyl acetate (PA) and dimethyl carbonate (DMC) to diphenyl carbonate (DPC) was prepared by a calcining method. The structure and catalytic properties of the catalyst synthesized at different temperatures were characterized by N2 absorption-desorption(BET), X-ray diffraction(XRD),scanning electron microscopy(SEM). The results showed that, the catalyst had an orthorhombic structure, with the increase of calcination temperature, the specific surface area of the catalyst was decreased, the diffraction intensity of the (110) and (021) faces decreased, and the diffraction intensity of the (020), (040), and (060) faces increased, and the face (021) and/or (110) are/is favorable to the transesterification of DMC and PA to DPC. And too high calcination temperature would deteriorate the structure and catalyst activity. Furthermore, a plausible mechanism for the transesterification of DMC and PA to DPC catalyzed by MoO3 was proposed by changing the feeding order of the materials and catalyst.
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