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Promoted effect of zinc-nickel bimetallic oxides supported on HZSM-5 catalysts in aromatization of methanol

机译:HZSM-5催化剂上负载的锌镍双金属氧化物对甲醇芳构化的促进作用

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摘要

Zn/ZSM-5 (NZ2) and Zn/Ni/ZSM-5 (NZ3) as the catalysts for methanol to aromatics (MTA) were synthesized by a simple ultrasonic impregnation.The textural and acid properties of all catalysts were characterized using XRD,HRTEM,NH3-TPD,Py-IR,XPS,XRF and TG techniques.The XRD and HRTEM results showed that the basic zeolite structures were not affected much with the incorporation of Zn and Ni species.However,great changes have taken place in acid properties.The Py-IR and XPS results indicated that the Zn-Lewis acid sites (ZnOH+ species),which have stronger interaction with the zeolite framework compared with ZnO species,were generated at the expense of B acid sites with the incorporation of zinc species.Moreover,the product analysis results showed that the incorporation of zinc species promoted the primary aromatization by enhancing the dehydroaromatization and suppressing the cracking and subsequent H-transfer reaction.Furthermore,the addition of Ni species well inhibited the loss of zinc species by converting partial ZnO species to ZnOH+ species,and thus improved the aromatization activity and catalyst stability.The catalytic performance results showed that the NZ3 possess higher conversion of methanol in a longer time and lower average rate of coke formation compared with NZ2.In addition,the NZ3 also exhibited the highest yield of BTX as the reaction proceeds.
机译:通过简单的超声浸渍法合成了甲醇制芳烃的催化剂Zn / ZSM-5(NZ2)和Zn / Ni / ZSM-5(NZ3),并用XRD表征了所有催化剂的结构和酸性质。 HRTEM,NH3-TPD,Py-IR,XPS,XRF和TG技术.XRD和HRTEM结果表明,基本的沸石结构不受Zn和Ni种类的影响。然而,酸发生了巨大变化Py-IR和XPS结果表明,与ZnO物种相比,与沸石骨架相互作用更强的Zn-Lewis酸位(ZnOH +物种)是通过掺入锌物种而以B酸性位为代价而产生的此外,产品分析结果表明,锌物种的掺入通过增强脱氢芳构化和抑制裂解以及随后的H-转移反应而促进了初级芳构化。此外,镍物种的加入很好地抑制了锌的流失。通过将部分ZnO物种转化为ZnOH +物种,从而提高了芳构化活性和催化剂稳定性。催化性能结果表明,与NZ2相比,NZ3在更长的时间内具有更高的甲醇转化率和更低的平均焦炭生成率。随着反应的进行,NZ3的BTX收率也最高。

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  • 来源
    《天然气化学(英文版)》 |2017年第3期|540-548|共9页
  • 作者单位

    College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, Shanxi, China;

    College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, Shanxi, China;

    State Key Laboratory of Coal Conversion, Institute of Coal Chemistry of CAS, Taiyuan 030001, Shanxi, China;

    College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, Shanxi, China;

    College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, Shanxi, China;

    College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, Shanxi, China;

    State Key Laboratory of Coal Conversion, Institute of Coal Chemistry of CAS, Taiyuan 030001, Shanxi, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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