...
首页> 外文期刊>Catalysis science & technology >Tailoring the selectivity in 2-butene conversion over supported d(0) group 4, 5 and 6 metal hydrides: from dimerization to metathesis
【24h】

Tailoring the selectivity in 2-butene conversion over supported d(0) group 4, 5 and 6 metal hydrides: from dimerization to metathesis

机译:根据受支持的D(0)组4、5和6金属氢化物来调整2-丁烯转化的选择性:从二聚化到元学

获取原文
获取原文并翻译 | 示例
           

摘要

2-Butenes are transformed in a continuous flow reactor over metal hydrides of zirconium, tantalum and tungsten supported on silica-alumina. Exceptionally high selectivity to dimeric products is obtained over supported zirconium hydride catalysts. Supported tantalum hydride gives high selectivity to dimeric products along with small amounts of metathesis products. Conversely, supported tungsten hydride leads only to metathesis products. The unprecedented selective production of mono-branched and di-branched octenes originates from the bi-functionality of the active sites, allowing isomerization of 2-butenes to 1-butene followed by fast insertion of 1-butene into the metal sec-butyl fragment.
机译:在二氧化硅 - 铝酸酯上支撑的锆,坦塔木和钨的金属氢化物上,将2丁烯转化为连续的流动反应器。 对二聚体产物的选择性异常高于氢化氢锆催化剂。 受支持的坦塔豪拉姆氢化物以及少量的元理解产物对二聚体产物具有高选择性。 相反,支持的钨氢化物仅导致元理解产物。 单分支和DI分支的八面体的前所未有的选择性生产起源于活性位点的双功能,从而使2-丁二烯到1-丁烯的异构化,然后将1-丁烯快速插入金属二丁烯中。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号