首页> 外文期刊>RSC Advances >Pt/Al2O3 coated with N-doped carbon as a highly selective and stable catalyst for catalytic hydrogenation of p-chloronitrobenzene to p-chloroaniline
【24h】

Pt/Al2O3 coated with N-doped carbon as a highly selective and stable catalyst for catalytic hydrogenation of p-chloronitrobenzene to p-chloroaniline

机译:涂有N-掺杂碳的Pt / Al 2 O 3,作为高精度且稳定的催化催化催化氢化对氯硝基苯催化加氢至对氯苯胺

获取原文
           

摘要

Selective catalytic hydrogenation of p -chloronitrobenzene on Pt-based catalysts is a green and high-efficient way for p -chloroaniline production. However, supported monometallic Pt catalysts often exhibit undesirable p -chloroaniline selectivity. We herein reported supported Pt catalysts with N-doped carbon (NC) as an overcoating (Pt/Al _(2) O _(3) @NC) to overcome the disadvantage. Three Pt/Al _(2) O _(3) @NC catalysts with different NC coating amounts were prepared by in situ carbonization of an ionic liquid. For comparison, Al _(2) O _(3) coated by NC and Pt/Al _(2) O _(3) coated by SiO _(2) were also prepared. A combination characterization confirmed that the NC overcoating was successfully formed on Pt/Al _(2) O _(3) surface and Pt particles were completely coated by NC layers when ion liquid amount increased to 25 μl per g catalyst. Due to the intimate contact of NC layers and Pt particles Pt-NC heterojunctions were effectively formed on the catalyst surface. For the catalytic hydrogenation of p -chloronitrobenzene, Pt/Al _(2) O _(3) @NC with 25 μl ionic liquid as the NC precursor exhibited 100% selectivity to p -chloroaniline at 100% conversion of p -chloronitrobenzene. A lower ionic liquid amount led to decreased selectivity to p -chloroaniline. Furthermore, no deactivation was observed on Pt/Al _(2) O _(3) @NC during 5 catalytic cycles. The findings in the study demonstrate that coating noble metal catalysts by N-doped carbon is a promising method to enhance the selectivity and stability for catalytic hydrogenation of p -chloronitrobenzene.
机译:对Pt基催化剂对P-氯苯硝基苯的选择性催化氢化是对对氯苯胺产生的绿色和高效的方式。然而,支持的单金属Pt催化剂通常表现出不希望的对氯苯胺选择性。我们在本文中,所谓的具有N-掺杂碳(NC)的支持的Pt催化剂作为覆盖(Pt / Al _(2)O _(3)o _(3))以克服缺点。通过离子液体的碳化制备具有不同Nc涂布量的三个Pt / Al _(2)O _(3)@ NC催化剂。为了比较,通过SiO_(2)涂覆的Nc和Pt / Al _(2)o _(3)涂覆的Al _(2)o _(3)也制备。组合表征证实,当离子液体量增加到每G催化剂25μl时,在Pt / Al _(2)O _(3)表面上成功形成了NC涂覆的成功形成,并且Pt颗粒通过NC层完全涂覆。由于NC层的紧密接触,并且Pt-NC杂交在催化剂表面上有效地形成。对于对氯苯硝基苯的催化氢化,具有25μL离子液体的Pt / Al _(2)O _(3)o _(3),因为Nc前体具有100%对对氯苯苯甲酸的100%的对氯苯胺的选择性。较低的离子液体量导致对对氯苯胺的选择性降低。此外,在5次催化循环期间,在Pt / Al _(2)O _(3)o _(3)o _(3)o _(3)上没有去活化。研究中的研究结果表明,通过N掺杂碳涂覆贵金属催化剂是提高对氯苯催化氢化的选择性和稳定性的有希望的方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
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