首页> 外文OA文献 >Synthesis of palladium nanoparticles over graphite oxide and carbon nanotubes by reduction in ethylene glycol and their catalytic performance on the chemoselective hydrogenation of para-chloronitrobenzene
【2h】

Synthesis of palladium nanoparticles over graphite oxide and carbon nanotubes by reduction in ethylene glycol and their catalytic performance on the chemoselective hydrogenation of para-chloronitrobenzene

机译:乙二醇还原在氧化石墨和碳纳米管上合成钯纳米粒子及其对对氯硝基苯化学选择性加氢的催化性能

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Pd nanoparticles have been synthesized over carbon nanotubes (CNT) and graphite oxide (GO) by reduction with ethylene glycol and by conventional impregnation method. The catalysts were tested on the chemoselective hydrogenation of p-chloronitrobenzene and the effect of the synthesis method and surface chemistry on their catalytic performance was evaluated. The catalysts were characterized by N2 adsorption/desorption isotherms at 77 K, TEM, powder X-ray diffraction, thermogravimetry, infrared and X-ray photoelectron spectroscopy and ICP-OES. It was observed that the synthesis of Pd nanoparticles employing ethylene glycol resulted in metallic palladium particles of smaller size compared to those prepared by the impregnation method and similar for both supports. The presence of oxygen groups on the support surface favored the activity and diminished the selectivity. It seems that ethylene glycol reacted with the surface groups of GO, this favoring the selectivity. The activity was higher over the CNT-based catalysts and both catalysts prepared by reduction in ethylene glycol were quite stable upon recycling.
机译:通过用乙二醇还原并通过常规浸渍方法,在碳纳米管(CNT)和氧化石墨(GO)上合成了Pd纳米颗粒。对催化剂进行了对氯硝基苯的化学选择性加氢测试,评价了合成方法和表面化学对其催化性能的影响。催化剂的特征是在77 K下具有N2吸附/解吸等温线,TEM,粉末X射线衍射,热重分析,红外和X射线光电子能谱以及ICP-OES。观察到,与通过浸渍方法制备的金属钯颗粒相比,使用乙二醇合成的钯纳米颗粒产生的金属钯颗粒尺寸更小,两种载体的钯含量均相似。载体表面上氧基团的存在有利于活性并降低了选择性。似乎乙二醇与GO的表面基团反应,这有利于选择性。与基于CNT的催化剂相比,活性更高,并且两种通过乙二醇还原制备的催化剂在再循环时都非常稳定。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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