首页> 外文期刊>Chemistry Select >Insight into the Catalytic Behavior in Nitroarenes Reduction over Non-Noble Metals Modified Polymer Carbon Nitride
【24h】

Insight into the Catalytic Behavior in Nitroarenes Reduction over Non-Noble Metals Modified Polymer Carbon Nitride

机译:洞悉非缺失金属修饰的聚合物氮化物的氮含量减少的催化行为

获取原文
获取原文并翻译 | 示例
       

摘要

Revealing the catalytic mechanism and dynamic process in heterogeneous catalysis is fundamental and tremendous important.Here,non-noble metals(Bi,Cu,Cu2O or CuO)hybrided polymer carbon nitride nanosheets(CNN)were fabricated through ions intercalation processes.The prepared Bi-CNN hybrid exhibits moderate catalytic activity compared with Cu–CNN in 4-nitrophenol(4-NP)reduction.The kinetic rate constant and apparent active energy of Bi-CNN are 0.04 min~(-1)(20 °C)and 53.6±4.8 kJmol~(-1),respectively.Cumodified CNN shows a rate of 0.65 min~(-1),which is 16 times higher than that of Bi-CNN and even higher than noble metal(Au,Ag)-CNN hybrids.More importantly,a new catalytic behavior that no delay time(usually reported by using noble metals and metal oxides)was observed in the 4-NP reduction over Bi-CNN and Cu–CNN hybrids.A possible catalytic mechanism elaborated this new catalytic phenomenon was proposed based on the chemical redox potentials.The CuO-CNN and Cu2O-CNN hybrids were further prepared to verify the proposed catalytic model.This work provides more insight into the mechanistic investigation of nitroarenes reduction over non-noble metal catalyst evolved photocatalytic systems.
机译:揭示异质催化中的催化机制和动态过程是基本的,并且非常重要。在此,非固定金属(BI,CU,CU2O或CUO)杂交聚合物氮含量氮含量(CNN),通过制备的生物构造过程。与4-硝基苯酚(4-np)还原中的CU – CNN相比,CNN杂化表现出适度的催化活性。BI-CNN的动力学速率常数和明显的活性能为0.04 min min〜(-1)(-1)(20°C)和53.6± 4.8 kJmol〜(-1)分别为0.65分钟〜(-1),比BI-CNN高16倍,甚至比Noble Metal(AU,AG)-CNN混合体高16倍。更重要的是,在BI-CNN和Cu-CNN杂交的4-NP降低中观察到了一种新的催化行为(通常使用贵金属和金属氧化物)。提出的基于化学氧化还原电势。CUO-CNN和CU2O-CNN杂种是进一步的这项工作为验证所提出的催化模型提供了更多的了解。对非差异金属催化剂进化的光催化系统的硝化碳还原的机械研究提供了更多的洞察力。

著录项

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