Bian Zhao-Yong, Bian Yu, Wang Hui, Ding Ai-Zhong
J Nanosci Nanotechnol. 2014 Sep;14(9):7279-85. doi: 10.1166/jnn.2014.8949.
Pd/graphene catalysts were prepared in situ from graphite oxide and palladium salts by the hydrogen-reduction method and were then used for the construction of Pd/graphene gas-diffusion electrodes (GDE). The prepared catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and differential pulse voltammetry (DPV) techniques. In the Pd/graphene catalysts, Pd particles, with an average size of 3.6 nm and an amorphous structure, were highly dispersed in the graphene. The Pd/graphene catalysts accelerated the two-electron reduction of O2 to H2O2 by feeding air, which favors the production of hydroxyl radicals (HO*). In the electrolytic system, HO* was determined in the reaction mixture by the electron spin resonance spectrum (ESR). The dechlorination degree of 4-chlorophenol reached approximately 90.5% after 80 min, and the removal efficiency and the average removal efficiency of 4-chlorophenol, in terms of total organic carbon (TOC) after 120 min, reached approximately 93.3% and 85.1%, respectively. Furthermore, based on the analysis of electrolysis intermediates by high performance liquid chromatography (HPLC) and ion chromatography (IC), a reaction scheme was proposed for the Pd/grapheme GDE catalytic degradation of 4-chlorophenol.
通过氢还原法由氧化石墨和钯盐原位制备了钯/石墨烯催化剂,然后将其用于构建钯/石墨烯气体扩散电极(GDE)。采用X射线衍射(XRD)、透射电子显微镜(TEM)和差分脉冲伏安法(DPV)技术对制备的催化剂进行了表征。在钯/石墨烯催化剂中,平均粒径为3.6 nm且具有非晶结构的钯颗粒高度分散在石墨烯中。通过通入空气,钯/石墨烯催化剂加速了O2的两电子还原生成H2O2,这有利于羟基自由基(HO*)的产生。在电解体系中,通过电子自旋共振谱(ESR)测定反应混合物中的HO*。80分钟后,4-氯苯酚的脱氯率达到约90.5%,120分钟后,以总有机碳(TOC)计,4-氯苯酚的去除率和平均去除率分别达到约93.3%和85.1%。此外,基于高效液相色谱(HPLC)和离子色谱(IC)对电解中间体的分析,提出了钯/石墨烯GDE催化降解4-氯苯酚的反应方案。