项目名称: 核壳结构Pt-M/REOx/C/Nafion阴极制备及苯电催化加氢还原规律研究
项目编号: No.51261012
项目类型: 地区科学基金项目
立项/批准年度: 2013
项目学科: 一般工业技术
项目作者: 杨滨
作者单位: 昆明理工大学
项目金额: 50万元
中文摘要: 加氢还原是柴油精制的重要步骤,使用核壳结构电解阴极可以增强对反应物-不饱和有机物(苯等)-的电吸附.由于传统研究方法难以对阴极上苯的双键活化以及氢的析出进行有效调控,因此尚未在水电解-苯加氢还原耦合过程中实用.本项目拟通过离子束溅射增强共沉积、化学修饰与涂覆固化技术制备核壳结构Pt-M/REOx/C/Nafion阴极,通过调控Pt壳压缩应变结构,调节苯分子在阴极-Nafion膜界面扩散通道形态以及二者间电荷交换行为,明确阴极表面结构组分和电解反应参量对苯电吸附性的调控机制,明确苯电催化加氢还原规律,增强苯加氢相对于阴极析氢的竞争优势,提高阴极的苯加氢选择性和还原速度.本项目的实施将有助于认识阴极表面结构与苯加氢还原效率的关系,强化水电解-有机物电催化还原耦合技术的应用理论基础,为苯加氢还原过程提供有效调制途径和新研究方法,对预期的催化电极制备和电催化耦合过程设计开发具有重要理论和现实意义.
中文关键词: 核壳结构;Pt-M/REOx/C/Nafion阴极;水电解-有机物还原耦合;电催化;苯加氢还原
英文摘要: Hydrogenation reduction is an important procedure in diesel refining manufacture process, and Water Electrolysis coupling Organics electro-catalysis Reduction (abbr. WE&OR) technology revealed definitely the available value for use in Hydrogenation reduction reactions. Core-shell structure electrolysis cathodes can be used to enhance adsorb reactant - unsaturated organics, such as Benzene, etc., - in these manufacture processes. But owing to it could not be regulated efficiently on activation of Benzene double bond and behavior of exhaustion hydrogen on the cathode by making use of traditional methods, in the today, regrettably, core-shell structure electrolysis cathodes have been difficult to use actually in WE&OR processes. So, in our project, we will produce core-shell structure Pt-M/REOx/C/Nafion cathodes by employ these technologies, Ion beam Sputtering Enhancing Cosedimentation (abbr. IBSEC), Chemical Modification (abbr. CM) and Depositing Solidifying (abbr. DS). We plan to regulate these technological conditions, such as sputtering voltage, Ion Beam current, oxygen partial pressure and deposition temperature in IBSEC, solution concentration and temperature and modificate time in CM, and dispersant concentration, Nafion / PTFE and pore-forming agent in DS, to control compression strain structure in Pt shel
英文关键词: Core-Shell structure;Pt-M/REOx/C/Nafion cathodes;Water electrolysis coupling organics reduction;Electro-catalysis;Benzene hydrogenation reduction