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作 者:李帅 杨声海 陈永明 唐朝波 赖延清 邓朝勇 王长红 Shuai LI;Sheng-hai YANG;Yong-ming CHEN;Chao-bo TANG;Yan-qing LAI;Chao-yong DENG;Chang-hong WANG(School of Metallurgy and Environment,Central South University,Changsha 410083,China;Ximei Resources Limited Company,Qingyuan 513000,China)
机构地区:[1]中南大学冶金与环境学院,长沙410083 [2]稀美资源(广东)有限公司,清远513000
出 处:《Transactions of Nonferrous Metals Society of China》2024年第5期1681-1693,共13页中国有色金属学报(英文版)
基 金:Science and Technology Innovation Program of Hunan Province,China(No.2021RC2002);Yangfan Plan,China(No.2017YT05C107)。
摘 要:作为一种具有广泛应用前景的高效电合成技术,耦合电溶解的铪醇盐合成(EHS)基于铪溶解/乙醇脱氢的同时非均相反应以及溶液中Hf^(4+)阳离子和烷氧阴离子的自发结合反应。为了阐明EHS过程的机制和动力学,通过电化学测试、扫描电镜、气相色谱和微观动力学模拟等手段,探究阳极铪溶解和阴极乙醇脱氢的电化学行为。结果表明,优选的支持电解质四乙基氯化铵(Et_(4)NCl)展现了钝化膜击穿与铪溶解协同的剧烈点蚀机制以及两段脱氢机制。为量化钝化膜击穿和铪点蚀的动力学参数,提取与钝化速率、钝化膜击穿敏感性和点蚀速率相关的3个指标,并通过建立微观动力学模型评估基于Et_(4)NCl体系的EHS工艺,其电能消耗为1.53~1.83 k W·h/kg Hf(OC_(2)H_(5))_(4)。Electrodissolution-coupled hafnium alkoxide synthesis(EHS)is a promising pathway for efficient electro-synthesis.It employs simultaneous heterogeneous reactions of Hf dissolution and ethanol dehydrogenation,and spontaneous solution-based combination reaction between Hf^(4+) cations and alkoxy anions.To elucidate the mechanism and kinetics of EHS process,the electrochemical behaviors of anodic Hf dissolution and cathodic ethanol dehydrogenation were explored through electrochemical measurements,SEM observations,gas chromatography,and micro-kinetics modeling.The results indicated the supporting electrolytes of tetraethylammonium chloride(Et_(4)NCl)to be preferable,which facilitated a passive-film-punctured pitting mechanism for Hf dissolution and a two-stage dehydrogenation mechanism.Three indicators related to passive rate,sensitivity towards puncture of the passive film,and pitting rate were extracted to quantify the kinetics of passive puncture and Hf corrosion.Micro-kinetics models were developed to evaluate the Et_(4)NCl-based EHS process,which achieved electric energy requirements of 1.53-1.83 kW·h/kg Hf(OC_(2)H_(5))_(4).
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