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作 者:冯丽婷[1] 苏畅[1] 冯绍彬[1] 李振兴[1] 王绍亮[1]
机构地区:[1]郑州轻工业学院材料与化学工程学院河南省表界面科学重点实验室,河南郑州450002
出 处:《材料保护》2010年第11期14-16,52,共4页Materials Protection
基 金:国家自然科学基金项目(20376077;20576126);河南省科技厅攻关项目(0524490018)资助
摘 要:为了研究腐蚀产物对青铜器腐蚀的影响,分别以多种不溶性铜盐作为活性催化物质,制备成了多孔氧电极,使之与青铜阳极组成原电池。以电流密度为0.01mA/cm2进行了连续115h以上的放电试验,并对氧电极进行了阴极极化测试。本试验较好地模拟了青铜器在大气条件下的电化学腐蚀过程,验证了铜盐中催化活性最高的是氯化亚铜而不是碱式氯化铜即粉状锈,粉状锈仅是腐蚀的最终产物。提出了多孔氧电极催化机理。Several kinds of insoluble nantokite were used as active catalysts to prepare porous oxygen electrodes. Resultant porous oxygen electrodes were combined with bronze anode to produce primary batteries. The primary batteries were continuously discharged at a current density of 0.01 mA/cm2 for more than 115 h, and the cathodic polarization of the porous oxygen electrodes was tested. The catalytic mechanism of the porous oxygen electrodes was discussed. It was found that the discharge test could be well used to simulate the electrochemical corrosion process of bronze wares under atmosphere. Cuprous chloride rather than basic cupric chloride was the nantokite with the highest catalytic activity for the corrosion process of bronze wares, and the powder-like rust was just the final corroded product.
关 键 词:青铜器腐蚀 粉状锈 原电池模拟 多孔氧电极 氯化亚铜
分 类 号:TG172[金属学及工艺—金属表面处理]
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