检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:李倩 林锦 赵梦珂 黎昌海[1] 陆守香[1] Qian LI;Jin LIN;Meng-ke ZHAO;Chang-hai LI;Shou-xiang LU(State Key Laboratory of Fire Science,University of Science and Technology of China,Hefei 230026,China)
机构地区:[1]中国科学技术大学火灾科学国家重点实验室,合肥230026
出 处:《Transactions of Nonferrous Metals Society of China》2024年第7期2304-2312,共9页中国有色金属学报(英文版)
基 金:financial support by the National Natural Science Foundation of China(No.52206180);the Fundamental Research Funds for the Central Universities,China(No.WK2320000050)。
摘 要:采用质量损失法研究聚氯乙烯火灾烟气环境中283.15~323.15 K温度范围内无铅Sn-3.0Ag焊料的腐蚀动力学、表面微观结构和腐蚀机理。结果表明,随着温度从283.15 K升高到323.15 K,Sn-3.0Ag焊料的质量损失从(22.09±2.01)g/m^(2)增加到(44.66±1.20)g/m^(2)。此外,腐蚀动力学符合阿伦尼乌斯定律。Sn-3.0Ag焊料表面腐蚀产物呈叠加生长趋势。在283.15 K,Sn-3.0Ag焊料的表面出现大量的腐蚀产物。Sn-3.0Ag无铅焊料的腐蚀过程为电化学腐蚀,阴极发生析氢和吸氧反应,阳极发生富锡相的溶解。腐蚀产物为Sn_(21)Cl_(16)(OH)_(14)O_(6)、SnO_(2)和SnO。The corrosion kinetics,surface microstructure,and corrosion mechanism of Sn−3.0Ag lead-free solder were investigated using mass-loss method in the temperature range from 283.15 to 323.15 K in polyvinyl chloride fire smoke environment.The results show that the Sn−3.0Ag solder exhibits an increase in mass-loss from(22.09±2.01)to(44.66±1.20)g/m^(2)as the temperature increases from 283.15 to 323.15 K.Moreover,the corrosion kinetics is in accordance with Arrhenius law.The surface corrosion products of Sn−3.0Ag solder show a superposition growth trend.At 283.15 K,the surface of Sn−3.0Ag solder shows significant corrosion products.The corrosion process of Sn−3.0Ag lead-free solder is an electrochemical corrosion.Hydrogen evolution and oxygen abstraction reactions occur in the cathode,and the dissolution of the Sn-rich phase occurs in the anode.The corrosion products are Sn_(21)Cl_(16)(OH)_(14)O_(6),SnO_(2),and SnO.
关 键 词:腐蚀 预测模型 Sn-3.0Ag焊料 火灾烟气 温度
分 类 号:TG172[金属学及工艺—金属表面处理]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.49