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
机构地区:[1]南京工业大学材料科学与工程学院,江苏南京210009 [2]陕西理工学院,陕西汉中723001
出 处:《材料保护》2006年第3期65-68,共4页Materials Protection
基 金:江苏省高校自然科学研究计划(03KJB430045;05KJB1300421);陕西省自然科学基金(2003E120)
摘 要:利用SEM、DSC、XRD、中性盐雾试验和显微硬度分析等手段,对Ni10.54%P及Ni9.25%Cu10.23%P化学镀层的组织特征、相结构转变、热稳定性、耐蚀性和硬度进行了比较。结果表明:(1)两种镀层均匀致密,均为胞状结构和非晶态组织;(2)NiP镀层仅发生从非晶相向稳定的Ni3P相转变,而NiCuP镀层则先生成NiCu固溶体和亚稳中间相Ni5P2,再向稳定相Ni3P转变;(3)NiCuP镀层的热稳定性高于NiP镀层;(4)镀态和低温热处理条件下两种镀层的硬度相差不大,NiP镀层经400℃、60min热处理时硬度达到最高值981.1HV,但NiCuP镀层经500℃、60min热处理时硬度达到最高值1144.8HV;(5)镀态时NiCuP镀层的腐蚀速率只有NiP镀层腐蚀速率的2.85%;经过400℃、120min相同条件的热处理,NiCuP镀层的腐蚀速率仅为NiP镀层腐蚀速率的0.351%。Microstructures, crystallization behaviors, thermal stabilities, hardness, and corrosion resistances of electroless plating Ni-10.54%P and Ni-9.25%Cu 10.23%P deposits were contrastively studied by using SEM, DSC, XRD, neutral salt spray and micro-hardness analysis. Results indicate that both as-plated deposits are compact and symmetrical, and all exhibit a cell structure and amorphous structure. It only occurs Ni_3P stable phase transformation from amorphous for Ni-P deposit during crystallization, but first forms Ni-Cu solid solution and Ni_5P_2 metastable phase and then transform to Ni_3P stable phase for Ni-Cu-P deposit. The thermal stability of Ni-Cu-P deposit is higher than Ni-P deposit. The hardness of both deposits is similar in as-plated and heat-treated under lower temperatures. The hardness of Ni-P deposit reaches the maximum 981.1 HV after treated under 400 ℃for 60 minutes, but that of Ni-Cu-P deposit reaches the maximum 1 144.8 HV. The corrosion rate of Ni-Cu-P deposit is only 2.85% of the Ni-P deposit in as-plated state, and is only 3.51‰ of the Ni-P deposit while both treated under 400 ℃ for 120 minutes.
关 键 词:化学镀 NI-P NI-CU-P 热稳定性 硬度 耐蚀性
分 类 号:TG174.44[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:216.73.216.145