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中国腐蚀与防护学报  2008, Vol. 28 Issue (6期): 351-354    
  研究报告 本期目录 | 过刊浏览 |
电泳涂装常温磷化工艺及磷化膜性能
陈泽民1;张巧云2;李志林2
1.廊坊师范学院化学与材料科学学院  廊坊 065000
2.河北大学化学与环境科学学院  保定 071002
PHOSPHATING TECHNOLOGY AND PHOSPHATING FILM PROPERTY AT ROOM TEMPERATURE BEFORE ELECTROPHORETIC COATING
CHEN Zemin1;ZHANG Qiaoyun2;LI Zhilin2
1.College of Chemistry and Materials Science; Langfang Teachers College; Langfang 065000
2.College of Chemistry and Environmental Science; Hebei University; Baoding 071002
全文: PDF(935 KB)  
摘要: 

在自制的低温锌系磷化液基础上,通过加入镍盐、锰盐和羧基聚合物,并以硝基苊为促进剂,研制出了一种适用于电泳涂装的低锌锰改性常温磷化工艺。用扫描电镜和能谱仪对低锌锰改性磷化膜与普通锌系磷化膜的形貌和组成进行对比分析。结果表明,该工艺制备出的磷化膜耐蚀性和耐碱性均优于普通锌系磷化膜;该磷化工艺可在常温下10 min内在金属表面形成完整、致密、耐碱性好的磷化膜,它是由Zn3(PO4)2、FeZn2(PO4)2、Mn Zn2(PO4)2组成的椭球状磷酸盐晶体薄膜。

关键词 电泳涂装常温磷化性能测试    
Abstract

A novel phosphating processing that nickel salt, manganese salt, nitro acenaphthene and carboxyl group polymer were contained in self-made Zn system phosphating, was developed for electrophoretic coating. Compared low Zn-Mn phosphating film with common phosphating film, the former in corrosion resistance and alkali resistance is better than the latter. The investigation and analysis of composition and structure of the low Zn-Mn phosphating film and common phosphating film are conducted by means of XPS and SEM. The experiment results demonstrated that by applying this phosphating process, a complete,alkaliproof and firm crystal film made up of Zn3(PO4)2、FeZn2(PO4)2 and Mn Zn2(PO4)2 sphere phosphide formed on metal surface in less than ten minutes at room temperature.

Key wordselectrophoretic coating    phosphating technology at room temperature    performance test
收稿日期: 2007-03-26     
ZTFLH: 

TG174

 
通讯作者: 陈泽民 zhangqy810@sina.com   
Corresponding author: CHEN Zemin   

引用本文:

陈泽民 张巧云 李志林. 电泳涂装常温磷化工艺及磷化膜性能[J]. 中国腐蚀与防护学报, 2008, 28(6期): 351-354.
CHEN Ze-Min. PHOSPHATING TECHNOLOGY AND PHOSPHATING FILM PROPERTY AT ROOM TEMPERATURE BEFORE ELECTROPHORETIC COATING. J Chin Soc Corr Pro, 2008, 28(6期): 351-354.

链接本文:

https://www.jcscp.org/CN/      或      https://www.jcscp.org/CN/Y2008/V28/I6期/351

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