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1、百度文库-让每个人平等地提升自我镁合金论文：AZ61镁合金的磷化及阴极电泳【中文摘要】镁合金作为优质的合金结构材料，在航空航天、汽 车、电子和医疗器材等行业得到广泛应用。但是镁的耐蚀性较差，制 约了镁合金的应用。镁合金磷酸盐转化膜具有多孔结构、附着力好，是有机涂层的有效基底。本文采用磷化与阴极电泳涂装相结合的方法 改善AZ61镁合金的表面性能。本研究的研究方法、研究内容和结果 分别叙述如下。在国内外锌系磷化研究的基础上 ，选取三种不同的磷 化体系。通过对三种磷化体系所得磷化膜的厚度、耐碱性、表面形貌 以及元素组成进行对比，选取适宜阴极电泳涂装的磷化膜。采用单因 素试验,分别研究磷化液中各物质对
2、磷化成膜的影响。研究表明： Zn(H2PO4)2的浓度对磷化膜的厚度有较大影响，浓度越大，厚度越大； NaNO3寸磷化过程具有良好的促进作用；硫酸羟胺是一种良好的磷化 氧化促进剂，且具有用量低的优点；NaF能够促进磷化、细化膜层。 间硝基苯磺酸钠与酒石酸添加后对磷化膜的成膜有利，但是添加的浓 度与成膜状况关系较小。采用正交设计的方法设计实验，正交表为 (L9(34),选取四种浓度对磷化过程影响较大的物质 NaF硫酸羟胺、 ZnH2PO4 NaNO3乍为正交试验的四个因素，物质的浓度为各因素的水 平。正交优化结果：NaF浓度为g-1、硫酸羟胺的浓度为g L-1、 ZnH2PO4勺浓度为g L-1
3、、NaNO3勺浓度为Q g L-1。在上述优化 物质浓度下，AZ61镁合金表面形成的磷化膜厚度适中、 w小、均匀 性好、腐蚀电流密度低、耐蚀性良好。在以上工作的基础上，采用上述磷化条件的磷化膜进行阴极电泳涂装，得到外观（颜色、光亮度、均 匀性）较好，厚度在35w m左右，硬度达到2H-3H,与基体的附着力为0 级，耐蚀性较好的复合电泳涂层。采用电涡流测厚仪测量磷化膜的厚 度；利用金相显微镜、扫描电镜（SEM网察磷化膜的表面形貌；利用 化学分析方法和能谱分析（EDS）分析磷化膜的成分组成；通过阳极极 化曲线、电化学阻抗谱（EIS）、腐蚀失重等方法评价磷化膜的耐腐蚀 性能。电泳部分采用电涡流测厚仪
4、测量有机涂层的厚度，采用EIS测试有机涂层的耐蚀性；按国家标准规定的方法测量有机涂层的附着 力、硬度和耐溶剂性。【英文摘要】 As a high-quality structural material, magnesium alloys have been used in lots of fields, especially in the aerospace, automobile, electronic and medical equipment. However, the use of magnesiumalloy was severely limited by its poor corr
5、osion resisting property. Magnesiumalloy phosphating conversion treatment was an effective substrate of organic coating because of its porous and binding force. In this dissertation, phosphating and cathode electrophoretic painting methods were applied to improve the surface performance of the magne
6、siumalloys. The experimental methods, main work and results were recounted as follows this dissertation, three phosphating systems were selected on the basis of investigation both at home and abroad. We select aoptimum phosphating coating for cathode electrophoretic painting by comparing the thickne
7、ss, weight loss in alkaline solution, surface morphology and elements of three phosphating coatings obtained in different phosphate influences of each substance in phosphate bath on phosphate coatings were researched with single factor test. The results are as follows:the concentration of Zn(H2PO4)2
8、 has an important effect on thickness of film, the film would be thicker with a higher the concentration of Zn(H2PO4)2; the concentration of NaNOJias effects on the accelerating of the phosphate process; hydroxylamine sulfate is a good accelerator which hascharacteristic of low consumption; The conc
9、entration of NaFcan promote the forming of phosphmefilm and thin crystalline grain. Tartaric acid and nitrobenzene sulfonate have important effects on the formation of phosphate coatings, but their concentrations have no effects on design was used to scheme experiment, the concentrations of four sub
10、stances were chosen as four factors of orthogonal design table (L9(34). The optimum orthogonal conditions were CNaF=g -L-1, z Chydroxylamine sulfate= g L-1, CznH2PO4= g L-1, CNaNO3=5 g - L-1. In the optimized conditions, test results showed that the phosphate coatings formed on magnesium alloys have
11、 moderate thickness, lower corrosion weight-loss, more detailed micro-structure and more excellent corrosion resistance than the contrastphosphate coatings. Electrophoretic composite coatings were prepared on basis of optimized phosphate coatings by cathodic electrophoretic. The appearances (color,
12、brightness, uniformity) of the electrophoretic composite coatings obtained in the optimized conditions were better than others, thethickness was 35 m, hardness was 2H-3H, adhesion was on zero level and the corrosion resistance was thickness of thephosphate coatings were measured by the eddy curreny
13、thickness meter. The surfaces morphologies of the phosphate coatings were observed by metallographic microscope and SEM; the compositions of the phosphate coatings were analyzed bytitrimetry and EDS. The corrosion resistance of the phosphatecoatings were assessed by anodic polarization curvesmeasure
14、ment, electronical impedance spectra(EIS) andcorrosion weight-loss test. The thickness of the organiccoatings were measured by the eddy curreny thickness meter. The corrosion resistance of the organic coatings were assessed byEIS. The thickness, weight loss and solvent resistance oforganic coatings
15、were tested according to the national standards.【关键词】镁合金 磷化表面形貌耐蚀性阴极电泳涂装【英文关键词】Magnesium alloys PhosphatingSurface morphologies Corrosion resistanceCathode electrophoretic painting【目录】AZ61镁合金的磷化及阴极电泳摘要10-12ABSTRACT12-1第一章 绪论14-30镁及镁合金的性质及分类 14-16镁及镁合金的性质14镁合金的分类14-16镁及镁合金的腐 蚀16-19镁及镁合金的腐蚀反应16-17负差数效
16、应17-18镁合金腐 蚀的类型18-19镁合金的腐蚀防护措施19-25改变合金的显微组织 19-20镁合金的表面处理20-25本课题的研究方向25-30镁合金磷 化的特点25-27镁合金阴极电泳涂装的特点27-28研究课题的提出 28-30第二章实验材料、工艺及研究方法30-44实验材料、药品及 仪器30基体材料30化学试剂30实验设备30实验方法30-44前 处理工艺30-33磷化工艺33-35阴极电泳工艺35测试方法35-44 第三章镁合金磷化工艺研究44-80磷化体系的选择44-49不同体 系得到的磷化膜的厚度分析45-46不同体系得到的磷化膜的耐碱性 试验46不同体系得到的磷化膜的金相
17、显微分析46-47不同体系得到的磷化膜的扫描电镜分析47-49磷化液中各成分对磷化的影响 49-70磷酸二氢锌浓度对磷化的影响 49-52有机胺对磷化的影响 52-58硝酸钠浓度对磷化的影响58-62氟化钠浓度对磷化的影响 62-66酒石酸浓度对磷化的影响66-68间硝基苯磺酸钠浓度对磷化 的影响68-70磷化体系优化70-78正交设计及实验结果70-73正交最佳配方的性能测试73-78本章小结78-80第四章 镁合金磷化膜上 的阴极电泳涂装80-91复合涂层的耐溶剂性80-81复合涂层的交流 阻抗测试81-88最佳磷化复合电泳涂层交流阻抗测试81-82对比磷化复合电泳复层交流阻抗测试 82-84表调复合电泳涂层交流阻抗测 试84-85镁合金电泳涂层交流阻抗测试 85-88阴极电泳复合涂层的 厚度分析88阴极电泳复合涂层的硬度分析 88阴极电泳复合涂层的 附着力分析88-89阴极电泳复合涂层的颜色分析89阴极电泳复合 涂层的光亮度分析89本章小结89-91第五章 结论91-93参考文献93-98致谢98-99附录：硕士期间发表学术论文99-100学位论文评阅 及答辩情况表100 6