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AZ91D镁合金化学复合镀Ni-P-ZrO2的工艺与性能 总被引:9,自引:2,他引:9
对镁合金传统化学镀工艺进行了改进,避免了使用氢氟酸和六价铬等有毒物质。采用化学镀与化学复合镀相结合方法,在AZ91D镁合金上获得了Ni-P-ZrO2纳米化学复合镀层,并研究了新工艺化学镀前处理和镍沉积机理及复合镀层的结构和性能。结果表明:新工艺方法获得的Ni-P镀层更均匀、致密,耐蚀性优于传统工艺化学镀层;Ni-P-ZrO2复合镀层与AZ91D合金基体在3.5%NaCl溶液中的动电位极化曲线对比表明,该复合镀层对镁合金可以起到明显的保护作用;从磨损实验结果可见,Ni-P镀层的磨损质量损失率几乎为Ni-P-ZrO2镀层的3倍,说明ZrO2纳米粉的加入能改善镀层的耐磨性。 相似文献
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AZ91D镁合金化学镀Ni-P及Ni-W-P镀层的结构与耐蚀性 总被引:1,自引:0,他引:1
在AZ91D镁合金上直接化学镀Ni-P和Ni-W-P镀层,并利用扫描电子显微镜、X射线衍射仪及电化学工作站研究后续热处理对化学镀层组织形貌、相组成及其耐蚀性的影响。结果表明,制备的Ni-P镀层为非晶态,而Ni-W-P镀层为纳米晶结构,两者在3.5%NaCl水溶液中的耐蚀性相当。热处理可以明显提高Ni-W-P镀层的耐蚀能力,但却稍微弱化Ni-P镀层的耐蚀能力,热处理后的Ni-W-P层自腐蚀电位相对于未处理的化学镀Ni-W-P或Ni-P层提高了约150 mV。 相似文献
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AZ91D镁合金化学镀镍 总被引:60,自引:6,他引:60
利用化学镀镍的方法,在AZ91D镁合金表面得到了均匀、致密,无明显表面缺陷的Ni-P涂层,X-ray衍射分析表明,镀层组织为单一的Ni;热震实验表明涂层与基体合金结合良好;动电位极化测试表明涂层的自腐蚀电位接近-0.4V(SCE),有明显的钝化区,而腐蚀性能优异,可对基体合金起到理想的防护作用。 相似文献
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AZ91D镁合金表面无铬化学转化膜的研究 总被引:1,自引:1,他引:1
在AZ91D镁合金表面利用无铬的KMnO4-Mn(H2PO4)2-pH值调整剂转化液进行化学转化,分析了转化膜的形成机理.经XRD分析结果显示,转化膜为非晶态结构,SEM观察发现,转化膜表面均匀,存在有利于增强涂装层附着力的网状裂纹.转化膜经EDS和XPS分析表明,主要元素为Mg、Al、Mn、O,由MgO、Mg(OH)2、MgAl2O4、Al2O3、Al(OH)3、MnO2组成.转化后的AZ91D镁合金在3.5%的NaCl溶液中全浸试验结果表明,其腐蚀速率低于其他化学转化膜. 相似文献
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采用常温碱性超声波清洗、酸洗和活化的前处理工艺在AZ91D镁合金表面化学镀镍,研究了辅助络合剂氨基乙酸和加速剂巯基乙酸对镀层耐蚀性的影响。结果表明:镀层表面由Ni-P固溶体组成,呈现尖锐的晶态峰,磷原子与镍原子形成置换固溶体,表面平整致密,无明显缺陷。氨基乙酸含量对镀层耐蚀性和腐蚀速率影响不大,随着巯基乙酸含量的增加,镀层腐蚀电位先升高后降低,腐蚀速率整体比镁合金基体慢,镀层总体呈现钝化趋势,在4 g/L时腐蚀电位最高。 相似文献
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《稀有金属材料与工程》2012,(Z1):183-186
Characterization of electroless nickel deposits on magnesium alloys was investigated by X-ray diffraction(XRD),scanning electron microscope(SEM),energy dispersive spectrometer(EDS)and electrochemical potentiodynamic polarization analysis.The result of XRD showed that the electroless nickel deposits on magnesium alloys were composed mostly of amorphous Ni-P and partially of microcrystalline nickel.The phosphorus content in the Ni-P deposits was 10.8%by the calculation of EDS.SEM micrographs showed that morphology of electroless nickel deposits on magnesium alloys was a typical cellular structure,and the growth of cellular structure was influenced by surface condition of substrate.Zinc layer between substrate and electroless nickel deposits was not found by the results of SEM and EDS,which indicated that the zinc layer on the surface of magnesium alloy was very thin,and the zinc would dissolved while being immersed in electroless nickel plating solution.The thin zinc layer was almost dissolved completely before Ni-P plating.The result of electrochemical potentiodynamic polarization analysis showed that the corrosion potential Ecorr of electroless nickel deposits in 3.5%NaCl solution was about-0.53 V,which was 1 V higher than that of magnesium alloys substrate.And corrosion current density of Ni-P deposits in 3.5%NaCl solution was much smaller than that of magnesium alloys substrate at the same potential value,which indicated that corrosion resistance of electroless Ni-P deposits was excellent.Discoloration time of concentrated nitric acid test for electroless nickel deposits on magnesium alloys was 445 s,which also indicated excellent corrosion resistance. 相似文献
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Corrosion and wear properties of electroless Ni-P plating layer on AZ91D magnesium alloy 总被引:2,自引:0,他引:2
A direct electroless Ni-P plating treatment was applied to AZ91D magnesium alloy for improving its corrosion resistance and wear resistance. Corrosion resistance of the Ni-P coatings was evaluated by potentiodynamic polarization and immersing experiments in 3.5% NaCl solution. The wear resistance of the coatings was investigated by the wear track and the mass change after ball-on-disk experiment. The results show that corrosion resistance and wear resistance of the AZ91D alloy are greatly improved after direct electroless Ni-P plating. No discoloration is noticed until 4 d of immersion in 3.5% NaC1 solution. Potentiodynamic polarization experiments show that the free corrosion potential of magnesium alloy is shifted from -1 500 mV to -250 mV and passivation occurs at 1 350 mV after direct electroless plating. The friction coefficients and wear rates of Ni-P coating and Ni-P coating after tempering are 0.10-0.351, 9.038×10^-3 mm^3/m and 0.13-0.177, 3.056×10^-4 mm^3/m, respectively, at a load of 1.5 N with dry sliding. Although minor hurt on corrosion resistance was caused, significant improvement of wear resistance was obtained after tempering treatment of the coating. 相似文献
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以AZ91D镁合金为基体,Al为合金粉末,采用激光表面改性技术对AZ91D镁合金进行表面改性,详细分析了镁合金改性后的表面组织,并通过盐雾实验对比了改性前后镁合金的耐蚀性,探讨了AZ91D镁合金基体及表面Mg-Al改性层的腐蚀机理,确定最佳激光功率参数为1.5 kW。 相似文献
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目的提高AZ91D镁合金的腐蚀防护性能。方法采用化学镀前处理在AZ91D镁合金表面制备一种保护性的Ni-Co合金镀层。分别采用环境扫描电镜(ESEM)、X射线衍射(XRD)和能量散射谱(EDS)分析合金镀层的表面形貌、微结构特点和化学成分。采用动电位极化(PC)和电化学阻抗谱(EIS),分析测试在模拟海洋环境(中性3.5%Na Cl溶液)中Ni-Co合金镀层对AZ91D镁合金的腐蚀防护性能。结果镁合金表面化学镀Ni-P镀层均匀覆盖,晶粒生长较致密,表面呈菜花状形貌,Ni-P镀层中P质量分数约为5.6%。Ni-Co合金镀层表面均匀且呈金字塔状形貌,形成了面心固溶体(FCC),镀层中Co质量分数约为31%。Ni-P镀层和Ni-Co合金镀层的厚度分别约为11μm和19μm。在模拟海洋(中性3.5%Na Cl溶液)环境中,镁合金裸基体、化学镀前处理Ni-P镀层、Ni-Co合金镀层的腐蚀电位分别为-1485、-372、-284 m V,其腐蚀电流密度分别是3.4×10-5、1.8×10-6、2.9×10~(-7) A/cm2,所拟合的电荷转移电阻分别为4.72×103、1.70×104、2.06×106?/cm2。结论化学镀前处理Ni-P镀层可为镁合金提供较好的腐蚀防护,Ni-Co合金镀层能够为镁合金提供更显著的腐蚀防护。 相似文献
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目的通过含有硬脂酸添加剂的阳极氧化工艺,获得耐蚀性优异的镁合金阳极氧化膜。方法采用直流电源阳极氧化法,在含有2 g/L硬脂酸的碱性氧化液中进行阳极氧化。通过SEM、ImageJ软件和TT230测厚仪分析氧化膜的微观形貌和膜厚,通过FTIR、XPS和XRD分析膜层成分,通过电化学测试检测膜层的耐蚀性能。结果氧化液中添加硬脂酸后,制备的氧化膜层孔隙率降低,孔径减小,孔洞数量下降,厚度增大,致密度提高。膜层的自腐蚀电流密度为3.15×10^–7 A/cm^2,与未加硬脂酸制备的氧化膜相比,降低了2个数量级,耐蚀性显著提升。结论硬脂酸添加剂通过提升成膜电压,增强火花放电效应、表面活性剂作用,改变膜层成分等机制,提升膜层耐蚀性能。 相似文献
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