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Formation of electrodeposited Ni-TiAlN/Si3N4 composite coating: effect of Si3N4 concentration

机译:电沉积Ni-TiAlN / Si3N4复合涂层的形成:Si3N4浓度的影响

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The Ni-TiAlN/Si3N4 composite coating has been investigated.The composites were deposited at fixed electrodeposition current of 3 mA for 15 minutes.The electrolyte consists of 0.49 mol/1 H3B03,0.17 M MC126H2O,0.38 M NiSO46H2O,0.2 gr/lit SDS,2 gr/lit A1N and 2 gr/lit TiN.The concentration of Si3N4nanofiber was varied into 10,20 and 30 gr/lit.The electrodes used were Pt wire as counter electrode,AgClwire as reference electrode and tungsten carbide(WC)rod as working electrode.The surface morphology and composition of composites were characterized by using Scanning Electron Microscopy(SEM)dan Energy Dispersive Spectroscopy(EDS),respectively.The crystal structure of composites was characterized by using X-Ray Diffraction(XRD)and the hardness was tested by using Vickers hardness tester.The results showed that the composite coating surface morphology was finer as the increase of Si3N4 concentration due to the decrease of Ni crystal size.The increase of S3N4 concentration indicating the formation of stable structure composed of Ni-TiAlN/Si3N4 caused the increase of the coating hardness.
机译:已经研究了Ni-TiAlN / Si3N4复合涂层。将复合材料沉积在固定电沉积电流为3 mA的15分钟。电解质由0.49mol / 1 H3b03,0.17M Mc126H2O,0.38M Niso46H2O,0.2 GR / Lit SDS组成。 ,2 GR / LIT A1N和2 GR / Lit TIN。Si3N4NoFiber的浓度变化为10,20和30 GR /点。使用的电极是PT线作为对电极,AgClWire作为参考电极和碳化钨(WC)杆作为工作电极。通过使用扫描电子显微镜(SEM)DAN能量分散光谱(EDS)来表征复合材料的表面形态和组成。通过使用X射线衍射(XRD)和硬度来表征复合材料的晶体结构通过使用维氏硬度测试仪进行测试。结果表明,由于Ni晶体尺寸的降低,复合涂层表面形态变得更精细。由于Ni晶体尺寸的降低,Si3N4浓度的增加。S3N4浓度的增加表明格式由Ni-TiAlN / Si3N4组成的稳定结构导致涂层硬度的增加。

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