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Silane with cerium obtained by sol-gel process for post-treatment on ZnNi coatings

机译:用溶胶 - 凝胶法得到铈,用于在Znni涂层上处理的溶胶加工

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A system constituted by a xerogel film on zinc-nickel electrodeposited coating (ZnNi/sol-gel) for corrosion protection of steel was studied. The aim of this work was to evaluate the effects of withdrawal speed substrates from the sol and addition of corrosion inhibitors to silane films on ZnNi coating obtained by dip-coating process. ZnNi (12 to 16 wt% of nickel and constituted of γ cubic phase) alloys were obtained by electrodeposition on steel (A-1008) substrate from alkaline electrolytes. The electrodeposition was carried out with at 2 A.dm-2 current density what resulted in a 13 ?μm thickness of ZnNi coating. Xerogel films were obtained on ZnNi coating by dipcoating process in a sol constituted with silane precursors as γ-methacryloxypropyltrimethoxysilane (MAP), tetraethoxysilane (TEOS) and 0.01 mol.L-1 of cerium. It was used three withdrawal speeds of substrates from the sol: 50cm.min-1, 20cm.min-1 and 10cm.min-1. The corrosion performance of the Sol-gel/ZnNi system has been evaluated by measurements of open circuit potentials with immersion times and polarization methods in a 5% NaCl solution. The ZnNi coatings were analysed for chemical composition by flame atomic-absorption spectrometry (FAAS) and for phase structure by X-ray diffraction. Scanning electron microscopy was used to study the morphology of the alloys. After drying in air under controlled temperature, the xerogel films was analysed from SEM. The increase in withdrawal speed involves a thickening of films and some cracks appears for the thicker coatings. The electrochemical analysis showed that the xerogel films have an inhibitory action depending on the operating conditions of dip coating. The measurements of open circuit potentials with immersion times noticed that Sol-gel/ZnNi/steel system has a better electrochemical performance than ZnNi/steel system and also superior to ZnNi post-treated with Zn-Ni coating post-treated with Cr (VI) conversion layers. The addition of small amounts of cerium salts to the solution (0.01 mol.L-1) promoted the corrosion potential (Ecorr) displacement in direction to more positive potentials but as a function of the withdrawal speed of substrates from the sol. The corrosion rate (icorr) was also affect by the withdrawal speed of substrates and the best corrosion performance was observed for ZnNi/sol-gel system with 10cm.min-1 of withdrawal speed of substrates from the sol.
机译:研究了用于锌 - 镍电沉积涂层(ZnNI /溶胶 - 凝胶)的Xerogel膜构成的系统,用于钢的腐蚀保护。这项工作的目的是评估通过浸涂工艺获得的溶胶从溶胶和腐蚀抑制剂对硅烷膜的腐蚀抑制剂的影响。通过从碱性电解质的钢(A-1008)底物上的电沉积获得ZnNI(12至16wt%的镍和由γ立方相)合金。电沉积在2A.dm-2电流密度下进行,导致13Ωμm厚度的ZnNI涂层。在ZnNI涂层上通过浸涂方法在ZnNI涂层中获得Xerogel薄膜,其用硅烷前体作为γ-甲基丙烯酰氧基丙基三甲氧基硅烷(MAP),四乙氧基硅烷(TEOS)和0.01mol.11的铈。它使用了来自溶胶的三种底物抽出速度:50cm.min-1,20cm.min-1和10cm.min-1。通过在5%NaCl溶液中测量浸入时间和偏振方法的开路电位测量来评估溶胶-GEL / ZnNI系统的腐蚀性性能。通过火焰原子吸收光谱法(FAAS)和通过X射线衍射进行化学组成分析ZnNI涂层。扫描电子显微镜用于研究合金的形态。在受控温度下在空气中干燥后,从SEM分析Xerogel薄膜。提取速度的增加涉及薄膜的增厚,厚涂层出现一些裂缝。电化学分析表明,Xerogel膜根据浸涂的操作条件具有抑制作用。具有浸入时间的开路电位的测量值注意到溶胶 - 凝胶/ ZnNI /钢系统具有比Znni /钢系统更好的电化学性能,并且在用Cr(VI)后用Zn-Ni涂层后处理的ZnNI优于ZnNI。转换层。向溶液(0.01mol.L-1)中加入少量铈盐(0.01mol.L-1)促进腐蚀电位(Ecorr)位移到更大的正电势,而是作为来自溶胶底物的剥离速度的函数。腐蚀速率(Icorr)也通过底物的取液速度影响,并且对于ZnNI /溶胶 - 凝胶系统的最佳腐蚀性,具有10cm.min-1的来自溶胶的衬底的剥离速度。

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