共查询到19条相似文献,搜索用时 333 毫秒
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在由FeSO4·7H2O 30 g/L、Co SO4·7H2O 30 g/L、H3BO3 30 g/L和抗坏血酸1 g/L组成的Co–Fe合金镀液中添加10 g/L自制纳米Zr O2溶胶,电沉积得到Co–Fe–Zr O2复合镀层。研究了电流密度对Co–Fe–Zr O2复合镀层微观结构、厚度、显微硬度和耐蚀性的影响。结果表明,随电流密度从5 mA/cm2增大到30 mA/cm2,Co–Fe–ZrO2复合镀层的晶粒细化,ZrO2颗粒复合量、厚度和显微硬度均增大,耐蚀性先改善后变差。当电流密度为25 mA/cm2时,Co–Fe–ZrO2复合镀层的厚度为18.6μm,显微硬度为349 HV,表面平整致密,耐蚀性最佳。 相似文献
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峰值电流密度对脉冲电沉积Ni-Co-CNTs复合镀层机械性能的影响 总被引:2,自引:0,他引:2
研究了峰值电流密度对脉冲电沉积Ni-Co-CNTs复合镀层机械性能的影响。结果表明:当峰值电流密度升高时,镀层表面变得粗糙;随着峰值电流密度的增加,镀层中碳的质量分数先增加后下降,当峰值电流密度为80 A/dm~2时,镀层中碳的质量分数达到最大值;镀层的显微硬度和抗拉强度均在峰值电流密度为100 A/dm~2附近时达到其最大值,且高于直流电沉积时所得镀层的显微硬度值和抗拉强度值。说明采用脉冲电沉积工艺可以提高镀层的机械性能。 相似文献
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采用脉冲电沉积技术在304不锈钢表面制备Ni-Cu合金镀层,镀液组成和工艺条件为:NiSO4ꞏ6H2O 200g/L,CuSO4ꞏ5H2O 10 g/L,十二烷基硫酸钠0.2 g/L,柠檬酸钠80 g/L,糖精0.2 g/L,pH 4.0,温度25°C,搅拌速率30 r/min,平均电流密度40~120 mA/cm2,脉冲频率0~100 Hz,占空比20%~90%,时间30 min。研究了平均电流密度、脉冲频率和占空比对Ni-Cu合金镀层的元素组成、表面形貌和显微硬度的影响,得到较优的工艺参数为:平均电流密度40 mA/cm2,脉冲频率50 Hz,占空比60%。该条件下所得Ni-Cu合金镀层由质量分数分别为56.53%和43.47%的Ni和Cu组成,呈“菜花”状形貌,结晶细致、均匀,显微硬度为614.4 HV。 相似文献
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《现代化工》2017,(4)
在络合-超滤处理含镍废水并得到镍离子质量浓度为418 mg/L浓缩液的基础上,考察了电沉积法处理含镍浓缩液过程中电流密度、初始pH、电解时间、温度、极距、搅拌等参数对电流效率和镍回收率的影响。结果表明:当电流密度、电解时间增加时,电流效率随之下降,而镍回收率增大;当pH、极距增大时,电流效率和镍回收率均先增大后减小;温度升高、低速搅拌均可提高电流密度与镍回收率。在电流密度为3.5 m A/cm~2,pH=4,温度为50℃,电解时间为130 min,极距为10 cm并加入低速搅拌的最优操作条件下,电流效率最高可达42%,镍回收率可达52%,并探讨了电沉积机理。 相似文献
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新型直接碳燃料电池阴极材料及其性能 总被引:2,自引:0,他引:2
考察了Ni-CeO2复合阴极对直接碳燃料电池(DCFC)输出性能的影响. 使用不同组成的Ni-CeO2复合阴极对DCFC性能进行了测试. 结果表明,使用Ni-CeO2复合阴极可显著提高DCFC在500和630℃工作时的电流密度、功率密度和燃料转化效率,500℃下DCFC最大电流密度、功率密度分别为328 mA/cm2和72 mW/cm2. 630℃下DCFC最大电流密度、功率密度分别为474 mA/cm2和108 mW/cm2,电流密度50 mA/cm2时燃料转化效率为70%. 用XRD和SEM对Ni-CeO2复合阴极材料进行了表征,并对Ni-CeO2复合阴极可能的作用机制进行了研究. 相似文献
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运用恒电流法在铜柱电极上研究了工业磷酸中毒性较大的As(Ⅲ)还原为无毒单质砷的电化学行为。实验表明,当电流密度控制在-0.044 mA/cm2以内时可以很好地将As(Ⅲ)转化为单质砷并抑制砷化氢析出。由塔费尔拟合推算得到As(Ⅲ)转化为单质砷的交换电流密度为-6.324×10-7mA/cm2,此过程为不可逆过程。采用表面积为15.8 cm2的铜柱电极,在电流密度为-0.038 mA/cm2,温度为80℃条件下,将磷酸中As(Ⅲ)含量由10.92×10-6降到0.47×10-6,电流效率达7.55%。 相似文献
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Nickel–tungsten nanocrystalline coatings were electrodeposited from a Watts type bath onto a copper substrate, at different
current densities selected from activation, mixed and diffusion controlled regions in the cathodic scan plot at room temperature.
The results confirm that tungsten codeposition proceeds via the adsorption and reduction of complexes produced in the bulk
of solution. The coatings obtained were single phase solid solutions and their grain sizes increased with current density.
A cauliflower-type surface morphology with highest hardness was obtained when the current density was in the activation controlled
region. The surface morphology obtained in the mixed controlled region was distorted, and then converted to a nodular morphology
in the diffusion controlled region. In the mixed control region, coatings with the highest corrosion resistance were obtained
due to the lowest exchange current density for water reduction. 相似文献
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采用直流电沉积法在高锰铝青铜基体上制得Cu-Ni合金镀层,镀液组成和工艺条件为:CuSO4·5H2O 20 g/L,NiSO4·6H2O 84 g/L,C6H5O7Na3·2H2O 75 g/L,十二烷基硫酸钠0.5 g/L,H3BO320 g/L,电流密度15~30 mA/cm^2,pH 7,温度55℃,搅拌速率300 r/min,时间60 min。研究了电流密度对Cu-Ni合金镀层元素成分、微观形貌和耐蚀性的影响。结果表明,在电流密度30 mA/cm^2下所得到的Cu-Ni合金镀层最厚,为25μm,耐蚀性最好,经乙酸盐雾试验168 h后表面仅有几个微小的腐蚀坑。 相似文献
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Effect of Electrodeposition Parameters on the Microstructure and Corrosion Behavior of DCPD Coatings on Biodegradable Mg–Ca–Zn Alloy
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Hamid Reza Bakhsheshi‐Rad Esah Hamzah Safaa N. Saud Mamoun Medraj 《International Journal of Applied Ceramic Technology》2015,12(5):1054-1064
In this study, DCPD (Brushite, CaHPO4.2H2O) coatings were prepared on the surface of a Mg–Ca–Zn alloy using different current density (0.15–1.2 mA/cm2) and deposition time (5–90 min). The results revealed that DCPD with needle‐like morphology was observed for the current density between 0.15 and 0.4 mA/cm2?, whereas ?plate‐like morphology was obtained at current density above 0.8 mA/cm2. The results showed that surface roughness increased with increasing current density. The lowest corrosion rate of 0.14 mm/year was obtained for the dense and uniform DCPD coating ?at 0.4 mA/cm2, while further increase has deleterious effect on the corrosion resistance. 相似文献
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羟基氧化镍的电解制备,结构表征和电化学性能研究 总被引:1,自引:0,他引:1
NiOOH was prepared by one-step electrolysis of spherical Ni(OH)2 and the effects of electrolysis parameters were examined. The highly pure NiOOH was obtained after electrolysis at a current density of 60mA.g^-1 and 30℃ with anodic potential controlled in the range of 1.73-1.85V (vs. Zn/ZnO) for 360min. The NiOOH samriles were characterized bv X-ray oowder diffraction (XRD) and scanning electron microscope (SEM) analysis.Resuits indicate that the electrolysis product is spherical NiOOH doped with graphite. Charge and discharge tests show that the prepared NiOOH offers a discharge capacity of over 270mAh·g^-1 at current density of 30mA·g^-1 and can be directly used as cathode material of alkaline Zn/NiOOH batteries. Galvanostatic charge/discharge and cyclic voltammetry (CV) tests reveal good cycling reversibility, of the NiOOH electrode. 相似文献
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Tungsten and nickel tungsten carbides were evaluated as the anode catalysts of a polymer electrolyte fuel cell (PEFC). These catalysts were prepared by the temperature-programmed carburization of tungsten and nickel tungsten oxides from 573 to 873-1073 K in a stream of 20% CH4/H2 and kept at temperature for 3 h. The 30% tungsten and nickel tungsten carbides mixed with Ketjen carbon (KC) were evaluated by cyclic voltammetry and linear sweep voltammetry using a rotating disk electrode and electrocatalytic activity (I-V performance) using a single cell. The W1023/KC catalyst achieved a power density of 6.4 mW/cm2 (current density: 15.2 mA/cm2) which corresponded to 5.7% of that achieved by a commercial 20% Pt/C catalyst in a single cell (20% Pt/C: 111.7 mW/cm2) using our setup. From the XRD data, α-W2C together with a small amount of WC was active during the anodic oxidation. The maximum power density of the 30 wt% 873 K-carburized NiW/KC was 8.2 mW/cm2 at the current density of 19.0 mA/cm2 which was 7.3% of the 20 wt% Pt/C. 相似文献