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首页> 外文期刊>Materials transactions >Effect of Dissolved Impurities on the Lightness and Surface Morphology of Nickel Deposits from Chloride Electrowinning Solutions
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Effect of Dissolved Impurities on the Lightness and Surface Morphology of Nickel Deposits from Chloride Electrowinning Solutions

机译:溶解杂质对氯化氯电解溶液镍沉积物的亮度和表面形态的影响

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摘要

This study investigated the effect of dissolved impurities on the lightness, surface morphology, and current efficiency of deposited nickel during electrowinning. Nickel electrodeposition was performed at a current density of 300 A . m(-2) and 7.2 x 10(5) C.m(-2) of charge in an unagitated chloride solution containing Mn2+, Cr3+, and SO42- ion impurities with a pH from 1 to 3, at a temperature of 333 K. Solutions containing 10 g dm-3 of Mn2+ resulted in a slight decrease in current efficiency for nickel deposition and smaller crystal sizes in the deposited nickel. The lightness of deposited nickel decreased for Mn2+ concentrations exceeding 1 g . dm(-3). When nickel deposition was performed using a soluble nickel anode to prevent the formation of MnO2 at the anode, greater nickel lightness resulted than with an insoluble anode, suggesting that MnO2 produced by the insoluble anode caused decreased lightness of nickel. In solutions containing Cr3+, the current efficiency of nickel gradually decreased with increasing Cr3+ concentrations and significantly decreased at Cr3+ concentrations above 0.1 g . dm(-3). The lightness of deposited Ni greatly decreased with increasing concentrations of Cr3+ above 0.001 g . dm(-3). Formation of Cr(OH)(3) at the cathode layer is presumed to suppress nickel deposition, resulting in some codeposition of NiO and Ni(OH) 2 along with Ni, which causes the nickel current efficiency and lightness to decrease. Conversely, solutions containing SO42- resulted in a moderate decrease in nickel current efficiency at SO42- concentrations above 50 g center dot dm-3 and a significant decrease above 100 g . dm(-3). The lightness of deposited nickel increased slightly at SO42- concentrations of 20 g center dot dm-3 and strongly increased above 20 g . dm(-3). Because the overpotential for nickel deposition increases with the concentration of SO4 2-, the surface of the deposited nickel becomes smooth, resulting in greater lightness.
机译:本研究研究了溶解的杂质对沉积镍在电热过程中沉积镍的电流效率的影响。镍电沉积在电流密度为300a。在含有Mn 2 +,Cr3 +和SO42离子杂质的未凝结氯化物溶液中的M(-2)和7.2×10(5)厘米(-2)电荷在333k溶液的温度下,含有Mn 2 +,Cr3 +和SO42离子杂质,其温度为1至3。含有10g DM-3的Mn2 +导致镍沉积的电流效率略微降低,并且在沉积的镍中的较小晶体尺寸。对于超过1g的Mn 2 +浓度,沉积镍的亮度降低。 DM(-3)。当使用可溶性镍阳极进行镍沉积以防止在阳极处形成MnO 2时,比用不溶的阳极形成更大的镍亮,表明通过不溶性阳极产生的MnO 2导致镍的亮度降低。在含CR3 +的溶液中,镍的电流效率随着Cr3 ​​+浓度的增加而逐渐降低,并且在0.1g的Cr3 +浓度下显着降低。 DM(-3)。沉积Ni的亮度随着CR3 +高于0.001g的浓度而大大降低。 DM(-3)。假定在阴极层的Cr(OH)(3)的形成以抑制镍沉积,导致NiO和Ni(OH)2的一些重质沉积以及Ni,这导致镍电流效率和亮度降低。相反,含有SO 42的溶液导致SO42-浓度在50g中心点DM-3高于50g中心点DM-3的镍电流效率下降,并显着降低100g。 DM(-3)。沉积镍的亮度略微增加到20g中心点DM-3的SO42-浓度,强大增加20g。 DM(-3)。因为镍沉积的过电位随着SO4 2的浓度而增加,所以沉积镍的表面变得光滑,导致较大的亮度。

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