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化学镀镍过程中丙酸作用的机理研究
引用本文:胡光辉,吴辉煌,杨防祖. 化学镀镍过程中丙酸作用的机理研究[J]. 高等学校化学学报, 2006, 27(3): 519-522
作者姓名:胡光辉  吴辉煌  杨防祖
作者单位:厦门大学化学化工学院,固体表面物理化学国家重点实验室,厦门 361005
摘    要:利用循环伏安法和红外漫反射光谱法研究化学镀镍过程中丙酸的作用机理. 不同丙酸浓度下的循环伏安曲线表明,丙酸能同时促进Ni2+的还原和H2PO-2的氧化.根据丙酸分别与NaH2PO2和NiSO4共存时镍基体上吸附物的红外漫反射光谱变化,推断丙酸是通过与NaH2PO2和Ni2+形成表面络合物来促进化学沉积的. 丙酸能与NaH2PO2形成分子间氢键,促使P-H键断裂并生成·PHO-2中间物,从而提高H2PO-2的氧化速度; 同时,丙酸以其-OCO-官能团与Ni2+生成桥式配合物,有利于加速Ni2+的沉积. H2PO-2氧化速度的提高有助于磷的沉积,从而增大了化学镀层中的磷含量.

关 键 词:丙酸   有机添加剂   化学镀镍   沉积速度,
文章编号:0251-0790(2006)03-0519-04
收稿时间:2005-04-06
修稿时间:2005-04-06

Mechanistic Studies on Mechanism of Propionic Acid Action in Elecroless Nickel Plating
HU Guang-Hui,WU Hui-Huang,YANG Fang-Zu. Mechanistic Studies on Mechanism of Propionic Acid Action in Elecroless Nickel Plating[J]. Chemical Research In Chinese Universities, 2006, 27(3): 519-522
Authors:HU Guang-Hui  WU Hui-Huang  YANG Fang-Zu
Affiliation:College of Chemistry and Chemical Engineering, State Key Laboratory of Physical Chemistry of the Solid Surfaces,  Xiamen University, Xiamen 361005, China
Abstract:Propionic acid as an additive in electroless nickel plating will accelerate chemical deposition and raise P contents in the deposits.  In this work, the action mechanism of propionic acid in the electroless plating were studied by cyclic voltammetry and infrared reflection spectroscopy.  The voltammetric curves at various concentrations of propionic acid indicate that propionic acid will promote both cathodic Ni2+ reduction and anodic NaH2PO2 oxidation.  According to the differences between the infrared reflection spectra of adsorbed propionic acid on Ni substrates and that of the adsorbed species when propionic acid co-exists with NaH2PO2 or NiSO4, it was proposed that the acceleration of chemical deposition was attributed to the formation of surface complexes of  propionic acid with NaH2PO2 and NiSO4,respectively.  Propionic acid could form intermolecular hydrogen bonds with NaH2PO2, which promotes splitting of P-H bond in the reductant and producing  PHO-2 intermediates, hence facilitates the oxidation of NaH2PO2.  At the same time, propionic acid is coordinated with Ni2+ via   its  —OCO— group to form bridge complexes so as to promote NiSO4 reduction.  The accelerating oxidation of NaH2PO2 in turn helps the deposition of P, as a result, P contents in the deposits increase with accelerating NaH2PO2 oxidation. 
Keywords:Propionic acid  Organic additive  Electroless nickel plating  Deposition rate
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