中国有色金属学报
中國有色金屬學報
중국유색금속학보
THE CHINESE JOURNAL OF NONFERROUS METALS
2013年
12期
3387-3393
,共7页
B95铝合金%交流阻抗%Ce转化膜%电极反应%成膜过程
B95鋁閤金%交流阻抗%Ce轉化膜%電極反應%成膜過程
B95려합금%교류조항%Ce전화막%전겁반응%성막과정
B95 aluminium alloys%electrochemical impedance spectroscope (EIS)%Ce conversion coating%electrode reaction%coating forming process
采用电化学阻抗谱(EIS)研究B95铝合金在10 mmol/L CeCl3溶液中转化膜的形成过程,在建立稀土转化膜成膜过程三阶段机理基础上,采用电化学阻抗谱(EIS)技术研究溶液中氧含量、H2O2、pH 值等各种条件变化对转化膜形成过程的影响。结果表明:O2参与的反应不是Ce转化膜形成速度的决定步骤,添加H2O2加快Ce转化膜形成速度,特别是形成过程的第一阶段;微阴极区氧主要按二电子途径还原,使局部 pH 上升,当 pH 达到或超过8.05时,Ce(Ⅲ)水合氢氧化物/氧化物开始沉积;Ce(Ⅲ)转化膜达到稳定平衡阶段,部分Ce(OH)3会被氧还原的中间产物H2O2氧化成CeO2;在中性或弱酸性溶液中,提高溶液的pH值对最终成膜有利。
採用電化學阻抗譜(EIS)研究B95鋁閤金在10 mmol/L CeCl3溶液中轉化膜的形成過程,在建立稀土轉化膜成膜過程三階段機理基礎上,採用電化學阻抗譜(EIS)技術研究溶液中氧含量、H2O2、pH 值等各種條件變化對轉化膜形成過程的影響。結果錶明:O2參與的反應不是Ce轉化膜形成速度的決定步驟,添加H2O2加快Ce轉化膜形成速度,特彆是形成過程的第一階段;微陰極區氧主要按二電子途徑還原,使跼部 pH 上升,噹 pH 達到或超過8.05時,Ce(Ⅲ)水閤氫氧化物/氧化物開始沉積;Ce(Ⅲ)轉化膜達到穩定平衡階段,部分Ce(OH)3會被氧還原的中間產物H2O2氧化成CeO2;在中性或弱痠性溶液中,提高溶液的pH值對最終成膜有利。
채용전화학조항보(EIS)연구B95려합금재10 mmol/L CeCl3용액중전화막적형성과정,재건립희토전화막성막과정삼계단궤리기출상,채용전화학조항보(EIS)기술연구용액중양함량、H2O2、pH 치등각충조건변화대전화막형성과정적영향。결과표명:O2삼여적반응불시Ce전화막형성속도적결정보취,첨가H2O2가쾌Ce전화막형성속도,특별시형성과정적제일계단;미음겁구양주요안이전자도경환원,사국부 pH 상승,당 pH 체도혹초과8.05시,Ce(Ⅲ)수합경양화물/양화물개시침적;Ce(Ⅲ)전화막체도은정평형계단,부분Ce(OH)3회피양환원적중간산물H2O2양화성CeO2;재중성혹약산성용액중,제고용액적pH치대최종성막유리。
The electrochemical impedance spectroscope (EIS) was used to study the conversion coating forming process of B95 aluminum alloy in 10 mmol/L CeCl3 solution. The formation process of rare earth (RE) conversion coating can be divided into three stages. Based on the three stages formation mechanism of the rare earth conversion coatings, the influences of O2 concentration, oxidant, pH etc on the formation process of conversion film were investigated. The result shows that the reaction caused by the O2 participation is not determinate step of the Ce conversion coating formation, the addition of H2O2 speeds up the formation of Ce conversion coating, especially in the first stage. The two electric ways of cathodic reaction are formed by the conversion coating on B95 aluminum alloy in CeCl3 solution, which reasonably explains the local pH rise in micro cathode area, Ce(Ⅲ) hydrous hydroxide/oxide begins to deposit when the pH reaches or exceeds 8.05. Part Ce(OH)3 can be oxidized into CeO2 by the intermediate products of H2O2 when Ce(Ⅲ) conversion coating achieves stable equilibrium. In neutral or subacidity solution, improving the pH of solution will beneficial to the final formation of the coating.