材料工程
材料工程
재료공정
JOURNAL OF MATERIALS ENGINEERING
2010年
3期
38-41
,共4页
衣晓红%樊占国%张景垒%李凤华%田昂
衣曉紅%樊佔國%張景壘%李鳳華%田昂
의효홍%번점국%장경루%리봉화%전앙
TC4钛合金%阳极氧化%TiO_2多孔膜%金红石型%锐钛型
TC4鈦閤金%暘極氧化%TiO_2多孔膜%金紅石型%銳鈦型
TC4태합금%양겁양화%TiO_2다공막%금홍석형%예태형
TC4 titanium alloy%anodic oxidation%TiO_2 porous film%rutile type%anatase type
以硫酸为电解液,钛合金(TC4)为阳极,不锈钢片为阴极,采用恒压的氧化方式在钛合金表面获得TiO_2多孔膜.通过扫描电镜(SEM)观察了多孔膜的微观形貌并用X射线衍射(XRD)对覆在钛合金基体上的氧化膜进行了物相分析,研究了氧化工艺参数电压、阳极氧化时间和硫酸浓度对TiO_2多孔膜相组成的影响.结果表明:TC4钛合金阳极氧化获得的氧化膜为非均一平面的TiO_2多孔膜,且膜的孔径分布在90~240nm,XRD分析表明在不同的氧化工艺参数下氧化膜均由锐钛相和金红石相双相晶型组成.在0.5mol/L硫酸溶液中,电压高于100V或氧化时间长于5min即出现锐钛相和金红石相TiO_2,随着电压的升高和时间的增长金红石相TiO_2的含量逐渐增加;在恒压120V时,硫酸溶液浓度为0.3mol/L即出现锐钛相和金红石相TiO_2,随着硫酸浓度的提高金红石相TiO_2的含量先增加后减少.
以硫痠為電解液,鈦閤金(TC4)為暘極,不鏽鋼片為陰極,採用恆壓的氧化方式在鈦閤金錶麵穫得TiO_2多孔膜.通過掃描電鏡(SEM)觀察瞭多孔膜的微觀形貌併用X射線衍射(XRD)對覆在鈦閤金基體上的氧化膜進行瞭物相分析,研究瞭氧化工藝參數電壓、暘極氧化時間和硫痠濃度對TiO_2多孔膜相組成的影響.結果錶明:TC4鈦閤金暘極氧化穫得的氧化膜為非均一平麵的TiO_2多孔膜,且膜的孔徑分佈在90~240nm,XRD分析錶明在不同的氧化工藝參數下氧化膜均由銳鈦相和金紅石相雙相晶型組成.在0.5mol/L硫痠溶液中,電壓高于100V或氧化時間長于5min即齣現銳鈦相和金紅石相TiO_2,隨著電壓的升高和時間的增長金紅石相TiO_2的含量逐漸增加;在恆壓120V時,硫痠溶液濃度為0.3mol/L即齣現銳鈦相和金紅石相TiO_2,隨著硫痠濃度的提高金紅石相TiO_2的含量先增加後減少.
이류산위전해액,태합금(TC4)위양겁,불수강편위음겁,채용항압적양화방식재태합금표면획득TiO_2다공막.통과소묘전경(SEM)관찰료다공막적미관형모병용X사선연사(XRD)대복재태합금기체상적양화막진행료물상분석,연구료양화공예삼수전압、양겁양화시간화류산농도대TiO_2다공막상조성적영향.결과표명:TC4태합금양겁양화획득적양화막위비균일평면적TiO_2다공막,차막적공경분포재90~240nm,XRD분석표명재불동적양화공예삼수하양화막균유예태상화금홍석상쌍상정형조성.재0.5mol/L류산용액중,전압고우100V혹양화시간장우5min즉출현예태상화금홍석상TiO_2,수착전압적승고화시간적증장금홍석상TiO_2적함량축점증가;재항압120V시,류산용액농도위0.3mol/L즉출현예태상화금홍석상TiO_2,수착류산농도적제고금홍석상TiO_2적함량선증가후감소.
TiO_2 porous films were prepared directly on the surface of TC4 titanium alloy by constant voltage anodic oxidation using sulfuric acid, TC4 and stainless steel plate as electrolyte, anode and cathode, respectively. The micro-morphology of the TiO_2 porous films on the substrate was observed by SEM. Meanwhile, phase composition of the porous films on the titanium alloy substrate was determined by XRD. The effects of oxidation process parameters such as the voltage, the anodization time and the concentration of sulphuric acid on the phase composition of TiO_2 porous films were investigated. The results showed that, oxide films of titanium alloy after anodic oxidation were heterogeneous TiO_2 porous films with pore size ranging from 90nm to 240nm. The XRD analysis showed that the oxide films prepared with different oxidation process parameters were all consisted of annatase and rutile phases. In 0.5mol/L sulfuric acid electrolyte, the annatase and rutile TiO_2 appeared when the voltage was higher than 100V or anodization time was longer than 5min, and with the voltage and time increasing the content of rutile TiO_2 increased gradually. The annatase and rutile TiO_2 appeared with 0.3mol/L sulfuric acid electrolyte at constant voltage (≥120V), and the content of rutile TiO_2 increased at first and then decreased with the increasing concentration of sulfuric acid.