稀有金属材料与工程
稀有金屬材料與工程
희유금속재료여공정
RARE METAL MATERIALS AND ENGINEERNG
2009年
z2期
560-563
,共4页
张荣发%黄隆%胡长员%柯科%巢强花%王为
張榮髮%黃隆%鬍長員%柯科%巢彊花%王為
장영발%황륭%호장원%가과%소강화%왕위
镁合金%微弧氧化%基体%性能
鎂閤金%微弧氧化%基體%性能
미합금%미호양화%기체%성능
magnesium alloys%micro arc oxidation%substrate%property
在环保型电解液中,采用电压-时间曲线、等离子体发射光谱仪(ICP)、扫描电镜(SEM)等方法研究了纯镁和AZ91HP两种基体材料对氧化过程、氧化膜表面形貌及成分的影响.根据电压-时间曲线,在氧化时间分别为1 min和5 min时,AZ91HP镁合金的电流效率比纯镁低,可能是由AZ91HP中的合金元素铝氧化并进入氧化膜中导致裂缝增加,成为析氧中心所导致的.在AZ91HP镁合金上生成的氧化膜孔的均匀性没有纯镁好,并且最大孔的直径比在纯镁上的氧化膜大.EDS分析表明,随着氧化时间延长,氧化膜中Si和P含量增加;而在氧化时间相同的情况下,两种基体上形成的氧化膜成分没有明显区别.ICP方法没有检测到氧化溶液中含有Mg~(2+)和Al~(3+),表明这两种离子在溶液中的浓度很低.
在環保型電解液中,採用電壓-時間麯線、等離子體髮射光譜儀(ICP)、掃描電鏡(SEM)等方法研究瞭純鎂和AZ91HP兩種基體材料對氧化過程、氧化膜錶麵形貌及成分的影響.根據電壓-時間麯線,在氧化時間分彆為1 min和5 min時,AZ91HP鎂閤金的電流效率比純鎂低,可能是由AZ91HP中的閤金元素鋁氧化併進入氧化膜中導緻裂縫增加,成為析氧中心所導緻的.在AZ91HP鎂閤金上生成的氧化膜孔的均勻性沒有純鎂好,併且最大孔的直徑比在純鎂上的氧化膜大.EDS分析錶明,隨著氧化時間延長,氧化膜中Si和P含量增加;而在氧化時間相同的情況下,兩種基體上形成的氧化膜成分沒有明顯區彆.ICP方法沒有檢測到氧化溶液中含有Mg~(2+)和Al~(3+),錶明這兩種離子在溶液中的濃度很低.
재배보형전해액중,채용전압-시간곡선、등리자체발사광보의(ICP)、소묘전경(SEM)등방법연구료순미화AZ91HP량충기체재료대양화과정、양화막표면형모급성분적영향.근거전압-시간곡선,재양화시간분별위1 min화5 min시,AZ91HP미합금적전류효솔비순미저,가능시유AZ91HP중적합금원소려양화병진입양화막중도치렬봉증가,성위석양중심소도치적.재AZ91HP미합금상생성적양화막공적균균성몰유순미호,병차최대공적직경비재순미상적양화막대.EDS분석표명,수착양화시간연장,양화막중Si화P함량증가;이재양화시간상동적정황하,량충기체상형성적양화막성분몰유명현구별.ICP방법몰유검측도양화용액중함유Mg~(2+)화Al~(3+),표명저량충리자재용액중적농도흔저.
In an environmentally friendly electrolyte, the effects of pure magnesium and AZ91HP substrate on anodizing process, surface morphologies and chemical compositions of anodic coatings were investigated by voltage-time curves, ICP and SEM. According to voltage-time curves, the current efficiency on AZ91HP was lower than that on pure magnesium for both 1 min and 5 min. The reason may be that the alloying element aluminium was anodized, subsequently entered into anodic coatings and therefore increased coating crack resulting in centers of oxygen evolution formed. The pore uniformity and the maximum diameter of anodic coatings formed on AZ91HP were separately worse and bigger than those on pure magnesium. EDX analysis showed that with anodizing prolonging, the content of Si and P on anodic coatings increased, too. For the same anodizing time, there was no distinct difference between the chemical compositions of anodic coatings formed on the two substrates. ICP analysis showed that Mg~(2+) or Al~(3+) was not detected in the anodizing solution, which indicated that their concentration in the solution was very low.