表面技术
錶麵技術
표면기술
SURFACE TECHNOLOGY
2014年
3期
31-36,47
,共7页
陈凯%刘小萍%范文娟%安康%邹鹏远%姚文苇
陳凱%劉小萍%範文娟%安康%鄒鵬遠%姚文葦
진개%류소평%범문연%안강%추붕원%요문위
Ti-6 Al-4 V%锆合金层%硬度%耐蚀性
Ti-6 Al-4 V%鋯閤金層%硬度%耐蝕性
Ti-6 Al-4 V%고합금층%경도%내식성
Ti-6Al-4V%Zr-alloyed layer%hardness%corrosion resistance
目的:通过等离子表面合金化渗锆,提高Ti-6 Al-4 V的表面硬度及在还原性酸中的耐蚀性能。方法分别在800,850,900℃渗锆,分析研究锆合金层的成分、相组成、显微硬度及在为10%(质量分数)H2SO4溶液中的腐蚀行为,并与未处理的基材进行对比。结果 Ti-6Al-4V在三种温度下渗锆后,形成的表面合金层主要由锆在α-Ti或β-Ti中形成的固溶体组成,元素组成呈梯度分布,表面粗糙度随渗锆温度的提高而增加,硬度由表及里呈梯度下降,表面硬度比未处理的Ti-6 Al-4 V提高了约200 HV0.1。与未处理的基材相比,Ti-6Al-4V渗锆后,在10%H2 SO4溶液中的自腐蚀电位均正移,钝化电流密度均有所减小。结论 Ti-6 Al-4 V渗锆后,硬度和耐蚀性较基体有所提高,其中,900℃渗锆后的耐蚀性最好,800℃与850℃渗锆试样的耐蚀性次之。
目的:通過等離子錶麵閤金化滲鋯,提高Ti-6 Al-4 V的錶麵硬度及在還原性痠中的耐蝕性能。方法分彆在800,850,900℃滲鋯,分析研究鋯閤金層的成分、相組成、顯微硬度及在為10%(質量分數)H2SO4溶液中的腐蝕行為,併與未處理的基材進行對比。結果 Ti-6Al-4V在三種溫度下滲鋯後,形成的錶麵閤金層主要由鋯在α-Ti或β-Ti中形成的固溶體組成,元素組成呈梯度分佈,錶麵粗糙度隨滲鋯溫度的提高而增加,硬度由錶及裏呈梯度下降,錶麵硬度比未處理的Ti-6 Al-4 V提高瞭約200 HV0.1。與未處理的基材相比,Ti-6Al-4V滲鋯後,在10%H2 SO4溶液中的自腐蝕電位均正移,鈍化電流密度均有所減小。結論 Ti-6 Al-4 V滲鋯後,硬度和耐蝕性較基體有所提高,其中,900℃滲鋯後的耐蝕性最好,800℃與850℃滲鋯試樣的耐蝕性次之。
목적:통과등리자표면합금화삼고,제고Ti-6 Al-4 V적표면경도급재환원성산중적내식성능。방법분별재800,850,900℃삼고,분석연구고합금층적성분、상조성、현미경도급재위10%(질량분수)H2SO4용액중적부식행위,병여미처리적기재진행대비。결과 Ti-6Al-4V재삼충온도하삼고후,형성적표면합금층주요유고재α-Ti혹β-Ti중형성적고용체조성,원소조성정제도분포,표면조조도수삼고온도적제고이증가,경도유표급리정제도하강,표면경도비미처리적Ti-6 Al-4 V제고료약200 HV0.1。여미처리적기재상비,Ti-6Al-4V삼고후,재10%H2 SO4용액중적자부식전위균정이,둔화전류밀도균유소감소。결론 Ti-6 Al-4 V삼고후,경도화내식성교기체유소제고,기중,900℃삼고후적내식성최호,800℃여850℃삼고시양적내식성차지。
Objective To improve the surface hardness and corrosion resistance of the Ti-6Al-4V in reducing acid solution by plasma surface zirconium alloying. Methods The chemical composition, phase structure and micro-hardness of the Zr-alloyed layer obtained at 800 ℃, 850 ℃ and 900 ℃ were studied. The electrochemical behaviors of alloyed and untreated matrix in 10 %H2 SO4 solution were also studied. Results The alloyed layers formed at three different temperatures exhibited a gradient composi-tion and mainly consisted of α( Ti, Zr) andβ( Ti, Zr) . The surface roughness of Zr-alloyed alloy increased with alloying tempera-ture. The hardness of the alloyed layer was increased by about 200HV0. 1 compared with untreated Ti-6Al-4V and was gradually decreased along the alloyed depth. The corrosion potential of the alloyed layer shifted markedly to positive direction in contrast to the untreated matrix, while the passivation current density was decreased. Conclusion The micro-hardness and the corrosion resis-tance of Zr-alloyed Ti-6Al-4V were improved compared with the untreated titanium alloy. Among the temperatures tested, the cor-rosion resistance of the alloyed layer treated at 900 ℃ was the best, followed by the alloyed layer treated at 800 ℃ and 850 ℃.