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
8期
2118-2124
,共7页
郑传波%益帼%高延敏%张克
鄭傳波%益幗%高延敏%張剋
정전파%익귁%고연민%장극
7075-T6铝合金%表观氢渗透系数%D-S双电解池%SSRT实验
7075-T6鋁閤金%錶觀氫滲透繫數%D-S雙電解池%SSRT實驗
7075-T6려합금%표관경삼투계수%D-S쌍전해지%SSRT실험
7075-T6 Al alloy%apparent hydrogen diffusivity%D-S double cell%SSRT experiment
采用D?S双电解池研究7075-T6铝合金的表观氢渗透系数,对表面镀镍厚度、充氢电流和循环次数对表观氢渗透系数的影响进行研究,进一步研究表面镀镍充氢试样的应力腐蚀敏感性。结果表明:表面镀镍厚度为220 nm 时,钝化电流最为稳定,镀镍层厚度对氢渗透电流的影响主要体现在对氢原子的氧化能力和对铝合金基体的保护能力上。表观氢渗透系数随充氢电流增大有增大的趋势,主要与表面氢原子深度增大、深度梯度增大以及加速氢向铝合金的渗透相关。但是增大幅度表观氢渗透系数有减小的趋势,主要原因是由于氢的表面覆盖度增大后,大部分的氢原子开始结合为氢气而脱离铝合金表面。随着循环次数的增加,表观氢渗透系数也随之增大,主要原因是随着循环次数增加,铝合金内部的不可扩散氢深度趋于稳定,可扩散氢的渗透速度增大。SSRT 实验分析和SEM电镜照片结果表明:随充氢时间的增长,SSRT敏感性增大,氢能够渗入铝合金内部,并使其脆性增大,且其脆性随着充氢时间延长而有所增大。
採用D?S雙電解池研究7075-T6鋁閤金的錶觀氫滲透繫數,對錶麵鍍鎳厚度、充氫電流和循環次數對錶觀氫滲透繫數的影響進行研究,進一步研究錶麵鍍鎳充氫試樣的應力腐蝕敏感性。結果錶明:錶麵鍍鎳厚度為220 nm 時,鈍化電流最為穩定,鍍鎳層厚度對氫滲透電流的影響主要體現在對氫原子的氧化能力和對鋁閤金基體的保護能力上。錶觀氫滲透繫數隨充氫電流增大有增大的趨勢,主要與錶麵氫原子深度增大、深度梯度增大以及加速氫嚮鋁閤金的滲透相關。但是增大幅度錶觀氫滲透繫數有減小的趨勢,主要原因是由于氫的錶麵覆蓋度增大後,大部分的氫原子開始結閤為氫氣而脫離鋁閤金錶麵。隨著循環次數的增加,錶觀氫滲透繫數也隨之增大,主要原因是隨著循環次數增加,鋁閤金內部的不可擴散氫深度趨于穩定,可擴散氫的滲透速度增大。SSRT 實驗分析和SEM電鏡照片結果錶明:隨充氫時間的增長,SSRT敏感性增大,氫能夠滲入鋁閤金內部,併使其脆性增大,且其脆性隨著充氫時間延長而有所增大。
채용D?S쌍전해지연구7075-T6려합금적표관경삼투계수,대표면도얼후도、충경전류화순배차수대표관경삼투계수적영향진행연구,진일보연구표면도얼충경시양적응력부식민감성。결과표명:표면도얼후도위220 nm 시,둔화전류최위은정,도얼층후도대경삼투전류적영향주요체현재대경원자적양화능력화대려합금기체적보호능력상。표관경삼투계수수충경전류증대유증대적추세,주요여표면경원자심도증대、심도제도증대이급가속경향려합금적삼투상관。단시증대폭도표관경삼투계수유감소적추세,주요원인시유우경적표면복개도증대후,대부분적경원자개시결합위경기이탈리려합금표면。수착순배차수적증가,표관경삼투계수야수지증대,주요원인시수착순배차수증가,려합금내부적불가확산경심도추우은정,가확산경적삼투속도증대。SSRT 실험분석화SEM전경조편결과표명:수충경시간적증장,SSRT민감성증대,경능구삼입려합금내부,병사기취성증대,차기취성수착충경시간연장이유소증대。
The apparent hydrogen diffusivity was studied by D?S double cell. The effect of thickness of plated Ni, charging current density and charging-uncharging cycles on apparent hydrogen diffusivity was studied. And the stress corrosion cracking (SCC) sensitivity of constant charging specimens was studied. The results show that the passivation current is steady while the thickness of plated Ni is 220 nm. The plated Ni can provide protection from pitting corrosion and catalysis effect on hydrogen. The apparent hydrogen diffusivity increases with the increase of charging current density. The surface hydrogen concentration increases with the increase of charging current density, and the concentration gradient also increases, the hydrogen permeation rate increases, while the increase trend becomes slow due to the surface coverage. The apparent hydrogen diffusivity increases with the increase of charging-uncharging cycles at the beginning, and then reaches a steady value due to the overflow of non-diffuse hydrogen and the increase of hydrogen permeation rate. And the SCC sensitivity of constant charging specimens increases with the increase of charging time.