7B04铝合金应力腐蚀敏感性研究

利用慢应变速率拉伸应力腐蚀实验方法研究7B04铝合金的应力腐蚀开裂敏感性。研究温度、腐蚀介质、电化学极化对应力腐蚀敏感性的影响,结果表明:随温度的升高7B04铝合金的应力腐蚀开裂敏感性增强;溶液的腐蚀性越强,7B04铝合金的应力腐蚀开裂敏感性越大;无论是阳极极化还是阴极极化都会增加7B04铝合金的应力腐蚀开裂敏感性。     

LC4高强铝合金的慢应变速率拉伸试验

采用慢应变速率拉伸 (SSRT)技术测试了LC4铝合金在空气和质量分数为 3.5 %的NaCl溶液中的应力腐蚀断裂 (SCC)行为 .研究了应变速率对铝合金SCC行为的影响和氢在LC4高强铝合金应力腐蚀断裂过程中的作用 .试验结果表明 ,LC4合金具有SCC敏感性 ,在潮湿空气中发生应力腐蚀断裂 ,而在干燥空气中不发生应力腐蚀断裂 .对于长横取向的LC4铝合金试样 ,在应变速率为 1.331× 10 6s 1时 ,其SCC敏感性比应变速率为 6 .6 5 5× 10 6s 1时的敏感性大 .在潮湿空气和阳极极化条件下 ,铝合金的应力腐蚀断裂机理是以阳极溶解为主 ,氢几乎不起作用 .在预渗氢或阴极极化条件下 ,氢脆起主要作用 ,预渗氢时间延长可加速LC4合金的应力腐蚀断裂 .     

8090铝锂合金的氢脆敏感性研究

采用Ｍ３５１测量系统测试８０９０铝锂合金在３．５％ＮａＣｌ溶液中的腐蚀行为,并用ＳＲＴ测试技术研究了阴极极化下合金的氢脆敏感性,结果表明：充氢介质和时效制度对合金的氢脆敏感性影响较大,强烈渗氢条件下,氢可能成为腐蚀新裂的主要因素 。     

电极极化对铝合金应力腐蚀断裂敏感性的影响

为了探讨极化对铝合金应力腐蚀断裂(SCC)敏感性的影响,采用慢应变速率拉伸技术研究了不同恒电位极化条件下7075T6,7075T7351,7075RRA铝合金的应力腐蚀行为.结果表明,在-1 200～-735 mV(vs SCE)电位范围内,无论是阳极极化还是阴极极化,甚至弱极化,都会增加7075铝合金在3.5% NaCl溶液中的应力腐蚀断裂敏感性,无论哪一种热处理状态的7075铝合金在极化电位下的ISSRT均明显高于腐蚀电位下的ISSRT.同时,有阴极极化时ISSRT值随电极极化增强而减小,阳极极化时ISSRT 值有随电极极化增强而增大的趋势.但不同热处理状态的7075铝合金受极化电位的影响程度不同.由此认为,阳极溶解和氢效应都是导致7075铝合金应力腐蚀开裂的重要因素,电化学保护方法并不适用于7075铝合金应力腐蚀断裂的防护.     

微量稀土Ce对Al-Zn-Mg铝合金组织和腐蚀性能的影响

采用金相(OM)和扫描电镜(SEM)分析、力学拉伸实验、剥落腐蚀实验、电化学阻抗谱实验以及慢应变速率拉伸实验研究了微量稀土Ce对AlZn-Mg铝合金组织和性能的影响。研究结果表明:在Al-Zn-Mg铝合金中添加微量的稀土Ce元素,合金的抗腐蚀性能显著提高,应力腐蚀断裂时间延长,应力腐蚀敏感性显著降低;添加0. 04%(质量分数,下同) Ce对Al-Zn-Mg铝合金力学性能影响较小,但可显著提高合金的抗腐蚀性能,合金的剥蚀等级由EC提升至N,钝化膜电阻(Rp)由14 655Ω·cm~2提升至36 839Ω·cm~2,应力腐蚀敏感指数由0. 612降至0. 219。     

20钢在H2S溶液中的应力腐蚀开裂行为研究

采用电化学极化、慢应变拉伸、外加极化电位等方法对20钢在饱和H2S溶液中的应力腐蚀及其预防措施进行了研究.研究结果表明,20钢在饱和H2S水溶液中具有很高的应力腐蚀敏感性;在饱和H2S水溶液中对20钢进行适当的阳极或阴极极化均可降低20钢的应力腐蚀开裂敏感性,但阳极极化效果最为明显;在饱和H2S水溶液中添加咪唑啉缓蚀剂、硫脲-吡啶复配缓蚀剂都能显著降低20钢的应力腐蚀开裂敏感性.     

富锌涂层、阴极极化对管线钢应力腐蚀开裂敏感性的影响

为加强对油气管线钢腐蚀失效机理的认识,采用动态慢应变速率拉伸试验(SSRT),研究了弱酸性环境中富锌涂层与阴极保护对16Mn和X80 2种不同强度级别管线钢应力腐蚀开裂(SCC)敏感性的影响,探讨了2种管线钢的SCC机理.结果表明:在5%NaCl 0.5%CH3 COOH 酸性溶液中,16Mn钢的SCC机理以阳极溶解为主,富锌涂层和阴极保护均能有效提高16Mn钢的SCC抗力,前者效果优于后者;X80钢的SCC机理以氢脆为主,富锌涂层和阴极极化均促进其SCC过程,但富锌涂层提高X80钢SCC敏感性的程度低于与涂层自腐蚀电位相近的阴极极化作用.     

钛合金慢应变速率拉伸应力腐蚀行为研究

对TA31和TC4ELI两合金分别在干燥空气、3.5% NaCl环境下进行慢应变速率拉伸试验。结合应力-应变曲线以及断口宏观、微观组织分析两种材料的应力腐蚀敏感性。结果表明:在35℃、3.5%(w,下同) NaCl溶液、应变速率为10-6/s条件下,TC4ELI合金应力腐蚀敏感性较高,在5×10-7/s和5×10-6/s的应变速率下应力腐蚀敏感性较低;TA31合金在上述3种应变速率下应力腐蚀敏感性均较低;在3.5% NaCl环境中,TA31合金断口形貌较空气中试验的断口形貌无明显的变化,TC4ELI则出现较明显的解理面。      

LY6铝合金的局部腐蚀行为研究

探讨LY6合金的局部腐蚀行为对扩大其应用范围意义重大,采用加速腐蚀试验和微观腐蚀形貌观察等方法,研究了经自然时效处理的LY6铝合金在含Cl-的典型环境中的点蚀、晶间腐蚀、应力腐蚀断裂和剥蚀等局部腐蚀行为,并讨论了它们的机理和相互关系.在试验环境下,LY6铝合金对点蚀、晶间腐蚀、剥蚀和应力腐蚀断裂都存在敏感性,合金中S相(Al2CuMg)、θ相(CuAl2)及MnAl6等第二相的存在是发生上述局部腐蚀的根本原因.研究表明,合金的剥蚀是一个从点蚀发展到晶间腐蚀,然后在应力协同作用下发生破坏的过程.恒载荷应力腐蚀拉伸法和断口形貌观察发现,LY6铝合金应力腐蚀断裂是由于阳极溶解作用的结果.     

Fe85Ga15多晶在模拟海水中的应力腐蚀行为研究

研究了新型磁致伸缩材料Fe-Ga合金的应力腐蚀性能。采用恒载荷和慢应变速率拉伸(SSRT)试验,结合电化学测试技术,研究了铸态Fe85Ga15多晶在模拟海水中的应力腐蚀。结果表明,开路电位下,模拟海水中薄板光滑试样恒载荷拉伸能够发生低于材料抗拉强度的断裂,且断裂时间明显依赖于外加应力的大小,外加应力愈大,断裂时间愈短。这表明铸态Fe85Ga15合金在模拟海水中能够发生应力腐蚀开裂(SCC),且SCC归一化门槛应力为σscc/σb=0.34。慢应变速率拉伸显示,SCC敏感性在应变速率为5×10-7/s时最大,用强度损失表示为Iσ=(1-σc/σb)×100%=35%。阴极极化升高而阳极极化降低恒载荷SCC断裂时间。这些结果初步表明铸态Fe85Ga15合金在模拟海水中的应力腐蚀为阳极溶解型。     

The corrosion behavior of Ti-6Al-3Nb-2Zr-1Mo alloy: Effects of HCl concentration and temperature

Investigation about the corrosion behavior of Ti alloys in different ambient environment is of great significance for their practical application.Herein,we systematically investigate the corrosion behavior of a newfound Ti-6Al-3Nb-2Zr-1 Mo (Ti80) alloy in hydrochloric acid (HCI) ranging from 1.37 to 7 M,and temperature ranging from 25 to 55 ℃,by means of electrochemical measurements,static immersion tests and surface analysis.Results manifest that increasing either HCI concentration or temperature can accelerate the corrosion of Ti80 alloy via promoting the breakdown of native protective oxide film and then further facilitating the active dissolution of Ti80 matrix.According to potentiodynamic polarization curves,Ti80 alloy displays a spontaneous passive behavior in 1.37 M HCI at 25 ℃,compared to a typical active-passive behavior under the other conditions.As indicated by cathodic Tafel slope,the rate determining step for cathodic hydrogen evolution reaction is likely the discharge reaction step.The apparent activation energies obtained from corrosion current density and maximum anodic current density for Ti80 alloy in 5 M HCI solution are 62.4 and 55.6 kJ mol-1,respectively,which signifies that the rate determining step in the corrosion process of Ti80 alloy is mainly determined by surface-chemical reaction rather than diffusion.Besides,the electrochemical impedance spectroscopy tests demonstrate that a stable and compact oxide film exists in 1.37 M HCl at 25 ℃,whereas a porous corrosion product film forms under the other conditions.Overall,the critical HCI concentration at which Ti80 alloy can maintain passivation at 25 ℃ can be determined as a value between 1.37 and 3 M.Furthermore,the corroded surface morphology characterization reveals that equiaxed α phase is more susceptible to corrosion compared to intergranular β3 phase due to a lower content of Nb,Mo,and Zr in the former.     

Mechanisms for corrosion fatigue crack propagation

ABSTRACT The corrosion fatigue crack growth (FCG) behaviour, the effect of applied potential on corrosion FCG rates, and the fracture surfaces were studied for high‐strength low‐alloy steels, titanium alloys, and magnesium alloys. During investigation of the effect of applied potential on corrosion FCG rates, polarization was switched on for a time period in which it was possible to register the change in the crack growth rate corresponding to the open‐circuit potential and to measure the crack growth rate under polarization. Due to the higher resolution of the crack extension measurement technique, the time rarely exceeded 300 s. This approach made possible the observation of a non‐single mode effect of cathodic polarization on corrosion FCG rates. Cathodic polarization accelerated crack growth when the maximum stress intensity (K_max) exceeded a certain well‐defined critical value characteristic for a given material‐solution combination. When K_max was lower than the critical value, the same cathodic polarization, with all other conditions (specimen, solution, pH, loading frequency, stress ratio, temperature, etc.) being equal, retarded or had no influence on crack growth. The results and fractographic observations suggested that the acceleration in crack growth under cathodic polarization was due to hydrogen‐induced cracking (HIC). Therefore, critical values of K_max, as well as the stress intensity range (ΔK) were regarded as corresponding to the onset of corrosion FCG according to the HIC mechanism and designated as K_HIC and ΔK_HIC. HIC was the main mechanism of corrosion FCG at K_max > K_HIC (ΔK > ΔK_HIC). For most of the material‐solution combinations investigated, stress‐assisted dissolution played a dominant role in the corrosion fatigue crack propagation at K_max < K_HIC (ΔK < ΔK_HIC).     

Corrosion behaviour of β-Ti20Mo alloy in artificial saliva

To evaluate the potential of β-Ti20Mo alloy as a dental material, we tested its corrosion behaviour in artificial saliva in comparison to that of cp-Ti. Open-circuit potential (E_OC), potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) were used as electrochemical methods to characterize the corrosion behaviour of Ti20Mo alloy and cp-Ti, respectively. Corrosion current and passive current densities obtained from the polarization curves showed low values indicating a typical passive behaviour for Ti20Mo alloy. The EIS technique enabled us to study the nature of the passive film formed on the binary Ti20Mo alloy at various imposed potentials. The Bode phase spectra obtained for Ti20Mo alloy in artificial saliva exhibited two-time constants at higher potential (0.5 V, 1.0 V), indicating a two-layer structure. According to our experimental measurements, Ti20Mo alloy appears to possess superior corrosion resistance to that of cp-Ti in artificial saliva.     

海水介质中高活性镁合金负极的电化学性能

研制了一种新型镁合金负极材料；用电化学方法测定了镁合金负极在人造海水介质中的电化学性能，用浸泡法测定了材料在人造海水介质中的自腐蚀速度，用扫描电子显微镜观察了镁合金腐蚀后的表面形貌，并与AP65合金和纯镁进行了比较。结果表明，新研制的镁合金在人造海水介质中的开路电位增加，自腐蚀速度降低，稳定工作电位提高，电极表面腐蚀均匀，可开发用于高电性能电池的负极材料。     

镁合金磷化处理对化学镀镍层性能的影响

为了有利于环保,采用磷化工艺对AZ31B镁合金进行化学镀镍前处理.采用直观法、扫描电子显微镜和阴极极化曲线法对磷化膜及其化学镀镍层进行了分析.结果表明:AZ31B镁合金表面经磷化处理后得到了良好的化学镀镍层;AZ31B镁合金化学镀镍层的耐蚀性随磷化时间的延长先增加后减小,当磷化时间为75 s时,化学镀镍层的腐蚀电势比直...     

Stress corrosion cracking behaviour of the duplex Fe-10Al-29Mn-0.4C alloy in 20% NaCl solution at 100° C

The stress corrosion cracking behaviour of the duplex Fe-10 Al-29 Mn-0.4 C alloy having two phases ( and) in an aqueous 20% NaCl solution (100° C) has been investigated using both the static constant load and dynamic slow strain rate tests. The constant load test shows that the duplex alloy investigated is immune to stress corrosion cracking in a 20% NaCl solution. However, the slow strain-rate test reveals that this alloy is susceptible to stress corrosion cracking at the stabilized corrosion potential, and also at potentials anodic and cathodic to this potential. Furthermore, the metallographic cross section of this duplex alloy after slow strainrate testing shows that the secondary cracks propagate transgranularly through the ferrite grains at and above the stabilized corrosion potential. However, the cracks propagate transgranularly in both the ferrite and austenite grains and also at the austenite-ferrite grain boundaries when the applied potential is cathodic to the stabilized corrosion potential.     

1 000 MPa级高强钢焊接件的氢脆敏感性研究

利用氢渗透试验、慢应变速率拉伸试验(SSRT)研究了1 000MPa级高强钢(HSS)焊接件在海水中的氢渗透行为及其应力腐蚀敏感性,结合SEM观察了试样的断口特征,并利用电化学试验和显微组织观察分析了焊接件不同区域的氢脆特征。结果表明:相对于焊缝区(WM)和母材区(BM),热影响区(HAZ)的自腐蚀电位最负、析氢电位最正,更容易发生腐蚀和析氢行为。热影响区的氢扩散系数最大,具有较强的吸氢倾向。动态电化学充氢对高强钢焊接件的影响主要体现在对塑性的损减方面;随着极化电位的负移,高强钢焊接件的强度没有明显变化,但断面收缩率、断后延伸率均减小,断裂方式逐渐由韧性断裂变为解理断裂;当极化电位约为-930mV(vs SCE)时,高强钢焊接件的氢脆系数达25%;在不同充氢极化电位下,焊接件试样的断裂位置多在热影响区。     

铜离子及电位对5083铝合金阴极保护行为的影响

目前有关船体防污涂料中的铜离子及阴极保护电位对铝合金船体的腐蚀电化学研究不够深入。通过极化试验、电化学阻抗谱(EIS)测试及外加恒电位阴极保护试验,并结合腐蚀形貌观察,研究了5083铝合金在有无Cu~(2+)的3.5%NaCl溶液中的极化及腐蚀特性,并结合不同电位下的阴极保护行为,探讨了其阴极保护电位范围。结果表明:防污剂中的Cu~(2+)沉积在铝合金基体表面会造成防腐蚀性能下降,降低铝合金舰船的阴极保护效果,应该避免Cu~(2+)的渗入;阴极保护电位过正,保护效果不佳,会造成铝合金表面发生点蚀,但若阴极保护电位过负,表面会发生析氢腐蚀,因此其合理的阴极保护电位范围为-1.00~-1.10 V(vs SCE)。     

FeCrMnNiTix高熵合金在NaCl溶液中的腐蚀行为研究

将Fe,Cr,Mn,Ni和Ti 5种金属纳米粉体经行星式球磨机混合后,采用真空熔铸法制备FeCrMnNiTi,FeCrMnNiTi_0.5,FeCrMnNi 3种高熵合金。为研究这3种合金在NaCl溶液中的腐蚀行为,运用电化学工作站测定3种合金在质量分数为3.5%的NaCl溶液中的开路电位、极化曲线和交流阻抗,利用金相显微镜和扫描电镜对腐蚀后的合金进行微观组织观察。电化学测试结果表明:当FeCrMnNiTi合金的自腐蚀电位为-0.301 V时,FeCrMnNiTi_0.5合金的自腐蚀电位为-0.443 V;腐蚀产物形貌观察表明:FeCrMnNiTi_0.5以晶界腐蚀为主,另外2种合金以点蚀为主。由此得出结论:FeCrMnNiTi耐蚀性最好,FeCrMnNiTi_0.5耐蚀性最差;加入Ti可能造成了合金晶格畸变。