AZ91D镁合金在含SO_2大气环境中的初期腐蚀行为

采用室内加速的方法,利用金相显微镜、扫描电镜和X射线衍射等手段对AZ91D镁合金在含微量SO2工业污染环境中的初期腐蚀层形貌以及腐蚀产物进行了分析和研究。结果表明:SO2加速镁合金的腐蚀,随着SO2含量增加,镁的腐蚀速率加快。镁合金的初期腐蚀具有局部腐蚀的特征。腐蚀优先从α相基体开始,腐蚀初期在材料表面生成一层保护性的含有MgO和Mg(OH)2的薄膜。SO2降低了薄液层的pH值,增强溶解过程,促进可溶性MgSO3·6H2O和MgSO4·6H2O腐蚀产物的生成,使表面膜失去保护作用,加速镁合金的后期腐蚀。     

Improvement of corrosion resistance of AZ91D magnesium alloy by gadolinium addition

Based on the previous investigation on beneficial introduction of holmium into magnesium alloy, the effect of gadolinium, an adjacent rare earth element, on corrosion resistance was examined. The corrosion behavior of two Mg-9Al-Gd alloys （Mg-9Al-0.45Gd and Mg-9Al-l.43Gd） was evaluated and compared with that of Mg-9Al alloy without Gd by means of specimen mass loss and hydrogen evolution in 3.5% NaCl solution saturated with Mg（OH）2. The Gd-containing alloys exhibit enhanced corrosion resistance with respect to the plain Mg-9Al alloy. The microstructures of Mg-9Al alloy and Mg-9Al-0.45 Gd alloy were observed by electron probe microanalysis （EPMA） and energy dispersion spectroscopy （EDS）. The alloys with Gd addition show a microstructure characterized by a phase solid solution, surrounded by minor amount of β phase and more grain-like Gd-containing phase. To illustrate the involved mechanism their polarization curves were recorded. The electrochemical investigations reveal that Gd addition shifts the corrosion potential of the alloy towards active, as Gd containing phase is more active and hence less cathodic. As a result, the micro-galvanic corrosion is suppressed. Moreover corrosion product films formed on the Gd containing alloys are more compact and provide a better protective effectiveness than that on the alloy without Gd against corrosion. Repassivation measurements in mixture solution of 0.21 mol/L K2CrO4＋0.6 mol/L NaCI also verify the beneficial role of Gd addition. Based on the present preliminary analysis, both the deposited Gd-containing phases and corrosion product films are believed to be responsible for the improved corrosion behaviour due to Gd addition.     

Influence of chemical composition on corrosion resistanceof AZ91D magnesium alloy ingots

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Electrochemical noise characteristics in corrosion process of AZ91D magnesium alloy in neutral chloride solution

The corrosion process of AZ91D magnesium alloy in neutral 1% (mass fraction) sodium chloride aqueous solution was investigated by electrochemical noise(EN), SEM and EDX. Fractal theory was primarily used to depict the corrosion process of the alloy. The fast wavelet transform(FWT), as well as the fast Fourier transform(FFT), was employed to analyze the EN data. The results show that the overall corrosion process can be described by three stages. The first stage corresponds to the pit nucleation and growth; the second stage involves the growth of a passive oxide layer; and the third stage involves reactivation. With increasing immersion time, fractal dimension increases fast initially, fluctuates in the medium and increases again at last. Pitting corrosion and fractal dimension increase due to the initiation and formation of pits in the initial and the end of immersion, while depresses due to the passivation in the medium period. The results of SEM and EDX support the above conclusions.     

Thixotropic behavior of semi-solid AZ91D magnesium alloy

The thixotropie behavior of semi-solid AZ91D slurry was studied through a Couette type viseometer.The results show that the apparent viscosity of semi-solid AZ91D magnesium alloy slurry increases after being isothermally held, but the apparent viscosity quickly falls down to a steady state value after being stirred again and it takes on a sharp shear-thinning behavior. With the same shearing rate and the rest time increasing, the steady apparent viscosity increases because of the agglomeration of the solid particles, and the time required for the slurry to reach the steady state also becomes longer. If the solid fraction increases, it takes longer time for the slurry to reach the steady apparent viscosity with the same shearing rate and the same rest time. If the solid fraction and the rest time are the same, but the shearing rate rises, it takes shorter time for the slurry to reach the steady apparent viscosity and the final steady apparent viscosity also decreases.     

AZ91D镁合金手汗腐蚀机理研究Ⅲ乳酸对AZ91D镁合金的腐蚀机制

通过电化学阻抗(EIS)和动电位极化曲线等方法研究了镁合金在乳酸和含有Cl^-的溶液中的电化学特性，发现镁合金腐蚀过程受到电极电位E、以β相为中心向外扩展的表面氧化膜的覆盖面积θ和MgH2的浓度Cm 3个表面状态变量的控制，在腐蚀过程中，β相表面氧化膜向四周扩展，覆盖了邻近很小范围的α相晶粒，从而使部分α相晶粒不受腐蚀．最后通过理论推导建立了一个新的镁合金腐蚀理论模型，并利用EIS实验证实了模型的可靠性。     

电解液组分对镁合金微弧氧化成膜及膜层耐蚀性的影响

基于单纯形重心设计改变Na₂SiO₃、NaOH、KF和NaAlO₂ 4种组分的搭配,在AZ91D镁合金上进行微弧氧化处理,研究了电解液配方对膜层成膜及耐蚀性能的影响。结果表明,所得到的回归方程非常显著,预测精度高。帕累托分析显示,4种电解质均对膜层耐蚀性影响显著。通过响应面分析可知,增大主盐Na₂SiO₃或者NaAlO₂的浓度可以显著提高膜层的耐蚀性。但二者复合却不利于耐蚀性的提高。主盐对于提高膜层成膜性及耐蚀性至关重要。当电解液中无主盐时,膜层的成膜性及耐蚀性都很差。当电解液中含有主盐时,适当增加NaOH与KF的浓度,膜层耐蚀性提高。通过Pearson相关分析可知,膜层耐蚀性主要受致密度及孔隙率的影响,同时也受膜厚、物相等其他特征参量的影响。而电解液各组分通过影响上述微观结构特征参量从而影响膜层性能。     

Fretting wear behavior of AZ91D magnesium alloy

The fretting behaviour of the AZ91D magnesium alloy was investigated. The influence of the number of cycles, normal load （contact pressure） and the amplitude of slip on the fretting behavior of the material were focused. Fretting tests were performed under various running conditions with regard to normal load levels and slip amplitudes. The friction coefficient between the surfaces at the fretting junction was continuously recorded. The freeing damage on the magnesium specimens was studied by SEM. The resultS show that the wear volume increases with the increase of slip amplitude, and linearly increases with the increase of normal load in the mixed and gross slip regime, but the normal load has no obvious effect on the wear volume in the partial slip regime. The predominant fretting wear mechanism of magnesium alloy in the slip regime is the oxidation wear, delaminated wear and abrasive wear.     

Influence of rare earth element Ce and La addition on corrosion behavior of AZ91 magnesium alloy

Two types of AZ91 magnesium alloys containing rare earth element Ce or La were fabricated. Hydrogen evolution and electrochemical tests were carried out to evaluate the corrosion behavior of new AZRE (RE = Ce or La) and AZ91 alloys in 3.5% NaCl solutions (pH 6.50). Various corrosion rate tests indicated that addition of RE obviously enhanced corrosion resistance of AZ91 magnesium alloy. The optimal content of RE was 0.92% for Ce and 0.66% for La. Scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), and low‐angle X‐ray diffraction (XRD) were used to characterize the effect of RE addition on microstructure and corrosion product film of AZ91 magnesium alloy. The refined β phase and formation of γ phase in AZRE alloy were observed by SEM, which resulted in the improvement of corrosion resistance due to the depression of microgalvanic couples. Moreover, the enhanced protective effectiveness of corrosion products was another reason for the improved corrosion resistance.     

AZ91D镁合金的均一化前处理与化学镀Ni-P

采用新型环保的均一化前处理工艺在AZ91D镁合金表面制备了化学镀Ni-P镀层。研究了前处理过程中AZ91D基体微观形貌、镀层沉积过程、成分和相结构。研究结果表明：基体表面的β相在前处理过程中被选择性去除,表面组织得到均一化,从而获得均匀致密的浸Zn层。Ni-P颗粒均匀形核生长,并最终形成致密的镀层。镀层具有优良的耐腐蚀性能。     

Organic-magnesium complex conversion coating on AZ91D magnesium alloy

An organic-magnesium complex conversion (OMCC) coating on AZ91D magnesium alloy was obtained by treating in a solution containing organic compounds. SEM, FESEM and XPS were used to examine the surface morphology, thickness and structure of the conversion coatings. The results show that the continuous and uniform conversion coating is deposited on AZ91D alloy and the main component of the coatings is organic compound containing benzene ring, which forms a chemical bond with magnesium. The polarization measurement and salt spray test show that the corrosion resistance of the conversion coating is much higher than that of traditional chromate conversion coating.     

Preparation and characterization of inorganic and organic coatings on AZ91D magnesium alloy with electroless plating pretreatment

In this paper, a protective coating scheme was applied for the corrosion protection of AZ91D magnesium alloy. Electroless Ni coating (EN coating) as bottom layer, electrodeposited Ni coating (ENN coating), and silane‐based coating (ENS coating) as top layer, respectively, were successfully prepared on AZ91D magnesium alloy by combination techniques. Scanning electron microscopy and X‐ray diffraction were employed to investigate the surface and phase structure of coatings, respectively. The electrochemical corrosion behaviors of coatings in neutral 3.5 wt% NaCl solution were evaluated by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization techniques. The corrosion testing showed that the three kinds of coatings all could provide corrosion protection for AZ91D magnesium alloy to a certain extent, and the corrosion resistance of ENN and ENS was superior to EN. In order to further study the corrosion protection properties of ENN and ENS, a comparative investigation on the evolution of EIS of ENN and ENS was carried out by dint of immersion test in neutral 3.5 wt% NaCl solution. The results indicated that, compared with ENN, the ENS could provide longer corrosion protection for AZ91D magnesium alloy. It is significant to determine the barrier effect of each coating, which could provide reference for industry applications.     

AZ91D镁合金微弧氧化膜在不同浓度NaCl溶液中的腐蚀行为(英文)

采用微弧氧化技术(MAO)在镁合金 AZ91D 表面制备微弧氧化陶瓷膜。利用电化学技术和浸泡实验研究该镁合金试样在不同浓度(0.1%,0.5%,1.0%,3.5%和 5.0%,质量分数) NaCl 溶液中的腐蚀行为。结果表明,试样的腐蚀速率随着氯离子浓度的升高而增大。在较高浓度(1.0%,3.5%和 5.0%)的 NaCl 溶液中的主要腐蚀形式是点蚀,而在较低浓度(0.1%和 0.5%)中是全面腐蚀。腐蚀过程可以分为两个阶段:亚稳态蚀点的出现和蚀点的生长。根据腐蚀过程中阻抗谱的特点,对镁合金微弧氧化膜试样在不同浓度 NaCl 溶液中浸泡 120 h 提出了不同的等效电路来模拟其腐蚀行为。     

Barium phosphate conversion coating on die-cast AZ91D magnesium alloy

Poor corrosion resistance limits the application of magnesium alloys.Conversion coating is widely used to protect magnesium alloys because of easy operation and low cost.A novel conversion coating on die-cast AZ91D magnesium alloy containing barium salts was studied.The optimum concentrations of Ba(NO_3)_2,Mn(NO_3)_2 and NH_4H_2PO_4 are 25 g/L,15 mL/L and 20 g/L,respectively,based on orthogonal test results.The treating time,solution temperature and pH value are settled to be 5-30 min, 50-70℃and 2.35-3.0...     

Anodization of AZ91 magnesium alloy in alkaline solution containing silicate and corrosion properties of anodized films

The anodization of AZ91 magnesium alloy in an alkaline electrolyte of 100g/L NaOH 20g/L Na2B4O7·10H2O 50g/L C6H5Na3O7·2H2O 60g/L Na2SiO3·9H2O was studied.The corrosion resistance of the anodized films was studied by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization techniques.The microstructure of the films was examined with scanning electronic microscope (SEM) and X-ray diffractometer (XRD).The results show that,under the experimental conditions,the optimum anodizing time and the optimum anodizing current density are 40min and 20mA/cm2 respectively for obtaining the anodic film with high corrosion resistance.The XRD pattern shows that the components of the anodized film consist of MgO and Mg2 (SiO4).     

电解质对AZ91D镁合金微弧氧化的影响

在Na2SiO3和NaAlO2为主成膜剂的硅铝复合电解液中,利用交流脉冲电源对AZ91D镁合金进行微弧氧化处理,研究主成膜剂含量的变化对微弧氧化过程及膜层特性的影响规律。利用扫描电镜(SEM)和膜层测厚仪分别研究了膜层的微观形貌和膜层厚度,通过电化学阻抗谱(EIS)测试膜层在3.5%NaCl中性溶液中的耐蚀性能。结果表明,随着主成膜剂含量的增加,微弧氧化过程中起弧电压和终止电压均呈下降的变化趋势,而膜层耐蚀性则基本呈先增大后降低的变化趋势,膜厚的变化趋势与其耐蚀性一致;Na2SiO3含量的变化对膜层内部致密层和外部疏松层的耐蚀性均有影响,而NaAlO2含量的变化则主要影响膜层内部致密层的耐蚀性;适量的主成膜剂含量是获得致密耐蚀膜层的关键。     

Effect of surface nanocrystallization on the microstructural and corrosion characteristics of AZ91D magnesium alloy

Surface distinct deformed layers with thicknesses up to 150 μm, with grain size in the top most surface is in the nanometer scale, were produced on AZ91D magnesium alloy using surface mechanical attrition treatment (SMAT). Effects of different ball size on the properties of the SMATed samples were investigated. The microstructural, grain size, hardness and roughness features of the treated surfaces were characterized using optical microscopy (OM), scanning electron microscopy (SEM), X-ray diffraction (XRD), micro-indenter and digital roughness meter, respectively. Corrosion behavior of the samples was evaluated using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) techniques. It is found that the ball diameter does not have a significant effect on the top surface grain size, but the thickness of the deformed layer increases with increase of ball size, from 50 μm for 2 mm balls to 150 μm for 5 mm balls. For all of the SMATed samples, the top surface microhardness value increased significantly and did not show any obvious change for samples treated with different balls. Corrosion studies show that the corrosion resistance of the sample treated with 2 mm balls is higher than that of those treated with 3 mm and 5 mm balls. This can be mainly attributed to the surface roughness and defects density of the samples, which are higher for the SMATed samples with 3 mm and 5 mm balls compared with that of sample SMATed with 2 mm balls.     

AZ91D镁合金的热压缩变形行为

在应变速率为0.005～1s~(-1)、温度250-350℃条件下,采用Instron-5500热模拟机对AZ91D镁合金的高温压缩特性进行研究,得到其真实应力-应变曲线.分析挤压温度和应变速率等对曲线的影响,得出本构方程的一系列常数,建立AZ91D镁合金在高温压缩中的本构方程关系式.结果表明:变形过程中AZ91D镁合金的流动应力随温度的升高而降低,随应变速率的升高而升高;该流动应力可以用双曲正弦函数来描述,其双曲正弦值随Zener-Hollomon参数自然对数的升高呈线性增大;AZ91D镁合金是正应变速率敏感材料,其应变速率敏感指数m=0.14.