Suspended electrode kinetics of mechanically activated pyrite

1　ＩＮＴＲＯＤＵＣＴＩＯＮＭｅｃｈａｎｉｃａｌａｃｔｉｖａｔｉｏｎｉｓｗｉｄｅｌｙａｐｐｌｉｅｄｉｎｅｎ ｈａｎｃｉｎｇｍｅｔａｌｌｕｒｇｉｃａｌｐｒｏｃｅｓｓ[1～ 3] ａｎｄｃｈｅｍｉｃａｌｓｙｎ ｔｈｅｓｉｓ[4 ,5] .Ｓｏｆａｒｉｔｉｓｄｉｆｆｉｃｕｌｔｔ     

微液滴现象与大气腐蚀——Ⅱ.微液滴现象的电化学表征

用扫描Kelyin探头和电化学极化等手段,研究了微液滴现象与大气腐蚀的电化学过程之间的相关性.扫描Kelvin探头测定主液滴周围的电位分布显示,微液滴只在表面的正电性区域出现;当有微液滴形成时,火山形电位分布的峰高且宽、谷深且窄;同时,峰变宽的速率与微液滴的扩展速率近似相等.电化学极化结果显示,微液滴的成核速率随极化电流的增加而线性加速,促使大气腐蚀过程发生的电位差和相应的腐蚀电流是微液滴形成和发展的推动力.     

Breakdown of passive film on nickel in borate solutions containing halide anions

The effect of Cl⁻, Br⁻ and I⁻ anions as aggressive agents on the anodic behaviour of nickel electrode in deaerated Na₂B₄O₇ solutions have been investigated by galvanostatic polarization technique. Lower concentrations of the halide anions have no effect on the mechanism of nickel passivation. An increase in the halide anions concentration causes oscillation of the potential in the oxygen evolution region. This could be attributed to the destruction of the passivity by halide anions and repassivation of the film by anodic current and/or OH⁻ anions. Higher aggressive anion concentrations cause breakdown of the passive film and initiated pitting corrosion. As the temperature increases, the breakdown potential is shifted towards the more negative direction. On the other hand, as the pH of the solution increases, the breakdown potential is shifted toward more positive direction, indicating increased protection of the passive film. The activation energy, , of the oxide film formation in the presence of Cl⁻ anions was calculated and was found to be 21 kJ/mol.     

稀土对A572 Gr.65钢电化学腐蚀行为的影响

目的提高A572 Gr.65钢的耐蚀性能。方法通过向A572 Gr.65钢中添加La和Ce的混合稀土,得到不同稀土含量的A572 Gr.65钢。以3.5%NaCl溶液为腐蚀介质,借助电化学工作站、XRD和SEM等手段分析表征了不同稀土含量的A572 Gr.65钢的电化学腐蚀行为。结果稀土能使A572 Gr.65钢腐蚀电位正移,腐蚀电流减小。当稀土质量分数为0.0047%时,腐蚀电位最正,为-0.50V,腐蚀电流密度最小,为2.77×10-6 A/cm2,极化曲线的阳极部分存在明显的活化-钝化过渡区,有明显的钝化过程。不同稀土含量的A572Gr.65钢的阻抗谱均由单一的容抗弧组成,容抗弧半径代表着对电荷传输的阻碍能力,稀土质量分数为0.0047%时,容抗弧半径最大,对电荷传输的阻碍能力最大。稀土可以使钢中的夹杂物变性,使夹杂物由Ca S和Al2O3-Ca O变为稀土的氧硫化物,夹杂物尺寸由5μm变为2μm,减小腐蚀发生的活性区。此外,稀土离子可以提高阴极极化率,使腐蚀产物中不稳定的γ-Fe OOH含量减少,增强锈层的稳定性、致密性和附着能力,增大电荷转移的阻力,有效阻碍侵蚀性Cl-的侵入。结论稀土的添加能有效提高A572Gr.65钢的耐蚀性,稀土质量分数为0.0047%时,试验钢的耐蚀性最好。腐蚀过程中,由点蚀逐渐转变为均匀腐蚀,活性点的形成和阳极溶解速度为整个腐蚀过程中的限制性环节。     

热变形参数对23Cr-6.2Mn-2.1Ni-0.28N节Ni型双相不锈钢点蚀行为的影响

采用热模拟、动电位极化曲线、交流阻抗谱等手段研究了热变形参数对23Cr-6.2Mn-2.1Ni-0.28N节Ni型双相不锈钢点蚀行为的影响。结果表明:实验钢的耐蚀性对应变速率、变形温度比较敏感,晶粒细化有利于提高试样的耐点蚀性能。在1和10 s-1的较高应变速率下,随变形温度升高,试样的耐蚀性先增加后降低,1050℃耐蚀性最好。随应变速率增加,再结晶晶粒细化程度降低,钝化膜稳定性减弱,试样耐蚀性逐渐降低。点蚀坑主要分布在δ相和δ/γ相界,随应变速率增加点蚀坑数量明显增多,尺寸变大。     

Molten pool and temperature field in CO_2 laser welding

0IntroductionCompared with conventional welding methods,laserwelding has many advantages,such as large penetrationratio,small HAZ,small welding deformation.Another ad-vantage of laser welding is easy to weld complicated com-ponents because laser can be transferred by mirrors andoptical fiber.The laser welding will find wide applicationswith the laser system developing.Induced-plasma,molten pool and keyhole are mainphenomena in study of laser welding process.The varietiesof them indicate the …     

Ni-W-P-SiC脉冲复合镀层的耐蚀性研究

采用腐蚀溶液浸泡、阳极极化曲线和中性盐雾试验3种方法较系统地研究了Ni-W-P-SiC脉冲复合镀层的耐蚀性.其结果表明：镀层在HCl、H2SO4、H3PO4溶液中的腐蚀速率都比较低，而镀层在FeCl3溶液中的腐蚀速率远大于前三者；镀层在H2SO4和H3PO4中的钝化区较宽，有过钝化区、二次钝化区和二次过钝化区出现，而在HCl和FeCl3中的钝化区较窄，且只有过钝化区；3种腐蚀试验方法均表明脉冲频率和占空比对试样的腐蚀速率都有不同程度的影响；不同脉冲参数条件下的400℃热处理镀层的腐蚀速率都比镀态镀层的腐蚀速率小得多.      

含菌介质中MDOPD对SRB菌及生物膜腐蚀的抑制作用

用动电位扫描极化曲线、原子力显微镜和电子探针等方法研究了SRB生物膜在培养基介质中对于含咪唑杂环的双季铵盐化合物MDOPD的敏感性．结果表明：含菌介质中，MDOPD吸附在电极表面，形成完整致密的有机保护膜，对电极的腐蚀反应具有良好的抑制作用，SRB的代谢及腐蚀产物也难以在电极表面直接吸附和沉积，从而降低了SRB生长代谢的次生过程（包括酸浸蚀等）对腐蚀的促进作用；同时也降低了介质中的SRB参与碳钢腐蚀的机会．     

十二烷基三甲基碘化铵对铝的缓蚀作用

1mol·L-1MgCl2溶液中,在30～50℃范围内用微分极化电阻和微分电容测量技术研究添加不同浓度的十二烷基三甲基碘化铵(DTMAI)对铝阳极过程的缓蚀作用,结果表明,DTMAI是铝的有效缓蚀剂,缓蚀效率随着浓度和温度的增加而增大;DTMAI吸附在铝表面上,且吸附服从Langmuir等温式发现这种吸附的特点是吸附过程的的总熵增加,且总熵随温度升高而增大,温度对缓蚀效率的影响是由于熵效应而不是焓效应,因此.DTMAI在铝表面的吸附是其具有良好缓蚀作用的基本原因     

Hydrogen effects on the passive film formation and pitting susceptibility of nitrogen containing type 316L stainless steels

The effects of hydrogen on the passivity and pitting susceptibility of type 316L stainless steels have been investigated with alloys containing different nitrogen contents (0.015, 0.198 and 0.556 wt.% N). The study revealed that electrochemically pre-charged hydrogen significantly reduced the pitting resistance of alloys conatining 0.015 and 0.198 wt.% nitrogen contents. In alloy with highest nitrogen content (0.556 wt.% N), an increase in the passive film current density with hydrogen was observed without affecting breakdown potential. Auger electron spectroscopy (AES) analysis of the passive film indicated the presence of nitrogen in the passive film. On other hand, for hydrogen charged samples, nitrogen was found to be significantly less in the passive film. In Electrochemical impedance spectroscopy (EIS) measurement, the decrease in semi-circle radius of Nyquist plot, and the polarization resistance, R_P associated with the resistance of the passive film was observed with hydrogen, indicating that hydrogen decreased the stability of the passive film. The present investigation indicated that precharged hydrogen deteriorated the passive film stability and pitting corrosion resistance in these alloys, and the increase in nitrogen content of the alloy offsets the deleterious effect of precharged hydrogen.