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机构地区:[1]中国科学院金属研究所金属腐蚀与防护国家重点实验室,沈阳110016
出 处:《金属学报》2011年第10期1321-1326,共6页Acta Metallurgica Sinica
基 金:国家自然科学基金资助项目51071160~~
摘 要:在除O_2的0.1 mol/L NaHCO_3,0.1 mol/L NaHCO_3+0.1 mol/L Na_2SO_4以及0.1 mol/L NaHCO_3+0.1 mol/L NaCl溶液中,用恒电位法在低碳钢电极表面制备腐蚀产物,并原位监测低碳钢的开路电位,用SEM观察腐蚀形貌,用XRD确定腐蚀产物的相组成.结果表明.在0.1 mol/L NaHCO_3溶液中,低碳钢的开路电位最终处于再钝化区间,其表面未观察到明显的腐蚀现象;在0.1 mol/L NaHCO_3+0.1 mol/L Na_2SO4溶液中,低碳钢的开路电位最终处于再活化区间,其表面发生均匀腐蚀;在0.1 mol/L NaHCO_3+0.1 mol/L NaCl溶液中,低碳钢的开路电位最终亦处于再活化区间,而其表面却发生局部腐蚀,XRD结果表明,低碳钢表面的腐蚀产物主要为Fe_3O_4和α-FeOOH.The corrosion behaviors of low carbon steel, a kind of materials used in making metal container sealing high level radioactive waste, in three deaerated bicarbonate solutions simulated the ground water, 0.1 mol/L NaHCO3 solution, 0.1 mol/L NaHCO3+0.1 mol/L Na2SO4 solution and 0.1 mol/L NaHC03+0.1 mol/L NaC1 solution, were examined. The results in potential evolution revealed that the low carbon steel moved up to the passive state in 0.1 mol/L NaHCO3 solution while moved up to the re active state in the other solutions. SEM observations showed that the low carbon steel was not corroded in 0.1 mol/L NaHCO3 solution, while homogeneous corrosion occurred in 0.1 mol/L NaHC03+0.1 mol/L Na2SO4 solution and local corrosion in the third solution. XRD analyses illustrated that the corrosion products are composed of Fe3O4 and α-FeOOH.
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