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Investigations of Fine Biomachining of Metals by using Microbially Influenced Corrosion

机译:使用微生物影响腐蚀来研究金属细菌的研究

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The biomachining mechanism of metals for mild steel and copper has been investigated both by electrochemical measurements in 9 K medium and ferrous oxidizing bacteria-cultured solution and by observations of the surface film. The results are as follows: (1) In all tested pH, passivation was found at near -450 mV vs. SCE on the anodic polarization curves of mild steel in 9 K medium. Great passivation was found also in the region of -500 to 0 mV vs. SCE on the anodic polarization curves of copper. (2) Cathodic polarization curves of mild steel depolarized greatly in the region of -750 to -900 mV vs. SCE in the bacteria-cultured solution. This depolarization caused by the reduction reaction of Fe~(3+) + e -> Fe~(2+) accelarated the dissolution of metals. (3) Passivation was not found on the anodic polarization curves of mild steel in the bacteria-cultured solution. Natural electrode potential of copper in the bacteria-cultured solution shifted to the noble dirrection of -30 to +50 mV vs. SCE. Passivation was not found also on the anodic polarization curves of copper. (4) Passivation at near -450 mV vs. SCE in 9 K medium seemed to be caused by the formation of FeSO_4 film from the results of EPMA of Fe and S. This film formation was remarkable on copper. (5) In 9 K medium the dissolution of mild steel and copper was prevented by FeSO_4 film, however, in the bacteria-cultured solution FeSO_4 film was not formed owing to the action of bacteria and the dissolution was accelerated by oxidizing effect of Fe~(3+). (6) The biomachining mechanism of metals for mild steel and copper seemed to be as follows. Fe_2 (SO_4)_3 which was formed by the culture of bacteria accelerated the dissolution of both mild steel and copper as the oxidizing agent. The dissolution progressed as the two following reactions.Fe_2 (SO_4)_3 + Fe -> 3FeSO_4 Fe_2 (SO_4)_3 + Cu -> CuSO_4 + 2FeSO_4
机译:通过9K中和氧化纤维型培养溶液中的电化学测量和表面膜的观察,通过电化学测量和表面膜的观察来研究用于温和钢和铜的金属的生物加工机制。结果如下:(1)在所有测试的pH中,在9k培养基中的温和钢的阳极偏振曲线接近-450mV与Sce附近的钝化。在铜的阳极偏振曲线上也发现了巨大的钝化。 (2)低于低于-750至-900 mV与SCE的低于极化钢的阴极偏振曲线在细菌培养的溶液中。这种由Fe〜(3+)+ e - > Fe〜(2+)的还原反应引起的去极化加速了金属的溶解。 (3)在细菌培养溶液中的低碳钢阳极偏振曲线上没有发现钝化。细菌培养溶液中铜的天然电极电位移至-30至+50mV与SCE的惰性桡骨。还找不到铜的阳极偏振曲线上未发现钝化。 (4)接近-450mV的钝化与9k培养基中的钝化似乎是由FESO_4薄膜从Fe和SePMA的结果形成引起的。这种成膜对铜显着显着。 (5)在9K中,通过FeSO_4膜防止低碳钢和铜的溶解,但是,在细菌培养的溶液中,由于细菌的作用,未形成FesO_4薄膜,并且通过Fe的氧化效应加速溶解。 (3+)。 (6)温和钢和铜金属的生物机机理似乎如下。由细菌培养形成的Fe_2(SO_4)_3加速了低碳钢和铜作为氧化剂的溶解。溶解作为后两个反应进行.Fe_2(SO_4)_3 + Fe - > 3Feso_4 Fe_2(SO_4)_3 + Cu - > Cuso_4 + 2Feso_4

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