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葡萄糖氧化酶存在下不锈钢的表面改性:界面过程的本质与作用

Ennoblement of stainless steel in the presence of glucose oxidase: nature and role of interfacial processes.

作者信息

Landoulsi J, Genet M J, Richard C, El Kirat K, Rouxhet P G, Pulvin S

机构信息

Laboratoire Roberval, CNRS UMR 6253, Université de Technologie de Compiègne, BP 20529, F-60205 Compiègne Cedex, France.

出版信息

J Colloid Interface Sci. 2008 Apr 15;320(2):508-19. doi: 10.1016/j.jcis.2008.01.038. Epub 2008 Feb 1.

Abstract

The ennoblement of the free corrosion potential (E(corr)) of AISI 316L stainless steel which did not occur in synthetic fresh water (SFW), was observed after introduction of glucose oxidase (Gox) and glucose, or of hydrogen peroxide (H(2)O(2)). The composition of the surface was monitored using AFM and XPS, a detailed XPS analysis being based on the discrimination between oxygen of organic and inorganic nature proposed in a previous study. In H(2)O(2) medium, the main changes regarding the inorganic phase were the increase of the oxygen concentration in the passive film, the increase of the molar concentration ratio of oxidized species Fe(ox)/Cr(ox) and the growth of nanoparticles, presumably made of ferric oxide/hydroxide. In Gox medium, no significant changes were observed in both oxygen concentration and Fe(ox)/Cr(ox) ratio, but the density of colloidal particles decreased, indicating a dissolution of Fe oxide/hydroxide under the influence of gluconate. In contrast with H(2)O(2), in SFW and Gox the amount of organic compounds increased due to the accumulation of polysaccharides and proteins. The influence of glucose oxidase on the ennoblement of stainless steel is not due to indirect effects of H(2)O(2) through the change of surface composition. The E(corr) ennoblement seems to be directly due to the presence of H(2)O(2) and to the electrochemical behavior of H(2)O(2) and related oxygen species. This consideration is important for understanding and controlling microbial influenced corrosion.

摘要

在添加葡萄糖氧化酶(Gox)和葡萄糖或过氧化氢(H₂O₂)后,观察到AISI 316L不锈钢在合成淡水(SFW)中未出现的自由腐蚀电位(E(corr))的升高。使用原子力显微镜(AFM)和X射线光电子能谱(XPS)监测表面成分,详细的XPS分析基于先前研究中提出的有机和无机性质氧的区分。在H₂O₂介质中,无机相的主要变化是钝化膜中氧浓度增加、氧化态物种Fe(ox)/Cr(ox)的摩尔浓度比增加以及纳米颗粒的生长,推测纳米颗粒由氧化铁/氢氧化铁制成。在Gox介质中,氧浓度和Fe(ox)/Cr(ox)比均未观察到显著变化,但胶体颗粒密度降低,表明在葡萄糖酸盐的影响下氧化铁/氢氧化铁发生溶解。与H₂O₂相反,在SFW和Gox中,由于多糖和蛋白质的积累,有机化合物的量增加。葡萄糖氧化酶对不锈钢电位升高的影响并非由于表面成分变化导致的H₂O₂间接作用。E(corr)升高似乎直接归因于H₂O₂的存在以及H₂O₂和相关氧物种的电化学行为。这一考虑对于理解和控制微生物影响的腐蚀很重要。

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