间四(4-羧基苯基)卟吩在碱性环境下对钢筋的协同防腐性能及机理研究

IF 1.5 4区 化学 Q4 CHEMISTRY, PHYSICAL International Journal of Chemical Kinetics Pub Date : 2024-06-17 DOI:10.1002/kin.21743
Xue-qi Zhang, Qing-xian Yue, Rui Ding, Jie Liu
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引用次数: 0

摘要

在碱性混凝土环境中保护钢筋免受腐蚀是海洋工程中的一项共同挑战。减轻钢筋腐蚀的一种方法是在混凝土中添加缓蚀剂。在碱性环境中,钢筋的钝化是通过阳极钝化和阴极氧还原反应(ORR)实现的。催化 ORR 可以加速阳极钝化。为了研究钢筋在碱性环境中的缓蚀作用,我们选择了具有 ORR 催化特性的中-四(4-羧基苯基)卟吩(TCPP)。TCPP 可在钢条表面形成吸附膜,促进钝化膜的形成。TCPP 主要吸附在钝化膜表面的活性位点上,在这些位点上,晶格铁离子已经浸出。吸附的 TCPP 可通过 ORR 催化作用加速钝化膜的形成,抑制钝化膜缺陷的产生,增强钝化膜的完整性和保护性。当 TCPP 的浓度为 0.5 mmol/L 时,效果最为明显。TCPP 的物理吸附主要由负电荷中心(即羧基 O 和吡咯 N)决定。然而,由于羧基苯不受限制地旋转所造成的立体阻碍,吡咯 N 在化学吸附中并不占主导地位。吸附过程大大降低了 TCPP 分子的扩散系数,使吸附结合牢固稳定。不含羧基苯的酞菁分子采用平面结构,可通过平面吸附在铁表面形成稳定的吸附构型。这一观察结果为设计新型金属酞菁分子提供了指导。具体来说,开发带有与酞菁环共面且旋转受限的修饰基团的金属酞菁分子,可以实现平面吸附,提高覆盖率,并增强吸附构型的稳定性。
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The synergistic anti-corrosion performance and mechanism of meso-tetra(4-carboxyphenyl)porphine on steel bars in alkaline environments

Corrosion protection of steel bars in alkaline concrete environments poses a common challenge in marine engineering. One approach to mitigate steel bar corrosion is the addition of corrosion inhibitors to the concrete. In alkaline environments, the passivation of rebars occurs through anodic passivation coupled with the cathodic oxygen reduction reaction (ORR). The catalysis of ORR can expedite anode passivation. To investigate the corrosion inhibition of steel bars in alkaline environments, meso-tetra(4-carboxyphenyl)porphine (TCPP), known for its ORR catalytic properties, is selected. TCPP forms adsorption films on the surface of steel bars, facilitating the formation of passivation films. TCPP primarily adsorbs onto active sites on the surface of the passivation film, where lattice iron ions have leached. The adsorbed TCPP accelerates the formation of the passivation film through ORR catalysis, inhibiting the development of passivation film defects and enhancing the integrity and protection of the passivation film. The most significant effect is observed when the concentration of TCPP is 0.5 mmol/L. The physical adsorption of TCPP is primarily determined by the negative charge centers, namely the carboxyl group O and the pyrrole N. However, due to steric hindrance caused by the unrestricted rotation of the carboxyl benzene, the pyrrole N does not play a dominant role in chemical adsorption. Instead, the active site for chemical adsorption is the carboxyl group O. The adsorption process significantly reduces the diffusion coefficient of TCPP molecules, providing a robust and stable adsorption binding. Phthalocyanine molecules without carboxyl benzene groups adopt a planar structure, allowing them to form stable adsorption configurations on the iron surface through flat adsorption. This observation provides guidance for the design of novel metal phthalocyanine molecules. Specifically, the development of metal phthalocyanine molecules with modifying groups that are coplanar with the phthalocyanine ring and possess restricted rotation can achieve flat adsorption, improve coverage rate, and enhance adsorption configuration stability.

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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
74
审稿时长
3 months
期刊介绍: As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.
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