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Molecular Assembly between Weak Crosslinking Cyclodextrin Polymer and trans-Cinnamaldehyde for Corrosion Inhibition towards Mild Steel in 3.5 NaCl Solution: Experimental and Theoretical Studies

机译:弱交联环糊精聚合物与反肉桂醛之间的分子组装对3.5%NaCl溶液中低碳钢的腐蚀抑制作用:实验和理论研究

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摘要

Constructing molecular assembly between a soluble cyclodextrin polymer (SCDP) and an anticorrosive component is conducive to increasing the availability of a corrosion inhibitor with low molecular polarity in aqueous solution. The SCDP was prepared via the weak crosslinking effect of glutaraldehyde using β-cyclodextrin as the subunit, whose structure was confirmed by proton nuclear magnetic resonance spectra (1H NMR), X-ray diffraction and morphology. An assembly between SCDP (host) and trans-cinnamaldehyde (guest, CA) was constructed, and the intermolecular interactions were disclosed by Fourier transform infrared spectra (FTIR). The corrosion inhibition of SCDP/CA assembly for mild steel in 3.5% NaCl solution was assessed through electrochemical and surface analyses. 1H NMR results showed that exterior hydroxyls of β-cyclodextrin were the active sites for crosslinking. Hydrogen bonds might be the binding force between SCDP and CA according to FTIR analyses. Electrochemical measurements revealed that SCDP/CA assembly could suppress both cathodic and anodic reactions and enhance the polarization impedance for mild steel in the corrosive medium with a maximum efficiency of 92.2% at 30 °C. Surface analyses showed that CA molecules could be released from the assembly followed by the energy competition mechanism, and solely adsorb on the steel surface in parallel form, which was further evidenced by theoretical modeling.
机译:在可溶性环糊精聚合物(SCDP)和防腐蚀组分之间构建分子组装体有助于提高水溶液中具有低分子极性的缓蚀剂的可用性。通过以β-环糊精为亚基的戊二醛的弱交联作用制备了SCDP,其结构通过质子核磁共振谱( 1 H NMR),X射线衍射和形态得以证实。构建了SCDP(宿主)和反肉桂醛(来宾,CA)之间的组装体,并通过傅立叶变换红外光谱(FTIR)揭示了分子间的相互作用。通过电化学和表面分析评估了SCDP / CA组件对3.5%NaCl溶液中低碳钢的腐蚀抑制作用。 1 1 H NMR结果表明,β-环糊精的外部羟基是交联的活性位点。根据FTIR分析,氢键可能是SCDP与CA之间的结合力。电化学测量表明,SCDP / CA组件可以抑制阴极和阳极反应,并提高腐蚀性介质中低碳钢的极化阻抗,在30°C时的最大效率为92.2%。表面分析表明,CA分子可以从装配体中释放出来,随后是能量竞争机制,并且仅以平行形式吸附在钢表面上,这在理论模型上得到了进一步证明。

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