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吡唑的氨基/酮基衍生物作为酸性介质中低碳钢的有效缓蚀剂:表面形态、电化学和计算研究

Amino/Keto Derivatives of Pyrazole as Effective Corrosion Inhibitors for Mild Steel in an Acidic Medium: Surface Morphological, Electrochemical, and Computational Studies.

作者信息

Kaur Navneet, Kaur Manvinder, Sohal Harvinder Singh, Husain Fohad Mabood, Bhowmik Pradip K, Verma Meenakshi, Han Haesook, Singh Kishanpal

机构信息

Medicinal and Natural Product Laboratory, Department of Chemistry, Chandigarh University, Gharuan, Mohali, Punjab 140413, India.

Department of Food Science and Nutrition, College of Food and Agriculture Sciences, King Saud University, Riyadh 11451, Saudi Arabia.

出版信息

ACS Omega. 2025 Mar 31;10(14):14343-14361. doi: 10.1021/acsomega.5c00552. eCollection 2025 Apr 15.

Abstract

The corrosion inhibition performance of two pyrazole derivatives, 3-methyl-1-pyrazol-5-amine (MPA) and 3-methyl-1-pyrazol-5-(4)-one (MPO), on mild steel (MS) in 1 M HSO was examined through weight loss, electrochemical methods (polarization and impedance), and quantum chemical analyses. The inhibition efficiency improved with an increasing concentration, achieving 92.28% for MPA and 88.14% for MPO at 0.8 mg/L and 303 K. The adsorption process adhered to the Freundlich model, indicating a heterogeneous interaction on the surface. Electrochemical tests revealed that MPA exhibited superior inhibition at 96.47%, compared to MPO's 85.55% at 0.8 g/L. UV-vis spectroscopy indicated that MPA decreased the band gap energy from 5.44 to 5.28 eV, suggesting a stronger interaction with the metal. Density functional theory further supported a higher adsorption potential of MPA due to its lower energy gap and increased softness. Although the presence of C=O groups in MPO improved adsorption through metal coordination, MPA formed a more stable protective layer, leading to better corrosion resistance. Further modifications with the polar groups on the pyrazole skeleton can lead to the formation of some potent corrosion inhibitors.

摘要

通过失重法、电化学方法(极化和阻抗)以及量子化学分析,研究了两种吡唑衍生物3-甲基-1-吡唑-5-胺(MPA)和3-甲基-1-吡唑-5-(4)-酮(MPO)在1 M硫酸中对低碳钢(MS)的缓蚀性能。缓蚀效率随浓度增加而提高,在0.8 mg/L和303 K时,MPA的缓蚀效率达到92.28%,MPO的缓蚀效率达到88.14%。吸附过程符合Freundlich模型,表明在表面存在非均相相互作用。电化学测试表明,在0.8 g/L时,MPA的缓蚀率为96.47%,优于MPO的85.55%。紫外可见光谱表明,MPA将带隙能量从5.44 eV降低到5.28 eV,表明其与金属的相互作用更强。密度泛函理论进一步支持了MPA具有更高的吸附潜力,因为其能隙更低且柔软度增加。尽管MPO中C=O基团的存在通过金属配位改善了吸附,但MPA形成了更稳定的保护层,从而具有更好的耐腐蚀性。对吡唑骨架上的极性基团进行进一步修饰可导致形成一些有效的缓蚀剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2353/12004140/e262130cc53c/ao5c00552_0018.jpg

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