Comparative study on corrosion inhibition of N doped and N,S codoped carbon dots for carbon steel in strong acidic solution

腐蚀 材料科学 碳钢 杂原子 碳纤维 兴奋剂 吸附 硫黄 化学工程 无机化学 冶金 化学 复合材料 有机化学 工程类 复合数 光电子学 戒指(化学)
作者
Siming Ren,Mingjun Cui,Xinyu Chen,Shixiang Mei,Yujie Qiang
出处
期刊:Journal of Colloid and Interface Science [Elsevier]
卷期号:628: 384-397 被引量:64
标识
DOI:10.1016/j.jcis.2022.08.070
摘要

Carbon steel is the most widely used engineering material, and its corrosion is one of the main areas of concern in many industries. The most practical approach to control this problem is to use corrosion inhibitors. Currently, because of their good water solubility, excellent chemical stability, low cost and nontoxic features, carbon dots (CDs), especially heteroatom-doped CDs, have been developed as green corrosion inhibitors, but the corrosion inhibition efficiency and underlying mechanisms of single- or dual-element doping have not yet been accurately compared and analyzed. Inspired by this, eco-friendly nitrogen-doped and nitrogen, sulfur codoped CDs (N-CDs and N,S-CDs) are prepared via a one-step hydrothermal process, and a comparative study on their inhibition performance for carbon steel corrosion in strong acidic solution is performed. The results show that both N-CDs and N,S-CDs can restrain the corrosion of carbon steel, and their inhibition efficiency increases with increasing concentration and immersion time, reaching approximately 87.9% (N-CDs) and 96.4% (N,S-CDs) at 200 ppm after 1 h of immersion. Molecular dynamics simulation indicates that the strong interaction ability between N,S-CDs and the Fe substrate leads to higher corrosion inhibition performance than the single N doping case, benefiting from the multi-anchor adsorption of N,S-CDs on carbon steel in a strong acidic solution. Therefore, the facile preparation, eco-friendliness and high corrosion inhibition performance of N,S-CDs will provide a new approach for designing highly efficient carbon dots and broadening the application of carbon dots in the corrosion field.
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