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Corrosivity and Corrosion Inhibiting Characteristics of Sulfonate-functionalized Triethylammonium and Pyridinium-type Brønsted Acidic Ionic Liquids

机译:磺酸盐官能化的三乙铵和吡啶鎓型布朗斯台德酸性离子液体的腐蚀和缓蚀特性

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The corrosion bebavior of mild steel in two Brønsted acidic ionic liquids (BAILs) with different cationic centers, triethylammonium and pyridinium-type, was electrochemically investigated in nonaqueous and aqueous conditions at 25°C. A relatively wide passivation region (0-2.1 V) was clearly observed for mild steel, along with a lower corrosion rate, for both BAILs at 25°C. The Bronsted acidity of these BAILs is not proportional to the corrosion rate of the tested mild steel specimens. In addition, the different adsorption centers on each BAIL molecule, namely their sulfonate group along with either a quaternary ammonium or pyridinium structural motif, means they can possess different inhibiting characteristics as well as modes of adsorption at metal surfaces. Based on these electrochemical results, the inhibition ability of both BAILs in 0.5 M HCI solution against acid corrosion of mild steel was investigated, at various concentrations at 25°C, using gravimetric measurements. The pyridinium-type sulfonate-functionalized IL did not contribute to corrosion protection of the steel surface, while the triethylammonium-type sulfonate-functionalized IL had an inhibition efficiency of ca. 40%.
机译:在25°C的非水和水条件下,电化学研究了软钢在两种阳离子中心不同的布朗斯台德酸性离子液体(BAIL)中的腐蚀行为,这些阳离子中心分别为三乙铵和吡啶鎓型。在25°C时,两种BAIL均明显观察到低碳钢的钝化区域相对较宽(0-2.1 V),并且腐蚀速率较低。这些BAIL的布朗斯台德酸度与所测试的低碳钢样品的腐蚀速率不成比例。另外,每个BAIL分子上不同的吸附中心,即它们的磺酸盐基团以及季铵或吡啶鎓结构基序,意味着它们可以具有不同的抑制特性以及在金属表面的吸附方式。基于这些电化学结果,使用重量分析法研究了在浓度为25°C的0.5M HCl溶液中两种BAIL对低碳钢酸腐蚀的抑制能力。吡啶鎓型磺酸盐官能化的IL对钢表面的腐蚀防护没有贡献,而三乙铵型磺酸盐官能化的IL的抑制效率约为。 40%。

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