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影响 Zn2Al 基层状双氢氧化物中 MoO4(2-) 抑制剂释放的因素及其在有机涂层保护热浸镀锌钢中的作用。

Factors Affecting MoO4(2-) Inhibitor Release from Zn2Al Based Layered Double Hydroxide and Their Implication in Protecting Hot Dip Galvanized Steel by Means of Organic Coatings.

机构信息

PSL Research University, Institut de Recherche Chimie Paris, CNRS - Chimie-ParisTech, 11 rue Pierre et Marie Curie, Paris 75005, France.

BASF Coatings GmbH , Glasuritstrasse 1, 48165 Münster, Germany.

出版信息

ACS Appl Mater Interfaces. 2015 Nov 18;7(45):25180-92. doi: 10.1021/acsami.5b06702. Epub 2015 Nov 3.

Abstract

Zn2Al/-layered double hydroxide (LDH) with intercalated MoO4(2-) was investigated as a potential source of soluble molybdate inhibitor in anticorrosion coatings for hot dip galvanized steel (HDG). The effect of solution pH, soluble chlorides, and carbonates on the release kinetics of the interleaved MoO4(2-) ions from the LDH powder immersed in solutions containing different anions was studied by X-ray diffraction, in situ attenuated total reflectance infrared (ATR-IR) spectroscopy, and inductively coupled plasma atomic emission spectroscopy (ICP-AES). The effect of the solution composition on the total release and the release kinetics was demonstrated. Less than 30% of the total amount of the intercalated MoO4(2-) was released after 24 h of the immersion in neutral 0.005-0.5 M NaCl and 0.1 M NaNO3 solutions whereas the complete release of MoO4(2-) was observed after 1 h in 0.1 M NaHCO3 or Na2SO4 and in alkaline solutions. The in situ ATR-IR experiments and quantification of the released soluble species by ICP-AES demonstrated the release by an anion exchange in neutral solutions and by the dissolution of Zn2Al/-LDH in alkaline solutions. The anion exchange kinetics with monovalent anions was described by the reaction order n = 0.35 ± 0.05 suggesting the diffusion control; for divalent anions, n = 0.70 ± 0.06 suggested the control by a surface reaction. Dissolution of Zn from coated HDG with and without Zn2Al/-MoO4(2-) fillers, leaching of MoO4(2-) from the coating, and the electrochemical impedance spectroscopy response of the coated systems were measured during the immersion in 0.5 M NaCl solutions with and without 0.1 M NaHCO3. Without carbonates, the release of soluble MoO4(2-) was delayed for 24 h with no inhibiting effect whereas with 0.1 M NaHCO3 the immediate release was accompanied by the immediate and strong inhibiting effect on Zn dissolution. The concept of controlling the inhibition performance of LDH hybrid coatings by means of the environment composition is discussed.

摘要

锌铝/-层状双氢氧化物 (LDH) 层间插层 MoO4(2-) 被研究作为热浸镀锌钢 (HDG) 防腐蚀涂层中可溶性钼酸盐抑制剂的潜在来源。通过 X 射线衍射、原位衰减全反射红外 (ATR-IR) 光谱和电感耦合等离子体原子发射光谱 (ICP-AES) 研究了溶液 pH 值、可溶性氯化物和碳酸盐对浸泡在含有不同阴离子溶液中的 LDH 粉末中插层 MoO4(2-) 离子释放动力学的影响。结果表明,溶液组成对总释放量和释放动力学有影响。在中性 0.005-0.5 M NaCl 和 0.1 M NaNO3 溶液中浸泡 24 小时后,仅释放了不到 30%的总插层 MoO4(2-),而在 0.1 M NaHCO3 或 Na2SO4 和碱性溶液中 1 小时后则完全释放了 MoO4(2-)。原位 ATR-IR 实验和 ICP-AES 对释放的可溶性物质进行定量分析表明,在中性溶液中通过阴离子交换和在碱性溶液中通过 Zn2Al/-LDH 的溶解来实现 MoO4(2-)的释放。用 ICP-AES 对释放的可溶性物种进行定量分析,并用 ICP-AES 对释放的可溶性物种进行定量分析,结果表明,在中性溶液中,MoO4(2-)的释放遵循反应级数 n = 0.35 ± 0.05,表明反应受扩散控制;而对于二价阴离子,n = 0.70 ± 0.06,表明反应受表面反应控制。在有和没有 Zn2Al/-MoO4(2-) 填充剂的涂覆 HDG 从涂层中浸出 MoO4(2-),以及在 0.5 M NaCl 溶液中有无 0.1 M NaHCO3 时的电化学阻抗谱响应。在没有碳酸盐的情况下,可溶性 MoO4(2-)的释放被延迟了 24 小时,但没有抑制作用,而在有 0.1 M NaHCO3 的情况下,MoO4(2-)的立即释放伴随着对 Zn 溶解的立即和强烈抑制作用。讨论了通过环境组成控制 LDH 杂化涂层抑制性能的概念。

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