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Photodegradation of 2-mercaptobenzothiazole and 1,2,3-benzotriazole corrosion inhibitors in aqueous solutions and organic solvents

机译:水溶液和有机溶剂中2-巯基苯并噻唑和1,2,3-苯并三唑缓蚀剂的光降解

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摘要

The photochemical degradation of 2-mercaptobenzothiazole (MBT) and 1,2,3-benzotriazole (BTA) inhibitors was studied in the present work in aqueous and in organic solutions. The extent of photo degradation was assessed by UV-Vis spectroscopy and the main reaction products were identified by tandem electrospray ionization mass spectrometry (ESI-MS/MS). The analysis of degradation products upon UV irradiation revealed the predominant formation of dimeric compounds from MBT and oligomeric structures from BTA, which were further converted into aniline. The increase of the quantum yield of MBT and BTA photodegradation reactions under aerobic conditions both in aqueous and organic solvents was explained by an increase of the spin-orbit conversion of the singlet radical pairs into the triplet radical pairs in the presence of oxygen. These triplet pairs further dissociate into free radicals, or convert to the parent compounds. At the early stage of UV irradiation, free radical coupling leads essentially to dimer formation in the case of MBT and to the formation of oligomers in the case of BTA irradiation.
机译:在目前的工作中,研究了2-巯基苯并噻唑(MBT)和1,2,3-苯并三唑(BTA)抑制剂的光化学降解。通过UV-Vis光谱法评估光降解的程度,并通过串联电喷雾电离质谱法(ESI-MS / MS)鉴定主要反应产物。紫外线照射下降解产物的分析表明,主要由MBT形成二聚化合物和BTA形成寡聚结构,然后进一步转化为苯胺。在有氧条件下,无论是在水性溶剂还是有机溶剂中,MBT和BTA光降解反应的量子产率都增加了,这是由于在氧存在下单线自由基对向三线态自由基对自旋轨道转化的增加所致。这些三重态对进一步解离成自由基,或转化为母体化合物。在紫外线照射的早期阶段,自由基偶联在MBT的情况下基本上导致二聚体的形成,在BTA照射的情况下导致低聚物的形成。

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