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首页> 外文期刊>Molecules >Degradation of Methyl 2-Aminobenzoate (Methyl Anthranilate) by H2O2/UV: Effect of Inorganic Anions and Derived Radicals
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Degradation of Methyl 2-Aminobenzoate (Methyl Anthranilate) by H2O2/UV: Effect of Inorganic Anions and Derived Radicals

机译:H2O2 / UV降解2-氨基苯甲酸甲酯(邻氨基苯甲酸甲酯):无机阴离子和衍生基团的影响

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This study shows that methyl 2-aminobenzoate (also known as methyl anthranilate, hereafter MA) undergoes direct photolysis under UVC and UVB irradiation and that its photodegradation is further accelerated in the presence of H2O2. Hydrogen peroxide acts as a source of hydroxyl radicals (·OH) under photochemical conditions and yields MA hydroxyderivatives. The trend of MA photodegradation rate vs. H2O2 concentration reaches a plateau because of the combined effects of H2O2 absorption saturation and ·OH scavenging by H2O2. The addition of chloride ions causes scavenging of ·OH, yielding Cl2·? as the most likely reactive species, and it increases the MA photodegradation rate at high H2O2 concentration values. The reaction between Cl2·? and MA, which has second-order rate constant k C l 2 ? ? + M A = (4.0 ± 0.3) × 108 M?1·s?1 (determined by laser flash photolysis), appears to be more selective than the ·OH process in the presence of H2O2, because Cl2·? undergoes more limited scavenging by H2O2 compared to ·OH. While the addition of carbonate causes ·OH scavenging to produce CO3·? ( k C O 3 ? ? + M A = (3.1 ± 0.2) × 108 M?1·s?1), carbonate considerably inhibits the photodegradation of MA. A possible explanation is that the elevated pH values of the carbonate solutions make H2O2 to partially occur as HO2?, which reacts very quickly with either ·OH or CO3·? to produce O2·?. The superoxide anion could reduce partially oxidised MA back to the initial substrate, with consequent inhibition of MA photodegradation. Fast MA photodegradation is also observed in the presence of persulphate/UV, which yields SO4·? that reacts effectively with MA ( k S O 4 ? ? + M A = (5.6 ± 0.4) × 109 M?1·s?1). Irradiated H2O2 is effective in photodegrading MA, but the resulting MA hydroxyderivatives are predicted to be about as toxic as the parent compound for aquatic organisms (most notably, fish and crustaceans). View Full-Text
机译:这项研究表明,2-氨基苯甲酸甲酯(也称为邻氨基苯甲酸甲酯,以下简称MA)在UVC和UVB照射下进行了直接光解,并且在H2O2存在下其光降解作用进一步加快。过氧化氢在光化学条件下充当羟基自由基(·OH)的来源,并生成MA羟基衍生物。由于H2O2吸收饱和和H2O2清除·OH的综合作用,MA光降解速率与H2O2浓度的趋势达到了平稳状态。氯离子的添加​​引起·OH的清除,产生Cl 2·α。作为最可能的反应物种,它会在高H2O2浓度下提高MA光降解速率。 Cl2·?之间的反应和MA,其具有二阶速率常数k C l 2? ? + M A =(4.0±0.3)×108 M?1·s?1(由激光闪光光解法确定),在存在H2O2的情况下似乎比·OH工艺更具选择性,因为Cl2·与·OH相比,H2O2的清除作用更有限。虽然添加碳酸盐会导致·OH清除产生CO3·? (k C O 3≥+ MA =(3.1±0.2)×108M≥1·s≤1),碳酸盐显着抑制了MA的光降解。可能的解释是碳酸盐溶液的升高的pH值使H2O2以HO2?的形式部分出现,它与·OH或CO3·?的反应非常快。产生O2·?。超氧阴离子可将部分氧化的MA还原回初始底物,从而抑制MA光降解。在过硫酸盐/紫外线的存在下,也观察到了MA的快速光降解,生成SO4·α。与MA有效反应(k S O 4≥α+ MA =(5.6±0.4)×109M≤1·s≤1)。辐照过的H2O2可以有效地降解MA,但是生成的MA羟基衍生物的毒性与水生生物(最显着的是鱼类和甲壳类)的母体化合物一样高。查看全文

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