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Fe(III)-草酸配合物在大气水相中介导的愈创木酚的光化学老化。

Photochemical Aging of Guaiacol by Fe(III)-Oxalate Complexes in Atmospheric Aqueous Phase.

机构信息

Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention, Department of Environmental Science and Engineering , Fudan University , Shanghai 200433 , China.

Department of Environmental Toxicology , University of California , Davis , California 95616 , United States.

出版信息

Environ Sci Technol. 2019 Jan 2;53(1):127-136. doi: 10.1021/acs.est.8b04507. Epub 2018 Dec 11.

Abstract

Fe(III)-oxalate complexes are likely abundant in clouds, fogs and aerosol water. They are photoreactive and can act as an important source of reactive oxygen species (OH, HO and HO·) in tropospheric aqueous phases. Although the mechanisms involved in ferrioxalate photolysis have been investigated extensively, few kinetic and mechanistic information is available on the aging of dissolved organic compounds by this photochemical system. In this work, the Fe(III)-oxalate mediated photooxidation of guaiacol (GUA), a model for phenolic compounds emitted from biomass burning, was investigated under typical pH conditions of the atmospheric water. The effect of Fe(III) concentration, oxalate concentration and pH on the photooxidation of GUA was studied in detail. Our results revealed that oxalate can inhibit the oxidation of GUA by Fe(III) under the dark condition. However, the iron-catalyzed photooxidation of GUA can be strongly promoted in the presence of oxalate due to the formation of photoactive Fe(III)-oxalate complexes. GUA was rapidly oxidized to form a number of polymeric, functionalized and open-ring products with low volatility. Detailed reaction pathways for the photooxidation of GUA by Fe(III)-oxalate complexes were proposed based on the results of high-resolution mass spectrometry. This work suggests that ferrioxalate photochemistry can play an important role in the transformation of dissolved organics in atmospheric aqueous phases.

摘要

草酸铁配合物可能在云、雾和气溶胶水中大量存在。它们具有光反应性,可以在对流层水相中充当重要的活性氧物质(OH、HO 和 HO·)的来源。尽管已经广泛研究了铁-草酸配合物光解的机制,但关于该光化学体系对溶解有机化合物老化的动力学和机制信息却很少。在这项工作中,研究了在大气水的典型 pH 值条件下,作为生物质燃烧排放的酚类化合物模型的愈创木酚(GUA)在草酸铁介导下的光氧化作用。详细研究了 Fe(III)浓度、草酸盐浓度和 pH 值对 GUA 光氧化的影响。我们的结果表明,在黑暗条件下,草酸盐可以抑制 Fe(III)对 GUA 的氧化。然而,由于形成了光活性的 Fe(III)-草酸根配合物,草酸根可以强烈促进铁催化的 GUA 光氧化。GUA 迅速氧化形成许多低挥发性的聚合、官能化和开环产物。根据高分辨率质谱的结果,提出了 Fe(III)-草酸根配合物对 GUA 光氧化的详细反应途径。这项工作表明,铁-草酸根光化学可以在大气水相中的溶解有机物转化中发挥重要作用。

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