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吸附在水铁矿上对溶解态黑碳光降解磺胺嘧啶光反应性的影响。

Effect of adsorption on ferrihydrite on the photoreactivity of dissolved black carbon for photodegradation of sulfadiazine.

机构信息

College of Earth and Environmental Sciences, Lanzhou University, Lanzhou, 730000, China.

College of Earth and Environmental Sciences, Lanzhou University, Lanzhou, 730000, China.

出版信息

Chemosphere. 2023 Oct;337:139359. doi: 10.1016/j.chemosphere.2023.139359. Epub 2023 Jun 26.

Abstract

The selective adsorption of dissolved black carbon (DBC) on inorganic minerals is a widespread geochemical process in the natural environment, which could change the chemical and optical properties of DBC. However, it remains unclear how selective adsorption affects the photoreactivity of DBC for photodegradation of organic pollutants. This paper was the first to investigate the effect of DBC adsorption on ferrihydrite at different Fe/C molar ratios (Fe/C molar ratios of 0, 7.50 and 11.25, and marked as DBC, DBC and DBC) on the photoproduction of reactive intermediates generated from DBC and their interaction with sulfadiazine (SD). Results showed that UV absorbance, aromaticity, molecular weight and contents of phenolic antioxidants of DBC were significantly decreased after adsorption on ferrihydrite, and higher decrease was observed at higher Fe/C ratio. Photodegradation kinetics experiments showed that observed photodegradation rate constant of SD (k) increased from 3.99 × 10 s in DBC to 5.69 × 10 s in DBC while decreased to 3.44 × 10 s in DBC, in which DBC* played an important role and O played a minor role, while ·OH was not involved in the reaction. Meanwhile, the second-order reaction rate constant between DBC* and SD (k) increased from 0.84 × 10 M s for DBC to 2.53 × 10 M s for DBC while decreased to 0.90 × 10 M s for DBC. The above results might be mainly attributed to the fact that the decrease of phenolic antioxidants in DBC weakened the back-reduction of DBC* and reactive intermediates of SD as the Fe/C ratio increased, while the decrease of quinones and ketones reduced the photoproduction of DBC*. The research revealed adsorption on ferrihydrite affected the photodegradation of SD by changing the reactivity of DBC*, which was helpful to understand the dynamic roles of DBC in the photodegradation of organic pollutants.

摘要

溶解态黑碳(DBC)在无机矿物上的选择性吸附是一种在自然环境中广泛存在的地球化学过程,它可以改变 DBC 的化学和光学性质。然而,对于选择性吸附如何影响 DBC 对有机污染物光降解的光反应性,目前还不清楚。本文首次研究了在不同 Fe/C 摩尔比(Fe/C 摩尔比分别为 0、7.50 和 11.25,标记为 DBC、DBC 和 DBC)条件下,DBC 在针铁矿上的吸附对 DBC 光生反应中间体的光产生及其与磺胺嘧啶(SD)相互作用的影响。结果表明,DBC 在针铁矿上吸附后,其紫外吸光度、芳香度、分子量和酚类抗氧化剂含量均显著降低,且在较高的 Fe/C 比下降低幅度更大。光降解动力学实验表明,磺胺嘧啶(SD)的表观光降解速率常数(k)从 DBC 中的 3.99×10 s 增加到 DBC 中的 5.69×10 s,而在 DBC 中降低到 3.44×10 s,其中 DBC起重要作用,O 起次要作用,而·OH 不参与反应。同时,DBC与 SD 的二级反应速率常数(k)从 DBC 中的 0.84×10 M s 增加到 DBC 中的 2.53×10 M s,而在 DBC 中降低到 0.90×10 M s。上述结果可能主要归因于随着 Fe/C 比的增加,DBC 中酚类抗氧化剂的减少削弱了 DBC和 SD 反应中间体的反还原作用,而醌和酮的减少则降低了 DBC 的光生成。该研究揭示了针铁矿上的吸附通过改变 DBC的反应性来影响 SD 的光降解,这有助于理解 DBC 在有机污染物光降解过程中的动态作用。

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