Environment Research Institute, Shandong University, Qingdao, 266237, China.
Atmospheric Chemistry Department (ACD), Leibniz-Institute for Tropospheric Research (TROPOS), Leipzig, 04318, Germany.
J Hazard Mater. 2021 Feb 5;403:123805. doi: 10.1016/j.jhazmat.2020.123805. Epub 2020 Sep 6.
P-nitrophenol (p-NP) is a recalcitrant organic compound attracted great environmental attention, but its degradation mechanism is indeterminacy, which challenges its treatment, migration, transformation and ecological impact in the environment. In the present study, the aqueous-phase decomposition process of p-NP initiated by O has been investigated by a theoretical calculation method. The detailed possible reaction pathways for the oxidative degradation of p-NP by ozone have been proposed. The chemical reaction thermodynamics results show that the reaction barriers of all ozone-initiated pathways are below 15 kcal·mol, indicating that ozone can completely initiate the oxidation of p-NP under natural conditions. However, the kinetic results show that the initiation reaction of p-NP by ozone alone is relatively slow compared to the reaction by OH. Interestingly, under ultraviolet (UV) radiation, the dissolved ozone interacts with water and produces two active radicals: OH and HO. The reaction rate of p-NP initiated with OH is much higher than that with ozone, implying that the OH produced in the photochemical process can improve the removal efficiency of p-NP. The intermediates generated in the ozone-initiated reaction have been found to decompose into small molecule organic acids, aldehydes and ketones. The potential carcinogenicities and teratogenicities of the transformation products have also been studied, and some of them still have carcinogenic activity, which deserve further attention. In addition, to our knowledge, this may be the first computational chemistry study on the degradation of p-NP initiated by HO. All the results provide a new fundamental understanding for the migration and transformation of p-NP in water environment, and indicate that further assessment is needed for the impact of p-NP and especially its transformation products on the ecological environment in a significant way.
对硝基苯酚(p-NP)是一种难降解的有机化合物,引起了人们的广泛关注,但其降解机制尚不确定,这给其在环境中的处理、迁移、转化和生态影响带来了挑战。本研究采用理论计算方法,研究了 O 引发的 p-NP 的水相分解过程,提出了臭氧氧化降解 p-NP 的详细可能反应途径。化学反应热力学结果表明,所有臭氧引发途径的反应势垒均低于 15 kcal·mol-1,表明臭氧在自然条件下可以完全引发 p-NP 的氧化。然而,动力学结果表明,与 OH 相比,臭氧单独引发 p-NP 的反应相对较慢。有趣的是,在紫外(UV)辐射下,溶解的臭氧与水相互作用产生两种活性自由基:OH 和 HO。与臭氧相比,OH 引发的 p-NP 反应速率要高得多,这意味着光化学过程中产生的 OH 可以提高 p-NP 的去除效率。在臭氧引发反应中生成的中间体已被发现分解为小分子有机酸、醛和酮。还研究了转化产物的潜在致癌性和致畸性,其中一些仍具有致癌活性,值得进一步关注。此外,据我们所知,这可能是首次采用计算化学方法研究 HO 引发的 p-NP 降解。所有结果为 p-NP 在水环境中的迁移和转化提供了新的基础认识,并表明需要进一步评估 p-NP 及其转化产物对生态环境的影响。