Tran Hai D, Nguyen Dinh Quan, Do Phuong T, Tran Uyen N P
Faculty of Environment, Ho Chi Minh University of Natural Resources and Environment Ho Chi Minh City Vietnam.
Laboratory of Biofuel and Biomass Research, Faculty of Chemical Engineering, Ho Chi Minh City University of Technology (HCMUT) 268 Ly Thuong Kiet, District 10 Ho Chi Minh City Vietnam
RSC Adv. 2023 Jun 5;13(25):16915-16925. doi: 10.1039/d3ra01970e.
Organic compounds are widespread pollutants in wastewater, causing significant risks for living organisms. In terms of advanced oxidation processes, photocatalysis is known as an effective technology for the oxidation and mineralization of numerous non-biodegradable organic contaminants. The underlying mechanisms of photocatalytic degradation can be explored through kinetic studies. In previous works, Langmuir-Hinshelwood and pseudo-first-order models were commonly applied to fit batch-mode experimental data, revealing critical kinetic parameters. However, the application or combination conditions of these models were inconsistent or ignored. This paper briefly reviews kinetic models and various factors influencing the kinetics of photocatalytic degradation. In this review, kinetic models are also systemized by a new approach to establish a general concept of a kinetic model for the photocatalytic degradation of organic compounds in an aqueous solution.
有机化合物是废水中广泛存在的污染物,对生物体构成重大风险。就高级氧化工艺而言,光催化是一种用于氧化和矿化众多不可生物降解有机污染物的有效技术。光催化降解的潜在机制可通过动力学研究来探索。在以往的研究中,朗缪尔 - 欣谢尔伍德模型和伪一级模型通常用于拟合间歇模式实验数据,以揭示关键的动力学参数。然而,这些模型的应用或组合条件并不一致或被忽视。本文简要回顾了动力学模型以及影响光催化降解动力学的各种因素。在本综述中,还通过一种新方法对动力学模型进行了系统化,以建立水溶液中有机化合物光催化降解动力学模型的一般概念。