Sarvothaman Varaha P, Velisoju Vijay K, Subburaj Janardhanraj, Panithasan Mebin S, Kulkarni Shekhar R, Castaño Pedro, Turner James, Guida Paolo, Roberts William L, Nagarajan Sanjay
Clean Combustion Research Center (CCRC), King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.
Multiscale Reaction Engineering (MuRE) Group, KAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.
Ultrason Sonochem. 2023 Oct;99:106548. doi: 10.1016/j.ultsonch.2023.106548. Epub 2023 Aug 3.
Phenols are recalcitrant compounds that constitute the majority of organic contaminants in industrial wastewaters. Their removal at large scales require a combination of various processes to reach the desired discharge quality. An extensive body of work has already been published in the area of phenol removal from wastewater, however none of them have focussed on a truly 'sensible' approach for coupling advanced oxidation processes (AOPs). Rather, a higher removal efficiency was targeted by unduly complicating the process by combining multiple AOPs. The most influential AOP as the primary method typically driven by the nature of the pollutant should form the basis for a hybrid AOP followed by a complementary AOP to intensify the oxidation process. This strategy is lacking in current literature. We address this knowledge gap directly by systematically identifying the best hybrid process for ZnO mediated photocatalysis of phenol. Either a cavitation mediated pre-treatment of ZnO or cavitation-photocatalysis-peroxide based hybrid AOP was investigated. While the pre-treatment approach led to >25% increase in phenol oxidation compared to bare ZnO photocatalysis, the hydrodynamic cavitation-photocatalysis-peroxide based system was found to have a cavitational yield 5 times higher than its acoustic cavitation counterpart. A new phenomenon known as the 'pseudo staggered effect' was also observed and established in hydrodynamic cavitation mediated photocatalysis-peroxide hybrid process for the first time. While we demonstrated that cavitation is a truly 'sensible' choice to enhance photocatalysis, the nature of the pollutant under investigation must always be the key driver when designing such hybrid AOPs.
酚类是难降解化合物,在工业废水中构成了大部分有机污染物。大规模去除这些污染物需要多种工艺相结合,以达到所需的排放质量。关于从废水中去除酚类的领域已经发表了大量的研究成果,然而,这些研究都没有聚焦于一种真正“合理”的方法来耦合高级氧化工艺(AOPs)。相反,人们试图通过将多种AOPs过度复杂化来实现更高的去除效率。作为主要方法的最具影响力的AOP通常由污染物的性质驱动,应作为混合AOP的基础,随后采用互补的AOP来强化氧化过程。目前的文献中缺乏这种策略。我们通过系统地确定用于氧化锌介导的苯酚光催化的最佳混合工艺,直接填补了这一知识空白。研究了氧化锌的空化介导预处理或基于空化-光催化-过氧化物的混合AOP。虽然预处理方法相比于单纯的氧化锌光催化使苯酚氧化率提高了>25%,但基于水力空化-光催化-过氧化物的系统的空化产率比其声空化对应物高5倍。一种被称为“伪交错效应”的新现象也首次在水力空化介导的光催化-过氧化物混合过程中被观察到并得以确立。虽然我们证明了空化是增强光催化的一种真正“合理”的选择,但在设计这种混合AOP时,所研究污染物的性质必须始终是关键驱动因素。