Unique effect of bromide ion on intensification of advanced oxidation processes for pollutants removal: A systematic review.

Advanced oxidation processes (AOPs) have been developed to decompose toxic pollutants to protect the aquatic environment. AOP has been considered an alternative treatment method for wastewater treatment. Bromine is present in natural waters posing toxic effects on human health and hence, its removal from drinking water sources is necessary. Of the many techniques advanced oxidation is covered in this review. This review systematically examines literature published from 1997 to April 2024, sourced from Scopus, PubMed, Science Direct, and Web of Science databases, focusing on the efficacy of AOPs for pollutant removal from aqueous solutions containing bromide ions to investigate the impact of bromide ions on AOPs. Data and information extracted from each article eligible for inclusion in the review include the type of AOP, type of pollutants, and removal efficiency of AOP under the presence and absence of bromide ion. Of the 1784 documents screened, 90 studies met inclusion criteria, providing insights into various AOPs, including UV/chlorine, UV/PS, UV/H2O2, UV/catalyst, and visible light/catalyst processes. The observed impact of bromide ion presence on the efficacy of AOP processes, alongside the AOP method under scrutiny, is contingent upon various factors such as the nature of the target pollutant, catalyst type, and bromide ion concentration. These considerations are crucial in selecting the best method for removing specific pollutants under defined conditions. Challenges were encountered during result analysis included variations in experimental setups, disparities in pollutant types and concentrations, and inconsistencies in reporting AOP performance metrics. Addressing these parameters in research reports will enhance the coherence and utility of subsequent systematic reviews.

Harnessing bromide ions to boost peroxymonosulfate for reactive yellow 145 dye degradation.

Bromide (Br-) was found in the fresh waters at concentrations from 0.1 to 1 mg/L and can be used to activate peroxymonosulfate (PMS) as a widely used chemical oxidation agent. In the present study, the reaction between PMS and Br- ions (PMS/Br- process) for the effective degradation of reactive yellow 145 (RY-145) dye was investigated by changing operational parameters vis solution pH, dosage of Br- ions and PMS, RY-145 concentration, and reaction time. Based on the results, the simultaneous presence of PMS and Br- ions in the solution led to efficient degradation of RY-145 with a synergistic index of 11.89. The degradation efficiency of RY-145 was decreased in severe basic pH and the presence of CO32- ions as a coexisting anion. Likewise, 4 mg/L of humic acid (HA), used as a classic scavenger, led to a 26.53% decrease in the RY-145 degradation efficiency. The free bromine (HOBr/OBr-), superoxide radical (●O2-), and singlet oxygen (1O2) was the dominant oxidation agents in RY-145 degradation, which confirmed the nonradical degradation pathway. In addition, PMS/Br- process showed excellent ability in mineralizing RY-145 in different aqueous solutions (total organic carbon (TOC) decreased 86.39% in deionized water and 78.23% in tap water). Although pollutants such as azo dyes can be effectively removed in the PMS/Br- process, the formation of byproducts should be strategically controlled and special attention should be paid when the PMS-based advance oxidation process is applied to treat Br- containing solutions.

Hydrothermally improved natural manganese-containing catalytic materials to degrade 4-chlorophenol.

Natural manganese-containing mineral (NMM) was used as a catalyst in heterogeneous catalytic ozonation for 4-chlorophenol (4-CP) degradation. The surface and structural properties of NMM were modified by the hydrothermal aging process and called H-NMM. The catalytic activity of NMM and H-NMM were evaluated for the catalytic ozonation process (COP). The synergistic effect of NMM and H-NMM in ozonation processes for 4-CP degradation under optimal conditions (pH of 7, 1 g/L of NMM and H-NMM, 0.85 mg/min of O3, and 15 min of reaction time) was measured by 3.04 and 4.34, respectively. During the hydrothermal process, Mn4+ and Fe2+ were converted to Mn2+ and Fe3+, which caused better performance of the H-NMM than the NMM. During the catalytic ozonation process, Mn2+ is completely oxidized, which increases the production of Hydroxyl radical (•OH). The reactive oxygen species (ROS) generated in the system were identified using radical scavenging experiments. •OH, superoxide radical (•O2-), and singlet oxygen (1O2) represented the dominant reactive species for 4-CP degradation. The O3/H-NMM process indicated a powerful ability in the mineralization of 4-CP (66.31% of TOC degradation). H-NMM exhibited excellent stability and reusability in consecutive catalytic cycles, and the NMM exhibited desirable performance. This study offers NMM and H-NMM as effective, stable, and competitive catalysts for hastening and enhancing the ozonation process to mitigate environmentally related pollutants of high concern.

Degradation of 4-chlorophenol using MnOOH and γ-MnOOH nanomaterials as porous catalyst: Performance, synergistic mechanism, and effect of co-existing anions.

Transition metal catalysts have been proven to be a highly-potent catalyst for peroxymonosulfate (PMS) activation. The present work aimed to synthesizes the γ-MnOOH and MnOOH based on the one-pot hydrothermal method as PMS activators for efficient degradation of 4-chlorophenol (4-CP). The effect of operational parameters including solution pH, γ-MnOOH and MnOOH dose, PMS dose, 4-CP concentration, and also mixture media composition was elaborated. The results showed that the combination of MnOOH and γ-MnOOH with PMS noticeably creates a synergistic effect (SF) in 4-CP degradation by both PMS/MnOOH and PMS/γ-MnOOH process, with a SF value of 48.14 and 97.42, respectively. In both systems, the removal of 4-CP decreased in severely alkaline and acidic conditions, while no significant changes were observed in pH 5 to 9. Also, coexisting PO43- significantly reduced the removal efficiency of both systems. In addition, the effect of humic acid (HA) as a classical scavenger was investigated and showed that presence of 4 mg/L HA reduced the removal efficiency of 4-CP in the PMS/MnOOH process from 97.44% to 79.3%. The three consecutive use of both catalysts turned out that MnOOH has better stability than γ-MnOOH with lower Mn ions leaching. More importantly, quenching experiment showed that both non-radical (1O2 and O2-) and radical (SO4- and OH) pathways are involved in 4-CP degradation and non-radical pathway was the dominant one in both systems.

Treatment of synthetic dye containing textile raw wastewater effluent using UV/Chlorine/Br photolysis process followed by activated carbon adsorption.

This study investigated the efficiency and feasibility of ultraviolet (UV)-assisted photolysis of synthetic dye containing textile raw wastewater effluent. For a said purpose, in-house developed UV/Chlorine/Br process was followed in the presence of activated carbon (AC) which additionally facilitate the dye adsorption. In UV/Chlorine process Cl•, Cl2•-, and HO• are generated in the solution and destroyed compounds that cannot be oxidized by the conventional oxidant. In this process, free bromine is formed and photolyzed by UV radiation and generate Br• and Br2•- that can enhance the rate of pollutant degradation. In the present study, the dye removal efficiency was contributed by dark bromide (7.18%), UV irradiation (26.8%), dark chlorination (78.67%), and UV/Chlorine/Br (87.01%), respectively. With increasing pH from 3.0 to 8.30, the dye removal efficiency was enhanced but decreased by further increasing pH values. In addition, magnetized activated carbon from pomegranate husk using dual-stage chemical activation was used for post-adsorption of the residual dye and its degradation byproducts. The adsorption of the dye residues by AC followed the second-order kinetics with the rate constant of 1.7 × 10-3. The phytotoxicity of the treated textile wastewater by UV irradiation, dark chlorination, and UV/Chlorine/Br was assessed by seed germination of Lepidium sativum seeds. The highest inhibition effect on seed germination was related to treated wastewater by UV irradiation (more than 90% inhibition) that alleviated to less than 10% when this effluent diluted to 5% v/v. The highest germination was observed when the seeds were irrigated by the effluent of the UV/Chlorine/Br process. The significant reduction in the toxicity of the treated wastewater revealed that the UV/Chlorine/Br process has a considerable potential to effectively detoxify textile wastewater. Graphical abstract.