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.

Hydrodynamic cavitation coupled with zero-valent iron produces radical sulfate radicals by sulfite activation to degrade direct red 83.

In the present research, hydrodynamic cavitation (HC) and zero-valent iron (ZVI) were used to generate sulfate radicals through sulfite activation as a new source of sulfate for the efficient degradation of Direct Red 83 (DR83). A systematic analysis was carried out to examine the effects of operational parameters, including the pH of the solution, the doses of ZVI and sulfite salts, and the composition of the mixed media. Based on the results, the degradation efficiency of HC/ZVI/sulfite is highly dependent upon the pH of the solution and the dosage of both ZVI and sulfite. Degradation efficiency decreased significantly with increasing solution pH due to a lower corrosion rate for ZVI at high pH. The corrosion rate of ZVI can be accelerated by releasing Fe2+ ions in an acid medium, reducing the concentration of radicals generated even though ZVI is solid/originally non-soluble in water. The degradation efficiency of the HC/ZVI/sulfite process (95.54 % + 2.87%) was found to be significantly higher under optimal conditions than either of the individual processes (<6% for ZVI and sulfite and 68.21±3.41% for HC). Based on the first-order kinetic model, the HC/ZVI/sulfite process has the highest degradation constant of 0.035±0.002 min-1. The contribution of radicals to the degradation of DR83 by the HC/ZVI/sulfite process was 78.92%, while the contribution of SO4•- and •OH radicals was 51.57% and 48.43%, respectively. In the presence of HCO3- and CO32- ions, DR83 degradation is retarded, whereas SO42- and Cl- ions promote degradation. To summarise, the HC/ZVI/sulfite treatment can be viewed as an innovative and promising method of treating recalcitrant textile wastewater.

Degradation of 2,4-diclorophenol via coupling zero valent iron and hydrodynamic cavitation for sulfite activation: A turbulence modeling.

The 2,4-dichlorophenol (2,4-DCP) is an important chemical precursor that can affect human endocrine system and induce pathological symptoms. This research reports the degradation of 2,4-DCP using lab-scale hydrodynamic cavitation (HC) approach, which is considered a green and effective method. To promote the degradation efficiency, the zero-valent iron (Fe0) as the catalyst for sulfate radical (SO4•-) generation via activation of sulfite (SO32-) salts was simultaneously used. Degradation efficiency was favorable in acidic pH than the alkaline pH due to higher production of active radicals and was dependent on the dose of Fe0 and SO32-. Under optimal condition, degradation efficiency by Fe0/HC/sulfite (96.67 ± 2.90%) was considerably enhanced compared to HC alone (45.37 ± 2.26%). Quenching experiments suggested that SO4•-, •OH, 1O2, and O2•- radicals were involved in the degradation of 2,4-DCP by Fe0/HC/sulfite process, but the dominant role was related to •OH (70.09% contribution) and SO4•- (29.91% contribution) radicals. From the turbulence model, turbulent pressure at venturi throat decreased from -0.42 MPa to -2.02 MPa by increasing the inlet pressure from 1.0 to 4.0 bar and increase in pressure gradient has intensified bubble collapse due to higher turbulence tension.