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.

New insights on the decolorization of waste flows by Saccharomyces cerevisiae strain - A systematic review.

One of the common causes of water pollution is the presence of toxic dye-based effluents, which can pose a serious threat to the ecosystem and human health. The application of Saccharomyces cerevisiae (S. cerevisiae) for wastewater decolorization has been widely investigated due to their efficient removal and eco-friendly treatments. This review attempts to create an awareness of different forms and methods of using Saccharomyces cerevisiae (S. cerevisiae) for wastewater decolorization through a systematic approach. Overall, some suggestions on classification of dyes and related environmental/health problems, and treatment methods are discussed. Besides, the mechanisms of dye removal by S. cerevisiae including biosorption, bioaccumulation, and biodegradation and cell immobilization methods such as adsorption, covalent binding, encapsulation, entrapment, and self-aggregation are discussed. This review would help to inspire the exploration of more creative methods for applications and modification of S. cerevisiae and its further practical applications.

Nitrate removal from aqueous solutions by cobalt ferrite nanoparticles synthesized by co-precipitation method: isotherm, kinetic and thermodynamic studies.

The purpose of this study was to examine the nitrate adsorption by cobalt ferrite (CFO) nanoparticles. The adsorbent was synthesized by co-precipitation method and its structure was characterized using scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction and vibrating-sample magnetometry. In batch adsorption studies, the effects of various parameters like pH (3-11), adsorbent dose (0.2-0.8 g/L), contact time (5-120 min), initial nitrate concentration (50-200 mg/L), and temperature (283-313 K) on the adsorption process were examined. The results of this study indicated that the maximum adsorption capacity was 107.8 mg/g (optimum condition pH = 3, adsorbent dosage: 0.2 g/L, nitrate concentration: 200 mg/L, contact time: 20 min and temperature: 313 K). The adsorption isotherm had a proper match with Langmuir (R2 = 0.99) and Freundlich (R2 = 0.99) models. The adsorption of nitrate by CFO followed pseudo-second-order kinetics. The results of the thermodynamics of the nitrate adsorption process by CFO showed that all the values of Gibbs free energy change, enthalpy change and entropy change were positive. Therefore, this process was endothermic and non-spontaneous.

A comparative study of using barberry stem powder and ash as adsorbents for adsorption of humic acid.

In the present research, investigation of the practical utility of barberry stem powder (BSP) and barberry stem ash (BSA) for humic acid (HA) removal from an aqueous medium by adsorption was carried out. The adsorption process was tested by varying of pH (3-11), reaction time (5-20 min), initial HA concentration (5-40 mg/L), adsorbent dosage (1-4 g/L), and temperature (15-35 °C). The isothermal results revealed that the adsorption process is favorable for both used adsorbents and it is highly described using the Freundlich and Langmuir models (R2 > 0.960). Also, the maximum uptakes of BSP and BSA for HA were 20.220 and 16.950 mg/g at the abovementioned optimized conditions (pH = 7, reaction time = 10 min, temperature = 15 °C, initial HA concentration = 40 mg/L, and adsorbent amount = 1.0 g/L), respectively. The results achieved from the fitting of the experimental data with Dubinin-Radushkevich isotherm model showed that the HA molecules are adsorbed onto the BSP and BSA by physiosorption process. From the thermodynamic study, it appeared that the biosorption process of the HA onto two studied adsorbents was of exothermic nature. The kinetics of the adsorption process of HA has been found to be pseudo-second-order model (R2 = 0.930-0.999). Thus, the results obtained from this paper elucidated that the BSP exhibited higher adsorption capacity in comparison to BSA, for HA removal up to permissible concentrations.

Synthesis and characterizations of a novel CoFe2O4@CuS magnetic nanocomposite and investigation of its efficiency for photocatalytic degradation of penicillin G antibiotic in simulated wastewater.

In the present study, efficiency of a new magnetic nanocomposite (CoFe2O4@CuS) for photocatalytic degradation of PG in aqueous solutions was investigated. Structural characteristics of synthesized magnetic nanoparticles were determined by scanning electron microscopy (SEM), transmission electron microscopy (TEM), fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), vibrating-sample magnetometer (VSM), Thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET), Energy-dispersive X-ray spectroscopy (EDX) and Raman spectroscopy. Also, the effect of important parameters such as pH (3-11), nanoparticle dosage (0.1-0.8 g/L), PG concentration (10-100 mg/L) and contact time (10-120 min) were investigated. Results of FT-IR, XRD, EDX and Raman analyses showed successful synthesis of CoFe2O4@CuS magnetic nanocomposite. SEM and TEM images showed that the size of CoFe2O4@CuS magnetic nanocomposite was below 100 nm. Also, results of VSM analyses showed that CoFe2O4@CuS magnetic nanocomposite still has magnetic properties (Ms = 7.76 emu/g). According to the results of study, in photocatalytic degradation process of PG by CoFe2O4@CuS magnetic nanocomposite by UV light and in optimum condition (pH = 5, nanocomposite dose: 0.2 g/L, PG concentration: 10 mg/L and contact time: 120 min), maximum degradation of PG was 70.7%. Also the photocatalytic reaction almost followed the pseudo-first order kinetics. In addition, after five consecutive runs, the catalyst efficiency wasn't reduced significantly.