Cotenygaard8697

The COVID-19 outbreak has triggered a massive research, but still urgent detection and treatment of this virus seems a public concern. The spread of viruses in aqueous environments underlined efficient virus treatment processes as a hot challenge. This review critically and comprehensively enables identifying and classifying advanced biochemical, membrane-based and disinfection processes for effective treatment of virus-contaminated water and wastewater. Understanding the functions of individual and combined/multi-stage processes in terms of manufacturing and economical parameters makes this contribution a different story from available review papers. Moreover, this review discusses challenges of combining biochemical, membrane and disinfection processes for synergistic treatment of viruses in order to reduce the dissemination of waterborne diseases. Certainly, the combination technologies are proactive in minimizing and restraining the outbreaks of the virus. It emphasizes the importance of health authorities to confront the outbreaks of unknown viruses in the future.In this study, a novel electrifying mode (divided power-on and power-off stage) was applied in the system of BDD activate sulfate to degrade tetracycline hydrochloride (TCH). The BDD electrode could activate sulfate and H2O to generate sulfate radicals (SO4•-) and hydroxyl radicals (•OH) to remove TCH, and SO4•- could dimerize to form S2O82-. Then, the S2O82- was activated by heat and quinones to generate SO4•- for the continuous degradation of TCH during the power-off stage. In addition, the intermittent time has a significant effect on the degradation of TCH. Factors, affecting the accumulation of S2O82-, were analyzed using a full factorial design, and the accumulation of S2O82- could reach 16.2 mM in 120 min. The results of electron spin resonance and radical quenching test showed that SO4•-, •OH, direct electron transfer (DET), and non-radical in the system could effectively degrade TCH, and SO4•- was dominated. The intermediate products of TCH were analyzed by HPLC-QTOF-MS/MS, and the TCH mainly underwent hydroxylation, demethylation and ring opening reactions to form small molecules, and finally mineralized. The results of the feasibility analysis revealed that some intermediates have high toxicity, but the system could improve the toxicity. The results of energy consumption indicated that the intermittent electrifying mode could make full use of the persulfate generated during the power-on stage and reduce about 30% energy consumption. In conclusion, this work demonstrated that it was economically feasible to degrade TCH in wastewater by activating sulfate with BDD electrodes with an intermittent electrifying mode.Phosphorus-modified biochars are considered as good materials for the removal of heavy metals from wastewater. However, the efficacy of ammonium polyphosphate-modified biochar in cadmium (Cd(II)) adsorption remains largely unknown. In this work, the biochar was respectively modified with ammonium polyphosphate (PABC), phosphoric acid (PHBC) and ammonium dihydrogen phosphate (PNBC) to enhance its adsorption performance for heavy metals from wastewater. The properties of biochar before and after modification and P speciation on the surface of the modified biochar were investigated with FTIR, SEM-EDS, XPS, XRD and 31P NMR, and the adsorption capacity was evaluated by batch adsorption experiments. The results demonstrated that the optimal adsorption performance could be achieved at the solution pH = 4, and the pseudo-second-order and Langmuir models could well describe the Cd(II) adsorption process. The maximum adsorption capacity of PABC, PHBC and PNBC for Cd(II) was 155, 138 and 99 mg g-1, which were 4.84, 4.32 and 3.10 folds that of original biochar, respectively. The 31P NMR showed that orthophosphate accounted for 82.1%, 62.8% and 54.5% of P in PABC, PHBC and PNBC, respectively, which decreased to 28.24%, 33.51% and 29.34% after Cd(II) adsorption, indicating that the orthophosphate ratio in P-modified biochar surface could significantly affect Cd adsorption by forming phosphate precipitate. This work implies that the PABC has greater potential in the removal of Cd from wastewater relative to PHBC and PNBC.Boron-doped diamond (BDD) electrodes are regarded as the most promising catalytic materials that are highly efficient and suitable for application in advanced electrochemical oxidation processes targeted at the removal of recalcitrant contaminants in different water matrices. Improving the synthesis of these electrodes through the enhancement of their morphology, structure and stability has become the goal of the material scientists. The present work reports the use of an ultranano-diamond electrode with a highly porous structure (B-UNCDWS/TDNT/Ti) for the treatment of water containing carbaryl. The application of the proposed electrode at current density of 75 mA cm-2 led to the complete removal of the pollutant (carbaryl) from the synthetic medium in 30 min of electrolysis with an electric energy per order of 4.01 kWh m-3 order-1. The results obtained from the time-course analysis of the carboxylic acids and nitrogen-based ions present in the solution showed that the concentrations of nitrogen-based ions were within the established maximum levels for human consumption. Under optimal operating conditions, the proposed electrode was successfully employed for the complete removal of carbaryl in real water. Thus, the findings of this study show that the unique, easy-to-prepare BDD-based electrode proposed in this study is a highly efficient tool which has excellent application potential for the removal of recalcitrant pollutants in water.Hexavalent chromium is widely used in industrial fields, but its pollution has posed a great threat to the environment due to its high toxicity. We created a chitosan-based microsphere biosorbent (CP) by combining polyethyleneimine with chitosan adopting inverse emulsion polymerization method. Under the optimal conditions (pH = 3), the maximum adsorption capacity of composite microspheres can reach 299.89 mg g-1, which is much higher than that of chitosan microspheres (168.91 mg g-1). When the amount of CP is 0.25 g L-1, the removal rate of 50 mg L-1 Cr(VI) and 50 mg L-1 Eriochrome blue-black R (EBBR) can reach 95% and 99%, respectively. The time required for CP to reach adsorption equilibrium (180 min) was significantly shorter than that of chitosan microspheres (540 min), and the adsorption rate was significantly improved. Langmuir isotherm model, pseudo-second-order kinetic model and thermodynamic calculation results penetrated an endothermic spontaneous, monolayer, and chemical adsorption process. Biomass composite microspheres CP has obvious selectivity and the adsorption capacity retention rate of CP was still 71.32% after four adsorption cycles. This work proposed an easily prepared and biomass-based microspheres for the effective removal of Cr(VI) in printing and dyeing wastewater pollution through adsorption.Starch-stablized and Fe/Mn bimetals modified biochar derived from corn straw (SFM@CBC and SFM@CBC-350) were firstly prepared, characterized (FTIR, XRD, SEM, EDS, BET and XPS), and applied in Pb removal from water and soil. SFM@CBC and SFM@CBC-350 displayed highly effective adsorption performance of Pb2+ from wastewater with the maximum adsorption capacity of 170.91 mg g-1 and 190.17 mg g-1, respectively, which were much greater than that of FM@CBC (149.25 mg g-1) and CBC (101.10 mg g-1). Studies of adsorption kinetics, isotherms and thermodynamics indicated that the absorption of Pb2+ by SFM@CBC and SFM@CBC-350 was spontaneous and endothermic reaction, and it was controlled by monolayer chemisorption. The mechanism studies indicated that Pb2+ removal involved with multiple mechanism, including complexation (dominant process confirmed by XPS analysis), physical adsorption, electrostatic attraction, and cation exchange. The reusability test demonstrated that SFM@CBC and SFM@CBC-350 had very good stability and reusability. In addition, in order to further explore Pb removal performance of the modified biochar, SFM@CBC-350 was used in soil-ryegrass pot systems. Compared with the controls, the addition of SFM@CBC-350 reduced Pb content in soil and ryegrass, increased the biomass and total chlorophyll content, reduced the activity of antioxidant enzymes (CAT, SOD, MDA and POD) and ROS fluorescence intensity of ryegrass, thus alleviating Pb stress of ryegrass. Besides, the addition of SFM@CBC-350 could increase the richness and diversity of soil microorganisms, which was beneficial to the growth of ryegrass. Hence, SFM@CBC-350 has the potential of being used as a green, efficient and promising adsorbent in Pb removal from wastewater and soil.Monoclinic BiVO4 (m-BiVO4) has been reported as promising phase for solar light driven photocatalysis. However, in the case of morphology guided BiVO4 with different synthetic conditions maintaining the m-BiVO4 phase remains a substantial challenge for achieving an efficient photocatalyst driven by solar light. Herein, a simple hydrothermal approach was used to produce well-defined template free m-BiVO4 dendrites with distinct branches for photo catalytically removal of organic pollutant and photocurrent generation. The development of monoclinic dendrite BiVO4 was confirmed after comprehensive structural, morphological, and optical examinations. FE-SEM images of m-BiVO4 revealed transformation of spherical to dendritic morphology with distinct branches by simply changing the HNO3 to NaOH ratios from 21 to 22, which are named as BVO 2-1 and BVO 2-2, respectively. The BVO 2-2 dendrites exhibited improved activity of 98% towards methylene blue (MB) photodegradation upon simulated solar light irradiation. The BVO 2-2 dendrites photoelectrode showed an outstanding photocurrent density of 1.4245 mAcm-2 than that of the BVO 2-1 spherical photoelectrode (0.7367 mAcm-2). Enhanced photocatalytic and photoelectrochemical action, could be ascribed to the unique morphological changes provides photoactive sites, harvest more light utilization together with higher separation of e-/h+ pairs. Furthermore, photocatalytic mechanism is investigated based on scavenger trapping agent, valence band XPS, UV Visible DRS and PL study. learn more Our findings could pave the way for the development of dendritic nanostructure photocatalysts with improved photocatalytic activity.From the 1950s to the 1970s, three Superfund sites discharged polychlorinated biphenyl (PCB)-contaminated waste upstream of the Mohawk Nation at Akwesasne, resulting in PCB contamination of groundwater, soil, and sediment in the surrounding area. Given the persistence of PCBs in the environment and in human tissues, there are continued concerns regarding PCB exposures and the potential for adverse health effects in the community. We developed an evidence map of PCB research at Akwesasne in order to characterize the available data and to highlight potential research needs. Human health and exposure biomarker studies were identified from a literature search based on population, exposure, comparator, and outcome (PECO) criteria. Data extracted from references that met the inclusion criteria after full-text review included study characteristics (e.g., sample size, study design, sampling years), details on PCB measurements (e.g., analytical method, number of congeners analyzed, method detection limits), and results (e.