Pre-oxidation has been reported to be an effective way to remove algal cells in water, but the released algal organic matter (AOM) could be oxidized and lead to the increment in disinfection by-product (DBP) formation...Pre-oxidation has been reported to be an effective way to remove algal cells in water, but the released algal organic matter (AOM) could be oxidized and lead to the increment in disinfection by-product (DBP) formation. The relationship between pre-oxidation and AOM-derived DBP formation needs to be approached more precisely. This study compared the impact of four pre-oxidants, ozone (O), chlorine dioxide (ClO), potassium permanganate(KMnO) and sodium hypochlorite (NaClO), on the formation of nitrogenous (N-) and carbonaceous (C-) DBPs in AOM chlorination. The characterization (fluorescent properties,molecular weight distribution and amino acids concentration) on AOM samples showed that the characterization properties variations after pre-oxidation were highly dependent on the oxidizing ability of oxidants. The disinfection experiments showed that Oincreased DBP formation most significantly, which was consistent with the result of characterization properties variations. Then canonical correspondent analysis (CCA) and Pearson’s correlation analysis were conducted based on the characterization data and DBP formation. CCA indicated that C-DBPs formation was highly dependent on fluorescent data. The formation of haloacetic acids (HAAs) had a positive correlation with aromatic protein-like component while trichloromethane (TCM) had a positive correlation with fulvic acid-like component.Pearson’s correlation analysis showed that low molecular weight fractions were favorable to form N-DBPs. Therefore, characterization data could provide the advantages in the control of DBP formation, which further revealed that KMnOand ClOwere better options for removing algal cells as well as limiting DBP formation.展开更多
Vacuum ultraviolet(VUV) photolysis is recognized as an environmental-friendly treatment process. Nitrate(NO-3) and natural organic matter(NOM) are widely present in water source.We investigated trichloronitromethane(T...Vacuum ultraviolet(VUV) photolysis is recognized as an environmental-friendly treatment process. Nitrate(NO-3) and natural organic matter(NOM) are widely present in water source.We investigated trichloronitromethane(TCNM) formation during chlorination after VUV photolysis, because TCNM is an unregulated highly toxic disinfection byproduct. In this study:(1) we found reactive nitrogen species that is generated under VUV photolysis of NO-3react with organic matter to form nitrogen-containing compounds and subsequently form TCNM during chlorination;(2) we found the mere presence of 0.1 mmol/L NO-3can result in the formation of up to 63.96 μg/L TCNM;(3) we found the changes in pH(6.0-8.0), chloride(1-4 mmol/L), and bicarbonate(1-4 mmol/L) cannot effectively diminish TCNM formation;and,(4) we established the quantitative structure-activity relationship(QSAR) model,which indicated a linear relationship between TCNM formation and the Hammett constant(σ) of model compounds;and,(5) we characterized TCNM precursors in water matrix after VUV photolysis and found 1161 much more nitrogen-containing compounds with higher aromaticity were generated. Overall, this study indicates more attention should be paid to reducing the formation risk of TCNM when applying VUV photolysis process at scale.展开更多
Lithium–sulfur(Li-S)batteries have been considered as promising candidates for large-scale high energy density devices due to the potentially high energy density,low cost,and more pronounced ecological compatibility....Lithium–sulfur(Li-S)batteries have been considered as promising candidates for large-scale high energy density devices due to the potentially high energy density,low cost,and more pronounced ecological compatibility.However,the complex Li-S conversion reactions,unsatisfactory battery performance,and unsafe metallic Li anode restrict the development of Li-S batteries to achieve commercialization.This review mainly focuses on three aspects which are the remaining challenges,recent advances,and applications in Li-S batteries.Firstly,this review portrays Li-S conversion chemistry involving the multi-step and multi-electron reaction mechanism,as well as the remaining challenges.Then,the scientific strategies and very recent advances of the cathode,electrolyte,lithium anode,and other constituent parts of Li-S batteries are detailly summed up,as well as their advantages and limitations.For the sake of promoting the Li-S batteries practicalization,next section is primarily concerned with problems,the corresponding solutions,and application scenarios of practical pouch cells.Finally,the important findings as guidelines and some future directions as trends for developing emerging Li-S batteries are briefly summarized.展开更多
A low-cost adsorbent modified kaolin clay(MKC) was synthesized and utilized for Cr(VI) removal from aqueous solution. Adsorption experiments were carried out as a function of adsorbent dosage, solution pH, Cr(VI) mass...A low-cost adsorbent modified kaolin clay(MKC) was synthesized and utilized for Cr(VI) removal from aqueous solution. Adsorption experiments were carried out as a function of adsorbent dosage, solution pH, Cr(VI) mass concentration, contact time, electrolyte, and temperature. It is found that the adsorption efficiency is high within a wide pH range of 2.5-11.5, and equilibrium is achieved within 180 min. Increases in temperature and electrolyte concentration decrease the adsorption. The adsorption follows the pseudo-second-order kinetic model. The Langmuir isotherm shows better fit than Freundlich isotherm. The maximum uptake capacities calculated from the Langmuir model are 15.82, 15.55 and 15.22 mg/g at 298, 308 and 318 K, respectively. Thermodynamic parameters reveals the spontaneous and exothermic nature of the adsorption. The FTIR study indicates that hydroxyl groups, NH4+ ions and NO3- ions on MKC surface play a key role in Cr(VI) adsorption. The Cr(VI) desorbability of 86.53% is achieved at a Na2CO3 solution. The results show that MKC is suitable as a low-cost adsorbent for Cr(VI) removal which has higher adsorption capacity and faster adsorption rate at pH close to that where pollutants are usually found in the environment.展开更多
Bisphenol(BP)analogues in wastewater effluent and groundwater pose a potential threat to human health due to their ability to disrupt steroidogenesis.A new solar-assisted electrochemical process(SECP)was developed and...Bisphenol(BP)analogues in wastewater effluent and groundwater pose a potential threat to human health due to their ability to disrupt steroidogenesis.A new solar-assisted electrochemical process(SECP)was developed and evaluated for the degradation of BP analogues.The effects of quenchers,current density,initial pH,supporting electrolyte,and aqueous matrix on the removal kinetics of bisphenol AF(BPAF)and bisphenol A(BPA)were investigated.The kinetic constants of BPAF,BPA,and bisphenol S(BPS)in the SECP with irradiation intensity of 500 mW cm^(-2) were 0.017±0.002 min^(-1),0.022±0.002 min^(-1),and 0.012±0.001 min^(-1),respectively.The changes in the degradation rates of BPAF,BPA,and BPS in the presence of quenchers indicated the relative contribution of hydroxyl radical(·OH)oxidation,anodic electrolysis,and singlet(^(1)O_(2))oxygenation in the degradation of BPs in the SECP.The enhanced rate of generation of ·OH and ^(1)O_(2) was observed in the SECP compared with those in the conventional electrochemical system.The identification of the transformation products(TPs)of BPAF demonstrated that hydroxylation,ring cleavage,b-scission,and defluorination were the major processes during the oxidation in the SECP.The conversion to fluoride ions(76%)and mineralization of total organic carbon(72%)in the SECP indicated further degradation of TPs.The results from this study improved our understanding of the degradation of BP analogues in the electrooxidation irradiated by solar light and help to establish the application potential of the SECP for the effective degradation of emerging contaminants in wastewater.展开更多
基金supported by the National Natural Science Foundation (Nos. 51878257, 52100007)the Natural Science Foundation of Hunan Province (No. 2021JJ40066) and the Natural Science Foundation of Hunan Province (No. 2021JJ40106)。
文摘Pre-oxidation has been reported to be an effective way to remove algal cells in water, but the released algal organic matter (AOM) could be oxidized and lead to the increment in disinfection by-product (DBP) formation. The relationship between pre-oxidation and AOM-derived DBP formation needs to be approached more precisely. This study compared the impact of four pre-oxidants, ozone (O), chlorine dioxide (ClO), potassium permanganate(KMnO) and sodium hypochlorite (NaClO), on the formation of nitrogenous (N-) and carbonaceous (C-) DBPs in AOM chlorination. The characterization (fluorescent properties,molecular weight distribution and amino acids concentration) on AOM samples showed that the characterization properties variations after pre-oxidation were highly dependent on the oxidizing ability of oxidants. The disinfection experiments showed that Oincreased DBP formation most significantly, which was consistent with the result of characterization properties variations. Then canonical correspondent analysis (CCA) and Pearson’s correlation analysis were conducted based on the characterization data and DBP formation. CCA indicated that C-DBPs formation was highly dependent on fluorescent data. The formation of haloacetic acids (HAAs) had a positive correlation with aromatic protein-like component while trichloromethane (TCM) had a positive correlation with fulvic acid-like component.Pearson’s correlation analysis showed that low molecular weight fractions were favorable to form N-DBPs. Therefore, characterization data could provide the advantages in the control of DBP formation, which further revealed that KMnOand ClOwere better options for removing algal cells as well as limiting DBP formation.
基金supported by Natural Science Foundation of Hunan Province (No. 2021JJ40066)National Natural Science Foundation (Nos. 51878257 and 52100007).
文摘Vacuum ultraviolet(VUV) photolysis is recognized as an environmental-friendly treatment process. Nitrate(NO-3) and natural organic matter(NOM) are widely present in water source.We investigated trichloronitromethane(TCNM) formation during chlorination after VUV photolysis, because TCNM is an unregulated highly toxic disinfection byproduct. In this study:(1) we found reactive nitrogen species that is generated under VUV photolysis of NO-3react with organic matter to form nitrogen-containing compounds and subsequently form TCNM during chlorination;(2) we found the mere presence of 0.1 mmol/L NO-3can result in the formation of up to 63.96 μg/L TCNM;(3) we found the changes in pH(6.0-8.0), chloride(1-4 mmol/L), and bicarbonate(1-4 mmol/L) cannot effectively diminish TCNM formation;and,(4) we established the quantitative structure-activity relationship(QSAR) model,which indicated a linear relationship between TCNM formation and the Hammett constant(σ) of model compounds;and,(5) we characterized TCNM precursors in water matrix after VUV photolysis and found 1161 much more nitrogen-containing compounds with higher aromaticity were generated. Overall, this study indicates more attention should be paid to reducing the formation risk of TCNM when applying VUV photolysis process at scale.
基金the Innovation-Driven Project of Central South University(No.2019CX033)the National Natural Science Foundation of China(No.51904344)。
文摘Lithium–sulfur(Li-S)batteries have been considered as promising candidates for large-scale high energy density devices due to the potentially high energy density,low cost,and more pronounced ecological compatibility.However,the complex Li-S conversion reactions,unsatisfactory battery performance,and unsafe metallic Li anode restrict the development of Li-S batteries to achieve commercialization.This review mainly focuses on three aspects which are the remaining challenges,recent advances,and applications in Li-S batteries.Firstly,this review portrays Li-S conversion chemistry involving the multi-step and multi-electron reaction mechanism,as well as the remaining challenges.Then,the scientific strategies and very recent advances of the cathode,electrolyte,lithium anode,and other constituent parts of Li-S batteries are detailly summed up,as well as their advantages and limitations.For the sake of promoting the Li-S batteries practicalization,next section is primarily concerned with problems,the corresponding solutions,and application scenarios of practical pouch cells.Finally,the important findings as guidelines and some future directions as trends for developing emerging Li-S batteries are briefly summarized.
基金Project(2012BAJ24B03)supported by the National Science and Technology Support Program of China
文摘A low-cost adsorbent modified kaolin clay(MKC) was synthesized and utilized for Cr(VI) removal from aqueous solution. Adsorption experiments were carried out as a function of adsorbent dosage, solution pH, Cr(VI) mass concentration, contact time, electrolyte, and temperature. It is found that the adsorption efficiency is high within a wide pH range of 2.5-11.5, and equilibrium is achieved within 180 min. Increases in temperature and electrolyte concentration decrease the adsorption. The adsorption follows the pseudo-second-order kinetic model. The Langmuir isotherm shows better fit than Freundlich isotherm. The maximum uptake capacities calculated from the Langmuir model are 15.82, 15.55 and 15.22 mg/g at 298, 308 and 318 K, respectively. Thermodynamic parameters reveals the spontaneous and exothermic nature of the adsorption. The FTIR study indicates that hydroxyl groups, NH4+ ions and NO3- ions on MKC surface play a key role in Cr(VI) adsorption. The Cr(VI) desorbability of 86.53% is achieved at a Na2CO3 solution. The results show that MKC is suitable as a low-cost adsorbent for Cr(VI) removal which has higher adsorption capacity and faster adsorption rate at pH close to that where pollutants are usually found in the environment.
基金the support from the State Key Laboratory of Urban Water Resource and Environment(QA201926)Youth program of the National Natural Science Foundation of China(51908164)+1 种基金support from the University of Cincinnati through a UNESCO co-Chair Professor position on“Water Access and Sustainability”the Herman Schneider Professorship in the College of Engineering and Applied Sciences.
文摘Bisphenol(BP)analogues in wastewater effluent and groundwater pose a potential threat to human health due to their ability to disrupt steroidogenesis.A new solar-assisted electrochemical process(SECP)was developed and evaluated for the degradation of BP analogues.The effects of quenchers,current density,initial pH,supporting electrolyte,and aqueous matrix on the removal kinetics of bisphenol AF(BPAF)and bisphenol A(BPA)were investigated.The kinetic constants of BPAF,BPA,and bisphenol S(BPS)in the SECP with irradiation intensity of 500 mW cm^(-2) were 0.017±0.002 min^(-1),0.022±0.002 min^(-1),and 0.012±0.001 min^(-1),respectively.The changes in the degradation rates of BPAF,BPA,and BPS in the presence of quenchers indicated the relative contribution of hydroxyl radical(·OH)oxidation,anodic electrolysis,and singlet(^(1)O_(2))oxygenation in the degradation of BPs in the SECP.The enhanced rate of generation of ·OH and ^(1)O_(2) was observed in the SECP compared with those in the conventional electrochemical system.The identification of the transformation products(TPs)of BPAF demonstrated that hydroxylation,ring cleavage,b-scission,and defluorination were the major processes during the oxidation in the SECP.The conversion to fluoride ions(76%)and mineralization of total organic carbon(72%)in the SECP indicated further degradation of TPs.The results from this study improved our understanding of the degradation of BP analogues in the electrooxidation irradiated by solar light and help to establish the application potential of the SECP for the effective degradation of emerging contaminants in wastewater.
