A homemade array surface plasmon resonance （SPR）-based imaging biosensor was used to develop sensitive and fast immunoassays to determine sulfamethoxazole （SMOZ） and sulfamethazine （SMT） in buffer. Two conjugati...A homemade array surface plasmon resonance （SPR）-based imaging biosensor was used to develop sensitive and fast immunoassays to determine sulfamethoxazole （SMOZ） and sulfamethazine （SMT） in buffer. Two conjugations of sulfonamide-bovine serum albumin （BSA） were separately immobilized on two different rows of the array chip with one row as reference. The immobilization was carried out in the instrument to monitor the quantity of the conjugations immobilized. The antibody mixed with the sulfonamide in the buffer was injected over the surface of the chip to get a relative response which was inversely proportional to the concentration of the sulfonamide in the PBS buffer. Two calibration curves were constructed and the limit of detection for sufamethoxazole in buffer was 3.5 ng/mL and for sulfamethazine 0.6 ng/mL. The stability and specificity of the antibody were also studied. The monoclonal antibody did not bind with BSA.展开更多
This study surveyed 180 samples of ultra high temperature （UHT） milk of four top Chinese dairy brands collected in the 25 cities in China in June 2011, and assessed their contamination with antibiotics, using the EL...This study surveyed 180 samples of ultra high temperature （UHT） milk of four top Chinese dairy brands collected in the 25 cities in China in June 2011, and assessed their contamination with antibiotics, using the ELISA method. The percentages of tetracyclines, sulfonamides, sulfamethazine, and quinolones detected in the samples were 0, 16.7, 40.6, and 100%, respectively. The maximum concentrations of the tetracyclines, sulfonamides, sulfamethazine and quinolones in UHT milk samples were 〈1.5, 26.2, 22.6, and 58.8 μg kg-1, respectively. None of the samples exceeded the maximum residue levels （MRLs） for these four veterinary drugs, according to the regulations set by China, the European Union （EU） and the Codex Alimentarius Commission （CAC）.展开更多
Intensive use of sulfamethazine(SM_2) in aquaculture has resulted in some detrimental effects to non-targeted organisms. In order to assess its potential ecological risk, it is crucial to have a good understanding on ...Intensive use of sulfamethazine(SM_2) in aquaculture has resulted in some detrimental effects to non-targeted organisms. In order to assess its potential ecological risk, it is crucial to have a good understanding on the bioaccumulation and biodegradation of SM_2 in Chlorella pyrenoidosa. The microalgae were treated with 2, 4, and 8 mg L^(-1) of sulfamethazine for 13 days, respectively, showing that the inhibition effects of sulfamethazine on the growth of Chlorella pyrenoidosa increased progressively as the concentrations of sulfamethazine increasing from 2 to 8 mg L^(-1). The peak concentrations of sulfamethazine accumulated in C. pyrenoidosa were 0.225, 0.325, and 0.596 ng per mg FW on day 13 for three treatment groups, respectively, showing a great ability to deplete sulfamethazine from the culture media. On day 13, the percentages of biotic degradation were 48.45%, 60.21% and 69.93%, respectively. The EC_(50) of 10.05 mg L^(-1) was derived which showed no significant risk for C. pyrenoidosa with a calculated risk quotient < 1. The activities of superoxide dismutase and catalase increased progressively in response to sulfamethazine and showed a positive correlation to the treatment concentrations. The highest superoxide dismutase activity was achieved at the concentration of 8 mg L^(-1) after 2 d of exposure, which was 1.89 folds higher than that of the control. The activity of catalase has a similar pattern to that of superoxide dismutase with the maximum activity achieved at day 2, which was 3.11 folds higher compared to that of the control. In contrast to superoxide dismutase and catalase, the maximum glutathione S-transferase activity was observed at day 6, showing 2.2 folds higher than that of the control.展开更多
In the present study,zinc molybdate(β‐ZnMoO4)and graphitic carbon nitride(g‐C3N4)‐modifiedβ‐ZnMoO4(β‐ZnMoO4/g‐C3N4)were prepared to decontaminate aqueous solutions from the antibiotic sulfamethazine(SMZ).Our ...In the present study,zinc molybdate(β‐ZnMoO4)and graphitic carbon nitride(g‐C3N4)‐modifiedβ‐ZnMoO4(β‐ZnMoO4/g‐C3N4)were prepared to decontaminate aqueous solutions from the antibiotic sulfamethazine(SMZ).Our results revealed that the hydrothermal synthesis method greatly influenced the photocatalytic activity of the resultant catalysts.The pristineβ‐ZnMoO4samples obtained under more intensive synthesis conditions(24h at280°C)showed higher photocatalytic activity than that prepared for12h at180°C(denotedβ‐ZnMoO4‐180).In the case of in situ hydrothermal synthesis ofβ‐ZnMoO4/g‐C3N4,a surface‐modified sample was only obtained under the reaction conditions of180°C for12h.Compared with the sheet‐likeβ‐ZnMoO4‐180sample,theβ‐ZnMoO4‐180/g‐C3N4composite showed enhanced photocatalytic activity for the degradation of SMZ.By contrast,the hydrothermal reaction at280°C caused the gradual decomposition of g‐C3N4.It is believed that the structural incorporation of g‐C3N4intoβ‐ZnMoO4at280°C might disrupt the crystal growth,thereby deteriorating the performance of the composite catalysts formed at this temperature.For the composite catalysts prepared by the ultrasonic method,a remarkable increase in the degradation rate of SMZ was only observed at a high g‐C3N4content of8mol%.The photocatalytic degradation of SMZ byβ‐ZnMoO4‐180/g‐C3N4composite catalysts followed pseudo‐first‐order kinetics.Further study of the photocatalytic mechanism revealed that holes and superoxide radicals were the dominant oxidative species in the photodegradation process.The enhanced photocatalytic performance of the composites was attributed to the higher separation efficiency of the photogenerated electron‐hole pairs at heterogeneous junctions.The degradation intermediates of SMZ were detected by liquid chromatography‐mass spectrometry,from which plausible reaction pathways for the photodegradation of SMZ were proposed.Our results indicated that the synthesis method for g‐C3N4composites should be carefully selected to achieve superior photocatalytic performance.展开更多
Two artificial antigens were synthesized successfully by diazotizing method, sulfamethazine（SM2）-human serum albumin （HSA） was used for the immunogen, and SM2-ovalbumin（OVA） was used for the coating antigen. The...Two artificial antigens were synthesized successfully by diazotizing method, sulfamethazine（SM2）-human serum albumin （HSA） was used for the immunogen, and SM2-ovalbumin（OVA） was used for the coating antigen. The coupled reaction was successful by confirmation of the ultraviolet scanning spectrometer, and the conjugation ratio of SM2 with HSA and OVA was 9：1 and 15：1, respectively. Using cell-fusion and limiting dilution method to reclone 5 times to get 3 hybridoma strains, which could stably secret monoclonal antibody （Mab）, named CBT, BC4 and BB12. The subtype of BC4 Mab was IgG1 and chain, the molecular weight was 162 ku, the numbers of chromosomal were about 90, the affinity constant was 6.1 × 10^12 M^-1. No cross reactivity was seen between the Mab and the other 4 sulfonamides, as well as the 2 carries proteins. The Mab antibody had excellent stability.展开更多
Sorption mechanisms of sulfamethazine(SMT)in different pH solutions are complicated.It has not been sufficiently investigated to enhance removal of SMT from alkalescent aqueous solution.In this study,sorption isotherm...Sorption mechanisms of sulfamethazine(SMT)in different pH solutions are complicated.It has not been sufficiently investigated to enhance removal of SMT from alkalescent aqueous solution.In this study,sorption isotherms and kinetics of SMT by corn biochars pyrolyzed at 300℃ and 600℃(300C,600C)under diverse pH conditions were compared.In order to improve the sorption efficiency of SMT from alkalescent aqueous solution,the biochar 300C was modified by acid or base.Different mathematic models were used to describe sorption driving force and sorption process.Results showed that the biochar 300C possessed more amorphous organic carbon and polar functional groups,which led to a higher sorption capacity than biochar 600C.The sorption rate of biochar 300C was greater than 600C under diverse pH as the physisorption of 300C outweighed 600C.The SMT presented stronger hydrophobicity at pH 5 and higher electrostatic repulsion at pH 1 or 8,which resulted in a higher combining capacity of SMT with both biochars at pH 5 than other pH values.In addition,the acid modified biochar had better removal effect on SMT than alkali at pH solution around 8.The research provides a theoretical basis for the removal of SMT from alkalescent aqueous solution.展开更多
In this study, various factors of ELISA for detection of sulfamethazine residues were explored, the coating antigen was diluted to 1：400, the best coating condition was at 4℃ overnight, the working concentration of ...In this study, various factors of ELISA for detection of sulfamethazine residues were explored, the coating antigen was diluted to 1：400, the best coating condition was at 4℃ overnight, the working concentration of HRP-IgG enzyme conjugate was 1 ： 7 000. The pre-incubation time and incubation time was 30 min and 120 min, respectively, the substrate solution working time was 20 min. Two moL · L^-1 H2SO4 was used to stop the reaction and checked. A standard curve of direct competitive ELISA had been established to detect the sulfamethazine residues in milk. The detection limit of this method was 1.97 ng · mL^-1. The mean concentration of sulfamethazine required to inhibit 30% antibody was 7.1 ng · mL^-1. The linear range of the detection was 5-200 ng · mL^-1. The recovery ratio was between 73.20% and 91.16%. The CV% of within array and between arrays was less than 10%.展开更多
In this work,boron(B)was used to promote Fe^(3+)/peracetic acid(Fe^(3+)/PAA)for the degradation of sulfamethazine(SMT).An SMT degradation efficiency of 9.1%was observed in the Fe^(3+)/PAA system over 60 min,which was ...In this work,boron(B)was used to promote Fe^(3+)/peracetic acid(Fe^(3+)/PAA)for the degradation of sulfamethazine(SMT).An SMT degradation efficiency of 9.1%was observed in the Fe^(3+)/PAA system over 60 min,which was significantly increased to 99.3%in the B/Fe^(3+)/PAA system over 10 min.The B/Fe^(3+)/PAA process also exhibited superior resistance to natural substances,excellent adaptability to different harmful substances,and good removal of antibiotics in natural fresh water samples.The mechanism of action of boron for Fe^(3+)reduction was determined using scanning electron microscopy(SEM),X-ray photoelectron spectroscopy(XPS),Fourier transform infrared(FT-IR)spectroscopy,density functional theory(DFT)calculations,and electrochemical tests.The dominant role of^(·)OH was confirmed using quenching experiments,electron spin resonance(EPR)spectroscopy,and quantitative tests.Organic radicals(R-O^(·))and Fe(IV)also significantly contribute to the removal of SMT.DFT calculations on the reaction between Fe^(2+)and the PAA were conducted to further determine the contribution from ^(·)OH,R-O^(·),and Fe(IV)from the perspective of thermodynamics and the reaction pathways.Different boron dosages,Fe^(3+)dosages,and initial pH values were also investigated in the B/Fe^(3+)/PAA system to study their effect of SMT removal and the production of the reactive species.Fe(IV)production determined the k_(R-O·+Fe(IV))value suggesting that Fe(IV)may play a more important role than R-O^(·).A comparison of the results with other processes has also proved that the procedure described in this study(B/Fe^(3+)/PAA)is an effective method for the degradation of antibiotics.展开更多
The S-scheme heterojunction has garnered increasing attention due to its remarkable oxidation capacity and efficient separation of photogenerated carriers.In this study,a one-pot glycerol-assisted hydrothermal process...The S-scheme heterojunction has garnered increasing attention due to its remarkable oxidation capacity and efficient separation of photogenerated carriers.In this study,a one-pot glycerol-assisted hydrothermal process was utilized to successfully synthesize S-scheme heterojunction photocatalysts comprising basic bismuth nitrate(BBN)and bismuth tungstate(BWO).Interestingly,the BBN/BWO heterogeneous photo-catalysts exhibited the highest photocatalytic properties.The optimized product achieved the degradation of sulfamethazine(SMZ)within 1 h,with a kinetic constant(k)value of 0.05818 min^(−1).The degradation process was influenced significantly by·O^(2)−and h^(+)species.To determine the degradation pathway of SMZ in the presence of BBN/BWO-0.6,liquid chromatography-mass spectrometry(LC-MS)analysis was performed,which revealed a decrease in the toxicity of intermediates and products.The enhanced pho-tocatalytic activity can be attributed to the internal electric field(IEF)of the S-scheme heterojunction between BBN and BWO,effectively promoting the separation of photogenerated carriers.This research presents a viable approach for developing S-scheme heterojunctions in SMZ photodegradation and other environmental applications.展开更多
基金The authors greatly acknowledge the financial support from the National Natural Science Foundation of China(No.60027001 and 60302003)the National High Technology Research and Development program of China(No.20060100Z3044).
文摘A homemade array surface plasmon resonance （SPR）-based imaging biosensor was used to develop sensitive and fast immunoassays to determine sulfamethoxazole （SMOZ） and sulfamethazine （SMT） in buffer. Two conjugations of sulfonamide-bovine serum albumin （BSA） were separately immobilized on two different rows of the array chip with one row as reference. The immobilization was carried out in the instrument to monitor the quantity of the conjugations immobilized. The antibody mixed with the sulfonamide in the buffer was injected over the surface of the chip to get a relative response which was inversely proportional to the concentration of the sulfonamide in the PBS buffer. Two calibration curves were constructed and the limit of detection for sufamethoxazole in buffer was 3.5 ng/mL and for sulfamethazine 0.6 ng/mL. The stability and specificity of the antibody were also studied. The monoclonal antibody did not bind with BSA.
基金funded by the Ministry of Agriculture of China (2013-Z10)Chinese Academy of Agricultural Sciences (2012ZL071)Institute of Animal Science, Chinese Academy of Agricultural Sciences (2013ywf-yb-4)
文摘This study surveyed 180 samples of ultra high temperature （UHT） milk of four top Chinese dairy brands collected in the 25 cities in China in June 2011, and assessed their contamination with antibiotics, using the ELISA method. The percentages of tetracyclines, sulfonamides, sulfamethazine, and quinolones detected in the samples were 0, 16.7, 40.6, and 100%, respectively. The maximum concentrations of the tetracyclines, sulfonamides, sulfamethazine and quinolones in UHT milk samples were 〈1.5, 26.2, 22.6, and 58.8 μg kg-1, respectively. None of the samples exceeded the maximum residue levels （MRLs） for these four veterinary drugs, according to the regulations set by China, the European Union （EU） and the Codex Alimentarius Commission （CAC）.
基金supported by the earmarked fund for the Modern Agro-Industry Technology Research System (CARS-47)the Program of Shandong Leading Talent (No.LJNY2015002)the AoShan Scientific and Technological Innovation Project which was financially backed by Qingdao National Laboratory for Marine Science and Technology (No.2015ASKJ02)
文摘Intensive use of sulfamethazine(SM_2) in aquaculture has resulted in some detrimental effects to non-targeted organisms. In order to assess its potential ecological risk, it is crucial to have a good understanding on the bioaccumulation and biodegradation of SM_2 in Chlorella pyrenoidosa. The microalgae were treated with 2, 4, and 8 mg L^(-1) of sulfamethazine for 13 days, respectively, showing that the inhibition effects of sulfamethazine on the growth of Chlorella pyrenoidosa increased progressively as the concentrations of sulfamethazine increasing from 2 to 8 mg L^(-1). The peak concentrations of sulfamethazine accumulated in C. pyrenoidosa were 0.225, 0.325, and 0.596 ng per mg FW on day 13 for three treatment groups, respectively, showing a great ability to deplete sulfamethazine from the culture media. On day 13, the percentages of biotic degradation were 48.45%, 60.21% and 69.93%, respectively. The EC_(50) of 10.05 mg L^(-1) was derived which showed no significant risk for C. pyrenoidosa with a calculated risk quotient < 1. The activities of superoxide dismutase and catalase increased progressively in response to sulfamethazine and showed a positive correlation to the treatment concentrations. The highest superoxide dismutase activity was achieved at the concentration of 8 mg L^(-1) after 2 d of exposure, which was 1.89 folds higher than that of the control. The activity of catalase has a similar pattern to that of superoxide dismutase with the maximum activity achieved at day 2, which was 3.11 folds higher compared to that of the control. In contrast to superoxide dismutase and catalase, the maximum glutathione S-transferase activity was observed at day 6, showing 2.2 folds higher than that of the control.
基金supported by the National Natural Science Foundation of China(51778505)the grants from Hubei Province of China(Special Grant for Technological Innovation(2016ACA162)the Natural Science Foundation,2015CFA017)~~
文摘In the present study,zinc molybdate(β‐ZnMoO4)and graphitic carbon nitride(g‐C3N4)‐modifiedβ‐ZnMoO4(β‐ZnMoO4/g‐C3N4)were prepared to decontaminate aqueous solutions from the antibiotic sulfamethazine(SMZ).Our results revealed that the hydrothermal synthesis method greatly influenced the photocatalytic activity of the resultant catalysts.The pristineβ‐ZnMoO4samples obtained under more intensive synthesis conditions(24h at280°C)showed higher photocatalytic activity than that prepared for12h at180°C(denotedβ‐ZnMoO4‐180).In the case of in situ hydrothermal synthesis ofβ‐ZnMoO4/g‐C3N4,a surface‐modified sample was only obtained under the reaction conditions of180°C for12h.Compared with the sheet‐likeβ‐ZnMoO4‐180sample,theβ‐ZnMoO4‐180/g‐C3N4composite showed enhanced photocatalytic activity for the degradation of SMZ.By contrast,the hydrothermal reaction at280°C caused the gradual decomposition of g‐C3N4.It is believed that the structural incorporation of g‐C3N4intoβ‐ZnMoO4at280°C might disrupt the crystal growth,thereby deteriorating the performance of the composite catalysts formed at this temperature.For the composite catalysts prepared by the ultrasonic method,a remarkable increase in the degradation rate of SMZ was only observed at a high g‐C3N4content of8mol%.The photocatalytic degradation of SMZ byβ‐ZnMoO4‐180/g‐C3N4composite catalysts followed pseudo‐first‐order kinetics.Further study of the photocatalytic mechanism revealed that holes and superoxide radicals were the dominant oxidative species in the photodegradation process.The enhanced photocatalytic performance of the composites was attributed to the higher separation efficiency of the photogenerated electron‐hole pairs at heterogeneous junctions.The degradation intermediates of SMZ were detected by liquid chromatography‐mass spectrometry,from which plausible reaction pathways for the photodegradation of SMZ were proposed.Our results indicated that the synthesis method for g‐C3N4composites should be carefully selected to achieve superior photocatalytic performance.
文摘Two artificial antigens were synthesized successfully by diazotizing method, sulfamethazine（SM2）-human serum albumin （HSA） was used for the immunogen, and SM2-ovalbumin（OVA） was used for the coating antigen. The coupled reaction was successful by confirmation of the ultraviolet scanning spectrometer, and the conjugation ratio of SM2 with HSA and OVA was 9：1 and 15：1, respectively. Using cell-fusion and limiting dilution method to reclone 5 times to get 3 hybridoma strains, which could stably secret monoclonal antibody （Mab）, named CBT, BC4 and BB12. The subtype of BC4 Mab was IgG1 and chain, the molecular weight was 162 ku, the numbers of chromosomal were about 90, the affinity constant was 6.1 × 10^12 M^-1. No cross reactivity was seen between the Mab and the other 4 sulfonamides, as well as the 2 carries proteins. The Mab antibody had excellent stability.
基金Funds for the Central Universities of China(No.201964004)the National Natural Science Foundation of China(No.41977315).
文摘Sorption mechanisms of sulfamethazine(SMT)in different pH solutions are complicated.It has not been sufficiently investigated to enhance removal of SMT from alkalescent aqueous solution.In this study,sorption isotherms and kinetics of SMT by corn biochars pyrolyzed at 300℃ and 600℃(300C,600C)under diverse pH conditions were compared.In order to improve the sorption efficiency of SMT from alkalescent aqueous solution,the biochar 300C was modified by acid or base.Different mathematic models were used to describe sorption driving force and sorption process.Results showed that the biochar 300C possessed more amorphous organic carbon and polar functional groups,which led to a higher sorption capacity than biochar 600C.The sorption rate of biochar 300C was greater than 600C under diverse pH as the physisorption of 300C outweighed 600C.The SMT presented stronger hydrophobicity at pH 5 and higher electrostatic repulsion at pH 1 or 8,which resulted in a higher combining capacity of SMT with both biochars at pH 5 than other pH values.In addition,the acid modified biochar had better removal effect on SMT than alkali at pH solution around 8.The research provides a theoretical basis for the removal of SMT from alkalescent aqueous solution.
基金Supported by Key Items of National Technology Research Project(2002BA518A06)Heilongjiang Provincial Science and Technology Tackle Key Problem Project(10541021)Harbin Technical Fund(2003AA6CN179)
文摘In this study, various factors of ELISA for detection of sulfamethazine residues were explored, the coating antigen was diluted to 1：400, the best coating condition was at 4℃ overnight, the working concentration of HRP-IgG enzyme conjugate was 1 ： 7 000. The pre-incubation time and incubation time was 30 min and 120 min, respectively, the substrate solution working time was 20 min. Two moL · L^-1 H2SO4 was used to stop the reaction and checked. A standard curve of direct competitive ELISA had been established to detect the sulfamethazine residues in milk. The detection limit of this method was 1.97 ng · mL^-1. The mean concentration of sulfamethazine required to inhibit 30% antibody was 7.1 ng · mL^-1. The linear range of the detection was 5-200 ng · mL^-1. The recovery ratio was between 73.20% and 91.16%. The CV% of within array and between arrays was less than 10%.
基金supported by the Natural Science Foundation of Jiangsu Province in China (No.BK20210952)the Jiangsu Provincial Key Laboratory of Environmental Engineering (No.ZX2022002)+2 种基金the National Natural Science Foundation of China (Nos.52200095,22176102,and 21806081)the China Postdoctoral Science Foundation Project (No.2020M681552)the Natural Science Foundation of Tianjin (No.19JCQNJC07900)。
文摘In this work,boron(B)was used to promote Fe^(3+)/peracetic acid(Fe^(3+)/PAA)for the degradation of sulfamethazine(SMT).An SMT degradation efficiency of 9.1%was observed in the Fe^(3+)/PAA system over 60 min,which was significantly increased to 99.3%in the B/Fe^(3+)/PAA system over 10 min.The B/Fe^(3+)/PAA process also exhibited superior resistance to natural substances,excellent adaptability to different harmful substances,and good removal of antibiotics in natural fresh water samples.The mechanism of action of boron for Fe^(3+)reduction was determined using scanning electron microscopy(SEM),X-ray photoelectron spectroscopy(XPS),Fourier transform infrared(FT-IR)spectroscopy,density functional theory(DFT)calculations,and electrochemical tests.The dominant role of^(·)OH was confirmed using quenching experiments,electron spin resonance(EPR)spectroscopy,and quantitative tests.Organic radicals(R-O^(·))and Fe(IV)also significantly contribute to the removal of SMT.DFT calculations on the reaction between Fe^(2+)and the PAA were conducted to further determine the contribution from ^(·)OH,R-O^(·),and Fe(IV)from the perspective of thermodynamics and the reaction pathways.Different boron dosages,Fe^(3+)dosages,and initial pH values were also investigated in the B/Fe^(3+)/PAA system to study their effect of SMT removal and the production of the reactive species.Fe(IV)production determined the k_(R-O·+Fe(IV))value suggesting that Fe(IV)may play a more important role than R-O^(·).A comparison of the results with other processes has also proved that the procedure described in this study(B/Fe^(3+)/PAA)is an effective method for the degradation of antibiotics.
基金supported by the National Natural Science Foundation of China(No.22278245)the Young Taishan Scholars Program of Shandong Province(No.tsqn.201909026)+1 种基金the Youth Interdisciplinary Science and Innovative Research Groups of Shandong University supported by the Fundamental Research Funds for the Central Universities(No.2020QNQT014)the Shandong University Future Youth Grant Program(No.61440089964189).
文摘The S-scheme heterojunction has garnered increasing attention due to its remarkable oxidation capacity and efficient separation of photogenerated carriers.In this study,a one-pot glycerol-assisted hydrothermal process was utilized to successfully synthesize S-scheme heterojunction photocatalysts comprising basic bismuth nitrate(BBN)and bismuth tungstate(BWO).Interestingly,the BBN/BWO heterogeneous photo-catalysts exhibited the highest photocatalytic properties.The optimized product achieved the degradation of sulfamethazine(SMZ)within 1 h,with a kinetic constant(k)value of 0.05818 min^(−1).The degradation process was influenced significantly by·O^(2)−and h^(+)species.To determine the degradation pathway of SMZ in the presence of BBN/BWO-0.6,liquid chromatography-mass spectrometry(LC-MS)analysis was performed,which revealed a decrease in the toxicity of intermediates and products.The enhanced pho-tocatalytic activity can be attributed to the internal electric field(IEF)of the S-scheme heterojunction between BBN and BWO,effectively promoting the separation of photogenerated carriers.This research presents a viable approach for developing S-scheme heterojunctions in SMZ photodegradation and other environmental applications.
