The title compounds, C7H4I2O2 1 and C13H7I2N2O3 2, have been synthesized and characterized by single-crystal X-ray diffraction. Compound 1 crystallizes in monoclinic, space group P21/c with a = 9.802（2）, b = 13.867...The title compounds, C7H4I2O2 1 and C13H7I2N2O3 2, have been synthesized and characterized by single-crystal X-ray diffraction. Compound 1 crystallizes in monoclinic, space group P21/c with a = 9.802（2）, b = 13.867（3）, c = 7.364（2） A, β = 109.74（3）°, V= 942.1（3） A^3, Dc= 2.636 g/cm^3, C7H4I2O2, Mr= 373.90, F（000） = 672, μ = 6.627 mm^-1, Z = 4, R = 0.0459 and wR = 0.1018 for 1805 observed reflections （I 〉 2 σ（I））. Compound 2 belongs to the monoclinic system, space group P21/n with a = 9.015（2）, b = 12.024（2）, c = 14.072（3） A, β = 103.91（3）°, V = 1480.6（5） A^3, Dc= 2.216 g/cm^3, C13H7I2N2O3, Mr= 494.01, F（000） = 920, p = 4.255 mm^-1, Z = 4, R = 0.0777 and wR = 0.1757 for 2896 observed reflections （I 〉 2σ（I））. Compounds 1 and 2 were assayed for antibacterial activities against three Gram positive bacterial strains （B. subtilis, S. aureus and S. faecalis） and three Gram negative bacterial strains （E. coli, P. aeruginosa and E. cloacae） by MTr method. Fortunately, compound 2 is found to show potent antibacterial activity against these six bacterial strains.展开更多
Wastewater with high NH_4^+-N is difficult to treat by traditional methods.So in this paper,a wild strain of photosynthetic bacteria was used for high NH_4^+-N wastewater treatment together with biomass recovery.Isola...Wastewater with high NH_4^+-N is difficult to treat by traditional methods.So in this paper,a wild strain of photosynthetic bacteria was used for high NH_4^+-N wastewater treatment together with biomass recovery.Isolation,identification,and characterization of the microorganism were carried out.The strain was inoculated to the biological wastewater treatment unit.The impacts of important factors were examined,including temperature,dissolved oxygen,and light intensity.Results showed that photosynthetic bacteria could effectively treat high NH_4^+-N wastewater.For wastewater with NH_4^+-N of 2300 mg·L^(-1),COD/N=1.0,98.3%of COD was removed,and cell concentration increased by 43 times.The optimal conditions for the strain's cell growth and wastewater treatment were 30℃,dissolved oxygen of 0.5-1.5 mg·L^(-1) and a light intensity of 4000 lx.Photosynthetic bacteria could bear a lower C/N ratio than bacteria in a traditional wastewater treatment process,but the NH_4^+-N removal was only 20%-40%because small molecule carbon source was used prior to NH_4^+-N.Also,the use of photosynthetic bacteria in chicken manure wastewater containing NH4+-N about 7000 mg·L^(-1) proved that photosynthetic bacteria could remove NH_4^+-N in a real case,finally,83.2%of NH_4^+-N was removed and 66.3%of COD was removed.展开更多
The treatment of domestic and industrial wastewater is one of the major sources of CH_4 in the Chinese waste sector. On the basis of statistical data and country-specific emission factors, using IPCC methodology, the ...The treatment of domestic and industrial wastewater is one of the major sources of CH_4 in the Chinese waste sector. On the basis of statistical data and country-specific emission factors, using IPCC methodology, the characteristics of CH_4 emissions from wastewater treatment in China were analyzed. The driving factors of CH_4 emissions were studied, and the emission trend and reduction potential were predicted and analyzed according to the current situation. Results show that in 2010, CH_4 emissions from the treatment of domestic and industrial wastewater were0.6110 Mt and 1.6237 Mt, respectively. Eight major industries account for more than 92% of emissions, and CH_4 emissions gradually increased from 2005 to 2010. From the controlling management scenario, we predict that in 2020, CH_4 emissions from the treatment of domestic and industrial wastewater will be 1.0136 Mt and 2.3393 Mt, respectively, and the reduction potential will be 0.0763 Mt and 0.2599 Mt, respectively.From 2010 to 2020, CH_4 emissions from the treatment of domestic and industrial wastewater will increase by 66% and 44%, respectively.展开更多
In this work, a coking wastewater was selected and a biochemical Az/O treatment device for fractional degradation was designed and employed. After each stage of the treatment, the products were analyzed through gas ch...In this work, a coking wastewater was selected and a biochemical Az/O treatment device for fractional degradation was designed and employed. After each stage of the treatment, the products were analyzed through gas chromatography-mass spectroscopy （GC-MS） to determine their composition. Finally, AgNO3 ＋ K2FeO4 was used as an advanced deep catalytic oxidation treatment. It was concluded from the analysis that cyclic organics could be degraded and the chemical oxygen demand （COD） was controlled within 50 mg. L-1, in line with the target value, Meanwhile, the spectra obtained from the GC-MS were in accordance with the conclusions reached based on the COD. The research results showed that all hard-degradable organics in coking wastewater could be eliminated through the A2/O bio-membrane treatment and the advanced treatment of making use of K2FeO4 as an oxidant and Ag＋ as a catalyst, the catalytic efficiency with Ag＋ as a catalyst of K2FeO4 was very high. Ag＋ could evidently improve the oxidation capacity of K2FeO4 to wastewater in its short stability time, and this is an important innovation.展开更多
In this study,a single dielectric barrier discharge(DBD)coaxial reactor was used to degrade 4,4'-sulfonylbis(TBBPS)in water using greenhouse gas(CO_(2))and argon as the carrier gases.The investigation focused on C...In this study,a single dielectric barrier discharge(DBD)coaxial reactor was used to degrade 4,4'-sulfonylbis(TBBPS)in water using greenhouse gas(CO_(2))and argon as the carrier gases.The investigation focused on CO_(2)conversion,reactive species formation,gas-liquid mass transfer mechanism,and degradation mechanism of TBBPS during the discharge plasma process.With the decrease of CO_(2)/Ar ratio in the process of plasma discharge,the emission spectrum intensity of Ar,CO_(2)and excited reactive species was enhanced.This increase promoted collision and dissociation of CO_(2),resulting in a series of chemical reactions that improved the production of reactive species such as·OH,^(1)O_(2),H_(2)O_(2)and O_(3).These reactive species initiated a sequence of reactions with TBBPS.Results indicated that at a gas flow rate of 240 mL/min with a CO_(2)/Ar ratio of 1:5,both the highest CO_(2)conversion rate(17.76%)and TBBPS degradation rate(94.24%)were achieved.The degradation mechanism was elucidated by determining types and contents of reactive species present in treatment liquid along with analysis of intermediate products using liquid chromatography-mass spectrometry techniques.This research provides novel insights into carbon dioxide utilization and water pollution control through dielectric barrier discharge plasma technology.展开更多
With the application of resins in various fields, numerous waste resins that are difficult to treat have been produced. The industrial wastewater containing Cr(Ⅵ) has severely polluted soil and groundwater environmen...With the application of resins in various fields, numerous waste resins that are difficult to treat have been produced. The industrial wastewater containing Cr(Ⅵ) has severely polluted soil and groundwater environments, thereby endangering human health. Therefore, in this paper, a novel functionalized mesoporous adsorbent PPR-Z was synthesized from waste amidoxime resin for adsorbing Cr(Ⅵ). The waste amidoxime resin was first modified with H3PO4 and ZnCl_(2), and subsequently, it was carbonized through slow thermal decomposition. The static adsorption of PPR-Z conforms to the pseudo-second-order kinetic model and Langmuir isotherm, indicating that the Cr(Ⅵ) adsorption by PPR-Z is mostly chemical adsorption and exhibits single-layer adsorption. The saturated adsorption capacity of the adsorbent for Cr(Ⅵ) could reach 255.86 mg/g. The adsorbent could effectively reduce Cr(Ⅵ) to Cr(Ⅲ) and decrease the toxicity of Cr(Ⅵ) during adsorption. PPR-Z exhibited Cr(Ⅵ) selectivity in electroplating wastewater. The main mechanisms involved in the Cr(Ⅵ) adsorption are the chemical reduction of Cr(Ⅵ) into Cr(Ⅲ) and electrostatic and coordination interactions. Preparation of PPR-Z not only solves the problem of waste resin treatment but also effectively controls Cr(Ⅵ) pollution and realizes the concept of “treating waste with waste”.展开更多
The Ru3(CO)12/PEDPA complex was firstly applied in the CO selective reduction of 4-propylthio-2-mitroaniline. The effects of reaction temperature, the pressure of CO and concentration of catalyst on the reduction were...The Ru3(CO)12/PEDPA complex was firstly applied in the CO selective reduction of 4-propylthio-2-mitroaniline. The effects of reaction temperature, the pressure of CO and concentration of catalyst on the reduction were investigated. Under the optimum conditions of T=140℃, Pco=5.0MPa and substrate/catalyst = 300 (molar ratio), the conversion and selectivity were 70% and 98%, respectively. After simple phase separation, the catalyst could be recycled.展开更多
[Objective] The aim was to research Chlorella properties in removing ni- trogen and phosphorus from wastewater. [Method] The effects of initial NH4＋-N and total P concentrations, N-to-P ratios, lightJdarkness ratios ...[Objective] The aim was to research Chlorella properties in removing ni- trogen and phosphorus from wastewater. [Method] The effects of initial NH4＋-N and total P concentrations, N-to-P ratios, lightJdarkness ratios and pH on the removal of NH4＋-N and total P were evaluated. [Result] The results showed that Chlorella al- most removed NH4＋-N and total P at 100% as initial concentrations of NH4＋-N and total P were no more than 55 and 7 mg/L, respectively, whereas the removal ratio of NH4＋-N decreased to 90% with initial NH4＋-N concentration coming up to 75 mg/L. With N-to-P ratios of 5：1, 10：1 and 25：1, Chlorella completely removed NH4＋-N within 4 d, while the removal ratio of total P reached almost 100% within 7 d, with different N-to-P ratios. With L./D ratios of 24 h： 0 h and 12 h： 12 h as well as the initial concentrations of NH4＋-N at 30 mg/L and total P at 7 mg/L, the removing ra- tio of NH4＋-N and total P almost achieved 100% by Chlorella, and the removing ra- tio under L/D ratio of 24 h：0 h proved much faster. The optimal pH range for Chlorella to remove NH4＋-N and total P was 7-8. [Conclusion] The research pro- vides references for wastewater treatment in biological way and highly-efficient and environment-friendly treatment in future.展开更多
Water pollution caused by highly toxic Cd(II), Pb(II), and Cr(VI) is a serious problem. In the present work,a green and low-cost adsorbent of g-C_3N_4 nanosheets was developed with superior capacity for both cationic ...Water pollution caused by highly toxic Cd(II), Pb(II), and Cr(VI) is a serious problem. In the present work,a green and low-cost adsorbent of g-C_3N_4 nanosheets was developed with superior capacity for both cationic and anionic heavy metals. The adsorbent was easily fabricated through one-step calcination of guanidine hydrochloride with thickness less than 1.6 nm and specific surface area of 111.2 m^2·g^(-1). Kinetic and isotherm studies suggest that the adsorption is an endothermic chemisorption process, occurring on the energetically heterogeneous surface based on a hybrid mechanism of multilayer and monolayer adsorption. The tri-s-triazine units and surface N-containing groups of g-C_3N_4 nanosheets are proposed to be responsible for the adsorption process.Further study on pH demonstrates that electrostatic interaction plays an important role. The maximum adsorption capacity of Cd(II), Pb(II), and Cr(VI) on g-C_3N_4 nanosheets is 123.205 mg·g^(-1), 136.571 mg·g^(-1),and 684.451 mg·g^(-1), respectively. The better adsorption performance of the adsorbent than that of the recently reported nanomaterials and low-cost adsorbents proves its great application potential in the removal of heavy metal contaminants from wastewater. The present paper developed a promising adsorbent which will certainly find applications in wastewater treatment and also provides guiding significance in designing adsorption processes.展开更多
基金supported by the National Natural Science Foundation of China (No 30772627)
文摘The title compounds, C7H4I2O2 1 and C13H7I2N2O3 2, have been synthesized and characterized by single-crystal X-ray diffraction. Compound 1 crystallizes in monoclinic, space group P21/c with a = 9.802（2）, b = 13.867（3）, c = 7.364（2） A, β = 109.74（3）°, V= 942.1（3） A^3, Dc= 2.636 g/cm^3, C7H4I2O2, Mr= 373.90, F（000） = 672, μ = 6.627 mm^-1, Z = 4, R = 0.0459 and wR = 0.1018 for 1805 observed reflections （I 〉 2 σ（I））. Compound 2 belongs to the monoclinic system, space group P21/n with a = 9.015（2）, b = 12.024（2）, c = 14.072（3） A, β = 103.91（3）°, V = 1480.6（5） A^3, Dc= 2.216 g/cm^3, C13H7I2N2O3, Mr= 494.01, F（000） = 920, p = 4.255 mm^-1, Z = 4, R = 0.0777 and wR = 0.1757 for 2896 observed reflections （I 〉 2σ（I））. Compounds 1 and 2 were assayed for antibacterial activities against three Gram positive bacterial strains （B. subtilis, S. aureus and S. faecalis） and three Gram negative bacterial strains （E. coli, P. aeruginosa and E. cloacae） by MTr method. Fortunately, compound 2 is found to show potent antibacterial activity against these six bacterial strains.
基金Supported by the National Natural Science Foundation of China(51278489)
文摘Wastewater with high NH_4^+-N is difficult to treat by traditional methods.So in this paper,a wild strain of photosynthetic bacteria was used for high NH_4^+-N wastewater treatment together with biomass recovery.Isolation,identification,and characterization of the microorganism were carried out.The strain was inoculated to the biological wastewater treatment unit.The impacts of important factors were examined,including temperature,dissolved oxygen,and light intensity.Results showed that photosynthetic bacteria could effectively treat high NH_4^+-N wastewater.For wastewater with NH_4^+-N of 2300 mg·L^(-1),COD/N=1.0,98.3%of COD was removed,and cell concentration increased by 43 times.The optimal conditions for the strain's cell growth and wastewater treatment were 30℃,dissolved oxygen of 0.5-1.5 mg·L^(-1) and a light intensity of 4000 lx.Photosynthetic bacteria could bear a lower C/N ratio than bacteria in a traditional wastewater treatment process,but the NH_4^+-N removal was only 20%-40%because small molecule carbon source was used prior to NH_4^+-N.Also,the use of photosynthetic bacteria in chicken manure wastewater containing NH4+-N about 7000 mg·L^(-1) proved that photosynthetic bacteria could remove NH_4^+-N in a real case,finally,83.2%of NH_4^+-N was removed and 66.3%of COD was removed.
基金supported by the National Natural Science Foundation of China (41175137)the Climate Change Working Program of MEP in 2015 (CC(2015)-9-3)the Climate Change Project of Beijing in 2014 (ZHCKT4)
文摘The treatment of domestic and industrial wastewater is one of the major sources of CH_4 in the Chinese waste sector. On the basis of statistical data and country-specific emission factors, using IPCC methodology, the characteristics of CH_4 emissions from wastewater treatment in China were analyzed. The driving factors of CH_4 emissions were studied, and the emission trend and reduction potential were predicted and analyzed according to the current situation. Results show that in 2010, CH_4 emissions from the treatment of domestic and industrial wastewater were0.6110 Mt and 1.6237 Mt, respectively. Eight major industries account for more than 92% of emissions, and CH_4 emissions gradually increased from 2005 to 2010. From the controlling management scenario, we predict that in 2020, CH_4 emissions from the treatment of domestic and industrial wastewater will be 1.0136 Mt and 2.3393 Mt, respectively, and the reduction potential will be 0.0763 Mt and 0.2599 Mt, respectively.From 2010 to 2020, CH_4 emissions from the treatment of domestic and industrial wastewater will increase by 66% and 44%, respectively.
文摘In this work, a coking wastewater was selected and a biochemical Az/O treatment device for fractional degradation was designed and employed. After each stage of the treatment, the products were analyzed through gas chromatography-mass spectroscopy （GC-MS） to determine their composition. Finally, AgNO3 ＋ K2FeO4 was used as an advanced deep catalytic oxidation treatment. It was concluded from the analysis that cyclic organics could be degraded and the chemical oxygen demand （COD） was controlled within 50 mg. L-1, in line with the target value, Meanwhile, the spectra obtained from the GC-MS were in accordance with the conclusions reached based on the COD. The research results showed that all hard-degradable organics in coking wastewater could be eliminated through the A2/O bio-membrane treatment and the advanced treatment of making use of K2FeO4 as an oxidant and Ag＋ as a catalyst, the catalytic efficiency with Ag＋ as a catalyst of K2FeO4 was very high. Ag＋ could evidently improve the oxidation capacity of K2FeO4 to wastewater in its short stability time, and this is an important innovation.
基金supported jointly by National Natural Science Foundation of China(No.51877208)Anhui Provincial Key R&D Programmers(No.202004a07020047)。
文摘In this study,a single dielectric barrier discharge(DBD)coaxial reactor was used to degrade 4,4'-sulfonylbis(TBBPS)in water using greenhouse gas(CO_(2))and argon as the carrier gases.The investigation focused on CO_(2)conversion,reactive species formation,gas-liquid mass transfer mechanism,and degradation mechanism of TBBPS during the discharge plasma process.With the decrease of CO_(2)/Ar ratio in the process of plasma discharge,the emission spectrum intensity of Ar,CO_(2)and excited reactive species was enhanced.This increase promoted collision and dissociation of CO_(2),resulting in a series of chemical reactions that improved the production of reactive species such as·OH,^(1)O_(2),H_(2)O_(2)and O_(3).These reactive species initiated a sequence of reactions with TBBPS.Results indicated that at a gas flow rate of 240 mL/min with a CO_(2)/Ar ratio of 1:5,both the highest CO_(2)conversion rate(17.76%)and TBBPS degradation rate(94.24%)were achieved.The degradation mechanism was elucidated by determining types and contents of reactive species present in treatment liquid along with analysis of intermediate products using liquid chromatography-mass spectrometry techniques.This research provides novel insights into carbon dioxide utilization and water pollution control through dielectric barrier discharge plasma technology.
基金supported by the National Natural Science Foundation of China (No.52364022)the Natural Science Foundation of Guangxi Province,China (Nos.2023JJA160192 and 2021GXNSFAA220096)+1 种基金the Guangxi Science and Technology Major Project,China (No.AA23073018)the Guangxi Chongzuo Science and Technology Plan,China (No.2023ZY00503).
文摘With the application of resins in various fields, numerous waste resins that are difficult to treat have been produced. The industrial wastewater containing Cr(Ⅵ) has severely polluted soil and groundwater environments, thereby endangering human health. Therefore, in this paper, a novel functionalized mesoporous adsorbent PPR-Z was synthesized from waste amidoxime resin for adsorbing Cr(Ⅵ). The waste amidoxime resin was first modified with H3PO4 and ZnCl_(2), and subsequently, it was carbonized through slow thermal decomposition. The static adsorption of PPR-Z conforms to the pseudo-second-order kinetic model and Langmuir isotherm, indicating that the Cr(Ⅵ) adsorption by PPR-Z is mostly chemical adsorption and exhibits single-layer adsorption. The saturated adsorption capacity of the adsorbent for Cr(Ⅵ) could reach 255.86 mg/g. The adsorbent could effectively reduce Cr(Ⅵ) to Cr(Ⅲ) and decrease the toxicity of Cr(Ⅵ) during adsorption. PPR-Z exhibited Cr(Ⅵ) selectivity in electroplating wastewater. The main mechanisms involved in the Cr(Ⅵ) adsorption are the chemical reduction of Cr(Ⅵ) into Cr(Ⅲ) and electrostatic and coordination interactions. Preparation of PPR-Z not only solves the problem of waste resin treatment but also effectively controls Cr(Ⅵ) pollution and realizes the concept of “treating waste with waste”.
文摘The Ru3(CO)12/PEDPA complex was firstly applied in the CO selective reduction of 4-propylthio-2-mitroaniline. The effects of reaction temperature, the pressure of CO and concentration of catalyst on the reduction were investigated. Under the optimum conditions of T=140℃, Pco=5.0MPa and substrate/catalyst = 300 (molar ratio), the conversion and selectivity were 70% and 98%, respectively. After simple phase separation, the catalyst could be recycled.
基金Supported by Shenzhen Exclusive Funds for Developing Emerging Industries of Strategic Importance(CXZZ20120618111150009)~~
文摘[Objective] The aim was to research Chlorella properties in removing ni- trogen and phosphorus from wastewater. [Method] The effects of initial NH4＋-N and total P concentrations, N-to-P ratios, lightJdarkness ratios and pH on the removal of NH4＋-N and total P were evaluated. [Result] The results showed that Chlorella al- most removed NH4＋-N and total P at 100% as initial concentrations of NH4＋-N and total P were no more than 55 and 7 mg/L, respectively, whereas the removal ratio of NH4＋-N decreased to 90% with initial NH4＋-N concentration coming up to 75 mg/L. With N-to-P ratios of 5：1, 10：1 and 25：1, Chlorella completely removed NH4＋-N within 4 d, while the removal ratio of total P reached almost 100% within 7 d, with different N-to-P ratios. With L./D ratios of 24 h： 0 h and 12 h： 12 h as well as the initial concentrations of NH4＋-N at 30 mg/L and total P at 7 mg/L, the removing ra- tio of NH4＋-N and total P almost achieved 100% by Chlorella, and the removing ra- tio under L/D ratio of 24 h：0 h proved much faster. The optimal pH range for Chlorella to remove NH4＋-N and total P was 7-8. [Conclusion] The research pro- vides references for wastewater treatment in biological way and highly-efficient and environment-friendly treatment in future.
基金Supported by the National Natural Science Foundation of China(21525625)the National Basic Research Program(973 Program) of China(2014CB745100)+3 种基金the(863) High Technology Project of China(2013AA020302)the Chinese Universities Scientific Fund(JD1417)China Postdoctoral Science Foundation funded project(2017M610038)the Fundamental Research Funds for the Central Universities(ZY1712,XK1701)
文摘Water pollution caused by highly toxic Cd(II), Pb(II), and Cr(VI) is a serious problem. In the present work,a green and low-cost adsorbent of g-C_3N_4 nanosheets was developed with superior capacity for both cationic and anionic heavy metals. The adsorbent was easily fabricated through one-step calcination of guanidine hydrochloride with thickness less than 1.6 nm and specific surface area of 111.2 m^2·g^(-1). Kinetic and isotherm studies suggest that the adsorption is an endothermic chemisorption process, occurring on the energetically heterogeneous surface based on a hybrid mechanism of multilayer and monolayer adsorption. The tri-s-triazine units and surface N-containing groups of g-C_3N_4 nanosheets are proposed to be responsible for the adsorption process.Further study on pH demonstrates that electrostatic interaction plays an important role. The maximum adsorption capacity of Cd(II), Pb(II), and Cr(VI) on g-C_3N_4 nanosheets is 123.205 mg·g^(-1), 136.571 mg·g^(-1),and 684.451 mg·g^(-1), respectively. The better adsorption performance of the adsorbent than that of the recently reported nanomaterials and low-cost adsorbents proves its great application potential in the removal of heavy metal contaminants from wastewater. The present paper developed a promising adsorbent which will certainly find applications in wastewater treatment and also provides guiding significance in designing adsorption processes.
