The synergetic effect and underlying mechanism of potassium ferrate(PF)with tea saponin(TS,a biosurfactant)in producing short chain fatty acids(SCFAs)from anaerobic fermentation of waste activated sludge(WAS)were expl...The synergetic effect and underlying mechanism of potassium ferrate(PF)with tea saponin(TS,a biosurfactant)in producing short chain fatty acids(SCFAs)from anaerobic fermentation of waste activated sludge(WAS)were explored in this work.Experimental results showed that 0.2 g PF(g TSS)^(-1)(total suspended solid)combined with 0.02 g TS(g TSS)^(-1) could further improve SCFAs’production,and the maximum SCFAs content reached 2008.7 mg COD L^(-1),which is 1.2 and 4.5 times higher than those with PF and TS individually added,respectively,and 5.3 times higher than that of blank WAS on Day 12.In the model substrates experiments,the degradation rates of bovine serum albumin and dextran with combination of PF and TS were 41.3%±0.1% and 48.5%±0.06%,respectively,on Day 3,which are lower than those in blank WAS(with degradation rates of 72.3%±0.5%and 90.3%±0.3%).It was revealed that the oxidative effect of PF and the solubilization of TS caused more organic matters to be dissolved out from WAS,providing a large number of biodegradable substances for subsequent SCFAs production.While WAS pretreated with the combination of PF and TS,the relative abundances of Firmicutes increased from 6.4%(blank)to 38.6%,and that of Proteobacteria decreased from 41.8%(blank)to 21.8%.The combination of PF and TS promoted the hydrolysis process of WAS by enriching Firmicutes,and then increased acetic acid production by inhibiting Proteobacteria that consumed SCFAs.Meanwhile,at the genus level,acidogenesis bacteria(e.g.,Proteiniclasticum and Petrimonas)were enriched whereas SCFAs consuming bacteria(e.g.,Dokdonella)were inhibited.展开更多
This paper investigated the effects of potassium ferrate(PF)on the flotation performances of chalcopyrite and galena.The flotation results showed that PF obviously depressed galena,but had little effects on the floata...This paper investigated the effects of potassium ferrate(PF)on the flotation performances of chalcopyrite and galena.The flotation results showed that PF obviously depressed galena,but had little effects on the floatability of chalcopyrite within pH range of 4.0–12.0.Zeta potential tests showed that the addition of PF induced the formation of more amounts of hydrophilic species on the surface of galena under an alkaline environment.Industrial grade O-isopropyl-N-ethyl thionocarbamate(IPETC)chemically adsorbed on the surface of the PF-treated chalcopyrite and galena after its addition.Contact angle measurements showed that with the addition of PF,the contact angle of the galena surface significantly decreased compared with the chalcopyrite surface.Localized electrochemical impedance spectroscopy(LEIS)tests showed that the addition of PF increased the impedance of the galena surface.X-ray photoelectron spectroscopy(XPS)analyses revealed that the formation of hydrophilic species,namely lead sulfite,lead hydroxide and ferric hydroxide,on the galena surface,decreased its floatability in the presence of PF,while the formation of hydrophobic species,namely copper disulfide and elemental sulfur,on the chalcopyrite surface,maintained its floatability.Finally,a descriptive model for the reaction of PF with chalcopyrite and galena was proposed.展开更多
This study evaluated the effect of potassium ferrate(PF)and low-temperature thermal hydrolysis co-pretreatment on the promotion of sludge hydrolysis process and the impact on acid production in the subsequent anaerobi...This study evaluated the effect of potassium ferrate(PF)and low-temperature thermal hydrolysis co-pretreatment on the promotion of sludge hydrolysis process and the impact on acid production in the subsequent anaerobic digestion process.The analytical investigations showed that co-pretreatment significantly facilitated the hydrolysis process of the sludge and contributed to the accumulation of short-chain fatty acids(SCFAs).The pretreatment conditions under the optimal leaching of organic matter from sludge were hydrothermal temperature of 75℃,hydrothermal treatment time of 12 h,and PF dosage of 0.25 g g^(−1)TSS(total suspended solids),according to the results of orthogonal experiments.By pretreatment under proper conditions,the removal rate of soluble chemical oxygen demand(SCOD)achieved 71.8%at the end of fermentation and the removal rate of total phosphorus(TP)was 69.1%.The maximum yield of SCFAs was 750.3 mg L^(−1),7.45 times greater than that of the blank group.Based on the analysis of the anaerobic digestion mechanism,it was indicated that the co-pretreatment could destroy the floc structure on the sludge surface and improve organic matter dissolving,resulting in more soluble organic substances for the acidification process.Furthermore,microbial community research revealed that the main cause of enhanced SCFAs generation was an increase in acidogenic bacteria and a reduction of methanogenic bacteria.展开更多
Potassium ferrate(K_(2)FeO_(4)) was used as a novel environmental-friendly depressant,and its inhibition effect on flotation performance of arsenopyrite and chalcopyrite using potassium ethyl xanthate(PEX)as a collect...Potassium ferrate(K_(2)FeO_(4)) was used as a novel environmental-friendly depressant,and its inhibition effect on flotation performance of arsenopyrite and chalcopyrite using potassium ethyl xanthate(PEX)as a collector was investigated by flotation experiments,contact angle measurements,adsorption measurements,localized electrochemical impedance spectroscopy(LEIS)measurements,and X-ray photoelectron spectroscopy(XPS)analyses.The results showed that K_(2)FeO_(4)strongly depressed arsenopyrite in a pH range of 4−11,and the flotation separation of chalcopyrite from arsenopyrite could be realized in the presence of 5×10^(−4)mol/L K_(2)FeO_(4)and 5×10^(−5)mol/L PEX at pH 8 or 10.In the presence of K_(2)FeO_(4) and PEX,the contact angle and the xanthate adsorption capacity of arsenopyrite decreased significantly.LEIS measurements showed that the addition of ferrate could significantly increase the impedance of the arsenopyrite surface.XPS analyses further confirmed that ferrate accelerated the oxidation of arsenopyrite surface.展开更多
In this work, the removal of thiophene from simulated oil has been studied by using the adsorption, extraction and oxidation/adsorption methods, respectively. In the adsorptive desulfurization process, different comme...In this work, the removal of thiophene from simulated oil has been studied by using the adsorption, extraction and oxidation/adsorption methods, respectively. In the adsorptive desulfurization process, different commercial adsorbents were used to eliminate thiophene at ambient pressure and mild temperature, and the results showed that carbon powder had the best adsorption ability. In the extractive desulfurization process, the best desulfurization result was obtained when DMF is used. In the oxidative/adsorptive desulfurization procedure using synthesized potassium ferrate as the oxidant and phosphomolybdic acid solution as the catalyst, thiophene was oxidized and removed from hydrocarbons in combination with active carbon adsorption, and the residual sulfur content of simulated oil could be reduced to 15.3mg/L from the original level of 200mg/L, with the desulfurization rate reaching 92.3%.展开更多
This study aims to optimize the treatment of phenol-contaminated soil by potassium ferrate. Variations in pH value can accurately reflect the state and reaction status of the entire treatment process. Therefore, the p...This study aims to optimize the treatment of phenol-contaminated soil by potassium ferrate. Variations in pH value can accurately reflect the state and reaction status of the entire treatment process. Therefore, the pH value could be an important variable for optimizing the reaction conditions and achieving the automatic control of the process. About 99.89% of phenol was removed after 10 min of the pH-contxolled reaction at a rotational speed of 40-70 r/min, with the initial phenol concentration equating to 10.0 g/kg and the total water consumption reaching 2.72 L （at a soil/water ratio of 1：0.68）. The test results could provide a basis for practical application of automatic reaction control by pH value.展开更多
As a high-valent iron compound with Fe in the highest accessible oxidation state,ferrate(VI)brings unique opportunities for a number of areas where chemical oxidation is essential.Recently,it is emerging as a novel ox...As a high-valent iron compound with Fe in the highest accessible oxidation state,ferrate(VI)brings unique opportunities for a number of areas where chemical oxidation is essential.Recently,it is emerging as a novel oxidizing agent for materials chemistry,especially for the oxidation of carbon materials.However,the reported reactivity in liquid phase(H2SO4 medium)is confusing,which ranges from aggressive to moderate,and even incompetent.Meanwhile,the solid-state reactivity underlying the“dry”chemistry of ferrate(VI)remains poorly understood.Herein,we scrutinize the reactivity of K2FeO4 using fullerene C60 and various nanocarbons as substrates.The results unravel a modest reactivity in liquid phase that only oxidizes the active defects on carbon surface and a powerful oxidizing ability in solid state that can open the inert C=C bonds in carbon lattice.We also discuss respective benefit and limitation of the wet and dry approaches.Our work provides a rational understanding on the oxidizing ability of ferrate(VI)and can guide its application in functionalization/transformation of carbons and also other kinds of materials.展开更多
The possibility of direct analytical applications of ferrate（Ⅵ） solution,which was freshly electrogenerated in low-concentration NaOH electrolyte,was studied by a flow-injection-chemiluminescence（FI-CL） system.It...The possibility of direct analytical applications of ferrate（Ⅵ） solution,which was freshly electrogenerated in low-concentration NaOH electrolyte,was studied by a flow-injection-chemiluminescence（FI-CL） system.It was found that some inorganic ions, organic molecule and biomolecule could enhance the chemiluminescence emission caused by ferrate（Ⅵ）-luminol reaction.V（Ⅴ）, Ca（Ⅱ）,Mg（Ⅱ）,phloroglucinol,and bovine hemoglobin（Hb） chosen as samples were successfully detected by this developed method.The analytical characteristics of the system for the analytes determination including linear ranges,correlation coefficients, limits of detection combined with FI analysis were studied.展开更多
β-Fe2O3·H2O is prepared by reacting FeCl3, K2CO3, an oxidizing agent HIO4 and a metal chelating agent K3PO4 at 65~ 70℃. The prepared β-Fe2O3' H2O is introduced into the mixture of KOH, KOCl and a ferrate s...β-Fe2O3·H2O is prepared by reacting FeCl3, K2CO3, an oxidizing agent HIO4 and a metal chelating agent K3PO4 at 65~ 70℃. The prepared β-Fe2O3' H2O is introduced into the mixture of KOH, KOCl and a ferrate stabilizer KI, and reacted at room temperature for 5 h to produce a ferrate-containing cake. The cake is dried to give a water-free dried potassium ferrate (VI).展开更多
In this study,a stepwise oxidation system of potassium ferrate(K_(2)FeO_(4))combined with ozone(O+3)was used to degrade ciprofloxacin(CIP).The effects of pH and pre-oxidation time of K_(2)FeO_(4) on the evolution of K...In this study,a stepwise oxidation system of potassium ferrate(K_(2)FeO_(4))combined with ozone(O+3)was used to degrade ciprofloxacin(CIP).The effects of pH and pre-oxidation time of K_(2)FeO_(4) on the evolution of K_(2)FeO_(4) reduction products(iron(hydr)oxides)and CIP degradation were investigated.It was found that in addition to its own oxidation capacity,K_(2)FeO_(4) can also influence the treatment effect of CIP by changing the catalyst content.The presence of iron(hydr)oxides effectively enhanced the mineralization rate of CIP by catalyzing ozonation.The pH value can influence the content and types of the components with catalytic ozonation effect in iron(hydr)oxides.The K_(2)FeO_(4) pre-oxidation stage can produce more iron(hydr)oxides with catalytic components for subsequent ozonation,but the evolution of iron(hydr)oxides components was influenced by O_(3) treatment.It can also avoid the waste of oxidation capacity owing to the oxidation of iron(hydr)oxides by O_(3) and free radicals.The intermediate degradation products were identified by Fourier transform ion cyclotron resonance mass spectrometry(FT-ICR-MS).Besides,the degradation pathways were proposed.Among the degradation products of CIP,the product with broken quinolone ring structure only appeared in the stepwise oxidation system.展开更多
Ferrate（VI） was employed for the oxidation of cyanide （CN） and simultaneous removal of copper or nickel in the mixed/complexed systems of CN-Cu, CN-Ni, or CN-Cu-Ni. The degradation of CN （1.00 mmol/L） and remova...Ferrate（VI） was employed for the oxidation of cyanide （CN） and simultaneous removal of copper or nickel in the mixed/complexed systems of CN-Cu, CN-Ni, or CN-Cu-Ni. The degradation of CN （1.00 mmol/L） and removal of Cu （0.095 mmol/L） were investigated as a function of Fe（Ⅵ） doses from 0.3-2.00 mmol/L at pH 10.0. It was found that Fe（Ⅵ） could readily oxidize CN and the reduction of Fe（Ⅵ） into Fe（Ⅲ） might serve efficiently for the removal of free copper ions. The increase in Fe（Ⅵ） dose apparently favoured the CN oxidation as well as Cu removal. Moreover, the pH dependence study （pH 10.0-13.0） revealed that the oxidation of CN was almost unaffected in the studied pH range （10.0-13.0）, however, the maximum removal efficiency of Cu was obtained at pH 13.0. Similarly, treatment was carded out for CN-Ni system having the initial Ni concentration of 0.170 mmol/L and CN concentration of 1.00 mmol with Fe（Ⅵ） dose 2.00 mmol at various pH values （10.0-12.0）. Results showed a partial oxidation of CN and partial removal of Ni. It can be observed that Fe（Ⅵ） can partially degrade the CN-Ni complex in this pH range. Further, Fe（Ⅵ） was applied for the treatment of simulated industrial waste/effluent waters treatment containing CN, Cu, and Ni.展开更多
基金supported by the National Natural Science Foundation of China(No.41276067)the Air Liquide(China)R&D Co.,Ltd.(No.20200216).
文摘The synergetic effect and underlying mechanism of potassium ferrate(PF)with tea saponin(TS,a biosurfactant)in producing short chain fatty acids(SCFAs)from anaerobic fermentation of waste activated sludge(WAS)were explored in this work.Experimental results showed that 0.2 g PF(g TSS)^(-1)(total suspended solid)combined with 0.02 g TS(g TSS)^(-1) could further improve SCFAs’production,and the maximum SCFAs content reached 2008.7 mg COD L^(-1),which is 1.2 and 4.5 times higher than those with PF and TS individually added,respectively,and 5.3 times higher than that of blank WAS on Day 12.In the model substrates experiments,the degradation rates of bovine serum albumin and dextran with combination of PF and TS were 41.3%±0.1% and 48.5%±0.06%,respectively,on Day 3,which are lower than those in blank WAS(with degradation rates of 72.3%±0.5%and 90.3%±0.3%).It was revealed that the oxidative effect of PF and the solubilization of TS caused more organic matters to be dissolved out from WAS,providing a large number of biodegradable substances for subsequent SCFAs production.While WAS pretreated with the combination of PF and TS,the relative abundances of Firmicutes increased from 6.4%(blank)to 38.6%,and that of Proteobacteria decreased from 41.8%(blank)to 21.8%.The combination of PF and TS promoted the hydrolysis process of WAS by enriching Firmicutes,and then increased acetic acid production by inhibiting Proteobacteria that consumed SCFAs.Meanwhile,at the genus level,acidogenesis bacteria(e.g.,Proteiniclasticum and Petrimonas)were enriched whereas SCFAs consuming bacteria(e.g.,Dokdonella)were inhibited.
基金supported by the National Natural Science Foun-dation of China(Nos.51964027 and 52264028)Basic Research Project for High-level Talents of Yunnan Province(No.KKS2202152011)open foundation of State Key Laboratory of Complex Nonferrous Metal Resources Clean Utilization(No.CNMRCUKF1602).
文摘This paper investigated the effects of potassium ferrate(PF)on the flotation performances of chalcopyrite and galena.The flotation results showed that PF obviously depressed galena,but had little effects on the floatability of chalcopyrite within pH range of 4.0–12.0.Zeta potential tests showed that the addition of PF induced the formation of more amounts of hydrophilic species on the surface of galena under an alkaline environment.Industrial grade O-isopropyl-N-ethyl thionocarbamate(IPETC)chemically adsorbed on the surface of the PF-treated chalcopyrite and galena after its addition.Contact angle measurements showed that with the addition of PF,the contact angle of the galena surface significantly decreased compared with the chalcopyrite surface.Localized electrochemical impedance spectroscopy(LEIS)tests showed that the addition of PF increased the impedance of the galena surface.X-ray photoelectron spectroscopy(XPS)analyses revealed that the formation of hydrophilic species,namely lead sulfite,lead hydroxide and ferric hydroxide,on the galena surface,decreased its floatability in the presence of PF,while the formation of hydrophobic species,namely copper disulfide and elemental sulfur,on the chalcopyrite surface,maintained its floatability.Finally,a descriptive model for the reaction of PF with chalcopyrite and galena was proposed.
基金supported by the National Natural Science Foundation of China(No.41276067)the Air Liquide(China)R&D Co.,Ltd.(No.20200216).
文摘This study evaluated the effect of potassium ferrate(PF)and low-temperature thermal hydrolysis co-pretreatment on the promotion of sludge hydrolysis process and the impact on acid production in the subsequent anaerobic digestion process.The analytical investigations showed that co-pretreatment significantly facilitated the hydrolysis process of the sludge and contributed to the accumulation of short-chain fatty acids(SCFAs).The pretreatment conditions under the optimal leaching of organic matter from sludge were hydrothermal temperature of 75℃,hydrothermal treatment time of 12 h,and PF dosage of 0.25 g g^(−1)TSS(total suspended solids),according to the results of orthogonal experiments.By pretreatment under proper conditions,the removal rate of soluble chemical oxygen demand(SCOD)achieved 71.8%at the end of fermentation and the removal rate of total phosphorus(TP)was 69.1%.The maximum yield of SCFAs was 750.3 mg L^(−1),7.45 times greater than that of the blank group.Based on the analysis of the anaerobic digestion mechanism,it was indicated that the co-pretreatment could destroy the floc structure on the sludge surface and improve organic matter dissolving,resulting in more soluble organic substances for the acidification process.Furthermore,microbial community research revealed that the main cause of enhanced SCFAs generation was an increase in acidogenic bacteria and a reduction of methanogenic bacteria.
基金the National Natural Science Foundation of China(Nos.52074139,51904129)Basic Research Project of Yunnan Province,China(No.202001AU070028)+2 种基金Basic Research Project for High-level Talents of Yunnan Province,China(No.KKS2202152011)Open Foundation of State Key Laboratory of Complex Nonferrous Metal Resources Clean Utilization,China(No.CNMRCUKF1602)the Testing and Analyzing Funds of Kunming University of Science and Technology,China(No.2020T20150055).
文摘Potassium ferrate(K_(2)FeO_(4)) was used as a novel environmental-friendly depressant,and its inhibition effect on flotation performance of arsenopyrite and chalcopyrite using potassium ethyl xanthate(PEX)as a collector was investigated by flotation experiments,contact angle measurements,adsorption measurements,localized electrochemical impedance spectroscopy(LEIS)measurements,and X-ray photoelectron spectroscopy(XPS)analyses.The results showed that K_(2)FeO_(4)strongly depressed arsenopyrite in a pH range of 4−11,and the flotation separation of chalcopyrite from arsenopyrite could be realized in the presence of 5×10^(−4)mol/L K_(2)FeO_(4)and 5×10^(−5)mol/L PEX at pH 8 or 10.In the presence of K_(2)FeO_(4) and PEX,the contact angle and the xanthate adsorption capacity of arsenopyrite decreased significantly.LEIS measurements showed that the addition of ferrate could significantly increase the impedance of the arsenopyrite surface.XPS analyses further confirmed that ferrate accelerated the oxidation of arsenopyrite surface.
基金financially supported by the Science and Technology Program of the Department of Education,Heilongjiang Province(11531012)
文摘In this work, the removal of thiophene from simulated oil has been studied by using the adsorption, extraction and oxidation/adsorption methods, respectively. In the adsorptive desulfurization process, different commercial adsorbents were used to eliminate thiophene at ambient pressure and mild temperature, and the results showed that carbon powder had the best adsorption ability. In the extractive desulfurization process, the best desulfurization result was obtained when DMF is used. In the oxidative/adsorptive desulfurization procedure using synthesized potassium ferrate as the oxidant and phosphomolybdic acid solution as the catalyst, thiophene was oxidized and removed from hydrocarbons in combination with active carbon adsorption, and the residual sulfur content of simulated oil could be reduced to 15.3mg/L from the original level of 200mg/L, with the desulfurization rate reaching 92.3%.
基金financially supported by the National Key R&D Plan of China (2017YFC1404605)the Natural Science Foundation of China (Grant No. 51579049 and 51509044)+4 种基金the High-Tech Ship Programthe Excellent Subject Leaders Foundation of Harbin Science and Technology Bureauthe Key Laboratory of Superlight Materials and Surface Technology of the Ministry of Educationthe Harbin Engineering University for their supportsupported by the Open Research Fund Program of Shandong Provincial Key Laboratory of Oilfield Produced Water Treatment and Environmental Pollution Control (SINOPEC Petroleum Eaguieering Corporation) (No.201801)
文摘This study aims to optimize the treatment of phenol-contaminated soil by potassium ferrate. Variations in pH value can accurately reflect the state and reaction status of the entire treatment process. Therefore, the pH value could be an important variable for optimizing the reaction conditions and achieving the automatic control of the process. About 99.89% of phenol was removed after 10 min of the pH-contxolled reaction at a rotational speed of 40-70 r/min, with the initial phenol concentration equating to 10.0 g/kg and the total water consumption reaching 2.72 L （at a soil/water ratio of 1：0.68）. The test results could provide a basis for practical application of automatic reaction control by pH value.
基金financial support from National Key Research and Development Program of China (2017YFA0207500)National Natural Science Foundation of China (51673114,51973111)Shanghai Science and Technology Committee (17ZR1447300)
文摘As a high-valent iron compound with Fe in the highest accessible oxidation state,ferrate(VI)brings unique opportunities for a number of areas where chemical oxidation is essential.Recently,it is emerging as a novel oxidizing agent for materials chemistry,especially for the oxidation of carbon materials.However,the reported reactivity in liquid phase(H2SO4 medium)is confusing,which ranges from aggressive to moderate,and even incompetent.Meanwhile,the solid-state reactivity underlying the“dry”chemistry of ferrate(VI)remains poorly understood.Herein,we scrutinize the reactivity of K2FeO4 using fullerene C60 and various nanocarbons as substrates.The results unravel a modest reactivity in liquid phase that only oxidizes the active defects on carbon surface and a powerful oxidizing ability in solid state that can open the inert C=C bonds in carbon lattice.We also discuss respective benefit and limitation of the wet and dry approaches.Our work provides a rational understanding on the oxidizing ability of ferrate(VI)and can guide its application in functionalization/transformation of carbons and also other kinds of materials.
基金supported by the National Natural Science Foundation of China(No.20005005)Hubei Biomass-Resource Chemistry and Environmental Biotechnology Key Laboratory(Wuhan University)(No. HBRCEBL2007004)the Opening Foundation of State Key Laboratory of Agricultural Microbiology(No. AML-200905)
文摘The possibility of direct analytical applications of ferrate（Ⅵ） solution,which was freshly electrogenerated in low-concentration NaOH electrolyte,was studied by a flow-injection-chemiluminescence（FI-CL） system.It was found that some inorganic ions, organic molecule and biomolecule could enhance the chemiluminescence emission caused by ferrate（Ⅵ）-luminol reaction.V（Ⅴ）, Ca（Ⅱ）,Mg（Ⅱ）,phloroglucinol,and bovine hemoglobin（Hb） chosen as samples were successfully detected by this developed method.The analytical characteristics of the system for the analytes determination including linear ranges,correlation coefficients, limits of detection combined with FI analysis were studied.
文摘β-Fe2O3·H2O is prepared by reacting FeCl3, K2CO3, an oxidizing agent HIO4 and a metal chelating agent K3PO4 at 65~ 70℃. The prepared β-Fe2O3' H2O is introduced into the mixture of KOH, KOCl and a ferrate stabilizer KI, and reacted at room temperature for 5 h to produce a ferrate-containing cake. The cake is dried to give a water-free dried potassium ferrate (VI).
基金supported by the National Natural Science Foundation of China (No.51878394)the Introduction and Cultivation Plan for Young Innovative Talents of Colleges and Universities by the Education Department of Shandong Province。
文摘In this study,a stepwise oxidation system of potassium ferrate(K_(2)FeO_(4))combined with ozone(O+3)was used to degrade ciprofloxacin(CIP).The effects of pH and pre-oxidation time of K_(2)FeO_(4) on the evolution of K_(2)FeO_(4) reduction products(iron(hydr)oxides)and CIP degradation were investigated.It was found that in addition to its own oxidation capacity,K_(2)FeO_(4) can also influence the treatment effect of CIP by changing the catalyst content.The presence of iron(hydr)oxides effectively enhanced the mineralization rate of CIP by catalyzing ozonation.The pH value can influence the content and types of the components with catalytic ozonation effect in iron(hydr)oxides.The K_(2)FeO_(4) pre-oxidation stage can produce more iron(hydr)oxides with catalytic components for subsequent ozonation,but the evolution of iron(hydr)oxides components was influenced by O_(3) treatment.It can also avoid the waste of oxidation capacity owing to the oxidation of iron(hydr)oxides by O_(3) and free radicals.The intermediate degradation products were identified by Fourier transform ion cyclotron resonance mass spectrometry(FT-ICR-MS).Besides,the degradation pathways were proposed.Among the degradation products of CIP,the product with broken quinolone ring structure only appeared in the stepwise oxidation system.
基金supported by the grant of the Basic Research Program of the Korea Science & Engineering Foundation (No R01-2006-000-10284-0)
文摘Ferrate（VI） was employed for the oxidation of cyanide （CN） and simultaneous removal of copper or nickel in the mixed/complexed systems of CN-Cu, CN-Ni, or CN-Cu-Ni. The degradation of CN （1.00 mmol/L） and removal of Cu （0.095 mmol/L） were investigated as a function of Fe（Ⅵ） doses from 0.3-2.00 mmol/L at pH 10.0. It was found that Fe（Ⅵ） could readily oxidize CN and the reduction of Fe（Ⅵ） into Fe（Ⅲ） might serve efficiently for the removal of free copper ions. The increase in Fe（Ⅵ） dose apparently favoured the CN oxidation as well as Cu removal. Moreover, the pH dependence study （pH 10.0-13.0） revealed that the oxidation of CN was almost unaffected in the studied pH range （10.0-13.0）, however, the maximum removal efficiency of Cu was obtained at pH 13.0. Similarly, treatment was carded out for CN-Ni system having the initial Ni concentration of 0.170 mmol/L and CN concentration of 1.00 mmol with Fe（Ⅵ） dose 2.00 mmol at various pH values （10.0-12.0）. Results showed a partial oxidation of CN and partial removal of Ni. It can be observed that Fe（Ⅵ） can partially degrade the CN-Ni complex in this pH range. Further, Fe（Ⅵ） was applied for the treatment of simulated industrial waste/effluent waters treatment containing CN, Cu, and Ni.
