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
Different concentrations of ferrate! with ClO- and without ClO- in alkaline solution were traced by visible spectrometry, and the conversion reaction of Fe! to Fe" was found to exist, in condition that cOH-was ≥...Different concentrations of ferrate! with ClO- and without ClO- in alkaline solution were traced by visible spectrometry, and the conversion reaction of Fe! to Fe" was found to exist, in condition that cOH-was ≥ 6 mol·L-1. ClO- would slow down the decomposition reaction rate of Ferrate! and increase the product concentration of Fe" in the system.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
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
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.
文摘Different concentrations of ferrate! with ClO- and without ClO- in alkaline solution were traced by visible spectrometry, and the conversion reaction of Fe! to Fe" was found to exist, in condition that cOH-was ≥ 6 mol·L-1. ClO- would slow down the decomposition reaction rate of Ferrate! and increase the product concentration of Fe" in the system.
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.
