Processing conditions of effectively separating indium from the leaching solution of a smelting antimony slag were studied. For the leaching solution containing indium and antimony and iron ions, indium was separated ...Processing conditions of effectively separating indium from the leaching solution of a smelting antimony slag were studied. For the leaching solution containing indium and antimony and iron ions, indium was separated by extracting with HDEHP kerosine solution, washing antimony and iron ions with oxalic acid solution and stripping indium with a dilute solution of hydrochloric acid. InCl 3 solution with purity above 90% is obtained. Indium can be enriched through a circulation of stripping with a dilute HCl solution. The concentration of InCl 3 solution is about 25～30 g/L.展开更多
Various molecular docking software packages are available for modeling interactions between small molecules and proteins.However,there have been few reports of modeling the interactions between metal ions and metallop...Various molecular docking software packages are available for modeling interactions between small molecules and proteins.However,there have been few reports of modeling the interactions between metal ions and metalloproteins.In this study,the AutoDock package was employed to example docking into a di-iron binding protein,bacterioferritin.Each binding site of this protein was tested for docking with iron ions.Blind docking experiments showed that all docking conformations converged into two clusters,one for internal iron binding in sites within the metalloprotein and the other for external iron binding on the protein surface.Local docking experiments showed that there were significant differences between two internal iron binding sites.Docking at one site gave a reasonable root-mean-square deviation(RMSD) distribution with relatively low binding energy.Analysis of the binding mode quality for this site revealed that more than half of the docking conformations were categorized as having good binding geometry,while no good conformations were found for the other site.Further investigations indicated that coordinating water molecules contributed to the stability of binding geometries.This study provides an empirical approach towards the study of molecular docking in metalloproteins.展开更多
Microporous chitosan （CS） membranes were directly prepared by extraction of poly（ethylene glycol） （PEG） from CS/PEG blend membrane and were examined for iron and manganese ions removal from aqueous solutions. Th...Microporous chitosan （CS） membranes were directly prepared by extraction of poly（ethylene glycol） （PEG） from CS/PEG blend membrane and were examined for iron and manganese ions removal from aqueous solutions. The different variables affecting the adsorption capacity of the membranes such as contact time, pH of the sorption medium, and initial metal ion concentration in the feed solution were investigated on a batch adsorption basis. The affinity of CS/PEG blend membrane to adsorb Fe（II） ions is higher than that of Mn（II） ions, with adsorption equilibrium achieved after 60 min for Fe（II） and Mn（II） ions. By increasing CS]PEG ratio in the blend membrane the adsorption capacity of metal ions increased. Among all parameters, pH has the most significant effect on the adsorption capacity, particularly in the range of 2.9-5.9. The increase in CS/PEG ratio was found to enhance the adsorption capacity of the membranes. The effects of initial concentration of metal ions on the extent of metal ions removal were investigated in detail. The experimental data were better fitted to Freundlich equation than Langmuir. In addition, it was found that the iron and manganese ions adsorbed on the membranes can be effectively desorbed in 0.1 mol/L HCl solution （up to 98% desorption efficiency） and the blend membranes can be reused almost without loss of the adsorption capacity for iron and manganese ions.展开更多
Highly photoluminescent nitrogen and sulfur co-doped carbon nanoparticles（CNPs） ca. 56 nm have been prepared through a green one-step hydrothermal synthesis route by using millet powder as carbon sources, in which t...Highly photoluminescent nitrogen and sulfur co-doped carbon nanoparticles（CNPs） ca. 56 nm have been prepared through a green one-step hydrothermal synthesis route by using millet powder as carbon sources, in which the nitrogen and sulfur co-doping improves the photoluminescent efficiency of the CNPs. The as-prepared CNPs display excellent fluorescent properties and low biotoxicity with a relatively high quantum yield of 30.4%, which have been applied for bioimaging and highly sensitive and selective detection of iron（III） ions.展开更多
The extracellular polymeric substances（EPS） of Acidithiobacillus ferrooxidans ATCC 23270,and iron and copper enclosed in EPS were extracted by ultrasonication and centrifugation methods to determine the interaction ...The extracellular polymeric substances（EPS） of Acidithiobacillus ferrooxidans ATCC 23270,and iron and copper enclosed in EPS were extracted by ultrasonication and centrifugation methods to determine the interaction mechanism of Cu2＋,Fe3＋ and EPS during bioleaching chalcopyrite.Generally,Cu2＋ ions can stimulate bacteria to produce more EPS than Fe3＋ ions.The mass ratio of Fe3＋/Cu2＋ enclosed in EPS decreased gradually from about 4：1 to about 2：1 when the concentration of Cu2＋ ions increased from 0.01 to 0.04 mol/L.The amount of iron and copper bound together by EPS in ferrous-free 9K medium containing 1% chalcopyrite was about 2 times of that in 9K medium containing 0.04 mol/L Cu2＋ ions.It was inferred that the EPS with jarosites on the surface of chalcopyrite gradually acted as a weak diffusion barrier for Cu2＋,Fe3＋ ions transference during bioleaching chalcopyrite.展开更多
Fe-doped TiO 2 coated on activated carbon （Fe-TiO 2 /AC, FTA） composites were prepared by an improved sol-gel method and characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, X-ray diffrac...Fe-doped TiO 2 coated on activated carbon （Fe-TiO 2 /AC, FTA） composites were prepared by an improved sol-gel method and characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, X-ray diffractometry, inductively coupled plasma mass spectrometry and BET surface area analysis. Obtained FTA composites were applied to the continuous treatment of dye wastewater in a dynamic reactor. The effects of Fe ion content, catalyst content, UV-lamp power and flowrate of the continuous treatment of dye wastewater on degradation efficiency were analyzed to determine the optimum operating conditions of dye wastewater degradation. Continuous photocatalytic experiments provided interesting results that FTA had a high chemical oxygen demand （COD） removal rate compared with TiO 2 , Fe doped TiO 2 （FT） and TiO 2 coated on activated carbon （TA）. In particular, when using the FTA catalyst with a Fe ion content of 0.33%, the kinetic content （k = 0.0376） of COD removal was more than the sum of both TA （0.0205） and 0.33% FT （0.0166）. FTA showed a high photoactivity because of a synergistic effect between Fe ions and AC on TiO 2 , which is higher than the individual effects of AC or Fe ions on TiO 2 . Additionally, for the photocatalytic degradation of dye wastewater, the optimum Fe ion content, catalyst content, UV-lamp power and flowrate were 0.33%, 6 g/L, 60 W （two lamps） and 300 mL/hr, respectively. An investigation of catalyst reuse revealed that the 0.33% FTA showed almost no deactivation in photocatalytic degradation of naturally treated wastewater.展开更多
The low efficiency of oxygen evolution reaction(OER) is regarded as one of the major roadblocks for metal-air batteries and water electrolysis.Herein,a high-performance OER catalyst of NiFe_(0.2)(oxy)hydroxide(NiFe_(0...The low efficiency of oxygen evolution reaction(OER) is regarded as one of the major roadblocks for metal-air batteries and water electrolysis.Herein,a high-performance OER catalyst of NiFe_(0.2)(oxy)hydroxide(NiFe_(0.2)-O_(x)H_(y)) was developed through topotactic transformation of a Prussian blue analogue in an alkaline solution,which exhibits a low overpotential of only 263 mV to reach a current density of 10 mA cm^(-2) and a small Tafel slope of 35 mV dec-1.Ex-situ/operando Raman spectroscopy results indicated that the phase structure of NiFe_(0.2)-O_(x)H_(y) was irreversibly transformed from the type of α-Ni(OH)_(2) to γ-NiOOH with applying an anodic potential,while ex-situ/operando 57Fe Mossbauer spectroscopic studies evidenced the in-situ production of abundant high-valent iron species under OER conditions,which effectively promoted the OER catalysis.Our work elucidates that the amount of high-valent iron species in-situ produced in the NiFe(oxy)hydroxide has a positive correlation with its water oxidation reaction performance,which further deepens the understanding of the mechanism of NiFe-based electrocatalysts.展开更多
Metal ions are physiologically essential,but excessive metal ions may cause severe risk to plants and animals.Here,we prepared gold nanoclusters（Au NCs） protected by 11-mercaptoundecanoic acid（11-MUA）,which have e...Metal ions are physiologically essential,but excessive metal ions may cause severe risk to plants and animals.Here,we prepared gold nanoclusters（Au NCs） protected by 11-mercaptoundecanoic acid（11-MUA）,which have excellent fluorescence properties for the detection of metal ions.The results showed that the copper ions（Cu^（2＋）） and iron ions（Fe^（3＋）） in the solution have obvious quenching effect on the fluorescence intensity of Au NCs.The detection range of Fe^（3＋） was 0.8-4.5 mmol/L（R^2= 0.992） and 4.5-11.0 mmol/L（R^2= 0.997）.And Cu^（2＋） has a lower linear range（0.1-1.0 mmol/L,R2= 0.993）.When EDTA was added into the reaction system,it was observed that the quenching effect of Cu^（2＋） and Fe^（3＋）on Au NCs showed different phenomenon.Then,the effect of metal ions on the fluorescence of Au NCs was investigated.The selective detection of Cu（2＋） was achieved by EDTA masking of Fe^（3＋）.In addition,we realized the metal ions detection application of Au NCs in the serum展开更多
The tinting phenomena of iron oxide contained glasses were studied from aspects of the electronic configuration, the iron ions coordination fields and the ions structure in glass. Several iron ion tinting forms at dif...The tinting phenomena of iron oxide contained glasses were studied from aspects of the electronic configuration, the iron ions coordination fields and the ions structure in glass. Several iron ion tinting forms at different redox or COD (chemical oxygen demand) conditions and their influential factors were given necessary explanations. The results reveal that the Fe^(3+)-O-Fe^(2+) structure is the real tinting reason of iron involved glasses, whereas the Si^(4+)-O-Fe^(3+) and Si^(4+)-O-Fe^(2+) formulations modify the glass colours. Under oxidizing melting condition, the amount of 4/6-coordinated Fe^(3+) increases and makes the glass colour yellowish. Conversely, reducing melting condition makes the 6-coordinated Fe^(2+) increased and gives much blue tint to the glass. The conventional tank furnace melting the very strong reducing condition, which is of high COD glass batch, is not suitable. The high ratio of ferrous/ferric in glass can be obtained with a new refining technology which contains no or little amount of refining agent.展开更多
A novel iron-hydrogen battery system, whose Fe^(3+)/Fe^(2+)cathode circumvents slowly dynamic oxygen reduction reaction and anode is fed with clean and cordial hydrogen, is systematically investigated. The maximum dis...A novel iron-hydrogen battery system, whose Fe^(3+)/Fe^(2+)cathode circumvents slowly dynamic oxygen reduction reaction and anode is fed with clean and cordial hydrogen, is systematically investigated. The maximum discharge power density of the iron-hydrogen battery reaches to 96.0 m W/cm^(2) under the room temperature. The capacity reaches to 17.2 Ah/L and the coulombic and energy efficiency are achieved to99% and 86%, respectively, during the galvanostatic charge-discharge test. Moreover, stable cycling test is observed for more than 240 h and 100 cycles with the iron sulfate in the sulfuric acid solutions. It is found that air plasma treatment onto the cathode carbon paper can generate the oxygen-containing groups and increase the hydrophilic pores proportion to ca. 40%, enlarging nearly 6-fold effective diffusion coefficient and improving the mass transfer in the battery performance. The simple iron-hydrogen energy storage battery design offers us a new strategy for the large-scale energy storage and hydrogen involved economy.展开更多
The acid bio-leaching process of vanadium extraction from clay vanadium water-leached residue was studied and the effect of the performance of iron transformation was investigated.Acidithiobacillus ferrooxidans affect...The acid bio-leaching process of vanadium extraction from clay vanadium water-leached residue was studied and the effect of the performance of iron transformation was investigated.Acidithiobacillus ferrooxidans affects the dissolution of vanadium through the catalytic effect on Fe^3+/Fe^2+couple and material exchange.The passivation of iron settling correlates with ferrous ion content in bio-leaching solution.In medium containing A.ferrooxidans and Fe(Ⅲ),the increment in Fe(Ⅱ)concentration leads to the formation of jarosite,generating a decline in vanadium extraction efficiency.Analysis of cyclic voltammetry shows that Fe(Ⅱ)ion is apt to be oxidized and translated into precipitate by A.ferrooxidans,which strongly adsorbed to the surface of the residue.Fe(Ⅲ)ion promotes the vanadium extraction due to its oxidizing activity.Admixing A.ferrooxidans to Fe(Ⅲ)medium elevates the reduction of low valence state vanadium and facilitates the exchange of substance between minerals and solution.This motivates 3.8%and 21.8%increments in recovery ratio and leaching rate of vanadium compared to the Fe(Ⅲ)exclusive use,respectively.Moreover,Fe(Ⅱ)ion impacts vanadium extraction slightly in sterile medium but negatively influences vanadium leaching in the presence of bacteria.展开更多
The coordination nature of a number of substituted sodiumphenoxides to iron （Ⅲ） ion has been studied. The o-nitrosodiumphenoxide was found to have different coordination behaviour from that the sodium salts of sali...The coordination nature of a number of substituted sodiumphenoxides to iron （Ⅲ） ion has been studied. The o-nitrosodiumphenoxide was found to have different coordination behaviour from that the sodium salts of salicylic acid and methylsalicylate showed. The structure of the complexes, the number of the ligands being coordinated to the metal ion, has also been determined by titration, uv-vis spectroscopy, atomic absorption and the flame test. In addition, other sodium phenoxides were also involved in this study for comparison. An electric conductivity study on the resulting complexes was carried out and all complexes were found to be semiconductors.展开更多
This study investigated the interaction between Cu^2＋and nano zero-valent iron（NZVI）coated with three types of stabilizers（i.e., polyacrylic acid [PAA], Tween-20 and starch） by examining the Cu^2＋ uptake, coll...This study investigated the interaction between Cu^2＋and nano zero-valent iron（NZVI）coated with three types of stabilizers（i.e., polyacrylic acid [PAA], Tween-20 and starch） by examining the Cu^2＋ uptake, colloidal stability and mobility of surface-modified NZVI（SM-NZVI） in the presence of Cu^2＋. The uptake of Cu^2＋ by SM-NZVI and the colloidal stability of the Cu-bearing SM-NZVI were examined in batch tests. The results showed that NZVI coated with different modifiers exhibited different affinities for Cu^2＋, which resulted in varying colloidal stability of different SM-NZVI in the presence of Cu^2＋. The presence of Cu^2＋ exerted a slight influence on the aggregation and settling of NZVI modified with PAA or Tween-20. However, the presence of Cu^2＋caused significant aggregation and sedimentation of starch-modified NZVI, which is due to Cu^2＋complexation with the starch molecules coated on the surface of the particles. Column experiments were conducted to investigate the co-transport of Cu^2＋ in association with SM-NZVI in water-saturated quartz sand. It was presumed that a physical straining mechanism accounted for the retention of Cu-bearing SM-NZVI in the porous media. Moreover, the enhanced aggregation of SM-NZVI in the presence of Cu^2＋ may be contributing to this straining effect.展开更多
In this work,a novel blue-green fluorescence phosphorous oxide quantum dots(PO QDs)was synthesized by solvothermal method in N-methyl-2-pyrrolidone(NMP)solution without any protection treatment during synthesis.Upon e...In this work,a novel blue-green fluorescence phosphorous oxide quantum dots(PO QDs)was synthesized by solvothermal method in N-methyl-2-pyrrolidone(NMP)solution without any protection treatment during synthesis.Upon excitation at 400 nm,PO QDs emitted blue-green fluorescence with quantum yield of 0.28.PO QDs exhibited the high inertness to air or moisture,the excellent water solubility,and stable emission intensity in a wide pH range and in high ionic strength solution.Interestingly,PO QDs could give the positive optical response to iron ions(Fe^(3+))and iodine ion(I^(-)).The photoluminescence(PL)of PO QDs could be directly quenched by Fe^(3+).While I^(-)quenched the PO QDs PL by means of Ag^(+)-mediated PO QDs system via the internal filtration effects(IFE)induced by the formation of AgI.Moreover,the biocompatibility and low toxicity of PO QDs verified in bean sprout and Hela cells indicated the promising application of PO QDs in medicine related fields.Furthermore,PO QDs could also be utilized in luminescent composite film for various application scenarios.展开更多
Anode modification plays a key role in higher power output in marine sediment microbial fuel cells(MSMFCs).A low-molecular organosilicon compound(3-aminopropyltriethoxysilane)was grafted onto the surface of carbon fel...Anode modification plays a key role in higher power output in marine sediment microbial fuel cells(MSMFCs).A low-molecular organosilicon compound(3-aminopropyltriethoxysilane)was grafted onto the surface of carbon felt using chemical method and a composite modified anode was prepared through organic ligands coordination Fe^(3+)for better electro-chemical per-formance.Results show that the biofilm resistance of the composite modified anode(2707Ω)is 1.3 times greater than that of the unmodified anode(2100Ω),and its biofilm capacitance also increases by 2.2 times,indicating that the composite modification pro-motes the growth and attachment of electroactive bacteria on the anode.Its specific capacitance(887.8 Fm^(−2))is 3.7 times higher than that of unmodified anode,generating a maximum current density of 1.5Am^(−2).In their Tafel curves,the composite modified anodic exchange current density(5.25×10^(−6)Acm^(−2))is 5.8 times bigger than that of unmodified anode,which suggests that the electro-chemical activity of redox,anti-polarization ability and electron transfer kinetic activity are significantly enhanced.The marine sediment microbial fuel cell with the composite modified anode generates the higher power densities than the blank(203.8mWm^(−2) versus 45.07mWm^(−2)),and its current also increases by 4.4 times.The free amino groups on the anode surface expands a creative idea that the modified anode ligates the natural Fe(Ⅲ)ion in sea water in the MSMFCs for its higher power output.展开更多
A facile and rapid approach for detecting low concentration of iron ion(Fe3+) with improved sensitivity was developed on the basis of plasmon enhanced fluorescence and subsequently amplified fluorescence quenching.Au1...A facile and rapid approach for detecting low concentration of iron ion(Fe3+) with improved sensitivity was developed on the basis of plasmon enhanced fluorescence and subsequently amplified fluorescence quenching.Au1Ag4@Si O2 nanoparticles were synthesized and dispersed into fluorescein isothiocyanate(FITC) solution. The fluorescence of the FITC solution was improved due to plasmon enhanced fluorescence. However, efficient fluorescence quenching of the FITC/Au1Ag4@Si O2 solution was subsequently achieved when Fe3+, with a concentration ranging from17 n M to 3.4 l M, was added into the FITC/Au1Ag4@Si O2 solution, whereas almost no fluorescence quenching was observed for pure FITC solution under the same condition. FITC/Au1Ag4@Si O2 solution shows a better sensitivity for detecting low concentration of Fe3+compared to pure FITC solution. The quantized limit of detection toward Fe3+was improved from 4.6 l M for pure FITC solution to 20 n M for FITC/Au1Ag4@Si O2 solution.展开更多
To address the lack of systematic studies on heavy metal fluorescent probes in typical buffer solutions,this study developed a Fe^(3+)and Cu^(2+)fluorescent probe,DHU‑NP‑4,based on a naphthalimide fluorophore.Comparat...To address the lack of systematic studies on heavy metal fluorescent probes in typical buffer solutions,this study developed a Fe^(3+)and Cu^(2+)fluorescent probe,DHU‑NP‑4,based on a naphthalimide fluorophore.Comparative analysis of the probe's performance in various buffer systems revealed that buffers with high organic content are unsuitable for evaluating such probes.Furthermore,the pH of the solvent system was found to significantly influence the probe's behavior.Under highly acidic conditions(pH≤2),DHU‑NP‑4 exhibited exceptional specificity for Fe^(3+),while in alkaline conditions,it demonstrated high specificity for Cu^(2+).Leveraging these properties,the probe enabled the quantitative detection of Fe^(3+)and Cu^(2+)in solution.展开更多
Nowadays,iron ions as a ubiquitous heavy metal pollutant are gradually concerned and the convenient and quick removal of excessive iron ions in groundwater has become a major challenge for the safety of drinking water...Nowadays,iron ions as a ubiquitous heavy metal pollutant are gradually concerned and the convenient and quick removal of excessive iron ions in groundwater has become a major challenge for the safety of drinking water.In this study,boron-doped biochar(B-BC)was successfully prepared at various preparation conditions with the addition of boric acid.The as-prepared material has a more developed pore structure and a larger specific surface area(up to 897.97 m2/g).A series of characterization results shows that boric acid effectively activates biochar,and boron atoms are successfully doped on biochar.Compared with the ratio of raw materials,the pyrolysis temperature has a greater influence on the amount of boron doping.Based on Langmuir model,the maximum adsorption capacity of 800 B-BC1:2 at25℃,40℃,55℃ are 50.02 mg/g,95.09 mg/g,132.78 mg/g,respectively.Pseudo-second-order kinetic model can better describe the adsorption process,the adsorption process is mainly chemical adsorption.Chemical complexation,ions exchange,and co-precipitation may be the main mechanisms for Fe2+removal.展开更多
A rhodamine-benzimidazole conjugate （RB） as a probe was investigated. UV-Vis analysis showed that a strong absorption band at 552 nm was formed with the addition of Cu^2＋, while other transition metal ions induced ...A rhodamine-benzimidazole conjugate （RB） as a probe was investigated. UV-Vis analysis showed that a strong absorption band at 552 nm was formed with the addition of Cu^2＋, while other transition metal ions induced a little more absorption. The absorption value of RB solution at 552 nm has a linear correlation with Cu^2＋ concentration between 35-70 μmol/L; the detection limit reached 6.82x 10-2 gmol/L, which is lower than the settled limitation for copper in the drinking water （-30 μmol/L） standardized by World Health Organization （WHO）. Moreover, FL analysis showed that only Fe^3＋ could induce large fluorescence intensity enhance- ment at 582 nm; other common metal ions including Cu^2＋ cannot induce the enhancement. There was a good linear correlation be Fe^3＋ tween relatwe fluorescence ntenslty and Fe concentration ranging from 2 μmol/L to 20 μmol/L, and the detection limit reached 1.70×10^-2 μmol/L. The results showed that RB could detect Cu^2＋ and Fe^3＋ simultaneously, with the UV-Vis and fluorescence spectroscopy, respectively.展开更多
The Fe3＋/Fe2＋ redox electrolyte for use in polyaniline/tin oxide （PANI/SnO2）supercapacitors was reported. The influences of redox electrolyte based on different Fe3＋/Fe2＋ ion pair concentrations in 1 mol/LH2SO4 ...The Fe3＋/Fe2＋ redox electrolyte for use in polyaniline/tin oxide （PANI/SnO2）supercapacitors was reported. The influences of redox electrolyte based on different Fe3＋/Fe2＋ ion pair concentrations in 1 mol/LH2SO4 solution on the pseudocapacitive behaviors of PANI/SnO2 supercapacitor were investigated. The electrochemical properties of the supercapacitor were studied by cyclic voltammetry （CV）, galvanostatic charge discharge （GCD）, and electrochemical impedance spectroscopy （EIS） techniques. It is found that the performance of the supercapacitor is the best when the Fe3＋/Fe2＋ concentrationis 0.4 mol/L and its initial specific capacitance is 1172 F/g at an applied current density of 1 A/g. The long-term cycling experiment shows good stability with the retention of initial capacitance values of 88% after 2000 galvanostatic cycles. The experimental results testify that using Fe3＋/Fe2＋ redox electrolyte has a good prospect for improving the performances of energy-storage devices.展开更多
文摘Processing conditions of effectively separating indium from the leaching solution of a smelting antimony slag were studied. For the leaching solution containing indium and antimony and iron ions, indium was separated by extracting with HDEHP kerosine solution, washing antimony and iron ions with oxalic acid solution and stripping indium with a dilute solution of hydrochloric acid. InCl 3 solution with purity above 90% is obtained. Indium can be enriched through a circulation of stripping with a dilute HCl solution. The concentration of InCl 3 solution is about 25～30 g/L.
基金Project (No. 2011-II-010) supported by the Fundamental Research Funds for the Central Universities,China
文摘Various molecular docking software packages are available for modeling interactions between small molecules and proteins.However,there have been few reports of modeling the interactions between metal ions and metalloproteins.In this study,the AutoDock package was employed to example docking into a di-iron binding protein,bacterioferritin.Each binding site of this protein was tested for docking with iron ions.Blind docking experiments showed that all docking conformations converged into two clusters,one for internal iron binding in sites within the metalloprotein and the other for external iron binding on the protein surface.Local docking experiments showed that there were significant differences between two internal iron binding sites.Docking at one site gave a reasonable root-mean-square deviation(RMSD) distribution with relatively low binding energy.Analysis of the binding mode quality for this site revealed that more than half of the docking conformations were categorized as having good binding geometry,while no good conformations were found for the other site.Further investigations indicated that coordinating water molecules contributed to the stability of binding geometries.This study provides an empirical approach towards the study of molecular docking in metalloproteins.
基金supported by the Housing & Building National Research Centre in EgyptCentral Metallurgical R & D Institute (CMRDI)
文摘Microporous chitosan （CS） membranes were directly prepared by extraction of poly（ethylene glycol） （PEG） from CS/PEG blend membrane and were examined for iron and manganese ions removal from aqueous solutions. The different variables affecting the adsorption capacity of the membranes such as contact time, pH of the sorption medium, and initial metal ion concentration in the feed solution were investigated on a batch adsorption basis. The affinity of CS/PEG blend membrane to adsorb Fe（II） ions is higher than that of Mn（II） ions, with adsorption equilibrium achieved after 60 min for Fe（II） and Mn（II） ions. By increasing CS]PEG ratio in the blend membrane the adsorption capacity of metal ions increased. Among all parameters, pH has the most significant effect on the adsorption capacity, particularly in the range of 2.9-5.9. The increase in CS/PEG ratio was found to enhance the adsorption capacity of the membranes. The effects of initial concentration of metal ions on the extent of metal ions removal were investigated in detail. The experimental data were better fitted to Freundlich equation than Langmuir. In addition, it was found that the iron and manganese ions adsorbed on the membranes can be effectively desorbed in 0.1 mol/L HCl solution （up to 98% desorption efficiency） and the blend membranes can be reused almost without loss of the adsorption capacity for iron and manganese ions.
基金financial supports of the National Natural Science Foundation of China(No.21535006)the Fundamental Research Funds for the Central Universities(No.XDJK2015B029)
文摘Highly photoluminescent nitrogen and sulfur co-doped carbon nanoparticles（CNPs） ca. 56 nm have been prepared through a green one-step hydrothermal synthesis route by using millet powder as carbon sources, in which the nitrogen and sulfur co-doping improves the photoluminescent efficiency of the CNPs. The as-prepared CNPs display excellent fluorescent properties and low biotoxicity with a relatively high quantum yield of 30.4%, which have been applied for bioimaging and highly sensitive and selective detection of iron（III） ions.
基金Project(50621063) supported by the National Natural Science Foundation of ChinaProject(2010CB630903) supported by the National Basic Research Program of China
文摘The extracellular polymeric substances（EPS） of Acidithiobacillus ferrooxidans ATCC 23270,and iron and copper enclosed in EPS were extracted by ultrasonication and centrifugation methods to determine the interaction mechanism of Cu2＋,Fe3＋ and EPS during bioleaching chalcopyrite.Generally,Cu2＋ ions can stimulate bacteria to produce more EPS than Fe3＋ ions.The mass ratio of Fe3＋/Cu2＋ enclosed in EPS decreased gradually from about 4：1 to about 2：1 when the concentration of Cu2＋ ions increased from 0.01 to 0.04 mol/L.The amount of iron and copper bound together by EPS in ferrous-free 9K medium containing 1% chalcopyrite was about 2 times of that in 9K medium containing 0.04 mol/L Cu2＋ ions.It was inferred that the EPS with jarosites on the surface of chalcopyrite gradually acted as a weak diffusion barrier for Cu2＋,Fe3＋ ions transference during bioleaching chalcopyrite.
基金supported by the National Natural Science Foundation of China (No. 50802034)the Educationaland Technological Department of Hunan Province (No.08B063)the Natural Science Foundation of Hunan Province (No. 09JJ6101)
文摘Fe-doped TiO 2 coated on activated carbon （Fe-TiO 2 /AC, FTA） composites were prepared by an improved sol-gel method and characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, X-ray diffractometry, inductively coupled plasma mass spectrometry and BET surface area analysis. Obtained FTA composites were applied to the continuous treatment of dye wastewater in a dynamic reactor. The effects of Fe ion content, catalyst content, UV-lamp power and flowrate of the continuous treatment of dye wastewater on degradation efficiency were analyzed to determine the optimum operating conditions of dye wastewater degradation. Continuous photocatalytic experiments provided interesting results that FTA had a high chemical oxygen demand （COD） removal rate compared with TiO 2 , Fe doped TiO 2 （FT） and TiO 2 coated on activated carbon （TA）. In particular, when using the FTA catalyst with a Fe ion content of 0.33%, the kinetic content （k = 0.0376） of COD removal was more than the sum of both TA （0.0205） and 0.33% FT （0.0166）. FTA showed a high photoactivity because of a synergistic effect between Fe ions and AC on TiO 2 , which is higher than the individual effects of AC or Fe ions on TiO 2 . Additionally, for the photocatalytic degradation of dye wastewater, the optimum Fe ion content, catalyst content, UV-lamp power and flowrate were 0.33%, 6 g/L, 60 W （two lamps） and 300 mL/hr, respectively. An investigation of catalyst reuse revealed that the 0.33% FTA showed almost no deactivation in photocatalytic degradation of naturally treated wastewater.
基金financially supported by the National Natural Science Foundation of China(21476232,21961142006)the International Partnership Program of Chinese Academy of Sciences(121421KYSB20170020)the State Key Laboratory of Catalysis in Dalian Institute of Chemical Physics(N-16-07)。
文摘The low efficiency of oxygen evolution reaction(OER) is regarded as one of the major roadblocks for metal-air batteries and water electrolysis.Herein,a high-performance OER catalyst of NiFe_(0.2)(oxy)hydroxide(NiFe_(0.2)-O_(x)H_(y)) was developed through topotactic transformation of a Prussian blue analogue in an alkaline solution,which exhibits a low overpotential of only 263 mV to reach a current density of 10 mA cm^(-2) and a small Tafel slope of 35 mV dec-1.Ex-situ/operando Raman spectroscopy results indicated that the phase structure of NiFe_(0.2)-O_(x)H_(y) was irreversibly transformed from the type of α-Ni(OH)_(2) to γ-NiOOH with applying an anodic potential,while ex-situ/operando 57Fe Mossbauer spectroscopic studies evidenced the in-situ production of abundant high-valent iron species under OER conditions,which effectively promoted the OER catalysis.Our work elucidates that the amount of high-valent iron species in-situ produced in the NiFe(oxy)hydroxide has a positive correlation with its water oxidation reaction performance,which further deepens the understanding of the mechanism of NiFe-based electrocatalysts.
基金financial support from the National Natural Science Foundation of China(Nos.61571426,61671435)the National Key Technology R&D Program(No.2015BAI23H00)+1 种基金Beijing Natural Science Foundation(No.4161003)Beijing Key Laboratory of Environmentally Harmful Chemical Analysis
文摘Metal ions are physiologically essential,but excessive metal ions may cause severe risk to plants and animals.Here,we prepared gold nanoclusters（Au NCs） protected by 11-mercaptoundecanoic acid（11-MUA）,which have excellent fluorescence properties for the detection of metal ions.The results showed that the copper ions（Cu^（2＋）） and iron ions（Fe^（3＋）） in the solution have obvious quenching effect on the fluorescence intensity of Au NCs.The detection range of Fe^（3＋） was 0.8-4.5 mmol/L（R^2= 0.992） and 4.5-11.0 mmol/L（R^2= 0.997）.And Cu^（2＋） has a lower linear range（0.1-1.0 mmol/L,R2= 0.993）.When EDTA was added into the reaction system,it was observed that the quenching effect of Cu^（2＋） and Fe^（3＋）on Au NCs showed different phenomenon.Then,the effect of metal ions on the fluorescence of Au NCs was investigated.The selective detection of Cu（2＋） was achieved by EDTA masking of Fe^（3＋）.In addition,we realized the metal ions detection application of Au NCs in the serum
文摘The tinting phenomena of iron oxide contained glasses were studied from aspects of the electronic configuration, the iron ions coordination fields and the ions structure in glass. Several iron ion tinting forms at different redox or COD (chemical oxygen demand) conditions and their influential factors were given necessary explanations. The results reveal that the Fe^(3+)-O-Fe^(2+) structure is the real tinting reason of iron involved glasses, whereas the Si^(4+)-O-Fe^(3+) and Si^(4+)-O-Fe^(2+) formulations modify the glass colours. Under oxidizing melting condition, the amount of 4/6-coordinated Fe^(3+) increases and makes the glass colour yellowish. Conversely, reducing melting condition makes the 6-coordinated Fe^(2+) increased and gives much blue tint to the glass. The conventional tank furnace melting the very strong reducing condition, which is of high COD glass batch, is not suitable. The high ratio of ferrous/ferric in glass can be obtained with a new refining technology which contains no or little amount of refining agent.
基金financial support granted by National Key R&D Program of China (No.2020YFB1505704)Dongyue Polymer Material Company of Dongyue Federation+2 种基金State Key Laboratory of Fluorinated Functional Membrane Materials (Dongyue Group institute)Dongyue Future Hydrogen Energy Materials Companysponsored by the Collaborative Innovation Center of Suzhou Nano Science and Technology。
文摘A novel iron-hydrogen battery system, whose Fe^(3+)/Fe^(2+)cathode circumvents slowly dynamic oxygen reduction reaction and anode is fed with clean and cordial hydrogen, is systematically investigated. The maximum discharge power density of the iron-hydrogen battery reaches to 96.0 m W/cm^(2) under the room temperature. The capacity reaches to 17.2 Ah/L and the coulombic and energy efficiency are achieved to99% and 86%, respectively, during the galvanostatic charge-discharge test. Moreover, stable cycling test is observed for more than 240 h and 100 cycles with the iron sulfate in the sulfuric acid solutions. It is found that air plasma treatment onto the cathode carbon paper can generate the oxygen-containing groups and increase the hydrophilic pores proportion to ca. 40%, enlarging nearly 6-fold effective diffusion coefficient and improving the mass transfer in the battery performance. The simple iron-hydrogen energy storage battery design offers us a new strategy for the large-scale energy storage and hydrogen involved economy.
基金Project(DY135-B2-15) supported by the China Ocean Mineral Resource R&D AssociationProject(2015ZX07205-003) supported by Major Science and Technology Program for Water Pollution Control and Treatment,ChinaProjects(21176242,21176026) supported by the National Natural Science Foundation of China
文摘The acid bio-leaching process of vanadium extraction from clay vanadium water-leached residue was studied and the effect of the performance of iron transformation was investigated.Acidithiobacillus ferrooxidans affects the dissolution of vanadium through the catalytic effect on Fe^3+/Fe^2+couple and material exchange.The passivation of iron settling correlates with ferrous ion content in bio-leaching solution.In medium containing A.ferrooxidans and Fe(Ⅲ),the increment in Fe(Ⅱ)concentration leads to the formation of jarosite,generating a decline in vanadium extraction efficiency.Analysis of cyclic voltammetry shows that Fe(Ⅱ)ion is apt to be oxidized and translated into precipitate by A.ferrooxidans,which strongly adsorbed to the surface of the residue.Fe(Ⅲ)ion promotes the vanadium extraction due to its oxidizing activity.Admixing A.ferrooxidans to Fe(Ⅲ)medium elevates the reduction of low valence state vanadium and facilitates the exchange of substance between minerals and solution.This motivates 3.8%and 21.8%increments in recovery ratio and leaching rate of vanadium compared to the Fe(Ⅲ)exclusive use,respectively.Moreover,Fe(Ⅱ)ion impacts vanadium extraction slightly in sterile medium but negatively influences vanadium leaching in the presence of bacteria.
文摘The coordination nature of a number of substituted sodiumphenoxides to iron （Ⅲ） ion has been studied. The o-nitrosodiumphenoxide was found to have different coordination behaviour from that the sodium salts of salicylic acid and methylsalicylate showed. The structure of the complexes, the number of the ligands being coordinated to the metal ion, has also been determined by titration, uv-vis spectroscopy, atomic absorption and the flame test. In addition, other sodium phenoxides were also involved in this study for comparison. An electric conductivity study on the resulting complexes was carried out and all complexes were found to be semiconductors.
基金supported by the Fundamental Research Funds for the Central Universities (531107040788)the National Natural Science Foundation of China (Nos. 51409100, 51039001, 51378190)the Program for Changjiang Scholars and Innovative Research Team in University (IRT-13R17)
文摘This study investigated the interaction between Cu^2＋and nano zero-valent iron（NZVI）coated with three types of stabilizers（i.e., polyacrylic acid [PAA], Tween-20 and starch） by examining the Cu^2＋ uptake, colloidal stability and mobility of surface-modified NZVI（SM-NZVI） in the presence of Cu^2＋. The uptake of Cu^2＋ by SM-NZVI and the colloidal stability of the Cu-bearing SM-NZVI were examined in batch tests. The results showed that NZVI coated with different modifiers exhibited different affinities for Cu^2＋, which resulted in varying colloidal stability of different SM-NZVI in the presence of Cu^2＋. The presence of Cu^2＋ exerted a slight influence on the aggregation and settling of NZVI modified with PAA or Tween-20. However, the presence of Cu^2＋caused significant aggregation and sedimentation of starch-modified NZVI, which is due to Cu^2＋complexation with the starch molecules coated on the surface of the particles. Column experiments were conducted to investigate the co-transport of Cu^2＋ in association with SM-NZVI in water-saturated quartz sand. It was presumed that a physical straining mechanism accounted for the retention of Cu-bearing SM-NZVI in the porous media. Moreover, the enhanced aggregation of SM-NZVI in the presence of Cu^2＋ may be contributing to this straining effect.
基金the National Natural Science Foundation of China(No.21808142)for financial support。
文摘In this work,a novel blue-green fluorescence phosphorous oxide quantum dots(PO QDs)was synthesized by solvothermal method in N-methyl-2-pyrrolidone(NMP)solution without any protection treatment during synthesis.Upon excitation at 400 nm,PO QDs emitted blue-green fluorescence with quantum yield of 0.28.PO QDs exhibited the high inertness to air or moisture,the excellent water solubility,and stable emission intensity in a wide pH range and in high ionic strength solution.Interestingly,PO QDs could give the positive optical response to iron ions(Fe^(3+))and iodine ion(I^(-)).The photoluminescence(PL)of PO QDs could be directly quenched by Fe^(3+).While I^(-)quenched the PO QDs PL by means of Ag^(+)-mediated PO QDs system via the internal filtration effects(IFE)induced by the formation of AgI.Moreover,the biocompatibility and low toxicity of PO QDs verified in bean sprout and Hela cells indicated the promising application of PO QDs in medicine related fields.Furthermore,PO QDs could also be utilized in luminescent composite film for various application scenarios.
基金This work was supported by the National Natural Sci-ence Foundation of China(No.22075262).
文摘Anode modification plays a key role in higher power output in marine sediment microbial fuel cells(MSMFCs).A low-molecular organosilicon compound(3-aminopropyltriethoxysilane)was grafted onto the surface of carbon felt using chemical method and a composite modified anode was prepared through organic ligands coordination Fe^(3+)for better electro-chemical per-formance.Results show that the biofilm resistance of the composite modified anode(2707Ω)is 1.3 times greater than that of the unmodified anode(2100Ω),and its biofilm capacitance also increases by 2.2 times,indicating that the composite modification pro-motes the growth and attachment of electroactive bacteria on the anode.Its specific capacitance(887.8 Fm^(−2))is 3.7 times higher than that of unmodified anode,generating a maximum current density of 1.5Am^(−2).In their Tafel curves,the composite modified anodic exchange current density(5.25×10^(−6)Acm^(−2))is 5.8 times bigger than that of unmodified anode,which suggests that the electro-chemical activity of redox,anti-polarization ability and electron transfer kinetic activity are significantly enhanced.The marine sediment microbial fuel cell with the composite modified anode generates the higher power densities than the blank(203.8mWm^(−2) versus 45.07mWm^(−2)),and its current also increases by 4.4 times.The free amino groups on the anode surface expands a creative idea that the modified anode ligates the natural Fe(Ⅲ)ion in sea water in the MSMFCs for its higher power output.
基金supported by the National Natural Science Foundation of China (51003069)Natural Science Foundation of Jiangsu Higher Education Institutions of China (10KJB430014)A Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions
文摘A facile and rapid approach for detecting low concentration of iron ion(Fe3+) with improved sensitivity was developed on the basis of plasmon enhanced fluorescence and subsequently amplified fluorescence quenching.Au1Ag4@Si O2 nanoparticles were synthesized and dispersed into fluorescein isothiocyanate(FITC) solution. The fluorescence of the FITC solution was improved due to plasmon enhanced fluorescence. However, efficient fluorescence quenching of the FITC/Au1Ag4@Si O2 solution was subsequently achieved when Fe3+, with a concentration ranging from17 n M to 3.4 l M, was added into the FITC/Au1Ag4@Si O2 solution, whereas almost no fluorescence quenching was observed for pure FITC solution under the same condition. FITC/Au1Ag4@Si O2 solution shows a better sensitivity for detecting low concentration of Fe3+compared to pure FITC solution. The quantized limit of detection toward Fe3+was improved from 4.6 l M for pure FITC solution to 20 n M for FITC/Au1Ag4@Si O2 solution.
文摘To address the lack of systematic studies on heavy metal fluorescent probes in typical buffer solutions,this study developed a Fe^(3+)and Cu^(2+)fluorescent probe,DHU‑NP‑4,based on a naphthalimide fluorophore.Comparative analysis of the probe's performance in various buffer systems revealed that buffers with high organic content are unsuitable for evaluating such probes.Furthermore,the pH of the solvent system was found to significantly influence the probe's behavior.Under highly acidic conditions(pH≤2),DHU‑NP‑4 exhibited exceptional specificity for Fe^(3+),while in alkaline conditions,it demonstrated high specificity for Cu^(2+).Leveraging these properties,the probe enabled the quantitative detection of Fe^(3+)and Cu^(2+)in solution.
基金the financial support by Open Research Fund of State Key Laboratory of Geomechanics and Geotechnical Engineering,Institute of Rock and Soil Mechanics,Chinese Academy of Sciences(No.Z019005)the Longjiang Scholars for young scientist。
文摘Nowadays,iron ions as a ubiquitous heavy metal pollutant are gradually concerned and the convenient and quick removal of excessive iron ions in groundwater has become a major challenge for the safety of drinking water.In this study,boron-doped biochar(B-BC)was successfully prepared at various preparation conditions with the addition of boric acid.The as-prepared material has a more developed pore structure and a larger specific surface area(up to 897.97 m2/g).A series of characterization results shows that boric acid effectively activates biochar,and boron atoms are successfully doped on biochar.Compared with the ratio of raw materials,the pyrolysis temperature has a greater influence on the amount of boron doping.Based on Langmuir model,the maximum adsorption capacity of 800 B-BC1:2 at25℃,40℃,55℃ are 50.02 mg/g,95.09 mg/g,132.78 mg/g,respectively.Pseudo-second-order kinetic model can better describe the adsorption process,the adsorption process is mainly chemical adsorption.Chemical complexation,ions exchange,and co-precipitation may be the main mechanisms for Fe2+removal.
基金Supported by National Natural Science Foundation of China(20901063,51203127)Wuhan Chenguang Scheme(Grant 201050231049)established under Wuhan Science and Technology BureauOutstanding youth project of Hubei Provincial Department of Education(20121509)
文摘A rhodamine-benzimidazole conjugate （RB） as a probe was investigated. UV-Vis analysis showed that a strong absorption band at 552 nm was formed with the addition of Cu^2＋, while other transition metal ions induced a little more absorption. The absorption value of RB solution at 552 nm has a linear correlation with Cu^2＋ concentration between 35-70 μmol/L; the detection limit reached 6.82x 10-2 gmol/L, which is lower than the settled limitation for copper in the drinking water （-30 μmol/L） standardized by World Health Organization （WHO）. Moreover, FL analysis showed that only Fe^3＋ could induce large fluorescence intensity enhance- ment at 582 nm; other common metal ions including Cu^2＋ cannot induce the enhancement. There was a good linear correlation be Fe^3＋ tween relatwe fluorescence ntenslty and Fe concentration ranging from 2 μmol/L to 20 μmol/L, and the detection limit reached 1.70×10^-2 μmol/L. The results showed that RB could detect Cu^2＋ and Fe^3＋ simultaneously, with the UV-Vis and fluorescence spectroscopy, respectively.
基金Project(51172190)supported by the National Natural Science Foundation of NationProject(07JJ6015)supported by the Natural Science Foundation of Hunan Province,China
文摘The Fe3＋/Fe2＋ redox electrolyte for use in polyaniline/tin oxide （PANI/SnO2）supercapacitors was reported. The influences of redox electrolyte based on different Fe3＋/Fe2＋ ion pair concentrations in 1 mol/LH2SO4 solution on the pseudocapacitive behaviors of PANI/SnO2 supercapacitor were investigated. The electrochemical properties of the supercapacitor were studied by cyclic voltammetry （CV）, galvanostatic charge discharge （GCD）, and electrochemical impedance spectroscopy （EIS） techniques. It is found that the performance of the supercapacitor is the best when the Fe3＋/Fe2＋ concentrationis 0.4 mol/L and its initial specific capacitance is 1172 F/g at an applied current density of 1 A/g. The long-term cycling experiment shows good stability with the retention of initial capacitance values of 88% after 2000 galvanostatic cycles. The experimental results testify that using Fe3＋/Fe2＋ redox electrolyte has a good prospect for improving the performances of energy-storage devices.
