This study investigates the compatibility and efficacy of combining ammonium molybdate(AM)with antagonistic bacteria Bacillus amyloliquefaciens B10W10 and Pseudomonas sp.B11W11 for brown rot control(Monilinia laxa).In...This study investigates the compatibility and efficacy of combining ammonium molybdate(AM)with antagonistic bacteria Bacillus amyloliquefaciens B10W10 and Pseudomonas sp.B11W11 for brown rot control(Monilinia laxa).In vitro experiments reveal variable mycelial growth inhibition rates compared to untreated controls,with B11W11+0.5%AM and B10W10+2%AM displaying the highest inhibition rates after 5 days.After 10 days,the 2%AM+B10W10 combination exhibits the highest inhibition rate.Microscopic observations show structural alterations in mycelium within inhibition zones,marked by vacuolization.The antagonistic bacteria,alone or with different ammonium molybdate concentrations,significantly impact M.laxa spore germination,with the B10W10 cell filtrate+2%ammonium molybdate combination achieving the most substantial inhibition.Conversely,the 0.5%ammonium molybdate treatment has the lowest inhibition rate while the combination of AM and bacteria is giving better results compared to the use of bacteria alone.Fruits treated with various antagonistic bacteria and ammonium molybdate combinations demonstrate a significant reduction in disease severity.The 0.5%AM+B10W10 combination exhibits the lowest severity.FT-IR spectra analysis identifies shifts in fungal biomass functional groups,with reduced lignin-related bands and increased phenols,lipids,polysaccharides,and carbohydrates.This highlights the structural modifications caused by the biological treatments.The study also evaluates the effects on fruit quality parameters.The 2%ammonium molybdate treatment yields the lowest weight loss.TSS levels are affected by salt concentration,while acid content remains consistent across treatments.All treatments influence fruit firmness compared to controls.These findings emphasize the potential of combining ammonium molybdate and antagonistic bacteria for effective brown rot control,highlighting their compatibility and effects on disease severity,fungal biomass,spore germination,and fruit quality.展开更多
Neutral oxygen evolution reaction(OER)is a crucial half-reaction for electrocatalytic chemical production under mild condition,but with limited development due to low activity and poor stability.Herein,a tungsten-dope...Neutral oxygen evolution reaction(OER)is a crucial half-reaction for electrocatalytic chemical production under mild condition,but with limited development due to low activity and poor stability.Herein,a tungsten-doped cobalt molybdate(WDCMO)catalyst was synthesized for efficient and durable OER under neutral electrolyte.It is demonstrated that catalyst reconstruction is suppressed by W doping,which stabilizes the Co-O-Mo point-to-point connection in CoMoO_(4) architecture and stimulates to a lower valence state of active sites over the surface phase.Thereby,the surface structure maintains to avoid compound dissolution caused by over-oxidation during OER.Meanwhile,the WDCMO catalyst promotes charge transfer and optimizes*OH intermediate adsorption,which improves reaction kinetics and intrinsic activity.Consequently,the WDCMO electrode exhibits an overpotential of 302 mV at 10 mA cm^(-2) in neutral electrolyte with an improvement of 182 mV compared with CoMoO4 electrode.Furthermore,W doping significantly improves the electrode stability from 50 h to more than 320 h,with a suppressive potential attenuation from 2.82 to 0.29 mV h^(-1).This work will shed new light on designing rational electrocatalysts for neutral OER.展开更多
Currently,endeavors to scale up the production of amorphous catalysts are still impeded by intricate synthesis conditions.Here,we have prepared a series of metal-based molybdate via one-step coprecipitation method.Aft...Currently,endeavors to scale up the production of amorphous catalysts are still impeded by intricate synthesis conditions.Here,we have prepared a series of metal-based molybdate via one-step coprecipitation method.After ingredient optimization,amorphous Co_(2)CeFe_(2)-MoO_(4) was identified as exhibiting the highest intrinsic activity among its counterparts.Modulation of electron structure enables Co_(2)CeFe_(2)-MoO_(4) to balance the adsorption behavior towards reactive intermediates.Ultimately,the obtained Co_(2)CeFe_(2)-MoO_(4) molybdate demonstrated a captivating OER performance,showcasing a low overpotential of 230 mV at 10 mA cm^(-2).Moreover,the alkaline electrolyzer employing the Co_(2)CeFe_(2)-MoO_(4) anode exhibited a low cell voltage of 1.50 V for water splitting and underwent an acceptable attenuation of 4.99% after 165 h of continuous operation,demonstrating its favorable catalytic activity and durability.This work provides a facile and eco-friendly synthesis pathway for crafting cost-effective and durable earth-abundant OER electrocatalysts tailored for water splitting to produce clean hydrogen.展开更多
Sodium percarbonate(Na_(2)CO_(3)·1.5H_(2)O_(2),SPC)has been extensively employed as a solid substitute of H_(2)O_(2)for Fenton process in water treatment,because of its high stability during the production,transp...Sodium percarbonate(Na_(2)CO_(3)·1.5H_(2)O_(2),SPC)has been extensively employed as a solid substitute of H_(2)O_(2)for Fenton process in water treatment,because of its high stability during the production,transport,storage and usage.In addition,SPC can be applied in a wider range of work pH,it is also applied as a buffer in Fenton reaction for preventing a drop in pH.Herein,we have synthesized basic copper molybdate(BCM)nanoblocks with the molecular formula of Cu_(3)(MoO_(4))_(2)(OH)_(2)as an efficient and heterogeneous catalyst for antibiotics degradation via percarbonate activation.First,fully physical characterizations confirmed BCM nanocomposite exhibited a structure of nanoblocks.We also found that BCM/SPC system could work in a much wider pH range,compared with H_(2)O_(2).Then,BCM/SPC system presented a good anti-interference ability for natural organic matter in OTC degradation.EPR results and Quenching tests confirmed that the co-presence of·CO_(3)-,·O_(2)-,1O_(2)and·OH in BCM/SPC system.展开更多
Novel silver/silver molybdate（Ag/Ag2MoO4） composites with surface plasmon resonance（SPR）-enhanced photocatalytic performance were successfully fabricated via a facile one-pot hydrothermal route with the presence o...Novel silver/silver molybdate（Ag/Ag2MoO4） composites with surface plasmon resonance（SPR）-enhanced photocatalytic performance were successfully fabricated via a facile one-pot hydrothermal route with the presence of sodium dodecyl sulfate（SDS） in this study.The as prepared silver/silver molybdate（Ag/Ag2MoO4） composites were systematically characterized by X-ray diffraction（XRD）,scanning electron microscopy（SEM） and ultraviolet-visible diffuse reflectance absorption spectroscopy（DRS） in order to investigate their crystal structure,morphology and optical property as well.The photocatalytic activities of the composites were subsequently evaluated by their ability to degrade rhodamine B（RhB） under visible-light irradiation.Varies of controlled experiments were then carefully operated to gain a deep insight into the assembling of Ag/Ag2MoO4composites.It was found that preparation conditions such as pH,reaction time,and the amount of surfactant played important roles in the formation of composites with octahedral microstructures.And the composite obtained at 160 ℃ using 0.5 g of sodium dodecyl sulfate exhibited the highest photocatalytic performance under visible-light irradiation.Capture experiments were also conducted to clarify the function of different active species generated on the surface of Ag/Ag2MoO4during the photocatalytic process,in which both holes and ·OH radicals were found to play crucial role in photocatalytic removal of RhB under visible light irradiation.A possible photocatalytic mechanism of Ag/Ag2MoO4 was finally proposed on the basis of all the results to explain the higher photocatalytic activity of the octahedral Ag/Ag2MoO4 composites.It was inferred that the photoinduced ＂hot＂ electrons can quickly transfer from the Ag NPs to the conduction band of Ag2MoO4 and react with oxygen and H2O to generate a large quality of active radicals such as ·OH and ·O2^- because of the SPR effects.Besides,this SPR effects of Ag nanoparticles deposited on the surface of Ag2MoO4 can not only dramatically amplify its light absorption,especially in the visible region,but also promote the separation of photoexcited electron-hole pairs and effectively decrease electron-hole recombination.展开更多
Transition metal molybdate(RMoO4)has been extensively studied in optics,electricity and catalysis due to its low cost and multivalent Mo atoms,while its poor electrical conductivity limits its application in electroma...Transition metal molybdate(RMoO4)has been extensively studied in optics,electricity and catalysis due to its low cost and multivalent Mo atoms,while its poor electrical conductivity limits its application in electromagnetic wave absorption(EMA).Compounding molybdate with conductive materials is an effective way to improve its electrical conductivity.In this work,a homogeneous coating on the molybdate surface was achieved by utilizing a pyrrole oxidation polymerization mechanism,and then stabilized composites of Molybdate@Carbon(RMoO4@C)were obtained by high-temperature pyrolysis.The EMA properties of the nanocomposites were tuned by substituting the species of transition metal elements(RMoO_(4)@C,R=Fe,Co,Cu).Among them,Fe_(2)(MoO_(4))_(3)@C has a minimum reflection loss of−60.62 dB at an ultra-low thickness of 1.7 mm,and the effective absorption bandwidth(EAB)can reach 4.75 GHz at 3.00 mm.This work expands the range of applications for molybdate and provides a new material basis for building high-performance EMA materials.展开更多
A new polyoxomolybdate compound,namely {[MnII（L）（4,4？-Hbipy）（H2O）2]2 [Mo5O15（PO4）2]}.2H2O 1（L = 3-（2-pyridyl）pyrazole,4,4＇-Hbipy = protonated 4,4＇-bipyridine）,was designed and synthesized under hydrothe...A new polyoxomolybdate compound,namely {[MnII（L）（4,4？-Hbipy）（H2O）2]2 [Mo5O15（PO4）2]}.2H2O 1（L = 3-（2-pyridyl）pyrazole,4,4＇-Hbipy = protonated 4,4＇-bipyridine）,was designed and synthesized under hydrothermal conditions.Single-crystal X-ray diffraction analysis result reveals that the [Mo5O15（PO4）2]6-cluster in compound 1 links to two MnII cations via the oxygen of PO43-,which is further coordinated by one 3-（2-pyridyl）pyrazole,one 4,4＇-Hbipyridine,and two water molecules.展开更多
A new polyoxomolybdate complex HNaT[Mo36O112（H2O）16]·47H2O 1 has been prepared in the beaker solution and characterized by single-crystal X-ray diffraction and elemental analyses. Crystal data： H127Mo36Na7O175...A new polyoxomolybdate complex HNaT[Mo36O112（H2O）16]·47H2O 1 has been prepared in the beaker solution and characterized by single-crystal X-ray diffraction and elemental analyses. Crystal data： H127Mo36Na7O175, Mr = 6542.79, monoclinic, C2/c, a = 40.891（6）, b = 17.900（3）, c = 25.580（4）A, β = 125.673（2）°, V = 15210（4）A3, Z = 4, Dc = 2.857 g/cm^3, F（000） = 12464,μ = 3.013 mm^-1, R = 0.0633 and wR = 0.1654 （I 〉 20（I））. With the bridging sodium cations, the [Mo36Ou2（H2O）16]^8- units in compound 1 are linked to form a one-dimensional structure, on the basis of which a three-dimensional architecture is further constructed via other sodium cations and complicated hydrogen bonds.展开更多
Two new polyoxomolybdate compounds,namely（CuIIL2）2[CuⅡ（HL）2]2[Mo8O26（HL）2].（H2O）4（1） and [CuⅡ（HL）2]2[β-Mo8O26]（HL）2（2）（HL=imidazole）,were designed and synthesized under hydrothermal conditions.X-r...Two new polyoxomolybdate compounds,namely（CuIIL2）2[CuⅡ（HL）2]2[Mo8O26（HL）2].（H2O）4（1） and [CuⅡ（HL）2]2[β-Mo8O26]（HL）2（2）（HL=imidazole）,were designed and synthesized under hydrothermal conditions.X-ray diffraction analyses reveal that compound 1 consists of one Mo8O26（HL）24-cluster,two CuL2,two Cu（HL）22＋,and four disassociated water molecules;and compound 2 is constructed by one β-Mo8O264-cluster,two Cu（HL）22＋,and two uncoordinated imidazole molecules.展开更多
Two new polyoxomolybdate compounds,namely CuII2（HL）3]2[Mo8O26]·（H2O）4（1） and [NiII（HL）3]2（Mo8O26）·（H2O）3（2）（HL = 3-（2-pyridyl）pyrazole）,were designed and synthesized under hydrothermal cond...Two new polyoxomolybdate compounds,namely CuII2（HL）3]2[Mo8O26]·（H2O）4（1） and [NiII（HL）3]2（Mo8O26）·（H2O）3（2）（HL = 3-（2-pyridyl）pyrazole）,were designed and synthesized under hydrothermal conditions.X-ray diffraction analyses reveal that compound 1 consists of one β-Mo8O264-cluster and a Cu2 dimer which is built from two Cu（II） ions linked by three 3-（2-pyridyl）pyrazole ligands.Compound 2 is generated by two kinds of polyoxomolybdate clusters of α-[Mo8O26]4-and β-[Mo8O26]4-.In complexes 1 and 2,the multi-dimensional frameworks are con-structed with the help of hydrogen-bonding links between the terminaloxygen atoms of [Mo8O26]4-,water molecules,and 3-（2-pyridyl）pyrazole ligands.Crystal data of 1：C24H25Cu2Mo4N9O15,Mr = 1190.37,monoclinic,space group P21/c,a = 10.850（2）,b = 18.510（4）,c = 17.230（3） ,β = 100.57（3）°,V = 3401.6（12） 3,Z = 4,Dc = 2.324 g/cm3,F（000） = 2312,μ = 2.742 mm-1,R = 0.0302 and wR = 0.0775（Ⅰ 〉 2σ（Ⅰ））;Crystal data for 2：C48H48Mo8N18Ni2O29,Mr = 2225.98,monoclinic,space group P21/n,a = 20.799（2）,b = 14.7970（13）,c = 23.141（2） ,β = 91.6180（10）°,V = 7119.0（11） 3,Z = 4,Dc = 2.077 g/cm3,F（000） = 4344,μ = 1.968 mm-1,R = 0.0309 and wR = 0.0696（Ⅰ〉 2σ（Ⅰ））.展开更多
The removal of tungsten(W)and vanadium(V)from molybdate solutions was studied using the poly hydroxyl chelating resin D403in batch and column experiments.The batch experiments indicated that tungsten and vanadium coul...The removal of tungsten(W)and vanadium(V)from molybdate solutions was studied using the poly hydroxyl chelating resin D403in batch and column experiments.The batch experiments indicated that tungsten and vanadium could be preferentially adsorbed by the D403resin for4h in molybdate solution at a pH of approximately9.25.Separation factors,αVMo andαWMo,wereabove45and18,respectively,when the molar ratios of Mo/V and Mo/W in the solution exceeded40.Elution tests illustrated that vanadium and tungsten could be easily eluted from the resin with1mol/L sodium hydroxide solution in only1h.To further explore the sorption mechanism of the resin,the experimental equilibrium isotherm data of the three metals fitted well with the Freundlich model.The column experiments confirmed the adaptability of the D403resin in the production of sodium molybdate with a removal rate of tungsten surpassing90%and that of vanadium of99.4%.展开更多
In order to effectively improve the corrosion resistance of aluminum alloys, anodic oxidation technique was used to generate the oxide film. We investigated the influences of two inorganic corrosion inhibitors(ammoniu...In order to effectively improve the corrosion resistance of aluminum alloys, anodic oxidation technique was used to generate the oxide film. We investigated the influences of two inorganic corrosion inhibitors(ammonium dihydrogen phosphate and sodium molybdate) on the corrosion resistance of anodic oxidation films on 2024 aluminum alloy, and studied the synergistic effect of two corrosion inhibitors. The corrosion resistance of anodic oxidation film in 3.5 wt% NaCl solution was evaluated by electrochemical impedance spectroscopy(EIS) and potentiodynamic polarization curves. Results show that, after adding the single ammonium dihydrogen phosphate or sodium molybdate of 0.01 M to oxalic acid electrolyte, inhibition efficiencies of the anodized samples are 10% and 47%, respectively. However, in the presence of two inhibitors with the same concentration of 0.01 M, inhibition efficiency can be as high as 92%. Therefore, we observed the significantly synergistic corrosion inhibition effect of molybdate and phosphate ions for anodic oxidation film formed on 2024 aluminum alloy.展开更多
Trivalent samarium ion (Sm^(3+)) activated calcium molybdate (CaMoO_4) phosphor was prepared by solid-state reaction in air. The XRD pattern of the powder CaMoO_4∶Sm shows that the CaMoO_4∶Sm single phase is develop...Trivalent samarium ion (Sm^(3+)) activated calcium molybdate (CaMoO_4) phosphor was prepared by solid-state reaction in air. The XRD pattern of the powder CaMoO_4∶Sm shows that the CaMoO_4∶Sm single phase is developed fully through our preparation procedure. The excitation spectrum of CaMoO_4∶Sm is composed of a broad absorption of host and some sharp lines of the f-f transition absorption of Sm^(3+). Illustrated in photoluminescence spectrum, CaMoO_4 doped with Sm^(3+) displays orange red emission that is ascribed to the inner 4f^5 electron transitions ~6H_(7/2)(orange)and ~6H_(9/2)(red)of Sm^(3+). Different from the sites of Sm^(3+) in CdWO_4, the Sm^(3+) ions substitute for the Ca^(2+) and form only one type emission center in the CaMoO_4 crystal lattice.展开更多
A novel transition metal ion bridging bis（diphosphopentamolybdates） has been synthesized and characterized by elemental analysis,IR spectrum,UV spectrum and single-crystal X-ray diffraction.The single-crystal struct...A novel transition metal ion bridging bis（diphosphopentamolybdates） has been synthesized and characterized by elemental analysis,IR spectrum,UV spectrum and single-crystal X-ray diffraction.The single-crystal structure analysis shows that the compound consists of seven charge-compensating 2,2＇-biimidazole cations （BIIM=2,2＇-biimidazole） and one dumbbell-like [Mn（H2O）4（P2Mo5O23）2]10-heteropolyanion which is constructed by two [P2Mo5O23]6-clusters bridged through one [Mn（H2O）4]2＋ cation.展开更多
Calcium molybdate(CaMoO4)is the main component of powellite and is a predominant intermediate in the pyrometallurgical and hydrometallurgical process of molybdenum.The extraction of Mo from CaMoO4 by a combination of ...Calcium molybdate(CaMoO4)is the main component of powellite and is a predominant intermediate in the pyrometallurgical and hydrometallurgical process of molybdenum.The extraction of Mo from CaMoO4 by a combination of phosphoric acid and hydrochloric acid was investigated.For further understanding of the leaching mechanism,the effects of five key factors were studied to describe the leaching kinetics.The results indicated that the dissolution rate of CaMoO4 was independent of the stirring speed.Mo extraction significantly increased with increasing HCl concentration and temperature,but decreased with increasing particle size.A shrinking core model with surface chemical reaction was found to withstand the dissolution of CaMoO4.The apparent activation energy was calculated to be 70.879 kJ/mol,and a semi-empirical equation was derived for the rate of reaction.展开更多
A mechanism study on MoO2 electrodeposition from ammonium molybdate solution was presented via linear sweep voltammetry,species distribution diagram,Raman spectra,Fourier transform infrared spectrometry and X-ray diff...A mechanism study on MoO2 electrodeposition from ammonium molybdate solution was presented via linear sweep voltammetry,species distribution diagram,Raman spectra,Fourier transform infrared spectrometry and X-ray diffractometry.The results show that there exist two reducible species in ammonium molybdate aqueous solution,i.e.Mo7 O24^6- and molybdenum ammonium complex.In weak acid medium without NH4^+,an obvious reduction peak denoting the reduction of Mo7 O24^6- to molybdenum(Ⅳ)oxides emerges at around-0.7 V(vs SCE).While in neutral and basic solutions without NH4^+,the dominant species changes to MoO4^2-,and accordingly,no reduction peak appears except hydrogen evolution.NH4^+ plays an important role in MoO2 electrodeposition.A new current peak appears at-1.25 V(vs SCE)in both acid and basic solutions,which is attributed to the reduction of molybdenum complex.The effects of solution composition and the electrodeposition conditions on the current efficiency were discussed systematically.By optimizing the electrodeposition conditions,the current efficiency can reach up to51.9%.展开更多
Considering the different geochemical enrichment behaviors of W and Mo,Fe?Mn binary oxide(FMBO),ferric hydroxide(Fe(OH)3)and manganese dioxide(MnO2)were studied to separate W from molybdate solution,respectively.The e...Considering the different geochemical enrichment behaviors of W and Mo,Fe?Mn binary oxide(FMBO),ferric hydroxide(Fe(OH)3)and manganese dioxide(MnO2)were studied to separate W from molybdate solution,respectively.The experimental results demonstrated that Fe?Mn binary oxide(FMBO)was the most suitable adsorbent for the separation.Under a wide pH(6.9?11.3)region,more than80%W removal efficiency and less than3%Mo loss could be obtained.In addition,the Fe?Mn binary oxide adsorbent can be regenerated by treating with3mol/L NaOH,and the W adsorption efficiency was retained after five adsorption?desorption?regeneration cycles.All these indicate that the Fe?Mn binary oxides have the potential for the separation of W from molybdate solution.展开更多
The equilibrium adsorption isotherm and kinetic of the sorption process for W and Mo on macro chelating resin D403 were investigated on single Na2 Mo O4 and Na2WO4 solutions.The sorption isotherm results show that the...The equilibrium adsorption isotherm and kinetic of the sorption process for W and Mo on macro chelating resin D403 were investigated on single Na2 Mo O4 and Na2WO4 solutions.The sorption isotherm results show that the adsorption process of W obeys the Freundlich model very well whereas the exchange process with Mo approximately follows the Henry model.The kinetic experiments show that the intraparticle diffusion process was the rate-determining step for W sorption on the resin,and the corresponding activation energy is calculated to be 21.976 k J/mol.展开更多
In order to prepare fluorescent material for white Light Emitting Diodes （LEDs）, a new Eu^3＋ activated molybdate phosphor SrMoO4 was fabricated with solid-state method. X-ray diffraction （XRD） showed that the dop...In order to prepare fluorescent material for white Light Emitting Diodes （LEDs）, a new Eu^3＋ activated molybdate phosphor SrMoO4 was fabricated with solid-state method. X-ray diffraction （XRD） showed that the doping of trivalent europium ion reduced the lattice parameters. The excitation and emission spectra indicated that this phosphor could be excited effectively by the visible light, and then emitted red light with the peaks located at 616 and 624 nm. The influence of Eu^3＋ concentration on the luminescent properties of Eu^3＋ doped SrMoO4 was investigated and the 25% （mole fraction） was the appropriate molar concentration. The reaction time and temperature had obvious effect on the luminescent properties. The luminescent intensity reached the strongest when it was sintered at 800 ℃ for 3 h.展开更多
The MoS_2 catalysts were prepared from various molybdate precursors including inorganic and organic molybdate compounds. The sulfidation degree and morphology of active phases of MoS_2 activated by various molybdate p...The MoS_2 catalysts were prepared from various molybdate precursors including inorganic and organic molybdate compounds. The sulfidation degree and morphology of active phases of MoS_2 activated by various molybdate precursors in H_2S/H_2 stream at different temperatures were studied by X-ray photoelectron spectroscopy(XPS) and high-resolution transmission electron microscopy(HRTEM). The organic molybdate precursors lead to MoS_2 catalysts with higher sulfidation degree and smaller active phases to demonstrate higher catalytic activity during hydrodesulfurizaiton(HDS) of 4,6-DMDBT.展开更多
基金supported by the Phytopathology Unit of the Department of Plant Protection(ENA-Meknes,Morocco).
文摘This study investigates the compatibility and efficacy of combining ammonium molybdate(AM)with antagonistic bacteria Bacillus amyloliquefaciens B10W10 and Pseudomonas sp.B11W11 for brown rot control(Monilinia laxa).In vitro experiments reveal variable mycelial growth inhibition rates compared to untreated controls,with B11W11+0.5%AM and B10W10+2%AM displaying the highest inhibition rates after 5 days.After 10 days,the 2%AM+B10W10 combination exhibits the highest inhibition rate.Microscopic observations show structural alterations in mycelium within inhibition zones,marked by vacuolization.The antagonistic bacteria,alone or with different ammonium molybdate concentrations,significantly impact M.laxa spore germination,with the B10W10 cell filtrate+2%ammonium molybdate combination achieving the most substantial inhibition.Conversely,the 0.5%ammonium molybdate treatment has the lowest inhibition rate while the combination of AM and bacteria is giving better results compared to the use of bacteria alone.Fruits treated with various antagonistic bacteria and ammonium molybdate combinations demonstrate a significant reduction in disease severity.The 0.5%AM+B10W10 combination exhibits the lowest severity.FT-IR spectra analysis identifies shifts in fungal biomass functional groups,with reduced lignin-related bands and increased phenols,lipids,polysaccharides,and carbohydrates.This highlights the structural modifications caused by the biological treatments.The study also evaluates the effects on fruit quality parameters.The 2%ammonium molybdate treatment yields the lowest weight loss.TSS levels are affected by salt concentration,while acid content remains consistent across treatments.All treatments influence fruit firmness compared to controls.These findings emphasize the potential of combining ammonium molybdate and antagonistic bacteria for effective brown rot control,highlighting their compatibility and effects on disease severity,fungal biomass,spore germination,and fruit quality.
文摘Neutral oxygen evolution reaction(OER)is a crucial half-reaction for electrocatalytic chemical production under mild condition,but with limited development due to low activity and poor stability.Herein,a tungsten-doped cobalt molybdate(WDCMO)catalyst was synthesized for efficient and durable OER under neutral electrolyte.It is demonstrated that catalyst reconstruction is suppressed by W doping,which stabilizes the Co-O-Mo point-to-point connection in CoMoO_(4) architecture and stimulates to a lower valence state of active sites over the surface phase.Thereby,the surface structure maintains to avoid compound dissolution caused by over-oxidation during OER.Meanwhile,the WDCMO catalyst promotes charge transfer and optimizes*OH intermediate adsorption,which improves reaction kinetics and intrinsic activity.Consequently,the WDCMO electrode exhibits an overpotential of 302 mV at 10 mA cm^(-2) in neutral electrolyte with an improvement of 182 mV compared with CoMoO4 electrode.Furthermore,W doping significantly improves the electrode stability from 50 h to more than 320 h,with a suppressive potential attenuation from 2.82 to 0.29 mV h^(-1).This work will shed new light on designing rational electrocatalysts for neutral OER.
基金supported by the National Natural Science Foundation of China (No. 21872153)。
文摘Currently,endeavors to scale up the production of amorphous catalysts are still impeded by intricate synthesis conditions.Here,we have prepared a series of metal-based molybdate via one-step coprecipitation method.After ingredient optimization,amorphous Co_(2)CeFe_(2)-MoO_(4) was identified as exhibiting the highest intrinsic activity among its counterparts.Modulation of electron structure enables Co_(2)CeFe_(2)-MoO_(4) to balance the adsorption behavior towards reactive intermediates.Ultimately,the obtained Co_(2)CeFe_(2)-MoO_(4) molybdate demonstrated a captivating OER performance,showcasing a low overpotential of 230 mV at 10 mA cm^(-2).Moreover,the alkaline electrolyzer employing the Co_(2)CeFe_(2)-MoO_(4) anode exhibited a low cell voltage of 1.50 V for water splitting and underwent an acceptable attenuation of 4.99% after 165 h of continuous operation,demonstrating its favorable catalytic activity and durability.This work provides a facile and eco-friendly synthesis pathway for crafting cost-effective and durable earth-abundant OER electrocatalysts tailored for water splitting to produce clean hydrogen.
基金Financial support from the NSFC(Nos.21972073,22136003,21805166 and 22206188)the 111 Project of China(No.D20015)and Natural Science Foundation of Hubei Province,China(No.2022CFB275)is gratefully acknowledged。
文摘Sodium percarbonate(Na_(2)CO_(3)·1.5H_(2)O_(2),SPC)has been extensively employed as a solid substitute of H_(2)O_(2)for Fenton process in water treatment,because of its high stability during the production,transport,storage and usage.In addition,SPC can be applied in a wider range of work pH,it is also applied as a buffer in Fenton reaction for preventing a drop in pH.Herein,we have synthesized basic copper molybdate(BCM)nanoblocks with the molecular formula of Cu_(3)(MoO_(4))_(2)(OH)_(2)as an efficient and heterogeneous catalyst for antibiotics degradation via percarbonate activation.First,fully physical characterizations confirmed BCM nanocomposite exhibited a structure of nanoblocks.We also found that BCM/SPC system could work in a much wider pH range,compared with H_(2)O_(2).Then,BCM/SPC system presented a good anti-interference ability for natural organic matter in OTC degradation.EPR results and Quenching tests confirmed that the co-presence of·CO_(3)-,·O_(2)-,1O_(2)and·OH in BCM/SPC system.
基金supported by Fundamental Research Funds for the Central Universities (2662014BQ061, 2015PY120, 2015PY047, 2016PY088)the National Natural Science Foundation of China (51572101, 21502059, 21607047)~~
文摘Novel silver/silver molybdate（Ag/Ag2MoO4） composites with surface plasmon resonance（SPR）-enhanced photocatalytic performance were successfully fabricated via a facile one-pot hydrothermal route with the presence of sodium dodecyl sulfate（SDS） in this study.The as prepared silver/silver molybdate（Ag/Ag2MoO4） composites were systematically characterized by X-ray diffraction（XRD）,scanning electron microscopy（SEM） and ultraviolet-visible diffuse reflectance absorption spectroscopy（DRS） in order to investigate their crystal structure,morphology and optical property as well.The photocatalytic activities of the composites were subsequently evaluated by their ability to degrade rhodamine B（RhB） under visible-light irradiation.Varies of controlled experiments were then carefully operated to gain a deep insight into the assembling of Ag/Ag2MoO4composites.It was found that preparation conditions such as pH,reaction time,and the amount of surfactant played important roles in the formation of composites with octahedral microstructures.And the composite obtained at 160 ℃ using 0.5 g of sodium dodecyl sulfate exhibited the highest photocatalytic performance under visible-light irradiation.Capture experiments were also conducted to clarify the function of different active species generated on the surface of Ag/Ag2MoO4during the photocatalytic process,in which both holes and ·OH radicals were found to play crucial role in photocatalytic removal of RhB under visible light irradiation.A possible photocatalytic mechanism of Ag/Ag2MoO4 was finally proposed on the basis of all the results to explain the higher photocatalytic activity of the octahedral Ag/Ag2MoO4 composites.It was inferred that the photoinduced ＂hot＂ electrons can quickly transfer from the Ag NPs to the conduction band of Ag2MoO4 and react with oxygen and H2O to generate a large quality of active radicals such as ·OH and ·O2^- because of the SPR effects.Besides,this SPR effects of Ag nanoparticles deposited on the surface of Ag2MoO4 can not only dramatically amplify its light absorption,especially in the visible region,but also promote the separation of photoexcited electron-hole pairs and effectively decrease electron-hole recombination.
基金the National Natural Science Foundation of China(No.52273267)the Fundamental Research Funds for the Central Universities(No.30920041102)。
文摘Transition metal molybdate(RMoO4)has been extensively studied in optics,electricity and catalysis due to its low cost and multivalent Mo atoms,while its poor electrical conductivity limits its application in electromagnetic wave absorption(EMA).Compounding molybdate with conductive materials is an effective way to improve its electrical conductivity.In this work,a homogeneous coating on the molybdate surface was achieved by utilizing a pyrrole oxidation polymerization mechanism,and then stabilized composites of Molybdate@Carbon(RMoO4@C)were obtained by high-temperature pyrolysis.The EMA properties of the nanocomposites were tuned by substituting the species of transition metal elements(RMoO_(4)@C,R=Fe,Co,Cu).Among them,Fe_(2)(MoO_(4))_(3)@C has a minimum reflection loss of−60.62 dB at an ultra-low thickness of 1.7 mm,and the effective absorption bandwidth(EAB)can reach 4.75 GHz at 3.00 mm.This work expands the range of applications for molybdate and provides a new material basis for building high-performance EMA materials.
基金supported by the Science and Technology Research Projects of the Education Department of Jilin Province (No.2009.272)
文摘A new polyoxomolybdate compound,namely {[MnII（L）（4,4？-Hbipy）（H2O）2]2 [Mo5O15（PO4）2]}.2H2O 1（L = 3-（2-pyridyl）pyrazole,4,4＇-Hbipy = protonated 4,4＇-bipyridine）,was designed and synthesized under hydrothermal conditions.Single-crystal X-ray diffraction analysis result reveals that the [Mo5O15（PO4）2]6-cluster in compound 1 links to two MnII cations via the oxygen of PO43-,which is further coordinated by one 3-（2-pyridyl）pyrazole,one 4,4＇-Hbipyridine,and two water molecules.
基金The work was supported by NNSFC (No. 20501011) Liaocheng University (31801)
文摘A new polyoxomolybdate complex HNaT[Mo36O112（H2O）16]·47H2O 1 has been prepared in the beaker solution and characterized by single-crystal X-ray diffraction and elemental analyses. Crystal data： H127Mo36Na7O175, Mr = 6542.79, monoclinic, C2/c, a = 40.891（6）, b = 17.900（3）, c = 25.580（4）A, β = 125.673（2）°, V = 15210（4）A3, Z = 4, Dc = 2.857 g/cm^3, F（000） = 12464,μ = 3.013 mm^-1, R = 0.0633 and wR = 0.1654 （I 〉 20（I））. With the bridging sodium cations, the [Mo36Ou2（H2O）16]^8- units in compound 1 are linked to form a one-dimensional structure, on the basis of which a three-dimensional architecture is further constructed via other sodium cations and complicated hydrogen bonds.
基金supported by Financial support from the Natural Science Foundation of Shandong Province (BR2010BQ023)Shandong Provincial Education Department,and Qilu Normal University
文摘Two new polyoxomolybdate compounds,namely（CuIIL2）2[CuⅡ（HL）2]2[Mo8O26（HL）2].（H2O）4（1） and [CuⅡ（HL）2]2[β-Mo8O26]（HL）2（2）（HL=imidazole）,were designed and synthesized under hydrothermal conditions.X-ray diffraction analyses reveal that compound 1 consists of one Mo8O26（HL）24-cluster,two CuL2,two Cu（HL）22＋,and four disassociated water molecules;and compound 2 is constructed by one β-Mo8O264-cluster,two Cu（HL）22＋,and two uncoordinated imidazole molecules.
基金Supported by the 973 Key Program of the MOST (2006CB932904,2007CB815304)the National Natural Science Foundation of China (20873150,20821061,and 50772113)+2 种基金the Chinese Academy of Sciences (KJCX2-YW-M05)the Chinese Academy of Sciences (''Hundred Talents Program'') Ministry of Science and Technology of China (Project of ''973'' plan,No. 2007CB607606),and Shandong Provincial Education Department and Qilu Normal University
文摘Two new polyoxomolybdate compounds,namely CuII2（HL）3]2[Mo8O26]·（H2O）4（1） and [NiII（HL）3]2（Mo8O26）·（H2O）3（2）（HL = 3-（2-pyridyl）pyrazole）,were designed and synthesized under hydrothermal conditions.X-ray diffraction analyses reveal that compound 1 consists of one β-Mo8O264-cluster and a Cu2 dimer which is built from two Cu（II） ions linked by three 3-（2-pyridyl）pyrazole ligands.Compound 2 is generated by two kinds of polyoxomolybdate clusters of α-[Mo8O26]4-and β-[Mo8O26]4-.In complexes 1 and 2,the multi-dimensional frameworks are con-structed with the help of hydrogen-bonding links between the terminaloxygen atoms of [Mo8O26]4-,water molecules,and 3-（2-pyridyl）pyrazole ligands.Crystal data of 1：C24H25Cu2Mo4N9O15,Mr = 1190.37,monoclinic,space group P21/c,a = 10.850（2）,b = 18.510（4）,c = 17.230（3） ,β = 100.57（3）°,V = 3401.6（12） 3,Z = 4,Dc = 2.324 g/cm3,F（000） = 2312,μ = 2.742 mm-1,R = 0.0302 and wR = 0.0775（Ⅰ 〉 2σ（Ⅰ））;Crystal data for 2：C48H48Mo8N18Ni2O29,Mr = 2225.98,monoclinic,space group P21/n,a = 20.799（2）,b = 14.7970（13）,c = 23.141（2） ,β = 91.6180（10）°,V = 7119.0（11） 3,Z = 4,Dc = 2.077 g/cm3,F（000） = 4344,μ = 1.968 mm-1,R = 0.0309 and wR = 0.0696（Ⅰ〉 2σ（Ⅰ））.
基金Project(2014CB643405)supported by the National Basic Research Program of China
文摘The removal of tungsten(W)and vanadium(V)from molybdate solutions was studied using the poly hydroxyl chelating resin D403in batch and column experiments.The batch experiments indicated that tungsten and vanadium could be preferentially adsorbed by the D403resin for4h in molybdate solution at a pH of approximately9.25.Separation factors,αVMo andαWMo,wereabove45and18,respectively,when the molar ratios of Mo/V and Mo/W in the solution exceeded40.Elution tests illustrated that vanadium and tungsten could be easily eluted from the resin with1mol/L sodium hydroxide solution in only1h.To further explore the sorption mechanism of the resin,the experimental equilibrium isotherm data of the three metals fitted well with the Freundlich model.The column experiments confirmed the adaptability of the D403resin in the production of sodium molybdate with a removal rate of tungsten surpassing90%and that of vanadium of99.4%.
基金Funded by the General Program of Natural Science Foundation of Jiangsu Province of China(No.BK20171440)the Natural Science Foundation of Nanjing University of Posts and Telecommunications(NY218039)
文摘In order to effectively improve the corrosion resistance of aluminum alloys, anodic oxidation technique was used to generate the oxide film. We investigated the influences of two inorganic corrosion inhibitors(ammonium dihydrogen phosphate and sodium molybdate) on the corrosion resistance of anodic oxidation films on 2024 aluminum alloy, and studied the synergistic effect of two corrosion inhibitors. The corrosion resistance of anodic oxidation film in 3.5 wt% NaCl solution was evaluated by electrochemical impedance spectroscopy(EIS) and potentiodynamic polarization curves. Results show that, after adding the single ammonium dihydrogen phosphate or sodium molybdate of 0.01 M to oxalic acid electrolyte, inhibition efficiencies of the anodized samples are 10% and 47%, respectively. However, in the presence of two inhibitors with the same concentration of 0.01 M, inhibition efficiency can be as high as 92%. Therefore, we observed the significantly synergistic corrosion inhibition effect of molybdate and phosphate ions for anodic oxidation film formed on 2024 aluminum alloy.
文摘Trivalent samarium ion (Sm^(3+)) activated calcium molybdate (CaMoO_4) phosphor was prepared by solid-state reaction in air. The XRD pattern of the powder CaMoO_4∶Sm shows that the CaMoO_4∶Sm single phase is developed fully through our preparation procedure. The excitation spectrum of CaMoO_4∶Sm is composed of a broad absorption of host and some sharp lines of the f-f transition absorption of Sm^(3+). Illustrated in photoluminescence spectrum, CaMoO_4 doped with Sm^(3+) displays orange red emission that is ascribed to the inner 4f^5 electron transitions ~6H_(7/2)(orange)and ~6H_(9/2)(red)of Sm^(3+). Different from the sites of Sm^(3+) in CdWO_4, the Sm^(3+) ions substitute for the Ca^(2+) and form only one type emission center in the CaMoO_4 crystal lattice.
基金Supported by the Natural Science Foundation of Henan Province (No. 0611011900)
文摘A novel transition metal ion bridging bis（diphosphopentamolybdates） has been synthesized and characterized by elemental analysis,IR spectrum,UV spectrum and single-crystal X-ray diffraction.The single-crystal structure analysis shows that the compound consists of seven charge-compensating 2,2＇-biimidazole cations （BIIM=2,2＇-biimidazole） and one dumbbell-like [Mn（H2O）4（P2Mo5O23）2]10-heteropolyanion which is constructed by two [P2Mo5O23]6-clusters bridged through one [Mn（H2O）4]2＋ cation.
基金Project(2017M610766)supported by China Postdoctoral Science FoundationProject(FRF-BD-17-010A)supported by the Fundamental Research Funds for the Central Universities,China
文摘Calcium molybdate(CaMoO4)is the main component of powellite and is a predominant intermediate in the pyrometallurgical and hydrometallurgical process of molybdenum.The extraction of Mo from CaMoO4 by a combination of phosphoric acid and hydrochloric acid was investigated.For further understanding of the leaching mechanism,the effects of five key factors were studied to describe the leaching kinetics.The results indicated that the dissolution rate of CaMoO4 was independent of the stirring speed.Mo extraction significantly increased with increasing HCl concentration and temperature,but decreased with increasing particle size.A shrinking core model with surface chemical reaction was found to withstand the dissolution of CaMoO4.The apparent activation energy was calculated to be 70.879 kJ/mol,and a semi-empirical equation was derived for the rate of reaction.
基金Project(51374185) supported by the National Natural Science Foundation of China
文摘A mechanism study on MoO2 electrodeposition from ammonium molybdate solution was presented via linear sweep voltammetry,species distribution diagram,Raman spectra,Fourier transform infrared spectrometry and X-ray diffractometry.The results show that there exist two reducible species in ammonium molybdate aqueous solution,i.e.Mo7 O24^6- and molybdenum ammonium complex.In weak acid medium without NH4^+,an obvious reduction peak denoting the reduction of Mo7 O24^6- to molybdenum(Ⅳ)oxides emerges at around-0.7 V(vs SCE).While in neutral and basic solutions without NH4^+,the dominant species changes to MoO4^2-,and accordingly,no reduction peak appears except hydrogen evolution.NH4^+ plays an important role in MoO2 electrodeposition.A new current peak appears at-1.25 V(vs SCE)in both acid and basic solutions,which is attributed to the reduction of molybdenum complex.The effects of solution composition and the electrodeposition conditions on the current efficiency were discussed systematically.By optimizing the electrodeposition conditions,the current efficiency can reach up to51.9%.
基金Projects(51334008,51304243,51604160)supported by the National Natural Science Foundation of ChinaProject(2016zzts037)supported by the Fundamental Research Funds for the Central Universities,China
文摘Considering the different geochemical enrichment behaviors of W and Mo,Fe?Mn binary oxide(FMBO),ferric hydroxide(Fe(OH)3)and manganese dioxide(MnO2)were studied to separate W from molybdate solution,respectively.The experimental results demonstrated that Fe?Mn binary oxide(FMBO)was the most suitable adsorbent for the separation.Under a wide pH(6.9?11.3)region,more than80%W removal efficiency and less than3%Mo loss could be obtained.In addition,the Fe?Mn binary oxide adsorbent can be regenerated by treating with3mol/L NaOH,and the W adsorption efficiency was retained after five adsorption?desorption?regeneration cycles.All these indicate that the Fe?Mn binary oxides have the potential for the separation of W from molybdate solution.
基金Project (2014CB643405) supported by National Research Development Program of China
文摘The equilibrium adsorption isotherm and kinetic of the sorption process for W and Mo on macro chelating resin D403 were investigated on single Na2 Mo O4 and Na2WO4 solutions.The sorption isotherm results show that the adsorption process of W obeys the Freundlich model very well whereas the exchange process with Mo approximately follows the Henry model.The kinetic experiments show that the intraparticle diffusion process was the rate-determining step for W sorption on the resin,and the corresponding activation energy is calculated to be 21.976 k J/mol.
基金Project supported by the Hebei Developing Foundation of Science &Technology (51215103b)
文摘In order to prepare fluorescent material for white Light Emitting Diodes （LEDs）, a new Eu^3＋ activated molybdate phosphor SrMoO4 was fabricated with solid-state method. X-ray diffraction （XRD） showed that the doping of trivalent europium ion reduced the lattice parameters. The excitation and emission spectra indicated that this phosphor could be excited effectively by the visible light, and then emitted red light with the peaks located at 616 and 624 nm. The influence of Eu^3＋ concentration on the luminescent properties of Eu^3＋ doped SrMoO4 was investigated and the 25% （mole fraction） was the appropriate molar concentration. The reaction time and temperature had obvious effect on the luminescent properties. The luminescent intensity reached the strongest when it was sintered at 800 ℃ for 3 h.
基金the financial support by the National Key Basic Research Development Program "973" Project (2012CB224800) of China
文摘The MoS_2 catalysts were prepared from various molybdate precursors including inorganic and organic molybdate compounds. The sulfidation degree and morphology of active phases of MoS_2 activated by various molybdate precursors in H_2S/H_2 stream at different temperatures were studied by X-ray photoelectron spectroscopy(XPS) and high-resolution transmission electron microscopy(HRTEM). The organic molybdate precursors lead to MoS_2 catalysts with higher sulfidation degree and smaller active phases to demonstrate higher catalytic activity during hydrodesulfurizaiton(HDS) of 4,6-DMDBT.
