Nano-porous ultra-high specific surface ul- trafine fibers are created by the method of “electrospin- ning-phase separation-leaching” (EPL) for the first time. First of all, polymer solutions of polyacrylonitrile (P...Nano-porous ultra-high specific surface ul- trafine fibers are created by the method of “electrospin- ning-phase separation-leaching” (EPL) for the first time. First of all, polymer solutions of polyacrylonitrile (PAN) and polyvinylpyrrolidone (PVP) blends dissolved in co-solvent are electrospun to make ultrafine fibers when charged to high voltages. The incompatibility of PAN and PVP induces phase separation to form microdomains of PVP in the poly- mer blend ultrafine fibers. Then, PVP microdomains in the blend fibers are leached out in water, and porous PAN ul- trafine fibers are obtained. Lastly, the surface and cross-section of the porous ultrafine fibers are observed in detail by field emission scanning electron microscope (FE- SEM), and the specific surface of the ultrafine fibers is measured by means of nitrogen absorption. With increasing the content of PVP, the specific surface area of the ultrafine fibers increases apparently. The specific surface area of the porous ultrafine fibers with the diameter of 2130 nm is more than 70 m2·g?1. The cross-section of the PAN porous ultrafine fibers after leaching of PVP microdomains from polymer blend fibers with the feed ratio of PAN/PVP of 10/20 shows the characteristic of porous structure with pore diameter of ca 30 nm according to FESEM photo.展开更多
Silicon has been recognized as the most promising anode material for high capacity lithium ion batteries. However, large volume variations during charge and discharge result in pulverization of Si electrodes and fast ...Silicon has been recognized as the most promising anode material for high capacity lithium ion batteries. However, large volume variations during charge and discharge result in pulverization of Si electrodes and fast capacity loss on cycling. This drawback of Si electrodes can be overcome by combination with well-organized graphene foam. In this work, hierarchical three-dimensional carbon-coated mesoporous Si nanospheres@graphene foam （C@Si@GF） nanoarchitectures were successfully synthesized by a thermal bubble ejection assisted chemical-vapor-deposition and magnesiothermic reduction method. The morphology and structure of the as-prepared nanocomposites were characterized by field emission scanning electron microscopy, transmission electron microscopy and Raman spectroscopy. When employed as anode materials in lithium ion batteries, C@Si@GF nanocomposites exhibited superior electrochemical per- formance including a high specific capacity of 1,200 mAh/g at the current density of 1A/g, excellent high rate capabilities and an outstanding cyclability. Post-mortem analyses identified that the morphology of 3D C@Si@GF electrodes after 200 cycles was well maintained. The synergistic effects arising from the combination of mesoporous Si nanospheres and graphene foam nanoarchitectures may address the intractable pulverization problem of Si electrode.展开更多
TiO2-Graphene Oxide intercalated composite (TiO2-Graphene Oxide) has been successfully prepared at low temperature (80°C) with graphite oxide (GO) and titanium sulfate (Ti(SO4)2) as initial reactants.GO was first...TiO2-Graphene Oxide intercalated composite (TiO2-Graphene Oxide) has been successfully prepared at low temperature (80°C) with graphite oxide (GO) and titanium sulfate (Ti(SO4)2) as initial reactants.GO was firstly exfoliated by NaOH and formed single and multi-layered graphite oxide mixture which can be defined as graphene oxide,[TiO]2+ induced by the hydrolysis of Ti(SO4)2 diffused into graphene oxide interlayer by electrostatic attraction.The nucleation and growth of TiO2 crystallites took place at low temperature and TiO2-Graphene Oxide composite was successfully synthesized.Furthermore,the photocatalytic properties of TiO2-Graphene Oxide under the irradiation of UV light were also studied.The results show that the degradation rate of methyl orange is 1.16 mg min-1 g-1(refer to the efficiency of the initial 15 min).Compared with P25 powder,this kind of intercalation composite owns much better efficiency.On the other hand,the reusable properties and stable properties of TiO2-Graphene Oxide intercalated composite are also discussed in this paper.At last,crystalline structure,interface status,thermal properties and microscopic structure of TiO2-Graphene Oxide were characterized by X-ray diffraction (XRD),X-ray photoelectron spectroscopy (XPS),thermogravimetric analysis (TGA),field emission scanning electron microscopy (FESEM) and high-resolution Transmission Electron Microscopy (HRTEM).Also,we have analyzed major influencing factors and mechanism of the composite structures which evidently improve the photocatalytic properties.展开更多
Faceted crystals with exposed highly reactive planes have attracted intensive investigations for applications. Herein, we demonstrate a general synthetic method to prepare mesocrystal Co3O4 with predominantly exposed ...Faceted crystals with exposed highly reactive planes have attracted intensive investigations for applications. Herein, we demonstrate a general synthetic method to prepare mesocrystal Co3O4 with predominantly exposed {111} reactive facets by the in situ thermal decomposition from Co（OH）2 nanoplatelets. The mesocrystal feature was identified by field emission scanning electron microscopy, transmission electron microscopy, selected area electron diffraction, and N2 isotherm analyses. When applied as anode material in lithium-ion batteries, mesocrystal Co3O4 nanoplatelets delivered a high specific capacity and an outstanding high rate performance. The superior electrochemical performance should be ascribed to the predominantly exposed {111} active facets and highly accessible surfaces. This synthetic strategy could be extended to prepare other mesocrystal functional nanomaterials.展开更多
Lithium-ion capacitors(LICs) were fabricated using mesocarbon microbeads(MCMB) as a negative electrode and a mixture of activated carbon(AC) and LiFePO4 as a positive electrode(abbreviated as LAC).The phase structure ...Lithium-ion capacitors(LICs) were fabricated using mesocarbon microbeads(MCMB) as a negative electrode and a mixture of activated carbon(AC) and LiFePO4 as a positive electrode(abbreviated as LAC).The phase structure and morphology of LAC samples were characterized by X-ray diffraction(XRD) and field emission scanning electron microscopy(FESEM).The electrochemical performance of the LICs was studied using cyclic voltammetry,charge-discharge rate measurements,and cycle performance testing.A LIC with 30 wt% LiFePO4 was found to have the best electrochemical performance with a specific energy density of 69.02 W h kg-1 remaining at 4 C rate after 100 cycles.Compared with an AC-only positive electrode system,the ratio of practical capacity to theoretical calculated capacity of the LICs was enhanced from 42.22% to 56.59%.It was proved that adding LiFePO4 to AC electrodes not only increased the capacity of the positive electrode,but also improved the electrochemical performances of the whole LICs via Li+ pre-doping.展开更多
Two types of metal-loaded visible-light-driven photocatalysts,Mo-BiVO4and Ag-BiVO4,were synthesized by wet impregnation method.Material poperties were characterized by UV-vis diffuse reflectance spectroscopy,X-ray dif...Two types of metal-loaded visible-light-driven photocatalysts,Mo-BiVO4and Ag-BiVO4,were synthesized by wet impregnation method.Material poperties were characterized by UV-vis diffuse reflectance spectroscopy,X-ray diffraction,field emission scanning electron microscopy,X-ray photoelectron spectroscopy and low temperature nitrogen adsorption-desorption.Photocatalytic activity of the obtained materials was investigated through degrading methylene blue(MB) solution under visible-light irradiation.The results reveal that both metal loaded-BiVO4catalysts have monoclinic scheelite structure.Mo and Ag exist as oxides on the surface of the particles.The changes of absorption in visible-light region,band gap(E g) and specific surface area(A BET) caused by loading Ag are more obvious than those caused by loading Mo.But the isoelectric point of Ag-BiVO4decreases less than that of Mo-BiVO4does.Both catalysts show higher photocatalytic activity than pure BiVO4,resulting in the significantly improved efficiency of degradation of MB.And the degradation efficiency of these two metal-loaded BiVO4photocatalysts is similar to each other.However,mechanisms of such enhancement are different.The decrease of isoelectric point helps Mo-BiVO4improve the degradation efficiency.As for Ag-BiVO4,the augmentation of absorption in visible-light region as well as the abatement of E g plays more important roles.展开更多
The present work is aimed at studying the microstructure and pitting corrosion behaviour of shielded metal arc welded high nitrogen steel made of Cromang-N electrode. Basis for selecting this electrode is to increase ...The present work is aimed at studying the microstructure and pitting corrosion behaviour of shielded metal arc welded high nitrogen steel made of Cromang-N electrode. Basis for selecting this electrode is to increase the solubility of nitrogen in weld metal due to high chromium and manganese content. Microscopic studies were carried out using optical microscopy(OM) and field emission scanning electron microscopy(FESEM). Energy back scattered diffraction(EBSD) method was used to determine the phase analysis, grain size and orientation image mapping. Potentio-dynamic polarization testing was carried out to study the pitting corrosion resistance in aerated 3.5% NaCl environment using a GillAC electrochemical system. The investigation results showed that the selected Cr-Mn-N type electrode resulted in a maximum reduction in delta-ferrite and improvement in pitting corrosion resistance of the weld zone was attributed to the coarse austenite grains owing to the reduction in active sites of the austenite/delta ferrite interface and the decrease in galvanic interaction between austenite and delta-ferrite.展开更多
Morphology controlled synthesis of nanoparticles of powerful high energetic compounds(HECs) such as l,3,5-trinitro-l,3,5-triazinane(RDX) and 1,3,5,7-tetranitro-l,3,5,7-tetrazocane(HMX) were achieved by a simple solven...Morphology controlled synthesis of nanoparticles of powerful high energetic compounds(HECs) such as l,3,5-trinitro-l,3,5-triazinane(RDX) and 1,3,5,7-tetranitro-l,3,5,7-tetrazocane(HMX) were achieved by a simple solvent—antisolvent interaction(SAI) method at 70 ℃.The effects of different solvents on particle size and morphology of the prepared nano-HECs were studied systematically.Particle size and morphology of the nano-HECs was characterized using field emission scanning electron microscopy(FE-SEM) imaging.X-ray diffraction(XRD) and Fourier transform infrared(FTIR) spectroscopy studies revealed that RDX and HMX were precipitated in their most stable polymorphic forms,i.e.a and P,respectively.Thermogravimetric analysis coupled with differential scanning calorimetry(TGA-DSC) studies showed that the thermal response of the nanoparticles was similar to the respective raw-HECs.HEC nanoparticles with spherical and rod shaped morphology were observed under different solvent conditions.The mean particle size also varied considerably with the use of different solvents.展开更多
p-Phenylenediamine(PPD)functionalized graphene oxide(GO)materials(PPDG)were prepared through a one-step solvothermal process and their application as supercapacitors(SCs)were studied.The PPD is not only as the spacers...p-Phenylenediamine(PPD)functionalized graphene oxide(GO)materials(PPDG)were prepared through a one-step solvothermal process and their application as supercapacitors(SCs)were studied.The PPD is not only as the spacers to prevent aggregating and restacking of the graphene sheets in the preparing process but also as nitrogen sources to obtain the nitrogen-doped graphene.The structures of PPDG were characterized by Fourier transformed infrared spectroscopy(FT-IR),X-ray diffraction spectroscopy(XRD),Raman spectroscopy and X-ray photoelectron spectroscopy(XPS)and the results show that the nitrogen-doped graphene was achieved with nitrogen content as high as 10.85 at.%.The field emission scanning electron microscopy(FE-SEM)and high resolution transmission electron microscopy(HR-TEM)have confirmed that the morphologies of PPDG were loose layered with less aggregation,indicating that PPD molecules,as spacers,effectively prevent the graphene sheets from restacking during the solvothermal reaction.The special loose textures make PPDG materials exhibit excellent electrochemical performance for symmetric SCs with superior specific capacitance(313 F/g at 0.1 A/g),rate capability and cycling stability.The present synthesis method is convenient and may have potential applications as ultrahigh performance SCs.展开更多
Porous anodic oxide films were fabricated galvanostatically on titanium alloy Ti-10V-2Fe-3Al in ammonium tartrate solution with different anodizing time.Scanning electron microscopy(SEM) and field emission scanning el...Porous anodic oxide films were fabricated galvanostatically on titanium alloy Ti-10V-2Fe-3Al in ammonium tartrate solution with different anodizing time.Scanning electron microscopy(SEM) and field emission scanning electron microscopy(FE-SEM) were used to investigate the morphology evolution of the anodic oxide film.It is shown that above the breakdown voltage,oxygen is generated with the occurrence of drums morphology.These drums grow and extrude,which yields the compression stress.Subsequently,microcracks are generated.With continuous anodizing,porous oxides form at the microcracks.Those oxides grow and connect to each other,finally replace the microcrack morphology.The depth profile of the anodic oxide film formed at 1 800 s was examined by Auger electron spectroscopy(AES).It is found that the film is divided into three layers according to the molar fractions of elements.The outer layer is incorporated by carbon,which may come from electrolyte solution.The thickness of the outer layer is approximately 0.2-0.3 μm.The molar fractions of elements in the intermediate layer are extraordinarily stable,while those in the inner layer vary significantly with sputtering depth.The thicknesses of the intermediate layer and the inner layer are 2 μm and 1.0-1.5 μm,respectively.Moreover,the growth mechanism of porous anodic oxide films in neutral tartrate solution was proposed.展开更多
文摘Nano-porous ultra-high specific surface ul- trafine fibers are created by the method of “electrospin- ning-phase separation-leaching” (EPL) for the first time. First of all, polymer solutions of polyacrylonitrile (PAN) and polyvinylpyrrolidone (PVP) blends dissolved in co-solvent are electrospun to make ultrafine fibers when charged to high voltages. The incompatibility of PAN and PVP induces phase separation to form microdomains of PVP in the poly- mer blend ultrafine fibers. Then, PVP microdomains in the blend fibers are leached out in water, and porous PAN ul- trafine fibers are obtained. Lastly, the surface and cross-section of the porous ultrafine fibers are observed in detail by field emission scanning electron microscope (FE- SEM), and the specific surface of the ultrafine fibers is measured by means of nitrogen absorption. With increasing the content of PVP, the specific surface area of the ultrafine fibers increases apparently. The specific surface area of the porous ultrafine fibers with the diameter of 2130 nm is more than 70 m2·g?1. The cross-section of the PAN porous ultrafine fibers after leaching of PVP microdomains from polymer blend fibers with the feed ratio of PAN/PVP of 10/20 shows the characteristic of porous structure with pore diameter of ca 30 nm according to FESEM photo.
文摘Silicon has been recognized as the most promising anode material for high capacity lithium ion batteries. However, large volume variations during charge and discharge result in pulverization of Si electrodes and fast capacity loss on cycling. This drawback of Si electrodes can be overcome by combination with well-organized graphene foam. In this work, hierarchical three-dimensional carbon-coated mesoporous Si nanospheres@graphene foam （C@Si@GF） nanoarchitectures were successfully synthesized by a thermal bubble ejection assisted chemical-vapor-deposition and magnesiothermic reduction method. The morphology and structure of the as-prepared nanocomposites were characterized by field emission scanning electron microscopy, transmission electron microscopy and Raman spectroscopy. When employed as anode materials in lithium ion batteries, C@Si@GF nanocomposites exhibited superior electrochemical per- formance including a high specific capacity of 1,200 mAh/g at the current density of 1A/g, excellent high rate capabilities and an outstanding cyclability. Post-mortem analyses identified that the morphology of 3D C@Si@GF electrodes after 200 cycles was well maintained. The synergistic effects arising from the combination of mesoporous Si nanospheres and graphene foam nanoarchitectures may address the intractable pulverization problem of Si electrode.
基金supported by the National Natural Science Foundation of China (50672066)
文摘TiO2-Graphene Oxide intercalated composite (TiO2-Graphene Oxide) has been successfully prepared at low temperature (80°C) with graphite oxide (GO) and titanium sulfate (Ti(SO4)2) as initial reactants.GO was firstly exfoliated by NaOH and formed single and multi-layered graphite oxide mixture which can be defined as graphene oxide,[TiO]2+ induced by the hydrolysis of Ti(SO4)2 diffused into graphene oxide interlayer by electrostatic attraction.The nucleation and growth of TiO2 crystallites took place at low temperature and TiO2-Graphene Oxide composite was successfully synthesized.Furthermore,the photocatalytic properties of TiO2-Graphene Oxide under the irradiation of UV light were also studied.The results show that the degradation rate of methyl orange is 1.16 mg min-1 g-1(refer to the efficiency of the initial 15 min).Compared with P25 powder,this kind of intercalation composite owns much better efficiency.On the other hand,the reusable properties and stable properties of TiO2-Graphene Oxide intercalated composite are also discussed in this paper.At last,crystalline structure,interface status,thermal properties and microscopic structure of TiO2-Graphene Oxide were characterized by X-ray diffraction (XRD),X-ray photoelectron spectroscopy (XPS),thermogravimetric analysis (TGA),field emission scanning electron microscopy (FESEM) and high-resolution Transmission Electron Microscopy (HRTEM).Also,we have analyzed major influencing factors and mechanism of the composite structures which evidently improve the photocatalytic properties.
文摘Faceted crystals with exposed highly reactive planes have attracted intensive investigations for applications. Herein, we demonstrate a general synthetic method to prepare mesocrystal Co3O4 with predominantly exposed {111} reactive facets by the in situ thermal decomposition from Co（OH）2 nanoplatelets. The mesocrystal feature was identified by field emission scanning electron microscopy, transmission electron microscopy, selected area electron diffraction, and N2 isotherm analyses. When applied as anode material in lithium-ion batteries, mesocrystal Co3O4 nanoplatelets delivered a high specific capacity and an outstanding high rate performance. The superior electrochemical performance should be ascribed to the predominantly exposed {111} active facets and highly accessible surfaces. This synthetic strategy could be extended to prepare other mesocrystal functional nanomaterials.
基金supported by the National Natural Science Foundation of China (51172160,50902102)the National High Technology Research and Development Program of China (2011AA11A232)the National Basic Research Program of China (2012CB720302)
文摘Lithium-ion capacitors(LICs) were fabricated using mesocarbon microbeads(MCMB) as a negative electrode and a mixture of activated carbon(AC) and LiFePO4 as a positive electrode(abbreviated as LAC).The phase structure and morphology of LAC samples were characterized by X-ray diffraction(XRD) and field emission scanning electron microscopy(FESEM).The electrochemical performance of the LICs was studied using cyclic voltammetry,charge-discharge rate measurements,and cycle performance testing.A LIC with 30 wt% LiFePO4 was found to have the best electrochemical performance with a specific energy density of 69.02 W h kg-1 remaining at 4 C rate after 100 cycles.Compared with an AC-only positive electrode system,the ratio of practical capacity to theoretical calculated capacity of the LICs was enhanced from 42.22% to 56.59%.It was proved that adding LiFePO4 to AC electrodes not only increased the capacity of the positive electrode,but also improved the electrochemical performances of the whole LICs via Li+ pre-doping.
基金supported by the National Natural ScienceFoundation of China (20876157)
文摘Two types of metal-loaded visible-light-driven photocatalysts,Mo-BiVO4and Ag-BiVO4,were synthesized by wet impregnation method.Material poperties were characterized by UV-vis diffuse reflectance spectroscopy,X-ray diffraction,field emission scanning electron microscopy,X-ray photoelectron spectroscopy and low temperature nitrogen adsorption-desorption.Photocatalytic activity of the obtained materials was investigated through degrading methylene blue(MB) solution under visible-light irradiation.The results reveal that both metal loaded-BiVO4catalysts have monoclinic scheelite structure.Mo and Ag exist as oxides on the surface of the particles.The changes of absorption in visible-light region,band gap(E g) and specific surface area(A BET) caused by loading Ag are more obvious than those caused by loading Mo.But the isoelectric point of Ag-BiVO4decreases less than that of Mo-BiVO4does.Both catalysts show higher photocatalytic activity than pure BiVO4,resulting in the significantly improved efficiency of degradation of MB.And the degradation efficiency of these two metal-loaded BiVO4photocatalysts is similar to each other.However,mechanisms of such enhancement are different.The decrease of isoelectric point helps Mo-BiVO4improve the degradation efficiency.As for Ag-BiVO4,the augmentation of absorption in visible-light region as well as the abatement of E g plays more important roles.
文摘The present work is aimed at studying the microstructure and pitting corrosion behaviour of shielded metal arc welded high nitrogen steel made of Cromang-N electrode. Basis for selecting this electrode is to increase the solubility of nitrogen in weld metal due to high chromium and manganese content. Microscopic studies were carried out using optical microscopy(OM) and field emission scanning electron microscopy(FESEM). Energy back scattered diffraction(EBSD) method was used to determine the phase analysis, grain size and orientation image mapping. Potentio-dynamic polarization testing was carried out to study the pitting corrosion resistance in aerated 3.5% NaCl environment using a GillAC electrochemical system. The investigation results showed that the selected Cr-Mn-N type electrode resulted in a maximum reduction in delta-ferrite and improvement in pitting corrosion resistance of the weld zone was attributed to the coarse austenite grains owing to the reduction in active sites of the austenite/delta ferrite interface and the decrease in galvanic interaction between austenite and delta-ferrite.
基金Financial assistance from ARMREB(DRDO) under grant No.ARMREB/CDSW/2012/149
文摘Morphology controlled synthesis of nanoparticles of powerful high energetic compounds(HECs) such as l,3,5-trinitro-l,3,5-triazinane(RDX) and 1,3,5,7-tetranitro-l,3,5,7-tetrazocane(HMX) were achieved by a simple solvent—antisolvent interaction(SAI) method at 70 ℃.The effects of different solvents on particle size and morphology of the prepared nano-HECs were studied systematically.Particle size and morphology of the nano-HECs was characterized using field emission scanning electron microscopy(FE-SEM) imaging.X-ray diffraction(XRD) and Fourier transform infrared(FTIR) spectroscopy studies revealed that RDX and HMX were precipitated in their most stable polymorphic forms,i.e.a and P,respectively.Thermogravimetric analysis coupled with differential scanning calorimetry(TGA-DSC) studies showed that the thermal response of the nanoparticles was similar to the respective raw-HECs.HEC nanoparticles with spherical and rod shaped morphology were observed under different solvent conditions.The mean particle size also varied considerably with the use of different solvents.
基金supported by the Ministry of Science and Technology (2012CB933401,2014CB643502)the National Natural Science Foundation of China (51273093,21374050,51373078)+2 种基金Natural Science Foundation of Tianjin (10ZCGHHZ00600)the Synergetic Innovation Center of Chemical Science and Engineering (Tianjin),Science and Technology Research Project of Higher Education of Hebei Province (z2012064)Science Research Project of Langfang Teachers College (LSZQ200908)
文摘p-Phenylenediamine(PPD)functionalized graphene oxide(GO)materials(PPDG)were prepared through a one-step solvothermal process and their application as supercapacitors(SCs)were studied.The PPD is not only as the spacers to prevent aggregating and restacking of the graphene sheets in the preparing process but also as nitrogen sources to obtain the nitrogen-doped graphene.The structures of PPDG were characterized by Fourier transformed infrared spectroscopy(FT-IR),X-ray diffraction spectroscopy(XRD),Raman spectroscopy and X-ray photoelectron spectroscopy(XPS)and the results show that the nitrogen-doped graphene was achieved with nitrogen content as high as 10.85 at.%.The field emission scanning electron microscopy(FE-SEM)and high resolution transmission electron microscopy(HR-TEM)have confirmed that the morphologies of PPDG were loose layered with less aggregation,indicating that PPD molecules,as spacers,effectively prevent the graphene sheets from restacking during the solvothermal reaction.The special loose textures make PPDG materials exhibit excellent electrochemical performance for symmetric SCs with superior specific capacitance(313 F/g at 0.1 A/g),rate capability and cycling stability.The present synthesis method is convenient and may have potential applications as ultrahigh performance SCs.
基金Project(50571003) supported by the National Natural Science Foundation of China
文摘Porous anodic oxide films were fabricated galvanostatically on titanium alloy Ti-10V-2Fe-3Al in ammonium tartrate solution with different anodizing time.Scanning electron microscopy(SEM) and field emission scanning electron microscopy(FE-SEM) were used to investigate the morphology evolution of the anodic oxide film.It is shown that above the breakdown voltage,oxygen is generated with the occurrence of drums morphology.These drums grow and extrude,which yields the compression stress.Subsequently,microcracks are generated.With continuous anodizing,porous oxides form at the microcracks.Those oxides grow and connect to each other,finally replace the microcrack morphology.The depth profile of the anodic oxide film formed at 1 800 s was examined by Auger electron spectroscopy(AES).It is found that the film is divided into three layers according to the molar fractions of elements.The outer layer is incorporated by carbon,which may come from electrolyte solution.The thickness of the outer layer is approximately 0.2-0.3 μm.The molar fractions of elements in the intermediate layer are extraordinarily stable,while those in the inner layer vary significantly with sputtering depth.The thicknesses of the intermediate layer and the inner layer are 2 μm and 1.0-1.5 μm,respectively.Moreover,the growth mechanism of porous anodic oxide films in neutral tartrate solution was proposed.
