An unexpected but welcome compound 1 obtained through organic synthesis, c an find a lot of applications in electrochemistry, industrial extracting agent f or gold and antiwear additive in lubricating oil. The Ni cent...An unexpected but welcome compound 1 obtained through organic synthesis, c an find a lot of applications in electrochemistry, industrial extracting agent f or gold and antiwear additive in lubricating oil. The Ni center in compound 1 ha s an octahedral geometry with a tetramethylammonium cation as a charge balance. CCDC: 252203.展开更多
The electrodeposition behaviors of nickel on glassy carbon（GC） and carbon steel（CS） electrodes were investigated in the14.3%-85.7%（mole fraction） betaine.HCl ethylene glycol（EG） ionic liquid using cyclic volta...The electrodeposition behaviors of nickel on glassy carbon（GC） and carbon steel（CS） electrodes were investigated in the14.3%-85.7%（mole fraction） betaine.HCl ethylene glycol（EG） ionic liquid using cyclic voltammetry and chronoamperometry.The results indicated that the reduction of Ni（Ⅱ） on CS electrode via a diffusion-controlled quasi-reversible process was much more facile and easier than that occurred on GC electrode,which followed a diffusion-controlled three-dimensional instantaneous nucleation and growth.Scanning electron microscopy was used to observe that the deposit was dense and contained fine crystallites with average size of（80±4） nm.Energy dispersive spectrometer analysis showed that the obtained deposit was metallic nickel.X-ray diffraction spectroscopy indicated that（111） plane was the most preferred crystal orientation.The nickel deposit was luminous and bright,and had good adhesion with the CS substrate.展开更多
LiNi0.8Co0.1Mn0.1O2 cathode was synthesized using transition metal acetates under different synthesis conditions. Simultaneous thermogravimetric–differential scanning calorimetry–derivative thermogravimetric analysi...LiNi0.8Co0.1Mn0.1O2 cathode was synthesized using transition metal acetates under different synthesis conditions. Simultaneous thermogravimetric–differential scanning calorimetry–derivative thermogravimetric analysis was applied to investigating the mixture of transition metal acetates. X-ray powder diffraction and charge–discharge test were adopted to characterize the as-prepared LiNi0.8Co0.1Mn0.1O2. The mixture of transition metal acetates undergoes dehydration and decomposition during heating. All the examined LiNi0.8Co0.1Mn0.1O2 samples have a layered structure with R3 m space group. LiNi0.8Co0.1Mn0.1O2 samples prepared with different lithium sources under different synthesis conditions exhibit very different charge–discharge performances. The sample synthesized via the procedure of sintering at 800 °C after heating lithium carbonate and transition metal acetates at 550 °C achieves a highest capacity of 200.8 m A·h/g and an average capacity of 188.1 mA ·h/g in the first 20 cycles at 0.2C.展开更多
To extract molybdenum and nickel from the roasted Ni-Mo ore, a process of hydrochloric acid leaching, sulphation roasting and water leaching was investigated. The results showed that this process could get a high leac...To extract molybdenum and nickel from the roasted Ni-Mo ore, a process of hydrochloric acid leaching, sulphation roasting and water leaching was investigated. The results showed that this process could get a high leaching rate of Mo and Ni. Under the optimum conditions of hydrochloric acid leaching （roasted Ni-Mo ore leached with 0.219 mL/g hydrochloric acid addition at 65 ℃ for 30 min with a L/S ratio of 3 mL/g）, sulphation roasting （51.9% sulfiaric acid addition, roasting temperature 240 ℃ for 1 h）, followed by leaching with the first stage hydrochloric acid leaching solution at 95 ℃ for 2 h, the leaching rates of Mo and Ni reached 95.8% and 91.3%, respectively.展开更多
A calcified roasting-acid leaching process was developed as a highly effective method for the extraction of valuable metals from low nickel matte in the presence of CaO additive. The influences of process parameters o...A calcified roasting-acid leaching process was developed as a highly effective method for the extraction of valuable metals from low nickel matte in the presence of CaO additive. The influences of process parameters on the metal extraction were studied, including the roasting temperature, roasting time, addition of CaO, H2SO4 concentration and liquid-solid ratio. Under the optimum condition, 94.2% of Ni, 98.1% of Cu, 92.2% of Co and 89.3% of Fe were recovered. Additionally, 99.6% of Fe was removed from the leachate as goethite by a subsequent goethite iron precipitation process. The behavior and mechanism of CaO additive in the roasting process was clarified. The role of CaO is to prevent the formation of nonferrous metal ferrite phases by a preferential reaction with Fe2O3 during the roasting process. The metal oxides(Cu O and NixCu1-xO) remained stable during high-temperature roasting and were subsequently efficiently leached using a sulfuric acid solution.展开更多
The liquid-phase hydrogenation of butyronitrile to saturated amines was studied on silica- supported Ni catalysts prepared by either incipient-wetness impregnation (Ni/SiO2-I) or ammonia (Ni/SiO2-A) methods. A Ni/SiO2...The liquid-phase hydrogenation of butyronitrile to saturated amines was studied on silica- supported Ni catalysts prepared by either incipient-wetness impregnation (Ni/SiO2-I) or ammonia (Ni/SiO2-A) methods. A Ni/SiO2-Al2O3-I sample was also used. Ni/SiO2-I was a non-acidic catalyst containing large Ni^0 particles of low interaction with the support, while Ni/SiO2-A was an acidic catalyst due to the presence of Ni^2+ species in Ni phyllosilicates of low reducibility. Ni/SiO2-I formed essentially butylamine (80%), and dibutylamine as the only byproduct. In contrast, Ni/SiO2-A yielded a mixture of dibutylamine (49%) and tributylamine (45%), being the formation of butylamine almost completely suppressed. The selective formation of secondary and tertiary amines on Ni/SiO2-A was explained by considering that butylamine is not release to the liquid phase during the reaction because it is strongly adsorbed on surface acid sites contiguous to Ni^0 atoms, thereby favoring the butylimine/butylamine condensation to higher amines between adsorbed species.展开更多
A number of synergistic solvent extraction （SSX） systems have been developed to recover nickel, cobalt, zinc and copper from sulphuric and chloride leach solutions by the solvent extraction team of CSIRO, Australia....A number of synergistic solvent extraction （SSX） systems have been developed to recover nickel, cobalt, zinc and copper from sulphuric and chloride leach solutions by the solvent extraction team of CSIRO, Australia. These in- clude （1） Versatic 10/CLXS0 system for the separation of Ni from Ca in sulphate solutions, （2） Versatic 10/4PC system for the separation of Ni and Co from Mn/Mg/Ca in sulphate solutions, （3） Cyanex 471X/HRJ-4277 system for the separation of Zn from Cd in sulphate solutions, （4） Versatic 10/LIX63 system for the separation of Co from Mn/Mg/Ca in sulphate solutions, （5） Versatic 10/LIX63/TBP system for separation of Ni and Co from Mn/Mg/Ca in sulphate solutions, （6） Versatic 10/LIX63 system for the separation of cobalt from nickel in sulphate solutions by difference in kinetics, （7） Cyanex 272/LIX84 system for the separation of Cu/Fe/Zn from Ni/Co in sulphate solutions, （8） Versatic 10/LIX63fFBP system to recover Cu/Ni from strong chloride solutions, and [9） Versatic 10/LIX63 system to separate Cu from Fe in strong chloride solutions. The synergistic effect on metal separation and efficiency is presented and possible industrial applications are demonstrated. The chemical stability of selected SSX systems is also reported.展开更多
Water-insoluble bagasse xanthates were prepared by xanthation of alkalified celluloses by treating bagasse with chromium hydroxide reauction effluent.The removel of nickel from both test solutions and electroplating i...Water-insoluble bagasse xanthates were prepared by xanthation of alkalified celluloses by treating bagasse with chromium hydroxide reauction effluent.The removel of nickel from both test solutions and electroplating industrial wastewater samples with BX was investigated. The process was studied taking into account such parameters as pH of water, precipitation time, xanthate dosage and storage time of BX. These products were found to be highly efficient in removing nickel. The residual con centration of nickel after treatment can be reduced to a value Of the ordor of 0. 01mg·1￣-1.展开更多
Rational design of low‐cost and efficient electrocatalysts for ethanol oxidation reaction(EOR)is imperative for electrocatalytic ethanol fuel cells.In this work,we developed a copper‐doped nickel oxyhydroxide(Cu‐do...Rational design of low‐cost and efficient electrocatalysts for ethanol oxidation reaction(EOR)is imperative for electrocatalytic ethanol fuel cells.In this work,we developed a copper‐doped nickel oxyhydroxide(Cu‐doped NiOOH)catalyst via in situ electrochemical reconstruction of a NiCu alloy.The introduction of Cu dopants increases the specific surface area and more defect sites,as well as forms high‐valence Ni sites.The Cu‐doped NiOOH electrocatalyst exhibited an excellent EOR performance with a peak current density of 227 mA·cm^(–2)at 1.72 V versus reversible hydrogen electrode,high Faradic efficiencies for acetate production(>98%),and excellent electrochemical stability.Our work suggests an attractive route of designing non‐noble metal based electrocatalysts for ethanol oxidation.展开更多
The crystal structure of the title complex having the stoichiometric formula [Ni\|(phen) 3]Pic 2·2CH 3CN (Pic=picrate anion; phen=1,10\|phenanthroline) has been determined by single-crystal X-ray diffraction. ...The crystal structure of the title complex having the stoichiometric formula [Ni\|(phen) 3]Pic 2·2CH 3CN (Pic=picrate anion; phen=1,10\|phenanthroline) has been determined by single-crystal X-ray diffraction. The crystal (C 52 H 34 N 14 O 14 Ni, M r=1137.63) belongs to the triclinic system, space group P1(#2) with the following crystallographic parameters: a = 14\^130(1), b=15\^256(3), c=13.673(2); α=109.11(1), β =90.92(4), γ=66.75(3)°; V=2537\^72 3, D c=1.489g/cm 3, μ(MoKα)=4.66cm -1 , F(000)=1168, Z=2, and final R=0.062 and R w=0.078 for 4917 observed reflections (I>2.00σ(I)). The analytical results of crystal structure and spectroscopic properties show that nickel(II) cation coordination environment is a distorted octahedral geometry, the Ni 2+ ion is coordinated with six nitrogen atoms~ of three phen directly, while two picrate anions and two acetonitrile molecules do not take part in coordination~.展开更多
NiFe(oxy)hydroxides nanosheets were synthesized on nickel foams via co-precipitation and electrochemical activation. It is found that the phosphate precursors(Na_(3)PO_(4), Na_(2)HPO_(4)and NaH_(2)PO_(4)) have diverse...NiFe(oxy)hydroxides nanosheets were synthesized on nickel foams via co-precipitation and electrochemical activation. It is found that the phosphate precursors(Na_(3)PO_(4), Na_(2)HPO_(4)and NaH_(2)PO_(4)) have diverse effects on the morphology and thus the oxygen evolution reaction activity of the formed final catalysts. The resulting NiFe(oxy)hydroxides nanosheets prepared with Na_(2)HPO_(4)demonstrate a low overpotential of 205 m V to achieve a current density of 50 mA/cm^(2) with a Tafel slope down to 30 mV/dec in 1 mol/L KOH, and remain stable for 20 h during stability test.展开更多
A novel two-dimensional compound [Ni0.5(H2O)1.5{Ni(en)2}3V18O42(Cl)]3.5H2O 1 has been hydrothermally synthesized and characterized by IR, elemental analysis, and single-crystal X-ray diffraction analysis. Crystal data...A novel two-dimensional compound [Ni0.5(H2O)1.5{Ni(en)2}3V18O42(Cl)]3.5H2O 1 has been hydrothermally synthesized and characterized by IR, elemental analysis, and single-crystal X-ray diffraction analysis. Crystal data for 1: monoclinic, space group C2/c with a = 12.824(3), b = 27.873(6), c = 21.092(4) , b = 92.93(3), V = 7529(3) 3, Z = 4, Dc = 2.012 g/cm3, Mr = 2280.56, F(000) = 4476 and m = 3.092 mm-1. The final R and wR are 0.0769 and 0.1783, respectively for 4203 observed reflections with I>2s(I). The structure consists of [V18O42(Cl)]7- clusters linked by trans- {Ni(en)2} groups into linear chains, while cis-{Ni(en)2} groups provide the cross-linking adjacent chains to form a two-dimensional structure.展开更多
文摘An unexpected but welcome compound 1 obtained through organic synthesis, c an find a lot of applications in electrochemistry, industrial extracting agent f or gold and antiwear additive in lubricating oil. The Ni center in compound 1 ha s an octahedral geometry with a tetramethylammonium cation as a charge balance. CCDC: 252203.
基金Projects(51274108,21263007,51204080)supported by the National Natural Science Foundation of ChinaProject(2011FA009)supported by the Applied Research Foundation of Yunnan Province,ChinaProject(14118441)supported by the Talents Cultivation Foundation of Kunming University of Science and Technology,China
文摘The electrodeposition behaviors of nickel on glassy carbon（GC） and carbon steel（CS） electrodes were investigated in the14.3%-85.7%（mole fraction） betaine.HCl ethylene glycol（EG） ionic liquid using cyclic voltammetry and chronoamperometry.The results indicated that the reduction of Ni（Ⅱ） on CS electrode via a diffusion-controlled quasi-reversible process was much more facile and easier than that occurred on GC electrode,which followed a diffusion-controlled three-dimensional instantaneous nucleation and growth.Scanning electron microscopy was used to observe that the deposit was dense and contained fine crystallites with average size of（80±4） nm.Energy dispersive spectrometer analysis showed that the obtained deposit was metallic nickel.X-ray diffraction spectroscopy indicated that（111） plane was the most preferred crystal orientation.The nickel deposit was luminous and bright,and had good adhesion with the CS substrate.
基金Project(2010ZC051)supported by the Natural Science Foundation of Yunnan Province,ChinaProject(20140439)supported by the Analysis and Testing Foundation from Kunming University of Science and Technology,ChinaProject(14118245)supported by the Starting Research Fund from Kunming University of Science and Technology,China
文摘LiNi0.8Co0.1Mn0.1O2 cathode was synthesized using transition metal acetates under different synthesis conditions. Simultaneous thermogravimetric–differential scanning calorimetry–derivative thermogravimetric analysis was applied to investigating the mixture of transition metal acetates. X-ray powder diffraction and charge–discharge test were adopted to characterize the as-prepared LiNi0.8Co0.1Mn0.1O2. The mixture of transition metal acetates undergoes dehydration and decomposition during heating. All the examined LiNi0.8Co0.1Mn0.1O2 samples have a layered structure with R3 m space group. LiNi0.8Co0.1Mn0.1O2 samples prepared with different lithium sources under different synthesis conditions exhibit very different charge–discharge performances. The sample synthesized via the procedure of sintering at 800 °C after heating lithium carbonate and transition metal acetates at 550 °C achieves a highest capacity of 200.8 m A·h/g and an average capacity of 188.1 mA ·h/g in the first 20 cycles at 0.2C.
基金Project(51104186)supported by the National Natural Science Foundation of ChinaProjects(2016zzts282,2016zzts283)supported by the Fundamental Research Funds for the Central Universities of Central South University,China
文摘To extract molybdenum and nickel from the roasted Ni-Mo ore, a process of hydrochloric acid leaching, sulphation roasting and water leaching was investigated. The results showed that this process could get a high leaching rate of Mo and Ni. Under the optimum conditions of hydrochloric acid leaching （roasted Ni-Mo ore leached with 0.219 mL/g hydrochloric acid addition at 65 ℃ for 30 min with a L/S ratio of 3 mL/g）, sulphation roasting （51.9% sulfiaric acid addition, roasting temperature 240 ℃ for 1 h）, followed by leaching with the first stage hydrochloric acid leaching solution at 95 ℃ for 2 h, the leaching rates of Mo and Ni reached 95.8% and 91.3%, respectively.
基金Projects(U1860203,U1860108,51574164) supported by the National Natural Science Foundation of China
文摘A calcified roasting-acid leaching process was developed as a highly effective method for the extraction of valuable metals from low nickel matte in the presence of CaO additive. The influences of process parameters on the metal extraction were studied, including the roasting temperature, roasting time, addition of CaO, H2SO4 concentration and liquid-solid ratio. Under the optimum condition, 94.2% of Ni, 98.1% of Cu, 92.2% of Co and 89.3% of Fe were recovered. Additionally, 99.6% of Fe was removed from the leachate as goethite by a subsequent goethite iron precipitation process. The behavior and mechanism of CaO additive in the roasting process was clarified. The role of CaO is to prevent the formation of nonferrous metal ferrite phases by a preferential reaction with Fe2O3 during the roasting process. The metal oxides(Cu O and NixCu1-xO) remained stable during high-temperature roasting and were subsequently efficiently leached using a sulfuric acid solution.
基金the Universidad Nacional del Litoral (UNL)Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)Agencia Nacional de Promoción Científica y Tecnológica (ANPCyT ), Argentina, for the financial support of this work
文摘The liquid-phase hydrogenation of butyronitrile to saturated amines was studied on silica- supported Ni catalysts prepared by either incipient-wetness impregnation (Ni/SiO2-I) or ammonia (Ni/SiO2-A) methods. A Ni/SiO2-Al2O3-I sample was also used. Ni/SiO2-I was a non-acidic catalyst containing large Ni^0 particles of low interaction with the support, while Ni/SiO2-A was an acidic catalyst due to the presence of Ni^2+ species in Ni phyllosilicates of low reducibility. Ni/SiO2-I formed essentially butylamine (80%), and dibutylamine as the only byproduct. In contrast, Ni/SiO2-A yielded a mixture of dibutylamine (49%) and tributylamine (45%), being the formation of butylamine almost completely suppressed. The selective formation of secondary and tertiary amines on Ni/SiO2-A was explained by considering that butylamine is not release to the liquid phase during the reaction because it is strongly adsorbed on surface acid sites contiguous to Ni^0 atoms, thereby favoring the butylimine/butylamine condensation to higher amines between adsorbed species.
文摘A number of synergistic solvent extraction （SSX） systems have been developed to recover nickel, cobalt, zinc and copper from sulphuric and chloride leach solutions by the solvent extraction team of CSIRO, Australia. These in- clude （1） Versatic 10/CLXS0 system for the separation of Ni from Ca in sulphate solutions, （2） Versatic 10/4PC system for the separation of Ni and Co from Mn/Mg/Ca in sulphate solutions, （3） Cyanex 471X/HRJ-4277 system for the separation of Zn from Cd in sulphate solutions, （4） Versatic 10/LIX63 system for the separation of Co from Mn/Mg/Ca in sulphate solutions, （5） Versatic 10/LIX63/TBP system for separation of Ni and Co from Mn/Mg/Ca in sulphate solutions, （6） Versatic 10/LIX63 system for the separation of cobalt from nickel in sulphate solutions by difference in kinetics, （7） Cyanex 272/LIX84 system for the separation of Cu/Fe/Zn from Ni/Co in sulphate solutions, （8） Versatic 10/LIX63fFBP system to recover Cu/Ni from strong chloride solutions, and [9） Versatic 10/LIX63 system to separate Cu from Fe in strong chloride solutions. The synergistic effect on metal separation and efficiency is presented and possible industrial applications are demonstrated. The chemical stability of selected SSX systems is also reported.
文摘Water-insoluble bagasse xanthates were prepared by xanthation of alkalified celluloses by treating bagasse with chromium hydroxide reauction effluent.The removel of nickel from both test solutions and electroplating industrial wastewater samples with BX was investigated. The process was studied taking into account such parameters as pH of water, precipitation time, xanthate dosage and storage time of BX. These products were found to be highly efficient in removing nickel. The residual con centration of nickel after treatment can be reduced to a value Of the ordor of 0. 01mg·1￣-1.
文摘Rational design of low‐cost and efficient electrocatalysts for ethanol oxidation reaction(EOR)is imperative for electrocatalytic ethanol fuel cells.In this work,we developed a copper‐doped nickel oxyhydroxide(Cu‐doped NiOOH)catalyst via in situ electrochemical reconstruction of a NiCu alloy.The introduction of Cu dopants increases the specific surface area and more defect sites,as well as forms high‐valence Ni sites.The Cu‐doped NiOOH electrocatalyst exhibited an excellent EOR performance with a peak current density of 227 mA·cm^(–2)at 1.72 V versus reversible hydrogen electrode,high Faradic efficiencies for acetate production(>98%),and excellent electrochemical stability.Our work suggests an attractive route of designing non‐noble metal based electrocatalysts for ethanol oxidation.
文摘The crystal structure of the title complex having the stoichiometric formula [Ni\|(phen) 3]Pic 2·2CH 3CN (Pic=picrate anion; phen=1,10\|phenanthroline) has been determined by single-crystal X-ray diffraction. The crystal (C 52 H 34 N 14 O 14 Ni, M r=1137.63) belongs to the triclinic system, space group P1(#2) with the following crystallographic parameters: a = 14\^130(1), b=15\^256(3), c=13.673(2); α=109.11(1), β =90.92(4), γ=66.75(3)°; V=2537\^72 3, D c=1.489g/cm 3, μ(MoKα)=4.66cm -1 , F(000)=1168, Z=2, and final R=0.062 and R w=0.078 for 4917 observed reflections (I>2.00σ(I)). The analytical results of crystal structure and spectroscopic properties show that nickel(II) cation coordination environment is a distorted octahedral geometry, the Ni 2+ ion is coordinated with six nitrogen atoms~ of three phen directly, while two picrate anions and two acetonitrile molecules do not take part in coordination~.
基金supported by the National Natural Science Foundation of China (Nos. 11904411, 52072308)the Fundamental Research Funds for the Central Universities, China (Nos. 3102021MS0404, 3102019JC001)。
文摘NiFe(oxy)hydroxides nanosheets were synthesized on nickel foams via co-precipitation and electrochemical activation. It is found that the phosphate precursors(Na_(3)PO_(4), Na_(2)HPO_(4)and NaH_(2)PO_(4)) have diverse effects on the morphology and thus the oxygen evolution reaction activity of the formed final catalysts. The resulting NiFe(oxy)hydroxides nanosheets prepared with Na_(2)HPO_(4)demonstrate a low overpotential of 205 m V to achieve a current density of 50 mA/cm^(2) with a Tafel slope down to 30 mV/dec in 1 mol/L KOH, and remain stable for 20 h during stability test.
基金This work was supported by NNSFC (No. 20271050 and 20171045) the Educational Ministry of China the Talents Program of the Chinese Academy of Sciences and NSF of Fujian province (E0210029)
文摘A novel two-dimensional compound [Ni0.5(H2O)1.5{Ni(en)2}3V18O42(Cl)]3.5H2O 1 has been hydrothermally synthesized and characterized by IR, elemental analysis, and single-crystal X-ray diffraction analysis. Crystal data for 1: monoclinic, space group C2/c with a = 12.824(3), b = 27.873(6), c = 21.092(4) , b = 92.93(3), V = 7529(3) 3, Z = 4, Dc = 2.012 g/cm3, Mr = 2280.56, F(000) = 4476 and m = 3.092 mm-1. The final R and wR are 0.0769 and 0.1783, respectively for 4203 observed reflections with I>2s(I). The structure consists of [V18O42(Cl)]7- clusters linked by trans- {Ni(en)2} groups into linear chains, while cis-{Ni(en)2} groups provide the cross-linking adjacent chains to form a two-dimensional structure.
