Extraction separation of germanium with hydroxamic acid HGS98

Ｔｈｅｓｅｐａｒａｔｉｏｎｏｆｇｅｒｍａｎｉｕｍｆｒｏｍａｃｉｄｉｃｌｅａｃｈｌｉｑｕｏｒｓ,ｅｓｐｅｃｉａｌｌｙｉｎｚｉｎｃｐｒｏｄｕｃｔｉｏｎ ,ｈａｓａｔｔｒａｃｔｅｄｇｒｅａｔａｔｔｅｎｔｉｏｎｂｅｃａｕｓｅｏｆｉｔｓｉｎｃｒｅａｓｉｎｇｌｙｉｍｐｏｒｔａｎｔｒｏｌｅｉｎｉｎ ｄｕｓｔｒｙ,ｓｕｃｈａｓｉｎｆｒａｒｅｄａｎｄｆｉｂｅｒｏｐｔｉｃｓ ,ｃａｔａｌｙｓｔｓａｎｄｓｅｍｉｃｏｎｄｕｃｔｏｒｄｅｖｉｃｅｓ.Ａｔｐｒｅｓｅｎｔ,ｔｈｅｂｅｓｔｗａｙｔｏｒｅｃｏ ｖｅｒｇｅｒｍａｎｉｕｍｉｓｔ…     

Dynamics of electrodeposition of tetraethylthioram disulphide (TETD) on pyrite surface

Ｄｉｅｔｈｙｌｄｉｔｈｉｏｃａｒｂａｍａｔｅ(ＤＤＴＣ)ｉｓｏｎｅｏｆｔｈｅｍｏｓｔｆｒｅｑｕｅｎｔｌｙｕｓｅｄｃｏｌｌｅｃｔｏｒｆｏｒｆｌｏｔａｔｉｏｎｏｆｈｅａｖｙ ｍｅｔａｌｓｕｌｆｉｄｅｍｉｎｅｒａｌｓ,ｓｕｃｈａｓｇａｌｅｎａ ,ｃｈａｌｃｏｐｙｒｉｔｅａｎｄｊａｍｅｓｏｎｉｔｅ ,ａｎｄｓｈｏｗｓｓｔｒｏｎｇｓｅ ｌｅｃｔｉｖｉｔｙ[1] .ＩｔｉｓｒｅｐｏｒｔｅｄｔｈａｔＤＤＴＣｉｓａｐｏｗｅｒｆｕｌｃｏｌｌｅｃｔｏｒｆｏｒｇａｌｅｎａａｎｄｖｅｒｙｓｅｌｅｃｔｉｖｅａｇａｉｎｓｔｐｙｒｉｔｅｉ…     

Mechanism of crud formation in copper solvent extraction

The authors investigated the mechanism of crud formation in copper solvent extraction. It is indicated that pH value of solution and the phase ratio (O/A) are the main factors affecting crud formation in solvent extraction. The amount of crud extraction increases with aqueous pH value increase, and reduces with the increase of the phase ratio. Fe3 , Mg2 , fine air bubble and suspended particulates in leaching solution contribute to crud formation. One case is that a series of reactions of hydrolization and polymerization occurs for Fe3 , while pH＞2.5, polyhydric complex or Fe-SO4 complex are formed. Then the complex-ions of FeOH2 , Fe2(OH)4 2 cause poly-reaction, which is likely to lead emulsion. The study on Zeta potential indicates the repulsion between electriferous droplets in solvent extraction prevents phase coalescence, which is one of the major reasons for emulsion.     

Solvent extraction of niobium from alkali solution by methyltrioctylammonium chloride

Ｏｆｔｈｅｔｒａｄｉｔｉｏｎａｌｐｒｏｃｅｓｓｅｓｏｆｎｉｏｂｉｕｍｅｘｔｒａｃｔｉｏｎ ,ｔｈｅｈｙｄｒｏｆｌｕｏｒｉｃａｃｉｄｄｉｓｓｏｌｕｔｉｏｎ ｓｏｌｖｅｎｔ (ＭＩＢＫ ,ＴＢＰｅｔｃ .)ｅｘｔｒａｃｔｉｏｎｐｒｏｃｅｓｓｉｓｗｉｄｅｌｙｕｔｉｌｉｚｅｄ[1] .ＢｅｃａｕｓｅｏｆｓｐｅｃｉａｌｐｒｏｐｅｒｔｉｅｓｏｆＨＦ ,ｈｏｗｅｖｅｒ ,ｔｈｉｓｐｒｏｃｅｓｓｇｉｖｅｓｒｉｓｅｔｏｍａｎｙｓｅｒｉｏｕｓｐｒｏｂｌｅｍｓ ,ｆｏｒｅｘａｍｐｌｅ ,ｓｅｒｉｏｕｓｃｏｒｒｏｓｉｏｎｏｆｐｒｏｄｕｃｔｉ…     

Synthesis and coloring properties of Cd（S1-xSex） pigments by precipitate-hydrothermal method

Cd（S1-xSex） pigments （red to yellow） were synthesized by precipitate-hydrothermal method. The structure, morphology and hue of the powder were characterized by X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, energy dispersive X-ray spectroscopy （EDAX） and CIE chromaticity. The optimum synthesis conditions were obtained and reaction mechanism was further analyzed as well. The results show that molar ratio of S to Se, pH value and hydrothermal reaction conditions have great effects on the hues of the pigments. Pigments with vivid hues are obtained under the conditions that pH value is about 13.0, hydrothermal reaction condition is at 140 ℃ for 4 h or at 160 ℃ for 6 h. The reaction mechanism is that Se^2- of Cd（S1-xSex） substitutes S^2- of CdS and then forms a continuous solid solution.     

Failure mode and strength anisotropic characteristic of stratified rock mass under uniaxial compressive situation

A stratified rock mass model was founded by FLAC^3D. The failure mode and anisotropic characteristic of strength for stratified rock mass were analyzed. The analysis results show that the numerical simulation can visually reflect the failure modes of rock samples under different inclination angles β of structural plane. The stiffness of rock sample before peak strength changes in the compressive procedure. With the increase of β, the compressive strength σ _c of rock sample decreases firstly and then increases; when β is in the range of 20°–30° and 80°–90°, σ _c has the largest sensitivity to β; while β falls in the range of 30°–70°, σ _c varies little. When ϕ _j <β<90° (β _j is friction angle of structure plane), the results obtained from numerical simulation and theoretical analysis are in almost the same values; while β⩽ ϕ _j or β=90°, they are in great different values. The results obtained from theoretical analysis are obvious larger than those from numerical simulation; and the results from numerical simulation can reflect the difference of compressive strength of rock samples for the two situations of β⩾ ϕ _j and β=90°, which is in more accordance with the real situation. Foundation item: Project (50099620) supported by the National Natural Science Foundation of China     

Physical simulation of hot deformation of TiAI based alloy

In order to establish a model between the grain size and the process parameters, the hot deformation behaviors of Ti-49.5Al alloy was investigated by isothermal compressive tests at temperatures ranging from 800 to 1 100 ℃ with strain rates of 10^-3-10^-1 s^-1. Within this range, the deformation behavior obeys the power law relationship, which can be described using the kinetic rate equation. The stress exponent, n, has a value of about 5.0, and the apparent activation energy is about 320 J/mol, which fits well with the value estimated in previous investigations. The results show that, the dependence of flow stress on the recrystallized grain size can be expressed by the equation: σ = K1 drex^-0.56. The relationship between the deformed microstructure and the process control parameter can be expressed by the formula: lgdrex= -0.281 1gZ 3.908 1.     

Synthesis of calixarenes and their extraction performance for ester catechins

A series of extractants (tert-butylcalix[6]arene, tert-butylcalix[8]arene and octeacetate of tert-butylcalix[8]arene) were synthesized, and their structures were identified by IR and 1H-NMR. The distribution behavior of ester catechins monomer in the aqueous and chloroform two-phase system containing one of calixarene was studied. The influences of different extractants, concentration of tert-butylcalix[8]arene and extraction temperature on the partition coefficients and the separation factors were investigated. The experiment results show that tert-butylcalix[8]arene is the best extractant that forms a more stable supramolecular compound with gallocatechin gallate (GCG) than with epigallocathechin gallate (EGCG) or epicatechin gallate (ECG). When the concentration of p-tert-butylcalix[8]arene is 3.79 mmol/L, the extraction temperature is 4 ℃, the partition coefficients of KGCG, KECG, KEGCG are 0.987, 0.629, 0.449,the separation factors of α1 and α2 are 1.450 and 1.596, respectively. The important factors influencing the extraction properties of calixarene are discovered to be its cavity size and hydrogen bonding.     

Spectra and DNA-binding properties of two novel mixed-ligand complexes containing organosulfonate

Two novel mixed-ligand complexes, [M(phen)₂(ans)₂]·H₂O (M = Cd(II) 1, Zn(II) 2; phen is 1, 10-phenanthroline, and ans is 4-aminonaphthalene-1-sulfonate), were obtained from the reaction of 1, 10-phenanthroline, sodium 4-aminonaphthalene-1-sulfonate tetrahydrate and acetate in mixed solvents. Interaction of the complexes with calf thymus DNA (ctDNA) were investigated using UV-vis absorption spectra, luminescence titrations, steady-state emission quenching by [Fe(CN)₆]⁴⁻, DNA competitive binding with ethidium bromide (EB) and viscosity measurements. The experimental results indicate that there exist two interaction modes between the complexes and DNA, namely the electrostatic interaction and intercalation, with the binding constants of 1.82 × 10⁵ M⁻¹ for 1 and 4.78 × 10⁴ M⁻¹ for 2 in buffer of 50 mM NaCl and 5 mM Tris-HCl (pH 7.0). Funded by Key Project of the National Natural Science Foundation of China (No. 60537050)     

Synthesis and characterization of arsenate antimonic acid AAAc(1 : 1)

The AAAc(1 : 1) was synthesized in water by As₂O₃ and Sb₂O₃ with molar ratio of 1 : 1. AAAc(1 : 1) was characterized by Raman, IR, TG/DTG, DSC, XPS and XRD. The results show that there are four peaks to v _s of As-OH, As-O-Sb, Sb-OH and Sb-O-Sb in Raman spectra of AAAc(1 : 1) at 100 – 1 000 cm⁻¹. The solution of AAAc(1 : 1) was also titrated with KOH solution. The titration results show that AAAc(1 : 1) is a hexabasic acid with dissociation constants of k ₁=3.62 × 10⁻², k ₂=3.05 × 10⁻³, k ₃=6.43 × 10⁻⁶, k ₄ =9.78 × 10⁻⁸, k ₅=1.32 × 10⁻¹¹, k ₆=3.87 × 10⁻¹². AAAc(1 : 1) has a good solubility and stability in water, its solid obtained by free volatilizing water from its solution under air at ambient temperature is amorphous. Chemical and thermal analysis show that the composition of AAAc(1 : 1) is As₂O₅ · Sb₂O₅ · 8H₂O in air at 25 °C. AAAc(1 : 1) has the structure of AsO(OH)₂-OH-Sb(OH)₄-O-Sb(OH)₄-OH-AsO(OH)₂ or As(OH)₃-O-Sb(OH)₄-O-Sb(OH)₄-O-As(OH)₃ (isomerism) through experimental determination and geometry optimization. Foundation item: Project(50274075) supported by the National Natural Science Foundation of China     

Electrochemical behavior of diverse vanadium ions at modified graphite felt electrode in sulphuric solution

PAN-based graphite felt (PGF) treated in 98% sulphuric acid for 5 h and then kept at 450 ℃ for 2 h was evaluated for their electrochemical performance as electrodes of vanadium redox battery (VRB). Structure and characteristic of treated PAN-based graphite felt (TPGF) were determined by means of Fourier Transform Infrared Spectroscopy, Scanning Electron Microscopy, Brunauer-Emmett-Teller surface area analysis and VRB test system. The results show that the acid and heat synergistic effect increase the number of —COOH functional groups on the PGF surface, and the PGF is eroded by sulphuric acid oxidation, resulting in the surface area increases from 0.31 m2/g to 0.45 m2/g. The V(Ⅱ)/V(Ⅲ) redox reaction is electrochemically reversible on the TPGF electrode, while the V(Ⅳ)/V(Ⅴ) couple is a quasi reversible process. The diffusion coefficients of the oxidation for V(Ⅳ)/V(Ⅴ) obtained from the scope of peak current Ip vs scan rate v1/2 is 4.4×10-5 cm2/s. The improvement of electrochemical activity for the electrode is mainly ascribed to the increase of the number of —COOH groups on the TPGF, which behaves as active sites catalyzing the vanadium species reactions and accelerating electron transfer reaction and oxygen transfer.     

Adsorption of Pb^2＋ on macroporous weak acid adsorbent resin from aqueous solutions： Batch and column studies

The adsorption properties of a novel macroporous weak acid resin (D152) for Pb²⁺ were investigated with chemical methods. The optimal adsorption condition of D152 resin for Pb²⁺ is at pH 6.00 in HAc-NaAc medium. The statically saturated adsorption capacity is 527 mg/g at 298 K. Pb²⁺ adsorbed on D152 resin can be eluted with 0.05 mol/L HCl quantitatively. The adsorption rate constants determined under various temperatures are k _{288 K}=2.22×10⁻⁵ s^t-1, k _{298 K}=2.51×10⁻⁵ s⁻¹, and k _{308 K}= 2.95×10⁻⁵ s⁻¹, respectively. The apparent activation energy, E _a is 10.5 kJ/mol, and the adsorption parameters of thermodynamics are ΔH ^Θ=13.3 kJ/mol, ΔS ^Θ=119 J/(mol·K), and ΔG ^Θ 298 K =−22.2 kJ/mol, respectively. The adsorption behavior of D152 resin for Pb²⁺ follows Langmuir model. Foundation item: Project(2008F70059) supported by the Scientific and Technological Research Planning of Zhejiang Province, China     

Effect of additive on synthesis of MnZn ferrite nanocrystal by hydrothermal crystallization

1　ＩＮＴＲＯＤＲＣＴＩＯＮＷｉｔｈｒｅｇａｒｄｔｏｔｈｅｓｔｕｄｙｏｆｃｒｙｓｔａｌｇｒｏｗｔｈｕｎｉｔｓ,ｒｅｓｅａｒｃｈｅｒｓｍａｉｎｌｙｃｏｎｃｅｎｔｒａｔｅｏｎｔｈｅｄｉｓｓｏｌｕｔｉｏｎｏｆｓｏｌｕｔｅ ,ｔｈｅｆｏｒｍａｔｉｏｎｏｆｇｒｏｗｔｈｕｎｉｔｓａｎｄｔｈｅｔｒａｎｓｐｏｒｔａｔｉｏｎｏｆｔｈｅｃｒｙｓｔａｌｇｒｏｗｔｈｕｎｉｔｔｏｔｈｅｉｎｔｅｒｆａｃｅ ,ａｓｗｅｌｌａｓｔｈｅｃｏｎｇｒｕｅｎｃｙｏｆｔｈｅｇｒｏｗｔｈｕｎｉｔｓｏｎｔｈｅｉｎｔｅｒ ｆａｃｅｓｏｆｔｈｅｃｒｙ…     

Mechanism of zinc electroplating in alkaline zincate solution

The cathodic deposition properties and mechanism of Zn in alkaline zincate solution were studied by electrochemical techniques. The results show that Zn2 exists in the alkaline solution in the form of Zn(OH)42-. The apparent activation energy of the electrode reaction is 38.93 kJ/mol, which indicates that the discharge of Zn(OH)42- on cathode is controlled by electrochemical polarization, and accompanied by a preceding chemical reaction. The diffusion coefficient of Zn(OH)42- is 2.452×10-6 cm2/s. Zn(OH)2 is the species directly discharged on the cathode surface. Based on the above results the mechanism of zinc electroplating in alkaline zincate solution was put forward. The discharged species is Zn(OH)2 formed from the preceding chemical reaction, which becomes Zn(OH)ad when gaining one electron, and then gaining the second electron to become Zn. The first electron gaining step is rate determining one.     

Biosorption mechanism of Cr （Ⅳ） onto cells of Synechococcus sp.

The biosorption mechanism of Cr （Ⅳ） ions on Synechococcus sp. biosorbent was studied by analyzing the biosorption kinetics as well as speciation change and bond formation during the biosorption process. The kinetics study shows that the adsorption process of Cr （Ⅳ） consists of a very fast stage in the first several minutes, in which more than half of the saturation adsorption is attained, and a slower stage that approximately follows the first order kinetic model, basically Freundlich isotherm models were observed. Comparative studies of FT-LR spectra of K2Cr2O7, free cells of Synechococcus sp., and Cr-bound cells of Synechococcus sp show that the speciation of chromium that binds to the cells ofSynechococcus sp. is Cr （Ⅲ）, instead of Cr （Ⅳ）, and the carboxylic, alcoholic, amido and amino groups may be involved in the binding of Cr （Ⅲ）. Integrative analyses of the surface electric potential, the effect of pH value on adsorption behavior of Cr （Ⅵ）, and the results of FT-IR show that the biosorption of Cr （Ⅵ） follows two subsequent steps, biosorption of Cr2O7 ^2- by electrostatical force at the protonated active sites and reduction of Cr2O7^2- to Cr^3＋ by the reductive groups on the surface of the biosorbents.     

Dynamic recrystallization behavior of 35CrMo structural steel

1　ＩＮＴＲＯＤＵＣＴＩＯＮＤｕｒｉｎｇｈｏｔｗｏｒｋｉｎｇ ,ｓｅｖｅｒａｌｍｅｔａｌｌｕｒｇｉｃａｌｐｈｅｎｏｍｅｎａｓｕｃｈａｓｗｏｒｋ ｈａｒｄｅｎｉｎｇ (ＷＨ ) ,ｄｙｎａｍｉｃｒｅｃｏｖｅｒｙ (ＤＲＶ) ,ａｎｄｄｙｎａｍｉｃｒｅ ｃｒｙｓｔａｌｌｉｚａｉｔｏｎ (ＤＲＸ )ｏｃｃｕｒｓｉｍｕｌｔａｎｅｏｕｓ ｌｙ[1 5 ] .Ｅｓｐｅｃｉａｌｌｙ ,ｔｈｅｏｃｃｕｒｒｅｎｃｅｏｆＤＲＸ ,ｃａｎｒｅｆｉｎｅｇｒａｉｎａｎｄｒｅｄｕｃｅｄｅｆｏｒｍａｔｉｏｎｒｅｓｉｓｔａｎｃｅｉｎｐｒａｃｔｉｃａｌｈｏｔ ｗ…     

Electrochemical behavior of K3Fe（CN）6 in water-in-oil microemulsion

A water-in-oil (W/O) microemulsion composed of Triton X-100, n-hexanol, n-hexane and water solution with hydrochloric acid was prepared. K₃Fe(CN)₆ was added in as a water-soluble electroactive probe, and its electrochemical behavior was investigated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). It is found that the H⁺ concentration of the water phase has a great effect on the conductivity of the W/O microemulsion, and hence influences the electrochemical behavior of K₃Fe(CN)₆. When the pH value of water phase is about 7, the electrical conductivity of the W/O microemulsion is only 1.2×10⁻⁶ S/cm, and K₃Fe(CN)₆ almost cannot react at the glassy carbon electrode. But when the H⁺ concentration is more than 3 mol/L, the W/O microemulsion has a good electrical conductivity and K₃Fe(CN)₆ shows good electrochemical performance in it. The results of CV and EIS studies indicate that the electrochemical behavior of Fe(CN)₆ ³⁻/Fe(CN)₆ ⁴⁻ in the W/O microemulsion is different from that in the aqueous solution. This may be due to the unique liquid structure of the W/O microemulsion and the unique mass transfer in the W/O microemulsion. Foundation item: Projects(20673036, J0830415) supported by the National Natural Science Foundation of China; Projects(05JT1026, 2007JT2013) supported by the Science Technology Project of Hunan Province, China     

Adsorption of D113 resin for dysprosium(III)

The adsorption behavior and mechanism of D113 resin for Dy(III) was investigated by using the method of resin adsorption. Experimental results show that the optimum medium pH of adsorption of D113 resin for Dy³⁺ is pH=6.00 in the HAc-NaAc medium. The static adsorption capacity of D113 resin for Dy³⁺ is 292.7 mg·g⁻¹. The optimum eluant is 0.5 mol·L⁻¹ HCl. The adsorption rate constant is k ₂₉₈=6.8×10⁻⁶s⁻¹. The apparent activation energy of D113 resin for Dy(III) is 14.79 kJ·mol⁻¹. The adsorption behavior of D113 resin for Dy(III) obeys the Freundlich isotherm. The adsorption parameters of thermodynamic are ΔH=14.48 kJ·mol⁻¹, ΔS=54.69 J·mol⁻¹·K⁻¹, ΔG=−1.82 kJ·mol⁻¹.The adsorption mechanism of D113 resin for Dy³⁺ was confirmed by chemical analysis and IR spectra. Funded by the Natural Science Foundation of Zhejiang Province (No.201027), Foundation of Zhejiang Provincial Education Bureau (No.20040551) and Zhoushan Science Technology Bureau (No.04114)     

水热辅助溶胶凝胶法制备纳米钛酸锌及其光催化性能

采用水热辅助的溶胶凝胶法制备纳米钛酸锌（ZnTiO₃）光催化剂,以罗丹明B为目标降解物,运用动力学模型分析罗丹明B（RhB）初始浓度对降解效果的影响。通过SEM、XRD、XPS、UV-Vis DRS对ZnTiO₃进行表征,并使用自由基捕获试验分析其降解机理。结果表明,ZnTiO₃为纯六方相,形貌为类球形,粒径50 nm左右。在催化剂用量为1 g/L、RhB初始浓度为5 mg/L、pH值为3的条件下,光催化反应150 min后,RhB降解率为93.2%。其动力学方程为k=0.132C₀^-1.253。ZnTiO₃光催化剂降解过程中,·OH、h⁺、·O₂^-均起到催化作用,产生·OH、h⁺的量相近且多于·O₂^-,说明·OH、h⁺在催化反应中起主要作用。     

HYDROPHOBICITY－HYDROPHILICITY BALANCE RELATIONSHIPSFORCOLLECTORLESSFLOTATIONOFSULPHIDEMINERALS

ＨＹＤＲＯＰＨＯＢＩＣＩＴＹ－ＨＹＤＲＯＰＨＩＬＩＣＩＴＹＢＡＬＡＮＣＥＲＥＬＡＴＩＯＮＳＨＩＰＳＦＯＲＣＯＬＬＥＣＴＯＲＬＥＳＳＦＬＯＴＡＴＩＯＮＯＦＳＵＬＰＨＩＤＥＭＩＮＥＲＡＬＳＨＹＤＲＯＰＨＯＢＩＣＩＴＹ－ＨＹＤＲＯＰＨＩＬＩＣＩＴＹＢＡＬＡ...