Electrochemical behaviors of gold and its associated elements in various complex agent solutions

1　INTRODUCTIONGoldisquitestableanddifficulttodissolveinacommonmineralacid .However ,becausethereisadelectroniclayerunfilledingoldatomicstructure ,goldcanbecombinedwithmanychemicalagentstoformstablecomplexions,causingthepotentialofgoldinasolutiontodecreaseandgoldtodissolveinthesolutioneasily .Basedonthisprinciple ,cyanideisanefficientlixiviatingagentofgold ,andhasbeenwidelyusedtoextractgoldfrom primaryandsecondaryresources .However ,itisthemosttoxicandnotbeneficialtoen vironmentprotection…     

SELECTIVE DISSOLUTION OF GOLD IN AN ALKALINETHIOUREA SOLUTION BY ELECTROLYSIS

Thioureawaswellknownasanlixiviantforgoldearlyin1932[fi.Thedissolutionofgoldinacidicthioureasolutionwasreportedin1941byPlaksin[Zj.Thioureahasbeenwidelypaidattentiontoasahighselectivenontoxicnovellixiviantofgoldsince197013j.Electrochemicalexperimentsongoldelectrodeshavebeenconductedbymanyresearches,showingthatgolddissolutionbythioureaismoreefficientinacidicsolutionthaninneutralandalkalinesolutions[4j.Theprocessforextract'inggoldfromtheoreorscrapbyacidicthioureasolution,however,demandedexcessive…     

Experiments and reaction characteristics of liquid phase simultaneous removal of SO<Subscript>2</Subscript> and NO

Experiments of simultaneous removal of SO₂ and NO from simulated flue gas, using NaClO₂ solution as the absorbent, were carried out in a self-designed bubble reactor, and high simultaneous removal efficiencies of SO₂ and NO were obtained under the optimal experimental conditions. The mechanism of simultaneous removal based on NaClO₂ acid solutions was proposed by analyzing the removal products. Possibility and limitation of the desulfurization and denitrification using NaClO₂ acid solutions were calculated by thermodynamic methods. Experimental results of reaction kinetics for simultaneous desulfurization and denitrification indicated that the oxidation-absorption processes of SO₂ and NO were divided into two zones, namely the fast and slow reaction zones. In the slow reaction zones both were zero order reactions, and in the fast reaction zones, the reaction order, rate constant and activation energy of SO₂ reaction with absorbent were 1.4, 1.22 (mol·L⁻¹)^−0.4·s⁻¹ and 66.25 kJ·mol⁻¹, respectively, and 2, 3.15×10³ (mol·L⁻¹) ⁻¹·s⁻¹, and 42.50 kJ·mol⁻¹ for NO reaction, respectively. Supported by the National High-Tech Research and Development Program of China (“863” Project) (Grant No. 2007AA061803)     

Thermodynamic equilibrium of bismuth hydrometallurgy in chloride and nitrate solutions

Simultaneous equilibrium was applied to the thermodynamic analysis and calculation of Bi( Ⅲ )-X(Cl- ,NO3- )-H2O systems, based on which the diagrams of the logarithm of equilibrium concentration of Bi( Ⅲ ) of series precipitation vs pH value of these two systems at 25 ℃ were obtained, and the pH ranges of the stable zones of various precipitations were analyzed and determined. In Bi( Ⅲ )-Cl -H2O system, the variations of c0 (Bi3 ) and c0 (Cl-) have little effect on the equilibria of Bi(OH)3-solution and BiOOH-solution, but has great influence on the equilibrium of BiOCl-solution. However, in Bi( Ⅲ )-NO3-H2O system, the variations of c0 (Bi3 ) and C0 (NO3-)have little effect on equilibria of Bi(OH)3-solution, BiOOH-solution and Bi2O3-solution. When pH value is high,Bi2O3 is the thermodynamic stable phase, its stable zone is the widest, almost including the stable zones of BiOCl or BiONO3, Bi(OH)3 and BiOOH. Bi(OH)3 cannot be obtained from Bi( Ⅲ )-Cl--H2O system, even strong alkaline media. Bi2O3 can be obtained from the solution directly, and highly pure BiOCl or BiONO3 can also be obtained through strictly controlling pH value.     

Study on the isothermal oxidation behavior in air of Ti3AlC2 sintered by hot pressing

The isothermal oxidation behavior at 900–1300°C for 20 h in air of bulk Ti₃AlC₂ with 2.8 wt% TiC sintered by means of hot pressing was investigated in the work. The isothermal oxidation behavior generally followed a parabolic rate law. The parabolic rate constants increased from 1.39×10⁻¹⁰ kg²·m⁻⁴·s⁻¹ at 900°C to 5.56×10⁻⁹ kg²·m⁻⁴·s⁻¹ at 1300°C. The calculated activation energy was 136.45 kJ/mol. It was demonstrated that Ti₃AlC₂ had excellent oxidation resistance due to the continuous, dense and adhesive protect scales consisted of a mass of α-Al₂O₃ and a little of TiO₂ and/or Al₂TiO₅. In principle, the oxide scale was grown by the inward diffusion of O²⁻ and the outward diffusion of Ti⁴⁺ and Al³⁺. The rapid outward diffusion of cations usually resulted in the formation of cracks, gaps, and holes.     

The mechanism of ground granulated blastfurnace slag preventing alkali aggregate reaction

Three different methods were applied to study the alkali content of gelpores in cement. In the closed system, the concentration of K⁺, Na⁺ and OH⁻ have not reduced with the increase of age. In the open system, the diffusion and transferring of K⁺ and Na⁺ towards free space leads to the decrease of total alkali content. In the micro-analysis system, the contents of K⁺ and Na⁺ in the first hydrated layer of ground granulated blastfurnace slag (GBFS) are very low, while the contents of calcium and magnesium are relatively high. This phenomenon shows that the mechanism of GBFS preventing alkali aggregate reaction (AAR) is: when GBFS is dissolved by alkali medium, SiO₂ and Al₂O₃ are dissolved into the cement matrix, then around GBFS particles form reaction rings rich in Ca²⁺ and Mg²⁺, and the C-S-H gel of positive charges formed in the area repulses K⁺ and Na⁺, which are forced to transfer to the mortar’s matrix, pore or mortar sample surface. The transferred K⁺ and Na⁺ form alkali gel products with other dissolved ions, then become evenly distributed in the mortar sample and react with Ca(OH)₂ in pore solutions to form (Na,K) _x−2z ·zCa·(SiO₂)_y·(OH)_x gel products; and thus changes the AAR gel products’ structure. The gel products will not expand, and so they can delay expansion destruction.     

Structure and electrochemical properties of LiCoO2 synthesized by microwave heating

Microwave synthesis method was applied to the fast preparation of LiCoO₂. The structure of the synthesized oxides was analyzed by using X-ray diffraction. Only single-phase LiCoO₂ was obtained. Electrochemical behaviors of LiCoO₂ were investigated by charge-discharge cycling properties in the voltage range of 3.00 – 4.35 V (vs Li). The results show that the prepared LiCoO₂ powders calcinated at 900 °C for 120 min exhibit an initial charge and discharge capacity of 168 and 162 mA · h · g⁻¹ at 0.1C current rate, respectively, as compared to 159 and 154 mA · h · g⁻¹ of LiCoO₂ synthesized by conventional means. In addition, more than 95% of the capacity is retained even after 10 cycles. But with the increase of calcinating time, its electrochemical properties deteriorate. Compared with the conventional method, the microwave heating method is simple, fast, and with high energy efficiency.     

Fabrication and microstructure of SiO2−GeO2 sol-gel glass coatings

SiO₂−GeO₂ sols and gel glass coatings with different contents of germanium dioxide were fabricated. Stable and transparent sols could only be obtained when the content of GeO₂ was under 35%. It is shown by SEM that only one continuous phase is observed in the coating of 65SiO₂·35GeO₂ and plenty of Ge, O and Si were all found in it. However, the separated phase is found in the coating of 60SiO₂·40GeO₂ and a large number of Ge and O. It is proved by the Raman scattering investigation that the separated phase in the coating of 60SiO₂ ·40GeO₂ is germanium dioxide. The congeries of hydrolystates of Cl₃ GeCH₂ CH₂ COOH play the main role in the formation of the separated phase when the proportion of GeO₂ is much higher. Si−O−Ge, Si−O−Si, and Ge−O−Ge bonds form in the coating of 65SiO₂·35GeO₂ and this coating is homogenous. Jing Cheng-bin: Born in 1974 This work was partly financially supported by the Foundation of Key Teachers of Ministry of Education, China     

Thermodynamics of chromite ore oxidative roasting process

To explicate the thermodynamics of the chromite ore lime-free roasting process,the thermodynamics of reactions involved in this process was calculated and the phrases of sinter with different roasting times were studied.The thermodynamics calculation shows that all the standard Gibbs free energy changes of the reactions to form Na2CrO4,Na2O·Fe2O3,Na2O·Al2O3 and Na2O·SiO2 via chromite ore and Na2CO3 are negative,and the standard Gibbs free energy changes of the reactions between MgO,Fe2O3 and SiO2 released f...     

Preparation of AgSnO2 composite powders by hydrothermal process

Silver-tin oxide powders were synthesized by the hydrothermal method with Ag（NH3）2^＋ solution and Na2SnO3 solution as raw materials and Na2SO3 as reductant. The precipitation conditions of Na2SnO3 solution and the reduction conditions of Ag（NH3）2^＋ were also investigated. The powders prepared were characterized by differential thermal analysis （DTA）, X-ray diffraction analysis （XRD）, scanning electron microscope （SEM） and energy spectrum analysis, The results show that pH value of the solution is a key parameter in the formation of Sn（OH）4 precipitate and the reduction reaction of Ag（NH3）2^＋ can release H^＋ ions, which results in synchronous precipitation of Sn（OH）6^2- as Sn（OH）4. The reduction of Ag（NH3）2^＋ and precipitation of Na2SnO3 occur simultaneously and the coprecipitation of silver and tin oxide is reached by the hydrothermal method. The silver-tin oxide composite powders have mainly flake shape of about 0.3 μm in thickness and there exists homogeneous distribution of tin oxide and silver in the powder synthesized.     

IR Spectra Analysis of SiO2-TiO2-GeO2 Gel Glass of CO2 Laser Transmitting Hollow Waveguide

Both titanium and germanium were introduced into silicon dioxide system by sol-gel method to move its region of anomalous dispersion caused by IR resonance absorption towards the wavelength of CO₂ laser. It is indicated by IR absorption spectra that as the content of SiO₂ decreases in this glass system TiO₂ and GeO₂ tends to exist in their own phases. As for the gel glass with a composition of 40 SiO₂·30TiO₂·30GeO₂, when the temperature is below 600°C, germanium atoms exist mainly in Ge−O−Ge bonds. With the temperature increasing from 800°C to 1000°C, titanium atoms in Si−O−Ti bonds abmost transform into Ti−O−Ti bonds. Furthermore, a large number of Si−O−Ti and Si−O−Ge bonds formed when the temperature approaches 800°C, which makes a notable IR absorption band round the wavelength of CO₂ laser. Therefore, sol-gel based SiO₂−TiO₂−GeO₂ gel glass is a candidate material for CO₂ laser hollow waveguide. JING Cheng-bin: Born in 1974. This work was partly financially supported by the Foundation of Key Teachers of Ministry of Education, China.     

Preparation of λ-MnO2 by Column Method and Its Ion-Sieve Property

λ-MnO₂ was prepared by column method from normal spinel LiMn₂O₄ with purity of 99.38%. The influence of LiMn₂O₄ grain size and acidity of leaching solution on the lithium leaching process was studied. The results show that the appropriate range of LiMn₂O₄ grain size was 60–160 meshes and the concentration of leaching solution HCl was 0.1 mol·L⁻¹. The adsorption capacity Q of λ-MnO₂ for lithium increased with the increase of pH and changed markedly at pH 6.0–10.0. It was 3.80mmol/g at pH 12.0 The distribution coefficients K_d of Li⁺ and Na⁺ were 3.406×10⁴ and 2.300 respectively, and the separation coefficient a _Na ^Li was 1.481 ×10⁴ at pH 6.5. As a result, λ-MnO₂ is a high performance ion-sieve material for lithium ion. LEI Jia-heng: Born in 1957. Funded by the National Natural Science Foundation of China (No. 59972027) and the Natural Science Foundation of Hubei Province (No. 2002AB074)).     

Chemial Bond and Stability of Adsorption of [Au（ AsS3 ）]^2- on the Surface of Kaolinite

Density function theory and discrete variation method (DFT-DVM) were used to study the adsorption of [Au( AsS3 )]^2- on the surface of kaolinite. The correlation among structure, chemical bond and stability was discussed. Several models were selected with [ Au( AsS3)]^2- in different directions and sites. The results show that the models with gold on the edge of kaolinite basal layer contain pincerlike bond among gold and several oxygen atoms and form strong Au - 0 covalent bond, so these models are more stable than those with gold above or under the layer. The models with gold near to [ AlO2(OH)4] octahedra are more stable than those with gold near to the vacancy withont aluminium. These two stable tendencies in kaolinite- [ Au( AsS3)]^2- are stronger than that in kaolinite-Au systems. The interaction between [ Au( AsS3 )]^2- and kaolinite is stronger than that between gold and kaolinite, and this interaction is strong enough to form the surface complexes.     

Preparation and thermoelectric properties of SiO<Subscript>2</Subscript>/<Emphasis Type="Italic">β</Emphasis>-Zn<Subscript>4</Subscript>Sb<Subscript>3</Subscript> nanocomposite materials

A series of SiO₂/β-Zn₄Sb₃ core-shell composite particles with 3, 6, 9, and 12 nm of SiO₂ shell in thickness were prepared by coating β-Zn₄Sb₃ microparticles with SiO₂ nanoparticles formed by hydrolyzing the tetraethoxysilane in alcohol-alkali-water solution. SiO₂/β-Zn₄Sb₃ nanocomposite thermoelectric materials were fabricated with these core-shell composite particles by spark plasma sintering (SPS) method. Microstructure, phase composition, and thermoelectric properties of SiO₂/β-Zn₄Sb₃ nanocomposite thermoelectric materials were systemically investigated. The results show that β-Zn₄Sb₃ microparticles are uniformly coated by SiO₂ nanoparticles, and no any phase transformation reaction takes place during SPS process. The electrical and thermal conductivity gradually decreases, and the Seebeck coefficient increases compared to that of β-Zn₄Sb₃ bulk material, but the increment of Seebeck coefficient in high temperature range remarkably increases. The thermal conductivity of SiO₂/β-Zn₄Sb₃ nanocomposite material with 12 nm of SiO₂ shell is the lowest and only 0.56 W·m⁻¹·K⁻¹ at 460 K. As a result, the ZT value of the SiO₂/β-Zn₄Sb₃ nanocomposite material reaches 0.87 at 700 K and increases by 30%.     

Localized electrochemical impedance spectroscopy study on the corrosion behavior of Fe-Cr alloy in the solution with Cl− and SO4 2−

The corrosion behaviors of Fe-Cr alloy under three different pH values solutions with Cl- and SO42- were investigated by localized electrochemical impedance spectroscopy (LEIS) measurements and the corrosion products were analyzed by laser Raman spectrometry. The results show that the high corrosion resistance of Fe-Cr Alloy is attributed to a passive film which is formed more easily when the alloy contains a large quantity of Cr element. However, its corrosion resistance varies in the solutions with different pH values, especially in the initial corrosion. The average impedance values in neutral and alkaline solution are much higher than that in acidic solution because the passive film is more likely to dissolve in the acidic condition. Moreover, the destructive effect of Cl- and SO42+ ions on the passive film is also demonstrated in corrosion process through the change of the impedance value with the steeping time.     

Electrochemical kinetics of gold dissolving in alkaline thiourea solution

1 INTRODUCTIONEssentially , determination of electrode reac-tion mechanism is just the determination of thecourse of electrode reaction and the rate-determi-ning step[1 5]. Based on the previous results[6 11],gold dissolution mechanism undergoes the follow-ing courses in alkaline thiourea solution: adsorp-tion of thiourea on active points of electrode sur-face and formation of Au[SC(NH2)2]ads; chargetransfer fromactive gold atomto thiourea moleculeand formation of Au[SC(NH2)2]a+ds; Au-…     

Synthesis of 1,4-benzenedicarbonyl thiourea resins and their adsorption properties for Ag（I）

Several 1,4-benzenedicarbonyl thiourea resins (BTR) were synthesized through interfacial polymerization between 1,4-benzenedicarbonyl diisothiocyanate and polyamine. Their structures were confirmed by FT-IR. The adsorption properties (including the effect of adsorption time, pH, initial concentrations and temperature) of BTR-1, BTR-2 and BTR-3 for Ag(I) were investigated by batch tests. The results show that the adsorption equilibria of BTR-1, BTR-2, BTR-3 for Ag(I) are achieved after about 10 h. Their equilibrium adsorption capacities are 7.11, 6.75 and 6.23, respectively, and the adsorption process accords with G. E. Boyd equation and Langmuir adsorption isotherm as well. The adsorption capacities increase with the increase of pH (the highest uptake values are observed at pH being about 6–7). The thermodynamic parameters of BTR-1 were calculated. The results show that ΔH ^Θ; and ΔS ^Θ are 6 958.8 J/mol and 64.28 J/(mol·K), respectively, and ΔG ^Θ at 20, 30, 40 and 50 °C are −11.79, −12.52, −13.16 and −13.8 kJ/mol, respectively. The silver-loaded resins can be quantitatively eluted by a solution containing 6% thiourea in 1 mol/L HNO₃.     

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     

Effect of corrosive solutions on C-S-H microstructure in portland cement paste with fly ash

By means of ²⁹Si and ²⁷Al magic angle spinning nuclear magnetic resonance (MAS NMR) combined with deconvolution technique, X-ray diffraction (XRD), scanning electron microscopy (SEM) as well as energy dispersive X-ray system(EDX), the effect of 5 wt% corrosive solutions (viz. 5 wt% Na₂SO₄, MgSO₄, Na2SO4+NaCl and Na₂SO₄+NaCl+Na₂CO₃) on C-S-H microstructure in Portland cement containing 30 wt% fly ash was investigated.The results show that, in MgSO₄ solution, Mg²⁺ promotes the decalcification of C-S-H by SO ₄ ^2- ,increasing silicate tetrahedra polymerization and mean chain length (MCL) of C-S-H. However, the substituting degree of Al³⁺ for Si⁴⁺ (Al[4]/Si) in the paste does not change evidently. Effect of Na²SO⁴ solution on C-S-H is not significantly influenced by NaCl solution, while the MCL and Al[4]/Si of C-S-H in fly ashcement paste slightly change. However, the decalcification of C-S-H by SO ₄ ^2- and CO ₃ ^2- attack, as well as the activation of fly ash by SO ₄ ^2- attack will increase the MCL and Al[4]/Si, which are both higher than that under Na₂SO₄ corrosion, MgSO₄ or Na₂SO₄ +NaCl coordination corrosion.     

Microstructure and microwave dielectric properties of CaO-B2O3-SiO2 glass ceramics with various B2O3 contents

The effects of B2O3 addition on both the sintering behavior and microwave dielectric properties of CaO-B2O3-SiO2 (CBS) glass ceramics were investigated by Fourier transform infrared spectroscopy (FTIR),X-ray diffractometry (XRD) and scanning electron microscopy (SEM).The results show that the increasing amount of B2O3 causes the increase of the contents of [BO3],[BO4] and [SiO4],which deduces the increase of CaB2O4 and α-SiO2 and the decrease of CaSiO3 correspondingly.No new phase is observed throughout the...