Leaching Mechanism of the Spodumene Sulphuric Acid Process

Leaching mechanism of acid roasted ore in the spodumene sulphuric acid process was investigated. Experimental results of leaching rates along with variations of leaching temperature in the acidized and neutral leaching processes were reported. Applying ion exchange mechanism in acidized roasting and absorption entrainment mechanism at high temperature, leaching mechanism was discussed. A better explanation of experimental results was given.

Role of dissolved oxygen reduction in improvement inhibition performance of ascorbic acid during copper corrosion in 0.50 mol/L sulphuric acid

The kinetics of dissolved O_2 reduction and hydrogen evolution reactions on copper surface was studied in naturally aerated and air and O_2-saturated 0.50 mol/L H_2SO_4 solutions using polarization measurements combined with the rotating disc electrode (RDE).The Koutecky-Levich plot indicated that the dissolved O_2 reduction at the copper electrode was an apparent four-electron process.A correlation between the presence of dissolved O_2 and the formation of Cu_2O,confirmed from XRD,was discussed. Ascorbic a...

Preparation of Cs-Rb-V series sulphuric acid catalyst

Cs Rb V series low temperature sulphuric acid catalyst was prepared for the first time by using carbonized mother liquor containing alkali metal salts. The results show that the conversion of SO 2 on catalyst prepared directly with carbonized mother liquor could reach to 24.8% at 410?℃. If n (Na)/ n (V) was adjusted properly, the conversion of SO 2 could be increased to 35.6% at 410?℃. Refined carbonized mother liquor could make the catalytic activity even higher at low temperature, the conversion of SO 2 could be increased to 36.65% at 410?℃. The catalyst was examined with differential thermal analysis. It was found that both endothermic peaks and exothermic peaks of catalyst shifted forward obviously and the catalyst possessed higher activity at low temperature.

Analysis of flowout gas field simulations and ignition methods for sulphuric gas wells

To avoid potential human casualties and environmental pollution,flowout gas from sulphuric gas wells showing high concentrations of volatile gas must be neutralized by controlled ignition.Simulation model is built by using CFD software for flowout gas,and ignition methods are analyzed.The simulation results indicate that the optimal ignition zone is located between 150mm and 570mm above the gas flowout device.Two ignition methods,electronical and chemical,are developed.12 and 6 experimental tests are performed respectively for these two methods.Results from the above tests verify that both approaches are successful in igniting the gas promptly and safely.In addition,our experience proves that the former way is more suitable for the fixed position ignition case,while the latter is more suitable for the long-distance or emergent ignition case.These two approaches can potentially be applied to a wide range of situations other than the fixed position ignition case and long distance ignition case.

Inhibition of Aluminium Corrosion Using <i>Carica papaya</i>Leaves Extract in Sulphuric Acid

Inhibition of aluminium corrosion using C. papaya leaves extract in 1.0 M H2SO4 was investigated by using gravimetric analysis at various concentrations and temperatures: 303 K, 313 K and 323 K. Characterization was done by using Scanning Electron Microscope (SEM) and Fourier Transform Infrared (FT-IR) spectroscopy. Results show that, inhibiting ability of the extract was due to its adsorption onto the metal surface through Langmuir adsorption isotherm. Thermodynamic (Gibbs energy, entropy and heats of adsorption) and kinetic parameters (activation energy and entropy of activation) were also determined. All of these agreed to physical adsorption of inhibitor onto the aluminium surface.

Electro-physical Properties of Super-thin Basalt Fiber Chemically Modified by Hydrochloric or Sulphuric Acid

The influence of hydrochloric or sulphuric acid treatment on the electro-physical properties of superthin basalt fiber (STBF) made from Armenian basalt rocks was studied. Specific electric resistance for direct and alternating currents, dielectric parameters of ε, and ε,, were measured. It is shown that specific resistance and dielectric parameters of super-thin basalt fiber change essentially after hydrochloric or sulphuric acid treatment. The temperature dependences of these parameters were studied, too, and their non–monotonic behavior was observed. The probable variation of mentioned STBF parameters is explained by different water absorption capacity of pores as a result of acid treatment.

Sulphuric Acid Bake-Leach Process for the Treatment of Mixed Copper-Cobalt Oxide Ores

A sulphuric acid bake–leach method for the treatment of mixed copper-cobalt oxide minerals was investigated as an alternative to the reductive leaching method. Sulphuric acid bake-leach process of the mixed copper-cobalt oxide ore was carried out by mixing the sample with sulphuric acid followed by baking of the mixture in a muffle furnace. Baking tests were conducted at different conditions such as temperature, time, and varying amounts of acid. The reacted samples were then subjected to water leaching at room temperature to determine the leachability of copper and cobalt from the baked material. The dissolutions of copper and cobalt were dependent on acid concentration with cobalt showing more sensitivity to the amount of acid. Both copper and cobalt were extracted from the baked material within short leaching times and without the addition of reducing agents. The outcome of this work has shown that the sulphuric acid bake-leach process is a possible alternative to the reductive leaching method for copper-cobalt oxide ores.

Thick and Dense Anodic Oxide Layers Formed on Aluminum in Sulphuric Acid Bath

Thick and dense oxide layers were obtained on aluminium in sulphuric acid electrolyte. For this purpose, the methodology of experimental design was used. A three-variables Doehlert design （bath temperature, anodic current density, sulphuric acid concentration）, was achieved. In order to maximize the growth rate and the density of the anodic oxide layer, optimum path study was conducted. Under the determined optimal anodizing conditions （5.7℃, 3 A.dm-2,Csul=140 g.L-1）, the estimated response values were 0.86 μmin-1 and 3.12 g.cm-2 for growth rate and density, respectively. The morphology of optimum layer was examined by scanning electron microscopy （SEM）. The compactness of the optimum anodic layer can be correlated with its morphology revealed by SEM observations.

Effect of Sn on Corrosion Behavior of Ultra-pure 17 mass% Cr Ferritic Stainless Steels in Sulphuric Acid

The effect of Sn on corrosion behavior of ferritic stainless steels in 20mass% H2SO4 was investigated by alternating current and direct current electrochemical methods and gravimetric tests at 25 ℃.The results show that Sn can effectively improve general corrosion resistance of ferritic stainless steels in H2SO4,mainly due to highly raised hydrogen evolution overpotential which is in favour of strong suppression of hydrogen evolution reaction,and inhibitive effect of dissolved Sn^2＋ on elementary anodic reactions.With increasing Sn content,the better corrosion resistance can be reached.The Electrochemical Impedance Spectroscopy（EIS）includes four time constants and can be perfectly fitted by equivalent circuit：Rs（CdlRct）（QadsRads（RL1（L1（RL2L2））））.

Reaction mechanism of fluoride conversion into BF^(4-) during sulphuric acid leaching of roasted bastnaesite

The bastnaesite used in hydrometallurgy usually contains 7%-11% fluorine,and the conversion of fluorine into high-value products is the key to achieving green production of rare earths and improving the comprehensive utilization of bastnaesite.In order to recover fluorine from bastnaesite in the form of KBF4,the mechanism of F^(-)conversion to BF^(4-)in sulphuric acid leaching solution of roasted bastnaesite was studied by using Eh-pH diagram and simulation experiment.It shows that the formation of BF^(4-)is affected by pH in the absence of rare earths.BF^(4-)is hydrolyzed to BF3 OH-and F-when the pH is greater than 3.9,and part of F-exists as HF^(2-)when pH is lower than 2.In the presence of La^(3+),the formation of BF^(4-)is mainly affected by LaF_(3) when pH is greater than 0,and in the case that the pH is lower than 2,it is mainly affected by HF^(2-).When Ce4+is present in solution,CeF_(2)^(2+) can exist stably in sulphuric acid solution.Bringing down the pH can reduce the stability of CeF_(2)^(2+) and increase the BF^(4-)conversion rate.Based on these results,KBF4 was prepared in the alkaline solution of bastnaesite,and the conversion of BF^(4-)is 84.31%.This provides a theoretical basis for the recovery of fluorine from bastnaesite in the form of KBF_(4).

Characteristics of Gold and Its Mineralization Style in the Boulon Djounga Eastern Perimeter of Liptako Mining Company (Central Southwestern Niger)

The Boulon Djounga eastern perimeter is part of the Tiawa operating permit of the Société des Mines du Liptako (SML), located in the central southwestern part of Liptako (Niger). In this study, we used field data, Reverse Circulation (RC) surveys and chemical analyzes of gold to determine the characteristics of gold and its mineralization style. The eastern perimeter of Boulon Djounga is represented by a succession of metabasalts and metasediments both intersected by intrusions of quartz and dolerite dykes, and covered by sandstone and clayey rocks. Gold is present in low contents (0.00 - 0.30 ppm) in the sedimentary cover and in medium (0.30 - 1.00 ppm) or high contents (1.00 - 4.534 ppm) in the metasediments, and in the gray quartz veins and locally in the volcanics. It exists in a disseminated state or in a concentrated state in the surrounding areas in the form of discrete grains associated with sulphurous minerals (pyrite: FeS2, chalcopyrite: CuFeS2 or arsenopyrite: FeAsS). The presence of gold in the quartz veins, and the NE-SW and NW-SE orientations of the ore bodies suggest that the eastern Boulon Djounga gold mineralization would be established during a late magmatic extensive phase.

Influence of the Partial Substitution of Bitumen by a Mixture of Sulphur and Tyre and Plastic Bottle Powders on the Behaviour of Bituminous Concrete

This article deals with the influence of the partial substitution of bitumen by a mixture of sulphur and tyre and plastic bottle powders on the characterization of asphalt concrete. The approach adopted was to subject a control asphalt concrete to level 2 formulation tests as well as those modified at 10%, 20%, 30% and 40% by substituting bitumen with a mixture of tyre powder, plastic bottle powder and sulphur at 40%, 28% and 32% respectively. The results of the PCG, Duriez and rutting tests carried out on the control and modified bituminous concretes (manufactured using the wet process) revealed three (03) major findings, in particular with regard to workability, resistance to simple compression and rutting. The experimental results show an increasing trend in the essential parameters. At 40% substitution, there was a 22.73% increase in compactness, reflecting a significant improvement in the material’s workability. With regard to simple compressive strength, the increase is 34.02% at 40% substitution, highlighting the limitation of crack formation and propagation under heavy precipitation. With regard to rutting, the 16% drop in susceptibility at 40% substitution reflects a significant improvement in the behaviour of the material under dynamic mechanical stresses in heavy precipitation. The improvement in these behaviours results from the insertion of the plastic bottle powder into the interstices of the granular skeleton, thus reducing its cellular structure, and also from the interactions between the sulphur with the tyre powder and the sulphur with the plastic bottle powder, i.e. cross-linking or vulcanisation.

Analysis on Concentration and Source Rate of Precursor Vapors Participating in Particle Formation and Growth at Xinken in the Pearl River Delta of China

Concentration and source rate of precursor vapors participating in particle formation and subsequent growth were investigated during the Pearl River Delta intensive campaign （PRD2004, October 2004） in southeastern China. Four new particle formation event days and a typical non-event day were selected for our analysis. Atmospheric sulphuric acid, the important precursor vapor in nucleation and growth, were simulated with a pseudo steady-state model based on the measurements of SO2, NOx, 03, CO, non-methane hydrocarbon （NMHC） and ambient particle number concentrations as well as modeled photolysis frequencies obtained from measurements. The maximum midday sulphuric acid concentrations vary from 4.53 × 10^7 to 2.17 × 10^8 molecules cm^-3, the corresponding source rate via reaction of OH and SO2 range between 2.37 × 10^6 and 1.16 × 10^7 molecules cm^-3 s^-1. Nucleation mode growth rate was derived from size spectral evolution during the events to be 6.8-13.8 nm h^-1. Based on the growth rate, concentration of the vapors participating in subsequent growth were estimated to vary from 1.32 × 10^8 to 2.80 × 10^8 molecules cm^-3 with corresponding source rate between 7.26 × 10^6 and 1.64 × 10^7 molecules cm^-3 s^-1. Our results show the degree of pollution is larger in PRD. Sulphuric acid concentrations are fairly high and have a close correlation with new particle formation events. Budget analysis shows that sulphuric acid alone is not enough for required growth; other nonvolatile vapors are needed. However, sulphuric acid plays an important role in growth; the contribution of sulphuric acid to growth in PRD is 12.4%-65.2%.

聚丙烯中硫酯类抗氧剂的质谱分析

采用齐格勒-钠塔催化剂使丙烯催化聚合得到聚丙烯.聚丙烯树脂本身具有优良的性能,如机械强度好,易加工成型,质量轻,成本低等,但也存在一些缺陷,如由于聚丙烯结构中存在叔碳原子,在造粒加工、贮存和使用过程中,易受热、光、氧等的作用而降解,导致材料的性能降低.……

Cu_2S-FeS-SiO_2-CaO系熔体氧化动力学及机理

在气体喷吹熔体表面的情况下,测定了Cu_2S-FeS-SiO_2-CaO系熔体氧化动力学。结果表明,熔体中FeS优先于Cu_2S氧化;硫的氧化反应对po_2为一级反应,对aFeS为零级反应,反应表观活化能为55.7kCal/mol;反应前期硫的氧化速率明显高于Fe^(2+)的氧化速率。随着反应的进行,Fe^(2+)的氧化速率显着增加。渣中CaO在一定范围内增加,脱硫速率及渣含Fe_3O_4提高;氧通过渣相的传递为总速率的控制步骤,氧的传递按两类机构来完成;气相氧浓度提高及渣中CaO增加的作用在于提高渣相中氧的传递速率。

Comparative Study of the Kinetics of Dissolution of Laterite in some Acidic Media

Studies on the kinetics of dissolution of a Nigerian lateritic soil in acids media including hydrochloric, nitric and sulphuric acids have been undertaken. The elemental and mineralogical characterization, loss of mass on ignition, moisture content and pH of the material suspension in water were determined. The effects of acid concentration, process temperature, stirring rate and particle size on the dissolution rate were investigated. Experimental results indicated that laterite dissolution was greatly influenced by hydrogen ion concentration and the leaching data fitted a diffusion model. The linear dependence of the rate constant k on 1/ro 2 supported the proposed kinetic model. Values of 60.23 kJmol-1, 64.31 kJmol-1 and 67.53 kJmol-1 were obtained for the activation energies of laterite dissolution in hydrochloric, nitric and sulphuric acids respectively;and the order of reaction was approximately one with respect to each of the three acids.

A DFT Study on the Reaction Mechanism Involved in the Synthesis of Sodium Azide via Hydrazine Hydrate Method

Sodium azide is a widely used inorganic compound. Besides the commonly used method of ＂Wislicenus process＂ which uses ammonia, nitrous and sodium as materials, the hydrazine hydrate route is also employed for the preparation of sodium azide particularly in laboratory. However, because many species are involved in the reaction system, the reaction details for the hydrazine hydrate route are still unclear. A comprehensive understanding of the reaction mechanism may provide meaningful help for optimizing the production process. In this work, the reaction mechanism for the synthesis of sodium azide by hydrazine hydrate route has been studied using density function theory（DFT） method. On the basis of our calculations, the reaction details, including the energetics of ten elementary steps, the structures of intermediates and transition states as well as the influence of inorganic acids and alcohols, were illuminated at the atomistic level. Both the two steps, the generation of key intermediate（NH2-NH-NO） and the trans-cistransformation of NH2-NH-NO, are suggested to be the possible rate-limiting step, corresponding to the energy barriers of 20.3 and 22.7 kcal/mol, respectively. In the early reaction steps to generate NH2-NH-NO, the main role of sulphuric acid is to donate proton, which can be replaced by nitric acid or hydrochloric acid. From the energy point of view, isopropanol has similar reactivity as methanol and ethanol.

Lignite oxidative desulphurization Notice 1.Process condition selection

The process of lignite desulphurization via its treatment by an oxidant(air or air–steam mixture)has been studied.The research objective was useful determination of steam application in oxidative lignite desulphurization.It has been proved that the water steam should be included in the oxidant composition to increase the hydrogen sulphide and combustible constituent content in the gases obtained during the processes under research.The impact of factors which affect the reactions between solid(in our case–lignite)and gaseous reagent(oxidant,i.e.air and or air–steam mixture)upon the research process has been investigated,if these reactions occur in the kinetic area.Such factors are linear rate of oxidant movement and coal grain size.The values of oxidant movement linear rate and coal grain size,which the reaction transfer from pyrite sulphur and organic content of lignite from diffusion into kinetic area occurs by,have been determined.Under these‘‘transfer’’conditions,the values of coefficients of oxidant mass transfer(β,m/s)as well as Sherwood criteria and boiling layer differences have been calculated.