铬铁矿在HCl-Na_(2)CrO_(4)体系中的多级浸出动力学研究

研究了在HCl-Na_(2)CrO_(4)体系中对铬铁矿进行多级浸出,并探讨了铬铁矿中主要金属元素的浸出动力学。结果表明:在粒径45~75μm、氧化剂Na_(2)CrO_(4)用量为理论量0.6倍、反应时间5h、反应温度453.15K、料球质量比1/1、搅拌速度30r/min、液固体积质量比4mL/1g最佳条件下进行3级循环浸出,铬、铁、铝、镁浸出率分别可达91.98%、94.54%、76.62%和78.03%;铬铁矿的酸浸反应受界面化学反应控制,温度在373.15~473.15K范围内,铬、铁、铝、镁的浸出表观活化能分别为45.80、40.43、42.08和43.54kJ/mol,浸出效果较好。

Effects of mechanical activation and oxidation-reduction on hydrochloric acid leaching of Panxi ilmenite concentration

The effects of oxidation-reduction treatment and mechanical activation on the hydrochloric acid leaching performance of Panxi ilmenite concentration were investigated.The results show that both of oxidation-reduction treatment and mechanical activation significantly accelerate the extraction of Fe,Ca and Mg from Panxi ilmenite concentration;however,the CaO and MgO contents of the calcined residues obtained from oxidized-reduced ilmenite concentration are higher than the standard values required by chlorination process.The Ca and Mg in oxidized-reduced ilmenite concentration can be leached much faster after mechanical activation,yielding a synthetic rutile which meets the requirements of chlorination process containing 90.50% TiO2 and 1.37% total iron as well as combined CaO and MgO of 1.00%.The optimum oxidation and reduction conditions are as follows：oxidization at 900 ℃ in the presence of oxygen for 15 min and reduction at 750 ℃ by hydrogen for 30 min.

Leaching behavior of heavy metals with hydrochloric acid fromfly ash generated in municipal waste incineration plants

The extraction behavior of heavy metals from municipal waste incineration （MWI） fly ash was investigated systematically. The extraction process includes two steps, namely, fly ash was firstly washed with water, and then subjected to hydrochloric acid leaching. The main parameters for water washing process were tested, and under the optimal conditions, about 86% Na, 70% K and 12% Ca were removed from fly ash, respectively. Hydrochloric acid was used for the extraction of valuable elements from the water-washed fly ash, and the optimal extraction was achieved for each heavy metal as follows： 86% for Pb, 98% for Zn, 82% for Fe, 96% for Cd, 62% for Cu, 80% for Al, respectively. And the main compositions of the finally obtained solid residue are Ca2PbO4, CaSi2Os, PbsSiO7, Ca3A12Si3012 and SiO2.

Extraction of molybdenum and nickel from roasted Ni-Mo ore by hydrochloric acid leaching, sulphation roasting and water leaching

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.

Hydrochloric acid recovery from rare earth chloride solutions by vacuum membrane distillation

The possibility of the recovery of hydrochloric acid from rare earth （RE） chloride solutions was first experimentally studied by batch vacuum membrane distillation （VMD）. The recovery by continuous VMD was also studied to devise methods that enabled the operation of VMD setup in a stable condition as well as to increase the membrane-operating life The results indicated that HCl separation with RE by VMD was possible, and the recovery ratio of 80% could be achieved by batch VMD. In continuous VMD, when the temperature of circular solutions, circular rate, and downstream pressure was 62-63℃, 5.4 cm/s, and 9.33 kPa, respectively, the HCl concentration in circular solutions and the processing capacity per membrane area were obtained. The mathematical results were in accordance with the experimental ones.

Corrosion Inhibition Synergism between Lanthanum(Ⅲ) Ion and 8-Hydroxyquinoline for Zinc in Hydrochloric Acid

The effects of La 3+ ion and chelate reagent 8 hydroxyquinoline on the corrosion rate of zinc in hydrochloric acid were investigated by using weight loss method and electrochemical method. It is found that in a specific concentration range of La 3+ ion and 8 hydroxyquinoline, the obvious corrosion inhibition synergism is obtained. The mechanism of corrosion inhibition synergism was discussed on basis of adsorption theory.

Extraction of Zr(IV) from hydrochloric acid with tri-octyl amine and Cyanex 921 in kerosene

This article reports the extraction of zirconium （IV） from aqueous HC1 solution by tri-octyl amine （TOA）, Cyanex 921, and their binary mixture using kerosene as the diluent. The effect of some parameters on the extraction of Zr（IV） was investigated such as equilibration time, aqueous phase acidity, extractant molarity, chloride ion concentration, nature of diluents, and temperature. The extraction of Zr（IV） was found to be 99% from 7.5 M HC1 using the mixture of extractants containing 0.1 M TOA and 0.02 M Cyanex 921 in kerosene. Kerosene was found to be the effective diluent for the extraction of Zr（IV） with the binary mixture of TOA and Cyanex 921. The positive enthalpy change and positive entropy change in the binary extraction system show the endothermic process with an increase in entropy. Stripping of Zr（IV） from the loaded organic phase containing the mixture of TOA （0.1 M） and Cyanex 921 （0.02 M） indicates that HNO3 and Na2CO3 are the best stripping agents.

Hydrochloric acid-enhanced radiofrequency ablation for treating a large hepatocellular carcinoma with spontaneous rapture:a case report

Background:A ruptured hepatocellular carcinoma(HCC)is often fatal.In addition to surgery and transarterial embo?lization,radiofrequency ablation(RFA)might be another option for treating a ruptured HCC.Unfortunately,conven?tional RFA has a limited ablation zone;as such,it is rarely used to treat ruptured tumors.Case presentation:This case was a 60?year?old man who had a large,ruptured HCC in which hydrochloric acid(HCl)?enhanced RFA successfully controlled the bleeding and made the tumor completely necrotic.Conclusion:Considering the effectiveness of HCl?enhanced RFA in achieving hemostasis and tumor ablation,it might be a new option for treating large,ruptured HCCs.

Leaching of chalcopyrite with hydrogen peroxide in hydrochloric acid solution

The aim of this work was to investigate the leaching of chalcopyrite concentrate in hydrochloric acid with hydrogen peroxide as a strong oxidizing agent. The effects of the leaching variables on metal extraction, such as stirring speed, solid-to-liquid ratio, temperature and HCl and H2O2 concentrations, were studied. The maximum final copper extraction of 33% was attained with 3.0 mol/L H2O2 in 0.5 mol/L HCl at room temperature after 180 min of the reaction. The results showed that the copper extraction was increased in the first 60 min of reaction, after which it essentially ceased due to the fast catalytic decomposition of hydrogen peroxide. Further, solid-to-liquid ratio affected the copper extraction significantly and the highest copper extraction was obtained in the most dilute suspension（i.e., S/L ratio of 1：100）. The dissolution process was described by the first order kinetics equation. The apparent activation energy of 19.6 k J/mol suggested that the dissolution process was under diffusion control. The reaction orders for HCl and H2O2 were established to be 0.30 and 0.53, respectively. The results of the XRD and SEM/EDS analysis of the leaching residue indicated the generation of the elemental sulphur on mineral surfaces which tended to inhibit the leaching rate.

Leaching of iron concentrate separated from kiln slag in zinc hydrometallurgy with hydrochloric acid and its mechanism

It is taken as a novel prospective process to treat iron concentrate from hydrometallurgical zinc kiln slag forcomprehensive utilization of valuable metals by a hydrochloric acid leaching-spray pyrolysis method.The leaching mechanism ofdifferent valuable metals was studied.The results revealed that the leaching rates of Ag,Pb,Cu,Fe,As and Zn were99.91%,99.25%,95.12%,90.15%,87.58%and58.15%,respectively with6mol/L HCl and L/S ratio of10:1at60°C for120min.The actionof SiO2in leaching solution was also studied.The results showed that the precipitation and settlement of SiO2(amorphous)adsorbedpart of metal ions in solution,which greatly inhibited the leaching of Cu,Fe,As and Zn,so it is crucial to control the precipitation ofamorphous SiO2.

Leaching kinetics of calcium molybdate with hydrochloric acid in presence of phosphoric acid

Calcium molybdate(CaMoO4)is the main component of powellite and is a predominant intermediate in the pyrometallurgical and hydrometallurgical process of molybdenum.The extraction of Mo from CaMoO4 by a combination of phosphoric acid and hydrochloric acid was investigated.For further understanding of the leaching mechanism,the effects of five key factors were studied to describe the leaching kinetics.The results indicated that the dissolution rate of CaMoO4 was independent of the stirring speed.Mo extraction significantly increased with increasing HCl concentration and temperature,but decreased with increasing particle size.A shrinking core model with surface chemical reaction was found to withstand the dissolution of CaMoO4.The apparent activation energy was calculated to be 70.879 kJ/mol,and a semi-empirical equation was derived for the rate of reaction.

Hydrochloric acid enhanced radiofrequency ablation for treatment of large hepatocellular carcinoma in the caudate lobe:Report of three cases

BACKGROUND To report on the use of percutaneous hydrochloric acid(HCl) enhanced radiofrequency ablation(HRFA) for the treatment of large(maximum diameter ≥5 cm) hepatocellular carcinoma(HCC) in the caudate lobe.CASE SUMMARY Between August 2013 and June 2016, three patients with a large HCC(maximum diameter: 5.0, 5.7, and 8.1 cm) in the caudate lobe were treated by transarterial chemoembolization followed by computer tomography(CT) guided RFA using a monopolar perfusion RF electrode, which was enhanced by local infusion of 10%HCl at 0.2 mL/min(total volume, 3 to 12 mL). The output power of HRFA reached 100 W, and the average ablation time was 39 min(range, 15 to 60 min).Two patients each underwent one session of HRFA and one patient two sessions.After treatment, CT/magnetic resonance imaging showed that all the three lesions were completely ablated. There was no major complication. Two patients had asymptomatic bile duct dilatation. One patient died of tongue cancer 24 mo after ablation. The remaining two patients were alive and no area of enhancement is detected in the caudate lobe at 28 and 60 mo after ablation, respectively.CONCLUSION Percutaneous CT-guided HRFA is safe and efficacious in treating large HCC in the caudate lobe.

Hydrochloric Acid Recovery from Rare Earth Chloride Solutions by Vacuum Membrane Distillation (1) Study on the Possibility

The equilibrium between the gas-liquid phases of the system of HCl-RECl_3-H_2O was analyzed,and the possibility of hydrochloric acid recovery from rare earth chloride solutions by vacuum membrane distillation (VMD) was experimentally studied in the laboratory scale. The results indicate that increasing initial concentrations of both hydrochloric acid and rare earth increase recovery ratio of hydrochloric acid,and recovery ratio of 80% can be achieved. Concentrated multiple of rare earth shows great influence on recovery ratio,leakage ratio of rare earth is less than 2% generally,and pure acid can be acquired in the permeate side. The two factors,namely flux and leakage ratio,which may determine the future use of VMD were also discussed.

Preparation of Butyl Chloride from Butanol and Hydrochloric Acid Using Ionic Liquids as Catalyst

The catalytic performance of some quaternary ammonium salts for the liquid phase reaction of butanol and hydrochloric acid at different conditions was studied experimentally and compared with the traditional catalyst （ZnCl2）. The organic ammonium catalysts investigated include ionic liquids N-butyl-N-methyl imidazolium fluoborate （[BMIM][BF4]） and N-butyl-N-methylimidazolium chloride （[BMIM]Cl） as well as hydrochloric salts of N-methylimidazol （[HMIM]Cl）, pyridine （[HPy]Cl） and triethylamine （[HEt3N]Cl）. It is shown that the intrinsic catalytic performance of all organic ammonium salts except [HEt3N]Cl is slightly superior to ZnCl2, while the selectivity of butyl chloride is nearly at the same level around 96%. The conversion of butanol increases slightly with temperature and the catalyst amount added while the variation of selectivity is not obvious. Based on the recycle experiments, the ionic liquids as catalyst for the reaction of butanol and hydrochloric acid can be used more than 5 times, which suggests great potential of using ionic liquids as novel catalyst for such reactions.

Direct Spectroscopic Determination of Europium（ Ⅱ ） Concentration During Europium（ Ⅲ ） Electro-Reduction in Hydrochloric Acid Medium

UV-Vis spectroscopy was used to directly determine the concentration of Eu（ Ⅱ） during electroreduction of Eu （ Ⅲ ） in hydrochloric acid medium. Electroreduction was carried out in a flow type electrolyzer with glassy carbon cathode at the constant potential of - 800 mV vs. Ag/AgCl. The effects of oxygen and concentration of hydrochloric acid on the system were investigated. For 0.01 mol· L^-1 hydrochloric acid, calibration curves for Eu （Ⅱ） absorption bands at 248 and 320 nm were constructed. Molar absorption coefficients were estimated to be 2016 and 648 L· mol^-1·cm^-1, respectively. The absorbance strongly decreased with decrease in pH of the solution, whereas concentration of chloride had only a negligible effect.

荞麦提取物对钢在HCl介质中的缓蚀机理

目的提取制备一种环境友好型缓蚀剂,并研究缓蚀剂对冷轧钢在1.0 mol/L盐酸溶液中的缓蚀性能。方法利用超声波提取法从荞麦中提取得到荞麦提取物。采用失重法和电化学法研究荞麦(Fagopyrum esculentum Moench.)提取物(FEME)对冷轧钢在HCl介质中的缓蚀性能,测试缓蚀溶液的紫外光谱(UV)、电导率及表面张力,并通过扫描电子显微镜(SEM)、原子力显微镜(AFM)、X–射线光电子能谱(XPS)、红外光谱(FTIR)表征钢表面的微观形貌、化学组成,用接触角测量仪测定钢表面的亲水/疏水性,分析FEME中的主要成分,进而深入探究了其缓蚀有效成分及作用机理。结果FEME在1.0 mol/L HCl中具有良好的缓蚀性能,100 mg/L FEME的缓蚀率达90.1%(30℃);FEME在钢表面的吸附服从Langmuir吸附等温式,标准吸附Gibbs自由能(?GΘ)为–32~–27 kJ/mol,电化学缓蚀机理为“几何覆盖效应”。添加FEME后,有效降低了钢/酸界面的双电层电容值,提升了电荷转移电阻。缓蚀钢表面的SEM和AFM微观形貌表明,其腐蚀程度明显下降,接触角变大,疏水性增强,FTIR和XPS证实了FEME能有效吸附在钢表面形成缓蚀膜层,且缓蚀膜层主要是通过FEME在钢表面的物理吸附和化学吸附而形成,FEME成分中含有大量的—OH,—OH的存在会使这些成分质子化,从而与带负电荷的钢表面通过静电引力而发生吸附,而且分子中含有大量的O、N等杂原子和不饱和基团结构,有大量的孤对电子可以与Fe的空d轨道配位,从而产生缓蚀剂在钢表面的化学吸附。与浸泡前相比,在钢腐蚀浸泡后,缓蚀溶液的表面张力增加,是由于浸泡后部分缓蚀剂分子在钢表面发生了吸附,致使溶液体相中的缓蚀剂分子浓度下降而引起。钢在腐蚀浸泡后,因H+的消耗,电导率明显降低,但浸泡钢表面后的缓蚀溶液随着FEME浓度的增加,电导率增加,说明缓蚀剂在钢表面吸附后,与钢表面发生腐蚀反应的H+消耗减少。20℃时,质量浓度为100 mg/L的芦丁的缓蚀率为57.8%,FEME的缓蚀性能优于其主成分芦丁,其机理为黄酮类化合物与其他成分的协同缓蚀作用。结论FEME是一种高效、环保的混合抑制型缓蚀剂。

Enhanced photocatalytic hydrogen production activity of highly crystalline carbon nitride synthesized by hydrochloric acid treatment

Crystalline carbon nitride(CCN)prepared by a molten-salt method is attracting increased attention because of its promising properties and excellent photocatalytic activity.In this work,we further improve the crystallinity of CCN through synthesis by the molten-salt method under the action of aqueous hydrochloric acid(HCl)solution.Our results showed that the crystallinity of the as-prepared samples increased with increasing HCl concentration and reached the maximum value at 0.1 mol L^-1.This can be attributed to the removal of some potassium ions(K+)from the terminal amino groups of CCN by the aqueous HCl solution,which results in a release of the polymerization sites.As a result,the crystallinity of the as-prepared samples further increased.Moreover,the obtained 0.1 highly crystalline carbon nitride(0.1HCCN;treated with 0.1 mol L^-1 aqueous HCl solution)exhibited an excellent photocatalytic hydrogen evolution of 683.54μmol h^-1 g^-1 and a quantum efficiency of 6.6%at 420 nm with triethanolamine as the sacrificial agent.This photocatalytic hydrogen evolution was 2 and 10 times higher than those of CCN and bulk carbon nitride,respectively.The enhanced photocatalytic activity was attributed to the improved crystallinity and intercalation of K+into the xHCCN interlayer.The improved crystallinity can decrease the number of surface defects and hydrogen bonds in the as-prepared sample,thereby increasing the mobility of the photoinduced carriers and reducing the recombination sites of the electron-hole pairs.The K+intercalated into the xHCCN interlayer also promoted the transfer of the photoinduced electrons because these ions can increase the electronic delocalization and extend theπ-conjugated systems.This study may provide new insights into the further development of the molten-salt method.

Vapor-Liquid Equilibria for Water+Hydrochloric Acid+Magnesium Chloride and Water+Hydrochloric Acid+Calcium Chloride Systems at Atmospheric Pressure

Vapor-liquid equilibria for water+hydrochloric acid+magnesium chloride and water+hydrochloric acid+calcium chloride systems at atmospheric pressure were measured using a Othmer-type equilibrium still. The experimental data are correlated using a modified Meissner’s method. Satisfactory agreements are obtained between the experimental and the calculated results.

Corrosion Studies on Stainless Steel (FE6956) in Hydrochloric Acid Solution

The effect of hydrochloric acid concentration on stainless steel (Fe6956) at temperature range 303 - 333 ± 1 K has been studied using weight loss, thermometric and electrochemical polarization techniques. The corrosion rate of the stainless steel was found to be dependent on both temperature variation and acid concentration. The potentiostatic study showed that the active passive transition depends strongly on acid concentration while the weight loss measurements revealed that 2 M HCl at temperature 333 K had an appreciable corrosion rate which corresponds to 14.04 × 10﹣3 reaction number (RN) got from thermometric monitoring. Arrhenius equation and transition state theory were used to calculate kinetic and thermodynamic parameter such as Ea, ΔH* and ΔS*. Results obtained showed that corrosion reaction of Fe6956 in HCl is spontaneous and there is good agreement between the data got from the techniques employed.

Corrosion Inhibition of Carbon Steel in Hot Hydrochloric Acid Solutions

The dissolution of carbon steel in 5% HCl in the temperature range of 30~90℃ was inhibited by two organic compounds having the general formula: ClR NH2(CH2)n NH2 RCl where R is a benzyl group. The behaviour of these inhibitors in acidic medium were investigated using weight loss method, open circuit potential and linear polarization technique. These inhibitors provided satisfactory corrosion inhibition for carbon steel in hydrochloric acid solutions even at higher temperature and acid concentration (10%). The electrochemical results showed that the polarization resistance (Rp) values increased with increasing inhibitor concentration, also the corrosion current decreased and a higher inhibition efficiency was obtained. The protective properties of these two organic inhibitors were attributed to the chemisorption mechanism