Mineralogy and geochemistry of hydrothermal sulphide from a submarine volcanic high at 18°36.4'S Central Lau Spreading Center, Southwest Pacific

We report the mineralogy and geochemistry of hydrothermal sulphide from the crater of a volcanic high near 18°36.4′S of the Central Lau Spreading Center.During 1990s,that volcanic structure was reported active and sulphide samples were collected by MIR submersible.A section of a chimney-like structure from the crater-floor was studied here.The Fe-depleted sphalerites,and Co-depleted pyrites in that chimney were similar to those commonly found in low to moderate temperature(<300℃)sulphides from sediment-starved hydrothermal systems.Bulk analyses of three parts of that chimney section showed substantial enrichment of Zn(18%–20%)and Fe(14%–27%)but depletion of Cu(0.8%–1.3%).In chondrite-normalized rare earth element-patterns,the significant negative Ce-anomalies(Ce/Ce*=0.27–0.39)and weakly positive Eu-anomalies(Eu/Eu*=1.60–1.68)suggested sulphide mineralisation took place from reduced low-temperature fluid.The depleted concentration of lithophiles in this sulphide indicates restricted contribution of sub-ducting plate in genesis of source fluid as compared to those from other parts of Lau Spreading Centre.Uniform mineralogy and bulk composition of subsamples across the chimney section suggests barely any alteration of fluid composition and/or mode of mineralisation occurred during its growth.

Correlation between the Sulphide Capacity Index and the Slag Basicity

The relationships between the sulphide capacity index and the optical basicity, the mole fraction of oxygen ion and the Bell's ratio were investigated based on extensive lab scale equilibrium and industry scale quasi-equilibrium experimental data in the temperature range of 1300 1600℃. Although the sulphide capacity index has good relations with different representations of slag basicity. according to the data obtained under the lab scale equilibrium experimental conditions,the similar relations do not exist according to the data obtained under the industry scale quasi-equilibrium experimental conditions. So it is concluded that the sulphide capacity index, which has been considered as a measure of the slag basicity. can not be used for virtually all oxide slags of interest in the field of ironmaking and steelmaking.

A Simple Two-Phase System Involving the Commercial Organophosphorous Extractant Cyanex 471x for the Preparation of Silver Sulphide Nanoparticles

The facile chemical synthesis of silver sulphide nanocrystals from metal-loaded organic media, containing a silver-selective organophosphorous ligand as extractant, is reported. The method involves the phase-transfer of silver species from aqueous nitrate media to organic solution using the commercial extractant Cyanex? 471x (tri-isobutylphosphine sulphide, Cytec Co.) as extractant, followed by precipitation stripping using ammonium sulphide as strip reagent. The nanoparticles were structurally characterized, and some aspects of the synthetical process, are briefly discussed. Under the conditions studied, the extractant Cyanex? 471x was able to act as stabilizer adsorbing on the particles surface, maintaining the size of the particles nanometrical.

FAULT TREE ANALYSIS OF SPONTANEOUS COMBUSTION OF SULPHIDE ORES AND ITS RISK ASSESSMENT

A logic fault tree of mine spontaneous combustion of sulphide ores was built by the fault tree analysis (FTA) based on a lot of mechanism investigation of sulphide ore spontaneous combustion in more than ten mines and review of a great amount of relevant

Leaching Behavior of Complex Copper Sulphide Concentrate with Ferric Chloride by Microwave Irradiation

Microwave assisted leaching of complex copper sulphide concentrate with ferric chloride was investigated, and its mechanism was analyzed. The results show that the leaching rate by microwave irradiation heating is much faster than that by conventional heating.

Mechanochemical sulfidization of a mixed oxide-sulphide copper ore by co-grinding with sulfur and its effect on the flotation efficiency

Mechanochemical sulfidization of a mixed sulfide/oxide copper ore by co-grinding with sulfur and additives including Mg(NO3)2 and Fe(NO3)3 salts and iron,aluminum and magnesium powders was investigated for the first time.Also,the influence of sulfidization during the wet-milling process was examined on the separation efficiency and recovery of copper in detail.The results demonstrated that co-grinding with sulfur solely had the best flotation performance at the value of 0.5 wt.%and it was attributed to the possible existence of S\\O bonding on copper oxides surfaces.In addition,adding magnesium nitrate salt,magnesium powder,iron nitrate salt and aluminum powder as additive associated with 0.5 wt%sulfur into ball milling caused the flotation improvement at the amounts of 0.2 wt%,0.2 wt%,0.5 wt%and 0.5 wt%,respectively.Also,the effect of grinding time and sulfidization pH with 0.5 wt%sulfur solely was determined and pH s of 7.5 to 8.5 gave the best results.The highest recovery(75.76%)and separation efficiency(63.44%)were achieved at pH of 7.5 and 8.5,respectively.

Massive Sulphide Deposits Related to the Volcano-Passive Continental Margin in the Altay Region

The Devonian volcano-passive continental margin in southern Altay is a significant volcanogenic massive sulphide metallogenic belt. Acidic volcanism has been dominant on the inner side of the volcano-passive continental margin, i.e., near the old land, resulting in a Pb-Zn metallogenic sub-belt, in which the ore deposits are hosted by sedimentary rocks in volcanic series, as represented by the large Koktal Pb-Zn deposits. In the central part of the margin far away from the old land, bimodal volcanic formations are well developed, forming volcanics-hosted Cu-Zn metallogenic sub-belts, e.g., the large-scale Ashele Cu-Zn deposit. The Qiaoxiahala sub-belt on the outer side of the margin near the ocean ridge is located at the spreading central trough, where ophiolite suites are developed. This type of deposits is rich in gold and copper, similar to the Cyprus-type Fe-Cu-Au metallogenic sub-belt in metallogenic environment (represented by the Qiaoxiahala medium-scale Fe-Cu-Au deposit). From the old land to the ocean, the mineralizing age becomes younger, i.e., from Early Devonian→Early and Middle Devonian→Middle Devonian, forming a complete metallogenic zoning series on the volcano-passive continental margin. Comparative studies show that the massive sulphide deposits distributed on the volcano-passive continental margin are different from those formed under a plate subduction regime and oceanic ridge environment; the former have their unique features and wide distributions, representing a new type of volcanogenic massive sulphide deposits—the Altay type.

Comparative study on the passivation layers of copper sulphide minerals during bioleaching

The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching as djurleite〉bomite〉pyritic chalcopyrite〉covellite〉porphyry chalcopyfite. The residues were characterized by X-ray diffraction （XRD） and scanning electron microscopy （SEM）. It is indicated that jarosite may not be responsible for hindered disso- lution. The elemental sulfur layer on the surface of pyritic chalcopyrite residues is cracked. The compact surface layer of porphyry chalcopy- rite may strongly hinder copper extraction. X-ray photoelectron spectroscopy （XPS） further confirms that the passivation layers of covellite, pyritic chalcopyrite, and porphyry chalcopyrite are copper-depleted sulphide Cu4S11, S8, and copper-rich iron-deficient polysulphide CtuFe2S9, resoectivelv. The ability of these oassivation layers was found as Cu4Fe2S9〉Cu4S11〉S8〉iarosite.

Effects of forced aeration on community dynamics of free and attached bacteria in copper sulphide ore bioleaching

Bacterial community dynamics and copper leaching with applied forced aeration were investigated during low-grade copper sulphide bioleaching to obtain better bioleaching efficiency.Results illustrated that appropriate aeration improved bacterial concentrations and leaching efficiencies.The highest bacterial concentration and Cu^(2+)concentration after 14-d leaching were 7.61×10^(7) cells·mL^(−1) and 704.9 mg·L^(−1),respectively,at aeration duration of 4 h·d^(−1).The attached bacteria played a significant role during bioleaching from 1 to 7 d.However,free bacteria dominated the bioleaching processes from 8 to 14 d.This phenomenon was mainly caused by the formation of passivation layer through Fe3+hydrolysis along with bioleaching,which inhibited the contact between the attached bacteria and ore.Meanwhile,16S rDNA analysis verified the effect of Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans on the bioleaching process.The results demonstrate the importance of free and attached bacteria in bioleaching.

IN SITU MEASUREMENT OF BREEDING-FIRE OF SULPHIDE ORE DUMPS

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EXPERIMENTAL INVESTIGATION ON CHEMICAL THERMODYNAMIC BEHAVIOUR OF SULPHIDE ORES DURING SPONTANEOUS COMBUST

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Mineral sulphide-lime reactions and effect of CaO/C mole ratio during carbothermic reduction of complex mineral sulphides

Mineral sulphide （MS）-lime （CaO） ion exchange reactions （MS ＋ CaO = MO ＋ CaS） and the effect of CaO/C mole ratio during carbothermic reduction （MS ＋ CaO ＋ C = M ＋ CaS ＋ CO（g）） were investigated for complex froth flotation mineral sulphide concentrates. Phases in the partially and fully reacted samples were characterised by X-ray diffraction （XRD） and scanning electron microscopy （SEM）. The primary phases during mineral sulphide-lime ion exchange reactions are Fe304, CaSO4 Cu2S, and CaS. A complex liquid phase of Ca2CuFeO3S forms during mineral sulphide-lime exchange reactions above 1173 K. The formation mechanisms of Ca2CuFeO3S liquid phase are determined by characterising the partially reacted samples. The reduction rate and extent of mineral sulphides in the presence of CaO and C increase with the increase in CaO/C ratio. The metallic phases are surrounded by the CaS rich phase at CaO/C 〉 1, but the metallic phases and CaS are found as separate phases at CaO/C 〈 1. Experimental results show that the stoichiometric ratio of carbon should be slightly higher than that of CaO. The reactions between CaO and gangue minerals （SiO2 and A1203） are only observed at CaO/C 〉 1 and the reacted samples are excessively sintered.

Hydrogen sulphide detection using near-infrared diode laser and compact dense-pattern multipass cell

Sub-ppmv level detection of hydrogen sulphide(H2 S) using a 1.578-μm distributed feedback tunable diode laser combining with wavelength modulation spectroscopy and second harmonic detection scheme is reported. A home-developed novel compact dense-pattern multipass gas cell with an effective optical path length of 29.37 m is used to improve sensitivity and reduce sample volume. Detection parameters are optimized, including modulation frequency and amplitude. The analysis of Allan variance shows that a minimum detectable concentration 60 ppbv is obtained with a lock-in time constant of 10 ms, and a detection limit of 13 ppbv can be achieved by average in 300 s. The demonstrated H2 S sensor has a strong penitential application in natural gas process for regulating and controlling H2 S concentration.

Study on sulphide capacity of CaO-SiO_2-Al_2O_3-MgO-Fe_tO slags

The sulphide capacity of CaO-SiO2-Al2O3-MgO-FetO slags was studied at 1773 K using gas-slag equilibrium techniques. Utilizing a Pt crucible, the slag was equilibrated with a mixture of gases, namely, CO, CO2, SO2 and N2 to provide the partial pressure of oxygen and sulphur. It was shown that at fixed FetO and Al2O3 contents and a fixed { （%CaO）＋（%MgO）}/（%SIO2） ratio, the sulphide capacity decreases with increasing MgO content. At a constant （%CaO）/（%SiO2） ratio and constant MgO and Al2O3 contents, increasing the FetO content of the slags also results in an increase of the sulphide capacity. The rising basicity of （%CaO）/（%SiO2） from 1.0 to 1.4 at fixed MgO, FetO and Al2O3 contents significantly increases the sulphide capacity.

Physical chemistry mechanisms of CDR system in sulphide mineral flotation

The flotation tests, zeta potential measurements, and Fourier transform infrared spectroscopy （FTIR） analysis on galena, sphalerite, and pyrite were studied in a collecting-depressing-reactivating （CDR） system. In this system, sulphide minerals were first collected and acti- vated by the collector, and then depressed strongly by Ca（OH）2 in a strong alkaline solution. Finally, they were reactivated by H2SO4. The flotation tests of pure minerals showed that in the Ca（OH）2 depressing process sulphide minerals had similar flotation characteristics because they had already been influenced by the collector. Hence, the flotability differences between them were reduced. However, in the H2SO4 re- activating process considerable differences in the flotability between galena and sphalerite/pyrite were produced. That is to say, galena was relatively easy to be reactivated by H2SO4, but sphalerite and pyrite were not reactivated at pH 〉 11. The zeta potentials of sulfide minerals measured by the Zeta Plus presented irreversible characteristics on the change of pH values. The results of the FTIR spectra analysis indi- cated that the collectors already adsorbed on the mineral surface were removed partially by Ca（OH）〉

A study of self-heating characteristics of a pyrrhotite-rich sulphide ore stockpile

Original surface chemistry of sulphidesis altered upon contact with air, leading to ''oxidation'', which is accompanied by evolution of heat. The current study reports results of an investigation on extent of exothermicity of an experimental nickel-copper sulphide stockpile that was formed at a mining site in Sudbury, Canada. The ore contained pentlandite and chalcopyrite that are accompanied by a large quantity of pyrrhotite. The self-heating characteristics were recorded by temperature sensors placed inside the stockpile. Ambient conditions such as temperature, humidity, and wind velocity were simultaneously recorded. The inner temperature of the stockpile indicated significant fluctuations due to rapid changes, particularly in the outside temperature. The minimum and maximum temperatures recorded in the outside and inside were 5 and 10.5, 44.3 and 32 ℃, respectively. The self-heating capacity of the sulphide ore stockpile observed represents a mild case compared to that experienced by coals. Possible reasons are discussed.

QUANTUM CHEMICAL MECHANISM ON THE SURFACE OXIDATION AND FLOTATION OF SULPHIDE MINERALS

The surfaces of galena and pyrite,the adsorption of oxygen,and the reactions of ethyl xanthate on the sulfides were studied using quantum chemical calculations.In addition,the surface electron structures of the minerals were discussed.According to the results,the mechanisms of ionic exchange reaction and dixanthogen adsorption for the xanthate notation of galena and pyrite were explained.The important role of oxygen in collector and collectorless flotation processes was also investigated.

Recent Advance in the Electrochemical Detection of Sulphide and Sulphhydryl Species

This article aims at providing a critical review of some most recent developments in the electrochemical detection and measurement of hydrogen sulphide and the related species, which are of great significance to a variety of industries and in environmental moitoring. The molecular recognition processes are initiated by using either an organic precursor or a catalytic complex, leading to extensive ranges of detection. A series of advanced chemical and simulation techniques are used to probe the mechanistic details of the analytical chemistry involved.

Free-standing ternary metallic sulphides/Ni/C-nanofiber anodes for high-performance lithium-ion capacitors

As a promising energy-storage device,the hybrid lithium-ion capacitor coupling with both a large energy density battery-type anode and a high power density capacitor-type cathode is attracting great attention.For the sake of improving the energy density of hybrid lithium-ion capacitor,the free-standing anodes with good electrochemical performance are essential.Herein,we design an effective electrospinning strategy to prepare free-standing MnS/Co4S3/Ni3S2/Ni/C-nanofibers(TMSs/Ni/C-NFs)film and firstly use it as a binder-free anode for hybrid lithium-ion capacitor.We find that the carbon nanofibers can availably prevent MnS/Co4S3/Ni3S2/Ni nanoparticles from aggregation as well as significantly improve the electrochemical performance.Therefore,the binder-free TMSs/Ni/C-NFs membrane displays an ultrahigh reversible capacity of 1246.9 m Ah g-1at 100 m A g-1,excellent rate capability(398 mAh g-1 at2000 mA g-1),and long-term cyclic endurance.Besides,we further assemble the hybrid lithium-ion capacitor,which exhibits a high energy density of 182.0 Wh kg-1at 121.1 W kg-1(19.0 Wh kg-1 at 3512.5 W kg-1)and remarkable cycle life.

LEACHING OF PRECIOUS METALS FROM COMPLEX SULPHIDE ORES——2.DIRECT LEACHING OF Cu SULFIDE CONCENTRATE BY ACIDIC THIOUREA SOLUTIONS

Recovery of gold and silver from a sulphide concentrate by thiourea leaching was investigat-ed.The effects of various parameters on the process,such as oxidants,the initial concentrationof thiourea and acidity in solutions as well as reaction temperature,were systematically exam-ined.From the results it was confirmed that(a)oxidants had no significant influence on the dis-solution of gold and silver at a fixed initial concentration of thiourea;(b)the initial concentra-tion of thiourea and acidity affected the dissolution rate only in the earliest period of leaching;(c)the rate of the process was controlled by reagent diffusion.The optimum operations wereworked out for the thiourea leaching process of the concentrate.