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By F. B. Waanders

Coal, as energy resource, possesses numerous characteristics and properties which all have an influence on its gasification behaviour. The two properties considered as critically important when evaluating a coal source for gasification is its mineral content and slagging behaviour. Research has indicated that slagging formation can be inhibited or even prevented by the addition of a fluxing agent. It is thus of great importance to understand the mineral interaction during gasification in order to select a suitable fluxing agent for the prevention of slagging and clinker formation in the gasifier. The aim of the present project is to evaluate the effect of iron as a fluxing agent and study the transformation of the mineral and added iron during gasification. A pre-determined amount of pure elemental iron (between 2wt% and 20wt%) was added to a base case coal sample in order to study the effect of the addition of iron to the coal. The transformation of the iron in conjunction with the possible iron containing minerals present in the coal was studied by means of Mössbauer analyses. Typical characterisation techniques included proximate analyses, ultimate analyses and ash composition analyses. The ash fusion temperature analyses (AFT) were used to study and predict the slagging behaviour of the iron-spiked coal samples. Even though AFT analyses only provide an average flow property, it gives a good indication of the changes that the iron addition induces on coal properties. FactSage modelling was carried out in conjunction with the Mössbauer and AFT analyses. From the proximate, ultimate and ash composition analyses it was clear that the coal used con-formed to the average characteristics measured over an extended time period. From the AFT values it was seen that an increase in the flow temperature occurred with the addition of pure elemental iron to the coal, which can be of importance for operational purposes as to raise the gasifier temperature and not to have slagging problems to occur in the gasifier. The Mössbauer data show that he-matite is the main Fe-component that forms from the pyrite originally present and from the added iron to the coal, consistent with FactSage modelling, which shows that the partial oxygen pressure determines which mineral species will form. This study opens up new possibilities when considering operational problems experienced in in-dustrial gasifiers. Successful completion of this study and a study to look at reducing conditions in the gasifier will also add to the knowledge that already exists regarding fluxing agents.

Jan 1, 2014

By Richard K. Komarek, Antonios Zavaliangos, Roman T. Dec

Roller presses are widely utilized in mineral industry for fine milling and compaction. Recently used models are providing only limited information about the material behavior in the roll bite. This paper introduces a 2-dimensional finite element model for analyzing those two basic processes. A pressure-dependent plasticity model with linear elasticity was used as a constitutive model for the particular material. Coulomb friction law was used to describe phenomena on the material/roller surface interface. Two basic roller geometries are considered: smooth (used for milling and compaction) and with cavities, commonly used for briquetting. Comparison of the results obtained from the model with experiment indicates that they are following the general trends of experimental values recorded with laboratory roller presses. It is shown, that the model is suitable to analyze material behavior through all stages of the rolling process: feeding zone, nip region, neutral plane and release section. It can predict pressure, shear stress, slip of the material over the roller surface, material velocity field, failure of the compact during release and the course of other important process variables. This allows the process engineer to gain an improved understanding, leading to a better process and equipment design and control.

Jan 1, 2003

By R. S. C. Smart

Surface chemical factors, including the balance of hydrophobic (e.g. collectors) and hydrophilic (e.g. oxidation products, precipitates) species, are major control determinants in flotation rates of specific minerals and therefore grade and recovery. There are a number of challenges involved with the surface analysis of different mineral phases from process streams in a flotation facility. The first is to collect samples that are representative of the process and retain their surface chemistry prior to introduction into the instrument. The second challenge in studying the surface chemistry of specific minerals is to find reliable methods of mineral phase recognition. In surface analysis of mineral particles, confident mineral selection can be difficult with many multi-metal minerals and with precipitated, adsorbed, reacted and contaminant species in the outermost molecular layers. The third challenge is to provide a statistical surface analysis of multiple grains of the same mineral. Methods to achieve these aims are described. Principal component analysis (PCA) of ToF-SIMS data provides improvement in phase recognition, particle selection and associated variations in surface species. Specific examples from both lab and plant operations, demonstrate that this technique can be utilized to differentiate surface chemical factors promoting (hydrophobic species) or inhibiting (hydrophilic species) flotation. A study of copper ion transfer (inadvertent activation) from chalcopyrite to pyrite and sphalerite clearly identified a statistical difference in copper intensities between the sphalerite and pyrite phases corresponding to their flotation response. The PCA analysis applied to concentrate and tails samples collected from the Inco Matte Concentrator demonstrated extensive CuOH and NiOH transfer between chalcocite and heazlewoodite minerals. The statistical analysis has been able to identify mechanisms controlling recovery and selectivity. High intensity conditioning (HIC) tests in which sphalerite was separated from a complex sulfide ore gave a 5% increase in the overall Zn recovery. The PCA/ToF-SIMS statistical analysis revealed the discriminating depressant action of adherent aluminosilicate (gangue) fine particles and adsorbed ions on the surface of sphalerite grains. HIC conditioning resulted in the removal of these gangue fines improving surface collector attachment efficiency.

Jan 1, 2014

By S. Q. Zhu

Coal Water Mixtures (CWMs) are densed suspensions of coal particles in water. Viscosity is one of the most important rheological properties of CWMs and it is desired to be as low as possible. The slurry viscosity was influenced significantly by additive formation, the particle size distribution and the ash content of the coal. However, the influence of dispersants is most obvious. At present, there are several kinds of dispersants such as polymeric styrene sulfuric sodium, lignin sulfonate, humate, polycarboxy salt, ethylene epoxide surfactant. In this paper, a newly synthesized CWM dispersant has been reported, which is an efficient anionic surfactants of polycarboxylic acid type. The synthesis process includes three steps. At the beginning, the polyglycol acetate ester has been performed by acetic acid and polyethylene glycol (PEO) on the condition of acetic-acid/PEO ratio 1:1.1, at 368~373K for 30 minutes. Then the macro-monomer is prepared through the esterification of 85.71% acrylic and 14.29% polyglycol acetate ester, at 368~373K for 10 minutes. After that, the polycarboxylic acid CWM dispersant is polymerized using proper proportion macro-monomer, acrylic (AA) and sulfonic styrol sodium, at 368~373K for 1 hour. This new dispersants are used in the coal water mixtures formulation. Four kinds of coal used in the experiment are Shuang Yashan, Tunliu, Luning, Changcun samples. ? The highest concentration for shuanyashan coal is 70% when the dosage of dispersant is 0.4%, and the content of -200 meshes particles is 75.53%. As the dosage of dispersant de-creases to 0.25%, the Shangyashan CWM concentration is 67%. ? For Tunliu coal CWM concentrations are in the range of 76% to 75% when dosage of the dispersant changes from 0.4% to 0.25% at the same particle size distribution of 83.5% minus 200 meshes. ? The highest concentration for Luning coal is 69% when dosage of the dispersant is 0.4%, and the content of -200 meshes particles is 88.86%. ? For Changcun sample, the coal concentration of CWM is 73%~75% when dosage range of the dispersant is 0.35%~0.5%. The experiments show that the synthesied dispersant is quite promising for some coals CWM preparation, but a little bit coal-dependent. The Proximate and Ultimate analysis, surface characteristic measurement have been made to investigate the interactions between coal and additives.

Jan 1, 2014

By Z. T. Yuan, S. L. Qi, Q. Y. Meng, G. X. Zou, L. X. Li, J. W. Lu

"The selective separation of pentlandite from serpentine was investigated using the magnetic coating-magnetic separation by conditioning slurry pH value, stirring speed, magnetic field intensity and controlling dosages of sodium hexametaphosphate (SHMP) and sodium oleate (SO). The optimal conditions were obtained as follows: the natural pH of 6.8-7.2, stirring speed of 2300 rpm, magnetic field intensity of 200 kA m-1, SHMP of 60 mg L-1, and SO of 400 mg L-1. Results showed that the Ni grade was 21.4% with the Ni recovery of 81.4% and MgO content of 3.8%. FTIR indicated that coagulant of SO preferentially adsorbed onto pentlandite and magnetite particles while hardly adsorbing onto serpentine particles when dispersant of SHMP was used. Thus, the selective magnetic coating of magnetite on pentlandite surfaces could be formed due to the formation of hydrophobic surfaces on pentlandite and magnetite particles. Calculations of DLVO (Derjaguin-Landau-Verwey-Overbeek) confirmed that interactions between magnetite and pentlandite particles were much stronger than that between magnetite and serpentine due to the existence of hydrophobic interactions with the addition of SO. Consequently, the pentlandite was successfully separated from serpentine. Therefore, this study exhibits the potential to separate pentlandite from serpentine minerals for practical applications and thus deserves further study.INTRODUCTION It has been well known that the separation of pentlandite from serpentine is a worldwide challenging issue in the processing of sulphide nickel-copper ores. Because the serpentine mainly causes the high pulp viscosity and slime coating on the pentlandite, which interferes with the flotation process of pentlandite (Cao et al., 2016; Feng et al., 2012). The fibrous mineral of serpentine preferentially attaches to the air bubble, forming bubble-macrofibers aggregates, which are easily floated into the nickel concentrates, resulting in the decline of Ni grade (Alvarez-Silva et al., 2016; Kusuma et al., 2014). In addition, the serpentine adheres to the pentlandite as hetero-aggregation or slime coating via the electrical interaction between a positively charged serpentine and a negatively charged pentlandite, which decreases the hydrophobicity of pentlandite and reduces the collector adsorption (Feng et al., 2013). In other words, the presence of serpentine or the occurrence of aggregates (including slime coating and bubble-macrofibers aggregates) seriously affects the flotation process and deteriorates the flotation of pentlandite. Therefore, we propose magnetic separation to recover pentlandite from serpentine with the magnetic coating technology, which is different from forth flotation."

Jan 1, 2018

By Wei Qu, Yongsheng Song, Xingyu Liu, Wenjuan Li, Shuang Liu, Guiying Zhou, Bowei Chen

The Pb,Sb,Zn multi-metal sulphide ore is processed in sequence of beneficiation of jamesonite, sphalerite . Due to relative large amount of collector (xanthate), activator (CuSO4) and regulator (lime) during different flotation stage, the flotation wastewater from sphalerite beneficiation stage can’t be directly recycled to the first lead flotation stage. In this paper, the flotation wastewater from sphalerite beneficiation stage was treated by Ozone and BAC technology, results showed that when the influent concentation of COD and copper ion were 850 mg/L, 10.48mg/L respectively, the Ozone and BAC technology could effectively treat such type of water. In the treated wastewater, the COD is 60mg/L, copper ion concentration is 0.023mg/L, pH is 7.0, which satisfy the need of Pb,Sb-Zn preferential floatation separation process. After recycle of the treated wastewater to Pb,Sb floatation circuit, qualified Pb,Sb concentrate and Zn concentrate were obtained.

Jan 1, 2014

By Y. M. Zhu

Lead in environment often causes a serious health hazard. The removal of Pb2+ from aqueous phase is a beneficial project. In this paper, deposited Saccharomyces cerevisiae (S.c.) was chosen as adsorbent, Pb2+ ions as adsorbate, and the process of biosorption was studied. The dynamics of the adsorption was investigated. The adsorption mechanism of Pb2+ by S.c. cells was also investigated by detecting microstructure, zeta potential under different pH value, FT-IR spectra of the S.c. particles before and after biosorption. It was shown that the biosorption of Pb2+ by deposited S. c. is a rapid process, and the adsorbing equilibrium is reached within 10 minutes. The Zero point of zeta potential of S.c. cells is pH=3.3. When 2.0<pH<3.3, there exists biosorption (biosorption rate 76%~88%), which means static bio-sorption been not the only kind of biosorption. FT-IR spectrum analysis showed that groups on bacteria surface were mainly characteristic groups of protein and amylase; oxo-groups and nitric-groups on S.c. cell surface could chelate with heavy metal ions. Chemical adsorption might exist in the process.

Jan 1, 2014

Gold thiosulfate complex is difference with gold cyanide complex, which is easily adsorbed on activated carbon while gold thiosulfate complex cannot be satisfactorily recovered by activated car-bon. However, Gold thiosulfate could be recovered by activated carbon if cyanide is added into the thiosulfate solution. To avoid the cyanide solution, this paper will review several possible processes to recover the gold from thiosuldate solution: such as the cementation with metals, ion exchange resin and solvent extraction. The gold cementation with the powders of zinc, copper, iron and aluminium will be discussed. The advantage and disadvantage of each are compared. The consumption of thiosulfate and copper and feasibility of solution recycling will be discussed. The gold recovery by some ion exchange resins will be suggested. The processing conditions, its applications and the resin elution methods will be presented. The gold recovery by using solvent ex-traction will be reviewed. The processing conditions of solvent extraction process are discussed and compared.

Jan 1, 2014

By P. M. Solozhenkin, V. N. Kovalev

Russia is a global antimony market leader. The three major antimony production provinces are Sakha Republic (Yakutia), Krasnoyarsk Territory and Trans-Baikal Territory. Russia’s largest antimony resources are Zhipkozhinsky and Solonechensky deposits in Sakha Republic (Yakutia) and Olimpiadinskoe deposit in Krasnoyarsk Territory. This work demonstrates the efficiency of computer programs and chemical technology aimed at the study of the behavior of collectors used in the processes of flotation of antimony, arsenic and Au (I – III) minerals. The most promising collectors for the flotation of ores containing antimony and gold on the basis of P(V) and compounds with S, O and N atoms were chosen. The mechanisms of interaction with the mixtures of two or three components of collectors were studied. High recovery of antimony and gold was reached in the processing of Au-Sb ores of Sarulah and Sentachan deposits in Sakha (Yakutia). X-ray radiometric methods of separation of antimony ores of Trans-Baikal Territory deposits were proposed. In order to choose the most cost-effective solvents for hydrometallurgical processing of Sb, Au-containing concentrates the method based on clusters formation between transition solvents and antimony minerals was suggested. The nature of Au losses was theoretically revealed in the sulfide-alkaline process. On the base of computer simulation, the formation of various complexes of (KAu) types was developed, for example, hydrosulphidic gold, thiosulfates of gold - Na3AuS4O6, antimony and arsenic gold, trithiostibate (III) and trythioarsenate (III) KAu were produced. The practice of processing of goldantimony concentrates to produce high-quality antimony trioxide and antimony-gold containing alloy (AGCA) regarding the special conditions of the Far North region, were analyzed. The affinage of AGCA was recommended. Creative project development of antimony industry in Russia in order to produce antimony compounds and pigments, including pyriform compounds and flame retardants (antipyrenes) is discussed.

Jan 1, 2018

By Kaioeng Wang, Qi Liu, Yahui Xiang

"In the differential metal sulfide ore flotation it is desirable to replace the toxic inorganic depressants with environmentally benign chemicals. Chitosan, as a natural and non-toxic polymer, has been proven to be an efficient depressant for chalcopyrite while allowing galena to be floated by xanthate collectors. However, the poor solubility of chitosan limits its potential applications as the flotation could only be carried out at about pH 4 where chitosan is soluble. A carboxymethyl derivative of chitosan, named N-carboxymethyl chitosan (N-CMC), was synthesized by substituting the amino groups of chitosan with carboxymethyl groups. The substitution significantly improved the solubility of chitosan. The structure of N-CMC was studied and compared with chitosan via Fourier transform infrared spectroscopy (FTIR). Flotation tests were performed on single minerals and mineral mixtures (with weight ratio of 1:1) with the addition of appropriate amount of potassium ethyl xanthate (KEX) and N-CMC. The solution pH was varied from neutral to alkaline. The flotation concentrates and tailings were collected and analysed for the contents of copper and lead. FTIR measurements showed that new peaks of C=O stretching of -COOH and N-H deformation of -NH- appeared in N-CMC, which indicated that the carboxymethyl groups were introduced and the amino groups were the sites for the substitution. Flotation results indicated that N-CMC could depress either chalcopyrite or galena depending on the pH. The results were not affected by the sequence of KEX and N-CMC addition. Therefore, N-CMC is potentially useful in Cu-Pb sulfide separation following a bulk Cu-Pb flotation. The N-CMC was also found to have surface cleaning functions, and was able to remove contaminating copper ions from galena surfaces. Therefore, its application in sulfide ore flotation is expected to be more robust than the original chitosan."

Jan 1, 2014

By X. Tan

In this paper, the application of the metallurgical residue produced from oceanic cobalt-rich crusts leaching process is studied in the area of wastewater treatment. The modification of the sulfuric acid leached residue and the adsorption behavior behaviour of heavy metal ions such as (Pb(II), Cu(II), Zn(II), Cd(II), Ni(II), Mn(II), Co(II), As(III)) in the waste-water on the surface of the residue are investigated. The rate of adsorption efficiency of heavy metal ions in the wastewater on the modified sulfuric acid leached residue is investigated. It is showed that when the initial pH value of wastewater containing heavy metal ions including Pb(II), Cu(II), Co(II), Ni(II), Mn(II), Zn(II), Cd(II) and As(III) range from 1.4 to 1.9, with the use of the modified leached residue, As(III) ion can be selectively separated from wastewater, and the separation efficiency can reach 90%~100%. The adsorption efficiency is affected by pH, reaction time, amount of adsorbent and the initial concentration of heavy metal ions in wastewater. The results showed that the optimum pH was natural pH value and the absorption equilibrium time was 2 hours. The adsorption efficiency of heavy metal ions increases with the addition of adsorbent and de- creases with the increase of the initial concentrations of heavy metal ions in wastewater. The heavy metal ions polluted wastewater, of which concentration is about 22.5~793.6 mg/L, can meet the national disposal standard for industrial wastewaters in China very well, after 2 hours treated by 3.75~7.50 g/L modified adsorbent at room temperature. Standard methods were used to investaged investigate the absorption behaviour between abosorbentabsorbent and metal ions in the wastewater. It is concluded that the adsorption behaviour of Co(II), Mn(II) and As(III) ion fits Freundlich iso-therm, while the adsorption behaviour of Pb(II), Cu(II), Zn(II), Cd(II) and Ni(II) ions fits Langmuir isotherm, and the saturated adsorption amount of the modified adsorbent is about 54.0~336.7mg metal/g?adsorbentabsorbent. It is suggested that the modified sulfuric acid leached residue produced from oceanic cobalt-rich crusts is environmentally attractive and meaningful as absorbent used in heavy metal ions polluted wastewater.

Jan 1, 2014

By Saeed Farrokhpay

It is known that the grinding condition has a major effect on the beneficiation characteristics of the minerals in subsequent processing, in particular, flotation. In the flotation process, particles surface and their condition can significantly influence collector adsorption and flotation performance. For example, particle shape and its surface roughness occurred during grinding may influence flotation characteristics of a specific ore. In fact, adsorption of different cationic and anionic species on mineral surfaces can be varied depending on the selected comminution procedure. The flotation performance of sulphide minerals can be detrimentally affected by the surface oxidation. The amount of surface oxidation may reduce the hydrophobicity of the mineral and makes adsorption of collectors less selective. Improved liberation may generally result in improved flotation recovery. However, this may result in finer grinding and slimes, and consequently, reduce the overall flotation recovery. This paper discusses the effect of wet and dry grinding on copper flotation of a complex Cu-Pb-Zn ore. Industrially, wet grinding is preferred due to its higher energy efficiency and owing to downstream processing requirements. In this study, series of flotation tests were conducted,and surface analysis (XPS and ToFSIMS) were performed after wet or dry grinding at two different P80 values. Mineralogical study was also conducted to investigate the liberation of valuable minerals after grinding. A higher copper flotation recovery was found for wet grinding. However, the copper recovery was increased by further grinding in both conditions (wet and dry). The results showed a higher collector adsorption on copper mineral surfaces after wet grinding. The surface analysis also revealed that the ore is slightly more oxidized after dry grinding probably due to higher temperature during dry grinding.

Sep 1, 2012

By John Nell, Paul den Hoed

Carbochlorination tests were conducted with matched particle-size fractions of rutile, ilmenite and high-titania slag in a small bubbling fluidized-bed reactor. The effects of temperature, the type and proportion of solid reductant in the charge, and the fraction of Cl2 in the fluidizing gas were investigated. Tests confirm the need for solid carbon in the bed if chlorination is to run at high rates. With solid carbon in the bed, CO supplied with the fluidizing gas does not increase significantly the degree of chlorination after 75 minutes. Ilmenite is chlorinated more quickly than titania slag, which in turn is chlorinated more quickly than rutile. Rates of chlorination at 1100°C and 1000°C are much the same and significantly higher than at 900°C. Chlorination is associated with significant increases in particle porosity (even for rutile), which is brought about by the rapid initial chlorination of FeO and MnO (in ilmenite and slag) and (it is argued) by the chlorination of Ti2O3 which forms at high-energy surface sites. A reaction mechanism is presented; where possible, its validity is demonstrated by the support of empirical observations.

Jan 1, 2003

By Herman D. Mendoza

"The removal of finely dispersed mercury from the effluent of small-scale gold mining operations and the eventual recycling of the recovered mercury was investigated. The conventional method of amalgamation, or “ball milling”, involves the mixing of a substantial amount of mercury with ore to recover free gold during the grinding stage. During grinding, a portion of the mercury is transformed into minute droplets, which readily float and disperse in the effluent. A kilo of gold ore containing 20-30 g Au/t, when ground with 3 g of mercury, yields 0.005 to 0.050 mg/l of mercury in the effluent, exceeding the concentration of 0.002 mg/l allowed by law for surface water.A rapid recovery/ recycling process was introduced using the surface-chemical properties of finely dispersed mercury in aqueous suspension. It was observed that fine droplets of mercury in an aqueous environment readily attached onto a collector having positive surface potentials for pH 3 to 10. An example of a suitable collector is alumina (Al2O3), which has an iso-electric point of pH 9.8. When an effluent, coming from a settling procedure after an amalgamation-grinding stage, was passed through a column-bed packed with alumina fiber, removal and subsequent collection of finely dispersed mercury occurred under acidic conditions, pH 3-6. Recovery was around 99.5%, yielding an acceptable quality of water safe for disposal into the aquatic environment. The collected droplets of mercury, which are left in the column-bed of alumina fiber, were subsequently treated with a cleansing solution at alkaline conditions pH 10 -12. At these conditions, both mercury and alumina fiber carry negative surface potentials, which results in the eventual detachment of attached mercury from the alumina collector. The effective recovery of attached mercury from the alumina collector by the detachment procedure is only 30-35%. The collected mercury from the cleansing stage can be collected, cleaned and can be used for subsequent amalgamation processes. The attachment and detachment behaviour of finely dispersed mercury onto and from the microscopic collector alumina is shown in Figure 1. The result of attachment and detachment were analyzed using existing interaction energy theories like the Darguin-Landau- Verwey- Overbeek (DLVO) Theory."

Jan 1, 2003

By Érica Linhares, Anderson Silveira Lopes, Aline Costa

In the production units of ferromanganese alloys wastewater are generated. They mainly arise from gutters of drainage water from warehouse of raw material (manganese ore, reducing agents and other), product and slag. This wastewater, in general, may contain particles that will suffer difficulty to naturally decant, giving the water turbidity and color characteristics. Thus, this study aims to characterize the effluent, the treated water and the sludge from the sedimentation tank from the one main Brazilian plant. The investigated characteristics were: turbidity, total solids (TS), suspended solids (SS), dissolved solids (DS), pH, Eh, COD (chemical oxygen demand), residue classification and chemical analysis by ICP - OES. The turbidity before treatment was 417 NTU and after passing through the tank, 44 NTU, a figure slightly higher than the emission standards for Class 1 regulated by the Brazilian environmental legislation in force. The values for TS, SS and DS of the effluent were 225, 114.3 and 110 mg/L, respectively. For the treated water the values were 93, 48.3 and 45 mg/L for TS, SS and DS, respectively. The sedimentation process was able to reduce by 21 % of the COD. In the test of loss on ignition (LOI) from the tank bottom sludge were observed losses of 29.35 %, while the volatile analysis found 20.70 % of volatiles in the sample. It was determined that the concentrations of Al, Fe, Mn and S are, respectively, 0.1875 mg.L-1, 0.3071 mg.L-1, 0,789 mg l-1 and 0.00828 mg.L-1, values above the maximum allowed by law. Based on the analysis of X-ray diffraction, the identified minerals in the sludge were quartz, muscovite, kaolinite, calcite and albite.

Jan 1, 2014

By Anuttam Patra, Romain Bordes, Andreas Fredriksson, Tommy Karlkvist, Krister Holmberg, Kota Hanumantha Rao

The present investigation aims to develop and distinguish mineral specific reagents with two functional groups for use in flotation of calcium containing minerals. For this purpose, a series of dicarboxylate-based surfactants with varying length between the carboxylate groups (one, two or three methylene groups) were synthesized. As reference, a surfactant with the same alkyl chain length but with only one carboxylate group in the polar part was synthesized. The adsorption behavior of these new reagents on pure apatite and calcite mineral surfaces was studied using Hallimond tube flotation, FTIR and ? potential measurements. The relation between the adsorption behavior of a given surfactant on a specific mineral surface and its molecular structure over a range of concentration and pH values, as well as the region of maximum recovery were established. It was found that one of the reagents, with a specific distance between the carboxylate groups, was much more selective for a particular mineral surface than the other homologues synthesized. This selective adsorption of a given surfactant to a particular mineral surface relative to other mineral surfaces as evidenced in flotation studies is substantiated by ? potential and infra-red spectroscopy data.

Jan 1, 2014

By S. Z. Khan, Veerendra Singh, Y. Rama Murthy, S. Prasad, Sunil Kumar Tripathy, Gajanan Kapure

"In this study, a low-grade ferruginous low-grade chromite ore was subjected to reduction roasting by using conventional heating as well as microwave heating. Sukinda chromite ore deposit contains majorly iron-bearing minerals as gangue phase. The magnetic susceptibility of these minerals enhances effectively after reduction roasting. Alteration of crystalline structure and magnetic property of these metals enables separation of low-grade ore by using magnetic separation. Conventional roasting studies by varying the temperature, time of reduction and reductant dosage were changed for low-grade ferruginous chromite ore. Similarly, microwave power, retention/exposure time and reductant dosage varied for reduction roasting studies under microwave environment. It is found that low-grade ferruginous chromite ore can be upgraded by reduction roasting and 61.2% Cr2O3 was recovered with a chromium-to-iron ratio of 1.93 from feed chromium-to-iron ratio of 1. Microwave reduction roasting studies resulted in upgradation of chromium-to-iron ratio to 1.73 with a recovery of 21% Cr2O3.INTRODUCTION The chromite ore occurs as a spinel containing oxides of chromium, iron, magnesium and aluminium. Most of the Indian chromite deposits are of ferruginous (rich in iron content) which indicates the abundance of ferruginous gangue minerals along with chromite. The primary use of chromite ore is towards the production of ferrochrome alloys. Chromite ores with less than 40% Cr2O3 and the chromium-to-iron ratio (Cr-to-Fe ratio) <1.8 is considered to be unsuitable for the smelting process (Tripathy et al. 2012, Tripathy et al. 2012a). A considerable amount of low-grade chromite ore and overburden excavated during chromite mining is getting accumulated every year, causing a threat to the environment. Its disposal poses a significant challenge and, hence, the beneficiation of low-grade chromite ore and its utilisation has been attracting a lot of attention. Different physical method of beneficiation methods is generally employed for the improvement of the Cr-to-Fe ratio (Tripathy et al. 2012, Murthy et al. 2011, Tripathy et al. 2012a, Tripathy et al. 2013, Tripathy et al. 2016, Tripathy et al. 2017, Tripathy et al. 2017a). It is observed that the enrichment of the chromite ore is carried out by using gravity and in some places by magnetic separation. However, the enrichment of Cr-to-Fe ratio from low-grade ferruginous chromite ore is difficult by using the above-mentioned beneficiation methods due to the presence of near gravity and near-magnetic susceptibility minerals along with chromite. However, an alternative beneficiation method is needed to explore for the beneficiation of such mineral deposits. Reduction roasting followed by magnetic separation is an alternative option for the separation of these types of ores which is widely reported for the iron and manganese ore (Li, et al., 2010; Chun, et al., 2014, Rath et al., 2018). These processes are majorly focussed on differentiating the magnetic susceptibility between minerals and subsequent separation by using magnetic field. The main advantage of such method is dry process option along with the pre-processed product for the costly smelting process. Also, the roasting of minerals in a microwave environment is also an active research topic in the recent time. So, the amenability of the separation feature of the roasting process by using conventional heating as well as microwave heating can be can be studied for the low grade ferruginous chromite ores."

Jan 1, 2018

By Y. G. Sun

This paper mainly reported separation manganese silver oxidized ores process by amylum de-gradation reduction and its influencing factors. When dosage is given according to nMn : nH2SO4 : n(C6H10O5)n : nH2O=1:k21.8: k116.66:30, the amount of up to 95.93% Mn leach rate and less than 2% silver loss can be obtained. Cyanidation process was used to extracted silver from leaching Mn residues. Silver leach rate could reach 94.15% at consumed amount of 1kg/t NaCN for 1h. Silver leach recovery rate was more than 92.27% by leaching Mn and cyanidation two-step processes so manganese and silver were separated effectively.

Jan 1, 2014

By L. J. Li, Q. Zhang, Z. H. Liu, Q. L. Chen

Phosphogypsum (PG) is an industrial waste from the production of phosphate fertilizer. The utilization of PG is restricted by its containing impurities, and the pretreatment is crucial to eliminating these impurities. The purpose of the research is to recycle pretreatment PG as raw material for preparation of a-calcium sulfate hemihydrate (a-HH) by salt solution method. The effect of pretreatment technologies of lime neutralization and washing on dehydration rate, phase composition and morphology evolution of a-HH were investigated by crystal water content analysis, XRD and SEM. Furthermore, the change of pH in the reaction process was also discussed in detail. The results show that the dehydration rate of conversion PG to a-HH increases and the corresponding induction period, crystal growth period and total time decrease with an increase in CaO dosage from 0.2% to 0.6%. In the presence of 0.4% CaO or 0.6% CaO, the a-HH presents a long hexagon-prism-shaped crystal with a purity of 94%, and the end face of a-HH presents polyhedron. The system pH sharply decreases with the reaction time under different CaO dosage, and the pH variation from the initial alkalinity to acidity. The main reason is that as the co-crystallized phosphorus dissolved and released HPO42-, and with the pH decreasing to 4-5, HPO42- transformed into H2PO4-. The dehydration rate of washing PG is lower than that of original PG. Compared with the original PG, a-HH with the larger width and smaller aspect ratio can be achieved from the pretreatment PG subjected to lime neutralization and washing, meanwhile the crystal surface is more smooth.

Jan 1, 2018

By Eduard Stefanescu, James M. Mwase, Egon Sehner, Stoyan Gaydardzhiev

"The study is focused on investigating the production of synthetic rutile of 95% purity or higher from a Norwegian ilmenite ore concentrate. This was to be achieved using a sequential process involving oxidative-reductive roasting at 975°C, followed by magnetic separation to further concentrate the sample and finally leaching with 20% HCl to remove mostly Fe-based impurities leaving behind synthetic rutile. The key process parameters considered were roasting time (1 and 2 hrs), leaching temperature (100, 125 and 145°C), pulp density (15 and 25wt%) and leaching time (3 and 6 hrs). The option of directly leaching the concentrate without pre-treatment was also evaluated. Test work was conducted using samples screened to a size fraction of 105-212 µm. Samples were leached in a 1 L glass autoclave. The reactor was hermetically sealed and thus the resulting pressure was not controlled but was dependent on the process temperature. The product from leaching was calcined and analysed via XRD and SEM to determine the purity of the product. The magnetic separation step was found to be ineffective and discontinued early in the study. Thus far a product with 97% synthetic rutile purity as analysed by SEM has been produced by directly leaching the concentrate at a temperature of 145°C, pulp density of 25wt% and leaching time of 6 hrs.INTRODUCTION The study investigates the use of a process route comprising oxidative-reductive roasting, followed by magnetic separation and then hydrochloric acid leaching and calcination to produce synthetic rutile from ilmenite concentrate. The grade of synthetic rutile produced should be suitable for chlorination to produce pigment grade TiO2. Hence the proposed process should produce a product consisting of no less than 95% synthetic rutile. Additionally, the product should have no more than 1.5wt% combined content of CaO and MgO (Zhang et al., 2011) as they tend to form high-boiling-point chloride leading to the malfunctioning of fluidized bed chlorinator (Cardarelli, 2008). Finally the product should have no more than 2.1wt% of Fe2O3."

Jan 1, 2018