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By Waraporn Piyawit

Grinding sludge from the sintered neodymium-iron-boron (NdFeB) magnets production process was enriched with critical rare earth elements (neodymium, dysprosium and praseodymium), which can be up to 30% in the magnets. The demand of NdFeB magnets are simultaneously growing. Therefore, rare earths recovered from waste residue would reduce the demand of rare earth elements from primary sources. In this study, the feasibility of recycling rare earths through a hydrometallurgical process was investigated. The selective leaching of Nd from grinding sludge can successfully raise the rare earths concentration to 70%. The necessity of an oxidation pretreatment to improve the selectivity between Nd and Fe will be described.

By Augusto Viana Leandro Teixeira

Rare Earth Elements (REE) are fundamental for modern life products and green technologies. Supply constraints and the price peak of 2011 boosted intensive research for alternatives for processing and separation. Complex monazite- type, rare earth ores usually contain high acid consumption impurities, such as iron and aluminum, and radioactive thorium in their composition. These impurities are not removed by conventional concentration processes due to fine, micro-level association between the REE carrying minerals and the gangue minerals. This work presents a selective process route for REE extraction from iron-rich, monazite ores. The process involves sulfation by addition of concentrated sulfuric acid and pyrohydrolysis at temperatures of approximately 700–750 °C. Experimental results show REE extraction higher than 70% and low iron (below 5%) and thorium extraction (below 10%). A method based on thermogravimetric analyses was shown to be adequate to predict the behavior of a given ore sample in the sulfationselective pyrolysis-leaching process.

By M. D. Stephens

A new, one-step process for extracting titanium from titaniferrous materials has been demonstrated. In the process, depleted uranium tetrafluoride (DUF 4), a solid, is mixed with ilmenite (FeTi03) and heated to 900°C. Titanium is extracted in the vapor phase as titanium tetrafluoride (TiF4) and the DUF4 is converted to uranium-iron oxide. The process has been found to selectively fluorinate the titanium in ilmenite and is capable of producing high purity TiF 4 with very low iron content. TiF 4 can be collected by condensation or through reaction with a fluoride salt such as NH4F, KF, or NaF. The TiF4 produced from the process can be used to make titanium metal, titanium oxide, or fluorotitanate compounds. Since the fluorination process is highly selective for titanium, it avoids many of the separations and waste issues common to other titanium extraction processes.

Jan 1, 2001

By J. D. Miller

Low-level radioactive contaminated soils (10-500 pci/gm) created by defense-related activities at certain superfund sites, such as Nevada Test Site (NTS), is a current environmental concern. Many of these contaminated sites may require appropriate cleanup and restoration, which could cost billions of dollars and put tremendous pressure on our limited financial resources. Therefore, the development of a selective flotation process to separate such radionuclides from contaminated soils should be considered. In this study, both a pure depleted UO2 sample and three synthetic UO2/soil mixtures were used to evaluate surface chemistry features and to examine the possibility for the flotation of fine UO2 particles from selected soils. It was intended that this model system would be a reasonable representation of contaminated soils such as those found at the Nevada Test Site which are reported to be contaminated by PuO2 fallout. The effect of reagent schedule, particle size distribution, and surface charge are discussed with respect to the flotation separation of the UO2/soil mixtures. It was found that both commercial fatty acids and reagent grade sodium oleate are effective collectors for UO2 flotation provided the pH is adjusted to the range of pH 8-9. The bench-scale flotation results successfully demonstrated that froth flotation technology can be used to remove UO2 from such model contaminated soils with appropriate flotation chemistry conditions which depend on the soil characteristics and other pretreatment procedures. In the best case, 90.2% of the UO2 was removed from a UO2/NTS soil mixture (119 ppm UO2) and the soil reduced in UO2 contamination from 119 ppm to 17 ppm in a single stage bench flotation. The impact of clay slimes present in the soil is revealed by the results which show that, for example, for a deslimed soil (28x400 mesh and 100 mg UO2/kg soil) 85¬90% UO2 recovery can be obtained with a reduction in contamination to 4.6 mg U02/kg soil.

Jan 1, 1995

By Kai Kang, Jun Bao, Shouping Liu, Xiao Sun

Powder characteristics have a significant influence on selective laser melting (SLM) process. In this research, particle size, surface contour and the microstructure of IN718 powder used in SLM were tested, and the physical and chemical changes during heating process of the powder were investigated as well. The shape characteristic and fluid properties of IN718 powder were defined and measured. It is shows that most particles of IN718 powder exhibited nearly spherical shapes, and the particle size is about 22.95μm. On this basis, IN718 sample was fabricated by SLM process using the powder and the microstructure of the fabricated sample was investigated. The results indicated that the sample has a dense microstructure, no macro-defects but a few micropores and porosity. Compared with the powder, there was no new phase formed in the sample and melting point of the sample was little less than that of the powder.

Jan 1, 2015

By Kejun Liu

Platinum and palladium are usually dissolved together and followed by separation. In this study, the selective leaching of platinum and palladium from a secondary resource, such as dental waste, by using chloride solution (hypochlorite and chlorate) has been developed. Results indicate that about 100% of palladium could be initially extracted by the combination of 0.3 mol/L sodium hypochlorite (NaClO) and 0.068 mol/L sodium chloride (NaCl) at pH 1.2 and 298K in 1.5 hours, or the combination of 0.005 mol/L sodium chlorate (NaClO3) and 6 mol/L hydrochloric acid (HCl) at 298K in 0.5 hour. About 100% of platinum could be extracted from the residue by the combination of 0.47 mol/L sodium chlorate (NaClO3) and 12 mol/L hydrochloric acid (HCl) at 298K in 2 hours.

Jan 1, 2003

By R. W. Harnmack

Hydrogen sulfide generated by the anaerobic respiration of sulfate-reducing bacteria was used to treat pH 2.2 water from the abandoned Rio Tinto copper mine in Nevada. The untreated water contained 550 mg/L Fe, 140 mg/L Al, 90 mg/L Cu, 80 mg/L Mn, 60 mg/L Zn, 4 mg/L Co, and 2 mg/L Ni. The bench-scale treatment system examined consisted of a bioreactor for H2S generation and three precipitator/clarifier units for metal sulfide precipitation and recovery. The treatment system reduced the concentrations of all metals except Mn to less than 0.1 mg/L. Manganese concentrations were reduced by 96 percent to 3.3 mg/L. A CUS/SO concentrate (33 pct Cu) and a ZnS/5° concentrate (28 pct Zn) were produced that may be suitable for metal recovery at existing smelters

Jan 1, 1994

02, NaCI03, H202, Na0CI and Ce+4 have been examined as oxidants in an alkaline carbonate system for uranium in in situ leaching. The South Texas and New Mexico ores contained up to 2.6 meqJg of reducing compounds which consume oxidants in the leading operation. Leaching rates did not increase linearly with the oxidation potential of the oxidants. A mild oxidant can be used to maximize uranium oxidation selectively and oxidant efficiency. 02 can oxidize most of the uranium mineral with an adequate rate and high oxidant efficiency.

Jan 1, 1990

By J. H. Huang

In this investigation, the selective precipitation of cobalt and molybdenum from Co-Mo aqueous solutions was studied in order to recover efficiently valuable elements from industrial effluents generated from a novel electrodeposition of nanocrystalline Co-based alloys process and reduce the effluent impact on environment. It was found that the behavior of cobalt in aqueous solutions was substantially affected by the presence of molybdenum. When adding 11.6 to 46.6g/L molybdenum to a 50g/L cobalt solution, the co-precipitation of molybdenum and cobalt started to occur at pH value of 3-4. However, without the presence of molybdenum, cobalt could only be precipitated out of the solution at about pH 6. Most of the molybdenum was found in the solid phase when the solution pH reached 5. After further increasing pH to greater than 7, the molybdenum dissolved back into the solution. Cobalt kept precipitating as the pH increased. When the pH was greater than 7, most of the cobalt was present in the solid phase. The chemical and physical characteristics of the precipitated materials were investigated by SEM, XRD, AAS and EDX. It was revealed that the precipitate was initially present as cobalt molybdate oxide hydrate and subsequently transformed as sodium cobalt molybdenum oxide. With further increasing the solution pH, the precipitate was transformed into cobalt hydroxide. Further investigation implied that most of molybdenum was chemically tied to the precipitate produced at the low pH, yet at the same time, physically entrapped at the high pH. The paper also presents the influence of reaction temperature and time on the precipitation process and kinetics.

Jan 1, 2003

By Gavin K. W. Freeman

The efficient separation of cobalt from nickel is a fundamental objective in the refining of cobalt. Based on recent experience at the Corefco refinery in Fort Saskatchewan, the identification of a novel process for the selective precipitation of cobalt from aqueous ammonia leach liquors is described. The addition of calcium sulphate, CaSO4.2H2O (gypsum), to an aqueous solution containing cobalt(III) hexammine sulphate, [Co(NH3)6]2(SO4)3, will result in the precipitation of a sparingly soluble double salt having the stoichiometry, [Co(NH3)6]2(SO4)3.2CaSO4.xH2O, where x = 4 or 6. Leach residues, which may contain a significant quantity of cobalt associated with the cobalt calcium double salt, can be washed with process solutions that contain ammonium carbonate. After contact with ammonium carbonate, the cobalt is recovered into solution, while the calcium is re-precipitated as the insoluble carbonate. The simplicity of this elemental separation and its high selectivity for cobalt, as well as the demonstrated usefulness in improving cobalt recoveries, are the basis for the potential applications of this process.

Jan 1, 2003

By D. R. Flynn

The recovery of nickel and cobalt from electromachining sludges in the form of relatively high-purity marketable products has been investigated. The investigation has shown that a series of metallurgical unit operations can be performed to recover nickel and cobalt from electromachining sludges in the form of al kal i nickel ic hydroxide and cobalt sulfate/cobal t metal, respectively. The recovery unit operations for nickel include high pH cyanide complexation, followed by oxidation and precipitation of alkali nickel hydroxide. The resultant filtrate can be treated for cobalt recovery by neutralization and acid baking to produce cobalt sulfate. The cobalt sulfate can then be treated for cobalt recovery by electrowinning. Results from laboratory bench scale test work are discussed in terms of appropriate operating conditions.

Jan 1, 1991

By Hongmin Zhu, Kai Huang, Shuqiang Jiao

"Garlic peel was used as the raw material to synthesize the biosorbent for the selective recovery of precious metals from the acid chloride solution. Garlic peel is rich in carboxyl-, amino- and thiol-groups, has the potential of exhibiting high affinity to Au(III) when appropriate chemical modification process was employed. Here in the present study, the biosorbent was prepared by cross-linking garlic peel particles with concentrated sulfuric acid. Adsorption tests for mixing different metal ions such as Au(III), Fe(III), Cu(II), Ni(II) and Zn(II) from various concentrations of hydrochloric acid media indicated that Au(III) was selectively adsorbed on the cross-linked garlic peel gel over the other coexisting base metal ions investigated. The crosslinking mechanism and selective adsorption of Au(III) were also investigated briefly.IntroductionPrecious metals are quite popularly applied in the modern industries such as jewelry, electronics and electrical devices, catalysts in chemical industry, etc. While their high values, limited deposit and quite large demand in industry makes its recovery from the industrial wastes, typically e-wastes, quite necessary. Actually, many techniques have been developed to recycle and recover the precious metals from various industrial wastes effectively in last decades, but the cleaning and ecofriendly processes are still seriously scarce [1]. Taking into account of the typical recovery processes using cyanide lixiviant in the alkaline media, or aqua regia, followed by the further recovery process using activated carbon adsorption or cementation with zinc, iron or aluminum plate or powder, though they both are quite effective recovery processes, if considering the special requirements on safety and ecofriendliness for the modern hydrometallurgical processes, various improved or novel extraction processes are greatly demanded [2]. Recently, the biosorption technology applied to the recover precious metals in the hydrometallurgical process has become a concern [3,4]. Inoue’s research group made great progress in the recovery of precious metals such as gold, palladium and platinum from the e-wastes such as spent mobile phone by using biosorption from the hydrochloric acid media [5,6]. This new hydrometallurgical process exhibits the prominent advantages of being cost-effective for its short process, easy operation and near-zero emission. In the above recycling process for e-wastes treatment, the preparation of biosorbents is the key and backbone of the whole recovery process. For this purpose, they developed a series of suitable sorbents for precious metals recovery by using the tanning-based or cellulose-based biomass such as persimmon peel, grape peel, orange juicing residue, waste cotton, waste paper through the crosslinking process with concentrated sulfuric acid and relative chemical modification processes [7-10]. In the present study, we also applied this technique to prepare the biosorbent of precious metal uptaking by using garlic peels as the raw materials, and investigated the adsorption properties of such-obtained gel in the hydrochloric acid media."

Jan 1, 2012

By Bo Jiang, Jiusan Xiao, Hongmin Zhu, Kai Huang, Shuqiang Jiao

Carbothermal selective reduction of simulative titanium slag and various titanium raw materials were presented and SiO2 was found to be partially reduced, forming a series of Fe-Si alloys during the process. Thermodynamic analysis of the selective reduction between TiO2 and SiO2 was performed using HSC 6.0 software, then a series of equilibrium experiments were designed and presented. The activity of Si reduced from SiO2 was affected by the presence of Fe reduced from FeOx and the generation of Fe-Si alloys, promoting the reduction of SiO2 in the whole process. The results of experiment are in great accordance with the calculated data obtained from thermodynamic analysis.

Jan 1, 2016

By Reed M. Izatt

SuperLig® materials are capable of individually separating Rh, Pd, and/or Pt in highly purified form (99.95 to 99.99%) from a variety of chloride-based feed streams in a single stage operation. The hydrophillicity and associated kinetics of the supported materials allow for operation at relatively high flow rates of both loading and elution in a packed bed format. Pilot and commercial systems have been operated with Rh, Pd, and/or Pt present in the feed from single digit ppm (mg/l) to tens of g/l. A dual SuperLig® system for one pass Au(CN)2- separation followed by Cu and CN- recovery for CN- recycle has also been tested up to a pilot level,

Jan 1, 1999

By XUEWEN WANG, Xingming Wang, Xuehui Liu, Mingyu Wang

The Panzhihua titanium concentrate contains high contents impurity of Mg and Al, and it is difficult to prepare high grade titanium slag. To solve this problem, a sodium salt roasting-acid leaching process was proposed for removing the impurities in titanium concentrate. Na2CO3 and titanium concentrate were mixed with the proportion of 1:4, and then the mixture was roasted at 700 for 2h. After roasting, the calcine was leached with HCl solution. The experimental results showed that the removal rate of silicon and aluminum can reach more than 85% and 80%, respectively, at leaching temperature of 70 , leaching time of 4h, HCl addition of 5ml and liquid-solid ratio of 4:1.

Jan 1, 2016

By Hylton McWhinney, Doanh Tran, Jewel Andrew Gomes, George Irwin, Sameer Pallavkar, Md Islam, David Cocke, Mohammad Rafiqul Islam

"High-performance nickel-based nanocrystalline zinc oxide adsorbents have been prepared adjusting Ni/Zn mol ratio of 1 :5 by thermal decomposition, coprecipitation and sol-gel method for selective adsorption of thiophene in liquid hydrocarbon fuels at ambient temperature and pressure. To understand the nature of reactive adsorption of thiophene (C4H4S) on Ni/ZnO, the effect of preparation techniques, morphological and textural structure on the desulfurization activity was investigated. A model fuel (20 mL) consisting of pentane (C5H12) and thiophene was prepared and adsorption experiments were performed by a batch method under ambient conditions. The physicochemical behaviors of the fresh adsorbents were obtained using X-ray diffraction (XRD) with EDAX, scanning electron microscopy (SEM). The sulfur concentration in the mixture was monitored by UV-vis spectrophotometry. The adsorption reaction confirmed that ZnO played a crucial role in taking up S element to convert it into ZnS. The deposition of nickel on ZnO is an innovative approach which takes advantage of the selectivity of Ni towards S-species and the high adsorptive capacity of ZnO support.IntroductionLow temperature deep desulfurization of fuels via selective adsorption of sulfur compounds keeping coexisting aromatic hydrocarbons and olefins intact is receiving increasing attention in the research community worldwide in order to satisfy the upcoming environmental regulations and fuel specifications. The sulfur compounds in the transportation fuels is a matter of concern when global crude oil slate is becoming heavier and sourer and environmental restrictions on both the refining process and the refined products are becoming more stringent. According to the current refinery technologies, the sulfur content in refinery fuel is typically around 300-500 ppm by weight (ppmw) [1-3]. Starting in 2006, sulfur limits in highway diesel and gasoline were set to 15 ppm and 30 ppm, respectively. During combustion sulfur in the fuel are converted to toxic sulfur oxide (SOx) and contributes to air pollution and acid rains [ 4]."

Jan 1, 2011

By Ph. Cauwe

This paper presents the experience that NESA and MECHIM have gained about recovery of non ferrous and precious metals from complex sulfide materials. Processed materials are from natural deposits or metallurgical by-products or residues. Roasting of these materials is closely related to the pyro or hydrometallurgical processes used downstream of the roasting. Conditions of a first step of roasting the SELECTIVE ROASTING, are analyzed and explained. The roasted products so obtained are characterised by an extended elimination of volatile sulfides (AS, Bi, Sb, Sn, Pb, Hg, ?? ) and are readily available for the pyrometallurgical recovery of non ferrous and precious metals. After the SELECTIVE ROASTING, thanks to. the high porosity obtained in the "selective calcine", the SULFATE ROASTING is per-formed in excellent conditions. Hydrometallurgical tests performed for the final calcine show a high recovery of non ferrous and precious? metals and require only simple and well known processes. Many experimental and commercial data are given.

Jan 1, 1983

By A. René Silva

The separation of Fe(III) from simulated Ni(II) solutions using different ion exchange resins was studied. The resins tested included cation exchangers with sulfonic and carboxylic groups and chelating resins with iminodiacetic, aminophosphonic, and mixed sulfonic and phosphonic groups. The dosage of resins was varied from 0.1 to 0.5 g/mL to study the impact of resin type and dosage on iron separation from simulated nickel leach solution containing 25 g/L Ni(II) and 25 g/L Fe(III) at pH 1.5. Also, the effects of different metal ion concentrations, Fe (III):Ni(II) ratios in solution, pH, and adsorption times were investigated. Experimental results demonstrate that all the chelating resins selected favored the adsorption of Fe(III) over Ni(II) with high Fe(III) loading. Soft cation exchange resins also favored the adsorption of Fe(III) over Ni(II), but no significant Fe(III) loading was observed. In contrast, strong cation exchange resins did not show adsorption preferences. The most efficient separation was observed using resin with aminophosphonic groups at resin dosage of 0.2 g/mL, having a Fe(III) adsorption over 94% and Ni(II) adsorption below 5%.

By Ephraim Jeya Kumari

The demand for the titanium dioxide pigments and the shortage of higher-grade titaniferous ores with low radioactivity and zircon sands worldwide has encouraged the development of new techniques for the beneficiation of lesser grade titaniferous ores. The inferior quality ores are invariably richer in radio-active and lanthanide oxides, which severely interfere with the fluidized bed chlorination reaction (FBCR), in which ultra-high purity titanium tetrachloride is distilled off for pigment manufacture. However the present beneficiation techniques require high quality ilmenite ores and are not suitable for upgrading lower grade ilmenite ores which do posses trace metals in the form of lanthanides and actinides as Al-phosphates and zirconium silicates, respectively. The presence of mineral hosts, zircon sand and monazite in ilmenite and anatase also increase in chlorine gas consumption in the FBCR and contribute to a larger volume of hazardous waste production, which must be neutralised at a significant cost before being disposed off safely. In view of the problems described for lanthanide (Ce, Nd etc) and actinide (Th, U) trace impurities in titaniferous ores, an alternative route, which is flexible and more accommodating for processing difficult ores, is discussed. In the new process, which may be used for richer grades of ores too, the ore is roasted in air with sodium carbonate below 950°C to promote the formation of water-soluble sodium ferrite and insoluble sodium titanate phases. In this investigation, the high-temperature roasting process and the ensuing hydrometallurgical leaching steps have been analysed in the context of selective separation of lanthanide and actinide minerals from the main titaniferous mineral structures. Evidences for the selective separation are presented based on the chemical (XRD, XRF, AA) and microstructural analysis (SEM, EDX, EPMA) of roasted mass and the leached product. The efficiency of selective separation is also reported based on the chemicals analysis and the particle size of the materials derived after leaching. The paper highlights the various thermodynamic aspects of reaction equilibrium in the Fe-Ti-O-Na system, and the effect of Eh-pH diagram in the determination of pH required for the better control of the removal of iron and sodium. Two different types of Ti ores, namely ilmenite and anatase, their crystal structure and the phase transformation will also be explained on the basis of wet chemical analysis, XRF, XRD, EPMA and SEM-EDX studies. The method developed examines the technological feasibility of the selective separation process.

Jan 1, 2006

By E. S. Peterson

The selective separations of trace metals- and organics from water are processes of importance to industry. The application of a new metals capture technology coupled with polymer membrane technology has proven to be one avenue to accomplish such selective separations. The polymers used in these studies are polyphosphazenes. Polyphosphazene polymers consist of an alternating backbone of nitrogen and phosphorus atoms. The polymers have high thermal and chemical stabilities. Experiments at the Idaho National Engineering Laboratory demonstrate that polyphosphazene membranes coupled with Chromato Chem,"Chelation Chromatography" process are capable of removing both chlorinated hydrocarbons and metal ions from process streams. These results point to a wide range of potential industrial and environmental applications for such systems. Data will be presented which show the efficiency and selectivity of separations, postulated separation mechanisms, and the initial designs of industrial demonstration units which are currently under construction. Parts of this work have been performed under a Cooperative Research and Development Agreement (CRADA) between ChromatoChem, Inc. and Idaho National Engineering Laboratory (INEL). The work at INEL was been sponsored by the United States Department of Energy's Office of Industrial Technologies

Jan 1, 1995