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By Xiaolong Lin, Yuanbo Zhang, Jiann-Yang Hwang, Guanghui Li, Hongjin Zhang, Jiaxing Yan, Zhiwei Peng, Tao Jiang

The pollution caused by the spent printed circuit boards (PCBs) is currently a concern of researchers and environmental managers due to its large quantity and exceptionally complex properties. This study characterized printed circuit boards (PCBs) from discarded computers using a number of characterization techniques, including chemical analysis, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), granulometric analysis and scanning electron microscopy (SEM).The PCBs contain approximately 50 wt% metals, 25 wt% glass fibers and 25 wt% polymers. The principal metals include copper, calcium, tin, aluminum, zinc and lead. They are still wrapped by brominated epoxy resin after the PCBs are preliminarily crushed. As precious metals, such as gold and silver, are barely found in the PCBs, copper and tin are the main metallic elements of recycling value which warrants extra attention.

Mar 1, 2017

Rotary kiln incinerators are widely used in the incineration of various types of hazardous wastes. However, the complex transport processes within the incinerator are not well understood. Due to large variations in waste types and difficulties in feed characterization, the incineration process meets great challenges in a smooth operation, and expects uncertainties in the process chemistry and emission control. In order to get better understanding of the incineration process, process simulation was made on the kiln behavior by using Computational Fluid-dynamics (CFD) to characterize gas flow, temperature distribution and waste combustion in the incinerator. Temperature measurement was conducted in an operating incinerator to validate the CFD model. This paper addresses the environmental issues related to the hazardous incineration process, and reports the recent simulation results on gas flow and mixing, combustion heat transfer, and potentials to reduce emissions.

Jan 1, 2002

By C. M. F. Viera

In this work the properties of a clayey ceramic incorporated, up to 10 wt.%, with three types of wastes from a water treatment plant was evaluated. To determine the physical and mechanical properties such as linear shrinkage, water absorption and diametrical compression, specimens were prepared by 18 MPa uniaxial pressure and then fired in laboratory furnace at 700oC. The results indicated that the wastes incorporation changed the properties of the clayey ceramic. From the results it was found it possible to recycle these wastes into clayey ceramic in low amounts to avoid deleterious effect on the quality of the fired product.

Jan 1, 2008

By Andrea Bernardes

Printed circuit boards (PCBs) of varying compositions have been converted by incineration and following melting into an environmental agreeable slag and a copper-nickel-tin alloy, containing the precious metals. The environmental compatibility of the slag was determined according to the German standard DIN 38414 - Part 4; pollutants' concentration in the lixiviates is smaller than the thresholds of drinking water (CE-Standards). Each experiment the charge were 500g scrap from PCBs and ca. 100g slag forming material. The products were a kind of mullite slag, poor on iron, which was recirculated, and an alloy containing up to 0.3% Gold. With a burner to the retort coal gas, the waste gas was burned without soot, and the produced mixed zinc-lead oxide containing silver was collected in the flue dust.

Jan 1, 1997

By T. Wang, R. G. Reddy

"The corrosion of stainless steel SS316L in a low melting point novel LiNO3-NaNO3-KNO3- NaNO2 eutectic molten salt mixture was investigated at 695K. After long-term isothermal dipping corrosion experiments, the SS316L samples were analyzed using scanning electron microscopy (SEM) equipped with energy dispersive spectrometer (EDS) to determine the topography and corrosion products. Dense and protective lithium iron oxide scale formed on the surface and prevented the SS316L sample from further severe corrosion. Therefore, SS316L is considered to be suitable construction material for solar thermal energy storage materials containers.IntroductionMolten salt mixtures have been considered as potential candidates for thermal energy storage and heat transfer media in solar energy applications. To apply the molten salt in the energy transfer process, the standard pipes made of stainless steel must be utilized to carry the molten salt mixtures in parabolic trough system of solar power production. The pipes encounter continuous flow of hot and cold molten salt every day. Thus corrosion of stainless steel in molten salt mixtures becomes extremely essential for the long-term utilization of the thermal energy storage media. The corrosion of passivity materials inside high temperature molten salt systems have been studied which gives fundamental understanding of basic mechanism about the corrosion process [1-8].The corrosion behavior of Fe-Ni-Cr alloys in an equi-molar LiNO3–NaNO3–KNO3 mixture was studied [9]. According to the XRD analyses, the major phases in the oxide scales were identified as LiFeO2, Fe3O4 and Cr2O3. A HITEC® salt mixture (NaNO3–NaNO2–KNO3) was also tested as a corrosion medium for stainless steel [10] and the corrosion rate was found to be affected by the protective oxide layer. In most cases, the alloys having more than 10wt% chromium show high resistance to corrosion in molten salts."

Jan 1, 2014

By Osamu Iida

Since 'start-up of the larger Mitsubishi Continuous Copper Smelting Process in 1991, furnace relining campaign was gradually prolonged to once every 2 years according to deregulation of governmental boiler inspection. On the other hand, in 1998 Naoshima smelter embarked on an intermediate strategic expansion plan to strengthell its international competitiveness. As part of this plan, modifications were implemented in the copper smelter designed to increase output of anodes from new charge source to 270,000 tpa. In May 1998, treatment of dried neutralized residue was started in C furnace, and during the shutdown for brick relining in April 1999, intensive modifications to the boilers as well as the installation of new spray coolers for furnace off gas treatment were implemented. Finally, the new larger oxygen plant was commenced its operation in May 2000 and the expansion was achieved around 30% increase of anode production from original design.

Jan 1, 2001

By Lingling Zhang, Daqiang Cang, Guizhou Zhao

Pilot trial ofthe detoxification ofchromium slag in cyclonefurnace and the preparation of glass-ceramics were investigated in a power plant in China. 10wt.%chromiumslagweremixedwithpulverizedbituminouscoalandlimestone as the raw materials of the cyclone furnace. Cr(VI) in chromium slag was reduced toCr O insidethecyclonefurnace.Themeltwaswater-quenchedintofritandthen 2 3 fired into glass-ceramics with a laboratory ceramicrollerkiln. The preparation and crystallization behavior of glass-ceramics were investigated with differential ther- mal analysis (DTA), physical and mechanical properties testing, X-ray diffraction (XRD) and scanning electron microscopy (SEM). The optimal flexural strength exceeding 90 MPa were achieved in firing temperature zone of 1170–1200 °C. Anorthite (CaAl Si O ) and diopside [Ca(Mg, Fe)Si O ] can be identified in the 2 2 8 2 6 glass-ceramicsandCaAl Si O isthepredominantcrystalphase.Fineparticleswith 2 2 8 average diameter of 200 nm distributed uniformly in the glass-ceramics. Granular crystals are intensively interconnected and constituted a crystal skeleton soaked in theglassmatrix.LeachingtoxicitytestdetectedCr(VI)of0.016and0.010 mg/Lof the water-quenched frit and glass-ceramics, respectively. This method provides an effective and comprehensive technique for the detoxification and utilization of chromium slag at low cost and large-scale. (cid:1) (cid:1)

Mar 1, 2018

By Rajesh Kumar Mishra

About 500,000 troy ounces of Platinum Group Metals (PGM) will be available for recycling each year from spent automobile catalytic converters in North America alone. Platinum Group Metals? from spent catalyst can be extracted by Hydrometallurgical, Pyrometallurgical or Gas Phase volatilization processes. This paper is a review and comparative study of various processes investigated for PGM extraction. A number of processes described in this paper have already been commercialized. The technical and environmental aspects of the important processes are discussed.

Jan 1, 1989

By Qixing Yang, Björn Haase, Fredrik Engström, Anita Wedholm

"MiMeR, the Minerals and Metals Recycling Research Centre at Luleå University of Technology, Sweden, started industry-related research work to stabilize an EAF slag from Höganäs AB with of CaO/SiO2 values near to 3.2. The intention was to determine the suitability of the EAF slag as construction material after stabilization. Some of the stabilizers effective for preventing disintegration of AOD slag were examined in laboratory tests for stabilization of the EAF slag. The EAF slag samples were mixed together with stabilizers for melting at 1600ºC and then cooling in a crucible system. With a laboratory granulation system, the liquid EAF slag was cooled rapidly using air. Samples from the tests were characterized by different techniques, including XRD and SEM. Some of the results from the work may be useful for preventing slag disintegration and, thus, enhancing utilization of the EAF slag as construction material, thereby saving valuable natural resources.IntroductionAt steel plants of some MiMeR member companies, steel grades with low carbon contents were produced in Electric Arc Furnaces (EAF). EAF slag was tapped out of the furnace to slag pots for transport to slag yards, where the slag was poured on the ground. Very often, the EAF slag disintegrated during cooling on the ground. Fines from the slag disintegration were often difficult to handle and use as material for road construction [1, 2]. The EAF slag disintegration was rather similar to the disintegration occurring in the slag tapped from some AOD (Argon Oxygen Decarburization) converter heats.Literature studies show that formation of dicalcium silicate (C2S) is the main reason for the disintegration or dusting of AOD slag from production of stainless steel [1-4]. The C2S can form while the content ratio of CaO to SiO2 of the slag, CaO/SiO2, exceeds 1.4 [1]. Values of CaO/SiO2 for the AOD slag are often near to 2.0, making the C2S a predominant slag component. The ß phase of C2S, ß-C2S, transforms into its low temperature ? form in the temperature range of 400-500°C, inducing a volume expansion of nearly 12% [1-4]. The volume expansion disintegrates the AOD slag."

Jan 1, 2008

By Charles A. Sorrell

Two red muds, two fly ashes, and several aluminosilicate minerals were subjected to direct treatment with concentrated H2SO4 at temperatures of 175°C and below. X-ray analysis showed that virtually all the sulfate reaction products remained in the solid residue because of their low solubilities in x SO Substantial portions of the Al2O3 Fe2O3TiO2, Na2O, and K2O components of the materials reacted to form water soluble sulfates, which were then removed by H2O leaching at 55°C. The solid residue after water leaching consisted largely of amorphous silica and, in lime bearing compounds, CaSO4, The reaction and leaching processes were effective in removing all or nearly all the Al2O3. Fe2O3, TiO2, Na2O, and in lime components in the fly ashes, red muds, china clay, bentonites, the nephelioe fraction of nepheline syenite, and a plaster insulating brick composed of anorthite and mullite. Reaction with potassium feldspar and petalite took place, with formation of alkali aluminum sulfates, but the reaction rates and yields were extremely low. Potassium feldspar can be heated with Na2O and x O in air at 700°C for 24 hours, or with CaO at 1000°C for 24 hours, after which the reaction product kaliophilite, nepheline, and leucite-like phases, prove to be very susceptible to H2SO4, reaction and H2O leaching, providing yields near 100% of the Al2O2 content. An alternative method of H SO treatment consists of heating the sample in a silica tube and passing H2SO4 vapor over it. Preliminary results indicate that this method can be effective in enhancing the kinetics of reaction with the Al O component of potassium feldspar and offer the possibility that formation of Al2 (SO ) Fe2(SO4)3 and TiOSO4 can be accomplished selectively by taking advantage of the fact that the upper stability limits of the respective sulfates in the presence of H2SO4 vapor will be different.

Jan 1, 1982

By Robert R. Grinstead

Two new ion exchange resins have been developed, which selectively absorb copper and nickel in preference to ferric iron from dilute sulfuric acid solutions of pH 1-3. The first absorbs copper and not nickel and can be readily eluted with 1-2N sulfuric acid. This resin is well adapted to the processing of copper leach liquors, including relatively low grade liquors obtained from dump leaching. The second resin absorbs nickel as well as copper in the same pH region, but only the nickel is eluted with 1-2N sulfuric acid. Elution of the copper requires much stronger (ca. ION) acid, altho both species are readily eluted with dilute (ca. lN) ammonium hydroxide. This resin, which should be useful in processing of certain types of copper-bearing solutions, may also be suitable for treating acidic nickel leach solutions of laterites and other non-sulfide ores.

Jan 1, 1976

By Cesimiro Fabian

The crystallite size of copper electrodeposits was determined by X-Ray powder diffraction analysis using a General Area Detector Diffraction Solution (GADDS) diffractometer. Crystallite size was calculated for copper thin films which were deposited on a 316 stainless steel rotating cylinder electrode (RCE) in the presence and absence of additive ?A?. The crystallite size was calculated from a corrected full width at half maximum (FWHM) of the [110] peak profile using the Scherrer equation. The test of significant difference on crystallite size was derived using Kruskal-Wallis method. It was found that in the absence of the additive the median crystallite size was 426, which decreased to 364 in the presence of the additive. As the additive degraded, the crystallite size increased to a size similar to that observed in the absence of additive.

Jan 1, 2003

By M. J. Collins

Pressure leaching of zinc sulphide concentrates has been practiced commercially for nearly two decades. The process, which includes direct leaching of concentrate with spent electrolyte in an autoclave, has been commercialized at four separate locations to date. In pilot studies carried out in the Dynatec lab in Fort Saskatchewan, dozens of additional zinc concentrates have been shown to be amenable to pressure leaching. This paper highlights recent improvements in zinc pressure leaching that have been identified through process development studies, and how the experience gained in these studies has been utilized in the development of a new copper pressure leach process.

Jan 1, 2000

By W. H. (Bill) Jay

The destruction of cyanide creates a significant impost on the financial returns of gold mines. These losses increase substantially when ores containing cyanide-soluble copper are treated. Failure to remove or destroy free or WAD cyanide before it is discharged into tailings dams has, on a number of occasions, led to significant fish, bird and animal deaths. Thus, the retention of cyanide within the leach circuit and the recovery or removal of stable metal cyanide complexes needs to become standard practice for all gold mining operations. Furthermore, reducing cyanide purchases will minimise the quantity of cyanide transported to the mine site thereby reducing the opportunity for spillage of this chemical. Many different physical and chemical methods have been investigated for the removal of cyanide from process solutions. All cyanide destruction methods create a financial impost on the economic viability of the gold mine. To reduce these costs, the recycle of cyanide and the economic recovery of the metals solubilised by cyanide is of prime importance. The alternative methods currently in use, or under consideration for the treatment of copper cyanide, entail high reagent costs, produce the recovered metal in a contaminated form and require the safe handling of hydrogen cyanide. These processes will be briefly discussed within this report Environmental and financial benefits are enhanced by recent laboratory and pilot plant studies conducted by Oretek Limited. The Oretek CPC process for the recovery of copper and the recycle of cyanide from copper cyanide-containing solutions does not require pH adjustment to the alkaline cyanide leach conditions. Copper ions are coordinated to a water-soluble and/or an organic soluble polychelating agent under alkaline conditions and the cyanide ions are displaced Membrane separation, or phase separation of the polychelated copper from the cyanide ions enables the cyanide ions to be recycled and the copper to be directly electrowon from the polychelating polymer. The polychelating polymer is then recycled. Ion exchange resins and solvent extraction systems which may be incorporated into the above process will also be discussed in detail.

Jan 1, 1998

By K. Moriyamo

Operation improvement efforts at Hyuga Smelting Co., Ltd. have focused on calcining capacity in the reduction rotary kilns ("the kilns"), whose limited feed rate capacity had capped production at around 18,000t-NiN since 1995. To improve the kilns' feed rate capacity of 80 wet t/hr, attempts were made to increase the gas flow in the kilns by increasing the capacity of the off-gas fans. However, as the increased gas flow resulted in only limited improvement of the kilns' feed rate, a scoop feeder was installed on each kiln to add coal to the middle of each kiln's interior to gain a higher efficiency of thermal supply and conversion. With these gas flow and coal charge addition operations, the kilns' feed rate capacity increased up to 120 wet t/hr, with burner fuel efficiency increasing by approx. 10% (approx. 5% in total with the additional coal included). As a result, production was raised to a level of 22.000t-Ni/Y Keywords: reduction rotary kiln, scoop feeder, additional coal charge.

Jan 1, 2004

By Yun Guo, Min-Min Lin, Bing Xie, Hong-Yi Li

The extraction of vanadium from vanadium-containing APV-precipitated wastewater by W/O microemulsion system was studied. In the N263/n-heptane/isoamyl alcohol/NaCl microemulsion system, N263 played double functions of cationic surfactant and extractant to form microemulsion in n-heptane, and isoamyl alcohol was added in the microemulsion as a cosurfactant. The extraction of vanadium by W/O microemulsion systems effectively accelerated the extraction and improved the extractatability because of the enormous increase in the micro-interfacial surface area. Due to ion association with extractant, vanadium was extracted into the microemulsion phase. The influence of different parameters on the extraction ratio (E%) were investigated, including the volume ratio of aqueous phase to microemulsion, surfactant concentration, pH value of the feed solutions, cosurfactant concentration, extraction time as well as temperature. In optimum conditions, the extraction ratio (E%) can reach 97.2%.

Mar 1, 2018

By C. Koopman

During the production of phosphoric acid from phosphate ore and sulfuric acid, large amounts of calcium sulfate are formed, in which impurities from the feedstock are incorporated. To use the calcium sulfate in, for example, the building industry, a lower concentration of impurities is desired. Mercury, copper, lead, and cadmium were extracted from clear industrial recrystallization acid (0.8-3.9 mol/kg H3PO4, 0.2-0:5 mol/kg H2SO4) by supported solvent extraction with the extracting agent Cyanex 302 in kerosene in a transverse flow hollow fiber module. The permeability for the mercury ion was 1.4.10-6 m/s, whereas that for the copper ion was calculated to be 1.5.10 m/s. Cadmium, lead, and copper were extracted during the recrystallization of calcium sulfate hemihydrate to dihydrate, an existing step within the ,phosphoric acid production process, by solvent extraction with the same extracting agent. The concentrations of cadmium and zinc in the newly formed calcium sulfate were proven to be decreased. Unfortunately, concentrations of mercury and lead were too low for analysis.

Jan 1, 1999

By Malsuzaki. Kenji

A mathematical simulation model of the Imperial Smelting Furnace operation has been developed for purpose of improving the furnace operation. The model consists of top, shaft and bottom regions. Analysis in the shaft region is based on differential heat and materials balances taking account of reaction kinetics and heat transfer rates, and those in the top and the bottom regions are based on heat and materials balances under a steady-state condition. Longitudinal distributions of process variables such as temperatures of gas, sinter and coke, gas composition and fractional conversion under a practical operating condition were calculated. With this model, the furnace performance under various operating conditions also can be shown reasonably predicted.

Jan 1, 2003

By Kenji Matsuzaki

A mathematical simulation model of the Imperial Smelting Furnace operation has been developed for purpose of improving the furnace operation. The model consists of top, shaft and bottom regions, Analysis in the shaft region is based on differential heat and materials balances taking account of reaction kinetics and heat transfer rates, and those in the top and the bottom regions are based on heat and materials balances under a steady-state condition, Longitudinal distributions of process variables such as temperatures of gas, sinter and coke, gas composition and fractional conversion under a practical operating condition were calculated, With this model, the furnace performance under various operating conditions also can be shown reasonably predicted,

Jan 1, 2003

By Andrew Wessman

Keywords: Recycling, Electrodeposition, Recovery, Dilute, Dissolved Metal Ions In order to facilitate the recovery of pure metals from solutions containing a mixture of dissolved metal ions, a pulsed electrodeposition method was developed. Using this method, it is possible to selectively remove metal ions from solution based upon the electrochemical potential of the particular ion desired. The use of pulsed electrodeposition rather than direct current electrodeposition creates an electrodeposited material with better morphology, increases electrical efficiency of the process, and avoids problems with short circuiting between electrodes. Using this method, it is possible to recover dissolved metal ions in a purified form in one simple step, and therefore maximizes recovery of the metal ions while obtaining them in a saleable form. This method is likely to be useful in improving the recycling process for numerous complex metal mixtures and alloys.

Jan 1, 2005