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By Emilia Visileanu, Eftalea Carpus

"Ecological economic policy shall be understood as the sum of political, economical and environmental measurements aimed at the entire economy dematerialization and the dematerialization shall be ""imposed"" since the designing stage of goods and services"". European textile and clothing industry with a long leading tradition in terms of innovation, fashion and creativity, continues to be one of Europe's major industrial sectors. Textile industry affects the environment by high consumption of water, energy and chemicals, as well as by the large amount of waste it generates as a result of using a large number of chemicals and technological processes.Textile waste prevention, reduction and ecological exploitation require the implementation of new management and education tools.Introduction“Europe must learn from the experience of global economic and financial crisis ""- this was the conclusion of the European Commission that has elaborated a ten-year strategy designed to reinvigorate the economy and make possible a growth which is ""intelligent, sustainable and favorable to inclusion"", by a better coordination of national and European policies.Adapting infrastructure and logistics that encourage the marketing of ""sustainable"", ""fair traded"" and ""green"" products as well as other special „green” products will facilitate the movement towards dematerialization and eco-efficiency among producers."

Jan 1, 2012

This symposium is dedicated to the lifetime achievements of Professor H.Y. Sohn. It covers the scientific fields, processing routes and investigation techniques in which Prof. Sohn has worked during his career and is based in the equally important three topical areas: Principles, Technologies, and Industrial practice. Professor Sohn was General Chair of the very first TMS Fall Extraction and Processing Symposium in 1983 in San Francisco which led to the Annual such symposia as this International symposium. Furthermore, the theme of that symposium was sulfide smelting, which is also included in this symposium. [ ] Professor Sohn was born in a beautiful dynastic capital Kaesung, Korea on August 21, 1941. He received his B.S. degree in 1962 from Seoul National University, M.Sc. in 1966 from the University of New Brunswick, Fredericton, N.B., Canada, and his Ph.D. degree in 1970 from theUniversity of California at Berkeley all in Chemical Engineering. After working as a Research Associate at the State University of New York at Buffalo and as a Research Engineer at Du Pont?s Engineering Technology Laboratory, Dr. Sohn joined the Department of Metallurgical Engineering at the University of Utah in 1974 and currently holds the ranks of Professor of Metallurgical Engineering and Adjunct Professor of Chemical Engineering.

Jan 1, 2006

By Kimio Itagaki

"As a contribution to understand the smelting of copper or nickel matte by blowing oxygen or oxygen-enriched air, the phase equilibrium and the distribution of minor elements between the iron-silicate based slag and the Cu2S-FeS or Ni3S2-FeS matte at 1573K were investigated in a magnesia crucible under controlled partial pressures of SO2 at 0.1, 0.5 and 1.atm. At a given matte grade, the solubility of copper in the slag was found to be independent of p5O2 while that of nickel was dependent on pSO2 and these behaviors were analysed thermodynainically based on a concept of oxidic and sulfidic dissolution of the components in the slag. When the matte grade was specified, the distribution ratios of X, defined as (wt pct X in slag)/(wt pct X in matte}, for As, Sb and Bi increased with increasing p5O2 while that for Ag was constant against p5O2.IntroductionA combination of intensive reactors with the use of oxygen or oxygen-.enriched air as the blowing gas has provided a number of improved copper and nickel smelting processes such as INCO-Flash, Outokumpu-Flash, Mitsubishi-Continuous and IBRC (top blown rotary converter) processes. Phase equilibrium and thermodynamic studies for the slag and the copper matte or the nickel matte under high partial pressure of SO2 are of practical importance for evaluating the behaviours of the related components in the oxygen-smelting.A series of experimental studies have been already conducted in a limited range of conditions for Pso2 around 0.1 atm, which corresponds to the smelting with air-Stowing [1-5]. However, there remain very few data on the phase equilibrium in the matteslag systems under higher partial pressures of SO2. Tavera and Davenport studied the phase equilibrium between the copper matte and fayalite slag phases under the partial pressure of SO2 controlled at 0.1 - 1 atrn but without controlling the partial pressures of sulfur and oxygen [6]. A potential diagram for the Cu-Fe-S-O-SiO2 system at 1523 - 1573K suggests that the partial pressure of S2 equilibrated with the matte and the fayalite slag with saturated SiO2 under the high SO2 pressure is considerably high at 10-4 - 10-2 atrn [7]. This condition must require controlling of p52 as well as Pso2, in the equilibrium experiments, otherwise, the equilibrium condition may be hardly attained due to the continuous flushing of sulfur from the system."

Jan 1, 2000

By Robert Corson

Zinc has a large solubility in Fe and a completely filled ?d? shell. With the discovery of dramatic increase of the magnetostriction in Fe by Ga addition, an examination of element Zinc that is adjacent to Ga in the periodic table is of significant interest. In this work, the effect of binary alloying of Zn with Fe on the magnetic and magnetostrictive properties is examined. The FeZn alloys were processed using powder metallurgy and vapor phase synthesis, and Zn contents were varied from 5% to 30%. An examination of the influence of different processing parameters and the Zn content on the resulting alloy properties is presented. The alloys were characterized using X-ray diffraction and SEM. Magnetostriction measurements were carried out at different pre-stress levels. Magnetic properties were measured using a vibrating sample magnetometer.

Jan 1, 2006

By D. E. Roberts

Over 425 million used automotive oil filters are discarded in the United States each year. Estimates prior to this research claim that 10% are recycled with the remainder typically being landfillcd. Surveys conducted with ferrous scrap users and oil filter processors as part of this research reveal that at least 15% are currently being recycled as ferrous scrap. Oil filter scrap is not being used by many operations because of concerns with scrap consistency and quality. These concerns stem from trials conducted in the infancy of the oil filter recycling movement. Consistent scrap quality depends both on the content of the used oil filters and the processing technique used to produce the scrap. Technology has advanced since the first recycling trials were conducted by steelmakers. Several different types of scrap are available, including pucks, bricks, cubes, and shred. This research conducted at the University of Missouri-Rolla investigated the content of used oil filters and compares the recyclability of different oil filter sizes and designs. Filters vary by application and vary between manufacturers for a particular application. An understanding of the scrap itself as well as the concerns and problems of both oil filter recyclers and oil filter processors is necessary to increase the number of used oil filters being recycled.

Jan 1, 1996

By Derek Fray

Molten salts have been used for the extraction of metals since the 19th century but, recently, many interesting processes have been investigated using mixtures of molten salts and different cathodic materials. In several existing processes, the cation is simply discharged from melt but, in some cases, complications arise when the electrode potentials of the cations are relatively close. For example, the co-deposition of sodium with aluminium in the Hall-Heroult process is discussed in terms of electrode potentials of the components in the molten electrolyte. Similar considerations will also be given to the anodic reactions with respect to chlorine, oxygen, carbon dioxide or monoxide evolution from chloride-oxide melts. In some cases, the cathodic product interacts with the cathode to produce new and exciting products such as nanotubes from carbon or titanates and reduced titanium oxides from titanium dioxide. Depending on the electrode potentials, it is also possible to completely change the cathodic reaction from discharge of the cation in the salt to ionisation of the anions in the cathode. Examples are given of the reduction of metal oxides to produce metals, high technology alloys and nanomaterials and the cathodic refining of liquid metals.

Jan 1, 2006

By Batric Pesic

A hydrometallurgical process for recovery of Zn and Mn from Bunker Hill Water Treatment Plant sludge was developed. The process is unique because it treats an unusual combination of metals, Zn and Mn. Another non-standard feature of the process is that leaching takes place with ~S04 in the presence of a reductant (SO2). Zn and Mn are recovered simultaneously by electrowinning, Zn on a cathode and Mn on an anode, as MnO2 The major purpose of the process is to detoxify the sludge by removing toxic heavy metals. The recovered metal values could be marketed to offset the overall costs of water and sludge processing. This work is presented in two separate parts, 1. Leaching and Solution Purification, and II. Electrowinning. This paper covers only the first part of the hydrometallurgical process: Leaching and Solution Purification. Initially, the paper briefly discusses the history of the pollution problem at the Bunker Hill Superfund Site, the origin of heavy metals in the mine waters, and the development and use of the water treatment plant. The leaching of sludge was examined as a function of the following parameters: constant vs. initial pH, initial vs. delayed addition of SO2, temperature, and pulp density. It was found that leaching with H2SO4 at pH 2.0 for 15 minutes (at 60°C), followed by S02 addition for another 15 minutes, could completely dissolve Zn and Mn. Solution purifIcation was done in three stages. In the first stage iron was removed by adjustment of pH (to pH 5.0) and oxidation offerrous to ferric iron (with H2O2). In the second stage, Cu and Cd were removed by Zn dust cementation. Finally, Co and Ni were precipitated with the organic reagents 1-2 nitroso-naphthol and nitroso, respectively. Electrowinning of Zn and Mn is discussed separately in Part II of this paper.

Jan 1, 1996

By Daniel Chen, Jewel Andrew Gomes, Venkata Palla, Sadia Afrin Jame, David Cocke, Paul Bemazzani

"Textile industries use various kinds of chemicals including dyestuffs and pigments during dyeing and finishing processes. The effluent from these processes includes suspended particles, strong color, high pH and high chemical oxygen demand (COD) that are extremely toxic and make environmental hazard. Although physical, chemical, photochemical, and biological methods are available for treating such wastewater, the electrochemical technique, electrocoagulation (EC), has emerged as an efficient, simple, and cost-effective technology in the last few decades. In this study we present the applicability of EC technique for removing dye, such as direct red dye using iron electrodes, and the optimized conditions such as dye concentration, current density and pH. The degradation of dye molecules was investigated using UV-visible spectroscopy. The EC-floe was also characterized using SEM/EDS, XRD and FTIR.IntroductionWastewaters generated by textile industries contain large amounts of toxic aromatic compounds, especially azo dyes. Azo dyes and their degradation products, such as aromatic amines, are highly carcinogenic. These effluents are also responsible for causing high levels of color. The colored wastewater released into the environment is also a source for disruption of aquatic life and aesthetic pollution as well [1].In most textile industries, dyeing and finishing are the two important processes which are generally applied. These two common processes generate significant amount of wastewater, which may contain, suspended particles, high pH, strong color and high chemical oxygen demand (COD) concentration [2]. Low pH and high temperature are other polluting factors from the waste water. Textile industries make use of about 10,000 dyes and pigments [3]. Disposal of these colored wastewaters poses a major problem for the industries as well as a threat to the environment. In textile industries, because of the low efficiency (60-90%) of dye fixing on textile fibers, substantial amounts of unfixed dyes are released in waste waters. The conventional method for treatment of textile wastewater was a combination of biological, physical and chemical methods [2]."

Jan 1, 2011

By Jr. Robison

"Aluminothermic (""thermite"") smelting became commercial with the development of tonnage aluminum, and prospered producing metals and alloys with higher cleanliness, consistency and elemental control than competing technologies. We explore the scope of thermite smelting, and metallothermic smelting in general; the thermochemistry of the process; and its advantages and limitations as applied to industrial production. We review currently-produced products of thermite smelting in several forms and a wide range of heat sizes. As these products serve several industries, we relate the demands of those industries to the requirements imposed on the thermite process, leading to process dynamics and mechanisms to control/alter those dynamics. We review ways to lower the process costs by altering process stoichiometry, using other energy sources and utilizing less costly materials while considering effects on product quality and customer requirements. Finally, we examine overall emissions control and waste disposal.IntroductionAluminothermic smelting is the reduction of various oxides by aluminum to produce metals or alloys with varying levels of residual aluminum. One of the earliest uses of the process was the production of liquid iron to weld railroad rails, later modified in ""thermite grenades"" used to ""spike"" artillery pieces in World War II. Then during the 50's, 60's and 70's the growth of jet aircraft created a demand for new superalloys and titanium alloys, both requiring master alloys for efficient production. Aluminothermic smelting grew with the aerospace industry and with the expansion of microalloyed steels. It is very much a niche industry, dependent on the specialized demands of the specialty steel, superalloy and titanium industries. In this paper we introduce the characteristics of aluminothermic smelting, the scope of smelting operations, the markets served, and the environmental aspects of the process, as seen through the eyes of a company using aluminothermic smelting for over fifty years"

Jan 1, 2012

By Xin-liang Gao, Qing Li, Gui-qin Fu, Duo Jin, Miao-yong Zhu

"Optical microscope together with alternative wet-dry cyclic accelerated corrosion tests and XRD, SEM were employed on bridge weathering steel samples with different Mn and Ni contents which were vacuum induction melted and rolled to study their effects on the microstructure and rust layer evolution in er' containing condition. The results show that the microstructure is mainly ferrite and pearlite when Mn and Ni contents are 0.75 %, 0.42 %, respectively. Both the increase of Mn and Ni contents will make pearlite disappear while granular bainite appear, meanwhile the grain size decreases. With the increase of Mn content, the corrosion rate decreases in the initial stage, but the effect becomes little in the later stage. The increase of Ni not only improves the corrosion resistance of steel base at the initial stage but also hinders the tendency of further corrosion. As Mn content increases, a-FeOOH contents in rust layer decreases. With increase of Ni content, the content of a-FeOOH in the rust increases while that ofy-FeOOH decreases.IntroductionWeathering steels had been ~radually applied in manufacture of bridges owing to reducing the corrosion rate remarkably [I- l .Good weldability was needed for high performance bridge weathering steels. Since carbon was thought to be bad for weldability, low carbon content steel was adopted and Mn was added to amend the mechanical strength loss. Some scholars[6, 7l believed that Mn was beneficial for increasing corrosion resistance performance of the steel in marine atmospheric environment. Some scholars [S, 9l thought that Mn had little effect on corrosion resistance in marine atmospheric environment. Presently, the effect of Mn on bridge weathering steel in marine atmospheric environment still remained poorly understood. Ni was considered to be beneficial for increasing corrosion resistance performance in marine atmospheric environment [JO-l4l However, the high cost limited its application range. What would bring to the rust and corrosion by decreasing Ni content needed further research.Most researchers assumed that microstructures only affected the corrosion behavior of bare steel. But the study of Guo et al. P5l showed that the homogenous microstructures were beneficial for the corrosion resistance of steels. The effect of Mn, Ni content change on microstructure and microstructure on corrosion still remained poorly understood. In the present work, the effect of Mn and Ni on the microstructures of steel matrix, as well as the microstructures on the rust and corrosion was investigated."

Jan 1, 2014

The paper concerns an unconventional, yet promising, use of waste magnesite dust and fines. In India a significant amount of this dust is generated from some of the integrated iron and steel industries, refractory and cement plants, during calcination of raw magnesite. However. it is possible to utilize this dust, which is normally a waste, conveniently and economically for the production of magnesium. chemicals. A bench scale study was carried out to determine the rate of formation of sulfated com¬pounds of Mg.Ca,and Fe, inter alla, present in the dust system containing MeO constituents (in which Me=Mg.Ca,Fe,Si,Al etc.) Effects of various process parameters, which affect the reaction rate as also the purity of the product ,were also studied. Some work carried out to develop the process flow charts involving the salient steps to produce magnesium chemicals commercially is reported in the paper .

Jan 1, 1992

By Hui-Gai Li

The fine Ti oxide inclusions precipitated during solidification are favorable for intragranular ferrite nucleation. The oxygen content before solidification affects the composition and size of inclusions. The composition of precipitated inclusions in Mn-Ti alloyed steel was studied by means of thermodynamic calculation and experiment in this paper. The micro-segregation of Mn, Ti and O during solidification was considered in calculation and unidirectional solidification apparatus was employed in experiment to ensure that alloy elements diffused along solidification direction. The results showed that: inclusions are mainly Ti oxide when oxygen content is 10ppm; they are Ti oxide and Mn-Ti oxide when it is 20ppm; Mn-Ti oxide dominates when it is 30ppm. With the increase of oxygen content, the size of inclusions increases. The maximum oxides size is about 3µm from statistical results of experiment.

Jan 1, 2008

By Chai Li-yuan

Anodizing behaviors of magnesium alloys AZ31 at constant applied current, based on the electrolyte solution free of chromate or fluoride, were investigated. The anodizing process was influenced by constituents of electrolyte greatly. Therein, the oxylate salts, which led to the occurrence of the two totally different processes, played a determinant role in anodizing. They were stable and sparking process respectively. The morphology of anodizing film was observed by SEM and the structure of film was analyzed by XRD. During the stable process, a brown thin film was formed, however the sparking process led to the formation of white hard thick film. The functions of some kinds of additives, such as ammonia, glyceryl alcohol and PVP etc were also studied. Some of them had great effect on surface morphology of anodic film and some of them affected stability of anodizing process significantly.

Jan 1, 2006

By Brandon R. Ball

An investigation of the effects of ozone and ozone-induced hydroxyl radical on reducing whole effluent toxicity is described and discussed relative to the application of ozone for industrial water treatment. Results from operation of an ozone system treating industrial effluent from a lead and zinc mine in Colorado are presented. The mine discharges 1,000 gpm of wastewater into a tributary of the Arkansas River and has historically exceeded Whole Effluent Toxicity (WET) limits and on occasion has exceeded numeric limits for copper, ammonia, and cyanide. Based on results of a Toxicity Identification Evaluation (TIE) conducted on the effluent and individual process waste streams, the source of effluent toxicity is believed to be primarily associated with organic reagents used in the milling process. Based on test results, an applied ozone to COD ratio of 3: 1 by weight and a contact time of 30 minutes was found to be effective for reducing whole effluent toxicity at pH 11 but not at pH 7, indicating oxidation by hydroxyl radical to be the dominant mechanism responsible for toxic-ity reduction. At an applied ozone to COD ratio of 3:1 and a pH of 11, toxicity was improved from 0 percent survival to 100 percent survival for Ceriodaphnia dubia and fathead minnow (Pimephales promelas) based

Jan 1, 1996

By Masafumi Maeda

Our aim in this project was to develop a new copper refining technology utilizing pyrometallurgical treatment and a raw materials preparation technique. In the recycling process; raw material is not an idealized concentrate of copper sulfide but is composed of various types of scrap, industrial wastes such as sludge, ash and slag, and municipal wastes. Since we cannot expect oxidation heat in this process as in sulfide smelting, organic materials are viewed as an alternative energy source. Quality of the copper produced is targeted as 99.99% and an intermediate grade will also be marketable. To benefit the plant, rare metals and other nonferrous metals will also be recovered The overall system is described in this paper, specific topics outlined and preliminary research presented. Current Japanese technology for recycling copper based materials is briefly reviewed.

Jan 1, 1995

By Christian Wögerer

For material or process development as well as for quality checking of materials, thermal diffusivity measurement may be the tool of choice in many applications. Especially if diffusivity is measured locally resolved, a lot of information can be read out of such a ?diffusivity image?. This paper explains the method to measure coplanar specimen like plates and lists some interpretations of diffusivity images, like inhomogeneity of sintered materials, structural voids or inclusions. Diffusivity is a material property, describing transportation of heat in solids in spatial and temporal terms. With thermo cameras it is possible, to measure diffusivity of larger areas simultaneously. The result is an area of diffusivity values that may be plotted or displayed like an image. Locations with lower diffusivity values could be caused by the presents of structural differences in the material, by decomposition of the material components or by inclusions of other material like air.

Jan 1, 2009

By T. Mason, R. Macko

Electroless nickel (EN) coatings are widely used in the manufacture of automotive parts, providing uniform coating, corrosion protection, wear resistance and lubrication. In contrast to EN plating benefits, the disposal and treatment of waste solutions can cause many difficulties. The use of electrochemical treatment technology greatly improves _the operation of the main wastewater treatment process and reduces operation costs. A new, state-of-the-art job shop in the Chicago area, which provides EN plating for the automotive industry, has installed a large separated electrolytic cell for the treatment of spent EN solution (from dumps and wastewater). The waste/wastewater is handled by the separated electrolytic cell, batch treatment system, filter press and neutralization station. The implementation of modem electrolytic technology and auxilliary equipment provides an effective waste treatment process that meets environmental compliance criteria.

Jan 1, 2000

By Jeffrey Shepherd, Scott R. Smith, Eduard Guerra

"Electrochemical and spectroscopic evidence for the dissolution of a Au electrode by meso-2,3- dimercaptosuccinic acid (DMSA) from an acidic LiCl04 electrolyte is presented. Near the potential of zero charge, DMSA was determined to form a stable layer on the metal surface but at more anodic polarizations, DMSA was displaced from the metal through an oxidative process. The anodic displacement of the layer from the electrode resulted in a small amount of Au that was detected in the electrolyte using atomic absorption analysis. The extent of Au dissolution, was monitored while holding the potential of the electrode for 24 hours at the thermodynamic Eo/H,O in LiCl04 electrolytes containing 10 mM DMSA. This routine resulted in detectable quantities of a soluble Au-DMSA complex in the electrolyte and the greatest leaching was observed at a pH = 2.0. At room temperature, the leaching rate was stable at 10.9 µg cm·2 hr·' however, upon increasing the temperature to 50.0°C, the rate of Au dissolution increased yielding an average rate of extraction of 40.1 µg cm·2 hr- 1. Interestingly, after the first 12 hours of leaching at 50.0°C, the leaching current decreased dramatically suggesting surface passivation which prevented further Au extraction. The implications of this process in the industrial leaching of Au will be discussed.IntroductionThe use of cyanide in the industrial process of leaching Au from ores has raised concerns regarding both operational safety and environmental issues surrounding the disposal of spent leaching eftluents in tailings ponds. Depending on the chemical nature of the processed ore, the spent solutions that are released into the tailings ponds can contain toxic cyanide, either dissolved or complexed with different metals and may pose serious risk to wildlife as well as freshwater contamination to nearby water systems. Because of these issues, some recent studies have focused on the exploration of more environmentally-friendly molecules to selectively leach Au with appropriate kinetics. However, to effectively leach Au into an aqueous solution, a suitable ligand that reacts to form a stable chemical bond with Au is needed to form soluble Au complexes that can be later recovered [I]. Recently several sulfur bearing alternatives have been shown to leach significant quantities of Au in aqueous solutions. These include thiourea [2], thiocyanate [3], and thiosulphate [4]. However, alkylthiols are also known to quickly form a stable covalent Au-S bond [5], but have been relatively understudied in term of their ability to leach Au in solution, even though some short chain thiols are water soluble and relatively nontoxic."

Jan 1, 2012

By S. Yin, A. Bogno, H. Henein, P. Natzke

Impulse Atomization (IA) (a single fluid atomization technique) was used to rapidly solidify Al- 4.5wt%Cu and Al-4.5wt%Cu-0.4wt%Sc under argon atmosphere. In addition to the IA-generated droplets, the same technique was used to produce strips by Spray Deposition (SD) of the same alloys on a copper substrate with and without oil coating. The rapid solidification microstructures were analyzed using Scanning Electron Microscopy (SEM). From the SEM images, the amount of eutectic and the secondary dendrite arm spacing (SDAS) were measured. These SDAS results lead to the estimation of cooling rate. The eutectic fraction coupled with the metastable extension of the solidus and liquidus lines of Al-Cu (Sc) phase diagram lead to the estimation of primary and eutectic undercoolings. A comparison of the solidification path of the droplets and the strips was done as well as the analysis of the effects of scandium.

Jan 1, 2015

By Ryosuke O. Suzuki

A combined process of electrolysis of CaO in the molten CaCl2 and of calciothermic reduction, so-called OS process, was applied to prepare metallic vanadium directly from V2O3. The fine metallic powder containing 1860 mass ppm oxygen was obtained using 0.5mol%CaO-CaCl2 melt for 10.8 ks at 1173 K. The oxygen level did not decrease further even when twice electricity was applied. Because the metallic vanadium could be electrochemically deoxidized to the level of 10 ppm oxygen from 1.48 %, the large amount of by-product, CaO, due to reduction and the large surface area of the fine particles are the reasons of high oxygen content in the reduced powder.

Jan 1, 2006