Search Documents

PRESIDENT WILLIAM L. SAUNDERS,1 NEW YORK, N. Y. PAST PRESIDENTS CHARLES F. RAND,1 NEW York , N. Y. BENJAMIN B. THAYER,2 . NEW YORK, N. Y. FIRST VICE-PRESIDENT PHILIP N. MOORE,1 ST. Louis, Mo. TREASURER GEORGE C. STONE,1 NEW YORK, N.Y. SECRETARY EMERITUS ROSSITER W. RAYMOND, NEW York, N. Y.

Jan 4, 1915

By Ching-Yi Tsai

The effect of various constituents on the pyrolysis and combustion of a pulverized coal in an entrained-flow reactor has been inves¬tigated. Predicted time-temperature histories of the coal' particles and experimental weight loss data indicate a strong coupling of heat and mass transfer to the pyrolysis and combustion rates. A higher combustion rate following ignition was observed as particle size was increased to 112 µm. This is related to a higher particle temperature after ignition for the larger particles. Although the heating rate prior to ignition decreases with increasing particle size, higher slip velocities and surrounding gas temperatures for the larger particles promote early ignition. The presence of liptinite in the coal increases the weight loss rate before and immediately after ignition. Similar behavior was observed for pyrolysis. Fractions of a HVA bituminous coal which were rich in mineral matter or semi-fusinite were found to have a higher heterogeneous char combustion rate than vitrinite rich samples.

Jan 1, 1984

By M. Kashiwada

The zinc leach residues are introduced into waelz kiln to fume volatile metals and before the end of 1967, the waelz-fume containing zinc, lead, cadmium and indium was directly recycled back to the leaching process for the production of electrolytic slab zinc. However, since 1968, we have been recovering with success those valuable metals contained in the fume separately instead of direct leaching. According to the improved process, the waelz-fume, after being mixed with chloridizing agents, is fed into the rotary kiln to be roasted, wherein most of lead and cadmium content is collected as fume and most of zinc remains in the calcine. Zinc calcine thus obtained, containing 70 to 75 per cent zinc and, less than 1.0 per cent lead is sent to zinc plant for further recovery and the fume containing 40 to 50 per cent lead and 3 to 6 per cent cadmium is further processed to recover lead, cadmium and indium. The advantage of this process can be secured to the utmost when it is combined with the following subsequent treatments. (a) Blast furnace smelting of non-magnetic waelz slag to recover copper, silver and gold as matte. (b) Gallium recovering process from magnetic waelz slag. (c) Soda process of lead bearing cake produced after removing cadmium and indium from the said fume. Thus the extractions of zinc, lead and cadmium from leach residues account for 87 per cent, 72 per cent and 85 per cent respectively.

Jan 1, 1970

By M. M. Ragin, B. J. Scheiner

The US Bureau of Mines (USBM) has been investigating the use of polyethylene oxide (PEO) as a flocculant for a variety of mineral wastes. As part of this investigation, the hydrodynamics of the flocculation process were studied. It was determined that to obtain optimum dewatering results, the factors of energy input into the stirrer, polymer concentration, and polymer dosage must be considered. It was found that at a given polymer concentration, there were an optimum stirrer speed and polymer dosage. With excess PEO, the amount of water removed in the trommel decreased, but no evidence for steric stabilization was observed.

Jan 1, 1987

Electrochemical behaviors of synthetic and natural enargite in buffer solutions have been investigated using open circuit potential, stationary polarization and cyclic voltammetry as functions of solution pH, scan direction, scan range, scan rate and dissolved O2. The results indicate that the electrochemical behaviors of synthetic and natural enargite are very similar; solution pH, scan direction, scan range and scan rate have remarkable effects on the electrochemical behavior of enargite while dissolved O2 has little effect on the electrochemical behavior of enargite. The potential range in which enargite possesses the ability of passivation is from ?0.9 V to + 0.83 V vs. SCE. Enargite is most stable in neutral and alkaline solution around potential ?0.2 V vs. SCE. The main oxidation products on enargite surface in alkaline solution are Cu(OH)2 while the potential imposed on it is within the range of ?0.2 V to 0.33 V vs. SCE and Cu(OH)2 + S0while the potential applied is higher than 0.52 V vs. SCE.

Jan 1, 2014

By A. P. Coldren, V. Biss

SINCE the r ? a transformation rates of many carbon-free ferrous alloys and low-carbon alloy steels are relatively fast, conventional equipment is not suitable for the dilatometric determination of continuous cooling transformation diagrams. On the other hand, a method based on metallographic analysis of quenched specimens would not be practicable because the various products of shear-dominated transformation are essentially indistinguishable in low-carbon iron-base alloys. Both problems may be avoided by a thermal analysis method employing gas quenching of small specimens austenitized in vacuo. The laboratory equipment employed in the present study consisted of a Tektronix Type 564 Storage Screen Oscilloscope and a Kinney high-vacuum evaporator, modified as shown in Fig. 1, to permit heating a small specimen and cooling it slowly by programmed cooling or rapidly (up to about 8000°F per sec) by a controlled quench with helium gas. The oscilloscope records the electromotive force of a 40-gage (0.003-in.-diam) Chromel-Alumel thermocouple in the specimen during cooling. The temperature at which the cooling curve begins to show the influence of the heat produced by the phase change in the specimen was arbitrarily taken as the transformation-start temperature.*

Jan 1, 1970

By R. B. Burt, J. A. Barr, I. S. Tillotson

DISCUSSION Howard Howie (Knoxville, Term.)—The authors are to be congratulated on the presentation of a paper containing so much valuable information on the pipeline transportation of phosphate, as there is very little literature on the subject. The writer is especially interested in the paper, as he conceived the arrangement of the Akin and Godwin plants and was in charge of the design work and the engineering incident to their construction. The Akin and other phosphate deposits in the Tennessee phosphate area lie on beds of limestone that are very irregular. The limestone beds, after the phosphate matrix has been removed, are similar in appearance to land severely eroded by the action of water and denuded of top soil. Depressions in the limestone, called cutters, are irregular in depth with vertical or overhanging walls, having the general appearance of cracks in dried clay. They change abruptly in direction, width, and depth, and vary on the Akin tract from 1 to 25 ft in depth and from 1 to 50 ft in width. Pinnacles of limestone commonly occur in the cutters which appear, when exposed, like small clifflike islands in a river. Limestone floats also occur. The phosphate matrix fills the cutters and covers the uncuttered areas, the thickness of the cover varying continually and sometimes rather abruptly. It occurs generally as stratifications of phosphate rock and clay of varying thickness. The phosphate rock in the matrix varies in hardness and in percents of silica, lime, iron oxides, and fluorine, and the clay varies in toughness. In some places the deposit consists of narrow strata of rock almost devoid of clay streaks. In other nearby locations the clay will predominate. When it is excavated, the phosphate rock breaks into thin irregular lumps, locally known as plate rock. Limestone lumps are also excavated with the matrix. Akin plate rock is generally much softer than that occurring in other deposits in the area. Because of the above described physical and chemical variations of the excavated material, the resultant slurry varies in size distribution, specific gravity, and percent of slimes. When the rock is soft or when there is an increase of clay, the slime fraction is greatly increased as it passes through pumps and pipelines, resulting in reduced pipe friction. It is obvious that the longer the pipeline the greater the reduction of coarse fractions into fines, causing a decrease in pipe friction that cannot be accurately evaluated. The matrix is mined with a dragline that drops it into a hopper with a grid composed of 9-in. parallel bar spacings located above the hammer mill. The matrix on, and passing through the grid, is subject to the action of powerful sprays which wash it down to the hammer mill, together with any limestone lumps that are not removed before passing through the grid. The hammer mill reduces the feed to lumps of plate rock and clay, most of which will pass through the 8-in. pump suction. The mixture discharges into a pool containing the pump suction pipe. Water from a hydraulic nozzle moves the mixture to the pump suction intake. The pump, driven by a variable speed motor, is the same size as the pumps mentioned on p. 279. Provision is made to remove any lumps that lodge in a bend in the suction pipe in a manner similar to that used in the Florida phosphate fields. The hammer mill and pump units are mounted on wide steel skids so that they can be moved as the mining operation progresses. The discharge from the pump flows through an abrasion-resistant spiral welded steel pipe 81/4 in. actual inside diam, 8 in. nominal diam, for a maximum distance of 2200 ft, which is the limiting pumping distance for one pump. This pipeline, referred to hereafter as pipeline A, discharges into a ball mill without balls, which in turn discharges into a rotary screen attached to it that separates the slurried matrix into 11/4-in. oversize and undersize fractions. The oversize is returned to the mill for further reduction; the undersize is pumped to a Dorrco washer and then flows into a hydroseparator 160 ft in diam. In spite of the size reduction in the hammer mill and the blunging and washing of the slurry in its passage through the pump, pipeline, mill, and washer, the discharge to the hydroseparator frequently contains mud balls almost perfectly spherical. Sometimes the discharge from the 16,000-ft pipeline at Godwin contains mud balls the size of bird shot and smaller. This pipeline will be referred to subsequently as line B. Liquid caustic is added to the slurry at the Akin plant before its passage through the hydro-separator, which decreases the size of particles in the overflow by dispersion. In passing through pumps 1, 2, and 3 and pipeline B, the slime fraction in the underflow is increased by abrasion and blunging and also by continuing dispersive action of the caustic. The matrix for use in the experimental tests referred to on p. 279 was obtained from three small surface openings on the Akin tract that were made previous to the purchase of the tract by the Authority. Matrix used in the 2 and 4-in. experimental pipeline tests was taken from the three openings and proportioned to obtain a sufficient quantity that would be fairly representative of the average in the Akin deposits. Prospecting samples of matrix had been obtained from drill holes which showed no small variation in physical and chemical properties. Some of the physical variation is evident from the size distribution of solids in samples taken during the tests covering line B flows so thoroughly made by the Authority und'er the direction of Mr. Burt, see Table V, p. 280. Hydraulic gradients for a pipe of 8-in. diam were derived from the 2 and 4-in. pipeline tests using the so-called representative matrix as above described, and plotted on the profile of pipeline B. Gradients of other materials in slurry form passing through pipelines that bore some similiarity to the Akin matrix slurry were also plotted. After a study had been made of the hydraulic gradients plotted on the profile and the varying slurry flow that would probably occur during actual operation, three pumps were ordered, referred to as No. 1, 2, and 3 on p. 279. No. 1 and 2 pumps were installed and the third kept in reserve should the operation of 1 and 2 pumps prove satisfactory, since installation of the third pump would require an attendant, as well as the laying of 5400 ft of pipe to supply it with seal-water from the Akin plant. Subsequently, it was found desirable to install the third pump to maintain capacity when the slime fraction was low and the coarse fractions were large. Reference to Fig. 6 will show that the flow in B line goes upgrade in three locations. At the outlet at Godwin, the slurry flows between two 45" bends for an approximate distance of 18 ft to rise above the ground a sufficient height to discharge into a launder feeding the first classifier. This condition requires extra energy, which is taken care of by keeping the hydraulic gradient a sufficient distance above the high points. Although there are rather heavy upgrades in the line, the choking condition that might occur at the

Jan 1, 1953

By Arthur F. Taggart, T. C. Fitt, A. W. Thomas

IT was noticed early by operators that high recoveries and flocculation of the sulphide minerals were closely correlated in agitation-froth flotation. Later, this readily visible flocculation was found almost invariably to be due to the binding together of the oiled sulphides by minute air bubbles, and is now known to be characteristic of pulps in which at least one of the mineral species is coated with an insoluble collecting oil. In 1930 it was reported1 that in differential flotation a correlation exists between Brownian movement of particles in the pulp and their nonfloatability, and that Brownian movement and dispersion are likewise correlated, whence it would appear to follow that dispersion of a mineral particle in a flotation pulp denotes a particle condition unfavorable to flotation. In 1934 it was postulated2 that Brownian movement, dispersion and nonfloatability all flow from the condition of the surface of the dispersed particles. It was also postulated at that time that the surfaces of dispersed particles are ionized, the ionized compound being a product of reaction between a component of the particle and a. component of the pulp, of a mass solubility of the general order of a fraction of a milligram to 15 to 20 mg. per liter. It was then further asserted, and has since been confirmed by Bankoff,3 that sulphides so conditioned with soluble collectors as to be floatable flocculate without the intervention of air bubbles as binding media. The present paper comprises an inquiry into the nature of the bound and counter ions in zinc sulphide dispersed by sodium arsenate. A part of its findings was mentioned in the 1934 paper above cited.2 The tests show that: I. When powdered granular zinc sulphide is immersed in aqueous solutions of sodium arsenate, arsenate ion is abstracted from solution and anchored to the solid surface, while sulphate and lower sulphoxy ions are concurrently displaced therefrom in substantially stoichiometric quantities. 2. The ion counterbalancing the anchored arsenate ion is zinc. 3. Dispersion and Brownian movement of zinc sulphide are concurrently maxima at an arsenate-ion concentration lying between 0.01 and 0.001-molar sodium arsenate. 4. Any condition or reaction that tends to remove the zinc arsenate coating from the zinc sulphide particles decreases dispersion and Brownian movement concurrently. EXPERIMENTAL Three samples of zinc sulphide were used. Lot I was C.P. zinc sulphide, washed well beyond absence of chloride, as shown by test with silver ion. Lot 2 was prepared by precipita-

Jan 1, 1943

By E. M. J. A. Pallone, F. N. Cunha, W. S. Resende, R. M. Stoll, R. C. Bradt

Utilization of the magnesium aluminate spinel in refractor' applications is briefly reviewed. The synthesis of a magnesia aluminate spinet aggregate from natural raw materials is considered in terms of the crystal chemistry of the spinet structure and expected impurities. Principles for the formation of this spinet refractory aggregate from different natural raw materials are presented. The basic concepts were then applied to the reaction of a bauxitic clay with a natural magnesite. This combination of raw materials has the potential to produce a low-cost refractor' aggregate that is a composite of spinel and forsterite. Experimental results are reported to produce a spinel refractor.' aggregate containing a small amount of forsterite. It possesses low apparent porosity and high bulk density suitable for industrial refractor' applications, including steelmaking, aluminum and copper foundries and cement production.

Jan 1, 2002

By C. P. Snyman

Three independent methods of coal classification can be distinguished, namely on the basis of grade, type and rank. The latter two can be determined accurately and unambiguously only by means of microscopical techniques. These three independent variables affect all the coal properties and therefore also the technological behaviour of a particular coal. The influence of the inorganic constituents of coal on the fusibility of the ash and on the length of the slag, and also on fouling and slagging, is discussed. The fractionation of the ash-forming constituents during combustion and gasification of pulverised coal shows that fouling and slagging are not related directly to the fusibility and composition of ash of the coal as a whole. The results of combustion experiments using a drop furnace technique indicate that the ignition temperatures of the light volatiles in the coal, and of the formed char, as well as the burn-out time of the char are more dependent on the rank than on the type or grade of the original coal. High-ash coals, however, apparently ignite at lower temperatures and are more reactive than low-ash coals of similar type and rank. The surface properties of coal, which are important in froth flotation and oil agglomeration, correlate well with the inherent moisture content (and by inference with the heat of wetting and the calorific value) and therefore with the type and rank of the coal. In coal exploration, variations of rank offer the possibility of predicting the presence of an intrusion near the seam, thus contributing to more effective exploration and mine planning.

Jan 1, 1991

By Donald K. Sparling, C. Edwin Baker

The White Mesa uranium/vanadium mill is six miles south of Blanding, UT, on the Colorado Plateau, which has historically spawned more than 200 uranium mines. As uranium prices approached an all-time high during the mill planning period, Energy Fuels Nuclear Inc. anticipated the reopening of many of these mines, whose low grade ore suddenly looked economic. The company located the White Mesa mill close to these mines, to minimize hauling distances to the mill and give vendors added incentive to reopen or expand mine operations. A receptive local community, a relatively unencumbered trip through the regulatory maze, and some mill circuit innovations all helped to make the White Mesa mill a well functioning reality. From a strategic standpoint, and to begin ore stockpiling as early as possible, Energy Fuels constructed two ore buying stations and began receiving ore in early 1977. The buying stations were located at Hanksville and at what is now the Blanding mill site. Ore receipts at Hanksville did not materialize as anticipated and the facility has since been closed. The Blanding ore buying station is now an integral part of the milling operation. All ores, whether company, vendor, or for toll milling, are received at the Blanding station. The Blanding site was central to the plateau mines, and was well received by area residents, who encouraged the introduction of industry to the area. Residents viewed mill construc¬tion as an economic blessing and were prepared to accept the associated im¬pacts. Energy Fuels hired as many local people as possible for mill opera¬tions.

Jan 4, 1981

By L. L. Handy

The most common method of identifying hydrocarbon-bearing strata in a well that penetrates many different formations involves measurement and interpretation of the electrical properties of the formations as determined by electrical logs. Even though this method is used extensively, and even though in a great many instances it is capable of indicating presence of oil or gas, situations arise for which it is extremely difficult, if not impossible, to deduce the presence of hydrocarbons. These situations may involve the following. 1. A thin formation, bounded by highly resistive formations, in which it is impossible to obtain the actual resistivity of the uninvaded zone with existing logging devices. 2. A formation in which invasion has been so extensive that a value for the uninvaded zone resistivity cannot be obtained. 3. A very shaly formation in which the resistivity index, I, is lower than that usually associated with productive formations. 4. Laminated formations comprised of thin productive sands separated by thin shale streaks in which the individual sand and shale streaks are too thin to permit measurement of uninvaded-zone resistivity with existing logging devices. 5. Productive formations in which the water saturation is high. To extend the utility of electric log interpretation to identification of hydrocarbons in all types of formations, there is strong incentive to find a method not subject to these limitations. Some time ago, in connection with research on the wettability of reservoir rock, an investigation was conducted in which the resistivities of cores were measured shortly after they were removed from a core barrel, and again after they had been extracted and restored to their original oil and brine saturation.' The resistivities after extraction were generally lower. Other tests made on the cores indicated that they were more nearly water wet after they were extracted; thus, it was assumed that the observed changes in resistivities were due to a change in wettability of the cores. Other experiments'," have shown that resistivities of rock samples are sharply dependent on wettability. These experiments have shown that oil-wet samples are more resistive than water-wet samples. To obtain an understanding of how the wetting properties of the surfaces of core material affect electrical resistivity, a series of experiments was conducted. Two groups of core samples were prepared for testing. One group contained brine, but no residual oil. The other group was saturated with brine, flooded with oil to a low water saturation, then flooded with brine to a final residual oil saturation. Resistivity measurements were made on each group. Both groups were then flooded with the original brine to which a chemical had been added that renders sand and clay surfaces preferentially oil wet, a so-called reverse-wetting agent. very little change in resistivity was observed in cores containing only water. The group containing residual oil, however, showed resistivity increases of 100 to 200 per cent. These experiments showed that the resistivity of a core containing oil could be altered by changing wet-tability of the core. Moreover, the possibility was introduced that reverse-wetting agents might be employed as the basis for a logging method for identification of oil-bearing strata. Since behavior of a porous rock containing gas and water might be expected to be similar to that of a rock containing oil and water, such a method should also be applicable to identification of gas-bearing zones. In principle the wettability of the invaded zone could be reversed without altering conductivity of the interstitial water or the hydrocarbon saturation therein. Those strata showing significantly increased invaded-zone resistivities would, therefore, contain hydrocarbons; those with no significant change would be filled only with water. Addition of a reverse-wetting agent to a hydro carbon -bearing zone which is, by nature, already preferentially oil wet would not result in an enhancement of its resistivity. It is generally believed, however, that most hydrocarbon-bearing strata are preferentially water wet.

By T. C. Eisele

The use of column flotation was considered for the ?reverse flotation? of iron ore, where the gangue (quartz) was recovered in the froth product. This use of the froth for carrying the gangue mineral rather than carrying the valuable concentrate significantly changes the operational requirements of the column. The objective of this work was to determine which of several column flotation technologies would be most suitable for this type of flotation operation. Studies were carried out using both the Jameson column and the Deister column. Comparative results are presented that show the capabilities of both column types in this application relative to conventional Wemco flotation cells. Columns were demonstrated to have grade-recovery performance superior to what could be achieved with conventional cells. Two-stage flotation with the columns could produce a concentrate that was up to 70.2% Fe at 87.5% iron recovery, compared to 70.4% Fe at only 77.7% iron recovery for four stages of flotation in conventional cells. It was shown to be particularly important to operate the columns to recover a maximum of the quartz gangue into the froth. It was noted that there are often problems in scale-up of laboratory columns to plant scale, because the increase in height and the decrease in the ratio of height to diameter at the larger scale allows more axial mixing and bubble coalescence, both of which degrade the column performance. Horizontal baffling was shown to improve column performance by reducing axial mixing and breaking up large bubbles, and so the use of such baffles in the reverse flotation application was investigated.

Jan 1, 2007

By C. A. Pickles, K. Mackowiak

Black Thor chromite ore from the Ring of Fire deposit in Northern Ontario was carbothermically reduced in a microwave system to produce a ferrochromium alloy. The as-received ore contained 43.0% Cr2O3, 19.9% Fe2O3, 14.5% MgO, 13.4% Al2O3, and 7.0% SiO2. Activated charcoal was utilized as the reducing agent. Firstly, TGA/DTA and permittivity studies were carried out in order to determine the relationship between the reduction process and the microwave susceptibility. Secondly, microwave reduction experiments were performed on the chromite ore. The variables investigated were; the amount of carbon, processing time, input power and type of atmosphere. A maximum chromium grade of 76.1% and a chromium metallization of 82.7% were obtained for a processing time of 20 minutes, a power input of 800 W, and a carbon addition of 15% in an argon atmosphere.

Jan 1, 2017

By R. A. L. Drew, J. P. Immarigeon, F. Jalilian, M. Jahazi

In the present work TLP bonding of Inconel 617 is investigated. The influence of the main processing parameters i.e. time and thickness of the interlayer were studied with optical and scanning electron microscopy. Boron containing interlayers with two different thicknesses were used and the influence of various holding times from 5 min to 24 hours on the microstructure of the bond region was investigated. The results indicated that, for the testing temperature of 1065°C and holding times above 2 hours with an interlayer of 25.4 microns thick no liquid phase was observed. The same phenomenon occurred only after 6 hours for a 76.2 microns thick interlayer. Precipitate growth started at grain boundaries and continued inside the grains. The composition, size and morphology of the precipitates were studied using electron microprobe analysis. No noticeable changes were observed in the grain size of the base metal with increasing holding times.

Jan 1, 2004

By M. S. Tsai, Y. D. Chuang, H. M. Wu

To contact the commercial OPAP-kerosene solution with CH3OH – H20 solution, we used the appropriate concentration of DOPAP / MOPAP solvent. By using this treated OPAP solvent, uranium can be recovered from wet-process phosphoric acid. Electric DC power is supplied on the dual side of the ion-exchange membrane of a specially designed box-type mixer settler. U(VI) is reduced to U(IV) in the cathode and U(IV) is oxidized to U(VI) in the anode. Uranium is extracted in the cathode by treating it with OPAP solvent. Next the uranium is stripped from the loaded OPAP solvent by concentrated phosphoric acid in the anode. After 300 hours of continuous operation total recovery of uranium is as much as 95%.

Jan 1, 1984

By Chuansheng Luo

If lead-zinc ores have high oxidation rate, separation of lead and zinc is very difficult. This paper studied the technology of preferential flotation by the coarse grinding and re-grinding. The lead concentrate grade is 51.40% and the lead recovery is 62.83% when feed grades Pb 1.74% and Zn 6.46% with oxidation rate being 13.75%. At same time, the zinc concentrate grade is 50.07% and its recovery is 90.01%.

Sep 1, 2012

By Albert F. J. Bordeaux

The following general survey of the character and present condition of the silver-mines of Mexico, though not offered as a detailed treatise, has been prepared with care, is believed to be generally up-to-date, and is offered as a summary which may be found useful by mining engineers. For several centuries Mexico has ranked first anlong the silver-producing countries. It is now second as a copper-producer, and seventh as a gold-producer, with a fast-increasing output every year. The total amount of capital invested in its mining- and smelting-works exceeds $250,000,000, while the value of the yearly metallic production is $160,000,000. There are more than 20,000 recorded mining properties. The silver-mines of Mexico represent deposits of three principal classes: (1) veins and stock-works in eruptive rocks; (2) fissure-veins crossing the crystalline schists, granite, diorite, etc.; and (3) veins and replacement-deposits in limestone. The true fissure-veins in some districts contain (in value) vol. xxr1x.—22

Jan 1, 1909

By Markus A. Reuter, Antoinette van Schaik

"Product design engineers select from a wide range of materials and combine them into multimaterial product designs. These include various materials (metals and non-metals) which are complexly integrated (e.g. welded, glued, alloyed, layered). The recycling/recovery rate of consumer products are determined by the different materials and alloys used, but also by the particle size and multi-material particle composition after shredding (combination of materials due to design). Eco-design (for recycling) and Design for Recycling (DfR) can only be conducted if the interconnectivity of material/metal in various unliberated materials is accounted for and its effect on material and energy recovery can be linked back to design. This paper will discuss the basic principles of these DfR models and it is shown how these tools (i) are linked Computer Aided Design (CAD) and Life Cycle Assessment (LCA) software, (ii) affect conceptual design specifications of products, (iii) integrate the complex detail of the recycling system and recyclate quality and hence (iv) make recycling an integrated part of the product system. Furthermore, it is shown how these assessment tools and models can be applied for benchmarking of the recyclability and environmental damage created by the recycling of end-oflife consumer goods in order to e.g. (i) provide the (original) equipment manufacturer with knowledge and solutions to support product stewardship and Extended Producer Responsibility; (ii) create awareness of the consequences/benefits of design, products and recycling systems to manufacturer, designer, legislator, recycler etc.; and (iii) assist the consumer in their choice of consumer goods from an end-of-life point of view.IntroductionA first-principles basis is required in order to be able to simulate and predict the recycling/recovery behaviour of products facilitating Design for Recycling (DfR) and Eco- Design. This links recycling technology and the environmental consequences of recycling directly to product design."

Jan 1, 2008

A general approach to the analysis of processing technology is presented using the concepts of Process Aims, Process Characteris- tics and Process Costs. From an examination of the processes used in extractive metallurgy a hierarchy of process aims is identified, these aims are separation, compound formation,, metal production and metal purification. The application of this methodology to process flowsheet development is described.

Jan 1, 1984