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By Tae-Hyun Kim, Kang-In Rhee, Jeong-Soo Sohn

The synthesis of Mn-Zn ferrite powder from spent zinc-carbon batteries was investigated using a series of physical treatment, sulfuric acid leaching and coprecipitation. Physical separation methods such as crushing, magnetic separation and sieving were applied to generate a non-magnetic material of 8- mesh undersize for subsequent leaching process. The 8-mesh undersize of the spent zinc-carbon batteries was assayed 23.9% Mn, 14.9% Zn, and 4% Fe. Metal extractions obtained in sulfuric acid leaching at the solid/liquid ratio of 1:10, 2 M H2SO4, and 60? with 6 vol.% H2O2 addition were 97.9% Mn, 98.0% Zn and 55.2% Fe. The leach liquor was finally adjusted to the Mn:Zn:Fe mole ratio of 1:1:4 suitable for producing MnZnFe4O8 ferrite powder by the addition of Mn, Zn and Fe sulfates followed by pH control. A co-precipitation test for Mn-Zn ferrite powder was performed at 80?, O2 gas flowing at 1.3 L/min. As a result of co-precipitation, Mn-Zn ferrite nanoparticles in 20 nm size with spinel structure were successfully synthesized. The saturation magnetizations of Mn-Zn ferrite powder (Mn1-xZnxFe2O4) were determined to be 39-91 emu/g with various zinc contents (X=0.2-0.8).

Jan 1, 2008

By Shaik Jeelani, Esperidiana A. B. Moura, Vijaya K. Rangari, Roberta A. Lima, Rene R. Oliveira

This work present the preparation and characterization of biodegradable nanocomposites based on aliphatic-aromatic copolyester (PBAT)/polylatic acid (PLA) blend reinforced by TiO2 nanoparticle. The biodegradable polymeric nanocomposites were prepared by melting extrusion process using a twin-screw extruder machine. The influence of the TiO2 nanoparticle addition on mechanical and thermal properties of PBAT/PLA blend was investigated by tensile and impact tests, SEM, DSC and XRD analysis and the correlation between properties was discussed.

Jan 1, 2015

By Tim Robinson, Michael S. Moats, Masatsugu Moritmitsu, Kathryn C. Sole, Lauri Palmu, Frank K. Crundwell

"Process technology and design trends for copper, zinc, and nickel electrowinning cellhouses include focusing on energy reduction, productivity, and acid mist abatement. Larger electrodes, longer cells, automation, and higher current densities are leading to more capital-effective designs. The latest cellhouse designs include installation of automated electrode-handling systems, thereby removing more operators from the cellhouse. These technology and design trends result in lower electrowinning operating costs and improved purity of electro won cathode.INTRODUCTIONTechnology transfer between similar industries is an important process in improving product quality and productivity, and reducing operating costs. The electrowinning (EW) recovery of base metals, such as zinc, copper and nickel, is no different. The zinc industry with its larger EW product-handling requirements as compared to nickel and copper, has been driven to automation technology and the use of larger equipment. This technology has been transferred to copper. Nickel has led development and application in large-scale anode and divided-cell technologies but, due to nickel being produced in multiple forms (not just cathode) and being a small part of the whole complex nickel process route, the quantities of electrowon nickel are small compared to copper and zinc. Copper process technology in acid mist abatement was recently transferred to nickel. The focus in copper EW has been on energy reduction and productivity."

Jan 1, 2012

By Dirk Verhulst

The Altair Hydrochloride Pigment Process is a new ?third route?, besides the established high-temperature chloride process and the older sulfate process, to manufacture TiO2 pigment from ilmenite ore. It has been tested at a scale of 5 t/day feed. The ore concentrate is digested in high-acid, high total chloride solution (+/- 39% Cl). Titanium and iron both go into solution. Iron is separated as FeCl2 crystals after reduction and cooling. Titanium is transferred by solvent extraction into a purified, high-Ti stream. It is spray-hydrolyzed to produce a TiO2 hydrate and further calcined with additives into high-quality pigment. HCl solutions generated by pyrohydrolysis and spray hydrolysis are treated by pressure-swing distillation to regenerate HCl gas for re-injection into the digestion reactor. All chloride streams are recycled. Recent work has concentrated on optimization, particularly in 3 areas: - Solvent extraction: a new organic mixture, including a new diluent, makes it possible to work at room temperature, to avoid TiO2 hydrolysis problems and to improve phase disengagement and impurity separation. - Pigment finishing: a systematic study of the parameters involved, followed by long runs in the best conditions confirm pigment quality. - Flow sheet optimization: innovative modifications of the conditions of spray hydrolysis and pyrohydrolysis, combined with re-routing of streams achieve significant energy savings. A 100 t/year pilot plant including these features as well as other process improvements is under construction.

Jan 1, 2006

By Katsuyoshi Kondoh

The synthesis processing of Mg2Si or Mg2SiIMgO at lower temperature from the elemental magnesium alloy powder/chips and Si or SiO2 powder mixture was established via the repeated plastic working (RPW) based on Powder Metallurgy (PIM) process. RPW is much effective on the mechanical breakage of MgO surface films, which prevent from the solid-state reaction between Mg and Si powder. The solid-state synthesized Mg2Si particle of 200nm-2um is extremely fine, compared to that via the conventional casting process, causing the coarse one of 50-100um. This is because of not coarsening during the solid-state synthesis of Mg2Si. By using in-situ fonning process of Mg2Si via RPW and pre-heating before hot working such as extrusion and forging, the magnesium composite material with Mg2Si or Mg2Si/MgO dispersions was developed in employing Si or SiO2 particles, respectively. For example, when employing AZ31 chips as raw materials of the matrix, it has low density of 1.85g/cm3 and extremely superior mechanical properties, such as tensile strength over 350MPa with 5-10% elongation and Young's modulus of 47-50GPa, to the conventional Mg-Al-Zn alloys. The Mg composite alloy wires and pipes were produced via the hot extrusion process in the manufacturing plant, and also showed excellent mechanical properties.

Jan 1, 2003

By Andre Thess, Oleg Zikanov

"Direct numerical simulation methods are applied to study the influence of a constant magnetic field on turbulent flows of liquid metals. The flow is assumed to be homogeneous and the problem is reduced to the classical case of the turbulent flow in a 3D box with periodic boundary conditions. The main subject of the study is the anisotropy developing in a liquid metal flow affected by constant magnetic field.To investigate the long-time evolution of initially isotropic flow the large-scale forcing is applied to maintain the flow energy at a statistically steady level. It is found that the flow evolution depend strongly on the magnetic interaction parameter (Stuart number). In the case of small Stuart number, the flow remains three-dimensional, turbulent, an approximately isotropic. At large Stuart number (strong magnetic field) the turbulence is suppressed rapidly and the flow becomes two-dimensional and laminar. Very interesting is the intermittent flow evolution at moderate Stuart number. Long periods of almost two-dimensional, laminar behavior are interrupted by strong turbulent three-dimensional bursts.The influence of a constant magnetic field on scalar transport properties of liquid metal turbulence is investigated using the simplified formulation of homogeneous flow driven by an imposed mean temperature gradient. Such a flow consists primarily of two turbulent antiparallel jets providing an effective mechanism for heat transfer. It is shown that the magnetic field parallel to the mean temperature gradient stabilizes the jets and, thus, enhances heat transfer considerably."

Jan 1, 1999

By Stanko Nikolic

Ferrous calcium silicate slags are potentially important for future practice in copper converting operations and processes and can be described by the ?Cu2O?-FeO-Fe2O3-CaO-SiO2 system. Despite its industrial importance the phase equilibria in this system have not been fully investigated. Characterization of this slag system is necessary to improve the design and optimization parameters of new processes, including fluxing and operating temperatures. Experimental methods have been developed to investigate the phase equilibria of these slags at copper saturation and without copper. This technique involved equilibration of samples at a fixed oxygen partial pressure, rapid quenching, and analysis of the compositions of phases using electron probe x-ray microanalysis (EPMA). Liquidus and solidus data are reported for the primary phase fields of spinel, wollastonite and tridymite at 1250oC and an oxygen partial pressure of 10-6atm. The resulting data has been used to construct liquidus isotherms in the ?FeO?-CaO-SiO2 system both in equilibrium with and without molten copper. The experimental results were compared with the predictions of a thermodynamic computer package utilizing a self consistent thermodynamic database. The predictions of the model were in good agreement with the experimental isotherms when projected onto the FeO-CaO-SiO2 section, however the copper concentrations in the liquid phase at copper saturation were lower than predicted using the current database of the model.

Jan 1, 2006

By M. Suzuki, M. Dobashi, M. Kahata, T. Yoshida

Almost 30% of steel in Japan is produced by electric arc furnace (EAF) treatment of iron scrap. EAF dust includes approximately 20 wt % of Zn and 3- 5 wt % of CI and is treated by the pyrometallurgical processes to recover Zn as Zn oxide. Direct hydrometallurgical processing is one of the most effective methods to recover high purity Zn. In this case, CI in the EAF dust is dissolved in the liquid phase by leaching, and the CI anion in electrolyte attacks anodes which are commonly made of a lead base alloy. Several processes have been proposed to remove CI anions from acidic sulfate solution. In this study, an electrolytic process was examined to eliminate CI anions from Zn sulfate electrolyte. From our study it can be said that the elimination rate of CI anion depends on the anode material ( i.e., the elimination rate is Pb-Ag alloy == Pb > DSE== Pt). In industrial Zn electrowinning process, the electrolyte contains Mn, which means the influence of Mn should be considered in the elimination of Cl. Mn dioxide deposition on an anode plate reduces the efficiency of CI removal. A periodical reverse current electrolytic system was examined to prevent this efficiency decrease, and deposited Mn dioxide could be removed very rapidly when the current is reversed. More than 95% of CI anion could be removed by this method in a shorter period than direct current method.

Jan 1, 1997

By Matsufumi Takaya, Yukihiro Sakamoto

"Electric field emission properties from CVD diamond fabricated using pulse-modulated microwave plasma CVD were studied. Diamond was synthesized by microwave plasma CVD apparatus equipped with a pulse-modulated microwave power supply. Pulse conditions were varied from 1 to 10 seconds for pulse periods and from 0.1 to lHz for pulse frequency either. Surface morphologies of the deposits were differed by pulse frequency and duty cycle. As a result, FE properties prepared by different pulse duty cycle were different from continuous film which synthesized using continuous microwave significantly. Highest current density was obtained from the uneven morphology diamond film prepared at 17.5% pulse duty cycle.FE properties of the CVD diamond were depended on surface morphologies that related to the pulse conditions.1. IntroductionDiamond has excellent physical and chemical properties as an industrial material. Especially, hydrogen terminated diamond had the negative electron affinity (NEA) 1) and CVD diamond has this NEA property either as deposited 2). So the electron emission source to the FED is expected as one of this application of CVD diamond as cold cathode of electric devices. We studied on FE properties of various CVD diamond, pulse microwave plasma CVD diamond showed better property than those of other CVD diamond 3).This report studied on· the effect of the duty-cycle of pulse modulate microwave condition on FE properties of the diamond fabricated by pulse modulated microwave plasma CVD."

Jan 1, 2000

By Daoxin Wu, Zhong Cao, Yan Shi, Yu Ding, Huanli Yang, Zhongliang Xiao

"2-substituted benzimidazole-zinc and 2-substituted benzimidazole-copper complexes were main components of organic solderability preservative (OSP) in PCB producing process and affect the thermal stability of OSP film. So these four complexes were prepared by 2-substitutedbenzimidazole reacting with zinc ion and copper ion, the complexes crystals were determined by IR, its thermal stabilities were studied by TG method. The results indicated that the thermal stability of 2-substituted benzimidazole-zinc is higher than the 2-substituted benzimidazole copper,and the thermal decomposition mechanism was presentedIntroductionImidazole compounds which is an important heterocyclic compound shows the important value and outstanding prospects[I-3l in field of biological engineering, medicine, and high-performance composites. It's said that imidazole compounds is an excellent new metal surface treatment[4] agent, because it has good reaction activity with metals and can form a chemical layer on the metal surface. The complexes of imidazole were main components of organic solderability preservative (OSP) in PCB producing process and affect the thermal stability of OSP film. The mechanism of imodazole combined with metal and film deposited has been reported, but the opinions about thermal stability of film have bifurcation, let alone the thermal decomposition mechanism of film at high temperature. The complexes were prepared by combining of 2- substituted-benzimidazole with zinc and copper iron, which were studied by IR and TG method, in order to get thermal stability of different complexes."

Jan 1, 2011

By C. T. Yavuz

Higher environmental standards have made the removal of arsenic from water an important problem for environmental engineering. Iron oxide is a particularly interesting sorbent to consider for this application. Its magnetic properties allow relatively routine dispersal and recovery of the adsorbent into and from groundwater or industrial processing facilities; in addition, iron oxide has strong and specific interactions with both As(III) and As(V). Finally, this material can be produced with nanoscale dimensions which enhance both its capacity and removal. The objective of this study was to evaluate the potential arsenic adsorption by nanoscale iron oxides, specifically magnetite (Fe3O4) nanoparticles. We focused on the effect of magnetite particle size on the adsorption and desorption behavior of As(III) and As(V). The results show that the nanoparticle size has a dramatic effect on the adsorption and desorption of arsenic. As particle size is decreased from 300 nm to 12 nm the adsorption capacities for both As(III) and As(V) increase nearly 1000 times. Interestingly, this increase is more than expected from simple considerations of surface area and suggest that nanoscale iron oxide materials sorb arsenic through different means than bulk systems. The desorption process however, exhibits some hysteresis with the effect becoming more pronounced with small nanoparticles. This hysteresis most likely results from a higher arsenic affinity for magnetite nanoparticles. This work suggests that magnetite nanocrystals and magnetic separations offer a promising method for arsenic removal.

Jan 1, 2006

By Evan Jamieson

The conditions under which various iron(III) oxy-hydroxides phases precipitate from iron(III) chloride and sulfate solutions at ambient temperatures (<60°C) are reviewed. Many of these precipitates are slow settling and gelatinous but ultimately transform into other more stable or crystalline phases. The phase that forms depends upon the rate of precipitation and pH. A comparison has been made of the iron(III) oxides formed upon the neutralisation of various iron(III) solutions with caustic, slaked lime or slaked magnesia which provide different rates of neutralisation and slowly dissolving solids with localised high pH. Mössbauer spectra of ferrihydrites precipitated under these different conditions are compared and interpreted. Particular attention is paid to the settling rate and settled volume which is likely to relate to industrial thickener and filter performance. It is shown that in pure chloride solutions, poorly settling ferrihydrite is usually produced at 20oC regardless of the choice of base. However in sulfate solutions fast settling precipitates are produced using lime and magnesia but not with caustic. In mixed chloride/sulfate solutions, optimum settling rates occur when the molar ratio of [SO4]2to Fe3+ is about 1:1 and when the sulfate concentration is <0.20 M. It is proposed that ?dense amorphous basic iron sulfate? or well-ordered ferrihydrite is formed on slowly dissolving lime or magnesia surfaces. Implications for industrial liquors are considered.

Jan 1, 2003

By Jr. Santafé, Lucas L. da Costa, Felipe P. D. Lopes, Sergio N. Monteiro

"Residual vegetable fibers as leftovers from crops, industrial activities and consumable items are realistic options to be incorporated into low cost polymeric composites with the aim of replacing other commonly used materials. The present work assesses the technical properties of epoxy composites reinforced with residual fibers from the coconut fruit, also known as coir fibers. Based on these properties, an evaluation was carried out on these coir fiber/epoxy matrix composites to be used as building panels and furniture in comparison with conventional materials.IntroductionThe utilization of waste from industrial activities is presently recognized as important way in preventing environmental pollution as well as developing new products. This utilization would also generate employment and contribute to environmental improvement in global scale. Among such wastes, those from lignocellulosic materials represent a considerable potential for practical application. In fact, about 2.5 billion tons of these materials are currently available [1], and their fiber content is an important option for composites fabrication. Actually, lignocellulosic fibers are now replacing synthetic fibers as reinforcement in resin matrix composites owing to specific advantages such as low cost, biodegradability and renewable characteristics [2,3]. Moreover, as abundant waste, some of these lingocellulosic fibers could help reducing the use of traditional materials like wood and plastics in many industrials applications. This would prevent further stress on the environment caused by depletion of dwindling resources associated with forests and petroleum."

Jan 1, 2008

By Xian-Dong Zhou, Guo-Sheng Sun, Jianzhong Luo, Hong-An Guan

"Oxygen utilization rate of the pretreatment process which adopts biological contact oxidation method for slightly polluted supply water is relatively low, less than 10%, usually lower than 3%. So the aeration amount is not determined by calculated value of oxygen demand when doing process design, but by the ratio of gas and water. The aeration way of the biological pretreatment process for slightly polluted supply water was introduced in this paper. In the foundation of the principles of mass transfer kinetic theory and experimental data, the change law of DO (dissolved oxygen) and ammonia in the aeration tank was analyzed to explore aeration method which will help to improve the overall effectiveness of handling capacity.IntroductionThere are many kinds of filler used in the biological contact oxidation process, such as flexible solid filler, composite filamentous filler, powdery clay filler, particle ceramic filler and so on. Regardless of the different forms of filler, there are a couple of common points in the function of the aeration[1,2]: (1) The aeration process in biochemical tank not only provides adequate oxygen for the biological reaction, but also plays as a role of stirring water; (2) Biochemical reactions mainly happen in the upper reaches of tank, but seldom at down-streams.This paper, from the perspective of changing aeration way, discussed the feasibility of improving the effectiveness of biochemical reactions without increasing aeration amount, which would have some leading significances for the operation and management of similar projects."

Jan 1, 2008

By Tiejun Chun, Marcus Emrich, Jian Pan, Deqing Zhu, Vinicius Mendes

"Joint projects of studies of hematite acid pellet have been implemented to develop technological solutions for using Vale hematite pellet feed in Chinese palletizing plant. Beneficial improvements on the pellets quality were achieved by adjusting the blends composition and using new technology of pre-treating the blended pellet feed with HPGR (High Pressure Grinding Roller) on rotary kiln pellet technology. The drop strength of green balls increased from 3.4 to 6.0 times from 0.5m height, at the same time, the bentonite dosage decreased from 1.5wt% to 0.7wt%. The compressive strength of roasted pellets reaches 2500 N/pellet. The reduction swelling index of roasted pellets is below 15%.IntroductionWith the fast development of steel industry in China, the production of pellets has been further expanded. Pellets are used as a high quality charge for blast furnace and the annual output is around 80Mt pellets [1]. According to the developmental trend, sinter will be replaced by pellets due to the larger environmental impact of sintering plants when compared to pelletizing plants. For example, the specific CO2 emission in sintering process is around 2.5 times higher than in pelletizing process. However, the steel industry of China has been confronted with a serious shortage of domestic pellet feed due to the low iron grade of Run-of-Mine ore despite of huge reserves of iron ores [2]. Therefore, more pellet feed, mainly hematite, has been imported to make pellets."

Jan 1, 2011

By Ju Shao-hua

Although nowadays gold extraction methods are very abundant, none of them is satisfying, especially, in the field of heap leaching of low grade gold ore. The traditional heap leaching method of cyanide method plays an inglorious role of badly environmental pollution. In this paper, a bran-new and innoxious method of gold extraction system, metal-ammonium-chloride-ammonia (MACA), was proposed, and also analyzed both thermodynamically and practically. Thermodynamically, according to the principles of simultaneous chemical equilibrium and electronic charge neutrality, the thermodynamics of Au-NH4Cl-NH3-H2O system was studied by using the exponential computation method and through MATLAB programming, and the solid figure of its potential - c(NH4Cl) - c(NH4OH) was drawn. The results showed when the concentrate of ammonia is higher than 0.6 mol?L-1, fAu+/Au is only about -0.2 v. Practically, the leaching results of a cuprous gold ore showed that the extraction of gold can reach to 80% in this system. The preliminary results of reduction of the rich solution with copper and zinc powders showed that with deoxygenizing, the reduction effects were relatively good. These new findings and results have established a theoretical and practical base for developing a new process for heap leaching of low grade gold ores in this system. And the new process owns a series of merits such as, non-cyanogens, nontoxic, broader applicability.

Jan 1, 2006

By Jeong-Soo Sohn

Physical treatment and chemical treatment of spent lithium-ion battery were studied in our research team. Especially we developed two types of acidic leaching for crushed powders containing LiCoO2 of spent lithium ion battery. One of them is sulfuric acid leaching with H2O2 as a reducing agent. The leaching rates of cobalt, lithium and the other metals were above 99 % at the condition of 2 M H2SO4, 10 vol. % H2O2, 75 °C, 300 rpm agitation speed, 250 g/5L solid liquid ratio and 75 minutes reaction time. And the other leaching process is the oxalic acid leaching. In this process more than 99% of Li and less than 1% of Co were dissolved at the condition of 3M oxalic acid, 80°C reaction temperature, 300rpm agitation speed, 50g/L initial solid/liquid ratio and 90min extraction time. Each process has its advantage and disadvantage. In sulfuric acid leaching, leaching reagent is very cheap and cobalt could be recovered into cobalt hydroxide. On the other hand, oxalic acid is more expensive than sulfuric acid but lithium could be dissolved selectively. Also cobalt could be recovered into cobalt oxalate and it could be changed into cobalt oxide after heat treatment. In order to select the effective recycling process, recovery rate and purity of cobalt hydroxide and cobalt oxalate were compared and it was investigated which process was more environment-friendly and economical.

Jan 1, 2006

By Yuhua Pan

Generic mathematical models have been developed for simulating heat transfer in two types of slag resistance heating electric furnaces for sulphide smelting: i) six-electrode-in-line rectangular furnaces and ii) three-electrode circular furnaces. The models are based on three-dimensional steady-state heat transfer of conduction, convection and radiation. Solidification of liquid slag into solid slag by water-cooling units, for use as freeze lining of furnace walls, is also considered in the models. The developed models are capable of providing predictions with reasonable accuracy for electric furnaces on 1) temperatures in slag, matte, cooling water, freeze lining and other solid regions as well as temperatures at various fluid/solid interfaces, 2) freeze lining thickness, 3) furnace smelting rate and 4) furnace heat loss rate. These computer models are built into executable application programs that are very efficient, with execution time less than one second, and can be easily portable to most computing platforms. This paper describes, as an example, the modelling results on heat transfer in six-electrode furnaces. The major modelling results show that in six-electrode furnaces uniform electric power inputs to the electrodes likely lead to low temperature regions close to slag and matte tapping ends of the furnaces, and the power input and the formation of air gaps between freeze lining and cooling units have significant influences on the thickness of freeze lining maintained by the cooling units.

Jan 1, 2006

By Tateo Usui

In the course of carbonization of coal under a rising temperature condition, volatile matter (V.M.) is released. The kind and amount of V.M. released depend on the kind of coal. Components of V.M. are tar, hydrocarbons (CH4, C2H4, C2H6, C3H8), CO, CO2 and H2, which are released in this order as a function of carbonization temperature. When the carbonization of coal under a rising temperature condition is interrupted at a certain temperature, TC, max, semi-coal-char with residual V.M. is obtained. If some optimum interruption-temperature is chosen, small but most suitable amount of V.M., namely H2, is retained. When the semi-coal-char thus obtained is heated again under the same rising temperature conditions but up to more than TC, max (1), the residual V.M. is released from just around TC, max (1). We propose novel iron ore agglomerate bearing such semi-coal-char with some strength. While simple iron ore agglomerate bearing coal char will start the reduction reaction as solid-solid reaction at somewhat higher temperature, the proposed one will start the reduction reaction as gas-solid reaction at somewhat lower temperature but a little higher than TC, max. Samples of semi-coal-char and novel iron ore agglomerate bearing such semi-coal-char have been prepared and evaluated.

Jan 1, 2006

By Larry M. Southwick

Pneumatic converting (Bessemerizing) of iron revolutionized the steel industry. Bessemerizing of copper (conversion of copper sulfide matte to copper metal) was proposed at almost the same time, but it was slow in being accepted. The differences between iron and copper converting were great and technical problems were substantial. It took 25 years for the process to become viable and another 25 years before a truly economical solution was found. A major economical and productivity problem was the short life for converter refractory linings. The first converters had acid (silica) linings, which were quickly consumed since silica was a flux for the process. Converters had to be relined at least once per day, a laboriously expensive manual process with only the most rudimentary mechanical aids available to assist. The industry was revolutionized almost overnight when finally a viable basic (magnesite) lining was developed. This lasted 100&apos;s of days versus less than one, leading to converters that were easier to operate and which handled larger charges. This change occurred after W.H. Peirce and E.A.C. Smith, with support from the Guggenheim interests, successfully operated a basic lined converter in a copper refinery in Baltimore. While Peirce and Smith are generally given credit for the development and explosive acceptance of this idea, a Pittsburgh industrialist, Ralph M. Baggaley, working in an independent smelter in Butte, Montana, successfully built and operated a basic lined converter four years before they did. In fact, the early support for Peirce and Smith likely occurred because Guggenheim&apos;s staff were encouraged after thoroughly examining Baggaley on his earlier successes. The questions of technology primacy between Baggaley and Peirce/Smith are ironically similar to those between Wm. Kelly and Bessemer in converting iron to steel. This paper will review what Baggaley (and other early researchers) accomplished, examine why he (or they) did not receive credit equal to Peirce and Smith and explore what his (their) place should be in the development of successful basic linings. More suspects than a Victorian Whodunit.

Jan 1, 1999