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By João Paulo Melo Silva

No beneficiamento de itabiritos pobres (%Fe˜44,0) um dos principais desafios para as usinas de tratamento é a produção de concentrado dentro das especificações de qualidade e com menor custo. Nas usinas de beneficiamento a moagem é a operação unitária com o maior custo. Além disso, a moagem secundária é a operação unitária na qual a granulometria do concentrado é adequada às especificações para a etapa de flotação cleaner e para o transporte em mineroduto. Dessa forma, o aumento da eficiência energética no circuito de remoagem permite reduzir os custos e aumentar a eficiência do circuito de flotação cleaner. Amostragens de rotina e testes de bancada realizados com amostras coletadas no concentrador I indicaram oportunidade de aumentar a eficiência energética (kWh/t) da remoagem e reduzir a granulometria na alimentação da flotação. Com esse objetivo, foram realizadas alterações no circuito de remoagem do pré-concentrado da flotação mecânica do concentrador I da Samarco. Essas alterações consistiram em moer todo o pré-concentrado em circuito fechado reverso e não mais em dois estágios, sendo um em circuito aberto e outro em circuito fechado. Essas alterações realizadas no circuito permitiram aumentar a eficiência energética do circuito de remoagem, reduzir o consumo energético em 9,3% e adequar as granulometria e grau de liberação para a etapa subsequente de flotação.

Aug 16, 2017

By Rodrigo Alberto Moreira Gomes

Para a purificação do níquel laterítico explorado na mina localizada em Niquelândia/GO, pela Votorantim Metais Níquel (VMN), utiliza-se solução amoniacal durante a etapa de lixiviação do minério, seguindo a rota hidrometalúrgica de produção. A amônia é recuperada em torres de destilação por arraste com vapor vivo, para ser reutilizada em um novo ciclo de produção. Este trabalho apresenta a aplicação de uma tecnologia baseada em lógica Fuzzy no conjunto de 6 torres de recuperação de amônia, com o objetivo de controlar as alimentações de solução a ser purificada e de vapor. A plataforma de controle avançado utilizada, Leaf, foi desenvolvida pela I.Systems Automação Industrial, empresa localizada em Campinas/SP, e não necessita da criação de modelos matemáticos fenomenológicos para geração e sintonia dos controladores. Com a automatização da operação das torres, o consumo de vapor da unidade foi reduzido em 3,5% e a intervenção manual foi reduzida.

Sep 25, 2017

By Saulo Brinco Diniz

O presente trabalho buscou explorar a influência de um tratamento térmico de ressolubilização (70 minutos / 510ºC), antes da laminação convencional de uma liga de alumínio 7475-T7351. Para tal, duas amostras (com e sem o tratamento térmico) foram laminadas de 12,5 mm até 3 mm de espessura, após 13 passes com uma redução aproximada de 10% por passe. Com base nos resultados obtidos via microscopia óptica (Olympus, modelo GX51) e dureza Vickers (durômetro EMCOTEST, modelo Duravision 300), conclui-se que o tratamento térmico de ressolubilização adotado antes da laminação convencional da liga em estudo, propiciou modificações microestruturais e incremento na dureza quando comparada a amostra laminada sem prévio tratamento térmico de ressolubilização.

Aug 17, 2017

By Carl Heinrich

I HAVE read with particular interest that portion of the discussion by Anton Eilers referring to the high-lime (and also high-alumina) slags made by August Raht in 1881, while smelting the Horn Silver ores at Franklin, Utah. The two analyses of such slags, furnished by Mr. Raht to Mr. Eilers are: Horn Silver Slags Oxygen(b) Oxygen(b) Average of I and. II Slag I percentage Slag II percentage Oxygen Si02 33.9 18.1 .35.0 18.7 34.50 18.40 FeO 26.8 6.0 25.4 5.7 26.10 5.80 CaO 26.1 7.5 24.9 7.1 25.50 7.30 BaO 3.2 (a) 0.3 3.2 0.3 3.20 0.30 A1203 10.8 5.1 9.3 4.4. 10.05 4.75 100.8 37.0 97.8 36.2

Jan 10, 1916

By Gustavo dos Santos Guimarães

Na Linha Leve da Laminação da Usina ArcelorMittal Cariacica o cintamento dos feixes de barras e perfis leves era feito manualmente através de cintadeiras pneumáticas envolvendo 8 operadores e representando um gargalo nos feixes mais leves de 1,0 e 1,5 t. Com a finalidade de eliminar o gargalo de produção e redução de mão de obra braçal foram implantadas 3 cintadeiras automáticas no trecho entre o empilhador de barras e o sistema de pesagem e etiquetagem.

Aug 16, 2017

By Dhyemila de Paula Mantovani

Hoje em dia, a necessidade de utilizar materiais ecologicamente corretos tem aumentando em paralelo com a constante busca de novas tecnologias para produzir materiais renováveis, economicamente viáveis e tecnologicamente avançados, o que justifica esse trabalho. O presente trabalho consiste em estudar o comportamento mecânico de compósitos de matriz poliéster reforçados com fibras de cânhamo e testadas com impacto Izod. Para a realização deste teste, foram feitas amostras com dimensões de 10 mm de largura, 63 mm de comprimento e 12,7 mm de espessura em diferentes frações volumétricas de fibra, 0%, 10%, 20% e 30%. As amostras foram testadas em um conjunto pendular PANTEC na configuração Izod, modelo XC-50 localizado no LAMAV/UENF. A energia de impacto Izod dos compósitos de poliéster de 30% de fibras de cânhamo foi de 169,4 J/m.

Oct 30, 2017

By Marcos Velho Ludolf

O projeto de Substituição dos Controladores Lógicos Programáveis da Sinterização tem como objetivo a substituição dos PLCs da Família S5 (Siemens) já obsoletos por novos PLCs de tecnologia atual. O projeto de substituição foi dividido em etapas, sendo que a primeira etapa ocorreu em 2012. Consequentemente, teremos novos e antigos PLCs na mesma plataforma de controle até o fim do projeto. Os maiores desafios foram fazer toda a migração e adaptação de hardware e software dos novos PLCs ao restante da planta adequando-se aos sistemas existentes tais como PIMS, comunicação com o Nível 2, comunicação com balanças já obsoletas, SCADA, outros PLCs e concluir toda a migração da primeira etapa do projeto em apenas 60 dias compreendendo desde a desmontagem do sistema anterior, montagem dos painéis novos, recomissionar todo o I/O substituído, conciliar todos os testes à frio e parciais com demais serviços de manutenção programados e realizar o comissionamento a quente de toda a sequência da planta nos últimos 04 dias de implantação, quando todas as linhas de operação foram liberadas para testes. Em 2014 foi iniciada uma segunda etapa, e um PLC de 600 pontos de I/O já foi substituído em apenas 80 h usando uma nova estratégia.

Jul 30, 2018

By Gyeonghye Moon, Inhyeok Choi, Jyothi Rajesh Kumar, Jin-Young Lee

"This paper deals with the recovery of the tungsten and vanadium from spent SCR catalyst leach liquors by different hydrometallurgical methods. The first part consists of pressure leaching of spent SCR catalyst using caustic soda followed by metal recovery by liquid-liquid extraction. In a leaching process, the following experimental parameters were tested and optimized: NaOH, particle size of feedstock, temperature, and solid to liquid ratio. The optimum condition for leaching of tungsten and vanadium was under the following conditions: NaOH 3 mol/L, temperature 250°C, particle size <300 µm, and solid to liquid ratio 0.4. From these optimum conditions in this experiment, the dissolution efficiency of vanadium and tungsten was 91.5and 87%, respectively. Liquid-liquid extraction following commercial extractants were tested: TBP, Cyanex 272, D2EHPA, Aliquat 336, Primeme JM-T, Alamine 308, Alamine 304-1, and methyl-tri-octyl-ammonium chloride. The conditions for both valuable metal recoveries were optimized.INTRODUCTIONSelective Catalytic Reduction (SCR) catalyst has become the most effective to reduce nitrogen oxide (NOx) emissions from stationary segments such as power plants and waste incinerations around the world due to the reinforcing regulatory trend and emerging environmental issues (Forzatti, 2001; Spivey, 2002; Li et al., 2011).Currently, the most widely used SCR catalyst is V2O5-WO3/TiO2 system due to its great catalytic properties (Li et al., 2011; Marshneva et al., 1995; Marbergeret al., 2015). In general, the composition of the SCR catalyst used in the stationary application is 0.5 to 1 wt% of V2O5and 7 to 10 wt% of WO3(Marberger et al., 2015; Chen &Yang, 1992, Vuurman et al., 1991; Alemany et al., 1991). Currently spent SCR catalysts are treated as waste and disposed of in landfills. This causes a lot of waste of secondary resources of vanadium and tungsten. In terms of industrial value of vanadium and tungsten (Gupta &Mukherjee, 1990; Moskalyk &Alfantazi, 2003) and reduction of pollutant emissions, it should not be disregarded for their recovery for their material recycling from spent SCR catalyst. However, investigations for recovery of metal values from spent SCR catalyst has been rarely carried out."

Jan 1, 2017

Domestic: Middle West-,11.. B. Newcombe Eastern District-J. French Robinson1 Kansas-Henry A. Ley 2 Oklahoma-Henry A. Ley 3 Texas, except Gulf Coast and Panhandle-M. G. Cheney 5 Texas Panhandle-W. E. Hubbard and H. E. Crum 6 Gulf Coast-L. P. Teas 7 South Arkansas, North Louisiana and Mississippi-H. K. Shearer 8 Foreign Mexico-V. R. Garfias and C. 0. Isakson 9 Canada-Line M. Farish 10 Venezuela-C. W. Hamilton 10 Colombia-J. T. Duce 12 Peru-O. B. Hopkins 12 Trindad-Williaim J. Millard 13 Dutch East Indies-Fred B. Ely 13 Rumania-I. I. Gardescu . .. . 14 India-Eric J. Bradshaw 14

Jan 1, 1931

By A. T. GRIFFIS, R. J. GRIFFIS

A large magnesite-talc body is locared in Delora Township, 11 km sourh-southeasr of Timmins, Onrario. The deposit occurs in part of an Archean greensrone belt dominated by volcanic and sedimenrary rocks and large bodies of ultramafic intrusions. The magnesite-talc zane is abour 1800 m long, has a maximum width of 300 m and has been drilled ro 120 m below surface. Chemical analyses of rhe main carbonate zane average 20 ro 28% soluble MgO (magnesia), 5 ro 6% rota/ iron oxide and less rhan 0.1 % CaO (lime). Mineralogically, the zane consists of approximately 54% magnesite, 28% rate, /5% quartz and 3% hematire. Perrographic srudies suggest that rhe various assemblages of magnesite, rate, quartz and serpentine were derived from a parenr serpenrinire (after dunire). An early carbonitization stage, which produced a high-magnesite, low-talc assemblage, preceded a farer decarbonitizarion stage, which formed rhe main magnesite-talc assemblage. Despite a favourably low calcium oxide content of rhe magnesite-talc rock, considerable iron in the magnesire /at rice has limited the quality of the beneficiared product: rhe besr flotation concentrate to dare yields 92 to 94% dead-burned MgO. Experimen- I L t r i i c:~:.•-4- -------- ? -_;> ,•----1---- ta/ work continues on finding a process whereby high-purity magnesia can be produced on a commercial scale.

Jan 1, 1984

By A. C. Halferdahl

The Granby ores may be divided into three groups or classes. The No. I ore is a heavy pyrite, chalcopyrite, pyrrhotite, sulphide carrying some free silica, and calcite. No. 2 ore carries the same general group of sulphides as does No. 1, but in a lesser amount. The gangue is an altered greenstone. No. 3 ore has a smaller amount of sulphides than either of the others. Analyses of these ores is as follows: Cu. Si02 Fe. CaO S. Al 203 MgO No. I. Per Cent. 1.8 17.5 33.0 5.7 34.5 2.3 1.3 No. 2 Per cent. 2. 0 35. 6 23. 9 4. 3 I .5. 0 9. 2 6 .. 0 No. 3, Per cent. 1 . 5 40. 9 21 . 7 3. 0 I 1 . 3 11 . 0 5 . 4 The sulphide minerals in No. 2 and No. 3 ores occur largely in bands in the gangue, and for these portions comparatively coarse grinding serves to release the gangue. Drill cores show a certain dissemination of sulphides in portions of the rock, so that grinding to 5 per cent. + 65 mesh with 65 per cent.-200 mesh liberates the sulphide minerals very completely. The association of the sulphides is fundamental. The pyrite was probably deposited first and was followed by a portion of the chalcopyrite, or these two portions of the sulphide minerals were deposited together.

Jan 1, 1924

By Carl Henrich

I have read with particular interest that portion of the discussion by Anton Eilers referring to the high-lime (and also high-alumina) slags made by August Raht in 1881, while smelting the Horn Silver ores at Franklin, Utah. The two analyses of such slags, furnished by Mr. Raht to Mr. Eilers are: (a) Not determined in this analysis. (b) Not given in Mr. Eilers&apos; paper. Oxygen ratio, A1 as base. I. 0 in acid: O in base:: 18.1:18.9:: 0.96:1 11. 0 in acid :O in base:: 18.7:17.5::1.06:1 Average: 18.4:18.15=1.01:l Oxygen ratio, AI as acid. I. O in acid: O in base: :23.2:13.8:: 1.68:1 11. O in acid: O in base::23.1:13.5:: 1.76:1 Average: 23.15:13.4 = 1.73:l By assigning to alumina the the of a base, Mr. Eilers deduces the formula 3Feo.-2SiOa + 4Cao.2SiO². The nearest approach to a simple formula expressing the average composition of these slags, which I can figure, is 9RO.Al2O3.6SiO2. Allowing a ratio of 4Feo : 5Cao, we have for this formula:

Jan 1, 1917

[nnuu,uIII) 111 thst?r5 Arr ~IYts, It ur t to 1rllliis% IbkI a:kNIII&apos; ti;Yrst k,aI t.LIIIIISC With :$&apos; ILIIIH111, ,Ir dclrlwns n,,ls Ix? nrit?~,s,il l, I&apos;¬ PC ,Irl;411ntI ,,rii iii Iklici ?I Lc y,ci,ri.al nullkII( kti :,s l,rl}?WS tiuouu,arS Ikkrluat Slrkktrkrrr Hackt,kuurul Sirr atstl { 3rr?.nLi:.,kinn ( I&apos;r,I]A]lhli l)kslrklklktl,ln I)l&apos;I1tiiriull,- [irutISl]rr ilir.tttt~n l .ti and V4-?ltl I rc 1ut l, t;~ k?&apos;.LILI,!,srslk+a, Mid OVA-1 101MIL11k t`llllkklt: I&apos;ru, ? ?inu Pn,rlnr&apos;r, 1nr 1 k ulr ,111,1 It1(Il1<Irl&apos; C:urrrnl Rt ir.,rrl, mtI AAIililit:,kir,II.]

Jan 1, 1985

By Virgil Miller, F. B. Petermann, S. F. Ravitz

The Cle Elum nickeliferous iron deposit is in Kittitas County, Washington, in a rugged, mountainous region about 23 miles north of the town of Cle Elum. The Biewett Pass deposit, which is similar in character and occurrence, is in Chelan County, about 18 miles east of the Cle Elum deposit. A more or less continuous ore zone may extend between the two deposits, since iron ore is reported to have been discovered at Iron Mountain, which lies directly between them. The ore probably was formed by meta-morphism of laterite resulting from Ieach-ing of serpentine derived from peridotite. It consists largely of magnetite grains distributed through a matrix of limonitic material containing a small amount of hematite and chromite. Many of the chromite grains have shells and inclusions of magnetite. The magnetite grains range in size from 1200-mesh to 1/4-in., the average size being 48 to 65-mesh; the chromite grains range from 20 to 150-mesh. The gangue minerals are olivine and serpentine with a small, amount of chlorite, and appear both as very thin bands in the ore and &apos;s minute fragments in the limonitic matrix. The nickel is present as minUte inclusions of a nickel silicate mineral within the magnetite and gangue par- ticles, varying in size from 1500 to about 280-mesh. Detailed analyses of 3000-lb. lots of Cle Elum and Blewett Pass ore are given in Table I. TABLE i.—Analyses of Ore Samples Per Cent Ore from Constituent cle Elum&apos; Blewett Pass Cr....................... 2.23 2-12 Ni...................... 1.43 0.9s Fe...................... 52.9 41.4 SiOz.................... 5.6 13.4 CaO.................... 0.3 0.8 MgO................... 4-1 7-5 AI2O3................... 7.0 2.g P...................... 0.022 0.034 S....................... O.O1 o.oa Mn..................... I.I 0.4 Ba..................... nil co..................... o.oa 0.02 CU..................... 0.02 0.03 As...................... 0.03 Au..................... nil Ag°..................... O.58 Pt...................... ml Fe++.................... 8.9 5-9 Fe+++.................. 44-0 35-5 « Ounces per ton, 1 sr,cte,so,","&&$ally absent: B, W, M~, T~, V, ~i, Bi, Pb. Sb. Sn. Be, In, Hg. Zn, Zr. Cd. Preliminary Tests Attempts to beneficiate the ore by ore-dressing methods, including various &apos;cornbinations of sink and float, tabling, jigging, flotation, and magnetic separation, were consistently unsuccessful. A wide variety of roasting and leaching tests were made on both raw and reduced ore, but in most of the tests little or no nickel was extracted, and in none did the extraction exceed 50 Per cent. No nickel could be volatilized as the carbonyl. by treating reduced ore with carbon monoxide. Fairly good sepa-

Jan 1, 1944

By Ting Lu, Gerard Laman

"This document compares the systems of coal classification described under ASTM standards used in Canada to GB standards used in China. A preliminary connection of metallurgical coal classes was set up between the two classifications. In GB classification system, there are nine metallurgical coal groups, namely PS, SM, JM, FM, ½ ZN, RN, 1/3 JM, and QM used in coal blending for coke production. PS coal is almost equivalent to the Low Volatile Bituminous coal; SM, JM, and FM coal groups fall into Low to Medium Volatile Bituminous range; ½ ZN, RN, 1/3 JM, and QM are equivalent to bituminous coal with medium to high volatile matters; QF contains higher volatile bituminous coal compared with High Volatile Bituminous coal. The caking properties commonly used in respective country are also compared in this document. These properties include free swelling index (FSI) and maximum fluidity used in Canada, as well as caking index (GR.I.), and the maximum plastic layer thickness (Y) mainly employed in China. It has been observed that the log of the maximum fluidity has a stronger correlation with the caking index than the Y values. Metallurgical coal processing strategy and typical coking coal product qualities are briefly discussed in the last section of this paper. Currently there is a trend to use heavy medium cyclone in both countries. In Canada the conventional two-product cyclone technology is the preferred practice; whereas in China the three-product heavy medium cyclone arrangement is widely used.INTRODUCTION Coal can be simply classified by applications into two categories: i) thermal coal used to provide heat energy in combustion, and ii) metallurgical coal which is converted to coke, in a carbonization process, and used mainly in the iron and steel industry. Metallurgical coal contains even higher heating values than thermal coal. In addition, it presents unique plastic properties during carbonization which in turn produces a porous solid, high in carbon referred to as coke. Coke is one of the most important raw materials in the iron and steel industry."

Jan 1, 2012

J. E. JOHNSON, JR., New York, N. Y. (communication to the Secretary*).-The discussion of Mr. Henrich&apos;s paper took place at a meeting from which I had the misfortune to be absent, and has just come to my attention. I do not wish to let the subject pass without contributing to it a little information which has come into my possession. In 1912, I published a brief note in the Transactions on The Effect of Alumina in Blast-Furnace Slags, giving in tabular form three typical slags used in iron blast-furnace practice, one of them the high alumina slag of, which Professor Richards speaks. That table is reproduced herewith. TABLE 1.-Composition of Slays. 1 3 3 4 5 6 7 CaO by Neutral Ratio Ratio Ratio Al2z03, SiO2, Differ- Substan- Cat Ca0 a A1203 Ratio Per Per ence, ces, CaO Cent. Cent. Per Per Al2O3 + Sioz Sit: SiO2 Cecil_ Cent. Virginia practice 6.5 36.0 54.0 3.5 1.27 1.6S 1.50 Lake-ore practice 13.5 33.0 50.0 3.5 1.08 1.92 1.51 Special experiment... 36.0 24.7 36.8 3.5 0.59 2.90 1.44 It supplies what seems to me convincing evidence that, for the purposes of the iron blast furnace, alumina can be regarded only as a neutral substance, dissolving in the slag and materially altering its viscosity, but not affecting its chemical activity. In subsequent experience with charcoal furnaces, I found the same rule to hold; that the chemical effect of alumina could be disregarded, providing the ratio of the lime and magnesia to the silica were kept constant. This is exactly the experience which Messrs. Dwight and Mathewson had in copper- and&apos; lead-smelting furnaces. I have never seen any evidence or argument adequate to support the contention of Professor Richards-that the alumina acted as a base in the charcoal iron furnace and as an acid in the coke furnace, and that the function of alumina in iron-furnace slags is inherently different from that in copper- and lead-furnace slags-and I am compelled to differ absolutely with his conclusions in that respect.

Jan 9, 1917

By Jheison Lopes dos Santos

Neste trabalho, pela primeira vez, o sistema cerâmico Al2O3-Nb2O5-LiF teve suas propriedades mecânicas investigadas. Foram investigadas diferentes composições, em peso, para o composto (Al2O3–4%Nb2O5)–nLiF, com n variando entre 0 e 1,50%, a três temperaturas de sinterização diferentes (1300, 1350 e 1400 ºC). Como caracterização mecânica, avaliou-se a microdureza Vickers para todas as composições. A adição de LiF que apresentou os maiores valores de densificação teve seus módulos de Young e de cisalhamento, e as velocidades de ondas elásticas determinadas. Os resultados mostraram que todas as adições de LiF elevaram a microdureza do composto Al2O3–4%Nb2O5. Este fato pode estar relacionado com a densificação e fases obtidas após a sinterização. A adição de 0,5% de LiF ao composto cerâmico Al2O3-4% Nb2O5, promovendo maior densificação, quando sinterizado a 1300 ºC obteve valores de propriedades elásticas comparáveis aos obtidos por Al2O3–4%Nb2O5 sem LiF, sinterizado a 1400 ºC. Os resultados relevaram ainda uma coerente correlação entre dureza, módulo de elasticidade e densificação. Dessa forma, a adição de fluoreto de lítio ao sistema cerâmico alumina-nióbia possibilitou a redução em pelo menos 100 ºC na temperatura de sinterização, com propriedades mecânicas comparáveis.

Oct 30, 2017

By Arthur F. Taggart

THIS paper proposes two units (believed to be new) for designating, respectively, capacity and efficiency for primary and intermediate crushers. CAPACITY Operators know that the tonnage of rock that can be put through a particular crusher in a given time depends primarily upon the crusher setting (open setting for jaw and primary gyratory types; closed setting for cones and rolls), and secondarily on the lithological character of the feed, its maximum size, the amount of fines that it carries, its moisture content, and the method of feeding. The proposed capacity formula states a relationship between all of these factors in one empirical equation, as follows: TR = TR80KK&apos;K" [I] in which TR, called "reduction tons per hour" is the new capacity unit; T = tons of feed per hour requiring crushing; R50 = "80-per cent reduction ratio"; and K, K&apos;, and K" are constants that approximate quantitatively lithological character, moisture content and method of feeding, respectively. T is the hourly weight of material in the feed that is coarser than the coarsest discharge of the crusher. (For marked departures from the normal specific-gravity range-2.5 to 2.7-T should be adjusted to corresponding volumes.) In the crushers under consideration, discharge from the crushing zone is limited by the minimum dimension of a particle. Passage of the particle through a square-mesh screen is limited by its intermediate dimension. Sheppard&apos; has shown that the ratio of maximum: intermediate: minimum average dimensions of broken rock fragments may be taken as about I.5: I: 0.6 for nonslabby rocks such as are normally crushed, while for slabby rocks, such as thin-bedded sedimentaries, foliated schists and gneisses, and the blocky metamorphics, the ratio is of the average order I.3:I:0.3, with the possibility of an even smaller relative value for the thickness. Gaudin2 finds the corresponding ratio for -150 + 200-mesh pyrite to be I.4: I : 0.6. The hourly tonnage of crusher-plant feed, therefore, should be diminished by the amount thereof that would pass a square-mesh screen of which the aperture is S times the crusher setting, where S is a shape factor with the value I.7 for rocks that break exceptionally cubic; 2 for ores and rocks that exhibit no appreciable tendency to slabbiness; and 2.5 to 3, or, in exceptional cases, even larger, when the tendency to slabbiness is marked. R80 is the quotient of the theoretical square-mesh aperture that would pass 8o per cent of the feed, divided by the aperture that would pass S0 per cent of the product. It is best determined from screen tests.

Jan 1, 1941

By Pei-Yung Huang, Carle R. Hayward

IN order to understand more fully the actual state of copper lost in copper reverberatory slags, a systematic study on the various reactions between certain metallurgically important copper compounds and synthetic copper reverberatory slags was undertaken by the authors in the Massachusetts Institute of Technology from 1942 to 1945.1 This paper, being only a part of the work completed, is published first because it furnishes the first experimental evidence of the formation of copper ferrite from reactions between cuprous oxide and copper reverberatory slags. CHOICE OF SLAG COMPOSITION The choice of the composition of the synthetic reverberatory slags to be used was much deliberated. Commercial copper reverberatory slags, neglecting minor constituents, average:2.3 45 to 47 pct FeO; 38 to 42 pct Si02; 5 to 6 pct CaO; 5 to 6 pct A1203. Since the ternary system CaO-FeO-SiO2 has been much more thoroughly studied4 and is much simpler than the quaternary system CaO-FeO-Si02-A1203, it was decided to use calcium oxide only instead of calcium oxide and alumina in the synthesis of the slags. Fortunately the composition of the average copper reverberatory slag with calcium oxide substituted for alumina lies in the region of the phase diagram clarified by the investigators. A survey of the phase diagram (Fig I) suggested two compositions: (I) the com¬position near the invariant point S, which is made up of 46 pct ferrous oxide, 37 pct silica and 17 pct calcium oxide; (2) the composition near the invariant point K with 45.5 pct ferrous oxide, 43 pct silica and 11.5 pct calcium oxide. Composition S has the advantage that the percentages of ferrous oxide and of silica almost exactly coincide with those of the average reverberatory slags, and that of the lowest melting point (1093° ± 3°C) in the whole ternary system. The calcium oxide content, however, obviously is high. Since we have already substituted calcium oxide for alumina, and since calcium oxide is more basic than alumina, the resulting slag is decidedly too basic. Composition K has a slightly higher melting point (1105° ± 3°C) and a higher silica content, but this is preferred because the slag is saturated with respect to tridymite and thus should not corrode siliceous refractories. Besides, it is less basic than composition S. The final slag composition, therefore, was chosen to

Jan 1, 1947

By J. Koster

[In lQ jG thc E&apos;lcct,ro:~(: L7.l :~u..-ic:ll S;%cti ?n of t?c :I. tcIl~tr,-;lcal 3:vi cioa, ?U~CE~U of lv!irtos, bc,~m an 9.ct iv.t In-:?*t ik7;5i GI of r.:ct.l-;c?;is for rccovcrin,; niclrel, cop?ir, an2 ?? cciou:; ~ot-1 c 1;-on or; :; of tile 3unl~crvi~.l~~ tiistrict in C1ni.k Coult:r, !Icl.r. ]

Jan 1, 1939