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By Nicholas J. Grant, Chih-Chung Wang

TO phase of the Ti-0 system has the structure of NaCl and has a wide range of solid solubility.' In the course of studying the Ti-Cr-0 ternary system, binary alloys were made of iodide titanium and high purity TiO,. It was found from X-ray studies of the binary alloys that a transformation of the TiO appears to take place at a temperature near 925°C. Evidence of this phase change is best seen in Fig. 1. Fig. 1A shows the X-ray spectrometer pattern (CUKa radiation) of an alloy of 25 wt pct 0 corresponding to the stoichiometric composition of TiO.

Jan 1, 1957

By R. S. Dean

AMONG naturally occurring inorganic compounds, magnetite has many unusual and interesting properties, and it is the purpose of this paper to call attention to these properties and review possible uses of magnetite that might be based on them; in other words, to see what uses may be found for magnetite as a physical rather than as a chemical entity, as a mineral rather than as an iron ore. The Mineral Physics Studies initiated in the Metallurgical Division of the U. S. Bureau of Mines a few years ago gathered together much information on mineral properties, and they are therefore the principal source of material for this paper.

Jan 1, 1937

By J. D. Forrester, Erich Sarapuu, T. C. Cheasley

RANKING high in the nation's wealth of natural resources, readily available liquid and gaseous hydrocarbons are nevertheless falling steadily in supply, while industrial requirements for hydro- carbon compounds are greater today than during the peak period of World War II. Theoretically, several processes will increase the future supply of liquid and gaseous fuels, but the practical application of these methods depends on two controlling factors: 1-that enough carbon- bearing material be available to warrant industrial exploitation, and 2-that the given process be physically, chemically, and economically applicable. With regard to the first factor, the Western Hemisphere is fortunately well supplied, see Table I.

Jan 9, 1954

D. C. JACKLING, the father of the porphyry coppers, has been honored for his pioneering in that field. There is another facet to Mr. Jackling's activities, one which now may prove an even greater monument than the big coppers-the story of his venture in taconite beneficiation. The essence of his porphyry development was mass handling of material. Not alone mining on a large scale, which was done on the Mesabi Range at the turn of the century, but the integration on a previously unknown scope of mining, milling, concentration, and in many cases, of final reduction to metal at the site. This was mass production applied to mining, treatment of a very low grade source material, previously considered submarginal.

Jan 1, 1954

By M. H. Gidel, D. C. Bard

These notes are based on the megascopic study of a suite of 2,400 specimens of minerals and ores from the Butte mines, combined with field observations at intervals over a period of several years. The estimate of average vein composition is based on field acquaintance with the veins. It is probably correct in its broader proportions, and should be of use for comparison. Chemical and Mineral Composition of Unoxidized Vein Matter. Per Cent. Oxygen,......48.00—Quartz, rhodonite, rhodochrosite, sericite, kaolinite, barite, calcite, and hübnerite. Silicon,...... 36.O0—Quartz, rhodonite, sericite, kaolinite, and willemite (very rare). Sulphur,.....5.0—Sulphides of iron, zinc, copper, lead, and sulphates of barium and rarely calcium. Iron,.......5.00—Ferric sulphides (pyrite, bornite, chalcopyrite), also in sphalerite, tetrahedrite, and rarely hematite and siderite. Manganese,.... 2.00—Rhodonite, rhodochrosite, and hübnerite. Zinc,.......1.00—Sphalerite, very rare wurtzite and willemite, and tetrahedrite and tennantite. Carbon,......0.50—Rhodochrosite and calcite. Capper,......0.75—Cuprous ( + ) and cupric (—) sulphides. Aluminum,.... 0.50—Sericite and kaolinite. Hydrogen,.... 0.50—Water, sericite, and kaolinite. Potassium,.....0.20—hicite. Lead,....... 0.20—Galena. Arsenic,......0.10—Tennantite and enargite. Barium,......0.10—Barite. Calcium,.....0.10—Fluorite, calcite, and rare gypsum. Antimony,.... 0.02—Tetrahedrite, famatinite, and silver sulphantimonites. Fluorine,.....0.05—Fluorite. Silver,.....1 —Argentite, and sulphantimonites. Tungsten,.... —Hübnerite. Phosphorus, • —Wavellite. Bismuth,' .... 0.05—Sulphide (?) Tellurium,... 1 —Telluride (?) Selenium,.... —Selenide (?) Cadmium,.... —Sulphide (?) Gold,..... —Native and telluride (?)

Jan 1, 1914

In opening the meeting I wish to express my greatest pleasure at being able to greet this joint session of the Mining and Electrical Engineers. As engineering develops, we find that the border lines between the different branches of engineering become more and more indistinct; the several fields overlap so much that they are three or four layers deep in places. It is only an accident that we couldn't have had the Mechanical Engineers also as a formal part of this gathering, because they are quite as much interested in this subject as the Electrical or Mining Engineers. A little history may enlighten some of those who have not been close to this work. A year ago last summer, there was brought to the attention

Jan 4, 1919

By Norman Hedley, Howard Tabachnick

The extraction of gold and silver from ores with alkaline cyanide solutions is well known. Cyanide solutions are also good solvents for many base metal minerals, particularly most of the copper minerals. Leaver and Woolf, who determined the solubilities of copper minerals in 0.10 pct sodium cyanide solution, showed that malachite, cuprite, chalcocite, and bornite are readily soluble in cyanide; least soluble are chalcopyrite and chrysocolla. The Mining Chemicals Laboratory of American Cyanamid Co. has studied the possibilities of using cyanide solutions for leaching base metals. In this article the authors present the results of their experiments with cyanide leaching to reduce the copper content of a zinc concentrate from 0.050 pct to the desired specification of less than 0.02 pct.

Jan 2, 1960

J. M. TIPPETT? Colorado Springs, Co1o.-There are several points which offer ground for discussion, although the authors' indicated results leave small chance for argument. Under classification of the ores as they come to the mill, it will be noted that these are classified according to their lime contents. In previous years the classification was based upon sulfur contents, CaO not being considered; class A would be called the oxidized ore and class B the sulfides. Classification according to CaO is the first public indication that a decided change in the ore has necessitated improved methods of treatment. The very serious effect that CaO, even in small quantities, has upon extraction has been noted for some years.

Jan 11, 1918

By Lawrence W. Teufel

An anelastic strain recovery technique is presented as a method of determining the directions and ratio of the maximum and minimum horizontal in-situ stresses from oriented cores from deep wells. Predictions of hydraulic fracture azimuth inferred from principal stress directions determined from both elastic and time-dependent (anelastic) strain relaxation measurements of volcanic tuff are consistent with the observed orientations of hydraulic fractures produced in simulation and mineback experiments, underground at the Nevada Test Site. In addition, anelastic strain recovery measurements on oriented cores of shale and sandstone from well depths of about 1680 meters show consistent relaxation directions of the principal horizontal strains and have enabled a prediction of the principal horizontal stress directions and hydraulic fracture azimuth.

Jan 1, 1982

By William E. Ford, Edward Salisbury Dana

The Niobates (Columbates) and Tantalates are chiefly salts of metaniobic and metatantalic acid, RNb2O6 and RTa2O6; also in part Pyroniobates, R2Nb2O7, etc. Titanium is prominent in a number of the species, which are hence intermediate between the niobates and titanates. Niobium and tanta¬lum also enter into the composition of a few rare silicates, as wöhlerite, låvenite, etc. The following groups may be mentioned: The isometric PYROCHLORE GROUP, including pyrochlore, microlite, etc. The tetragonal FERGUSONITE Group, including fergusonite and sipylite. The orthorhombic COLUMBITE Group, including columbite and tantalite. Also the orthorhombic SAMARSKITE GROUP, including yttrotantalite, samarskite, and ånnerodite. The species belonging in this class are for the most part rare, and are hence but briefly described.

Jan 1, 1922

By R. V. Ramani, C. J. Bise

The potential of deep-mineable coal reserves in the western United States for meeting future energy needs has been recognized for quite some time. However, two of the major constraints tending to limit the development of these underground reserves are the great thicknesses of the coal seams encountered and their high pitch. Although new mining methods may need to be developed to recover these reserves, at least in the short-term the industry has to incorporate presently available equipment not originally designed for thick-seam mining. The purpose of this paper is to present an analysis of the various equipment in use today and their possible application to thick-seam mining. The paper also addresses various ground control and safety considerations unique to thick-seam extraction.

Jan 1, 1984

By Cyril Smith

FOR several years an investigation has been in progress in the research laboratory of The American Brass Co. to determine the thermal and electrical conductivities of most copper alloys of commercial importance and several of scientific interest. This paper contains such data on the binary alloys of copper with silicon, aluminum, manganese and nickel, and on a large number of ternary or more complex alloys. Some inter-esting general relationships between the thermal and electrical conductivi-ties for all copper alloys at all temperatures are pointed out. The data for the copper-zinc, copper-phosphorus and copper-tin binary systems have already been published1,2 ? except for the electrical conductivity at 200° C., which is given in the appendix of this paper.

Jan 1, 1935

By G. A. Hellstrand

IN 1915, H. A. Guess, Vice President of American Smelting & Refining Co., in charge of its Mining Department, learned that the Anglo-New-foundland Development Co., Ltd., a pulpwood and paper-mill enterprise, had found upon its large concession in Newfoundland, and had opened up by shaft to the third level and some drifting, a lenticular orebody indicat-ing about 100,000 tons, as an extremely fine-grained sulfide ore, averaging about 0.05 oz. Au, 4 oz. Ag, 1.5 per cent Cu, 10 per cent Pb, 18 per cent Zn; and that having sent parcels of this ore to Minerals Separation, Ltd., and various other metallurgical testing concerns without obtaining any success in commercial separations thereon, had discontinued work thereon and let the workings fill. Mr. Guess wrote to the general manager of that company and obtained a few hundred pounds of the typical ore, which he sent to his company's metallurgical testing laboratory at Flat River, Mo., outlining various flotation tests desired thereon, in an endeavor to obtain separation into a commercial lead concentrate and a zinc concentrate. But the art of flotation had not then progressed far enough to treat such ore, the galena and zinc blende being so fine grained that grinding to about 300 mesh was required to release the mineral particles in their gangue. Mr. Guess had flotation and other tests continued upon this ore from time to time with whatever new reagents and flotation devices were evolved as time went on, and finally, in 1925, he succeeded in effecting in his company's testing plant, then at Wallace, Idaho, separations into lead concentrates and zinc concentrates of satisfactory commercial grade. Mr. Guess then proceeded to unwater, examine and sample the property and made with the owners a partnership operating agreement upon the mine itself and a considerable area surrounding it, and in the early summer of 1926 began to prospect for additional orebodies, utilizing for such prospecting geophysical methods, under the direction of Hans Lundberg, methods which up to that time had been little used in mining in the western hemisphere.. This geophysical work found two large flat-lying orebodies of a type precisely similar to the smaller body of the original discovery. The larger orebody, some 3500 ft. west of the original

Jan 1, 1934

By C. A. Stewart

PAGE. I. Introduction............ 241 II. Location. TopoGRaphy. and History....... 243 III. DescRiption of the Rocks......... 245 1. Altered Sediments.......... 245 2. Alaskite........... 246 3. Alaskite.Porphyry.....255 4. Quartz Dikes........... 257 5. Biotite.Granite.......... 256 6. Quartz.Porphyryl......... 260 7. Andesite........... 262 8. Miscellaneous Dikes......... 263 IV. Age oF the Rocks and Comparison with other Localities.. 263 V. AlteRation............ 265 1. Sericitization........... 265 2. Silicification........... 266 VI. StRuctuRes........267 1. Dip of the Limestone......... 267 2. Faulting........... 267 VII. Contact - metamorhism,.......... 269 1. Endomorphism.......... 269 2. Exomorphism......... 271 Recrystallization and Loss of Color...... 271 New ,Minerals.......... 272 Addition of Material........ 274 Volume.Changes.... 276 Locus of Metamorhism........ 277 Method of Precipitation.........278 VIII. ORe-Deposits............ 278 1. Contact-Metamorphic Copper.Ores,..... 279 General..........279 Shape and Distribution........ 279 Minerals........... 281 Secondary Enrichment........ 282 2. Disseminated Copper.Ores........ 283 3. Origin of the Copper.Orcs........ 284 4. Lead-Silver Ores.......... 287 IX. Bibliography............ 288

Jan 1, 1913

By Jasper Johnson

Taken in all its bearings there is, perhaps, no more interesting coal-field than that locally known and designated as " Wilmington," both on account of the superior qualities of its product as a household and steam fuel, when compared with other Illinois coal, and its geological position. The territory underlaid with coal, to which this name was originally given, embraced a very small area, including only the south half of sections 31 and 32 (township 33 north, range 9 east) in Wilmington township, and sections 5, 6, 7, 8, 17, 18, 19, 30, and 31, with occasional outliers in sections 3, 4, and 9, and, possibly, in sections 20, 28, 29, 30, and 32 (township 32 north, range 9 east) of Reed township, in Will County, comprising eleven square miles of workable coal within the known basin. Borings indicate the presence of coal on sections 30 and 33 in Wilmington

By Jasper Johnson

TAKEN in all its bearings there is, perhaps, no more interesting coal-field than that locally known and designated as " Wilmington," both on account of the superior qualities of its product as a house- hold and steam fuel, when compared with other Illinois coal, and its geological position. The territory underlaid with coal, to which this name was originally given, embraced a very small area, including only the south half of sections 31 and 32 (township 33 north, range 9 east) in Wilmington township, and sections 5, 6, 7, 8, 17, 18, 19, 30, and 31, with occasional outliers in sections 3, 4, and 9, and, possibly, in sections 20, 28, 29,30, and 32 (township 32 north, range 9 east) of Reed township, in Will County, comprising eleven square miles of workable coal within the known basin. Borings indicate the presence of coal on sections 30 and 33 in Wilmington

Jan 1, 1875

Prof. Dr. H. Seger and Mr. E. Cramer, Chemisches Laboratorium fur Thonindustrie, Berlin, Prussia (communication to the President)* : We have learned, with much interest, from the pamphlet sent to us, of the work of Messrs. Hofman and Demond, particularly as we observe from their experiments that these gentlemen recognize the usefulness of the Seger cones, and that this method of determining temperatures in the furnaces of the ceramic industry and in the tests of refractory clays is valued, not only in all parts of Germany, but also in other countries. Permit us to say, with reference to the crucibles employed in tests for refractoriness, that we have used of late, besides the magnesia crucibles, also those made of Zettlitz kaolin, with the addition of alumina, previously calcined, with regard to which we beg to refer to our article in the Thonindustrie-Zeitung of December 9, 1893.

Jan 1, 1895

By Frank C. Frischknecht

Most early development and application of electromagnetic prospecting methods took place in Scandinavia, where geological conditions favor their use. In other parts of the world these methods have aroused cycles of interest, but in Scandinavia they have been used continuously and successfully since the 1920's. Electromagnetic methods may be classified into two general groups. One group includes methods in which the source of the electromagnetic field remains stationary while the receivers are moved about to explore the area. The other includes procedures in which the energizing and receiving systems are moved together. Other classifications could be based on the size of the energizing source, the particular components of the electromagnetic field which are measured, or the mode of trans- porting the equipment. The difference between fixed-source and moving-source methods, however, is of such great fundamental importance that it will be emphasized in this discussion.

Jan 9, 1959

By Toshio Kurikami, Charles A. Brockmiller, John E. FitzSimmons

In the manufacture of sulfuric acid from SO2 bearing gases, the presence of mercury vapor in the gases may lead to unacceptably high mercury levels in product acid. Anticipating inception of regulations requiring low mercury acid, St. Joe Minerals Corporation and Toho Zinc Company, Ltd. independently developed new mercury removal technology. The processes may be used individually or in combination, depending upon the mercury content of the SO2 gases and the required mercury level in acid, for efficient control of maximum mercury levels in sulfuric acid. The St. Joe B Process removes mercury from roaster off-gas streams, while Toho’s NAK Process precipitates Hg from concentrated sulfuric acid. The combined process is commercially operated at St. Joe's zinc smelter in Monaca, Pennsylvania, and the NAK Process at Toho’s Chigirishima lead smelter and Onahama zinc roasting plant in Japan. Product acid mercury levels of 0.5 mg/kg are economically achieved.

Jan 1, 1976

[SWEETSER, R. H.: Discussions: on Evaluation of Coal for Blast furnace Coke, 94, 378, 394,385 on Mt. Union Sand Flotation Plant for Preparing Bituminous Coal, 74, 591 on Need for Research in Foundry Pig Iron, 76, 450 on Pig Iron Low in Total Carbon, Is in Demand for Use in Various Industries 75,471 on Properties of Coal Which Affect Its Use in the Ceramic Industry, 101, 254 on Relation of Ash Composition to the Uses of Coal, 74, 471 on Research on Blastfurnace Slags 100, 137.138 on Selection of Coals for the Manufacture of Coke, 74, 637 on Sinter in Blast-furnace Burdens, 100, 54 on Sintering Limonitic Iron Ores at Ironton, Minnesota, 90, 355, 356 on Slag Control in the Making of Iron and Steel, 116, 104, 115, 116 on Solubility of Nitrogen in Liquid Iron, 116, 193, 194 on A Statistical Analysis of Blast-furnace Data, 96, 70]

Jan 1, 1936