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p. 169-207
Received: 30 March 2012; in revised form: 7 June 2012 / Accepted: 20 June 2012 / Published: 29 June 2012
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| Download PDF Full-text (1347 KB) | Download XML Full-text Abstract: The epigenetic Zn-Pb deposits in the Lycksele-Storuman ore district, northern Sweden, are hosted by Paleoproterozoic basement near the margin of the Caledonian mountains. A paleogeographic reconstruction suggests that platform sediments, including Cambrian shales, overlaid the mineralised basement. The mineralisation type, containing sphalerite, galena, calcite and fluorite, is confined to veins and breccias and interpreted to be of Mississippi Valley Type (MVT) style. There is no appreciable wall rock alteration. Fluid inclusion work reveals coexisting aqueous and hydrocarbon fluids. Ore deposition is interpreted to have occurred during mixing of two fluids; a cool (
p. 208-227
Received: 22 June 2012; in revised form: 26 July 2012 / Accepted: 31 July 2012 / Published: 13 August 2012
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| Download PDF Full-text (1499 KB) | Download XML Full-text Abstract: Frothers are surfactants commonly used to reduce bubble size in mineral flotation. This paper describes a methodology to characterize frothers by relating impact on bubble size reduction represented by CCC (critical coalescence concentration) to frother structure represented by HLB (hydrophile-lipophile balance). Thirty-six surfactants were tested from three frother families: Aliphatic Alcohols, Polypropylene Glycol Alkyl Ethers and Polypropylene Glycols, covering a range in alkyl groups (represented by n, the number of carbon atoms) and number of Propylene Oxide groups (represented by m). The Sauter mean size (D32 ) was derived from bubble size distribution measured in a 0.8 m3 mechanical flotation cell. The D32 vs. concentration data were fitted to a 3-parameter model to determine CCC95, the concentration giving 95% reduction in bubble size compared to water only. It was shown that each family exhibits a unique CCC95-HLB relationship dependent on n and m. Empirical models were developed to predict CCC95 either from HLB or directly from n and m. Commercial frothers of known family were shown to fit the relationships. Use of the model to predict D32 is illustrated.
p. 228-243
Received: 28 June 2012; in revised form: 27 July 2012 / Accepted: 3 August 2012 / Published: 14 August 2012
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| Download PDF Full-text (993 KB) | Download XML Full-text Abstract: Tertiary low sulfidation (LS) epithermal deposits in the western USA often show evidence of the former presence of nanoparticle-sized precious-metal and silica phases in the highest grade (bonanza) ores. Here, nanoparticles are defined to have a size less than ~10− 7 m. The ore-mineral textures that formed from aggregation of nanoparticles (or colloids) observed to date in these ores include electrum and naumannite (Ag2 Se). Here it is proposed that chalcopyrite also forms nanoparticles in these ores, but sulfide nanoparticles apparently have significantly different physical (surface) properties than the precious-metal phases, and thus exhibit different mineral textures (e.g. , no textural evidence of previous chalcopyrite nanoparticles). Textures described here show that nanoparticles of precious-metal phases and silica were episodically and often repeatedly deposited to form the banded bonanza veins typical of many western USA epithermal deposits. Chalcopyrite is the most abundant metal-sulfide mineral in these bonanza ores, and it was also deposited episodically as well, and it appears to replace earlier formed naumannite dendrites. However, this apparent “replacement” texture may just be the result of naumannite dendrite limbs trapping chalcopyrite nanoparticles that later recrystallized to the apparent replacement texture. The episodic and repetitive nature of the metal-depositing events may record periodic “degassing” of magma chambers at depth, where metals are repeatedly delivered to the shallow epithermal environment by “vapor-phase” metal (loid) transport.
p. 244-257
Received: 11 July 2012; in revised form: 31 July 2012 / Accepted: 2 August 2012 / Published: 14 August 2012
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| Download PDF Full-text (648 KB) | Download XML Full-text Abstract: The review presents synthetic approaches to modern rhenium-based catalysts. Creation of an active center is considered as a process of obtaining a nanoparticle or a molecule, immobilized within a matrix of the substrate. Selective chemical routes to preparation of particles of rhenium alloys, rhenium oxides and the molecules of alkyltrioxorhenium, and their insertion into porous structure of zeolites, ordered mesoporous MCM matrices, anodic mesoporous alumina, and porous transition metal oxides are considered. Structure-property relationships are traced for these catalysts in relation to such processes as alkylation and isomerization, olefin metathesis, selective oxidation of olefins, methanol to formaldehyde conversion, etc.
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