NATIVE METALS IN THE MUSKOX INTRUSION

1965 ◽  
Vol 2 (3) ◽  
pp. 188-215 ◽  
Author(s):  
J. A. Chamberlain ◽  
C. R. McLeod ◽  
R. J. Traill ◽  
G. R. Lachance

The following native metals have been identified in the Muskox intrusion: native iron, native nickel–iron (awaruite), native cobalt–iron (wairauite), and native copper. Mineral distributions and textures indicate that the native metals formed more or less contemporaneously, during the period of serpentinization of the host dunites and related rocks.Conditions during serpentinization must have been more reducing in the central and lower parts of the layered series than in the margins and upper parts of the intrusion. This is indicated by the fact that most native metals are abundant in the central regions and are essentially lacking elsewhere, even in strongly serpentinized zones. This zoning suggests that reducing conditions may have been generated internally, possibly as a result of the serpentinization process itself. The composition of the primary olivine of forsterite80–88 together with the presence of abundant secondary magnetite in equivalent serpentinites indicates that a redox reaction, olivine + water = serpentine + magnetite + hydrogen, contributed to the development of a progressively more reducing, or hydrogen-rich, fluid phase.Natural phase relations indicate that each native metal formed primarily in situ as a result of the decomposition of specific earlier formed minerals that had become unstable in the reducing environment. Native iron appears to have been formed by the reduction of magnetite; awaruite by the reduction of pentlandite; wairauite by the reduction of an unknown phase, possibly cobalt pentlandite or cobaltian pyrite; and native copper by the reduction of chalcopyrite. The feasibility of most of these reactions was confirmed by experimental studies carried out in systems open to moist hydrogen.

Author(s):  
O. Yu. Kichigina

At production of stainless steel expensive alloying elements, containing nickel, are used. To decrease the steel cost, substitution of nickel during steel alloying process by its oxides is an actual task. Results of analysis of thermodynamic and experimental studies of nickel reducing from its oxide presented, as well as methods of nickel oxide obtaining at manganese bearing complex raw materials enrichment and practice of its application during steel alloying. Technology of comprehensive processing of complex manganese-containing raw materials considered, including leaching and selective extraction out of the solution valuable components: manganese, nickel, iron, cobalt and copper. Based on theoretical and experiment studies, a possibility of substitution of metal nickel by concentrates, obtained as a result of hydrometallurgical enrichment, was confirmed. Optimal technological parameters, ensuring high degree of nickel recovery out of the initial raw materials were determined. It was established, that for direct steel alloying it is reasonable to add into the charge pellets, consisting of nickel concentrate and coke fines, that enables to reach the through nickel recovery at a level of 90%. The proposed method of alloying steel by nickel gives a possibility to decrease considerably steel cost at the expense of application of nickel concentrate, obtained out of tails of hydrometallurgical enrichment of manganese-bearing raw materials, which is much cheaper comparing with the metal nickel.


1972 ◽  
Vol 68 (2_Supplb) ◽  
pp. S9-S25 ◽  
Author(s):  
John Urquhart ◽  
Nancy Keller

ABSTRACT Two techniques for organ perfusion with blood are described which provide a basis for exploring metabolic or endocrine dynamics. The technique of in situ perfusion with autogenous arterial blood is suitable for glands or small organs which receive a small fraction of the animal's cardiac output; thus, test stimulatory or inhibitory substances can be added to the perfusing blood and undergo sufficient dilution in systemic blood after passage through the perfused organ so that recirculation does not compromise experimental control over test substance concentration in the perfusate. Experimental studies with the in situ perfused adrenal are described. The second technique, termed the pilot organ method, is suitable for organs which receive a large fraction of the cardiac output, such as the liver. Vascular connections are made between the circulation of an intact, anaesthetized large (> 30 kg) dog and the liver of a small (< 3 kg) dog. The small dog's liver (pilot liver) is excised and floated in a bath of canine ascites, and its venous effluent is continuously returned to the large dog. Test substances are infused into either the hepatic artery or portal vein of the pilot liver, but the small size of the pilot liver and its blood flow in relation to the large dog minimize recirculation effects. A number of functional parameters of the pilot liver are described.


2013 ◽  
Vol 1514 ◽  
pp. 151-156
Author(s):  
Darío Pieck ◽  
Lionel Desgranges ◽  
Yves Pontillon ◽  
Pierre Matheron

ABSTRACTIn the present work, we focus on δ-Gd6UO12 phase and its stability under reducing conditions. This later point is interesting regarding reducing environment that could exist in some nuclear storage sites and that could possibly degrade δ–compounds. A polycrystalline δ-Gd6UO12 sample was prepared by sintering cubic-Gd2O3 and UO2 mixed powders under an air atmosphere. The resulting pellets were then characterized and reduced by heat treatment under an Ar with H2 5% atmosphere. XRD analysis of the sample after reduction did not confirm the reduction into Gd6UO11 but a decomposition of the δ-compound. Preliminary characterizations of these decomposition products are presented.


2020 ◽  
Vol 90 (3) ◽  
pp. 434
Author(s):  
А.Н. Ищенко ◽  
С.А. Афанасьева ◽  
Н.Н. Белов ◽  
В.В. Буркин ◽  
С.В. Галсанов ◽  
...  

In this work, computational and experimental studies of the process of destruction of composite firing pin of porous alloy tungsten+nickel+iron+cobalt with 10 % content of titanium tungsten carbide at high-speed collision with steel barriers. It is shown that at ballistic tests with the broad range of speeds, significant exceeding of penetration of these firing pins in steel barriers in comparison with a mass-dimensional analog of the W-Ni-Fe-90 alloy. Based on the analysis of the crater morphology and structure of the striker fragments after penetration into the barrier, the assumption of implementation of the self-sharpenings mode of the firing pin, by means of localization of plastic deformation is made that leads to decrease in the effective area of interaction and increase in depth of penetration. Modification of a mathematical model of a porous ideal elasto-plastic solid with complex structure for the description of destruction with a possibility of accounting of the adiabatic shift mechanism in the course of interaction of the firing pin and a barrier is carried out.


2021 ◽  
Author(s):  
Nhan Nu Hong Ton ◽  
Binh Khanh Mai ◽  
Thanh Vinh Nguyen

Abstract: Hydroboration reaction of alkynes is one of the most synthetically powerful tools to access organoboron compounds, versatile precursors for cross coupling chemistry. This type of reaction has traditionally been mediated by transition metal or main group catalysts. Herein, we report a novel method using tropylium salts, typically known as organic oxidants and Lewis acids, to efficiently promote the hydroboration reaction of alkynes. A broad range of vinylboranes can be easily accessed via this metal-free protocol. Similar hydroboration reactions of alkenes and epoxides can also be efficiently catalyzed by the same tropylium catalysts. Experimental studies and DFT calculations suggested that the reaction follows an uncommon mechanistic paradigm, which is triggered by a hydride abstraction of pinacolborane with tropylium ion. This is followed by a series of <i>in situ</i> counterion-activated substituent exchanges to generate boron intermediates that promote the hydroboration reaction.


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