scholarly journals Investigation of composition and properties of EAF dust for metal reduction

2021 ◽  
Vol 1155 (1) ◽  
pp. 012082
Author(s):  
D A Kalganov ◽  
D A Pavlov ◽  
A P Anzulevich ◽  
L N Butko ◽  
V A Tolkachev ◽  
...  
Keyword(s):  
2020 ◽  
Author(s):  
Lucas A. Freeman ◽  
Akachukwu D. Obi ◽  
Haleigh R. Machost ◽  
Andrew Molino ◽  
Asa W. Nichols ◽  
...  

The reduction of the relatively inert carbon–oxygen bonds of CO<sub>2</sub> to access useful CO<sub>2</sub>-derived organic products is one of the most important fundamental challenges in synthetic chemistry. Facilitating this bond-cleavage using earth-abundant, non-toxic main group elements (MGEs) is especially arduous because of the difficulty in achieving strong inner-sphere interactions between CO<sub>2</sub> and the MGE. Herein we report the first successful chemical reduction of CO<sub>2</sub> at room temperature by alkali metals, promoted by a cyclic(alkyl)(amino) carbene (CAAC). One-electron reduction of CAAC-CO<sub>2</sub> adduct (<b>1</b>) with lithium, sodium or potassium metal yields stable monoanionic radicals clusters [M(CAAC–CO<sub>2</sub>)]<sub>n</sub>(M = Li, Na, K, <b> 2</b>-<b>4</b>) and two-electron alkali metal reduction affords open-shell, dianionic clusters of the general formula [M<sub>2</sub>(CAAC–CO<sub>2</sub>)]<sub>n </sub>(<b>5</b>-<b>8</b>). It is notable that these crystalline clusters of reduced CO<sub>2</sub> may also be isolated via the “one-pot” reaction of free CO<sub>2</sub> with free CAAC followed by the addition of alkali metals – a reductive process which does not occur in the absence of carbene. Each of the products <b>2</b>-<b>8</b> were investigated using a combination of experimental and theoretical methods.<br>


2021 ◽  
Vol 1096 (1) ◽  
pp. 012091
Author(s):  
F Leilan ◽  
T Revina ◽  
I Dimassetya ◽  
A Rahmanissa
Keyword(s):  

FEBS Journal ◽  
2007 ◽  
Vol 274 (14) ◽  
pp. 3728-3738 ◽  
Author(s):  
Jimmy Borloo ◽  
Bjorn Vergauwen ◽  
Lina De Smet ◽  
Ann Brigé ◽  
Bart Motte ◽  
...  

2017 ◽  
Vol 83 (18) ◽  
Author(s):  
Angela Chen ◽  
Lydia M. Contreras ◽  
Benjamin K. Keitz

ABSTRACT The biological synthesis of metal nanoparticles has been examined in a wide range of organisms, due to increased interest in green synthesis and environmental remediation applications involving heavy metal ion contamination. Deinococcus radiodurans is particularly attractive for environmental remediation involving metal reduction, due to its high levels of resistance to radiation and other environmental stresses. However, few studies have thoroughly examined the relationships between environmental stresses and the resulting effects on nanoparticle biosynthesis. In this work, we demonstrate cell-free nanoparticle production and study the effects of metal stressor concentrations and identity, temperature, pH, and oxygenation on the production of extracellular silver nanoparticles by D. radiodurans R1. We also report the synthesis of bimetallic silver and gold nanoparticles following the addition of a metal stressor (silver or gold), highlighting how production of these particles is enabled through the application of environmental stresses. Additionally, we found that both the morphology and size of monometallic and bimetallic nanoparticles were dependent on the environmental stresses imposed on the cells. The nanoparticles produced by D. radiodurans exhibited antimicrobial activity comparable to that of pure silver nanoparticles and displayed catalytic activity comparable to that of pure gold nanoparticles. Overall, we demonstrate that biosynthesized nanoparticle properties can be partially controlled through the tuning of applied environmental stresses, and we provide insight into how their application may affect nanoparticle production in D. radiodurans during bioremediation. IMPORTANCE Biosynthetic production of nanoparticles has recently gained prominence as a solution to rising concerns regarding increased bacterial resistance to antibiotics and a desire for environmentally friendly methods of bioremediation and chemical synthesis. To date, a range of organisms have been utilized for nanoparticle formation. The extremophile D. radiodurans, which can withstand significant environmental stresses and therefore is more robust for metal reduction applications, has yet to be exploited for this purpose. Thus, this work improves our understanding of the impact of environmental stresses on biogenic nanoparticle morphology and composition during metal reduction processes in this organism. This work also contributes to enhancing the controlled synthesis of nanoparticles with specific attributes and functions using biological systems.


Tetrahedron ◽  
1984 ◽  
Vol 40 (10) ◽  
pp. 1701-1711 ◽  
Author(s):  
C. Schnieders ◽  
K. Müllen ◽  
W. Huber
Keyword(s):  

2020 ◽  
Vol 61 (2) ◽  
pp. 145-151
Author(s):  
Alexander S. Vusikhis ◽  
◽  
Evgeny N. Selivanov ◽  
Stanislav N. Tyushnyakov ◽  
Viktor P. Chentsov ◽  
...  

Thermodynamic modeling is used to describe the metal reduction processes by hydrogen from oxide melt in the B2O3-CaO- MeO (Me – Ni, Zn, Pb, Cu) system. Open systems approximation with periodic removal of metal particles and gases from the working melt composition is used in the method. By this work we present the thermodynamic modeling results of metal reduction processes (Ni, Cu, Pb, Zn) by Hydrogen. The reducible metals oxides content in the all melts was 3 mass %, and the mass ratio of B2O3/CaO was taken as 3 to be close to eutectic composition. The calculations made it possible to determine such parameters as oxide melt compositions and elements reduction degree depending on the induced gas quantity. of the Nickel, Copper, Lead and Zinc reduction process simulation from B2O3-CaO-MeO melts proved the reduction process by Hydrogen is similar to that which was earlier established when Carbon monoxide was used as the reducing agent. When Copper is reduced from CuO, the process occurs with intermediate Cu2O oxide formation (CuO → Cu2O → Cu). The Nickel (NiO → Ni), Lead (PbO → Pbs + Pbg) and Zinc (ZnO → Zng) recovery have been realized by one stage. The non-ferrous metals change content in the oxide melt and the degrees of its reduction depending on temperature and reducing agent quantity introduced are described by the second-order polynomial functional equations. Comparison of the Carbon monoxide and Hydrogen used for Nickel, Copper, Lead, and Zinc reducing to 90% metallization degree proved much less Hydrogen consumption.


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