scholarly journals A Mineralogical Investigation on Volatilization of Impurity Elements from Cu-Rich Polymetallic Concentrates During Roasting in Inert Atmosphere

Author(s):  
Pande Nishant Prasad ◽  
Iris McElroy ◽  
Andreas Lennartsson ◽  
Caisa Samuelsson

AbstractFour different Cu-rich polymetallic concentrates are tested for volatilization of Sb and As during laboratory-scale roasting. The experiments are performed between 200 °C and 700 °C, at intervals of 100 °C and in an inert atmosphere. Sb volatilization is much less (maximum approximately 45 pct) than As volatilization (maximum approximately 95 pct) in these conditions at 700 °C. As volatilization is however limited from the concentrate having As mainly in a tetrahedrite solid solution ((Cu,Ag,Fe,Zn)12(Sb,As)4S13). Sb and As retained in the roasted calcine are found in the low-melting liquid phase, formed at approximately 500 °C. This melt phase gets enlarged and enriched in Sb with an increase in temperature. However, there is noticeable As volatilization from this melt phase with the temperature approaching 700 °C. Furthermore, there is an early and relatively high Sb volatilization from the concentrate having Sb substantially as gudmundite. Micron-scale elemental redistribution in gudmundite in the 350 °C roasted calcine confirms its transformation at this temperature. Other Sb minerals did not undergo any detectable transformation at this temperature, suggesting that the significant Sb volatilization starting between 300 °C and 400 °C was primarily from gudmundite. This benign attribute of gudmundite featured in this work in the context of roasting should also be relevant from the geometallurgical perspective during concentrate production, where concentrates bearing Sb are considered substandard for further Cu extraction irrespective of the Sb mineralogy.

2020 ◽  
Vol 51 (4) ◽  
pp. 1446-1459 ◽  
Author(s):  
Pande Nishant Prasad ◽  
Andreas Lennartsson ◽  
Caisa Samuelsson

AbstractFour different Cu-rich polymetallic concentrates (additionally comprising Zn, Pb and impurity elements As, Sb) from various deposits in Sweden are examined, in particular for the sintering tendency during roasting in inert atmosphere. Experiments performed in a laboratory-scale roasting setup between 200 °C and 700 °C in intervals of 100 °C revealed that significant sintering initiates from 500 °C for all four concentrates. Two sintering mechanisms are determined from the examination of the sintered calcines: (1) solid-state assimilation of Cu-, Zn- and Fe-bearing main sulphide minerals to form a high-temperature solid solution, the iss phase belonging to the Cu-Fe-Zn-S system; (2) low-melting liquid phase formation due to partial melting of galena facilitated by the presence of impurity-bearing minerals, mainly the arsenopyrite and Sb sulphosalts such as tetrahedrite. Galena also forms a melt below 700 °C with the iss phase. Therefore, the presence of galena in polymetallic concentrates generally increases the susceptibility to early sintering. These experiments in inert atmosphere facilitate a fundamental study with practical relevance to the roasting in low oxidation potential environments, favourable for volatilization of impurity elements such as As and Sb.


1986 ◽  
Vol 47 (C1) ◽  
pp. C1-441-C1-445
Author(s):  
E. KOSTIĆ ◽  
S. J. KISS ◽  
D. CEROVIĆ

2021 ◽  
Vol 2 (1) ◽  
pp. 39-48
Author(s):  
Nguyen H. H. Phuc ◽  
Takaki Maeda ◽  
Tokoharu Yamamoto ◽  
Hiroyuki Muto ◽  
Atsunori Matsuda

A solid solution of a 100Li3PS4·xLi3PO4 solid electrolyte was easily prepared by liquid-phase synthesis. Instead of the conventional solid-state synthesis methods, ethyl propionate was used as the reaction medium. The initial stage of the reaction among Li2S, P2S5 and Li3PO4 was proved by ultraviolet-visible spectroscopy. The powder X-ray diffraction (XRD) results showed that the solid solution was formed up to x = 6. At x = 20, XRD peaks of Li3PO4 were detected in the prepared sample after heat treatment at 170 °C. However, the samples obtained at room temperature showed no evidence of Li3PO4 remaining for x = 20. Solid phosphorus-31 magic angle spinning nuclear magnetic resonance spectroscopy results proved the formation of a POS33− unit in the sample with x = 6. Improvements of ionic conductivity at room temperature and activation energy were obtained with the formation of the solid solution. The sample with x = 6 exhibited a better stability against Li metal than that with x = 0. The all-solid-state half-cell employing the sample with x = 6 at the positive electrode exhibited a better charge–discharge capacity than that employing the sample with x = 0.


1981 ◽  
Vol 7 ◽  
Author(s):  
G. Battaglin ◽  
A. Carnera ◽  
G. Della Mea ◽  
P. Mazzoldi ◽  
Animesh K. Jain ◽  
...  

ABSTRACTWe present a comparative study (by 1.8 MeV 4He+ ion channeling) of virgin, self and Eu implanted single crystals of nickel, under irradiation with single ruby laser pulses. The as implanted Eu is nearly non-substitutional and remains so, even after laser treatment. The comparative defect dechanneling behaviour provides explicit evidence of defect-impurity interaction which may be suppressing the formation of an expected metastable solid solution in the Eu-Ni system, which possesses miscibility in the liquid phase. A clear surface Eu peak appears at 2.1 J/cm2.


2020 ◽  
Vol 6 (9) ◽  
pp. 10-17
Author(s):  
A. Razzakov ◽  
A. Matnazarov ◽  
M. Latipova ◽  
A. Japakov

Abstract. Single-crystal films of a graded-gap solid solution Si1-xGex (0 <x <1) was grown on Si substrates from limited tin, gallium solution-melt. Accordingly, liquid phase epitaxy method was applied in the process. The formation of dislocations, grown under various technological conditions, at the substrate-film interface along the growth direction of the Si1-xGex solid solution was studied. Optimal technological growth modes for obtaining crystalline perfect epitaxial layers and structures are given.


1976 ◽  
Vol 7 (5) ◽  
Author(s):  
G. M. KUZNETSOV ◽  
L. S. TSURGAN ◽  
A. A. PEDOS ◽  
T. N. SELIKHOVA ◽  
V. A. ROTENBERG

2013 ◽  
Vol 813 ◽  
pp. 364-371 ◽  
Author(s):  
Qiong Zhu Huang ◽  
Gui Min Lu ◽  
Jian Guo Yu

Effect of LiCl·H2O on sintering properties of MgO prepared from natural brine from Qarhan Salt Lake, crystalline bischofite and MgCl2·6H2O(AR) was studied. The results showed that LiCl·H2O of addition exceeded 1 wt% had promoting effect on sintering of magnesia prepared from MgCl2·6H2O(AR). While 1.5 wt% LiCl·H2O was added, the bulk density of magnesia was 3.40 g/cm3, and the relative density was 95.0%. With 0.5 wt% LiCl·H2O, the bulk densities of magnesia prepared from crystalline bischofite and brine were 3.04 and 3.10 g/cm3, and the relative densities increased by 8.4% and 14.8%, respectively. The main mechanism for promoting MgO sintering with LiCl·H2O was that Li2O produced by hydrolysis solubilized in MgO to form solid solutions and oxygen vacancies which were favorable to sintering. The main reasons for promoting sintering of brine magnesia with LiCl·H2O were solid solution and liquid phase sintering, while the main reason was solid solution for magnesia from crystalline bischofite and MgCl2·6H2O(AR).


2014 ◽  
Vol 33 (6) ◽  
pp. 525-529 ◽  
Author(s):  
X.Y. Gu ◽  
Z.Z. Duan ◽  
X.P. Gu ◽  
D.Q. Sun

AbstractIn the present study microstructural evolution in transient liquid phase (TLP) bonded Ti3Al-Nb alloy joints using a pure copper as interlayer was investigated. TLP bonded Ti3Al-Nb alloy joints composed of intermetallic compound layers were produced. Microstructural evolution of joints depended on both bonding time and bonding temperature. With increasing bonding time and bonding temperature, the joint width increased and amount of compounds in the joint decreased. The joint microstructure at 1173 K × 1 min mainly consisted of Ti (solid solution) + Ti2Cu + TiCu + Ti3Cu4 + Ti2Cu3 + TiCu4 + Cu (solid solution) phase and it changed to Ti (solid solution) + Ti2Cu + TiCu at 1223 K × 60 min. Compounds formed on cooling from the bonding temperature by liquid phase were eliminated from the joint at 1223 K × 60 min due to isothermal solidification of liquid phase. The increase of the width of joint is attributed to the composition difference between the isothermal solidification production and its adjacent base material.


Sign in / Sign up

Export Citation Format

Share Document