scholarly journals Recovery of zinc from zinc oxide dust containing multiple metal elements by carbothermal reduction

2021 ◽  
pp. 49-49
Author(s):  
F.-G. Lei ◽  
M.-T. Li ◽  
C. Wei ◽  
Z.-G. Deng ◽  
X.-B. Li ◽  
...  
Keyword(s):  
Zinc Oxide ◽  
Carbothermal Reduction ◽  
Carbothermic Reduction ◽  
Reduction Process ◽  
Zinc Content ◽  
Holding Time ◽  
Reduction Condition ◽  
Reduction Experiment ◽  
Effects Of Temperature ◽  
Optimal Reduction

A carbothermal reduction process simulating EAF process is used to handle the zinc oxide dust, and the zinc in the dust can be extracted and recovered efficiently. The crude zinc and lead-tin alloy were obtained finally. The effects of temperature, holding time, and reductant dosage on zincvolatilization rate were investigated, and the ?Pelletizing -Calcination-Carbothermic reduction? experiment was conducted. The resultsfound the optimal reduction condition was as follows: the temperature of 1300?C, reductant dosage of 14.04% and holding time of 120 min. After the calcination at 900?C for 120 min, the removal rates of fluorine, chlorine and sulfur in the dust were 98.18%, 96.38% and 28.58% respectively, and the volatilization rate of zinc was 99.83% in reduction process. The zinc content of the crude zinc was 68.48%.

Preparation of Phosphorus by Carbothermal Reduction Mechanism in Vacuum

2011 ◽  
Vol 361-363 ◽  
pp. 268-274 ◽  
Author(s):  
Yu Cheng Liu ◽  
Qiu Xia Li ◽  
Yong Cheng Liu
Keyword(s):  
Carbothermal Reduction ◽  
Carbothermic Reduction ◽  
Reduction Process ◽  
Molar Ratio ◽  
Main Reaction ◽  
Reduction Mechanism ◽  
Element Analysis ◽  
Reaction Phase ◽  
System Pressure ◽  
Increasing Temperature

The purpose of this work was to investigated the carbothermic reaction of fluorapatite process by the means of thermodynamics analyses, XRD and element analysis, respectively. Thermodynamic calculations indicated that phosphorus can be prepared by heating the mixture of Ca5(PO4)3F2 and C at 1173K under the system pressure of 100Pa. CO cannot react with Ca5(PO4)3F2 in the carbothermic reduction process at 973-1873K and 100Pa. Experimental results demonstrated that phosphorus can be produced by the reaction between Ca5(PO4)3F2 and C, the main reaction phase is P2(g), CO(g), CaO and CaF2, and with increasing temperature, the greater degree of response. The best technology conditions, the molar ratio of Ca5(PO4)3F2 to C is 1:7.5 at 1723K for 1h when the system pressure was about 100Pa. This study to provide experimental evidence for preparation of phosphorus by carbothermal reaction of fluorapatite in vacuum.

scholarly journals Calculation Model for Activity of FeO in Quaternary Slag System SiO2-CaO-Al2O3-FeO

Metals ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 714 ◽  
Author(s):  
Zhi Li ◽  
Guojun Ma ◽  
Mengke Liu ◽  
Jingjing Zou
Keyword(s):  
Carbothermal Reduction ◽  
Theoretical Basis ◽  
Reduction Process ◽  
Slag System ◽  
Copper Slag ◽  
Calculation Model ◽  
Al2o3 Content ◽  
Coexistence Theory ◽  
Slag Structure ◽  
Effects Of Temperature

According to the coexistence theory of slag structure, a calculation model for the activity of FeO in the quaternary system SiO2-CaO-Al2O3-FeO of depleted copper slag was established. The model was used to calculate and analyze the effects of temperature (T), basicity (B), and Al2O3 content on the activity of FeO (NFeO). The results show that temperature has little impact on NFeO. With increased basicity, NFeO first increased slightly, then increased sharply, and finally decreased. It is easier for CaO to combine with SiO2 than FeO to form calcium silicate, which replaces FeO in 2FeO·SiO2 and increases NFeO. However, when basicity is higher than 2.0, CaO not only reacts with SiO2, but also combines with FeO to form calcium ferrate compounds to decrease NFeO. In addition, the activity of FeO decreases with increased Al2O3 content because of the reaction between CaO and Al2O3. The results can be used as a theoretical basis to guide the carbothermal reduction process of copper slag.

Synthesis of Al4SiC4-Al8SiC7 Composite Powders by Carbothermal Reduction Process

2011 ◽  
Vol 399-401 ◽  
pp. 813-816 ◽  
Author(s):  
Chao Yu ◽  
Wen Jie Yuan ◽  
Jun Li ◽  
Hong Xi Zhu ◽  
Cheng Ji Deng
Keyword(s):  
Carbon Black ◽  
Carbothermal Reduction ◽  
Carbothermic Reduction ◽  
Heating Temperature ◽  
Reduction Process ◽  
Composite Powders

Tabular structure of Al4SiC4-Al8SiC7composites was successfully synthesized using a mixture of calcined bauxite, SiC and carbon black by a carbothermal reduction process. The effects of the amount of SiC addition and the heating temperature on synthesis of Al4SiC4-Al8SiC7composites by carbothermic reduction were investigated. The results show that SiC amount played an important role in the content of the final products. With the increasing of heating temperature, the Al4SiC4content increased and Al8SiC7content decreased in the products, which indicated the formation and growth of Al4SiC4were promoted.

Phase Behaviors of Talc Minerals in Carbothermal Reduction Process

2012 ◽  
Vol 512-515 ◽  
pp. 123-126
Author(s):  
Wen Juan Li ◽  
Zhao Hui Huang ◽  
Zi He Pan ◽  
Yan Gai Liu ◽  
Ming Hao Fang
Keyword(s):  
Silicon Carbide ◽  
Carbothermal Reduction ◽  
Acid Leaching ◽  
Reduction Process ◽  
Magnesium Silicate ◽  
Raw Material ◽  
Carbon Powder ◽  
Carbon Addition ◽  
Effects Of Temperature ◽  
Phase Behaviors

In this paper, we focus on the phase behaviors of talc minerals by carbothermal reduction (CR) method. The effects of temperature and carbon addition are both discussed in our work. In the experiment, acid-leaching talc was employed as raw material, carbon coke powders were adopted as reducing agent. The XRD results show that: When acid-leaching talc was used as raw material, quartz and few enstatite can be obtained at 1300 °C, with the temperature increasing, the diffraction intensities of enstatite increased. At 1550 °C, enstatite transformed to magnesium silicate and obvious β-SiC can be detected. At 1600 °C, the main phases in the final product are magnesium silicate and β-SiC. The SEM results reveal that the preferred, as-fabricated silicon carbide has morphology of irregular shape. Relatively pure β-SiC can be obtained by using acid-leaching talc mixed together with excess 50% of theoretical quantity of carbon powder sintered at 1550 °C for 4 h.

scholarly journals Ultrafast carbothermal reduction of silica to silicon using a CO2 laser beam

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Seok-Ho Maeng ◽  
Hakju Lee ◽  
Min Soo Park ◽  
Suhyun Park ◽  
Jaeki Jeong ◽  
...  
Keyword(s):  
Carbon Black ◽  
Laser Beam ◽  
Carbothermal Reduction ◽  
Gas Flow ◽  
Crystalline Silicon ◽  
Reduction Process ◽  
Reaction Chamber ◽  
Raman Shift ◽  
Influence Of Process Parameters ◽  
Laser Beam Intensity

AbstractWe report the extraction of silicon via a carbothermal reduction process using a CO2 laser beam as a heat source. The surface of a mixture of silica and carbon black powder became brown after laser beam irradiation for a few tens of seconds, and clear peaks of crystalline silicon were observed by Raman shift measurements, confirming the successful carbothermal reduction of silica. The influence of process parameters, including the laser beam intensity, radiation time, nitrogen gas flow in a reaction chamber, and the molar ratios of silica/carbon black of the mixture, on the carbothermal reduction process is explained in detail.

scholarly journals Titanium Carbide Nanocrystals Synthesized from a Metatitanic Acid-Sucrose Precursor via a Carbothermal Reduction

2015 ◽  
Vol 2015 ◽  
pp. 1-11 ◽  
Author(s):  
Hyunho Shin ◽  
Jun-Ho Eun
Keyword(s):  
Process Control ◽  
Titanium Carbide ◽  
Specific Surface ◽  
Surface Area ◽  
Pore Volume ◽  
Carbothermal Reduction ◽  
Crystal Size ◽  
Reduction Process ◽  
Specific Pore Volume ◽  
Metatitanic Acid

A TiC powder is synthesized from a micron-sized mesoporous metatitanic acid-sucrose precursor (precursor M) by a carbothermal reduction process. Control specimens are also prepared using a nanosized TiO2-sucrose precursor (precursor T) with a higher cost. When synthesized at 1500°C for 2 h in flowing Ar, the characteristics of the synthesized TiC from precursor M are similar to those of the counterpart from precursor T in terms of the crystal size (58.5 versus 57.4 nm), oxygen content (0.22 wt% versus 0.25 wt%), and representative sizes of mesopores: approximately 2.5 and 19.7–25.0 nm in both specimens. The most salient differences of the two specimens are found in the TiC from precursor M demonstrating (i) a higher crystallinity based on the distinctive doublet peaks in the high-two-theta XRD regime and (ii) a lower specific surface area (79.4 versus 94.8 m2/g) with a smaller specific pore volume (0.1 versus 0.2 cm3/g) than the counterpart from precursor T.

High surface area mesoporous SiC synthesized via nanocasting and carbothermal reduction process

2005 ◽  
Vol 40 (18) ◽  
pp. 5091-5093 ◽  
Author(s):  
AN-HUI LU ◽  
WOLFGANG SCHMIDT ◽  
WOLFGANG KIEFER ◽  
FERDI SCHÜTH
Keyword(s):  
Surface Area ◽  
Carbothermal Reduction ◽  
High Surface ◽  
High Surface Area ◽  
Reduction Process

On the carbo-thermal reduction of silica for carbon nano-fibre formation via CVD

2011 ◽  
Vol 1284 ◽  
Author(s):  
Alicja Bachmatiuk ◽  
Felix Börrnert ◽  
Imad Ibrahim ◽  
Bernd Büchner ◽  
Mark H. Rümmeli
Keyword(s):  
Chemical Vapor Deposition ◽  
Vapor Deposition ◽  
Carbothermal Reduction ◽  
Carbon Nanostructures ◽  
Reduction Process ◽  
Chemical Vapor ◽  
Deposition Process ◽  
Thermal Reduction ◽  
Fibre Formation ◽  
Quartz Substrates

ABSTRACTThe formation of carbon nanostructures using silica nanoparticles from quartz substrates as a catalyst in an aerosol assisted chemical vapor deposition process was examined. The silica particles are reduced to silicon carbide via a carbothermal reduction process. The recyclability of the explored quartz substrates is also presented. The addition of triethyl borate improves the efficiency of the carbothermal reduction process and carbon nanotubes formation. Moreover, the addition of hydrogen during the chemical vapor deposition leads to the helical carbon nanostructures formation.

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