Carbothermic Reduction of Zinc Sulfide in the Presence of Calcium Oxide and Lithium Carbonate

碩士 === 國立臺灣科技大學 === 化學工程系 === 93 === Carbothermic reduction of zinc sulfide in the presence of lithium carbonate and calcium oxide was carried out in a thermogravimetic analysis system (TGA). Solid sample before and after reaction were analyzed by an X-ray diffractometer (XRD), an atomic absorption...

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Main Authors: Yu-Chain Peng, 彭鈺謙
Other Authors: Chun-I Lin
Format: Others
Language:zh-TW
Published: 2005
Online Access:http://ndltd.ncl.edu.tw/handle/85384307237175169596
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spelling ndltd-TW-093NTUST3420452015-10-13T12:56:37Z http://ndltd.ncl.edu.tw/handle/85384307237175169596 Carbothermic Reduction of Zinc Sulfide in the Presence of Calcium Oxide and Lithium Carbonate 碳酸鋰與氧化鈣存在下硫化鋅的碳熱還原反應 Yu-Chain Peng 彭鈺謙 碩士 國立臺灣科技大學 化學工程系 93 Carbothermic reduction of zinc sulfide in the presence of lithium carbonate and calcium oxide was carried out in a thermogravimetic analysis system (TGA). Solid sample before and after reaction were analyzed by an X-ray diffractometer (XRD), an atomic absorption spectrometer (AAS), a carbon and sulfur determinator (CSD), an elemental analyzer (EA), a scanning electron microscope (SEM) and a surface area analyzer (SAA). Experimental results revealed that reaction rate was enhanced about four times in the Li2CO3 catalyzed system. The results of TGA, AAS, CSD and EA were found to be close to each other. The results of SEM indicated that zinc containing grains, carbon grains and the calcium containing grains were covered by a layer of liquid film of lithium carbonate. The results of SAA indicated that the pore surface area and average pore diameter of a solid sample reduced drastically and the pore volume increased rapidly in the initial stage. When the reaction time elapsed, the changes of the pore surface and average pore diameter become mild and the pore volume reduced drastically and then remain unchanged. The effects of reaction temperature on the variations of pore surface area, pore diameter and average pore diameter were similar to that of reaction times. A mechanism and a model were proposed to interpret this reaction. The study on the kinetics of the carbothermic reduction was based on the data of the TGA. Experimental results indicated that the reduction rate could not be changed by the variation of argon flow rate. However, it could be increased by the reaction temperature, the initial molar ratio of C/ZnS, the initial molar ratio of CaO/ZnS, or the initial molar ratio of Li2CO3/ZnS and decreasing the sample height, the size of carbon aggregate, or initial bulk density. The effects of the operating variables, excluding the initial molar ratio of Li2CO3/ZnS, on the reaction rate in Li2CO3 catalyzed system were found to be close to those of uncatalyzed system. Chun-I Lin 林俊一 2005 學位論文 ; thesis 142 zh-TW
collection NDLTD
language zh-TW
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description 碩士 === 國立臺灣科技大學 === 化學工程系 === 93 === Carbothermic reduction of zinc sulfide in the presence of lithium carbonate and calcium oxide was carried out in a thermogravimetic analysis system (TGA). Solid sample before and after reaction were analyzed by an X-ray diffractometer (XRD), an atomic absorption spectrometer (AAS), a carbon and sulfur determinator (CSD), an elemental analyzer (EA), a scanning electron microscope (SEM) and a surface area analyzer (SAA). Experimental results revealed that reaction rate was enhanced about four times in the Li2CO3 catalyzed system. The results of TGA, AAS, CSD and EA were found to be close to each other. The results of SEM indicated that zinc containing grains, carbon grains and the calcium containing grains were covered by a layer of liquid film of lithium carbonate. The results of SAA indicated that the pore surface area and average pore diameter of a solid sample reduced drastically and the pore volume increased rapidly in the initial stage. When the reaction time elapsed, the changes of the pore surface and average pore diameter become mild and the pore volume reduced drastically and then remain unchanged. The effects of reaction temperature on the variations of pore surface area, pore diameter and average pore diameter were similar to that of reaction times. A mechanism and a model were proposed to interpret this reaction. The study on the kinetics of the carbothermic reduction was based on the data of the TGA. Experimental results indicated that the reduction rate could not be changed by the variation of argon flow rate. However, it could be increased by the reaction temperature, the initial molar ratio of C/ZnS, the initial molar ratio of CaO/ZnS, or the initial molar ratio of Li2CO3/ZnS and decreasing the sample height, the size of carbon aggregate, or initial bulk density. The effects of the operating variables, excluding the initial molar ratio of Li2CO3/ZnS, on the reaction rate in Li2CO3 catalyzed system were found to be close to those of uncatalyzed system.
author2 Chun-I Lin
author_facet Chun-I Lin
Yu-Chain Peng
彭鈺謙
author Yu-Chain Peng
彭鈺謙
spellingShingle Yu-Chain Peng
彭鈺謙
Carbothermic Reduction of Zinc Sulfide in the Presence of Calcium Oxide and Lithium Carbonate
author_sort Yu-Chain Peng
title Carbothermic Reduction of Zinc Sulfide in the Presence of Calcium Oxide and Lithium Carbonate
title_short Carbothermic Reduction of Zinc Sulfide in the Presence of Calcium Oxide and Lithium Carbonate
title_full Carbothermic Reduction of Zinc Sulfide in the Presence of Calcium Oxide and Lithium Carbonate
title_fullStr Carbothermic Reduction of Zinc Sulfide in the Presence of Calcium Oxide and Lithium Carbonate
title_full_unstemmed Carbothermic Reduction of Zinc Sulfide in the Presence of Calcium Oxide and Lithium Carbonate
title_sort carbothermic reduction of zinc sulfide in the presence of calcium oxide and lithium carbonate
publishDate 2005
url http://ndltd.ncl.edu.tw/handle/85384307237175169596
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