Mechanistic study on the significant difference in flotation collector consumption of different coal gasification fine slag

被引:0
|
作者
Cai, Shuangji [1 ]
Dong, Lianping [1 ]
Li, Haipeng [1 ]
Fan, Panpan [2 ]
Yang, Runquan [1 ]
Xue, Zhonghua [3 ,4 ]
Wang, Jiancheng [2 ]
Bao, Weiren [2 ]
Fan, Minqiang [1 ]
Gao, Feng [1 ]
机构
[1] Taiyuan Univ Technol, Coll Min Engn, Taiyuan 030024, Shanxi, Peoples R China
[2] Taiyuan Univ Technol, Coll Chem Engn & Technol, Taiyuan, Shanxi, Peoples R China
[3] Univ Sci & Technol Beijing, Sch Civil & Resource Engn, Beijing, Peoples R China
[4] Chinese Acad Sci, Inst Proc Engn, Key Lab Biochem Engn, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Coal gasification fine slag; flotation; pore structure; pore adsorption; surface energy; INVERSE GAS-CHROMATOGRAPHY;
D O I
10.1080/19392699.2024.2365850
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Froth flotation, a prevalent technique for the separation of fine materials, is employed in the decarburization process of coal gasification fine slag (CGFS). This process is known to consume significant quantities of reagents. This study investigates the pronounced variance in collector consumption during the flotation decarbonization of two distinct CGFS samples, where a tenfold difference was observed when the tailings ash content surpassed 95%. A comprehensive set of analyses, including XPS, BET, SEM, wettability tests, LF-NMR and IGC-SEA, was conducted on the residual charcoal from CGFS to elucidate the mechanism behind reagent consumption. The findings reveal that the reagent's ability to alter the surface hydrophobicity of residual charcoal is contingent upon the adsorption saturation of micropores and transition pores. Furthermore, variations in porosity and surface energy significantly impact collector consumption, independent of differences in the type and quantity of oxygen-containing functional groups. This investigation aims to provide a theoretical framework for reducing the dosage of reagents in the flotation decarburization of CGFS.
引用
收藏
页数:18
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