Extraction of Humic Acid from Lignite by KOH-Hydrothermal Method

被引:70
作者
Cheng, Gan [1 ,2 ]
Niu, Zeyu [3 ]
Zhang, Chuanxiang [1 ,2 ]
Zhang, Xiaoming [1 ]
Li, Xusheng [4 ]
机构
[1] Henan Polytech Univ, Coll Chem & Chem Engn, Jiaozuo 454000, Peoples R China
[2] Henan Polytech Univ, Henan Key Lab Coal Green Transformat, Jiaozuo 454000, Peoples R China
[3] Cent South Univ Forestry & Technol, Coll Food Sci & Engn, Changsha 410004, Hunan, Peoples R China
[4] China Univ Min & Technol, Sch Chem Engn & Technol, Xuzhou 221116, Jiangsu, Peoples R China
来源
APPLIED SCIENCES-BASEL | 2019年 / 9卷 / 07期
基金
中国博士后科学基金;
关键词
humic acid; hydrothermal; lignite; XRD; FTIR; COAL; ADSORPTION; OXIDATION; GASIFICATION; SUBSTANCES; ACTIVATION; REMOVAL; SURFACE; IMPACT; STATE;
D O I
10.3390/app9071356
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Humic acid (HA) was extracted by a hydrothermal method from Huolinhe lignite from Inner Mongolia. The effects of the alkali-to-carbon mass ratio, water-to-coal mass ratio, reaction temperature, and reaction time on the HA yield were investigated. The physicochemical characterization of the products was performed, and the reaction mechanism was explored. Raw coal, HA, and residual coal were characterized using Fourier-transform infrared spectroscopy (FTIR), ultraviolet-visible spectroscopy (UV-VIS), elemental composition, and X-ray diffraction (XRD) analyses and compared to each other. The maximum HA yield (90.2%) was obtained from the 0.250-0.180 mm size fraction of the coal sample at a reaction temperature and time of 190 degrees C and 7 h. Proximate analysis proved that the ash and sulfur of lignite can be removed by hydrothermal treatment. Elemental analysis showed that the O/C and H/C ratios were highest for HA, followed by those for residual coal and raw coal, indicating an increase in the oxygen and hydrogen content of HA. FTIR and UV-VIS analyses showed that hydrothermal extraction destroyed the macromolecular structure of lignite. Moreover, the organics were degraded and hydrolyzed during the reaction process.
引用
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页数:13
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