Steam gasification of hydrochar derived from hydrothermal carbonization of fruit wastes

被引:32
|
作者
Salaudeen, Shakirudeen A. [1 ]
Acharya, Bishnu [2 ]
Dutta, Animesh [1 ]
机构
[1] Univ Guelph, Sch Engn, Mech Engn Program, Guelph, ON N1G 2W1, Canada
[2] Univ Saskatchewan, Dept Chem & Biol Engn, 57 Campus Dr, Saskatoon, SK S7N 5A9, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Hydrochar gasification; Steam gasification; Fruit wastes; Syngas; Waste conversion;
D O I
10.1016/j.renene.2021.02.115
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study presents a numerical investigation of steam gasification of hydrochar derived from fruit wastes. Four fruit wastes, apple chip pomace, grape pomace, rotten apple, and apple juice pomace, were used as feedstocks. Aspen Plus was used to simulate the gasification process. The syngas composition, hydrogen to CO ratio (H-2/CO), CO to CO2 ratio (CO/CO2), and heating value (HHV) of the resulting syngas were analyzed. Results show that hydrothermal carbonization (HTC) increases the CO and reduces the CO2 content of the syngas after gasification. Accordingly, H-2/CO reduces, and CO/CO2 increases after HTC treatment. Hydrothermal treatment also improves the HHV of the syngas. The obtained HHV of syngas from hydrochar gasification ranged from 10.1 to 15.3 MJ/Nm(3) depending on the process parameters. Additionally, effects of process parameters were studied. Increasing the steam to biomass ratio (SBR) leads to a higher H-2/CO, enriching the syngas with hydrogen (up to 64.7 vol%). Higher SBR also lowers the CO/CO2 ratio due to the consumption of CO and a rise in CO2. HHV increases with increasing pressure, and hydrochars exhibit more changes in HHV than raw feedstocks. The reaction temperature contributes to an increase in the fraction of CO in the syngas (up to 39.6 vol%). Although hydrogen increased initially with temperature, a slight reduction was observed for the gas at elevated temperatures, reducing the H2/ CO ratio and increasing the CO/CO2 ratio. (c) 2021 Elsevier Ltd. All rights reserved.
引用
收藏
页码:582 / 591
页数:10
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