Conversion of tomato-peel waste into solid fuel by hydrothermal carbonization: Influence of the processing variables

被引:192
作者
Sabio, E. [1 ]
Alvarez-Murillo, A. [1 ]
Roman, S. [1 ]
Ledesma, B. [1 ]
机构
[1] Univ Extremadura, Dept Appl Phys, Sch Ind Engn, Badajoz 06006, Spain
关键词
Hydrothermal carbonization; Tomato waste; Surface response methods; TG-FTIR; SEWAGE-SLUDGE; WOOD LIGNIN; PYROLYSIS; DEGRADATION; BIOMASS;
D O I
10.1016/j.wasman.2015.04.016
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this work, the influence of the variables temperature, residence time, and biomass/water ratio on the hydrothermal carbonization (HTC) of tomato peel was investigated. The implementation of a Design of Experiments - Response Surface Methodology approach allowed to identify the importance of each variable, as well as their interactions, in both the reactivity (solid yield) and energy densification (increase in higher heating value). The HTC residence time and specially temperature had a major effect on the process, increasing the solid yield and promoting energy densification. Ratio had a minor effect although under certain temperature and time conditions, it was a decisive parameter. Solid yields in the range 27.6% and 87.7% with corresponding high heating values 23.6-34.6 MJ kg(-1) were obtained. From the statistical processing of the experimental data obtained pseudo-second order models were developed. It was proven that these approaches envisaged the hydrochar final characteristics successfully. From the elemental analysis and the FTIR spectra, it was possible to investigate the HTC pathway, which was defined as a combination of several processes; considering dehydration and decarboxylation reactions and especially lignin depolimerization reactions, which lead to the formation of monomeric radicals. Moreover, the surface morphology of selected hydrochars by Scanning Electron Microscopy (SEM) showed the original structure scaffold, with minor changes between hydrochars prepared under different conditions.(c) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:122 / 132
页数:11
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