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Co-pyrolysis of de-oiled microalgal biomass residue and waste tires: Deeper insights from thermal kinetics, behaviors, drivers, bio-oils, bio-chars, and in-situ evolved gases analyses

热解 生物质燃烧 残留物(化学) 生物量(生态学) 废物管理 化学 环境科学 环境化学 动力学 原位 有机化学 生态学 工程类 生物 物理 气溶胶 量子力学
作者
Akash Kumar,Beibei Yan,Junyu Tao,Jian Li,Lata Kumari,Belay Tafa Oba,Moses Akintayo Aborisade,Imtiaz Ali Jamro,Guanyi Chen
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:446: 137160-137160 被引量:46
标识
DOI:10.1016/j.cej.2022.137160
摘要

• The residual microalgal biomass was further pyrolyzed with WT as a zero-waste biorefinery concept. • The optimal blends were given based on pyrolytic behaviors and average activation energies. • Evolved behavior of gaseous species were quantified as a function of temperature. • The interaction of fuels promoted hydrocarbons and inhibited N- and O- compounds. • The pore size of biochar rose with increasing NSR share in the blends. The effective utilization of biomass and waste streams has drawn significant attention in light of the energy crisis and requirement for carbon footprint reduction. This study aimed to characterize the pyrolytic behaviors, drivers, kinetics, in-situ evolved gases characteristics, bio-oils, bio-chars, and product distributions of the de-oiled Nannochloropsis sp. residue (NSR) and waste tires (WT) via TG-FTIR-MS and Fixed bed reactor. The D(TG) analysis of the co-pyrolysis was characterized by two decomposition stages: the first stage was the degradation of NSR (150–350 °C), and the second stage (350–550 °C) was ascribed to the degradation of NSR-WT blends. The discrepancy in experimental and theoretical weight loss (ΔW) was less than zero for the blends containing 80, 60, and 50% NSR when the temperature exceeded 210 °C, which confirmed the existence of a strong synergistic effect. The average activation energy (E avg ) was 167.37 kJ/mol and 221.79 kJ/mol for the NSR and WT devolatilization, respectively. To gain more insight into the pyrolytic performance, solid, liquid, and gas products were analyzed by different analytical techniques. The results revealed that the co-pyrolysis significantly modified the chemical composition of bio-oil, leading to an increase in bio-oil yield up to 48.96 wt%. Meanwhile, it seemed conceivable to modify the structure and improve the quality of bio-oils and biochar by co-pyrolysis. This work provides a practical and theoretical understanding of optimizing energy generation, emission control, and products recovery during the co-pyrolysis process.
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