木质素
化学
热解
碱金属
碳纤维
化学工程
有机化学
磺酸盐
傅里叶变换红外光谱
碳-13核磁共振
钠
材料科学
复合数
工程类
复合材料
作者
Huiming Yin,Xiankun Huang,Lin Mei,Xi Xi,Ming Dong,Zhaoyi Huo
出处
期刊:Fuel
[Elsevier]
日期:2023-07-01
卷期号:343: 127944-127944
被引量:2
标识
DOI:10.1016/j.fuel.2023.127944
摘要
The release characteristics of inorganic minerals during the thermochemical transformation of organic solid wastes are one of the key issues for their resource utilization. This study concentrated on the chemical structure of three kinds of industrial lignin and the release pattern and mechanism of alkali metal elements during heat treatment by means of 13C NMR, FTIR, XRD, SEM, and chemical thermodynamic equilibrium simulation. The microstructures of the three lignin samples were studied using 13C NMR and FTIR. The three lignin samples contained much more aliphatic and aromatic carbon than carbonyl carbon, and the aliphatic carbon moieties contained the most oxygenated carbon. The lignin samples mainly had aromatic molecular structures with aromaticity (fa) of 55.76% (sodium lignin sulfonate, SL), 52.62% (calcium lignin sulfonate, CL), and 63.93% (de-alkalized lignin, DL), respectively. Carbonyl content in DL was lower than lignin sulfonate SL and CL. The benzene ring content of SL was lower than the other two lignin samples. Na+ metal salts promoted the pyrolysis of lignin samples, while Ca2+ metal salts inhibited the pyrolysis of lignin samples. Microstructural studies showed that the structure of SL evolved from columnar and granular coexistence breaking into filamentous protrusions and lamellar structures with the increase of pyrolysis temperature. The CL and DL samples became ash presented in granular state and the particle size continued to become smaller with increasing temperature as the distribution gap became larger. The chemical thermodynamic equilibrium calculations showed that the variation in the initial concentrations of Na+ and Ca2+ in the three lignin samples led to different release characteristics of the three lignin samples. Na+ release rate was higher than that of Ca2+, and the valence state of the metal ions was an important reason for this phenomenon. This study provides data support and theoretical basis for the migration and release pattern of alkali metal during the thermal conversion reaction of organic solid waste applications.
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