کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
210032 461697 2013 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Study on carbonization of lignin by TG-FTIR and high-temperature carbonization reactor
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
Study on carbonization of lignin by TG-FTIR and high-temperature carbonization reactor
چکیده انگلیسی

Biomass charcoal is dominantly made from lignin. It is necessary to study lignin carbonization process to improve the quality of biomass charcoal. A Thermo-Gravimetric Analyzer coupled with a Fourier Transform Infrared Spectrometry (TG-FTIR) was applied to investigate the kinetics of lignin carbonization. Three mass loss stages (drying, pyrolysis and carbonization) were observed below 900 °C and another stage (structural rearrangement stage) with a slight mass loss was noticed between 900 and 1200 °C. Charcoal obtained at different temperatures was analyzed by FTIR to track the variation of functional groups. The pyrolysis of lignin started at 200 °C and charcoal was initially formed till 500 °C together with the intensive evolution of volatiles including various phenyl compounds. Amorphous carbon was formed between 500 and 900 °C, while most benzene rings structures were transformed into aromatic structures with emission of CO. When the temperature increased from 900 °C to 1400 °C, most CC bonds were cleaved and a new charcoal structure, between amorphous carbon and graphite structures, was probably formed. The activation energies of the above three stages were estimated to be 54 kJ/mol, 70 kJ/mol and 178 kJ/mol.


► Pyrolysis, amorphous carbon forming and structure reforming are important stages.
► Amorphous carbon formed at 500 ~ 900 °C as benzene rings became aromatic structure.
► A structure between amorphous carbon and graphite appeared at 900 ~ 1400 °C.
► Most CC bonds broke when the temperature increased from 900 to 1400 °C.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Fuel Processing Technology - Volume 106, February 2013, Pages 41–47
نویسندگان
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