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Journal ArticleDOI

A unified, global model for the pyrolysis of cellulose

James P. Diebold
- 01 Jan 1994 - 
- Vol. 7, Iss: 1, pp 75-85
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TLDR
In this article, the authors present cellulose pyrolysis as a comprehensible interaction of time, temperature, and pressure, and develop a mathematical model to predict results and trends observed in both slow and fast reactions.
Abstract
Complex interactions occur between the many competing and sequential chemical reactions during the pyrolysis of cellulose, making the prediction of the pyrolysis products relatively difficult. The purpose of this paper is to present cellulose pyrolysis as a comprehensible interaction of time, temperature and pressure. Appropriate kinetic data for seven first-order global reactions for the pyrolysis of cellulose were found in the literature. A mathematical model was developed, in which the seven reactions occurred simultaneously so long as the feedstock for the particular reaction existed. The seven differential equations representing the reaction rates were numerically integrated simultaneously to obtain the products of pyrolysis as a function of time, temperature, heating rate and pressure. This program was used to predict many results and trends observed in both slow and fast pyrolysis: very high yields of condensible vapors (primary oils) were predicted under high heating rates to modest final temperatures; high char yields were predicted for slow heating rates at low temperatures; high gas yields were predicted for fast pyrolysis at high temperatures.

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Citations
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Journal ArticleDOI

Synthesis of transportation fuels from biomass: chemistry, catalysts, and engineering.

TL;DR: Hydrogen Production by Water−Gas Shift Reaction 4056 4.1.
Journal ArticleDOI

Lignocellulosic biomass pyrolysis mechanism: A state-of-the-art review

TL;DR: A broad review of the state-of-the-art biomass pyrolysis research can be found in this article, where three major components (cellulose, hemicellulose and lignin) are discussed in detail.
Journal ArticleDOI

Biomass pyrolysis kinetics: A comparative critical review with relevant agricultural residue case studies

TL;DR: A critical review of kinetic models and mathematical approximations currently employed in solid state thermal analysis is provided and analysis of thermal decomposition data obtained from two agricultural residues, nutshells and sugarcane bagasse reveals the inherent difficulty and risks involved in modeling heterogeneous reaction systems.
Journal ArticleDOI

Thermal decomposition kinetics of natural fibers: Activation energy with dynamic thermogravimetric analysis

TL;DR: In this article, a dynamic TG analysis under nitrogen was used to investigate the thermal decomposition processes of 10 types of natural fibers commonly used in the polymer composite industry, including wood, bamboo, agricultural residue, and bast fibers.
Journal ArticleDOI

Kinetics and mechanism of cellulose pyrolysis

TL;DR: In this article, the authors report the kinetics and chemistry of cellulose pyrolysis using both a Pyroprobe reactor and a thermogravimetric analyzer mass spectrometer (TGA-MS).
References
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Journal ArticleDOI

Molecular characterization of the pyrolysis of biomass

Robert J. Evans, +1 more
- 01 Mar 1987 - 
TL;DR: Application de la spectrometrie de masse a faisceau a l'etude des mecanismes moleculaires de la pyrolyse du bois and de ses principaux constituants (cellulose, lignine et hemicellulose).
Journal ArticleDOI

A kinetic model for pyrolysis of cellulose.

TL;DR: In this article, it was shown that the pyrolysis of cellulose at low pressure (1.5 Torr) can be described by a three reaction model, where an initialization reaction leads to formation of an active cellulose which subsequently decomposes by two competitive first-order reactions, one yielding volatiles and the other char and a gaseous fraction.
Journal ArticleDOI

Thermal degradation of cellulose in air and nitrogen at low temperatures

TL;DR: This paper showed that at temperatures above 300°C, the rate of pyrolysis is essentially the same in both air and nitrogen, indicating that thermal degradation is independent of the oxidative reactions.
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