Conventional pyrolysis of beech wood has been carried out for heating temperatures in the range 600-900 K, reproducing conditions of interest in countercurrent fixed-bed gasification. The yields of liquids (water and tars) increase with the heating temperature from about 40 to 55% of dry wood mass, confirming results previously obtained with a laboratory-scale gasifier. Apart from qualitative identification of 90 species, GC/MS techniques have been applied to quantify 40- 43% of tars (40 species, with major contributions from acetic acid, hydroxypropanone, hydroxyacetaldehyde, levoglucosan, formic acid, syringol, and 2-furaldehyde). Decomposition of holocellulose leads to the formation of furan derivatives and carbohydrates, with a temperaturedominated selectivity toward hydroxyacetaldehyde against levoglucosan. Syringols and guaiacols, originating from primary degradation of lignin, present a maximum for heating temperatures of about 750-800 K whereas, owing to secondary degradation, phenols continuously increase. A comparison is also provided with fast pyrolysis liquids obtained from four commercial plants.

GC/MS Characterization of Liquids Generated from Low-Temperature Pyrolysis of Wood

Carmen Branca;
2003

Abstract

Conventional pyrolysis of beech wood has been carried out for heating temperatures in the range 600-900 K, reproducing conditions of interest in countercurrent fixed-bed gasification. The yields of liquids (water and tars) increase with the heating temperature from about 40 to 55% of dry wood mass, confirming results previously obtained with a laboratory-scale gasifier. Apart from qualitative identification of 90 species, GC/MS techniques have been applied to quantify 40- 43% of tars (40 species, with major contributions from acetic acid, hydroxypropanone, hydroxyacetaldehyde, levoglucosan, formic acid, syringol, and 2-furaldehyde). Decomposition of holocellulose leads to the formation of furan derivatives and carbohydrates, with a temperaturedominated selectivity toward hydroxyacetaldehyde against levoglucosan. Syringols and guaiacols, originating from primary degradation of lignin, present a maximum for heating temperatures of about 750-800 K whereas, owing to secondary degradation, phenols continuously increase. A comparison is also provided with fast pyrolysis liquids obtained from four commercial plants.
2003
Istituto di Ricerche sulla Combustione - IRC - Sede Napoli
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/7476
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