The thermal decompositions of sugarcane bagasse and waste-wood samples are studied using thermogravimetric analysis. Assuming the addition of three independent parallel decompositions, these corresponding to three pseudocomponents linked to the hemicellulose, cellulose, and lignin, the weight loss associated with the pyrolysis process is simulated. First, an irreversible firstorder reaction model is assumed for each pseudocomponent. Results show that the modelsimulated curves do not fit well to the experimental data. Consequently, a further kinetic study is carried out for the pure lignin (Kraft alkali lignin), which demonstrates that the pyrolysis of lignin is better described by a third-order reaction rate law. The reformulation of the lignin kinetic model, and its subsequent implementation in the summative model (for the third pseudocomponent), has allowed one to reach a good agreement between simulated and experimental data.

A fibrous form of poly d(A):poly d(T) has a heteronomous secondary structure which is the first to be confirmed for a polynucleotide duplex: although both chains are 10(1) helices, mutually hydrogen-bonded in the standard (Watson-Crick) fashion, each has a quite different conformation. One chain -- probably poly d(A) -- has C3'-endo-puckered furanose rings characteristic of the A family of polynucleotide secondary structures while the other -- probably poly d(T) -- has the C2'-endo-puckered rings of the B family. Since analogous heteronomous structures could be assumed by DNA-DNA or DNA-RNA duplexes containing more general base sequences the polymorphic range of polynucleotide double-helices may be even greater than we have come to suppose.

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