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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Hydrated fractions of cellulosics probed by infrared spectroscopy coupled with dynamics of deuterium exchange

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Autor(es):
Driemeier, Carlos [1] ; Mendes, Fernanda M. [1] ; Ling, Liu Yi [1]
Número total de Autores: 3
Afiliação do(s) autor(es):
[1] Lab Nacl Ciencia & Tecnol Bioetanol CTBE CNPEM, BR-13083970 Sao Paulo - Brazil
Número total de Afiliações: 1
Tipo de documento: Artigo Científico
Fonte: Carbohydrate Polymers; v. 127, p. 152-159, AUG 20 2015.
Citações Web of Science: 2
Resumo

This article presents a novel method to selectively probe the non-crystalline, hydrated fractions of cellulosic biomass. The method is based on time-resolved infrared spectra analyzed to provide information on spectral and dynamical features of deuterium exchange (OH -> OD) in D2O atmosphere. We assign deuterium exchange spectral regions (700-3800 cm(-1)) and explore changes due to relative humidity, different cellulosic samples, and infrared polarization. Here, two results are highlighted. First, a wide range of celluloses isolated from plants show remarkable spectral similarities whatever the relative amounts of cellulose and xylan. This result supports an inherent type of hydrated disorder which is mostly insensitive to the molecular identities of the associated polysaccharides. Second, polarized infrared analysis of cotton reveals hydrated cellulose having chains preferentially aligned with those of crystals, while the hydroxyls of hydrated cellulose present much more randomized orientation. Our results provide new insights on molecular and group orientation and on hydrogen bonding in hydrated fractions of cellulosic biomass. (C) 2015 Elsevier Ltd. All rights reserved. (AU)

Processo FAPESP: 13/07932-6 - Componentes desordenados de lignoceluloses: caracterização por espectroscopia de infravermelho associada à dinâmica de troca isotópica
Beneficiário:Carlos Eduardo Driemeier
Modalidade de apoio: Auxílio à Pesquisa - Regular