Microwave-Assisted Derivatization of Cellulose in an Ionic Liquid: An Efficient, Expedient Synthesis of Simple and Mixed Carboxylic Esters


Autoria(s): POSSIDONIO, Shirley; FIDALE, Ludmila C.; SEOUD, Omar A. El
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Microwave (MW)-assisted cellulose dissolution in ionic liquids (ILs) has routinely led either to incomplete biopolymer solubilization, or its degradation. We show that these problems can be avoided by use of low-energy MW heating, coupled with efficient stirring. Dissolution of microcrystalline cellulose in the IL 1-allyl-3-methylimidazolium chloride has been achieved without changing its degree of polymerization; regenerated cellulose showed pronounced changes in its index of crystallinity, surface area, and morphology. MW-assisted functionalization of MCC by ethanoic, propanoic, butanoic, pentanoic, and hexanoic anhydrides has been studied. Compared with conventional heating, MW irradiation has resulted in considerable decrease in dissolution and reaction times. The value of the degree of substitution (DS) was found to be DS(ethanoate) > DS(propanoate) > DS(butanoate). The values of DS(pentanoate) and DS(hexanoate) were found to be slightly higher than DS(ethanoate). This surprising dependence on the chain length of the acylating agent has been reported before, but not rationalized. On the basis of the rate constants and activation parameters of the hydrolysis of ethanoic, butanoic, and hexanoic anhydrides in aqueous acetonitrile (a model acyl transfer reaction), we suggest that this result may be attributed to the balance between two opposing effects, namely, steric crowding and (cooperative) hydrophobic interactions between the anhydride and the cellulosic surface, whose lipophilicity has increased, due to its partial acylation. Four ethanoate-based mixed esters were synthesized by the reaction with a mixture of the two anhydrides; the ethanoate moiety predominated in all products. The DS is reproducible and the IL is easily recycled. (C) 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 134-143, 2010

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP

CNPq

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CAPES-DAAD[256/2009]

DAAD

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Identificador

JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, v.48, n.1, p.134-143, 2010

0887-624X

http://producao.usp.br/handle/BDPI/31391

10.1002/pola.23770

http://dx.doi.org/10.1002/pola.23770

Idioma(s)

eng

Publicador

JOHN WILEY & SONS INC

Relação

Journal of Polymer Science Part A-polymer Chemistry

Direitos

restrictedAccess

Copyright JOHN WILEY & SONS INC

Palavras-Chave #1-allyl-3-(1-butyl)ismidazolium chloride #biomaterials #biopolymers #carboxylic anhydride, hydrolysis of #cellulose carboxylic esters #cellulose mixed esters #cellulose solution in ionic liquids #cellulose, microwave-assisted acylation #cellulose, microwave-assisted dissolution #esterification #ionic liquids #microwave #polysaccharides #structure-reactivity #DILUTE-SOLUTION PROPERTIES #1-ALLYL-3-METHYLIMIDAZOLIUM CHLORIDE #RHEOLOGICAL PROPERTIES #REACTION VELOCITIES #ORGANIC-SYNTHESIS #ACID ANHYDRIDES #ALKYL-GROUPS #SOLVENT #DISSOLUTION #DERIVATIVES #Polymer Science
Tipo

article

original article

publishedVersion