Polymer Interdiffusion vs Cross-Linking in Carboxylic Acid−Carbodiimide Latex Films

1999 ◽  
Vol 32 (22) ◽  
pp. 7692-7695 ◽  
Author(s):  
Hung H. Pham ◽  
Mitchell A. Winnik
Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4445
Author(s):  
Tiphaine Wong ◽  
Lorette Brault ◽  
Eric Gasparotto ◽  
Romuald Vallée ◽  
Pierre-Yves Morvan ◽  
...  

Marine polysaccharides are part of the huge seaweeds resources and present many applications for several industries. In order to widen their potential as additives or bioactive compounds, some structural modifications have been studied. Among them, simple hydrophobization reactions have been developed in order to yield to grafted polysaccharides bearing acyl-, aryl-, alkyl-, and alkenyl-groups or fatty acid chains. The resulting polymers are able to present modified physicochemical and/or biological properties of interest in the current pharmaceutical, cosmetics, or food fields. This review covers the chemical structures of the main marine polysaccharides, and then focuses on their structural modifications, and especially on hydrophobization reactions mainly esterification, acylation, alkylation, amidation, or even cross-linking reaction on native hydroxyl-, amine, or carboxylic acid functions. Finally, the question of the necessary requirement for more sustainable processes around these structural modulations of marine polysaccharides is addressed, considering the development of greener technologies applied to traditional polysaccharides.


Holzforschung ◽  
2006 ◽  
Vol 60 (1) ◽  
pp. 47-52 ◽  
Author(s):  
Francisco López-Suevos ◽  
Charles E. Frazier

Abstract Parallel-plate rheological analysis was conducted on two types of cross-linking poly(vinyl acetate) latex films: dry freestanding films, and dry films bonded directly to wood (composites). For each sample type, three levels of cross-linking were used: (1) little or no cross-linking of unaltered latex; (2) substantial cross-linking through AlCl3 catalysis of N-methylolacrylamide co-monomer; and (3) greater cross-linking from a phenol-formaldehyde resol additive, in addition to AlCl3 catalysis. Simple thermal scans revealed a strong wood/adhesive interaction; wood increased the base polymer T g by ∼5°C in all adhesives. Relative to the simple thermal scans, time-temperature master curves provided more insight and information about the wood/adhesive interaction. Storage modulus and tan δ master curves both indicated that wood retarded adhesive cross-linking. Using time-temperature superposition, a segmental coupling analysis demonstrated that wood actually narrowed the breadth of the glass transition, or reduced segmental coupling. Cross-linking influenced segmental coupling, but in a fashion that was dependent on the presence or absence of wood. Wood-induced reductions in cross-linking and in segmental coupling were attributed to the diffusion of water-soluble reactive compounds away from the adhesive layer and into the bulk wood. Time/temperature equivalence provides a sensitive means to detect interactions between wood and viscoelastic adhesives.


2001 ◽  
Vol 11 (3) ◽  
pp. 736-740 ◽  
Author(s):  
Robert A. Hunter ◽  
Peter D. Turner ◽  
Stephen Rimmer

2022 ◽  
Vol 164 ◽  
pp. 106691
Author(s):  
Yang Liu ◽  
Kenneth Tran ◽  
Kevin Ho ◽  
Jessica Emsermann ◽  
Margaret Zhang ◽  
...  

2004 ◽  
Vol 37 (16) ◽  
pp. 6141-6152 ◽  
Author(s):  
Florence Mazuel ◽  
Chuong Bui ◽  
Bernadette Charleux ◽  
Eva Cabet-Deliry ◽  
Mitchell A. Winnik
Keyword(s):  

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