Complexes of starch polysaccharides and poly(ethylene co-acrylic acid): Structure and stability in solution
β Scribed by R. L. Shogren; R. V. Greene; Y. V. Wu
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 698 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
SYNOPSIS
Chiroptical methods have been used to study the conformation and interactions of amylose and amylopectin with poly( ethylene co-acrylic acid) (EAA) in aqueous solution. These studies, along with X-ray diffraction and solid-state NMR data, show that amylose and EAA, as well as amylopectin and EAA, form helical V-type inclusion complexes when mixed in aqueous suspension. This structure apparently accounts for the partial compatibility observed in films containing starch and EAA. About 3 by weight of EAA does not interact with amylose and probably represents the ethylene-rich central core of the EAA micelle. EAA/amylose complexes in 10 m M NaOH were stable to temperatures > 90Β°C, whereas EAA/ amylopectin complexes in the same solvent were largely disrupted a t this temperature. Urea, at a concentration of 8 M, further destabilized both EAA/amylopectin and EAA/amylose complexes. Solutions with an alkaline pH (> 9.5) dispersed EAA optimally and allowed maximum complexing with amylose. At pH values > 13, the EAA/ amylose complexes were weaker, most likely due to electrostatic repulsion between ionized hydroxyl groups of amylose and carboxyl groups of EAA.
(1988). (1984).
π SIMILAR VOLUMES
## SYNOPSIS X-ray diffraction, CP/MAS C-13 NMR, DSC, FTIR and fluorescence microscopy have been used to study the structure, compatibility, and morphology of films made from starch, poly (ethylene-co-acrylic acid) (EAA), and polyethylene (PE) before and after exposure to a mixture of highly amylol
Interpolymer reactions between poly(acrylic acid) and poly(vinyl ether) of ethylene glycol were studied by viscometric and spectroturbidimetric methods in aqueous and organic solutions of different nature. It is shown that the formation of interpolymer complexes strongly depends on the strength of t