Chemical Modification of a Poly(ethylene terephthalate) Surface by the Selective Alkylation of Acid Salts
β Scribed by Jun Li; Yasunari Maekawa; Tetsuya Yamaki; Masaru Yoshida
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 112 KB
- Volume
- 203
- Category
- Article
- ISSN
- 1022-1352
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β¦ Synopsis
Abstract
Chemical modification of the hydrophilic surface of poly(ethylene terephthalate) (PET) was examined by the selective alkylation of the acid salt on the surface using acyl bromides as an electrophile with catalytic potassium fluoride. The hydrophobicity of the PET surface increased as the alkylation reaction of the hydrolyzed surface proceeded. The chemical incorporation of the alkylation reagents was confirmed by the presence of fluorine peaks in Xβray photoelectron spectroscopy (XPS) from the fluorinated reagents. Exponential increases were observed in the emission and excitation intensities of fluorescence spectra during the reaction of the surface with a fluorescent reagent. This indicated that the esterification of carboxylic acids on the surface proceeded without deterioration of the reaction even at the later stages. The relation between changes in contact angles and the fluorescence spectra revealed that the hydrophobicity of a surface was quickly restored at the beginning of a reaction.
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π SIMILAR VOLUMES
Six organic solvents with solubility parameters close to those of poly(ethy1ene terephthalate) (PET), namely, dimethyl sulfoxide, y-butyrolactone, dimethyl formamide, pyridine, tetrachlorethane, and chlorobezene, were selected as swelling agents to promote the incorporation and the subsequent polyme
Blends of carboxyl functionalized poly(phenylene sulfide) (PPS) and poly-(ethylene terephthalate) (PET) were shown to undergo an ester interchange reaction during melt blending. Pendent carboxyl functionality randomly incorporated along the PPS chain reacts with the ester moiety of PET to form a gra