Poly(ethylene terephthalate) (PET) was synthesized by self-condensation of bis-(2-hydroxyethyl) terephthalate (BHET). Copolymerization of BHET with ethyl, bis-3,5-(2-hydroxyethoxy) benzoate (EBHEB) and ethyl, 3-(2-hydroxyethoxy) benzoate (E3HEB) yielded copolymers that contain varying amounts of bra
Synthesis and Characterisation of Branched Poly(ethylene terephthalate)
β Scribed by Rosu, Ruxandra F.; Shanks, Robert A.; Bhattacharya, Sati N.
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 387 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0959-8103
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β¦ Synopsis
Branched poly(ethylene terephthalate)s (PET) were synthesised with a variety of molar masses and with a large range of degree of branching by introduction of mono-, tri-(glycerol) and tetra-functional (pentaerythritol) comonomers to dimethyl terephthalate and ethylene glycol. The monofunctional alcohols, dodecanol and benzyl alcohol, were used as terminating agents to minimise gelation. The e β ect of various reaction parameters, such as percentage glycerol or pentaerythritol and polymerisation time, on limiting viscosity number [g] and weight average molar mass were investigated. The thermal behaviour (M 1 w ) of branched PET was studied by di β erential scanning calorimetry ; all samples showed a characteristic double endothermic melting peak and the glass transition temperature was not observed. Some branched PETs were subjected to solid-state polymerisation to increase the molar mass of previously prepared branched polymers. The solid-state polymerisation technique showed that the process not only promoted the molar mass but, more importantly, it increased the crystallinity of the polymer. Overall, the solid-state reaction rate was governed by initial molar mass, crystallinity, reaction temperature and time.
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Branched poly(ethylene terephthalate)s (BPET) of varying molar mass have been synthesized with glycerol and pentaerythritol as branching comonomers, and their rheological behaviour has been measured. In this study, we describe the use of dynamic and steady shear measurements to examine the inΒ―uence
## Abstract Poly(ethylene isophthalateβ__co__βethylene terephthalate) (PEIPET) copolymers of various compositions and molecular weights were synthesized by melt polycondensation and characterized in terms of chemical structure and thermal and rheological properties. At room temperature, all copolym
A series of branched poly(ethylene terephthalate) samples was prepared by employing 0.07-0.42 mol % trimethylolpropane (TMP) for melt polycondensation. These polymers were characterized with respect to molar mass, intrinsic viscosity, and melt viscosity. Spinning into fibers took place at spinning s
The effect of branching on the crystallization behavior of poly(ethylene terephthalate) has been examined by nonisothermal crystallization studies, using DSC. It was found that branching causes a significant change in the crystallization behavior, in that the Avrami exponent n lies between 1 and 2,