New Technology for Solid-state Polymerization of Polymers: Polyethylene terephthalate–Solid-state Polyaddition
✍ Scribed by Hussain Al Ghatta; Sandro Cobror; Tonino Severini
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 664 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1042-7147
No coin nor oath required. For personal study only.
✦ Synopsis
This article introduces the new M&G technology for Solid state polyaddition (SSPA) of polyethylene terephthalate (PET). The new SSPA is characterized by the following:
(1) It is based on a novel chemical process, SSPA.
(2) It is suitable for high-performance polyesters.
(3) It enables separate control of many different key properties of the polyester (molecular weight, rheology, crystallinity, etc.).
This intrinsic flexibility has already been exploited to produce tailor-made polyesters suitable for most important applications in packaging and related fields.
It is also a powerful tool for the upgrading of recycled PET.
The SSPA reaction has a much faster kinetic than the standard solid-state upgrading process so that accordingly the intrinsic viscosity (I.V.) built up in the solid state is much faster than that of solid-state polycondensation. This raises the possibility of solid-state upgrading at lower temperatures, where standard solid-state polycondensation reactions are barely noticeable.
The accelerating reactions used in this process could be utilized to de-bottleneck the existing production plants in order to attain greater productivity, more flexibility, lower costs and higher quality.
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## Abstract A simple kinetic model capable of describing the behaviors of solid‐state polymerization (SSP) of poly(ethylene terephthalate) (PET) has been developed. According to this model, there are two types of end groups, namely active end groups and inactive end groups, and the solid‐state poly
A mathematical model for solid-state polymerization of poly(ethylene terephthalate) was developed. The effects of temperature and chain entanglement on chain mobility were considered to estimate the rate constants of chemical reactions. The diffusivities of volatile byproducts could be determined us
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