In this article, the chemical modification of poly(2,6-dimethyl-l,4-phenylene oxide) (PPO) was carried out by incorporating a n amine group into the PPO backbone. A maximum monosubstitution degree of 65 mol % was reached. The effects of reaction conditions on the functional group content in PPO is d
Synthesis and characterization of poly[(2,6-dimethyl-1,4-phenylene oxide)-block-isoprene] diblock copolymers
✍ Scribed by Emmanuelle Servens; Dennis Löwik; Anton Bosman; Laurent Nelissen; Piet J. Lemstra
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 821 KB
- Volume
- 198
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
As a first stage in the synthesis of a new class of thermoplastic elastomers, a suitable synthetic route for elastomeric tailor‐made diblock copolymers based on poly(2,6‐dimethyl‐1,4‐phenylene oxide), PPE, as the thermoplastic block and on 1,4‐polyisoprene, PIP, as the elastomeric block, is outlined. The 2,6‐dimethyl‐1,4‐phenylene oxide‐block‐isoprene diblock copolymers were synthesized via an amidation coupling route between the ammonium salt of PPE and the monocarboxylic acid of PIP in the presence of dicyclohexylcarbodiimide, DCC. Preliminary studies were focused on the synthesis of a welldefined low molar mass diblock copolymer (M~n~ = 10000) in order to facilitate the quantitative characterization by proton NMR spectroscopy. The developed amidation coupling route was successively applied to the synthesis of a similar diblock copolymer with a number‐average molar mass of 40000 in order to obtain optimum overall properties.
📜 SIMILAR VOLUMES
Poly(2,6-dimethyl-1,4 -phenylene oxide) (PPO) is a chemically resistant polymer and, therefore, an attractive material for the formation of membranes. However, membranes of unmodified PPO prepared by an immersion precipitation possess very low hydraulic permeabilities at the filtration processes. T
## Abstract A series of poly(ether–ester) copolymers were synthesized from poly(2,6 dimethyl‐1,4‐phenylene oxide) (PPO) and poly(ethylene terephthalate) (PET). The synthesis was carried out by two‐step solution polymerization process. PET oligomers were synthesized via glycolysis and subsequently u
Dicarboxy-terminated poly(2,6-dimethyl-l ,Cphenylene oxide) (PPO) macromonomers were prepared and subjected to the preparation of tailor-made aromatic thermotropic liquid-crystalline (LC) polyester-graft-PPO copolymers. The macromonomers were obtained by hydrolysis of dimethyl carboxylate-terminated
The thermal degradation and kinetics of poly(2,6-dimethylphenylene oxide) (PPO) were studied by high-resolution thermogravimetry. The thermogravimetry measurements were conducted at an initial heating rate of 50°C min Ϫ1 , resolution 4.0, and sensitivity 1.0 in both nitrogen and air from room temper