POLY(2,6-DIMETHYL-1,4-PHENYLENE OXIDE) manufacturers
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| | POLY(2,6-DIMETHYL-1,4-PHENYLENE OXIDE) Basic information |
| Product Name: | POLY(2,6-DIMETHYL-1,4-PHENYLENE OXIDE) | | Synonyms: | 2,6-dimethyl-phenohomopolymer;Phenol,2,6-dimethyl-,homopolymer;POLY(2,6-DIMETHYL-1,4-PHENYLENE OXIDE);POLY(2,6-DIMETHYLENE-P-PHENYLENE OXIDE);POLY(2,6-DIMETHYL-P-PHENYLENE OXIDE);2,6-DIMETHYL-1,4-PHENYLENE OXIDE POLYMER;POLY(2,6-DIMETHYL-1,4-PHENYLENE OXIDE), SECONDARY STANDARD;Poly(2,6-dimethyl-1,4-phenylene oxide), approx. M.W. 50,000 | | CAS: | 25134-01-4 | | MF: | C8H10O | | MW: | 122.1644 | | EINECS: | | | Product Categories: | Poly(phenylene oxide) Thermoplastic Resins;Engineering Polymers;Polymer Science;Polymers | | Mol File: | 25134-01-4.mol |  |
| | POLY(2,6-DIMETHYL-1,4-PHENYLENE OXIDE) Chemical Properties |
| Melting point | 258-261 °C | | density | 1.06 g/mL at 25 °C(lit.) | | form | powder | | InChI | InChI=1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3 | | InChIKey | NXXYKOUNUYWIHA-UHFFFAOYSA-N | | SMILES | C1(O)=C(C)C=CC=C1C | | EPA Substance Registry System | Phenol, 2,6-dimethyl-, homopolymer (25134-01-4) |
| WGK Germany | 3 | | TSCA | TSCA listed | | Storage Class | 11 - Combustible Solids |
| | POLY(2,6-DIMETHYL-1,4-PHENYLENE OXIDE) Usage And Synthesis |
| Chemical Properties | white to off-white powder | | Chemical Properties | Poly(2,6-dimethyl-l,4-phenylene oxide) is characterized by high tensile
strength, stiffness, impact strength and creep resistance; it also has good
dielectric properties. These properties are maintained over a broad temperature
range (about -45-120°C). The polymer is self-extinguishing. The polymer
has a high glass-transition temperature (Tg = 208°C) which restricts
crystallization in normal moulding techniques. Crystalline material may be
obtained by heating the amorphous material or from solutions. One notable
feature of the polymer is its good dimensional stability; it has a very low
coefficient of thermal expansion and low water absorption.
Poly(2,6-dimethyl-l,4-phenylene oxide) is soluble in aromatic hydrocarbons
and chlorinated solvents and several aliphatic hydrocarbons cause
environmental stress cracking. The polymer is outstandingly resistant to
most aqueous reagents, being unaffected by acids, alkalis and detergents. | | Uses | At the present time, most poly(2,6-dimethyl-l,4-phenylene oxide) intended
for commercial use is blended with polystyrene (principally in the form of
high-impact polystyrene). The two materials are miscible over the complete
composition range. The effect of blending is to facilitate melt-processing (by
lowering melt viscosity) and to lower cost whilst the desirable properties of
the straight polymer are largely retained. In one recent product, the polystyrene
is grafted on to the polyether. Polystyrene-modified poly(2,6-
dimethyl-l,4-phenylene oxide) (commonly referred to as PPO) has found a
variety of uses, which include telecommunication and business equipment
housings and components and automotive parts. | | Uses | Imidazolium modified PPO with liquid ionic graphene oxide can be used as an anion exchange membrane (AEM) composite with a peak power density of 136 mW cm2 for use in the fabrication of high performance fuel cells. It may also be sulfonated to form a long chained polymeric structure with an efficiency of 81.8% at a current density of 120 mA cm2 for potentiall use in vanadium redox flow batteries (VRFBs) as effective energy storage systems. It may also be used in the formation of AEMs, which can be used in the development of microbial desalination cell system (MDCS). | | Preparation | Oxidative coupling is readily accomplished by passing oxygen into a reaction
mixture containing 2,6-xylenol, pyridine and cuprous chloride. (The molar
ratio of pyridine to cuprous ion is generally in the range 10: 1 to 100: 1.)
External heating is unnecessary; during the course of the reaction the
temperature rises to about 70C. The polymer is precipitated with dilute
hydrochloric acid and collected by filtration.
It is generally accepted that aryloxy radicals are intermediates in the
polymerization reaction since ESR studies have shown the presence of both
monomeric and polymeric aryloxy radicals in polymerizing solutions of 2,6-
xylenol. The simplest mechanism that can be suggested for the reaction is
aromatic substitution:
| | Definition | ChEBI: 2,6-Dimethylphenol is a hydroxytoluene. | | General Description | Poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) is an anion exchange membrane (AEM) material that is mainly used as a cross-linker in which the methyl groups are used to bond with ultraviolet (UV) excited ketones. |
| | POLY(2,6-DIMETHYL-1,4-PHENYLENE OXIDE) Preparation Products And Raw materials |
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