GB1117327A - Poly-(phenylene oxides) - Google Patents

Poly-(phenylene oxides)

Info

Publication number
GB1117327A
GB1117327A GB3424465A GB3424465A GB1117327A GB 1117327 A GB1117327 A GB 1117327A GB 3424465 A GB3424465 A GB 3424465A GB 3424465 A GB3424465 A GB 3424465A GB 1117327 A GB1117327 A GB 1117327A
Authority
GB
United Kingdom
Prior art keywords
polymer
oxide units
chlorophenol
pyridine
percent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB3424465A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
3M Co
Original Assignee
Minnesota Mining and Manufacturing Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Minnesota Mining and Manufacturing Co filed Critical Minnesota Mining and Manufacturing Co
Publication of GB1117327A publication Critical patent/GB1117327A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/34Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
    • C08G65/38Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols

Abstract

The invention comprises amorphous poly-(phenylene oxides) containing from 0 to 75 mole per cent para-phenylene oxide units with the remainder being ortho-phenylene oxide units, in which up to 30% of the units may carry the side groups phenyl, carbonylaryl or sulphonylaryl, the polymer having a softening range below 150 DEG C., an inherent viscosity measured as a 1% solution of polymer in sulphuric acid of at least 0.3, complete solubility in benzene at 25 DEG C., and a temperature of at least 500 DEG C. for a 10% weight loss in air, as determined by Thermogravimetric Analysis at a rate of temperature rise of 5 DEG C. per minute. The polymers are prepared from very pure potassium o- and p-chlorophenolates containing not more than 0.05% of water, in the presence of 0.01 to 0.5 mole per cent of a cuprous or cupric salt and of 2 to 100 weight per cent of pyridine or quinoline, in the absence of oxygen and air, by heating to 160 DEG to 175 DEG C. for 2 to 24 hours and then at 200 DEG to 275 DEG C. for one or more hours. The molecular weight of the polymer may be increased by dissolving it in a solvent and oxidizing with sodium hypochlorite or lead tetraacetate, or with oxygen and cuprous chloride or potassium ferricyanide, or with lead dioxide and caustic alkali. The polymer may be cured by heating with dicumyl peroxide, di-t-butyl peroxide, benzoyl peroxide, lauroyl peroxide or azobisiso-butyronitrile. In examples, the purified potassium salts of p-chlorophenol, o-chlorophenol, 2 - chloro - 4 - phenyl phenol, 2 - chloro - 6-phenyl phenol, 2 - benzenesulphonyl - 4 - chlorophenol and 2 - benzoyl - chlorophenol, are heated in the presence of cuprous chloride and pyridine (in some instances pyridine is present in some of the monomers as pyridine of crystallization); the molecular weight of two polymers is increased by reacting them in solution with sodium hypochlorite and with cuprous chloride and oxygen.ALSO:Polyphenylene oxide polymers containing 0 to 75 mole percent paraphenylene oxide units with the remainder being ortho-phenylene oxide units, in which up to 30 percent of the units may carry the side groups phenyl, carboxyl aryl or sulphonyl aryl, may be coated on metal, ceramic, glass, plastics and laminate surfaces. In an Example a polymer containing 60 percent para- and 40 percent ortho-phenylene oxide units is dissolved in methylene chloride and xylene, t-butyl peroxide is added and the composition is coated on aluminium sheet and heated.
GB3424465A 1964-08-28 1965-08-10 Poly-(phenylene oxides) Expired GB1117327A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US39293764A 1964-08-28 1964-08-28

Publications (1)

Publication Number Publication Date
GB1117327A true GB1117327A (en) 1968-06-19

Family

ID=23552628

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3424465A Expired GB1117327A (en) 1964-08-28 1965-08-10 Poly-(phenylene oxides)

Country Status (2)

Country Link
DE (1) DE1570992A1 (en)
GB (1) GB1117327A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997028905A1 (en) * 1996-02-12 1997-08-14 Akzo Nobel N.V. Heat treatment of polyphenylene oxide-coated metal

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997028905A1 (en) * 1996-02-12 1997-08-14 Akzo Nobel N.V. Heat treatment of polyphenylene oxide-coated metal

Also Published As

Publication number Publication date
DE1570992A1 (en) 1970-03-19

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