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US5096979A Expired / Lapsed US ⏱️ 0.0 years remaining

Epoxytriazine-capped polyphenylene ethers and method of preparation

Assignee: SABIC Global Technologies BV
•
Filing: 1989-05-15
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Granted: 1992-03-17
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Expires: 2009-05-15
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Abstract

Abstract Epoxytriazine-capped polyphenylene ethers are prepared by reaction of a polyphenylene ether with an epoxychlorotriazine such as diglycidyl chlorocyanurate, n-butyl glycidyl chlorocyanurate or mesityl glycidyl chlorocyanurate. The products undergo reaction with nucleophilic polymers such as polyamides and polyesters, to form copolymer-containing compositions which have excellent properties and which find utility as molding compositions and as compatibilizers for blends of similar polymers.

Inventors

  • 👤 Sterling B. Brown
  • 👤 Richard C. Lowry

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-03 12:08
CPC Classifications
C; C08; C08L; C08L63/00; C08G; C08G59/00; C08G59/02; C08G59/04; C08G59/06; C08G59/063; C08G65/00; C08G65/34; C08G65/48; C08G65/485; C08L71/00; C08L71/08; C08L71/10; C08L71/12; C08L71/126; C08L67/00; C08L77/00; Y; Y10; Y10S; Y10S525/00; Y10S525/905

Claims Analysis

Total Claims: 22
Claim 1
Independent Claim 93 words
An epoxytriazine-capped polyphenylene ether composition comprising polymer molecules having end groups of the formula ##STR15## wherein: each Q 1 is independently halogen, primary or secondary lower alkyl, phenyl, haloalkyl, aminoalkyl, hydrocarbonoxy, or halohydrocarbonoxy wherein at least two carbon atoms separate the halogen and oxygen atoms; each Q 2 is independently hydrogen, halogen, primary or secondary lower alkyl, phenyl, haloalkyl, hydrocarbonoxy or halohydrocarbonoxy as defined for Q 1 ; X is an alkyl, cycloalkyl or aromatic radical or ##STR16## R 1 is a divalent aliphatic, alicyclic, heterocyclic or unsubstituted or substituted aromatic hydrocarbon radical.
Claim 2
Dependent Claim 93 words
An epoxytriazine-capped polyphenylene ether composition comprising polymer molecules having end groups of the formula ##STR15## wherein: each Q 1 is independently halogen, primary or secondary lower alkyl, phenyl, haloalkyl, aminoalkyl, hydrocarbonoxy, or halohydrocarbonoxy wherein at least two carbon atoms separate the halogen and oxygen atoms; each Q 2 is independently hydrogen, halogen, primary or secondary lower alkyl, phenyl, haloalkyl, hydrocarbonoxy or halohydrocarbonoxy as defined for Q 1 ; X is an alkyl, cycloalkyl or aromatic radical or ##STR16## R 1 is a divalent aliphatic, alicyclic, heterocyclic or unsubstituted or substituted aromatic hydrocarbon radical.
Claim 3
Dependent Claim 74 words
A composition according to claim 1 wherein the polyphenylene ether comprises a plurality of structural units having the formula ##STR17## wherein each Q 1 is independently halogen, primary or secondary lower alkyl, phenyl, haloalkyl, aminoalkyl, hydrocarbonoxy, or halohydrocarbonoxy wherein at least two carbon atoms separate the halogen and oxygen atoms; and each Q 2 is independently hydrogen, halogen, primary or secondary lower alkyl, phenyl, haloalkyl, hydrocarbonoxy or halohydrocarbonoxy as defined for Q 1 .
Claim 4
Dependent Claim 14 words
A composition according to claim 2 wherein R 1 is a lower alkylene radical.
Claim 5
Dependent Claim 14 words
A composition according to claim 3 wherein the polyphenylene ether is a poly(2,6-dimethyl-1,4-phenylene ether).
Claim 6
Dependent Claim 11 words
A composition according to claim 4 wherein R 1 is methylene.
Claim 7
Dependent Claim 16 words
A composition according to claim 5 wherein X is a lower alkyl or aromatic hydrocarbon radical.
Claim 8
Dependent Claim 13 words
A composition according to claim 6 wherein X is methyl, n-butyl or 2,4,6-trimethylphenyl.
Claim 9
Dependent Claim 11 words
A composition according to claim 5 wherein X has formula II.
Claim 10
Independent Claim 59 words
A method for preparing an epoxytriazine-capped polyphenylene ether composition which comprises contacting under reactive conditions, in the presence of a basic reagent, at least one polyphenylene ether with an epoxychlorotriazine of the formula ##STR18## wherein: X is an alkyl or aromatic radical or ##STR19## R 1 is a divalent aliphatic, alicyclic, heterocyclic or unsubstituted or substituted aromatic hydrocarbon radical.
Claim 11
Independent Claim 59 words
A method for preparing an epoxytriazine-capped polyphenylene ether composition which comprises contacting under reactive conditions, in the presence of a basic reagent, at least one polyphenylene ether with an epoxychlorotriazine of the formula ##STR18## wherein: X is an alkyl or aromatic radical or ##STR19## R 1 is a divalent aliphatic, alicyclic, heterocyclic or unsubstituted or substituted aromatic hydrocarbon radical.
Claim 12
Dependent Claim 14 words
A method according to claim 9 wherein the polyphenylene ether is a poly(2,6-dimethyl-1,4-phenylene ether.
Claim 13
Dependent Claim 38 words
A method according to claim 10 wherein the reaction is conducted in solution in a non-polar organic liquid at a temperature in the range of about 80°-150° C., and the basic reagent is soluble in the organic liquid.
Claim 14
Dependent Claim 18 words
A method according to claim 11 wherein the basic reagent is pyridine and the organic liquid is toluene.
Claim 15
Dependent Claim 38 words
A method according to claim 12 wherein the amount of epoxychlorotriazine is in the range of about 1-20% by weight, based on polyphenylene ether, and the amount of basic reagent is about 1.0-1.1 equivalent per mole of chloroepoxytriazine.
Claim 16
Dependent Claim 47 words
A method according to claim 10 wherein the reaction is conducted interfacially at a temperature in the range of about 20°-100° C., in a medium comprising water and a non-polar organic liquid, the basic reagent is a water-soluble base, and a phase transfer catalyst is also employed.
Claim 17
Dependent Claim 40 words
A method according to claim 14 wherein the basic reagent is sodium hydroxide, the organic liquid is toluene and the phase transfer catalyst is a tetraalkylammonium chloride wherein at least two alkyl groups per molecule contain about 5-20 carbon atoms.
Claim 18
Dependent Claim 50 words
A method according to claim 15 wherein the amount of epoxychlorotriazine is in the range of about 2-6% by weight based on polyphenylene ether, the ratio of equivalents of base to moles of epoxychlorotriazine is about 0.5-1.5:1, and the weight ratio of phase transfer catalyst to base is about 0.01-5.0.
Claim 19
Dependent Claim 17 words
A method according to claim 10 wherein the reaction mixture is subsequently neutralized with an acidic compound.
Claim 20
Dependent Claim 13 words
A method according to claim 17 wherein the acidic compound is carbon dioxide.
Claim 21
Dependent Claim 9 words
A composition prepared by the method of claim 9.
Claim 22
Dependent Claim 9 words
A composition prepared by the method of claim 11.

References Cited (Backward Citations)

US4895945A Cited

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