High performance thermoplastic compositions with improved melt flow properties
AssigneeGeneral Electric Company
InventorsFranciscus Johannes Maria van Beek, Glen D. Merfeld, Alan Oshinski, Robert Puyenbroek, Kenneth Paul Zarnoch
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Abstract
A high performance thermoplastic polymer composition having improved melt flow properties, comprising a thermoplastic polymer resin and a low intrinsic viscosity poly(arylene ether). Preferred thermoplastic polymers are poly(imide) polymers.
Claims35
A thermoplastic resin composition, comprising, based upon the total weight of the composition
- about 40 wt % to about 99.9 wt % of a high Tg amorphous thermoplastic polymer resin wherein the high Tg amorphous thermoplastic polymer resin is selected from the group consisting of poly (imide) polymers, poly(amide imide) polymers, poly(sulfone) polymers, poly(ether sulfone) polymers, poly(etherimide) polymers, and combinations of the foregoing high Tg amorphous thermoplastic polymer resins;
- and about 0.1 wt % to about 50 wt % of an unfunctionalized poly(arylene ether) having an intrinsic viscosity of about 0.10 to about 0.15 dl/g, as measured in chloroform at 25° C.
A thermoplastic resin composition comprising, based upon the total weight of the composition, about 0.1 wt % to about 50 wt % of an unfunctionalized poly(arylene ether) having an intrinsic viscosity of about 0.10 to about 0.15 dug, as measured in chloroform at 25° C, wherein the poly(arylene ether) polymer comprises a plurality of structural units of the formula (XII):
- wherein each Q1 is independently a halogen, primary or secondary lower alkyl having from one to four carbon atoms, phenyl, haloalkyl, aminoalkyl, hydrocarbonoxy, or halohydrocarbonoxy wherein at least two carbon atoms separate the halogen and oxygen atoms;
- each Q2 is independently a hydrogen, halogen, primary or secondary lower alkyl, phenyl, haloalkyl, hydrocarbonoxy or halohydracarbonoxy wherein at least two carbon atoms separate the halogen and oxygen atoms;
- and n is less than 50;
- and
- about 40 wt % to about 99.9 wt % of a high Tg amorphous thermoplastic polymer resin, wherein the high Tg amorphous thermoplastic polymer resin comprises structural units of the formula (V):
- wherein T is —O— or a group of the formula —O—Z—O— wherein the divalent bonds of the —O— or the —O—Z—O— group are in the 3,3′, 3,4′, 4,3′, or the 4,4′positions;
- and wherein Z is one or more of the divalent radicals of formula (III):
- and
- R is a divalent organic radical selected from the group consisting of (a) aromatic hydrocarbon radicals having about 6 to about 20 carbon atoms or halogenated derivatives thereof, (b) straight or branched chain alkylene radicals having about 2 to about 20 carbon atoms;
- (c) cycloalkylene radicals having about 3 to about 20 carbon atoms, and (d) divalent radicals of the formula (IV):
- wherein Q is a divalent moiety selected from the group consisting of —O—, —S—, —C(O)—, —SO2—, CyH2y—, CyH2y-2—, and halogenated derivatives thereof wherein y is an integer from 1 to 10.
A method of preparing a thermoplastic resin composition comprising:
- melt mixing about 40 wt % to about 99.9 wt % of a high Tg amorphous thermoplastic polymer resin selected from the group consisting of poly (imide) polymers, poly(sulfone) polymers, and combinations of the foregoing high Tg amorphous thermoplastic polymer resins and about 0.1 wt % to about 50 wt % of an unfunctionalized poly(arylene ether) having an intrinsic viscosity/of about 0.10 to about 0.15 dl/g, as measured in chloroform at 25° C., to form a mixture;
- and molding the mixture.
A thermoplastic resin composition, comprising the reaction product of, based upon the total weight of the composition:
- about 40 wt % to about 99.9 wt % of a high Tg amorphous thermoplastic polymer resin selected from the group consisting of poly (imide) polymers, poly(sulfone) polymers, and combinations of the foregoing high Tg amorphous thermoplastic polymer resins;
- and about 0.1 wt % to about 50 wt % of an unfunctionalized poly(arylene ether) having an intrinsic viscosity of about 0.10 to about 0.15 dl/g, as measured in chloroform at 25° C.
Dependencies are inferred from the claim text.