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US4661564A Expired / Lapsed US ⏱️ 0.0 years remaining

Modified styrenic polymer beads

Assignee: Lyondell Chemical Technology LP
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Filing: 1986-07-17
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Granted: 1987-04-28
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Expires: 2006-07-17
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Abstract

Abstract Styrenic polymer beads that are useful in forming foamed cups with improved strength and thermal properties are prepared by forming an aqueous suspension of initial styrenic polymer beads and adding thereto an emulsion of a comonomer solution of styrenic monomer and divinylbenzene, which emulsion also contains free-radical-producing catalysts, and the suspension with added monomers is heated to copolymerize the styrenic monomer and divinylbenzene within and on the initial beads and form modified beads.

Inventors

  • 👤 Adolph V. DiGiulio

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 15:53
CPC Classifications
C; C08; C08J; C08J9/00; C08J9/16; C08J9/18; C08F; C08F257/00; C08F257/02; C08J2351/00

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 298 words
A bead product comprising a polystyrene bead having a styrene monomer-divinylbenzene copolymer relatively uniformly dispersed throughout the bead; said copolymer consisting essentially of styrene monomer and 0.02 to 0.85 percent by weight of divinylbenzene and said copolymer comprising 8 to 35 percent by weight of the total bead product; said bead product produced by the process comprising: (a) forming an aqueous suspension of initial styrene polymer beads having a weight average molecular weight of 230,000 to 350,000 with a polydispersity (Mw/Mn) of 2 to 3.1, with the aid of a suitable suspending agent system; said initial styrene polymer beads selected from the group consisting of polymers of styrene, alpha-methylstyrene, nuclear-methylstyrene, para-tert-butylstyrene, chlorostyrene, dichlorostyrene, mixtures of these, and copolymers of at least 50% styrene and up to 50% of other mono-ethylenically unsaturated monomers copolymerizable the therewith; (b) forming a comonomer solution of a styrene monomer and divinylbenzene; said styrene monomer being selected from the group consisting of sytrene, alpha-methylstyrene, nuclearmethylstyrene, para-tert-butylstyrene, monochlorostyrene, dichlorostyrene and mixtures thereof; (c) forming an emulsion comprising a suitable emulsifier and a portion of said comonomer solution; (d) adding the emulsion to the styrene polymer bead suspension at 25°-75° C. to allow the comonomers to be absorbed into the beads; (e) forming a second emulsion comprising a suitable emulsifier, the remaining portion of said comonomer solution, and free-radical-producing catalysts; (f) adding the second emulsion to the suspension of said beads absorbed with comonomers at 25°-75° C., at a rate such that the rate of absorption of comonomer/catalyst by said beads is at least equivalent to the rate of addition of emulsified comonomer/catalyst solution, then allowing said subpension to stand for 30 minutes to 4 hours, and then raising the temperature to 80°-95° C., and maintaining the suspension at said temperature to polymerize said comonomers; and
Claim 2
Dependent Claim 298 words
A bead product comprising a polystyrene bead having a styrene monomer-divinylbenzene copolymer relatively uniformly dispersed throughout the bead; said copolymer consisting essentially of styrene monomer and 0.02 to 0.85 percent by weight of divinylbenzene and said copolymer comprising 8 to 35 percent by weight of the total bead product; said bead product produced by the process comprising: (a) forming an aqueous suspension of initial styrene polymer beads having a weight average molecular weight of 230,000 to 350,000 with a polydispersity (Mw/Mn) of 2 to 3.1, with the aid of a suitable suspending agent system; said initial styrene polymer beads selected from the group consisting of polymers of styrene, alpha-methylstyrene, nuclear-methylstyrene, para-tert-butylstyrene, chlorostyrene, dichlorostyrene, mixtures of these, and copolymers of at least 50% styrene and up to 50% of other mono-ethylenically unsaturated monomers copolymerizable the therewith; (b) forming a comonomer solution of a styrene monomer and divinylbenzene; said styrene monomer being selected from the group consisting of sytrene, alpha-methylstyrene, nuclearmethylstyrene, para-tert-butylstyrene, monochlorostyrene, dichlorostyrene and mixtures thereof; (c) forming an emulsion comprising a suitable emulsifier and a portion of said comonomer solution; (d) adding the emulsion to the styrene polymer bead suspension at 25°-75° C. to allow the comonomers to be absorbed into the beads; (e) forming a second emulsion comprising a suitable emulsifier, the remaining portion of said comonomer solution, and free-radical-producing catalysts; (f) adding the second emulsion to the suspension of said beads absorbed with comonomers at 25°-75° C., at a rate such that the rate of absorption of comonomer/catalyst by said beads is at least equivalent to the rate of addition of emulsified comonomer/catalyst solution, then allowing said subpension to stand for 30 minutes to 4 hours, and then raising the temperature to 80°-95° C., and maintaining the suspension at said temperature to polymerize said comonomers; and
Claim 3
Dependent Claim 35 words
(g) heating said suspension to a temperature of 115° to about 135° C. to substantially complete the polymerization of said styrene monomer and divinylbenzene to form beads having copolymer relatively uniformly distributed throughout the beads.
Claim 4
Dependent Claim 35 words
(g) heating said suspension to a temperature of 115° to about 135° C. to substantially complete the polymerization of said styrene monomer and divinylbenzene to form beads having copolymer relatively uniformly distributed throughout the beads.
Claim 5
Dependent Claim 276 words
A bead product comprising a polystyrene bead having a styrene monomer-divinylbenzene copolymer relatively uniformly dispersed throughout the bead; said copolymer consisting essentially of styrene monomer and 0.02 to 0.85 percent by weight of divinylbenzene and said copolymer comprising 8 to 35 percent by weight of the total bead product; said bead product produced by the process comprising: (a) forming an aqueous suspension of initial styrene polymer beads having a weight average molecular weight of 230,000 to 350,000 with a polydispersity (Mw/Mn) of 2 to 3.1, with the aid of a suitable suspending agent system; said initial styrene polymer beads being selected from the group condisting of polymers of styrene, alpha-methylstyrene, nuclear-methylstyrene, para-tert-butylstyrene, chlorostyrene, dischlorostyrene, mixtures of these, and copolymers of at least 50% styrene and up to 50% of other mono-ethylenically unsaturated monomers copolymerizable therewith; (b) forming a comonomer solution of styrene monomer and divinylbenzene; said styrene monomer being selected from the group consisting of styrene, alpha-methylstyrene, nuclearmethylstyrene, para-tert-butylstyrene, monochlorostyrene, dichlorostyrene and mixtures thereof; (c) forming an emulsion comprising suitable emulsifier and a portion of said comonomer solution with free-radical-producing catalysts dissolved therein; (d) adding the emulsion to the styrene polymer bead suspension at 25°-75° C. and allowing said suspension to stand for 30 minutes to 4 hours to allow the comonomers and catalysts to be absorbed into the beads; (e) heating the suspension to 80°-95° C. and maintaining said temperature for 0.10 to 6 hours to copolymerize said comonomers; and (f) heating said suspension to a temperature of 115° to about 135° C. to substantially complete the polymerization of said styrene monomer and divinylbenzene to form beads having copolymers relatively uniformly distributed throughout the beads.
Claim 6
Dependent Claim 276 words
A bead product comprising a polystyrene bead having a styrene monomer-divinylbenzene copolymer relatively uniformly dispersed throughout the bead; said copolymer consisting essentially of styrene monomer and 0.02 to 0.85 percent by weight of divinylbenzene and said copolymer comprising 8 to 35 percent by weight of the total bead product; said bead product produced by the process comprising: (a) forming an aqueous suspension of initial styrene polymer beads having a weight average molecular weight of 230,000 to 350,000 with a polydispersity (Mw/Mn) of 2 to 3.1, with the aid of a suitable suspending agent system; said initial styrene polymer beads being selected from the group condisting of polymers of styrene, alpha-methylstyrene, nuclear-methylstyrene, para-tert-butylstyrene, chlorostyrene, dischlorostyrene, mixtures of these, and copolymers of at least 50% styrene and up to 50% of other mono-ethylenically unsaturated monomers copolymerizable therewith; (b) forming a comonomer solution of styrene monomer and divinylbenzene; said styrene monomer being selected from the group consisting of styrene, alpha-methylstyrene, nuclearmethylstyrene, para-tert-butylstyrene, monochlorostyrene, dichlorostyrene and mixtures thereof; (c) forming an emulsion comprising suitable emulsifier and a portion of said comonomer solution with free-radical-producing catalysts dissolved therein; (d) adding the emulsion to the styrene polymer bead suspension at 25°-75° C. and allowing said suspension to stand for 30 minutes to 4 hours to allow the comonomers and catalysts to be absorbed into the beads; (e) heating the suspension to 80°-95° C. and maintaining said temperature for 0.10 to 6 hours to copolymerize said comonomers; and (f) heating said suspension to a temperature of 115° to about 135° C. to substantially complete the polymerization of said styrene monomer and divinylbenzene to form beads having copolymers relatively uniformly distributed throughout the beads.

References Cited (Backward Citations)

US2405817A Cited
US3324052A Cited
US3259595A Cited
US3259594A Cited
US3960784A Cited
US4525486A Cited
US4579872A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-04-27 1990-10-27 1991-04-28 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-04-27 1994-10-27 1995-04-28 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-04-27 1998-10-27 1999-04-28 $7700.00 Window Closed / Lapsed

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