WO1980000083A1 - Reinforced impact modified polycarbonates - Google Patents

Reinforced impact modified polycarbonates Download PDF

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Publication number
WO1980000083A1
WO1980000083A1 PCT/US1979/000371 US7900371W WO8000083A1 WO 1980000083 A1 WO1980000083 A1 WO 1980000083A1 US 7900371 W US7900371 W US 7900371W WO 8000083 A1 WO8000083 A1 WO 8000083A1
Authority
WO
WIPO (PCT)
Prior art keywords
ethylene
copolymers
propylene
group
polycarbonate
Prior art date
Application number
PCT/US1979/000371
Other languages
English (en)
French (fr)
Inventor
F Holub
P Wilson
Original Assignee
Gen Electric
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 Gen Electric filed Critical Gen Electric
Publication of WO1980000083A1 publication Critical patent/WO1980000083A1/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00Compositions of polycarbonates; Compositions of derivatives of polycarbonates

Definitions

  • thermoplastic molding composi ⁇ tions having improved notched Izod impact strength comprising
  • polyolefins such as ethylene-propylene copolymers, ethylene-butadiene copolymers, propylene-butadiene copolymers, ethylene-propylene-butadiene terpolymers, ethylene-acrylic acid copolymers, propylene-acrylic acid cop
  • bisphenol-A polycarbonates as molding composi ⁇ tions, both with and without reinforcing agents is well known and these materials have been widely employed in the manufacture of various thermoplastic molded articles.
  • the present invention provides for a novel thermoplastic molding composition which comprises Q (a) a bisphenol-A polycarbonate;
  • polystyrene resin has recurring units of the formula
  • each -R- is selected from the group consisting of phenylene, halo-substituted phenylene and alky! substituted phenylene
  • X and Y are each selected from the group consist ⁇ ing of hydrogen, hydrocarbon radicals free from aliphatic unsaturation and of radicals which together with the adjoining
  • the preferred polycarbonate resins may be derived from the reaction of bisphenol-A and phosgene. These polycarbonates have from 10-400 recurring units of the formula:
  • the polycarbonate should have an intrinsic vis ⁇ cosity between 0.2 and 1.0, preferably from 0.30 to 0.65 as measured at 20°C in methylene chloride.
  • a reinforcing amount of the reinforcing agent in the compositions of the present invention from 1-60 parts by weight of the total weight of the resultant molding composition may comprise the reinforcing 5 agent.
  • a preferred range is from 5-40 parts by weight.
  • the preferred reinforcing agents for use in the present invention are of glass, and it is preferred to use fibrous glass filaments, glass beads, or mixtures of these.
  • the pre ⁇ ferred glass filaments for plastics reinforcements are made ° by mechanical pulling, and have filament diameters in the range of from about (0.000112) 0.000284cm to about (0.00075 inch 0.0019cm. However, this is not critical to the present inven ⁇ tion.
  • the glass beads which may be advantageously employed either 5 alone or together with the treated glass fibers described above will have diameters on the order of 0.0003cm (0.0001) to about . 0.025cm (O.OlOinches) and are generally prepared via spraying of the molten glass as fine droplets into liquid baths.
  • the glass fibers may be employed in amounts up to about 0 40 parts by weight of the total composition and the glass beads may be employed in amounts up to about 60 parts by weight of the total composition.
  • the glass fibers and glass beads may be advantageously employed in varying proportions such that the combined quantity of glass fibers and glass beads make up from 5 about 1 to about 60 parts by weight of the total composition.
  • the preferred range of the combined glass fibers and glass beads is from about 5 to about 40 parts by weight of the total mold ⁇ ing composition.
  • polyolefin copolymers such as ethyl ene-propylene ' copolymers
  • olefin terpolymers such as ethylene-propylene- butadiene terpolymers, which may be suitably employed in practicing the present invention are all commercially available products whose preparation is well known.
  • the olef in-acrylic acid copolymers such as ethylene- acryl ic acid copolymers
  • di olef in-acrylic acid terpolymers such as ethyl ene-propylene-acryl ic acid terpolymers and other olefin based thermoplastic elastomers , which may be suitably employed in practicing the present invention are also commercial ⁇ ly available products whose preparation is well known, as will be readily apparent to those skilled in the art.
  • propylene block copolymers al l of which are manufactured and sold by Hercules , Inc. :, US ⁇ LB 342 and USp-R.B 703, both ethylene homopolymers, manu ⁇
  • compositions of the present invention may contain from about 0.5 to about 10 percent by weight of combined impact modifying component(s) described above, without taking into account the amount of reinforcing agents to be employed, and will preferentially contain from about 2 to about 6 percent by weight of the combined impact modifying component(s).
  • compositions of the present invention may be prepared by any standard procedure and the particular method employed is not critical.
  • the compositions of the present invention may also include flame retardants such as those described in U.S. Patent No. 3,915,926 which is incorporated herin by reference. Description of the ; 'Preferred Embodiments
  • Example I Control A blend of 91 parts by weight of bisphenol-A polycarbonate and 9 parts by weight of chopped glass fibers was prepared, extruded in a twin screw extruder and molded into sample parts of approximately 0.3cm (1/8 inch) thickness. The results of impact and flexural tests on the resultant molded parts are set forth in Table I.
  • Examples II - XXIII A blend of 91 parts by weight of bisphenol-A polycarbonate and 9 parts by weight of chopped glass fibers was blended with 4 parts per 100 by weight of various commercially available compositions as impact modifying agents as set forth in Table I. The various resultant blends were extruded and molded -in the • same manner as in Example I. The results of impact and flexur ⁇ al tests on the resultant molded parts are also set forth in Table I.
  • V indicates that at least one sample did not fall when subjected to the machine l imit of 40 ft. -lb. /in.
  • Exa ple XXIV - Control A blend of 60 parts by weight of bisphenol-A polycarbonate, 20 parts by weight of chopped glass fibers and 20 parts by weight of glass beads was prepared, extruded and molded into sample parts in the same manner as in Example I. The results of impact and flexural tests performed on the resultant molded parts are set forth in Table II.
  • Examples XXV - XXX Blends of 60 parts by weight of bisphenol-A polycarbonate, 20 parts by weight of chopped glass fibers and 20 parts by weight of glass beads in admixture with 4 parts per 100 by weight of various compositions as impact modifying agents were prepared, extruded and molded in the same manner as in Example XXIV.
  • the results of impact and flexural tests performed on the resultant molded parts are set forth in Table II.
  • Base 60 Parts by Weight Po1y(BPA Carbonate) 8 , 20 Parts by Weight Chopped Glass Fibers and 20 Parts by Weight Glass Beads -
  • Example XXXI - Control A blend of 70 parts by weight of bisphenol-A polycarbonate and 30 parts by weight of glass beads was prepared, extruded and molded into sample parts in the same manner as in Example I. The results of impact and flexural tests performed on the re- sultant molded parts are set forth in Table III.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
PCT/US1979/000371 1978-06-16 1979-05-30 Reinforced impact modified polycarbonates WO1980000083A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US91609978A 1978-06-16 1978-06-16
US916099 1978-06-16

Publications (1)

Publication Number Publication Date
WO1980000083A1 true WO1980000083A1 (en) 1980-01-24

Family

ID=25436698

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1979/000371 WO1980000083A1 (en) 1978-06-16 1979-05-30 Reinforced impact modified polycarbonates

Country Status (3)

Country Link
EP (1) EP0016058A4 (enrdf_load_stackoverflow)
JP (1) JPS55500811A (enrdf_load_stackoverflow)
WO (1) WO1980000083A1 (enrdf_load_stackoverflow)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0063769A3 (en) * 1981-04-29 1983-03-02 Mobay Chemical Corporation Glass-filled polycarbonate with impact resistance
US4401785A (en) * 1982-01-29 1983-08-30 General Electric Company Polyolefin-poly(ester-carbonate) composition
US4464512A (en) * 1982-01-29 1984-08-07 General Electric Company Composition comprising an aromatic polyester-carbonate resin and a linear low density polyolefin polymer
EP0119533A1 (en) * 1983-03-22 1984-09-26 General Electric Company Polycarbonate resin mixture
EP0376921A3 (de) * 1983-08-31 1990-08-16 Bayer Ag Thermoplastische Formmassen auf Basis von Polysiloxan-Polycarbonat-Blockcopolymeren
EP0472064A3 (en) * 1990-08-22 1992-08-05 Bayer Ag Ternary blends
US9667364B2 (en) 2008-05-14 2017-05-30 Sony Interactive Entertainment Inc. Broadcast seeding for peer-to-peer networks
CN111548619A (zh) * 2019-02-12 2020-08-18 柯尼卡美能达株式会社 树脂组合物、其制造方法以及成型品

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000063639A (ja) * 1998-08-13 2000-02-29 Mitsui Chemicals Inc α−オレフィン/共役ジエン系共重合体組成物

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1010043A (en) * 1963-04-08 1965-11-17 Organico Soc Improved organic thermoplastic material and process for its manufacture
CA879152A (en) * 1971-08-24 L. Peterson Douglas Glass-filled polycarbonate/polyethylene resin
US3875107A (en) * 1971-09-29 1975-04-01 Bayer Ag Flame-resistant thermoplastic molding compositions and moldings made therefrom
US4014849A (en) * 1973-11-05 1977-03-29 Basf Aktiengesellschaft Self-extinguishing reinforced polycarbonate molding compositions
US4110299A (en) * 1976-10-15 1978-08-29 General Electric Company Flame-retardant polycarbonate composition
US4122131A (en) * 1977-09-14 1978-10-24 General Electric Company Polyblend composition comprising aromatic polycarbonate, polyolefin, selectively hydrogenated block copolymer and olefinic copolymer

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US879152A (en) * 1906-07-09 1908-02-18 Alexander S Diack Toy.
US3437631A (en) * 1967-02-13 1969-04-08 Mobay Chemical Corp Body protective device composed of polycarbonate resins admixed with polyolefins and pigments
BE743678A (enrdf_load_stackoverflow) * 1968-12-26 1970-05-28
DE2704875A1 (de) * 1976-02-09 1977-08-11 Mobay Chemical Corp Polycarbonatformmassen mit dauerhaft verbesserter kerbschlagzaehigkeit

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA879152A (en) * 1971-08-24 L. Peterson Douglas Glass-filled polycarbonate/polyethylene resin
GB1010043A (en) * 1963-04-08 1965-11-17 Organico Soc Improved organic thermoplastic material and process for its manufacture
US3875107A (en) * 1971-09-29 1975-04-01 Bayer Ag Flame-resistant thermoplastic molding compositions and moldings made therefrom
US4014849A (en) * 1973-11-05 1977-03-29 Basf Aktiengesellschaft Self-extinguishing reinforced polycarbonate molding compositions
US4110299A (en) * 1976-10-15 1978-08-29 General Electric Company Flame-retardant polycarbonate composition
US4122131A (en) * 1977-09-14 1978-10-24 General Electric Company Polyblend composition comprising aromatic polycarbonate, polyolefin, selectively hydrogenated block copolymer and olefinic copolymer

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP0016058A4 *

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0063769A3 (en) * 1981-04-29 1983-03-02 Mobay Chemical Corporation Glass-filled polycarbonate with impact resistance
US4401785A (en) * 1982-01-29 1983-08-30 General Electric Company Polyolefin-poly(ester-carbonate) composition
US4464512A (en) * 1982-01-29 1984-08-07 General Electric Company Composition comprising an aromatic polyester-carbonate resin and a linear low density polyolefin polymer
EP0119533A1 (en) * 1983-03-22 1984-09-26 General Electric Company Polycarbonate resin mixture
EP0376921A3 (de) * 1983-08-31 1990-08-16 Bayer Ag Thermoplastische Formmassen auf Basis von Polysiloxan-Polycarbonat-Blockcopolymeren
EP0472064A3 (en) * 1990-08-22 1992-08-05 Bayer Ag Ternary blends
US5202374A (en) * 1990-08-22 1993-04-13 Bayer Aktiengesellschaft Ternary mixtures
US9667364B2 (en) 2008-05-14 2017-05-30 Sony Interactive Entertainment Inc. Broadcast seeding for peer-to-peer networks
CN111548619A (zh) * 2019-02-12 2020-08-18 柯尼卡美能达株式会社 树脂组合物、其制造方法以及成型品

Also Published As

Publication number Publication date
EP0016058A1 (en) 1980-10-01
EP0016058A4 (en) 1980-10-16
JPS55500811A (enrdf_load_stackoverflow) 1980-10-23

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