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WO1982002895A1 - Flame retardant polyester-carbonate compositions - Google Patents

Flame retardant polyester-carbonate compositions Download PDF

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Publication number
WO1982002895A1
WO1982002895A1 PCT/US1982/000078 US8200078W WO8202895A1 WO 1982002895 A1 WO1982002895 A1 WO 1982002895A1 US 8200078 W US8200078 W US 8200078W WO 8202895 A1 WO8202895 A1 WO 8202895A1
Authority
WO
WIPO (PCT)
Prior art keywords
aromatic
composition
carbonate
polyester
sulfonic acids
Prior art date
Application number
PCT/US1982/000078
Other languages
English (en)
French (fr)
Inventor
Electric Co General
Niles Richard Rosenquist
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
Priority to NL8220052A priority Critical patent/NL8220052A/nl
Priority to DE19823233716 priority patent/DE3233716A1/de
Publication of WO1982002895A1 publication Critical patent/WO1982002895A1/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/41—Compounds containing sulfur bound to oxygen
    • C08K5/42—Sulfonic acids; Derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C08L27/18—Homopolymers or copolymers or tetrafluoroethene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
    • C08L69/005—Polyester-carbonates

Definitions

  • This invention is directed to an improved flame retardant polyester-carbonate composition of an aromatic polyester-carbonate in admixture with an organic alkali metal salt of sulfonic acid or an organic alkaline earth metal salt of sulfonic acid or a mixture therof, which composition has in admixture therewith a fluorinated polyolefin in sufficient quantity to render the polyester-carbonate composition non-dripping.
  • polyester-carbonate resins are quite different from polycarbonate resins.
  • polyester-carbonates have a higher heat distortion temperature under load (generally from about 50 oF. to about 60°F. higher) than polycarbonates, and are usually more difficult to process (because of their higher intrinsix viscosity) than polycarbonates.
  • polyester-carbonates in place of polycarbonates in certain applications. This is particularly true where there is a high temperature environment.
  • polyester-carbonates it is still preferred over the polycarbonate resin in these applications because of its higher heat distortion temperature.
  • this main advantage of polyester-carbonates makes it especially important that they be made flame retardant and non-dripping since they are used in high temperature environments where the chances of ignition and burning are increased.
  • an aromatic polyester-carbonate can be made both flame retardant and non-dripping by incorporating with the aromatic polyester-carbonate (i) an organic alkali metal salt of sulfonic acid, an organic alkaline earth metal salt of a sulfonic acid, or mixtures thereof, and (ii) a fluorinated polyolefin.
  • polyester-carbonates which find use in the instant invention and the methods for their preparation are well known in the art as disclosed in U.S. Patents 3,303,331; 3,169,121; 4,194,038 and 4,156,069 as well as in copending application Serial No. 33,389 filed April 26, 1979 and assigned to the same assignee as the instant application, all of which are incorporated herein by reference.
  • the polyester-carbonates can generally be termed co-polyesters containing carbonate groups, carboxylate groups, and aromatic carbocyclic groups in the polymer chain, in which at least .some of the carboxylate groups and at least some of the carbonate groups are bonded directly to ring carbon atoms of the aromatic carbocyclic groups.
  • These polyester-carbonates are, in general, prepared by reacting a difunctional carboxylic acid or a reactive derivative of the. acid such as the acid dihalide, a dihydric phenol and a carbonate precursor.
  • the dihydric phenols useful in formulating the polyester-carbonates which are of use in the practice of the present invention are in general represented, by the general formula
  • A represents an aromatic group such as phenylene, biphenylene, naphthylene, etc.
  • E may be an alkylene or alkylidene group such as methylene, ethylene, propylene, propylidene, isopropylidene, butylene, butylidene, isobutylidene, amylene, isoamylene, amylidene, isoamylidene, etc.
  • E is an alkylene or alkylidene group, it may also consist of two or more alkylene or alkylidene groups connected by a non-alkylene or non-alkylidene group such as an aromatic linkage, a tertiary amino linkage, an ether linkage, a carbonyl linkage, a silicon-containing linkage, or by a sulfur- containing linkage such as sulfide, sulfoxide, sulfone, etc.
  • E may be a cycloaliphatic group
  • R represents hydrogen or a monovalent hydrocarbon group such as alkyl (methyl, ethyl, propyl, etc.), aryl (phenyl, naphthyl, etc.), aralkyl (benzyl, ethylphenyl, etc.), alkaryl, or cycloaliphatic (cyclopentyl, cyclohexyl, etc.).
  • Y may be an inorganic atom such as halogen (fluorine, bromine, chlorine, iodine), an inorganic group such as the nitro group, an organic group such as R above, or an oxy group such as OR, it being only necessary that Y be inert to and unaffected by the reactants and reaction conditions.
  • the letter m represents any integer from and including zero through the number of positions on A available for substitution; p represents an integer from and including zero through the number of positions on E available for substitution; t represents an integer equal to at least one; s is either zero or one; and u represents any integer including zero.
  • dihydric phenols falling within the scope of Formula I include: 2,2-bis(4-hydroxyphenyl)propane (bisphenol A); 2,4'-dihydroxydiphenylmethane; bis(2-hydroxyphenyl)methane; bis (4-hydroxyphenyl)methane; bis (4-hydroxy-5 ⁇ -nitro ⁇ henyl)methane; bis (4-hydroxy-2,6-dimethyl-3-methoxyphenyl)methane; 1,1-bis(4-hydroxyphenyl) ethane; 1,1-bis(4-hydroxy-2-chlorophenyl)ethane; 2,2-bis(3-phenyl-4-hydroxyphenyl)propane; bis (4-hydroxyphenyl)cyclohexylmethane; and 2,2-bis (4-hydroxy ⁇ henyl)-1-phenylpropane.
  • bisphenol A 2,4'-dihydroxydiphenylmethane
  • bis(2-hydroxyphenyl)methane bis (4-hydroxyphenyl)methane
  • dihydric phenols may be used alone or as mixtures of two or more different dihydric phenols.
  • any difunctional carboxylic acid or its reactive, derivative such as the acid dihalide conventionally used in the preparation of polyesters may be used for the preparation of the polyester-carbonates useful in formulating the flame retardant non-dripping compositions of the present invention.
  • the carboxylic acids which may be used are aliphatic carboxylic acids, aliphatic-aromatic carboxylic acids, or aromatic carboxylic acids.
  • the aromatic dicarboxylic acids or their reactive derivatives such as the aromatic acid dihalides are preferred as they produce the aromatic polyester-carbonates which are most useful in the practice of the present invention.
  • R 1 represents an alkylene, alkylidene or cycloaliphatic group in the same manner as set out above for E in Formula I; an alkylene, alkylidene or cycloaliphatic group containing ethylenic unsaturation; an aromatic radical such as phenylene, nathylene, biphenylene, substituted phenylene, etc.; two or more aromatic groups connected through non-aromatic linkages such as those defined by E in formula I; or an aralkyl radical such as tolylene, xylene, etc.
  • R 2 is either a carboxyl or a hydroxyl group.
  • the letter q represents one where R 2 is a hydroxyl group and either zero or one wherein R 2 is a carboxyl group.
  • the difunctional acid will either be a monohydroxy monocarboxylic acid or a dicarboxylic acid.
  • the dicarboxylic acids or their reactive derivatives such as the acid dihalides are preferred, with the aromatic dicarboxylic acids or their dihalides being more preferred.
  • R 2 is a carboxyl group and R 1 is a divalent aromatic radical such as phenylene, naphthylene, biphenylene, substituted phenylene, etc.; two or more aromatic groups connected through non-aromatic linkages; or a divalent aralkyl group.
  • suitable preferred aromatic and aliphatic-aromatic dicarboxylic acids which may be used in preparing the polyester-carbonates useful in the practice of the present invention include phthalic acid, isophthalic acid, terephthalic acid, homophthalic acid, p-, m-, and p-phenylenediacetic acid; the polynuclear aromatic acids such as diphenic acid, and 1,4-naphthalic acid.
  • These acids may be used either individually or as a mixture of two or more different acids.
  • the carbonate precursor may be a carbonyl haiide, a carbonate ester or a haloformate.
  • the carbonyl halides which can be employed herein are carbonyl chloride, carbonyl bromide and mixtures thereof.
  • Typical of carbonate esters which may be employed herein are diphenyl carbonate, di(halophenyl)carbonates such as di(chlorophenyl)carbonate, di(bromophenyl) carbonate, di(trichlorophenyl) carbonate, di(tribromophenyl)carbonate, etc; di(alkylphenyl) carbonates such as di(tolyl)carbonate, etc., di(naphthyl) carbonate, di(chloronaphthyl)carbonate, phenyl tolyl carbonate, chlorophenyl chloronaphthyl carbonate, etc., or mixtures thereof.
  • haloformates suitable for use herein include bishaloformates of dihydric phenols (bischloroformates of hydroquinone, etc.) or glycols. (bishaloformates of ethylene glycol, neopentyl glycol, polyethylene glycol, etc.). Carbonyl chloride, also known as phosgene, is preferred. Also present during the co-reaction between the dihydric phenol, the carbonate precursor and the dicarboxylic acid or its reactive derivative are catalysts, molecular weight regulators, and acid acceptors. Examples of suitable molecular weight regulators include phenol, p-tertiary butyl phenol, etc.
  • polyester-carbonates which are useful in the practice of the present invention are the aromatic polyester-carbonates derived from dihydric phenols, aromatic dicarboxylic acids or their reactive derivatives such as the aromatic acid dihalides, e.g. dichloride, and phosgene.
  • a quite useful class of aromatic polyester- carbonates are those derived from bisphenol A; terephthalic acid, isophthalic acid, or a mixture thereof or terephthaloyl dichloride, isophthaloyl dichloride, or a mixture thereof; and phosgene. If a mixture of terephthaloyl and isophthaloyl dichloride is utilized the ratio by weight of terephthaloyl dichloride to isophthaloyl dichloride is from about 5:95 to 95:5.
  • the instant invention is directed to novel flame retardant and non-dripping compositions containing, in admixture:
  • the fluorinated polyolefins used in this invention as drip retarding agents are commercially available or can be prepared by known processes. They are white solids obtained by polymerization of tetrafluoroethylene, for example, in aqueous media with free radical catalysts, e.g., sodium, potassium or ammonium peroxydisulfates at 100 to 1,000 psi at 0-200oC and preferably at 20-100oC. See Brubaker, U.S. Patent 2,393,967, which is incorporated herein by reference. While not essential, it is preferred to use the fluorinated polyolefins in the form of relatively large particles, e.g., of average size of 0.3 to 0.7 mm, mostly 0.5 mm.
  • polytetrafluoroethylene powders which have particles of from 0.05 to 0.5 millimicrons, in diameter. It is especially preferred to use the relatively large particle size material because it tends to disperse readily in polymers and bond them together into fibrous materials.
  • preferred polytetrafluoroethylenes are designated by ASTM as Type 3, and are available commercially from the E. I. DuPont de Nemour and Company under the tradename Teflon.
  • the amount of the fluorinated polyolefin used in the compositions of the present invention is a drip retarding amount.
  • an amount of fluorinated polyolefin effective to retard the dripping of flaming particles from a burning aromatic polyester-carbonate formed article ranges from about 0.01 to about 3 weight percent based on the weight of the aromatic polyester-carbonate resin.
  • the composition contains from about 0.02 to about 2 weight percent of the polyolefin based on the weight of the polyester-carbonate, and more preferably from about 0.05 to about 0.50 weight percent of the polyolefin.
  • These salts are used in a flame retarding amount.
  • an amount of the salt effective to provide flame retardant properties to the aromatic polyester- carbonate composition ranges from about 0.01 to about 10 weight percent based on the weight of the aromatic polyester-carbonate resin, and preferably from about 0.1 to about 5 weight percent based on the weight of the aromatic polyester-carbonate resin, and more preferably from about 0.2 to about 2%.
  • Preferred salts include sodium 2,4,5-trichlorobenzene sulfonate; sodium benzene sulfonate; disodium naphthalene-2,6-disulfonate; sodium p-iodobenzenesulfonate; sodium 4,4'-dibromobiphenyl-3-sulfonate; sodium 2,3,4,5,6-pentachlorobetastyrenesulfonate; sodium 4,4'-dichlorodiphenylsulfide-3-sulfonate; disodium tetrachlorodiphenyletherdisulfonate; disodium 4,4'-dichlorobenzophenone-3, 3'-disulfonate; sodium 2,5-dichlorothiophene-3-sulfonate; sodium salt of diphenylsulfone-3-sulfonic acid; sodium dimethyl 2,4,6-trichloro-5-sulfoisophthalate; potassium
  • the flame retardant non-dripping compositions of the instant invention may optionally contain the commonly known and used additives such as antioxidants, antistatic agents, mold release agents, colorants, impact modifiers, ultraviolet light stabilizers, plasticizers, fillers, glass fibers, color stabilizers and hydrolytic stabilizers.
  • additives such as antioxidants, antistatic agents, mold release agents, colorants, impact modifiers, ultraviolet light stabilizers, plasticizers, fillers, glass fibers, color stabilizers and hydrolytic stabilizers.
  • the pH is maintained in the range of 8.5 to 11.5 by the addition of 25% aqueous sodium hydroxide.
  • the resulting reaction mixture is then phosgenated by the introduction of phosgene at the rate of 36 grams/minute for 15 minutes with the pH controlled at 9.5 to 12 by the addition of the aqueous sodium hydroxide.
  • phosgenation is terminated 6 liters of methylene chloride are added, the brine, layer is separated by centrifuge and the resin solution is washed with aqueous acid and with water.
  • the resin is steam precipitated and dried in a nitrogen fluid bed drier at approximately 240°F.
  • Examples 2-7 illustrate compositions falling outside the scope of the instant invention because these compositions, while containing the alkali or alkaline earth metal salt of sulfonic acid, do not contain the fluorinated polyolefin.
  • EXAMPLE 2 To the aromatic polyester-carbonate prepared substantially in accordance with the procedure of Example 1 is added 0.25 parts by weight of sodium 2,4,5-trichlorobenzenesulfonate per hundred parts by weight of polyester-carbonate resin. The mixture is extruded and molded into test samples in the same manner as described in Example 1.
  • Example 2 To the aromatic polyester-carbonate prepared substantially in accordance with the procedure of Example 1 is added 0.5 parts by weight of sodium 2,4,5-trichlorobenzenesulfonate per hundred parts by weight of polyester-carbonate resin. The mixture is extruded and molded into test samples in the same manner as described in Example 1.
  • EXAMPLE 4 To the aromatic polyester-carbonate prepared substantially in accordance with the procedure of Example 1 is added 0.75 parts by weight of sodium 2,4,5-trichlorobenzenesulfonate per hundred parts by weight of polyester-carbonate resin. The mixture is extruded and molded into test samples in .the same manner as described in Example 1.
  • EXAMPLE.5 To the aromatic polyester-carbonate resin prepared substantially in accordance with the procedure of Example 1 is added 0.5 parts by weight of a mixture of (i) the potassium salt of diphenyl sulfone-3-sulfonic acid and (ii) the dipotassium salt of diphenyl sulfone-3,3'-disulfonic acid per hundred parts by weight of polyester-carbonate resin..
  • Examples 8-10 are illustrative of the flame retardant non-dripping compositions of the instant invention.
  • EXAMPLE 8 To the aromatic polyester-carbonate prepared substantially in accordance with the procedure of Example 1 are added 0.75 parts by weight of sodium 2,4,5-trichlorobenzenesulfonate and 0.12 parts by weight of polytetrafluoroethylene per hundred parts by weight of polyester-carbonate resin. The mixture is extruded and molded into test samples in the same manner as described in Example 1.
  • Example 10 To the aromatic polyester-carbonate prepared substantially in accordance with the procedure of Example 1 are added 0.5 parts by weight of sodium 2,4,5-trichlorobenzenesulfonate and 0.24 parts by weight of polytetra- fluoroethylene per hundred parts by weight of polyester- carbonate resin. The mixture is extruded and molded into test samples in the same manner as described in Example 1.
  • EXAMPLE 10 To the aromatic polyester-carbonate prepared substantially in accordance with the procedure of Example 1 are added 0.75 parts by weight of sodium 2,4,5-trichlorobenzenesulfonate and 0.24 parts by weight of polytetrafluoroethylene per hundred parts by weight of polyester-carbonate resin. The mixture is extruded and molded into test samples in the same manner as described in Example 1.
  • Example 1 To the aromatic polyester-carbonate prepared substantially in accordance with the procedure of Example 1 are added 0.5 parts by weight of a mixture of (i) the potassium salt of diphenyl sulfone-3-sulfonic acid and (ii) the dipotassium salt of diphenyl sulfone-3,3'-disulfonic acid, 0.24 parts by weight of polytetra- fluoroethylene, and.1.5 parts by weight of fiber glass per hundred parts by weight of polyester-carbonate resin.
  • the mixture is extruded and molded into test samples in the same manner as described in Example.1.
  • the test samples prepared in Examples; 1-11 are subjected to a test procedure to determine the flammability and dripping characteristics of these samples.
  • This test procedure is a modified ASTM D-3713. - The modification consists in that only.5 samples of each, lot are tested and only for a 60 second flame impingement time. In accordance with this modified test procedure, materials so investigated are rated as either "passing” or “failing” based on the results obtained from the testing of 5 specimens.
  • the criteria for passing or failing is briefly as follows:
  • the composition of the instant invention may optionally contain fiber glass.
  • fiber glass it is understood that glass silk, as well as all glass fiber materials derived therefrom including glass fiber fabrics, rovings, stable fibers and glass fiber mats are included.
  • fibrous glass filaments they may first be formed and gathered into a bundle known as a strand.
  • a binder or binding agent is applied to the glass filaments.
  • the strand can be chopped into various lengths as desired. It is convenient to use the strands..in lengths of from about 1/8" to about 1" long, preferably less than 1/4"
  • the composition contains from about 1 to about 50 weight percent of the glass fibers.

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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/US1982/000078 1981-02-20 1982-01-22 Flame retardant polyester-carbonate compositions WO1982002895A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
NL8220052A NL8220052A (nl) 1981-02-20 1982-01-22 Vlamvertragende, polyestercarbonaat bevattende samenstellingen.
DE19823233716 DE3233716A1 (de) 1982-01-22 1982-01-22 Feuerhemmende polyester-cabonat-zubereitung

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US23659181A 1981-02-20 1981-02-20
US236591810220 1981-02-20

Publications (1)

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WO1982002895A1 true WO1982002895A1 (en) 1982-09-02

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JP (1) JPS58500286A (ja)
NL (1) NL8220052A (ja)
WO (1) WO1982002895A1 (ja)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0103123A1 (en) * 1982-08-11 1984-03-21 General Electric Company Flame retardant copolyester-carbonate compositions
EP0132629A3 (en) * 1983-08-01 1985-11-06 General Electric Company Improved flame retardant copolyester-carbonate compositions
EP0643096A1 (de) * 1993-08-24 1995-03-15 Bayer Ag Stabilisierte, flammwidrige Polycarbonatformmassen
WO2005017043A3 (en) * 2003-08-11 2005-04-21 Gen Electric Flame retardant fiber reinforced composition with improved flow
US7259201B2 (en) 2003-08-28 2007-08-21 General Electric Company Flame retardant thermoplastic films and methods of making the same
US7649040B2 (en) 2002-04-11 2010-01-19 Sabic Innovative Plastics Ip B.V. Flame retardant fiber reinforced composition with improved flow

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3169121A (en) * 1957-08-22 1965-02-09 Gen Electric Carbonate-carboxylate copolyesters of dihydric phenols and difunctional carboxylic acids
US3835089A (en) * 1972-06-23 1974-09-10 Gen Electric Polylactone-modified linear polyesters and molding compositions containing the same
US3876580A (en) * 1971-09-29 1975-04-08 Bayer Ag Flame-resistant thermoplastic molding compositions and moldings made therefrom
US3940366A (en) * 1973-12-28 1976-02-24 General Electric Company Flame retardant polycarbonate composition
US4156069A (en) * 1976-04-02 1979-05-22 Allied Chemical Corporation Bisphenol-A/terephthalate/carbonate melt processable copolymers
US4223100A (en) * 1979-04-18 1980-09-16 Mobay Chemical Corporation Flame retardant aromatic polycarbonate with good mechanical properties and melt stability
US4297455A (en) * 1977-03-22 1981-10-27 Bayer Aktiengesellschaft Process for the preparation of carbonic acid aryl esters of polyester-diols lengthened via carbonate groups and their use for the preparation of polyester-diol bis-diphenol carbonates and polyester/polycarbonates

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3023818A1 (de) * 1980-06-25 1982-01-28 Bayer Ag Flammwidrige formmassen auf basis thermoplastischer aromatischer polyester und polyestercarbonate, verfahren zu ihrer herstellung und ihre verwendung zur herstellung von formkoerpern

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3169121A (en) * 1957-08-22 1965-02-09 Gen Electric Carbonate-carboxylate copolyesters of dihydric phenols and difunctional carboxylic acids
US3876580A (en) * 1971-09-29 1975-04-08 Bayer Ag Flame-resistant thermoplastic molding compositions and moldings made therefrom
US3835089A (en) * 1972-06-23 1974-09-10 Gen Electric Polylactone-modified linear polyesters and molding compositions containing the same
US3940366A (en) * 1973-12-28 1976-02-24 General Electric Company Flame retardant polycarbonate composition
US4156069A (en) * 1976-04-02 1979-05-22 Allied Chemical Corporation Bisphenol-A/terephthalate/carbonate melt processable copolymers
US4297455A (en) * 1977-03-22 1981-10-27 Bayer Aktiengesellschaft Process for the preparation of carbonic acid aryl esters of polyester-diols lengthened via carbonate groups and their use for the preparation of polyester-diol bis-diphenol carbonates and polyester/polycarbonates
US4223100A (en) * 1979-04-18 1980-09-16 Mobay Chemical Corporation Flame retardant aromatic polycarbonate with good mechanical properties and melt stability

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0103123A1 (en) * 1982-08-11 1984-03-21 General Electric Company Flame retardant copolyester-carbonate compositions
EP0132629A3 (en) * 1983-08-01 1985-11-06 General Electric Company Improved flame retardant copolyester-carbonate compositions
EP0643096A1 (de) * 1993-08-24 1995-03-15 Bayer Ag Stabilisierte, flammwidrige Polycarbonatformmassen
US7649040B2 (en) 2002-04-11 2010-01-19 Sabic Innovative Plastics Ip B.V. Flame retardant fiber reinforced composition with improved flow
WO2005017043A3 (en) * 2003-08-11 2005-04-21 Gen Electric Flame retardant fiber reinforced composition with improved flow
EP1860145A1 (en) * 2003-08-11 2007-11-28 General Electric Company Flame retardant fiber reinforced composition with improved flow
US7259201B2 (en) 2003-08-28 2007-08-21 General Electric Company Flame retardant thermoplastic films and methods of making the same

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JPS58500286A (ja) 1983-02-24
NL8220052A (nl) 1983-01-03

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