WO2013176868A1 - Antimony-free flame-retarded styrenic thermoplastic polymer composition, article containing same and method of making same - Google Patents

Antimony-free flame-retarded styrenic thermoplastic polymer composition, article containing same and method of making same Download PDF

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Publication number
WO2013176868A1
WO2013176868A1 PCT/US2013/039474 US2013039474W WO2013176868A1 WO 2013176868 A1 WO2013176868 A1 WO 2013176868A1 US 2013039474 W US2013039474 W US 2013039474W WO 2013176868 A1 WO2013176868 A1 WO 2013176868A1
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Prior art keywords
flame
thermoplastic polymer
retarded
styrenic thermoplastic
polymer composition
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PCT/US2013/039474
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French (fr)
Inventor
Pierre Georlette
Eyal EDEN
Rachel Shtekler
Marc LEIFER
Sergei V. Levchik
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Icl-Ip America, Inc.
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Priority to EP13723622.0A priority Critical patent/EP2855571A1/en
Priority to CN201380026574.XA priority patent/CN104334622A/en
Priority to US14/400,118 priority patent/US20150126650A1/en
Publication of WO2013176868A1 publication Critical patent/WO2013176868A1/en

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00Compositions 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 an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02Homopolymers or copolymers of hydrocarbons
    • C08L25/04Homopolymers or copolymers of styrene
    • C08L25/06Polystyrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0066Flame-proofing or flame-retarding additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0091Complexes with metal-heteroatom-bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/02Halogenated hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/49Phosphorus-containing compounds
    • C08K5/51Phosphorus bound to oxygen
    • C08K5/53Phosphorus bound to oxygen bound to oxygen and to carbon only
    • C08K5/5317Phosphonic compounds, e.g. R—P(:O)(OR')2
    • C08K5/5333Esters of phosphonic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions 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
    • C08L27/02Compositions 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
    • C08L27/12Compositions 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
    • C08L27/18Homopolymers or copolymers or tetrafluoroethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/04Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L55/00Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
    • C08L55/02ABS [Acrylonitrile-Butadiene-Styrene] polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/02Flame or fire retardant/resistant
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00Applications
    • C08L2203/20Applications use in electrical or conductive gadgets

Definitions

  • the present invention relates to flame-retarded thermoplastic compositions and more particularly to flame-retarded styrenic thermoplastic polymer compositions and articles containing the same.
  • Sty.re.nic polymers and more specifically high impact polystyrene (HIPS) and HIPS high impact polystyrene
  • acrylonitriie, butadiene, styrene polymers (ABS) plastics axe used for the production of electronic parts such as housings, cases and internal parts, amongst others, in most of these applications, flame retardancy is needed and is usually provided by flame retardant systems based on a combination of brominated flame retardants with antimony trioxide as a synergist.
  • this type of flame retardant system has limitations, because antimon trioxide. being a very efficient synergist, tends to significantly increase smoke yield, which impairs visibility which could create problems for evacuation of people in the case of a fire.
  • antimony trioxide has a very high bulk density which increases the specific gravity of molded parts containing the same. This is especially undesirable in transportation and aviation applications.
  • antimony trioxide has significantly increased in price in recent years. Still further, some recently introduced ecolabels require elimination of antimony trioxide from thermoplastic pails.
  • a combination of brominated flame retardant, a high phosphorus-content flame retardani and an antidripping agent provides an excellent flame retardant additive composition for use in styrenic thermoplastic polymers, more specifically HIPS and ABS thermoplastics, such flame-retardant additive compositions provide flame retardant efficiency adequate to styrenic thermoplastic resins in electrical and electronic applications without (lie use of antimony trioxide.
  • the present invention is directed to an antimony irio ide-free flame-retarded styrenic thermoplastic polymer composition
  • an antimony irio ide-free flame-retarded styrenic thermoplastic polymer composition comprising:
  • thermoplastic polymer (a) at least one styrenic thermoplastic polymer
  • At least one antidripping agent more specifically, polytetrafluoroethyiene (PTFE)
  • the flame-retarded styrenic thermoplastic polymer composition can optionally further comprise impact modifiers, heat stabilizers, antioxidants, processing aids, and other additives enhancing physical properties of the resin.
  • the present invention is also directed to a molded article comprising a styrenic thermoplastic polymer, a brominated flame retardant, aluminum methyl methyiphosphonate, PTFE, and optionally one or more of an antioxidant, processing aid, and colorant.
  • the present invention is directed to a method of making a flame-retarded article comprising blending a thermoplastic polymer, a brominated flame retardant, a metal phosphonaie, e.g. , aluminum methyl methyiphosphonate and an antidripping agent, e.g., PTFE.
  • any reference to a flame-retarded styrenic thermoplastic polymer composition is such that the composition is in the absence of antimony trioxide.
  • the present, invention is directed to a flame retardant: additive composition that comprises a unique and unexpected combination of a bromine compound, a high phosphorus-content compound and an antidripping agent, e.g., poiytetrafluoroethylene.
  • a flame retardant additive composition can be used in styrenic thermoplastic polymers and compositions containing styrenic thermoplastic polymers, to provide flame retardancy without use of antimony irioxide.
  • Styrenic thermoplastic polymer (a) refers to polymers, and specifically copolymers (including terpolymers), which contain (optionally substituted) a styrenic structural unit, however combined with one or more oilier structural units. More specific examples of styrenic thermoplastic polymer (a) are st rene -based copolymers belonging to the following classes:
  • HIPS rubber-modified copolymers of styrenic monomers, obtainable, for example, by mixing an elastomer (butadiene) with the (optionally substituted) styrenic monomer(s) prior to polymerization.
  • the styrenic thermoplastic polymer (a) generally comprise between 40 wt.% and 85 wt3 ⁇ 4, more specifically between 50 wt% and 85 ⁇ vt% HIPS resins having a melt flow index (MFI) between 1 and 50 g/l Omm (measured according to ISO 1 133; 200°C/5kg).
  • ABS copolymers and terpolymers that include the structural units corresponding to (optionally substituted) stymie, acrylonitrile and butadiene, regardless of the composition and method of production of said polymers.
  • the styrenic thermoplastic polymer (a) can comprise between 40 wt% and 85 wt%, more specifically between 50 ⁇ vt% and 83 wl% ABS having an MFI between 1 and 50 g/l Omin (measured according to ISO 1 133 at: 220°C/I 0 kg).
  • SAN copolymer of acrylonitrile and sty ie, and SMA; copolymer of stymie with maleic anhydride.
  • the styrenic thermoplastic polymer (a) can in one embodiment comprise between 40 wt% and 85 wt% SAN, and in another embodiment can comprise between 40 wt.% and 85 wt% SMA.
  • the flame-retarded styrenic thermoplastic polymer composition of the invention can contain as the styrenic thermoplastic polymer (a) an alloy of styrene-containing polymers, namely, a blend of a styrene-eontaining polymer as set forth above with a second polymer or copolymer (such blends are obtained by extruding pellets of the styrene-eontaining polymer (a) and pellets of the second polymer in desired proportions).
  • a an alloy of styrene-containing polymers, namely, a blend of a styrene-eontaining polymer as set forth above with a second polymer or copolymer (such blends are obtained by extruding pellets of the styrene-eontaining polymer (a) and pellets of the second polymer in desired proportions).
  • Some non-limiting examples of such blends include a blend of MIPS
  • thermoplastic styrenic polymer (a) is different from brorninated flame retardant (b). in one embodiment the thermoplastic styrenic polymer (a) is non- haiogenated,
  • Brorninated flame retardant (b) includes any flame retardant which contains a bromine atom in its chemical stmcture.
  • the most specific brorninated flame retardant compounds (h) have the following formulae.
  • Tetrabromobisphenol A sold under the trade name FR-1524
  • the brominated flame reiardant (b) is present in the flarne- retarded styreni thermoplastic polymer composition in the range of from about 5 wt% to about 40 wt% and specificall in the range from about 5 wt% to about 30 wt% based on the total weight of the flame-retarded styrenic thermoplastic polymer composition.
  • the metal phosphonate (c) used herein can be a salt of alky 1 alkylphosphonic acid or a salt of aryl alkylphosphonic acid.
  • the salt of alky] alkylphosphonic acid or salt of aryl alkylphosphonic acid can be such that the alkyi group and/or aryl group contains up to about 12 carbon atoms.
  • the metal phosphonate (c) is represented by general formula (1):
  • R 1 is a linear or branched alkyi of up to about 12 carbon atoms, specifically from 1 to about 4 carbon atoms
  • R- is a linear or branched alkyi of up to about 12 carbon atoms, specifically from 1 to about 4 carbon atoms or a substituted aryl or an uusubstit ted aryl of general formula (II): where R 3 is hydrogen, or a branched or linear alkyi of up to about 4 carbon atoms, or NH 2 or CN or NO.
  • R 1 and/or R" are each independently methyl or ethyl radicals.
  • Metals i.e.. Me of the above formula (I), Include alkaline earth or transition metals such as the non-limiting group consisting ofCa, Mg ? Zn, Al, Fe, Ni, Cr, Ti. The most specific metal is
  • the metal phosphonate (c) of the formula ( ⁇ ) is an aluminum salt of methyl methylphosphonic acid (AMMP), where Me is aluminum, R' and R 2 are both methyl and iv : -"3, AMMP contains a high level (i.e., 26 weight percent) of active phosphorus.
  • AMMP can be synthesized either by reacting methyl methylphosphonate with an aqueous solution of sodium hydroxide followed by precipitation with aluminum chloride, or by direct reaction of aluminum hydroxide with methyl methylphosphonate at about 180° C in high shear mixer.
  • the metal phosphonate (c) is a powder with an average particle size of less than about 25 microns, specifically less than about 10 microns, and even more specifically less than about 5 microns.
  • the most specific metal phosphonate (c) average particle size according to the present, embodiments comprises an average size in the range of from about 0.1 microns to about 3 microns. It will be understood that any of the aforementioned average particle size ranges can have a lower end poi nt of from about 0.1 microns.
  • the metal phosphonate (c) is present in the flame-retarded styrenie thermoplastic pol mer composition in the range from about 1 wt% to about 15 wt% and more specifically in the range from about 2 wt% to about. 10 wr% based on the total weight of the flame-retarded styrenie thermoplastic polymer composition.
  • Antidripping agent (d) is generally a fluoropolymer or copolymer containing a fluoro- ethyienie structure.
  • the antidripping agent include difluoroethyiene polymers, tetrafluaroethylene polymers, tetrafluoroethylene-hexafluoropropylene copolymers, and copolymers of tetrafluoroethylene with fluorine- tree etliylenic monomers. More specifically the antidripping agent (d) is polytetrafiuoroethylene (PTFE). Any and every type of
  • polytetrafiuoroeth lene known at present in the art is usable for antidripping agent (d).
  • polytetrafiuoroethylene used herein is not specificall limited.
  • Specific examples of the polytetTafiuoroethylene capable of forming fibrils include Teflon 6C (registered trademark of DuPont) or Hostaflon 2071 (registered trademark of Dynon).
  • the content of the antidripping agent (d) the flame-retarded styrenie titer mo plastic polymer composition is generally from 0.05 percent by weight to 2 percent by weight, specifically between 0.1 percent by weight to 0.5 percent by weight.
  • the amount of the fluororesin may be suitably detennined depending on the required flame retardancy of the article formed from the flame-retarded styrenic thermoplastic polymer composition, for example, based or».
  • V-O V-l or V-2 In UL-94 in consideration with the amount of the other components,
  • the antimony trioxide-free flame retarded styrenic thermoplastic polymer composition may also further comprise impact modifiers such as elastomers and core-shell polymers.
  • elastomers can be thermoplastic elastomers, which can be melt-mixed with thermoplastic styrenic resin (a) because they are solids having rubber-like elasticity at normal temperature, but heating them decreases the viscosity thereof.
  • the specific thermoplastic elastomer used is not particularly restricted, and olefin-, styrene-, polyester-, polyamide-and urethane-based
  • elastomers may be used as non-limiting examples.
  • ingredients that can be employed in amounts less than 10 percent by weight of the antimony irioxide-free flame retarded styrenic thermoplastic polymer composition, specifically less than 5 percent by weight include the non-limiting examples of lubricants, heat stabilizers, light stabilizers and other additi ves used to enhance the properties of the resin. Such other ingredients may be specifically utilized in amounts from 0,01 to 5 percent by weight of the total weight of the antimony trioxide-free flame-retarded styrenic thermoplastic polymer composition and include specific examples such as hindered phenols and phosphites.
  • thermoplastic polymer composition comprises styrenic thermoplastic polymer (a), ,g. , HIPS, ABS, SAN or SMA resin in an amount of from about 40 wt% to about 85 wt%; brominated flame retardant (b) in an amount of from about. 5 wt% to about 40 wt%; metal phosphonate (c) in an amount of from about 1 wt% to about 15 t% and antidripping agent (d), e.g., PTFE in an amount of from about 0.05 wt% to abou 2 wt% all based on the total weight of the antimony trioxide-free flame retarded styrenic thermoplastic polymer composition.
  • the antimony trioxide-free flame-retarded styrenic thermoplastic polymer composition comprises styrenic thermoplastic polymer (a), e.g., HIPS, ABS, SAN or SMA resin in an amount of from about 50 wt% to about 85 wt%; brominated rlaine retardant (b) in an amount of Irons about 5 wt% to about 30 wt%; the metal phosphonate (c) in an amount of from about 2 wt% to about 10 wt.% weight percent and antidripping agent(d). e.g. , PTFE in an amount of from about 0.1. wt% to about 0.5 wt% all based on the total weight of the antimony trioxide-free flame retarded styrenic thermoplastic polymer composition.
  • styrenic thermoplastic polymer e.g., HIPS, ABS, SAN or SMA resin in an amount of from about 50 wt% to about 85 wt
  • the antimony trioxide-free flam -retarded styrenic thermoplastic polymer composition or articles made therefrom herein can have a flame retardancy classification of one or more of MB, V-2, V-l , V-0 and 5.VA according to UL-94 protocol.
  • the antimony trioxide-free flame retarded styrenic thermoplastic polymer composition can have a flame retardancy of at least V-l or V-0,
  • a .flame-retarded article comprising blending the flame-retarded styrenic thermoplastic polymer compositions of this invention, tire manner of which is not critical, and can be carried out by conventional techniques.
  • One convenient method comprises blending the styrenic polymer (a) and oilier ingredients in powder or granular form, extruding the blend and comminuting the blend into pellets or other suitable shapes.
  • the best resul ts are obtained if the ingredients (a), (b), (c) and (d) are precompounded, pelletized and then molded into desirable article.
  • Precompoimding can be carried out in conventional equipment.
  • the styrenic polymer (a), other ingredients (b), (c) and (d), and, optionally, other additives are fed into a twin screw extruder in the form of a dry blend of the composition, the screw employed having a long transition section to insure proper melting.
  • a twin screw extrusion machine e.g., a ZE25 with L/D ⁇ 32 ex Berstorff extruder can be fed with the styrenic resins and additives at the feed port.
  • a generally suitable machine temperature will be about 180° to 250° C.
  • the antimony trioxide-free flame-retarded styrenic thermoplastic polymer composition can be molded in any equipment conventionally used for thermoplastic compositions. For example, good results will be obtained in an injection molding machine, e.g. of the Arburg 320S Allrounder 500-150 type, at conventional temperatures, e.g., 20(5 to 270 C. If necessary, depending on the molding properties of the styrenic polymer (a), the amount of additives, resin flow and the rate of solidification of the styrenic polymer (a), those skilled in the art will be able to make the conventional adjustments in molding cycles to accommodate the composition.
  • a molded article comprising antimony trioxide-free flame-retarded styrenic thermoplastic polymer composition, specifically where the molded article is made by injection molding the contents of the blended flame-retarded styrenic thermoplastic polymer composition.
  • the antimony trioxide-free flame-retarded styrenic thermoplastic polymer composition of the present invention is useful, for example, in the production of electronic components, such as for example, housings and frames and the like.
  • Injection molded components e.g., electronic components, comprising a styrenic polymer (a), and a flame retardant additive composition, which flame retardant additive composition comprises brommated flame retardant (b), e.g.. tribromophenol triazine, metal phosphonate (e), e.g., aluminum methyl
  • flame retardant additive composition comprises brommated flame retardant (b), e.g.. tribromophenol triazine, metal phosphonate (e), e.g., aluminum methyl
  • a flame retarded article e.g., an electronic component, preferably an injection molded electronic component, as described herein, made by the above-described method.
  • the polymers pellets, AM P, PT.FE and stabilizers were weighted on semi analytical, scales with consequent manual mixing in plastic bags.
  • the mixtures were introduced into the main feeding port of the extruder via feeder N°l .
  • FR-245 introduced into the main feeding port of the extruder via feeder N°2.
  • the compounding was performed in a twin screw co-rotating r./D ⁇ 32 ex Berstorif ZE25 at J 80°- 220°C
  • the obtained pellets of compounded mixtures were dried in a circulating air oven ex i i ' eraeus instruments at 120' J C for 4 hours.
  • Test specimens were prepared by injection molding the pellets of compounded mixtures in A [[rounder 500-150 ex. Arburg at 200-220 C
  • % phosphorus coming from aluminum phosphonate resulted in a V-l rating in HIPS.
  • a V-l rating is required for most electronic equipment applications.
  • This formulation was antimony trioxide-free and had a relatively low Br content

Abstract

There is provided herein an antimony trioxide-free flame -retarded styrenic thermoplastic polymer composition comprising: (a) at least one styrenic thermoplastic polymer; (b) at least one brominated flame retardant, (c) at least one metal phosphonate; and, (d) at least one antidripping agent. There is also provided a method of making said flame retarded styrenic thermoplastic polymer composition; and, an article comprising the styrenic thermoplastic polymer composition.

Description

ANTIMONY-FREE FLAME-RETARDED STYRENIC
THERMOPLASTIC POLYMER. COMPOSITION, ARTICLE
CONTAINING SAME AND METHOD OF MAKING SAME
The present application claims priority to U.S. Provisional Application No. 61/651.244 filed May 24, 2012 which is herein incorporated by reference in its entirety.
FIELD OF THE INVENTION
The present invention relates to flame-retarded thermoplastic compositions and more particularly to flame-retarded styrenic thermoplastic polymer compositions and articles containing the same.
BACKGROUND OF THE INVENTION
Sty.re.nic polymers and more specifically high impact polystyrene (HIPS) and
acrylonitriie, butadiene, styrene polymers (ABS) plastics axe used for the production of electronic parts such as housings, cases and internal parts, amongst others, in most of these applications, flame retardancy is needed and is usually provided by flame retardant systems based on a combination of brominated flame retardants with antimony trioxide as a synergist. But this type of flame retardant system has limitations, because antimon trioxide. being a very efficient synergist, tends to significantly increase smoke yield, which impairs visibility which could create problems for evacuation of people in the case of a fire. Further, antimony trioxide has a very high bulk density which increases the specific gravity of molded parts containing the same. This is especially undesirable in transportation and aviation applications. Furthermore, antimony trioxide has significantly increased in price in recent years. Still further, some recently introduced ecolabels require elimination of antimony trioxide from thermoplastic pails.
Although there is a clear need for low antimony trioxide or antimony trioxideTree flame retardant plastics, such plastics usually requires a significant increase in the loading of brominated flame retardant which Is also undesirable. SUMMARY OF THE INVENTION
It has been unexpectedly discovered by the inventors herein that a combination of brominated flame retardant, a high phosphorus-content flame retardani and an antidripping agent provides an excellent flame retardant additive composition for use in styrenic thermoplastic polymers, more specifically HIPS and ABS thermoplastics, such flame-retardant additive compositions provide flame retardant efficiency adequate to styrenic thermoplastic resins in electrical and electronic applications without (lie use of antimony trioxide.
The present invention is directed to an antimony irio ide-free flame-retarded styrenic thermoplastic polymer composition comprising:
(a) at least one styrenic thermoplastic polymer;
(b) at least one brominated flame reiardant;
(c) at least one metal phosphonate and,
(d) at least one antidripping agent, more specifically, polytetrafluoroethyiene (PTFE)
Further, the flame-retarded styrenic thermoplastic polymer composition can optionally further comprise impact modifiers, heat stabilizers, antioxidants, processing aids, and other additives enhancing physical properties of the resin.
Further, the present invention is also directed to a molded article comprising a styrenic thermoplastic polymer, a brominated flame retardant, aluminum methyl methyiphosphonate, PTFE, and optionally one or more of an antioxidant, processing aid, and colorant.
Still further, the present invention is directed to a method of making a flame-retarded article comprising blending a thermoplastic polymer, a brominated flame retardant, a metal phosphonaie, e.g. , aluminum methyl methyiphosphonate and an antidripping agent, e.g., PTFE.
It will be understood herein that any reference to a flame-retarded styrenic thermoplastic polymer composition is such that the composition is in the absence of antimony trioxide. DETAILED DESCRIPTIO OF THE INVENTION
The present, invention is directed to a flame retardant: additive composition that comprises a unique and unexpected combination of a bromine compound, a high phosphorus-content compound and an antidripping agent, e.g., poiytetrafluoroethylene. Such flame retardant additive compositions can be used in styrenic thermoplastic polymers and compositions containing styrenic thermoplastic polymers, to provide flame retardancy without use of antimony irioxide.
Styrenic thermoplastic polymer (a), as used herein, refers to polymers, and specifically copolymers (including terpolymers), which contain (optionally substituted) a styrenic structural unit, however combined with one or more oilier structural units. More specific examples of styrenic thermoplastic polymer (a) are st rene -based copolymers belonging to the following classes:
1 . HIPS: rubber-modified copolymers of styrenic monomers, obtainable, for example, by mixing an elastomer (butadiene) with the (optionally substituted) styrenic monomer(s) prior to polymerization. The styrenic thermoplastic polymer (a) generally comprise between 40 wt.% and 85 wt¾, more specifically between 50 wt% and 85 \vt% HIPS resins having a melt flow index (MFI) between 1 and 50 g/l Omm (measured according to ISO 1 133; 200°C/5kg).
2. ABS: copolymers and terpolymers that include the structural units corresponding to (optionally substituted) stymie, acrylonitrile and butadiene, regardless of the composition and method of production of said polymers. The styrenic thermoplastic polymer (a) can comprise between 40 wt% and 85 wt%, more specifically between 50 \vt% and 83 wl% ABS having an MFI between 1 and 50 g/l Omin (measured according to ISO 1 133 at: 220°C/I 0 kg).
3. SAN: copolymer of acrylonitrile and sty ie, and SMA; copolymer of stymie with maleic anhydride. The styrenic thermoplastic polymer (a) can in one embodiment comprise between 40 wt% and 85 wt% SAN, and in another embodiment can comprise between 40 wt.% and 85 wt% SMA.
In one embodiment the flame-retarded styrenic thermoplastic polymer composition of the invention can contain as the styrenic thermoplastic polymer (a) an alloy of styrene-containing polymers, namely, a blend of a styrene-eontaining polymer as set forth above with a second polymer or copolymer (such blends are obtained by extruding pellets of the styrene-eontaining polymer (a) and pellets of the second polymer in desired proportions). Some non-limiting examples of such blends include a blend of MIPS and polypheny lene oxide or a blend of ABS with polycarbonate. For an ABS/polyearbonate alloy, such can comprise the styrene-eontaining polymer (ABS) at a concentration in the range between 5 wt% and 85 wt%. hi one embodiment thermoplastic styrenic polymer (a) is different from brorninated flame retardant (b). in one embodiment the thermoplastic styrenic polymer (a) is non- haiogenated,
Brorninated flame retardant (b) includes any flame retardant which contains a bromine atom in its chemical stmcture. The most specific brorninated flame retardant compounds (h) have the following formulae.
Decabromodiphenyl oxide sold under the trade name FR-1210
Figure imgf000005_0001
Tetrabromobisphenol A sold under the trade name FR-1524
Figure imgf000005_0002
Tetrabromobisphenol A bis (23-dibromo ropyl ether) sold under the trade name FR.-720
Figure imgf000005_0003
(ΪΟ) Tri.s(iribromo heiioxy)l"riazine sold under the trade name PR
Figure imgf000006_0001
Tris(tribromoneopenyl) phosphate sold under the trade name F ~
GHjBr O CH3Br
I II I
-C-CH2— 0~ P—O— CI¾— C— -CHjBr
C¾Br O CHjBr
CI¾
BrCH -C CHjBr
CiWir
Brominated poiyaerylate sold under the trade name F.R-1025
Figure imgf000006_0002
(VI)
Brominated olystyrene sold under the trade name F -803P
Figure imgf000006_0003
(VII) Brominated epoxy polymers sold under the trade name F-2000 series
OI , , , 9» Ci!, , o
CM;- CMS- CI t. j )— 0—CH-~ i!C— Cii:
CM,
(VIII)
Bromhiated end-capped epoxy polymers sold under the trade naiite F-3000
Figure imgf000007_0001
Phenoxy -terminated carbonate oligomer of tetrabromobis phenol A
Figure imgf000007_0002
(X)
Deeabromodlpheny'leihane
Figure imgf000007_0003
T r r t
Teiradeeabromodiphenoxy benzene
Figure imgf000007_0004
(XI?) Ethyienebistetrabromop thaiixTjide
Figure imgf000008_0001
Tetrabromobisphenot S bis (2,3-dibroH!Oprapyl ether)
Figure imgf000008_0002
Poly-dibro oplieriylerie oxide
Figure imgf000008_0003
2-eihylhexyl tetrabroniophthalate ester
Figure imgf000008_0004
Bis (tribroniophenoxy) ethane
Figure imgf000008_0005
Preferably, the brominated flame reiardant (b) is present in the flarne- retarded styreni thermoplastic polymer composition in the range of from about 5 wt% to about 40 wt% and specificall in the range from about 5 wt% to about 30 wt% based on the total weight of the flame-retarded styrenic thermoplastic polymer composition.
The metal phosphonate (c) used herein can be a salt of alky 1 alkylphosphonic acid or a salt of aryl alkylphosphonic acid. In one embodiment the salt of alky] alkylphosphonic acid or salt of aryl alkylphosphonic acid can be such that the alkyi group and/or aryl group contains up to about 12 carbon atoms. In a further embodiment the metal phosphonate (c) is represented by general formula (1):
Figure imgf000009_0001
where Me is a metal, n is equal to the valency of the racial which is in the range of from 1 to 4, specifically 2 or 3, R1 is a linear or branched alkyi of up to about 12 carbon atoms, specifically from 1 to about 4 carbon atoms, R- is a linear or branched alkyi of up to about 12 carbon atoms, specifically from 1 to about 4 carbon atoms or a substituted aryl or an uusubstit ted aryl of general formula (II):
Figure imgf000009_0002
where R3 is hydrogen, or a branched or linear alkyi of up to about 4 carbon atoms, or NH2 or CN or NO..
In one specific embodiment, R1 and/or R" are each independently methyl or ethyl radicals.
Metals, i.e.. Me of the above formula (I), Include alkaline earth or transition metals such as the non-limiting group consisting ofCa, Mg? Zn, Al, Fe, Ni, Cr, Ti. The most specific metal is
AL
In one embodiment the metal phosphonate (c) of the formula (Ϊ) is an aluminum salt of methyl methylphosphonic acid (AMMP), where Me is aluminum, R' and R2 are both methyl and iv:-"3, AMMP contains a high level (i.e., 26 weight percent) of active phosphorus. AMMP can be synthesized either by reacting methyl methylphosphonate with an aqueous solution of sodium hydroxide followed by precipitation with aluminum chloride, or by direct reaction of aluminum hydroxide with methyl methylphosphonate at about 180° C in high shear mixer.
Specifically, the metal phosphonate (c) is a powder with an average particle size of less than about 25 microns, specifically less than about 10 microns, and even more specifically less than about 5 microns. The most specific metal phosphonate (c) average particle size according to the present, embodiments comprises an average size in the range of from about 0.1 microns to about 3 microns. It will be understood that any of the aforementioned average particle size ranges can have a lower end poi nt of from about 0.1 microns.
Specifically, the metal phosphonate (c) is present in the flame-retarded styrenie thermoplastic pol mer composition in the range from about 1 wt% to about 15 wt% and more specifically in the range from about 2 wt% to about. 10 wr% based on the total weight of the flame-retarded styrenie thermoplastic polymer composition.
Antidripping agent (d) is generally a fluoropolymer or copolymer containing a fluoro- ethyienie structure. Examples of the antidripping agent include difluoroethyiene polymers, tetrafluaroethylene polymers, tetrafluoroethylene-hexafluoropropylene copolymers, and copolymers of tetrafluoroethylene with fluorine- tree etliylenic monomers. More specifically the antidripping agent (d) is polytetrafiuoroethylene (PTFE). Any and every type of
polytetrafiuoroeth lene known at present in the art is usable for antidripping agent (d).
Among polytetraiTuoroethyienes, the use of those which are capable of forming fibrils can impart especially high melt-dripping preventing ability. The fibril-forming
polytetrafiuoroethylene used herein is not specificall limited. Specific examples of the polytetTafiuoroethylene capable of forming fibrils include Teflon 6C (registered trademark of DuPont) or Hostaflon 2071 (registered trademark of Dynon).
The content of the antidripping agent (d) the flame-retarded styrenie titer mo plastic polymer composition is generally from 0.05 percent by weight to 2 percent by weight, specifically between 0.1 percent by weight to 0.5 percent by weight. The amount of the fluororesin may be suitably detennined depending on the required flame retardancy of the article formed from the flame-retarded styrenic thermoplastic polymer composition, for example, based or». V-O V-l or V-2 In UL-94 in consideration with the amount of the other components,
The antimony trioxide-free flame retarded styrenic thermoplastic polymer composition may also further comprise impact modifiers such as elastomers and core-shell polymers. These elastomers can be thermoplastic elastomers, which can be melt-mixed with thermoplastic styrenic resin (a) because they are solids having rubber-like elasticity at normal temperature, but heating them decreases the viscosity thereof. The specific thermoplastic elastomer used is not particularly restricted, and olefin-, styrene-, polyester-, polyamide-and urethane-based
elastomers may be used as non-limiting examples.
Other ingredients that can be employed in amounts less than 10 percent by weight of the antimony irioxide-free flame retarded styrenic thermoplastic polymer composition, specifically less than 5 percent by weight, include the non-limiting examples of lubricants, heat stabilizers, light stabilizers and other additi ves used to enhance the properties of the resin. Such other ingredients may be specifically utilized in amounts from 0,01 to 5 percent by weight of the total weight of the antimony trioxide-free flame-retarded styrenic thermoplastic polymer composition and include specific examples such as hindered phenols and phosphites.
In one embodiment herein, the antimony trioxide-free flame retarded styrenic
thermoplastic polymer composition comprises styrenic thermoplastic polymer (a), ,g. , HIPS, ABS, SAN or SMA resin in an amount of from about 40 wt% to about 85 wt%; brominated flame retardant (b) in an amount of from about. 5 wt% to about 40 wt%; metal phosphonate (c) in an amount of from about 1 wt% to about 15 t% and antidripping agent (d), e.g., PTFE in an amount of from about 0.05 wt% to abou 2 wt% all based on the total weight of the antimony trioxide-free flame retarded styrenic thermoplastic polymer composition.
In a more specific embodiment, the antimony trioxide-free flame-retarded styrenic thermoplastic polymer composition comprises styrenic thermoplastic polymer (a), e.g., HIPS, ABS, SAN or SMA resin in an amount of from about 50 wt% to about 85 wt%; brominated rlaine retardant (b) in an amount of Irons about 5 wt% to about 30 wt%; the metal phosphonate (c) in an amount of from about 2 wt% to about 10 wt.% weight percent and antidripping agent(d). e.g. , PTFE in an amount of from about 0.1. wt% to about 0.5 wt% all based on the total weight of the antimony trioxide-free flame retarded styrenic thermoplastic polymer composition.
These amounts of flame retardant additives (b), (c) and (d) in the antimony trioxide-Jfree flame-retarded styrenic thermoplastic polymer composition or articles made therefrom are flanie-retardant effective amounts thereof.
The antimony trioxide-free flam -retarded styrenic thermoplastic polymer composition or articles made therefrom herein can have a flame retardancy classification of one or more of MB, V-2, V-l , V-0 and 5.VA according to UL-94 protocol. In one embodiment, the antimony trioxide-free flame retarded styrenic thermoplastic polymer composition can have a flame retardancy of at least V-l or V-0,
There is als provided herein method of making a .flame-retarded article comprising blending the flame-retarded styrenic thermoplastic polymer compositions of this invention, tire manner of which is not critical, and can be carried out by conventional techniques. One convenient method comprises blending the styrenic polymer (a) and oilier ingredients in powder or granular form, extruding the blend and comminuting the blend into pellets or other suitable shapes.
Although it is not essential, the best resul ts are obtained if the ingredients (a), (b), (c) and (d) are precompounded, pelletized and then molded into desirable article. Precompoimding can be carried out in conventional equipment. For example, the styrenic polymer (a), other ingredients (b), (c) and (d), and, optionally, other additives are fed into a twin screw extruder in the form of a dry blend of the composition, the screw employed having a long transition section to insure proper melting. In one specific embodiment, a twin screw extrusion machine e.g., a ZE25 with L/D~32 ex Berstorff extruder can be fed with the styrenic resins and additives at the feed port. In either ease, a generally suitable machine temperature will be about 180° to 250° C.
The antimony trioxide-free flame-retarded styrenic thermoplastic polymer composition can be molded in any equipment conventionally used for thermoplastic compositions. For example, good results will be obtained in an injection molding machine, e.g. of the Arburg 320S Allrounder 500-150 type, at conventional temperatures, e.g., 20(5 to 270 C. If necessary, depending on the molding properties of the styrenic polymer (a), the amount of additives, resin flow and the rate of solidification of the styrenic polymer (a), those skilled in the art will be able to make the conventional adjustments in molding cycles to accommodate the composition.
In another embodiment herein there is provided a molded article comprising antimony trioxide-free flame-retarded styrenic thermoplastic polymer composition, specifically where the molded article is made by injection molding the contents of the blended flame-retarded styrenic thermoplastic polymer composition.
The antimony trioxide-free flame-retarded styrenic thermoplastic polymer composition of the present invention is useful, for example, in the production of electronic components, such as for example, housings and frames and the like.
In a specific embodiment herein there are provided Injection molded components, e.g., electronic components, comprising a styrenic polymer (a), and a flame retardant additive composition, which flame retardant additive composition comprises brommated flame retardant (b), e.g.. tribromophenol triazine, metal phosphonate (e), e.g., aluminum methyl
methylphosphonate and antidripping agent (d), e.g., P IPE.
In another embodiment there is provided a flame retarded article, e.g., an electronic component, preferably an injection molded electronic component, as described herein, made by the above-described method.
The following examples are used to illustrate the present invention.
EXAMPLES
in order to prepare samples of flame-retarded HIPS and ABS that illustrate the invention, the following procedures have been used.
1. Materials.
The materials used in this study are presented in Table 1.
2. Compounding
The polymers pellets, AM P, PT.FE and stabilizers were weighted on semi analytical, scales with consequent manual mixing in plastic bags. The mixtures were introduced into the main feeding port of the extruder via feeder N°l . FR-245 introduced into the main feeding port of the extruder via feeder N°2.
The compounding was performed in a twin screw co-rotating r./D~32 ex Berstorif ZE25 at J 80°- 220°C
The obtained pellets of compounded mixtures were dried in a circulating air oven ex i i'eraeus instruments at 120'JC for 4 hours.
3. injection molding.
Test specimens were prepared by injection molding the pellets of compounded mixtures in A [[rounder 500-150 ex. Arburg at 200-220 C
4. Conditioning
Specimens were conditioned at 23°C for 168 hours before testing,
5. Flammahility test
Flamrnability was tested on 1.6 mm standard bars according to IJL-94 vertical ignition protocol. 6, Results
Composition and tests results -for HIPS and ABS are presented in Table 2. As it is shown in comparative example 3 the formulation without PTFE required 1 1 wt. % Br and 4.4 \vt. % Sb20i to pass V-0 rating. The addition of 0.1 wt. % PTFE (comparative example 4) allowed a decrease of Sb,0, content to 1 wt. % with only a modest increase in Br content to 15 vvt %. However, complete elimination of Sb203 (Comparative Example 5) required 20 wt. % Br in order to pass V-0. In contrast, the use of a formulation containing 1 wt. ¾ Br and 1.3 wt . % phosphorus coming from aluminum phosphonate (examples 1 and 2) resulted in a V-l rating in HIPS. A V-l rating is required for most electronic equipment applications. This formulation was antimony trioxide-free and had a relatively low Br content,
A very similar trend was observed with the use of ABS polymer. 21 vvt. % Br was required to pass a V-0 rating in an antimony trioxide-free formulation (coinparative example 10), but only 16 wt. % Br and 1.3 vvt. % phosphorus was needed for an antimony-free formulation containing aluminum methyl methyl phosphonate.
TABLE 1 Materials
Figure imgf000015_0001
TABLE 2 Fiammability performance and physical properties of flame retardant HIPS and ABS
Figure imgf000016_0001
While the above description comprises many specifics, these specifics should not be construed as limitations, but merely as exemplifications of specific embodiments thereof. Those skilled in the art will, envision many other embodiments within the sco of the description as defined by the claims appended hereto,

Claims

CLAIMS:
1. An antimony trioxide-iree flame -retarded styrenic thermoplastic polymer
composition comprising:
(a) at least one styrenic thermoplastic polymer;
(b) at least one brominated flame retardant;
(c) at least one metal phosplionate; and,
(d) at least one anti dripping agent.
2. The flame-retarded styrenic thermoplastic polymer composition of Claim 1 , wherein sty renic thermoplastic polymer (a) is at least one selected from the group consisting of high impact polystyrene (HIPS), acrylomtrile-biitedieiie-styrene copolymer (ABS), styrene- acryionitrile copolymer (SAN), styrene-maleic anhydride copolymer (SMA).
3. The flame-retarded styrenic thermoplastic polymer compositio of Claim 1, wherein brominated flame retardant (b) is at least one compound selected from the group consisting of decabromodiphenyl oxide, tetrabromobisphenol A, tetrabromobisphenol A bis (2,3- dibromopropyl ether). tris{tribromophenoxy)triazuie> tris(tribromoneopenyl) phosphate, brominated polyacr late, brominated polystyrene, broniinated epoxy polymers, brominated end- capped epoxy polymers, phenoxy-terminated carbonate- oligomer of tetrabromobisphenol A, decabromodiphenylethane, tetradecabromodiphenoxybenzeiie,
ethylenebistetrabromophthalimide, tetrabroinobisphenol S bis (2 ,3 -dibromopropy I ether), poly- dibromophenylene oxide, 2-ethylhexyl tetrabromop thalate ester and bis (tribromophenoxy) ethane.
4. The flame-regarded styrenic thermoplastic polymer composition of Claim 1, wherein the metal phosphonate (c) Is a salt of alkyl alkylphosphonic acid or aryl alkylphosphonic acid, wherein each alkyl and/or aryl contains up to 12 carbon atoms.
5. The flame-retarded styrenic thermoplastic polymer composition of Claim 4. wherein the salt of alky i alky, phosphonic acid or ar l alky 1 phosphonic acid is represented by general formula (I);
Figure imgf000018_0001
wherein Me is a metal, "n is equal to the valency of the metal and is an integer of from 1 to 4, R' is a linear or branched alkyl of up to about 12 carbon atoms, R2 is a linear or branched alkyl of up to about 12 cai'bon atoms or substituted ary l o an unsubstituted aryl of general formula (II):
ri where R5 is selected from hydrogen, a branched or linear alkyl of up to about 4 carbon atoms, NI L. CN and NO,.
6. The flame-retarded styrenic thermoplastic polymer composition of Claim 5, wherein n is 2 or 3, and/or wherein R1 is a linear or branched alkyl of up to 4 carbon atoms.
7. The flame-retarded styrenic thermoplastic polymer composition of Claim 4, wherein the metal phosphonate (c) is aluminum methyl rnethylphosphonate.
8. The flame-retarded styrenic thermoplastic polymer composition of Claim 1, wherei the antidripping agent (d) is polytetrafluoroethylene.
9. The flame-retarded styrenic thermoplastic polymer composition of Claim 1 further comprising an impact modifier.
10. The flame-retarded, styrenic thermoplastic polymer composition of Claim 1 further comprising a heat stabilizer and/or an antioxidant.
1 1 . The flame-retarded styrenic thermoplastic polymer composition of Claim 1 wherein the styrenic polymer (a) is present in an amount, of from about 40 t about 85 weight percent; the brominated flame retardant (b) is present in an amount of from about 5 to about 40 weight percent, the metal phosphonate (c) is present in an amount from about 1 to about 15 weight percent and the anti dripping agent (d) is present in the amount from 0,01 to 2 weight percent wherein said weight percents are based on the total weight of the flame-retarded styrenic thermoplastic polymer composition.
12. The flame-retarded styrenic thermoplastic polymer composition of Claim 1 wherein the styrenic polymer (a) is present in an amount of front about 50 to about 85 weight percent; the brominated flame retardant b) is present in an amount of from about 5 to about 30 weight percent, the metal phosphonate (c) is present in an amount from about 2 to about 10 weight percent, and the antidripping agent (d) is present in the amount from 0.1 to 0.5 weight percent wherein said weight percents are based on the total weight of the flame- retarded styrenic thermoplastic polymer composition,.
13. A molded article comprising the flame-retarded styrenic thermoplastic polymer compositio of Claim 1.
14. A method of making a flame-retarded article comprising blending
(a) at least one thermoplastic styrenic polymer;
(b) at least one brominated flame retardant,
(c) at least one metal phosphonate
(d) at least one antidripping agent; and,
optionally at least one of an impact modifier, antioxidant, heat stabilizer and light stabiliser, wherein blending occurs in the absence of antimony tri-oxide.
15. A flame-retarded article made by the method of Claim 14.
16. The flame-retarded article of Claim 15 wherein the article is an injection-molded electric component.
PCT/US2013/039474 2012-05-24 2013-05-03 Antimony-free flame-retarded styrenic thermoplastic polymer composition, article containing same and method of making same WO2013176868A1 (en)

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