WO2005120165A2 - Fire retardant formulations - Google Patents

Fire retardant formulations Download PDF

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Publication number
WO2005120165A2
WO2005120165A2 PCT/IL2005/000612 IL2005000612W WO2005120165A2 WO 2005120165 A2 WO2005120165 A2 WO 2005120165A2 IL 2005000612 W IL2005000612 W IL 2005000612W WO 2005120165 A2 WO2005120165 A2 WO 2005120165A2
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WO
WIPO (PCT)
Prior art keywords
concentration
fire
antimony trioxide
retardant formulation
formulation
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/IL2005/000612
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French (fr)
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WO2005120165A3 (en
Inventor
Yoav Bar-Yaakov
Ita Finberg
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bromine Compounds Ltd
Original Assignee
Bromine Compounds Ltd
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 Bromine Compounds Ltd filed Critical Bromine Compounds Ltd
Priority to US11/597,784 priority Critical patent/US7695650B2/en
Priority to CN2005800189455A priority patent/CN1965055B/en
Priority to KR1020067025825A priority patent/KR101146876B1/en
Priority to JP2007526694A priority patent/JP2008501844A/en
Priority to EP05750315A priority patent/EP1784474A4/en
Publication of WO2005120165A2 publication Critical patent/WO2005120165A2/en
Publication of WO2005120165A3 publication Critical patent/WO2005120165A3/en
Anticipated expiration legal-status Critical
Priority to US12/706,311 priority patent/US8663509B2/en
Ceased legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K21/00Fireproofing materials
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K21/00Fireproofing materials
    • C09K21/14Macromolecular materials
    • 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
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477Six-membered rings
    • C08K5/3492Triazines
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K21/00Fireproofing materials
    • C09K21/02Inorganic materials
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K21/00Fireproofing materials
    • C09K21/06Organic materials
    • 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
    • C08K5/03Halogenated hydrocarbons aromatic, e.g. C6H5-CH2-Cl
    • 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

Definitions

  • the present invention relates to improved fire-retardant formulations. More specifically, the present invention relates to improved fire-retardant
  • HIPS Polystyrene
  • ABS Acrylonitrile-Butadiene-Styrene terpolymer
  • Styrenic resins are widely used in many applications including those where fireproof materials are necessary. Such applications include for
  • FR-245 decabromodiphenyl oxide and more recently tris(2,4,6-tribromophenoxy)-s- triazine the latter known as FR-245.
  • the advantages of FR-245 are good balance of properties, high level of mechanical properties, high processing heat stability, good light stability, high melt flow and no blooming.
  • JP 11323064 discloses the incorporation of fire-retardant formulation comprising tris(2,4,6-tribromophenoxy)-s-triazine known as FR-245, tris(3-
  • bromo-2,2(bromomethyl)propyl)phosphate known as FR-370, antimony
  • antimony trioxide serving as a synergist
  • UL-94V is UL (Underwriter Laboratories) Standard for Safety for Tests for Parts in Devices and Appliances.
  • a fire-retardant formulation containing FR-245 with 11.5 wt. % Br, 0.08 wt. % PTFE and 3.5 wt. % antimony trioxide is also rated UL-94 V-0, but reducing the bromine content to 10.5 wt. % Br results in derating to UL-94 V-1 because of long afterglow time.
  • JP 11323064 overcomes this problem by introducing FR-370 to the formulation, which effectively reduces that time, while keeping relatively low levels of bromine-based fire-retardant.
  • JP 11323064 states that incorporation of FR-370 in the
  • Still another object of the present invention is to provide a fire-retardant formulation with improved technical and mechanical properties.
  • Still another object of the present invention is to provide a fire-retardant formulation that is cost-effective.
  • Still anther object of the present invention is to provide a fire-retarded
  • styrene-containing polymer for injection molding or extrusion essentially comprising said fire-retardant formulation.
  • Still another object of the present invention is to provide fire-retarded
  • styrene-containing polymer that may be HIPS or ABS.
  • the present invention provides a fire-retardant formulation that meets
  • the formulation comprises FR-245, antimony trioxide, PTFE and optionally carbon black pigment, in which
  • the acceptable concentrations of bromine range between about 9.0 and about 10.5 wt. % and those of antimony trioxide range between about 1.8 and about 3.2 wt. %.
  • FR-HIPS FR-HIPS
  • carbon black a preferred pigment
  • halogen based fire retardant In addition to the polystyrenic polymer, halogen based fire retardant,
  • additives are: fillers, pigments, dyes, impact modifiers,
  • UV stabilizers antioxidants, processing aids, nucleating agents, lubricants and the like.
  • the flame retarded formulations may be shaped into the final object by
  • test samples as well as the methods and conditions for their preparation. Flammability was tested according to UL-94V.
  • Antimony trioxide is added as 80% concentrate in polystyrene carrier.
  • Carbon black is added as 35% concentrate in polystyrene carrier.
  • the components are weighed on Sartorius semi- analytical scales with consequent manual mixing in plastic bags. All the components are introduced into an extruder via K-SFS 24 gravimetric feeding system ex.
  • Test specimens were prepared by injection molding in an Allrounder 500
  • test specimens Prior to UL-94 testing test specimens are conditioned at 70 °C for 168
  • Table 4 summarizes several composition and flammability test results of prior art related fire-retardant formulations as well as of formulations relating to the present invention. From this table it is clearly
  • Reference Example 8 Reference Example 9, Reference Example 10 and Example 2 to Example 3 relate to FR-245 containing formulations having varying concentrations of the components Further reduction of FR-245 to 10 wt. % bromine while keeping the antimony trioxide concentration relatively high (Reference Example 8) results in derating to V-1. Omission of PTFE from this formulation (Reference Example 9) results in dripping with cotton ignition and V-2 rating. Further addition of carbon black to Reference Example 8 (Reference Example 10) results in long afterglow effect and a rating of V-1. However, reduction of antimony trioxide to 2.5 wt.
  • Example 2 surprisingly improves flammability retardation and is rated V-0. Further reduction of antimony trioxide to 1 wt. % (Reference Example 12) results in total burning of the specimen up to the clamps and in a HB rating.
  • the upper concentration limit of antimony trioxide is tested in Reference Example 11 vs. Example 1; at antimony trioxide concentration of 3.2 wt. % the formulation is rated V-1 because of long after glow time (Reference Example 11); at antimony trioxide concentration of 3.0 wt. % the formulation is rated V-0 (Example 1).
  • the concentration limits of PTFE are tested in formulations Reference Example 13, 0.02 wt. %, and Reference Example 14, 0.4 wt. %.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Inorganic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Fireproofing Substances (AREA)

Abstract

A fire-retardant formulation for styrene-containing polymers comprising tris(2,4,6-tribromophenoxy)-s-triazine (FR-245), antimony trioxide and polytetrafluoroethylene (PTFE), wherein the bromine concentration in said fire-retardant formulation is from about 9.0 to about 10.5 wt. %, said antimony trioxide concentration being lower than about 3.2 wt. %.

Description

FIRE RETARDANT FORMULATIONS
Field of the invention
The present invention relates to improved fire-retardant formulations. More specifically, the present invention relates to improved fire-retardant
formulations for styrene polymers and more particularly for High Impact
Polystyrene (HIPS) and Acrylonitrile-Butadiene-Styrene terpolymer (ABS).
Background
Styrenic resins are widely used in many applications including those where fireproof materials are necessary. Such applications include for
example TV cabinets, in which there is a need for the incorporation of fire- retardants (FR) in styrene-polymeric materials.
Traditional FRs for these applications include, inter alia,
decabromodiphenyl oxide and more recently tris(2,4,6-tribromophenoxy)-s- triazine the latter known as FR-245. The advantages of FR-245 are good balance of properties, high level of mechanical properties, high processing heat stability, good light stability, high melt flow and no blooming.
However, unlike formulations based on decabromodiphenyl oxide, the
formulations based on FR-245 tend to induce long after glow time. This effect is enhanced when carbon black is added to the formulation. JP 11323064 discloses the incorporation of fire-retardant formulation comprising tris(2,4,6-tribromophenoxy)-s-triazine known as FR-245, tris(3-
bromo-2,2(bromomethyl)propyl)phosphate known as FR-370, antimony
trioxide (Sb2O3) and PTFE (polytetrafluoroethylene) in rubber reinforced polystyrene also known as HIPS, wherein the bromine content, the main component responsible for fire retardation, is between 9.5 and 11 wt. %
and wherein antimony trioxide, serving as a synergist, is between 3.5 and
3.7 wt. %.
This formulation is claimed to successfully meet the requirement of UL-94 class V-0 according to the flammability tests, where five specimens are ignited, twice each, and the fulfillment of 5 requirements is necessary to
pass a UL-94 V-0 standard, namely:
1. Maximum after flame time < 10 seconds (for each ignition).
2. Total after flame time of 10 ignitions less or equal to 50 seconds.
3. Maximum after flame + after glow time less or equal to 30 seconds.
4. None of the test specimens burns or glows up to the holding clamp.
5. No cotton ignition by dripping.
UL-94V is UL (Underwriter Laboratories) Standard for Safety for Tests for Parts in Devices and Appliances.
A fire-retardant formulation containing FR-245 with 11.5 wt. % Br, 0.08 wt. % PTFE and 3.5 wt. % antimony trioxide is also rated UL-94 V-0, but reducing the bromine content to 10.5 wt. % Br results in derating to UL-94 V-1 because of long afterglow time. JP 11323064 overcomes this problem by introducing FR-370 to the formulation, which effectively reduces that time, while keeping relatively low levels of bromine-based fire-retardant.
Although JP 11323064 states that incorporation of FR-370 in the
formulation allows maintaining low levels of bromine, which enhances technical properties of articles incorporating it and leads to cost-effective FR formulations, the inventors of the present invention note that FR-370
is a very expensive material and its use in fire-retardant formulations offers a high-cost non-economical solution for reducing or eliminating the afterglow phenomenon and for achieving V-0 flammability test rating.
Summary of the Invention
The applicants have surprisingly found that by lowering the concentration
levels of antimony trioxide to certain ranges while maintaining low levels of bromine, a fire-retardant formulation that essentially meets the
requirement UL-94 class V-0 standards is achieved without evoking the need for high-cost or other materials. In particular, it has also been found
that even when incorporating additives to the formulation as carbon black
pigment those concentration ranges of the respective components still allow to successfully pass the standard flammability tests. It is therefore an object of the present invention to provide a fire-retardant formulation that essentially meets the requirement standard according to the flammability tests.
It is yet another object of the present invention to provide a pigmented
fire-retardant formulation that essentially meets the requirement standard according to the flammability tests.
Still another object of the present invention is to provide a fire-retardant formulation with improved technical and mechanical properties.
Still another object of the present invention is to provide a fire-retardant formulation that is cost-effective.
Still anther object of the present invention is to provide a fire-retarded
styrene-containing polymer for injection molding or extrusion essentially comprising said fire-retardant formulation.
Still another object of the present invention is to provide fire-retarded
styrene-containing polymer that may be HIPS or ABS.
This and other objects of the invention will become apparent as the description proceeds. Detailed description of the invention
The present invention provides a fire-retardant formulation that meets
the requirement UL-94 V-0 standard according to the flammability tests and which is also cost-effective.
According to the present invention the formulation comprises FR-245, antimony trioxide, PTFE and optionally carbon black pigment, in which
the acceptable concentrations of bromine range between about 9.0 and about 10.5 wt. % and those of antimony trioxide range between about 1.8 and about 3.2 wt. %.
Styrene rubber reinforced polymers containing fire-retardant formulations
(FR-HIPS) are often required to possess a black or gray color. This is achieved by the incorporation of carbon black, a preferred pigment, to
these formulations. However, a side-effect of carbon black when introduced in a fire-retardant formulation is long period of time afterglow
effect, where the formulation comprises essentially the same components having the same concentrations as disclosed in JP 11323064, excluding the
presence of FR-370.
In addition to the polystyrenic polymer, halogen based fire retardant,
antimony oxide, PTFE and the carbon black there can be present in the formulation conventional additives in their conventional amounts. Examples of such additives are: fillers, pigments, dyes, impact modifiers,
UV stabilizers, antioxidants, processing aids, nucleating agents, lubricants and the like.
The flame retarded formulations may be shaped into the final object by
processes that are well known to the person skilled in the art; non limiting examples of such processes are: injection molding, extrusion, press
molding, vacuum forming, etc.
Examples
The present invention will now be described in more detail with Examples and Reference Examples.
Tables 1-3 below summarize the materials used for the preparation of the
test samples as well as the methods and conditions for their preparation. Flammability was tested according to UL-94V.
Table 1 Materials
Figure imgf000008_0001
* Antimony trioxide is added as 80% concentrate in polystyrene carrier. *Carbon black is added as 35% concentrate in polystyrene carrier.
Compounding
All formulations were prepared under the same conditions.
The components are weighed on Sartorius semi- analytical scales with consequent manual mixing in plastic bags. All the components are introduced into an extruder via K-SFS 24 gravimetric feeding system ex.
K-Tron.
Compounding is performed in a co-rotating twin-screw extruder ZE25 ex Berstorff with L/D=32. The compounding conditions are presented in
Table 2. The extruded strands are pelletized in pelletizer 750/3 ex Accrapak Systems Limited. The obtained pellets are dried in a circulating air oven ex Heraeus
Instruments at 75°C for 4 hours. Table 2 Compounding conditions
Figure imgf000009_0001
Injection molding
Test specimens were prepared by injection molding in an Allrounder 500
150 ex. Arburg. All test specimens were prepared under the same conditions. The injection molding conditions are presented in Table 3.
Table 3 Injection molding conditions
Figure imgf000010_0001
Conditioning
Prior to UL-94 testing test specimens are conditioned at 70 °C for 168
hours and at 23°C for 168 hours.
Compositions and flammability test results are presented in Table 4 for
HIPS compositions and in Table 5 for ABS compositions.
Table 4 HIPS compositions and flammability test results
Figure imgf000011_0001
Figure imgf000011_0002
Figure imgf000012_0001
Table 4 (Continued) HIPS compositions and test flammability results
Figure imgf000012_0002
Table 4 above summarizes several composition and flammability test results of prior art related fire-retardant formulations as well as of formulations relating to the present invention. From this table it is clearly
seen that:
(a) Formulations (Reference Example-6) based on JP 11323064 pass successfully the V-0 flammability test, but introducing 1 wt. % carbon black pigment (Reference Example- 7), results in derating to V-1 due to long afterglow time.
(b) In fire-retardant FR-1210 (decabromodiphenyl oxide) based formulations - Reference Examples 1-5 - the first two formulations substantially having the same bromine, antimony trioxide and PTFE concentrations as in Reference Examples 6 and 7 pass V-0 tests, even when containing carbon black pigment (Reference Example 2). Reducing bromine content to 10 wt. % and then further elimination of PTFE from this formulation result in V-0 and V-2 rating, respectively (Reference Example 3 and Reference Example 4), the latter is due to burning drops ignited cotton effect. Addition of carbon black to Reference Example 3 does not derate the formulation and it passes V-0 tests (Reference Example 5). It should be noted that the antimony trioxide remains essentially unchanged in all those formulation variations. (c) Reference Example 8, Reference Example 9, Reference Example 10 and Example 2 to Example 3 relate to FR-245 containing formulations having varying concentrations of the components Further reduction of FR-245 to 10 wt. % bromine while keeping the antimony trioxide concentration relatively high (Reference Example 8) results in derating to V-1. Omission of PTFE from this formulation (Reference Example 9) results in dripping with cotton ignition and V-2 rating. Further addition of carbon black to Reference Example 8 (Reference Example 10) results in long afterglow effect and a rating of V-1. However, reduction of antimony trioxide to 2.5 wt. % (Example 2) surprisingly improves flammability retardation and is rated V-0. Further reduction of antimony trioxide to 1 wt. % (Reference Example 12) results in total burning of the specimen up to the clamps and in a HB rating. The upper concentration limit of antimony trioxide is tested in Reference Example 11 vs. Example 1; at antimony trioxide concentration of 3.2 wt. % the formulation is rated V-1 because of long after glow time (Reference Example 11); at antimony trioxide concentration of 3.0 wt. % the formulation is rated V-0 (Example 1). The concentration limits of PTFE are tested in formulations Reference Example 13, 0.02 wt. %, and Reference Example 14, 0.4 wt. %. In the first an effect of burning drops ignited cotton leads to V-2 rating. The second is rated V-1 due to long afterglow time. (d) The employment of both FR-245 and F-3020 (MBEO endcapped brominated epoxy resin) as the bromine fire-retardants, the first contributing about 7 wt. % and the second about 3 wt. % of the bromine content, leads to long afterglow time (Reference Example 15) when incorporating 3.5 wt. % antimony trioxide, i.e. V-1 rating, and to successful results (Example 3) when lowering antimony trioxide concentration to 2.5 wt. %, i.e. V-0. These two results are similar to the ones achieved for formulations containing only FR- 245, i.e. Reference Example 10 and Example 2, and further stress the optimal relation between bromine fire-retardant and antimony trioxide synergist contents.
Table 5 ABS compositions and results of flammability results
Figure imgf000016_0001
Table 5 demonstrates that the same effects, which are observed in HIPS
formulations, are also applied in ABS based formulations.
HIPS and ABS containing fire-retardant formulations containing FR-245 or a combination of FR-245 and BEO's at low bromine content and with
the incorporation of carbon black do not pass UL-94 V-0 because of long
after glow time. It is surprisingly found that at low antimony trioxide concentrations it is possible to pass UL-94 V-0 and get economic cost- effective formulations with good mechanical, thermal and processing properties. While examples of the invention have been described for purposes of illustration, it will be apparent that many modifications, variations and adaptations can be carried out by persons skilled in the art, without
exceeding the scope of the claims.

Claims

1. A fire-retardant formulation for styrene-containing polymers comprising tris(2,4,6-tribromophenoxy)-s-triazine (FR-245), antimony trioxide and polytetrafluoroethylene (PTFE), wherein the bromine concentration in said fire-retardant formulation is from about 9.0 to about 10.5 wt. %, said antimony trioxide concentration being lower than about 3.2 wt. %.
2. A formulation according to claim 1, wherein the antimony trioxide concentration is from about 1.8 to about 3.2 wt. % and the PTFE concentration is from about 0.03 to about 0.2 wt. %.
3. The fire-retardant formulation of any one of claims 1 or 2, wherein the bromine concentration is about 10 wt. %, the antimony trioxide concentration is about 3.0 wt. %, and the PTFE concentration is about 0.1 wt. %.
4. The fire-retardant formulation of any one of claims 1 or 2, wherein the bromine concentration is about 10 wt. %, the antimony trioxide concentration is about 2.5 wt. %, and the PTFE concentration is about 0.1 wt. %.
5. A fire-retardant formulation according to claim 1, further comprising carbon black, wherein the bromine concentration in said fire-retardant formulation is from about 9.0 to about 10.5 wt. %, said antimony trioxide concentration being lower than about 3.2 wt. %.
6. The fire-retardant formulation of claim 5, wherein the carbon black concentration is from about 0.3 to about 2 wt. %.
7. The fire-retardant formulation of any one of claims 5 or 6, wherein the bromine concentration is about 10 wt. %, the antimony trioxide concentration is about 3.0 wt. %, the PTFE concentration is about 0.1 wt. % and the carbon black concentration is about 1.0 wt. %.
8. The fire-retardant formulation of any one of claims 5 or 6, wherein the bromine concentration is about 10 wt. %, the antimony trioxide concentration is about 2.5 wt. %, the PTFE concentration is about 0.1 wt. % and the carbon black concentration is about 1.0 wt. %.
9. The fire-retardant formulation according to any one of claims 1 to 8, further comprising brominated epoxy resin (BEO) or endcapped brominated epoxy resin (MBEO).
10. The fire-retardant formulation of claim 9, wherein said bromine of said BEO or MBEO is at least 3 wt. %.
11. Fire-retarded styrene-containing polymer comprising fire-retardant formulation for injection-molding or extrusion, wherein said fire- retardant formulation comprises tris(2,4,6-tribromophenoxy)-s-triazine (FR-245), antimony trioxide and polytetrafluoroethylene (PTFE) and optionally carbon black, wherein the bromine concentration in said fire-retardant formulation is from about 9.0 to about 10.5 wt. % and the antimony trioxide concentration lower than about 3.2 wt. %.
12. The polymer of claim 11, wherein the antimony trioxide concentration is from about 1.8 to about 3.2 wt. % and the PTFE concentration is from about 0.03 to about 0.2 wt. %.
13. The fire-retarded styrene-containing polymer of claim 12, wherein the fire-retardant formulation further comprises brominated epoxy resin (BEO).
14. The fire-retarded styrene-containing polymer of claim 13, wherein the bromine concentration of said BEO is about 3 wt. %.
15. A fire-retarded styrene-containing polymer according to any one of claims 11 to 14, wherein the carbon black concentration is from about 0.3 to about 2 wt. %.
16. A fire-retarded styrene-containing polymer according to claim 11, said polymer comprising a fire-retardant formulation for injection- molding or extrusion, said formulation comprising bromine in a concentration of about 10 wt. % essentially comprised in tris(2,4,6-tribromophenoxy)- s-triazine (FR-245), antimony trioxide in a concentration of about 3.0 wt. %, PTFE in a concentration of about 0.1 wt. % and carbon black in a concentration of about 1.0 wt. %.
17. A fire-retarded styrene-containing polymer according to claim 11, said polymer comprising a fire-retardant formulation for injection-molding or extrusion, said formulation comprising bromine in concentration of about 10 wt. % essentially comprised in tris(2,4,6-tribromophenoxy)-s- triazine (FR-245), antimony trioxide in a concentration of about 2.5 wt. %, PTFE in a concentration of about 0.1 wt. % and carbon black in a concentration of about 1.0 wt. %.
18. A fire-retarded styrene-containing polymer according to claim 11, said polymer comprising a fire-retardant formulation for injection- molding or extrusion, said formulation comprising bromine in a concentration of about 10 wt. % essentially comprised in tris(2,4,6-tribromophenoxy)- s-triazine (FR-245) and BEO, antimony trioxide in a concentration of about 2.5 wt. %, PTFE in a concentration of about 0.1 wt. % and carbon black in a concentration of about 1.0 wt. %.
19. A fire-retarded styrene-containing polymer according to any one of claims 11 to 18, wherein said polymer is high-impact polystyrene (HIPS).
20. A fire-retarded styrene-containing polymer according to any one of claims 11 to 18, wherein said polymer is acrylonitrile-butadiene- styrene polymer (ABS).
21. A method for upgrading fire-retardation in styrene-containing polymer, said polymer comprising a fire-retardant formulation, said fire-retardant formulation comprising tris(2,4,6-tribromophenoxy)-s- triazine (FR-245), antimony trioxide and polytetrafluoroethylene (PTFE) and optionally carbon black and brominated epoxy resin (BEO) or endcapped brominated epoxy resin (MBEO), wherein said upgrading comprises decreasing said antimony trioxide concentration in said fire- retardant formulation, to a level equal to or below 3.2 wt%.
22. A method according to claim 21, wherein the bromine concentration in the fire-retardant formulation is from about 9.0 to about 10.5 wt. %, the antimony trioxide concentration is from about 1.8 to about 3.2 wt. % and the PTFE concentration is from about 0.03 to 0.2 wt. %.
23. The method according to claim 21 or 22, wherein the bromine concentration from the BEO or MBEO is about 3 wt. %.
24. The method according to any one of claims 21 to 23, wherein the styrene-containing polymer is HIPS.
25. The method according to any one of claims 21 to 23, wherein the styrene-contaimng polymer is ABS.
26. A flame-retardant formulation for styrene-containing polymer, substantially as described and exemplified.
27. A flame-retarded styrene-containing polymer, substantially as described and exemplified.
PCT/IL2005/000612 2004-06-10 2005-06-09 Fire retardant formulations Ceased WO2005120165A2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
US11/597,784 US7695650B2 (en) 2004-06-10 2005-06-09 Fire retardant formulations
CN2005800189455A CN1965055B (en) 2004-06-10 2005-06-09 Flame Retardant Preparations
KR1020067025825A KR101146876B1 (en) 2004-06-10 2005-06-09 Fire retardant formulations
JP2007526694A JP2008501844A (en) 2004-06-10 2005-06-09 Flame retardant composition
EP05750315A EP1784474A4 (en) 2004-06-10 2005-06-09 FLAME RETARDANT
US12/706,311 US8663509B2 (en) 2004-06-10 2010-02-16 Fire retardant formulations

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IL162449 2004-06-10
IL162449A IL162449A (en) 2004-06-10 2004-06-10 Fire retardant formulations and styrene polymer compositions containing them

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