WO2009100232A1 - Flame-retardant polyolefin / thermoplastic polyurethane composition - Google Patents

Flame-retardant polyolefin / thermoplastic polyurethane composition Download PDF

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Publication number
WO2009100232A1
WO2009100232A1 PCT/US2009/033236 US2009033236W WO2009100232A1 WO 2009100232 A1 WO2009100232 A1 WO 2009100232A1 US 2009033236 W US2009033236 W US 2009033236W WO 2009100232 A1 WO2009100232 A1 WO 2009100232A1
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Prior art keywords
flame
thermoplastic polyurethane
polyolefin
polyphosphate
composition
Prior art date
Application number
PCT/US2009/033236
Other languages
French (fr)
Inventor
Geoffrey Brown
Robert Eaton
Original Assignee
Union Carbide Chemicals & Plastics Technology Llc
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 Union Carbide Chemicals & Plastics Technology Llc filed Critical Union Carbide Chemicals & Plastics Technology Llc
Priority to CN2009801116572A priority Critical patent/CN101981128A/en
Priority to MX2010008715A priority patent/MX2010008715A/en
Priority to US12/865,055 priority patent/US9758672B2/en
Priority to KR1020167002650A priority patent/KR101840574B1/en
Priority to BRPI0905902A priority patent/BRPI0905902B1/en
Priority to CA2714100A priority patent/CA2714100C/en
Priority to JP2010545998A priority patent/JP5666917B2/en
Priority to EP09707926.3A priority patent/EP2247668B1/en
Publication of WO2009100232A1 publication Critical patent/WO2009100232A1/en

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04—Polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04—Polyurethanes
    • C08L75/06—Polyurethanes from polyesters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04—Homopolymers or copolymers of ethene
    • C08L23/08—Copolymers of ethene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04—Homopolymers or copolymers of ethene
    • C08L23/08—Copolymers of ethene
    • C08L23/0846—Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
    • C08L23/0853—Vinylacetate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04—Polyurethanes
    • C08L75/08—Polyurethanes from polyethers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L85/00—Compositions of macromolecular compounds obtained by reactions forming a linkage in the main chain of the macromolecule containing atoms other than silicon, sulfur, nitrogen, oxygen and carbon; Compositions of derivatives of such polymers
    • C08L85/02—Compositions of macromolecular compounds obtained by reactions forming a linkage in the main chain of the macromolecule containing atoms other than silicon, sulfur, nitrogen, oxygen and carbon; Compositions of derivatives of such polymers containing phosphorus
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/302—Polyurethanes or polythiourethanes; Polyurea or polythiourea
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/44—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
    • H01B3/441—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins from alkenes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B7/00—Insulated conductors or cables characterised by their form
    • H01B7/17—Protection against damage caused by external factors, e.g. sheaths or armouring
    • H01B7/29—Protection against damage caused by extremes of temperature or by flame
    • H01B7/295—Protection against damage caused by extremes of temperature or by flame using material resistant to flame
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00—Properties
    • C08L2201/02—Flame or fire retardant/resistant
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00—Applications
    • C08L2203/20—Applications use in electrical or conductive gadgets
    • C08L2203/202—Applications use in electrical or conductive gadgets use in electrical wires or wirecoating

Definitions

  • This invention relates to flame retardant formulations for wire and cable applications. Specifically, it relates to halogen-free, flame retardant polyolefin / thermoplastic polyurethane formulations for jacketing for wires, jacketing for cables, extruded sheeting, and extruded profiles.
  • Metal hydrate-based polyolefin compounds and intumescent-based polyolefin compounds do not achieve simultaneously industry-required flame and mechanical properties.
  • the addition of flame retardant fillers at loadings of 40-50 weight percent to achieve good burn test performance will cause the resulting polyolefin compound to have poor mechanical properties.
  • the presently invented composition comprising a polyolefin, a thermoplastic polyurethane, and an intumescent, polyphosphate flame retardant.
  • the present invention achieves elongations > 400% and tensile strengths > 1500 psi while the same polyolefin only achieved 100% elongation and ⁇ 1000 psi tensile strength.
  • the present invention shows improved tape extrusion performance versus a comparable TPU only composition, indicating improved melt rheology / fabrication capability for extrusion applications.
  • the present invention is particularly useful in the preparation of wire-and-cable jackets and other extruded articles, such as sheeting and profiles.
  • composition of the present invention comprises a polyolefin, a thermoplastic polyurethane, and an intumescent, polyphosphate flame retardant composition.
  • the presently described composition is halogen-free.
  • the polyolefin may be polar, nonpolar, or a mixture thereof.
  • the polyolefin is present in an amount of about 5 to about 90 weight percent.
  • Suitable polar polyolefins include (i) copolymers of ethylene and an unsaturated ester, (ii) copolymers of ethylene and an unsaturated acid such as acrylic or methacrylic acid, (iii) copolymers of ethylene and a vinyl silane (e.g., vinyltrimethoxysilane and vinyltriethoxysilane), and (iv) interpolymers of any of these comonomers.
  • the polyolefin is a polar, copolymer of ethylene and an unsaturated ester.
  • the portion of the copolymer attributed to the ester comonomer can be in the range of about 5 to about 50 percent by weight based on the weight of the copolymer, and is preferably in the range of about 15 to about 40 percent by weight.
  • the melt index of the ethylene/unsaturated ester copolymers can be in the range of about 0.5 to about 50 grams per 10 minutes.
  • the alkyl groups can have 1 to 8 carbon atoms and preferably have 1 to 4 carbon atoms.
  • the acrylates and methacrylates are ethyl acrylate, methyl acrylate, methyl methacrylate, t-butyl acrylate, n-butyl acrylate, n-butyl methacrylate, and 2- ethylhexyl acrylate.
  • the unsaturated ester is a vinyl carboxylate
  • the carboxylate group can have 2 to 8 carbon atoms and preferably have 2 to 5 carbon atoms.
  • the vinyl carboxylates are vinyl acetate, vinyl propionate, and vinyl butanoate.
  • Suitable nonpolar polyolefins include (i) homopolymers of ethylene, (ii) copolymers of ethylene and one or more alpha-olefins, and, optionally, a diene, (iii) ethylene copolymers with carbon monoxide, propylene, and butene, (iv) homopolymers of propylene, (v) copolymers of propylene and other olefins, and (vi) terpolymers of propylene, ethylene, and dienes.
  • Thermoplastic polyurethane polymers are known in the art and are typically obtained by the reaction of a linear hydroxyl-terminated polyol, an organic diisocyanate, and a chain extender.
  • Thermoplastic polyurethanes (TPUs) useful in the present invention include polyester TPUs and polyether TPUs.
  • polyesters TPUs can be made with di-acids like adipic acid and diols like ethylene glycol, propane diol, and butane diol while the polyether TPUs can be made with polyols of polyethylene oxide, propylene oxide, and butylene oxide.
  • the TPU is present in an amount of about 0.1 to 95 weight percent.
  • the intumescent, polyphosphate flame retardant composition is a blend of (i) an intumescent, nitrogen-containing polyphosphate and (ii) a melamine or a melamine-derivative co-additive.
  • the intumescent, nitrogen-containing polyphosphate is an ammonium polyphosphate, a piperazine polyphosphate, or derivatives thereof. More preferably, the intumescent, nitrogen-containing polyphosphate is piperazine polyphosphate.
  • the nitrogen-containing polyphosphate has the character of swelling and charring when exposed to flame.
  • the intumescent, polyphosphate flame retardant composition is present in an amount of about 0.1 to about 70 weight percent.
  • composition of the present invention may further comprise other non- halogen flame retardants, such as metal oxides, metal oxide hydrates, metal carbonates, a carbonate plus an acid or acid-generating material, cement, urea, and polyalcohols.
  • non-halogen flame retardants such as metal oxides, metal oxide hydrates, metal carbonates, a carbonate plus an acid or acid-generating material, cement, urea, and polyalcohols.
  • the composition may further comprise other polymers such as non-olefin polymers, polyvinyl chloride, ester-ether block copolymers, ester/amide block copolymers, olefin block copolymers, and engineering plastics such as polycarbonates, polysulfones, and polyimides.
  • the composition may also further comprise other additives such as minerals and peroxides.
  • the present invention is a cable comprising one or more electrical conductors or a core of one or more electrical conductors, each conductor or core being surrounded by a flame retardant layer comprising the flame - retardant polyolefin / thermoplastic polyurethane composition described herein.
  • the present invention is an extruded article comprising the flame-retardant polyolefin / thermoplastic polyurethane composition described herein.
  • the burn tests were performed by a vertical strip test for a 45-sec perpendicular UL94 ignition @ bottom.
  • the test specimens were prepared to be a 100-mil strip of 75-mil plaque with embedded wire and 8" long.
  • test specimens were prepared using the following components:
  • PELLETHANETM 2102-75A caprolactone polyester thermoplastic polyurethane having a Shore A Hardness of 77A, a specific gravity of 1.17, and available from The Dow Chemical Company;
  • FP-2100TM intumescent, nitrogen-containing polyphosphate-based flame retardant which is a blend of piperazine polyphosphate and a phosphoric acid compound and available Amfine Chemical Corporation or Adeka Corporation.
  • Table 1 shows two comparative examples (Comp. Ex. 1 and 2) and three examples of the present invention (Example 3-5). Each amount is shown in weight percent.
  • Desired mechanical properties include a tensile strength > 1500 psi and elongation > 200 percent. For flame retardancy performance, an overall flame rating of 2 or less is acceptable.

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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)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Organic Insulating Materials (AREA)
  • Insulated Conductors (AREA)

Abstract

The present invention is a flame-retardant polyolefin / thermoplastic polyurethane formulation made from or containing a polyolefin, a thermoplastic polyurethane, and an intumescent, polyphosphate flame retardant composition. The invented system achieves elongations > 400% and tensile strengths > 1500 psi while the same polyolefin only achieved 100% elongation and <1000 psi tensile strength. Also, the present invention shows improved tape extrusion performance versus a comparable TPU only composition, indicating improved melt rheology / fabrication capability for extrusion applications.

Description

FLAME-RETARDANT POLYOLEFIN / THERMOPLASTIC POLYURETHANE COMPOSITION
This invention relates to flame retardant formulations for wire and cable applications. Specifically, it relates to halogen-free, flame retardant polyolefin / thermoplastic polyurethane formulations for jacketing for wires, jacketing for cables, extruded sheeting, and extruded profiles.
Metal hydrate-based polyolefin compounds and intumescent-based polyolefin compounds do not achieve simultaneously industry-required flame and mechanical properties. Notably, the addition of flame retardant fillers at loadings of 40-50 weight percent to achieve good burn test performance will cause the resulting polyolefin compound to have poor mechanical properties. As such, it is desirable to provide a polyolefin composition with excellent mechanical properties, such as high elongation, high flexibility (low modulus), good tensile strength, and improved deformation temperature as well as excellent burn performance.
To that end, the presently invented composition is provided, comprising a polyolefin, a thermoplastic polyurethane, and an intumescent, polyphosphate flame retardant. Specifically, the present invention achieves elongations > 400% and tensile strengths > 1500 psi while the same polyolefin only achieved 100% elongation and <1000 psi tensile strength. Also, the present invention shows improved tape extrusion performance versus a comparable TPU only composition, indicating improved melt rheology / fabrication capability for extrusion applications. The present invention is particularly useful in the preparation of wire-and-cable jackets and other extruded articles, such as sheeting and profiles.
The composition of the present invention comprises a polyolefin, a thermoplastic polyurethane, and an intumescent, polyphosphate flame retardant composition. Preferably, the presently described composition is halogen-free.
The polyolefin may be polar, nonpolar, or a mixture thereof. The polyolefin is present in an amount of about 5 to about 90 weight percent.
Suitable polar polyolefins include (i) copolymers of ethylene and an unsaturated ester, (ii) copolymers of ethylene and an unsaturated acid such as acrylic or methacrylic acid, (iii) copolymers of ethylene and a vinyl silane (e.g., vinyltrimethoxysilane and vinyltriethoxysilane), and (iv) interpolymers of any of these comonomers. Preferably, the polyolefin is a polar, copolymer of ethylene and an unsaturated ester. The portion of the copolymer attributed to the ester comonomer can be in the range of about 5 to about 50 percent by weight based on the weight of the copolymer, and is preferably in the range of about 15 to about 40 percent by weight. The melt index of the ethylene/unsaturated ester copolymers can be in the range of about 0.5 to about 50 grams per 10 minutes.
When the unsaturated ester is an alkyl acrylate or an alkyl methacrylate, the alkyl groups can have 1 to 8 carbon atoms and preferably have 1 to 4 carbon atoms. Examples of the acrylates and methacrylates are ethyl acrylate, methyl acrylate, methyl methacrylate, t-butyl acrylate, n-butyl acrylate, n-butyl methacrylate, and 2- ethylhexyl acrylate.
When the unsaturated ester is a vinyl carboxylate, the carboxylate group can have 2 to 8 carbon atoms and preferably have 2 to 5 carbon atoms. Examples of the vinyl carboxylates are vinyl acetate, vinyl propionate, and vinyl butanoate.
Suitable nonpolar polyolefins include (i) homopolymers of ethylene, (ii) copolymers of ethylene and one or more alpha-olefins, and, optionally, a diene, (iii) ethylene copolymers with carbon monoxide, propylene, and butene, (iv) homopolymers of propylene, (v) copolymers of propylene and other olefins, and (vi) terpolymers of propylene, ethylene, and dienes.
Thermoplastic polyurethane polymers are known in the art and are typically obtained by the reaction of a linear hydroxyl-terminated polyol, an organic diisocyanate, and a chain extender. Thermoplastic polyurethanes (TPUs) useful in the present invention include polyester TPUs and polyether TPUs.
Notably, the polyesters TPUs can be made with di-acids like adipic acid and diols like ethylene glycol, propane diol, and butane diol while the polyether TPUs can be made with polyols of polyethylene oxide, propylene oxide, and butylene oxide. The TPU is present in an amount of about 0.1 to 95 weight percent.
The intumescent, polyphosphate flame retardant composition is a blend of (i) an intumescent, nitrogen-containing polyphosphate and (ii) a melamine or a melamine-derivative co-additive. Preferably, the intumescent, nitrogen-containing polyphosphate is an ammonium polyphosphate, a piperazine polyphosphate, or derivatives thereof. More preferably, the intumescent, nitrogen-containing polyphosphate is piperazine polyphosphate. As an intumescent flame retardant, the nitrogen-containing polyphosphate has the character of swelling and charring when exposed to flame. The intumescent, polyphosphate flame retardant composition is present in an amount of about 0.1 to about 70 weight percent.
The composition of the present invention may further comprise other non- halogen flame retardants, such as metal oxides, metal oxide hydrates, metal carbonates, a carbonate plus an acid or acid-generating material, cement, urea, and polyalcohols.
The composition may further comprise other polymers such as non-olefin polymers, polyvinyl chloride, ester-ether block copolymers, ester/amide block copolymers, olefin block copolymers, and engineering plastics such as polycarbonates, polysulfones, and polyimides. The composition may also further comprise other additives such as minerals and peroxides.
In another embodiment, the present invention is a cable comprising one or more electrical conductors or a core of one or more electrical conductors, each conductor or core being surrounded by a flame retardant layer comprising the flame - retardant polyolefin / thermoplastic polyurethane composition described herein.
In yet another embodiment, the present invention is an extruded article comprising the flame-retardant polyolefin / thermoplastic polyurethane composition described herein.
EXAMPLES
The following non-limiting examples illustrate the invention.
Testing
(1) Yield Strength (psi);
(2) Tensile Strength @ Peak (psi);
(3) Tensile Strength @ Break (psi);
(4) Elongation @ Break (%);
(5) 1% Secant Modulus (psi);
(6) 2% Secant Modulus (psi);
(7) 5% Secant Modulus (psi); and
(8) Burn property of Not Burn Flag;
(9) Time to Flag (sec);
(10) Burn property of Total Time (sec);
(11) Not Fully Burned;
(12) Uncharred (mm below flag);
(13) No Flaming Drip; (14) High Melt Flow, wherein 1 no flow (best), 5 high flow; and
(15) Overall Rating**; Best(l)»Worst(5), wherein #1 No Flaming Drip; #2 Char Length; #3a No melt flow; #3b not burn to flag; #3c time to flag.
Burn Test
The burn tests were performed by a vertical strip test for a 45-sec perpendicular UL94 ignition @ bottom. The test specimens were prepared to be a 100-mil strip of 75-mil plaque with embedded wire and 8" long.
Exemplified Compositions The test specimens were prepared using the following components:
(1) PELLETHANE™ 2102-75A caprolactone polyester thermoplastic polyurethane, having a Shore A Hardness of 77A, a specific gravity of 1.17, and available from The Dow Chemical Company;
(2) PELLETHANE™ 2103 -80AE polyether thermoplastic polyurethane, having a Shore A Hardness of 82A, a specific gravity of 1.13, and available from The Dow Chemical Company;
(3) ELV AX™ 40L-03 ethylene/vinyl acetate copolymer having a vinyl acetate content of 40 percent and a melt index of 3 dg/m measured at 190 degrees Celsius and 2.16 kg, available from E. I. du Pont de Nemours and Company; and
(4) FP-2100™ intumescent, nitrogen-containing polyphosphate-based flame retardant, which is a blend of piperazine polyphosphate and a phosphoric acid compound and available Amfine Chemical Corporation or Adeka Corporation.
Table 1 shows two comparative examples (Comp. Ex. 1 and 2) and three examples of the present invention (Example 3-5). Each amount is shown in weight percent.
Desired mechanical properties include a tensile strength > 1500 psi and elongation > 200 percent. For flame retardancy performance, an overall flame rating of 2 or less is acceptable. TABLE 1
Figure imgf000006_0001

Claims

What is claimed is:
1. A flame-retardant polyolefin / thermoplastic polyurethane composition comprising:
(a) a polyolefin;
(b) a thermoplastic polyurethane; and
(c) an intumescent, polyphosphate flame retardant composition.
2. The flame-retardant polyolefin / thermoplastic polyurethane composition of Claim 1 wherein the composition is halogen-free.
3. The flame-retardant polyolefin / thermoplastic polyurethane composition of Claim 1 or Claim 2 wherein the polyolefin is polar.
4. The flame-retardant polyolefin / thermoplastic polyurethane composition of Claim 3 wherein the polar polyolefin is a copolymer of ethylene and an unsaturated ester.
5. The flame-retardant polyolefin / thermoplastic polyurethane composition of Claim 1 or Claim 2 wherein the intumescent, polyphosphate flame retardant composition comprises:
(i) an intumescent, nitrogen-containing polyphosphate and (ii) a melamine or a melamine-derivative co-additive.
6. The flame-retardant polyolefin / thermoplastic polyurethane composition of Claim 5 wherein the intumescent, nitrogen-containing polyphosphate is selected from the group consisting of ammonium polyphosphate and piperazine polyphosphate.
7. The flame-retardant polyolefin / thermoplastic polyurethane composition of Claim 6 wherein the intumescent, nitrogen-containing polyphosphate is piperazine polyphosphate.
8. A cable comprising one or more electrical conductors or a core of one or more electrical conductors, each conductor or core being surrounded by a flame retardant layer comprising the flame-retardant polyolefin / thermoplastic polyurethane composition according to any of Claims 1 to 7.
9. An extruded article comprising the flame-retardant polyolefin / thermoplastic polyurethane composition according to any of Claims 1 to 7.
PCT/US2009/033236 2008-02-08 2009-02-05 Flame-retardant polyolefin / thermoplastic polyurethane composition WO2009100232A1 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
CN2009801116572A CN101981128A (en) 2008-02-08 2009-02-05 Flame-retardant polyolefin / thermoplastic polyurethane composition
MX2010008715A MX2010008715A (en) 2008-02-08 2009-02-05 Flame-retardant polyolefin / thermoplastic polyurethane composition.
US12/865,055 US9758672B2 (en) 2008-02-08 2009-02-05 Flame-retardant polyolefin/thermoplastic polyurethane composition
KR1020167002650A KR101840574B1 (en) 2008-02-08 2009-02-05 Flame-retardant polyolefin/thermoplastic polyurethane composition
BRPI0905902A BRPI0905902B1 (en) 2008-02-08 2009-02-05 flame retardant thermoplastic polyureline / polyurethane composition, cable and extruded article
CA2714100A CA2714100C (en) 2008-02-08 2009-02-05 Flame-retardant polyolefin / thermoplastic polyurethane composition
JP2010545998A JP5666917B2 (en) 2008-02-08 2009-02-05 Flame retardant polyolefin / thermoplastic polyurethane composition
EP09707926.3A EP2247668B1 (en) 2008-02-08 2009-02-05 Flame-retardant polyolefin / thermoplastic polyurethane composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US2722108P 2008-02-08 2008-02-08
US61/027,221 2008-02-08

Publications (1)

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EP (1) EP2247668B1 (en)
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KR (2) KR101840574B1 (en)
CN (2) CN105713377A (en)
BR (1) BRPI0905902B1 (en)
CA (1) CA2714100C (en)
MX (1) MX2010008715A (en)
TW (1) TW200938579A (en)
WO (1) WO2009100232A1 (en)

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EP2510055A1 (en) * 2009-12-11 2012-10-17 Dow Global Technologies LLC Thermoplastic polymer blends comprising crosslinked polar olefin polymers in a thermoplastic polyurethane matrix
EP2513914A1 (en) * 2009-12-18 2012-10-24 Dow Global Technologies LLC Halogen-free, flame retardant compositions for wire and cable applications
EP2576694A1 (en) * 2010-05-24 2013-04-10 Dow Global Technologies LLC HALOGEN-FREE, FLAME RETARDANT COMPOSITION COMPRISING CROSSLINKED SILANE-g-EVA
JP2013515827A (en) * 2009-12-31 2013-05-09 ダウ グローバル テクノロジーズ エルエルシー Halogen-free flame retardant thermoplastic composition for wire and cable applications
JP2014208821A (en) * 2014-05-27 2014-11-06 ダウ グローバル テクノロジーズ エルエルシー Halogen-free frame-retardant thermoplastic composition for wire and cable applications
JP2015212390A (en) * 2015-06-10 2015-11-26 ダウ グローバル テクノロジーズ エルエルシー Halogen-free fire retardant thermoplastic composition for wire and cable application

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