[go: up one dir, main page]

WO2005049716A1 - Flame retardant polyolefin blends - Google Patents

Flame retardant polyolefin blends Download PDF

Info

Publication number
WO2005049716A1
WO2005049716A1 PCT/IN2003/000365 IN0300365W WO2005049716A1 WO 2005049716 A1 WO2005049716 A1 WO 2005049716A1 IN 0300365 W IN0300365 W IN 0300365W WO 2005049716 A1 WO2005049716 A1 WO 2005049716A1
Authority
WO
WIPO (PCT)
Prior art keywords
blends
melamine
polyolefin
flame retardant
blend
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/IN2003/000365
Other languages
French (fr)
Inventor
Sujit Banerji
Anand Kumar Kulshreshtha
Manjeet Singh Choudhary
Sodagudi Francis Xavier
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.)
Indian Petrochemicals Corp Ltd
Reliance Industries Ltd
Original Assignee
Indian Petrochemicals Corp Ltd
Reliance Industries 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 Indian Petrochemicals Corp Ltd, Reliance Industries Ltd filed Critical Indian Petrochemicals Corp Ltd
Priority to EP03808345A priority Critical patent/EP1687367A1/en
Priority to AU2003304555A priority patent/AU2003304555A1/en
Priority to PCT/IN2003/000365 priority patent/WO2005049716A1/en
Publication of WO2005049716A1 publication Critical patent/WO2005049716A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • 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
    • C08K5/34928Salts
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/32Phosphorus-containing compounds
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/38Boron-containing compounds

Definitions

  • the present invention relates to a flame retardant polyolefin blend and a process for the preparation thereof.
  • the blends of this invention neither drip nor glow when ignited and pass UL94 V- 0 test with low emission of nontoxic fumes.
  • Background of the Invention The concept of fire-retardancy is remarkably old. Herodotus, the Greek Historian, in 484-431 BC recorded that the Egyptians imparted fire-resistance to wood by soaking it in a solution of alum (potassium aluminum sulfate). Vitruvius in the 1 st Century BC described some military applications of fire retardant materials such as plaster of clay reinforced with hair.
  • Wild was issued a British patent in 1735 for his process of treating wood with a mixture of alum, ferrous sulfate and borax (sodium tetra borate decahydrate). And Gay-Lussac in 1821 showed that a solution of ammonium phosphate, ammonium chloride and borax acts as a fire retardant for wood.
  • the key ingredients are the elements from Group HI (B and Al) of the periodic table. Even at the beginning of the 21 st Century, with so much of research activity for better fire retardants, the most effective elements are still found in Group: 111 (B and Al), V (N , P and Sb) and VII (Cl and Br).
  • FR flame retardant
  • Certain compounds such as melamine (2,4,5-triamino- 1,3,5-triazine) and its derivatives are also found to be effective flame-retardants, because of their ability to employ various modes of flame retardant action.
  • the growing interest for melamine based flame retardants is further more driven by the particular advantages these products offer over existing flame retardants: cost effective, low smoke density and toxicity, low corrosion and safe handling.
  • melamine and/or its derivatives when used in conjunction with an inorganic hydroxide was found to impart flame retardancy to the polyolefms.
  • Inorganic non-halogen FR compounds such as zinc borate; ammonium phosphate and organic phosphorous-based chemicals are also being used for providing flame resistivity to polymers.
  • US Patent 3,936,416 (1976) issued to Brady described a process for preparing no burning, no dripping, char-forming polypropylene composition with melamine pyrophosphate dipentacrythritol and other systems.
  • US Patent 4,010,137 (1977) granted to Brady again illustrates phosphorus containing flame retardant along with melamine for synthetic resins.
  • the present invention provides a fire-resistant polyolefin blend comprising a polyolefin and melamine or it's derivative along with a melt flow improver and having melt flow index in the range: 2 - 15g/10 min. when tested according to ASTM D1238.
  • the base polymer of the polyolefin blend is a homopolymer of propylene or ethylene, or a block or a random copolymer of ethylene and propylene and is present in a concentration range of from 30 to 88 wt.%.
  • the blend comprises of (i) a polyolefin base polymer (ii) melamine or its derivative (iii) a flame retardant and (iv) a compatibilizer.
  • the polyolefin base polymer is selected from an isotactic or syndiotactic polypropylene homopolymer or a blend of the two; said melamine derivative is selected from melamine cyanurate or melamine phosphate; said flame retardant is selected from magnesium hydroxide and/or aluminum trihydroxide, zinc borate and ammonium phosphate and said compatibilizer comprises a maleic anhydride grafted polypropylene (MAH-g-PP) or a suitable organo silane.
  • MAH-g-PP maleic anhydride grafted polypropylene
  • said polyolefin polymer has a melt flow index in the range of 12 to 40 g/10 min. when tested at 230°C at 2.16 kg load (according to ASTM D1238).
  • said melamine or its derivative is present in the concentration range of 10 to 50wt %.
  • said flame retardant preferably an inorganic hydroxide, is present in the concentration range of 2 to lOwt %.
  • the blend additionally includes a processing aid such as a fluoroelastomer in the concentration range of 1 to 2wt %.
  • the blend additionally includes an antioxidant, preferably trinonyl phenylphosphites, in a concentration range of 0-3 wt %.
  • an antioxidant preferably trinonyl phenylphosphites.
  • This invention also provides a process for preparation of polypropylene blends with melamine and/or its derivatives along with other ingredients extruded in a twin screw extruder or a Buss co-kneader all together or in separate batches, wherein for example, twin screw extruder temperature is maintained in the range: 180 - 250°C and the screws are rotated at a speed of: 50 - 100 rpm.
  • the FR blends qualify the flame retardancy test, UL94 V-0.
  • polyolefin polymer received in the form of granules/spheri-beads, after adequately adding the stabilizers and anti-oxidants after polymerization in the plant.
  • polyolefin is used to refer to polypropylene homopolymer, polyethylene (such as low density polyethylene, LDPE, high density polyethylene, HDPE) and reactor copolymers (both random and block copolymers) of propylene and ethylene.
  • the copolymer granules are dehumidified at 80 (+/-) 5°C for two hours, in an oven, preferably, with an air circulation facility.
  • melt blending is to uniformly disperse melamine or melamine derivative and other additives throughout the polymer matrix. This is achieved by means of a twin-screw extruder, or a Buss co-kneader with a specially designed screw profile that facilitates intimate mixing of the ingredients.
  • PO polyolefin
  • melamine/melamine derivative metal hydroxide
  • fluoroelastomer fluoroelastomer
  • a compatibilizer a compatibilizer
  • PO 30-88 wt%
  • melamine/melamine derivative 10-50wt %
  • metal hydroxide 2-10 wt%
  • MAH-g-PP maleic anhydride - grafted - polypropylene
  • organo silane compatibilizer 0-10wt% all together 100% by weight, and in addition other additives viz.
  • a Buss co-kneader or a co- rotating twin screw extruder with a preferred screw profile that would enhance intimate mixing of ingredients was used under the following conditions: temperature range: 180-250 °C, screw speed: 50-100 rpm, residence time: 2-5 min.
  • the extrudates were dipped in circulating cold water and later chopped into granules of length 2-4 mm.
  • the extrudates granules were dried and were injection molded into ASTM standard test specimens for evaluating various performance properties such as burning test, tensile, flexural, Izod impact, heat deflection temperature etc.
  • the dried granules were also used to measure melt flow index, thermal stability (using thermo gravimetric analyzer).
  • Computer controlled injection molding machine was used with temperature profile (with four heating zones) in the temperature range: 180 - 230°C, injection pressure (applied in six stages): 15-125 kg/cm 2 , injection time (in six stage): 2.5 - 5.0 sec, with screw speed (in two stages) in the range: 80-100 rpm.
  • Standard test specimens were used for evaluating various performance properties of the compounds following the ASTM standard test methods.
  • Melamine based flame retardants are growing in their popularity as end-use customers discover their virtues, which includes low smoke and toxic gas evolution in fire situations, low corrosion to metals such as those used in extruders and molding machines and low corrosion to metal contacts or wires in electrical and electronic applications. These virtues of melamine-based flame-retardants are inherent in their flame retarding mechanism: multiple actions such as endothermic decomposition and reactions in the solid and gas phases in fire situations. These nitrogen based environment friendly flame-retardants also offer a way to reuse/recycle the polyolefin blends. The present invention will now be illustrated with reference to the following non-restrictive Examples.
  • Example - 1 Dried granules of polypropylene homopolymer (50-75 wt %) were mixed with dry melamine or melamine based compound, in the concentration range: 20-40 wt % and metal hydroxide in the concentration range: 2-10 wt% in a high-speed sigma- mixer.
  • the dry mixture was extruded in a Buss co-kneader with a preferred screw profile.
  • the extrusion was carried out with the extruder operating in the temperature range: 150 -215°C with screw rotating at 60 rpm.
  • the extrudate strands (say Blend-A) were dipped in a trough of water that was circulated in order to keep them cool.
  • Blend-A The dry granules of Blend-A were injection molded to get ASTM standard test specimens using FRK-85, Klockner-Windsor injection molding machine under the molding conditions given below in Table -I.
  • Table -I Typical injection molding condition for preparing ASTM test specimens No. Processing Parameter Units Typical Value 1. Injection pressure kg/cm 2 70-120 2. Temperature maintained °C 150-230 3. Injection time sec. 3-10
  • Example-2 Pre-dried granules of copolymer of propylene and ethylene (PPCP) (50-80 wt%), melamine/ melamine derivative (20-45 wt%) and Aluminum tri-hydroxide (0-5 wt%) were mixed in a high-speed sigma mixer along with other additives viz. processing aid and antioxidants.
  • the entire dry blended mixture was melt extruded in a Buss co-kneader as described in Example-1, using similar extrusion conditions and the granules of this blend (say Blend-B) were later injection molded on a Klockner- Windsor machine (FRK-85), under identical conditions described previously.
  • the injection molded ASTM test specimens were used to evaluate the performance properties of the Blend-B given in Table-Ill. Table -IE. Typical properties of Blend-B
  • Example-3 Dried granules of PPCP (50-70wt.%) were mixed with dried melamine (20-40 wt.%) and Aluminum tri hydrate (5-10 wt.%).To this mixture was added MAH-g-PP (2-5 wt.%), processing aid, antioxidants and other additives mentioned above. The ingredients were mixed thoroughly in a high speed Sigma mixer and extruded in a similar fashion as described in Example-1, on a Buss co-kneader. The extrudate strands (say Blend-C) was granulated following the same procedure as in the previous experiment. ASTM standard test specimens were prepared using the same injection- molding machine under identical conditions described earlier. The typical properties of Blend-C are given in Table-IV.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A Flame retardant composition and a process for the preparation thereof is disclosed. The blends of the invention are prepared by melt-mixing (I) a base polymer which is a polyolefin polymer or a blend of two polyolefin polymers (ii) melamine or its derivative such as melamine cyanurate or melamine phosphate (iii) a metal hydroxide, where the metal involved could be magnesium or aluminum and (iv) a compatibilizer, in a Buss co-kneader (or a twin screw extruder). The polyolefin blends of this invention exhibit flame retardancy by passing UL 94 V-0 test, with balanced mechanical Properties.

Description

FLAME RETARDANT POLYOLEFIN BLENDS Field of Invention: The present invention relates to a flame retardant polyolefin blend and a process for the preparation thereof. The blends of this invention neither drip nor glow when ignited and pass UL94 V- 0 test with low emission of nontoxic fumes. Background of the Invention: The concept of fire-retardancy is remarkably old. Herodotus, the Greek Historian, in 484-431 BC recorded that the Egyptians imparted fire-resistance to wood by soaking it in a solution of alum (potassium aluminum sulfate). Vitruvius in the 1st Century BC described some military applications of fire retardant materials such as plaster of clay reinforced with hair. Wild was issued a British patent in 1735 for his process of treating wood with a mixture of alum, ferrous sulfate and borax (sodium tetra borate decahydrate). And Gay-Lussac in 1821 showed that a solution of ammonium phosphate, ammonium chloride and borax acts as a fire retardant for wood. In all these processes the key ingredients are the elements from Group HI (B and Al) of the periodic table. Even at the beginning of the 21st Century, with so much of research activity for better fire retardants, the most effective elements are still found in Group: 111 (B and Al), V (N , P and Sb) and VII (Cl and Br). Research efforts are on to find new and improved flame retardant (FR) agents for synthetic and natural polymers. Certain compounds such as melamine (2,4,5-triamino- 1,3,5-triazine) and its derivatives are also found to be effective flame-retardants, because of their ability to employ various modes of flame retardant action. The growing interest for melamine based flame retardants is further more driven by the particular advantages these products offer over existing flame retardants: cost effective, low smoke density and toxicity, low corrosion and safe handling. In the present process, melamine and/or its derivatives when used in conjunction with an inorganic hydroxide was found to impart flame retardancy to the polyolefms. Inorganic non-halogen FR compounds such as zinc borate; ammonium phosphate and organic phosphorous-based chemicals are also being used for providing flame resistivity to polymers. Several attempts have been made for developing fire retardant polyolefins. US Patent 3,936,416 (1976) issued to Brady described a process for preparing no burning, no dripping, char-forming polypropylene composition with melamine pyrophosphate dipentacrythritol and other systems. US Patent 4,010,137 (1977) granted to Brady again illustrates phosphorus containing flame retardant along with melamine for synthetic resins. US Patent 5,124,404 (1992) granted to Atwell, Ray W., et al, of Great Lakes Chemical Corp. describes flame-retardant polypropylene (with grafted side chain having brominated monomer units) molding compositions, which exhibit good physical properties in combination with flame retardancy. Imahasi et al, (1996) described in their US Patent No.5,583,172 flame-retardant composition in which aluminum or magnesium hydroxide was used to impart color stability against heat. Chapline et α .(1994) in their US Patent No. 5,342,874 described flame retardant polymer formulation in which synergistic mix of flame-retardants such as aluminum or magnesium hydroxide of trioxide etc. were used. A novel magnesium hydroxide as fϊre-retardant for thermoplastic synthetic resins and aqueous paints was disclosed by Miyata et al. (1979) in their US Patent No. 4,145,404. US Patent No. 6,414,070 (2002) issued to Charles Kausch, et al, of Omnova Solution Inc., presents flame-resistant nanocomposite polyolefin composition containing organically modified clays. In all these above inventions the use of melamine or its derivatives in conjunction with a metal hydroxide as flame-retardant for polyolefins was not reported. The synergistic effect of such combination in the presence of certain other chemicals is described here. Objects of the Invention It is an object of the invention to obtain polyolefin blends with melamine and other additives that allow injection molding, compression molding, thermoforming and other conventional techniques to be applied for making end-products such as, electrical meter housings, various furniture/general items that can be used in cars, buses, railway coaches and other motorized vehicles. It is another object of the invention to develop a process for the preparation of flame retarded polyolefin blends with melamine and other additives that provide a synergistic effect in flame retardancy along with balanced mechanical properties, using a twin- screw extruder or a Buss co-kneader. Summary of the Invention The present invention provides a fire-resistant polyolefin blend comprising a polyolefin and melamine or it's derivative along with a melt flow improver and having melt flow index in the range: 2 - 15g/10 min. when tested according to ASTM D1238. In an embodiment, the base polymer of the polyolefin blend is a homopolymer of propylene or ethylene, or a block or a random copolymer of ethylene and propylene and is present in a concentration range of from 30 to 88 wt.%. In an embodiment, the blend comprises of (i) a polyolefin base polymer (ii) melamine or its derivative (iii) a flame retardant and (iv) a compatibilizer. In a preferred embodiment, the polyolefin base polymer is selected from an isotactic or syndiotactic polypropylene homopolymer or a blend of the two; said melamine derivative is selected from melamine cyanurate or melamine phosphate; said flame retardant is selected from magnesium hydroxide and/or aluminum trihydroxide, zinc borate and ammonium phosphate and said compatibilizer comprises a maleic anhydride grafted polypropylene (MAH-g-PP) or a suitable organo silane. In an embodiment, said polyolefin polymer has a melt flow index in the range of 12 to 40 g/10 min. when tested at 230°C at 2.16 kg load (according to ASTM D1238). In an embodiment, said melamine or its derivative is present in the concentration range of 10 to 50wt %. In another preferred embodiment, said flame retardant, preferably an inorganic hydroxide, is present in the concentration range of 2 to lOwt %. In an embodiment, the blend additionally includes a processing aid such as a fluoroelastomer in the concentration range of 1 to 2wt %. In an embodiment, the blend additionally includes an antioxidant, preferably trinonyl phenylphosphites, in a concentration range of 0-3 wt %. This invention also provides a process for preparation of polypropylene blends with melamine and/or its derivatives along with other ingredients extruded in a twin screw extruder or a Buss co-kneader all together or in separate batches, wherein for example, twin screw extruder temperature is maintained in the range: 180 - 250°C and the screws are rotated at a speed of: 50 - 100 rpm. In another embodiment of the invention, the FR blends qualify the flame retardancy test, UL94 V-0. Detailed Description of the Invention This invention is carried out with a polyolefin polymer, received in the form of granules/spheri-beads, after adequately adding the stabilizers and anti-oxidants after polymerization in the plant. The term polyolefin is used to refer to polypropylene homopolymer, polyethylene (such as low density polyethylene, LDPE, high density polyethylene, HDPE) and reactor copolymers (both random and block copolymers) of propylene and ethylene. The copolymer granules are dehumidified at 80 (+/-) 5°C for two hours, in an oven, preferably, with an air circulation facility. Melamine or one of its derivatives (melamine cyanurate or melamine polyphosphate) was also dried separately in an oven at a preferred temperature 80 (+/-) 5°C for a period of at least two hours. Similarly, metal hydroxide was also pre-dried at the same above-mentioned conditions. The objective of melt blending is to uniformly disperse melamine or melamine derivative and other additives throughout the polymer matrix. This is achieved by means of a twin-screw extruder, or a Buss co-kneader with a specially designed screw profile that facilitates intimate mixing of the ingredients. Dried polyolefin (PO) granules, melamine/melamine derivative, metal hydroxide, fluoroelastomer and a compatibilizer were tumble-mixed along with other ingredients in the composition given here: PO: 30-88 wt%; melamine/melamine derivative: 10-50wt %; metal hydroxide: 2-10 wt%; maleic anhydride - grafted - polypropylene (MAH-g-PP) or an organo silane compatibilizer: 0-10wt% all together 100% by weight, and in addition other additives viz. glycerinemono-stearate, calcium stearate, Tinuvin-770, Timιvin-327, Blend- 225 and Chimmasorb, a combination of Tinuvin 622 and Benzophenone 0.01 - 0.1 phr. each. A Buss co-kneader or a co- rotating twin screw extruder with a preferred screw profile that would enhance intimate mixing of ingredients was used under the following conditions: temperature range: 180-250 °C, screw speed: 50-100 rpm, residence time: 2-5 min. The extrudates were dipped in circulating cold water and later chopped into granules of length 2-4 mm. The extrudates granules were dried and were injection molded into ASTM standard test specimens for evaluating various performance properties such as burning test, tensile, flexural, Izod impact, heat deflection temperature etc. The dried granules were also used to measure melt flow index, thermal stability (using thermo gravimetric analyzer). Computer controlled injection molding machine was used with temperature profile (with four heating zones) in the temperature range: 180 - 230°C, injection pressure (applied in six stages): 15-125 kg/cm2, injection time (in six stage): 2.5 - 5.0 sec, with screw speed (in two stages) in the range: 80-100 rpm. Standard test specimens, thus obtained, were used for evaluating various performance properties of the compounds following the ASTM standard test methods. Melamine based flame retardants are growing in their popularity as end-use customers discover their virtues, which includes low smoke and toxic gas evolution in fire situations, low corrosion to metals such as those used in extruders and molding machines and low corrosion to metal contacts or wires in electrical and electronic applications. These virtues of melamine-based flame-retardants are inherent in their flame retarding mechanism: multiple actions such as endothermic decomposition and reactions in the solid and gas phases in fire situations. These nitrogen based environment friendly flame-retardants also offer a way to reuse/recycle the polyolefin blends. The present invention will now be illustrated with reference to the following non-restrictive Examples. Example - 1: Dried granules of polypropylene homopolymer (50-75 wt %) were mixed with dry melamine or melamine based compound, in the concentration range: 20-40 wt % and metal hydroxide in the concentration range: 2-10 wt% in a high-speed sigma- mixer. The dry mixture was extruded in a Buss co-kneader with a preferred screw profile. The extrusion was carried out with the extruder operating in the temperature range: 150 -215°C with screw rotating at 60 rpm. The extrudate strands (say Blend-A) were dipped in a trough of water that was circulated in order to keep them cool. Then the strands were dried and granulated. The dry granules of Blend-A were injection molded to get ASTM standard test specimens using FRK-85, Klockner-Windsor injection molding machine under the molding conditions given below in Table -I. Table -I Typical injection molding condition for preparing ASTM test specimens No. Processing Parameter Units Typical Value 1. Injection pressure kg/cm2 70-120 2. Temperature maintained °C 150-230 3. Injection time sec. 3-10
4. Cooling time sec. 25-100
5. Screw speed rpm. 70-100 The properties of the blends injection molded under the above conditions are given in Table -II. Table -II Typical properties of Blend-A
No. Property ASTM method Unit Blend-A
1. Melt flow index D1238 h/lOmin. 1.5
2. Tensile strength D638 kg/cm2 173
3. Tensile modulus D638 kg/cm2 -
4. Flexural strength D790 kg/cm2 318
5. Flexural modulus D790 kg/cm2 -
6. Notched Izod impact strength 3.2mm thick specimens* D256 kg. cm/cm 1.88 6.4mm thick specimens
7. Heat deflection temperature At 4.6 kgf stress D648 °C 120 At 18.2 kgf stress
8. Flammability UL94 — V-O
(^Middle portions of the injection molded ASTM standard tensile specimens were used)
Example-2 Pre-dried granules of copolymer of propylene and ethylene (PPCP) (50-80 wt%), melamine/ melamine derivative (20-45 wt%) and Aluminum tri-hydroxide (0-5 wt%) were mixed in a high-speed sigma mixer along with other additives viz. processing aid and antioxidants. The entire dry blended mixture was melt extruded in a Buss co-kneader as described in Example-1, using similar extrusion conditions and the granules of this blend (say Blend-B) were later injection molded on a Klockner- Windsor machine (FRK-85), under identical conditions described previously. The injection molded ASTM test specimens were used to evaluate the performance properties of the Blend-B given in Table-Ill. Table -IE. Typical properties of Blend-B
No. Property ASTM method Unit Blend-B
1. Melt flow index D1238 g/lOmin. 9.92
2. Tensile strength (at break) D638 kg/cm2 180
3. Flexural modulus D790 kg/cm2 24,250
4. Notched Izod impact strength 6.4mm thick specimens. D256 kg. cm/cm 3.22 Heat deflection temperature At 4.6 kgf stress D648 °C 110.5 At 18.2 kgf stress
6. Flammability UL94 -- V-0.
Example-3. Dried granules of PPCP (50-70wt.%) were mixed with dried melamine (20-40 wt.%) and Aluminum tri hydrate (5-10 wt.%).To this mixture was added MAH-g-PP (2-5 wt.%), processing aid, antioxidants and other additives mentioned above. The ingredients were mixed thoroughly in a high speed Sigma mixer and extruded in a similar fashion as described in Example-1, on a Buss co-kneader. The extrudate strands (say Blend-C) was granulated following the same procedure as in the previous experiment. ASTM standard test specimens were prepared using the same injection- molding machine under identical conditions described earlier. The typical properties of Blend-C are given in Table-IV.
Table -IV. Typical properties of Blend-C
No. Property ASTM method Unit Blend-C 1. Melt flow index D1238 g/lOmin. 7.56 2. Tensile strength(at break) D638 kg/cm2 170.6 3. Flexural modulus D790 kg/cm2 19,770 4. Notched Izod impact strength 3.2mm thick specimens. * D256 kg.cm cm 3.3
5. Heat deflection temperature At 4.6 kgf stress D648 At 18.2 kgf stress
6. Flammability UL94 V-0.
(^Middle portions of the injection molded ASTM standard tensile specimens were tised)

Claims

Claims:
1. Fire resistant polyolefin blends which comprise of a blend of (i) a polyolefin base polymer (ii) melamine or its derivative (iii) a flame retardant and (iv) a compatibilizer all put together constitute 100 wt% of the blend.
2. Blends as claimed in claim 1, wherein the said polyolefin comprises polypropylene homopolymer, polyethylene, more preferably a high density polyethylene, random as well as block copolymers of propylene and ethylene.
3. Blends as claimed in claim 1, wherein the said polyolefin polymer has a melt flow index in the range of 12 to 40 g/lOmin. when tested at 230°C at 2.16 kg load (according to ASTM D 1238).
4. Blends as claimed in claim 1, wherein the said melamine derivative is selected from melamine cyanurate or melamine phosphate.
5. Blends as claimed in claims 1 to 4, wherein the said melamine or its derivative is present in the concentration range 10 to 50 wt%.
6. Blends as claimed in claims 1 to 5, wherein the said flame retardant is selected from magnesium hydroxide and / or aluminum trihydroxide, zinc borate and ammonium phosphate.
7. Blends as claimed in claims 1 to 6, wherein the said flame retardant is present in the concentration range of 2 to 10 wt%.
8. Blends as claimed in claims 1 to 7, wherein the said compatibilizer comprises a maleic anhydride grafted polypropylene (MAH-g-PP) or an organo silane.
9. Blends as claimed in claims 1 to 8, wherein the said compatibilizer is present in an amount from 0 to 10-wt%.
10. Blends as claimed in any preceding claim, wherein a processing aid such as a fluoroelastomer is present in the concentration range of 1 .to 2 wt% over and above the total blend.
11. Blends as claimed in above claims, wherein an antioxidant is present in the concentration range of 0-3 wt% over and above the total blend.
12. A process for preparation of fire-resistant polyolefin blends, which comprise melt mixing of a polyolefin, melamine or its derivative, a flame retardant and a compatibilizer in a Buss co-kneader or a twin screw extruder.
13. A process as claimed in claim 12, wherein the said polyolefin comprises a polypropylene homopolymer, polyethylene, more preferably ' a high-density polyethylene, random as well as block copolymers of propylene and ethylene.
14. A process as claimed in claim 12, wherein the said polyolefin polymer has a melt flow index in the range of 12 to 40 g/lOmin. when tested at 230°C at 2.16 kg load (according to ASTM D1238).
15. A process as claimed in any one of claims 12 to 14, wherein the said melamine derivative is selected from melamine cyanurate or melamine phosphate.
16. A process as claimed in any one of claims 12 to 15, -wherein the said melamine or its derivative is present in the concentration range 10 to 50 wt%.
17. Processes as claimed in any one of claims 12 to 16, wherein said flame retardant is selected from magnesium hydroxide and / or aluminum trihydroxide, zinc borate and ammonium phosphate.
18. A process as claimed in any one of claims 12 to 17, wherein the said flame retardant is present in the concentration range of 2 to 10 wt%.
19. A process as claimed in any one of claims 12 to 18, wherein the said compatibilizer comprises a maleic anhydride grafted polypropylene (MAH-g- PP) or an organo silane.
20. A process as claimed in any one of claims 12 to 19, wherein the said compatibilizer is present in an amount from 0 to 10-wt%.
21. A process as claimed in any one of claims 12 to 20, wherein said melt mixing is carried out at a temperature in the range of 180 to 250°C in a Buss co-kneader or a twin screw extruder.
22. A process as claimed in claim 21, wherein said kneader / extruder speed is 50 to 100 rpm.
23. An article of manufacture whenever made of a fire-resistant polypropylene blend as claimed in any one of claims 1 to 11.
PCT/IN2003/000365 2003-11-21 2003-11-21 Flame retardant polyolefin blends Ceased WO2005049716A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP03808345A EP1687367A1 (en) 2003-11-21 2003-11-21 Flame retardant polyolefin blends
AU2003304555A AU2003304555A1 (en) 2003-11-21 2003-11-21 Flame retardant polyolefin blends
PCT/IN2003/000365 WO2005049716A1 (en) 2003-11-21 2003-11-21 Flame retardant polyolefin blends

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/IN2003/000365 WO2005049716A1 (en) 2003-11-21 2003-11-21 Flame retardant polyolefin blends

Publications (1)

Publication Number Publication Date
WO2005049716A1 true WO2005049716A1 (en) 2005-06-02

Family

ID=34611184

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IN2003/000365 Ceased WO2005049716A1 (en) 2003-11-21 2003-11-21 Flame retardant polyolefin blends

Country Status (3)

Country Link
EP (1) EP1687367A1 (en)
AU (1) AU2003304555A1 (en)
WO (1) WO2005049716A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1991613A4 (en) * 2006-02-22 2009-12-23 Ls Cable Ltd PROPYLENE RESIN COMPOSITION WITH FLAME RESISTANCE AND ABRASION STRENGTH
CN112852106A (en) * 2021-03-03 2021-05-28 平顶山学院 Epoxy resin-boron nitride heat-conducting flame-retardant composite material and preparation method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997041173A1 (en) * 1996-04-26 1997-11-06 Akzo Nobel N.V. Flame retardant composition for polymers
US6538054B1 (en) * 1996-10-21 2003-03-25 Basf Aktiengesellschaft Flame-proof moulding compounds
WO2003050175A2 (en) * 2001-12-10 2003-06-19 Ciba Specialty Chemicals Holding Inc. Flame retardant conpositions

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997041173A1 (en) * 1996-04-26 1997-11-06 Akzo Nobel N.V. Flame retardant composition for polymers
US6538054B1 (en) * 1996-10-21 2003-03-25 Basf Aktiengesellschaft Flame-proof moulding compounds
WO2003050175A2 (en) * 2001-12-10 2003-06-19 Ciba Specialty Chemicals Holding Inc. Flame retardant conpositions

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1991613A4 (en) * 2006-02-22 2009-12-23 Ls Cable Ltd PROPYLENE RESIN COMPOSITION WITH FLAME RESISTANCE AND ABRASION STRENGTH
CN112852106A (en) * 2021-03-03 2021-05-28 平顶山学院 Epoxy resin-boron nitride heat-conducting flame-retardant composite material and preparation method thereof

Also Published As

Publication number Publication date
AU2003304555A1 (en) 2005-06-08
EP1687367A1 (en) 2006-08-09

Similar Documents

Publication Publication Date Title
CN101268138B (en) Flame retardant polymeric compositions
US20050075442A1 (en) Fire retarded polymer composition
EP1239005B1 (en) Fire-retardant polyolefin compositions
EP1270613A2 (en) Flame retardant polyolefin resin composition
CN116218031A (en) Halogen-free flame retardant composition and preparation method of polyolefin-based master batch thereof
US4719045A (en) Flame retardants for polyolefins
JPS61272254A (en) Flame-retardant polyolefin resin composition
KR100435935B1 (en) Flame resistant polypropylene resin composition having low toxicity and excellent flame resistance and heat resistance
WO2005049716A1 (en) Flame retardant polyolefin blends
JPH10195254A (en) Flame-retardant polyolefin composition
KR20070091037A (en) Fire retardant composition
CN115975296A (en) A kind of halogen-free flame-retardant polyolefin composition and preparation method thereof
JP4012431B2 (en) Flame retardant olefin resin composition
JPH0657774B2 (en) Flame-retardant polypropylene resin composition
JP2000169729A (en) Flame-retardant resin composition and method for producing the same
KR100796730B1 (en) Flame retardant polypropylene resin composition excellent in blooming resistance
JPS62167338A (en) Flame-retardant polyolefin composition
CN117229587B (en) Flame retardant polyolefin composition and preparation method thereof
JPH01163230A (en) Flame-retardant polyolefin composition
CN117164999A (en) Flame-retardant master batch and preparation of polyolefin-based material thereof
KR100528082B1 (en) Flame Retardant Polypropylene Resin Composition_
JPH06184374A (en) Flame-retardant polypropylene resin composition
CN117165000A (en) Low-smoke flame-retardant polyolefin composition and preparation method thereof
JP2622737B2 (en) Heat-resistant polyolefin composition
JPH01163231A (en) Flame-retardant polyolefin composition

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): BW GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 492/MUMNP/2006

Country of ref document: IN

WWE Wipo information: entry into national phase

Ref document number: 2003304555

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 2003808345

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 200380110727.5

Country of ref document: CN

NENP Non-entry into the national phase

Ref country code: DE

WWW Wipo information: withdrawn in national office

Ref document number: DE

WWP Wipo information: published in national office

Ref document number: 2003808345

Country of ref document: EP

WWW Wipo information: withdrawn in national office

Ref document number: 2003808345

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: JP