EP1687367A1 - Flame retardant polyolefin blends - Google Patents
Flame retardant polyolefin blendsInfo
- Publication number
- EP1687367A1 EP1687367A1 EP03808345A EP03808345A EP1687367A1 EP 1687367 A1 EP1687367 A1 EP 1687367A1 EP 03808345 A EP03808345 A EP 03808345A EP 03808345 A EP03808345 A EP 03808345A EP 1687367 A1 EP1687367 A1 EP 1687367A1
- Authority
- EP
- European Patent Office
- 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.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 49
- 239000003063 flame retardant Substances 0.000 title claims abstract description 33
- 229920000098 polyolefin Polymers 0.000 title claims abstract description 31
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title claims abstract description 22
- 229920000877 Melamine resin Polymers 0.000 claims abstract description 24
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims abstract description 24
- 238000000034 method Methods 0.000 claims abstract description 22
- 229920000642 polymer Polymers 0.000 claims abstract description 9
- 238000002156 mixing Methods 0.000 claims abstract description 6
- 229920005601 base polymer Polymers 0.000 claims abstract description 5
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 claims abstract description 5
- 238000002360 preparation method Methods 0.000 claims abstract description 5
- XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical compound OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229920001911 maleic anhydride grafted polypropylene Polymers 0.000 claims description 8
- -1 polyethylene Polymers 0.000 claims description 8
- 150000007974 melamines Chemical class 0.000 claims description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical group [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 6
- 239000000347 magnesium hydroxide Substances 0.000 claims description 6
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 6
- 239000004254 Ammonium phosphate Substances 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 5
- 239000004743 Polypropylene Substances 0.000 claims description 5
- 229910000148 ammonium phosphate Inorganic materials 0.000 claims description 5
- 235000019289 ammonium phosphates Nutrition 0.000 claims description 5
- 239000003963 antioxidant agent Substances 0.000 claims description 5
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims description 5
- 229920005629 polypropylene homopolymer Polymers 0.000 claims description 5
- 239000006057 Non-nutritive feed additive Substances 0.000 claims description 4
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 claims description 4
- 230000009970 fire resistant effect Effects 0.000 claims description 4
- 229920001903 high density polyethylene Polymers 0.000 claims description 4
- 239000004700 high-density polyethylene Substances 0.000 claims description 4
- 239000000155 melt Substances 0.000 claims description 4
- 150000001282 organosilanes Chemical class 0.000 claims description 4
- 229920001155 polypropylene Polymers 0.000 claims description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 4
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 3
- 229920001400 block copolymer Polymers 0.000 claims description 3
- 229920001973 fluoroelastomer Polymers 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 229920005604 random copolymer Polymers 0.000 claims description 3
- 230000003078 antioxidant effect Effects 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 238000012360 testing method Methods 0.000 abstract description 10
- 229910000000 metal hydroxide Inorganic materials 0.000 abstract description 6
- 150000004692 metal hydroxides Chemical class 0.000 abstract description 6
- 229910052782 aluminium Inorganic materials 0.000 abstract description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052751 metal Inorganic materials 0.000 abstract description 3
- 239000002184 metal Substances 0.000 abstract description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 1
- 229910052749 magnesium Inorganic materials 0.000 abstract 1
- 239000011777 magnesium Substances 0.000 abstract 1
- 239000008187 granular material Substances 0.000 description 11
- 238000002347 injection Methods 0.000 description 11
- 239000007924 injection Substances 0.000 description 11
- 239000000654 additive Substances 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 238000001746 injection moulding Methods 0.000 description 5
- 235000006708 antioxidants Nutrition 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 235000010339 sodium tetraborate Nutrition 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- YQEMORVAKMFKLG-UHFFFAOYSA-N 2-stearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229940037003 alum Drugs 0.000 description 2
- 229940024548 aluminum oxide Drugs 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 229910001853 inorganic hydroxide Inorganic materials 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- FIBDHOZDBPHCLW-UHFFFAOYSA-N 1,3,5-triazine-2,4,6-triamine 2H-1,3,5-triazine-1,2,4-triamine Chemical compound NC1N=C(N)N=CN1N.NC1=NC(N)=NC(N)=N1 FIBDHOZDBPHCLW-UHFFFAOYSA-N 0.000 description 1
- SWZOQAGVRGQLDV-UHFFFAOYSA-N 4-[2-(4-hydroxy-2,2,6,6-tetramethylpiperidin-1-yl)ethoxy]-4-oxobutanoic acid Chemical compound CC1(C)CC(O)CC(C)(C)N1CCOC(=O)CCC(O)=O SWZOQAGVRGQLDV-UHFFFAOYSA-N 0.000 description 1
- UJNOBVSDBJIWKX-UHFFFAOYSA-N CCCCCCCCCOP(OCCCCCCCCC)(OCCCCCCCCC)C1=CC=CC=C1 Chemical class CCCCCCCCCOP(OCCCCCCCCC)(OCCCCCCCCC)C1=CC=CC=C1 UJNOBVSDBJIWKX-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- RREGISFBPQOLTM-UHFFFAOYSA-N alumane;trihydrate Chemical compound O.O.O.[AlH3] RREGISFBPQOLTM-UHFFFAOYSA-N 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- CDMADVZSLOHIFP-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane;decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 CDMADVZSLOHIFP-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920005674 ethylene-propylene random copolymer Polymers 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000002114 nanocomposite Substances 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 125000005461 organic phosphorous group Chemical group 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- XZTOTRSSGPPNTB-UHFFFAOYSA-N phosphono dihydrogen phosphate;1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(N)=N1.OP(O)(=O)OP(O)(O)=O XZTOTRSSGPPNTB-UHFFFAOYSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34928—Salts
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/38—Boron-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.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
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
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.
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 |
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| EP1687367A1 true EP1687367A1 (en) | 2006-08-09 |
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| JP2009527620A (en) * | 2006-02-22 | 2009-07-30 | エルエス ケーブル リミテッド | Flame retardant polypropylene resin composition with wear resistance |
| CN112852106B (en) * | 2021-03-03 | 2023-07-21 | 平顶山学院 | A kind of epoxy resin-boron nitride thermally conductive flame retardant composite material and preparation method thereof |
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| WO1997041173A1 (en) * | 1996-04-26 | 1997-11-06 | Akzo Nobel N.V. | Flame retardant composition for polymers |
| DE19643280A1 (en) * | 1996-10-21 | 1998-04-23 | Basf Ag | Flame retardant molding compounds |
| DE60230922D1 (en) * | 2001-12-10 | 2009-03-05 | Ciba Holding Inc | FLAME-REDUCING COMPOSITIONS |
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