ZA200610741B - Use of fluoropolymers for rotomolding - Google Patents
Use of fluoropolymers for rotomolding Download PDFInfo
- Publication number
- ZA200610741B ZA200610741B ZA200610741A ZA200610741A ZA200610741B ZA 200610741 B ZA200610741 B ZA 200610741B ZA 200610741 A ZA200610741 A ZA 200610741A ZA 200610741 A ZA200610741 A ZA 200610741A ZA 200610741 B ZA200610741 B ZA 200610741B
- Authority
- ZA
- South Africa
- Prior art keywords
- weight
- polyolefin
- rotomolding
- fluoropolymer
- polymer
- Prior art date
Links
- 238000001175 rotational moulding Methods 0.000 title claims abstract description 38
- 229920002313 fluoropolymer Polymers 0.000 title claims description 13
- 239000004811 fluoropolymer Substances 0.000 title claims description 13
- 229920000098 polyolefin Polymers 0.000 claims abstract description 37
- 239000000203 mixture Substances 0.000 claims abstract description 29
- 239000012963 UV stabilizer Substances 0.000 claims abstract description 16
- 238000000465 moulding Methods 0.000 claims abstract description 10
- 229920000642 polymer Polymers 0.000 claims description 29
- 238000000280 densification Methods 0.000 claims description 21
- 229920001577 copolymer Polymers 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 17
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 11
- 239000005977 Ethylene Substances 0.000 claims description 11
- 229920001223 polyethylene glycol Polymers 0.000 claims description 9
- 239000002202 Polyethylene glycol Substances 0.000 claims description 3
- 239000004433 Thermoplastic polyurethane Substances 0.000 claims description 3
- 229920006018 co-polyamide Polymers 0.000 claims description 3
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 3
- 239000012968 metallocene catalyst Substances 0.000 claims description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 abstract description 12
- 239000004952 Polyamide Substances 0.000 description 27
- 229920002647 polyamide Polymers 0.000 description 27
- 229920000570 polyether Polymers 0.000 description 26
- 239000004721 Polyphenylene oxide Substances 0.000 description 25
- -1 polyethylene Polymers 0.000 description 17
- 238000005245 sintering Methods 0.000 description 14
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 13
- 239000002253 acid Substances 0.000 description 10
- 239000004698 Polyethylene Substances 0.000 description 9
- 229920000573 polyethylene Polymers 0.000 description 9
- 239000000654 additive Substances 0.000 description 8
- 150000002009 diols Chemical group 0.000 description 6
- 239000002243 precursor Substances 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000004581 coalescence Methods 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 229920001451 polypropylene glycol Polymers 0.000 description 4
- 239000004711 α-olefin Substances 0.000 description 4
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 3
- JLZIIHMTTRXXIN-UHFFFAOYSA-N 2-(2-hydroxy-4-methoxybenzoyl)benzoic acid Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1C(O)=O JLZIIHMTTRXXIN-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 125000004427 diamine group Chemical group 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 229920001973 fluoroelastomer Polymers 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 230000000750 progressive effect Effects 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 2
- 229920006370 Kynar Polymers 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- VPGLGRNSAYHXPY-UHFFFAOYSA-L zirconium(2+);dichloride Chemical compound Cl[Zr]Cl VPGLGRNSAYHXPY-UHFFFAOYSA-L 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- VTDMBRAUHKUOON-UHFFFAOYSA-N 4-[(4-carboxyphenyl)methyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1CC1=CC=C(C(O)=O)C=C1 VTDMBRAUHKUOON-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 229920006347 Elastollan Polymers 0.000 description 1
- UAUDZVJPLUQNMU-UHFFFAOYSA-N Erucasaeureamid Natural products CCCCCCCCC=CCCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-UHFFFAOYSA-N 0.000 description 1
- RYECOJGRJDOGPP-UHFFFAOYSA-N Ethylurea Chemical compound CCNC(N)=O RYECOJGRJDOGPP-UHFFFAOYSA-N 0.000 description 1
- 229920002449 FKM Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002266 Pluriol® Polymers 0.000 description 1
- 229920002614 Polyether block amide Polymers 0.000 description 1
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-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
- 238000003490 calendering Methods 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 125000001142 dicarboxylic acid group Chemical group 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- JZZIHCLFHIXETF-UHFFFAOYSA-N dimethylsilicon Chemical group C[Si]C JZZIHCLFHIXETF-UHFFFAOYSA-N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical class C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical class CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 1
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920006146 polyetheresteramide block copolymer Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 238000010094 polymer processing Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- ZAKVZVDDGSFVRG-UHFFFAOYSA-N prop-1-en-2-ylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CC(=C)C1=CC=CC=C1 ZAKVZVDDGSFVRG-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- 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
- C08L23/06—Polyethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
- C08L2666/06—Homopolymers or copolymers of unsaturated hydrocarbons; Derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Moulding By Coating Moulds (AREA)
- Laminated Bodies (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04102385A EP1600474A1 (fr) | 2004-05-28 | 2004-05-28 | Utilisation de polymères fluorés pour rotomoulage |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200610741B true ZA200610741B (en) | 2008-05-28 |
Family
ID=34929144
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200610741A ZA200610741B (en) | 2004-05-28 | 2006-12-20 | Use of fluoropolymers for rotomolding |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US20080018019A1 (fr) |
| EP (2) | EP1600474A1 (fr) |
| JP (1) | JP5112055B2 (fr) |
| KR (1) | KR100849055B1 (fr) |
| CN (1) | CN100591718C (fr) |
| AT (1) | ATE427979T1 (fr) |
| CA (1) | CA2567270C (fr) |
| DE (1) | DE602005013769D1 (fr) |
| EA (1) | EA012390B1 (fr) |
| MX (1) | MXPA06013797A (fr) |
| WO (1) | WO2005118707A1 (fr) |
| ZA (1) | ZA200610741B (fr) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2023129464A1 (fr) * | 2022-01-01 | 2023-07-06 | Cytec Industries Inc. | Compositions polymères comprenant des accélérateurs de densification et procédés de moulage par rotation pour fabriquer des articles creux à partir de celles-ci |
Family Cites Families (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL8004958A (nl) * | 1980-08-30 | 1982-04-01 | Stamicarbon | Polyolefinepoedersamenstellingen, in het bijzonder polyetheenpoedersamenstellingen met verbeterde hechting en daarvan te vervaardigen en vervaardigde voorwerpen. |
| US4973626A (en) * | 1982-09-29 | 1990-11-27 | Wilkus Edward V | Crosslinked polymer interdispersions containing polyolefin and method of making |
| JPS63110257A (ja) * | 1986-10-28 | 1988-05-14 | Idemitsu Petrochem Co Ltd | 難燃性樹脂組成物 |
| JPH01254748A (ja) * | 1988-04-04 | 1989-10-11 | Nippon Steel Chem Co Ltd | オレフィン系樹脂組成物 |
| US4855360A (en) * | 1988-04-15 | 1989-08-08 | Minnesota Mining And Manufacturing Company | Extrudable thermoplastic hydrocarbon polymer composition |
| JPH03269029A (ja) * | 1990-03-16 | 1991-11-29 | Nippon Petrochem Co Ltd | 難燃性発泡組成物、難燃性発泡体およびその製造法 |
| US5550193A (en) * | 1994-12-07 | 1996-08-27 | Novacor Chemicals Ltd. | Melt fracture elimination in film production |
| US5587429A (en) * | 1995-04-04 | 1996-12-24 | E. I. Dupont De Nemours And Company | Processing aid system for polyolefins |
| US6335490B1 (en) * | 1995-06-07 | 2002-01-01 | Mitsubishi Cable Industries, Ltd. | Insulating material for coaxial cable, coaxial cable and method for producing coaxial cable |
| CA2259308C (fr) * | 1996-06-28 | 2007-04-24 | Alan V. Bray | Materiau composite a forte densite |
| EP0839623B1 (fr) * | 1996-10-30 | 2001-01-31 | Ciba SC Holding AG | Combinaison de stabilisateurs pour le procédé rotomolding |
| US6294604B1 (en) * | 1998-03-06 | 2001-09-25 | Dyneon Llc | Polymer processing additive having improved stability |
| GB9818316D0 (en) * | 1998-08-21 | 1998-10-14 | Borealis As | Polymer |
| US6734252B1 (en) * | 1999-01-29 | 2004-05-11 | 3M Innovative Properties Company | Melt processable thermoplastic polymer composition employing a polymer processing additive containing a fluorothermoplastic copolymer |
| US6444733B1 (en) * | 1999-03-01 | 2002-09-03 | Ciba Specialty Chemicals Corporation | Stabilizer combination for the rotomolding process |
| JP2001089615A (ja) * | 1999-07-16 | 2001-04-03 | Mitsui Chemicals Inc | 回転成形用ポリエチレン樹脂組成物およびその組成物を用いた回転成形体 |
| US6362270B1 (en) * | 1999-08-12 | 2002-03-26 | The Dow Chemical Company | Thermoplastic compositions for durable goods applications |
| US6538069B2 (en) * | 2000-06-05 | 2003-03-25 | Immix Technologies, Inc. | Polymer blends of PVDF thermoplastics blended with FKM fluoroelastomers |
| TW552435B (en) * | 2000-06-12 | 2003-09-11 | Asahi Glass Co Ltd | Plastic optical fiber |
| US6679695B2 (en) * | 2001-05-29 | 2004-01-20 | University Of North Carolina At Chapel Hill | Pultrusion apparatus for continuous fabrication of fiber-reinforced plastic articles having a non-linear shape, methods of fabricating such articles and compositions used therein |
| US6602452B2 (en) * | 2001-07-18 | 2003-08-05 | Mcghan Medical Corporation | Rotational molding of medical articles |
| JP4163112B2 (ja) * | 2001-09-26 | 2008-10-08 | 日本ポリオレフィン株式会社 | ポリオレフィン系樹脂材料およびそれを用いた積層体ならびにその製造方法、それらの成形体 |
| US7323502B2 (en) * | 2002-03-12 | 2008-01-29 | Ciba Specialty Chemicals Corporation | Flame retardant compositions |
| JP2003312625A (ja) * | 2002-04-24 | 2003-11-06 | Japan Polychem Corp | 高密度ポリエチレン系樹脂製食品容器 |
| US6743865B2 (en) * | 2002-06-28 | 2004-06-01 | Atofina Chemicals, Inc. | Fluoropolymer blends |
| JP3756133B2 (ja) * | 2002-07-29 | 2006-03-15 | 旭化成ケミカルズ株式会社 | グラフト共重合体およびその樹脂組成物 |
| ATE459680T1 (de) * | 2002-10-01 | 2010-03-15 | Exxonmobil Chem Patents Inc | Polyethylenmischungen zum spritzgiessen |
| US20050101722A1 (en) * | 2003-11-06 | 2005-05-12 | 3M Innovative Properties Company | Melt processable compositions |
| US20050113486A1 (en) * | 2003-11-26 | 2005-05-26 | Sandieson Kevin R. | Molded articles having a granular or speckled appearance and process therefor |
-
2004
- 2004-05-28 EP EP04102385A patent/EP1600474A1/fr not_active Withdrawn
-
2005
- 2005-05-30 KR KR1020067024375A patent/KR100849055B1/ko not_active IP Right Cessation
- 2005-05-30 EP EP05756666A patent/EP1749059B1/fr not_active Not-in-force
- 2005-05-30 JP JP2007513951A patent/JP5112055B2/ja not_active Expired - Fee Related
- 2005-05-30 AT AT05756666T patent/ATE427979T1/de not_active IP Right Cessation
- 2005-05-30 WO PCT/EP2005/052455 patent/WO2005118707A1/fr active Application Filing
- 2005-05-30 CN CN200580017072A patent/CN100591718C/zh not_active Expired - Fee Related
- 2005-05-30 MX MXPA06013797A patent/MXPA06013797A/es active IP Right Grant
- 2005-05-30 DE DE602005013769T patent/DE602005013769D1/de active Active
- 2005-05-30 CA CA2567270A patent/CA2567270C/fr not_active Expired - Fee Related
- 2005-05-30 EA EA200601965A patent/EA012390B1/ru not_active IP Right Cessation
- 2005-05-30 US US11/596,426 patent/US20080018019A1/en not_active Abandoned
-
2006
- 2006-12-20 ZA ZA200610741A patent/ZA200610741B/en unknown
-
2012
- 2012-10-29 US US13/663,086 patent/US20130049262A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20080018019A1 (en) | 2008-01-24 |
| WO2005118707A1 (fr) | 2005-12-15 |
| EP1600474A1 (fr) | 2005-11-30 |
| EA012390B1 (ru) | 2009-10-30 |
| KR20070050868A (ko) | 2007-05-16 |
| JP2008501052A (ja) | 2008-01-17 |
| MXPA06013797A (es) | 2007-04-16 |
| CN1980994A (zh) | 2007-06-13 |
| EP1749059A1 (fr) | 2007-02-07 |
| DE602005013769D1 (en) | 2009-05-20 |
| ATE427979T1 (de) | 2009-04-15 |
| CN100591718C (zh) | 2010-02-24 |
| EA200601965A1 (ru) | 2007-06-29 |
| EP1749059B1 (fr) | 2009-04-08 |
| KR100849055B1 (ko) | 2008-07-30 |
| CA2567270A1 (fr) | 2005-12-15 |
| US20130049262A1 (en) | 2013-02-28 |
| CA2567270C (fr) | 2013-01-08 |
| JP5112055B2 (ja) | 2013-01-09 |
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