ZA200610731B - Use of polyetheresters for rotomolding - Google Patents

Use of polyetheresters for rotomolding Download PDF

Info

Publication number: ZA200610731B
Authority: ZA; South Africa
Prior art keywords: weight; polyolefin; polyetherester; rotomolding; blocks
Prior art date: 2004-05-28

Application number

ZA200610731A

Other languages

English (en)

Inventor

Maziers Eric

Original Assignee

Total Petrochemicals Res Feluy

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.)

2004-05-28

Filing date

2006-12-22

Publication date

2008-05-28

2006-12-22 Application filed by Total Petrochemicals Res Feluy filed Critical Total Petrochemicals Res Feluy

2008-05-28 Publication of ZA200610731B publication Critical patent/ZA200610731B/en

Links

238000001175 rotational moulding Methods 0.000 title claims description 33
229920000098 polyolefin Polymers 0.000 claims description 36
239000000203 mixture Substances 0.000 claims description 29
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
239000012963 UV stabilizer Substances 0.000 claims description 14
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 12
239000005977 Ethylene Substances 0.000 claims description 12
229920001223 polyethylene glycol Polymers 0.000 claims description 12
238000000465 moulding Methods 0.000 claims description 9
239000002202 Polyethylene glycol Substances 0.000 claims description 6
229920002313 fluoropolymer Polymers 0.000 claims description 4
239000004811 fluoropolymer Substances 0.000 claims description 4
239000004433 Thermoplastic polyurethane Substances 0.000 claims description 3
229920006018 co-polyamide Polymers 0.000 claims description 3
239000012968 metallocene catalyst Substances 0.000 claims description 3
229920002803 thermoplastic polyurethane Polymers 0.000 claims description 3
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
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 15
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
238000005245 sintering Methods 0.000 description 14
239000006057 Non-nutritive feed additive Substances 0.000 description 11
239000002253 acid Substances 0.000 description 10
239000000654 additive Substances 0.000 description 8
239000004698 Polyethylene Substances 0.000 description 7
229920000573 polyethylene Polymers 0.000 description 7
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
238000004581 coalescence Methods 0.000 description 5
238000009826 distribution Methods 0.000 description 5
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 5
239000000178 monomer Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
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
125000004427 diamine group Chemical group 0.000 description 3
150000002148 esters Chemical class 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
229920002635 polyurethane Polymers 0.000 description 3
239000004814 polyurethane Substances 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
229920010930 Hytrel® 5556 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
239000003054 catalyst Substances 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
229920001973 fluoroelastomer Polymers 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
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
229920002449 FKM Polymers 0.000 description 1
229920006370 Kynar 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
238000007278 cyanoethylation reaction Methods 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
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
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
- 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
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
- C08L67/025—Polyesters derived from dicarboxylic acids and dihydroxy compounds containing polyether sequences

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)
Moulding By Coating Moulds (AREA)
Polyesters Or Polycarbonates (AREA)
Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)

ZA200610731A 2004-05-28 2006-12-22 Use of polyetheresters for rotomolding ZA200610731B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP04102389A EP1600476A1 (de)	2004-05-28	2004-05-28	Verwendung von Polyetherestern in Rotoformen

Publications (1)

Publication Number	Publication Date
ZA200610731B true ZA200610731B (en)	2008-05-28

Family

ID=34929146

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200610731A ZA200610731B (en)	2004-05-28	2006-12-22	Use of polyetheresters for rotomolding

Country Status (13)

Country	Link
US (2)	US8105525B2 (de)
EP (2)	EP1600476A1 (de)
JP (1)	JP5112057B2 (de)
KR (1)	KR100849054B1 (de)
CN (1)	CN1980995B (de)
AT (1)	ATE414736T1 (de)
CA (1)	CA2567279C (de)
DE (1)	DE602005011129D1 (de)
EA (1)	EA012143B1 (de)
MX (1)	MXPA06013799A (de)
PL (1)	PL1751227T3 (de)
WO (1)	WO2005118709A1 (de)
ZA (1)	ZA200610731B (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1600476A1 (de) *	2004-05-28	2005-11-30	Total Petrochemicals Research Feluy	Verwendung von Polyetherestern in Rotoformen
EP1721739A1 (de) *	2005-05-09	2006-11-15	Total Petrochemicals Research Feluy	Doppelschichtige rotationsgeformte Anwendungen
EP1721931A1 (de) *	2005-05-09	2006-11-15	Total Petrochemicals Research Feluy	Einschichtige, rotoverformte Gegenstände hergestellt aus polyethylenenthaltenden Mischungen
EP2172513A1 (de)	2008-10-02	2010-04-07	Total Petrochemicals Research Feluy	Verfahren zum Hinzufügen von Polymeren bei Rotationsformanwendungen
KR101529706B1 (ko) *	2008-12-31	2015-06-29	코오롱플라스틱 주식회사	내후성 폴리에스테르 탄성체 수지 조성물
KR101405525B1 (ko) *	2013-11-29	2014-06-27	화인케미칼 주식회사	분말 슬러쉬 몰딩 조성물
WO2023129464A1 (en) *	2022-01-01	2023-07-06	Cytec Industries Inc.	Polymer compositions having densification accelerators and rotational molding processes for making hollow articles therefrom

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL136115C (de) *	1968-03-25
US3536689A (en) *	1968-04-24	1970-10-27	Monsanto Co	Densification of polyolefins
US4472545A (en) *	1982-12-28	1984-09-18	E. I. Du Pont De Nemours And Company	Leather-like articles made from cellulosic filler loaded ethylene interpolymers
US4988740A (en) *	1989-06-15	1991-01-29	E. I. Du Pont De Nemours And Company	Low density foamed thermoplastic elastomers
US5574104A (en) *	1990-01-05	1996-11-12	The B. F. Goodrich Company	Chain extended low molecular weight polyoxiranes and electrostatic dissipating blend compositions based thereon
JPH0733484B2 (ja) *	1990-05-07	1995-04-12	第一工業製薬株式会社	樹脂組成物
JPH06226763A (ja) *	1993-02-08	1994-08-16	Du Pont Mitsui Polychem Co Ltd	スラッシュ成形品の製造方法
US6015356A (en) *	1997-01-13	2000-01-18	Lisco, Inc.	Golf ball and method of producing same
US5550193A (en) *	1994-12-07	1996-08-27	Novacor Chemicals Ltd.	Melt fracture elimination in film production
IL129929A0 (en)	1996-12-17	2000-02-29	Du Pont	Polymerization of ethylene with specific iron or cobalt complexes novel pyridinebis (imines) and novel complexes of pyridinebis(imines) with iron and cobalt
US6103946A (en)	1997-07-15	2000-08-15	E. I. Du Pont De Nemours And Company	Manufacture of α-olefins
GB9818316D0 (en) *	1998-08-21	1998-10-14	Borealis As	Polymer
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
US6486295B1 (en) *	2000-01-24	2002-11-26	Richard A. Gross	Lipase-catalyzed transesterifications to regulate copolymer structure
GB0004044D0 (en) *	2000-02-21	2000-04-12	Borealis Polymers Oy	Polymer
US7004854B2 (en) *	2001-10-09	2006-02-28	Acushnet Company	Golf ball with vapor barrier layer and method of making same
EP1402861A1 (de) *	2002-09-24	2004-03-31	The Procter & Gamble Company	Flexibler saugfähiger Einwegartikel
JP2006501352A (ja) *	2002-10-01	2006-01-12	エクソンモービル・ケミカル・パテンツ・インク	射出成形用ポリエチレン組成物
EP1600476A1 (de) *	2004-05-28	2005-11-30	Total Petrochemicals Research Feluy	Verwendung von Polyetherestern in Rotoformen

2004
- 2004-05-28 EP EP04102389A patent/EP1600476A1/de not_active Withdrawn
2005
- 2005-05-30 AT AT05747860T patent/ATE414736T1/de not_active IP Right Cessation
- 2005-05-30 EA EA200601970A patent/EA012143B1/ru not_active IP Right Cessation
- 2005-05-30 EP EP05747860A patent/EP1751227B1/de not_active Not-in-force
- 2005-05-30 KR KR1020067024392A patent/KR100849054B1/ko not_active IP Right Cessation
- 2005-05-30 JP JP2007513955A patent/JP5112057B2/ja not_active Expired - Fee Related
- 2005-05-30 DE DE602005011129T patent/DE602005011129D1/de active Active
- 2005-05-30 WO PCT/EP2005/052460 patent/WO2005118709A1/en active Application Filing
- 2005-05-30 MX MXPA06013799A patent/MXPA06013799A/es active IP Right Grant
- 2005-05-30 US US11/597,227 patent/US8105525B2/en not_active Expired - Fee Related
- 2005-05-30 CA CA2567279A patent/CA2567279C/en not_active Expired - Fee Related
- 2005-05-30 PL PL05747860T patent/PL1751227T3/pl unknown
- 2005-05-30 CN CN2005800170730A patent/CN1980995B/zh not_active Expired - Fee Related
2006
- 2006-12-22 ZA ZA200610731A patent/ZA200610731B/en unknown
2011
- 2011-08-26 US US13/218,861 patent/US8703854B2/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
EA012143B1 (ru)	2009-08-28
MXPA06013799A (es)	2007-04-16
CA2567279A1 (en)	2005-12-15
EP1600476A1 (de)	2005-11-30
JP2008501054A (ja)	2008-01-17
KR100849054B1 (ko)	2008-07-30
US20110313096A1 (en)	2011-12-22
US20080103264A1 (en)	2008-05-01
EP1751227B1 (de)	2008-11-19
PL1751227T3 (pl)	2009-04-30
CN1980995A (zh)	2007-06-13
ATE414736T1 (de)	2008-12-15
KR20070050869A (ko)	2007-05-16
US8703854B2 (en)	2014-04-22
JP5112057B2 (ja)	2013-01-09
US8105525B2 (en)	2012-01-31
CN1980995B (zh)	2010-09-01
WO2005118709A1 (en)	2005-12-15
CA2567279C (en)	2013-07-16
EA200601970A1 (ru)	2007-06-29
DE602005011129D1 (de)	2009-01-02
EP1751227A1 (de)	2007-02-14

Publication	Publication Date	Title
CA2567276C (en)	2012-12-18	Use of thermoplastic composition comprising polyether-block copolyamides as additive
US8703854B2 (en)	2014-04-22	Use of polyetheresters for rotomolding
CA2567568C (en)	2013-05-21	Use of thermoplastic composition comprising thermoplastic polyurethanes as additive
CA2567270C (en)	2013-01-08	Use of fluoropolymers for rotomolding
US8182733B2 (en)	2012-05-22	Use of thermoplastic composing polyethlene glycol as additive