CA1249897A - Compositions de type polymere pouvant servir a la fabrication de canalisation pour eau chaude - Google Patents

Compositions de type polymere pouvant servir a la fabrication de canalisation pour eau chaude

Info

Publication number: CA1249897A
Authority: CA; Canada
Prior art keywords: percent; weight; filler; pigment; butene
Prior art date: 1983-09-12
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.): Expired

Application number

CA000454432A

Other languages

English (en)

Inventor

Ananda M. Chatterjee

Earl E. Hayden

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Shell USA Inc

Original Assignee

Shell Oil Co

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.)

1983-09-12

Filing date

1984-05-16

Publication date

1989-02-07

1984-05-16 Application filed by Shell Oil Co filed Critical Shell Oil Co

1989-02-07 Application granted granted Critical

1989-02-07 Publication of CA1249897A publication Critical patent/CA1249897A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 43
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title abstract description 15
239000002667 nucleating agent Substances 0.000 claims abstract description 18
229920001519 homopolymer Polymers 0.000 claims abstract description 17
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims abstract description 13
239000000049 pigment Substances 0.000 claims abstract description 12
239000002253 acid Substances 0.000 claims abstract description 7
RRZCFXQTVDJDGF-UHFFFAOYSA-N dodecyl 3-(3-octadecoxy-3-oxopropyl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC RRZCFXQTVDJDGF-UHFFFAOYSA-N 0.000 claims abstract description 7
239000012764 mineral filler Substances 0.000 claims abstract description 6
229920001903 high density polyethylene Polymers 0.000 claims description 18
239000004700 high-density polyethylene Substances 0.000 claims description 18
239000000945 filler Substances 0.000 claims description 16
239000003963 antioxidant agent Substances 0.000 claims description 15
230000003078 antioxidant effect Effects 0.000 claims description 9
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 6
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical group [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 6
239000000454 talc Substances 0.000 claims description 5
229910052623 talc Inorganic materials 0.000 claims description 5
239000006229 carbon black Substances 0.000 claims description 4
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 claims description 4
239000000391 magnesium silicate Substances 0.000 claims description 4
229910052919 magnesium silicate Inorganic materials 0.000 claims description 4
235000019792 magnesium silicate Nutrition 0.000 claims description 4
XYXJKPCGSGVSBO-UHFFFAOYSA-N 1,3,5-tris[(4-tert-butyl-3-hydroxy-2,6-dimethylphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C)=C1CN1C(=O)N(CC=2C(=C(O)C(=CC=2C)C(C)(C)C)C)C(=O)N(CC=2C(=C(O)C(=CC=2C)C(C)(C)C)C)C1=O XYXJKPCGSGVSBO-UHFFFAOYSA-N 0.000 claims description 3
235000012206 bottled water Nutrition 0.000 claims description 2
239000003651 drinking water Substances 0.000 claims description 2
238000010438 heat treatment Methods 0.000 claims description 2
229910052751 metal Inorganic materials 0.000 claims 2
239000002184 metal Substances 0.000 claims 2
239000004408 titanium dioxide Substances 0.000 claims 2
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims 1
239000000758 substrate Substances 0.000 claims 1
239000002530 phenolic antioxidant Substances 0.000 abstract description 4
239000004615 ingredient Substances 0.000 description 15
238000009472 formulation Methods 0.000 description 13
229920000642 polymer Polymers 0.000 description 11
239000011347 resin Substances 0.000 description 10
229920005989 resin Polymers 0.000 description 10
235000006708 antioxidants Nutrition 0.000 description 8
239000003381 stabilizer Substances 0.000 description 8
229940063583 high-density polyethylene Drugs 0.000 description 7
SCKHCCSZFPSHGR-UHFFFAOYSA-N cyanophos Chemical compound COP(=S)(OC)OC1=CC=C(C#N)C=C1 SCKHCCSZFPSHGR-UHFFFAOYSA-N 0.000 description 6
230000007774 longterm Effects 0.000 description 6
MQQKTNDBASEZSD-UHFFFAOYSA-N 1-(octadecyldisulfanyl)octadecane Chemical compound CCCCCCCCCCCCCCCCCCSSCCCCCCCCCCCCCCCCCC MQQKTNDBASEZSD-UHFFFAOYSA-N 0.000 description 5
239000000370 acceptor Substances 0.000 description 4
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
239000007983 Tris buffer Substances 0.000 description 3
238000001125 extrusion Methods 0.000 description 3
230000006872 improvement Effects 0.000 description 3
239000000155 melt Substances 0.000 description 3
238000009428 plumbing Methods 0.000 description 3
230000035882 stress Effects 0.000 description 3
PXBFMLJZNCDSMP-UHFFFAOYSA-N 2-Aminobenzamide Chemical compound NC(=O)C1=CC=CC=C1N PXBFMLJZNCDSMP-UHFFFAOYSA-N 0.000 description 2
229940076442 9,10-anthraquinone Drugs 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 2
BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000032683 aging Effects 0.000 description 2
239000003570 air Substances 0.000 description 2
RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
150000004056 anthraquinones Chemical class 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
235000019241 carbon black Nutrition 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
238000013461 design Methods 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
230000002706 hydrostatic effect Effects 0.000 description 2
239000000463 material Substances 0.000 description 2
238000000034 method Methods 0.000 description 2
LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 2
-1 polybutylene Polymers 0.000 description 2
229920001748 polybutylene Polymers 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
238000012545 processing Methods 0.000 description 2
GUEIZVNYDFNHJU-UHFFFAOYSA-N quinizarin Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2O GUEIZVNYDFNHJU-UHFFFAOYSA-N 0.000 description 2
239000000700 radioactive tracer Substances 0.000 description 2
JOWXNCPELQZFHF-UHFFFAOYSA-N 2-[3,3-bis(3-tert-butyl-4-hydroxyphenyl)butanoyloxy]ethyl 3,3-bis(3-tert-butyl-4-hydroxyphenyl)butanoate Chemical compound C1=C(O)C(C(C)(C)C)=CC(C(C)(CC(=O)OCCOC(=O)CC(C)(C=2C=C(C(O)=CC=2)C(C)(C)C)C=2C=C(C(O)=CC=2)C(C)(C)C)C=2C=C(C(O)=CC=2)C(C)(C)C)=C1 JOWXNCPELQZFHF-UHFFFAOYSA-N 0.000 description 1
ZLFHNCHMEGLFKL-UHFFFAOYSA-N 3,3-bis(3-tert-butyl-4-hydroxyphenyl)butanoic acid Chemical compound C1=C(O)C(C(C)(C)C)=CC(C(C)(CC(O)=O)C=2C=C(C(O)=CC=2)C(C)(C)C)=C1 ZLFHNCHMEGLFKL-UHFFFAOYSA-N 0.000 description 1
RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 description 1
VRQPMDKCBNYRLJ-UHFFFAOYSA-N C(CC)(=S)SCCCCCCCCCCCCCCCCCCCCCCC Chemical compound C(CC)(=S)SCCCCCCCCCCCCCCCCCCCCCCC VRQPMDKCBNYRLJ-UHFFFAOYSA-N 0.000 description 1
NJIDLJRHMJCJIV-UHFFFAOYSA-N C.C(CC)(=O)O Chemical compound C.C(CC)(=O)O NJIDLJRHMJCJIV-UHFFFAOYSA-N 0.000 description 1
XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
239000004594 Masterbatch (MB) Substances 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
SKZKKFZAGNVIMN-UHFFFAOYSA-N Salicilamide Chemical compound NC(=O)C1=CC=CC=C1O SKZKKFZAGNVIMN-UHFFFAOYSA-N 0.000 description 1
WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
239000012080 ambient air Substances 0.000 description 1
JPICKYUTICNNNJ-UHFFFAOYSA-N anthrarufin Chemical compound O=C1C2=C(O)C=CC=C2C(=O)C2=C1C=CC=C2O JPICKYUTICNNNJ-UHFFFAOYSA-N 0.000 description 1
XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical compound C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 description 1
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
230000008859 change Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229910000423 chromium oxide Inorganic materials 0.000 description 1
238000013329 compounding Methods 0.000 description 1
238000000748 compression moulding Methods 0.000 description 1
239000012967 coordination catalyst Substances 0.000 description 1
239000013078 crystal Substances 0.000 description 1
230000009849 deactivation Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
VFQXVTODMYMSMJ-UHFFFAOYSA-N isonicotinamide Chemical compound NC(=O)C1=CC=NC=C1 VFQXVTODMYMSMJ-UHFFFAOYSA-N 0.000 description 1
WRIRWRKPLXCTFD-UHFFFAOYSA-N malonamide Chemical compound NC(=O)CC(N)=O WRIRWRKPLXCTFD-UHFFFAOYSA-N 0.000 description 1
YASWBJXTHOXPGK-UHFFFAOYSA-N n-(4-hydroxyphenyl)octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NC1=CC=C(O)C=C1 YASWBJXTHOXPGK-UHFFFAOYSA-N 0.000 description 1
RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 description 1
SGMHGVVTMOGJMX-UHFFFAOYSA-N n-naphthalen-2-yl-2-sulfanylacetamide Chemical compound C1=CC=CC2=CC(NC(=O)CS)=CC=C21 SGMHGVVTMOGJMX-UHFFFAOYSA-N 0.000 description 1
229960003966 nicotinamide Drugs 0.000 description 1
235000005152 nicotinamide Nutrition 0.000 description 1
239000011570 nicotinamide Substances 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
238000010525 oxidative degradation reaction Methods 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
238000010926 purge Methods 0.000 description 1
239000000376 reactant Substances 0.000 description 1
229960000581 salicylamide Drugs 0.000 description 1
GGCZERPQGJTIQP-UHFFFAOYSA-M sodium 2-anthraquinonesulfonate Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)[O-])=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-M 0.000 description 1
229940037312 stearamide Drugs 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000003017 thermal stabilizer Substances 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
230000009466 transformation Effects 0.000 description 1
239000000326 ultraviolet stabilizing agent Substances 0.000 description 1

Landscapes

Compositions Of Macromolecular Compounds (AREA)

CA000454432A 1983-09-12 1984-05-16 Compositions de type polymere pouvant servir a la fabrication de canalisation pour eau chaude Expired CA1249897A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US53152783A	1983-09-12	1983-09-12
US531,527		1983-09-12

Publications (1)

Publication Number	Publication Date
CA1249897A true CA1249897A (fr)	1989-02-07

Family

ID=24118002

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
CA000454431A Expired CA1237225A (fr)	1983-09-12	1984-05-16	Composition a base de polymere pour la fabrication de canalisations pour eau chaude
CA000454432A Expired CA1249897A (fr)	1983-09-12	1984-05-16	Compositions de type polymere pouvant servir a la fabrication de canalisation pour eau chaude

Family Applications Before (1)

Application Number	Title	Priority Date	Filing Date
CA000454431A Expired CA1237225A (fr)	1983-09-12	1984-05-16	Composition a base de polymere pour la fabrication de canalisations pour eau chaude

Country Status (1)

Country	Link
CA (2)	CA1237225A (fr)

1984
- 1984-05-16 CA CA000454431A patent/CA1237225A/fr not_active Expired
- 1984-05-16 CA CA000454432A patent/CA1249897A/fr not_active Expired

Also Published As

Publication number	Publication date
CA1237225A (fr)	1988-05-24

Legal Events

Date	Code	Title	Description
2006-02-07	MKEX	Expiry

Publication	Publication Date	Title
US4812500A (en)	1989-03-14	Polyolefin compositions for water pipes and for wire and cable coatings
CA2236634C (fr)	2003-07-01	Composition de polymere olefinique generant peu de fumee et fibres et films prepares a partir de celle-ci
DE60212064T2 (de)	2007-01-04	Polyolefinmischung mit verbesserten Eigenschaften
US4746692A (en)	1988-05-24	Polyolefin compositions for use with water systems
DE69916313T2 (de)	2005-05-12	Thermoplastische harze stabilisiert durch mischungen aus sterisch gehinderten phenolen, sekundären aminen und thioethern
US5132344A (en)	1992-07-21	Stabilized polyethylene composition
US4963605A (en)	1990-10-16	Stabilized polyolefin composition
US4579900A (en)	1986-04-01	Polymeric composition useful for hot water pipe service
US4145373A (en)	1979-03-20	Stress crack resistant polycarbonates
US4576983A (en)	1986-03-18	Polymeric composition useful for hot water pipe service
US5070129A (en)	1991-12-03	Polyolefin composition containing fluoropolymer
JP4801830B2 (ja)	2011-10-26	ポリオレフィン系樹脂組成物
CA1237225A (fr)	1988-05-24	Composition a base de polymere pour la fabrication de canalisations pour eau chaude
US3772232A (en)	1973-11-13	Flame-retardant polymers
US4555539A (en)	1985-11-26	Fireproof polymer material
JPH04220446A (ja)	1992-08-11	安定化されたフィルム成形用ポリオレフィン系樹脂組成物
DE69600400T2 (de)	1998-10-29	Kristalline Propylenpolymerzusammensetzung
JPS645063B2 (fr)	1989-01-27
JP2859346B2 (ja)	1999-02-17	多孔性フイルム
JP2661164B2 (ja)	1997-10-08	無機充填剤含有ポリオレフィン組成物
JP2615830B2 (ja)	1997-06-04	ポリオレフィン組成物
JPH08311259A (ja)	1996-11-26	難燃性樹脂組成物
JPH0515737B2 (fr)	1993-03-02
KR100236923B1 (ko)	2000-01-15	신발 뒷축용 수지 조성물
US3622539A (en)	1971-11-23	Stabilized polyolefin resin compositions