NO312967B1 - Peroksidholdige blandinger for herding av polymerer - Google Patents
Peroksidholdige blandinger for herding av polymerer Download PDFInfo
- Publication number
- NO312967B1 NO312967B1 NO19991880A NO991880A NO312967B1 NO 312967 B1 NO312967 B1 NO 312967B1 NO 19991880 A NO19991880 A NO 19991880A NO 991880 A NO991880 A NO 991880A NO 312967 B1 NO312967 B1 NO 312967B1
- Authority
- NO
- Norway
- Prior art keywords
- ethylene
- copolymers
- peroxide
- curing
- mixtures according
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 35
- 229920000642 polymer Polymers 0.000 title claims description 20
- 150000002978 peroxides Chemical class 0.000 title claims description 17
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 10
- 239000005977 Ethylene Substances 0.000 claims description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 8
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 8
- 239000000654 additive Substances 0.000 claims description 7
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- -1 phenylene, ethylene Chemical group 0.000 claims description 6
- PJANXHGTPQOBST-VAWYXSNFSA-N trans-stilbene Chemical compound C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 claims description 6
- 125000005418 aryl aryl group Chemical group 0.000 claims description 4
- 239000012764 mineral filler Substances 0.000 claims description 4
- 150000001451 organic peroxides Chemical class 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
- DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 claims description 3
- 230000000996 additive effect Effects 0.000 claims description 3
- 239000003963 antioxidant agent Substances 0.000 claims description 3
- 229920001684 low density polyethylene Polymers 0.000 claims description 3
- 239000004702 low-density polyethylene Substances 0.000 claims description 3
- PJANXHGTPQOBST-UHFFFAOYSA-N trans-Stilbene Natural products C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 claims description 3
- BIISIZOQPWZPPS-UHFFFAOYSA-N 2-tert-butylperoxypropan-2-ylbenzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC=C1 BIISIZOQPWZPPS-UHFFFAOYSA-N 0.000 claims description 2
- 239000004709 Chlorinated polyethylene Substances 0.000 claims description 2
- 229920002943 EPDM rubber Polymers 0.000 claims description 2
- 229920005549 butyl rubber Polymers 0.000 claims description 2
- DDTBPAQBQHZRDW-UHFFFAOYSA-N cyclododecane Chemical class C1CCCCCCCCCCC1 DDTBPAQBQHZRDW-UHFFFAOYSA-N 0.000 claims description 2
- 150000001934 cyclohexanes Chemical class 0.000 claims description 2
- 229920001038 ethylene copolymer Polymers 0.000 claims description 2
- 229920001903 high density polyethylene Polymers 0.000 claims description 2
- 239000004700 high-density polyethylene Substances 0.000 claims description 2
- 229920001179 medium density polyethylene Polymers 0.000 claims description 2
- 239000004701 medium-density polyethylene Substances 0.000 claims description 2
- 229940070710 valerate Drugs 0.000 claims description 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims description 2
- HSLFISVKRDQEBY-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)cyclohexane Chemical compound CC(C)(C)OOC1(OOC(C)(C)C)CCCCC1 HSLFISVKRDQEBY-UHFFFAOYSA-N 0.000 claims 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 claims 1
- 125000005396 acrylic acid ester group Chemical group 0.000 claims 1
- 230000002028 premature Effects 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 241001441571 Hiodontidae Species 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 230000001934 delay Effects 0.000 description 2
- 125000000687 hydroquinonyl group Chemical class C1(O)=C(C=C(O)C=C1)* 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000010355 oscillation Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- NALFRYPTRXKZPN-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane Chemical compound CC1CC(C)(C)CC(OOC(C)(C)C)(OOC(C)(C)C)C1 NALFRYPTRXKZPN-UHFFFAOYSA-N 0.000 description 1
- ODBCKCWTWALFKM-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhex-3-yne Chemical compound CC(C)(C)OOC(C)(C)C#CC(C)(C)OOC(C)(C)C ODBCKCWTWALFKM-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 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
-
- 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
- C08K5/01—Hydrocarbons
-
- 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
- C08K5/14—Peroxides
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymerisation Methods In General (AREA)
- Polymerization Catalysts (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 |
---|---|---|---|
IT1998MI000844A IT1305320B1 (it) | 1998-04-21 | 1998-04-21 | Composizioni perossidiche con migliorata resistenza allo scorch perla reticolazione di elastomeri e poliolefine |
Publications (3)
Publication Number | Publication Date |
---|---|
NO991880D0 NO991880D0 (no) | 1999-04-20 |
NO991880L NO991880L (no) | 1999-10-22 |
NO312967B1 true NO312967B1 (no) | 2002-07-22 |
Family
ID=11379858
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO19991880A NO312967B1 (no) | 1998-04-21 | 1999-04-20 | Peroksidholdige blandinger for herding av polymerer |
Country Status (9)
Country | Link |
---|---|
US (1) | US6207776B1 (fr) |
EP (1) | EP0952181A1 (fr) |
JP (1) | JPH11335416A (fr) |
KR (1) | KR19990083316A (fr) |
CN (1) | CN1117805C (fr) |
BR (1) | BR9901390A (fr) |
CA (1) | CA2269454A1 (fr) |
IT (1) | IT1305320B1 (fr) |
NO (1) | NO312967B1 (fr) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20130074454A1 (en) | 2011-09-26 | 2013-03-28 | Cryovac, Inc. | Polyolefin Films for Packaging and Administering Medical Solutions |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB945717A (en) * | 1959-01-14 | 1964-01-08 | Koppers Co Inc | Process for the production of polymeric materials |
US3674884A (en) * | 1967-08-04 | 1972-07-04 | Ube Industries | Process for the preparation of aromatic hydrocarbons containing monoethylenic unsaturated radicals |
CA1047696A (fr) | 1974-11-27 | 1979-01-30 | Union Carbide Corporation | Produits a base de peroxyde de dicumyle et procede pour eviter le dessechement d'un produit polymerique a base d'ethylene |
CA1047200A (fr) | 1974-11-27 | 1979-01-23 | Donald L. Schober | Produits comportant des peroxydes et procede pour eviter le dessechement de produits polymeriques a base d'ethylene |
US3954907A (en) * | 1974-11-27 | 1976-05-04 | Union Carbide Corporation | Composition with selected vinyl compounds and process for avoiding scorching of ethylene polymer composition |
US4994539A (en) * | 1984-10-03 | 1991-02-19 | Nippon Petrochemicals Co., Ltd. | Method for improving impulse destructive stength of electrical insulating materials |
US5245084A (en) | 1988-06-14 | 1993-09-14 | Luperox Gmbh | Mixture suited for crosslinking polymers and process for crosslinking polymers with extension of scorch time |
IT1251502B (it) | 1991-09-19 | 1995-05-15 | Akrim S R L | Composizioni perossidiche liquide |
ITMI960029U1 (it) | 1996-01-18 | 1997-07-18 | Atochem Elf Italia | Composizioni perossidiche con resistenza allo scorch |
US5859160A (en) * | 1997-01-09 | 1999-01-12 | Lord Corporation | Additives for controlling cure rate of polymerizable composition |
-
1998
- 1998-04-21 IT IT1998MI000844A patent/IT1305320B1/it active
-
1999
- 1999-04-16 EP EP99107662A patent/EP0952181A1/fr not_active Withdrawn
- 1999-04-19 CA CA002269454A patent/CA2269454A1/fr not_active Abandoned
- 1999-04-19 KR KR1019990013885A patent/KR19990083316A/ko not_active Application Discontinuation
- 1999-04-19 US US09/293,937 patent/US6207776B1/en not_active Expired - Fee Related
- 1999-04-20 NO NO19991880A patent/NO312967B1/no not_active IP Right Cessation
- 1999-04-20 BR BR9901390-8A patent/BR9901390A/pt not_active IP Right Cessation
- 1999-04-21 CN CN99107403A patent/CN1117805C/zh not_active Expired - Fee Related
- 1999-04-21 JP JP11114255A patent/JPH11335416A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
ITMI980844A1 (it) | 1999-10-21 |
NO991880D0 (no) | 1999-04-20 |
KR19990083316A (ko) | 1999-11-25 |
EP0952181A1 (fr) | 1999-10-27 |
CN1117805C (zh) | 2003-08-13 |
CA2269454A1 (fr) | 1999-10-21 |
BR9901390A (pt) | 2001-03-20 |
CN1237589A (zh) | 1999-12-08 |
IT1305320B1 (it) | 2001-05-04 |
NO991880L (no) | 1999-10-22 |
JPH11335416A (ja) | 1999-12-07 |
US6207776B1 (en) | 2001-03-27 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM1K | Lapsed by not paying the annual fees |