GB1294154A - Improvements in or relating to the cross-linking of olefin homopolymers and copolymers - Google Patents
Improvements in or relating to the cross-linking of olefin homopolymers and copolymersInfo
- Publication number
- GB1294154A GB1294154A GB4728570A GB4728570A GB1294154A GB 1294154 A GB1294154 A GB 1294154A GB 4728570 A GB4728570 A GB 4728570A GB 4728570 A GB4728570 A GB 4728570A GB 1294154 A GB1294154 A GB 1294154A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bis
- acenaphthylene
- butylperoxy
- crosslinking
- peroxide
- 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.)
- Expired
Links
- 238000004132 cross linking Methods 0.000 title abstract 4
- 150000001336 alkenes Chemical class 0.000 title 1
- 229920001577 copolymer Polymers 0.000 title 1
- 229920001519 homopolymer Polymers 0.000 title 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title 1
- 125000004054 acenaphthylenyl group Chemical group C1(=CC2=CC=CC3=CC=CC1=C23)* 0.000 abstract 5
- HXGDTGSAIMULJN-UHFFFAOYSA-N acetnaphthylene Natural products C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 abstract 4
- 239000003795 chemical substances by application Substances 0.000 abstract 4
- 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 abstract 3
- 125000006267 biphenyl group Chemical group 0.000 abstract 3
- 229920000642 polymer Polymers 0.000 abstract 3
- 239000004698 Polyethylene Substances 0.000 abstract 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 abstract 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 2
- 150000002978 peroxides Chemical group 0.000 abstract 2
- -1 polyethylene Polymers 0.000 abstract 2
- 229920000573 polyethylene Polymers 0.000 abstract 2
- 229920000098 polyolefin Polymers 0.000 abstract 2
- YXUGBTHHXGQXPO-UHFFFAOYSA-N 1-tert-butylperoxy-3-(2-tert-butylperoxypropan-2-yl)benzene Chemical compound CC(C)(C)OOC1=CC=CC(C(C)(C)OOC(C)(C)C)=C1 YXUGBTHHXGQXPO-UHFFFAOYSA-N 0.000 abstract 1
- HQOVXPHOJANJBR-UHFFFAOYSA-N 2,2-bis(tert-butylperoxy)butane Chemical compound CC(C)(C)OOC(C)(CC)OOC(C)(C)C HQOVXPHOJANJBR-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000003963 antioxidant agent Substances 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- 229920001971 elastomer Polymers 0.000 abstract 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 229940070710 valerate Drugs 0.000 abstract 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 abstract 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
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)
- Processes Of Treating Macromolecular Substances (AREA)
- Graft Or Block Polymers (AREA)
Abstract
1294154 Crosslinking olefin polymers SIEMENS AG 5 Oct 1970 [16 Oct 1969] 47285/70 Heading C3P Olefin polymers are crosslinked by heating in the presence of at least one tertiary peroxide and 0À1 to 20 weight per cent, based on the polymer, of at least one radical transfer agent selected from acridine and acenaphthylene and halogen and aryl derivatives thereof. The radical transfer agent reacts with alkyl radicals formed during the crosslinking to form a resonance stabilized radical intermediate which is then saturated by hydrogen split off from the polymer. Specified peroxides are dicumyl peroxide, di - t - butyl peroxide, 2,5 - bis - t - butylperoxy - 2,5 - dimethylhexane, 1,3 - bis - (tbutylperoxy) isopropyl benzene, n-butyl-4,4- bis-(t-butylperoxy) valerate and 2,2-bis-(t-butylperoxy) butane. The transfer agents may be blended directly with a polymer melt, or added as a solution or dispersion in a liquid medium, e.g. chlorinated diphenyl, which enhances the effect of the agent. Examples describe the crosslinking of (1) polyethylene with dicumyl peroxide or 1,3-bis-(t-butylperoxy) isopropylbenzene in the presence of acenaphthylene, with and without chlorinated diphenyl; (2) polyethylene with dicumyl peroxide in the presence of acenaphthylene; and (3) ethylene/propylene rubber with 1,3-bis-(t-butyl peroxy isopropyl benzene in the presence of acenaphthylene, with and without chlorinated diphenyl. The acenaphthylenes are said to function additionally as antioxidants.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19691952073 DE1952073C3 (en) | 1969-10-16 | 1969-10-16 | Process for crosslinking polyolefins and olefin copolymers |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1294154A true GB1294154A (en) | 1972-10-25 |
Family
ID=5748325
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4728570A Expired GB1294154A (en) | 1969-10-16 | 1970-10-05 | Improvements in or relating to the cross-linking of olefin homopolymers and copolymers |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPS5023063B1 (en) |
AT (1) | AT307723B (en) |
DE (1) | DE1952073C3 (en) |
FR (1) | FR2066029A5 (en) |
GB (1) | GB1294154A (en) |
NL (1) | NL7015153A (en) |
TR (1) | TR16943A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9150682B2 (en) | 2010-07-22 | 2015-10-06 | Borealis Ag | Modified polymer compositions, modification process and free radical generating agents for i.a. wire and cable applications |
US9388296B2 (en) | 2012-06-04 | 2016-07-12 | National Institute Of Clean-And-Low-Carbon Energy | Crosslinked polyethylene composition having improved processability |
US9617356B2 (en) | 2012-06-13 | 2017-04-11 | National Institute Of Clean-And-Low-Carbon Energy | Crosslinked polyethylene composition |
EP2064279B2 (en) † | 2007-07-12 | 2018-07-18 | Borealis Technology OY | Polymer composition comprising an organic peroxide free radical generating agent, preparation of the composition, crosslinkable cable produced using the composition and organic peroxides |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5871904A (en) * | 1981-10-23 | 1983-04-28 | Asahi Chem Ind Co Ltd | Improved linear medium-to-low density polyethylene composition |
-
1969
- 1969-10-16 DE DE19691952073 patent/DE1952073C3/en not_active Expired
-
1970
- 1970-10-05 AT AT896870A patent/AT307723B/en not_active IP Right Cessation
- 1970-10-05 TR TR1694370A patent/TR16943A/en unknown
- 1970-10-05 GB GB4728570A patent/GB1294154A/en not_active Expired
- 1970-10-15 NL NL7015153A patent/NL7015153A/xx unknown
- 1970-10-15 FR FR7037296A patent/FR2066029A5/fr not_active Expired
- 1970-10-16 JP JP9062570A patent/JPS5023063B1/ja active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2064279B2 (en) † | 2007-07-12 | 2018-07-18 | Borealis Technology OY | Polymer composition comprising an organic peroxide free radical generating agent, preparation of the composition, crosslinkable cable produced using the composition and organic peroxides |
US9150682B2 (en) | 2010-07-22 | 2015-10-06 | Borealis Ag | Modified polymer compositions, modification process and free radical generating agents for i.a. wire and cable applications |
US9388296B2 (en) | 2012-06-04 | 2016-07-12 | National Institute Of Clean-And-Low-Carbon Energy | Crosslinked polyethylene composition having improved processability |
US9617356B2 (en) | 2012-06-13 | 2017-04-11 | National Institute Of Clean-And-Low-Carbon Energy | Crosslinked polyethylene composition |
Also Published As
Publication number | Publication date |
---|---|
DE1952073C3 (en) | 1974-05-02 |
DE1952073B2 (en) | 1973-09-06 |
NL7015153A (en) | 1971-04-20 |
AT307723B (en) | 1973-06-12 |
FR2066029A5 (en) | 1971-08-06 |
TR16943A (en) | 1973-11-01 |
JPS5023063B1 (en) | 1975-08-05 |
DE1952073A1 (en) | 1971-04-22 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |