GB538871A - Improvements in or relating to halogenated polymers of ethylene - Google Patents
Improvements in or relating to halogenated polymers of ethyleneInfo
- Publication number
- GB538871A GB538871A GB970/40A GB97040A GB538871A GB 538871 A GB538871 A GB 538871A GB 970/40 A GB970/40 A GB 970/40A GB 97040 A GB97040 A GB 97040A GB 538871 A GB538871 A GB 538871A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polymers
- stabilizer
- polymer
- halogenated
- ethylene
- 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
- 229920000642 polymer Polymers 0.000 title abstract 12
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 title abstract 3
- 239000005977 Ethylene Substances 0.000 title abstract 3
- 239000003381 stabilizer Substances 0.000 abstract 5
- 239000002904 solvent Substances 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 239000000126 substance Substances 0.000 abstract 3
- 239000004709 Chlorinated polyethylene Substances 0.000 abstract 2
- 238000000354 decomposition reaction Methods 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- -1 iodine chloride Chemical class 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 abstract 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- UVQTYWZUAWYSET-UHFFFAOYSA-N (2,3-dibenzoyloxyphenyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C=1OC(=O)C=2C=CC=CC=2)=CC=CC=1OC(=O)C1=CC=CC=C1 UVQTYWZUAWYSET-UHFFFAOYSA-N 0.000 abstract 1
- SUQGLJRNDJRARS-UHFFFAOYSA-N (3-benzoyloxyphenyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C=1)=CC=CC=1OC(=O)C1=CC=CC=C1 SUQGLJRNDJRARS-UHFFFAOYSA-N 0.000 abstract 1
- PLXMOAALOJOTIY-FPTXNFDTSA-N Aesculin Natural products OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)[C@H]1Oc2cc3C=CC(=O)Oc3cc2O PLXMOAALOJOTIY-FPTXNFDTSA-N 0.000 abstract 1
- YFDUWSBGVPBWKF-UHFFFAOYSA-N Butyl salicylate Chemical compound CCCCOC(=O)C1=CC=CC=C1O YFDUWSBGVPBWKF-UHFFFAOYSA-N 0.000 abstract 1
- QZRGKCOWNLSUDK-UHFFFAOYSA-N Iodochlorine Chemical compound ICl QZRGKCOWNLSUDK-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 238000010292 electrical insulation Methods 0.000 abstract 1
- XHCADAYNFIFUHF-TVKJYDDYSA-N esculin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC(C(=C1)O)=CC2=C1OC(=O)C=C2 XHCADAYNFIFUHF-TVKJYDDYSA-N 0.000 abstract 1
- 229940052296 esters of benzoic acid for local anesthesia Drugs 0.000 abstract 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 238000001704 evaporation Methods 0.000 abstract 1
- 239000004744 fabric Substances 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 150000002366 halogen compounds Chemical class 0.000 abstract 1
- 239000011872 intimate mixture Substances 0.000 abstract 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 229960000969 phenyl salicylate Drugs 0.000 abstract 1
- 229920000573 polyethylene Polymers 0.000 abstract 1
- 230000001376 precipitating effect Effects 0.000 abstract 1
- 229960004889 salicylic acid Drugs 0.000 abstract 1
- DQFBYFPFKXHELB-VAWYXSNFSA-N trans-chalcone Chemical compound C=1C=CC=CC=1C(=O)\C=C\C1=CC=CC=C1 DQFBYFPFKXHELB-VAWYXSNFSA-N 0.000 abstract 1
- 239000008096 xylene Substances 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
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Insulating Materials (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL59869D NL59869C (OSRAM) | 1940-01-16 | ||
| FR885120D FR885120A (OSRAM) | 1940-01-16 | ||
| GB970/40A GB538871A (en) | 1940-01-16 | 1940-01-16 | Improvements in or relating to halogenated polymers of ethylene |
| US373380A US2316481A (en) | 1940-01-16 | 1941-01-06 | Halogenated polymers of ethylene |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB970/40A GB538871A (en) | 1940-01-16 | 1940-01-16 | Improvements in or relating to halogenated polymers of ethylene |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB538871A true GB538871A (en) | 1941-08-20 |
Family
ID=9713721
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB970/40A Expired GB538871A (en) | 1940-01-16 | 1940-01-16 | Improvements in or relating to halogenated polymers of ethylene |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US2316481A (OSRAM) |
| FR (1) | FR885120A (OSRAM) |
| GB (1) | GB538871A (OSRAM) |
| NL (1) | NL59869C (OSRAM) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2502841A (en) * | 1946-02-05 | 1950-04-04 | Visking Corp | Method of modifying the surface characteristics of polyethylene structures and product resulting therefrom |
| US2578904A (en) * | 1949-03-18 | 1951-12-18 | Du Pont | Stabilization of chlorinated ethylene polymer |
-
0
- FR FR885120D patent/FR885120A/fr not_active Expired
- NL NL59869D patent/NL59869C/xx active
-
1940
- 1940-01-16 GB GB970/40A patent/GB538871A/en not_active Expired
-
1941
- 1941-01-06 US US373380A patent/US2316481A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US2316481A (en) | 1943-04-13 |
| FR885120A (OSRAM) | 1943-09-06 |
| NL59869C (OSRAM) |
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