GB1020873A - Dry polymerisation of ª‡-olefines - Google Patents
Dry polymerisation of ª‡-olefinesInfo
- Publication number
- GB1020873A GB1020873A GB4741962A GB4741962A GB1020873A GB 1020873 A GB1020873 A GB 1020873A GB 4741962 A GB4741962 A GB 4741962A GB 4741962 A GB4741962 A GB 4741962A GB 1020873 A GB1020873 A GB 1020873A
- Authority
- GB
- United Kingdom
- Prior art keywords
- propylene
- ether
- ethylene
- catalyst
- methoxypropylamine
- 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
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 5
- 239000003054 catalyst Substances 0.000 abstract 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 abstract 2
- WEGYGNROSJDEIW-UHFFFAOYSA-N 3-Acetylpyridine Chemical compound CC(=O)C1=CC=CN=C1 WEGYGNROSJDEIW-UHFFFAOYSA-N 0.000 abstract 2
- FAXDZWQIWUSWJH-UHFFFAOYSA-N 3-methoxypropan-1-amine Chemical compound COCCCN FAXDZWQIWUSWJH-UHFFFAOYSA-N 0.000 abstract 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 abstract 2
- -1 Polypropylene Polymers 0.000 abstract 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Substances OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 abstract 2
- 229920001155 polypropylene Polymers 0.000 abstract 2
- ABDKAPXRBAPSQN-UHFFFAOYSA-N veratrole Chemical compound COC1=CC=CC=C1OC ABDKAPXRBAPSQN-UHFFFAOYSA-N 0.000 abstract 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 abstract 1
- RBKHNGHPZZZJCI-UHFFFAOYSA-N (4-aminophenyl)-phenylmethanone Chemical compound C1=CC(N)=CC=C1C(=O)C1=CC=CC=C1 RBKHNGHPZZZJCI-UHFFFAOYSA-N 0.000 abstract 1
- VWGNFIQXBYRDCH-UHFFFAOYSA-N 1,4-diethoxybenzene Chemical compound CCOC1=CC=C(OCC)C=C1 VWGNFIQXBYRDCH-UHFFFAOYSA-N 0.000 abstract 1
- HJORCZCMNWLHMB-UHFFFAOYSA-N 1-(3-aminopropyl)pyrrolidin-2-one Chemical compound NCCCN1CCCC1=O HJORCZCMNWLHMB-UHFFFAOYSA-N 0.000 abstract 1
- XDQZKTCRPTYJNY-UHFFFAOYSA-N 1-(cyclohexylamino)hexan-2-one Chemical compound C1(CCCCC1)NCC(CCCC)=O XDQZKTCRPTYJNY-UHFFFAOYSA-N 0.000 abstract 1
- MFBMAFBMODVDKF-UHFFFAOYSA-N 1-(diethylamino)pentan-2-one Chemical compound CCCC(=O)CN(CC)CC MFBMAFBMODVDKF-UHFFFAOYSA-N 0.000 abstract 1
- RRPYHFHHVVWXIX-UHFFFAOYSA-N 1-aminopentan-2-one Chemical compound CCCC(=O)CN RRPYHFHHVVWXIX-UHFFFAOYSA-N 0.000 abstract 1
- WGYWCLNFFONDQZ-UHFFFAOYSA-N 2-(2-hexan-3-yloxyethoxy)ethanol Chemical compound CCCC(CC)OCCOCCO WGYWCLNFFONDQZ-UHFFFAOYSA-N 0.000 abstract 1
- PZIGWBNYQKBPTG-UHFFFAOYSA-N 2-[2-[3-(ethylamino)propoxy]ethoxy]ethanol Chemical compound C(C)NCCCOCCOCCO PZIGWBNYQKBPTG-UHFFFAOYSA-N 0.000 abstract 1
- CGNJNFZTDWGNSF-UHFFFAOYSA-N 2h-pyrimidin-1-amine Chemical compound NN1CN=CC=C1 CGNJNFZTDWGNSF-UHFFFAOYSA-N 0.000 abstract 1
- LPUBRQWGZPPVBS-UHFFFAOYSA-N 3-butoxypropan-1-amine Chemical compound CCCCOCCCN LPUBRQWGZPPVBS-UHFFFAOYSA-N 0.000 abstract 1
- JJCAXAMFVUFDKS-UHFFFAOYSA-N 4-(2-ethoxyethyl)aniline Chemical compound CCOCCC1=CC=C(N)C=C1 JJCAXAMFVUFDKS-UHFFFAOYSA-N 0.000 abstract 1
- YHTUIJUPUWSDQA-UHFFFAOYSA-N 4-ethoxypyridine Chemical compound CCOC1=CC=NC=C1 YHTUIJUPUWSDQA-UHFFFAOYSA-N 0.000 abstract 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 abstract 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 abstract 1
- 239000004743 Polypropylene Substances 0.000 abstract 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical class NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000007796 conventional method Methods 0.000 abstract 1
- HQWPLXHWEZZGKY-UHFFFAOYSA-N diethylzinc Chemical group CC[Zn]CC HQWPLXHWEZZGKY-UHFFFAOYSA-N 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 239000012467 final product Substances 0.000 abstract 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 abstract 1
- 239000004312 hexamethylene tetramine Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 239000003701 inert diluent Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- KMBPCQSCMCEPMU-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-methylpropane-1,3-diamine Chemical compound NCCCN(C)CCCN KMBPCQSCMCEPMU-UHFFFAOYSA-N 0.000 abstract 1
- SKGXKLYDSBFYPZ-UHFFFAOYSA-N n-(2-phenoxyethyl)aniline Chemical compound C=1C=CC=CC=1NCCOC1=CC=CC=C1 SKGXKLYDSBFYPZ-UHFFFAOYSA-N 0.000 abstract 1
- SBOJXQVPLKSXOG-UHFFFAOYSA-N o-amino-hydroxylamine Chemical class NON SBOJXQVPLKSXOG-UHFFFAOYSA-N 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 229920005606 polypropylene copolymer Polymers 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 abstract 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/04—Monomers containing three or four carbon atoms
- C08F110/06—Propene
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB65263A DE1214401B (de) | 1961-12-20 | 1961-12-20 | Verfahren zur Polymerisation von Propylen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1020873A true GB1020873A (en) | 1966-02-23 |
Family
ID=6974705
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4741962A Expired GB1020873A (en) | 1961-12-20 | 1962-12-17 | Dry polymerisation of ª‡-olefines |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE626253A (enrdf_load_stackoverflow) |
| DE (1) | DE1214401B (enrdf_load_stackoverflow) |
| GB (1) | GB1020873A (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3669948A (en) * | 1970-09-04 | 1972-06-13 | Chisso Corp | Method for producing poly{60 -olefins |
| US4065609A (en) | 1975-04-17 | 1977-12-27 | Imperial Chemical Industries Limited | Polymerization process |
| US4189556A (en) * | 1976-06-16 | 1980-02-19 | Standard Oil Company (Indiana) | Polymerization process |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT967867B (it) * | 1972-09-26 | 1974-03-11 | Montedison Spa | Procedimento per la polimerizzazio ne stereospecifica delle alfa ole fine |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE594407A (enrdf_load_stackoverflow) * | ||||
| FR1253455A (fr) * | 1958-09-17 | 1961-02-10 | Chemical Investors Sa | Procédé de production de polyoléfines cristallines |
-
0
- BE BE626253D patent/BE626253A/xx unknown
-
1961
- 1961-12-20 DE DEB65263A patent/DE1214401B/de active Pending
-
1962
- 1962-12-17 GB GB4741962A patent/GB1020873A/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3669948A (en) * | 1970-09-04 | 1972-06-13 | Chisso Corp | Method for producing poly{60 -olefins |
| US4065609A (en) | 1975-04-17 | 1977-12-27 | Imperial Chemical Industries Limited | Polymerization process |
| US4189556A (en) * | 1976-06-16 | 1980-02-19 | Standard Oil Company (Indiana) | Polymerization process |
Also Published As
| Publication number | Publication date |
|---|---|
| BE626253A (enrdf_load_stackoverflow) | |
| DE1214401B (de) | 1966-04-14 |
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