GB917096A - - Google Patents
Info
- Publication number
- GB917096A GB917096A GB917096DA GB917096A GB 917096 A GB917096 A GB 917096A GB 917096D A GB917096D A GB 917096DA GB 917096 A GB917096 A GB 917096A
- Authority
- GB
- United Kingdom
- Prior art keywords
- magnesium
- magnesium iodide
- titanium
- iodide
- magnesium bromide
- 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.)
- Active
Links
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 6
- 239000003054 catalyst Substances 0.000 abstract 5
- 229910052719 titanium Inorganic materials 0.000 abstract 5
- 239000010936 titanium Substances 0.000 abstract 5
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 abstract 4
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 4
- -1 titanium halides Chemical class 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 abstract 2
- AFABGHUZZDYHJO-UHFFFAOYSA-N 2-Methylpentane Chemical compound CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 abstract 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 abstract 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 abstract 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
- 229910052794 bromium Inorganic materials 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 150000004795 grignard reagents Chemical class 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract 2
- 229910001641 magnesium iodide Inorganic materials 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- 230000000379 polymerizing effect Effects 0.000 abstract 2
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 abstract 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 abstract 1
- PBGDIBQPASXECU-UHFFFAOYSA-N Br.Br.I.I Chemical compound Br.Br.I.I PBGDIBQPASXECU-UHFFFAOYSA-N 0.000 abstract 1
- KMUJBUGXVZQPEB-UHFFFAOYSA-N Br.I.I.I Chemical compound Br.I.I.I KMUJBUGXVZQPEB-UHFFFAOYSA-N 0.000 abstract 1
- MNVJLJILXBISNA-UHFFFAOYSA-M CCCCCCCCCCCCCCCCCC[Mg]I Chemical compound CCCCCCCCCCCCCCCCCC[Mg]I MNVJLJILXBISNA-UHFFFAOYSA-M 0.000 abstract 1
- YSTLQQXWCYWSRE-UHFFFAOYSA-M CCCCCCCCC[Mg]Cl Chemical compound CCCCCCCCC[Mg]Cl YSTLQQXWCYWSRE-UHFFFAOYSA-M 0.000 abstract 1
- JDDGTBZDTZYWKM-UHFFFAOYSA-N CCCC[Mg]CC1=CC=CC=C1 Chemical compound CCCC[Mg]CC1=CC=CC=C1 JDDGTBZDTZYWKM-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- JVTVMLDMNFACIG-UHFFFAOYSA-N Cl.Cl.I.I Chemical compound Cl.Cl.I.I JVTVMLDMNFACIG-UHFFFAOYSA-N 0.000 abstract 1
- 239000007818 Grignard reagent Substances 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000005062 Polybutadiene Substances 0.000 abstract 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 abstract 1
- 235000021355 Stearic acid Nutrition 0.000 abstract 1
- MSAQSJXMDMTPBO-UHFFFAOYSA-M [Br-].CCCCCCCCCCCCCC[Mg+] Chemical compound [Br-].CCCCCCCCCCCCCC[Mg+] MSAQSJXMDMTPBO-UHFFFAOYSA-M 0.000 abstract 1
- LOYRQSGAOKAWHT-UHFFFAOYSA-M [Cl-].C(CCCCCCCCCCCCCCC)[Mg+] Chemical compound [Cl-].C(CCCCCCCCCCCCCCC)[Mg+] LOYRQSGAOKAWHT-UHFFFAOYSA-M 0.000 abstract 1
- TUWXWQHYZVBUPC-UHFFFAOYSA-M [I-].C(CCCCCCCC)[Mg+] Chemical compound [I-].C(CCCCCCCC)[Mg+] TUWXWQHYZVBUPC-UHFFFAOYSA-M 0.000 abstract 1
- CLGLRNZWNSOYFG-UHFFFAOYSA-M [I-].C(CCCCCCCCC)[Mg+] Chemical compound [I-].C(CCCCCCCCC)[Mg+] CLGLRNZWNSOYFG-UHFFFAOYSA-M 0.000 abstract 1
- VBTGVCXMSMDEFP-UHFFFAOYSA-M [I-].C(CCCCCCCCCCCCCCC)[Mg+] Chemical compound [I-].C(CCCCCCCCCCCCCCC)[Mg+] VBTGVCXMSMDEFP-UHFFFAOYSA-M 0.000 abstract 1
- KZRBNZDKAHWUJJ-UHFFFAOYSA-M [I-].CCCCCCCCCCCC[Mg+] Chemical compound [I-].CCCCCCCCCCCC[Mg+] KZRBNZDKAHWUJJ-UHFFFAOYSA-M 0.000 abstract 1
- FEAXVNMZZBOUNO-UHFFFAOYSA-M [I-].CCCCCC[Mg+] Chemical compound [I-].CCCCCC[Mg+] FEAXVNMZZBOUNO-UHFFFAOYSA-M 0.000 abstract 1
- CDKFWIMBZAUBRS-UHFFFAOYSA-M [I-].CC[Mg+] Chemical compound [I-].CC[Mg+] CDKFWIMBZAUBRS-UHFFFAOYSA-M 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000006229 carbon black Substances 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 229910001623 magnesium bromide Inorganic materials 0.000 abstract 1
- BLQJIBCZHWBKSL-UHFFFAOYSA-L magnesium iodide Chemical compound [Mg+2].[I-].[I-] BLQJIBCZHWBKSL-UHFFFAOYSA-L 0.000 abstract 1
- CFPKVQBKKLRQHZ-UHFFFAOYSA-M magnesium;3-methanidylheptane;bromide Chemical compound [Mg+2].[Br-].CCCCC([CH2-])CC CFPKVQBKKLRQHZ-UHFFFAOYSA-M 0.000 abstract 1
- VXWPONVCMVLXBW-UHFFFAOYSA-M magnesium;carbanide;iodide Chemical compound [CH3-].[Mg+2].[I-] VXWPONVCMVLXBW-UHFFFAOYSA-M 0.000 abstract 1
- MBHQEXPGNCWWBP-UHFFFAOYSA-M magnesium;dodecane;bromide Chemical compound [Mg+2].[Br-].CCCCCCCCCCC[CH2-] MBHQEXPGNCWWBP-UHFFFAOYSA-M 0.000 abstract 1
- FRIJBUGBVQZNTB-UHFFFAOYSA-M magnesium;ethane;bromide Chemical compound [Mg+2].[Br-].[CH2-]C FRIJBUGBVQZNTB-UHFFFAOYSA-M 0.000 abstract 1
- YLERVAXAQFOFRI-UHFFFAOYSA-M magnesium;propa-1,2-diene;bromide Chemical compound [Mg+2].[Br-].[CH2-]C#C YLERVAXAQFOFRI-UHFFFAOYSA-M 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000002808 molecular sieve Substances 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract 1
- 239000007800 oxidant agent Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- QUPCNWFFTANZPX-UHFFFAOYSA-M paramenthane hydroperoxide Chemical compound [O-]O.CC(C)C1CCC(C)CC1 QUPCNWFFTANZPX-UHFFFAOYSA-M 0.000 abstract 1
- ANRQGKOBLBYXFM-UHFFFAOYSA-M phenylmagnesium bromide Chemical compound Br[Mg]C1=CC=CC=C1 ANRQGKOBLBYXFM-UHFFFAOYSA-M 0.000 abstract 1
- 229920002857 polybutadiene Polymers 0.000 abstract 1
- 239000002002 slurry Substances 0.000 abstract 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 abstract 1
- 239000008117 stearic acid Substances 0.000 abstract 1
- NLLZTRMHNHVXJJ-UHFFFAOYSA-J titanium tetraiodide Chemical compound I[Ti](I)(I)I NLLZTRMHNHVXJJ-UHFFFAOYSA-J 0.000 abstract 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 1
- 239000011787 zinc oxide Substances 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
- C08F136/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F136/02—Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F136/04—Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
- C08F136/06—Butadiene
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 |
|---|---|---|---|
| US3841760A | 1960-06-24 | 1960-06-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB917096A true GB917096A (enrdf_load_stackoverflow) |
Family
ID=21899828
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB917096D Active GB917096A (enrdf_load_stackoverflow) | 1960-06-24 |
Country Status (4)
| Country | Link |
|---|---|
| DE (1) | DE1219686B (enrdf_load_stackoverflow) |
| GB (1) | GB917096A (enrdf_load_stackoverflow) |
| NL (5) | NL6610066A (enrdf_load_stackoverflow) |
| SE (1) | SE308615B (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2257786A1 (de) * | 1971-11-26 | 1973-05-30 | Snam Progetti | Stereospezifische polymerisationsprodukte von diolefinen, verfahren zu deren herstellung und zur polymerisation von olefinen |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT549009A (enrdf_load_stackoverflow) * | 1954-08-16 | Du Pont |
-
0
- GB GB917096D patent/GB917096A/en active Active
- NL NL128408D patent/NL128408C/xx active
- NL NL266229D patent/NL266229A/xx unknown
- NL NL126767D patent/NL126767C/xx active
-
1961
- 1961-06-07 DE DET20266A patent/DE1219686B/de active Pending
- 1961-06-14 SE SE623761A patent/SE308615B/xx unknown
-
1966
- 1966-07-18 NL NL6610066A patent/NL6610066A/xx unknown
- 1966-07-18 NL NL6610065A patent/NL6610065A/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2257786A1 (de) * | 1971-11-26 | 1973-05-30 | Snam Progetti | Stereospezifische polymerisationsprodukte von diolefinen, verfahren zu deren herstellung und zur polymerisation von olefinen |
Also Published As
| Publication number | Publication date |
|---|---|
| NL128408C (enrdf_load_stackoverflow) | |
| NL126767C (enrdf_load_stackoverflow) | |
| NL266229A (enrdf_load_stackoverflow) | |
| SE308615B (enrdf_load_stackoverflow) | 1969-02-17 |
| NL6610065A (enrdf_load_stackoverflow) | 1966-09-26 |
| DE1219686B (de) | 1966-06-23 |
| NL6610066A (enrdf_load_stackoverflow) | 1966-09-26 |
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