NO120489B - - Google Patents
Download PDFInfo
- Publication number
- NO120489B NO120489B NO156058A NO15605864A NO120489B NO 120489 B NO120489 B NO 120489B NO 156058 A NO156058 A NO 156058A NO 15605864 A NO15605864 A NO 15605864A NO 120489 B NO120489 B NO 120489B
- Authority
- NO
- Norway
- Prior art keywords
- dispersant
- polyolefin
- polyolefins
- compound
- double bonds
- Prior art date
Links
- 229920000098 polyolefin Polymers 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 17
- 239000002270 dispersing agent Substances 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 7
- 239000000843 powder Substances 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 238000009835 boiling Methods 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 3
- 150000001451 organic peroxides Chemical class 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 239000011574 phosphorus Substances 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- 238000005406 washing Methods 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 230000007717 exclusion Effects 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 238000000605 extraction Methods 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 4
- 238000005984 hydrogenation reaction Methods 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- 150000003377 silicon compounds Chemical class 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- CBCXFOMAFPBKOF-UHFFFAOYSA-N C(CCCCCCCCCCC)P(CCCCCCCCCCCC)Cl Chemical compound C(CCCCCCCCCCC)P(CCCCCCCCCCCC)Cl CBCXFOMAFPBKOF-UHFFFAOYSA-N 0.000 description 1
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 description 1
- 239000003508 Dilauryl thiodipropionate Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 230000004520 agglutination Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- JDOXUXDGEFQQII-UHFFFAOYSA-N benzyl(dichloro)phosphane Chemical compound ClP(Cl)CC1=CC=CC=C1 JDOXUXDGEFQQII-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- XGRJZXREYAXTGV-UHFFFAOYSA-N chlorodiphenylphosphine Chemical compound C=1C=CC=CC=1P(Cl)C1=CC=CC=C1 XGRJZXREYAXTGV-UHFFFAOYSA-N 0.000 description 1
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- MJEQIIGWDHUZJW-UHFFFAOYSA-N dichloro(cyclohexyl)phosphane Chemical compound ClP(Cl)C1CCCCC1 MJEQIIGWDHUZJW-UHFFFAOYSA-N 0.000 description 1
- PVNZKNQSKGENAP-UHFFFAOYSA-N dichloro(dodecyl)phosphane Chemical compound CCCCCCCCCCCCP(Cl)Cl PVNZKNQSKGENAP-UHFFFAOYSA-N 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 235000019304 dilauryl thiodipropionate Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000002638 heterogeneous catalyst Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- FUKUFMFMCZIRNT-UHFFFAOYSA-N hydron;methanol;chloride Chemical compound Cl.OC FUKUFMFMCZIRNT-UHFFFAOYSA-N 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/40—Introducing phosphorus atoms or phosphorus-containing groups
-
- 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
- C08K5/49—Phosphorus-containing compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEV0025296 | 1964-01-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO120489B true NO120489B (ru) | 1970-10-26 |
Family
ID=7581821
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO156058A NO120489B (ru) | 1964-01-31 | 1964-12-19 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3356639A (ru) |
| AT (1) | AT257157B (ru) |
| BE (1) | BE656198A (ru) |
| CH (1) | CH435747A (ru) |
| DE (1) | DE1545159A1 (ru) |
| GB (1) | GB1087150A (ru) |
| NL (1) | NL6501023A (ru) |
| NO (1) | NO120489B (ru) |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2811514A (en) * | 1954-12-21 | 1957-10-29 | Eastman Kodak Co | Addition products of thermally degraded polyethylene |
| US2829137A (en) * | 1955-11-14 | 1958-04-01 | Du Pont | Polyalkylenepolyphosphinic acids |
| NL98888C (ru) * | 1957-01-30 | |||
| US3008939A (en) * | 1957-12-27 | 1961-11-14 | Union Carbide Corp | Phosphorylated olefin polymers |
-
1964
- 1964-01-31 DE DE19641545159 patent/DE1545159A1/de active Pending
- 1964-11-23 CH CH1508664A patent/CH435747A/de unknown
- 1964-11-25 BE BE656198D patent/BE656198A/xx unknown
- 1964-12-19 NO NO156058A patent/NO120489B/no unknown
-
1965
- 1965-01-25 GB GB3184/65A patent/GB1087150A/en not_active Expired
- 1965-01-26 US US428239A patent/US3356639A/en not_active Expired - Lifetime
- 1965-01-27 NL NL6501023A patent/NL6501023A/xx unknown
- 1965-01-27 AT AT68065A patent/AT257157B/de active
Also Published As
| Publication number | Publication date |
|---|---|
| GB1087150A (en) | 1967-10-11 |
| AT257157B (de) | 1967-09-25 |
| CH435747A (de) | 1967-05-15 |
| BE656198A (ru) | 1965-03-16 |
| NL6501023A (ru) | 1965-08-02 |
| DE1545159A1 (de) | 1969-08-28 |
| US3356639A (en) | 1967-12-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69935591T2 (de) | Propylenpolymer und zusammensetzung die dieses enthält, geformter gegenstand und laminat die dieses enthalten sowie verfahren zur herstellung von polypropylen un dessen zusammensetzung | |
| KR101657925B1 (ko) | 폴리올레핀-폴리스티렌 블록공중합체를 포함하는 유기 아연 화합물 및 이의 제조 방법 | |
| EP0941257B1 (de) | Polar modifizierte polypropylen-wachse | |
| DE68911812T2 (de) | Katalysatorbestandteil für Olefinpolymerisation, Verfahren zur Herstellung davon, Olefinpolymerisationskatalysator und Verfahren zur Polymerisation von Olefinen. | |
| DE69026558T2 (de) | Thermoplastisches Olefinpolymer und Verfahren zu seiner Herstellung | |
| DE3888145T2 (de) | Katalysator-Feststoff für Olefinpolymerisation und Olefinpolymerisationskatalysator. | |
| DE10061727A1 (de) | Verfahren zur Herstellung von Polyisobutenen | |
| NO120602B (ru) | ||
| EP1347995B1 (de) | Verfahren zur herstellung von homo- und copolymeren des isobutens | |
| NO156153B (no) | Fremgangsmaate for fremstilling av et farmasoeytisk preparat med langvarig frigjoering. | |
| DE3119713C2 (de) | Verfahren zur Polymerisation von mindestens eines α-Olefins mit 3-6 Kohlenstoffatomen oder einer Mischung aus mindestens einem dieser α-Olefine und Äthylen | |
| NO120489B (ru) | ||
| EP1297025B1 (de) | Oxidierte polyolefinwachse | |
| JPS6341511A (ja) | 熱安定化α−オレフィン（共）重合体の製法 | |
| DE1158714B (de) | Verfahren zur Herstellung von Mischpolymerisaten des AEthylens mit 1-Olefinen | |
| DE69027652T2 (de) | Verfahren zur Herstellung von syndiotaktischen Copolymeren aus Propylen und Olefinen | |
| DE69921083T2 (de) | Polypropylen/acryl pfropfpolymere, die stabil gegen thermische oxidation sind und verfahren zu ihrer herstellung | |
| DE1111393B (de) | Verfahren zur Polymerisation von olefinisch ungesaettigten Kohlenwasserstoffen | |
| DE4431644A1 (de) | Katalysatorsystem und Verfahren zur Polymerisation von Olefinen | |
| NO156057B (no) | Uopploeselig anode for anvendelse ved elektrolytisk utvinning av metaller, og fremgangsmaate til fremstilling av samme | |
| DE60108346T2 (de) | Verbessertes Verfahren zur Herstellung von Butylkautschuk unter Verwendung von Alkylaluminiumdihalogeniden und Aluminoxanen | |
| JPH02232207A (ja) | プロピレンの連続重合方法 | |
| DE1301526B (de) | Verfahren zur Polymerisation von alpha-Olefinen | |
| EP0973810A1 (de) | Katalysatorzubereitungen für die herstellung von olefin(co)polymeren | |
| WO2001062806A1 (de) | Verfahren zur herstellung von polyethylenwachsen |