SU1227119A3 - Способ получени полиаминамидов - Google Patents
Способ получени полиаминамидовInfo
- Publication number
- SU1227119A3 SU1227119A3 SU813247700A SU3247700A SU1227119A3 SU 1227119 A3 SU1227119 A3 SU 1227119A3 SU 813247700 A SU813247700 A SU 813247700A SU 3247700 A SU3247700 A SU 3247700A SU 1227119 A3 SU1227119 A3 SU 1227119A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- reactor
- polymer
- polyaminoamides
- producing
- nbd
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 7
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 9
- 239000010948 rhodium Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 5
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 229920000768 polyamine Polymers 0.000 description 4
- 229910052703 rhodium Inorganic materials 0.000 description 4
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- 239000005062 Polybutadiene Substances 0.000 description 3
- 150000001408 amides Chemical group 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 229920002857 polybutadiene Polymers 0.000 description 3
- AVFZOVWCLRSYKC-UHFFFAOYSA-N 1-methylpyrrolidine Chemical compound CN1CCCC1 AVFZOVWCLRSYKC-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 229920002521 macromolecule Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- -1 nitrogen anions Chemical class 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 125000002924 primary amino group Chemical class [H]N([H])* 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920003060 Poly(vinyl benzyl chloride) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- XTLNYNMNUCLWEZ-UHFFFAOYSA-N ethanol;propan-2-one Chemical compound CCO.CC(C)=O XTLNYNMNUCLWEZ-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003284 rhodium compounds Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000004448 titration Methods 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
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
- C08F8/32—Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polyamides (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/123,740 US4312965A (en) | 1980-02-22 | 1980-02-22 | Process for forming amine/amide containing polymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1227119A3 true SU1227119A3 (ru) | 1986-04-23 |
Family
ID=22410590
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU813247700A SU1227119A3 (ru) | 1980-02-22 | 1981-02-20 | Способ получени полиаминамидов |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4312965A (enExample) |
| BE (1) | BE887628A (enExample) |
| DE (1) | DE3106109A1 (enExample) |
| ES (1) | ES8202844A1 (enExample) |
| FI (1) | FI67868C (enExample) |
| FR (1) | FR2476655A1 (enExample) |
| GB (1) | GB2070025B (enExample) |
| IT (1) | IT1141108B (enExample) |
| NL (1) | NL8006490A (enExample) |
| SE (1) | SE444440B (enExample) |
| SU (1) | SU1227119A3 (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4442421A (en) * | 1981-07-31 | 1984-04-10 | Jacobus Otha J | Semiconducting coordination polymers and electrical applications thereof |
| US4513122A (en) * | 1983-03-18 | 1985-04-23 | W. R. Grace & Co. | Retention and drainage aid |
| US4566943A (en) * | 1983-03-18 | 1986-01-28 | W. R. Grace & Co. | Wet strength material |
| US4513121A (en) * | 1983-03-18 | 1985-04-23 | W. R. Grace & Co. | Wet strength material |
| US4526936A (en) * | 1983-03-18 | 1985-07-02 | W. R. Grace & Co. | Process for the preparation of polymeric amine containing products |
| US4565604A (en) * | 1983-03-18 | 1986-01-21 | W. R. Grace & Co. | Retention and drainage aid |
| US4503217A (en) * | 1983-11-10 | 1985-03-05 | Texaco Inc. | Process for selective preparation of polymeric polyamines |
| EP0186975A3 (en) * | 1984-12-24 | 1987-10-28 | The Standard Oil Company | 3-pentenamides from 1,3-butadienes |
| DE3611230A1 (de) * | 1986-04-04 | 1987-10-08 | Basf Ag | Polybutyl- und polyisobutylamine, verfahren zu deren herstellung und diese enthaltende kraft- und schmierstoffzusammensetzungen |
| US4866177A (en) * | 1986-11-24 | 1989-09-12 | Texaco Inc. | Process for one-step synthesis of amides |
| GB8706369D0 (en) * | 1987-03-18 | 1987-04-23 | Exxon Chemical Patents Inc | Crude oil |
| CA2086527A1 (en) * | 1990-07-26 | 1992-01-27 | Samuel J. Tremont | Polymeric drug delivery system |
| ES2113997T3 (es) * | 1992-07-08 | 1998-05-16 | Shell Int Research | Procedimiento para la preparacion de aminas secundarias y composiciones cataliticas para utilizacion en tal procedimiento. |
| EP0603146B1 (en) * | 1992-12-14 | 1998-02-04 | Monsanto Company | Controlled functional density poly(secondary amines) and method for preparation thereof |
| US5646332A (en) * | 1992-12-17 | 1997-07-08 | Exxon Chemical Patents Inc. | Batch Koch carbonylation process |
| US5643859A (en) * | 1992-12-17 | 1997-07-01 | Exxon Chemical Patents Inc. | Derivatives of polyamines with one primary amine and secondary of tertiary amines |
| US5650536A (en) * | 1992-12-17 | 1997-07-22 | Exxon Chemical Patents Inc. | Continuous process for production of functionalized olefins |
| IL107810A0 (en) * | 1992-12-17 | 1994-02-27 | Exxon Chemical Patents Inc | Functionalized polymers and processes for the preparation thereof |
| US5559193A (en) * | 1993-12-20 | 1996-09-24 | Monsanto Company | Controlled functional density polyamines and method for preparation thereof |
| US5767046A (en) * | 1994-06-17 | 1998-06-16 | Exxon Chemical Company | Functionalized additives useful in two-cycle engines |
| US5773567A (en) * | 1996-06-17 | 1998-06-30 | Exxon Chemical Patents Inc | Carboxylic amide-containing polymers for use as fuel or lubricating oil additives and processes for their preparation |
| SG11202101326VA (en) | 2018-12-31 | 2021-03-30 | Halliburton Energy Services Inc | Perturbation based well path reconstruction |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2422631A (en) * | 1944-11-07 | 1947-06-17 | Sharples Chemicals Inc | Manufacture of aliphatic amines and acid amides |
| US3383426A (en) | 1963-09-09 | 1968-05-14 | Exxon Research Engineering Co | Hydroformylation process for polymers |
| FR1494136A (fr) | 1966-05-17 | 1967-09-08 | Auxiliaire De L Inst Francais | Procédé de modification des polymères insaturés par réaction avec l'oxyde de carbone, et produits obtenus |
| US3513200A (en) * | 1968-11-25 | 1970-05-19 | Union Oil Co | Preparation of tertiary amines |
| US3776981A (en) | 1971-02-03 | 1973-12-04 | Shell Oil Co | Hydroformylated block copolymers |
| FR2211002A5 (enExample) * | 1972-12-20 | 1974-07-12 | Rhone Progil | |
| FR2324615A2 (fr) | 1974-07-04 | 1977-04-15 | Rhone Progil | Procede de preparation d'amines tertiaires |
-
1980
- 1980-02-22 US US06/123,740 patent/US4312965A/en not_active Expired - Lifetime
- 1980-11-28 NL NL8006490A patent/NL8006490A/nl not_active Application Discontinuation
- 1980-12-03 IT IT26423/80A patent/IT1141108B/it active
- 1980-12-18 FR FR8026969A patent/FR2476655A1/fr active Granted
- 1980-12-23 SE SE8009109A patent/SE444440B/sv not_active IP Right Cessation
- 1980-12-30 FI FI804063A patent/FI67868C/fi not_active IP Right Cessation
-
1981
- 1981-02-19 DE DE19813106109 patent/DE3106109A1/de active Granted
- 1981-02-20 ES ES499655A patent/ES8202844A1/es not_active Expired
- 1981-02-20 BE BE0/203879A patent/BE887628A/fr unknown
- 1981-02-20 SU SU813247700A patent/SU1227119A3/ru active
- 1981-02-20 GB GB8105491A patent/GB2070025B/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB2070025A (en) | 1981-09-03 |
| FI67868B (fi) | 1985-02-28 |
| BE887628A (fr) | 1981-06-15 |
| IT8026423A0 (it) | 1980-12-03 |
| FR2476655A1 (fr) | 1981-08-28 |
| US4312965A (en) | 1982-01-26 |
| SE444440B (sv) | 1986-04-14 |
| DE3106109A1 (de) | 1981-12-24 |
| GB2070025B (en) | 1984-02-01 |
| DE3106109C2 (enExample) | 1989-04-27 |
| FR2476655B1 (enExample) | 1985-03-29 |
| NL8006490A (nl) | 1981-09-16 |
| FI804063L (fi) | 1981-08-23 |
| ES499655A0 (es) | 1982-02-01 |
| FI67868C (fi) | 1985-06-10 |
| IT1141108B (it) | 1986-10-01 |
| SE8009109L (sv) | 1981-08-23 |
| ES8202844A1 (es) | 1982-02-01 |
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