CH628358A5 - Procede de preparation d'un oligomere aminolyse. - Google Patents
Procede de preparation d'un oligomere aminolyse. Download PDFInfo
- Publication number
- CH628358A5 CH628358A5 CH27678A CH27678A CH628358A5 CH 628358 A5 CH628358 A5 CH 628358A5 CH 27678 A CH27678 A CH 27678A CH 27678 A CH27678 A CH 27678A CH 628358 A5 CH628358 A5 CH 628358A5
- Authority
- CH
- Switzerland
- Prior art keywords
- oligomer
- aminolysed
- units
- amine
- water
- Prior art date
Links
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 10
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 9
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- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 229910000754 Wrought iron Inorganic materials 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000011938 amidation process Methods 0.000 description 1
- 150000001408 amides Chemical group 0.000 description 1
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000008135 aqueous vehicle Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- XNNQFQFUQLJSQT-UHFFFAOYSA-N bromo(trichloro)methane Chemical compound ClC(Cl)(Cl)Br XNNQFQFUQLJSQT-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- BELZJFWUNQWBES-UHFFFAOYSA-N caldopentamine Chemical compound NCCCNCCCNCCCNCCCN BELZJFWUNQWBES-UHFFFAOYSA-N 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- HHFAWKCIHAUFRX-UHFFFAOYSA-N ethoxide Chemical compound CC[O-] HHFAWKCIHAUFRX-UHFFFAOYSA-N 0.000 description 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical class CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000001030 gas--liquid chromatography Methods 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 description 1
- 150000003893 lactate salts Chemical class 0.000 description 1
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000007069 methylation reaction Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 239000002687 nonaqueous vehicle Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-M oxidooxomethyl Chemical compound [O-][C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-M 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical group NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- PIOSEDPFJPAJKQ-UHFFFAOYSA-M sodium;toluene;hydroxide Chemical compound [OH-].[Na+].CC1=CC=CC=C1 PIOSEDPFJPAJKQ-UHFFFAOYSA-M 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
- MBYLVOKEDDQJDY-UHFFFAOYSA-N tris(2-aminoethyl)amine Chemical compound NCCN(CCN)CCN MBYLVOKEDDQJDY-UHFFFAOYSA-N 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 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
-
- 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
- C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
- C08F2800/20—Copolymer characterised by the proportions of the comonomers expressed as weight or mass percentages
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/263—Coating layer not in excess of 5 mils thick or equivalent
- Y10T428/264—Up to 3 mils
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)
- Paints Or Removers (AREA)
- Epoxy Resins (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- General Preparation And Processing Of Foods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/758,894 US4120839A (en) | 1977-01-13 | 1977-01-13 | Oligomeric amino-containing aminolysis products of polymethacrylates or polyacrylates, and epoxy resin coating compositions containing such aminolysis products as curing agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH628358A5 true CH628358A5 (fr) | 1982-02-26 |
Family
ID=25053527
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH27678A CH628358A5 (fr) | 1977-01-13 | 1978-01-11 | Procede de preparation d'un oligomere aminolyse. |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4120839A (enExample) |
| JP (2) | JPS5388089A (enExample) |
| AU (1) | AU516177B2 (enExample) |
| BE (1) | BE862855A (enExample) |
| CA (1) | CA1120643A (enExample) |
| CH (1) | CH628358A5 (enExample) |
| DE (1) | DE2801491C2 (enExample) |
| DK (1) | DK162289C (enExample) |
| ES (2) | ES465860A1 (enExample) |
| FR (1) | FR2377421A1 (enExample) |
| GB (1) | GB1598703A (enExample) |
| IT (1) | IT1106964B (enExample) |
| NL (1) | NL184956C (enExample) |
| NO (1) | NO780093L (enExample) |
| NZ (1) | NZ186162A (enExample) |
| PH (1) | PH15671A (enExample) |
| SE (1) | SE7800266L (enExample) |
| ZA (1) | ZA7814B (enExample) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2407899A1 (fr) * | 1977-11-03 | 1979-06-01 | Jacques Guerrini | Procede pour la fabrication du verre feuillete et produit obtenu selon ledit procede |
| AT365218B (de) * | 1979-11-09 | 1981-12-28 | Vianova Kunstharz Ag | Waesserige beschichtungsmittel fuer holzoberflaechen |
| US4285849A (en) * | 1979-11-27 | 1981-08-25 | Ppg Industries, Inc. | Amidation reaction products of polyamines and polycarboxyl containing materials and coating compositions containing same |
| US4352898A (en) * | 1980-04-25 | 1982-10-05 | Deft, Inc. | Water-reducible epoxy coating compositions without emulsifier |
| US4495317A (en) * | 1980-04-25 | 1985-01-22 | Deft Chemical Coatings, Inc. | Warer reducible epoxy coating composition |
| US4501832A (en) * | 1980-04-25 | 1985-02-26 | Deft Chemical Coatings, Inc. | Water-reducible epoxy coating compositions |
| US4740536A (en) * | 1985-09-06 | 1988-04-26 | Rohm And Haas Company | Water-based binder, coating and adhesive compositions from alkaline-curable latex polymers, epoxies and amines |
| US4731419A (en) * | 1986-02-24 | 1988-03-15 | Nalco Chemical Company | Alkoxylated/cationically modified amide-containing polymers |
| GB8617879D0 (en) * | 1986-07-22 | 1986-08-28 | Buchardt O | Polymer modification |
| DE3740934A1 (de) * | 1987-12-03 | 1989-06-15 | Rhein Chemie Rheinau Gmbh | Mehrschichtenverbund |
| US4957677A (en) * | 1987-12-09 | 1990-09-18 | Mitsubishi Yuka Badische Co., Ltd. | Process for producing composite laminate comprising insert part and injection-molded part |
| DE3827587A1 (de) * | 1988-08-13 | 1990-03-01 | Basf Lacke & Farben | Aminogruppenhaltige copolymerisate, verfahren zu ihrer herstellung sowie ihre verwendung in beschichtungsmitteln |
| US5476885A (en) * | 1989-07-25 | 1995-12-19 | Nippon Shokubai Co., Ltd. | Cement additive, method for producing the same, and cement composition |
| DE69224907D1 (de) * | 1991-07-17 | 1998-04-30 | Nat Diagnostics | Polyacrylamid-matrix-gel |
| DE69208976T2 (de) * | 1991-08-23 | 1997-04-17 | Nippon Shokubai Co. Ltd., Osaka | Biologisch abbaubares, hydrophiles, vernetztes Polymer, Verfahren zu seiner Herstellung und seine Verwendung |
| EP0721004B1 (en) * | 1995-01-06 | 2001-03-21 | Rohm And Haas Company | Water-dispersible powder composition for water-resistant coatings |
| US5516826A (en) * | 1995-03-13 | 1996-05-14 | Westvaco Corporation | Polyamine condensates of styrene-acrylic acid copolymers as corrosion inhibitors |
| US5569687A (en) * | 1995-03-16 | 1996-10-29 | Rohm And Haas Company | Waterborne zinc-rich primer compositions |
| DE19721728C2 (de) * | 1997-05-24 | 2001-07-12 | Byk Chemie Gmbh | Dispergiermittel für Pigmente oder Füllstoffe auf der Basis von Acrylsäurealkylester-Polymeren, Verwendung und Verfahren zur Herstellung |
| EP1123942B1 (en) | 2000-02-10 | 2004-05-06 | Nippon Shokubai Co., Ltd. | Amino-group-containing polymer (salt) and production process therefor |
| AU5200401A (en) * | 2000-07-03 | 2002-01-10 | Rohm And Haas Company | Semi-telechelic nitrogen-functional oligomer |
| US7517934B2 (en) * | 2003-07-31 | 2009-04-14 | Basf Corporation | Modified anionically polymerized polymers |
| WO2011120156A1 (en) * | 2010-04-02 | 2011-10-06 | Alberta Innovates - Technology Futures | Polyamine-containing polymers and methods of synthesis and use |
| WO2019224356A1 (en) * | 2018-05-24 | 2019-11-28 | Universiteit Gent | Amidation of polymers containing ester side chains using functionalized amines |
| US10865172B1 (en) * | 2019-09-04 | 2020-12-15 | Eastman Chemical Company | Aromatic enol ethers |
| WO2021122978A1 (en) | 2019-12-19 | 2021-06-24 | Allnex Netherlands B.V. | Non aqueous crosslinkable composition |
| KR20240024222A (ko) | 2021-06-22 | 2024-02-23 | 알넥스 네덜란드 비. 브이. | 비수성 가교성 조성물 |
| CN122422391A (zh) | 2023-12-19 | 2026-07-17 | 湛新荷兰有限公司 | 非水性涂料组合物 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2912416A (en) * | 1954-07-12 | 1959-11-10 | Shell Dev | Amide containing copolymers and their preparation |
| US2845408A (en) * | 1954-08-04 | 1958-07-29 | Rohm & Haas | Linear polymeric amides and methods of making them |
| NL127158C (enExample) * | 1962-04-23 | |||
| US3406155A (en) * | 1965-05-18 | 1968-10-15 | Gaf Corp | Cationic vinyl lactam-acrylamide copolymers |
| US4018847A (en) * | 1975-10-01 | 1977-04-19 | The B. F. Goodrich Company | Flexible coating compositions |
-
1977
- 1977-01-13 US US05/758,894 patent/US4120839A/en not_active Expired - Lifetime
- 1977-12-22 GB GB53433/77A patent/GB1598703A/en not_active Expired
-
1978
- 1978-01-03 ZA ZA00780014A patent/ZA7814B/xx unknown
- 1978-01-04 CA CA000294333A patent/CA1120643A/en not_active Expired
- 1978-01-05 NZ NZ186162A patent/NZ186162A/xx unknown
- 1978-01-09 PH PH20630A patent/PH15671A/en unknown
- 1978-01-10 ES ES465860A patent/ES465860A1/es not_active Expired
- 1978-01-10 SE SE7800266A patent/SE7800266L/xx unknown
- 1978-01-10 FR FR7800546A patent/FR2377421A1/fr active Granted
- 1978-01-11 DK DK013178A patent/DK162289C/da active
- 1978-01-11 AU AU32362/78A patent/AU516177B2/en not_active Expired
- 1978-01-11 NO NO780093A patent/NO780093L/no unknown
- 1978-01-11 CH CH27678A patent/CH628358A5/fr not_active IP Right Cessation
- 1978-01-12 JP JP160778A patent/JPS5388089A/ja active Granted
- 1978-01-12 BE BE184270A patent/BE862855A/xx not_active IP Right Cessation
- 1978-01-12 IT IT67055/78A patent/IT1106964B/it active
- 1978-01-13 DE DE2801491A patent/DE2801491C2/de not_active Expired - Fee Related
- 1978-01-13 NL NLAANVRAGE7800440,A patent/NL184956C/xx not_active IP Right Cessation
- 1978-10-14 ES ES474217A patent/ES474217A1/es not_active Expired
-
1985
- 1985-12-24 JP JP60289511A patent/JPS61166874A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| DK162289B (da) | 1991-10-07 |
| NL184956B (nl) | 1989-07-17 |
| JPH0218685B2 (enExample) | 1990-04-26 |
| SE7800266L (sv) | 1978-07-14 |
| US4120839A (en) | 1978-10-17 |
| DK13178A (da) | 1978-07-14 |
| DE2801491C2 (de) | 1995-02-16 |
| JPS6361321B2 (enExample) | 1988-11-29 |
| DK162289C (da) | 1992-03-16 |
| NZ186162A (en) | 1980-10-08 |
| PH15671A (en) | 1983-03-11 |
| ES465860A1 (es) | 1979-01-01 |
| IT1106964B (it) | 1985-11-18 |
| FR2377421A1 (fr) | 1978-08-11 |
| AU3236278A (en) | 1979-07-19 |
| FR2377421B1 (enExample) | 1980-09-19 |
| GB1598703A (en) | 1981-09-23 |
| BE862855A (fr) | 1978-07-12 |
| NL7800440A (nl) | 1978-07-17 |
| NL184956C (nl) | 1989-12-18 |
| JPS61166874A (ja) | 1986-07-28 |
| AU516177B2 (en) | 1981-05-21 |
| ZA7814B (en) | 1979-02-28 |
| IT7867055A0 (it) | 1978-01-12 |
| NO780093L (no) | 1978-07-14 |
| ES474217A1 (es) | 1979-05-16 |
| JPS5388089A (en) | 1978-08-03 |
| CA1120643A (en) | 1982-03-23 |
| DE2801491A1 (de) | 1978-07-20 |
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