DE1922626C3 - Verfahren zur Herstellung von Bindemitteln - Google Patents
Verfahren zur Herstellung von BindemittelnInfo
- Publication number
- DE1922626C3 DE1922626C3 DE1922626A DE1922626A DE1922626C3 DE 1922626 C3 DE1922626 C3 DE 1922626C3 DE 1922626 A DE1922626 A DE 1922626A DE 1922626 A DE1922626 A DE 1922626A DE 1922626 C3 DE1922626 C3 DE 1922626C3
- Authority
- DE
- Germany
- Prior art keywords
- weight
- parts
- polyurethane
- nco
- reaction
- 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
- 238000000034 method Methods 0.000 title claims description 12
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 239000011230 binding agent Substances 0.000 title claims description 6
- 239000004814 polyurethane Substances 0.000 claims description 25
- 229920002635 polyurethane Polymers 0.000 claims description 25
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 16
- 239000012948 isocyanate Substances 0.000 claims description 15
- 150000002513 isocyanates Chemical class 0.000 claims description 15
- 239000003973 paint Substances 0.000 claims description 15
- 229920000570 polyether Polymers 0.000 claims description 13
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 12
- 238000001035 drying Methods 0.000 claims description 11
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- 150000001298 alcohols Chemical class 0.000 claims description 6
- 229920001228 polyisocyanate Polymers 0.000 claims description 6
- 239000005056 polyisocyanate Substances 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 125000001033 ether group Chemical group 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 10
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 7
- 239000008096 xylene Substances 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000499 gel Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 5
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000004922 lacquer Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 150000005846 sugar alcohols Polymers 0.000 description 4
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 3
- -1 Thio alcohols Chemical class 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- RHUYHJGZWVXEHW-UHFFFAOYSA-N 1,1-Dimethyhydrazine Chemical compound CN(C)N RHUYHJGZWVXEHW-UHFFFAOYSA-N 0.000 description 1
- DIIIISSCIXVANO-UHFFFAOYSA-N 1,2-Dimethylhydrazine Chemical compound CNNC DIIIISSCIXVANO-UHFFFAOYSA-N 0.000 description 1
- 235000009161 Espostoa lanata Nutrition 0.000 description 1
- 240000001624 Espostoa lanata Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000243251 Hydra Species 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- IPTNXMGXEGQYSY-UHFFFAOYSA-N acetic acid;1-methoxybutan-1-ol Chemical compound CC(O)=O.CCCC(O)OC IPTNXMGXEGQYSY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- QRXWMOHMRWLFEY-UHFFFAOYSA-N isoniazide Chemical compound NNC(=O)C1=CC=NC=C1 QRXWMOHMRWLFEY-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000011527 polyurethane coating Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Substances CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/80—Masked polyisocyanates
- C08G18/8003—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen
- C08G18/8006—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32
- C08G18/8009—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32 with compounds of C08G18/3203
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6666—Compounds of group C08G18/48 or C08G18/52
- C08G18/667—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/6674—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
- Paints Or Removers (AREA)
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1922626A DE1922626C3 (de) | 1969-05-03 | 1969-05-03 | Verfahren zur Herstellung von Bindemitteln |
| AT381770A AT297327B (de) | 1969-05-03 | 1970-04-27 | Verfahren zur Herstellung von tertiäre Stickstoffatome aufweisenden Polyurethanisocyanaten |
| GB2029670A GB1310754A (en) | 1969-05-03 | 1970-04-28 | Process for the production of polyurethane-based one-compo nent systems which are stable on storage and which dry quickly in contact with atmospheric moisture |
| NL7006378.A NL165777C (nl) | 1969-05-03 | 1970-04-29 | Werkwijze voor het lakken van substraten met eencomponent-laksystemen. |
| SE05966/70A SE364516B (cg-RX-API-DMAC7.html) | 1969-05-03 | 1970-04-29 | |
| BE749822D BE749822A (fr) | 1969-05-03 | 1970-04-30 | Procede de preparation de systemes a un composant a base de polyurethanes, sechant rapidement avec l'humidite de l'air et stablesa l'entreposage |
| FR7016022A FR2047195A5 (cg-RX-API-DMAC7.html) | 1969-05-03 | 1970-04-30 | |
| JP45036932A JPS4843198B1 (cg-RX-API-DMAC7.html) | 1969-05-03 | 1970-05-01 | |
| US00265907A US3792023A (en) | 1969-05-03 | 1972-06-23 | Process for the production of storagestable polyurethane isocyanates |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1922626A DE1922626C3 (de) | 1969-05-03 | 1969-05-03 | Verfahren zur Herstellung von Bindemitteln |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE1922626A1 DE1922626A1 (de) | 1970-11-05 |
| DE1922626B2 DE1922626B2 (de) | 1978-04-06 |
| DE1922626C3 true DE1922626C3 (de) | 1983-01-13 |
Family
ID=5733157
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1922626A Expired DE1922626C3 (de) | 1969-05-03 | 1969-05-03 | Verfahren zur Herstellung von Bindemitteln |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US3792023A (cg-RX-API-DMAC7.html) |
| JP (1) | JPS4843198B1 (cg-RX-API-DMAC7.html) |
| AT (1) | AT297327B (cg-RX-API-DMAC7.html) |
| BE (1) | BE749822A (cg-RX-API-DMAC7.html) |
| DE (1) | DE1922626C3 (cg-RX-API-DMAC7.html) |
| FR (1) | FR2047195A5 (cg-RX-API-DMAC7.html) |
| GB (1) | GB1310754A (cg-RX-API-DMAC7.html) |
| NL (1) | NL165777C (cg-RX-API-DMAC7.html) |
| SE (1) | SE364516B (cg-RX-API-DMAC7.html) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4426487A (en) | 1981-10-08 | 1984-01-17 | Bayer Aktiengesellschaft | Mixtures of NCO prepolymers containing tertiary nitrogen atoms and the use thereof as adhesives or coatings |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1751574B1 (de) * | 1968-06-21 | 1970-09-24 | Schoppe Fritz | Verbrennungsvorrichtung (Brennkegel),insbesondere fuer Muell |
| US3971764A (en) * | 1974-12-26 | 1976-07-27 | Akzona Incorporated | Process for producing a cationic polyurethane |
| DE2507682A1 (de) * | 1975-02-22 | 1976-09-02 | Bayer Ag | Isocyanate |
| DE2555535C2 (de) * | 1975-12-10 | 1978-01-05 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Überzügen |
| DE2623401C3 (de) * | 1976-05-25 | 1981-07-16 | Bayer Ag, 5090 Leverkusen | Verfahren zur lösungsmittelfreien Herstellung von massiven Kunststoff-Formteilen |
| DE2651089C3 (de) * | 1976-11-09 | 1980-06-12 | Bayer Ag, 5090 Leverkusen | Selbsthältendes Material für Stutzverbände |
| DE2705751C2 (de) * | 1977-02-11 | 1979-03-08 | Bayer Ag, 5090 Leverkusen | Patrone zum Befestigen von Ankerstangen in Bohrlöchern |
| US4123421A (en) * | 1977-03-21 | 1978-10-31 | Witco Chemical Corporation | Stable tertiary amine containing terminally unsaturated polyurethane resins |
| CH636235B (de) | 1977-09-06 | 1900-01-01 | Sandoz Ag | Verfahren zur herstellung von polyurethanen und deren verwendung in binderdispersionen zum verkleben von fasern in vliesstoffen. |
| US4163815A (en) * | 1977-09-19 | 1979-08-07 | Ford Motor Company | Catalyzed polyisocyanate coating compositions |
| DE2758114A1 (de) * | 1977-12-24 | 1979-07-05 | Basf Ag | Verfahren zur herstellung von formstabilen einkomponentenpolyurethanschaumstoffen |
| US4411262A (en) * | 1978-04-21 | 1983-10-25 | Bayer Aktiengesellschaft | Constructional material |
| DE2843377A1 (de) * | 1978-10-05 | 1980-04-24 | Bayer Ag | Verwendung von gegebenenfalls aethergruppen aufweisenden hydroxylalkylaminen bzw. derer salze als den wasserdampfdiffusionswiderstand reduzierende zusaetze in beschichtungsmitteln auf polyurethanbasis |
| US4273912A (en) * | 1979-09-24 | 1981-06-16 | Minnesota Mining And Manufacturing Company | Polyurethane floor varnish and floor materials coated therewith |
| US4383070A (en) * | 1982-05-27 | 1983-05-10 | Mobay Chemical Corporation | Storage stable polyurethane compositions |
| US5236994A (en) * | 1991-03-28 | 1993-08-17 | Miles Inc. | Process for sealing and/or priming concrete with aqueous polyisocyanate dispersions and the concrete obtained by this process |
| DE4129953A1 (de) * | 1991-09-10 | 1993-03-11 | Bayer Ag | Polyisocyanatgemische, ein verfahren zu ihrer herstellung und ihre verwendung |
| DE4308332A1 (de) * | 1993-03-16 | 1994-09-22 | Basf Ag | Härtungsmittel für Zweikomponenten-Polyurethansysteme, insbesondere Zweikompenenten-Polyurethanlacke, sowie ein Verfahren zu ihrer Herstellung |
| US6368714B1 (en) | 1993-10-14 | 2002-04-09 | John Russell Robertson | Moisture-activated adhesive compositions |
| CN101287783B (zh) * | 2005-10-14 | 2011-11-09 | 陶氏环球技术有限责任公司 | 复合制品和使用异氰酸酯基封端的预聚物作为粘结剂的制备方法 |
| DE102007028922A1 (de) | 2007-06-22 | 2008-12-24 | Bayer Materialscience Ag | Polyisocyanatmischungen |
| DE102008018160A1 (de) | 2008-04-10 | 2009-10-15 | Bayer Materialscience Ag | Polyisocyanatgemische |
| DE102009058463A1 (de) | 2009-12-16 | 2011-06-22 | Bayer MaterialScience AG, 51373 | Polyisocyanatmischungen |
| DE102010019504A1 (de) | 2010-05-06 | 2011-11-10 | Bayer Materialscience Ag | Polyisocyanatprepolymere und deren Verwendung |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3112281A (en) * | 1957-09-17 | 1963-11-26 | Wyandotte Chemicals Corp | Polyurethane foams and process for preparing same |
| US3049515A (en) * | 1959-03-26 | 1962-08-14 | Wyandotte Chemicals Corp | Hydroxy-terminated polyether-based urethane compositions |
| US3211585A (en) * | 1961-06-16 | 1965-10-12 | Schenectady Chemical | Electric conductor coated with the reaction product of a dibasic polycarboxylic acid and tris(2-hydroxyethyl) isocyanurate together with an organic polyisocyanate or an alkyl titanate |
| GB1126094A (en) * | 1966-09-12 | 1968-09-05 | Ici Ltd | Moisture-curing polyurethane compositions |
-
1969
- 1969-05-03 DE DE1922626A patent/DE1922626C3/de not_active Expired
-
1970
- 1970-04-27 AT AT381770A patent/AT297327B/de not_active IP Right Cessation
- 1970-04-28 GB GB2029670A patent/GB1310754A/en not_active Expired
- 1970-04-29 SE SE05966/70A patent/SE364516B/xx unknown
- 1970-04-29 NL NL7006378.A patent/NL165777C/xx not_active IP Right Cessation
- 1970-04-30 FR FR7016022A patent/FR2047195A5/fr not_active Expired
- 1970-04-30 BE BE749822D patent/BE749822A/xx unknown
- 1970-05-01 JP JP45036932A patent/JPS4843198B1/ja active Pending
-
1972
- 1972-06-23 US US00265907A patent/US3792023A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4426487A (en) | 1981-10-08 | 1984-01-17 | Bayer Aktiengesellschaft | Mixtures of NCO prepolymers containing tertiary nitrogen atoms and the use thereof as adhesives or coatings |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1922626B2 (de) | 1978-04-06 |
| FR2047195A5 (cg-RX-API-DMAC7.html) | 1971-03-12 |
| DE1922626A1 (de) | 1970-11-05 |
| GB1310754A (en) | 1973-03-21 |
| NL165777C (nl) | 1981-05-15 |
| JPS4843198B1 (cg-RX-API-DMAC7.html) | 1973-12-17 |
| NL165777B (nl) | 1980-12-15 |
| BE749822A (fr) | 1970-10-01 |
| SE364516B (cg-RX-API-DMAC7.html) | 1974-02-25 |
| US3792023A (en) | 1974-02-12 |
| NL7006378A (cg-RX-API-DMAC7.html) | 1970-11-05 |
| AT297327B (de) | 1972-03-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1922626C3 (de) | Verfahren zur Herstellung von Bindemitteln | |
| EP1134247B1 (de) | Hochfunktionelle Polyisocyanate | |
| EP0154768B1 (de) | Verfahren zur Herstellung von Polyurethanen, Polyurethane mit aromatischen Aminoendgruppen und ihre Verwendung | |
| DE1519432C3 (cg-RX-API-DMAC7.html) | ||
| EP0172362B1 (de) | Kaltvernetzende PUR-Dispersionen, ihre Herstellung und Verwendung | |
| EP0010248A1 (de) | Isocyanatgemisch und seine Verwendung als Bindemittel in Einkomponenten-Lacken | |
| DE1494465C3 (de) | Feuchtigkeitstrocknende Eintopfüberzugs- und -klebemasse | |
| DE2165023C3 (de) | Verfahren zur Herstellung hochmolekularer allophanat- und gegebenenfalls urethangrupenhaltiger -verbindungen | |
| DE1150517B (de) | Verfahren zur Herstellung von Urethan- und Semicarbazidgruppierungen aufweisenden Polymeren | |
| DE2633396A1 (de) | Verfahren zur herstellung einer anionischen waessrigen polyurethanemulsion | |
| DE4438351A1 (de) | Verwendung von partiell dehydratisierten Rizinusölen zur Herstellung von wäßrigen Polyurethandispersionen sowie unter Verwendung dieser wäßrigen Polyurethandispersionen hergestellte Beschichtungen | |
| DE2632544A1 (de) | Verfahren zum herstellen einer waessrigen, in der waerme haertbaren polyurethanemulsion | |
| DE2632708A1 (de) | Verfahren zum herstellen einer waessrigen kationischen waermehaertbaren polyurethanemulsion | |
| EP0868463B1 (de) | Verbindungen mit isocyanatgruppen und verkappten gegenüber isocyanaten reaktiven gruppen | |
| DE102017108730A1 (de) | Verfahren zur lösemittelfreien Herstellung einer Polyurethandispersion | |
| DE1028772B (de) | Verfahren zur Herstellung hochmolekularer vernetzter Kunststoffe | |
| DE1595701A1 (de) | Verfahren zur Herstellung von vernetzbaren Polymerisations-Polykondensations- und Polyadditionsprodukten | |
| DE2900031A1 (de) | Verfahren zur herstellung von formkoerpern und ueberzuegen | |
| DE2415467A1 (de) | Fluessiger klebstoff | |
| DE2238741A1 (de) | Verfahren zur linearisierung vernetzter isocyanat-polyadditionsprodukte mit polyisocyanaten | |
| DE1694221A1 (de) | Polyurethan-Kunststoffe und Verfahren zu ihrer Herstellung | |
| US2907752A (en) | Synthetic rubbery polyester-polyisocyanate polymers | |
| DE955094C (de) | Verfahren zur Herstellung von Flaechengebilden aus Polyisocyanaten und Verbindungen m mehr als einem reaktionsfaehigen Wasserstoffatom | |
| DE2633294A1 (de) | Vernetzte, ungesaettigte blockpolyamide | |
| DE1145353B (de) | Verfahren zur Herstellung von homogenen Kunststoffen einschliesslich Flaechengebilden nach dem Isocyanat-Polyadditionsverfahren |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) |