GB887387A - Adhesive sheets - Google Patents
Adhesive sheetsInfo
- Publication number
- GB887387A GB887387A GB6609/58A GB660958A GB887387A GB 887387 A GB887387 A GB 887387A GB 6609/58 A GB6609/58 A GB 6609/58A GB 660958 A GB660958 A GB 660958A GB 887387 A GB887387 A GB 887387A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compound
- functional groups
- pentadecyl
- octadecyl
- linkages
- 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
- 239000000853 adhesive Substances 0.000 title 1
- 230000001070 adhesive effect Effects 0.000 title 1
- KVVSCMOUFCNCGX-UHFFFAOYSA-N cardol Chemical compound CCCCCCCCCCCCCCCC1=CC(O)=CC(O)=C1 KVVSCMOUFCNCGX-UHFFFAOYSA-N 0.000 abstract 8
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
- GDJMJAKVVSGNLA-UHFFFAOYSA-N 5-n-pentacosylresorcinol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCC1=CC(O)=CC(O)=C1 GDJMJAKVVSGNLA-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000000524 functional group Chemical group 0.000 abstract 4
- 229940126062 Compound A Drugs 0.000 abstract 3
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 abstract 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 abstract 2
- PTFIPECGHSYQNR-UHFFFAOYSA-N 3-Pentadecylphenol Chemical compound CCCCCCCCCCCCCCCC1=CC=CC(O)=C1 PTFIPECGHSYQNR-UHFFFAOYSA-N 0.000 abstract 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 abstract 2
- -1 sulphonamido Chemical group 0.000 abstract 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 abstract 2
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 abstract 1
- QWDQYHPOSSHSAW-UHFFFAOYSA-N 1-isocyanatooctadecane Chemical compound CCCCCCCCCCCCCCCCCCN=C=O QWDQYHPOSSHSAW-UHFFFAOYSA-N 0.000 abstract 1
- XQITUXIEASXIMZ-UHFFFAOYSA-N 2-sulfooctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(C(O)=O)S(O)(=O)=O XQITUXIEASXIMZ-UHFFFAOYSA-N 0.000 abstract 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 229920000877 Melamine resin Polymers 0.000 abstract 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 abstract 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 abstract 1
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 abstract 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 1
- 150000005215 alkyl ethers Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 239000004202 carbamide Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 239000008199 coating composition Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- CTXKDHZPBPQKTD-UHFFFAOYSA-N ethyl n-(carbamoylamino)carbamate Chemical compound CCOC(=O)NNC(N)=O CTXKDHZPBPQKTD-UHFFFAOYSA-N 0.000 abstract 1
- 229940075507 glyceryl monostearate Drugs 0.000 abstract 1
- ZBRRLVWJAPULGW-UHFFFAOYSA-N henicosane-2,4-dione Chemical compound CCCCCCCCCCCCCCCCCC(=O)CC(C)=O ZBRRLVWJAPULGW-UHFFFAOYSA-N 0.000 abstract 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 abstract 1
- 150000002466 imines Chemical class 0.000 abstract 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 abstract 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 1
- 235000010935 mono and diglycerides of fatty acids Nutrition 0.000 abstract 1
- WZLRSHAZJIUYQJ-UHFFFAOYSA-N n-(4,6-diamino-1,3,5-triazin-2-yl)octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NC1=NC(N)=NC(N)=N1 WZLRSHAZJIUYQJ-UHFFFAOYSA-N 0.000 abstract 1
- 125000000962 organic group Chemical group 0.000 abstract 1
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 abstract 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 239000001593 sorbitan monooleate Substances 0.000 abstract 1
- 235000011069 sorbitan monooleate Nutrition 0.000 abstract 1
- 229940035049 sorbitan monooleate Drugs 0.000 abstract 1
- 229950003429 sorbitan palmitate Drugs 0.000 abstract 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 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
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/201—Adhesives in the form of films or foils characterised by their carriers characterised by the release coating composition on the carrier layer
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/21—Paper; Textile fabrics
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
A release coating composition for a pressure-sensitive adhesive sheet or tape comprises the reaction product of a polyfunctional compound A, the molecules of which are unreactive with each other and consist essentially of an organic group to which is attached a long, straight chain alkyl group of 12 to 24 carbon atoms and at least two functional groups; and a polyfunctional compound B, the molecules of which are unreactive with each other and consist essentially of at least one atom to which are attached at least two functional groups, the functional groups of compound A being reactive with the functional groups of compound B to form polar linkages between the respective nuclei of compound A and compound B, said linkages being ester, ether, amide, ureido, urethane and/or sulphonamido linkages. Examples describe the preparation of release agents by reacting tolylene diisocyanate (in toluene \sB acetone, with a triethylamine catalyst) with (1) and (2) 5-n-pentadecyl resorcinol; (3) N-methyl-N-(2,3,4,5,6-pentahydroxyhexyl)-N1-octadecyl urea; (4) an alkyl ether R-O-(CH2)n-NH2 of M.W. 310 to 330; (4) alpha-sulphostearic acid; (6) kojyl palmitate; (7) mono- and diglycerides of fatty acids; (9) octadecylamine; (10) N,N-diethanol -N1-octadecyl urea; (11) sorbitan palmitate; (12) sorbitan mono-oleate; (13) polyoxyethylene sorbitan monostearate; (16) glyceryl monostearate. Other release agents are obtained from (8 and 15) p,p1-diisocyanato-diphenylmethane with N,N1-ethylene-bis-stearamide and 5-n-pentadecyl resorcinol; (14) 5-n-pentadecyl resorcinol and p,p1,p11-triisocyanato-triphenylmethane; (20) 3-n-pentadecyl phenol and formaldehyde in alkaline aqueous propanol; (21) p-aminophenol, octadecyl isocyanate and formaldehyde in aqueous alkalineisopropanol; (23) 5-n-pentadecyl resorcinol and tetraisopropyl titanate in toluene. Water, ammonia, imines, alcohol, phenol, urea, melamine, hydrogen sulphide, mercaptan, thionic or thioic acid, thiothiolic acid, 2,4-diketo-heneicosane, N-monostearoyl-melamine, 3-n-octadecyl glutardi-aldehyde and compounds with activated methylene groups are other specified reactants.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US887387XA | 1957-02-28 | 1957-02-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB887387A true GB887387A (en) | 1962-01-17 |
Family
ID=22213155
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB6609/58A Expired GB887387A (en) | 1957-02-28 | 1958-02-28 | Adhesive sheets |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB887387A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0189978A1 (en) * | 1985-01-10 | 1986-08-06 | United Merchants and Manufacturers, Inc. | Aqueous based release coating compositions |
| GB2262056A (en) * | 1991-11-15 | 1993-06-09 | Standard Check Book Company Li | Release coated products |
| WO2014160905A1 (en) * | 2013-03-29 | 2014-10-02 | E. I. Du Pont De Nemours And Company | Non-fluorinated urethane based coatings |
| US9845410B2 (en) | 2014-06-12 | 2017-12-19 | The Chemours Company Fc, Llc | Wax and urethane based extender blends for surface effect compositions |
| US9938431B2 (en) | 2014-09-26 | 2018-04-10 | The Chemours Company Fc, Llc | Use of non-fluorinated or partially fluorinated urethanes in coatings |
| US10047245B2 (en) | 2014-09-26 | 2018-08-14 | The Chemours Company Fc, Llc | Non-fluorinated and partially fluorinated polymers |
| US10138594B2 (en) | 2014-09-26 | 2018-11-27 | The Chemours Company Fc, Llc | Partially fluorinated urethane based coatings |
| US10208155B2 (en) | 2014-09-26 | 2019-02-19 | The Chemours Company Fc, Llc | Sulfonated fluorinated, non-fluorinated or partially fluorinated urethanes |
| US10246608B2 (en) | 2014-09-26 | 2019-04-02 | The Chemours Company Fc, Llc | Non-fluorinated urethane based coatings |
| US10308898B2 (en) | 2014-09-26 | 2019-06-04 | The Chemours Company Fc, Llc | Method of imparting water repellency with non-fluorinated laundry treatment compositions |
-
1958
- 1958-02-28 GB GB6609/58A patent/GB887387A/en not_active Expired
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0189978A1 (en) * | 1985-01-10 | 1986-08-06 | United Merchants and Manufacturers, Inc. | Aqueous based release coating compositions |
| GB2262056A (en) * | 1991-11-15 | 1993-06-09 | Standard Check Book Company Li | Release coated products |
| GB2262056B (en) * | 1991-11-15 | 1995-11-08 | Standard Check Book Company Li | A coated product |
| US10138392B2 (en) | 2013-03-29 | 2018-11-27 | The Chemours Company Fc, Llc | Non-fluorinated urethane based coatings |
| WO2014160905A1 (en) * | 2013-03-29 | 2014-10-02 | E. I. Du Pont De Nemours And Company | Non-fluorinated urethane based coatings |
| JP2016524628A (en) * | 2013-03-29 | 2016-08-18 | ザ ケマーズ カンパニー エフシー リミテッド ライアビリティ カンパニー | Non-fluorinated urethane coating |
| EP3231828A1 (en) * | 2013-03-29 | 2017-10-18 | The Chemours Company FC, LLC | Method for preparing non-fluorinated urethane based coatings |
| EP4592448A3 (en) * | 2013-03-29 | 2025-08-06 | The Chemours Company FC, LLC | Non-fluorinated urethane based coatings |
| CN105377935B (en) * | 2013-03-29 | 2018-08-31 | 得凯莫斯公司弗罗里达有限公司 | Non-fluorinated urethane-based coating |
| US9845410B2 (en) | 2014-06-12 | 2017-12-19 | The Chemours Company Fc, Llc | Wax and urethane based extender blends for surface effect compositions |
| US10047245B2 (en) | 2014-09-26 | 2018-08-14 | The Chemours Company Fc, Llc | Non-fluorinated and partially fluorinated polymers |
| US10138594B2 (en) | 2014-09-26 | 2018-11-27 | The Chemours Company Fc, Llc | Partially fluorinated urethane based coatings |
| US10208155B2 (en) | 2014-09-26 | 2019-02-19 | The Chemours Company Fc, Llc | Sulfonated fluorinated, non-fluorinated or partially fluorinated urethanes |
| US10246608B2 (en) | 2014-09-26 | 2019-04-02 | The Chemours Company Fc, Llc | Non-fluorinated urethane based coatings |
| US10308898B2 (en) | 2014-09-26 | 2019-06-04 | The Chemours Company Fc, Llc | Method of imparting water repellency with non-fluorinated laundry treatment compositions |
| US9938431B2 (en) | 2014-09-26 | 2018-04-10 | The Chemours Company Fc, Llc | Use of non-fluorinated or partially fluorinated urethanes in coatings |
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