DE2905430C2 - Verwendung eines selbsthärtenden ungesättigten Polyesters als Schmelzklebstoff - Google Patents
Verwendung eines selbsthärtenden ungesättigten Polyesters als SchmelzklebstoffInfo
- Publication number
- DE2905430C2 DE2905430C2 DE2905430A DE2905430A DE2905430C2 DE 2905430 C2 DE2905430 C2 DE 2905430C2 DE 2905430 A DE2905430 A DE 2905430A DE 2905430 A DE2905430 A DE 2905430A DE 2905430 C2 DE2905430 C2 DE 2905430C2
- Authority
- DE
- Germany
- Prior art keywords
- adhesive
- polyester
- curing
- resin
- additive
- 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
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- JOVOSQBPPZZESK-UHFFFAOYSA-N phenylhydrazine hydrochloride Chemical compound Cl.NNC1=CC=CC=C1 JOVOSQBPPZZESK-UHFFFAOYSA-N 0.000 description 1
- MLCHBQKMVKNBOV-UHFFFAOYSA-N phenylphosphinic acid Chemical compound OP(=O)C1=CC=CC=C1 MLCHBQKMVKNBOV-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 235000013446 pixi Nutrition 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000012985 polymerization agent Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- RLJWTAURUFQFJP-UHFFFAOYSA-N propan-2-ol;titanium Chemical compound [Ti].CC(C)O.CC(C)O.CC(C)O.CC(C)O RLJWTAURUFQFJP-UHFFFAOYSA-N 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- YPVDWEHVCUBACK-UHFFFAOYSA-N propoxycarbonyloxy propyl carbonate Chemical compound CCCOC(=O)OOC(=O)OCCC YPVDWEHVCUBACK-UHFFFAOYSA-N 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 230000035943 smell Effects 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- JIWBIWFOSCKQMA-UHFFFAOYSA-N stearidonic acid Natural products CCC=CCC=CCC=CCC=CCCCCC(O)=O JIWBIWFOSCKQMA-UHFFFAOYSA-N 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- XTVMZZBLCLWBPM-UHFFFAOYSA-N tert-butylcyclohexane Chemical compound CC(C)(C)C1CCCCC1 XTVMZZBLCLWBPM-UHFFFAOYSA-N 0.000 description 1
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N tetraisopropyl titanate Substances CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 238000001029 thermal curing Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/682—Polyesters containing atoms other than carbon, hydrogen and oxygen containing halogens
- C08G63/6824—Polyesters containing atoms other than carbon, hydrogen and oxygen containing halogens derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/6828—Polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/66—Polyesters containing oxygen in the form of ether groups
- C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/676—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
-
- 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
- C09J167/00—Adhesives based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Adhesives based on derivatives of such polymers
- C09J167/06—Unsaturated polyesters having carbon-to-carbon unsaturation
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1412278A JPS54107935A (en) | 1978-02-13 | 1978-02-13 | Hot-melt adhesive |
JP10141978A JPS5529515A (en) | 1978-08-22 | 1978-08-22 | Adhesive composition |
JP10188178A JPS5529541A (en) | 1978-08-23 | 1978-08-23 | Composite adhesive |
Publications (2)
Publication Number | Publication Date |
---|---|
DE2905430A1 DE2905430A1 (de) | 1979-08-23 |
DE2905430C2 true DE2905430C2 (de) | 1982-07-01 |
Family
ID=27280537
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2905430A Expired DE2905430C2 (de) | 1978-02-13 | 1979-02-13 | Verwendung eines selbsthärtenden ungesättigten Polyesters als Schmelzklebstoff |
Country Status (5)
Country | Link |
---|---|
CH (1) | CH641490A5 (fr) |
DE (1) | DE2905430C2 (fr) |
FR (1) | FR2416930A1 (fr) |
GB (1) | GB2014170B (fr) |
IT (1) | IT1113002B (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0397494A2 (fr) * | 1989-05-12 | 1990-11-14 | Hoechst Celanese Corporation | Copolymères polyacétal du trioxanne et de dérivés du formal de 1'1,2,6-hexanetriol |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10144524B4 (de) * | 2001-09-05 | 2008-11-20 | Jowat Ag | Verkleben von Kunststoffextrudaten mit Werkstoffoberflächen |
FR2960546B1 (fr) * | 2010-05-28 | 2012-07-13 | Saint Gobain Rech | Composition adhesive renfermant un polyester insature hydrosoluble ou dispersable dans l'eau et un monomere ethyleniquement insature, et utilisations. |
US8906999B2 (en) | 2011-02-17 | 2014-12-09 | Ccp Composites Us Llc | Styrene-free unsaturated polyester |
EP2821454B1 (fr) * | 2013-07-02 | 2017-03-29 | Nitto Europe N.V | Composition adhésive à base biologique photodurcissable non saturée |
EP2957303A1 (fr) * | 2014-06-20 | 2015-12-23 | Nitto Denko Corporation | Composition durcissable et adhésif de la peau |
GB201718470D0 (en) * | 2017-11-08 | 2017-12-20 | Provost Fellows Found Scholars And The Other Members Of Board Of The College Of The Holy And Undivid | Adhesive formulations |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2578690A (en) * | 1949-10-04 | 1951-12-18 | Pittsburgh Plate Glass Co | Accelerators for addendum type resins |
US2610168A (en) * | 1951-08-17 | 1952-09-09 | Libbey Owens Ford Glass Co | Polyesters stabilized with substituted p-benzoquinones |
US2852487A (en) * | 1955-08-05 | 1958-09-16 | Glidden Co | Polymerizable solution of an allyl ether and an unsaturated alkyd resin |
FR1334978A (fr) * | 1962-05-10 | 1963-08-16 | Sorepe Soc | Nouvelles méthodes d'obtention de résines de polyesters insaturés dépourvues de monomère de pontage et utilisation de celles-ci |
FR1534128A (fr) * | 1967-07-05 | 1968-07-26 | Eastman Kodak Co | Nouveaux assemblages par composition thermoadhésive et procédé de fabrication |
US3660528A (en) * | 1970-02-12 | 1972-05-02 | Alla Elisbarovna Kostenko | Unsaturated polyester resins method of their production and application |
JPS5645951B2 (fr) * | 1973-05-21 | 1981-10-29 | ||
JPS5328177B2 (fr) * | 1974-06-11 | 1978-08-12 | ||
JPS5743879B2 (fr) * | 1975-02-05 | 1982-09-17 | ||
JPS558022B2 (fr) * | 1975-02-10 | 1980-03-01 | ||
NL7510817A (en) * | 1975-09-15 | 1977-03-17 | Eastman Kodak Co | Hot melt adhesives for seams of metal cans - comprising terephthalic acid-dimeric acid component, ethylene glycol copolyester and polystyrene |
-
1979
- 1979-02-13 FR FR7903626A patent/FR2416930A1/fr active Granted
- 1979-02-13 DE DE2905430A patent/DE2905430C2/de not_active Expired
- 1979-02-13 IT IT20150/79A patent/IT1113002B/it active
- 1979-02-13 CH CH138179A patent/CH641490A5/de not_active IP Right Cessation
- 1979-02-13 GB GB7905014A patent/GB2014170B/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0397494A2 (fr) * | 1989-05-12 | 1990-11-14 | Hoechst Celanese Corporation | Copolymères polyacétal du trioxanne et de dérivés du formal de 1'1,2,6-hexanetriol |
EP0397494A3 (fr) * | 1989-05-12 | 1991-05-15 | Hoechst Celanese Corporation | Copolymères polyacétal du trioxanne et de dérivés du formal de 1'1,2,6-hexanetriol |
Also Published As
Publication number | Publication date |
---|---|
FR2416930B1 (fr) | 1983-01-28 |
IT7920150A0 (it) | 1979-02-13 |
GB2014170A (en) | 1979-08-22 |
GB2014170B (en) | 1982-11-24 |
CH641490A5 (de) | 1984-02-29 |
DE2905430A1 (de) | 1979-08-23 |
FR2416930A1 (fr) | 1979-09-07 |
IT1113002B (it) | 1986-01-20 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
OAP | Request for examination filed | ||
OD | Request for examination | ||
D2 | Grant after examination | ||
8328 | Change in the person/name/address of the agent |
Free format text: STREHL, P., DIPL.-ING. DIPL.-WIRTSCH.-ING. SCHUEBEL-HOPF, U., DIPL.-CHEM. DR.RER.NAT., PAT.-ANW., 8000 MUENCHEN |
|
8331 | Complete revocation |