SE439319B - Sett att framstella overdrag pa och hopklistringar av metalliska material samt polyvinylklorid-plastisol till anvendning vid settet - Google Patents
Sett att framstella overdrag pa och hopklistringar av metalliska material samt polyvinylklorid-plastisol till anvendning vid settetInfo
- Publication number
- SE439319B SE439319B SE7713634A SE7713634A SE439319B SE 439319 B SE439319 B SE 439319B SE 7713634 A SE7713634 A SE 7713634A SE 7713634 A SE7713634 A SE 7713634A SE 439319 B SE439319 B SE 439319B
- Authority
- SE
- Sweden
- Prior art keywords
- fatty acid
- adhesives
- condensation products
- mixture
- plastisols
- Prior art date
Links
- 229920001944 Plastisol Polymers 0.000 title claims description 23
- 239000004999 plastisol Substances 0.000 title claims description 23
- 239000007769 metal material Substances 0.000 title claims description 7
- 229920002554 vinyl polymer Polymers 0.000 title 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 61
- 229930195729 fatty acid Natural products 0.000 claims description 61
- 239000000194 fatty acid Substances 0.000 claims description 61
- 150000004665 fatty acids Chemical class 0.000 claims description 61
- 239000000203 mixture Substances 0.000 claims description 36
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 claims description 25
- 239000000853 adhesive Substances 0.000 claims description 15
- 230000001070 adhesive effect Effects 0.000 claims description 14
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 13
- 239000004800 polyvinyl chloride Substances 0.000 claims description 13
- 238000000576 coating method Methods 0.000 claims description 12
- 239000007859 condensation product Substances 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 8
- 239000004014 plasticizer Substances 0.000 claims description 8
- 229920000768 polyamine Polymers 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 5
- 239000000945 filler Substances 0.000 claims description 5
- 229920001281 polyalkylene Polymers 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 3
- 150000002576 ketones Chemical class 0.000 claims description 3
- 150000001299 aldehydes Chemical class 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims 2
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 125000003700 epoxy group Chemical group 0.000 claims 1
- 239000003292 glue Substances 0.000 claims 1
- 150000001412 amines Chemical class 0.000 description 22
- 239000000047 product Substances 0.000 description 20
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 19
- 229960001124 trientine Drugs 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 239000002253 acid Substances 0.000 description 13
- 239000013638 trimer Substances 0.000 description 11
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 150000007513 acids Chemical class 0.000 description 8
- 239000000539 dimer Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 150000002118 epoxides Chemical class 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 238000010304 firing Methods 0.000 description 4
- 238000007127 saponification reaction Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 235000019445 benzyl alcohol Nutrition 0.000 description 3
- -1 for example Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 3
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 2
- 239000002318 adhesion promoter Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 229940106691 bisphenol a Drugs 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 150000002081 enamines Chemical class 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000004658 ketimines Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 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
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- 239000004808 2-ethylhexylester Substances 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000002262 Schiff base Substances 0.000 description 1
- 150000004753 Schiff bases Chemical class 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000001030 gas--liquid chromatography Methods 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 150000002894 organic compounds Chemical class 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
- 230000035515 penetration Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000003022 phthalic acids Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/04—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C09D127/06—Homopolymers or copolymers of vinyl chloride
-
- 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
- C09J127/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Adhesives based on derivatives of such polymers
- C09J127/02—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J127/04—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Adhesives based on derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C09J127/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/14—Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2654871A DE2654871C3 (de) | 1976-12-03 | 1976-12-03 | Polyvinylchlorid-Plastisole mit verbesserter Haftung |
Publications (2)
Publication Number | Publication Date |
---|---|
SE7713634L SE7713634L (sv) | 1978-06-04 |
SE439319B true SE439319B (sv) | 1985-06-10 |
Family
ID=5994626
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE7713634A SE439319B (sv) | 1976-12-03 | 1977-12-01 | Sett att framstella overdrag pa och hopklistringar av metalliska material samt polyvinylklorid-plastisol till anvendning vid settet |
Country Status (12)
Country | Link |
---|---|
US (1) | US4146520A (en:Method) |
BE (1) | BE861449A (en:Method) |
DE (1) | DE2654871C3 (en:Method) |
DK (1) | DK493877A (en:Method) |
FR (1) | FR2372862A1 (en:Method) |
GB (1) | GB1577583A (en:Method) |
IE (1) | IE46099B1 (en:Method) |
IT (1) | IT1089313B (en:Method) |
LU (1) | LU78615A1 (en:Method) |
NL (1) | NL185675C (en:Method) |
PL (1) | PL110670B1 (en:Method) |
SE (1) | SE439319B (en:Method) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4427802A (en) | 1981-07-27 | 1984-01-24 | Hexcel Corporation | Heterocyclic multifunctional amine adducts and curable compositions containing the same |
DE3201265A1 (de) * | 1982-01-16 | 1983-07-28 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Verfahren zum herstellen von ueberzuegen und klebeverbindung mit polyvinylchlorid-plastisolen mit verbesserter haftung und plastisole fuer das verfahren |
DE3221354A1 (de) * | 1982-06-05 | 1983-12-08 | Schering AG, 1000 Berlin und 4709 Bergkamen | Verfahren zum herstellen von ueberzuegen und klebeverbindungen mit polyvinylchlorid-plastisolen mit verbesserter haftung und plastisole fuer das verfahren |
DE3319849C1 (de) * | 1983-06-01 | 1984-11-22 | Degussa Ag, 6000 Frankfurt | Beschichtungsmassen aus Plastisolen oder Organosolen und Verfahren zur Verbesserung der Haftung dieser Massen auf metallischen Untergruenden |
IT1180214B (it) * | 1984-08-02 | 1987-09-23 | Chem Plast Spa | Promotori d'adesione per plastisols in grado di mantenere stabile il colore dei plastisols all'effetto del trattamento termico d'applicazione |
US4824700A (en) * | 1986-09-02 | 1989-04-25 | Sherex Chemical Company, Inc. | Paintable adhesion promoter system for polyvinyl chloride plastisols |
US4851464A (en) * | 1986-09-02 | 1989-07-25 | Sherex Chemical Company, Ltd. | Paintable adhesion promoter system for polyvinyl chloride plastisols |
US4959399A (en) * | 1988-05-20 | 1990-09-25 | W. R. Grace & Co.-Conn. | Acidic adhesion promoters for PVC plastisols |
CA2007328A1 (en) * | 1989-01-10 | 1990-07-10 | Don S. Wozniak | Adhesion and paintability improvements in pvc plastisols at low bake temperatures |
DE4004477A1 (de) * | 1990-02-14 | 1991-08-22 | Schering Ag | Verfahren zur herstellung von loesungen oligomerer methylaluminoxane |
US5475056A (en) * | 1991-04-19 | 1995-12-12 | Teroson Gmbh | Plastisols which prevent the yellowing of top coats, process for their preparation and use |
DE4112823C2 (de) * | 1991-04-19 | 1996-11-21 | Henkel Teroson Gmbh | Vergilbung von Decklacken verhindernde Plastisole, Verfahren zu ihrer Herstellung und ihre Verwendung |
EP0683803B1 (en) * | 1993-02-10 | 1997-05-02 | Air Products And Chemicals, Inc. | Adhesion promoters |
DE4342672A1 (de) * | 1993-12-15 | 1995-06-22 | Akzo Nobel Nv | Haftverbesserer |
US6238789B1 (en) * | 1994-03-22 | 2001-05-29 | Omnova Solutions Inc. | Breathable wallcovering |
US6162504A (en) * | 1997-12-04 | 2000-12-19 | Henkel Corporation | Adhesives and sealants containing adhesion promoter comprising waste powder prime |
US6103309A (en) * | 1998-01-23 | 2000-08-15 | Henkel Corporation | Self-levelling plastisol composition and method for using same |
US20040034143A1 (en) * | 2001-05-17 | 2004-02-19 | James Hubert | Plastisol composition and method for using same |
AU2003268942A1 (en) * | 2002-08-21 | 2004-03-11 | Hunstman Advanced Materials (Switzerland) Gmbh | Adhesion promoters for plastisols |
KR102135392B1 (ko) | 2013-03-11 | 2020-07-17 | 비와이케이-케미 게엠베하 | 요변성-증진 첨가제 및 상기 첨가제를 함유하는 조성물 |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1129153B (de) * | 1959-07-04 | 1962-05-10 | Bayer Ag | Verfahren zur Herstellung von ª-Cyan-ª-Alkyl-ª-phenylacrylsaeureestern |
BE608993A (en:Method) * | 1960-10-11 | 1900-01-01 | ||
US3168491A (en) * | 1960-11-01 | 1965-02-02 | Grace W R & Co | Printing plate compositions |
US3234156A (en) * | 1961-05-24 | 1966-02-08 | Grace W R & Co | Liquid polymeric printing plate compositions comprising a vinyl chloride polymer, a 2-imidazoline and a polyesteramine containing reaction mixture |
US3135796A (en) * | 1961-08-31 | 1964-06-02 | Goodrich Co B F | Production of n, n'-di(1-methylalkylidene)-p-phenylenediamine |
US3216969A (en) * | 1961-10-27 | 1965-11-09 | Universal Oil Prod Co | Polymers stabilized with o-hydroxybenzalaminodiphenylamines or metal coordination complexes thereof |
US3260692A (en) * | 1963-02-19 | 1966-07-12 | Frank C Magne | Vinyl chloride polymers plasticized with morpholides of fatty acids and dimerized fatty acids |
US3349110A (en) * | 1963-06-17 | 1967-10-24 | Universal Oil Prod Co | Nu-(2-hydroxyphenylmethylene)-or-gano aryl amines and metal salts thereof |
US3324158A (en) * | 1963-06-17 | 1967-06-06 | Universal Oil Prod Co | N-(2-hydroxyphenylmethylene)-2-hydroxy-organo-aryl amine and metal salts thereof |
US3398170A (en) * | 1964-05-21 | 1968-08-20 | Universal Oil Prod Co | Mixed chelates of a schiff base, an amine, and a transition series metal |
US3368974A (en) * | 1964-12-30 | 1968-02-13 | Universal Oil Prod Co | Pyrenyl compounds and use thereof |
US3478096A (en) * | 1966-04-18 | 1969-11-11 | Universal Oil Prod Co | Sec.-alkyl- or cycloalkyl-alkoxy-alkylamines |
DE1811657C3 (de) * | 1968-11-29 | 1979-03-01 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von in a-Stellung substituierten !minen |
DE1923708C3 (de) * | 1969-05-09 | 1978-07-20 | Basf Ag, 6700 Ludwigshafen | Elektroisoliermassen auf der Basis von Olefinpolymerisaten |
DE2123171C3 (de) | 1971-05-11 | 1975-08-07 | Roehm Gmbh, 6100 Darmstadt | Polyvinylchloridplastisole |
US3785855A (en) * | 1972-01-14 | 1974-01-15 | D Sausaman | Method for coating steel |
DE2327958A1 (de) | 1973-06-01 | 1975-01-02 | Henkel & Cie Gmbh | Haftvermittler enthaltende plastisole |
US3937716A (en) * | 1973-07-09 | 1976-02-10 | Rohm And Haas Company | Oxazolidine derivatives |
DE2402037B1 (de) * | 1974-01-17 | 1975-05-28 | Teroson Gmbh, 6900 Heidelberg | Polyvinylchloridplastisole |
-
1976
- 1976-12-03 DE DE2654871A patent/DE2654871C3/de not_active Expired
-
1977
- 1977-10-03 NL NLAANVRAGE7710812,A patent/NL185675C/xx not_active IP Right Cessation
- 1977-11-07 DK DK493877A patent/DK493877A/da not_active Application Discontinuation
- 1977-11-29 US US05/855,805 patent/US4146520A/en not_active Expired - Lifetime
- 1977-12-01 LU LU78615A patent/LU78615A1/xx unknown
- 1977-12-01 SE SE7713634A patent/SE439319B/sv not_active IP Right Cessation
- 1977-12-01 PL PL1977202572A patent/PL110670B1/pl unknown
- 1977-12-01 IT IT30258/77A patent/IT1089313B/it active
- 1977-12-02 BE BE183128A patent/BE861449A/xx not_active IP Right Cessation
- 1977-12-02 GB GB50349/77A patent/GB1577583A/en not_active Expired
- 1977-12-02 IE IE2444/77A patent/IE46099B1/en not_active IP Right Cessation
- 1977-12-05 FR FR7736524A patent/FR2372862A1/fr active Granted
Also Published As
Publication number | Publication date |
---|---|
GB1577583A (en) | 1980-10-29 |
IE46099B1 (en) | 1983-02-23 |
DK493877A (da) | 1978-06-04 |
BE861449A (fr) | 1978-06-02 |
NL185675B (nl) | 1990-01-16 |
SE7713634L (sv) | 1978-06-04 |
US4146520A (en) | 1979-03-27 |
IE46099L (en) | 1978-06-03 |
PL202572A1 (pl) | 1978-08-28 |
DE2654871C3 (de) | 1984-10-04 |
DE2654871A1 (de) | 1978-06-08 |
PL110670B1 (en) | 1980-07-31 |
LU78615A1 (en:Method) | 1978-04-20 |
NL7710812A (nl) | 1978-06-06 |
DE2654871B2 (de) | 1979-12-13 |
FR2372862B1 (en:Method) | 1981-01-16 |
IT1089313B (it) | 1985-06-18 |
NL185675C (nl) | 1990-06-18 |
FR2372862A1 (fr) | 1978-06-30 |
Similar Documents
Publication | Publication Date | Title |
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