DE4423309A1 - Verfahren zur Herstellung einer sterisch stabilisierten, nichtwäßrigen Dispersion eines Polyepoxids und diese Dispersion enthaltende Beschichtungsmittel - Google Patents
Verfahren zur Herstellung einer sterisch stabilisierten, nichtwäßrigen Dispersion eines Polyepoxids und diese Dispersion enthaltende BeschichtungsmittelInfo
- Publication number
- DE4423309A1 DE4423309A1 DE4423309A DE4423309A DE4423309A1 DE 4423309 A1 DE4423309 A1 DE 4423309A1 DE 4423309 A DE4423309 A DE 4423309A DE 4423309 A DE4423309 A DE 4423309A DE 4423309 A1 DE4423309 A1 DE 4423309A1
- Authority
- DE
- Germany
- Prior art keywords
- epoxy resin
- component
- stage
- dispersion
- epoxy
- 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.)
- Withdrawn
Links
- 229920000647 polyepoxide Polymers 0.000 title claims abstract description 67
- 239000006185 dispersion Substances 0.000 title claims abstract description 49
- 238000000034 method Methods 0.000 title claims abstract description 48
- 239000008199 coating composition Substances 0.000 title claims description 7
- 238000002360 preparation method Methods 0.000 title claims 2
- 239000003822 epoxy resin Substances 0.000 claims abstract description 54
- 150000002009 diols Chemical class 0.000 claims abstract description 26
- 239000003381 stabilizer Substances 0.000 claims abstract description 16
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 14
- 239000004593 Epoxy Substances 0.000 claims abstract description 9
- 125000003700 epoxy group Chemical group 0.000 claims abstract description 9
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 3
- 239000003960 organic solvent Substances 0.000 claims abstract description 3
- 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 claims description 23
- 239000011248 coating agent Substances 0.000 claims description 18
- 238000000576 coating method Methods 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 238000009835 boiling Methods 0.000 claims description 9
- 238000004806 packaging method and process Methods 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 3
- 239000005062 Polybutadiene Substances 0.000 claims description 3
- 235000013305 food Nutrition 0.000 claims description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
- 229920002857 polybutadiene Polymers 0.000 claims description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims 2
- 229920001519 homopolymer Polymers 0.000 claims 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 13
- 239000011347 resin Substances 0.000 description 13
- 239000002904 solvent Substances 0.000 description 12
- 239000013065 commercial product Substances 0.000 description 11
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 11
- 239000003054 catalyst Substances 0.000 description 8
- 150000002118 epoxides Chemical class 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 3
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000120 polyethyl acrylate Polymers 0.000 description 2
- 150000008442 polyphenolic compounds Polymers 0.000 description 2
- 235000013824 polyphenols Nutrition 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Inorganic materials [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 2
- -1 potassium hydroxide quaternary ammonium salts Chemical class 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 1
- 229940114072 12-hydroxystearic acid Drugs 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- BWLUMTFWVZZZND-UHFFFAOYSA-N Dibenzylamine Chemical compound C=1C=CC=CC=1CNCC1=CC=CC=C1 BWLUMTFWVZZZND-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 101150049168 Nisch gene Proteins 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000012674 dispersion polymerization Methods 0.000 description 1
- SLAFUPJSGFVWPP-UHFFFAOYSA-M ethyl(triphenyl)phosphanium;iodide Chemical compound [I-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CC)C1=CC=CC=C1 SLAFUPJSGFVWPP-UHFFFAOYSA-M 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000005028 tinplate Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 150000003752 zinc compounds Chemical class 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
- C08G59/06—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
- C08G59/066—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols with chain extension or advancing agents
-
- 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
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
- Epoxy Resins (AREA)
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4423309A DE4423309A1 (de) | 1994-07-02 | 1994-07-02 | Verfahren zur Herstellung einer sterisch stabilisierten, nichtwäßrigen Dispersion eines Polyepoxids und diese Dispersion enthaltende Beschichtungsmittel |
| JP8503665A JPH10502403A (ja) | 1994-07-02 | 1995-06-29 | 滅菌安定化されたポリエポキシド非水性分散液の製造法および該分散液を含有する被覆剤 |
| PCT/EP1995/002531 WO1996001292A1 (fr) | 1994-07-02 | 1995-06-29 | Procede de fabrication d'une dispersion non aqueuse, steriquement stabilisee, d'un polyepoxy, et agent de revêtement renfermant cette dispersion |
| BR9508204A BR9508204A (pt) | 1994-07-02 | 1995-06-29 | Processo para a preparação de uma dispersão não-aquosa estericamente estabilizada de um poliepóxido e composições de revestimento que contêm essa dispersão |
| CA002189864A CA2189864A1 (fr) | 1994-07-02 | 1995-06-29 | Procede de fabrication d'une dispersion non aqueuse, steriquement stabilisee, d'un polyepoxy, et agent de revetement renfermant cette dispersion |
| AU29788/95A AU693915B2 (en) | 1994-07-02 | 1995-06-29 | Method of producing a sterically stabilized non-aqueous dispersion of a polyepoxide, and coating materials containing such a dispersion |
| EP95925787A EP0769037A1 (fr) | 1994-07-02 | 1995-06-29 | Procede de fabrication d'une dispersion non aqueuse, steriquement stabilisee, d'un polyepoxy, et agent de rev tement renfermant cette dispersion |
| TR95/00792A TR199500792A2 (tr) | 1994-07-02 | 1995-06-30 | Bir poliepoksitin sterik stabilize, susuz dispersiyonunun elde edilmesine iliskin yöntem ve bu dispersiyonu ihtiva eden kaplama maddesi. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4423309A DE4423309A1 (de) | 1994-07-02 | 1994-07-02 | Verfahren zur Herstellung einer sterisch stabilisierten, nichtwäßrigen Dispersion eines Polyepoxids und diese Dispersion enthaltende Beschichtungsmittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE4423309A1 true DE4423309A1 (de) | 1996-01-04 |
Family
ID=6522149
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE4423309A Withdrawn DE4423309A1 (de) | 1994-07-02 | 1994-07-02 | Verfahren zur Herstellung einer sterisch stabilisierten, nichtwäßrigen Dispersion eines Polyepoxids und diese Dispersion enthaltende Beschichtungsmittel |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP0769037A1 (fr) |
| JP (1) | JPH10502403A (fr) |
| AU (1) | AU693915B2 (fr) |
| BR (1) | BR9508204A (fr) |
| CA (1) | CA2189864A1 (fr) |
| DE (1) | DE4423309A1 (fr) |
| TR (1) | TR199500792A2 (fr) |
| WO (1) | WO1996001292A1 (fr) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997031952A1 (fr) * | 1996-02-28 | 1997-09-04 | Ppg Industries, Inc. | Dispersion non aqueuse stabilisee steriquement et materiau de revetement a base de celle-ci |
| EP3124515A1 (fr) | 2015-07-28 | 2017-02-01 | Evonik Degussa GmbH | Dispersions reactives non aqueuses pour peintures, materiaux d'etancheite et adhesifs |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6173726A (ja) * | 1984-09-19 | 1986-04-15 | Nippon Oil & Fats Co Ltd | 非水系エポキシ樹脂分散体の製造方法 |
| US4568735A (en) * | 1984-11-05 | 1986-02-04 | Shell Oil Company | Process for preparing polyepoxides (II) |
| US4579887A (en) * | 1985-02-26 | 1986-04-01 | The Dow Chemical Company | Non-aqueous dispersions of relatively high molecular weight epoxy resins |
| ES2061686T3 (es) * | 1987-12-04 | 1994-12-16 | Ici Plc | Progreso de epoxidos. |
| NZ244069A (en) * | 1991-08-26 | 1995-04-27 | Dow Chemical Co | Flexibilized epoxy resin comprising a residue of at least one polyaromatic hydroxy compound and at least one polyglycidyl ether of such compounds and a polybutylene glycol derivative; electrodeposition coatings |
-
1994
- 1994-07-02 DE DE4423309A patent/DE4423309A1/de not_active Withdrawn
-
1995
- 1995-06-29 AU AU29788/95A patent/AU693915B2/en not_active Ceased
- 1995-06-29 JP JP8503665A patent/JPH10502403A/ja active Pending
- 1995-06-29 CA CA002189864A patent/CA2189864A1/fr not_active Abandoned
- 1995-06-29 WO PCT/EP1995/002531 patent/WO1996001292A1/fr not_active Ceased
- 1995-06-29 EP EP95925787A patent/EP0769037A1/fr not_active Withdrawn
- 1995-06-29 BR BR9508204A patent/BR9508204A/pt not_active Application Discontinuation
- 1995-06-30 TR TR95/00792A patent/TR199500792A2/xx unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997031952A1 (fr) * | 1996-02-28 | 1997-09-04 | Ppg Industries, Inc. | Dispersion non aqueuse stabilisee steriquement et materiau de revetement a base de celle-ci |
| DE19607435A1 (de) * | 1996-02-28 | 1997-09-04 | Basf Lacke & Farben | Sterisch stabilisierte, nicht-wäßrige Dispersion, und Beschichtungsmittel auf deren Basis |
| EP3124515A1 (fr) | 2015-07-28 | 2017-02-01 | Evonik Degussa GmbH | Dispersions reactives non aqueuses pour peintures, materiaux d'etancheite et adhesifs |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2978895A (en) | 1996-01-25 |
| AU693915B2 (en) | 1998-07-09 |
| JPH10502403A (ja) | 1998-03-03 |
| EP0769037A1 (fr) | 1997-04-23 |
| CA2189864A1 (fr) | 1996-01-18 |
| BR9508204A (pt) | 1997-12-23 |
| WO1996001292A1 (fr) | 1996-01-18 |
| TR199500792A2 (tr) | 1996-06-21 |
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Owner name: PPG INDUSTRIES, INC., PITTSBURGH, PA., US |
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Representative=s name: PATENTANWAELTE STERNAGEL & FLEISCHER, 51429 BERGIS |
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| 8139 | Disposal/non-payment of the annual fee |