CA2010822A1 - Revetements pouvant etre appliques par cathophorese et contenants des teintures hydrophobes - Google Patents
Revetements pouvant etre appliques par cathophorese et contenants des teintures hydrophobesInfo
- Publication number
- CA2010822A1 CA2010822A1 CA002010822A CA2010822A CA2010822A1 CA 2010822 A1 CA2010822 A1 CA 2010822A1 CA 002010822 A CA002010822 A CA 002010822A CA 2010822 A CA2010822 A CA 2010822A CA 2010822 A1 CA2010822 A1 CA 2010822A1
- Authority
- CA
- Canada
- Prior art keywords
- coating
- solvent
- dye
- group
- bath
- 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.)
- Abandoned
Links
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- 238000004070 electrodeposition Methods 0.000 claims abstract description 30
- 125000002091 cationic group Chemical group 0.000 claims abstract description 6
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- 238000000034 method Methods 0.000 claims description 32
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
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- 241000254173 Coleoptera Species 0.000 description 3
- 239000004971 Cross linker Substances 0.000 description 3
- 229920003270 Cymel® Polymers 0.000 description 3
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 3
- UOACKFBJUYNSLK-XRKIENNPSA-N Estradiol Cypionate Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H](C4=CC=C(O)C=C4CC3)CC[C@@]21C)C(=O)CCC1CCCC1 UOACKFBJUYNSLK-XRKIENNPSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-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
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
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- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 3
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- 238000003756 stirring Methods 0.000 description 3
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- 150000002739 metals Chemical class 0.000 description 1
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- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
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- WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 238000006116 polymerization reaction Methods 0.000 description 1
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- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 239000005720 sucrose Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical class CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
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- 238000012546 transfer Methods 0.000 description 1
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Landscapes
- Paints Or Removers (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002010822A CA2010822A1 (fr) | 1989-01-31 | 1990-02-23 | Revetements pouvant etre appliques par cathophorese et contenants des teintures hydrophobes |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US30467489A | 1989-01-31 | 1989-01-31 | |
| CA002010822A CA2010822A1 (fr) | 1989-01-31 | 1990-02-23 | Revetements pouvant etre appliques par cathophorese et contenants des teintures hydrophobes |
| AU52193/90A AU634760B2 (en) | 1989-01-31 | 1990-03-23 | Cathodic electrodepositable coatings containing hydrophobic dyes |
| EP90105734A EP0448747A1 (fr) | 1989-01-31 | 1990-03-26 | Revêtements cathodiques électrodéposables contenant des colorants hydrophobes |
| JP2080539A JPH03281673A (ja) | 1989-01-31 | 1990-03-28 | 疎水性染料を含有する陰極電着性被覆物 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2010822A1 true CA2010822A1 (fr) | 1991-08-23 |
Family
ID=27507015
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002010822A Abandoned CA2010822A1 (fr) | 1989-01-31 | 1990-02-23 | Revetements pouvant etre appliques par cathophorese et contenants des teintures hydrophobes |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2010822A1 (fr) |
-
1990
- 1990-02-23 CA CA002010822A patent/CA2010822A1/fr not_active Abandoned
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |