DE2449473A1 - Verwendung von epsilon-hydroxycapronsaeureestern niederer alkohole als loesungsmittel fuer lacke - Google Patents
Verwendung von epsilon-hydroxycapronsaeureestern niederer alkohole als loesungsmittel fuer lackeInfo
- Publication number
- DE2449473A1 DE2449473A1 DE19742449473 DE2449473A DE2449473A1 DE 2449473 A1 DE2449473 A1 DE 2449473A1 DE 19742449473 DE19742449473 DE 19742449473 DE 2449473 A DE2449473 A DE 2449473A DE 2449473 A1 DE2449473 A1 DE 2449473A1
- Authority
- DE
- Germany
- Prior art keywords
- paint
- solvent
- lower alcohols
- acid esters
- epsilon
- 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- Withdrawn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
- 239000003973 paint Substances 0.000 title claims description 19
- 150000001298 alcohols Chemical class 0.000 title claims description 6
- 239000002904 solvent Substances 0.000 title description 14
- NYHNVHGFPZAZGA-UHFFFAOYSA-N 2-hydroxyhexanoic acid Chemical class CCCCC(O)C(O)=O NYHNVHGFPZAZGA-UHFFFAOYSA-N 0.000 title 1
- 150000002148 esters Chemical class 0.000 claims description 10
- IWHLYPDWHHPVAA-UHFFFAOYSA-N 6-hydroxyhexanoic acid Chemical compound OCCCCCC(O)=O IWHLYPDWHHPVAA-UHFFFAOYSA-N 0.000 claims description 9
- 229920003002 synthetic resin Polymers 0.000 claims description 3
- 239000000057 synthetic resin Substances 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- VFGRALUHHHDIQI-UHFFFAOYSA-N butyl 2-hydroxyacetate Chemical compound CCCCOC(=O)CO VFGRALUHHHDIQI-UHFFFAOYSA-N 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- -1 glycol ethers Chemical class 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 150000003903 lactic acid esters Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- YDJZXHZRXDLCEH-UHFFFAOYSA-N methyl 6-hydroxyhexanoate Chemical compound COC(=O)CCCCCO YDJZXHZRXDLCEH-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 238000000643 oven drying Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/20—Diluents or solvents
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT891073A AT331941B (de) | 1973-10-22 | 1973-10-22 | Losungsmittel fur lacke |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2449473A1 true DE2449473A1 (de) | 1975-04-24 |
Family
ID=3609568
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19742449473 Withdrawn DE2449473A1 (de) | 1973-10-22 | 1974-10-19 | Verwendung von epsilon-hydroxycapronsaeureestern niederer alkohole als loesungsmittel fuer lacke |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS50111122A (enExample) |
| AT (1) | AT331941B (enExample) |
| BE (1) | BE821343A (enExample) |
| BR (1) | BR7408752D0 (enExample) |
| DE (1) | DE2449473A1 (enExample) |
| ES (1) | ES431218A1 (enExample) |
| FR (1) | FR2248305B3 (enExample) |
| GB (1) | GB1489364A (enExample) |
| IT (1) | IT1030727B (enExample) |
| NL (1) | NL7413721A (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4314918A (en) * | 1980-06-26 | 1982-02-09 | Ppg Industries, Inc. | Coating compositions containing organic alcoholic reactive diluents |
-
1973
- 1973-10-22 AT AT891073A patent/AT331941B/de not_active IP Right Cessation
-
1974
- 1974-10-18 NL NL7413721A patent/NL7413721A/xx unknown
- 1974-10-19 DE DE19742449473 patent/DE2449473A1/de not_active Withdrawn
- 1974-10-21 BR BR8752/74A patent/BR7408752D0/pt unknown
- 1974-10-21 FR FR7435347A patent/FR2248305B3/fr not_active Expired
- 1974-10-22 IT IT28648/74A patent/IT1030727B/it active
- 1974-10-22 BE BE149767A patent/BE821343A/xx unknown
- 1974-10-22 GB GB45681/74A patent/GB1489364A/en not_active Expired
- 1974-10-22 ES ES431218A patent/ES431218A1/es not_active Expired
- 1974-10-22 JP JP49121066A patent/JPS50111122A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| FR2248305A1 (enExample) | 1975-05-16 |
| FR2248305B3 (enExample) | 1977-07-29 |
| ES431218A1 (es) | 1977-02-16 |
| ATA891073A (de) | 1975-12-15 |
| IT1030727B (it) | 1979-04-10 |
| BR7408752D0 (pt) | 1975-08-05 |
| AT331941B (de) | 1976-08-25 |
| JPS50111122A (enExample) | 1975-09-01 |
| BE821343A (fr) | 1975-02-17 |
| NL7413721A (nl) | 1975-04-24 |
| GB1489364A (en) | 1977-10-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8141 | Disposal/no request for examination |