DE1745340A1 - Verfahren zur Herstellung von Alkydharzen hoher Viskositaet - Google Patents
Verfahren zur Herstellung von Alkydharzen hoher ViskositaetInfo
- Publication number
- DE1745340A1 DE1745340A1 DE19671745340 DE1745340A DE1745340A1 DE 1745340 A1 DE1745340 A1 DE 1745340A1 DE 19671745340 DE19671745340 DE 19671745340 DE 1745340 A DE1745340 A DE 1745340A DE 1745340 A1 DE1745340 A1 DE 1745340A1
- Authority
- DE
- Germany
- Prior art keywords
- alkyd
- weight
- resin
- alkyd resins
- parts
- 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.)
- Pending
Links
- 229920000180 alkyd Polymers 0.000 title claims description 34
- 238000000034 method Methods 0.000 title claims description 9
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 4
- -1 glycidyl compound Chemical class 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 238000009833 condensation Methods 0.000 description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- 239000008096 xylene Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 235000019241 carbon black Nutrition 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- JAGPZOQWDSRFPM-UHFFFAOYSA-N C(C1CO1)N(CC(CN(C(C)C)CC1CO1)O)C(C)C Chemical compound C(C1CO1)N(CC(CN(C(C)C)CC1CO1)O)C(C)C JAGPZOQWDSRFPM-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 238000004939 coking Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000004992 fission Effects 0.000 description 1
- 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 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
- DXAUPHVMJXKRRE-UHFFFAOYSA-N n,n-bis(oxiran-2-ylmethyl)propan-2-amine Chemical compound C1OC1CN(C(C)C)CC1CO1 DXAUPHVMJXKRRE-UHFFFAOYSA-N 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- 238000000643 oven drying Methods 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C08G63/91—Polymers modified by chemical after-treatment
- C08G63/914—Polymers modified by chemical after-treatment derived from polycarboxylic acids and polyhydroxy compounds
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
- Epoxy Resins (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DER0046680 | 1967-08-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1745340A1 true DE1745340A1 (de) | 1971-09-02 |
Family
ID=7408129
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19671745340 Pending DE1745340A1 (de) | 1967-08-09 | 1967-08-09 | Verfahren zur Herstellung von Alkydharzen hoher Viskositaet |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3639314A (cg-RX-API-DMAC7.html) |
| BE (1) | BE719292A (cg-RX-API-DMAC7.html) |
| CH (1) | CH522724A (cg-RX-API-DMAC7.html) |
| DE (1) | DE1745340A1 (cg-RX-API-DMAC7.html) |
| ES (1) | ES356204A1 (cg-RX-API-DMAC7.html) |
| FR (1) | FR1576174A (cg-RX-API-DMAC7.html) |
| GB (1) | GB1173734A (cg-RX-API-DMAC7.html) |
| NL (1) | NL6811198A (cg-RX-API-DMAC7.html) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3839249A (en) * | 1970-07-13 | 1974-10-01 | Texaco Ag | Process for the production of plastics and lacquer resins from basic nitrogen-containing glycidyl compounds and dicarboxylic anhydrides |
| US4020122A (en) * | 1973-01-05 | 1977-04-26 | General Electric Company | Process for the preparation of polyester compositions having increased melt elasticity |
| DE2710993C3 (de) * | 1977-03-14 | 1981-05-14 | Henkel KGaA, 4000 Düsseldorf | Wäßrige Dispersion von als Überzugsmittel bzw. Lackbindemittel geeigneten Harzen |
| US4154709A (en) * | 1978-03-06 | 1979-05-15 | Hitachi Chemical Company, Ltd. | Water-dispersible epoxy modified alkyd resins |
-
1967
- 1967-08-09 DE DE19671745340 patent/DE1745340A1/de active Pending
-
1968
- 1968-07-11 CH CH1037468A patent/CH522724A/de not_active IP Right Cessation
- 1968-07-16 ES ES356204A patent/ES356204A1/es not_active Expired
- 1968-07-19 GB GB34644/68A patent/GB1173734A/en not_active Expired
- 1968-08-07 NL NL6811198A patent/NL6811198A/xx unknown
- 1968-08-09 FR FR1576174D patent/FR1576174A/fr not_active Expired
- 1968-08-09 BE BE719292D patent/BE719292A/xx unknown
-
1970
- 1970-04-28 US US31819A patent/US3639314A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| NL6811198A (cg-RX-API-DMAC7.html) | 1969-02-11 |
| BE719292A (cg-RX-API-DMAC7.html) | 1969-02-10 |
| GB1173734A (en) | 1969-12-10 |
| US3639314A (en) | 1972-02-01 |
| FR1576174A (cg-RX-API-DMAC7.html) | 1969-07-25 |
| ES356204A1 (es) | 1970-01-01 |
| CH522724A (de) | 1972-06-30 |
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