US2315347A - Coating composition - Google Patents
Coating composition Download PDFInfo
- Publication number
- US2315347A US2315347A US284094A US28409439A US2315347A US 2315347 A US2315347 A US 2315347A US 284094 A US284094 A US 284094A US 28409439 A US28409439 A US 28409439A US 2315347 A US2315347 A US 2315347A
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- US
- United States
- Prior art keywords
- oil
- acid
- cellulose nitrate
- compositions
- resin
- 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.)
- Expired - Lifetime
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- 239000008199 coating composition Substances 0.000 title description 14
- 239000000203 mixture Substances 0.000 description 33
- 229920001220 nitrocellulos Polymers 0.000 description 23
- 239000003921 oil Substances 0.000 description 23
- 235000019198 oils Nutrition 0.000 description 23
- 239000000020 Nitrocellulose Substances 0.000 description 22
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 22
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 17
- 239000002253 acid Substances 0.000 description 17
- 229920000180 alkyd Polymers 0.000 description 17
- 238000002845 discoloration Methods 0.000 description 13
- 229920005989 resin Polymers 0.000 description 13
- 239000011347 resin Substances 0.000 description 13
- 239000000049 pigment Substances 0.000 description 12
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 9
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 9
- 210000003298 dental enamel Anatomy 0.000 description 9
- 239000001630 malic acid Substances 0.000 description 8
- 235000011090 malic acid Nutrition 0.000 description 8
- 239000004014 plasticizer Substances 0.000 description 8
- 150000007513 acids Chemical class 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- -1 aliphatic dicarboxylic acids Chemical class 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 235000019441 ethanol Nutrition 0.000 description 6
- 235000015112 vegetable and seed oil Nutrition 0.000 description 6
- 239000008158 vegetable oil Substances 0.000 description 6
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 5
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 5
- 239000002480 mineral oil Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 239000004359 castor oil Substances 0.000 description 4
- 235000019438 castor oil Nutrition 0.000 description 4
- 235000019864 coconut oil Nutrition 0.000 description 4
- 239000003240 coconut oil Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 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 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 238000005498 polishing Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 230000003245 working effect Effects 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000001464 adherent effect Effects 0.000 description 2
- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 235000010980 cellulose Nutrition 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- XLLIQLLCWZCATF-UHFFFAOYSA-N ethylene glycol monomethyl ether acetate Natural products COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 2
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- MXHKJQTYOAFPBY-UHFFFAOYSA-N 2-(2,3-dihydroxypropoxycarbonyl)benzoic acid Chemical compound OCC(O)COC(=O)C1=CC=CC=C1C(O)=O MXHKJQTYOAFPBY-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004421 aryl sulphonamide group Chemical group 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000001055 blue pigment Substances 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
- 239000006229 carbon black Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- PCYQQSKDZQTOQG-NXEZZACHSA-N dibutyl (2r,3r)-2,3-dihydroxybutanedioate Chemical compound CCCCOC(=O)[C@H](O)[C@@H](O)C(=O)OCCCC PCYQQSKDZQTOQG-NXEZZACHSA-N 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N ferric oxide Chemical compound O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000000266 injurious effect Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002691 malonic acids Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- PMDKYLLIOLFQPO-UHFFFAOYSA-N monocyclohexyl phthalate Chemical compound OC(=O)C1=CC=CC=C1C(=O)OC1CCCCC1 PMDKYLLIOLFQPO-UHFFFAOYSA-N 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 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
- 229920000223 polyglycerol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- C09D101/00—Coating compositions based on cellulose, modified cellulose, or cellulose derivatives
- C09D101/08—Cellulose derivatives
- C09D101/16—Esters of inorganic acids
- C09D101/18—Cellulose nitrate
Definitions
- This invention relates to improved coating compositions and more particularly to cellulose nitrate coating compositions which are to discoloration from contact with oils and greases.
- composition which affords a finish highly to "oil spott or discoloration from contact with mineral oils and greases.
- Another object of the invention is the provision of a cellulose nitrate coating composition which afiords a finish durability including superior excellent outdoor further object is the provi- I sion'oi a cellulose nitrate coating composition which affords a finish that may be readily rubbed and polished.
- a still further object is the provi sion of a cellulose nitrate coating composition which ailords a finish that is adherent, flexible and substantially non-thermoplastic under a buffing wheel.
- This inventiomtherefore has as a primary object the provision of a cellulose nitrate coating prising cellulose nitrate, certain non-drying vegetable oil modified alkyd resins and an aliphatic dicarboxylic acid.
- compositions which normally tend to gel rapidly during shelf storage, particularly in basic pigments such as zinc oxide.
- These compositions may include also certain vegetable oil modified alkyd resins which increase gelation tendencies probably because of a high acid hum her or because they are modified with an oxidizing oil such as linseed oil.
- the present invention is directed to cellulose nitrate compositions which do not'normally gel in the complete absence or an for any inhibiting agent.
- an entirely un- 45,-'expected and important improvement is now made available through the use of the aforementioned acids for the express purpose ofv providing e. finish which is highly resistant to discoloration from mineral oils and greases, a desirable property which bears no relation whatsoever to gelation tendencies.
- the malic acid solution consisted of a 30% solution of malic acid in denatured ethyl alcohol.
- the resin solution oi. the above example consisted of a mixture of 30 parts of toluol and 70 parts of a synthetic resin which is a reaction product Per cent Giycerine 18.2 Phthalic anhydride 36.6 Coconut oil 47.2
- This resin was prepared by first heating the glycerlne and coconut oil at a temperature between 380 and 400 F. until a homogeneous solution was obtained. The phthalic anhydride was then added and heating continued at about 480 F. until an acid number oi 5-6 was obtained.
- the charge was blanketed with carbon dioxide during the preparation of the resin.
- Example 1 which contains cellulose nitrate, resin, plasticizer and malic acid in the ratio of parts by weight of cellulose nitrate, 9 parts by weight oimodified alkyd resin, 2.5 parts by weight of plasticizer, and 0.23 part by weight of malic acid, was prepared by first dispersing the pigment in a cellu lose nitrate colloid adjusted to a suitable consistency by the addition of solvents and diluents by a kneading treatment described in U. S. Patent 2,052,470. This pigmented intermediate was then placed in an agitator mixer together with the remaining ingredients including the synthetic resin and malic acid solutions, and the mixture thoroughly agitated until a homogeneous enamel product was obtained.
- Example 2 which contains cellulose nitrate, resin, softener, and
- the viscosity characteristic of the cellulose nitrates utilized in the examples was about 3 seconds as determined in accordance with A. S. T. M. Specifications D-301-33T, Formula 3.
- the aliphatic dicarboxylic acids both unsaturated and saturated including hydroxy acids of this class, appear to aflord the desired results of markedly reducing or completely eliminating discoloration from oils and greases in'the com- Positions of the present invention.
- Malic, malonic, maleic, tartaric, adipic, succinic. and oxalic are exemplary of the types of acids which have been found suitable. Malic and malonic acids are particularly effective.
- the resin should be modified with from not less than to not more than 60% and prererably with from 40 to of coconut oil or similar non-gelling, nonhydro non-drying oil such as cottonseed or with blown oils of these types.
- the non-gelling, non-drying oil modified alkyd resin must be prepared so that the acid number is kept as low as possible, preferably not mor than 5 or 6 and, in any event, should be kept below 10.
- Resins of substantially higher acid number have a. tendency to gel and also cannot be used with reactive type pigments such as 7 zinc oxidebecause ofpoor stability of the compositionsduring store-seas evidenced by gelling and/orthe'formationof grit.
- reactive type pigments as referred to in the trade indicate pig- .ments which chemically react with the liquid or solid. ingredients in the composition in which they are incorporated.
- Optimum resistance to oil spotting combined with maximum durability including superior chalk resistance are obtained when the cellulose nttrate aik'yd resin-plasticizer ratios and the non-gelling, non-hydroxy, non-drying vegetable oil modified alkyd resin compositions which include the commonly used pigments or other coloring matter such as antimony oxide, titanium dioxide, titanate, pigments, iron blue pigments.
- dicarboxyiic acid employed are kept within definite limits. These ratios should be such that for each 10 parts by weight of cellulose nitrate. the amount of alkyd resin is kept below 10 parts but not less than about 5 parts. If the roons, carbon black, ultramarine blue, burnt umber, iron oxide, etc. If zinc oxide, a basic type pigment, is employed to any considerable extent 'inthe compositions of the present invention, little if any improvement in resistance to oil-spotting is obtained by the use of the above described dicarboxyiic acids which are otherwise so outstandingiy effective. The invention is particularly valuable when employed with the light colored socalled pastel shade andmetallic enamels which proportion of alkyd resin to cellulose nitrate is increased by a small amount as. for instance, to 1 part of alkyd resin to 1 'partof cellulose nitrate,
- the compositionswhile possibly useful for some industrial purposes even with somewhat higher proportions of the modified alkyd resin are of no value practically for the present primary purpose of finishing automobiles because the conventional sanding, rubbing and polishing operations employed in this industry cannot be satisfactorily practiced.
- the amount of plasticizer is about 2 parts when the maximum quantity of resin is used and about 5 parts when'the minimum amount of resin is used.
- These acids are preferably incorporated in an amount between 0.2% and 2.0% based on the a total weight of the composition to be treated.
- Suitable solvents and 'diluents include esters of lower fatty acids. for example, ethyl acetate,
- ketones such as methyl ethyl ketone, alcohol ethers and their esters, such as ethylene glycol monoethyl ether acetate and ethylene glycol monomethyl ether acetate.
- alcohol ethers and their esters such as ethylene glycol monoethyl ether acetate and ethylene glycol monomethyl ether acetate.
- lower aliphatic alcohols and aliphatic and aromatic hydrocarbon diluents such as petroleum naphtha and toluene.
- plasticizers and softeners which may be I employed in the compositions of the present invention include conventional materials such as castor oil, blown castor oil, aryl sulfonamides including ortho, meta and para toluene ethyl sulfonamides and mixtures of these, aryl and alkyl esters of phosphoric acid, dibutyl tartrate, di-
- cyclohexyl phthalate diethyl phthalate and the phthalate esters of ether alcohols, such as the phthalate, ester of ethylene glycol monomethyl ether.
- the invention is operative for cellulose nitratehave been a considerable source of complaint in the previously available enamels because of poor resistance to oils and greases where discoloration is more pronounced.
- phthalic anhydride is the preferred acid radical in the alkyd resin ingredient of the improved compQsitionsother'acids such as succinic, malic, adipic, maleic, sebacic, etc may be substituted wholly or in, part for the phthalic anhydride, but best results are secured when phthalic anhydride is present in preponderant proportionss J
- Suitable resins for the improved compositions may also be prepared using other poiyhydric alcohols including ethylene glycol and higher homologs, diethylene g ycol and other polyslycols;
- polyglycerols pentaerythritol and sorbitol.
- compositions of the invention are generally useful in finishing surfaces which may be exposed to direct contact-with oils and greases. They are particularly useful for finishing automobiles where contact with lubricating o ls and greases and oil-containing rubbing compounds is more frequently encountered.
- the new compositions have shown a number of important advantages when employed in the suggested utilities. In the first place, they have exhibited an unexpected and decisively superior resistance to spotting or discoloration of the finish from oily rubbing and polishing compounds and from direct contact with oils and greases which sometimes reach the finish of an automobile through careless servicing of the car before or after delivery to the customer. This defect of "oil spotting was quite common in commercial finishes heretofore'available and caused frequent consumer complaint and costly rejections in the final inspection in the manufacture of new automobiles. Furthermore, the new compositions are adherent andfiexible and afford excellent durability, including superior resistance to chalking,
- the enamels of the present invention provide finishes of satisfactory working properties which do not become thermoplastic or soften under the rubbing and polishing operations normally practiced in the automotive industry.
- the satisfactory working properties of the improved compositions as controlled by the particular proportions previously indicated are of considerable importance inasmuch as previously known compositions containing related'ingredicuts are usually quite defective. in this respect,
- a coating composition which is highly resistant to oils and greases consisting of (A) a normally non-gelling coating composition containing cellulose nitrate and a non-gelling, nonhydroxy, non-drying vegetable oil modified alkyd resin characterized by an acid number or less than 10 and (B) in addition-thereto an aliphatic dicarboxylic acid in the proportions of between 0.2 and 20% by weight of the total coating composition.
- composition of claim 1 in which the alkyd resin is modified with coconut oil is modified with coconut oil.
- composition of claim 1'in which said modified alkyd resin is a glyceryl phthalate resin.
- composition of claim 1 in which the aliphatic dicarboxylic acid is present in an amount of about 0.5% by weight of the total coating composition.
- a normally non-gelling, weather-resistant cellulose nitrate coating composition which is highly resistant to oils and greases consisting of (A) a normally non-gelling composition containing cellulose nitrate, a plasticizer, an alkyd resin modified with 35-60% of a non-hydroxy, nondrying vegetable oil, said resin having an acid number of less than 10 and being present in said composition in a proportion by weight of at least 5 parts as a minimum but less than 10 parts as a maximum for each 10 parts of cellulose nitrate, said plasticizer being present in the proportion by weight of about 2 partsvas a minimum and 5 parts as a maximum and (B) in addition thereto an aliphatic dicarboxylic acid in the proportion of between 0.2 and 2.0% by weight of the total coating composition.
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Description
Patented Mar. 30, 1943 COATING comrosrnon Walter K. Moflett, South River, N. 3..
EJ. du Pont de Ncmours & Company, Wilmington, Del., a corporation of Delaware Application July i2, 19s9,
' No Drawing.
assignor to Serial No. 284,094 8 Claims, (01. 260-16) This invention relates to improved coating compositions and more particularly to cellulose nitrate coating compositions which are to discoloration from contact with oils and greases.
Recent advances in the development of cellulose nitrate enamels for automotive and industrial finishing fields and especially for-the finishin of automobiles have provided outstanding improvements in general durability and more particularly in the "elimination or reduction in chalking tendencies, a deficiency generally encountered in the earlier finishes when exposed to the atmospher'ic elements. This defect has been largely overcome through the use of special'or specially treated pigments on specific types of vehicles. However, in certain instances, these finishes which exhibit superior chalk resistance have proven to be defective in their resistanceto "oil spotting" or discoloration when mineral oils or reases are broughtin direct contact therewith.
This defect is particularly significant and more frequently encountered in automobile finishes where grease and oil may inadvertently come in contact with the finish from overhead conveyor systems used in assembling the car or during servicing and lubricating of the automobile before or after delivery to the consumer. The new hypoid gear lubricants are quite injurious in this respect. Oilspotting is also sometimes caused by the oil-containing rubbing compounds employed in conventional rubbing operations performed after application of the coating composition to bringout high lustre in the finish. Discoloration from this source is particularly a parent when the rubbing compound is permitted to remain on the finish during temporary shutdown periods.
The effect of such all or grease on the finish is not a softening or destructive action on the film but rather an unsightly discoloration which increases in intensity on exposure to light and which is especiallypronounced in the light colored finishes, including metallicFflnishes consisting of low pigmented enamels containing finely ground aluminum, which are, generally popular at the present time. The effect seems highly resistant I chalk resistance.
composition which affords a finish highly to "oil spott or discoloration from contact with mineral oils and greases. Another object of the invention is the provision of a cellulose nitrate coating composition which afiords a finish durability including superior excellent outdoor further object is the provi- I sion'oi a cellulose nitrate coating composition which affords a finish that may be readily rubbed and polished. A still further object is the provi sion of a cellulose nitrate coating composition which ailords a finish that is adherent, flexible and substantially non-thermoplastic under a buffing wheel.
These objects are accomplished by means of a composition which is normally non-gelling, com
to be permanent since it cannot beremoved'by' any known cleaning or polishing means without removing excessive amounts of the finish film and, thereiore presents a serious problem in the finishing of surfaces which may be exposed to contact, with mineral oils and greases. v
This inventiomtherefore, has as a primary obiect the provision of a cellulose nitrate coating prising cellulose nitrate, certain non-drying vegetable oil modified alkyd resins and an aliphatic dicarboxylic acid.
Some oi the aforementioned acids have been proposed as gel inhibitors in cellulose nitrate compositions which normally tend to gel rapidly during shelf storage, particularly in basic pigments such as zinc oxide. These compositions may include also certain vegetable oil modified alkyd resins which increase gelation tendencies probably because of a high acid hum her or because they are modified with an oxidizing oil such as linseed oil.
In contra-distinction, the present invention is directed to cellulose nitrate compositions which do not'normally gel in the complete absence or an for any inhibiting agent. However, an entirely un- 45,-'expected and important improvement is now made available through the use of the aforementioned acids for the express purpose ofv providing e. finish which is highly resistant to discoloration from mineral oils and greases, a desirable property which bears no relation whatsoever to gelation tendencies. a
The preferred embodiment of the invention is illustrated by the following examples which are not intended to limit the invention except as indicated in the appended claims, since variathe presence of tions will occur to those skilled in the art without departing from. the spirit and scope thereof.
The malic acid solution consisted of a 30% solution of malic acid in denatured ethyl alcohol.
The resin solution oi. the above example consisted of a mixture of 30 parts of toluol and 70 parts of a synthetic resin which is a reaction product Per cent Giycerine 18.2 Phthalic anhydride 36.6 Coconut oil 47.2
This resin was prepared by first heating the glycerlne and coconut oil at a temperature between 380 and 400 F. until a homogeneous solution was obtained. The phthalic anhydride was then added and heating continued at about 480 F. until an acid number oi 5-6 was obtained.
The charge was blanketed with carbon dioxide during the preparation of the resin.
The enamel composition of Example 1 which contains cellulose nitrate, resin, plasticizer and malic acid in the ratio of parts by weight of cellulose nitrate, 9 parts by weight oimodified alkyd resin, 2.5 parts by weight of plasticizer, and 0.23 part by weight of malic acid, was prepared by first dispersing the pigment in a cellu lose nitrate colloid adjusted to a suitable consistency by the addition of solvents and diluents by a kneading treatment described in U. S. Patent 2,052,470. This pigmented intermediate was then placed in an agitator mixer together with the remaining ingredients including the synthetic resin and malic acid solutions, and the mixture thoroughly agitated until a homogeneous enamel product was obtained.
Erample 2 I Per cent by weight Cellulose nitrate (low viscosity) 13.1 Ethyl alcohol (denatured) 6.9 Chrome yellow pigment 12.0 Isobutyl acetate 14.4 Methyl ethyl ketone 19.5 Petroleum naphtha (till-129 C.) 5.1 Ethyl acetate 6.4 Isobutyl alcohol 5.0 Malonic acid solution 1.0 Castor oil 2.9 Dibutyl phthalate 4.3 Synthetic resin solution 9.4
The enamel composition of Example 2 which contains cellulose nitrate, resin, softener, and
m-alonic acid in the ratioof 10 parts by weight of cellulose nitrate, 5 parts by weight of modified alkyd resin, 3.3 parts by weight of plasticizer and 0.23 part by weight or malonic acid, was prepared in accordance with the procedure described for Example 1.
The viscosity characteristic of the cellulose nitrates utilized in the examples was about 3 seconds as determined in accordance with A. S. T. M. Specifications D-301-33T, Formula 3.
In order to determine whether a finish is reslstant to oils and greases an arbitrary test was devised which consists of soaking a felt pad one inch square and 1 inch in thickness with a heavy automotive transmission 011, preferably a hypoid gear lubricant and placing this oil-soaked pad on the surface 01 a finished panel for 24 hours atroom temperature. The pad is removed and excess oil wiped oil with a dry cloth or with a cloth wetted with petroleum naphtha. The, finish is then examined for discoloration. A
short exposure to direct sunlight seems to accentuate the discoloration if any is present.
The application of this test to finishes prepared byspraying 3 coats suitably thinned of the compositions of Examples 1 and 2 on steel panels primed and surfaced with conventional undercoats failed to show any discoloration whatsoever, whereas finishes prepared in the same manner with compositions in which no malic acid or equivalent described herein was included an i which were otherwise identical with the composi-- tions of Examples 1 and 2 showed serious disv coloration.
The aliphatic dicarboxylic acids both unsaturated and saturated including hydroxy acids of this class, appear to aflord the desired results of markedly reducing or completely eliminating discoloration from oils and greases in'the com- Positions of the present invention. Malic, malonic, maleic, tartaric, adipic, succinic. and oxalic are exemplary of the types of acids which have been found suitable. Malic and malonic acids are particularly effective. Phthalic acid, an arcmatic dicarboxylic acid, or its anhydrlde, is also of utility although somewhat less effective than malic or malonic acid.
Other methods 01 dispersing the pigment in the vehicles of the invention may be employed 11 desired such as by grinding in ball mills, roller mills,
buhrstone mills or from pigment pulps-according' to the process described in U. S. Patent 2,110,745.
In order to provide a superior enamel which maintains highest chalk resistance combined with resistance to mineral oils and greases when the dicarboxylic acids or the present invention are included and which aflords satisfactory working properties, the resin should be modified with from not less than to not more than 60% and prererably with from 40 to of coconut oil or similar non-gelling, nonhydro non-drying oil such as cottonseed or with blown oils of these types. Compositions containing alkyd resins modified with hydroxy oils, such as castor oil,
are not preferred in the present invention because oi the poor durability and reactivity with reactive type pigments which are imparted to :ellulose nitrate coating compositions by such modified resins.
Inany event, the non-gelling, non-drying oil modified alkyd resin must be prepared so that the acid number is kept as low as possible, preferably not mor than 5 or 6 and, in any event, should be kept below 10. Resins of substantially higher acid number have a. tendency to gel and also cannot be used with reactive type pigments such as 7 zinc oxidebecause ofpoor stability of the compositionsduring store-seas evidenced by gelling and/orthe'formationof grit. Such reactive type pigments as referred to in the trade indicate pig- .ments which chemically react with the liquid or solid. ingredients in the composition in which they are incorporated.
Optimum resistance to oil spotting combined with maximum durability including superior chalk resistance are obtained when the cellulose nttrate aik'yd resin-plasticizer ratios and the non-gelling, non-hydroxy, non-drying vegetable oil modified alkyd resin compositions which include the commonly used pigments or other coloring matter such as antimony oxide, titanium dioxide, titanate, pigments, iron blue pigments.
' chrome pigments, para and toluidine toners, ma-
amount of dicarboxyiic acid employed are kept within definite limits. These ratios should be such that for each 10 parts by weight of cellulose nitrate. the amount of alkyd resin is kept below 10 parts but not less than about 5 parts. If the roons, carbon black, ultramarine blue, burnt umber, iron oxide, etc. If zinc oxide, a basic type pigment, is employed to any considerable extent 'inthe compositions of the present invention, little if any improvement in resistance to oil-spotting is obtained by the use of the above described dicarboxyiic acids which are otherwise so outstandingiy effective. The invention is particularly valuable when employed with the light colored socalled pastel shade andmetallic enamels which proportion of alkyd resin to cellulose nitrate is increased by a small amount as. for instance, to 1 part of alkyd resin to 1 'partof cellulose nitrate,
the compositionswhile possibly useful for some industrial purposes even with somewhat higher proportions of the modified alkyd resin, are of no value practically for the present primary purpose of finishing automobiles because the conventional sanding, rubbing and polishing operations employed in this industry cannot be satisfactorily practiced. The amount of plasticizer is about 2 parts when the maximum quantity of resin is used and about 5 parts when'the minimum amount of resin is used.
These acids are preferably incorporated in an amount between 0.2% and 2.0% based on the a total weight of the composition to be treated. In
most cases an amount of between 0.2% and 0.6% is quite effective, particularly in the case of the more preferred acids, namely, malic acid and malonic acid. Excessive proportions are to be avoided since in such cases there may be a tendency for the acid to exude on the surface of the widely used in the art, and many other equivalent materials may be satisfactorily substituted therefor. Suitable solvents and 'diluents include esters of lower fatty acids. for example, ethyl acetate,
butyl acetate, amyi acetate, isobutyl acetate, butyl proplonate and the like, ketones such as methyl ethyl ketone, alcohol ethers and their esters, such as ethylene glycol monoethyl ether acetate and ethylene glycol monomethyl ether acetate. lower aliphatic alcohols and aliphatic and aromatic hydrocarbon diluents such as petroleum naphtha and toluene. v
The plasticizers and softeners which may be I employed in the compositions of the present invention include conventional materials such as castor oil, blown castor oil, aryl sulfonamides including ortho, meta and para toluene ethyl sulfonamides and mixtures of these, aryl and alkyl esters of phosphoric acid, dibutyl tartrate, di-
cyclohexyl phthalate, diethyl phthalate and the phthalate esters of ether alcohols, such as the phthalate, ester of ethylene glycol monomethyl ether.
The invention is operative for cellulose nitratehave been a considerable source of complaint in the previously available enamels because of poor resistance to oils and greases where discoloration is more pronounced.
Although phthalic anhydride is the preferred acid radical in the alkyd resin ingredient of the improved compQsitionsother'acids such as succinic, malic, adipic, maleic, sebacic, etc may be substituted wholly or in, part for the phthalic anhydride, but best results are secured when phthalic anhydride is present in preponderant proportionss J Suitable resins for the improved compositions may also be prepared using other poiyhydric alcohols including ethylene glycol and higher homologs, diethylene g ycol and other polyslycols;
polyglycerols; pentaerythritol and sorbitol.
The compositions of the invention are generally useful in finishing surfaces which may be exposed to direct contact-with oils and greases. They are particularly useful for finishing automobiles where contact with lubricating o ls and greases and oil-containing rubbing compounds is more frequently encountered.
The new compositions have shown a number of important advantages when employed in the suggested utilities. In the first place, they have exhibited an unexpected and decisively superior resistance to spotting or discoloration of the finish from oily rubbing and polishing compounds and from direct contact with oils and greases which sometimes reach the finish of an automobile through careless servicing of the car before or after delivery to the customer. This defect of "oil spotting was quite common in commercial finishes heretofore'available and caused frequent consumer complaint and costly rejections in the final inspection in the manufacture of new automobiles. Furthermore, the new compositions are adherent andfiexible and afford excellent durability, including superior resistance to chalking,
thus preserving the original gloss and lustre for extended periods during exposure to atmospheric conditions. The enamels of the present invention provide finishes of satisfactory working properties which do not become thermoplastic or soften under the rubbing and polishing operations normally practiced in the automotive industry. The satisfactory working properties of the improved compositions as controlled by the particular proportions previously indicated are of considerable importance inasmuch as previously known compositions containing related'ingredicuts are usually quite defective. in this respect,
making them entirely unsuited for the'present purpose. Substantial economies are represented in the new finishes in that assembly line rejections and consumer complaints necessitating touching up or refinishing of automobiles because of oil spotting" discoloration are practi' cally eliminated.
As many widely different embodiments of the invention may be made without departing from the spirit and scope thereof, it will be understood that the invention is not limited to the specific embodiments thereof except as defined in the appended claims.
I claim:
l. A coating composition which is highly resistant to oils and greases consisting of (A) a normally non-gelling coating composition containing cellulose nitrate and a non-gelling, nonhydroxy, non-drying vegetable oil modified alkyd resin characterized by an acid number or less than 10 and (B) in addition-thereto an aliphatic dicarboxylic acid in the proportions of between 0.2 and 20% by weight of the total coating composition.
2. Composition of claim 1 in which the aliphatic dicarboxylic acid is malic acid.
3. Composition of claim 1 in which the aliphatic dicarboxylic acid is malonic acid.
4. The composition of claim 1 in which the alkyd resin is modified with from 85 to 60 per cent of the non-hydroxy, non-drying vegetable oil.
5. Composition of claim 1 in which the alkyd resin is modified with coconut oil.
6. Composition of claim 1'in which said modified alkyd resin is a glyceryl phthalate resin.
'7. Composition of claim 1 in which the aliphatic dicarboxylic acid is present in an amount of about 0.5% by weight of the total coating composition.
8. A normally non-gelling, weather-resistant cellulose nitrate coating composition which is highly resistant to oils and greases consisting of (A) a normally non-gelling composition containing cellulose nitrate, a plasticizer, an alkyd resin modified with 35-60% of a non-hydroxy, nondrying vegetable oil, said resin having an acid number of less than 10 and being present in said composition in a proportion by weight of at least 5 parts as a minimum but less than 10 parts as a maximum for each 10 parts of cellulose nitrate, said plasticizer being present in the proportion by weight of about 2 partsvas a minimum and 5 parts as a maximum and (B) in addition thereto an aliphatic dicarboxylic acid in the proportion of between 0.2 and 2.0% by weight of the total coating composition.
' WALTER K. MOFFETT.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US284094A US2315347A (en) | 1939-07-12 | 1939-07-12 | Coating composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US284094A US2315347A (en) | 1939-07-12 | 1939-07-12 | Coating composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2315347A true US2315347A (en) | 1943-03-30 |
Family
ID=23088833
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US284094A Expired - Lifetime US2315347A (en) | 1939-07-12 | 1939-07-12 | Coating composition |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2315347A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE971564C (en) * | 1952-03-26 | 1959-02-19 | Metallgesellschaft Ag | Process for applying top coats to base coats in an electrostatic field |
| US2920054A (en) * | 1956-06-14 | 1960-01-05 | Du Pont | Coating composition comprising nitrocellulose and alkyd resin and article coated therewith |
-
1939
- 1939-07-12 US US284094A patent/US2315347A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE971564C (en) * | 1952-03-26 | 1959-02-19 | Metallgesellschaft Ag | Process for applying top coats to base coats in an electrostatic field |
| US2920054A (en) * | 1956-06-14 | 1960-01-05 | Du Pont | Coating composition comprising nitrocellulose and alkyd resin and article coated therewith |
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