NZ198482A - Propellant-active carrier system for aerosol paint compositions - Google Patents
Propellant-active carrier system for aerosol paint compositionsInfo
- Publication number
- NZ198482A NZ198482A NZ198482A NZ19848281A NZ198482A NZ 198482 A NZ198482 A NZ 198482A NZ 198482 A NZ198482 A NZ 198482A NZ 19848281 A NZ19848281 A NZ 19848281A NZ 198482 A NZ198482 A NZ 198482A
- Authority
- NZ
- New Zealand
- Prior art keywords
- composition
- water
- weight
- propellant
- present
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 104
- 239000003973 paint Substances 0.000 title claims description 26
- 239000000443 aerosol Substances 0.000 title claims description 23
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 64
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 40
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 29
- 239000003380 propellant Substances 0.000 claims description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 26
- 229920000642 polymer Polymers 0.000 claims description 26
- 229920005989 resin Polymers 0.000 claims description 26
- 239000011347 resin Substances 0.000 claims description 26
- 239000000049 pigment Substances 0.000 claims description 18
- 239000002904 solvent Substances 0.000 claims description 16
- 239000003495 polar organic solvent Substances 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 12
- 239000004925 Acrylic resin Substances 0.000 claims description 11
- 229920000178 Acrylic resin Polymers 0.000 claims description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 10
- 239000000758 substrate Substances 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 239000007921 spray Substances 0.000 claims description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 8
- 239000003960 organic solvent Substances 0.000 claims description 8
- 125000001931 aliphatic group Chemical group 0.000 claims description 7
- 239000004094 surface-active agent Substances 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 claims description 6
- 239000004014 plasticizer Substances 0.000 claims description 6
- 239000004593 Epoxy Substances 0.000 claims description 5
- 229920000180 alkyd Polymers 0.000 claims description 5
- 239000002518 antifoaming agent Substances 0.000 claims description 5
- 239000003381 stabilizer Substances 0.000 claims description 5
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- 244000093965 Triphasia trifolia Species 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 238000007605 air drying Methods 0.000 claims 1
- 239000012071 phase Substances 0.000 description 11
- 238000009472 formulation Methods 0.000 description 10
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 9
- 229960004592 isopropanol Drugs 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- -1 such as Substances 0.000 description 5
- DAFHKNAQFPVRKR-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylpropanoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)C DAFHKNAQFPVRKR-UHFFFAOYSA-N 0.000 description 4
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 229910017974 NH40H Inorganic materials 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000001055 blue pigment Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000013530 defoamer Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 2
- 125000005609 naphthenate group Chemical group 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 230000019612 pigmentation Effects 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 235000020354 squash Nutrition 0.000 description 2
- 239000012463 white pigment Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-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
- 235000019485 Safflower oil Nutrition 0.000 description 1
- 229920004890 Triton X-100 Polymers 0.000 description 1
- 229920004896 Triton X-405 Polymers 0.000 description 1
- 229920004897 Triton X-45 Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 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
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 230000001236 detergent effect Effects 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 239000008266 hair spray Substances 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000001053 orange pigment Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
- C09D5/021—Aerosols
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
-
- 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)
- Dispersion Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Cosmetics (AREA)
Description
New Zealand Paient Spedficaiion for Paient Number 1 98482 198 482 prbrf,,, - 30-1 -to; Cor.-.; ■ ri a.-** wk&°®.r,L9Xt?.
Pub&ston Dats: P.O. Jotirr-:-:, He: ....
Hf. A*.r & Ss rwa*, »***> /r*; *=■"« *** TO ?JT- f?\; jiin^ *MSS"i* iUa'.jijS Patents Fonn No.5.
Patents Act 1953 COMPLETE SPECIFICATION "Propellant-Active Carrier System fo^ Water-Eased Paints" WE, CCL INDUSTRIES INC., a company organised and existing under the laws of Canada, of 26 Waterman Avenue, Toronto, Ontario, Canada M4B 1Y5, hereby declare :.he invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement 198 482 - PROPELLANT-ACTIVE CARRIER SYSTEM FOR WATER-BASED PAINTS The present invention relates to aerosol paint compositions, and in particular to a novel propellant-active carrier system therefor.
Aerosol paint compositions are well known but have used volatile organic solvents as the carrier for the film-forming polymer. Toxicity and flammability problems arise .from the use of such organic solvents and governmental regulatory authorities are moving towards severe restric-10 tions on the use of organic solvents in such compositions.
In prior United States patent application Serial No. 09 7,152 filed November 23, 19 79, the disclosure of which is incorporated herein by reference, (.now U.S. Patent No. 4 , 265, 797 )/there is described a water-based aerosol paint 15 formulation which satisfactorily produces a high gloss and excellent durability paint film on a substrate surface. The compositions defined therein are restricted to a narrow range of film-forming polymers.
It has now surprisingly been found that a novel 2 0 single phase propellant-active carrier composition can be utilized to form satisfactory spray-applied films based on a wide■ variety of water-dilutable film-forming polymers, which may be in solution form or emulsified form.
The novel propellant composition of the invention con-25 sists essentially of: (a) about 20 to about 7 5% by weight of a propellant comprising dimethyl ether and from 0 to about 50% by weight of the dimethyl ether of another liquid propellant; (b) about 10 to about 50% by weight of water; (c) about 0.1 to about 45% by weight of at least one k 198 48 2 I ' 3- water-soluble polar organic solvent. The proportions of the components total 100% and are sufficient to provide a single phase. The composition, together with auxiliary gaseous pro-pellants, if present, exerts a vapor pressure in a pressurized 5 aerosol dispensing container in the range of about 30 to about 85 psig at ±>out 20°C (70°F).
In a preferred embodiment of the invention, the novel propellant composition consists essentially of: (a) about 20 to about 75% by weight of dimethyl ether; 10 (b) about 10 to about 50% by weight of water; (c) about 1 to about 30% by weight of at least one aliphatic monohydric alcohol of the formula: R-OH wherein R is an unsubstituted straight or branched chain alkyl group containing from 1 to 6 carbon atoms; and 15 (d) about 1 to about 15% by weight of at least one water-soluble organic coalescing solvent. The proportions of the components total 100% and are sufficient to provide a single phase.
While the present invention is primarily directed to 20 the provision of aerosol paint compositions, nevertheless the propellant-active carrier composition may be used for the spray dispensing of a variety of- other active components, such as, in hair sprays and deodorants.
The essential components of the propellant composition 25 of this inT'9n„ion are dimethyl ether, water, and at least one water-soluble polar organic solvent. Dimethyl ether is a colorless, odorless, stable molar liquid with a boiling point of -25°C and a vapor pressure of 4.2 bar at 20°C.
It has been previously suggested to use this liquid as 30 a propellant. U.S. Patent No. 1, 800,156 discloses the use of dimethyl ether alone as the propella-nt for a large variety of materials and' paints are mentioned. U.S. Patent No. 3,207,386 discloses the utilization of a combination of dimethyl ether and water as a propellant for a wide variety 35 of products including paints, the proportions being chosen to provide a homogeneous solution of the dimethyl ether and water as the propellant and this restriction results in a - 4- 198 48 2 composition consisting of 5 to 35% by weight of dimethyl ether and 9 5 to 6 5% by weight of water. No other solvent or propellant components are used in this prior art composition.
In the present invention, the dimethyl ether is used in a combination with water and at least one water-soluble polar organic solvent, preferably a mixture of an alcohol and a water-soluble organic coalescing solvent, to provide a single phase propellant-active carrier composition for a water-10 dilutable film-forming polymer which is in aqueous solution or aqueous emulsion form, and hence the present invention involves quite a different application of the dimethyl ether in different proportions for a different purpose.
The dimethyl ether constitutes about 20 to about 75% 15 by weight of the propellant-active carrier composition, preferably about 25 to about 40% by weight, typically about 40% by weight.
Although the presence of conventional liquid propellants and other organic solvents, such as, aliphatic hydrocarbons 20 and fluorinated hydrocarbons, often introduces instability to the system and hence dimethyl ether is preferred to be the sole propellant, under sonre circumstances there may be present in the composition up to about 50% by weight of the dimethyl ether of another liquid propellant.
A gaseous phase propellant, such as, nitrogen, carbon dioxide or nitrous oxide, may be used to enhance the propellant effect of the dimethyl ether or combination of dimetnyl ether and other liquid propellant.
Another essential component of the propellant compo-30 sition of the invention is water. This component is present in a concentration of about 10 to about 50% by weight, preferably about 2 0 to about 35% by weight, typically about 30% by weight.
In a preferred embodiment of the invention, a 35 water-soluble lower aliphatic monohydric alcohol also is used in the composition. The monohydric alcohols used in this invention are those having the formula: R-OH wherein R is an unsubstituted straight or branched chain alkyl group containing from 1 to 6 carbon atoms. Examples 198 48 2 of suitable monohydric alcohols are methanol, ethanol, n-propanol, iso-propanol and n-butanol, preferably ethanol or iso-propanol.
The concentration of the monohydric alcohol used in 5 the compositions of this invention may vary widely from about 1 to about 3 0% by weight, preferably about 5 to about 20% by weight, typically about 15% by weight.
In a preferred embpdiment of the invention, a water-soluble organic coalescing solvent is present along with the 10 alcohol. A coalescing organic solvent is one which assists in film formation and which acts as an agent to render the polymer water-soluble.
The coalescing solvent may be any water-soluble polar organic solvent. Such materials include glycol ethers, esters, 15 ketones and certain modified alcohols and may have a boiling point in the range of about 365° to about 572°F. (about 185° to about 300aC).' Suitable solvents include lower monoalkyl ethers of ethylene or propylene glycol, such as, propylene glycol methyl ether and propylene glycol methyl ethyl 20 ether, diacetone alcohol and ester alcohols.
The coalescing solvent is present in an amount of from about 1 to about 15% -by weight, preferably about 5 to about 10% by weight, typically about 6% by weight. The combination of the monohydric alcohol and coalescing solvent 25 is present in an amount of about 2 to about 30% by weight and, in combination with the chosen proportions of dimethyl ether and water forms a single phase composition which is suitable for dissolving or suspending the active components to be dispensed.
In many instances, both an alcohol and a coalescing solvent are required. However, certain resins providing the film-forming component of the composition may be utilized when one or the other of these components is absent.
In the broadest aspect of the invention, therefore, the 35 composition contains at ieast one water-soluble polar organic solvent to achieve coupling of the organic and aqueous phases to ensure a single-phase active carrier propellant composition. The concentration of the at least one polar organic solvent may vary widely, from about 0.1 to about 45% by weight. 4 0 The propellant-active carrier composition of the invention 198 482 -b- exerts a vapor pressure when packaged in a pressurized container sufficient to effect dispensing of the contents of the container. Generally, the vapor pressure is in the range of about 30 to about 3 5 psig at 20°C (70°F) and preferably 5 about 40 to about 60 psig.
The dimethyl ether constitutes the main propellant component of the composition. The water provides the primary solvent and/or suspension phase for the active components, which include a film-forming polymer in the case of 10 an aerosol paint. The water-soluble organic solvents mainly act as solvents for the propellant and the water, so that there results a substantially single phase mixture of components, which resists separation into separate liquid phases on standing. A single phase propellant-active 15 carrier composition enables active components to be readily and efficiently dispensed from the aerosol container.
The propellant-active carrier composition of this invention has particular utility in the provision of aerosol water-based paint compositions. Such compositions comprise 20 the single-phase propellant-active carrier composition and a film-forming polymer dissolved and/or suspended therein. Pigments also may be included to impart pigmentation to the sprayed film.
Such water-based aerosol paints generally comprise 25 about 6 to about 25% by weight, preferably about 12 to about 20% by weight, of the film-forming polymers and about 92 to about 75% by weight, preferably about 88 to about 80% by weight, of propellant-active carrier and, optional components, such as, pigments, surfactants, stabilizers, antifoam agents 30 and plasticizers, as discussed in more detail below.
The propellant-active carrier composition is quite versatile and is effective to permit the spray application of a wide variety of film-forming polymers onto a substrate surface to form a continuous film of excellent durability, 35 including high flexibility retention. Depending on the nature of the polymer and the other components of the formulation, the films may be of high gloss, medium gloss, low gloss or flat.
Aerosol compositions formulated using the propellant-40 active carrier system of the composition are preferably sub- 1 98.48.2 -i- stantially non-flammable, as tested according to standard flammability tests for aerosols. For example, the spray blows out a candle.
The film-forming polymer may be any water-dilutable polymer, in-5 eluding water-soluble polymers and water-dilutable emulsified polymers, which is capable of spray application to form a continuous film on a substrate _ surface. Many classes of polymer may be employed, including acrylic resins, alkyds, epoxy esters and polyvinyl copolymers.
Acrylic resins are thermoplastic or thermosetting 10 polymers or copolymers of acrylic acid, methacrylic acid, esters of these acids, or acrylonitrile. Such resins may be modified by the presence of an aromatic monovinylidene compound, usually, styrene. Acrylic resins generally have molecular weights in the range of about 100,000 to about 15 1,000,000.
One example of an acrylic resin which is suitable for the formulation of a water-based aerosol paint composition in accordance with this invention is available from Rohm and Haas Inc., under the designation '"W.L. 91". Another 20 example is the resin available from Reichold Chemicals under the designation "90-587 Resin".
AlJcyd resins are made by combining dibasic acids or their anhydrides, usually phthalic anhydride, with a polyhydric alcohol, such as glycerol. AlJcyd resins often 25 are modified by natural drying oils, such as, linseed oil, soya oil and safflower oil, in concentrations of 30 to 60% by weight.
Examples of alkyd resins which are suitable for the formulation of a water-based aerosol paint composition in 30 accordance with this invention are available from Ashland Oil Inc., under the Trademark "AROLON" such as those designated "580" and "585".
Epoxy ester resins are resins containing a reactive epoxy group and derived from polyols and epoxy-group 35 containing compounds. Other comonomers, such as, styrene may be copolymerized, Thes.e resins may be modified by natural drying oils in the same manner as alkyd resins.
An example of an epoxy resin which may be used is sold by Reichold Chemicals under the designation "38-690". 1 98 482 * Polyvinyl copolymers are formed by copolymerizing vinyl chloride or vinyl acetate with copolymerizable monomers. One example of such a material suitable for the formulation of a water-based aerosol paint composition in 5 accordance with this invention is available from B.F.
Goodrich Company under the designation "514H".
Mixtures of two or more resins or resin types may be used in the aerosol water-based paint formulations of this invention.
As mentioned above, an optional component which may be present in the paint composition is a pigment for pigmentation of the film formed on spraying the composition onto a substrate surface. When employed, up to about 15% by weight of the total composition of the pigment may be used, 15 preferably about 5 to about 15% by weight of pigment.
When such pigment is present, the quantity of polymer used is generally towards the lower end of the range recited above. When such pigment is omitted and a clear film is required, then quantities of'polymer towards the higher end 2 0 of the range are used.
The presence of the pigment usually requires the presence of added surfactant to ensure suspension of the pigment in the liquid vehicle. Some surfactant may be present with the film-forming polymer, if the latter is in 25 emulsion form, but the quantity involved usually is insufficient to effect suitable suspension of added pigment.
The overall quantity of surfactant present in the composition should be sufficient to maintain solids in suspension and usually varies up to about 3% by weight of 30 the composition.
A pH stabilizer may also be present in the composition to provide an overall pH value greater than about 7.2 and up to about 10 to assist in inhibition of corrosion of the conventional pressurized metal container in which the paint 35 composition is located for spray application. Suitable pH stabilizer materials ihclude morpholine, ammonia and triethanolamine. This component may be present in an amount of up to about 2% by weight of the total composition.
An antifoam agent may be included to alter the 1 198 482 W surface tension of the composition to permit ready release of dissolved gases upon spraying of the composition onto the substrate surface and to counteract the detergent effect of the surfactants present in the composition. A 5 non-ionic blend of mineral oils and silica derivatives has been found to'be suitable for use for defoaming. When an antifoam agent is present, quantities up to about 2% by weight of the total composition may be used, preferably about 0.4% by weight.
Another component which may be added to the aerosol paint composition is a plasticizer to promote flexibility. Any one of a wide range of plasticizers may be used, for example, dioctyl phthalata. The plasticizer may be present in an amount of up to about 2% by weight of the 15 total composition, preferably about 1% by weight.
The aerosol water-based paint compositions provided in accordance with this invention, therefore, are characterized by a pH of about 7.2 to abo.ut 10, preferably about 7.4 to about 7.9, and consist essentially of: about 6 to about 25 wt.% of at least one watar- dilutable film-forming polymer (calculated as the nonvolatile content thereof], about 20 to about 60 wt.% of a propellant comprising dimethyl ether and from 0 to about 50 wt.% of the dimethyl 25 ether of another liquid propellant, about 10 to about "40 wt.% of water, about 0.1 to about 30 wt.% of at least one water-soluble polar organic- solvent, 0 to about 3 wt.% of at least one surfactant, 3 0 0 to about 15 wt.% of at least one pigment, in the composition in proportions to provide a single phase propellant-active carrier system in which the remainder of the components are dissolved or suspended.
Preferably, the composition contains, as the polar organic solvent component: 0 to about 1 wt.% of at least one pH stabilizer, 0 to about 2 wt.% of at least one antifoam agent, and 0 to about 2 wt.% of at least one plasticizer.
The dimethyl ether, water and polar solvent, are present 198 48 2 about 1 to about 20 wt.% of at least one aliphatic monohydric alcohol containing from 1 to 6 carbon atoms, and about 1 to about 10 wt.% of at least one water-soluble organic coalescing solvent.
The aerosol water-based paint composition, which is formulated as described above using the propellant-active carrier system of the invention, may be sprayed onto a substrate surface without foaming occurring and the: pigmented or unpigmented continuous film touch dries rapidly, usually in 10 about 15 to 30 minutes, and exhibits complete water resistance in an acceptable period of time, usually in about 3 to 5 hours.
The invention is illustrated by the following Exairples: Examples 1 to 14 A number of aerosol water-based paint formulations were prepared using various film-forming polymers and pigments and packaged in aerosol cans. The films were sprayed onto substrate surfaces. In each case, a continuous film was formed which was dry to the touch in 30 minutes, 20exhibited water resistance within 3 hours of application and had a salt spray resistance (ASTM test B117) of more than 50 hours. ! The following are the formulations: 198 48 2 - 1# " Example 1 - Red oxide primer - Mixed acrylic-epoxy resin Comoonent ~ wt.
% WL91 Resin ("1) 3. 38-690 Resin 14.
Water 13.
Isopropyl alcohol is".' 0 Butylcellosolve 4. 0 Texanol 0. 7 Red Oxide pigment . 0 Driers - Mn 6%, Co 6% 0.
L475 C3) 0. 2 Triethanolamine 1. 0 Dioctyl phthalate 0. 0K412 2. 0 Dimethyl ether 40. 0 Total 100 . 0 Notes: CD Acrylic resin made by Rohm and Haas; C2) Epoxy resin made by Reichold Chemicals; (3) Defoamer - Dow Chemical; (4) Silica flattening agent. 198 482 - Example 2 - Blue - Acrylic resin Comoonent wt WL91 Resin 22 .0 Water . 0 Isopropyl alcohol .0 Butylcellosolve 4 .5 Texanol 0 .7 White pigment 2 .3 Blue pigment 4 .6 L475 0 .2 % NH4OH 0 .2 Dioctyl phthalate 0 .2 Dimethyl ether _ 40 .0 Total 100 . 0 Examples 3 to 7 Ponnulations similar to Example 2 were prepared using WL91 as the resin with differing pigments, as follows: Example 3 - White Example 4 - Red Example 5 - Green Example 5 - Black Example 7 - Orange Example 8 - Flat black - Acrylic resin Comoonent wt.
%' WL91 Resin 21. 8 .
Water 9.
Isopropyl alcohol . 0 Butylcellosolve 4.
Texanol 0. 7 Black pigment . 0 L475 0. 4 % NH40H 0.
Dioctyl phthalate 0.
OK412 2. 0 Triton X-45 0. 1 Dimethyl ether 40. 0 Total 100. 0 Note:' CD Rohm & Haas non-ionic surfactant _,3. 198 482 Example 9 - Fira orange fluorescent - Acrylic resin Component wt. % 90-587 Resin^~^ 15.0 Watar 12.7 Isopropyl alcohol 15.0 Butylcellosolve 4. 0 Fire orange pigment 11.7 L475 0.2 NH4OH tcone.) 1.2 Triton X 405 0 .1 Dimethyl ether 40.0 Total 100.0 Notes: (1). Reichold Chemicals acrylic resin; C21 Rohm & Haas nonionic surfactant.
Example 10 - Red oxide primer - Alkyd-Acrylic resin mixture Component wt. % WL91 Resin 18.00 Arolon 585 ^ 5.75 Water 15.03 Isopropyl alcohol 15.00 Butylcellosolve 4.50 Texanol - 0.70 Red oxide pigment 8.00 L475 0.40 % NH40H 0-02 Dioctyl phthalate 0.50 OK412 2.00 Triton X10 0 0.1-0 Dimethyl ether 30.00 Total 100.00 Note: (1) Ashland Oil alkyd resin \ 198 48 2 Example II - Blue - AUcyd resin Component wt. % Arolon 580 ^ 27.0 Arolon 585 ^ .2 Water 8.8 Isopropyl alcohol 7.7 Butylcellosolve 2.3 Blue pigment 2.1 White pigment 1.1 Drier 0.3 L475 0.2 % NH4OH 0.1 Triton X100" 0.3 Dimethyl ether 40.0 Total 100. 0 Note: HI and (_2L AlJcyd resins made by Ashland Oil .Example 12 - Red Oxide primer - Epoxy resin In the formulation of Example 1, the WL91 resin was replaced wholly by an increased amount of 3 8-690 resin to provide 18.1 wt.% of such resin in the resulting formulation. Example 13 - clear - PVC resin Component wt. % 415H Resin(il 25.0 Water 2 4.7 Isopropyl alcohol 15.0 Butylcellosolve 5.0 L475 0.2 % Ammonia 0.1 Dimethyl ether 30.0 Total 100.0 Note: (1) Carboxy modified polyvinyl chloride terpolymer made by B.F. Goodrich.
A 198 482 Example 14 Component wt. % Styrenated epoxy ester^ 13.0 Water 31.0 White tinter^ 13.5 Driers (Cu naphthenate 6%, Mn naphthenate 6%) 0.2 Active 8 0.1 Concentrated ammonia 1.0 Byk 020. (defoamer) 0.2 Byk 351 (flow agent) 1.0 Dimethyl ether 40.0 Total 100.00 Notes: (1) 453V8 by C.P.V. - comprises 70% solids and 30% Butylcellosolve (2) v Tinter comprises: Styrenated epoxy ester 23.5 Concentrated ammonia 1.5 Water 15.0 TiO„ 60.0 2 100.<5 In summary of this disclosure, the present invention, therefore, provides a novel propellant-active carrier composition useful for the spray application of water-based paints to substrate surfaces. Modifications are possible within the scope of this invention.
Claims (23)
1. A single phase liquid propellant-active carrier composition suitable for the spray application of an active ingredient from a pressurized container onto a substrate surface, comprising, to a total of 100% by weight, (a) 20 to 75% by weight of a propellant comprising dimethyl ether and from 0 to 50% by weight of the dimethyl ether of another liquid propellant; (b( 10 to 50% by weight of water*, and (c) 0.1 to 45% by weight of at least one polar water-soluble organic solvent; the composition, together with any gaseous propellant present, exerting a vapor pressure within the pressurized container in the range of 30 to 85 psig at 70°F.;
2. A composition as claimed in Claim 1, in which the polar organic solvent comprises at least one aliphatic monohydric alcohol of the formula: R-OH in which R is an unsubstituted straight or branched chain alkyl group containing from 1 to;6 carbon atoms.;
3. A composition as claimed in Claim 1, in which the polar organic solvent is a monoalkyl ester with a carbon chain length of 1. to 6 carbon atoms of ethylene glycol or propylene glycol, diacetone alcohol, a ketone or an ester alcohol.;
4. A composition as claimed in claim 1, in which the polar organic solvent comprises a mixture of at least one aliphatic monohydric alcohol of the formula: R-OH in which R is an unsubstituted straight or branched chain alkyl group containing from 1 to 6 carbon atoms and a different water-soluble polar organic solvent.;
5. A composition as claimed in Claim 1 in which the polar organic solvent comprises 1 to 30% by weight of the total composition and which organic solvent comprises at least one aliphatic monohydric alcohol of the formula: R-OH wherein R is an unsubstituted straight or branched chain alkyl group containing from 1 to 6 carbon atoms, and 1 to 15% by weight of the total composition of at least one water-soluble polar organic coalescing solvent.;
6. A composition as claimed in claim 5, in which the monohydric alcohol is ethanol or isopropanol.;
7. A composition as claimed in claim 5 or 6, in which the coalescing solvent is a monoalkyl ester with a carbon chain length of 1 to 16 carbon atoms of ethylene glycol or ropylene glycol, diacetone alcohol or an ester alcohol.;■ ' 198482;-i7-;
8. A single phase liquid propellant-active carrier composition substantially as hereinbefore described with reference to any one of the Examples.;
9. A water-based aerosol paint composition suitable for spray application from a pressurized container to a substrate surface and air drying to a continuous film thereon, comprising: (a) 6 to 25% by weight of at least one water-dilutable film-forming polymer, and (b) 92 to 75% by weight of a propellant-active carrier composition as claimed in any one of claims 1 to 8.;
10. A composition as claimed in claim 9, in which the film-forming polymer is present in an amount of from 12 to 20% by weight and the propellant-active carrier composition is present in an amount of 88 to 80% by weight.;
11. A composition as claimed in claim 9 which has a pH of 7.2 to 10 and which consists essentially of (a) 6 to 25 wt.% of at least one water-dilutable film-forming polymer; (b) 20 to 60 wt.% of a propellant comprising dimethyl ether and from 0 to 50% by weight of the dimethyl ether of another liquid propellant? (c) 10 to 40 wt.% of water; (d) 0.1 to 30 wt.% of at least one water-soluble polar organic solvent; (e) 0 to 3 wt.% of at least one surfactant; (f) 0 to 15 wt.% of at least one pigment; (c) 0 to 1 wt.% of at least one pH stabilizer; (h) 0 to 2 wt.% of at least one antifoam agent;"and (i) 0 to 2 wt.% of at least one plasticizer? the propellant, water and polar organic agent being present in proportions to provide a single phase propellant-active carrier composition in which the remainder of the components of the composition are dissolved or suspended, the composition, together with any gaseous propellant present,;exerting a vapor pressure within the pressurized container in the range of 30 to 85 psig at 70°F.;
12. A composition as claimed in claim 11, In which component (d) comprises 1 to 20 wt.% of the total -composition of at least one aliphatic monohydric alcohol of the formula: R-OH wherein R is an unsubstituted straight or branched chain alkyl group containing 1 to 6 carbon atoms and 1 to 10 wt.% of the; total;Pmposit-ion of at least one water-soluble polar organic coal-;W. , ,;es-cmg solvent.;% J;:t* / 198 482
13. A composition as claimed in claim 12, in which the monohydric alcohol is present in an amount of 5 to 2 0% by weight.
14. A composition as claimed in claim 12 or 13, in which the alcohol is ethanol or isopropanol.
15. A composition as claimed in any one of claims 12 to 14, in which the coalescing solvent is present in an amount of . 5 to 10% by weight.
16. A composition as claimed in any one of claims 11 to 15, in which the dimethyl ether is present in an amount of 20 to 40% by weight.
17. A composition as claimed in any one of claims 11 to 16, in which the water is present in an amount of 2 0 to 35% by weight.
18. A composition as claimed in any one of claims 11 to 17, wherein the pH is 7.4 to 7.9.
19. A composition as claimed in any one of claims 11 to 18, in which the continuous film is pigmented and the at least one pigment is present in the composition in an amount of 5 to 15 wt.%.
20. A composition as claimed in any one of claims 9 to 19, in which the film-forming polymer is a water-soluble resin.
21. A composition as claimed in any one of claims 9 to 19, in which the film-forming polymer is a water-dilutable emulsified resin.
22. A composition as claimed in any one of claims 9 to 21, in which the film-forming polymer is an acrylic resin, an alkyd, an epoxy ester or a polyvinyl copolymer.
23. A water-based aerosol paint composition substantially as hereinbefore described with reference to any one of the Examples. CCL INDUSTRIES INC by their authorised agents: P.L.BERRY & ASSOCIATES per:
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US19245480A | 1980-09-30 | 1980-09-30 | |
US23579281A | 1981-02-25 | 1981-02-25 | |
US23718981A | 1981-03-03 | 1981-03-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
NZ198482A true NZ198482A (en) | 1984-03-30 |
Family
ID=27393054
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NZ198482A NZ198482A (en) | 1980-09-30 | 1981-09-29 | Propellant-active carrier system for aerosol paint compositions |
Country Status (14)
Country | Link |
---|---|
AT (1) | AT392076B (en) |
AU (1) | AU548700B2 (en) |
BE (1) | BE890564A (en) |
BR (1) | BR8106291A (en) |
CH (1) | CH648586A5 (en) |
DE (1) | DE3138298C2 (en) |
FR (1) | FR2500471A1 (en) |
GR (1) | GR75009B (en) |
IE (1) | IE51595B1 (en) |
IT (1) | IT1139625B (en) |
MX (1) | MX159291A (en) |
NZ (1) | NZ198482A (en) |
PT (1) | PT73751B (en) |
SE (1) | SE8105703L (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4420575A (en) * | 1982-07-26 | 1983-12-13 | Plasti-Kote Company, Inc. | Water reducible aerosol paints |
US5830440A (en) * | 1991-11-21 | 1998-11-03 | L'oreal | Aqueous aerosol hair spray |
US6428844B1 (en) * | 1993-02-03 | 2002-08-06 | Rohm And Haas Company | Reduction of microfoam in a spray-applied waterborne composition |
JP4776757B2 (en) | 1999-10-01 | 2011-09-21 | 株式会社ダイゾー | Aerosol composition |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3207386A (en) * | 1962-06-01 | 1965-09-21 | Aerosol Tech Inc | Aerosol dispenser producing non-flammable spray with fluid system having a flammable propellant |
DE2849590C2 (en) * | 1978-11-15 | 1981-11-19 | Schwarzkopf, Hans, 2000 Hamburg | Aerosol preparation under pressure in a container, process for its manufacture and use of the aerosol preparation under pressure in a container (aerosol can) |
CA1102466A (en) * | 1978-12-06 | 1981-06-02 | Albert Suk | Aerosol water-based paint composition |
-
1981
- 1981-03-25 FR FR8106020A patent/FR2500471A1/en active Granted
- 1981-09-23 CH CH6122/81A patent/CH648586A5/en not_active IP Right Cessation
- 1981-09-24 IE IE2226/81A patent/IE51595B1/en not_active IP Right Cessation
- 1981-09-25 DE DE3138298A patent/DE3138298C2/en not_active Expired - Lifetime
- 1981-09-28 SE SE8105703A patent/SE8105703L/en unknown
- 1981-09-29 AU AU75767/81A patent/AU548700B2/en not_active Expired
- 1981-09-29 NZ NZ198482A patent/NZ198482A/en unknown
- 1981-09-29 GR GR66150A patent/GR75009B/el unknown
- 1981-09-29 AT AT0417581A patent/AT392076B/en active
- 1981-09-30 BR BR8106291A patent/BR8106291A/en unknown
- 1981-09-30 IT IT24240/81A patent/IT1139625B/en active
- 1981-09-30 MX MX189427A patent/MX159291A/en unknown
- 1981-09-30 BE BE0/206120A patent/BE890564A/en not_active IP Right Cessation
- 1981-09-30 PT PT73751A patent/PT73751B/en unknown
Also Published As
Publication number | Publication date |
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IT8124240A0 (en) | 1981-09-30 |
GR75009B (en) | 1984-07-12 |
PT73751B (en) | 1982-12-30 |
PT73751A (en) | 1981-10-01 |
AU7576781A (en) | 1982-04-08 |
SE8105703L (en) | 1982-03-31 |
AT392076B (en) | 1991-01-25 |
DE3138298C2 (en) | 1990-12-06 |
IE812226L (en) | 1982-03-30 |
FR2500471A1 (en) | 1982-08-27 |
BR8106291A (en) | 1982-06-22 |
ATA417581A (en) | 1990-07-15 |
FR2500471B1 (en) | 1985-10-04 |
IE51595B1 (en) | 1987-01-21 |
BE890564A (en) | 1982-01-18 |
CH648586A5 (en) | 1985-03-29 |
DE3138298A1 (en) | 1982-06-16 |
AU548700B2 (en) | 1986-01-02 |
IT1139625B (en) | 1986-09-24 |
MX159291A (en) | 1989-05-15 |
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