US2739903A - Paint killer - Google Patents
Paint killer Download PDFInfo
- Publication number
- US2739903A US2739903A US316049A US31604952A US2739903A US 2739903 A US2739903 A US 2739903A US 316049 A US316049 A US 316049A US 31604952 A US31604952 A US 31604952A US 2739903 A US2739903 A US 2739903A
- Authority
- US
- United States
- Prior art keywords
- paint
- water
- surface active
- killer
- active agent
- 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
Links
- 239000003973 paint Substances 0.000 title claims description 53
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 48
- 239000000463 material Substances 0.000 claims description 35
- 239000007921 spray Substances 0.000 claims description 29
- 239000000203 mixture Substances 0.000 claims description 28
- 239000004094 surface-active agent Substances 0.000 claims description 22
- 235000019832 sodium triphosphate Nutrition 0.000 claims description 14
- 239000002245 particle Substances 0.000 description 32
- 239000003921 oil Substances 0.000 description 18
- 239000003599 detergent Substances 0.000 description 12
- 229930195733 hydrocarbon Natural products 0.000 description 12
- 150000002430 hydrocarbons Chemical class 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 11
- 239000004215 Carbon black (E152) Substances 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000002518 antifoaming agent Substances 0.000 description 9
- 229920001296 polysiloxane Polymers 0.000 description 8
- 125000000129 anionic group Chemical group 0.000 description 7
- 230000001681 protective effect Effects 0.000 description 7
- 229910019142 PO4 Inorganic materials 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 235000021317 phosphate Nutrition 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 229920000388 Polyphosphate Polymers 0.000 description 4
- 239000013043 chemical agent Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- 239000001205 polyphosphate Substances 0.000 description 4
- 235000011176 polyphosphates Nutrition 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- -1 2-ethylhexyl Chemical group 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 239000011343 solid material Substances 0.000 description 3
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 3
- JHWIEAWILPSRMU-UHFFFAOYSA-N 2-methyl-3-pyrimidin-4-ylpropanoic acid Chemical compound OC(=O)C(C)CC1=CC=NC=N1 JHWIEAWILPSRMU-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000009849 deactivation Effects 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 230000002147 killing effect Effects 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- 125000004437 phosphorous atom Chemical group 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 235000019830 sodium polyphosphate Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- VRTLTXSZIJATNC-UHFFFAOYSA-N [K].[K].[Na].[Na].[Na] Chemical compound [K].[K].[Na].[Na].[Na] VRTLTXSZIJATNC-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 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
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 1
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 235000020030 perry Nutrition 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- KNXVOGGZOFOROK-UHFFFAOYSA-N trimagnesium;dioxido(oxo)silane;hydroxy-oxido-oxosilane Chemical compound [Mg+2].[Mg+2].[Mg+2].O[Si]([O-])=O.O[Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O KNXVOGGZOFOROK-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/71—Paint detackifiers or coagulants, e.g. for the treatment of oversprays in paint spraying installations
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/02—Organic and inorganic agents containing, except water
Definitions
- Substantial efiort has been expanded in an attempt to deactivate the paint particles. These attempts have met with limited success. But all of the methods heretofore proposed fall far short from filling the requirements of an ideal paint killer, as these materials are called.
- One method of deactivation is to utilize chemical agents which at least partially destroy the paint particles, such as sodium hydroxide. Sodium hydroxide is undesirable as an additive agent for several reasons. It is dangerous to use in commercial establishments, and the resulting saponification of the resins in the paint material produces soaps that are at least partially soluble in the water causing increased foaming of the spray booth water. Moreover, the water in the spray booth system becomes increasingly contaminated 'by the presence of these soluble soaps which gradually precipitate out and collect upon the various surfaces of the system.
- Paint killer compounded and used in accordance with this invention deactivates the paint particles instantly when they strike the water and does not require heavy concentrations of chemicals in the water supply so that a large reserve can be maintained in the system and it is necessary to add the chemical agents only infrequently.
- the amount of reserve material which can be maintained in the Water of the spray booth is not severely limited either by lack of solubility or by pH such as is the case with sodium hydroxide.
- the paint particles are so thoroughly deactivated that they will not stick to each other or to the surfaces of the spray booth. It is particularly important that the protective films form substantially instantaneous around each individual particle. This is particularly important in spray booths in which the water moves over the water curtain at a high velocity. After the particles of paint have been killed by the formation of the protective film, the particles form into larger conglomerates, for example of A; to /2 inch in diameter, so that the material can be readily removed from the water. The paint remains deactivated for a substantial period of time, and the solvent action from within the paint particle does not reactivate it.
- the material is capable of deactivating a wide varietyof materials, such as various types of paints, varnishes, lacquers, enamels, and the like, and also of operating effectively with different types of pigments.
- composition of the paint materials that are used in spray booths may vary widely, no single composition can be set forth with the optimum proportions to be used for each application. Although the examples set forth here will give satisfactory results in a wide variety of applications, the particular proportions of the ingredients may be modified in order to better suit the conditions of a particular use or in order to further reduce the cost of the agent while giving satisfactory results for the. particular paint material being used in that particular spray booth.
- anionic surface active agent In order to form a film around each particle of the paint as it strikes the water, I prefer to use an. anionic surface active agent together with a non-ionic surface active agent.
- the anionic surface active agent serving to form a film instantaneously around the particle as it strikes the water, and the non-ionic film serving to reinforce this film to subsequent action.
- an organic phosphorous compound For example, compounds containing sodium phosphorous and oxygen coupled to an organic hydrocarbon.
- One such material is manufactured by the Victor Chemical Company, 141 W. Jackson Boulevard, Chicago 4, Illinois, and is sold under the trade-name Victawet b.
- the composition of this compound is Na3R5(PsOio)2, where R is either 2-ethylhexyl or oc'tyl-2, and is described in Surface Active Agents by Schwartz and Perry (Interscience Publishers, New York, 1949) at page 145 in chapter 6.
- This material forms a continuous film around each of the paint particles without dispersing them into fine separated particles which would be ditlicult to agglomerate.
- the non-ionic surface active agent also can be formed advantageously of an organic phosphate of the non-ionic. type.
- Medium chain alkyl groups attached to a phos phate group are suitable.
- Iv prefer to use a detergent manufactured by the Victor Chemical Company and sold under the trade-narne Victor T12.
- This material includes sodium tripolyphosphate an inorganic phosphates as Well as the non-ionic organic component.
- This active surface. active agent in the detergent T12 is designated in the Handbook of Material Trade Names by Zimmerman and Lavine on page.
- R Alkyl group-:-OP O
- potassium tripolyphosphate or tetraso- -dium monopotassium tripolyphosphate (NasKPsOio) or trisodium dipotassium tripolyphosphate (NasKzPsOrn) or other similar phosphates may be used.
- sodium tripolyphosphate (NazPaOm) is the most versatile for all-around application.
- a low specific gravity lubricating oil is. included which. forms an addition protective film on the solid interfaces.
- Shell Tellus oil. which contains an anti-oxidantsurface active agent, and a. blend of hydrocarbons that have a high adhesionto the surface interfaces.
- Other hydrocarbon oils can be employed. if desired.
- the hydrocarbon oil together with the surface active agents, form a strong permanent isolating film around each of the paint particles so that. even in the presence of the vehicle within the paint particle, the protective film. is not ruptured and the paint. particles 'do not coalesce into a sticky mass that would be difii'cult to handle.
- composition is given as one example: 30 to 60 pounds of an alkali metal polyphosphate, preferably sodium tripol-yphosphate, and 10 to 20 pounds of light hydrocarbon lubricating oil.
- an alkali metal polyphosphate preferably sodium tripol-yphosphate
- 10 to 20 pounds of light hydrocarbon lubricating oil preferably water
- the polyphosphate preferably mixed with a small amount of water and then emulsified by mixing with the oil. This mixture can then be added to the water in. the spray booth: the above quantity being suflicient in most instances to treat l000 gallons of water.
- a somewhat more versatile formulation is as follows: sodium tripolyphosphate-61.5 pounds; alkyl phosphate substituted non-ionic surface active agent with 88 to 90 percent inorganic polyphosphates, such as Victor T12 detergent- 308 pounds; Shell Tellus oil 33-35 pounds.
- the sodium tripolyphosphate and the T12. detergent were first added to a relatively small quantity of water, and when thoroughly dispersed therein, the oil was added gradually to form a relatively stable emulsion. This emulsion was then added to the water of the spray, which in this particular example contained 2800 gallons of water.
- the organic silicone anti-foam agents to be the most sati's factory for this purpose.
- Simi-' lar organic silicones sold by the Dow Company have also been found tobe satisfactory.
- Certain other anti-foam agents maybe used'if desired, but they must be compatible with the solution, suppress the foam, and not interfere with the film-building action of the other materials.
- Octyl alcohol has been used with good results, but a relatively large volume of the anti-foam material. is required and the odor may be objectionable; Generally, the silicone anti-foam agents will be found more satisfactory.
- the material contains surface active agents so that the metal of the spray booth is thoroughly wet by the water, it is important to include in the spray booth solution a suitable amount of rust inhibitor, such as sodium dichromate. Accordingly, I have found that improved results are obtained if about 1.5 pounds of anti-foam emulsion General Electric No. 81224 are added to the above compositions, along with 0.1 pound of sodium dichromate rust inhibitor.
- rust inhibitor such as sodium dichromate
- the agent is packed and sold in two separate packages, one of which contains the solid components and the other of which contains the oil and antifoam emulsions.
- the solid material may be formulated by weight as follows: sodium tripolyphosphate-50 to 75%; detergent Victawet 35b--2 /2 to 5%; Victor T12 detergent25 to 35%; rust inhibitor.l% or less.
- the anti-foam silicone emulsion such as GE 81224, may be added to the oil in the proportion of about one pound of organic silicone to 300 pounds of oil.
- a paint killer composition for the purpose of altering the characteristics of overspray material in paint spray booths to enable easier handling of the overspray material comprising water containing sodium tripolyphosphate, an anionic surface active agent, and a non-ionic surface active agent.
- a paint killer composition as claimed in claim 4 and wherein said water also contains from 10 to 20 parts of low specific gravity hydrocarbon oil.
- a paint killer composition for use in collecting and disposing of overspray material in a spray both comprising water having in solution therein the following ingredients in the following proportions by weight: about pounds of sodium tripolyphosphate; about 30 pounds of Victor T12 detergent; and about 35 pounds of light hydrocarbon oil per about 2800 gallons of water.
- a paint killer composition as claimed in claim 6 and wherein said water also contains from 2 to 4 pounds of detergent Victawet 35b.
- a paint killer composition as claimed in claim 4 and wherein said non-ionic surface active agent is Victor T12 detergent.
- a paint killer composition for deactivating and collecting organic overspray material from a spray booth comprising a water solution containing 30 to 60 pounds of an alkali metal phosphate and 10 to 20 pounds of light hydrocarbon oil per about 1000 gallons of water.
- a paint killer composition for deactivating and collecting organic overspray material from a spray booth comprising a water solution containing per 1000 gallons of water between about 10 and about 20 pounds of light hydrocarbon oil containing about 1 part by weight of organic silicone per 300 parts of oil and between about 30 and about 50 pounds of a mixture comprising between about 50 and about sodium tripolyphosphate; between about 2 /2% and about 5% of Victawet 35b detergent and between about 25% and about 35% of Victo T12 detergent.
- a composition for use in deactivating and recovering overspray of coating materials comprising a solution of sodium polyphosphate in water emulsified with light hydrocarbon oil.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
Description
nited PAINT KILLER No Drawing. Application October 21, 1952, Serial No. 316,049
15 Claims. (Cl. 106-287) This invention relates to chemical agents which are added to the water used in a spray booth to trap the particles of paint which do not adhere to the articles being sprayed. These chemical agents are for the purpose of deactivating the paint particles so that they will not coalesce into a sticky mass that is difiicult to handle, and so that neither the individual particles nor any coalesced masses of it will adhere to the spray booth or parts of the water circulating system.
Substantial efiort has been expanded in an attempt to deactivate the paint particles. These attempts have met with limited success. But all of the methods heretofore proposed fall far short from filling the requirements of an ideal paint killer, as these materials are called. One method of deactivation is to utilize chemical agents which at least partially destroy the paint particles, such as sodium hydroxide. Sodium hydroxide is undesirable as an additive agent for several reasons. It is dangerous to use in commercial establishments, and the resulting saponification of the resins in the paint material produces soaps that are at least partially soluble in the water causing increased foaming of the spray booth water. Moreover, the water in the spray booth system becomes increasingly contaminated 'by the presence of these soluble soaps which gradually precipitate out and collect upon the various surfaces of the system.
Another approach to the system has been the addition of finely divided inert materials to the water such as graphite, 'bentonite, asbestine, and the like. Such particles may act somewhat as an absorbent of liquid or gaseous ingredients and as a solid protective coating about the solid particles which are recovered, but they are relatively ineffective in deactivating the various paints and finishing materials and relatively large quantities must be added to the water in the spray booth system before even partial deactivation is obtained.
Another approach has been to add agents to the spray 'atent booth water which will form a protective film around each particle of paint as it is taken in by the water. This film, in theory, would then remain around the particle of paint and would prevent the paint from coalescing into a large mass and would also prevent it from sticking to the surfaces of the spray booth. For example, Saunders in U. S. Patent No. 2,086,514 proposes the use of a mineral oil comprising an emulsion of soluble oil in waterand in his Patent 2,208,647 proposes that an alkali salt of a sulphonated hydrocarbon of the resin class he added to the water of the spray booth. In U. S. Patent No. 2,161,122, Anderson describes the use of aluminum hydroxide for this purpose. However, this and other materials heretofore proposed and to some extent utilized,
"have been relatively inefiective. For example, some materials which immediately deactivate or kill each of the paint particles as it strikes the water gradually lose their protective effect, either because of the release of solvent from within the paint particle or because the film eventually is ruptured or otherwise removed from the particle: the particles then coalesce and form a sticky mass that 2,739,93 Patented Mar. 27, 1956 ice is diflicult to handle and which adheres to the surfaces of the spray booth.
Other'materials which form somewhat more stable films do not form the films rapidly enough, so that after the particles strike the water, there is a substantial amount of coalescence before the formation of the surface film, at which time the ratio of the mass to surface area is so great that the film cannot effectively kill the paint particle. Moreover, if the paint particles is not deactivated immediately upon striking the water, some of the particles will adhere to the surfaces of the spray booth before the formation of the deactivating film. With a large volume of over-spray, the paint must be fairly permenently deactivated or it will sink to the bottom of the water and form a sticky mass very diflicult to remove.
In accordance with the present invention, a method of killing paint is provided which has substantial advantages over the prior methods and additive agents.
Paint killer compounded and used in accordance with this invention deactivates the paint particles instantly when they strike the water and does not require heavy concentrations of chemicals in the water supply so that a large reserve can be maintained in the system and it is necessary to add the chemical agents only infrequently. The amount of reserve material which can be maintained in the Water of the spray booth is not severely limited either by lack of solubility or by pH such as is the case with sodium hydroxide.
It is preferred, however, to add the paint killer continually and automatically thus preventing any possibility of the solution decreasing below the minimum concentration required for complete killing action. The addition of the reagents at the rate of only a few milliliters per minute will maintain the necessary concentration in spray booths of the usual capacity.
The paint particles are so thoroughly deactivated that they will not stick to each other or to the surfaces of the spray booth. It is particularly important that the protective films form substantially instantaneous around each individual particle. This is particularly important in spray booths in which the water moves over the water curtain at a high velocity. After the particles of paint have been killed by the formation of the protective film, the particles form into larger conglomerates, for example of A; to /2 inch in diameter, so that the material can be readily removed from the water. The paint remains deactivated for a substantial period of time, and the solvent action from within the paint particle does not reactivate it. The material is capable of deactivating a wide varietyof materials, such as various types of paints, varnishes, lacquers, enamels, and the like, and also of operating effectively with different types of pigments.
In general, it is much easier to remove the killed paint if it is caused to float on the surface of the water. Overspray treated in the manner described herein is formed into a conglomerate curdy mass that contains substantial air, and this trapped air causes the mass of the conglomerate to be substantially less than that of water, so that even heavy paint such as red-oxide primer and the like temporarily, but if no other film formation took place, the particle would soon be reactivated and would then return it its former sticky condition. However, other agents are added to the water of the spray booth, so that a second and more permanent film forms at a somewhat.
slower rate. This multiple film formation also permits the formulation of materials having a much wider range of operability than when only a single layer is to be formed. These and other objects and advantages of the present invention will be apparent from a consideration of the following specific examples of preferred embodiments of the invention.
Because the composition of the paint materials that are used in spray booths may vary widely, no single composition can be set forth with the optimum proportions to be used for each application. Although the examples set forth here will give satisfactory results in a wide variety of applications, the particular proportions of the ingredients may be modified in order to better suit the conditions of a particular use or in order to further reduce the cost of the agent while giving satisfactory results for the. particular paint material being used in that particular spray booth.
In order to form a film around each particle of the paint as it strikes the water, I prefer to use an. anionic surface active agent together with a non-ionic surface active agent. The anionic surface active agent serving to form a film instantaneously around the particle as it strikes the water, and the non-ionic film serving to reinforce this film to subsequent action.
For the anionic surface active agent, I prefer to use an organic phosphorous compound. For example, compounds containing sodium phosphorous and oxygen coupled to an organic hydrocarbon. One such material is manufactured by the Victor Chemical Company, 141 W. Jackson Boulevard, Chicago 4, Illinois, and is sold under the trade-name Victawet b. The composition of this compound is Na3R5(PsOio)2, where R is either 2-ethylhexyl or oc'tyl-2, and is described in Surface Active Agents by Schwartz and Perry (Interscience Publishers, New York, 1949) at page 145 in chapter 6. This material forms a continuous film around each of the paint particles without dispersing them into fine separated particles which would be ditlicult to agglomerate. Only relatively small concentrations of this material are required in order to produce the thin protective film. The chemical structure of this compound is such as to provide a desirable balance in the relationship between the polar groups which are soluble in water, and the organic groups which form the interface with the paint particles. Another material, sold by the same company under the trade designation Victawet 34b, is also suitable and has the same. general formula but in which the R is iso-octyl. Similar compounds in which the R represents. normal butyl', isoamyl, l-heptyl, capryl alkyl radicals, or the like are also suitable.
The non-ionic surface active agent also can be formed advantageously of an organic phosphate of the non-ionic. type. Medium chain alkyl groups attached to a phos phate group are suitable. For this purpose, Iv prefer to use a detergent manufactured by the Victor Chemical Company and sold under the trade-narne Victor T12. This material includes sodium tripolyphosphate an inorganic phosphates as Well as the non-ionic organic component. There is approximately ten to twelve percent of this non-ionic organic phosphate surface active agent in the detergent T12. This active surface. active agent in the detergent T12 is designated in the Handbook of Material Trade Names by Zimmerman and Lavine on page. 604, as a substituted phosphate in which one of the oxygens is connected to the phosphorous atom and also to an alkyl group which may vary in the sizes of the medium chain hydrocarbons. Two of the other oxygens in the orthophosphate are connected onto the phosphorous atom and alsoto a water solubilizing group designated in this case as R. The general structure maybe written as follows:
R Alkyl group-:-OP=O Alternatively, potassium tripolyphosphate or tetraso- -dium monopotassium tripolyphosphate (NasKPsOio) or trisodium dipotassium tripolyphosphate (NasKzPsOrn) or other similar phosphates may be used. However, I have found sodium tripolyphosphate (NazPaOm) to be the most versatile for all-around application. As an alkaline builder, which supplies additional phosphates and which also serves to control the pH of the solution for maximum film building action, I use sodium tripolyphosphate (NasPsOro) together with the surface active agents just mentioned.
In addition to the above components, a low specific gravity lubricating oil is. included which. forms an addition protective film on the solid interfaces. For this purpose,
I have used the oil sold under the trade-name Shell Tellus oil.,33 which contains an anti-oxidantsurface active agent, and a. blend of hydrocarbons that have a high adhesionto the surface interfaces. Other hydrocarbon oils can be employed. if desired.
The hydrocarbon oil, together with the surface active agents, form a strong permanent isolating film around each of the paint particles so that. even in the presence of the vehicle within the paint particle, the protective film. is not ruptured and the paint. particles 'do not coalesce into a sticky mass that would be difii'cult to handle.
The following composition is given as one example: 30 to 60 pounds of an alkali metal polyphosphate, preferably sodium tripol-yphosphate, and 10 to 20 pounds of light hydrocarbon lubricating oil. In use the polyphosphate preferably mixed with a small amount of water and then emulsified by mixing with the oil. This mixture can then be added to the water in. the spray booth: the above quantity being suflicient in most instances to treat l000 gallons of water. a i
The above formulation, although working well with some organic coating materials, does not give ideal results with all materials. A somewhat more versatile formulation is as follows: sodium tripolyphosphate-61.5 pounds; alkyl phosphate substituted non-ionic surface active agent with 88 to 90 percent inorganic polyphosphates, such as Victor T12 detergent- 308 pounds; Shell Tellus oil 33-35 pounds. The sodium tripolyphosphate and the T12. detergent were first added to a relatively small quantity of water, and when thoroughly dispersed therein, the oil was added gradually to form a relatively stable emulsion. This emulsion was then added to the water of the spray, which in this particular example contained 2800 gallons of water.
If desired, from two to four pounds of detergent. Victawet.
the organic silicone anti-foam agents to be the most sati's factory for this purpose. For example, the silicone antifoam materials sold by General Electric under the numbers 81224 or 81066 'have'been'found satisfactory. Simi-' lar organic silicones sold by the Dow Company have also been found tobe satisfactory. Certain other anti-foam agents maybe used'if desired, but they must be compatible with the solution, suppress the foam, and not interfere with the film-building action of the other materials. Octyl alcohol has been used with good results, but a relatively large volume of the anti-foam material. is required and the odor may be objectionable; Generally, the silicone anti-foam agents will be found more satisfactory.
Because the material contains surface active agents so that the metal of the spray booth is thoroughly wet by the water, it is important to include in the spray booth solution a suitable amount of rust inhibitor, such as sodium dichromate. Accordingly, I have found that improved results are obtained if about 1.5 pounds of anti-foam emulsion General Electric No. 81224 are added to the above compositions, along with 0.1 pound of sodium dichromate rust inhibitor.
Preferably, the agent is packed and sold in two separate packages, one of which contains the solid components and the other of which contains the oil and antifoam emulsions. In general, the solid material may be formulated by weight as follows: sodium tripolyphosphate-50 to 75%; detergent Victawet 35b--2 /2 to 5%; Victor T12 detergent25 to 35%; rust inhibitor.l% or less. The anti-foam silicone emulsion, such as GE 81224, may be added to the oil in the proportion of about one pound of organic silicone to 300 pounds of oil.
In use, about 30 to 50 pounds of the solid material are used for each thousand gallons of water in the spray booth equipment, and from to pounds of the oil containing the organic silicone anti-foam agent as set forth above.
I have found also that sodium aluminate may be added to the formulation and will provide better suspension and more effective film-building properties. The sodium' aluminate may be added in the proportions between 2 /2 to 10% by weight of the total amount of solid material, the preferred range being between 3 and 4%. The pH may range between 7 and 10 or even as high as 12, but is preferably maintained between 8 and 9. The resulting solution is harmless so far as possible injury to the workmen is concerned.
I claim:
1. A paint killer composition for the purpose of altering the characteristics of overspray material in paint spray booths to enable easier handling of the overspray material comprising water containing sodium tripolyphosphate, an anionic surface active agent, and a non-ionic surface active agent.
2. A paint killer composition as claimed in claim 1 wherein said water contains the said ingredients in the following relative proportions by weight: 50 to 75 parts of sodium tripolyphosphate; 2.5 to 5 parts of anionic surface active agent; and to 35 parts of non-ionic surface active agent.
3. A paint killer composition as claimed in claim 2 wherein said anionic surface agent is Victawet 35b and said non-ionic surface active agent is Victor T12 detergent.
4. A paint killer composition for use in handling the overspray material in a spray booth comprising water containing by weight: 50 to 75 parts of a sodium polyphosphate; 2.5 to 5.0 parts of Na3R5(P3O1o)2, where R is 2- ethylhexyl, and from 25 to 35 parts of a non-ionic surface active agent.
5. A paint killer composition as claimed in claim 4 and wherein said water also contains from 10 to 20 parts of low specific gravity hydrocarbon oil.
6. A paint killer composition for use in collecting and disposing of overspray material in a spray both comprising water having in solution therein the following ingredients in the following proportions by weight: about pounds of sodium tripolyphosphate; about 30 pounds of Victor T12 detergent; and about 35 pounds of light hydrocarbon oil per about 2800 gallons of water.
7. A paint killer composition as claimed in claim 6 and wherein said water also contains from 2 to 4 pounds of detergent Victawet 35b.
8. A paint killer composition as claimed in claim 4 and wherein said non-ionic surface active agent is Victor T12 detergent.
9. A paint killer composition for deactivating and collecting organic overspray material from a spray booth comprising a water solution containing 30 to 60 pounds of an alkali metal phosphate and 10 to 20 pounds of light hydrocarbon oil per about 1000 gallons of water.
10. A paint killer composition as claimed in claim 9 and wherein said alkali metal is sodium.
11. A paint killer composition as claimed in claim 10 wherein the alkali metal polyphosphate is sodium tripolyphosphate.
12. A paint killer composition as claimed in claim 11 wherein said solution includes a non-ionic surface active agent.
13. A paint killer composition as claimed in claim 12 and wherein said solution includes an anionic surface active agent.
14. A paint killer composition for deactivating and collecting organic overspray material from a spray booth comprising a water solution containing per 1000 gallons of water between about 10 and about 20 pounds of light hydrocarbon oil containing about 1 part by weight of organic silicone per 300 parts of oil and between about 30 and about 50 pounds of a mixture comprising between about 50 and about sodium tripolyphosphate; between about 2 /2% and about 5% of Victawet 35b detergent and between about 25% and about 35% of Victo T12 detergent.
15. A composition for use in deactivating and recovering overspray of coating materials comprising a solution of sodium polyphosphate in water emulsified with light hydrocarbon oil.
References Cited in the file of this patent UNITED STATES PATENTS 2,208,647 Saunders July 23, 1940 2,348,625 Hoffman May 9, 1944 2,362,964 Affieck Nov. 21, 1944 2,550,691 Harris May 1, 1951 2,586,897 Woodstock Feb. 26, 1952
Claims (1)
1. A PAINT KILLER COMPOSITION FOR THE PURPOSE OF ALTERING THE CHARACTERISTICS OF OVERSPRAY MATERIAL IN PAINT SPRAY BOOTHS TO ENABLE EASIER HANDLING OF THE OVERSPRAY MATERIAL COMPRISING WATER CONTAINING SODIUM TRIPOLYPHOSPHATE, AN ANIONIC SURFACE ACTIVE AGENT, AND A NON-IONIC SURFACE ACTIVE AGENT.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US316049A US2739903A (en) | 1952-10-21 | 1952-10-21 | Paint killer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US316049A US2739903A (en) | 1952-10-21 | 1952-10-21 | Paint killer |
Publications (1)
Publication Number | Publication Date |
---|---|
US2739903A true US2739903A (en) | 1956-03-27 |
Family
ID=23227251
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US316049A Expired - Lifetime US2739903A (en) | 1952-10-21 | 1952-10-21 | Paint killer |
Country Status (1)
Country | Link |
---|---|
US (1) | US2739903A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2877866A (en) * | 1954-08-26 | 1959-03-17 | Phillips Petroleum Co | Improved quenching method |
US2982723A (en) * | 1954-12-31 | 1961-05-02 | Ajem Lab Inc | Method for handling overspray materials |
US2983685A (en) * | 1956-09-19 | 1961-05-09 | Ajem Lab Inc | Absorbent solution for core oven fumes |
US3110677A (en) * | 1959-04-23 | 1963-11-12 | Olin Mathieson | Chlorinated trisodium phosphate |
US3421940A (en) * | 1961-01-27 | 1969-01-14 | Bohme Fettchemie Gmbh | Washing agents and process for machine washing of dishes |
US4090001A (en) * | 1973-03-28 | 1978-05-16 | Air-Industrie | Compositions for denaturing paints, especially for cleaning painting cabins |
US4125476A (en) * | 1977-03-10 | 1978-11-14 | Dean Ralph R | Paint spray booth composition |
US4185970A (en) * | 1977-03-10 | 1980-01-29 | Dean Ralph R | Paint spray booth composition |
US5092928A (en) * | 1990-05-25 | 1992-03-03 | Caterpillar Inc. | Process for recovering paint overspray particles |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2208647A (en) * | 1937-10-15 | 1940-07-23 | Chrysler Corp | Coating material recovery process |
US2348625A (en) * | 1939-07-06 | 1944-05-09 | Harry E Hoffman | Method for the recovery of sprayed paint material |
US2362964A (en) * | 1940-08-02 | 1944-11-21 | Gregor S Afflcck | Recovery addition agent and method of making |
US2550691A (en) * | 1951-05-01 | Nongorrosive detergent | ||
US2586897A (en) * | 1948-07-03 | 1952-02-26 | Victor Chemical Works | Detergent composition |
-
1952
- 1952-10-21 US US316049A patent/US2739903A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2550691A (en) * | 1951-05-01 | Nongorrosive detergent | ||
US2208647A (en) * | 1937-10-15 | 1940-07-23 | Chrysler Corp | Coating material recovery process |
US2348625A (en) * | 1939-07-06 | 1944-05-09 | Harry E Hoffman | Method for the recovery of sprayed paint material |
US2362964A (en) * | 1940-08-02 | 1944-11-21 | Gregor S Afflcck | Recovery addition agent and method of making |
US2586897A (en) * | 1948-07-03 | 1952-02-26 | Victor Chemical Works | Detergent composition |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2877866A (en) * | 1954-08-26 | 1959-03-17 | Phillips Petroleum Co | Improved quenching method |
US2982723A (en) * | 1954-12-31 | 1961-05-02 | Ajem Lab Inc | Method for handling overspray materials |
US2983685A (en) * | 1956-09-19 | 1961-05-09 | Ajem Lab Inc | Absorbent solution for core oven fumes |
US3110677A (en) * | 1959-04-23 | 1963-11-12 | Olin Mathieson | Chlorinated trisodium phosphate |
US3421940A (en) * | 1961-01-27 | 1969-01-14 | Bohme Fettchemie Gmbh | Washing agents and process for machine washing of dishes |
US4090001A (en) * | 1973-03-28 | 1978-05-16 | Air-Industrie | Compositions for denaturing paints, especially for cleaning painting cabins |
US4125476A (en) * | 1977-03-10 | 1978-11-14 | Dean Ralph R | Paint spray booth composition |
US4185970A (en) * | 1977-03-10 | 1980-01-29 | Dean Ralph R | Paint spray booth composition |
US5092928A (en) * | 1990-05-25 | 1992-03-03 | Caterpillar Inc. | Process for recovering paint overspray particles |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4564464A (en) | Hectorite based paint spray booth detackifying slurries and methods of use thereof | |
US2739903A (en) | Paint killer | |
US4220456A (en) | Paint removal composition spray method for paint booths | |
DE69006853T2 (en) | METHOD FOR RECOVERY OF PARTICLES OF SPRAYED COLOR. | |
US4185970A (en) | Paint spray booth composition | |
US4629477A (en) | Coagulating compositions containing a cyanamide component for coagulating lacquers, waxes and coating compositions | |
US4125476A (en) | Paint spray booth composition | |
EP0312987A2 (en) | A method for paint removal using oil-in-water emulsions | |
US6294104B1 (en) | Liquid for the prevention of freezing of aircrafts and runways | |
US2362964A (en) | Recovery addition agent and method of making | |
DE3719929A1 (en) | USE OF AN ORGANOPHILIC CLAY FOR SEPARATING THE OIL PHASE FROM OEL-IN-WATER SUSPENSIONS | |
US5863456A (en) | Fluid, formulation and method for dust control and dewatering of particulate materials | |
US4380495A (en) | Method of treating spray paint collection water in paint spray booths and composition therefor | |
US4714564A (en) | High performance multifunctional corrosion inhibitors especially for combining at 20 to 50 weight percent with soap or paint | |
US4409119A (en) | Process for regenerating cleaning solutions | |
TW364013B (en) | Low-foaming, liquid cleaning composition | |
US3010907A (en) | Alkaline cleaning compositions | |
EP1064334B1 (en) | Aqueous composition for removing coatings | |
US3609089A (en) | Process for cleaning road vehicles and composition | |
US2585407A (en) | Spray booth wash and a process of making it | |
US3341467A (en) | Method of inhibiting foaming in aqueous systems | |
JPH06500132A (en) | Two-component coagulant for paints, waxes and coating compositions | |
CA2072061C (en) | Paint denaturant | |
JPH0631281A (en) | Additive for circulating water of wet coating booth | |
CA1207217A (en) | Paint detackification using oil-in-water emulsions |