CA2068571C - Method for removing paint solids from water-based paint systems using aluminum salts - Google Patents
Method for removing paint solids from water-based paint systems using aluminum salts Download PDFInfo
- Publication number
- CA2068571C CA2068571C CA002068571A CA2068571A CA2068571C CA 2068571 C CA2068571 C CA 2068571C CA 002068571 A CA002068571 A CA 002068571A CA 2068571 A CA2068571 A CA 2068571A CA 2068571 C CA2068571 C CA 2068571C
- Authority
- CA
- Canada
- Prior art keywords
- water
- paint
- aluminum
- alkalinity
- aluminum salt
- Prior art date
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Links
- 239000003973 paint Substances 0.000 title claims abstract description 104
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 83
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 title claims abstract description 39
- 238000000034 method Methods 0.000 title claims abstract description 28
- 239000007787 solid Substances 0.000 title description 33
- 239000007921 spray Substances 0.000 claims abstract description 33
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims abstract description 10
- 239000010802 sludge Substances 0.000 claims abstract description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims abstract description 7
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 24
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 14
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 12
- 235000017550 sodium carbonate Nutrition 0.000 claims description 12
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 229920002401 polyacrylamide Polymers 0.000 claims description 10
- LVYZJEPLMYTTGH-UHFFFAOYSA-H dialuminum chloride pentahydroxide dihydrate Chemical compound [Cl-].[Al+3].[OH-].[OH-].[Al+3].[OH-].[OH-].[OH-].O.O LVYZJEPLMYTTGH-UHFFFAOYSA-H 0.000 claims description 9
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 8
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 7
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 5
- 125000002091 cationic group Chemical group 0.000 claims description 4
- 235000011118 potassium hydroxide Nutrition 0.000 claims description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims description 3
- 229920001577 copolymer Polymers 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- 235000011121 sodium hydroxide Nutrition 0.000 claims description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- 229920000867 polyelectrolyte Polymers 0.000 claims description 2
- GDTSJMKGXGJFGQ-UHFFFAOYSA-N 3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound O1B([O-])OB2OB([O-])OB1O2 GDTSJMKGXGJFGQ-UHFFFAOYSA-N 0.000 claims 2
- 229920000642 polymer Polymers 0.000 description 14
- 229910052782 aluminium Inorganic materials 0.000 description 12
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 9
- 229940001593 sodium carbonate Drugs 0.000 description 9
- 239000008394 flocculating agent Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- -1 ALUMINUM SALTS Chemical class 0.000 description 6
- 238000005187 foaming Methods 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000006228 supernatant Substances 0.000 description 4
- 238000002834 transmittance Methods 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- 229940037003 alum Drugs 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- YIOJGTBNHQAVBO-UHFFFAOYSA-N dimethyl-bis(prop-2-enyl)azanium Chemical compound C=CC[N+](C)(C)CC=C YIOJGTBNHQAVBO-UHFFFAOYSA-N 0.000 description 3
- 238000007667 floating Methods 0.000 description 3
- 238000012812 general test Methods 0.000 description 3
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- FZGFBJMPSHGTRQ-UHFFFAOYSA-M trimethyl(2-prop-2-enoyloxyethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCOC(=O)C=C FZGFBJMPSHGTRQ-UHFFFAOYSA-M 0.000 description 3
- RRHXZLALVWBDKH-UHFFFAOYSA-M trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)OCC[N+](C)(C)C RRHXZLALVWBDKH-UHFFFAOYSA-M 0.000 description 3
- UZNHKBFIBYXPDV-UHFFFAOYSA-N trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)NCCC[N+](C)(C)C UZNHKBFIBYXPDV-UHFFFAOYSA-N 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229920006317 cationic polymer Polymers 0.000 description 2
- 239000003518 caustics Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000005188 flotation Methods 0.000 description 2
- 238000011221 initial treatment Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 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 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 235000019687 Lamb Nutrition 0.000 description 1
- 239000004614 Process Aid Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 150000001449 anionic compounds Chemical class 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
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 1
- IOMDIVZAGXCCAC-UHFFFAOYSA-M diethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](CC)(CC)CC=C IOMDIVZAGXCCAC-UHFFFAOYSA-M 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 229910001412 inorganic anion Inorganic materials 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- ITFGZZGYXVHOOU-UHFFFAOYSA-N n,n-dimethylmethanamine;methyl hydrogen sulfate Chemical compound C[NH+](C)C.COS([O-])(=O)=O ITFGZZGYXVHOOU-UHFFFAOYSA-N 0.000 description 1
- PZNOBXVHZYGUEX-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine;hydrochloride Chemical compound Cl.C=CCNCC=C PZNOBXVHZYGUEX-UHFFFAOYSA-N 0.000 description 1
- 238000011369 optimal treatment Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920003009 polyurethane dispersion Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 235000019795 sodium metasilicate Nutrition 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000000954 titration curve Methods 0.000 description 1
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 1
- 239000012855 volatile organic compound Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/54—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using organic material
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/5236—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/5236—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents
- C02F1/5245—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents using basic salts, e.g. of aluminium and iron
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/14—Paint wastes
-
- 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
- Y10S210/00—Liquid purification or separation
- Y10S210/93—Paint detackifying
Abstract
Methods of treating circulating water containing oversprayed, water-borne paint, such as in a paint spray booth operation, with aluminum salts such as aluminum chloride or polyaluminum chloride and a flocculant, resulting in removal of sludge from the paint spray booth water.
Description
~~b~~~~
TITLE OF THE INVENTION
°'METHOD FOR REMOVING PAINT SOLIDS FROM
WATER-BASED PAINT SYSTEMS USING' ALUMINUM SALTS"
BACKGROUND OF THE INVENTION
Automobile bodies and many industrial and consumer articles are conventionally spray painted in areas called spray booths, wherein water is employed to cleanse the air of over-sprayed paint. The wash water is then treated to remove paint solids, and the treated water is recirculated. The circulating water typically contains less than about 10,000 ppm of suspended .t 0 solids. A well run system generally contains less than about 500 ppm of suspended solids in the circulating water.
Fine droplets of over-sprayed paint, emitted by a spray gun, contact and are captured by the water. The amount of paint contacting a water curtain may change depending on a number of variables, including plant or ~~~~~71 rocess shutdowns, the size and shape of the object being painted, the type of spray equipment used, the spraying and purge technique used, the water flow rate and the type of paint used.
Tn the past, solvent-based or solvent-borne paints have commonly been employed in spray booths. Federal regulations now limit the amount of volatile organic compounds (i.e., vocs) that can be released at a given plant site. Since organic solvent diluents used in solvent-based paint are a major source of vocs, water-borne or water-based paints are now being used in spray booth operations to help comp~.y with t~aese regulations.
The term "water-based paints°°, as used herein, refers to all varieties of coatings which contain in excess of approximately 10$ water in the coating formulation, including, but not limited to, water-reducible alkyd and epoxy ester compositions, water-borne thermoplastic compositions using acrylic polymer/copolymers; water-based polyurethane dispersions, and blends of such compositions. As used herein, the terms °'water-based paints°° and "water-borne paints" are synonymous.
~0~~~'~l ~.
g -C°1496 A primary treatment objective relative to solvent-based paints concerns the tacky or adhesive nature of the over-sprayed coating material. Due to their hydrophobicity, solvent-based solids tend to coalesce and adhere to the walls, ceilings, floors or spray areas of spray booth systems and in their scrubber sections. Thus, the over-sprayed paint mist captured in the water system of a spray booth must be detackified, or "killed," to prevent accumulation on the walls, piping, etc. of the spray booth system.
Paint that sticks to spray booth surfaces usually cannot be easily removed from equipment and tends to build up over time, thereby hampering spray booth efficacy.
In contrast, the primary treatment objective ,0 relative to water-based paints is to capture and collect finely-dispersed paint solids. Water-based paints are not tacky in nature. However, without treatment, these paints tend to remain dispersed due to their compatability with water. Ultimately, uncaptured solids accumulate~in the system and settle in sludge recovery pits and in booth weirs. such solids encourage the growth of anaerobic bacteria colonies which may result in odor problems. This treatment problem is aggravated by the use of water-based paints because such paints generally contain resins and dyes which are highly compatible with water.
4 _ Other problems which severely interfere with spray booth operations occur in areas of high agitation where foaming occurs and in areas where foam accumulates.
Foaming is caused by chemical additives, surfactants, solvents or combinations thereof. Also, finely dispersed paint solids which are not captured and removed tend to stabilize foam, which aggravates foaming problems. Foaming generally mandates that copious amounts of defoamers be used, which results in higher operating costs. Water--based paints generally tend to cause foaming to a greater extent than solvent-based paints.
A wide variety of chemicals have been proposed as treating agents for circul<~ting wet spray booth waters containing over-spray paint, including compositions containing polymers and amphoteric metal salts which farm insoluble hydroxides at pH~s greater than about 7. The use of combinations of this type are described in the following U.S. Pats.; 3,861,887 to Forney;
3,990,986 to Gabel et al; 4,002,490 to Miahalski et al;
25 4,130,674 to Robeirts et al; and 4,440,647 to Puchalski. Further, U.S. Pat. Ido. 4,637,824 to Pominville discloses the use of silicates and polydiallyldialkylammonium halides with amphoteric metal salts, and U.S. Pat. No. 4,853,132 to Merrell et al discloses the use of precipitates formed by the reaction of cationic polymers and salts of inorganic anions to detackify solvent-based paints. Benton~.te ~0~~~~~
c-149s clays, aluminum salts and zinc salts have also been used with cationic polymers. U.S. Pat. No. 4,401,574 to Farrington et al discloses the use of polyaluminum chloride to flocculate and settle dispersed paint solids resulting from the production of latex paints and U.S. Pat. No. 4,026,794 to Mauceri discloses water soluble salts of amphoteric metals in combination with dimethyl diallyl ammonium polymers to bxeak oil-in-water emulsions. ~P52071538 discloses 'the use of coagulants such as aluminum sulphate, aluminum polychloride and calcium hydroxide in combination with 15 polymer accelerators to aggregate coating particles in coating booth waste water steams. U.S. Pat. Nos.
4,759,855 arid 4,880,471 disclose the use of alkaline zinc solutions containing ammonium hydroxide and ammonium chloride to treat .over-sprayed paint.
DESCRIPTTON OF THE DRAWINGS
Figure 1 shows relationship between pH and alkalinity using various alkalinity sources in a system ~5 containing water-borne paints. In this figure, the pH
for optimum paint collection is that pH where water clarity and paint flotation are maximized, with minimal suspended solids. This figure represents a system containing a cIL white water-borne paint with 1000 ppm 80 of aluminum chlorohydrate.
TITLE OF THE INVENTION
°'METHOD FOR REMOVING PAINT SOLIDS FROM
WATER-BASED PAINT SYSTEMS USING' ALUMINUM SALTS"
BACKGROUND OF THE INVENTION
Automobile bodies and many industrial and consumer articles are conventionally spray painted in areas called spray booths, wherein water is employed to cleanse the air of over-sprayed paint. The wash water is then treated to remove paint solids, and the treated water is recirculated. The circulating water typically contains less than about 10,000 ppm of suspended .t 0 solids. A well run system generally contains less than about 500 ppm of suspended solids in the circulating water.
Fine droplets of over-sprayed paint, emitted by a spray gun, contact and are captured by the water. The amount of paint contacting a water curtain may change depending on a number of variables, including plant or ~~~~~71 rocess shutdowns, the size and shape of the object being painted, the type of spray equipment used, the spraying and purge technique used, the water flow rate and the type of paint used.
Tn the past, solvent-based or solvent-borne paints have commonly been employed in spray booths. Federal regulations now limit the amount of volatile organic compounds (i.e., vocs) that can be released at a given plant site. Since organic solvent diluents used in solvent-based paint are a major source of vocs, water-borne or water-based paints are now being used in spray booth operations to help comp~.y with t~aese regulations.
The term "water-based paints°°, as used herein, refers to all varieties of coatings which contain in excess of approximately 10$ water in the coating formulation, including, but not limited to, water-reducible alkyd and epoxy ester compositions, water-borne thermoplastic compositions using acrylic polymer/copolymers; water-based polyurethane dispersions, and blends of such compositions. As used herein, the terms °'water-based paints°° and "water-borne paints" are synonymous.
~0~~~'~l ~.
g -C°1496 A primary treatment objective relative to solvent-based paints concerns the tacky or adhesive nature of the over-sprayed coating material. Due to their hydrophobicity, solvent-based solids tend to coalesce and adhere to the walls, ceilings, floors or spray areas of spray booth systems and in their scrubber sections. Thus, the over-sprayed paint mist captured in the water system of a spray booth must be detackified, or "killed," to prevent accumulation on the walls, piping, etc. of the spray booth system.
Paint that sticks to spray booth surfaces usually cannot be easily removed from equipment and tends to build up over time, thereby hampering spray booth efficacy.
In contrast, the primary treatment objective ,0 relative to water-based paints is to capture and collect finely-dispersed paint solids. Water-based paints are not tacky in nature. However, without treatment, these paints tend to remain dispersed due to their compatability with water. Ultimately, uncaptured solids accumulate~in the system and settle in sludge recovery pits and in booth weirs. such solids encourage the growth of anaerobic bacteria colonies which may result in odor problems. This treatment problem is aggravated by the use of water-based paints because such paints generally contain resins and dyes which are highly compatible with water.
4 _ Other problems which severely interfere with spray booth operations occur in areas of high agitation where foaming occurs and in areas where foam accumulates.
Foaming is caused by chemical additives, surfactants, solvents or combinations thereof. Also, finely dispersed paint solids which are not captured and removed tend to stabilize foam, which aggravates foaming problems. Foaming generally mandates that copious amounts of defoamers be used, which results in higher operating costs. Water--based paints generally tend to cause foaming to a greater extent than solvent-based paints.
A wide variety of chemicals have been proposed as treating agents for circul<~ting wet spray booth waters containing over-spray paint, including compositions containing polymers and amphoteric metal salts which farm insoluble hydroxides at pH~s greater than about 7. The use of combinations of this type are described in the following U.S. Pats.; 3,861,887 to Forney;
3,990,986 to Gabel et al; 4,002,490 to Miahalski et al;
25 4,130,674 to Robeirts et al; and 4,440,647 to Puchalski. Further, U.S. Pat. Ido. 4,637,824 to Pominville discloses the use of silicates and polydiallyldialkylammonium halides with amphoteric metal salts, and U.S. Pat. No. 4,853,132 to Merrell et al discloses the use of precipitates formed by the reaction of cationic polymers and salts of inorganic anions to detackify solvent-based paints. Benton~.te ~0~~~~~
c-149s clays, aluminum salts and zinc salts have also been used with cationic polymers. U.S. Pat. No. 4,401,574 to Farrington et al discloses the use of polyaluminum chloride to flocculate and settle dispersed paint solids resulting from the production of latex paints and U.S. Pat. No. 4,026,794 to Mauceri discloses water soluble salts of amphoteric metals in combination with dimethyl diallyl ammonium polymers to bxeak oil-in-water emulsions. ~P52071538 discloses 'the use of coagulants such as aluminum sulphate, aluminum polychloride and calcium hydroxide in combination with 15 polymer accelerators to aggregate coating particles in coating booth waste water steams. U.S. Pat. Nos.
4,759,855 arid 4,880,471 disclose the use of alkaline zinc solutions containing ammonium hydroxide and ammonium chloride to treat .over-sprayed paint.
DESCRIPTTON OF THE DRAWINGS
Figure 1 shows relationship between pH and alkalinity using various alkalinity sources in a system ~5 containing water-borne paints. In this figure, the pH
for optimum paint collection is that pH where water clarity and paint flotation are maximized, with minimal suspended solids. This figure represents a system containing a cIL white water-borne paint with 1000 ppm 80 of aluminum chlorohydrate.
2~~~~~1 _6_ Figure 2 shows the optimum operating window for a system containing a CIL white water-borne paint, sodium carbonate as the alkalinity source and aluminum chlorohydrate as the aluminum salt.
Figure 3 shows the titration curves of various aluminum salts with a sodium car-bonate alkalinity source.
Figure 4 shows the impact of pH on treatment performance, in terms of subnatant clarity. In the 1g system represented by this :Figure, a CIL white water-based paint was treated with soda ash and aluminum chlorohydrate.
SUMMARY OF THE INVENTION
ao The instant inventor ha;a discovered that aluminum salts, in conjunction with ;specified polymeric flocculants, applied within designated pH and alkalinity ranges, can be used with improved results to ~5 treat water which. collects and/or contains water-based paints. The relationship between paint addition and aluminum addition is not believed to be critical due to the non-tacky nature of the paint. The water, after capture and removal of the oversprayed, water- barne 3p paint therefrom, is typically recirculated in paint spray booth operations.
~0~~~~~
More particularly, the present invention relates to a method of treating the circulating water of a paint spray booth system used to capture over-sprayed, water-borne paint, which water contains or will contain aver-sprayed water-borne paint, to facilitate removal of over-sprayed, water-borne paint from such water.
The method comprises a) maintaining the pH of the circulating paint spray booth water being treated between about 5.0 to about 9.0, preferably about 6.0 to about 8.0, by adding an appropriate acid or base, while maintaining alkalinity within the range of 50 - 2,000, on a calcium carbonate basis, preferably 100-1000 ppmp b) adding an effective amount of a designated aluminum salt to the water being treated; c) contacting the over-sprayed, water-borne paint with the pH and alkalinity-maintained paint spray booth water before the addition of an effective amount of the aluminum salt or contacting the over-sprayed water-borne paint with the pH and alkalinity-maintained water after the addition of an effective amount of the aluminum salt;
d) adding an effective amount of a flocculant to the ~5 treated paint spray booth water; and e) removing the resulting sludge from the paint spray booth watery The method of the present invention is highly efficient for treating systems containing a wide variety of water-based paints, Additionally, the present method generally produces a well-flocculated ~o~~~~~~.
_8_ sludge which may be readily disposed of in land fills or by incineration.
These and additional advantages will be more apparent in view of the following detailed description.
DETRILED DESCRIPTION
The present invention relates to a method for treating circulating paint spray booth water containing or which will contain over-sprayed, water-based paint 1S to facilitate the removal of the over-sprayed paint from the water being treated, i.e.,,the water of a spray booth system or operation. The present method comprises: a) maintaining t:he p~I of the water in the aqueous system being treated, namely circulating paint spray booth water, between about 5.0 and 9:0, preferably about 6.0 to abc:ut 8.0, by adding an appropriate acid or base, while maintaining alkalinity within the range of 50-2,000 ppm on a calcium carbonate basis, preferably 100-1000 ppmp b) adding to said ~5 circulating water. an effective amount of an aluminum salt; c) contacting over-sprayed water-borne paint with the pH and alkalinity-maintained paint spray booth water of step a) before or after addition of an effective amount of said aluminum salt; d) adding an effective amount of a flocculan~t to the pH and alkalinity-maintained circulating paint spray booth water, preferably after or simultaneous with addition 2~~8~"l~.
_ c-2495 of the aluminum salto and e) removing the resulting g sludge from the paint spray booth water.
The pH of the water being treated should be maintained between about 5.0 and about 9.0, preferably between about 5.0 and about 8Ø As the pH is lowered below about 5.0, corrosion in the system generally increases. Paint treated at pH less than 5 tends to be more adherent and stringy. These characteristics are not conducive to goad sludge recovery. On the other hand, a pH of greater than about 9.0 generally results in greater solids dispersion, thus creating less efficient solids capture, and causes greater foam generation. Caustic and sulfuric acid are the preferred pI-I-adjustment ags.nts, though other acids or bases can be used.
Aside from pH, the alkalinity of the system being treated should be maintain~:d between about 50 and 2,000 ppm, preferably 100-1,000 ppm, on a calcium carbonate basis, based on the total weight of the water in the system being treated. The inventor has discovered that, for a given alkalinity agent and a given system, optimal treatment may be represented by a graph similar to Figure d, which shows effecti~re alkalinity dosages vs. pH for the system represented. This figure also demonstrates that the impact of various alkalinity agents on pH can vary substantially.
0°1496 The inventor has discovered that optimum performance of the instant aluminum salt program is dependent on the aluminum salt used, the alkalinity and the pH. There is a preferred range of alkalinity/
aluminum salt weight ratios for various alkalinity agent/aluminum salt combinations which can be used.
These depend, among other things, on the ability of a given alkalinity agent to disperse the paints) being treated. As Figure 2 shows, paint treated with too high of an aluminum/alkalinity ratio tends to result in a water high in suspended solids, whereas too low of an aluminum/alkalinity ratio generates flocculated paint solids which settle (instead of float), leaving behind a clear supernatant. The optimum aluminum/alkalinity ratio range varies depending on the type of alkalinity agent and the amount and type of aluminum salt used in treating the paint solids. As used. herein, optimum performance is defined as that which yields floating paint solids, clear subnata;nt water (as measured by transmittance, for example) and low suspended solids.
This is shown as the center are of Figure 2.
Alkalinity, in addition to that normally present in the system being treated, can be provided by NaoH, KOH, sodium bicarbonate, sodium carbonate, sodium tetrabora~e, sodium metasilicate, or calcium carbonate ~0 (among others) and blends thereof. The preferred alkalinity sources are NaOH, KOH, sodium bicarbonate and sodium carbonate.
While any aluminum salt can be used, the aluminum salts of this invention preferably contain a chloride anion. The preferred aluminum salts are aluminum chloride, aluminum chlorohydrate, polyaluminum chloride (PAC), also called basic aluminum chloride and is represented by the empirical formula Aln(OH)mClgn-m (n? 1.0 and m:n ratio = 0 to 2.5) and blends thereof. An advantage of the polymeric aluminum salts compared to other aluminum salts such as alum is that less pH adjustment is required. (See, for example, Figure 3.) In addition, it has been discovered that the polymeric aluminum salts form a larger, more efficient floc than alum. The improved efficiency of these products reduces the chemical demand and results in less dissolved solids being added to the system. This is very important since most 2p plants operate on total water recycle and one parameter that controls blowdown of the system is the accumulation of dissolved materials. Hlowdown refers to the replacement of recycle water with fresh makeup water. Additianally, the preferred aluminum salts produce a better solids removal on an equivalent A12o3 basis.
An effective amount of the aluminum salt is added.
As used herein, the term "effective amount" refers to that amount of aluminum salt necessary to treat the paint solids present an a given system so as to yield a floc which floats, a clear subnatant and an acceptable level of suspended solids. Generally, about 1:20 to ~0~~~7~.
°- 12 -about 20:1 paint solids:aluminum salt is required, on a dry solids basis. Preferably, the dosage ranges from about 1:4 to about 4:1 paint solids:aiuminum salt, and most preferably from about 1:3 to about 3:1 paint solids: aluminum salt. The aluminum salts may be added by any suitable means. Additionally, the aluminum salt/alkalinity source caeight ratio is believed to be critical, as shown in Figure 2. This figure shows that an aluminum chlorohydrate/sodium carbonate system has a specific aluminum salt/alkalinity ratio range wherein a clear subnatant is produced with a floc that floats.
An effective aluminum salt/alkalinity ratio should be used. As used herein, an effective.aluminum salt/alkalinity ratio is a ratio which gives a clear subnatant and a floc which floats, as exemplified by the center region of Figure 2.
After oversprayed, water-based paint contacts the aluminum salt added to the circulating water, an effective amount of a polymer flocculant is added to the paint spray booth water system. The flocculant promotes the formation of a buoyant floc structure by binding the aluminum salt-conditioned paint particles while allowing air to be incorporated into the floc structure. The resulting floating floc facilitates the removal of paint solids from the circulating water system.
According to this invention, the type and molecular weight of the polymeric flocculant used are not 2~~8~°~~.
C°1496 believed to be critical. Generally, polymeric flocculants having weight average molecular weights o~
at least 2 X 106 are preferred. More preferably, the molecular weight should exceed about 6 X 106.
Exam~,les of suitable flocculants include long chain high molecular weight polyacrylamides and copolymers of acrylic acid and acrylamide or long chain poly-methacrylamides. Preferred flocculants are nonionic or slightly anionic polyacrylamides (hydrolyzed polyacrylamides) having a weight average molecular is weight ranging from about 6 X 106 to about 20 X
106. Generally, the anionic functionality of such hydrolyzed polyacrylamides should not exceed about 30%, by weight.
Typical cationic polyelectrolytes which may be used as flocculants in true instant invention include but are not limited to polyphosphonium compounds, polysulfonium compounds, quaternary ammonium compounds, polymers of methacryloyloxethyl trimethyl ammonium methyl sulfate (METAMSj, polymers of methacrylamido propyl trimethylammonium chloride (MAPTAC), polymers of acryloyloxyethyl trimethyl ammonium chloride (AETAC), polymers of methacryloyloxyethyl trimethyl ammonium chloride (METAL) and polymers prepared from 30 combinations of METAMS, MAPTAC, AETAC and/or METAL with ac-rylamide and/or methacrylamide Representative of quaternary ammonium compounds are diethyl diallyl C°1496 ammonium and dimethyl diallyl ammonium polymers and salts thereof.
Other acceptable flocculants are quaternary ammonium polymers such as polydimethyl diallyl ammonium chloride (polyDMDAAC), poly dimethyl diallyl ammonium bromide (polyDMDAAB), poly diethyl diallyl ammonium chloride (polyDEDAAB), or any of the same copolymerized with acrylamide or methacrylamide. The preferred molecular weights for the quaternary ammonium polymers are in excess of about 2,000,000.
mhe most preferred cationic flo~culant is a polymer comprising dimethyl diallyl ammonium chloride and acrylamide, or a homologue thereof, having a weight average molecular weight in excess of about 4,000,000.
The ratio of the nonionic moiety (for example, acrylamide or methacrylamide) to the cationic moiety should be greater than about 1:1, on an active weight basis.
Blends of the,above listed flocculants can also be used.
An effective amount of the polymeric flocculant should be added. The effective amount depends primarily upon the quantity of over-sprayed paint and aluminum salt present in the system being treated.
Preferably, the effective flocculant dosage will range 2~~~~~
from about .O1 to about 150 parts (active weight basis) of the polymeric flocculant per part paint, and morepreferably, 0.1 to 20 parts, on an active polymer: paint basis.
The function of the polymeric flocculant is two-fold: it interacts with the aluminum salt and the paint to form a large, buoyant, easily-captured floc, and it generally reduces foam formation in the system by removing colloidal particulates present in the water.
x5 A requirement of the present invention is that the flocculant be added to the paint spray booth water after the over-sprayed, water-borne paint is contacted with the pH and alkalinity-maintained paint spray booth water. Thus, the flocculant: can be added along with or after addition of the aluminum salt. The flocculant can be added by any convenient means. Once the treated paint solids have been contacted with at least one polymeric flocculant, the resulting sludge is removed from the water. This removal may be facilitated by any means known in the art, including but not limited to, flotation and filtration.
Other additives commonly used for the treatment of 3n water containing oversprayed paint may generally be used in conjunction with the instant method. For example, bentonite clays, carbon black, talc, gums starch, dextrin, lime, aluminum oxide, silica solids, - is _ C-149s and casein among other additives, may be used as additional process aids in conjunction with the primary steps of the instant method. Additives from the class of amphoteric metal salts, including, but not limited to, ferric sulfate and ferric chloride, can also be used to enhance the performance of the instant invention. .
EXAMPLES
The following examples are intended to further 1~ demonstrate the instant invention. They are not, however, intended to in any way limit the instant invention. In these examples,, the following general procedure was followed:
2p 1. The alkalinity of the water was adjusted the desired range with the designated alkalinity agent; the pH was adjusted, if necessary, t~
the desired value using caustic or sulphura.c acid.
2. 200 mls of the alkalinity-adjusted water was added to a 400 ml wide mouth jar.
Figure 3 shows the titration curves of various aluminum salts with a sodium car-bonate alkalinity source.
Figure 4 shows the impact of pH on treatment performance, in terms of subnatant clarity. In the 1g system represented by this :Figure, a CIL white water-based paint was treated with soda ash and aluminum chlorohydrate.
SUMMARY OF THE INVENTION
ao The instant inventor ha;a discovered that aluminum salts, in conjunction with ;specified polymeric flocculants, applied within designated pH and alkalinity ranges, can be used with improved results to ~5 treat water which. collects and/or contains water-based paints. The relationship between paint addition and aluminum addition is not believed to be critical due to the non-tacky nature of the paint. The water, after capture and removal of the oversprayed, water- barne 3p paint therefrom, is typically recirculated in paint spray booth operations.
~0~~~~~
More particularly, the present invention relates to a method of treating the circulating water of a paint spray booth system used to capture over-sprayed, water-borne paint, which water contains or will contain aver-sprayed water-borne paint, to facilitate removal of over-sprayed, water-borne paint from such water.
The method comprises a) maintaining the pH of the circulating paint spray booth water being treated between about 5.0 to about 9.0, preferably about 6.0 to about 8.0, by adding an appropriate acid or base, while maintaining alkalinity within the range of 50 - 2,000, on a calcium carbonate basis, preferably 100-1000 ppmp b) adding an effective amount of a designated aluminum salt to the water being treated; c) contacting the over-sprayed, water-borne paint with the pH and alkalinity-maintained paint spray booth water before the addition of an effective amount of the aluminum salt or contacting the over-sprayed water-borne paint with the pH and alkalinity-maintained water after the addition of an effective amount of the aluminum salt;
d) adding an effective amount of a flocculant to the ~5 treated paint spray booth water; and e) removing the resulting sludge from the paint spray booth watery The method of the present invention is highly efficient for treating systems containing a wide variety of water-based paints, Additionally, the present method generally produces a well-flocculated ~o~~~~~~.
_8_ sludge which may be readily disposed of in land fills or by incineration.
These and additional advantages will be more apparent in view of the following detailed description.
DETRILED DESCRIPTION
The present invention relates to a method for treating circulating paint spray booth water containing or which will contain over-sprayed, water-based paint 1S to facilitate the removal of the over-sprayed paint from the water being treated, i.e.,,the water of a spray booth system or operation. The present method comprises: a) maintaining t:he p~I of the water in the aqueous system being treated, namely circulating paint spray booth water, between about 5.0 and 9:0, preferably about 6.0 to abc:ut 8.0, by adding an appropriate acid or base, while maintaining alkalinity within the range of 50-2,000 ppm on a calcium carbonate basis, preferably 100-1000 ppmp b) adding to said ~5 circulating water. an effective amount of an aluminum salt; c) contacting over-sprayed water-borne paint with the pH and alkalinity-maintained paint spray booth water of step a) before or after addition of an effective amount of said aluminum salt; d) adding an effective amount of a flocculan~t to the pH and alkalinity-maintained circulating paint spray booth water, preferably after or simultaneous with addition 2~~8~"l~.
_ c-2495 of the aluminum salto and e) removing the resulting g sludge from the paint spray booth water.
The pH of the water being treated should be maintained between about 5.0 and about 9.0, preferably between about 5.0 and about 8Ø As the pH is lowered below about 5.0, corrosion in the system generally increases. Paint treated at pH less than 5 tends to be more adherent and stringy. These characteristics are not conducive to goad sludge recovery. On the other hand, a pH of greater than about 9.0 generally results in greater solids dispersion, thus creating less efficient solids capture, and causes greater foam generation. Caustic and sulfuric acid are the preferred pI-I-adjustment ags.nts, though other acids or bases can be used.
Aside from pH, the alkalinity of the system being treated should be maintain~:d between about 50 and 2,000 ppm, preferably 100-1,000 ppm, on a calcium carbonate basis, based on the total weight of the water in the system being treated. The inventor has discovered that, for a given alkalinity agent and a given system, optimal treatment may be represented by a graph similar to Figure d, which shows effecti~re alkalinity dosages vs. pH for the system represented. This figure also demonstrates that the impact of various alkalinity agents on pH can vary substantially.
0°1496 The inventor has discovered that optimum performance of the instant aluminum salt program is dependent on the aluminum salt used, the alkalinity and the pH. There is a preferred range of alkalinity/
aluminum salt weight ratios for various alkalinity agent/aluminum salt combinations which can be used.
These depend, among other things, on the ability of a given alkalinity agent to disperse the paints) being treated. As Figure 2 shows, paint treated with too high of an aluminum/alkalinity ratio tends to result in a water high in suspended solids, whereas too low of an aluminum/alkalinity ratio generates flocculated paint solids which settle (instead of float), leaving behind a clear supernatant. The optimum aluminum/alkalinity ratio range varies depending on the type of alkalinity agent and the amount and type of aluminum salt used in treating the paint solids. As used. herein, optimum performance is defined as that which yields floating paint solids, clear subnata;nt water (as measured by transmittance, for example) and low suspended solids.
This is shown as the center are of Figure 2.
Alkalinity, in addition to that normally present in the system being treated, can be provided by NaoH, KOH, sodium bicarbonate, sodium carbonate, sodium tetrabora~e, sodium metasilicate, or calcium carbonate ~0 (among others) and blends thereof. The preferred alkalinity sources are NaOH, KOH, sodium bicarbonate and sodium carbonate.
While any aluminum salt can be used, the aluminum salts of this invention preferably contain a chloride anion. The preferred aluminum salts are aluminum chloride, aluminum chlorohydrate, polyaluminum chloride (PAC), also called basic aluminum chloride and is represented by the empirical formula Aln(OH)mClgn-m (n? 1.0 and m:n ratio = 0 to 2.5) and blends thereof. An advantage of the polymeric aluminum salts compared to other aluminum salts such as alum is that less pH adjustment is required. (See, for example, Figure 3.) In addition, it has been discovered that the polymeric aluminum salts form a larger, more efficient floc than alum. The improved efficiency of these products reduces the chemical demand and results in less dissolved solids being added to the system. This is very important since most 2p plants operate on total water recycle and one parameter that controls blowdown of the system is the accumulation of dissolved materials. Hlowdown refers to the replacement of recycle water with fresh makeup water. Additianally, the preferred aluminum salts produce a better solids removal on an equivalent A12o3 basis.
An effective amount of the aluminum salt is added.
As used herein, the term "effective amount" refers to that amount of aluminum salt necessary to treat the paint solids present an a given system so as to yield a floc which floats, a clear subnatant and an acceptable level of suspended solids. Generally, about 1:20 to ~0~~~7~.
°- 12 -about 20:1 paint solids:aluminum salt is required, on a dry solids basis. Preferably, the dosage ranges from about 1:4 to about 4:1 paint solids:aiuminum salt, and most preferably from about 1:3 to about 3:1 paint solids: aluminum salt. The aluminum salts may be added by any suitable means. Additionally, the aluminum salt/alkalinity source caeight ratio is believed to be critical, as shown in Figure 2. This figure shows that an aluminum chlorohydrate/sodium carbonate system has a specific aluminum salt/alkalinity ratio range wherein a clear subnatant is produced with a floc that floats.
An effective aluminum salt/alkalinity ratio should be used. As used herein, an effective.aluminum salt/alkalinity ratio is a ratio which gives a clear subnatant and a floc which floats, as exemplified by the center region of Figure 2.
After oversprayed, water-based paint contacts the aluminum salt added to the circulating water, an effective amount of a polymer flocculant is added to the paint spray booth water system. The flocculant promotes the formation of a buoyant floc structure by binding the aluminum salt-conditioned paint particles while allowing air to be incorporated into the floc structure. The resulting floating floc facilitates the removal of paint solids from the circulating water system.
According to this invention, the type and molecular weight of the polymeric flocculant used are not 2~~8~°~~.
C°1496 believed to be critical. Generally, polymeric flocculants having weight average molecular weights o~
at least 2 X 106 are preferred. More preferably, the molecular weight should exceed about 6 X 106.
Exam~,les of suitable flocculants include long chain high molecular weight polyacrylamides and copolymers of acrylic acid and acrylamide or long chain poly-methacrylamides. Preferred flocculants are nonionic or slightly anionic polyacrylamides (hydrolyzed polyacrylamides) having a weight average molecular is weight ranging from about 6 X 106 to about 20 X
106. Generally, the anionic functionality of such hydrolyzed polyacrylamides should not exceed about 30%, by weight.
Typical cationic polyelectrolytes which may be used as flocculants in true instant invention include but are not limited to polyphosphonium compounds, polysulfonium compounds, quaternary ammonium compounds, polymers of methacryloyloxethyl trimethyl ammonium methyl sulfate (METAMSj, polymers of methacrylamido propyl trimethylammonium chloride (MAPTAC), polymers of acryloyloxyethyl trimethyl ammonium chloride (AETAC), polymers of methacryloyloxyethyl trimethyl ammonium chloride (METAL) and polymers prepared from 30 combinations of METAMS, MAPTAC, AETAC and/or METAL with ac-rylamide and/or methacrylamide Representative of quaternary ammonium compounds are diethyl diallyl C°1496 ammonium and dimethyl diallyl ammonium polymers and salts thereof.
Other acceptable flocculants are quaternary ammonium polymers such as polydimethyl diallyl ammonium chloride (polyDMDAAC), poly dimethyl diallyl ammonium bromide (polyDMDAAB), poly diethyl diallyl ammonium chloride (polyDEDAAB), or any of the same copolymerized with acrylamide or methacrylamide. The preferred molecular weights for the quaternary ammonium polymers are in excess of about 2,000,000.
mhe most preferred cationic flo~culant is a polymer comprising dimethyl diallyl ammonium chloride and acrylamide, or a homologue thereof, having a weight average molecular weight in excess of about 4,000,000.
The ratio of the nonionic moiety (for example, acrylamide or methacrylamide) to the cationic moiety should be greater than about 1:1, on an active weight basis.
Blends of the,above listed flocculants can also be used.
An effective amount of the polymeric flocculant should be added. The effective amount depends primarily upon the quantity of over-sprayed paint and aluminum salt present in the system being treated.
Preferably, the effective flocculant dosage will range 2~~~~~
from about .O1 to about 150 parts (active weight basis) of the polymeric flocculant per part paint, and morepreferably, 0.1 to 20 parts, on an active polymer: paint basis.
The function of the polymeric flocculant is two-fold: it interacts with the aluminum salt and the paint to form a large, buoyant, easily-captured floc, and it generally reduces foam formation in the system by removing colloidal particulates present in the water.
x5 A requirement of the present invention is that the flocculant be added to the paint spray booth water after the over-sprayed, water-borne paint is contacted with the pH and alkalinity-maintained paint spray booth water. Thus, the flocculant: can be added along with or after addition of the aluminum salt. The flocculant can be added by any convenient means. Once the treated paint solids have been contacted with at least one polymeric flocculant, the resulting sludge is removed from the water. This removal may be facilitated by any means known in the art, including but not limited to, flotation and filtration.
Other additives commonly used for the treatment of 3n water containing oversprayed paint may generally be used in conjunction with the instant method. For example, bentonite clays, carbon black, talc, gums starch, dextrin, lime, aluminum oxide, silica solids, - is _ C-149s and casein among other additives, may be used as additional process aids in conjunction with the primary steps of the instant method. Additives from the class of amphoteric metal salts, including, but not limited to, ferric sulfate and ferric chloride, can also be used to enhance the performance of the instant invention. .
EXAMPLES
The following examples are intended to further 1~ demonstrate the instant invention. They are not, however, intended to in any way limit the instant invention. In these examples,, the following general procedure was followed:
2p 1. The alkalinity of the water was adjusted the desired range with the designated alkalinity agent; the pH was adjusted, if necessary, t~
the desired value using caustic or sulphura.c acid.
2. 200 mls of the alkalinity-adjusted water was added to a 400 ml wide mouth jar.
3. The water was mixed, using a Fisher Science Thermix Magnetic Stirrer Model 120M (setting 9 was used).
w
w
4, The designated aluminum salt was aided.
5. 0.2 grams of the paint were added,
6. The dispersibility of the paint was noted.
7. The system was mixed for 45 seconds.
8. A flocculant solution [2 ml of 1 g/1 polyacrylamide solution (active basis)] was added. A commercially available polyacrylamide having a molecular weight of 10-15 mm was used to prepare the flocculant solution.
9. The system was mixed for 30 seconds.
10. The stirrer was turned off.
11. The floc rise rate and sludge characteristics were noted.
12. The system was allowed to stand for 2 minutes.
13. The water clarity was measured, as %
transmittance using a Bausch and Lamb 3p Spectronic mini 20 spectrophotometer @ 450 nzn.
Examples 1-5 1. A CIL white water-borne paint was dispersed in water containing 500 ppm sodium carbonate as the alkalinity source and was then treated with 3900 ppm of aluminum chlorohydrate. The treated paint solids were then flocculated with a nonionic polyacrylamide according to the general test procedure given above. All of the captured paint floated, the supernatant clarity was 93% and the final pH was 8.2.
2. A CIL white water-borne paint was dispersed in water containing 1500 ppm sodium bicarbonate as the alkalinity source and was then treated with 2000 ppm of aluminum chlorohydrate. The treated paint solids were flocculatedl with a nonionic polyacrylamide according to the general test procedure given above. All of the captured paint floated, the supernatant clarity was 97% and the final pH was 7.5.
2~
3. A CIL metallic silver water-borne paint was dispersed in water containing 400 ppm sodium carbonate as the alkalinity source and was then treated with 1000 ppm of an .~1CL3/polyacrylamide blend, which resulted in 80% supernatant clarity and 100% of the captured paint floating.
~~~~~7~.
-~~9s 4. A CIL white water-borne paint was dispersed in S water containing various amounts of sodium carbonate alkalinity. The treated paint solids were then flocculated with a nonionic poly-aerylamide according to the general test procedure given above. The final pH was recorded and related to the water clarity. The results are illustrated in Figure 4.
5. A blend of BASF water-borne paints was run according to the general procedure given above.
1S The pH of each test was maintained at about 7.B.
The alkalinity was adjusted to accommodate the different dosages of aluminum salt using sodium carbonate. Various aluminum salts were evaluated for performance and the relative equivalent dosage required to produce comparable water clarity was established. Equivalent dosage (for this example) is defined as the amount of aluminum salt required to produce a water with 90% transmittance. The relative equivalent dosage relates the dosage of 2S the various aluminum salts to that of alum.
The results are summarized in Tabie I:
c-149s TABLE d Relative Dosage Transmittance Equivalent SAluminumSalt (Dpm~ @ 480 nm tfa) Dosage PolyAluminum Chloride 500 30 0.70X
Aluminum Sulfate 500 28 1.00X
Aluminum Chlorohydrate 500 60 0.28X
Aluminum Chloride 500 35 0.84X
loo0 46
transmittance using a Bausch and Lamb 3p Spectronic mini 20 spectrophotometer @ 450 nzn.
Examples 1-5 1. A CIL white water-borne paint was dispersed in water containing 500 ppm sodium carbonate as the alkalinity source and was then treated with 3900 ppm of aluminum chlorohydrate. The treated paint solids were then flocculated with a nonionic polyacrylamide according to the general test procedure given above. All of the captured paint floated, the supernatant clarity was 93% and the final pH was 8.2.
2. A CIL white water-borne paint was dispersed in water containing 1500 ppm sodium bicarbonate as the alkalinity source and was then treated with 2000 ppm of aluminum chlorohydrate. The treated paint solids were flocculatedl with a nonionic polyacrylamide according to the general test procedure given above. All of the captured paint floated, the supernatant clarity was 97% and the final pH was 7.5.
2~
3. A CIL metallic silver water-borne paint was dispersed in water containing 400 ppm sodium carbonate as the alkalinity source and was then treated with 1000 ppm of an .~1CL3/polyacrylamide blend, which resulted in 80% supernatant clarity and 100% of the captured paint floating.
~~~~~7~.
-~~9s 4. A CIL white water-borne paint was dispersed in S water containing various amounts of sodium carbonate alkalinity. The treated paint solids were then flocculated with a nonionic poly-aerylamide according to the general test procedure given above. The final pH was recorded and related to the water clarity. The results are illustrated in Figure 4.
5. A blend of BASF water-borne paints was run according to the general procedure given above.
1S The pH of each test was maintained at about 7.B.
The alkalinity was adjusted to accommodate the different dosages of aluminum salt using sodium carbonate. Various aluminum salts were evaluated for performance and the relative equivalent dosage required to produce comparable water clarity was established. Equivalent dosage (for this example) is defined as the amount of aluminum salt required to produce a water with 90% transmittance. The relative equivalent dosage relates the dosage of 2S the various aluminum salts to that of alum.
The results are summarized in Tabie I:
c-149s TABLE d Relative Dosage Transmittance Equivalent SAluminumSalt (Dpm~ @ 480 nm tfa) Dosage PolyAluminum Chloride 500 30 0.70X
Aluminum Sulfate 500 28 1.00X
Aluminum Chlorohydrate 500 60 0.28X
Aluminum Chloride 500 35 0.84X
loo0 46
Claims (10)
1. A method of treating circulating water in a paint spray booth system used to capture over-sprayed, water-borne paint, which method comprises:
(a) maintaining the pH of the circulating water between 5 and 9, while using an alkalinity agent to maintain the alkalinity of said circulating water within the range of 50-2,000 ppm, on a calcium carbonate basis;
(b) adding to said circulating water an effective amount of an aluminum salt;
(c) contacting said over-sprayed, water-borne paint with said circulating water, after completing step (a) and before or after completing step (b):
(d) adding an effective amount of a flocculant to said circulating water after completing steps (a), (b) and (c) to obtain a resulting sludge; and (e) removing the resulting sludge from said circulating water.
(a) maintaining the pH of the circulating water between 5 and 9, while using an alkalinity agent to maintain the alkalinity of said circulating water within the range of 50-2,000 ppm, on a calcium carbonate basis;
(b) adding to said circulating water an effective amount of an aluminum salt;
(c) contacting said over-sprayed, water-borne paint with said circulating water, after completing step (a) and before or after completing step (b):
(d) adding an effective amount of a flocculant to said circulating water after completing steps (a), (b) and (c) to obtain a resulting sludge; and (e) removing the resulting sludge from said circulating water.
2. The method of Claim 1, wherein said aluminum salt is selected from the group consisting of aluminum chlorohydrate, aluminum chloride, polyaluminum chloride and blends thereof.
3. The method of Claim 2, wherein said aluminum salt is a polyaluminum chloride.
4. The method of Claim 2, wherein said aluminum salt is a blend.
5. The method of Claim 2, wherein said flocculant is selected from the group consisting of long chain polyacrylamides, copolymers of acrylic acid and acrylamide and polymethacrylamides, wherein said copolymers possess an anionic functionality less than or equal to 30%, by weight.
6. The method of Claim 2, wherein a cationic polyelectrolyte is used.
7. The method of Claim 2, wherein the pH of said water is adjusted to between 6 and 9.
8. The method of Claim 5, wherein said alkalinity agent is selected from the group consisting of NaOH, KOH, Na2CO3, NaHCO3, Na metasilicate, calcium carbonate, Na tetraborate and blends thereof.
9. The method of Claim 6, wherein said alkalinity agent is selected from the group consisting of NaOH, KOH, Na2CO3, NaHCO3, Na metasilicate, calcium carbonate, Na tetraborate and blends thereof.
10. The method of Claim 1, wherein the aluminum salt and the flocculant are added simultaneously.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US699,549 | 1991-05-14 | ||
US07/699,549 US5250189A (en) | 1991-05-14 | 1991-05-14 | Method for removing paint solids from water-based paint systems using aluminum salts |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2068571A1 CA2068571A1 (en) | 1992-11-15 |
CA2068571C true CA2068571C (en) | 2003-07-15 |
Family
ID=24809829
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002068571A Expired - Fee Related CA2068571C (en) | 1991-05-14 | 1992-05-13 | Method for removing paint solids from water-based paint systems using aluminum salts |
Country Status (9)
Country | Link |
---|---|
US (1) | US5250189A (en) |
EP (1) | EP0514132B1 (en) |
JP (1) | JP2510812B2 (en) |
KR (1) | KR100201511B1 (en) |
AT (1) | ATE144275T1 (en) |
AU (1) | AU1624592A (en) |
CA (1) | CA2068571C (en) |
DE (1) | DE69214507T2 (en) |
ES (1) | ES2092638T3 (en) |
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FR2705661B1 (en) * | 1993-05-24 | 1995-08-25 | Rhone Poulenc Chimie | Composition based on aluminum polychloride and iron salt, its method of preparation and its use in water treatment. |
DE4216352A1 (en) * | 1992-05-18 | 1993-11-25 | Henkel Kgaa | Process for detackifying coagulation of paints |
US5462672A (en) * | 1992-08-13 | 1995-10-31 | Chemical Grouting Co., Ltd. | Process for treating sludge and system for the same |
US5458778A (en) * | 1992-12-23 | 1995-10-17 | Partner Gmbh | Method of treating waste water from a car wash at a vehicle refueling station |
US5614103A (en) * | 1993-06-22 | 1997-03-25 | Betzdearborn, Inc. | Methods for detackifying paint spray booth water |
US5562833A (en) * | 1995-02-03 | 1996-10-08 | Betz Laboratories, Inc. | Dual feed paint detackification program |
US5474703A (en) * | 1995-02-27 | 1995-12-12 | Warner-Lambert Company | Flocculating agent containing aluminum and a polybasic carboxylic acid |
US5660734A (en) * | 1996-01-17 | 1997-08-26 | Betzdearborn Inc. | Paint spray booth treatment program for waterborne and/or solventborne paints |
US5985154A (en) * | 1998-01-29 | 1999-11-16 | Betz Dearborn Inc. | Methods and compositions for treating paint spray booth water |
US6228269B1 (en) | 1999-10-19 | 2001-05-08 | Steven Cort | Methods for treating wastewater containing hard-to-filter solids, in particular photoresist and paint sludges |
US6471871B1 (en) | 1999-10-28 | 2002-10-29 | Finnchem Usa, Inc | Method for the removal of silicon and heavy metals from aqueous streams |
CZ2000155A3 (en) * | 2000-01-17 | 2001-10-17 | Asio Spol. S R.O. | Recycling process of disperse coating compositions or adhesives from waste water and apparatus for making the same |
US6742720B2 (en) | 2000-11-17 | 2004-06-01 | Safe Foods Corp. | Spray application system |
DE10217428A1 (en) * | 2002-04-18 | 2003-11-06 | Fabricius Pro Terra Gmbh | Recovery of color pigment and/or dispersant from waste water (e.g. from spray coloration of concrete tiles) involves flocculation and conventional separation |
WO2007072502A2 (en) * | 2005-12-19 | 2007-06-28 | Maharani Paints (India) Pvt. Ltd. | Composition and process for conversion of paint sludge into reusable paint |
US7967988B1 (en) * | 2007-01-03 | 2011-06-28 | Innovative Environmental Products, Inc. | Method for treatment of waste latex |
AU2008274885A1 (en) * | 2007-07-06 | 2009-01-15 | Duluxgroup (Australia) Pty Ltd | Coagulation of paint |
KR100953863B1 (en) | 2008-08-27 | 2010-04-20 | 한국과학기술원 | REMOVAL METHOD OF pH-SENSITIVE POWDER COATING USED FOR LEAKAGE TEST |
DE102008046409C5 (en) * | 2008-09-04 | 2013-08-22 | Eisenmann Ag | Method of removing solids from overspray resulting from painting articles |
US10093562B2 (en) * | 2009-06-24 | 2018-10-09 | Ecolab Usa Inc. | Methods and compositions for the treatment and recovery of purge solvent |
US8591744B2 (en) * | 2009-06-24 | 2013-11-26 | Nalco Company | Composition and process for removing impurities from a circulating water system |
US8404753B2 (en) * | 2009-11-17 | 2013-03-26 | Robert Joseph Hanlon, JR. | Method for degrading water-soluble polymeric films |
CN102951710A (en) * | 2011-08-22 | 2013-03-06 | 天津立昌科技有限公司 | Coating workshop circulating water treatment agent and its application |
US8933005B2 (en) * | 2012-04-16 | 2015-01-13 | Stefanie Slade | Method and composition for removing latex paint |
KR102414040B1 (en) | 2016-07-01 | 2022-06-27 | 에코랍 유에스에이 인코퍼레이티드 | Low Chloride Paint Anti-Tacking Agent |
CN106583348A (en) * | 2016-12-15 | 2017-04-26 | 南京工业职业技术学院 | Recovery technology of abandoned film-forming cleaning agent |
US10954399B2 (en) | 2018-06-14 | 2021-03-23 | Ecolab Usa Inc. | Addition of caustic soda for improving detackifier stability |
KR102207099B1 (en) * | 2019-03-12 | 2021-01-25 | 박상은 | Eco-friendly detackification agent for paint having excellent viscocity reduction effect and treatment method of the painting booth circulating water using the same |
KR20200126065A (en) | 2019-04-29 | 2020-11-06 | 금오공과대학교 산학협력단 | Manufacturing methods of paint floating composition comprising cetyltrimethylammonium chloride |
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US3956171A (en) * | 1973-07-30 | 1976-05-11 | E. I. Du Pont De Nemours And Company | Process for preparing stable positively charged alumina coated silica sols and product thereof |
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US3990986A (en) * | 1974-12-19 | 1976-11-09 | Nalco Chemical Company | Composition for the clarification and detackification of paint spray booth wastes |
US4002490A (en) * | 1975-02-20 | 1977-01-11 | Nalco Chemical Company | Paint spray booth chemical treatment |
US4026794A (en) * | 1976-08-30 | 1977-05-31 | Nalco Chemical Company | Process for resolving oil-in-water emulsions by the use of a cationic polymer and the water soluble salt of an amphoteric metal |
US4130674A (en) * | 1977-08-17 | 1978-12-19 | Detrex Chemical Industries, Inc. | Process of controlling organic coatings in aqueous spray booth systems |
US4401574A (en) * | 1981-07-21 | 1983-08-30 | Drew Chemical Corporation | Flocculation of aqueous paint waste |
US4440647A (en) * | 1983-02-09 | 1984-04-03 | Betz Laboratories, Inc. | Paint spray booth detackification composition and method |
JPS61108698A (en) * | 1984-11-01 | 1986-05-27 | 栗田工業株式会社 | Wet spray booth treatment agent |
US4637824A (en) * | 1985-06-21 | 1987-01-20 | Atlantic Richfield Company | Paint detackification method |
US4629572A (en) * | 1986-02-27 | 1986-12-16 | Atlantic Richfield Company | Paint detackification method |
DE3872055T2 (en) * | 1987-05-26 | 1992-12-03 | Calgon Corp | METHOD FOR DETECTING WASTE FROM SPRAY PAINT METHOD WITH MELAMINE FORMALDEHYDE. |
US4880471A (en) * | 1987-07-24 | 1989-11-14 | Calgon Corporation | Method for detackification of paint spray operation wastes |
US4759855A (en) * | 1987-07-24 | 1988-07-26 | Calgon Corporation | Method for detackification of paint spray operation wastes |
US4853132A (en) * | 1988-02-29 | 1989-08-01 | Betz Laboratories, Inc. | Paint spray booth treatment |
-
1991
- 1991-05-14 US US07/699,549 patent/US5250189A/en not_active Expired - Lifetime
-
1992
- 1992-05-12 DE DE69214507T patent/DE69214507T2/en not_active Expired - Fee Related
- 1992-05-12 ES ES92304262T patent/ES2092638T3/en not_active Expired - Lifetime
- 1992-05-12 AT AT92304262T patent/ATE144275T1/en active
- 1992-05-12 EP EP92304262A patent/EP0514132B1/en not_active Expired - Lifetime
- 1992-05-13 AU AU16245/92A patent/AU1624592A/en not_active Abandoned
- 1992-05-13 KR KR1019920008035A patent/KR100201511B1/en not_active IP Right Cessation
- 1992-05-13 CA CA002068571A patent/CA2068571C/en not_active Expired - Fee Related
- 1992-05-14 JP JP4165274A patent/JP2510812B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
AU1624592A (en) | 1992-11-19 |
CA2068571A1 (en) | 1992-11-15 |
JP2510812B2 (en) | 1996-06-26 |
KR920021673A (en) | 1992-12-18 |
DE69214507D1 (en) | 1996-11-21 |
US5250189A (en) | 1993-10-05 |
EP0514132B1 (en) | 1996-10-16 |
EP0514132A1 (en) | 1992-11-19 |
DE69214507T2 (en) | 1997-03-27 |
ATE144275T1 (en) | 1996-11-15 |
ES2092638T3 (en) | 1996-12-01 |
KR100201511B1 (en) | 1999-06-15 |
JPH07970A (en) | 1995-01-06 |
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