ZA200300973B - Method of making a composition, a product from such method, and the use thereof in removing or dissolving a contaminant from an environment. - Google Patents
Method of making a composition, a product from such method, and the use thereof in removing or dissolving a contaminant from an environment. Download PDFInfo
- Publication number
- ZA200300973B ZA200300973B ZA200300973A ZA200300973A ZA200300973B ZA 200300973 B ZA200300973 B ZA 200300973B ZA 200300973 A ZA200300973 A ZA 200300973A ZA 200300973 A ZA200300973 A ZA 200300973A ZA 200300973 B ZA200300973 B ZA 200300973B
- Authority
- ZA
- South Africa
- Prior art keywords
- water
- glycolic acid
- hydrogen peroxide
- weight percent
- composition
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 203
- 238000000034 method Methods 0.000 title claims abstract description 100
- 239000000356 contaminant Substances 0.000 title claims abstract description 82
- 238000004519 manufacturing process Methods 0.000 title description 19
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims abstract description 192
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 181
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 162
- 230000008569 process Effects 0.000 claims abstract description 76
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims abstract description 27
- 238000007639 printing Methods 0.000 claims abstract description 22
- 150000002894 organic compounds Chemical class 0.000 claims abstract description 5
- 238000012545 processing Methods 0.000 claims description 22
- 239000002253 acid Substances 0.000 claims description 19
- 241000233866 Fungi Species 0.000 claims description 14
- 241000195493 Cryptophyta Species 0.000 claims description 13
- 230000009182 swimming Effects 0.000 claims description 13
- 241000894006 Bacteria Species 0.000 claims description 11
- 238000004806 packaging method and process Methods 0.000 claims description 11
- 239000004094 surface-active agent Substances 0.000 claims description 11
- 239000000853 adhesive Substances 0.000 claims description 10
- 230000001070 adhesive effect Effects 0.000 claims description 10
- 235000013305 food Nutrition 0.000 claims description 9
- 229920002472 Starch Polymers 0.000 claims description 8
- 235000019698 starch Nutrition 0.000 claims description 8
- 150000007513 acids Chemical class 0.000 claims description 7
- 238000004061 bleaching Methods 0.000 claims description 6
- -1 hydrogen 2 peroxide Chemical class 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- 235000013365 dairy product Nutrition 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 235000013372 meat Nutrition 0.000 claims description 5
- 238000005272 metallurgy Methods 0.000 claims description 5
- 239000000575 pesticide Substances 0.000 claims description 5
- 244000144977 poultry Species 0.000 claims description 5
- 150000001277 beta hydroxy acids Chemical class 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 229920001206 natural gum Polymers 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- 150000002978 peroxides Chemical class 0.000 claims description 4
- 238000011012 sanitization Methods 0.000 claims description 4
- 239000008107 starch Substances 0.000 claims description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 4
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 239000000835 fiber Substances 0.000 claims description 3
- 230000005484 gravity Effects 0.000 claims description 3
- 230000002262 irrigation Effects 0.000 claims description 3
- 238000003973 irrigation Methods 0.000 claims description 3
- 239000010865 sewage Substances 0.000 claims description 3
- 229910052709 silver Inorganic materials 0.000 claims description 3
- 239000004332 silver Substances 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000012425 OXONE® Substances 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 229910021480 group 4 element Inorganic materials 0.000 claims description 2
- 229910021474 group 7 element Inorganic materials 0.000 claims description 2
- 229910021472 group 8 element Inorganic materials 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- HJKYXKSLRZKNSI-UHFFFAOYSA-I pentapotassium;hydrogen sulfate;oxido sulfate;sulfuric acid Chemical compound [K+].[K+].[K+].[K+].[K+].OS([O-])(=O)=O.[O-]S([O-])(=O)=O.OS(=O)(=O)O[O-].OS(=O)(=O)O[O-] HJKYXKSLRZKNSI-UHFFFAOYSA-I 0.000 claims description 2
- 229940061720 alpha hydroxy acid Drugs 0.000 claims 2
- 150000001280 alpha hydroxy acids Chemical class 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 150000001261 hydroxy acids Chemical class 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- 229910021476 group 6 element Inorganic materials 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 description 42
- 229960004275 glycolic acid Drugs 0.000 description 39
- 239000000243 solution Substances 0.000 description 27
- 239000000126 substance Substances 0.000 description 25
- 239000003292 glue Substances 0.000 description 20
- 238000007774 anilox coating Methods 0.000 description 15
- 239000000123 paper Substances 0.000 description 15
- 229910052500 inorganic mineral Inorganic materials 0.000 description 13
- 239000011707 mineral Substances 0.000 description 13
- 235000010755 mineral Nutrition 0.000 description 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 11
- 239000001301 oxygen Substances 0.000 description 11
- 229910052760 oxygen Inorganic materials 0.000 description 11
- 230000000087 stabilizing effect Effects 0.000 description 10
- 238000002156 mixing Methods 0.000 description 9
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 8
- 239000011575 calcium Substances 0.000 description 8
- 229910052791 calcium Inorganic materials 0.000 description 8
- 239000000976 ink Substances 0.000 description 8
- 230000003134 recirculating effect Effects 0.000 description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 7
- 229910052801 chlorine Inorganic materials 0.000 description 7
- 238000007647 flexography Methods 0.000 description 7
- 230000012010 growth Effects 0.000 description 7
- 238000001223 reverse osmosis Methods 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 241000251468 Actinopterygii Species 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000003139 biocide Substances 0.000 description 6
- 241000195628 Chlorophyta Species 0.000 description 5
- 230000005791 algae growth Effects 0.000 description 5
- 230000001580 bacterial effect Effects 0.000 description 5
- 238000004140 cleaning Methods 0.000 description 5
- 239000012530 fluid Substances 0.000 description 5
- 241000252210 Cyprinidae Species 0.000 description 4
- 230000003115 biocidal effect Effects 0.000 description 4
- 238000010297 mechanical methods and process Methods 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 241000218645 Cedrus Species 0.000 description 3
- 239000003619 algicide Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000005422 blasting Methods 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 238000001459 lithography Methods 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000011435 rock Substances 0.000 description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
- 208000004434 Calcinosis Diseases 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 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 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000007844 bleaching agent Substances 0.000 description 2
- 239000011449 brick Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000007667 floating Methods 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
- 244000045947 parasite Species 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000009877 rendering Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 2
- 235000019345 sodium thiosulphate Nutrition 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000002604 ultrasonography Methods 0.000 description 2
- MJVIZWIQHKRBPI-UHFFFAOYSA-N 1-(aziridin-1-yl)but-3-en-2-ol Chemical compound C=CC(O)CN1CC1 MJVIZWIQHKRBPI-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 235000014653 Carica parviflora Nutrition 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241000243321 Cnidaria Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000002242 deionisation method Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000002635 electroconvulsive therapy Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011066 ex-situ storage Methods 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 229910021478 group 5 element Inorganic materials 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000002147 killing effect Effects 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 229910001338 liquidmetal Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 238000009372 pisciculture Methods 0.000 description 1
- 235000013594 poultry meat Nutrition 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000008400 supply water Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 239000011273 tar residue Substances 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000004506 ultrasonic cleaning Methods 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/261—Alcohols; Phenols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/265—Carboxylic acids or salts thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Paper (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
- Cleaning Or Drying Semiconductors (AREA)
Abstract
A composition which is effective in removing a wide variety of contaminants, such as organic compounds, from a wide variety of environments, such as printing systems, is provided. A process of preparing such composition includes contacting hydrogen peroxide, glycolic acid, and water. The process can additionally include contacting with one or more additional components such as isopropyl alcohol.
Description
1 METHOD OF MAKING A COMPOSITION, A PRODUCT FROM SUCH METHOD, 2 AND THE USE THEREOF IN REMOVING OR DISSOLVING A CONTAMINANT 3 FROM AN ENVIRONMENT 4 RELATED APPLICATIONS ) 5 This application claims priority from provisional U.S. application serial number 6 60/223,064 filed August 4, 2000. 7 BACKGROUND OF THE INVENTION 8 The invention relates to a method of making a composition and a product from such 9 method wherein such composition is effective in reducing the concentration of a contaminant in an environment. 11 It is known that various processes used to produce printed materials such as printing 12 processes and lithography processes utilize various machinery that contain several parts such 13 as rollers, apparatus to contain and move fluids (such as hoses and trays), and other moving 14 parts (such as gears and the like). Such machinery becomes contaminated with various contaminants, such as organic deposits, calcium deposits, bacteria, fungi, and additional 16 residue created from the use of various organic-based inks and printing production fluids 17 known in the art. Great difficulty is encountered in attempting to reduce the concentration of, 18 preferably remove, such contaminants from the various parts of the machinery due, in part, to 19 the difficulty in accessing the internal parts of such machinery.
In addition, when such contaminant residue is not removed on a consistent basis, it is 21 known that such residue can accumulate and harden over time creating a residue which is 22 difficult to remove and can cause undesirable chemical reactions to occur in the various 23 processes. Processes used in the past to remove such residue have included mechanical 24 removal that requires disassembling the machinery to access parts that contain such residue and then removing such residue by mechanical methods such as by hammering, chiseling, and 26 the like. Such mechanical methods require significant downtime of the machinery and
SUBSTITUTE SHEET (RULE 26)
. o
1 involve increased risk to the equipment and the personnel involved with removing such 2 residue.
. 3 It is also known that various methods for removing such residue, other than 4 mechanical methods, usually involve the use of fluids such as various solvents and surfactants.
However, such solvents and surfactants do not completely remove such residue. 6 Further, when such solvents and surfactants do not completely remove such residue, such 7 residue begins to accumulate as discussed above.
Thus, a composition and process of using 8 such composition for removing contaminants from machinery such as printing and g lithography equipment that does not require mechanical methods of removing such residue, provides for a substantially complete removal of such residue, and helps to prevent the 11 accumulation of such residue, would be of significant contribution to the art and to the 12 economy. 13 It is also known that various industrial processes used to produce goods utilize various 14 systems, such as packaging systems, flexographic systems, food processing systems, bleaching systems, metallurgy systems, acid washing systems, veterinary product systems, 16 pesticide systems, meat processing systems, poultry processing systems, dairy processing 17 systems, sanitizing systems, and the like and combinations thereof, which contain several 18 parts such as gears, rollers, and the like.
Such parts can become contaminated with various 19 contaminants such as organic and calcium deposits, calcium and starch-based glues, and the like and combinations thereof.
Various compositions known to reduce the concentration of
} 21 or remove, such contaminants utilize compositions which are difficult to dispose of due to 22 environmental regulations and can present significant safety hazards.
Thus, a composition,
23 useful for removing such contaminants from such systems, which is non-toxic, easy to 24 prepare, and capable of being disposed of without costly disposal procedures would also be of significant contribution to the art and to the economy.
1 It is also known that various industrial processes used to produce goods such as paper 2 and pulp products utilize various water-containing systems. Such water-containing systems . 3 are also found in various printing systems, water treating systems, drainage systems, boiler 4 systems, chiller systems, and the like. Use of such water-containing systems presents several problems relating to the fouling of such water-containing systems with various contaminants 6 such as scale, algae, fungi, bacteria, surfactants, various organic compounds, and the like. 7 The contaminants can foul such water-containing systems to such an extent that such water- 8 containing systems require extensive cleaning to remove such contaminants, which results in 9 adecrease in production of goods.
Various known compositions that can be used for reducing the concentration of, 11 preferably removing or dissolving, such contaminants from such water-containing systems 12 frequently utilize chlorine. However, use of such chlorine-based compositions present 13 various environmental and safety hazards and further, disposal of such products produced 14 using such chlorine-based compositions requires close environmental scrutiny and regulation.
In addition, such chlorine-based compositions are frequently utilized in gaseous form which 16 requires extensive safety and training procedures to be utilized. Thus, a composition, useful 17 for removing or dissolving one or more contaminants from an environment that contains 18 water-based systems, which is non-toxic, inexpensive, and easy to prepare and use would be 19 of significant value to the art and to the economy.
In addition, compositions, useful in reducing the concentration of, preferably } 21 removing or dissolving, contaminants from an environment, which contain more than one 22 component commonly require one of the components to be added to the environment first, 23 followed by the addition of a second component. The two components must then react “in 24 situ” to thereby provide a composition that can remove or dissolve the contaminants contained within the environment. Such compositions can be difficult to use due to the
1 difficulty in determining how much of each component of the composition should be added. 2 Thus, a composition useful in reducing the concentration of, preferably removing or . 3 dissolving, contaminants from an environment and that can be prepared “ex situ” in various 4 concentrations, which can then be added to an environment to remove or dissolve contaminants would be of significant contribution to the art and to the economy. 6 In addition, a composition useful in reducing the concentration of, preferably 7 removing or dissolving, contaminants from an environment which is prepared from easily 8 accessible components and which can be prepared by a simple procedure utilizing a minimum 9 of preparation apparatus would also be of significant contribution to the art and to the economy. 11 SUMMARY OF THE INVENTION 12 An object of the present invention is to provide a process for preparing a composition 13 which is useful for reducing the concentration of, preferably removing or dissolving, one or 14 more contaminants from an environment. Such process utilizes components which are inexpensive to use and easy to prepare. Another object of the present invention is to provide 16 a process for preparing a composition which utilizes a simple and effective method which 17 provides a composition having desirable properties such as enhanced capabilities for reducing 18 the concentration of, preferably removing or dissolving, a contaminant from an environment 19 when compared to a composition prepared by other methods.
A further object of the present invention is to provide an improved process of . 21 reducing the concentration of, preferably removing or dissolving, a contaminant from an 22 environment. 23 An embodiment of the present invention is a novel composition prepared by a process 24 comprising contacting hydrogen peroxide, glycolic acid (also referred to as hydroxy acetic acid), and water.
1 Another embodiment of the present invention is a process of preparing a novel 2 composition comprising contacting hydrogen peroxide, glycolic acid, and water. The process . 3 can further comprise contacting with one or more additional components such as isopropyl 4 alcohol.
A novel composition of the present invention can be used for reducing the 6 concentration of, preferably removing or dissolving, a wide variety of contaminants from a 7 wide variety of environments. Such contaminants can include Groups II-VI of the Periodic 8 Table of the Elements, algae, fungi, bacteria, surfactants, natural gums, synthetic gums, 9 organic compounds, paper fillers, paper filters, clays, sulfites, sulfates, oxides, adhesives, starches, and the like and combinations thereof. Such environments can include water- 11 containing systems, paper producing systems, pulp producing systems, printing systems, 12 packaging systems, flexographic systems, food processing systems, bleaching systems, 13 metallurgy systems, acid washing systems, veterinary product systems, pesticide systems, 14 meat processing systems, poultry processing systems, dairy processing systems, sanitizing systems, and the like and combinations thereof. Such water-containing systems can include 16 swimming pools, water treating systems, drainage systems, boiler systems, chiller systems, 17 ~~ sewage treating systems, irrigation systems, agriculture systems, cooling tower systems, and 18 the like and combinations thereof. 19 Other objects and advantages of the present invention will become apparent from the detailed description of the invention and the appended claims.
Co
1 DETAILED DESCRIPTION OF THE INVENTION 2 It has been discovered that the performance of a composition when reducing the
. 3 concentration of, preferably removing or dissolving, one or more contaminants from an
4 environment can be improved by utilizing a novel process of preparing such composition which comprises contacting hydrogen peroxide and glycolic acid. 6 Generally, a process of preparing a composition of the present invention comprises 7 contacting hydrogen peroxide, glycolic acid, and water.
The hydrogen peroxide is generally 8 present as a hydrogen peroxide solution comprising hydrogen peroxide and water.
Such 9 hydrogen peroxide solution generally comprises at least about 0.1 weight percent hydrogen peroxide in water and at most about 20 weight percent hydrogen peroxide in water, preferably 11 at least about 0.5 weight percent hydrogen peroxide in water and at most about 15 weight 12 percent hydrogen peroxide in water, and more preferably at least about 1 weight percent 13 hydrogen peroxide in water and at most about 15 weight percent hydrogen peroxide in water. 14 An example hydrogen peroxide solution which can be used in a process of the present invention can be prepared by adding a stabilizing amount of water to a commercially 16 available 35 weight percent technical grade solution of hydrogen peroxide in water from FMC 17 Corporation, Philadelphia, Pennsylvania, to thereby obtain a hydrogen peroxide solution 18 suitable for use in a process of the present invention. 19 The water suitable for use in a process of the present invention is preferably a low solids water generally comprising less than about 10 parts per million (ppm) dissolved solids,
} 21 preferably less than about 5 ppm dissolved solids, more preferably less than about 1 ppm 22 dissolved solids, and most preferably about 0 ppm dissolved solids.
An example low solids 23 water which can be used in a process of the present invention can be obtained commercially 24 from PGT Inc., Cedar Hill, Texas, which is a low solids water produced by reverse osmosis having less than about 0.1 ppm dissolved solids.
1 The water, preferably low solids water, can be prepared by any suitable means known 2 in the art for preparing water which can be used in a process of the present invention. . 3 Generally, the low solids water can be prepared by subjecting a high solids water to a treating 4 means selected from the group consisting of reverse osmosis, deionization, and the like and combinations thereof.
The high solids water generally comprises more dissolved solids than 6 the low solids water.
Generally, the high solids water comprises more than about 200 ppm of 7 dissolved solids. 8 Generally, water is present in a stabilizing amount which allows for the contacting of e¢ hydrogen peroxide and glycolic acid according a process as described herein.
Generally, a stabilizing amount of water as described herein should be large enough to prevent an 11 uncontrollable or unpredictable reaction between the hydrogen peroxide and glycolic acid 12 which can occur in a non-dilute environment as known in the art.
However, a stabilizing 13 amount of water as described herein should be small enough to prevent the resulting 14 composition from being so dilute that such resulting composition no longer has the ability to reduce the concentration of, preferably remove or dissolve, a contaminant from an . 16 environment as described herein.
Thus, a novel aspect of the present invention is the 17 presence of a stabilizing amount of water, preferably low solids water, which is large enough 18 to allow the contacting of such hydrogen peroxide and glycolic acid in a predictable and 19 controllable manner, yet, is small enough to prevent a significant dilution of the resulting composition so that such composition is effective in reducing the concentration of, preferably } 21 removing or dissolving, a contaminant from an environment as described herein. 22 Generally, a stabilizing amount of water, preferably low solids water, is present in an 23 amount of at least about 50 percent by weight water based on the total weight of the hydrogen 24 peroxide, glycolic acid, and water, and at most about 99.9 percent by weight water based on the total weight of the hydrogen peroxide, glycolic acid, and water.
Preferably, a stabilizing
1 amount of water is present in an amount of at least about 60 percent by weight water based on 2 the total weight of the hydrogen peroxide, glycolic acid, and water, and at most about 97 . 3 percent by weight, and more preferably a stabilizing amount of water is present in an amount ] 4 of at least about 70 percent by weight water based on the total weight of the hydrogen peroxide, glycolic acid, and water, and at most about 95 percent by weight water based on the 6 total weight of the hydrogen peroxide, glycolic acid, and water.
7 The glycolic acid is preferably a glycolic acid solution comprising glycolic acid and 8 water.
Such glycolic acid solution generally comprises at least about 1 weight percent 9 glycolic acid and at most about 15 weight percent glycolic acid, preferably at least about 1 weight percent glycolic acid and at most about 10 weight percent glycolic acid, and more 11 preferably comprises at least about 1 weight percent glycolic acid and at most about 5 weight 12 percent glycolic acid.
An example glycolic acid solution which can be used in a process of 13 the present invention can be obtained by adding low solids water as described herein to a 14 commercially available 70 weight percent technical grade solution of glycolic acid obtained from DuPont Chemical, Wilmington, Delaware, to thereby obtain a 5 weight percent glycolic
16 acid solution. 17 The hydrogen peroxide, glycolic acid, and water can be contacted by any suitable 18 means and in any suitable order which provides for a composition of the present invention 19 effective in reducing the concentration of, preferably removing or dissolving, a contaminant from an environment.
Preferably, such contacting comprises mixing utilizing any suitable } 21 mixing means known in the art for mixing an aqueous solution with another aqueous solution. 22 More preferably, a hydrogen peroxide solution as described herein is mixed with a glycolic 23 acid solution as described herein.
During contacting, the weight ratio of hydrogen peroxide to 24 glycolic acid is generally at least about 1:1 and at most about 30:1, preferably at least about
1 2:1 and at most about 20:1, more preferably at least about 2:1 and at most about 10:1, and 2 most preferably at least about 2:1 and at most about 6:1. . 3 The temperature during contacting of the hydrogen peroxide, glycolic acid, and water, . 4 preferably during the contacting of the hydrogen peroxide solution and glycolic acid solution, can be any temperature which provides a composition effective in reducing the concentration 6 of, preferably removing or dissolving, a contaminant from the environment as described 7 herein. Generally, the temperature during contacting is at least about 0°F and at most about 8 100°F, preferably at least about 10°F and at most about 90°F, and more preferably at least o about 20°F and at most about 80°F. The pressure during contacting can be any pressure which provides for a composition as described herein. The pressure is generally at least about 11 atmospheric and at most about 100 pounds per square inch absolute (psia), preferably about 12 atmospheric. The time period of contacting can be any time period capable of providing for a 13 composition as described herein. The time period of contacting is generally at least about 0.1 14 minute and at most about 60 minutes, preferably at least about 0.1 minute and at most about 30 minutes. 16 A process of providing a composition of the present invention can further comprise 17 contacting with an additional component comprising isopropyl alcohol. Generally, the 18 isopropyl alcohol has a purity of at least about 95 percent, preferably at least about 98 percent, 19 and more preferably at least about 99 percent.
In addition to, or in lieu of, contacting with isopropyl alcohol, a process of the present ) 21 invention can further comprise contacting with one or more components selected from the 22 group consisting of potassium monopersulfate, silver, acids, esters, alcohols, alpha hydroxy 23 acids, beta hydroxy acids, and the like and combinations thereof. Examples of suitable esters 24 include, but are not limited to, ethoxylated esters and the like and combinations thereof.
Examples of suitable acids include, but are not limited to, acetic, sulfuric, formic,
1 peroxyacetic, and the like and combinations thereof. Examples of suitable alpha hydroxy and 2 beta hydroxy acids include, but are not limited to, citric, lactic, maleic, and the like and ) 3 combinations thereof. 4 Such additional component(s) can be added in any amount(s) as long as such amount(s) provides a composition effective in reducing the concentration of, preferably 6 removing or dissolving, a contaminant from an environment as described herein. Generally, 7 when such additional component(s) is present, such additional component(s) is present in an 8 amount of at least about 0.1 weight percent based on the total weight of the final composition 9 and at most about 20 weight percent based on the total weight of the final composition, preferably in an amount of at least about 0.1 weight percent based on the total weight of the 11 final composition and at most about 10 weight percent based on the total weight of the final 12 composition, and more preferably in an amount of at least about 0.1 weight percent based on 13 the total weight of the final composition and at most about 5 weight percent based on the total 14 weight of the final composition.
A preferred method of preparing a composition of the present invention comprises 16 mixing a 35 weight percent solution of hydrogen peroxide in water with a stabilizing amount 17 of low solids water comprising less than about 1 ppm dissolved solids to thereby provide a 18 resulting mixture comprising about 80 weight percent low solids water and the rest 19 comprising the hydrogen peroxide solution. The resulting mixture is then contacted with a 5 weight percent glycolic acid solution prepared by contacting a 70 weight percent glycolic acid 21 solution with low solids water comprising less than about 1 ppm dissolved solids to provide a 22 composition having a pH of about 1.9 to about 3.5. Such composition is particularly suitable 23 for use in reducing the concentration of, preferably removing or dissolving, calcium and 24 starch glues and organic substances and mineral residue typically found in corrugated box manufacturing and printing and flexography processes.
1 Another preferred method of preparing a composition of the present invention 2 comprises mixing a 35 weight percent solution of hydrogen peroxide in water with a . 3 stabilizing amount of low solids water comprising less than about 1 ppm dissolved solids to 4 thereby provide a resulting mixture comprising about 43 weight percent low solids water and the rest comprising the hydrogen peroxide solution. The resulting mixture is then contacted 6 with a 5 weight percent glycolic acid solution prepared by contacting a 70 weight percent 7 glycolic acid solution with low solids water comprising less than about 1 ppm dissolved 8 solids to provide a composition having a pH of about 1.9 to about 3.5. Such resulting © composition is particularly suitable for use in reducing the concentration of, preferably removing or dissolving, contaminants typically found in water-containing systems. 11 An additional preferred process of preparing such composition is to further contact the 12 resulting composition with isopropyl alcohol having a purity of about 99 percent in an amount 13 to provide a resulting composition containing such isopropyl alcohol in an amount of about 5 14 weight percent based on the total weight of the final composition.
A composition of the present invention generally has a pH of at least about 1.5 and at 16 most about 4.5, preferably at least about 1.7 and at most about 4, and more preferably at least 17 about 1.9 and at most about 3.8. 18 A composition of the present invention generally has a specific gravity of at least 19 about 1.0 and at most about 1.5, preferably at least about 1.1 and at most about 1.4, more preferably at least about 1.3 and at most about 1.4, and most preferably about 1.35. 21 While not intending to be bound by theory, it is believed that a composition of the 22 present invention comprises a molecule containing two carbon atoms, four hydrogen atoms, 23 and four oxygen atoms. It is further believed that two of the four hydrogen atoms and two of 24 the four oxygen atoms are present as hydroxyl groups (OH).
1 A composition of the present invention prepared by a process of the present invention 2 described herein can be utilized to reduce the concentration of, preferably remove or dissolve, . 3 a wide array of contaminants from a wide array of environments. Such process generally 4 comprises contacting such contaminant(s) with a concentration of a composition of the present invention, prepared according to a process as described herein, in a concentration 6 effective in reducing the concentration of, preferably removing or dissolving, such 7 contaminant(s) from such environment. Examples of suitable contaminants include, but are 8 not limited to, elements of Groups II-VIII of the Periodic Table of the Elements (also referred g to as Group II elements, Group III elements, Group IV elements, Group V elements, Group
VI elements, Group VII elements, and Group VIII elements), algae, fungi, bacteria, 11 surfactants, natural gums, synthetic gums, organic compounds, paper fibers, paper filters, 12 clays, sulfites, sulfates, oxides, adhesives, starches, and the like and combinations thereof. 13 Examples of a suitable environment include, but are not limited to, water-containing 14 systems, paper producing systems, pulp producing systems, printing systems, packaging systems, flexographic systems, food processing systems, bleaching systems, metallurgy 16 systems, acid washing systems, veterinary product systems, pesticide systems, meat 17 processing systems, poultry processing systems, dairy processing systems, sanitizing systems, 18 and the like and combinations thereof. The term “system” refers to any method, process, 19 apparatus, components, and the like and combinations thereof related in any way or manner to the disclosed type of system. For example, the term “water-containing systems” refers to any 21 method, process, apparatus, components, and the like and combinations thereof known in the 22 art related in any way or manner to water containing or containment. Also for example, the 23 term “food processing systems” refers to any method, process, apparatus, components, and 24 the like and combinations thereof known in the art related in any way or manner to food processing. Also for example, the term “printing systems” refers to any method, process,
1 apparatus, components, and the like and combinations thereof known in the art related in any 2 way or manner to printing.
: 3 Examples of suitable water-containing systems include, but are not limited to,
4 swimming pools, water treating systems, drainage systems, boiler systems, chiller systems, sewage treating systems, irrigation systems, agricultural systems, cooling tower systems, and 6 the like and combinations thereof. 7 A composition of the present invention can be contacted with one or more 8 contaminants as described herein by any suitable means and under any suitable conditions 9 which are effective in reducing the concentration of, preferably removing or dissolving, such contaminants from an environment.
The contacting condition, also referred to as the 11 contaminant contacting condition, which comprises a concentration of a composition as 12 described herein, a contacting temperature, a contacting pressure, and a contacting time 13 period can be any contacting condition effective in reducing the concentration of, preferably 14 removing or dissolving, a contaminant from an environment as described herein.
The contacting condition will generally depend on the type and concentration of contaminant and 16 type of environment.
For example, the contacting condition will generally have an increased 17 composition concentration, temperature, pressure, and time period when the concentration of 18 one or more contaminants is increased compared to the contacting condition necessary when 19 such contaminants are present in a reduced concentration.
For example, when a composition of the present invention is used as a swimming pool shock treatment to help initially reduce
; 21 the concentration of, preferably remove or dissolve, a contaminant, the composition 22 concentration will be significantly increased and the time period decreased compared to when 23 a composition of the present invention is used to maintain the reduction in concentration of 24 contaminants in such swimming pool over, for example, a thirty day period.
Selecting the
1 proper contacting condition based on the concentration of contaminants within an 2 environment is within the skill in the art.
. 3 When the environment comprises a liquid medium, such as the water-containing
4 systems described herein, the concentration of composition is generally at least about 0.1 part composition by volume per million parts environment (ppmv) and at most about 25 volume 6 percent, preferably at least about 0.5 ppmv and at most about 20 volume percent, and more 7 preferably at least about 1 ppmv and at most about 15 volume percent.
When the 8 environment does not comprise a liquid medium, such as when the composition is applied 9 directly to a contaminant, the concentration of composition is generally at least about 0.1 part composition by weight per million parts environment (ppm) and at most about 20 weight 11 percent, preferably at least about 0.5 ppm and at most about 10 weight percent, and more 12 preferably at least about 1 ppm and at most about 5 weight percent. 13 Generally, the contacting temperature, also referred to as the contaminant contacting 14 temperature, is at least about 50°F and at most about 200°F, preferably at least about 70°F and at most about 150°F.
The contacting pressure, also referred to as the contaminant 16 contacting pressure, is generally at least about atmospheric and at most about 100 pounds per 17 square inch absolute (psia), preferably about atmospheric.
The contacting time, also referred 18 to as the contaminant contacting time, is generally at least about 0.1 minute and at most about 18 30 days, preferably at least about 0.5 minute and at most about 20 days, and more preferably at least about 1 minute and at most about 10 days.
. 21 Examples of suitable uses of a composition of the present invention include, but are 22 not limited to, the following. 23 A composition of the present invention can be used as a descalant, biocide, slimicide, 24 flocculant, and the like and combinations thereof to reduce the concentration of, preferably
1 remove or dissolve, scale, algae, and the like and combinations thereof from machinery and 2 apparatus used to produce paper and pulp.
: 3 A composition of the present invention can be used as a descalant, biocide and/or
} 4 algaecide to reduce the concentration of, preferably remove or dissolve, various contaminants from water-containing systems used in the printing industry.
For example, a composition of 6 the present invention can be used as a calcium and surfactant remover to reduce the 7 concentration of, preferably remove or dissolve, calcium, dissolved minerals, surfactants, 8 bacteria, and the like and combinations thereof from the lines and tanks of water-containing 9 systems used in the printing industries, packaging industries, and the like and combinations thereof.
Also for example, a composition of the present invention can be used to reduce the 11 concentration of, preferably remove or dissolve, various surfactants, natural gums, calcium 12 carbonate, polymer-containing residue, and the like and combinations thereof from 13 lithographic plate surfaces.
A composition of the present invention can also be used as a 14 rubber roller rinse to reduce the concentration of, preferably remove or dissolve, organic contaminants, water-based contaminants, and liquid metal precipitants including, but not 16 limited to, paper fiber, paper fillers, clay coatings, sulfites, sulfates, titanium dioxide, 17 chromium, barium, calcium carbonate, and the like and combinations thereof.
The reduction 18 in concentration, preferably the removing or dissolving, of these contaminants results in 19 improved consistency of ink transfer and aids in restricting the neutralization of acid fountain chemistries commonly used in lithography and lithographic processes.
) 21 A composition of the present invention can be used for reducing the concentration of, 22 preferably removing or dissolving, a contaminant such as scale, algae, fungi, bacteria, 23 minerals, and the like and combinations thereof from water-containing systems such as 24 water tanks, water lines, pumps, and the like and combinations thereof.
Such contaminants are known to exist in such water-containing systems commonly utilized in the printing and
1 paper industries and the like because of the high contact rate with paper products which 2 contain mold, fungi spores and bacteria which are commonly found in the wood used to : 3 produce such paper products. 4 A composition of the present invention can be used to reduce the concentration of, preferably remove or dissolve, an adhesive.
In various processes, such as the process of 6 manufacturing corrugated boxes and packaging, glues and adhesives containing organic 7 compounds and starches are commonly used.
A composition of the present invention can be 8 contacted, such as by spraying, with such glues and adhesives and, after a time period 9 effective for allowing a composition of the present invention to penetrate such glues and adhesives, can thus provide for easy removal of such glues and adhesives. 11 A composition of the present invention can be used to treat anilox rolls, particularly 12 the cells contained by, or within, such anilox rolls, commonly found in flexographic 13 situations.
Anilox rolls commonly utilized in flexographic situations commonly contain 14 organic substances of microscopic size found in various concentrations.
There are various methods of applying various compositions to remove such substances which include spraying 16 onto the surface being treated, mechanically applying to the surface, immersion treating, and 17 the like and combinations thereof.
Utilizing a composition of the present invention provides 18 an improvement over existing technologies of cleaning anilox rolls which are currently being 19 used such as baking soda blasting, ultra-sonic cleaning, and utilizing chemicals of high alkalinity concentration. . 21 A composition of the present invention can be used to reduce the concentration of, 22 preferably remove or dissolve, various contaminants commonly found in food processing and 23 food packaging environments and the like. 24 A composition of the present invention can be used in waste sludge treatment processes to help break down solids and provide biocide effects.
1 A composition of the present invention can be used as an industrial biocide treatment 2 to kill various fungi such as the bottrus fungi, mold or bacteria. - 3 A composition of the present invention can be used to enhance the bleaching 4 processes commonly found in the textile industries, paper and pulp industries, and the like and combinations thereof. 6 A composition of the present invention can be used to enhance the effectiveness of 7 known descalants, slimicides, antimicrobials, and the like and combinations thereof. 8 A composition of the present invention can be used in fish farming and agricultural 9 processes as a pesticide for killing microorganisms and/or parasites, including bacteria and fungi, found to exist within such processes.
Such agricultural processes include, but are not 11 limited to, agricultural rendering and growing, including various related holding areas which 12 can contain such bacteria, fungi, and parasites. 13 A composition of the present invention can be used to reduce the concentration of, 14 preferably remove or dissolve, various contaminants commonly found in meat, poultry, and dairy rendering and processing facilities. 16 A composition of the present invention can be used to reduce the concentration of, 17 preferably remove or dissolve, various contaminants commonly found in metallurgy 18 processes involving copper or other metals. 19 A composition of the present invention can be used to reduce the concentration of, preferably remove or dissolve, various contaminants commonly found in processes . 21 comprising the acid-washing of concrete. 22 A composition of the present invention can be used to reduce the concentration of, 23 preferably remove or dissolve, various contaminants commonly found in processes to produce 24 veterinary products.
1 A composition of the present invention can be used to reduce the concentration of, 2 preferably remove or dissolve, various contaminants commonly found in beer processing . 3 systems, wine processing systems, and the like such as removing contaminants from various i 4 vats.
A composition of the present invention can be used to reduce the concentration of, 6 preferably remove or dissolve, various contaminants from the surfaces of automobiles such as 7 removing bug and tar residue from an external surface, e.g., a bumper, of a car or truck. 8 A composition of the present invention can be used as an additive in various products 9 used in the cosmetic industry such as face-peel products.
A composition of the present invention can be used to reduce the concentration of, 11 preferably remove or dissolve, contaminants such as calcium-based and organic-based 12 substances commonly found in the marine industry such as from the ‘external surfaces of 13 ships. 14 Preferably, a composition of the present invention is used to reduce the concentration of, preferably remove or dissolve, contaminants from printing systems. A composition of the 16 present invention can be used in addition to, or preferably as an alternative to, various 17 mechanical means and the use of various solvents and/or various surfactants, such as sodium 18 hydroxide, to remove such contaminants. 19 Also preferred, a composition of the present invention is used as a sanitizer, fungicide, algaecide, and the like and combinations thereof to reduce the concentration of, preferably . 21 remove or dissolve, contaminants from water-containing systems such as swimming pools, 22 water gardens, and the like and combinations thereof. A composition of the present invention 23 can be used in addition to, or preferably as an alternative to, chlorine-based, or bromide- 24 based, or biguianide-based compositions.
1 Also preferred, a composition of the present invention is used as a sanitizer, fungicide, 2 algaecide, and the like and combinations thereof to reduce the concentration of, preferably ; 3 remove or dissolve, contaminants from water-containing systems commonly found in 4 municipal water treating systems, commercial drainage systems, industrial boiler systems, industrial chiller systems, cooling tower systems, and the like and combinations thereof. A 6 composition of the present invention can be used in addition to, or preferably as an alternative 7 to, chlorine-based, or bromide-based, or biguianide-based compositions. 8 The following examples are presented to further illustrate this invention and are not to 9 be construed as unduly limiting the scope of this invention. 11 EXAMPLE I 12 This example illustrates a preparation of a composition of the present invention. 13 A 55-gallon quantity of a composition of the present invention was prepared by 14 mixing 8.25 gallons of 35 weight percent hydrogen peroxide solution (obtained from FMC
Corporation, Philadelphia, Pennsylvania, as a 35 weight percent technical grade solution of 16 hydrogen peroxide in water) with 34.675 gallons of low solids water comprising less than 17 about 0.1 ppm dissolved solids (obtained from PGT Inc., Cedar Hill, Texas, the low solids 18 water had been produced by reverse osmosis) at room temperature (about 70°F) and 1¢ atmospheric pressure to thereby provide a resulting mixture. Total mixing time was about 15 minutes. The resulting mixture was then contacted with 11.55 gallons of a 5 weight percent ] 21 glycolic acid solution which had been prepared by contacting 0.825 gallons of approximately 22 70 weight percent glycolic acid solution (obtained from DuPont Chemical, Wilmington, 23 Delaware, as a 70 weight percent technical grade solution of glycolic acid in water) with 24 10.725 gallons of low solids water comprising less than about 0.1 ppm dissolved solids (obtained from PGT Inc., the low solids water had been produced by reverse osmosis) at
1 room temperature (about 70°F) and atmospheric pressure to thereby obtain about 55 gallons 2 of a composition of the present invention referred to herein as "Composition A" having a pH . 3 of about 3.3. 4
EXAMPLE II
6 This example illustrates the use of a composition of the present invention 7 (Composition A as described herein) to reduce the concentration of, preferably remove or 8 dissolve, calcium and/or starch glues and substances from corrugating equipment used in o manufacturing corrugated boxes.
Equipment was obtained from Packaging Corporation of America (PCA) located in 11 Waco, Texas and had been in use for several years. A significant amount of glue residue 12 (color of such residue was a dirty-white due to the glue drying to a semi-translucent 13 appearance over time) was observed. A significant concentration of glue residue was located 14 on a cross-member of the adhesive application device of such equipment about 10 inches under the glue applicator which applied the glue to the web paperboard to form a corrugated 16 box sheet. The glue residue level had accumulated to such an extent that production 17 problems were encountered. PCA had requested assistance from several chemical companies 18 to develop a product which would remove or allow removal of the glue residue. It is believed 19 that twenty unsuccessful attempts were made by the various chemical vendor companies to do so. Composition A was then applied directly to the glue residue using a trigger sprayer ] 21 Within about 5 minutes, the semi-translucent appearance of the glue residue turned to a white 22 color as such glue residue originally appeared (i.e., the appearance of the glue before it dried). 23 Layer by layer the accumulated glue residue turned white. Within about 20 minutes, the 24 layers of residue were all visibly re-hydrated and could be removed by hand by peeling each layer from the cross-member. When Composition A reached the bottom layer of residue
1 which had been estimated as having initially formed over 20 years prior, such bottom layer 2 was able to be removed which enabled the equipment to be operated again.
Overall, . 3 maintenance problems for the equipment based on glue residue was minimized.
Before the 4 application of Composition A, the preferred and possibly only means to remove this residue was with a hammer and chisel.
The hammer and chisel were used to chisel the layers away 6 from the cross-member section of the adhesive application device. 7 8 EXAMPLE ITI 9 This example illustrates another use of a composition of the present invention (Composition A as described herein) to remove organic substances and mineral residue from 11 equipment such as anilox rolls used in flexography processes. 12 Equipment utilizing anilox rolls was provided by Packaging Corporation of America 13 (PCA) located in Waco, Texas.
Such equipment had been used for several years.
An 14 inherent problem which exists in flexography processes is various contaminants have a tendency to accumulate and bond to small laser-etched cells within the anilox rolls.
These 16 cells supply water and solvent-based flexography inks to the raised image photo-polymer 17 printing plate.
After removal of excess flexography inks, there are multiple procedures used 18 to remove scalants and residue from the anilox rolls.
The anilox rolls of the PCA equipment 19 had various mineral and ink component deposits which could not be easily removed by previous methods, such as baking soda blasting and using ultrasound equipment. . 21 In a first method, Composition A was sprayed directly onto the surface of the anilox 22 roll cells having a concentration of 145 cells per linear inch of anilox roll.
The anilox roll 23 was hydrated with Composition A and remained hydrated for about 5 minutes.
Thereafter, a 24 standard aqueous-based flexographic wash was used to rinse the contamination out of the cells.
The application of Composition A appeared to decompose the bonded minerals and
1 deposits, allowing such bonded minerals and deposits to be removed by washing with normal 2 alkaline types of flexography wash. This process allowed for recovery of cell depth and cell . 3 volume of the anilox rolls. Composition A allowed for the anilox equipment to be cleaned on 4 press, without the costly purchase of cleaning equipment, which provided a reduction in down-time and capital expenditure costs for PCA. 6 The second method of applying Composition A was by adding Composition A to the 7 flexography printing unit ink reservoir contacting the ink pump. The contact time was about 8 five minutes followed by rinsing using standard aqueous-based flexographic wash 9 procedures. Previously, methods such as baking soda blasting and using ultrasound equipment were utilized, but had only cleaned the surface of the anilox cells. Composition A 11 performed better than such previous methods and opened the cells to a like-new condition. 12 13 EXAMPLE IV 14 This example illustrates another preparation of a composition of the present invention.
A 55-gallon quantity of a composition of the present invention was prepared by 16 mixing 18.15 gallons of a 35 weight percent hydrogen peroxide solution (obtained from FMC 17 Corporation, Philadelphia, Pennsylvania, as a 35 weight percent technical grade solution of 18 hydrogen peroxide in water) with 13.75 gallons of low solids water comprising less than 19 about 0.1 ppm dissolved solids (obtained from PGT Inc., Cedar Hill, Texas, the low solids water had been produced by reverse osmosis) at room temperature (about 70°F) and ) 21 atmospheric pressure to thereby provide a resulting mixture. Total mixing time was about 15 22 minutes. The resulting mixture was then contacted with 23.1 gallons of a 5 weight percent 23 glycolic acid solution which had been prepared by contacting 1.65 gallons of 70 weight 24 percent glycolic acid solution (obtained from DuPont Chemical, Wilmington, Delaware, as a 70 weight percent technical grade solution of glycolic acid in water) with 21.45 gallons of
1 low solids water comprising less than about 0.1 ppm dissolved solids (obtained from PGT
2 Inc, Cedar Hill, Texas, the low solids water had been produced by reverse osmosis) at room . 3 temperature (about 70°F) and atmospheric pressure to thereby obtain about 55 gallons of a
4 composition of the present invention referred to herein as "Composition B" having a pH of about2.2.
6
7 EXAMPLE V
8 This example illustrates a use of a composition of the present invention (Composition
9 Bas described herein) to remove residue and bacterial growth and fungi from a printing press fountain solution recirculating system (a water-containing system).
11 A printing press was obtained from Rock Tenn Company, Waxahachie, Texas, and
12 contained a Man Roland fountain solution recirculating system, also referred to as a
13 dampening system, which comprised a blender, chiller, and recirculating unit containing an
14 approximately 30 gallon reservoir with a total capacity of 200 gallons of water.
The equipment has been used almost continuously for about 20 years.
A significant amount of
16 mineral substance residue, such as mineral deposits consisting of calcium and lime deposits,
17 and bacterial and fungi growth was observed, including hair algae, which were white, green,
18 brown and various other colors which are common to the industry.
Various solvents had been
19 used in an attempt to remove the residue and growth before such residue had accumulated and caused production interruptions.
Common industry products used for cleaning such printing ] 21 press recirculating systems included products comprising a mixture of sodium hydroxide,
22 glycol ethers, and various biocides, such as those sold by various chemical manufacturers, 23 including Varn International (a worldwide chemical manufacturer which manufactures
24 pressroom and printing chemicals and distributes such products throughout the world).
1 However, use of such solvents was unsuccessful in removing the mineral residue and 2 bacterial and fungal growth. The mineral residue and growth had accumulated to a point that ) 3 such had become hardened within the water lines and could not be removed. The lines had 4 become plugged, making production difficult. An additional option of replacing the water lines and/or flushing the water system with bleach would have been an option, but the amount 6 of water which would have to be consumed would have amounted to thousands of gallons of 7 water. In addition, production-related issues resulting from bleach residue would have been 8 difficult to alleviate, making the bleaching option undesirable and economically unfeasible. 9 A five-gallon quantity of Composition B described herein was supplied for the following procedure. Composition B was poured directly, in one-pint quantities, into each of 11 the six water trays of the recirculating system. Upon contact of Composition B with the 12 mineral residue and bacterial and algae growth, it was observed that within about 15 to 30 13 seconds, water immediately began flowing in the return line from the press back to the 14 recirculating system indicating that Composition B was removing the various contaminants.
Then, the drain of the recirculating system became unplugged so that water could easily flow. 16 An additional four-gallon quantity of Composition B was then added directly to the 30-gallon 17 reservoir. Within about 15 to 30 seconds, water immediately began flowing in the return line 18 from the press back to the reservoir indicating that Composition B was removing the various 19 contaminants. It was observed that the substance being removed by Composition B contained paper dust, slime, fungus, algae, ink components, and the like. About 35 gallons of such 21 substance were collected in an empty barrel. In about 30 minutes, about 200 gallons of fresh 22 water were passed through the water system to further help remove the debris and remains of 23 dead algae and bacterial growth and minerals which had been dislodged and/or dissolved by 24 Composition B.
1 The recirculating system was then recharged with a standard fountain solution having 2 a pH of about 3.8. The press was immediately placed into production. Normal startup ] 3 recovery time had previously been about 20 to 25 printed sheets before production. After use 4 of Composition B, startup recovery time was about 2 to 3 sheets. It is believed that the better startup was because the pH of Composition B was at or near the recommended pH of the 6 fountain solution. Before use of Composition B, products previously used comprised sodium 7 hydroxide, glycol ethers and biocides, with some of these products containing foaming agents 8 or alkalines such as caustic soda. The residual pH left in the water system after using 9 traditional cleaning products would normally be in a range of about 9 to about 10.5. Thus, since the pH of fountain solutions is typically in a range of about 3.8 to about 4.0 and since 11 Composition B has a similar residual pH, use of Composition B provides a direct benefit to 12 production ability, print quality, and reduction of water costs. 13 14 EXAMPLE VI
This example illustrates a use of a composition of the present invention (Composition 16 B as described herein) to remove a contaminant from a swimming pool. 17 The test site consisted of a swimming pool which contained 25,000 gallons of water 18 which was substantially free of chlorine and other chemical substances. The swimming pool 19 was rectangular in shape with a shallow end depth of approximately three feet and a deep end depth of approximately nine feet. The swimming pool had been covered and dormant for 21 about nine months. Before treatment, the water appeared blackish in color and emitted a 22 strong foul odor. The surface areas of the pool under water were covered with a green algae 23 growth which was about 1.5 inches thick. The green algae growth appeared to cover an 24 underlying gray-colored algae-type substance. Due to the extensive algae growth, the bottom surface of the pool and the surfaces of the first and second steps of the pool were not visible.
1 The filter media contained in the swimming pool filtration system was diametaceous earth. 2 The pH of the water was 7.2 and the temperature of the water was about 78°F.
. 3 A ten-gallon quantity of Composition B described herein was then added to the pool 4 by pouring Composition B at a steady rate into the pool from a plastic bucket while walking around the edges of the pool from the shallow to the deep end.
After approximately twenty- 6 five minutes, the color of the water turned to a light oreen “pea-soup” color.
Debris began to 7 float to the top and such debris appeared to be large pieces of the green algae and gray- 8 colored algae-type substance.
The clarity of the water continued to improve.
After gs approximately twenty-four hours, the water appeared to be somewhat cloudy or “milky” in color.
The green algae and gray-colored algae-type substance appeared to have been “killed” 11 with the remains of such algae appearing as a white skeletal debris which covered the bottom 12 of the pool with some of the debris floating on top.
The pH of the pool was 6.8. A flocculent 13 was then added in an amount of about two fluid quarts to aid in the removal of the floating 14 debris.
After approximately seventy-two hours from the addition of Composition B, the bottom of the pool was vacuumed and the vacuumed debris was exhausted into an area next 16 to the pool.
The pH of the pool was 6.8. Tap water was then added to the pool until the pH 17 of the pool water was 7.0.
18 The pool water remained uncovered, dormant, and was not circulated for two weeks. 19 After the two-week period, the dissolved oxygen (DO) was 106 parts per million (ppm), the water appeared to very clear (the bottom surface of the deep end was visible), and the pump 21 used to circulate the pool water was started and set to circulate the pool water for two hours 22 each day.
One week later (three weeks total time from the addition of Composition B), which
23 included a two-inch rain, the DO was 98 ppm.
After one more week (four weeks total time 24 from the addition of Composition B), the DO was 44 ppm.
The water was still clear, but
1 several small areas of green algae growth on the surface areas of the pool underwater were 2 observed.
X 3 A 2.5 gallon “maintenance dose” of Composition B described herein was then added 4 to the pool by pouring from a plastic bucket at one end of the pool After adding, the DO was 100 ppm (which was the desired reading) and the pH was 7.4. The pool was then maintained 6 atadosage rate of 2.5 gallons of Composition B added every two weeks. 7 8 EXAMPLE VII 9 This example demonstrates the effect of various increases in concentration of a composition of the present invention. 11 Two test sites (1 and 2) were utilized to determine the toxicity of a composition of the 12 present invention. Test site 1 consisted of an outdoor water garden comprising a circular- 13 shaped fiberglass molded tank having a diameter of about 5 feet and which contained 14 approximately 500 gallons of water. The tank also contained soil, rock, several bricks, and 36 minnows. The water was foul-smelling and black in color. A substance which appeared to 16 be a black mold or algae covered the soil and rocks at the bottom of the tank. 17 An eight fluid ounce quantity of Composition B described herein was then 18 added to the tank by pouring Composition B directly from a plastic bottle into the water at 19 one end of the tank . The temperature of the water during addition was about 78°F. Upon addition, the water immediately began to bubble. The bubbling began on one end of the tank 21 and proceeded to the other end of the tank within about 15 minutes. After 24 hours had 22 elapsed, the water appeared to be clear and the bricks and rock contained within the tank were 23 completely visible and were no longer covered with the black mold or algae. The minnows 24 appeared to be unaffected by the addition of Composition B. Skeletal debris appeared to cover the bottom of the tank. A pH reading and dissolved oxygen reading were not obtained.
1 Based on the observations, a recommended dosage rate of eight ounces of Composition B 2 applied every two to three weeks was developed. . 3 Test site 2 consisted of a standard 29-gallon aquarium containing six gallons of 4 crushed coral gravel. To such aquarium was charged 29 gallons of reverse osmosis treated water. The pH was 8.0. The growth medium used in the tank included a General Electric 6 brand Gro-Lite bulb (which had a UV spectrum similar to sunlight) and TETRA-MIN tropical 7 fish food. The water was allowed to cycle through the aquarium for about five days without 8 the addition of any chemicals, live fish, or plants. After five days, twenty-four small bait 9 shop minnows were added to the water and left alone for about two days (about 48 hours).
Then, Composition B was added in an amount of 100 parts Composition B by weight per 11 million parts water (i.e., 100 ppm). About thirty minutes after such addition, the dissolved 12 oxygen level was 106 ppm. 13 After twenty-four hours, the dissolved oxygen level was about 44 ppm and an 14 additional 200 ppm amount of Composition B was added. After thirty minutes, the dissolved oxygen was about 210 ppm. The minnows were observed to be swimming near the bottom 16 of the tank. After an additional twenty-four hours, the dissolved oxygen was 86 ppm. An 17 additional 500 ppm amount of Composition B was then added. Thereafter, a reading for the 18 dissolved oxygen could not be obtained because the dissolved oxygen was so high that the 19 titration medium being used (sodium thiosulfate) kept turning black which prevented an accurate dissolved oxygen reading from being obtained. Even after six hours had passed and 21 over 600 ppm of sodium thiosulfate had been used, a dissolved oxygen reading still could not 22 be obtained. 23 No additional chemicals were added to the tank for a period of four days. After ten 24 days had passed from the initial application of Composition B, the fish present in the tank began to expire at a rate of about one fish per day over the next two weeks. The scales of
1 about three of the fish appeared to be expanded away from the. bodies of such fish.
After four
2 weeks had passed since the initial application of Composition B to the tank, the water was . 3 still very clear and free of algae growth.
The dissolved oxygen was 44 ppm.
4° The results shown in the above examples clearly demonstrate that the present invention is well adapted to carry out the objects and attain the ends and advantages
6 mentioned as well as those inherent therein.
7 Reasonable variations, modifications, and adaptations can be made within the scope
8 of the disclosure and the appended claims without departing from the scope of this invention.
Claims (1)
- WHAT IS CLAIMED IS:1 1. A process of producing a composition comprising contacting hydrogen 2 peroxide, glycolic acid, and water wherein said water is present in an amount of least about 3 50 weight percent based on the total weight of said hydrogen peroxide, glycolic acid, and 4 water and at most about 99.9 weight percent based on the total weight of said hydrogen peroxide, glycolic acid, and water.1 2. The process according to claim 1 wherein the weight ratio of said hydrogen 2 peroxide to said glycolic acid is at least about 1:1 and at most about 30:1.1 3. The process according to claim 1 wherein the weight ratio of said hydrogen 2 peroxide to said glycolic acid is at least about 2:1 and at most about 20:1. 1 4, The process according to claim 1 wherein the weight ratio of said hydrogen 2 peroxide to said glycolic acid is at least about 2:1 and at most about 10:1.1 5. The process according to claim 1 wherein said hydrogen peroxide is present as 2 a hydrogen peroxide solution of said hydrogen peroxide and said water and wherein said 3 hydrogen peroxide solution comprises at least about 0.1 weight percent said hydrogen 4 peroxide and at most about 20 weight percent said hydrogen peroxide, and further wherein 5 said glycolic acid is present as a glycolic acid solution of said glycolic acid and said water and 6 wherein said glycolic acid solution comprises at least about 1 weight percent said glycolic 7 acid and at most about 15 weight percent said glycolic acid.1 6. The process according to claim 1 wherein said hydrogen peroxide is present as 2 a hydrogen peroxide solution of said hydrogen peroxide and said water and wherein said 3 hydrogen peroxide solution comprises at least about 0.5 weight percent said hydrogen 4 peroxide and at most about 15 weight percent said hydrogen peroxide, and further wherein said glycolic acid is present as a glycolic acid solution of said glycolic acid and said water 6 wherein said glycolic acid solution comprises at least about 1 weight percent said glycolic. 7 acid and at most about 10 weight percent said glycolic acid.1 7. The process according to claim 1 further comprising contacting with isopropyl 2 alcohol.1 8. The process according to claim 7 wherein said isopropyl alcohol has a purity 2 of at least about 99 percent.1 9. The process according to claim 2 wherein said water is present in an amount of 2 least about 60 weight percent based on the total weight of said hydrogen peroxide, glycolic 3 acid, and water and at most about 97 weight percent based on the total weight of said 4 hydrogen peroxide, glycolic acid, and water. 1 10. The process according to claim 1 wherein said hydrogen peroxide is present as 2 a hydrogen peroxide solution of said hydrogen peroxide and said water and wherein said 3 hydrogen peroxide solution comprises at least about 1 weight percent said hydrogen peroxide 4 and at most about 15 weight percent said hydrogen peroxide, and further wherein said 5 glycolic acid is present as a glycolic acid solution of said glycolic acid and said water and 6 wherein said glycolic acid solution comprises at least about 1 weight percent said glycolic 7 acid and at most about 5 weight percent said glycolic acid.. 1 11. The process according to claim 1 wherein said water is present in an amount of 2 least about 70 weight percent based on the total weight of said hydrogen peroxide, glycolic 3 acid and water and at most about 95 weight percent based on the total weight of said 4 hydrogen peroxide, glycolic acid and water.1 12. The process according to claim 1 further comprising contacting with a 2 component selected from the group consisting of potassium monopersulfate, silver, acids, ) 3 esters, alcohols, alpha hydroxy acids, beta hydroxy acids, and combinations thereof. , 1 13. The process according to claim 12 wherein said acids are selected from the 2 group consisting of acetic, sulfuric, formic, peroxyacetic, and combinations thereof. 1 14. The process according to claim 12 wherein said alpha hydroxy and beta 2 hydroxy acids are selected from the group consisting of citric, lactic, maleic, and 3 combinations thereof. 1 15. The process according to claim 1 wherein said composition has a pH of at least 2 about 1.5 and at most about 4.5. 1 16. The process according to claim 1 wherein said composition has a specific 2 gravity of at least about 1.0 and at most about 1.5. 1 17. A composition prepared by the process of contacting hydrogen peroxide, 2 glycolic acid, and water wherein said water is present in an amount of least about 50 weight 3 percent based on the total weight of said hydrogen peroxide, glycolic acid, and water and at 4 most about 99.9 weight percent based on the total weight of said hydrogen peroxide, glycolic acid, and water. 1 18. The composition according to claim 17 wherein the weight ratio of said ’ 2 hydrogen peroxide to said glycolic acid is at least about 1:1 and at most about 30:1. 1 19. The composition according to claim 17 wherein the weight ratio of said 2 hydrogen peroxide to said glycolic acid is at least about 2:1 and at most about 20:1.1 20. The composition according to claim 17 wherein the weight ratio of said 2 hydrogen peroxide to said glycolic acid is at least about 2:1 and at most about 10:1. 1 21. The composition according to claim 17 wherein said hydrogen peroxide is : 2 present as a hydrogen peroxide solution of said hydrogen peroxide and said water and3 wherein said hydrogen peroxide solution comprises at least about 0.1 weight percent said 4 hydrogen peroxide and at most about 20 weight percent said hydrogen peroxide, and further wherein said glycolic acid is present as a glycolic acid solution of said glycolic acid and said 6 water and wherein said glycolic acid solution comprises at least about 1 weight percent said 7 glycolic acid and at most about 15 weight percent said glycolic acid.1 22. The composition according to claim 17 wherein said hydrogen peroxide is 2 present as a hydrogen peroxide solution of said hydrogen peroxide and said water and 3 wherein said hydrogen peroxide solution comprises at least about 0.5 weight percent said 4 hydrogen peroxide and at most about 15 weight percent said hydrogen peroxide, and further 5 wherein said glycolic acid is present as a glycolic acid solution of said glycolic acid and said 6 water wherein said glycolic acid solution comprises at least about 1 weight percent said 7 glycolic acid and at most about 10 weight percent said glycolic acid.1 23. The composition according to claim 17 wherein the process further comprises 2 contacting with isopropyl alcohol.1 24. The composition according to claim 23 wherein said isopropyl alcohol has a 2 purity of at least about 99 percent. :1 25. The composition according to claim 18 wherein said water is present in an 2 amount of least about 60 weight percent based on the total weight of said hydrogen peroxide,3 glycolic acid, and water and at most about 97 weight percent based on the total weight of said 4 hydrogen peroxide, glycolic acid, and water. ) 1 26. The composition according to claim 17 wherein said hydrogen peroxide is ‘ 2 present as a hydrogen peroxide solution of said hydrogen peroxide and said water and 3 wherein said hydrogen peroxide solution comprises at least about 1 weight percent said 4 hydrogen peroxide and at most about 15 weight percent said hydrogen peroxide, and further wherein said glycolic acid is present as a glycolic acid solution of said glycolic acid and said 6 water and wherein said glycolic acid solution comprises at least about 1 weight percent said 7 glycolic acid and at most about 5 weight percent said glycolic acid. 1 27. The composition according to claim 17 wherein said water is present in an 2 amount of least about 70 weight percent based on the total weight of said hydrogen peroxide, 3 glycolic acid and water and at most about 95 weight percent based on the total weight of said 4 hydrogen peroxide, glycolic acid and water. 1 28. The composition according to claim 17 wherein the process further comprises 2 contacting with a component selected from the group consisting of potassium 3 monopersulfate, silver, acids, esters, alcohols, alpha hydroxy acids, beta hydroxy acids, and 4 combinations thereof. 1 29. The composition according to claim 28 wherein said acids are selected from 2 the group consisting of acetic, sulfuric, formic, peroxyacetic, and combinations thereof. 1 30. The composition according to claim 28 wherein said alpha hydroxy and beta 2 hydroxy acids are selected from the group consisting of citric, lactic, maleic, and 3 combinations thereof. :1 31. The composition according to claim 17 wherein said composition has a pH of2 atleast about 1.5 and at most about 4.5.1 32. The composition according to claim 17 wherein said composition has a ‘ 2 specific gravity of at least about 1.0 and at most about 1.5.1 33. A composition comprising a molecule consisting of two carbon atoms, four2 hydrogen atoms, and four oxygen atoms.1 34. A composition according to claim 33 wherein two of said four hydrogen atoms2 and two of said four oxygen atoms are present as hydroxyl groups.1 35. A process of removing or dissolving a contaminant from an environment2 comprising:3 selecting a composition of hydrogen peroxide, glycolic acid, and water, wherein said4 water is present in an amount of least about 50 weight percent based on the total weight of said hydrogen peroxide, glycolic acid, and water and at most about 99.9 weight percent based6 on the total weight of said hydrogen peroxide, glycolic acid, and water to provide a7 composition and8 contacting said contaminant with a concentration of said composition, wherein said9 concentration is effective in removing at some of said contaminant from said environment.1 36. A process according to claim 35 wherein said contaminant is selected from the2 group consisting of Group II elements, Group Ill elements, Group IV elements, Group V 3 elements, Group VI elements, Group VII elements, Group VIII elements, algae, fungi, : 4 bacteria, surfactants, natural gums, synthetic gums, organic compounds, paper fibers, paper5 filters, clays, sulfites, sulfates, oxides, adhesives, starches, and combinations thereof.1 37. A process according to claim 35 wherein said environment is selected from the 2 group consisting of water-containing Systems, paper producing systems, pulp producing . 3 systems, printing systems, packaging systems, flexographic systems, food processing systems, 4 bleaching systems, metallurgy systems, acid washing systems, veterinary product systems, pesticide systems, meat processing systems, poultry processing systems, dairy processing 6 systems, sanitizing systems, and combinations thereof. 1 38. A process according to claim 37 wherein said water-containing systems are 2 selected from the group consisting of swimming pools, water treating systems, drainage 3 systems, boiler systems, chiller systems, sewage treating systems, irrigation systems, 4 agricultural systems, cooling tower systems, and combinations thereof. 1 39. A process according to claim 35 wherein said contaminant comprises algae 2 and said environment comprises a water-containing system. 1 40. A process according to claim 39 wherein said water-containing system 2 comprises a swimming pool. 1 41. A process according to claim 35 wherein said contaminant comprises a Group 2 Il element and said environment comprises a printing system. 1 42. A process according to claim 35 wherein said contaminant comprises a Group 2 Il element and said environment comprises a packaging system. ) 1 43. A process according to claim 35 wherein said contaminant comprises a starch . 2 and said environment comprises a packaging system.1 44. A process of producing a composition comprising contacting hydrogen ” 2 peroxide, glycolic acid, and water wherein said water is present in an amount of least about . 3 50 weight percent based on the total weight of said hydrogen peroxide, glycolic acid, and 4 water.
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EP (1) | EP1409632B1 (en) |
JP (2) | JP5614912B2 (en) |
CN (1) | CN1261555C (en) |
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AU (1) | AU8316501A (en) |
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CY (1) | CY1107765T1 (en) |
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US7029588B2 (en) * | 2003-03-19 | 2006-04-18 | Samuel Rupert Owens | Oxidizing solution and process for contaminants |
US8398781B2 (en) * | 2004-08-27 | 2013-03-19 | Ecolab Usa Inc. | Methods for cleaning industrial equipment with pre-treatment |
GEP20237469B (en) * | 2020-11-10 | 2023-02-10 | Dzala Llc | Novel compositions for neutralizing toxic effects of hydrogen peroxide in living cells or tissues |
DE102021129678A1 (en) | 2021-11-15 | 2023-05-17 | Knieler & Team Gmbh | Ready-to-use aqueous disinfectant composition |
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US2720441A (en) * | 1953-09-21 | 1955-10-11 | Du Pont | Peroxygen bleaching of nylon |
US4609475A (en) * | 1984-02-24 | 1986-09-02 | Halliburton Company | Method of improving the permeability of a subterranean formation by removal of polymeric materials therefrom |
US5122538A (en) * | 1990-07-23 | 1992-06-16 | Ecolab Inc. | Peroxy acid generator |
DE4026806A1 (en) * | 1990-08-24 | 1992-02-27 | Henkel Kgaa | Cleaning carpet by impregnation with aq. soln. - contg. solid inorganic peroxide, activator for peroxide, and surfactant |
JP3397383B2 (en) * | 1992-10-28 | 2003-04-14 | 花王株式会社 | Liquid bleaching detergent composition |
GB9302441D0 (en) * | 1993-02-08 | 1993-03-24 | Warwick Int Group | Oxidising agents |
US5409713A (en) * | 1993-03-17 | 1995-04-25 | Ecolab Inc. | Process for inhibition of microbial growth in aqueous transport streams |
US5961736A (en) * | 1993-04-05 | 1999-10-05 | Active Environmental Technologies, Inc. | Method for removal of contaminants from surfaces |
NZ260144A (en) * | 1993-04-12 | 1995-10-26 | Colgate Palmolive Co | Cleaning composition; contains three liquid phases which merge at a tricritical point; use for removing tar or grease from articles |
US5567444A (en) * | 1993-08-30 | 1996-10-22 | Ecolab Inc. | Potentiated aqueous ozone cleaning and sanitizing composition for removal of a contaminating soil from a surface |
EP0659876A3 (en) * | 1993-12-24 | 1996-12-04 | Procter & Gamble | Detergent additive composition. |
US5759975A (en) * | 1996-08-26 | 1998-06-02 | Gage Products Company | Paint line cleaner |
US5958984A (en) * | 1996-10-10 | 1999-09-28 | Devillez; Richard L. | Method and composition for skin treatment |
JPH115995A (en) * | 1997-04-21 | 1999-01-12 | Lion Corp | Liquid oxygenic bleaching agent composition |
JP3370571B2 (en) * | 1997-09-03 | 2003-01-27 | クリーンケミカル株式会社 | Disinfectant cleaning agents for medical equipment and disinfecting cleaning methods |
JPH1180794A (en) * | 1997-09-08 | 1999-03-26 | Kao Corp | Liquid bleaching composition |
JP3766746B2 (en) * | 1997-12-24 | 2006-04-19 | ライオン株式会社 | Liquid bleach composition |
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ATE367431T1 (en) | 2007-08-15 |
ES2288980T3 (en) | 2008-02-01 |
EP1409632A4 (en) | 2004-08-25 |
PT1409632E (en) | 2007-10-11 |
CN1261555C (en) | 2006-06-28 |
AU2001283165B2 (en) | 2006-10-26 |
DK1409632T3 (en) | 2007-11-12 |
AU8316501A (en) | 2002-02-18 |
PL366164A1 (en) | 2005-01-24 |
CA2417927C (en) | 2012-05-22 |
BR0113031B1 (en) | 2012-01-24 |
MXPA03001038A (en) | 2004-09-10 |
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JP2004519529A (en) | 2004-07-02 |
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IL154269A (en) | 2007-03-08 |
JP2014224265A (en) | 2014-12-04 |
PL199174B1 (en) | 2008-08-29 |
BR0113031A (en) | 2004-11-09 |
EP1409632B1 (en) | 2007-07-18 |
EP1409632A1 (en) | 2004-04-21 |
NZ545460A (en) | 2008-07-31 |
IL154269A0 (en) | 2003-09-17 |
CN1447852A (en) | 2003-10-08 |
JP5976731B2 (en) | 2016-08-24 |
WO2002012428A1 (en) | 2002-02-14 |
JP5614912B2 (en) | 2014-10-29 |
CY1107765T1 (en) | 2013-04-18 |
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