CA2396170A1 - Self-indicating neutralizing compositions - Google Patents
Self-indicating neutralizing compositions Download PDFInfo
- Publication number
- CA2396170A1 CA2396170A1 CA002396170A CA2396170A CA2396170A1 CA 2396170 A1 CA2396170 A1 CA 2396170A1 CA 002396170 A CA002396170 A CA 002396170A CA 2396170 A CA2396170 A CA 2396170A CA 2396170 A1 CA2396170 A1 CA 2396170A1
- Authority
- CA
- Canada
- Prior art keywords
- composition
- present
- neutralizing
- weight
- solution
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 87
- 230000003472 neutralizing effect Effects 0.000 title claims abstract description 46
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 19
- 239000007793 ph indicator Substances 0.000 claims abstract description 15
- 239000011230 binding agent Substances 0.000 claims abstract description 13
- 239000007884 disintegrant Substances 0.000 claims abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 16
- 239000000945 filler Substances 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 11
- 230000007935 neutral effect Effects 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 6
- 239000000377 silicon dioxide Substances 0.000 claims description 5
- -1 clays Inorganic materials 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
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- 229910000323 aluminium silicate Inorganic materials 0.000 claims description 3
- 239000004033 plastic Substances 0.000 claims description 3
- 229920003023 plastic Polymers 0.000 claims description 3
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- 150000004760 silicates Chemical class 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 235000019738 Limestone Nutrition 0.000 claims description 2
- 239000000404 calcium aluminium silicate Substances 0.000 claims description 2
- 235000012215 calcium aluminium silicate Nutrition 0.000 claims description 2
- WNCYAPRTYDMSFP-UHFFFAOYSA-N calcium aluminosilicate Chemical compound [Al+3].[Al+3].[Ca+2].[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O WNCYAPRTYDMSFP-UHFFFAOYSA-N 0.000 claims description 2
- 229940078583 calcium aluminosilicate Drugs 0.000 claims description 2
- 239000000919 ceramic Substances 0.000 claims description 2
- 239000006028 limestone Substances 0.000 claims description 2
- 239000004576 sand Substances 0.000 claims description 2
- 239000010457 zeolite Substances 0.000 claims description 2
- 239000010881 fly ash Substances 0.000 claims 1
- 238000006386 neutralization reaction Methods 0.000 abstract description 3
- 239000000243 solution Substances 0.000 description 13
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- 238000005056 compaction Methods 0.000 description 8
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- 238000007792 addition Methods 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 2
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- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
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- 239000001099 ammonium carbonate Substances 0.000 description 2
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- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
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- KYKNRZGSIGMXFH-ZVGUSBNCSA-M potassium bitartrate Chemical compound [K+].OC(=O)[C@H](O)[C@@H](O)C([O-])=O KYKNRZGSIGMXFH-ZVGUSBNCSA-M 0.000 description 2
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- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
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- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- RTZZCYNQPHTPPL-UHFFFAOYSA-N 3-nitrophenol Chemical compound OC1=CC=CC([N+]([O-])=O)=C1 RTZZCYNQPHTPPL-UHFFFAOYSA-N 0.000 description 1
- OLQIKGSZDTXODA-UHFFFAOYSA-N 4-[3-(4-hydroxy-2-methylphenyl)-1,1-dioxo-2,1$l^{6}-benzoxathiol-3-yl]-3-methylphenol Chemical compound CC1=CC(O)=CC=C1C1(C=2C(=CC(O)=CC=2)C)C2=CC=CC=C2S(=O)(=O)O1 OLQIKGSZDTXODA-UHFFFAOYSA-N 0.000 description 1
- CJIJXIFQYOPWTF-UHFFFAOYSA-N 7-hydroxycoumarin Natural products O1C(=O)C=CC2=CC(O)=CC=C21 CJIJXIFQYOPWTF-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
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- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- BELBBZDIHDAJOR-UHFFFAOYSA-N Phenolsulfonephthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2S(=O)(=O)O1 BELBBZDIHDAJOR-UHFFFAOYSA-N 0.000 description 1
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- 235000021355 Stearic acid Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
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- LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 description 1
- TVWHNULVHGKJHS-UHFFFAOYSA-N Uric acid Natural products N1C(=O)NC(=O)C2NC(=O)NC21 TVWHNULVHGKJHS-UHFFFAOYSA-N 0.000 description 1
- FZQSLXQPHPOTHG-UHFFFAOYSA-N [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 Chemical compound [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 FZQSLXQPHPOTHG-UHFFFAOYSA-N 0.000 description 1
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- HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
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- 150000008064 anhydrides Chemical class 0.000 description 1
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- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- BITYAPCSNKJESK-UHFFFAOYSA-N potassiosodium Chemical compound [Na].[K] BITYAPCSNKJESK-UHFFFAOYSA-N 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000343 potassium bisulfate Inorganic materials 0.000 description 1
- 229940081543 potassium bitartrate Drugs 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- IWZKICVEHNUQTL-UHFFFAOYSA-M potassium hydrogen phthalate Chemical compound [K+].OC(=O)C1=CC=CC=C1C([O-])=O IWZKICVEHNUQTL-UHFFFAOYSA-M 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086065 potassium hydrogentartrate Drugs 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
- WKZJASQVARUVAW-UHFFFAOYSA-M potassium;hydron;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [K+].OC(=O)CC(O)(C(O)=O)CC([O-])=O WKZJASQVARUVAW-UHFFFAOYSA-M 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- ALMQPZAZAZTVLI-UHFFFAOYSA-N sodium;4-benzamido-2-hydroxybenzoic acid Chemical compound [Na+].C1=C(O)C(C(=O)O)=CC=C1NC(=O)C1=CC=CC=C1 ALMQPZAZAZTVLI-UHFFFAOYSA-N 0.000 description 1
- IAAKNVCARVEIFS-UHFFFAOYSA-M sodium;4-hydroxynaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(O)=CC=C(S([O-])(=O)=O)C2=C1 IAAKNVCARVEIFS-UHFFFAOYSA-M 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- MSLRPWGRFCKNIZ-UHFFFAOYSA-J tetrasodium;hydrogen peroxide;dicarbonate Chemical compound [Na+].[Na+].[Na+].[Na+].OO.OO.OO.[O-]C([O-])=O.[O-]C([O-])=O MSLRPWGRFCKNIZ-UHFFFAOYSA-J 0.000 description 1
- JADVWWSKYZXRGX-UHFFFAOYSA-M thioflavine T Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C1=[N+](C)C2=CC=C(C)C=C2S1 JADVWWSKYZXRGX-UHFFFAOYSA-M 0.000 description 1
- CPWJKGIJFGMVPL-UHFFFAOYSA-K tricesium;phosphate Chemical compound [Cs+].[Cs+].[Cs+].[O-]P([O-])([O-])=O CPWJKGIJFGMVPL-UHFFFAOYSA-K 0.000 description 1
- TWQULNDIKKJZPH-UHFFFAOYSA-K trilithium;phosphate Chemical compound [Li+].[Li+].[Li+].[O-]P([O-])([O-])=O TWQULNDIKKJZPH-UHFFFAOYSA-K 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- ORHBXUUXSCNDEV-UHFFFAOYSA-N umbelliferone Chemical compound C1=CC(=O)OC2=CC(O)=CC=C21 ORHBXUUXSCNDEV-UHFFFAOYSA-N 0.000 description 1
- HFTAFOQKODTIJY-UHFFFAOYSA-N umbelliferone Natural products Cc1cc2C=CC(=O)Oc2cc1OCC=CC(C)(C)O HFTAFOQKODTIJY-UHFFFAOYSA-N 0.000 description 1
- 229940116269 uric acid Drugs 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/66—Treatment of water, waste water, or sewage by neutralisation; pH adjustment
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2209/00—Controlling or monitoring parameters in water treatment
- C02F2209/06—Controlling or monitoring parameters in water treatment pH
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Detergent Compositions (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paints Or Removers (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicinal Preparation (AREA)
Abstract
A unitized, self-indicating, neutralizing composition comprises a neutralizi ng agent, a binding agent, and a pH indicator. The composition may optionally further include a disintegrant. The composition is convenient to use and is especially useful in the neutralization of wash water from cementitious compositions.
Description
SELF-INDICATING NEUTRALIZING COMPOSITIONS
Background of Invention Wash water that has been used to clean equipment that has been exposed to substances which are highly alkaline or acidic, for example, water used to wash cement mixing equipment, will o$en not be at a neutral pH at the end of washing. The wash water will thus require neutralization before disposal, to comply with environmental regulations, This is usually achieved by addition of a neutralizing agent, and the achievement of an appropriate pH is verified by testing. This can be time-consuming. In addition, in the case of cement mixing equipment, such as mixer trucks, stationary mixers and chutes at job sites, the quantity of residual material is variable, and this makes estimating the amount of neutralizing agent difficult. This means that multiple additions of neutralizing agent and subsequent testing are often needed.
What is needed in the art is a neutralizing agent that can indicate when the solution is neutralized without the need for measuring pH.
Summary of Invention The present invention provides a unitized, self indicating, neutralizing composition comprising a neutralizing agent, a binding agent, and a pH indicator.
The present invention also provides a method of neutralizing a solution to about a neutral pH
comprising adding a sufficient amount of a unitized, self indicating, neutralizing composition comprising a neutralizing agent, a binding agent, and a pH
indicator to the solution, until the solution has about a neutral pH as indicated by the pH
indicator, wherein the neutralizing composition dissolves into the solution to effect neutralization.
Background of Invention Wash water that has been used to clean equipment that has been exposed to substances which are highly alkaline or acidic, for example, water used to wash cement mixing equipment, will o$en not be at a neutral pH at the end of washing. The wash water will thus require neutralization before disposal, to comply with environmental regulations, This is usually achieved by addition of a neutralizing agent, and the achievement of an appropriate pH is verified by testing. This can be time-consuming. In addition, in the case of cement mixing equipment, such as mixer trucks, stationary mixers and chutes at job sites, the quantity of residual material is variable, and this makes estimating the amount of neutralizing agent difficult. This means that multiple additions of neutralizing agent and subsequent testing are often needed.
What is needed in the art is a neutralizing agent that can indicate when the solution is neutralized without the need for measuring pH.
Summary of Invention The present invention provides a unitized, self indicating, neutralizing composition comprising a neutralizing agent, a binding agent, and a pH indicator.
The present invention also provides a method of neutralizing a solution to about a neutral pH
comprising adding a sufficient amount of a unitized, self indicating, neutralizing composition comprising a neutralizing agent, a binding agent, and a pH
indicator to the solution, until the solution has about a neutral pH as indicated by the pH
indicator, wherein the neutralizing composition dissolves into the solution to effect neutralization.
Brief Description of Drawings Figure 1 illustrates one embodiment of the present invention wherein the self indicating neutralizing composition is severable into smaller units.
Detailed Description The composition is unitized to provide ease of use for adding the composition to the solution. By "unitized" it is meant that the composition is solid and in a single unit of suitable size, as opposed to, say, a powder. Such units are generally prepared by compaction. Any known method of compacting powdered or flake solid materials may be used to produce the self indicating neutralizing compositions. Examples of such methods include extrusion moulding ofthe self indicating neutralizing composition, pressing, stamping or tabletting, and moulding, such as by melting and pouring into a shaped mould.
The composition can be unitized into any desired shape, preferably a tablet or puck shape.
There are cases where compaction is unnecessary; these will be further discussed hereinunder.
The result of any such compaction should be that the composition has sufficient strength to allow handling, but is also sufficiently friable to break down under conditions of use and allow the composition to perform its function.
The composition is added to a solution that is not at a neutral pH to bring it to a pH that is about neutral, that is, between about 5.5 and about 8.5.
The neutralizing agent may be an acid or a base. Preferably, the neutralizing agent comprises an organic chemical.
Examples of suitable neutralizing agents include, but are not limited to, citric acid, acetic acid, phosphoric acid, succinic acid, phthalic acid, uric acid, stearic acid, lauric acid, pahnitic acid, oleic acid, oxalic acid, tartaric acid, malic acid, lactic acid, carbonic acid, boric acid, sulfuric acid, nitric acid, hydrochloric acid, benzoic acid, monosodium citrate, monopotassium citrate, KHS04, NaHS04, KHZPO~, and mixtures thereof. Generally, the neutralizing agent is present to the extent of from 45% to 85% based on the weight of the composition. Preferably, the neutralizing agent is present to the extent of from 65% to 75%
based on the weight of the composition.
Examples of the binding agent include, but are not limited to, polyethylene glycol, polyoxypropylene glycol adducts, polyoxyethylenestearate, polyvinylbutyral, polyvinyl alcohols, paraffin, polyvinylacetate, polyvinyl methyl ether-malefic anhydride (PVMIMA), cellulose,~talc, clays, silicates, silica fume, fumed silica such as "Aerosil"
(trade mark), precipitated silica gel, organic pigments, synthetic resins, and mixtures thereof. Generally, the binding agent is present from 5% to 25% based on the weight of the composition.
Preferably, the binding agent is present from 6% to 15% based on the weight of the composition.
Examples of the pH indicator include, but are not limited to, phenol red, phenolphthalein, cresol red; metanil yellow; m-nitrophenol; curcurmin; alizarin; alizarin yellow R; alizarin blue; methyl orange; litmus; Congo red; bromthymol blue; chlorphenol red;
cresol purple;
brilliant diazol yellow; salts of phenolphthalein; neutral red; acid R
phosphine, Gleves acid;
coumaric acid; 3,6-dioxyphthalic dinitrile; magnesium 8-hydroxyquinolinate; j3-methylumbelliferone; 1-naphthol 4-sulfonic acid; orcinaurine; patent phosphine; thioflavine;
umbelliferone; and mixtures thereof. Preferably, the salts of phenolphthalein are selected from the group consisting of sodium, disodium, potassium, and mixtures thereof. Generally, the pH indicator is present from 0.001% to 0.8% based on the weight ofthe composition.
Preferably, the pH indicator is present from 0.1 % to 0.8% based on the weight of the composition. More preferably, the pH indicator is present from 0. I % to 0.4%
based on the weight of the composition.
Additionally, the composition may include a disintegrant to aid in dissolving the composition in the solution. Preferably, the disintegrant is an effervescing disintegrant, activated by contact with the aqueous solution to be neutralized. Examples of suitable disintegrants include, but are not limited to, lithium carbonate, lithium bicarbonate, sodium carbonate, sodium bicarbonate, potassium carbonate, potassium bicarbonate, caesium carbonate, caesium bicarbonate, ammonium carbonate, ammonium bicarbonate, lithium phosphate, sodium phosphate, potassium phosphate, caesium phosphate, ammonium phosphate, borax, magnesium carbonate with citric acid, potassium bitartrate, potassium biphtbalate, potassium oxalate, potassium hydrogen phthalate, alkaline perborates, perchlorates, permaganates, chlorates, potassium tetraborate, sodium carbonate peroxide, tarfiaric acid, Rochelle salt (potassium sodium tarixate), citric acid, potassium hydrogen tartrate, NR.q.+ carbonate ((NR4~ZC03), NR4''~ bicarbonate ({N12~.~2C03), peroxides, hyperoxides, materials that liberate nitrogen, and mixtures thereof, wherein R--C,lH2n+1, ~6H4CnH2n+1~ or C6H4X,.~'c'herein n is an integer from 1 to 24, and X is selected from the group consisting of COOH, polyethylene oxide, alkyl sulfonate, and mixtures thereof.
Preferably, n is an integer from 8 to 18. Suitable examples of materials that liberate nitrogen include, but are not limited to, hydrazine, compounds containing an azo group, and azides.
Generally, the disintegrant is present to the extent of from 1% to 30% based on the weight of the composition. Preferably, the disintegrant is present to the extent of from 3% to 21%
based on the weight of the composition.
The composition can also include other additives for manufacturing as needed.
Examples of the other additives include, but are not limited to, dyes, pigments, dyeing assistants, colorants, tannins, colloidal material, toners, clays, tales, barytes, whitening agents, mould release agents, lubricants, and mixtures thereof. Generally, the quantity of additives present is up to 70% based on the weight of the composition. Preferably, the additives are present to the extent of up to 12% based on the weight of the composition.
When the unitized composition is to be formed by compaction, it is preferable to add inert .
fillers to the self indicating neutralizing composition. This helps render individual units structurally stable for physical handling and storage, and/or facilitate the rapid breakdown by dissolution and/or fragmentation of the unit when added to an aqueous solution. These characteristics are obtained by balancing the addition percentage of inert filler and the compacting pressure, to provide a self indicating neutralizing composition unit of desired physical integrity and stability, and of desired solubility, friability or fragmentability. The provision of a suitable structural stability is within the routine skill of the art.
S
Fillers may be present in the self indicating neutralizing composition in an amount of up to 50% by the weight of the composition, if the sole function of the filler is as a filler.
However, if the filler performs another function in the composition in addition to acting as a filler, it can be present in an amount of up to 95% based on the weight of the composition.
Preferably, the amount of filler in the composition is from 5% to 15% based on the weight of the composition.
Examples of suitable fillers include silica sand, silica fume, other natural or synthetic silica-based materials, "Micro-Cell" (trade mark) E silica (Celite Corp.), silicates, calcium aluminosilicate, aluminosilicates, clays, alumina, .ALUNDUM (trade mark) aluminosilicates (Norton), zeolites, ceramic spheres, ffy ash, limestone powder, and finely divided or powdered plastic.
Preferably, the neutralizing agent, the pH indicator, the binder, the disintegrant, and any other additive in the composition are solids. If it is desired to use liquid components, these may be processed into solid compacted units by adsorbing them on to carriers, which are advantageously the inert fillers hereinabove described. The carriers are contacted by the liquid components, and preferably at least partially dried, such as by air drying, prior to compaction. For water-alcohol-borne materials, the carriers are fully dried to prevent reaction with other components when compacted. Carriers are preferably present in the composition from 5% to 25% by weight of the composition.
In yet another embodiment of the present invention, soluble solid self indicating neutralizing composition materials may be dissolved in a suitable liquid solvent, such as water, and the resulting solution impregnated or adsorbed on to carriers by contacting the carrier with the solution, and preferably at least partially drying, prior to compaction.
Similarly, insoluble solid admixtures may be slurried in a liquid and the carrier contacted with the slurry to form a coated carrier prior to compaction.
The self indicating neutralizing composition units according to the present invention are sized so as to deliver a selected amount of pre-measured self indicating neutralizing composition to a desired or standardized volume of aqueous solution.
It is within the scope of the invention to use multiple units for a given volume of aqueous solution. It is further within the scope of the present invention for the self indicating neutralizing composition 11 to be compacted into a unit 10 which is severable, such as by S providing perforations 12 of the compact or the like, to provide selected, structurally stable fractions for smaller volumes of aqueous solution. (Fig. l .) For practical considerations, the unit size is preferably small, so as to provide the most efficient packing and ease of handling. A preferred size of the unit is such that it can deliver sufficient self indicating neutralizing composition for about 15 litres.
For ease of handling and storability, the self indicating neutralizing composition compacted units are preferably somewhat moisture resistant. Such moisture resistance may be imparted by the selection of an appropriate binder, preferably a binder which breaks down at a pH
experienced by the unit in the aqueous solution, which may be at pH 11 and above. If such a binder is used, it is possible to produce a self indicating neutralizing composition article without compaction.
For situations where the composition units must be stored in a substantially water-free environment, they may be stored individually, but preferably in number, in a sealable plastic bag such as those sold under the trademark "Zip-Loc". Any water-insoluble container, however, is suitable for such storage, so long as it is water-impermeable and not water-degradable.
In a further embodiment of the invention, the compacted unit is coated with a material that is at least partially insoluble in water. Coating the compacted unit with a material that is substantially insoluble in water enhances the storage capabilities of the compacted unit in a moist environment and protects any hydroscopic components present in the self indicating neutralizing composition. Such a water-insoluble coating should be capable of breaking or dissolving at the pH of the aqueous solution, and should preferably be thin, of the order of 0.025-0.25mm. In addition, the material should not be deleterious to the properties desired for the final product. The coating may be selected so as to protect the compacted unit, and/or to protect the user from any hazardous materials in the self indicating neutralizing composition. Examples of suitable substantially water-insoluble materials include clays, latexes, polystyrenes, polyurethanes, and celluloses wherein the hydroxyl groups have been substituted with alkyls.
More information regarding unitization of materials can be found in United States Patent No.
Detailed Description The composition is unitized to provide ease of use for adding the composition to the solution. By "unitized" it is meant that the composition is solid and in a single unit of suitable size, as opposed to, say, a powder. Such units are generally prepared by compaction. Any known method of compacting powdered or flake solid materials may be used to produce the self indicating neutralizing compositions. Examples of such methods include extrusion moulding ofthe self indicating neutralizing composition, pressing, stamping or tabletting, and moulding, such as by melting and pouring into a shaped mould.
The composition can be unitized into any desired shape, preferably a tablet or puck shape.
There are cases where compaction is unnecessary; these will be further discussed hereinunder.
The result of any such compaction should be that the composition has sufficient strength to allow handling, but is also sufficiently friable to break down under conditions of use and allow the composition to perform its function.
The composition is added to a solution that is not at a neutral pH to bring it to a pH that is about neutral, that is, between about 5.5 and about 8.5.
The neutralizing agent may be an acid or a base. Preferably, the neutralizing agent comprises an organic chemical.
Examples of suitable neutralizing agents include, but are not limited to, citric acid, acetic acid, phosphoric acid, succinic acid, phthalic acid, uric acid, stearic acid, lauric acid, pahnitic acid, oleic acid, oxalic acid, tartaric acid, malic acid, lactic acid, carbonic acid, boric acid, sulfuric acid, nitric acid, hydrochloric acid, benzoic acid, monosodium citrate, monopotassium citrate, KHS04, NaHS04, KHZPO~, and mixtures thereof. Generally, the neutralizing agent is present to the extent of from 45% to 85% based on the weight of the composition. Preferably, the neutralizing agent is present to the extent of from 65% to 75%
based on the weight of the composition.
Examples of the binding agent include, but are not limited to, polyethylene glycol, polyoxypropylene glycol adducts, polyoxyethylenestearate, polyvinylbutyral, polyvinyl alcohols, paraffin, polyvinylacetate, polyvinyl methyl ether-malefic anhydride (PVMIMA), cellulose,~talc, clays, silicates, silica fume, fumed silica such as "Aerosil"
(trade mark), precipitated silica gel, organic pigments, synthetic resins, and mixtures thereof. Generally, the binding agent is present from 5% to 25% based on the weight of the composition.
Preferably, the binding agent is present from 6% to 15% based on the weight of the composition.
Examples of the pH indicator include, but are not limited to, phenol red, phenolphthalein, cresol red; metanil yellow; m-nitrophenol; curcurmin; alizarin; alizarin yellow R; alizarin blue; methyl orange; litmus; Congo red; bromthymol blue; chlorphenol red;
cresol purple;
brilliant diazol yellow; salts of phenolphthalein; neutral red; acid R
phosphine, Gleves acid;
coumaric acid; 3,6-dioxyphthalic dinitrile; magnesium 8-hydroxyquinolinate; j3-methylumbelliferone; 1-naphthol 4-sulfonic acid; orcinaurine; patent phosphine; thioflavine;
umbelliferone; and mixtures thereof. Preferably, the salts of phenolphthalein are selected from the group consisting of sodium, disodium, potassium, and mixtures thereof. Generally, the pH indicator is present from 0.001% to 0.8% based on the weight ofthe composition.
Preferably, the pH indicator is present from 0.1 % to 0.8% based on the weight of the composition. More preferably, the pH indicator is present from 0. I % to 0.4%
based on the weight of the composition.
Additionally, the composition may include a disintegrant to aid in dissolving the composition in the solution. Preferably, the disintegrant is an effervescing disintegrant, activated by contact with the aqueous solution to be neutralized. Examples of suitable disintegrants include, but are not limited to, lithium carbonate, lithium bicarbonate, sodium carbonate, sodium bicarbonate, potassium carbonate, potassium bicarbonate, caesium carbonate, caesium bicarbonate, ammonium carbonate, ammonium bicarbonate, lithium phosphate, sodium phosphate, potassium phosphate, caesium phosphate, ammonium phosphate, borax, magnesium carbonate with citric acid, potassium bitartrate, potassium biphtbalate, potassium oxalate, potassium hydrogen phthalate, alkaline perborates, perchlorates, permaganates, chlorates, potassium tetraborate, sodium carbonate peroxide, tarfiaric acid, Rochelle salt (potassium sodium tarixate), citric acid, potassium hydrogen tartrate, NR.q.+ carbonate ((NR4~ZC03), NR4''~ bicarbonate ({N12~.~2C03), peroxides, hyperoxides, materials that liberate nitrogen, and mixtures thereof, wherein R--C,lH2n+1, ~6H4CnH2n+1~ or C6H4X,.~'c'herein n is an integer from 1 to 24, and X is selected from the group consisting of COOH, polyethylene oxide, alkyl sulfonate, and mixtures thereof.
Preferably, n is an integer from 8 to 18. Suitable examples of materials that liberate nitrogen include, but are not limited to, hydrazine, compounds containing an azo group, and azides.
Generally, the disintegrant is present to the extent of from 1% to 30% based on the weight of the composition. Preferably, the disintegrant is present to the extent of from 3% to 21%
based on the weight of the composition.
The composition can also include other additives for manufacturing as needed.
Examples of the other additives include, but are not limited to, dyes, pigments, dyeing assistants, colorants, tannins, colloidal material, toners, clays, tales, barytes, whitening agents, mould release agents, lubricants, and mixtures thereof. Generally, the quantity of additives present is up to 70% based on the weight of the composition. Preferably, the additives are present to the extent of up to 12% based on the weight of the composition.
When the unitized composition is to be formed by compaction, it is preferable to add inert .
fillers to the self indicating neutralizing composition. This helps render individual units structurally stable for physical handling and storage, and/or facilitate the rapid breakdown by dissolution and/or fragmentation of the unit when added to an aqueous solution. These characteristics are obtained by balancing the addition percentage of inert filler and the compacting pressure, to provide a self indicating neutralizing composition unit of desired physical integrity and stability, and of desired solubility, friability or fragmentability. The provision of a suitable structural stability is within the routine skill of the art.
S
Fillers may be present in the self indicating neutralizing composition in an amount of up to 50% by the weight of the composition, if the sole function of the filler is as a filler.
However, if the filler performs another function in the composition in addition to acting as a filler, it can be present in an amount of up to 95% based on the weight of the composition.
Preferably, the amount of filler in the composition is from 5% to 15% based on the weight of the composition.
Examples of suitable fillers include silica sand, silica fume, other natural or synthetic silica-based materials, "Micro-Cell" (trade mark) E silica (Celite Corp.), silicates, calcium aluminosilicate, aluminosilicates, clays, alumina, .ALUNDUM (trade mark) aluminosilicates (Norton), zeolites, ceramic spheres, ffy ash, limestone powder, and finely divided or powdered plastic.
Preferably, the neutralizing agent, the pH indicator, the binder, the disintegrant, and any other additive in the composition are solids. If it is desired to use liquid components, these may be processed into solid compacted units by adsorbing them on to carriers, which are advantageously the inert fillers hereinabove described. The carriers are contacted by the liquid components, and preferably at least partially dried, such as by air drying, prior to compaction. For water-alcohol-borne materials, the carriers are fully dried to prevent reaction with other components when compacted. Carriers are preferably present in the composition from 5% to 25% by weight of the composition.
In yet another embodiment of the present invention, soluble solid self indicating neutralizing composition materials may be dissolved in a suitable liquid solvent, such as water, and the resulting solution impregnated or adsorbed on to carriers by contacting the carrier with the solution, and preferably at least partially drying, prior to compaction.
Similarly, insoluble solid admixtures may be slurried in a liquid and the carrier contacted with the slurry to form a coated carrier prior to compaction.
The self indicating neutralizing composition units according to the present invention are sized so as to deliver a selected amount of pre-measured self indicating neutralizing composition to a desired or standardized volume of aqueous solution.
It is within the scope of the invention to use multiple units for a given volume of aqueous solution. It is further within the scope of the present invention for the self indicating neutralizing composition 11 to be compacted into a unit 10 which is severable, such as by S providing perforations 12 of the compact or the like, to provide selected, structurally stable fractions for smaller volumes of aqueous solution. (Fig. l .) For practical considerations, the unit size is preferably small, so as to provide the most efficient packing and ease of handling. A preferred size of the unit is such that it can deliver sufficient self indicating neutralizing composition for about 15 litres.
For ease of handling and storability, the self indicating neutralizing composition compacted units are preferably somewhat moisture resistant. Such moisture resistance may be imparted by the selection of an appropriate binder, preferably a binder which breaks down at a pH
experienced by the unit in the aqueous solution, which may be at pH 11 and above. If such a binder is used, it is possible to produce a self indicating neutralizing composition article without compaction.
For situations where the composition units must be stored in a substantially water-free environment, they may be stored individually, but preferably in number, in a sealable plastic bag such as those sold under the trademark "Zip-Loc". Any water-insoluble container, however, is suitable for such storage, so long as it is water-impermeable and not water-degradable.
In a further embodiment of the invention, the compacted unit is coated with a material that is at least partially insoluble in water. Coating the compacted unit with a material that is substantially insoluble in water enhances the storage capabilities of the compacted unit in a moist environment and protects any hydroscopic components present in the self indicating neutralizing composition. Such a water-insoluble coating should be capable of breaking or dissolving at the pH of the aqueous solution, and should preferably be thin, of the order of 0.025-0.25mm. In addition, the material should not be deleterious to the properties desired for the final product. The coating may be selected so as to protect the compacted unit, and/or to protect the user from any hazardous materials in the self indicating neutralizing composition. Examples of suitable substantially water-insoluble materials include clays, latexes, polystyrenes, polyurethanes, and celluloses wherein the hydroxyl groups have been substituted with alkyls.
More information regarding unitization of materials can be found in United States Patent No.
5,728,209 to Bury et al., which is incorporated herein by reference.
The present invention also includes a method of neutralizing a solution to about a neutral pH.
A unitized composition is added to the solution and allowed to dissolve in the solution. If the pH indicator does not change color to indicate a pH of about neutral, then additional unitized compositions may be added until the pH indicator indicates a pH of about neutral.
A further advantage of the compacted units of self indicating neutralizing composition according to the present invention, is that, unlike liquid compositions, they are not prone to freeze, slush or separate at low temperature. The use of compacted units of self indicating neutralizing composition according to the present invention overcomes job site dusting problems associated with powders, avoids the use of bullcy measuring dispensing equipment at the job site for liquids or solid free-flowing components, and overcomes spillage concerns associated with using components of the self indicating neutralizing composition separately.
The present invention also includes a method of neutralizing a solution to about a neutral pH.
A unitized composition is added to the solution and allowed to dissolve in the solution. If the pH indicator does not change color to indicate a pH of about neutral, then additional unitized compositions may be added until the pH indicator indicates a pH of about neutral.
A further advantage of the compacted units of self indicating neutralizing composition according to the present invention, is that, unlike liquid compositions, they are not prone to freeze, slush or separate at low temperature. The use of compacted units of self indicating neutralizing composition according to the present invention overcomes job site dusting problems associated with powders, avoids the use of bullcy measuring dispensing equipment at the job site for liquids or solid free-flowing components, and overcomes spillage concerns associated with using components of the self indicating neutralizing composition separately.
Claims (10)
1. A unitized, self indicating, neutralizing composition comprising a neutralizing agent, a binding agent, and a pH indicator.
2. The composition of claim 1 further comprising at least one of a disintegrant, a filler, and a carrier.
3. The composition of claim 2, wherein if present, the disintegrant is a effervescing agent.
4. The composition of claim 1, wherein the neutralizing agent is present from 45% to 85% by weight of the composition, the binding agent is present from 5% to 25%
by weight of the composition, and the pH indicator is present from 0.001 % to 0.8% by weight of the composition.
by weight of the composition, and the pH indicator is present from 0.001 % to 0.8% by weight of the composition.
5. The composition of claim 2, wherein if present, the filler is present up to 95% by weight of the composition, the disintegrant is present from 1% to 30% by weight of the composition, and the carrier is present from 5% to 25% by weight of the composition.
6. The composition of claim 1, wherein the neutralizing agent comprises an organic chemical.
7. The composition of claim 2, wherein if present, the filler is selected from the group consisting of silica sand, silica fume, natural or synthetic silica-based materials, silicates, calcium aluminosilicate, aluminosilicates, clays, alumina, zeolites, ceramic spheres, fly ash, limestone powder, finely divided or powdered plastic, and mixtures thereof.
8. The composition of claim 1, wherein the composition further comprises a coating that is at least partially insoluble in water disposed over the composition.
9. A method of neutralizing a solution to about a neutral pH comprising:
adding a sufficient amount of a unitized, self-indicating, neutralizing composition comprising a neutralizing agent, a binding agent, and a pH indicator to the solution until the solution has about a neutral pH as indicated by the pH indicator, wherein the neutralizing composition dissolves into the solution.
adding a sufficient amount of a unitized, self-indicating, neutralizing composition comprising a neutralizing agent, a binding agent, and a pH indicator to the solution until the solution has about a neutral pH as indicated by the pH indicator, wherein the neutralizing composition dissolves into the solution.
10. A method according to claim 9, wherein the solution is wash water from a cementitious composition.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US70894600A | 2000-11-08 | 2000-11-08 | |
US09/708,946 | 2000-11-08 | ||
PCT/EP2001/010983 WO2002038506A2 (en) | 2000-11-08 | 2001-11-02 | Self-indicating neutralizing compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2396170A1 true CA2396170A1 (en) | 2002-05-16 |
Family
ID=24847809
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002396170A Abandoned CA2396170A1 (en) | 2000-11-08 | 2001-11-02 | Self-indicating neutralizing compositions |
Country Status (8)
Country | Link |
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EP (1) | EP1335883A2 (en) |
JP (1) | JP2004512950A (en) |
AU (1) | AU2002214987A1 (en) |
BR (1) | BR0107466A (en) |
CA (1) | CA2396170A1 (en) |
EC (1) | ECSP024284A (en) |
MX (1) | MXPA02006743A (en) |
WO (1) | WO2002038506A2 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006102705A (en) * | 2004-10-08 | 2006-04-20 | Noda:Kk | Cement draining sheet and cement draining treatment method |
JP2010274150A (en) * | 2009-05-26 | 2010-12-09 | Panasonic Electric Works Co Ltd | Additive for water treatment and water treatment apparatus |
AU2013203799B2 (en) * | 2012-02-27 | 2014-12-04 | Zodiac Group Australia Pty Limited | Water treatment product and method |
JP5571138B2 (en) * | 2012-08-13 | 2014-08-13 | 株式会社Kensyo | Wastewater neutralization buffer treatment agent, wastewater neutralization buffer treatment additive water and wastewater treatment method |
WO2020093172A1 (en) | 2018-11-08 | 2020-05-14 | Neovasc Tiara Inc. | Ventricular deployment of a transcatheter mitral valve prosthesis |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6181497A (en) * | 1983-09-22 | 1986-04-25 | 樋口 泰義 | Method of discriminating neutralization easily by neutralizing agent by use of viscous acid detergent containing ph indicator |
EP0376126B1 (en) * | 1988-12-30 | 1996-10-09 | Purotech Ltd. | Improvements in water purification systems |
JPH05305286A (en) * | 1992-04-28 | 1993-11-19 | Konica Corp | Flocculation treatment of waste liquid of processed photosensitive material |
US5267532A (en) * | 1992-05-05 | 1993-12-07 | Anitox Corporation | pH-indicating material and cat litter containing same |
JPH06246278A (en) * | 1993-02-24 | 1994-09-06 | Hazama Gumi Ltd | Treatment of mine wastewater and hot spring water |
EP0909555B1 (en) * | 1996-06-17 | 2004-05-26 | Otsuka Pharmaceutical Factory, Inc. | Package for container of liquid medicine containing bicarbonate |
US5792384A (en) * | 1997-01-31 | 1998-08-11 | Warren; James R. | Concrete masons' hand rinse |
-
2001
- 2001-11-02 AU AU2002214987A patent/AU2002214987A1/en not_active Abandoned
- 2001-11-02 MX MXPA02006743A patent/MXPA02006743A/en unknown
- 2001-11-02 BR BR0107466-0A patent/BR0107466A/en not_active Application Discontinuation
- 2001-11-02 EP EP01983495A patent/EP1335883A2/en not_active Withdrawn
- 2001-11-02 WO PCT/EP2001/010983 patent/WO2002038506A2/en not_active Application Discontinuation
- 2001-11-02 CA CA002396170A patent/CA2396170A1/en not_active Abandoned
- 2001-11-02 JP JP2002541047A patent/JP2004512950A/en active Pending
-
2002
- 2002-07-08 EC ECSP024284 patent/ECSP024284A/en unknown
Also Published As
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MXPA02006743A (en) | 2002-10-23 |
BR0107466A (en) | 2002-11-19 |
WO2002038506A2 (en) | 2002-05-16 |
WO2002038506A3 (en) | 2002-08-01 |
ECSP024284A (en) | 2002-09-27 |
EP1335883A2 (en) | 2003-08-20 |
AU2002214987A1 (en) | 2002-05-21 |
JP2004512950A (en) | 2004-04-30 |
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