WO2002038506A2 - Self-indicating neutralizing compositions - Google Patents

Self-indicating neutralizing compositions Download PDF

Info

Publication number
WO2002038506A2
WO2002038506A2 PCT/EP2001/010983 EP0110983W WO0238506A2 WO 2002038506 A2 WO2002038506 A2 WO 2002038506A2 EP 0110983 W EP0110983 W EP 0110983W WO 0238506 A2 WO0238506 A2 WO 0238506A2
Authority
WO
WIPO (PCT)
Prior art keywords
composition
present
neutralizing
weight
self
Prior art date
Application number
PCT/EP2001/010983
Other languages
English (en)
French (fr)
Other versions
WO2002038506A3 (en
Inventor
Julie K. Buffenbarger
Runhai Lu
Zvi Grauer
Original Assignee
Mbt Holding Ag
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mbt Holding Ag filed Critical Mbt Holding Ag
Priority to BR0107466-0A priority Critical patent/BR0107466A/pt
Priority to CA002396170A priority patent/CA2396170A1/en
Priority to EP01983495A priority patent/EP1335883A2/en
Priority to JP2002541047A priority patent/JP2004512950A/ja
Priority to MXPA02006743A priority patent/MXPA02006743A/es
Priority to AU2002214987A priority patent/AU2002214987A1/en
Publication of WO2002038506A2 publication Critical patent/WO2002038506A2/en
Publication of WO2002038506A3 publication Critical patent/WO2002038506A3/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/66Treatment of water, waste water, or sewage by neutralisation; pH adjustment
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2209/00Controlling or monitoring parameters in water treatment
    • C02F2209/06Controlling or monitoring parameters in water treatment pH

Definitions

  • 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 often 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.
  • 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.
  • the present invention provides a unitized, self-indicating, neutralizing composition
  • a neutralizing agent 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.
  • Figure 1 illustrates one embodiment of the present invention wherein the self-indicating neutralizing composition is severable into smaller units.
  • the composition is unitized to provide ease of use for adding the composition to the solution.
  • 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 of the self-indicating neutralizing composition, pressing, stamping or tahletting, 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 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.
  • 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.
  • the neutralizing agent comprises an organic chemical.
  • neutralizing agents include, but are not limited to, citric acid, acetic acid, phosphoric acid, succinic acid, phthalic acid, uric acid, stearic acid, lauric acid, palmitic 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, KHSO4, NaHSO 4 , KH 2 PO , and mixtures thereof.
  • the neutralizing agent is present to the extent of from 45% to 85% based on the weight of the composition.
  • the neutralizing agent is present to the extent of from 65% to 75% based on the weight of the composition.
  • the binding agent examples include, but are not limited to, polyethylene glycol, polyoxypropylene glycol adducts, polyoxyethylenestearate, polyvinylbutyral, polyvinyl alcohols, paraffin, polyvinylacetate, polyvinyl methyl ether-nialeic anhydride PNM/MA), cellulose, talc, clays, silicates, silica fume, fumed silica such as "Aerosil" (trade mark), precipitated silica gel, organic pigments, synthetic resins, and mixtures thereof.
  • the binding agent is present from 5% to 25% based on the weight of the composition.
  • the binding agent is present from 6% to 15% based on the weight of the composition.
  • pH indicator examples 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, Cleves acid; coumaric acid; 3,6-dioxyphthalic dinitrile; magnesium 8-hycIroxyqumolinate; ⁇ - methylumbelliferone; l-naphthol-4-sulfonic acid; orcinaurine; patent phosphine; thioflavine; umbelliferone; and mixtures thereof.
  • the salts of phenolphthalein are selected from the group consisting of sodium, disodium, potassium, and mixtures thereof.
  • the pH indicator is present from 0.001% to 0.8% based on the weight of the composition.
  • 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 0J % to 0.4% based on the weight of the composition.
  • the composition may include a disintegrant to aid in dissolving the composition in the solution.
  • the disintegrant is an effervescing disintegrant, activated by contact with the aqueous solution to be civilized.
  • 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 biphthalate, potassium oxalate, potassium hydrogen phthalate, alkaline perborates, perchlorates, permaganates, chlorates, potassium tetraborate, sodium carbonate peroxide, tartaric acid, Rochelle salt (potassium-sodium tartrate), citric acid, potassium hydrogen tart
  • n is an integer from 8 to 18.
  • materials that liberate nitrogen include, but are not limited to, hydrazine, compounds containing an azo group, and azides.
  • the disintegrant is present to the extent of from 1% to 30% based on the weight of the composition.
  • 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.
  • the other additives include, but are not limited to, dyes, pigments, dyeing assistants, colorants, tannins, colloidal material, toners, clays, talcs, barytes, whitening agents, mould release agents, lubricants, and mixtures thereof.
  • the quantity of additives present is up to 70% based on the weight of the composition.
  • the additives are present to the extent of up to 12% based on the weight of the composition.
  • inert fillers 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. 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.
  • 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.
  • the amount of filler in the composition is from 5% to 15% based on the weight of the composition.
  • suitable fillers include silica sand, silica fume, other natural or synthetic silica- based materials, "Micro-Cell” (trade mark) E silica (Celite Corp.), silicates, calcium alurriinosilicate, aluminosilicates, clays, alumina, ALUNDUM (trade mark) aluminosilicates (Norton), zeolites, ceramic spheres, fly ash, limestone powder, and finely divided or powdered plastic.
  • the neutralizing agent, the pH indicator, the binder, the disintegrant, and any other additive in the composition are solids.
  • 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.
  • 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.
  • 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.
  • a suitable liquid solvent such as water
  • 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 providing perforations 12 of the compact or the like, to provide selected, structurally stable fractions for smaller volumes of aqueous solution. (Fig. 1.)
  • 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.
  • the self-indicating neutralizing composition compacted units are preferably somewhat moisture resistant.
  • 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
  • composition units 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.
  • 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.
  • 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.
  • 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.
  • suitable substantially water-insoluble materials include clays, latexes, polystyrenes, polyurethanes, and celluloses wherein the hydroxyl groups have been substituted with alkyls.
  • the present invention also includes a method of neutralizing a solution to about a neutral pH.
  • a v-initized 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 neutrahzing 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 bulky 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.

Landscapes

  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Environmental & Geological Engineering (AREA)
  • Water Supply & Treatment (AREA)
  • Chemical & Material Sciences (AREA)
  • Hydrology & Water Resources (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Detergent Compositions (AREA)
  • Paints Or Removers (AREA)
  • Medicinal Preparation (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
PCT/EP2001/010983 2000-11-08 2001-11-02 Self-indicating neutralizing compositions WO2002038506A2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
BR0107466-0A BR0107466A (pt) 2000-11-08 2001-11-02 Composições neutralizantes auto-indicadoras
CA002396170A CA2396170A1 (en) 2000-11-08 2001-11-02 Self-indicating neutralizing compositions
EP01983495A EP1335883A2 (en) 2000-11-08 2001-11-02 Self-indicating neutralizing compositions
JP2002541047A JP2004512950A (ja) 2000-11-08 2001-11-02 自動指示中性化組成物
MXPA02006743A MXPA02006743A (es) 2000-11-08 2001-11-02 Composiciones neutralizantes de autoindicacion.
AU2002214987A AU2002214987A1 (en) 2000-11-08 2001-11-02 Self-indicating neutralizing compositions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US70894600A 2000-11-08 2000-11-08
US09/708,946 2000-11-08

Publications (2)

Publication Number Publication Date
WO2002038506A2 true WO2002038506A2 (en) 2002-05-16
WO2002038506A3 WO2002038506A3 (en) 2002-08-01

Family

ID=24847809

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2001/010983 WO2002038506A2 (en) 2000-11-08 2001-11-02 Self-indicating neutralizing compositions

Country Status (8)

Country Link
EP (1) EP1335883A2 (es)
JP (1) JP2004512950A (es)
AU (1) AU2002214987A1 (es)
BR (1) BR0107466A (es)
CA (1) CA2396170A1 (es)
EC (1) ECSP024284A (es)
MX (1) MXPA02006743A (es)
WO (1) WO2002038506A2 (es)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140339176A1 (en) * 2012-02-27 2014-11-20 Zodiac Group Australia Pty Limited Water treatment product and method

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006102705A (ja) * 2004-10-08 2006-04-20 Noda:Kk セメント排水シート及びセメント排水処理方法
JP2010274150A (ja) * 2009-05-26 2010-12-09 Panasonic Electric Works Co Ltd 水処理用添加剤および水処理装置
JP5571138B2 (ja) * 2012-08-13 2014-08-13 株式会社Kensyo 排水中和緩衝処理剤、排水中和緩衝処理剤添加水及び排水処理方法
CN113271890A (zh) 2018-11-08 2021-08-17 内奥瓦斯克迪亚拉公司 经导管二尖瓣假体的心室展开

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0376126A2 (en) * 1988-12-30 1990-07-04 Purotech Ltd. Improvements in water purification systems
EP0569232A1 (en) * 1992-05-05 1993-11-10 Anitox Corporation pH-indicating material and cat litter containing same
US5792384A (en) * 1997-01-31 1998-08-11 Warren; James R. Concrete masons' hand rinse
EP0909555A1 (en) * 1996-06-17 1999-04-21 Otsuka Pharmaceutical Factory, Inc. PACKAGE FOR CONTAINER OF LIQUID MEDICINE CONTAINING BICARBONATE AND pH INDICATOR

Family Cites Families (3)

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Publication number Priority date Publication date Assignee Title
JPS6181497A (ja) * 1983-09-22 1986-04-25 樋口 泰義 Ph指示薬を含む粘ちょう性の酸洗浄剤を使用して,中和剤による中和が簡単に識別できる方法。
JPH05305286A (ja) * 1992-04-28 1993-11-19 Konica Corp 感光材料の処理廃液の凝集処理方法
JPH06246278A (ja) * 1993-02-24 1994-09-06 Hazama Gumi Ltd 坑廃水又は温泉水の処理方法

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0376126A2 (en) * 1988-12-30 1990-07-04 Purotech Ltd. Improvements in water purification systems
EP0569232A1 (en) * 1992-05-05 1993-11-10 Anitox Corporation pH-indicating material and cat litter containing same
EP0909555A1 (en) * 1996-06-17 1999-04-21 Otsuka Pharmaceutical Factory, Inc. PACKAGE FOR CONTAINER OF LIQUID MEDICINE CONTAINING BICARBONATE AND pH INDICATOR
US5792384A (en) * 1997-01-31 1998-08-11 Warren; James R. Concrete masons' hand rinse

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN vol. 018, no. 111 (C-1170), 23 February 1994 (1994-02-23) & JP 05 305286 A (KONICA CORP), 19 November 1993 (1993-11-19) *
PATENT ABSTRACTS OF JAPAN vol. 018, no. 639 (C-1282), 6 December 1994 (1994-12-06) & JP 06 246278 A (HAZAMA GUMI LTD), 6 September 1994 (1994-09-06) *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140339176A1 (en) * 2012-02-27 2014-11-20 Zodiac Group Australia Pty Limited Water treatment product and method
US9988289B2 (en) * 2012-02-27 2018-06-05 Zodicac Group Australia Pty Limited Water treatment product and method

Also Published As

Publication number Publication date
EP1335883A2 (en) 2003-08-20
JP2004512950A (ja) 2004-04-30
ECSP024284A (es) 2002-09-27
WO2002038506A3 (en) 2002-08-01
MXPA02006743A (es) 2002-10-23
BR0107466A (pt) 2002-11-19
AU2002214987A1 (en) 2002-05-21
CA2396170A1 (en) 2002-05-16

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