AU643278B2 - Water treatment blend in solid form - Google Patents
Water treatment blend in solid form Download PDFInfo
- Publication number
- AU643278B2 AU643278B2 AU77368/91A AU7736891A AU643278B2 AU 643278 B2 AU643278 B2 AU 643278B2 AU 77368/91 A AU77368/91 A AU 77368/91A AU 7736891 A AU7736891 A AU 7736891A AU 643278 B2 AU643278 B2 AU 643278B2
- Authority
- AU
- Australia
- Prior art keywords
- solid
- composition
- blend
- chlorine
- hypochlorite
- 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.)
- Ceased
Links
Landscapes
- Treatment Of Water By Oxidation Or Reduction (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Detergent Compositions (AREA)
Description
AUSTRALIA
PATENTS ACT 1952 COMPLETE SPECIFICATION
(ORIGINAL)
FOR OFFICE USE Short Title: Int. Cl: Application Number: Lodged: Complete Specification Lodged: Accepted: Lapsed: Published: S* Tvbrity: 6 *.Related Art: Form 43278 TO BE COMPLETED BY APPLICANT Epe of Applicant: ELTECH SYSTEMS CORPORATION 'Ad'dress of Applicant: 6100 Glades Road, Suite 305, BOCA RATON, Florida 33434, USA
S
Actual Inventors: CHARLES G. PARSONS *4dress for Service: CALLINAN LAWRIE, Patent Attorneys, 278 High Street, Kew, Victoria 3101, Australia.
Complete Specification for the invention entitled: WATER TREATMENT BLEND IN SOLID
FORM.
The following statement is a full description of this invention, including the best method of performing it known to me:- WATER TRELTMENT BLEND IN SOLID FORM BACKGROUND OF THE INVENTION 0* Compositions which release chlorine into aqueous media have been found to be generally useful, such as for preparing a sterilizing solution. For example it S" has been taught in U.S. Patent No. 4,104,024 to sterilize an article at a temperature below that of boiling water with a sterilizing solution having active chlorine. A variety of ingredients have been proposed for such a sterilizing solution. These ingredients S* include hypochlorite salts, toluene S 10 sulfochloroamide compounds, chlorine dioxide, chlorinated hydantoin, and trichloroisocyanuric acid and salts thereof.
Chlorine-containing compositions may also be utilized for treatment of specific miedia, e.g., 15 swimming pools. In such use, compounds can be provided in a dispenser and the chemicals for water treatment thereby dispensed to the swimming pool.
Suitable chlorine donor chemicals that have been disclosed, in British Patent No. 1,327,763, include the chlorocyanuric acids, calcium hypochlorite and the halogenated hydantoins. It has also been known to provide a chemical dispenser of disinfecting agent for a toilet tank. As disclosed in U.S. Patent No.
4,709,423 such a dispenser for providing a disinfectant solution may contain a disinfectant such as halogenated hydantoin, trichloroisocyanuric acid, and inorganic hypochlorite salts, the salts of calcium, lithium and magnesium.
Compositions providing available chlorine may also be useful in dishwasher detergent compositions. Thus there has been disclosed in U.S. Patent No. 4,284,524 a cleaning composition for automatic dishwashers, which composition can contain available chlorine at a level of from about 0.5 to about 3 percent. To provide the available chlorine, there may be used chlorinated trisodium phosphate as well as other materials such as 15 chloroisocyanurates, chlorinated hydantoin, toluene sulfodichloroamides, hypochlorite salts, chlorinated melamine, chlorinated succinimide, or N-chloroacetyl urea and the like.
It has usually been proposed to provide various blends or mixtures of ingredients for these specific treating composition. For example U.S. Patent No.
4,709,423 recommends a mixture of trichloroisocyanuric acid plus cyanuric acid. British Patent No. 1,327,763 recommends a mixture containing cyanuric acid or salt thereof. U.S. Patent No. 3, 629,408 discloses a combination of hypochlorite salt with a chlorinated glycoluril.
It would however still be desirable to provide a disinfectant composition that combines a great variety of desirable characteristics, economy of manufacture, enhanced disinfectant quality and controlled dissolve rate.
SUMMARY OF THE INVENTION There has now been devised a wator troat:r.et- -3a method of treating an aqueous medium in a one-pass treatment method to provide available chlorine and bromine thereto, which method comprises flowing the medium into contact with a solid composition having active components of blended particles consisting of 75 to 99 weight percent of calcium hypochlorite with 1-25 weight percent of one or more N,N-halogenated dialkylhydantoin having chlorine or bromine halogenation, or both, one of which is N-brominated, basis 100 percent of the composition active ingredients, wherein said solid composition is in the form of particles having size within the range of from about 12 to about 100 mesh.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The composition of the present invention can be used for treating a variety of fluid media. For example in water treatment, it may be used generally to provide available chlorine to media containing biologically active components such as bacteria and viruses, it may be utilised for treating aqueous sewage media, plant effluent, cooling towers, lagoons and secondary water recovery. The composition can also be used for specialty water treatment, in swimming pools. In general, the composition will be utilised for providing available chlorine to media for bleaching, sterilising and disinfecting applications.
The composition will provide available chlorine to the media to be treated.
It is to be understood that S 0* S the composition might not only dispense available chlorine, but may also provide bromine. Whether the composition provides chlorine or bromine or both, for purposes of convenience, unless otherwise expressly detailed, this will be referred to hereinafter simply as available chlorine. It will thereby be understood that when the word "halogen" is used herein, such will refer to chlorine, bromine, or both.
The availab'- chlorine is expressed as the amount, as a percentage, of the halogen, chlorine or bromine or both, that is available based upon the total of such halogens present in the solid composition. This availability may be determined by titration of an aqueous solution of the composition, such as with sodium 15 thiosulphate. This available chlorine may therefore also be referred to as titratible chlorine. Although providing a high degree of available chlorine, the composition of the present invention has a most desirable low toxicity. Yet it will nevertheless provide excellent disinfection as well as viricidal characteristics while providing for bacteriological stabilization of aqueous media.
The hypochlorite, which may also be referre-d to herein as the hypochlorite salt, will be an alkali metal 25 or alkaline earth metal hypochlorite. The metal of the salt will most often be sodium, potassium, lithium, calcium or magnesium. Mixtures of these salts may also be used, such as mixtures including alkali metal plus alkaline earth metal salts, lithium hypochlorite mixed with calcium hypochlorite. Preferably for economy of the composition as well as efficiency of available chlorine, the hypochlorite salt will simply be calcium hypochlorite. In the blended, solid composition the hypochlorite salt can be expected to provide from about 65 to 75 percent available chlorine, or about 55 to percent available chlorine in the composition.
The hydantoin used will be an N-halogenated dialkylhydantoin. The halogen for this hydantoin will be one or more of chlorine or bromine. For example, there may be used l-bromo-3-chloro-5,5-dimethylhydantoin (which may be referred to hereinafter simply as "BCDMH"). Advantageously for economy, the alkyl of the dialkylhydantoin will be either or both of methyl or ethyl. For example there may be supplied as the hydantoin 1,3-dichloro-5-ethyl-5-methylhydantoin. The hydantoin used can be expected to provide from 48 to 72 percent available chlorine or about 0.5 to 18 percent available chlorine in the composition as either bromine or chlorine or both. In addition to the hydantoins mentioned above, other suitable compounds that may be 15 used include 1,3-dibromo-5,5-dimethylhydantoin and 1,3dichloro-5,5-dimethylhydantoin. Additionally, mixtures Sof hydantoins may be utilized in the composition. For example a mixture containing a minor amount of 1,3may be useful where the major portion of the mixture is supplied by 1,3dichloro-5,5-dimethylhydantoin. It is to be understood that for economy the hydantoins that will be used will most always be the commercially available materials that can range from about 90 to more than 99 percent active 25 ingredient, with a balance typically of incidental inerts. Preferably for efficient dispensing of available chlorine, the hydantoin used will be BCDMH.
The hypochlorite salt may be available in powder or flake form. However, other particulate, solid form, granules, can be particularly serviceable, especially where such are comminuted prior to use.
Usually, for blending with the hydantoin, the hypochlorite salt will be a free-flowing particulate having particle size within the range from about 12 to about 100 mesh. Hypochlorite salt more finely divided than about 100 mesh can lead to problems such as dusting when blending with the hydantoin. Salt particles of greater size than about 12 mesh will most always detract from obtaining a uniform blend of the solid particulates. Preferably, for best blending the hypochlorite salt will be a granular material having a particle size within the range of from about 16 mesh to about 40 mesh.
The hydantoins are usually commercially available as dry, free-flowing solids in powder or granular or flake form. Typically, as with the hypochlorite salts, the hydantoin will be in granular form and will have particle size from about 12 to 100 mesh. For initiating preparation of the composition, as with the hypochlorite salt, it is preferred to start with a hydantoin in 15 granular form, to avoid dusting during blending.
In preparing the composition, there will be used from 75 to 99 weight percent of the hypochlorite salt and from 1 to 25 weight percent of the hydantoin, basis 100 weight percent of these ingredients. Use of less than about 75 weight percent of the hypochlorite salt will be insufficient for providing desireable available S" chlorine. On the other hand, less than about I weight percent of hydantoin will be insufficient to provide beneficial effect from the hydantoin. These materials 25 in finely divided form, as granules, can then be brought together by any mixing means, preferably by mechanical mixing means which are typically utilized for forming blends of dry ingredients. These may include, for example, stirring and tumbling means or the like.
It is advantageous that mixing be carried out in such a manner that the particle size of the ingredients being mixed is not appreciably altered during the mixing of the dry materials. A preferred dry blending operation is accomplished with a ribbon blender. Particularly where the blending is initiated with ingredients in very finely divided form, and the blending operation is to form granules of the ingredients in mixture, there may be utilized a granulating operation, roller compacting of a moistened ingredient mix followed by granulating. By any manner of blending there will result a solid, particulate composition which will typically have a highly desirable shelf stability on storage, as a packaged blend of particulate solids. In use, the particles may for example be simply mixed with a liquid medium for desired treatment, or the liquid can flow by, through or ever, the solid, water treatment blend particles.
It is to be understood that there may be present in the composition additional ingredients, such as binding agents, surface active agents, and the like.
15 For a representative composition there was blended together a commercial grade, granular calcium hypochlorite having a particle size between 16-40 mesh and containing 72-75 percent available chlorine. With this calcium hypochlorite there was blended a commercially available, l-bromo-3-chloro-5,5dimethylhydantoin (BCDMH). This commercial BCDMH was 93.5 percent active ingredient, with a balance of incidental inerts, having about 59 percent available chlorine and was a granular material having particle size between 12-40 mesh. The blending was done for about 10 minutes in a double spiral blade ribbon blender. The resulting blend was a white granular solid and contained 5 weight percent BCDMH anc' 95 weight percent calcium hypochlorite, the water having been essentially volatilized during the blending operation.
This solid granular composition was 70 percent minimum active halogen, expressed as available chlorine. The pH of a 1 percent solution of this solid, granular mixture, as determined by dissolving 1 gram of the blend in 100 milliliters of deionized water, was 9.15 at 200 C.
Claims (4)
1. A method of treating an aqueous medium in a one-pass treatment method to provide available chlorine and bromine thereto, which method comprises flowing the medium into contact with a solid composition having active components of blended particles consisting of 75 to 99 weight percent of calcium hypochlorite with 1-25 weight percent of one or more N,N-halogenated dialkylhydantoin having chlorine or bromine halogenation, or both, one of which is N-brominated, basis 100 percent of the composition active ingredients, wherein said solid composition is in the form of particles having size within the range of from 12 to 100 mesh.
2. The method of claim 1, wherein said solid composition of blended particles treats an aqueous medium of one or more of sewage media, plant effluent, cooling tower liquid or secondary water media.
3. The method of claim 1, wherein said aqueous medium is treated with a solid composition of particles of calcium hypochlorite blended with a hydantoin having N-chlorination and N-bromination and having alkyl groups of one or more of methyl or ethyl. 9 DATED this 7th day of September, 1993. ELTECH SYSTEMS CORPORATION By their Patent Attorneys: CALLINAN LAWRIE 9
4 I WATER TREATMENT BLEND IN SOLID FORM Abstract of the Disclosure There is now provided a water treatment blend in solid form for disinfection and bacteriological stabilization of aqueous media. The solid is an intimate blend of solid particulates and can provide 5 prolonged release of both chlorine and bromine in aqueous media. The blend contains one or more alkali metal or alkaline earth metal hypochlorite with one or more N-halogenated dialkylhydantoin. The solid composition can combine excellent shelf stability with desirable disinfection property in use. A blend of calcium hypochlorite with l-bromo-3-chloro-5, dimethylhydantoin io especially preferred. 0 O
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US52985090A | 1990-05-29 | 1990-05-29 | |
US529850 | 1990-05-29 |
Publications (2)
Publication Number | Publication Date |
---|---|
AU7736891A AU7736891A (en) | 1991-12-05 |
AU643278B2 true AU643278B2 (en) | 1993-11-11 |
Family
ID=24111501
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU77368/91A Ceased AU643278B2 (en) | 1990-05-29 | 1991-05-28 | Water treatment blend in solid form |
Country Status (2)
Country | Link |
---|---|
AU (1) | AU643278B2 (en) |
CA (1) | CA2042430A1 (en) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1277757C (en) * | 1998-09-28 | 2006-10-04 | 株式会社荏原制作所 | Method and apparatus for disinfecting drainage |
US6638959B2 (en) | 2000-01-18 | 2003-10-28 | Albemarle Corporation | Microbiological control in aqueous systems |
US6495698B1 (en) | 2000-01-18 | 2002-12-17 | Albemarle Corporation | Binder-free compacted forms of 1,3-dihalo-5,5-dimethylhydantoins |
US6448410B1 (en) | 2000-01-18 | 2002-09-10 | Albemarle Corporation | Production of compacted biocidal agent from particulate biocidal agent without using a binder |
US6565868B1 (en) | 2000-01-18 | 2003-05-20 | Albemarle Corporation | Methods for microbiological control in aqueous systems |
US6508954B1 (en) | 2000-01-18 | 2003-01-21 | Albemarle Corporation | 1,3-dibromo-5,5-dimethylhydantoin of enhanced properties |
US7999118B2 (en) | 2000-01-18 | 2011-08-16 | Albemarle Corporation | Process for producing N-halogenated hydantoins |
US7579018B2 (en) | 2000-01-18 | 2009-08-25 | Albemarle Corporation | Microbiological control in aqueous systems |
US6680070B1 (en) | 2000-01-18 | 2004-01-20 | Albemarle Corporation | Particulate blends and compacted products formed therefrom, and the preparation thereof |
US6809205B1 (en) | 2000-01-18 | 2004-10-26 | Albemarle Corporation | Process for producing N-halogenated organic compounds |
US6908636B2 (en) | 2001-06-28 | 2005-06-21 | Albermarle Corporation | Microbiological control in poultry processing |
US6965035B1 (en) | 2002-07-25 | 2005-11-15 | Albemarle Corp | Compacted forms of halogenated hydantoins |
US7901276B2 (en) | 2003-06-24 | 2011-03-08 | Albemarle Corporation | Microbiocidal control in the processing of meat-producing four-legged animals |
FI20055120A0 (en) * | 2005-03-16 | 2005-03-16 | Bim Kemi Ab | Procedure for inhibiting the growth of microorganisms |
BRPI0620851B1 (en) | 2005-12-01 | 2016-08-23 | Albemarle Corp | Method for microbial control in the meat production process of four-legged animals |
CN107912432A (en) * | 2017-10-19 | 2018-04-17 | 鄄城康泰化工有限公司 | A kind of bromochloroin compound disinfectant |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU5924890A (en) * | 1989-06-16 | 1991-01-08 | University Of Houston, The | Biocidal methods and compositions for recirculating water systems |
AU7309491A (en) * | 1990-01-22 | 1991-08-05 | Auburn University | N,n'-dihaloimidazolidin-4-ones |
-
1991
- 1991-05-13 CA CA 2042430 patent/CA2042430A1/en not_active Abandoned
- 1991-05-28 AU AU77368/91A patent/AU643278B2/en not_active Ceased
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU5924890A (en) * | 1989-06-16 | 1991-01-08 | University Of Houston, The | Biocidal methods and compositions for recirculating water systems |
AU7309491A (en) * | 1990-01-22 | 1991-08-05 | Auburn University | N,n'-dihaloimidazolidin-4-ones |
Also Published As
Publication number | Publication date |
---|---|
AU7736891A (en) | 1991-12-05 |
CA2042430A1 (en) | 1991-11-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU643278B2 (en) | Water treatment blend in solid form | |
US8048435B2 (en) | Preparation of concentrated aqueous bromine solutions and biocidal applications thereof | |
US7534368B2 (en) | Oxidizing composition including a gel layer | |
US5614528A (en) | Compositions and methods for inhibiting the formation of chloramines and trihalomethanes in aqueous media | |
US8492419B2 (en) | Multifunctional solid formulations for water conditioning | |
US5817337A (en) | Disinfectant effervescent tablet formulation | |
WO2002056728A1 (en) | Toilet bowl cleaner effervescent tablet | |
JP2010189393A (en) | Stabilized hypobromous acid solution | |
WO2001074988A1 (en) | Foaming garbage disposal sanitizer tablet and method of cleaning garbage disposals | |
US6291397B1 (en) | Algaecide compositions and methods of removing algae | |
EP2079666B1 (en) | Solid composition for treating water | |
WO2005051850A1 (en) | Multi-functional oxidizing composition | |
JPH0826917A (en) | Sterilizing cleaner composition | |
JPS5846003A (en) | Germicidal cleaning agent having immediate effect and durability | |
JPS59155311A (en) | Production of foamed granules | |
AU729617B2 (en) | Disinfectant effervescent tablet formulation | |
US20040118787A1 (en) | Method for stabilizing chlorine in aqueous solution | |
WO1998053679A1 (en) | Solid disinfectant material/surfactant compositions | |
US20070032397A1 (en) | Fragrant monopersulfate compositions for water treatment and articles containing them | |
US8293795B1 (en) | Preparation of concentrated aqueous bromine solutions and biocidal applications thereof | |
CN101547870A (en) | Solid composition for treating water | |
EP0723396A1 (en) | Compositions and methods for inhibiting the formation of chloramines and trihalomethanes in aqueous media |