AU3076397A - Method for sanitizing swimming pools and recirculating water systems - Google Patents
Method for sanitizing swimming pools and recirculating water systemsInfo
- Publication number
- AU3076397A AU3076397A AU30763/97A AU3076397A AU3076397A AU 3076397 A AU3076397 A AU 3076397A AU 30763/97 A AU30763/97 A AU 30763/97A AU 3076397 A AU3076397 A AU 3076397A AU 3076397 A AU3076397 A AU 3076397A
- Authority
- AU
- Australia
- Prior art keywords
- water
- halogenated
- pool
- skimmer basket
- halogenated compound
- 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.)
- Granted
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 58
- 238000000034 method Methods 0.000 title claims description 37
- 230000009182 swimming Effects 0.000 title claims description 21
- 230000003134 recirculating effect Effects 0.000 title claims description 13
- 238000011012 sanitization Methods 0.000 title description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 36
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 35
- 229910052794 bromium Inorganic materials 0.000 claims description 35
- 150000001469 hydantoins Chemical class 0.000 claims description 26
- 239000000203 mixture Substances 0.000 claims description 21
- 150000001875 compounds Chemical class 0.000 claims description 20
- 229920006317 cationic polymer Polymers 0.000 claims description 18
- PQRDTUFVDILINV-UHFFFAOYSA-N bcdmh Chemical compound CC1(C)N(Cl)C(=O)N(Br)C1=O PQRDTUFVDILINV-UHFFFAOYSA-N 0.000 claims description 17
- 239000004215 Carbon black (E152) Substances 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 239000000460 chlorine Substances 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- 125000002252 acyl group Chemical group 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 6
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052740 iodine Chemical group 0.000 claims description 3
- 239000011630 iodine Chemical group 0.000 claims description 3
- -1 iodine, hydrogen Chemical group 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 2
- 229940125898 compound 5 Drugs 0.000 claims 1
- PIEXCQIOSMOEOU-UHFFFAOYSA-N 1-bromo-3-chloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Br)C(=O)N(Cl)C1=O PIEXCQIOSMOEOU-UHFFFAOYSA-N 0.000 description 35
- 241000195493 Cryptophyta Species 0.000 description 19
- 230000015572 biosynthetic process Effects 0.000 description 18
- 239000000126 substance Substances 0.000 description 13
- 239000004576 sand Substances 0.000 description 11
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 7
- 229940091173 hydantoin Drugs 0.000 description 6
- 125000002091 cationic group Chemical group 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000000645 desinfectant Substances 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 230000000249 desinfective effect Effects 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 3
- 239000011505 plaster Substances 0.000 description 3
- 238000009428 plumbing Methods 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 238000005352 clarification Methods 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 230000002906 microbiologic effect Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000003826 tablet Substances 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- YRIZYWQGELRKNT-UHFFFAOYSA-N 1,3,5-trichloro-1,3,5-triazinane-2,4,6-trione Chemical compound ClN1C(=O)N(Cl)C(=O)N(Cl)C1=O YRIZYWQGELRKNT-UHFFFAOYSA-N 0.000 description 1
- OMJKWVKPIOIQDM-UHFFFAOYSA-N 3-bromo-1-chloroimidazolidine-2,4-dione Chemical compound ClN1CC(=O)N(Br)C1=O OMJKWVKPIOIQDM-UHFFFAOYSA-N 0.000 description 1
- YIROYDNZEPTFOL-UHFFFAOYSA-N 5,5-Dimethylhydantoin Chemical compound CC1(C)NC(=O)NC1=O YIROYDNZEPTFOL-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 230000005791 algae growth Effects 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 150000003842 bromide salts Chemical class 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000008395 clarifying agent Substances 0.000 description 1
- 239000007891 compressed tablet Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- VRNCRGHDRGGBLW-UHFFFAOYSA-N cyclopenta-1,2-diene Chemical compound C1CC=C=C1 VRNCRGHDRGGBLW-UHFFFAOYSA-N 0.000 description 1
- 238000002716 delivery method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 230000003442 weekly effect Effects 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
- C02F1/50—Treatment of water, waste water, or sewage by addition or application of a germicide or by oligodynamic treatment
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)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Description
METHOD FOR SANITIZING SWIMMING POOLS AND RECIRCULATING WATER SYSTEMS
FIELD OF THE INVENTION
The present invention relates generally to methods for sanitizing recirculating water systems, and more particularly to a method of using N-halogenated hydantoins to sanitize swimming pools.
BACKGROUND OF THE INVENTION
N-halogenated hydantoins such as bromochlorodimethyl- hydantoin have long been recognized as effective disinfectants for circulating water systems. For example, in 1964 Paterson disclosed the use of bromochlorodimethylhydantoins as disinfectants for swimming pool water after recognizing that organo-bromo-chlorinated compounds appeared to have enhanced bacteriacidal activity when compared to disinfecting compositions containing bromine or chlorine alone. See. U.S. Patent No. 3,147,219.
Unfortunately, it has also long been recognized that there are significant problems associated with effectively delivering N-halogenated hydantoins to swimming pool water. Paterson initially studied and "solved" the problem with respect to bromochlorodimethylhydantoin in U.S. Patent No. 3,412,021, issued in 1968, by suggesting that bromochlorodimethyl- hydantoins should be delivered as a solid agglomerate disposed in a reservoir "so that the surface area of the agglomerates exposed to the impure water is held substantially constant." See, U.S. Patent No. 3,412,021 at col. 3. lines 44-51.
In recognition of the accepted view that N-halogenated hydantoins such as bromochlorodimethylhydantoins should be delivered by placing an agglomerate of the disinfectant in a reservoir constructed so that a constant surface area of the agglomerate is exposed to the water, the prior art developed the use of separate "brominator" chemical dispensing devices to dispense the N-halogenated hydantoin product. Examples of such "brominators" include the Di-Halo® Automatic Swimming Pool Disinfecting System and the Aquabrome® Brominator .
Certain disadvantages are known to be associated with brominator dispensing systems. For example, swimming pools in geographical areas prone to freezing temperatures must winterize all plumbing equipment, including the brominator chemical dispensing device. This is a time consuming process, and may subject the pool owner and/or operator to unnecessary chemical exposure when purging the brominator of agglomerated or tableted hydantoin. In addition, the consumption rate of dimethylhydantoin is greater than necessary when brominator units are used.
A need therefore exists for a method of disinfecting swimming pools with N-halogenated hydantoins such as dihalodimethylhydantoins , whereby disinfectant consumption is reduced, the need for associated plumbing and equipment is eliminated, and superior water quality is maintained. The present invention addresses that need.
SUMMARY OF THE INVENTION
Briefly describing one preferred embodiment of the present invention, there is provided a method of treating the water of a swimming pool by putting an agglomerate of bromochlorodimethylhydantoin in the skimmer basket, and a cationic polymer in the pool, and allowing a substantial portion of the agglomerate to dissolve before replenishing the supply of agglomerate in the skimmer basket.
One object of the present invention is to provide an improved method of delivering N-halogenated hydantoin to swimming pool water.
Another object of the present invention is to provide an improved method of delivering BCDMH to swimming pool water.
Further objects and advantages of the present invention will be apparent from the following description.
DESCRIPTION OF THE PREFERRED EMBODIMENT
For the purpose of promoting an understanding of the principles of the invention, reference will now be made to preferred embodiments and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the invention is thereby intended, such alterations and further modifications in the illustrated device, and such further applications of the principles of the invention as illustrated therein being contemplated as would normally occur to one skilled in the art to which the invention relates.
One preferred embodiment of the present invention relates to an improved method of effectively providing bromochloro-5, 5- dimethylhydantoin ("BCDMH" or bromochloro-5, 5-dimethyl-2,4- imidazolidinedione) to swimming pool water. In the prior art, a special "brominator" dispensing apparatus was understood to be required to provide a bed of BCDMH agglomerate that contacts the pool water as it is pumped through the pool filter. In another preferred embodiment other N-halogenated hydantoins are used.
The present invention eliminates the requirement to have a separate chemical dispensing device for delivering dihalodimethylhydantoins to the pool. Instead, one preferred embodiment of the present invention effectively delivers bromochlorodimethylhydantoin to swimming pool water by placing one or more pucks of BCDMH in the pool's skimmer basket and replacing the pucks only after they have substantially dissolved. With this method the surface area of the BCDMH is not constant as it would be with prior art methods .
In another preferred embodiment, bromochlorodimethyl¬ hydantoin is effectively delivered by placing pucks of BCDMH in the skimmer basket in conjunction with the addition of a
cationic polymer to the pool water. Here too, the surface area of the BCDMH is not constant as it would be with prior art methods.
In a third preferred embodiment, an N-halogenated composition is added to a recirculating water system by contacting the recirculating water with solid pieces of the N-halogenated composition, wherein the surface area of the N-halogenated composition is allowed to vary over time (i.e.. the surface area is not kept substantially constant). In this embodiment the N-halogenated composition need not be placed in the skimmer basket, but may be maintained in contact with the recirculating water at any convenient location by placing the N-halogenated composition in a receptacle which allows the recirculating water to freely flow therethrough.
In one aspect of the present invention a method is provided for reducing the consumption of N-halogenated hydantoins when the same are used to treat recirculating water. For example, the use of prior art brominator chemical dispensing devices is difficult to regulate and results in an average consumption of 3 to 5 pounds of bromochlorodimethylhydantoin per week per 10,000 gallons. In contrast, the skimmer-fed application of tableted bromochlorodimethylhydantoin accompanied by the biweekly addition of cationic polymeric compounds results in an average BCDMH consumption rate of only 1 to 2 pounds per week per 10,000 gallons.
As to the compositions themselves, the N-halogenated hydantoin is preferably of the formula:
where :
X is chlorine, bromine or iodine;
Y is chlorine, bromine, iodine, hydrogen, a lower (C1_8) alkyl, a lower (C, „) acyl, or a lower (C, „) alkoxy; and
R 1, and R2- are each C,1—oD mono- or multivalent hydrocarbon radicals of the group consisting of alkyl and/or saturated or unsaturated monocyclic hydrocarbon radicals having five or six carbon atoms per cycle, which radicals can be substituted with lower alkyl, lower acyl, lower alkoxy, carboxy and/or sulfonic acid groups.
As previously indicated, bromochlorodimethylhydantoin is preferably used. Other N-halogenated hydantoins with higher order straight or branched chain alkyl groups in Position 5 of the heterocyclic imidazolidinedione ring may be more or less desired according to the particular characteristics desired to be achieved, and according to other technical and economic considerations.
The N-halogenated hydantoin may be provided in either dry or liquid form. When provided as a dry composition, the hydantoin may be agglomerated, compressed, extruded or tableted into essentially any size or shape. Preferably, the N-halogenated hydantoin is formed into tablets weighing from 1 to 500 grams. More preferably, the N-halogenated hydantoin is provided as an agglomerated, compressed, extruded or tableted product of undefined dimension, size and/or shape weighing from 10 to 200 grams. Most preferably, the N-halogenated hydantoin is provided as an agglomerated, compressed, extruded or tableted product of undefined dimension, size and/or shape weighing from 20 to 125 grams. The N-halogenated hydantoin used in certain of the following examples was provided as a 1" diameter, 20 gram compressed tablet or a 2 3/4" diameter, 120 gram compressed puck. in one preferred embodiment of the present invention,
one or more pucks of bromochlorodimethylhydantoin agglomerate are placed directly in the skimmer basket of a pool. The pucks are allowed to dissolve in the pool water over a period of between about three days and about seven days before new pucks are added to the skimmer basket to replenish the supply. In this embodiment of the invention the agglomerate is provided in an amount and in a form such that the surface area of the agglomerate exposed to the water changes over time as the pucks dissolve, and is not substantially constant.
In another preferred embodiment the N-halogenated hydantoin is delivered to the recirculating water via a device which holds the hydantoin and is placed in the recirculating water flow. For example, the N-halogenated hydantoin may be placed in a reusable or a disposable container which holds the hydantoin while simultaneously allowing water to flow freely therethrough. The container is preferably corrosion resistant, and may be an interlocking clam shell device, or a twist-open or permeable mesh bag-type assembly. The receptacle may be maintained in contact with the water at essentially any location in the pool or its associated plumbing. Most preferably, the receptacle is placed in the skimmer basket.
The total halogen is preferably between 0.1 and 10.0, expressed as mg/liter Br.. More preferably, total halogen is between 0.25 and 2.5 mg/liter Br_ . In one preferred embodiment the total halogen is between 0.40 to 0.80 mg/liter Br_ .
In one preferred embodiment of the present invention, a secondary composition is provided to the pool water to work in conjunction with the bromochlorodimethylhydantoin. In the most preferred of these embodiments the bromochlorodimethylhydantoin agglomerate is delivered through the skimmer basket technique previously described, and the secondary composition is added directly to the
pool. The secondary composition is preferably added to the pool at least once a month, more preferably every ten to twenty days, and most preferably biweekly.
The secondary composition preferably exhibits properties such as water clarification, halogen residual stabilization, etc., in circulating water systems. Preferably the secondary composition is a polymer; most preferably a cationic polymer. Polymeric and/or non-polymeric substances that are rigid, water soluble clarifying agents in any physical form such as aluminum sulfate, ferric salts, iron III compounds, etc., may advantageously be used.
In certain preferred embodiments the secondary composition is a water soluble cationic polymer such as poly(hexamethylammonium chloride), poly(dodecamethylene- dimethylimino chloride), poly[ (oxyethylene dimethylimino) ethylene-(dimethylimino) ethylene dichloride] , l,3-diaza-2,4-cyclopentadiene (with l-chloro-2, 3-epoxypropane to assist in water clarification and filtration), polyvinyl amine, chitosan, polyethylene amine or a polymer of
1, 6-hexanediamine-N,N,N' ,N'-tetramethyl . Alternatively, the fluoride, chloride, or bromide salts of these compounds may also be used.
The molecular weight of the cationic polymer is preferably between about 500 Da to 100,000 Da, with polymers having a molecular weight of between about 1,000 Da and 20,000 Da being most preferred.
The cationic polymer is preferably provided at a concentration of about 0.10 to 10.0 mg/liter as active cationic. More preferably, the polymeric cationics should be present in a concentration of about 0.75 to 7.5 mg/liter as active cationic. Most preferably, the polymeric cationics should be present in a concentration of about 1.0 to 4.0 mg/liter as active cationic. Reference will now be made to specific examples using
the processes described above. It is to be understood that the examples are provided to more completely describe preferred embodiments, and that no limitation to the scope of the invention is intended thereby.
Examples 1 through 4
The field performance of prior art methods of delivering bromochloro-5, 5-dimethylhydantoin was evaluated. The compound was delivered by placing 20 gram, 1" diameter tablets in a "brominator" chemical dispensing device.
The following information was recorded during each pool visit. (1) Date and time of pool inspection; (2) pH; (3) total alkalinity as mg/l CaCO_ ; (4) calcium hardness as mg/l CaCO_; (5) observed total bromine residual as ppm bromine; (6) water temperature (F°); (7) total dissolved solids; (8) copper and iron content; (9) cyanuric acid
(Stabilizer) content as mg/l cyanuric acid; (10) turbidity as NTU's; (11) pounds of N-halogenated compound added; (12) Brominator Chemical Dispensing Device setting; and (13) general pool appearance (visual). The test period was June-September, with most pools being tested weekly over a 12-15 week period.
EXAMPLE 1
The system represented in Example 1 is a 14,770 gallon, outdoor pool. This pool is a vinyl-lined, in-ground system equipped with a filtering system and a pump. The pool was equipped with an AQUABROME® Brominator Chemical Dispensing device CR8.19AT plumbed in a pressure-suction configuration. The pool operated approximately 12 hours per day. During the trial period the average consumption rate of tableted bromochloro-5, 5-dimethylhydantoin was 4.7 pounds
per week per 10,000 gallons. The average observed turbidity ranged between 0.05 and 0.49, with an average observed turbidity of 0.17 for the trial period. The average observed total residual bromine was 1.48 ppm. No algae formation was observed during the test period.
EXAMPLE 2
The system represented in Example 2 is a 21,000 gallon, outdoor pool. This pool is a vinyl-lined, in-ground system equipped with a high rate sand filter and a pump. The pool was originally treated with stabilized chlorine (e.g., trichloro-s-triazinetrione) via skimmer feed, but was fitted with an AQUABROME® Brominator Chemical Dispensing Device CR8.19AT plumbed in a pressure-suction configuration. The pool operated approximately 12 to 14 hours per day. During the trial period the average consumption rate of tableted Bromochloro-5, 5-dimethylhydantoin was 5.0 pounds per week per 10,000 gallons. The average observed turbidity ranged between 0.06 and 0.47, with an average observed turbidity of 0.19 for the trial period. The average observed total residual bromine was 1.59 ppm. No algae formation was observed during the test period.
EXAMPLE 3
The system represented in Example 3 is a 21,500 gallon, outdoor pool. This pool is a vinyl-lined, in-ground system equipped with a high rate sand filter and a pump. The pool was equipped with an AQUABROME® Brominator Chemical Dispensing Device CR8.19AT plumbed in a pressure-suction configuration. The pool operated routinely from 12 to 24 hours . During the trial period the average consumption rate of tableted bromochloro-5, 5-dimethylhydantoin was 4.43 pounds per week per 10,000 gallons. The average observed turbidity ranged between 0.10 and 0.43, with an average observed
turbidity of 0.20 for the trial period. The average observed total residual bromine was 1.46 ppm. No algae formation was observed during the test period.
EXAMPLE 4
The system represented in Example 4 is a 15,400 gallon, outdoor pool. This pool is a vinyl-lined, in-ground system equipped with a cartridge filter system and a pump. The pool was fitted with an AQUABROME® Brominator Chemical Dispensing Device CR8.19AT plumbed in a pressure-suction configuration. The pool operated routinely from 12 to 24 hours per day.
During the trial period the average consumption rate of tableted bromochloro-5, 5-dimethylhydantoin was 4.35 pounds per week per 10,000 gallons. it can be seen from the above that the methods of the prior art provide bromochlorodimethylhydantoin to swimming pool water at an average consumption rate of about 4.2 pounds per week per 10,000 gallons for outdoor residential swimming pools of between about 10,000 and about 25,000 gallons. The average observed turbidity ranged between 0.09 and 0.49, with an average observed turbidity of 0.26 for the trial period. The average observed total residual bromine was 4.01 ppm. No algae formation was observed during the test period.
Examples 5 through 14
Test pools were treated with compressed pucks containing bromochloro-5, 5-dimethylhydantoin agglomerate as the active ingredient via skimmer-fed application, and by the direct biweekly addition of 200 ml of a cationic polymeric compound (specifically, poly[hexamethylammonium] chloride) per 10,000 gal. of pool water. The consumption of bromochlorodimethyl¬ hydantoin was reduced without sacrificing water quality.
EXAMPLE 5
The system represented in Example 5 is a 29,000 gallon, outdoor pool. The pool is a vinyl-lined, in-ground system equipped with a sand filter and a pump. The pool operated routinely for 12 hours per day, and was facilitated by a timer .
During the trial period the average consumption of BCDMH was 1.39 pounds per week per 10,000 gallons. The average observed turbidity ranged between 0.10 and 0.58, with an average observed turbidity of 0.23 for the trial period. The average observed total residual bromine was 0.57 ppm. No algae formation was observed during the test period.
EXAMPLE 6
The system represented in Example 6 is a 20,000 gallon, outdoor pool. This pool is a vinyl-lined, in-ground system equipped with a filter, and a pump. The pool operated approximately 12 hours per day and was not equipped with a timer .
During the trial period the average consumption of BCDMH was 0.98 pound per week per 10,000 gallons. The average observed turbidity ranged between 0.10 and 0.60, with an average observed turbidity of 0.24 for the trial period.
The average observed total residual bromine was 0.60 ppm.
No algae formation was observed during the test period.
EXAMPLE 7
The system represented in Example 7 is a 10,000 gallon, outdoor pool. This pool is a vinyl-lined, above-ground system equipped with a makeshift sand filter, and a 1.5 horsepower pump. The pool operated approximately 18 hours per day and was not equipped with a timer.
During the 14-week trial period the average consumption of BCDMH was 0.72 pounds per week per 10,000 gallons. The average observed turbidity ranged between 0.14 and 0.55, with an average observed turbidity of 0.30 for the trial period. The average observed total residual bromine was 0.31 ppm. No algae formation was observed during the test period.
EXAMPLE 8
The system represented in Example 8 is a 27,000 gallon, outdoor pool. This pool is a plaster in-ground system equipped with a cartridge filter and a 1.5 horsepower pump.
The pool operated approximately 24 hours per day and was equipped with a timer.
During the trial period the average consumption of BCDMH was 1.45 pounds per week per 10,000 gallons. The average observed turbidity ranged between 0.10 and 0.31, with an average observed turbidity of 0.16 for the trial period.
The average observed total residual bromine was 1.49 ppm.
No algae formation was observed during the test period.
EXAMPLE 9
The system represented in Example 9 is a 20,000 gallon, outdoor pool. This pool is a vinyl-lined, in-ground system equipped with a sand filter and a 1.5 horsepower pump. The pool operated approximately 12 hours per day and was equipped with a timer.
During the trial period the average consumption of BCDMH was 1.10 pounds per week per 10,000 gallons. The average observed turbidity ranged between 0.08 and 0.51, with an average observed turbidity of 0.32 for the trial period. The average observed total residual bromine was 0.63 ppm. No algae formation was observed during the test period.
EXAMPLE 10
The system represented in Example 10 is a 20,000 gallon, outdoor pool. This pool is a vinyl-lined, in-ground system equipped with a sand filter and a 0.75 horsepower pump. The pool operated approximately 24 hours per day and was not equipped with a timer.
During the trial period the average consumption of BCDMH was 1.93 pounds per week per 10,000 gallons. The average observed turbidity ranged between 0.09 and 0.56, with an average observed turbidity of 0.29 for the trial period. The average observed total residual bromine was 1.17 ppm. No algae formation was observed during the test period.
EXAMPLE 11
The system represented in Example 11 is a 32,500 gallon, outdoor pool. This pool is a plaster, in-ground system equipped with a D.E. filter, and a 1.0 horsepower pump. The filtration system operated approximately 10 hours per day and was equipped with a timer.
During the 14-week trial period the average consumption of BCDMH was 1.05 pounds per week per 10,000 gallons. The average observed turbidity ranged between 0.11 and 0.37, with an average observed turbidity of 0.17 for the trial period. The average observed total residual bromine was 0.59 ppm. No algae formation was observed during the test period.
EXAMPLE 12
The system represented in Example 12 is a 15,100 gallon outdoor pool. This pool is a vinyl-lined, in-ground system equipped with a filter and a pump. The pool operated
approximately 24 hours per day and was not equipped with a timer.
During the trial period the average consumption of BCDMH was 1.02 pounds per week per 10,000 gallons. The average observed turbidity ranged between 0.14 and 0.60, with an average observed turbidity of 0.25 for the trial period. The average observed total residual bromine was 0.71 ppm. No algae formation was observed during the test period.
EXAMPLE 13
The system represented in Example 13 is a 27,000 gallon, outdoor pool. This pool is a plaster, in-ground system equipped with a D.E. filter and a pump. The pool operated approximately 10 hours per day and was not equipped with a timer . During the trial period the average consumption of BCDMH was 1.69 pounds per week per 10,000 gallons. The average observed turbidity ranged between 0.07 and 0.18, with an average observed turbidity of 0.11 for the trial period. The average observed total residual bromine was 1.38 ppm. No algae formation was observed during the test period.
EXAMPLE 14
The system represented in Example 14 is a 20,000 gallon, outdoor pool. This pool is a vinyl-lined, in-ground system equipped with a sand filter and a pump. The pool operated approximately 24 hours per day and was equipped with a timer .
During the trial period the average consumption of BCDMH was 1.08 pounds per week per 10,000 gallons. The average observed turbidity ranged between 0.06 and 0.61, with an average observed turbidity of 0.33 for the trial period. The average observed total residual bromine was 0.77 ppm.
No algae formation was observed during the test period.
It can be seen from the above that the present invention provides for more finely tuned product delivery rate facilitating a more efficient use of N-halogenated compound than can be obtained by prior art delivery methods. For example, Examples 1 through 4 show that the tested outdoor pool systems using a Brominator Chemical Dispensing Device as directed in Paterson Patent No. 3,412,021 had an average consumption of about 4.6 pounds of tableted Bromochloro-5, 5-dimethylhydantoin per week per 10,000 gallons. In contrast, examples 5-14 show that the tested outdoor pool systems using the skimmer-fed application of tableted Bromochloro-5, 5-dimethylhydantoin and the biweekly addition of cationic polymeric compounds resulted in average consumption rate of about 1.2 pounds per week per 10,000 gallons. This is a significant advantage that was not taught or suggested by the prior art.
It can also be seen that water quality was maintained with the inventive skimmer-feed method. In particular, Examples 1 through 4 show that the tested outdoor pool systems using a Brominator Chemical Dispensing Device had an average observed turbidity of 0.21, while examples 5-14 show that the tested outdoor pool systems using the skimmer-fed application of tableted bromochlorodimethylhydantoin and the biweekly addition of cationic polymeric compounds resulted in average observed turbidity of 0.24.
Finally, it can be seen that the skimmer-fed systems of the present invention effectively inhibited algae growth, even when operating at lower-than-conventional total bromine residuals. In particular, effective algae inhibition was observed at residual bromine levels of less than 1.5 ppm, and more particularly at residual bromine levels of less than 1.0 ppm, including at residual bromine levels as low as about 0.3 ppm. The prior art does not teach or suggest
that effective algael inhibition can be obtained at these low residual bromine levels when bromochlorodimethylhydantoins are used.
EXAMPLE 15
The Table below shows bactericidal performance when bromochloro-5 , 5-dimethylhydantoin is applied at lower residual bromine concentrations. The average bromine residual for examples 6-14 is 0.73 mg/liter. These extremely low bacterial counts provide further support to the proposition that lower residuals of bromochloro-5 , 5-Dimethylhydantoin are effective in controlling the propagation of bacterial and microbiological contaminants .
TABLE
Microbiological Results (CFU's)
Example 10° 10 -1 10 -2 lO"3 No.
6 CNR CNR 0 11
7 0 0 0 0
8 CNR CNR CNR 0
9 0 0 0 0
10 0 0 0 0
11 0 0 0 0
12 0 0 0 0
13 0 0 0 0
14 0 0 0 0
15 0 0 0 0
CNR - Cannot Read
Examples 16-19 represent test pools that were treated with compressed pucks containing bromochloro-5, 5-dimethylhydantoin agglomerate as the active ingredient via skimmer-fed application, without the additional use of a cationic polymer. The consumption of bromochlorohydantoin was reduced without sacrificing water quality.
EXAMPLE 16
The syrte'ϊi represented in Example 16 is an 18,400 gallon, outdoor pool. The pool is a vinyl-lined, in-ground system equipped with a sand filter and pump. The pool operated r jutinely for 24 hours per day and was not equipped with a timer.
During the trial period, the average consumption rate of tableted BCDMH was 1.09 pounds per week per 10,000 gallons. The average observed turbidity was between 0.06 and 0.21, with an average observed turbidity of 0.10 for the trial period. The average observed total residual bromine was 0.39 ppm. The average observed cationic polymer concentration was 0.40 ppm. No algae formation was observed during this period.
EXAMPLE 17
The system represented in Example 17 is an 18,000 gallon, outdoor pool. The pool is a vinyl-lined, in-ground system equipped with a sand filter and pump. The pool operated routinely for 24 hours per day and was not equipped with a timer.
During the trial period, the average consumption rate of tableted BCDMH was 1.70 pounds per week per 10,000 gallons. The average observed turbidity was between 0.06 and 0.25,
with an average observed turbidity of 0.10 for the trial period. The average observed total residual bromine was 0.92 ppm. The average observed cationic polymer concentration was 0.48 ppm. No algae formation was observed during this period.
EXAMPLE 18
The system represented in Example 18 is a 22,000 gallon, outdoor pool. The pool is a vinyl-lined, in-ground system equipped with a sand filter and pump. The pool operated routinely for 24 hours per day and was not equipped with a timer.
During the trial period, the average consumption rate of tableted BCDMH was 1.35 pounds per week per 10,000 gallons. The average observed turbidity was between 0.05 and 0.18, with an average observed turbidity of 0.11 for the trial period. The average observed total residual bromine was 1.25 ppm. The average observed cationic polymer concentration was 0.40 ppm. No algae formation was observed during this period.
EXAMPLE 19
The system represented in Example 19 is a 16,000 gallon, outdoor pool. The pool is vinyl-lined, in-ground system equipped with a sand filter and pump. The pool operated routinely for 24 hours per day and was not equipped with a timer.
During the trial period, the average consumption rate of tableted BCDMH was 1.28 pounds per week per 10,000 gallons. The average observed turbidity was between 0.45 and 0.11, with an average observed turbidity of 0.20 for the trial period. The average observed total residual bromine was 0.85 ppm. The average observed cationic polymer concentration
was 0.42 ppm. No algae formation was observed during this period.
In view of the above it can be seen that with the methods of the present invention substantially lower residuals of bromine concentration may be used to effectively sanitize swimming pool water when bromochlorodimethylhydantoin is applied via the skimmer-fed application described herein.
While the invention has been illustrated and described in detail in the foregoing description, the same is to be considered as illustrative and not restrictive in character, it being understood that only the preferred embodiment has been shown and described and that all changes and modifications that come within the spirit of the invention are desired to be protected.
Claims (15)
1. A method of treating the water of a swimming pool equipped with a skimmer basket, comprising the steps of: (a) putting into the skimmer basket an N-halogenated hydantoin of the formula:
where:
X is chlorine, bromine or iodine;
Y is chlorine, bromine, iodine, hydrogen, a Ci,—o_ alkyl, a C, _ acyl, or a C, „ alkoxy; and R and R_ are each independently a C, fi monovalent or multivalent hydrocarbon radical selected from the group consisting of alkyl hydrocarbon radicals and saturated or unsaturated monocyclic hydrocarbon radicals having five or six carbon atoms per cycle; wherein said radicals are optionally substituted with one or more substituents selected from the group consisting of C._8 alkyl, C. acyl, C, fl alkoxy, carboxy and sulfonic acid groups; and
(b) allowing a substantial portion of the N-halogenated hydantoin to dissolve before replenishing the supply of N-halogenated hydantoin in the skimmer basket.
2. The method of claim 1 wherein said N-halogenated compound is a bromochlorodimethylhydantoin.
3. The method of claim 1 wherein said N-halogenated compound is provided as an agglomerate, and wherein said "allowing" step comprises allowing a substantial portion of the agglomerate to dissolve before replenishing the supply of agglomerate in the skimmer basket.
5 4. The method of claim 1 wherein said N-halogenated compound is provided to the skimmer basket by placing the N-halogenated compound in a container effective to allow water to flow therethrough, and placing said container in the skimmer basket.
° 5. In a method of treating the water of a swimming pool equipped with a skimmer basket, wherein the swimming pool water is treated with both an N-halogenated compound and an additional water clarifying composition, the improvement comprising providing the N-halogenated compound 5 to the pool water by placing the N-halogenated compound in the skimmer basket and allowing a substantial portion of the N-halogenated hydantoin to dissolve before replenishing the supply of N-halogenated hydantoin in the skimmer basket.
6. The method of claim 5 wherein said additional water 0 clarifying composition is a cationic polymer.
7. The method of claim 5 wherein said N-halogenated compound is a bromochlorodimethylhydantoin.
8. The method of claim 6 wherein said cationic polymer is added to the water biweekly.
5 9. The method of claim 5 wherein said N-halogenated compound is provided to the skimmer basket by placing the N-halogenated compound in a container effective to allow water to flow therethrough, and placing said container in the skimmer basket.
10. A method of treating the water of a swimming pool equipped with a skimmer basket, said method comprising the step of providing an N-halogenated compound to the skimmer basket of a swimming pool in an amount and form effective to provide between about 0.2 and 1.0 ppm of the N-halogenated compound to the water.
11. The method of claim 10 wherein said N-halogenated compound is a bromochlorodimethylhydantoin.
12. The method of claim 10, and additionally including the step of providing a secondary composition to the pool water to work in conjunction with the N-halogenated composition; wherein said secondary composition is provided to the pool water by placing the secondary composition directly in the pool water.
13. The method of claim 12, wherein said secondary composition is a cationic polymer.
14. The method of claim 10 wherein said N-halogenated compound is provided to the skimmer basket by placing the N-halogenated compound in a container effective to allow water to flow therethrough, and placing said container in the skimmer basket.
15. A method of treating a recirculating water system, said method comprising the steps of:
(a) contacting the recirculating water with an N-halogenated hydantoin of the formula:
where:
X is chlorine, bromine or iodine;
Y is chlorine, bromine, iodine, hydrogen, a C,i—oQ alkyl, a C, _ acyl, or a C,_fi alkoxy; and R and R_ are each independently a C, ft monovalent or multivalent hydrocarbon radical selected from the group consisting of alkyl hydrocarbon radicals and saturated or unsaturated monocyclic hydrocarbon radicals having five or six carbon atoms per cycle; wherein said radicals are optionally substituted with one or more substituents selected from the group consisting of C,_fi alkyl, C, R acyl, C- R alkoxy, carboxy and sulfonic acid groups; and
(b) allowing a substantial portion of the N-halogenated hydantoin to dissolve before replenishing the supply of N-halogenated hydantoin in the recirculating water
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US64897296A | 1996-05-17 | 1996-05-17 | |
| US08/648972 | 1996-05-17 | ||
| PCT/US1997/008712 WO1997043215A1 (en) | 1996-05-17 | 1997-05-16 | Method for sanitizing swimming pools and recirculating water systems |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU3076397A true AU3076397A (en) | 1997-12-05 |
| AU735824B2 AU735824B2 (en) | 2001-07-19 |
Family
ID=24602977
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU30763/97A Ceased AU735824B2 (en) | 1996-05-17 | 1997-05-16 | Method for sanitizing swimming pools and recirculating water systems |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0909260A4 (en) |
| AU (1) | AU735824B2 (en) |
| CA (1) | CA2255928A1 (en) |
| WO (1) | WO1997043215A1 (en) |
| ZA (1) | ZA974174B (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6303038B1 (en) | 1999-06-01 | 2001-10-16 | Albemarle Corporation | Solid mixtures of dialkylhydantoins and bromide ion sources for water sanitization |
| US6986910B2 (en) | 2001-06-28 | 2006-01-17 | Albemarle Corporation | Microbiological control in poultry processing |
| US6908636B2 (en) | 2001-06-28 | 2005-06-21 | Albermarle Corporation | Microbiological control in poultry processing |
| US6749758B2 (en) | 2001-12-05 | 2004-06-15 | Albemarle Corporation | Methods and systems for uniform-control of bromine concentrations in water |
| US7901276B2 (en) | 2003-06-24 | 2011-03-08 | Albemarle Corporation | Microbiocidal control in the processing of meat-producing four-legged animals |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3412021A (en) * | 1964-09-15 | 1968-11-19 | Laurene O. Paterson | Water-treating method and agglomerates of n-halogenated organic compounds for use therein |
| US4530120A (en) * | 1975-06-30 | 1985-07-23 | Kenji Etani | Methods and apparatus for bathing |
| DE3380290D1 (en) * | 1983-10-17 | 1989-09-07 | Lonza Ag | Agglomerated halo-hydantoins |
| MX173174B (en) * | 1989-11-06 | 1994-02-04 | Bio Lab Inc | N-HALOGEN COMPOSITIONS WITH STABLE BLUE PIGMENT |
-
1997
- 1997-05-14 ZA ZA9704174A patent/ZA974174B/en unknown
- 1997-05-16 EP EP97925700A patent/EP0909260A4/en not_active Withdrawn
- 1997-05-16 AU AU30763/97A patent/AU735824B2/en not_active Ceased
- 1997-05-16 CA CA002255928A patent/CA2255928A1/en not_active Abandoned
- 1997-05-16 WO PCT/US1997/008712 patent/WO1997043215A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| EP0909260A4 (en) | 1999-11-17 |
| EP0909260A1 (en) | 1999-04-21 |
| WO1997043215A1 (en) | 1997-11-20 |
| AU735824B2 (en) | 2001-07-19 |
| CA2255928A1 (en) | 1997-11-20 |
| ZA974174B (en) | 1997-12-10 |
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