CA1118984A - Method for sanitizing toilets - Google Patents

Method for sanitizing toilets

Info

Publication number
CA1118984A
CA1118984A CA000329502A CA329502A CA1118984A CA 1118984 A CA1118984 A CA 1118984A CA 000329502 A CA000329502 A CA 000329502A CA 329502 A CA329502 A CA 329502A CA 1118984 A CA1118984 A CA 1118984A
Authority
CA
Canada
Prior art keywords
water
flush
dye
dispensing means
bowl
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.)
Expired
Application number
CA000329502A
Other languages
French (fr)
Inventor
David J. Kitko
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
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 Procter and Gamble Co filed Critical Procter and Gamble Co
Application granted granted Critical
Publication of CA1118984A publication Critical patent/CA1118984A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/48Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L9/00Disinfection, sterilisation or deodorisation of air
    • A61L9/015Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone
    • A61L9/04Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating
    • A61L9/05Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating specially adapted to be released by contact with a liquid, e.g. for toilets
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047Detergents in the form of bars or tablets
    • C11D17/0056Lavatory cleansing blocks
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/395Bleaching agents
    • C11D3/3953Inorganic bleaching agents
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40Dyes ; Pigments
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/22Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S4/00Baths, closets, sinks, and spittoons
    • Y10S4/09Methods

Abstract

ABSTRACT

A method for sanitizing toilets wherein a hypochlorite sanitizing agent and an oxidizabie dye are dispensed from separate dispensing means into the toilet flush water to provide a color to the bowl water. The color disappears within a short time after the flush, thereby providing a visual indicator of the activity of the sanitizing agent.

Description

- 2 - -, -METHOD FOR SANITIZING TOILETS

David ~. Kitko _ ;
:, ~',' TEC~NICAL FIELD
The present invention relatas to the automatic sanitizing of flush toilets by the dispensing of a bleach~ -able dye and a hypochlorite sanitizing agent to the toilet bowl with each flush. The dye is bleached by the hypo-chlorite to a colorless state within a short time after 1ushi~g, thereby providing a visual signal o~ the activity o the hypochlorite.
' BACKGROUND ART

This invention relates to a method of sanitizing a toilet bowl. More particularly, it relates to a method wherein a hypochlorite sanitizing agent and a water-soluble dye, which is oxidizable by the hypochlorite from a color~d to a colorless state, are automatically dispensed from separate dispe~sing means to the toilet bowl during flushing. The water in the bowl at ~he end o the ~lush is ~`
colored by the dye. However, the dye is oxid:ized to a colorless ~tate within a short time thereby p:roviding a visual signal that ~he hypochlorite sanitizinq ag~nt is present and "acting" in the bowl.
Automatically dispensed toile~ bowl cleaning and~or sanitizing products, which contain dyes to provide a visual signal to the user that product is ~eing dispensed, are well known. Such products are sold in the United ~5 States under the ~rand names VANISH AUTO~TIC ~Drackett Products), TY-D-BOL AUTOMATIC (Xnomark, Inc.) and SANIFLUSH
AUTO~TIC (Boyle-Midway). None of these products contains 1. Trademark -2. Trademark
3. Trademark .', ' ~

.

i~ ~
. _ 3 _ a hypochlorite sanitizing agent and all of them provide a color to the bowl wa-ter which persists between flushings.
U.S. Patent 3,504,384, Radley et al., issued April 7, 1970, discloses a dual comparbment dispenser for automatically dispensing a hypochlorite solution and a surfactant/dye ; solution to the toilet bowl during flushin~. The dye which is taught in the patent is Disulfide Blue VN150. It is believed that the dye referred to in Radley et al. is - -actually Disulphine Blue VN150 (Color Index No. 42045).
This dye has been found by the present applicant to be quite resistant to oxidation -to a colorless state by hypochlorite; thus, it too provides a persistent color to the toilet bowl waterS even in the presence of the hypochlorite.
A persistent color in the toilet bowl water has certain attendant negatives. The dye can cause staining cf the toilet bowl itsalf or of deposit3 tsuc~l as wa~e~
hardness deposits) which acc~nulate on the surfaces of the - ~owl between manual cleanings. Also, colored water in the bowl will tend to obscure medical symptoms such as the passing of blood during excretion or urination. Furthe~, a persistent color in the toilet bowl water tends to obscure otherwise visible evidence of soiling on suxfaces of the toilet ~owl which are below the water line.
An object of the present invention is to provide a method of automatically sanitizing a toilet bowl with each flush.
Another object of the invention is to provide a visual color signal to indicate that the sanitizing agent is present and acting in the toilet bowl.
Another object of the invention is to provide a visual color signal which persists in the toilet bowl for only a short time after flushing.
Another object of the invention is to provide, i~ 35 by a visual color signal, a means by which the consumer will know when a new supply of sanitizing agent needs to be provided for the toilet.

lllE~5~l34 DISCLOSURE OF INVENTION

The present invention reLates to a method of treating a flush ~oilet, which comprises a flu.sh tank and bowl, with a hypochlorite sanitizing agent each time the toilet is 1ushed, and providing a ~ransitory visual signal to indica~e the activity of the sanitizing agen~
in the bowl. The said method comprises the step of dis-pensing from separate dispensing means, into the flush water; (A) an aqueous solution of a compound which produces ~: hypochlorite ion in aqueous solution; and (B) a solution of a dye, the said dye being one which is oxidize~ from a colored state to a colorless state in the bowl within about 5 seconds to lO minutes ~preferably about 10 seconds ~o about 5 minutes) after contact with the hypochlorite. If desired, the dye solution can also contain a water-soluble .
bromide sait ~o catalyze the ac~ivity of ~he hypochlorite.
In a more particular aspect the present invention resides in a method of sanitizing a toilet which comprises a flush tank and a bowl, with a hypochlorite sanitizing agent each time the toilet is flushed, and providing a transitory visual signal to indicate the activity of the sanitizing agen~ in the bowl, said met:hod comprlsing the step of dispensingj from separate dispensing means, into the flush water, (A) an aqueous solu-tion of a compound which produces - hypochlorite ion in aqueous solution, and (B) a solution of a dye selected from the group consisting of those identified by Colc~r Index nu~bers 24401 and 42040, and Color Inclex name Basic Blue 80; the amount of (A) bein~ sufficient to produce a concentration of from about 2 to about 30 ppm available chlorine in the bowl water at the end of the flush, the amount oi (B) being suficient to produce a dye concentral~:ion of from about 0.02 to about 2 ppm and an avai:l.able chlorine;dye ratio of from about 2~ o about 150:1, and the pH of the solution forr~led in the toilet bowl being from about 6 to about 9.

L8~

.
- 4a -The present invention, in a further apsect, resides in an article OI manufacture designed ror placement in the water of the flusn tan~ of a toilet, said article comprising two disp2nsi~g ~.eans, the first dispensing means containing a solia composition which is soluble in water and comprises a compound which provides hypochlorite ions in aqueous solution, and a second dispensing means contain-ins a solid composition ~hich is soluble in water and wnich ~ontains a dye selected from the group consisting of those identi~ied by Color Inde~ numbers 24401, 42040 and Color Inde~ name Basic Blue 80, said first dispensins means and second dispensing means each having a chamber for receiving water fro~ the flush tan'~ wnen said flush tank reills after a flush and for maintaining said received wat.er in contact . with the respective solid compositions in said first and second dis-pensins means during the quiescent period bet~een ~lushes so as to form concentrated 501utions of said com-positions in said respective dispensing means between flushes, said firs~ dispensing means and second dispensing means each having means for retaining said concentrated :~
solutions in substantial isolation :Erom each other and from : the bcdy of water in the flush tank during the quiescent period between flushes, said first dispensing means. and ~ -said second dis-ensing means each having means for releasing said concentrated solutions into the water in the flush tank wl~en said wa er f~sws frc.~ ,ne tan~ durins rlushing, said irst and second dispensing means cooperating to produce, in the bowl water at the end of the flush, a concentration of from about 2 to about 30 ppm available chlorine, a concen-tration of from about 0.02 to about 2 ppm of said dye, an available chlorine:dye ratio of from about 2:1 to about ; 150:1, and a pH of about 6 to about 9.
~:

; h~ ~
~v 9~:
-4b-The Sanitizing Agent The sanitizing agent of the present invention can be any compound which provides the hypochlorite ion (OCl ) in aqueous solution~ Such compounds include alkali me~al and alkaline earth metal hypochlorites, hypochlorite addition products, chloramines, chlorimines, chloramides, and chlorimides. Specific e~.amples of compounds of this type include sodium hypochlorite, potassium hypochlorite, lithium hypochlorite, calcium hypochlorite, calcium hypoe chlorite dihydrate, monobasic calcium hypochlorite, dibasic magnesium hypochlorite, chlorinated trisodium phosphate dodecahydrate, potassium dichloroisocyanurate, sodium dichloroisocyanurate, sodium dichloroisocyanurate dihydrate, 1,3-dichloro-5,5-dimethylhydantoin, N-chlorosulfamide, Chloramine T, Dichloramine T, Chloramine B, Dichloramine B, and Di-~ialo (bromochlorodimethyl hydantoin). A particularly preferred sanitizing agent composition suitable for use in ~ -the practice of the present invention is described in the '. ;
,, {~L ' ' .t.

`:
:;

commonly assigned Canadian patent application of John Daniel Nyquist en~itled DISINFECTING COMPOSITION, Serial No.
325,625, filed April 17, 1979. Th~.~ composition . _ . . _ _ . . . _ . _ described in the Nyquist application is a cc~mpacted cake comprising lithium hypochlorite and calcium hypochlorite in a ratio of lithium hypochlorite:calcium hypochlorite of from a~out 0.58:1 to about 0.17:1, by welght. ;~
By virtue of the strong oxidizing power of the hypochlorite ion, it is highly effective in bleaching stains, breaking down and removing soils and killing microorganisms, thereby pro~iding effec~ive sanitizing ~ ~
action to the toilet bowl. ;
The amount of hypochlorite-pro~idi.ng compound '~
15 dispensed to the toilet in the process of the invention can ~ ,~
vary over a wide range, but preferably should be sufficient ~o p~ovide from about 2 to about ~0 ppm (pre!fer~ly rom about 4 to about 8 ppm) available chlorine in the bowl water a~ the end of the flush~ Only a very small amoun~ o 20 the available chlorine which is delivered to the bowl will ,~
be utilized in oxidizing the dye~ The sanii:izing agent can be formulated as an aqueous'liquid if it: is to be dispensed from a dispensing means designed t:o receive liquids. The sanitizing agent can also be ~'ormulated into 25 the form of a solid ~ake or use in dispensing means which ~;
are designed to receive a cake of solid mate!rial (see description of dispensing means below). The le~el of available chlorine in the bowl water can be measured by well-known methods such as the DPD Ferrous Titrimetric Method or the Stabilized Neutral Orthotolidi,ne Method~
described, respectively, at pages 129 and 1~6 Qf Standard Methods for the Examination of Water and Was,tewater, 13th Ed., published by American Public Health Association.
If desirea, the activity of the hypochlorite ~`
can be catalyzed by addition of bromide ion to the process of the invention. This will enhance the sanitizing activity of hypochlo,.r~ h~....~5i~ wl r and will , 9E~

; speed up the oxidation of the dye. Generally, any com-pound which produces bromide ion in aqueous solu~ion can be used as the souxce of bromide ion~ Examples of such compounds are inorganic bromide salts such as sodium -bromide, potassium bromide, calcium bromide, zinc bromide;
magnesium bromide and lithium bromide, a~ well as organic salts such as cetylpyridinium bromide and cetyltrimethyl-~ammonium bromide~ The hromide salt is kept separate from the hypochlorite sanitizing agent until the sanitizing agent is dispensed into the flush water, i.e., the bromide and sanitizing agen~ are dispensed from separate dispensing means. Preferably, the bromide salt is dispensed to the ; toilet from the same dispensing ~eans as the dye. When a bromide catalyst is used; ~he ~lount which is ~Ised prefer-ably should be sufficient to provide a weight xatio of available chlorine to bromide ion of from about 2:1 to about 150:1, and most preferably from about 4:1 to ahout 13:1 in the toilet bowlO (~ll percentages and ratios herein are "by weight" unless specified otherwise.) ~y~
~ .
A water-soluble bleachable dye is an essential feature of the present invention. The dye should be soluble in water to the exten~ of at least 0.01% by weight in water at 25Co The amount of dye dispensed to the toilet in the process of the invention will depend on ~he color in~ensity desiredl the amount of sanitizing agent dispensed into the toilet with the dye, and on the quickness with which it is desired to have the color disappear. Genera].ly, the amoun~
of dye dispensed will be sufficient -to produce a dye con-centration of from about .02 to about 2 ppm, preferably ~rom about 0.2 ppm to about 1.5 ppm in the toilet bowl. Gen-; erally, the dye should be present in a ra-tio of available chlorine:dye of from 2:1 to about 150:1, prefexably from about S:l to about 25:1 D Dye concentration and ratios herein are based upon the amount of the ac-tual dye compound, J
, .

8~

unless speciEied otherwise~ ~yes are normally sold in the form of mixtures of dye compound and inert diluent.
Dyes which are suitable for use in the method of the present inven-tion are those which are oxidized by the sanitizing agent to a colorless state within a period of from about 5 seconds to 10 minutes from the time they come into contact with the saniti.zing a~ent during the flushing of the toilet. A wide variety of oxidizable dyes can be utilized in the present process.
The following screening -test can be used for ~` i determining the suitability of any particular dye for use ¦ in the method of the present inventi.on. The test is con-ducted at pH 6 and pH 9, since thi.s rep:cesents the range j of pH's likely to be found in tap water.
I 15 Three liters of deionized water at 65F are placed in a four liter beaker, and the 1;~ater is kep~ in stirrin~ motion with a magneti.c stirrer. 65F wa~ ~hosT~n because it is approximately the median temperature ~or toilet flush water, which generally can vary in the range of ~TO F to 80F. The appropri.ate amoun~ of sodium hypo-chlorite is added via a pipe~te to the ,~ater from a 1 available chlorine aqueous stock solutilon of sodium hypochlvrite. The pH is then adjusted to 6 or 9 with a one~percent aqueous solution of NaOH or H2SO4, as needed.
I~bromide catalysis is utilized, ~he appropriate a~ount of sodium bromide is added from an aqueous stock solution ~1%
NaBr in water). The color change react:ion is initiated by the addition of the appropriate amount of a stock solution of dye (0.1% dye, on an "as received" basis, in water).
The solution is then observed to determine the time for disappearance of color.
The fol].owing table presents clata on the testing of various dyes for suitability for use in the present invention with an available chlorine le~el of 5 ppm, cataly2ed with 1.0 ppm bromide io~, and uncatalyzed.
The dye level in all instances was l ppm on an "as received"

,, .

basis. Based upon information provided by suppliers of the dyes, ~he approximate concentratlons of actual dye were calcula~ed and are shown in the table. The table records the time inter~al (M = minutes, S = seconds) from ` 5 when the dye solution is added until the col.or disappears in the beakerO
TABLE I
pH 6 pH !~ :
S ppm 5 ppm 5 ppm AV.C12 5 pEm Av~C12 Dye* ~ AvoC12 1.0 p~m Br Av.Cl~ ? p~ Br 1 0.92 >10 M ~10 M>10 M ~10 M
~ 2 0.90 >10 M >10 M 6 M lS S
3 0.88 >10 M >10 M~10 M >10 M
15 4 0.68 >10 M . >10 M>1~ M~10 M :
O.9S>10 M 1 M 8 M 1.3M - :~
-6 0.251 ~1 4 M 6 M 15 S
7 0.90>10 M 9 M 2 M 1.5 8 1.04.5M 2.5M 1.8M 1.8M
.: . 20 9 0.13>10 M 3.5M 7 M 1 M
0.291.5M 10 S 8 M 1.5M : ~;
11 0.856 ~1 2 M >10 M 3 M
12 0.75>10 M 3.5M 6 M 1.5M
*Dye identification (C. I . reEers to the Color : 25 Index listing name or number) : 1 FD&C Blue ~1 C.I. 42090 2 FD&C Blue ~2 C.I. 73015 3 FD&C Green #3 C.I. 42053
4. Disulphine Blue VN C.I. 42045
5 Alizarine Light Blue B C.I. 63010 . 6 Carta Blue VP C.I. 24401 ,.: 7 Acid Green 2G C.I. 42085 8 "Astrazon Green D"* C.I. 4~040 9 Supranol Cyanine 7B C . I ~ 42675 35 10 "Maxilon Blue 3RL" ** C.I. Basic Blue 80 11 Drim2rene Blue Z-RL C.I. Reactive Blue 17 12 Alizarine Light Blue H~RL C.I. Acid Blue 182 **~ra~emark .~

g From these data it can be seen -that for uncata-lyzed hypochlorite at 5 ppm Av. C12, dyes 6 r 8~ and 10 provide a color-to-colorless signal in the required time frame at both pH's. For bromide~catalyzed hypochlorite at 5 ppm Av.C12 and 1 ppm bromide, dyes 5, 6, 7, 8, 9, 10, 11, and 12 provide a colox-to-colorless signal in the required ~ time frame at both p~'sO
Optionally, the dyes used in the method of the --present inventio.n can be formulated into composition5 con-taining other ingredients which it is desired to dispenseinto the toilet bowl, such as, for example, surfactants, sequestering agents, perfumes r and diluents such as water, organic solvents such as ethanol~ and organi.c or .inorganic salts such as sodium sulfate, sodium chloride and sodium acetate.
Surfactants can provide enhanced sanitizing per:Eormance through breakup and emulsification ol. soils, ~ and also provide some sudsing in the toilet bowl, which : ~ may be-aesthetically desirable. Perfumes provide a pleasant smell to the area surrounding the toilet and also help to obscure the "bleach" smell of the sanitizin~
agent. Sequestrants aid soil removal by sequestration o~
; multivalent metal i.ons.
. When the dyes herein are formulated with surfacr ` 25 tants f the resul~ing compositions will generally comprise from about 5% to about 9g~ surfactant and from about 0.2%
to about 15~ dye. Perfumes will no~nally be used at levels of up to about 25%.and inert diluents at levels up to about 90~. Sequestering agents such as potassium pyrophos 30 phate, sodium tripolyphosphate and ethylenediamine penta-acetate can be used at levels up to about 25~.
Compositions comprising the dye and a surfactant and/or o~her ingredients can be conveniently pressed into the form of a cake ~or use in dispensers which are designed 35 to receive a cake of solid material (see description of . dispensing means, below). Such cakes can be made by ", 8~
'`

extrusion or hydraulic stamping, or by pouring a melt of the composition into a mold and solidif~ing the compositi-on by cooling.
If it is desired to use a dispensing means which is designed to receive liquids, the dye and any optional ingredients such as surfactants, etc., can be formulated into li~uid compositions.

. .

' .~ .

:
,;

Dyes 8 and lO in Table I are c:ationic dyes, whereas the remainder are anionic. ~en surfactants are to be used in the present invention, it is important that dye and surfactant be selected so as to be compatible with each other. Cationic dyes should not be used with anionic surfactants, and anionic dyes should not be used with ca-tionic surfactants.
Anionic surfactan-ts operable in compositions suitable for use in practicing the present invention can be broadly described as the water~soluble salts, particu-larly the alkali metal salts, of organic sulfuric acid reaction products having in their molecular structure an alkyl or alkaryl radical containing from about 8 ~o about 22 carbon atoms and a radical selected from the group con~
sisting of sulfonic acid and sulfuric acid ester radicals.
; (Included in the term alkyl is the alkyl portion o higher ~ acyl radicals.) Important examrles of the anionic surfac-i tants which can be employed in the practicing of the present invention are the sodium or potassium alkyl sulfates, especially those obtained by sulfating the hiyher alcohols (C8-Cl8 carbon atoms) produced by reducing the ~lycerides o~ tallow or coconut oil; sodium or potassium alkyl ben2ene sulfonates, in which the alkyl group contains from about ' 9 to about lS carbon atoms, ~the alkyl radical can be a straight or branched aliphatic chain); paraffin sulfona-te surfactants having the general formula RS03M, wherein R
is a primary or secondary alkyl group containing from about 8 to about 22 carbon atoms (preferably 10 to 18 carbo~
atoms) and M is an alkali metal, e.g.~ sodium or potassium;
sodium alkyl glyceryl ether sulfonates, especially those ethers of the higher alcohols derived from tallow and coconut oil; sodium coconut oil fatty acid monoglyceride sulfates and sulfonates; sodium or potassium salts of sulfuric acid esters of the reaction product of one mole of a higher fatty alcohol ~e.g., tallow or coconut oil alcohols) and about l to lO moles of ethylene oxide;
sodium or potassium salts of alkyl phenol ethylene oxide 9t~

ether sulfates with about 1 to about 10 units of ethylene oxide per molecule and in which the alkyl radicals contain from about 8 to about 12 carbon atoms; the xeaction products of fatty acids esterified with isethionic acid and neutral-ized with sodium hydroxide where, for example, the-fatty acids are derived from coconut oil; sodium or potassium salts of fatty acid amides of a methyl tauride in which ~ the fatty acids, for exampler are derived from coconut oil :
, and sodium or potassium ~-acetoxy- or ~-acetamido~alkane-sulfonates where the alkane has from ~ to 22 car~on atoms.
Nonionic surfactants which can be used in practicing the present invention can be of three basic types -- the alkylenc oxide condensates, the amides an~
the semi~polar nonlonics.
The alkylene oxide condensates are broadly defined as compounds produced by the con~ensa~ion o ; alkylene oxide groups (hydrophilic in nature) with an organic hydrophobic compound, which can be aliphatic or ~ alkyl aromatic in nature. The length of the hydrophilic .~ 20 or polyoxyalkylene radical which is condensed with any , .
particular hydropho~ic group can be readily adjusted to yield a water-soluble~compound having the desired deyree of balance between hydrophilic and hydrophobic elements.
Examples of such alkylene oxicle condensates include:
1. The condensation products of aliphatic alcohols with ethylene oxide. The alky] chain of the ali-. .~ .
; phatic alcohol can either be straight or branched and generally contains from about 8 to about 22 carbon atoms.
:i 30 Examples of such ethoxylated alcohols illclude the condensa~
tion product of about 6 moles of ethylene oxide with 1 mole of tridecanol, myristyl alcohol condensed V~ith about 10 moles of ethylene oxide per mole of myr:istyl alcohol, the - condensation product of ethylene oxide with coconut fatty alcohol wherein the coconut alcohol is a mixture of fatty alcohols with alkyl chains varying from 10 to 14 carbon :

~ ~L$~S~

atoms and wherein the condensate contains about 6 moles of ethylene oxide per mole of alcohol and the condensation product of about 9 moles of ethylene oxide with the above-described coconut alcohol. Examples of co~nercially available nonionic surf~ctants of this type include"Tergitol 15-S-9"~arketed by the Union Carblde Corporation," ~eodol 23-6.5"~arke~ed by the Shell Chemical Comp~.rly and'Xyro EOB'j6 marketed by The Proctex & Gamble Company.
The polyethylene oxide conder~sates of alkyl phenols. These compounds include the condensation products o~ alkyl phenols having an alXyl group containing ~ro~ about
6 to about 12 carbon atoms in either a strai.gh~ chain or - branched chain con~iguration, with ethylene oxide, the said ethylene oxide being pre~ent in amounts equ~ o S to 25 moles c;f ethylene oxide per mole of alkyl p}~enol. The alkyl substituent in such compounds can be ~leriv~d, ~ox axample, from polymerized propylene, diisob~;ltylenet octene, or nonene~ Examples of compounds of this t~pe include nonyl phenol conde~sed with abou~ 9.5 moles o ethylene oxide per mole of nonyl phenol, dodecyl phenol condensed with about 12 moles of e~hylene oxide per mc~le of phenol, dinonyl phenol condensed with about 15 molè~ of ethylene ;~ oxide per mole of phenol, di-isooctylphenol condensed ~` with about 15 moles o ethylene oxide per mole of phenol.
Commercially available nonionic surfactants of this type include'`Igepal CO-61~"~ar~eted by the GAF Corpora~ion;
andl~Trito~ -45r X-114, X-100 and X-102 all marketed by the Rohm and Haas Company.
3. The condensation products of e~hylene oxide with a hydrophobic base formed by the condensation of propy-lene oxide with propylene glycol. The hydrophobic por~ion of these compounds has a molecular weight oi rom abou~
1500 to 1800 and of course exhibits water insolubility~
The addition of polyoxyethylene moieties of this hydrophobic portion tends to increase the water-solubility of the mole-cule. Examples of compounds of this type include certain 4 - 8 inclusive. The terms bearing these superscript numerals - are all trademarks.

L8~

:
of the commercially available"Pluronicl~surfactants marketed - by ~he Wyandotte Chemicals Corporation.
4. The condensation products of ethylene oxide ~ with the product resulting from the reaction of propylene - S oxide and ethylene diamine. The hydrophobic base of these ~ products consists of the reaction product o ethylene ; diamine and excess propylene oxide, said base having a molecular weight of from about 2500 to about 3000. This -~ base is condensed wi~h ethylene oxide to the extent that i; 10 the condensation product contains from about 40~ to about .~ 80~ by weight of polyoxyet`hylene and has a molecular weight of from about 5,000 to about 11,000~ Examples o~ this t~pe o nonionic sur~actant include certain o the Gomn~er-~; cially available"Tetronic"compounds marXeted by the ~yandotte Chemicals Corporation.
; Examples of the amide type of nonionic surfac-tants include the a~monia, monoethanol and diethanoi amides ,~ _ of fatty acids havin~ an acyl moiety of from abou~ 8 to about 18 carbo~ atoms. These acyl moieties are normally derived from naturally occurring glycerides, e.g., coconut i oil, palm oil, soybean oil and tallow, but can be derived , ~, .
synthetically, e.g., by the oxidation of petroleum, or by `~
hydrogenation of carbon monoxide by ~he Fischer-Tropsch `:i; process.
Examples of the semi-polar type of nonionic sur-factants are the amine oxides, phosphine oxides and sulfoxides. These materials are described more fully in U.S. Patent 3,819,528, Berry, issued ~une 25, 1974, Ampholytic surfactants which can be used in practicing the present invention can be broadly described as derivativas of aliphatic amines which contain a long chain of about 8 ~o about 18 carbon atoms and an anionic ~ water-solu~ilizing group, e.g., car~oxy, sulfo and sulfato.
m 35 Examples of compounds falling within this definition are sodium-3-dodecylamino-propionate, sodium-3-dodecylamino propane sulfonate, and dodecyl dimethylammoni~m hexanoate.
* Trademark Zwitterionic surfactants which can be used in .; .
practicing the present invention are broadly described as internally-neutralized derivatives of aliphatic quaternary ammonium and phosphonium and tertiary sufonium compounds, 5 in which the aliphatic radical can be straight chain-or branched, and wherei~ one of the aliphatic substituents contains from about 8 to about 18 carbon atoms and one contains an anio~ic water-solubilizing group, e.g., carboxy, sulfo, sulfato, phosphato, or phosphono.
Cationic surfactants which can he used in prac~
ticing the present invention include stearyl dimethyl benzyl ammonium chloride~ coconut dimethyl benzyl ammonium chloride~ cetyl pyridi~iunl chloride and cetyl trimethyl ammonium chloride.
Bleach-stable (i.e., hypochlorite-stable) sur-factants which are especially resistant to oxidation are the al~yl sulLates anu paraffin suion~l~s. Alkyl sulfates are the water-soluble salts of sulfated fatty alcohols containing from a~out 8 to about 18 carbon atoms in the alkyl group. Examples of suitable alcohols which Gan be employed in alkyl sulfate manufacture i~,clude decyl, lauryl, myristyl, palmityl and stearyl alcohols and the mix~ures of fatty alcohols deri~ed by reducing the glycerides o tallow and coconut oil.
Specific examples of alkyl sulfate salts which can be employed in the instant surfactant/dye compositions include sodium lauryl alkyl sulfate, sodium s~earyl alkyl sulfate, sodium palmityl alkyl sulfate, sodium decyl sulfate, sodium myristyl alkyl sulfate, potassium lauryl alkyl sulfate, potassi~ stearyl alkyl sulfate, potassium decyl sulfate, potassium palmityl alkyl sulate, potassium myristyl alkyl sulfate, sodium dodecyl sulfate, potassium dodecyl sulfate, potassium tallow alkyl sulfate, sodium tallow alkyl sulfate, sodium coconut alkyl sulfate, ~-potassium coconut alkyl sulfate and mixtures of these surfactants. Highly preferred alkyl su]fates are sodium 9~3~

- 16 - ~
:

coconut alkyl sulfate, potassi~m coconut alkyl sulfate, - potassium lauryl alkyl sulfate and sodium lauryl alkyl sulfate.
Paraffin sulfonate surfactants have the general formula RSO3M, wherein R is a primary or secondary alkyl group containing from about 8 to about 22 carbon atoms (preferably 10 to 18 car~on atoms) and M is an alkali metal, e.g., sodium or potassium. Para~in sulfonate sux-~ factants and methods for their preparation are well known `I 10 in the ar~. They may be prepared, for exam~le, by reaction o hydrocarbons with sulfur dioxicle, oxygen and a sulo-nation reaction initiator. Alternatively, -they may be prepared by reacting an alkene ancl a sodium bisulfite ~ under suitable radiation or catalysis, as disclosed in `
,~ lS British Patent 1,451,228 publishecl September 2~ 76;
;~' Paraf~in ;-~ sulfonate surfactants are commercially available, e.g., '' from Farbwerk~-~Hoechst A.G.
Preferred paraffin sulfonates her~3in are ., secondary paraf~in sulfonates. Examples of specific paraffin sulfonates herein are:
Sodium-l-decane sulfonate:
Potassium-2-decane sulfonate;
Lithium-l-dodecane sulfonate;
Sodium-6-trid~cane sulfonate;
Sodium-2-tetradecane sulfonate;
Sodium-l-hexadecane sulfonate;
Sodium-4-octadecane sulfona~e;
Sodium-3 octadecane sulfonate. ~;
Normally, the paraffin sulfonates are available as mixtures of individual chain lengths and position isomers t and such mixtures are suitable for use herein.

!

. . . . ..

Dispensing Means `. In order to provide automatic sanitizing of the toilet bowl in accordance with the presen-t inven-tion, it is essential that the hypochlor:ite sanitizing agent and the dye, in the form of relatively concentrated solutions, be dispensed into the flush wa.ter e~ch time the toilet is flushed. --, It is within the contemplation o~ the present invention that the concentrated solution of one of the components (i.e., either the dye or the sanitizing agent) i be dispensed into the flush tank during the reill after a r,~` flush ~thereby forming a dilut:e solution of one oomponent . in the flush water which is stored in the tank between flushes) and that the concentrated sol.u~ion of the other component be dispensed into this treated flush water during `. the time lt 15 ~lowing from the -~clnk to 1.. he ~owl during -t~le next succeeding flush. Dispensing means which operate to dispense solutions into a toilet tank during the time it is refilling are described, for example, in U.S. Patents 1,798,090, Lebegue, issued March 24, 19~1; 3,339,801r ~ronas, i.ssued September 5, 1967; and 3,121,2361 Yodro et al., issued February 18, 1964.
It is preferred that both of the concentrated solutions be dispensed into the flush water on the down-: flush, i~e., that they be di.spensed into the flush water during the time the flush water is flowing from the tank into the bowl~ In this preferred mode of operation, it is additionally preferred that the dispensing of the hypo- -.: chlori~e and dye should occur near the end of the flush in order to avoid wastage of dye and hypochlorite and to keep to a minimum the time of contact between dye and hypochlorite before they enter the bowl. The xespective dispensing means for the hypochlorite and dye solutions should pref~-: erably be positioned relative to each o~her in the toilet tank so -that these concentrated solutions will be diluted by flush water during the flush before they come into .

~iLlB984 .

contact with each other, i.e., intimate mixture of streams of the two concentrated solutions in the flush tank should preferably be avoided. Dispensing means for automatically dispensing solutions of chemicals into the flush water dur-ing the down-flush are well known to th~ art. U.S. Patent 3,504,384, Radley et al., issued April 7, 1970, discloses a dual dispenser for separately dispensing a detergent/dye solution and a hypochlorite solution into the flush water ; during the flush. Water from the flush tank flows into the respective dispenser chambers as the tank fills a~ter a flush, where it comes into contact with a soli.d deter-genttdye composition and a solid hypochlorite-producing composition in the respective char~rs~ Durill~ the in~erval between flushes, relatively concentrated solutions o the lS hypochlorite and detergent/dye compositions form in the respective cham~ers, and these solutions are discharged into the flush water on the next flush. It should be noted tha~
- the inlet and outlet ports of the dispenser chambers in the Radley et al. dual dispenser are not closed between flush-ings, and therefore there is opportunit~ for ingredients in the respective concentrated solutions in the chambers to diffuse into the tank water between f:lushes, whereby there is also opportunity for ingredient:s from one dispenser chamber to ultimately find their way int:o the solution in the other dispenser chamber. The longer the time interval between ~lushes, the more likelihood the!re is that some portion of the contents of the two dispenser chambers will have an opportunity to come into contact with each other : before -they are dispensed into the flush water on the next flush. ~hile dispensing devices of the type disclosed in Radley et alO can be used in the method of the present invention, they are not preferred. Because of the high reactivity between the dye and the hypochlorite, the color intensity and duration of the color signal in the bowl will be less reproducible from one flush to the next than if the dye and saniti lng agent are substantialLy completely isolated from the tank water (and, therefore, from each .~;

:

-- 19 -- , other) between flushesO This isolation can be accomplished in the dispensing means by providing a blocking means such as an air bubble or a mechanical seal which, during t~e period between flushes, blocks the ports by which liquid flow~ into and ou~ of the dispensing means. Depending on the type dispensing means used, and the mat~?rials used in constructing it, complete isolation of the concentrated solutions from ~he tank water may not always be possible since some small amount of solution may escape by capillaxy action, imper~ect sealing of th inlet and outlet ports, etc.
. Dispensers which completely or substan~ially com-pletely isolate their contents from the tank water during the quiescent period bet~een flushes are known to the ar~ :
and are the pre~erred type for use in the present inven~ion.
Such dispensers are disclosed, ~or example, in U~S. Patent : ;
3,831,20S, issued August 27, 1Y7~, to Foley; U.S. Paten~ :
: 3,341,074, issued Septem~er 12, 1967, to Panutti; U.S.
Paten~ 4,036,407, issued July 19, 1977, to Slone; U.S.
Patent No. 4,171,546, Dirksing, entitled PASSIVE DOSING DIS~
PENSER, i.ssued Octo~er 23, 1979; and Canadian Application No.
325,630, Dirksing, entitled PASSIVE DOSING DISPE~SER EMPLOYING
TRAPPED AIR BUBBLE TO PROVIDE AIR-LOCK, filed April 17, . 25 ~: 1979. Preferably, the ~mount o~ sanitizing composition placed in the sanitizing composition dispensing means should be chosen so as to last at least as long as ~i.e., through at least as many flushes as) the amount of dye composition 30 in the dye composition dispensing means. When the consumer ::
no longer sees any color appear in the bowl when f lushing the toilet, this indlcates that it is time to replace the system (dye and sanitizer). Conversely, i t:he consume~
sees that color persists in the toilet bowl r this is also an indication that the supply of sanitizing agent has been exhausted and the system should be replaced. As indicated previously, it is undesirable to have a persi.sten~ color 9~3~

in the toilet bowl between flushes, and, therefore, it is preferable that the supply of sanitizer last ~or at least as long as the supply of dye.
The dye and sanitizing agents can be formulated in-to the form of liquid or solid composition for use in the present method. The form of the composition will depend upon the type of dispenser used. The most preferred ; dispense~s are those which are designed to receive a solid composition. With this type of dispenser, wa,ter from the flush tank enters into the dispenser during t:he refill of the flush tank at the end of the f]ush. Water within the dispenser remains in contact with the solid composition between flushes, thereby forming a concentra1ed SOlUtiOIl :-within the dispenserO When the toilet is flushed, a pre-determined amount of the concentrated solut:ion is dis charged into the flush water as it flows from the tank to the bowl. Particularly preferred dispensers which are ; designed to receive a solid composition are 1:hose of the ~ b type disclosed in Dirksing's U.S. Patent 4,171,546 an~ Canadian ~;~
`
~pplication 325,630 previously referred to. In a preferrecl ~x~iment, these tw~ ~ypes of dispensing means are constructed into a dual dispenser unit, as is set forth in Example I, herein.
:~ EXAMPLE I
-- ' A solid, compacted sanitizing composition cake was prepared by dry-mixing FO~I-2*llthium hypochlorite (30% LiOCl), as available from Lithium Corporation of America, Bessemer City, North Carolina, with HTH calcium -- hypochlorite ~65% Ca(OCl)2], as available from Olin Mathieson Chemical Corp., NaCl and Na2SO4 in the propor-tions hereinafter set forth and subjecting the granular mi~ture io a compaction pressure OI about 2.5 ~ons per square inch on a Stokes Model R Tablet Press * Trademark .~
, .. . .

8~a .
.
.
;. - 21 ~ ~
,,~ ~ '.

Ingredient Grams . LiOCl (Form 2) 27.2 HT~ ~65% Ca(OCl)2] 43.9 NaCl 21.7 Na2S4 7.2 100.0 This composition had a LiOCl:Ca(OCl)2 weight ratio of about 0.29:1, and an available chlorine level ~ ;~
; tAVC12) of about 38% to 39~. The cake had a speci~ic :~ gravity of about 1.7, and dimensions of about 3.5 inch.es . 10 by about 1.5 inches by about 0.625 inGhes.
- A solid, compacted cake containin~ dye was pre-pared by mixing the ingredients he.reina~ter set orth in ~ a batch amalgamator, ~ollowed by milling and then extrusion . to-orm a rectangular slab having dimensions of about ~ 15 3.625 inches in width by about 2.0 inches i:n heigh~ by about 0.5 inches thick, and a speciflc gravlty of about :
1.1~ ` ~
~ .,.

Ingredlent Grams : Sodium paraffin sulfonate 52.2 . 20 (~Hostapur"**ap roximately .
: 8~ actlve, as available from American Hoechst, : Somerville, N.J. ) Acid Green 2G Conc.3.,'*
(as available from Sandoz, Hanover, N.J.) : NaBr 1.9 .; Perfume 7.2 . 65.0 *The dye sample contained 10~ diluent, therefore, ;~
the actual dye level was 3.3 grams.
-!- ~ Trademark ' ' , , ~ , - 22 - ;

This dye cake was thereater coated with talcum powder to prevent it from sticking to the sides of the dispensing apparatus.
The solid sanitizer caXe and dye cake were incor~
porated, respectively, into separately dispensing compart-ments of a dual dispensing apparatus which was vacuum thermoformed in two segments from 0.01S inch thick poly~inyl chloride. The conriguration of the integral:Ly formed dual comparbment dispenser was such that the dye cake was placed vertically overhead the sanitizer cake. The portion of the dispensing apparatus housing the dye cake was o~ a ~ -configuration generally similar to those described in con-nection with Figures 1 and 15 of the aforementioned U.S. Patent ~o. 4~171,546 of Robert S. Dirksing, granted on October 23, 1979, lS while the portion of the dispensing apparatus housing the sanitizer ca~e was of a configuration generally slmilar to that described in connection with Figure 12 of the aforem~ltioned Canadian patent application of Robert S. Dirksing, Seria~ No. 325,630, filed April 17, 1979. ~ :
These separate portions of the dispensing appara~us (actually two separate dispensing means) produce concen-trated solutions, respecti~ely, of the sanitizer composi-tion and dye composition in water which enters the apparatus when the toilet tank is filling after a flush. ~he respec tive dispensing means serve to isolate the concentrated solutions from each other and from the tanX water during ~`~
the period between flushes, although a very small amoun~ of dye solution was found to migrate into the flush tank between flushes. The positioning of the respective dis-pensing means of the dual dispenser is such as to prevent mixing o~ the dispensed sanitizer and dye 501ution5 during the flush until they have been dilu~ea with flush water.
The measuring cavity and inlet conduit of the sanitizer-containing portion of the dual dispenser is so sized that approximately 9 cubic centimeters of sani-tizer-containing solution is dispensed with each flush cycle of the toilet.
, 8~L
, :

The dye-containing portion of the dispenser is so sized that approximately two cubic centimeters of dye-containing -solution is dispensed into the flush water as it leaves the tank during each flush cycle of the toilet.
The aforedescribed exemplary embodiment of a dual ~;
dispenser for carrying out the cleansing and disinfecting method of the present invention provides an excellent ~; release of both the sanitizer-containing so~ution and the ~ `
surfactant-containing solution throughout the life of the unit~
A conventional toilet comprising a flush tank and a bowl was e~uipped with this type of dual dispenser by placing the dispenser into the tank. Over a 20-day period the toilet was flushed daily at predetermined time inter-vals during each day. Observations of color in the bowlduring and after flushing were made periodic:ally. The toilet was flushed a total of 281 times. The first seven flushes are required to prime the dispensing means for the hypochlorite sanitizer. Accordingly, on the first seven flushes very little, if any, hypochlorite was delivered to -the bowl, and the color which was delivered to the bowl persisted between flushes. After the seventh flush, color observations were made on 47 of the remainin,g flushes. Out of this total of 47 observations, there was one instance in '~ 25 which no color was seen in the bowl, either during or after the flush was complete. In all other instances color was observed during the flush and at the end of the flush. The time of color persistence ranged from 10 sec:onds to 120 seconds from the end of flush (i.e., from the time when the siphon breaks and the bowl begins to refill). The flush itself takes about 13 seconds (from beginning of tank water flow until siphon break), therefore, the total time for -color persistence was from about 23 seconds to about 133 seconds. The amount of available chlorine in the bowl at the end of the flush averaged about 6 ppm.
,. ~

Claims (22)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. A method of sanitizing a toilet which comprises a flush tank and a bowl, with a hypochlorite sanitizing agent each time the toilet is flushed, and providing a transitory visual signal to indicate the activity of the sanitizing agent in the bowl, said method comprising the step of dispensing, from separate dispensing means, into the flush water, (A) an aqueous solution of a compound which produces hypochlorite ion in aqueous solution, and (B) a solution of a dye selected from the group consisting of those identified by Color Index numbers 24401 and 42040, and Color Index name Basic Blue 80; the amount of (A) being sufficient to produce a concentration of from about 2 to about 30 ppm available chlorine in the bowl water at the end of the flush, the amount of (B) being sufficient to produce a dye concentration of from about 0.02 to about 2 ppm and an available chlorine:dye ratio of from about 2:1 to about 150:1, and the pH of the solution formed in the toilet bowl being from about 6 to about 9.
2. The method of Claim 1 wherein the respective solutions, (A) and (B), are both dispensed into the flush water during the down-flush.
3. The method of Claim 2, wherein the respective solutions, (A) and (B), are substantially completely isolated from the flush water in the toilet tank during the quiescent period between flushes of the toilet.
4. The method of Claim 3 wherein the amount of sanitizing agent dispensed is sufficient to produce a con-centration of from about 4 to about 8 ppm available chlorine in the bowl water at the end of the flush.
5. The method of Claim 4 wherein the available chlorine to dye ratio is from about 5:1 to about 25:1.
6. A method of sanitizing a toilet bowl which comprises a flush tank and a bowl, with a bromide catalyzed hypochlorite sanitizing agent each time the toilet is flushed, and providing a transitory visual signal to indicate the activity of the sanitizing agent in the bowl, said method comprising the step of dispensing, from separate dispensing means, into the flush water, (A) an aqueous solution of a compound which produces hypochlorite ion in aqueous solution, and (B) a solution comprising a dye and a water-soluble bromide salt, the said bromide salt being present in sufficient quantity to catalyze the oxidizing action of the hypochlorite-producing compound of (A) in the bowl, the said dye being selected from the group of those identified by Color Index numbers 24401, 42040, 63010, 42085, 42675, and those having Color Index names Basic Blue 80, Reactive Blue 17 and Acid Blue 182;
the amount of (A) being sufficient to produce a concentration of from about 2 to about 30 ppm available chlorine in the bowl, the amount of (B) being sufficient to produce a dye concentration of from about 0.2 to about 2ppm and an avail-able chlorine:dye ratio of from about 2:1 to 150:1 in the bowl, and the pH of the solution formed in the bowl being from about 6 to about 9.
7. The method of Claim 6 wherein the respective solutions, (A) and (B), are both dispensed into the flush water during the down-flush.
8. The method of Claim 7 wherein the respective solutions, (A) and (B), are substantially completely isolated from the flush water in the toilet tank water during the quiescent period between flushes of the toilet.
9. The method of claim 8 wherein the amount of bromide salt in (B) is sufficient to produce a weight ratio of available chlorine to bromide ion of from about 2:1 to about 150:1 in the toilet bowl water at the end of the flush.
10. The method of Claim 8 wherein the amount of hypochlorite-producing compound dispensed is sufficient to produce a concentration of from about 4 to about 8 ppm available chlorine in the toilet bowl at the end of the flush, and the amount of bromide salt dispensed is suffi-cient to produce a weight ratio of available chlorine to bromide of from about 4:1 to about 13:1.
11. The method of Claim 10 wherein the available chlorine to dye ratio is from about 5:1 to about 25:1.
12. The method of Claim 6 wherein the dye is Color Index number 42085.
13. The method of Claim 11 wherein the dye is Color Index number 42085.
14. An article of manufacture designed for placement in the water of the flush tank of a toilet, said article comprising two dispensing means, the first dispensing means containing a solid composition which is soluble in water and comprises a compound which provides hypochlorite ions in aqueous solution, and a second dispensing means contain-ins a solid composition which is soluble in water and which contains a dye selected from the group consisting of those identified by Color Index numbers 24401, 42040 and Color Index name Basic Blue 80, said first dispensing means and second dispensing means each having a chamber for receiving water from the flush tank when said flush tank refills after a flush and for maintaining said received water in contact with the respective solid compositions in said first and second dispensing means during the quiescent period between flushes so as to form concentrated solutions of said com-positions in said respective dispensing means between flushes, said first dispensing means and second dispensing means each having means for retaining said concentrated solutions is substantial isolation from each other and from the body of water in the flush tank during the quiescent period between flushes, said first dispensing means and said second dispensing means each having means for releasing said concentrated solutions into the water in the flush tank when said water flows from the tank during flushing, said first and second dispensing means cooperating to produce, in the bowl water at the end of the flush, a concentration of from about 2 to about 30 ppm available chlorine, a concentration of from about 0.02 to about 2 ppm of said dye, an available chlorine:dye ratio of from about 2:1 to about 150:1, and a pH
of about 6 to about 9.
15. An article of manufacture designed for placement in the water of the flush tank of a toilet, said article comprising two dispensing means, the first dispensing means containing a solid composition which is soluble in water and comprises a compound which provides hypochlorite ions in aqueous solution, and a second dispensing means contain-ins a solid composition which is soluble in water and which contains a water-soluble bromide salt and a dye selected from the group consisting of those identified by Color Index numbers 24401, 42040, 63010, 42085, 42675, and those having Color Index names Basic Blue 80, Reactive Blue 17 and Acid Blue 182; said first dispensing means and second dispensing means each having a chamber for receiving water from the flush tank when said flush tank refills after a flush and for maintaining said received water in contact with the respective solid compositions in said first and second dis-pensing means during the quiescent period between flushes so as to form concentrated solutions of said compositions in said respective dispensing means between flushes, said first dispensing means and second dispensing means each having means for retaining said concentrated solutions in substantial isolation from each other and from the body of water in the flush tank during the quiescent period between flushes, said first dis-pensing means and said second dispensing means each having means for releasing said concentrated solutions into the water in the flush tank when said water flows from the tank during flushing said first and second dispensing means cooperating to produce, in the bowl water at the end of the flush, a concentration of from about 2 to about 30 ppm available chlorine, a concentration of from about 0.02 to about 2 ppm of said dye, an available chlorine:dye ratio of from about 2:1 to about 150:1, a concentration of bromide ion sufficient to catalyze the oxidizing action of the available chlorine and a pH
of from about 6 to about 9.
16. The article of Claim 14 wherein said first and second dispensing means cooperate to produce an available chlorine concentration of from about 4 to about 8 ppm and an available chlorine to dye ratio of from about 5:1 to about 25:1 in the bowl water at the end of the flush.
17. The article of Claim 16 wherein the dye is selected from the group of those having Color Index Numbers 24401, 42040 and Color Index name Basic Blue 80.
18. The article of Claim 15 wherein said first and second dispensing means cooperate to produce a weight ratio of available chlorine to bromide ion of from about 2:1 to about 150:1 in the bowl water at the end of the flush.
19. The article of Claim 18 wherein the dye in said second dispensing means is Color Index number 42085.
20. The article of 18 wherein said first and second dispensing means cooperate to produce an available chlorine concentration of from about 4 ppm to about 8 ppm and an available chlorine bromide ion weight ratio of from about 4:1 to about 13:1 in the bowl water at the end of the flush.
21. The article of Claim 20 wherein said first and second dispensing means cooperate to produce an available chlorine:dye ratio of from about 5:1 to about 25:1 in the bowl water at the end of the flush.
22. The article of Claim 21 wherein the dye is Color Index 42085.
CA000329502A 1978-06-12 1979-06-11 Method for sanitizing toilets Expired CA1118984A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US05/915,027 US4248827A (en) 1978-06-12 1978-06-12 Method for sanitizing toilets
US915,027 1978-06-12

Publications (1)

Publication Number Publication Date
CA1118984A true CA1118984A (en) 1982-03-02

Family

ID=25435098

Family Applications (1)

Application Number Title Priority Date Filing Date
CA000329502A Expired CA1118984A (en) 1978-06-12 1979-06-11 Method for sanitizing toilets

Country Status (2)

Country Link
US (1) US4248827A (en)
CA (1) CA1118984A (en)

Families Citing this family (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4353866A (en) * 1980-11-05 1982-10-12 The Procter & Gamble Company Activation of hypochlorite bleaching of dyes
US4384869A (en) * 1980-11-05 1983-05-24 The Procter & Gamble Company Activation of hypochlorite bleaching of dyes
US4420412A (en) * 1980-11-05 1983-12-13 The Procter & Gamble Company Activation of hypochlorite bleaching of dyes
US4434136A (en) 1982-03-08 1984-02-28 The Proctor & Gamble Company Tapered-bottom bleach cake for sanitation dosing dispenser
US4668475A (en) * 1982-04-02 1987-05-26 Twinoak Products, Inc. Cleaning and disinfecting method and article of manufacture including color display
US4709423A (en) * 1982-11-08 1987-12-01 The Drackett Company Toilet tank dispenser
US4485500A (en) * 1983-01-06 1984-12-04 Knomark, Inc. Gas binding resistant chemical dispenser
US4450594A (en) * 1983-05-02 1984-05-29 The R. T. French Co. Tank dispenser with end-of-life indicator
FR2548682B1 (en) * 1983-07-08 1985-11-08 Lesieur Cotelle COMPOSITION FOR AUTOMATIC CLEANING OF WC TOILETS
FR2552328A1 (en) * 1983-09-23 1985-03-29 Eparco Sa PROCESS FOR PRODUCING A PERFUMED COMPOSITION AND COMPOSITION OBTAINED THEREBY
US4587069A (en) * 1983-10-31 1986-05-06 Twinoak Products, Inc. Process for producing color display means
US4605534A (en) * 1983-11-02 1986-08-12 Twinoak Products, Inc. Cleaning and disinfecting systems including color display means
US4595536A (en) * 1983-12-09 1986-06-17 The Hilton-Davis Chemical Co. Triphenylmethane dyestuff
US4536367A (en) * 1983-12-09 1985-08-20 The Hilton-Davis Chemical Co. Method for sanitizing toilets
US4536368A (en) * 1983-12-09 1985-08-20 The Hilton-Davis Chemical Co. Method for sanitizing toilets
US4597941A (en) * 1984-03-28 1986-07-01 The Drackett Company Toilet cleaning article and method for codispensing disinfectant and dye having resistance to spectral degradation
GB8417183D0 (en) * 1984-07-05 1984-08-08 Bush Boake Allen Ltd Perfumery compositions
US4755354A (en) * 1984-07-20 1988-07-05 The Procter & Gamble Company Bromide activated hypochlorite cleaning of soiled toilet bowls
US4722801A (en) * 1986-06-20 1988-02-02 Kiwi Brands, Inc. Toilet bowl cleaner in cake form containing a polyethyleneglycol distearate
US4780236A (en) * 1986-06-20 1988-10-25 Kiwi Brands, Inc. Lavoratory cleansing block containing polyethylene gycol disteatrate, guar gum and sodium chloride
GB2209942A (en) * 1987-09-23 1989-06-01 Johnson & Son Inc S C Air refreshening compositions containing indicators
AU4969990A (en) * 1989-01-27 1990-08-24 Trans Delta Corporation Stabilized sterilizing or disinfecting halogen containing composition, method and apparatus
FR2673640B1 (en) * 1991-03-07 1994-08-19 Reckitt Colman NEW HOUSEHOLD COMPOSITIONS, THEIR PREPARATION PROCESS AND THEIR APPLICATIONS, PARTICULARLY IN THE FIELD OF HOUSEHOLD CARE.
EP0619367A1 (en) * 1993-04-06 1994-10-12 The Procter & Gamble Company Lavatory blocks containing enzymes
US5578559A (en) * 1993-05-14 1996-11-26 Block Drug Company, Inc. Lavatory cleaning block
US5538629A (en) * 1994-12-15 1996-07-23 Kimberly-Clark Corporation Process and article for disinfecting water
US5755330A (en) * 1995-05-22 1998-05-26 Block Drug Company, Inc. Multiple compacted solids and packages thereof
WO1998035006A1 (en) * 1997-02-11 1998-08-13 The Procter & Gamble Company Liquid cleaning composition
US5863876A (en) * 1997-02-11 1999-01-26 S. C. Johnson & Son, Inc. In-tank toilet cleansing block having polyacrylic acid/acrylate
AU6322098A (en) * 1997-02-11 1998-08-26 Procter & Gamble Company, The A cleaning composition
WO1998035004A1 (en) * 1997-02-11 1998-08-13 The Procter & Gamble Company Solid detergent compositions
AU6321098A (en) * 1997-02-11 1998-08-26 Procter & Gamble Company, The Cleaning compositions
GB2321900A (en) * 1997-02-11 1998-08-12 Procter & Gamble Cationic surfactants
GB9712680D0 (en) * 1997-06-18 1997-08-20 Reckitt & Colmann Prod Ltd Improvements in or relating to disinfecting materials
WO1999040170A1 (en) * 1998-02-04 1999-08-12 Unilever Plc Lavatory cleansing compositions
JP2001334254A (en) * 2000-05-29 2001-12-04 Japan Organo Co Ltd Method for controlling concentration of chemical for water treatment
US6528466B1 (en) 2000-08-15 2003-03-04 Biolab Services, Inc. Solid oxidizer with dissolution indicator
GB2372046A (en) * 2001-02-09 2002-08-14 Jeyes Group Ltd Liquid dispensing unit for a toilet bowl
NZ527289A (en) 2001-02-14 2005-05-27 Gw Pharma Ltd Lipophilic medicaments and their administration via mucosal surfaces
JP6423789B2 (en) 2012-09-04 2018-11-14 ルブリゾル アドバンスド マテリアルズ, インコーポレイテッド Polyurethane-acrylic / styrene hybrid dispersions for glossing applications in home care
ES2915274T3 (en) 2015-01-21 2022-06-21 Innovative Water Care Llc Methods of using calcium hypochlorite compositions with transient color indicators
WO2017205474A1 (en) * 2016-05-24 2017-11-30 Smartwash Solutions, Llc Process and system for managing water in a food preparation sink

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1798090A (en) * 1930-02-20 1931-03-24 Lebegue Herbert Sanitary wash-down closet disinfector
US3121236A (en) * 1959-12-17 1964-02-18 Frank G Yadro Chemicals feed device for flush tank
US3243377A (en) * 1963-08-30 1966-03-29 Warner Lambert Pharmaceutical Denture cleansing composition
US3355392A (en) * 1963-10-18 1967-11-28 West Laboratories Inc Alkaline germicidal cleaner with color indicator
US3504384A (en) * 1963-10-23 1970-04-07 Russell Research Ltd Toilet bowl cleaning and disinfecting device
US3318815A (en) * 1965-07-21 1967-05-09 Drackett Co Germicidal toilet bowl cleaning composition
US3339801A (en) * 1965-08-20 1967-09-05 Calgon Corp Feeding apparatus for liquid treating agent
US3341074A (en) * 1965-10-21 1967-09-12 Antone D Pannutti Solution dispenser
ZA672910B (en) * 1966-05-18
US3378495A (en) * 1966-07-08 1968-04-16 Fred H. Buck Jr. Deodorant and germicidal bodies for toilets and urinals
US3444566A (en) * 1967-06-08 1969-05-20 Clifton T Spear Device for introducing substances into a toilet bowl trap
US3578499A (en) * 1968-08-02 1971-05-11 Grace W R & Co Gelling composition for general purpose cleaning and sanitizing
DE2133710C3 (en) 1971-07-07 1978-03-02 Kukident Kurt Krisp Kg, 6940 Weinheim Cleaning tablet for dentures
US3793211A (en) * 1971-07-23 1974-02-19 Carter Wallace Effervescent composition
US3831205A (en) * 1972-04-03 1974-08-27 Clorox Co Automatic dispensing apparatus
US3936385A (en) * 1973-08-09 1976-02-03 Colgate-Palmolive Company Denture cleanser
US4036407A (en) * 1976-03-26 1977-07-19 The Procter & Gamble Company Dosing valve
US4216027A (en) * 1978-04-18 1980-08-05 The Procter & Gamble Company Method and apparatus for cleansing and disinfecting a flushing toilet

Also Published As

Publication number Publication date
US4248827A (en) 1981-02-03

Similar Documents

Publication Publication Date Title
CA1118984A (en) Method for sanitizing toilets
US4308625A (en) Article for sanitizing toilets
US4200606A (en) Method for sanitizing toilets
CA1183435A (en) Activation of hypochlorite bleaching of dyes
CA1106257A (en) Method and apparatus for cleansing and disinfecting a flushing toilet
US4249274A (en) Apparatus for sanitizing toilets
US4578207A (en) Two component cleaner and disinfectant tablet
US4420412A (en) Activation of hypochlorite bleaching of dyes
EP1902123B1 (en) Lavatory block composition
CA1219184A (en) Inhibition of the staining of porcelain surfaces by manganese
CA2150458C (en) Lavatory cleansing blocks
GB2226827A (en) Toilet bowl cleaner
AU2005268628A1 (en) Improvements in lavatory block compositions
CA1148057A (en) Method and composition to inhibit staining of porcelain surfaces by manganese
NZ242448A (en) Solid cleansing block for a lavatory, containing a chlorine releasing agent and a solubility control agent
US4755354A (en) Bromide activated hypochlorite cleaning of soiled toilet bowls
CA1209156A (en) Method for sanitizing toilets
US4428872A (en) Composition to inhibit staining of porcelain surfaces by manganese
US6184192B1 (en) Chlorinated in-tank toilet cleansing block
US4278571A (en) Surfactant cake compositions
US4384869A (en) Activation of hypochlorite bleaching of dyes
US4536368A (en) Method for sanitizing toilets
US4595536A (en) Triphenylmethane dyestuff
US4374572A (en) Method and composition to inhibit staining of porcelain surfaces by manganese
US5817611A (en) Lavatory cleansing blocks

Legal Events

Date Code Title Description
MKEX Expiry