AU607813B2 - Sanitizer - Google Patents

Sanitizer Download PDF

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Publication number
AU607813B2
AU607813B2 AU23454/88A AU2345488A AU607813B2 AU 607813 B2 AU607813 B2 AU 607813B2 AU 23454/88 A AU23454/88 A AU 23454/88A AU 2345488 A AU2345488 A AU 2345488A AU 607813 B2 AU607813 B2 AU 607813B2
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AU
Australia
Prior art keywords
composition according
composition
weight ratio
weight
alkali metal
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
AU23454/88A
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AU2345488A (en
Inventor
Johannes Jacobus Maria De Ridder
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.)
Unilever PLC
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Unilever PLC
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Application filed by Unilever PLC filed Critical Unilever PLC
Publication of AU2345488A publication Critical patent/AU2345488A/en
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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
    • C11D3/395Bleaching agents
    • C11D3/3956Liquid compositions

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

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O68L99tCI-' x~~sb0U111 61), zAXMAnis80dONW fio~~ 1HO CW 'd 8 O68L9g1C[ zAXMAnsjbdouwp!!q5Jepxqo ZAxMAnisNdONWINrIH0 10ODV 'Id 01.
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AUSTRALIA
PATENTS ACT 1952 COMPLETE SPECIFICATION Form
(ORIGINAL)
FOR OFFICE USE urn-c') tent contains the amendments made tinder Section 49 and is cprrect for printing Short Title: Int. Cl: Application Number: Lodged: Complete Specification-Lodged: Accepted: Lapsed: Published: *~Priority: :'"Related Art: TO B "Name of Applicant: .'"Addre~ss of Applicant: I f ,,Actual inventor: 4jfAddress for Service: E COMPLETED BY APPLICANT UNILEVER PLC UNILEVER HOUSE
BLACKFRIARS
LONDON EC4
ENGLAND
GRIFFITH HACK CO., 601 St. Kilda Road, Melbourne, Victoria 3004, Australia.
Complete Specification for the invention entitled:
SANITIZER
The following statement is a full description of this invention including the best method of performing it known to me:- M00345 05/ 10/8
I
li v I-.1 -i Imnmax: 1 II;- 1. I C 3194 (R)
SANITIZER
The present invention is concerned with a sanitizing product which contains a hypohalite bleach.
In industrial machines for bulk warewashing or fabrics washing, it is often desired to add a bleach-based sanitizing product during one or more wash cycles, to ensure an acceptable level of hygiene.
to Unfortunately, for optimum sanitizing performance and acceptable cost, it is necessary to use a hypohalite bleach which, with prolonged use, can lead to spot corrosion of some stainless steel parts. This especially occurs when the machine is not operating, and particularly at spots which are near the spray nozzles 5 for tle sanitizer solution.
t .9 ,a 1 O 9 1 o9 0 9 eo t. Although it has been known in the past to use an agent like sodium metasilicate to inhibit corrosion, there are problems in using this effectively in sanitizers of the aforementioned kind. First, any putative corrosion inhibitor must be soluble in an aqueous liquid (such sanitizers must be dosed as liquids). Second, an insufficient level of such inhibitor actually increases corrosion as compared to that observed with equivalent products totally devoid of any inhibitor. Third, at effective levels of inhibitor, there is a real danger of premature decomposition of the bleach.
We have now found that these problems can be overcome by providing a liquid sanitizer composition comprising at least 2% by weight of a caustic agent, from 0 to 1% of a surfactant and at least 3% by weight of a hypohalite bleach and an amount of an alkali metal neutral silicate such that the weight ratio of silicate ions to free halogen is at least 1:5 and the weight ratio of the :r
S;;
i do C 3194 (R) 2 hypohalite bleach to other water-soluble electrolyte in the composition is at most 1:1.
Hypohalites, such as sodium hypochlorite, exert their sanitizing action by release of free oxygen to leave sodium chloride. Commercially available hypochlorites do indeed contain trace impurities of the corresponding Schloride. Thus, in the context of the present invention, the term "free halogen" means the total halogen in the composition, whether as a halide ion or in the form of S the corresponding hypohalite.
t t t t Commercially available hypochlorite compositions are characterized by their content of "available chlorine".
i'riS Methods for determining the "available chlorine" of S compositions containing chlorine bleach are well known in the art. In accordance with usual practice, the available chlorine is defined in this application as the S amount of chlorine which can be liberated from a S ',20 composition by acidification and addition of at least one molar equivalent of chloride ions.
For the best corrosion inhibition performance, it is preferred that the weight ratio of silicate ions to free j halogen is from 1:5 to 1:1.5.
To guard against premature decomposition of the bleach, it is most preferred that the weight ratio of hypohalite bleach to other water-soluble electrolyte in the j 30 composition is from 1:2 to 1:1.
The most preferred hypohalite bleaches are the alkali metal hypochlorites, especially the sodium salt.
Preferably also, to inhibit calcium deposits on metal surfaces, especially aluminium, the composition further comprises from 1 to 5% of an alkali metal condensed ""f~lW r t; r; I C 3194 (R) phosphate builder, such as sodium or potassium tripolyphosphate.
For optimum bleach stability and performance, it is also preferred that the pH of the composition is at least 12.0.
The caustic agent in the composition is an alkali metal hydroxide or metasilicate, such as sodium hydroxide, potassium hydroxide, sodium metasilicate or potassium S metasilicate. The relative amount of sodium and potassium ions in the total composition should be chosen such that there is no precipitation of any tripoly phosphate present, in the form of a precipitate of the sodium salt.
The surfactant, which may be present in an amount of 0.1% by weight, is essentially a foam depressor.
St i The term alkali metal neutral silicate means one in which the ratio of silicate to alkali metal oxide species is greater than 3:1. A typical example is sodium neutral silicate having an SiO 2 :Na20 ratio of 3.4:1.
The present invention will now be explained better by way of the following Examples.
s"h i r i; C 3194 (R) Examples 1-8* The following compositions were formulated using 6% by weight of a concentrated stock solution of potassium hydroxide containing 50% by weight of potassium hydroxide, and 31.3% by weight of a concentrated stock solution of sodium hypochlorite containing 19.2% by weight of sodium hypochlorite-(calculated as available chlorine).
Examples 1-4 were formulated using a low sodium chloride impurity bleach, whereas Examples 5-8 were formulated using a regular grade, resulting in NaCl contents in the total composition of 3 and 5% by weight, respectively.
The sodium silicate was added as a concentrated stock solution containing 34% by weight of active SiO 2 :Na20 in a ratio of 3.4:1.
t t I The solution was applied neat to stainless steel discs and left for sufficient time for visible corrosion to be apparent. The corrosion apparent was rated on an arbitrary scale of 1-10 where 1 refers to no corrosion and 10 refers to severe attack.
Examples 9-12 The following compositions were prepared using the same stock solutions as in Examples 1-8, but additionally containing potassium tripolyphosphate. The latter was added as a concentrated stock solution containing 50% by weight of potassium tripolyphosphate. Clear solutions were obtained without any signs of precipitates being formed. The corrosion ratings were similar to those of Examples 1-4 or 5-8, depending on the amount of NaCl impurity of the sodium hypochlorite solution used.
i
I
I I1' C 3194 (R) Ex 1 2 3 4 6 7 8 Wt.% silicate* Wt.% SiO 2 0 0 4 1.05 8 2.10 12 3.15 0 0 4 1.05 8 2.10 12 3.15 Wt.% NaCi Impurity 3.0 of It 5.0 if It Wt. ratio Si2:free halogen 1:4.59 1:2.30 1:1.53 1:5.74 1:2.87 1:1.91 Wt. ratio bleach other electrolyte 1:0.95 1:1.17 1:1.38 1:1.60 1:1.27 1:1.49 1:1.70 1:1.92 corrosion rating 6 1 2 2 6 4 3 2 34% active SiO 2 :Na 2 o 3.4:1 -i
U
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4
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II
ii ii
H
2 0 KOH (50%) KTPP (50%) Na-silicate (34%) NaOC1 (19.2%) pH Ex 9 59.7 6 3 0 31.3 13 .65 (by weight) 10 11 55.7 51.7 6 6 3 3 4 8 31.3 31.3 13.60 13.55 C 3194 (R) 12 47.7 6 3 12 31.3 13 I 4
I,

Claims (7)

1. A liquid sanitizer composition comprising at least 2% by weight of a caustic agent selected from the group consisting of sodium hydroxide, potassium hydroxide, sodium metasilicate and potassium-metasilicate, from 0 to 1% of a foam depressing surfactant and at least 3% by weight of a hypohalite bleach and an amount of an alkali metal neutral silicate such that the weight ratio of silicate ions to free halogen is at least 1:5 and the weight ratio of the hypohalite bleach to other water-soluble electrolyte in the composition is at most 1:1.
2. A composition according to Claim 1, wherein the weight ratio of silicate ions to free halogen is from to 1:1.5.
3. A composition according to Claim 1 or Claim 2, wherein the weight ratio of hypohalite bleach to other water-soluble electrolyte in the composition is from 1:2 to 1:1.
4. A composition according to any preceding claim, wherein the hypohalite bleach is an alkali metal hypochlorite.
A composition according to any preceding claim, further comprising from 1 to 5% of an alkali metal S condensed phosphate builder. c
6. A composition according to any preceding claim, b r" wherein the pH is at least 12.0. It I 2. A opsto codn oCam1 hri h wegh raitfslct ost fe aoe sfo If,, 8
7. A process of mechanical warewashing comprising dosing an effective sanitizing amount of a composition according to any preceding claim into the wash liquor in a warewashing machine. DATED THIS 11TH DAY OF DECEMBER 1990 UNILEVER PLC By its Patent Attorneys: GRIFFITH HACK CO. Fellows Institute of Patent Attorneys of Australia. i *000 o *o 0 0 000 0 C. Ci 0 0 01 0 00r *r S 0 @0 01 I 11 l.i i i iii~ 1
AU23454/88A 1987-10-08 1988-10-05 Sanitizer Ceased AU607813B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8723675 1987-10-08
GB878723675A GB8723675D0 (en) 1987-10-08 1987-10-08 Sanitizer

Publications (2)

Publication Number Publication Date
AU2345488A AU2345488A (en) 1989-04-13
AU607813B2 true AU607813B2 (en) 1991-03-14

Family

ID=10625009

Family Applications (1)

Application Number Title Priority Date Filing Date
AU23454/88A Ceased AU607813B2 (en) 1987-10-08 1988-10-05 Sanitizer

Country Status (9)

Country Link
EP (1) EP0311175B1 (en)
JP (1) JPH01128907A (en)
AU (1) AU607813B2 (en)
BR (1) BR8805157A (en)
DE (1) DE3886873T2 (en)
ES (1) ES2061634T3 (en)
GB (1) GB8723675D0 (en)
NO (1) NO173023C (en)
ZA (1) ZA887548B (en)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3802127C1 (en) * 1988-01-26 1988-12-01 Kaiser, H.-G.
JPH0214298A (en) * 1988-06-30 1990-01-18 Matsushita Electric Ind Co Ltd Detergent for vessel of cleaner and method for cleaning thereof
GB9213578D0 (en) * 1992-06-26 1992-08-12 Unilever Plc Improvements to bleaching compositions
US5843190A (en) * 1993-11-11 1998-12-01 The Procter & Gamble Company Hypochlorite bleaching compositions
EP0892042A1 (en) * 1993-11-11 1999-01-20 The Procter & Gamble Company The use of silicates in hypochlorite bleaching compositions
US6297209B1 (en) 1996-05-10 2001-10-02 The Clorox Company Sequesterants as hypochlorite bleach enhancers
GB0222501D0 (en) 2002-09-27 2002-11-06 Unilever Plc Composition and method for bleaching a substrate
DE102005062008B3 (en) 2005-12-22 2007-08-30 Henkel Kgaa Odor reduction of hypochlorite-containing agents
DE102005063065A1 (en) * 2005-12-29 2007-07-12 Henkel Kgaa Corrosion inhibition of liquid hypochlorite detergent
DE102005063177A1 (en) 2005-12-30 2007-07-05 Henkel Kgaa Use of diethylene-penta-methylene phosphonic acid for the stabilization of optical brightener in aqueous liquid detergent containing alkali hypochlorite

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU458559B2 (en) * 1970-12-09 1975-02-27 Kao Soap Co., Ltd Cleaning and bleaching liquid composition
AU7742787A (en) * 1986-09-05 1988-03-10 Colgate-Palmolive Company, The Thixotropic clay aqueous suspensions

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB490092A (en) * 1936-10-10 1938-08-09 Ig Farbenindustrie Ag Process for the production of cleansing agents
GB1320919A (en) * 1969-11-07 1973-06-20 Albright & Wilson Detergent composition
US3697431A (en) * 1971-01-22 1972-10-10 Clorox Co Liquid drain opening composition and method
US4339235A (en) * 1979-12-06 1982-07-13 Economics Laboratory, Inc. Methods and compositions for bleaching of mycological stain
JPS5690898A (en) * 1979-12-25 1981-07-23 Nippon Rasukatsuto Kk Cleaning agent for household bath tub
JPS58196297A (en) * 1982-05-12 1983-11-15 ア−ス製薬株式会社 Bath boiler detergent

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU458559B2 (en) * 1970-12-09 1975-02-27 Kao Soap Co., Ltd Cleaning and bleaching liquid composition
AU7742787A (en) * 1986-09-05 1988-03-10 Colgate-Palmolive Company, The Thixotropic clay aqueous suspensions

Also Published As

Publication number Publication date
EP0311175A2 (en) 1989-04-12
BR8805157A (en) 1989-05-16
EP0311175B1 (en) 1994-01-05
ES2061634T3 (en) 1994-12-16
DE3886873T2 (en) 1994-05-19
NO173023B (en) 1993-07-05
NO884451D0 (en) 1988-10-06
EP0311175A3 (en) 1990-04-11
AU2345488A (en) 1989-04-13
DE3886873D1 (en) 1994-02-17
JPH01128907A (en) 1989-05-22
NO173023C (en) 1993-10-13
ZA887548B (en) 1990-06-27
NO884451L (en) 1989-04-10
GB8723675D0 (en) 1987-11-11

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