JPH01128907A - Sanitizer - Google Patents
SanitizerInfo
- Publication number
- JPH01128907A JPH01128907A JP63253623A JP25362388A JPH01128907A JP H01128907 A JPH01128907 A JP H01128907A JP 63253623 A JP63253623 A JP 63253623A JP 25362388 A JP25362388 A JP 25362388A JP H01128907 A JPH01128907 A JP H01128907A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- alkali metal
- agent
- silicate
- weight ratio
- 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.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/395—Bleaching agents
- C11D3/3956—Liquid compositions
Landscapes
- 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)
Abstract
Description
【発明の詳細な説明】
本発明は、次1止ハロゲン酸塩漂白剤を含むIfli牛
化剤(San!jiZ!n(l product)に関
する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an Ifli bovineizer (San!jiZ!n (l product)) containing a subhalogenate bleach.
嵩の大ぎい物品洗浄(warewashina)もしく
は織物洗浄用のJ、榮用機械にJ3いて、衛生状態をl
[宵口I能なレベルにするために、1回らしくはそれ以
上の洗浄ザイクルで漂白剤を基にl)た1j11生化剤
を慮するど次亜ハ1−1ゲン酸塩漂白剤を使用すること
が必東ぐあるが、都合の恕いことに、継続して使用する
とステンレス鋼のある部分にスポット腐食を生じる。こ
れ【ま1!1に機械が作動していないとさ゛、特にリニ
タイリ゛−溶’a (sanitizcr 5olut
ion)のスプレーノズルの近くにあるスポットに生じ
る。J3 is used for washing large items (warewashina) or washing textiles.
[In order to achieve a functional level, use hypochlorite 1-1 genate bleach, considering the bleach-based l) 1j11 biogenic agent, in at least one or more washing cycles. Unfortunately, continued use will cause spot corrosion in certain parts of the stainless steel. If the machine is not working, especially the linear melter (sanitizcr 5olut)
ion) in spots near the spray nozzle.
Im良さけないJ、うにするためメタケイ酸ナトリウム
のような剤を使用Jることが過去にJ3いて知られてい
るが、十記したよう4I−リニタイヂーにおいにれを効
果的に使用するには問題がある。第1に、iff宇土の
腐食抑制剤はいずれも水性液体において可溶f1でなけ
ればならない(リニタイリ゛−は液体として添加されな
ければならない)。第2に該抑制剤の不−1分な吊は、
いかなる抑制剤をも全く欠いている等^1のリニタイ1
F−に比較して事実上腐食を増加さける1、第3に、抑
制剤の効果的なレベルにおいては、漂白剤の9明分解と
いう現実的な危険がある。。It has been known in the past that agents such as sodium metasilicate have been used to remove the irritants, but as mentioned above, in order to effectively use the 4I-linitai There's a problem. First, all corrosion inhibitors in the IF UTO must be soluble f1 in aqueous liquids (the linitalyte must be added as a liquid). Second, the indefinite suspension of the inhibitor is
Linitai 1, which is completely devoid of any inhibitors.
Third, at effective levels of inhibitor, there is a real risk of bleach degradation. .
本発明名らは、少なくとも2 =l’ lf1%のr1
1性剤、0〜1%の界面活f1剤、少なくとも3壬;d
%の次亜ハIIゲン酸塩漂白剤とアルカリ金1+1中性
ケイ醇塩を含み、タイ酸イオン対遊離ハ11ゲンの干は
比が少なくとも1:5であり、次曲ハ【コゲン酸塩漂白
剤対組成物中の他の水溶性゛市解質の中M比が多くとも
1:1であるJ、うな液体号二りイIJ’−組成物(!
記供1°ることIニJ、−)で、これらの問題を克ロロ
し1!7ることを知見し/j 。The present invention provides that r1 of at least 2 = l'lf1%
1 agent, 0-1% of surfactant f1 agent, at least 3 tons; d
% of hypochlorite II genate bleach and alkali gold 1+1 neutral silicate salt, the ratio of taic acid ion to free chlorine salt is at least 1:5, J, eel liquid No. 2 IJ'-composition (!
I discovered that these problems can be overcome and 1!7 can be achieved by writing the following notes.
次亜ハ【1ゲン酸塩例えば次1IIi塩メ・j酸プ1−
1911番よ′1ri1!l11の酸素を放出して塩化
プ]・リウムとなってその衛生化作用を発揮する。市販
されている次亜塩′A酸塩は実際は対応する塩化物の不
純物を微吊含む。本発明におい(、ii@離ハ]:1ゲ
ンパという用、110.1、ハ11ゲンイΔンどしでか
ムしくは対応りる次111iハ11ゲンM塩の形態のい
ずれであろうと、組成物中の仝(のハL1ゲン庖意味す
る。Hypochlorite monogenate, e.g.
Number 1911'1ri1! The oxygen of l11 is released to form chloride, which exerts its sanitizing effect. Commercially available hypochlorite A salts actually contain traces of the corresponding chloride impurity. In the present invention (, ii@Riha): 1 Genpa, 110.1, 110.1, 110.1, 110.1, 110.1, 110.1, regardless of whether it is in the form of the corresponding 111i 11 Gen M salt, In the composition, the term "(") means "L1" in the composition.
市販されている次411塩累酸塩組成物titその゛利
用ii(能な塩素″の吊にJ、って特徴(=i &]ら
れる。塩水漂白剤を含む組成物のパ利用iij能な塩水
゛の定イ【りとも1モル当M添加りることによって組成
物から遊離しjtする塩水の串とし゛C利用可能な塩素
を定義する。The commercially available 411-salt cumulative salt compositions are characterized by their ability to utilize chlorine (=i &). The available chlorine is defined as the amount of chlorine liberated from the composition by adding at least 1 mole per M of brine.
最す良好な腐食抑制効果を得るためには、ケイ酸イオン
ズ・1遊離ハロゲンの重量比は1:5〜1:15が好ま
しい。In order to obtain the best corrosion inhibiting effect, the weight ratio of silicate ions to 1 free halogen is preferably 1:5 to 1:15.
漂白へ11の”?’ Iv1分解を防ぐためには、次亜
ハ1]ゲン酸塩標白剤対組成物中の他の水溶性電解r′
■の・−Eh目ヒは1−2・〜・1:1であるのbc最
し好−ましい、。To prevent the degradation of 11'Iv1 to bleaching, use the hypochlorite 1]genate whitening agent versus other water-soluble electrolytes in the composition.
It is most preferable that the ratio of (1) to (Eh) is 1:2 to 1:1.
hi b好ましい次亜ハ11ゲンl1i12塩漂白剤(
まアルhり金属次亜基本M 1m、特にす1〜リウム塩
である。hi b preferred hypochlorite bleach (
Aluminum metals are hypobasic M 1m, especially lithium salts.
好ましくは、金属表面特にアルミニウムにカルシウムが
jtl積するのを妨げるため、組成物はさらに1・〜5
%のアルカリ全屈縮合リン酸塩ビルダー例えばトリポリ
リン酸ナトリウムもしくはカリーンムを含む。Preferably, the composition further contains 1-5 to prevent calcium deposition on metal surfaces, particularly aluminum.
% of alkaline total condensed phosphate builders such as sodium tripolyphosphate or kareem.
最適の漂白剤安定ヤla3よび効果を1116ためには
、さらに組成物の011は少なくと1912.OCある
のが11(ましい。For optimum bleach stability and effectiveness, the composition should also have a 011 content of at least 1912. 11 (preferably) with OC.
組成物中のIE剤は、アルカリ金属の水酸化物もしくは
メタケイ酸塩例えば、水酸化ナトリウム。The IE agent in the composition is an alkali metal hydroxide or metasilicate such as sodium hydroxide.
水酸化カリ1クム、メタケイ酸ナトリウムもしくはメタ
ケイ酸カリウムである。全組成物中のり一トリウムおJ
、びカリウムイオンの相対垣は、存在する1へリボリリ
ンIll!塩がナトリウム塩の沈殿の形態で沈殿し4T
い、にうに選択するべきである。1 cum of potassium hydroxide, sodium metasilicate or potassium metasilicate. Noritrium J in the whole composition
, and the relative barrier of potassium ions is 1 heribolyrin Ill! The salt precipitates in the form of a sodium salt precipitate and 4T
You should choose the right one.
0.1重量%の帛で存在し1qる界面活性剤は本質的に
tよ消泡剤である。The surfactant present at 0.1% by weight of the fabric is essentially an antifoaming agent.
用語゛アルカリ舎属中性ケイ酸塩°′は、ケイ酸In対
アルカリ金属酸化物の比が3:1よりb大ぎいものを意
味する。、典型的な例tよ、SiO:Na Oが3.
4:1の比である中性ライ酸ナトリつ11である。。The term ``alkaline neutral silicates'' means those in which the ratio of In silicate to alkali metal oxide is greater than 3:1. , a typical example is that SiO:NaO is 3.
Neutral sodium lyate and 11 in a 4:1 ratio. .
本発明を以1この実施例によって更に説明する。The invention will now be further explained by way of this example.
【1鼠ユニ1
5(li[71%の水酸化カリ1クムを含む水酸化カリ
ウt1の濃縮ストック溶液を6重量%および19.2重
14%(利用可能な塩素としてi’ii n )の次亜
塩素酸す1−リウムを含む次亜塩素酸ナトリウムの淵縮
ストック溶液を31.3手h1%使用して双手の組成物
を配合しIこ。[1 Mouse Uni 1 5 (li [71% Potassium hydroxide 1 cum of potassium hydroxide t1 concentrated stock solution containing 6% by weight and 19.2% by weight 14% (i'ii n as available chlorine)] A two-handed composition was formulated using a 31.3% stock solution of sodium hypochlorite containing 1-lium hypochlorite.
塩化ナトリウム不純物が少ない漂白剤を使用しC実施例
1〜4を配合し、通常の等級の漂白剤を使用して実施例
5・−E3を配合し、それぞれのNaCfJ含!21含
金21物において3 J3よび5重;危%となるJ、う
にした。C Examples 1 to 4 were formulated using a bleaching agent with low sodium chloride impurities, and Examples 5 and -E3 were formulated using a normal grade bleach and their respective NaCfJ-containing! In 21 metal-containing materials, 3 J3 and 5 heavy;
うイ酸ナトリウムを、活性SiO:Na 0(比+、
L3.4 : 1 )を34重ψ%含む哨ス1−ツク
溶液として添加した。Sodium oxalate was added to active SiO:Na 0 (ratio +,
L3.4:1) was added as a 1-tox solution containing 34% by weight.
溶液をそのままステンレス鋼ディスクに塗イoし、腐食
が明らかに識別できるように一1分46時間をおいた。The solution was directly applied to a stainless steel disk and allowed to stand for 11 minutes and 46 hours so that corrosion was clearly visible.
腐食の程度を1〜10の段階で評価した。ここで1は全
く腐食がないことを示し、10は激しい腐食を示す。The degree of corrosion was evaluated on a scale of 1 to 10. Here, 1 indicates no corrosion and 10 indicates severe corrosion.
実施例9〜12
実施例1〜8と同じであるが、トリポリリン酸カリウム
をさらに合むストック溶液を使用して以Fの組成物を1
!J造した。トリポリリン酸カリ・クムは50小吊%含
む濃ストック溶液として添加した。Examples 9-12 Same as Examples 1-8, but using a stock solution containing additionally potassium tripolyphosphate, the following compositions were made into 1
! I built J. Potassium cum tripolyphosphate was added as a concentrated stock solution containing 50% suspension.
沈殿を全く生成することなく透明な溶液を得た。A clear solution was obtained without any precipitate formation.
腐食の評価は使用しに次亜塩;+J酸J−トリウム溶液
のN a Cβ不純物の品に依存り゛る実施例1へ・4
ま7、、: f、i 5・−8の6のと同じであった。Corrosion evaluation depends on the product of NaCβ impurities in the hypochlorite +J acid J-thorium solution used.Example 1-4
Ma7, ,: f,i It was the same as 6 of 5・-8.
Claims (7)
性剤と、少なくとも3重量%の次亜ハロゲン酸塩漂白剤
とアルカリ金属中性ケイ酸塩を含み、ケイ酸イオン対遊
離ハロゲンの重量比が少なくとも1:5であり、次亜ハ
ロゲン酸塩漂白剤対組成物中の他の水溶性電解質の重量
比が多くとも1:1であるような液体サニタイザー組成
物。(1) Contains at least 2% by weight caustic agent, 0-1% surfactant, and at least 3% by weight hypohalite bleach and alkali metal neutral silicate, silicate ions versus free halogens. and the weight ratio of hypohalite bleach to other water-soluble electrolytes in the composition is at most 1:1.
1:1.5であることを特徴とする特許請求の範囲第1
項に記載の組成物。(2) Weight ratio of silicate ion to free halogen is 1:5 or more
Claim 1 characterized in that the ratio is 1:1.5.
The composition described in Section.
電解質の重量比が1:2〜1:1であることを特徴とす
る特許請求の範囲第1項もしくは第2項に記載の組成物
。(3) Claims 1 or 2, characterized in that the weight ratio of the hypohalite bleach to other water-soluble electrolytes in the composition is from 1:2 to 1:1. Compositions as described.
酸塩であることを特徴とする特許請求の範囲第1項〜第
3項のいずれかに記載の組成物。(4) The composition according to any one of claims 1 to 3, wherein the hypohalite bleach is an alkali metal hypochlorite.
さらに含むことを特徴とする特許請求の範囲第1項〜第
4項のいずれかに記載の組成物。(5) The composition according to any one of claims 1 to 4, further comprising 1 to 5% of an alkali metal condensed phosphate builder.
る特許請求の範囲第1項〜第5項のいずれかに記載の組
成物。(6) The composition according to any one of claims 1 to 5, which has a pH of at least 12.0.
項〜第6項のいずれかに記載の組成物を効果的に衛生化
する量添加することを特徴とする機械的物品洗浄方法。(7) Claim No. 1 to the cleaning liquid in the article washing machine
7. A method for mechanically cleaning articles, which comprises adding the composition according to any one of items 1 to 6 in an amount that effectively sanitizes the composition.
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 (1)
| Publication Number | Publication Date |
|---|---|
| JPH01128907A true JPH01128907A (en) | 1989-05-22 |
Family
ID=10625009
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63253623A Pending JPH01128907A (en) | 1987-10-08 | 1988-10-07 | 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) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0214298A (en) * | 1988-06-30 | 1990-01-18 | Matsushita Electric Ind Co Ltd | Detergent for vessel of cleaner and method for cleaning thereof |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3802127C1 (en) * | 1988-01-26 | 1988-12-01 | Kaiser, H.-G. | |
| 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 |
| EP0653483B1 (en) * | 1993-11-11 | 1999-04-14 | 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 (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3697431A (en) * | 1971-01-22 | 1972-10-10 | Clorox Co | Liquid drain opening composition and method |
| 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 |
Family Cites Families (5)
| 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 |
| JPS4926688B1 (en) * | 1970-12-09 | 1974-07-11 | ||
| US4339235A (en) * | 1979-12-06 | 1982-07-13 | Economics Laboratory, Inc. | Methods and compositions for bleaching of mycological stain |
| US4752409A (en) * | 1985-06-14 | 1988-06-21 | Colgate-Palmolive Company | Thixotropic clay aqueous suspensions |
-
1987
- 1987-10-08 GB GB878723675A patent/GB8723675D0/en active Pending
-
1988
- 1988-09-27 ES ES88202094T patent/ES2061634T3/en not_active Expired - Lifetime
- 1988-09-27 EP EP88202094A patent/EP0311175B1/en not_active Expired - Lifetime
- 1988-09-27 DE DE3886873T patent/DE3886873T2/en not_active Expired - Fee Related
- 1988-10-05 AU AU23454/88A patent/AU607813B2/en not_active Ceased
- 1988-10-06 BR BR8805157A patent/BR8805157A/en not_active IP Right Cessation
- 1988-10-06 NO NO884451A patent/NO173023C/en unknown
- 1988-10-07 JP JP63253623A patent/JPH01128907A/en active Pending
- 1988-10-07 ZA ZA887548A patent/ZA887548B/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3697431A (en) * | 1971-01-22 | 1972-10-10 | Clorox Co | Liquid drain opening composition and method |
| 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 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0214298A (en) * | 1988-06-30 | 1990-01-18 | Matsushita Electric Ind Co Ltd | Detergent for vessel of cleaner and method for cleaning thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| NO884451L (en) | 1989-04-10 |
| AU2345488A (en) | 1989-04-13 |
| EP0311175A2 (en) | 1989-04-12 |
| EP0311175A3 (en) | 1990-04-11 |
| NO884451D0 (en) | 1988-10-06 |
| AU607813B2 (en) | 1991-03-14 |
| BR8805157A (en) | 1989-05-16 |
| GB8723675D0 (en) | 1987-11-11 |
| ES2061634T3 (en) | 1994-12-16 |
| ZA887548B (en) | 1990-06-27 |
| NO173023C (en) | 1993-10-13 |
| DE3886873T2 (en) | 1994-05-19 |
| NO173023B (en) | 1993-07-05 |
| EP0311175B1 (en) | 1994-01-05 |
| DE3886873D1 (en) | 1994-02-17 |
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