JPH11229271A - Washing of hospital bedclothes - Google Patents

Washing of hospital bedclothes

Info

Publication number
JPH11229271A
JPH11229271A JP3470098A JP3470098A JPH11229271A JP H11229271 A JPH11229271 A JP H11229271A JP 3470098 A JP3470098 A JP 3470098A JP 3470098 A JP3470098 A JP 3470098A JP H11229271 A JPH11229271 A JP H11229271A
Authority
JP
Japan
Prior art keywords
acid
cleaning
washing
cloth
hospital
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
Application number
JP3470098A
Other languages
Japanese (ja)
Inventor
Eijiro Yamazaki
英二郎 山崎
Yoshiko Saito
佳子 齋藤
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.)
Nicca Chemical Co Ltd
Original Assignee
Nicca Chemical Co Ltd
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 Nicca Chemical Co Ltd filed Critical Nicca Chemical Co Ltd
Priority to JP3470098A priority Critical patent/JPH11229271A/en
Publication of JPH11229271A publication Critical patent/JPH11229271A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To provide a method for washing hospital bedclothes, capable of removing chlorhexidine gluconate adhered to the hospital bedclothes to prevent the generation of stained marks due to a chlorine-based bleaching agent by preliminarily washing the hospital bedclothes with an aqueous solution containing a polybasic carboxylic acid or a hydroxycarboxylic acid and subsequently mainly washing the hospital bedclothes. SOLUTION: This method for washing hospital bedclothes comprises preliminarily washing the hospital bedclothes with an aqueous solution containing a polybasic carboxylic acid or a hydroxycarboxylic acid and subsequently mainly washing the hospital bedclothes with an aqueous solution containing a bleaching agent, an alkali builder and a detergent. The polybasic carboxylic acid includes oxalic acid, malonic acid and succinic acid, and the hydroxycarboxylic acid includes lactic acid, malic acid, tartaric acid and citric acid. The preliminary washing may be carried out with an aqueous solution containing both the polybasic carboxylic acid and the hydroxycarboxylic acid.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、病院寝具類の洗浄
方法に関する。さらに詳しくは、本発明は、消毒剤とし
て用いられるグルコン酸クロルヘキシジンが付着した病
院寝具類を、塩素系漂白剤を含む洗浄水を用いて洗浄し
ても、汚染痕を残すことなく洗浄することができる病院
寝具類の洗浄方法に関する。
The present invention relates to a method for cleaning hospital bedding. More specifically, the present invention is capable of cleaning hospital bedding to which chlorhexidine gluconate used as a disinfectant has been attached without leaving traces of contaminants even when washed with cleaning water containing a chlorine bleach. The present invention relates to a method for cleaning hospital bedding that can be performed.

【0002】[0002]

【従来の技術】従来より、リネンサプライにおいて、シ
ーツ、包布、枕カバー、病衣、白衣、手術衣などの病院
寝具類は、漂白剤、アルカリビルダー及び洗剤を含む水
溶液で洗浄されている。この際にシミ抜きのために使用
される漂白剤としては、過炭酸ソーダ、過酸化水素、過
硼酸ソーダなどの酸素系漂白剤、次亜塩素酸ソーダ、亜
塩素酸ソーダなどの塩素系漂白剤、ハイドロサルファイ
ト、チオ硫酸ソーダなどの還元漂白剤などが用いられて
いる。健常者の血液、飲料の色素、調味料などの除去し
やすいシミについては、一般には酸素系漂白剤が用いら
れている。しかし、病院寝具類は、入院患者の血液など
が、その治療薬などの影響により、酸素系漂白剤では充
分に除去し得ない場合があるために、塩素系漂白剤が用
いられる場合がある。グルコン酸クロルヘキシジンは、
皮膚の一般消毒及び滅菌器具の保存のために、0.05
〜0.5%液として病院において広く用いられている
が、グルコン酸クロルヘキシジンが付着した病院寝具類
を、塩素系漂白剤を含む洗浄水を用いて洗浄すると、無
色ないし微赤色であったグルコン酸クロルヘキシジンの
痕跡が、濃黒褐色に変色して落ちなくなるという問題を
生じている。このために、グルコン酸クロルヘキシジン
が付着した病院寝具類を、塩素系漂白剤を含む洗浄水を
用いて洗浄しても、汚染痕を残すことなく洗浄すること
ができる病院寝具類の洗浄方法が求められていた。
2. Description of the Related Art Conventionally, in bed linen supplies, hospital bedding such as sheets, wrappers, pillowcases, sick coats, white coats, and surgical coats have been washed with an aqueous solution containing a bleaching agent, an alkali builder, and a detergent. In this case, bleaching agents used for removing stains include oxygen-based bleaching agents such as sodium percarbonate, hydrogen peroxide and sodium perborate, and chlorine-based bleaching agents such as sodium hypochlorite and sodium chlorite. And reducing bleaching agents such as hydrosulfite and sodium thiosulfate. An oxygen-based bleach is generally used for easily removing stains such as blood of healthy persons, pigments of beverages, and seasonings. However, in hospital bedding, chlorine bleach may be used because the blood of an inpatient may not be sufficiently removed with an oxygen bleach due to the effect of the therapeutic agent or the like. Chlorhexidine gluconate,
0.05 for general disinfection of the skin and storage of sterile instruments.
Although chlorhexidine gluconate is widely used in hospitals as a 0.5% solution, hospital bedding to which chlorhexidine gluconate has adhered is washed out with washing water containing a chlorine bleach to give gluconic acid that is colorless or slightly red. There is a problem that traces of chlorhexidine are discolored to dark black brown and cannot be dropped. Therefore, there is a need for a method of cleaning hospital bedding to which hospital bedding to which chlorhexidine gluconate has adhered can be cleaned without leaving traces of contamination even when the cleaning is performed using cleaning water containing a chlorine bleach. Had been.

【0003】[0003]

【発明が解決しようとする課題】本発明は、病院寝具類
に付着したグルコン酸クロルヘキシジンを除去し、塩素
系漂白剤を使用しても汚染痕が生ずることなく、延いて
は、再洗い枚数を減らし、作業性、経済性の面で寄与す
ることができる病院寝具類の洗浄方法を提供することを
目的としてなされたものである。
SUMMARY OF THE INVENTION The present invention removes chlorhexidine gluconate adhering to hospital bedding, and does not cause stains even if a chlorine bleach is used. It is an object of the present invention to provide a method for cleaning hospital bedding which can reduce the amount of work and contribute to workability and economy.

【0004】[0004]

【課題を解決するための手段】本発明者らは、上記の課
題を解決すべく鋭意研究を重ねた結果、グルコン酸クロ
ルヘキシジンが付着した布地を、多価カルボン酸又はオ
キシカルボン酸を含む水溶液で予備洗浄したのち、本洗
浄することにより、被洗物に変色した汚染痕を残すこと
なく美麗に洗浄することが可能となることを見いだし、
この知見に基づいて本発明を完成するに至った。すなわ
ち、本発明は、(1)病院寝具類を、多価カルボン酸又
はオキシカルボン酸を含む水溶液で予備洗浄したのち、
漂白剤、アルカリビルダー及び洗剤を含む水溶液で本洗
浄することを特徴とする病院寝具類の洗浄方法、及び、
(2)多価カルボン酸又はオキシカルボン酸が、シュウ
酸、マロン酸、コハク酸、乳酸、リンゴ酸、酒石鹸又は
クエン酸である第(1)項記載の病院寝具類の洗浄方法、
を提供するものである。
Means for Solving the Problems The inventors of the present invention have conducted intensive studies to solve the above-mentioned problems, and as a result, the cloth to which chlorhexidine gluconate has been adhered is treated with an aqueous solution containing a polycarboxylic acid or an oxycarboxylic acid. After pre-cleaning, it is found that by performing the main cleaning, it is possible to clean beautifully without leaving discolored contamination marks on the object to be washed,
Based on this finding, the present invention has been completed. That is, the present invention provides (1) preliminarily cleaning hospital bedding with an aqueous solution containing a polyvalent carboxylic acid or an oxycarboxylic acid,
A method for cleaning hospital bedding characterized by main cleaning with an aqueous solution containing a bleach, an alkali builder and a detergent, and
(2) The method for cleaning hospital bedding according to (1), wherein the polycarboxylic acid or oxycarboxylic acid is oxalic acid, malonic acid, succinic acid, lactic acid, malic acid, tartar soap or citric acid.
Is provided.

【0005】[0005]

【発明の実施の形態】本発明の病院寝具類の洗浄方法に
おいては、多価カルボン酸又はオキシカルボン酸を含む
水溶液を用いて予備洗浄を行う。使用する多価カルボン
酸は、水溶性を有するものであれば特に制限はなく、例
えば、シュウ酸、マロン酸、コハク酸、グルタル酸など
の飽和脂肪族ジカルボン酸、マレイン酸などの不飽和脂
肪族ジカルボン酸、1,2,3−プロパントリカルボン酸
などの脂肪族トリカルボン酸などを挙げることができ
る。これらの中で、シュウ酸、マロン酸及びコハク酸を
特に好適に使用することができる。使用するオキシカル
ボン酸は、水溶性を有するものであれば特に制限はな
く、例えば、グリコール酸、乳酸、3−ヒドロキシプロ
ピオン酸、2−ヒドロキシ酪酸、3−ヒドロキシ酪酸、
グリセリン酸、タルトロン酸、リンゴ酸、酒石酸、クエ
ン酸などの脂肪族オキシカルボン酸などを挙げることが
できる。これらの中で、乳酸、リンゴ酸、酒石酸及びク
エン酸を特に好適に使用することができる。本発明方法
において、多価カルボン酸又はオキシカルボン酸は、1
種を単独で使用することができ、あるいは2種以上を組
み合わせて使用することもできる。
BEST MODE FOR CARRYING OUT THE INVENTION In the method of cleaning hospital bedding of the present invention, preliminary cleaning is performed using an aqueous solution containing a polyvalent carboxylic acid or an oxycarboxylic acid. The polyvalent carboxylic acid used is not particularly limited as long as it has water solubility.For example, oxalic acid, malonic acid, succinic acid, saturated aliphatic dicarboxylic acid such as glutaric acid, unsaturated aliphatic such as maleic acid, etc. Examples thereof include aliphatic tricarboxylic acids such as dicarboxylic acid and 1,2,3-propanetricarboxylic acid. Among these, oxalic acid, malonic acid and succinic acid can be particularly preferably used. The oxycarboxylic acid used is not particularly limited as long as it has water solubility. For example, glycolic acid, lactic acid, 3-hydroxypropionic acid, 2-hydroxybutyric acid, 3-hydroxybutyric acid,
Examples include aliphatic oxycarboxylic acids such as glyceric acid, tartronic acid, malic acid, tartaric acid, and citric acid. Among them, lactic acid, malic acid, tartaric acid and citric acid can be particularly preferably used. In the method of the present invention, the polycarboxylic acid or oxycarboxylic acid is
The species can be used alone, or two or more can be used in combination.

【0006】本発明方法において、病院寝具類を予備洗
浄する条件には特に制限はなく、被洗物の汚れの状態な
どに応じて適宜選択することができるが、通常は多価カ
ルボン酸又はオキシカルボン酸を、被洗物100重量部
に対して0.2〜1.0重量部すなわち0.2〜1.0%ow
f使用し、浴比を1:3〜1:10とし、洗浄温度を室
温〜40℃として、2〜10分洗浄することが好まし
い。病院寝具類を多価カルボン酸又はオキシカルボン酸
を含む水溶液で予備洗浄することにより、本洗浄におい
て塩素系漂白剤を用いた際の着色や変色を防止すること
ができる。多価カルボン酸又はオキシカルボン酸を含む
水溶液で予備洗浄することにより、本洗浄における着色
や変色を防止し得る機構は明らかではないが、着色して
汚染痕の原因となる物質、例えば、グルコン酸クロルヘ
キシジン
In the method of the present invention, the conditions for pre-cleaning hospital bedding are not particularly limited, and can be appropriately selected according to the condition of dirt on the articles to be washed. The carboxylic acid is used in an amount of 0.2 to 1.0 parts by weight, that is, 0.2 to 1.0% ow, based on 100 parts by weight of the object to be washed.
f, it is preferable to wash at 2 to 10 minutes at a bath ratio of 1: 3 to 1:10 and a washing temperature of room temperature to 40 ° C. Preliminary cleaning of hospital bedding with an aqueous solution containing a polyvalent carboxylic acid or oxycarboxylic acid can prevent coloring and discoloration when a chlorine bleach is used in the main cleaning. The mechanism by which pre-washing with an aqueous solution containing a polyvalent carboxylic acid or oxycarboxylic acid can prevent coloring and discoloration in the main washing is not clear, but a substance that becomes colored and causes contamination marks, for example, gluconic acid Chlorhexidine

【化1】 を、より水溶性の大きい塩として、被洗物から除去する
ものと推定される。
Embedded image Is presumed to be removed from the object to be washed as a salt having higher water solubility.

【0007】本発明方法においては、予備洗浄に続い
て、漂白剤、アルカリビルダー及び洗剤を含む水溶液を
用いて本洗浄を行う。本洗浄に用いる漂白剤には特に制
限はなく、例えば、過炭酸ソーダ、過酸化水素、過硼酸
ソーダ、過酸化ソーダなどの酸素系漂白剤、次亜塩素酸
ソーダ、亜塩素酸ソーダ、サラシ粉などの塩素系漂白
剤、ハイドロサルファイト、チオ硫酸ソーダ、重亜硫酸
ソーダなどの還元漂白剤などを挙げることができる。病
院寝具類にグルコン酸クロルヘキシジンなどが付着して
いる場合、塩素系漂白剤を含む洗浄水を用いて本洗浄を
行うと、本洗浄直後にすでに被洗物に着色した汚染痕が
発生するが、本発明方法にしたがってあらかじめ予備洗
浄を行うことにより、着色物質を除去して被洗物の汚染
痕の発生を防止することができる。また、酸素系漂白剤
又は還元漂白剤を用いて本洗浄を行った場合は、本洗浄
直後の被洗物の着色は顕著ではないが、洗浄後被洗物を
放置することにより徐々に着色した汚染痕が現れる。多
価カルボン酸又はオキシカルボン酸を含む水溶液で予備
洗浄を行う本発明方法により、このように洗浄後徐々に
出現する着色をも防止することができる。
In the method of the present invention, subsequent to the preliminary cleaning, the main cleaning is performed using an aqueous solution containing a bleaching agent, an alkali builder and a detergent. There is no particular limitation on the bleaching agent used in the main washing, and for example, oxygen-based bleaching agents such as sodium percarbonate, hydrogen peroxide, sodium perborate, and sodium peroxide, sodium hypochlorite, sodium chlorite, and ground bean powder And a reducing bleach such as hydrosulfite, sodium thiosulfate and sodium bisulfite. If chlorhexidine gluconate is adhered to hospital bedding and main cleaning is performed using cleaning water containing a chlorine-based bleach, stains already stained on the item to be washed will occur immediately after main cleaning. By performing pre-cleaning in advance according to the method of the present invention, it is possible to remove colored substances and prevent the occurrence of contamination marks on the object to be cleaned. When the main washing was performed using an oxygen-based bleach or a reducing bleach, the color of the object to be washed immediately after the main washing was not remarkable, but the object to be washed was gradually colored by leaving the object to be washed. Contamination marks appear. According to the method of the present invention in which pre-washing is performed with an aqueous solution containing a polyvalent carboxylic acid or an oxycarboxylic acid, coloring that gradually appears after washing can also be prevented.

【0008】本発明方法において、本洗浄に用いるアル
カリビルダーには特に制限はなく、例えば、メタケイ酸
ソーダ、ケイ酸ソーダ、炭酸ソーダ、リン酸ソーダなど
を挙げることができる。これらの中で、メタケイ酸ソー
ダを好適に使用することができる。本洗浄に用いる洗剤
には特に制限はなく、例えば、α−オレフィンスルホン
酸塩、直鎖アルキルベンゼンスルホン酸塩、ポリオキシ
エチレンアルキル硫酸塩などの合成界面活性剤や石鹸な
どを単独に使用することができ、あるいは、アルカリビ
ルダー、消泡剤、蛍光増白剤、酵素などを含む市販の洗
剤を使用することができる。本発明方法において、本洗
浄の条件には特に制限はなく、被洗物の汚れの状態など
に応じて適宜選択することができるが、例えば、漂白剤
を0.05〜1.0%owf、アルカリビルダーを0.05〜
1.0%owf、洗剤を0.1〜1.0%owf使用し、浴比を
1:3〜1:10とし、洗浄温度を50〜80℃とし
て、5〜20分洗浄することができる。このような条件
で本洗浄を行うことにより、病院寝具類などの被洗物の
汚れを、再汚染を生ずることなく除去し、さらに漂白効
果を発揮することができる。本洗浄後の被洗物は、公知
の方法により濯ぎ、脱水、乾燥を行うことが好ましい。
本発明方法によれば、殺菌消毒剤のグルコン酸クロルヘ
キシジンが付着した病院寝具類も、良好な洗浄性、漂白
性及び再汚染防止性を確保し、かつグルコン酸クロルヘ
キシジンに起因する着色を生ずることなく洗浄すること
ができる。
In the method of the present invention, the alkali builder used for the main washing is not particularly limited, and examples thereof include sodium metasilicate, sodium silicate, sodium carbonate, and sodium phosphate. Among them, sodium metasilicate can be preferably used. There is no particular limitation on the detergent used for the main washing, and for example, a synthetic surfactant such as α-olefin sulfonate, linear alkylbenzene sulfonate, polyoxyethylene alkyl sulfate, soap and the like can be used alone. Alternatively, commercially available detergents containing alkaline builders, defoamers, optical brighteners, enzymes and the like can be used. In the method of the present invention, the conditions for the main washing are not particularly limited, and can be appropriately selected depending on the condition of the stain on the article to be washed. Alkali builder
1.0% owf, 0.1 ~ 1.0% owf detergent, bath ratio 1: 3 ~ 1: 10, washing temperature 50 ~ 80 ° C, can be washed for 5 ~ 20 minutes. . By performing the main washing under such conditions, the stains on the articles to be washed such as hospital bedding can be removed without recontamination, and the bleaching effect can be further exhibited. The object to be washed after the main washing is preferably rinsed, dehydrated and dried by a known method.
According to the method of the present invention, hospital bedding to which chlorhexidine gluconate as a germicidal disinfectant has adhered also has good cleaning properties, bleaching properties and anti-recontamination properties, and does not cause coloring caused by chlorhexidine gluconate. Can be washed.

【0009】[0009]

【実施例】以下に、実施例を挙げて本発明をさらに詳細
に説明するが、本発明はこれらの実施例によりなんら限
定されるものではない。 実施例1 10cm×10cmの綿布の中央に、グルコン酸クロルヘキ
シジンの5重量%水溶液0.12mlをスポット状に付着
させ、80℃で30分間乾燥してテスト布を調製した。
グルコン酸クロルヘキシジンが付着した中央のスポット
部分について、測色機[ミノルタカメラ(株)、ミノルタ
CR−200]を用いて測色したところ、L値91.5
8、a値0.69、b値0.58であった。ラウンダ・オ
・メーター[大栄科学精器製作所(株)、L−20]のポ
ットに、クエン酸と水を、クエン酸の濃度が0.5%ow
f、浴比が1:10になるように入れ、さらにスチール
ボール20個とテスト布10枚とを入れて、30℃で3
分間予備洗浄した。別のラウンダ・オ・メーターのポッ
トに、次亜塩素酸ソーダ(有効塩素12重量%)、メタ
珪酸ソーダ9水塩、無リン粉末洗剤[日華化学(株)、シ
ロックAN−55]及び水を、次亜塩素酸ソーダ(有効
塩素12重量%)の濃度が1.0%owf、メタ珪酸ソーダ
9水塩の濃度が0.5%owf、無リン粉末洗剤の濃度が
0.5%owf、浴比が1:10になるように入れ、さらに
スチールボール20個と予備洗浄を終えたテスト布10
枚を脱水せずに入れた。60℃で10分間本洗浄したの
ち、2分間濯ぎをし、80℃で30分間乾燥した。乾燥
後のテスト布の中央のスポット部分について測色したと
ころ、L値91.59、a値−0.81、b値2.53で
あった。この洗浄後のテスト布の中央のスポット部分
に、次亜塩素酸ソーダの12重量%水溶液0.08mlを
滴下し、80℃で30分乾燥した。乾燥後のテスト布の
中央のスポット部分について測色したところ、L値9
2.41、a値−1.38、b値1.79であった。実施
例2予備洗浄において、クエン酸の代わりにシュウ酸を
用いた以外は、実施例1と同じ操作を繰り返した。本洗
浄後のテスト布の中央のスポット部分は、L値91.8
1、a値−0.88、b値2.26であった。さらに、次
亜塩素酸ソーダ水溶液を滴下し、乾燥したのちの中央の
スポット部分は、L値92.58、a値−1.40、b値
1.55であった。 比較例1 予備洗浄を行うことなく、テスト布を直接本洗浄にかけ
て、実施例1と同じ操作を繰り返した。本洗浄後のテス
ト布の中央のスポット部分は、L値88.33、a値−
0.11、b値9.78であった。さらに、次亜塩素酸ソ
ーダ水溶液を滴下し、乾燥したのちの中央のスポット部
分は、L値90.16、a値−0.95、b値6.59で
あった。 比較例2 予備洗浄において、クエン酸の代わりに酢酸を用いた以
外は、実施例1と同じ操作を繰り返した。本洗浄後のテ
スト布の中央のスポット部分は、L値89.00、a値
−0.25、b値9.04であった。さらに、次亜塩素酸
ソーダ水溶液を滴下し、乾燥したのちの中央のスポット
部分は、L値90.46、a値−1.03、b値6.10
であった。 実施例3 本洗浄において、次亜塩素酸ソーダ(有効塩素12重量
%)の代わりに35重量%−過酸化水素水を用いた以外
は、実施例1と同じ操作を繰り返した。本洗浄後のテス
ト布の中央のスポット部分は、L値92.70、a値−
0.85、b値−0.32であった。さらに、次亜塩素酸
ソーダ水溶液を滴下し、乾燥したのちの中央のスポット
部分は、L値92.29、a値−1.50、b値2.10
であった。 実施例4 予備洗浄において、クエン酸の代わりにシュウ酸を用い
た以外は、実施例3と同じ操作を繰り返した。本洗浄後
のテスト布の中央のスポット部分は、L値92.97、
a値−0.79、b値−0.43であった。さらに、次亜
塩素酸ソーダ水溶液を滴下し、乾燥したのちの中央のス
ポット部分は、L値92.56、a値−1.42、b値
1.73であった。 比較例3 予備洗浄を行うことなく、テスト布を直接本洗浄にかけ
て、実施例3と同じ操作を繰り返した。本洗浄後のテス
ト布の中央のスポット部分は、L値92.11、a値−
0.93、b値1.09であった。さらに、次亜塩素酸ソ
ーダ水溶液を滴下し、乾燥したのちの中央のスポット部
分は、L値90.99、a値−1.16、b値5.31で
あった。実施例1〜4及び比較例1〜3の結果を、第1
表に示す。
EXAMPLES The present invention will be described in more detail with reference to the following Examples, which should not be construed as limiting the present invention. Example 1 0.12 ml of a 5% by weight aqueous solution of chlorhexidine gluconate was applied in the form of a spot to the center of a 10 cm × 10 cm cotton cloth and dried at 80 ° C. for 30 minutes to prepare a test cloth.
When the color of the central spot to which chlorhexidine gluconate was attached was measured using a colorimeter [Minolta Camera Co., Ltd., Minolta CR-200], the L value was 91.5.
8, the a value was 0.69 and the b value was 0.58. Citric acid and water were added to a pot of Rounder O-Meter [Daei Kagaku Seiki Seisakusho Co., Ltd., L-20], and the citric acid concentration was 0.5% ow.
f, put so that the bath ratio becomes 1:10, further put 20 steel balls and 10 test cloths, and at 30 ° C 3
Pre-washed for minutes. In another rounder-o-meter pot, sodium hypochlorite (effective chlorine 12% by weight), sodium metasilicate 9-hydrate, phosphorus-free powder detergent [Nichika Chemical Co., Ltd., Siroc AN-55] and water The concentration of sodium hypochlorite (effective chlorine 12% by weight) is 1.0% owf, the concentration of sodium metasilicate 9-hydrate is 0.5% owf, and the concentration of phosphorus-free powder detergent is 0.5% owf. The test cloth 10 was placed so that the bath ratio was 1:10, and further 20 steel balls and the pre-cleaning were completed.
The sheets were placed without dehydration. After main washing at 60 ° C. for 10 minutes, rinsing was performed for 2 minutes, and drying was performed at 80 ° C. for 30 minutes. When the color of the spot portion at the center of the dried test cloth was measured, the L value was 91.59, the a value was -0.81, and the b value was 2.53. After washing, 0.08 ml of a 12% by weight aqueous solution of sodium hypochlorite was dropped into the center spot of the test cloth, and dried at 80 ° C. for 30 minutes. When the color of the center spot portion of the test cloth after drying was measured, the L value was 9
2.41, a value -1.38, and b value 1.79. Example 2 The same operation as in Example 1 was repeated, except that oxalic acid was used instead of citric acid in the preliminary cleaning. The center spot of the test cloth after the main cleaning has an L value of 91.8.
1, the a value was -0.88, and the b value was 2.26. Further, after the sodium hypochlorite aqueous solution was dropped and dried, the central spot portion had an L value of 92.58, an a value of -1.40, and a b value of 1.55. Comparative Example 1 The test cloth was directly subjected to main cleaning without performing preliminary cleaning, and the same operation as in Example 1 was repeated. The spot at the center of the test cloth after the main cleaning has an L value of 88.33 and an a value of-.
It was 0.11 and the b value was 9.78. Further, after the sodium hypochlorite aqueous solution was dropped and dried, the central spot portion had an L value of 90.16, an a value of -0.95, and a b value of 6.59. Comparative Example 2 The same operation as in Example 1 was repeated, except that acetic acid was used instead of citric acid in the preliminary washing. The spot at the center of the test cloth after the main cleaning had an L value of 89.00, an a value of -0.25, and a b value of 9.04. Further, after the sodium hypochlorite aqueous solution was dropped and dried, the central spot portion had an L value of 90.46, an a value of -1.03, and a b value of 6.10.
Met. Example 3 The same operation as in Example 1 was repeated, except that 35% by weight-hydrogen peroxide solution was used instead of sodium hypochlorite (effective chlorine 12% by weight) in the main cleaning. The spot at the center of the test cloth after the main cleaning has an L value of 92.70 and an a value of-
It was 0.85 and the b value was -0.32. Further, after the sodium hypochlorite aqueous solution was dropped and dried, the central spot portion had an L value of 92.29, an a value of -1.50, and a b value of 2.10.
Met. Example 4 The same operation as in Example 3 was repeated, except that oxalic acid was used instead of citric acid in the preliminary washing. The spot at the center of the test cloth after the main cleaning has an L value of 92.97,
The a value was -0.79 and the b value was -0.43. Further, after the sodium hypochlorite aqueous solution was dropped and dried, the central spot portion had an L value of 92.56, an a value of -1.42, and a b value of 1.73. Comparative Example 3 The test cloth was directly subjected to main cleaning without performing preliminary cleaning, and the same operation as in Example 3 was repeated. The spot at the center of the test cloth after the main cleaning has an L value of 92.11 and an a value of −
0.93 and b value 1.09. Further, after the sodium hypochlorite aqueous solution was dropped and dried, the central spot portion had an L value of 90.99, an a value of -1.16, and a b value of 5.31. The results of Examples 1 to 4 and Comparative Examples 1 to 3
It is shown in the table.

【0010】[0010]

【表1】 [Table 1]

【0011】被洗物の汚染痕の状態は、黄〜緑の指標で
あるb値に最も顕著に現れるほかに、明るさの指標であ
るL値にも現れる。塩素系漂白剤である次亜塩素酸ソー
ダを用いた実施例1、2及び比較例1、2の結果を見る
と、クエン酸又はシュウ酸を用いて予備洗浄を行った実
施例では本洗浄後のb値が2.53、2.26と低い値で
あるのに対して、予備洗浄を行わない比較例1では本洗
浄後のb値が9.78、酢酸を用いて予備洗浄を行った
比較例2では本洗浄後のb値が9.04といずれも高
く、目視によっても比較例のテスト布の中央のスポット
部分の強い着色が認めらる。また、L値も実施例の方が
比較例より高く、実施例のテスト布の方が比較例のテス
ト布より明るい状態に洗浄されていることが分かる。次
亜塩素酸ソーダの滴下により、実施例、比較例ともにス
ポット部分が漂白されてb値が小さくなるが、比較例の
テスト布のb値は6.59及び6.10となお大きく、次
亜塩素酸ソーダの滴下によっても漂白されない汚染物が
残存していることが分かる。また、酸素系漂白剤である
過酸化水素を用いた実施例3、4及び比較例3の結果を
見ると、本洗浄後のb値はいずれも−0.32、−0.4
3及び1.09と低く、目視によっては顕著な差は認め
られないが、次亜塩素酸ソーダを滴下すると、実施例、
比較例ともにスポット部分のb値が大きくなり、特に比
較例のテスト布のb値は5.31と大きく、目視によっ
ても黄変が認められ、汚染物が除去されずに残存してい
ることが分かる。 実施例5 負荷量が50kgである5槽式の連続洗濯機を用いて病院
寝具の洗濯を行う際に、下記(1)〜(5)のテスト布を同
時に投入して洗濯を行い、洗浄性、漂白性、再汚染防止
性及び発色性を評価した。この試験で用いたテスト布
は、以下のように調製した。 (1)標準汚染布 綿布又はE/C布(ポリエステル/綿=65/35)
に、牛脂0.2%owf、流動パラフィン0.9%owf、カー
ボン0.03%owfを付着した布。 (2)人工汚染布 綿布又はE/C布(ポリエステル/綿=65/35)
に、牛脂脂肪酸0.2%owf.、牛脂0.2%owf.、コレス
テロール0.07%owf.、51oFワックス0.15%ow
f、カーボン0.01%owf、関東ローム層0.7%owf、
酸化鉄0.07%owfを付着した布。 (3)漂白性テスト布 綿ワイン汚染布[EMPA社製]及び綿血液汚染布[E
MPA社製]。 (4)再汚染防止性テスト布 綿白布及びE/C白布(ポリエステル/綿=65/3
5)。 (5)発色性テスト布 綿布の中央に、グルコン酸クロルヘキシジンの5重量%
水溶液0.12mlをスポット状に付着させ、80℃で3
0分間乾燥させた布。また、評価は下記の方法により行
った。なお、反射率は、測色機[(株)村上色彩技術研究
所、CM−53D]を用いて550nmにおいて測定し
た。 (1)洗浄性 綿及びE/Cの標準汚染布及び人工汚染布の洗浄前後の
反射率と綿及びE/Cの白布の反射率を測定し、次式に
より洗浄率を求める。 洗浄率(%)={(D'−D)/(W−D)}×100 ただし、Wは白布の反射率、Dは洗浄前の汚染布の反射
率、D'は洗浄後の汚染布の反射率である。 (2)漂白性 綿ワイン汚染布及び綿血液汚染布の洗浄前後の反射率と
綿の白布の反射率を測定し、次式により漂白率を求め
る。 漂白率(%)={(D'−D)/(W−D)}×100 ただし、Wは白布の反射率、Dは洗浄前の汚染布の反射
率、D'は洗浄後の汚染布の反射率である。 (3)再汚染防止性 洗浄前後の綿及びE/Cの白布の反射率を測定し、次式
により再汚染防止率を求める。 再汚染率(%)={(W−W')/W}×100 ただし、Wは洗浄前の白布の反射率、W'は洗浄後の白
布の反射率である。 (4)発色性 発色性テスト布の中央のスポット部分の本洗浄後の反射
率と、本洗浄後の布の中央のスポット部分に次亜塩素酸
ソーダの12重量%水溶液0.08mlを滴下し、80℃
で30分間乾燥した布のスポット部分について反射率を
測定し、綿白布の反射率に対する百分率を発色性(%)
とする。なお、洗浄前の発色性テスト布の中央のスポッ
ト部分の発色性は、86%であった。5槽式の連続洗濯
機の第1槽に、シュウ酸と水を、シュウ酸が0.32%o
wfの濃度になるようにいれ、被洗物である病院寝具と各
テスト布を投入し、28℃で6分間予備洗浄を行った。
第2槽及び第3槽に、次亜塩素酸ソーダ(有効塩素12
重量%)、無リン粉末アルカリビルダー[日華化学
(株)、ニッカミラクルビルダー]、無リン粉末洗剤[日
華化学(株)、シロックAN−55]及び水を、次亜塩素
酸ソーダ(有効塩素12重量%)の濃度が0.32%ow
f、無リン粉末アルカリビルダーの濃度が0.08%ow
f、無リン粉末洗剤の濃度が0.16%owfになるように
入れ、予備洗浄後の被洗物を投入し、60℃で6分間ず
つ2回の本洗浄を行い、さらに、第4槽と第5槽で濯ぎ
を2回行ったのち、シーツロールを用いて180℃で3
0秒間乾燥した。洗浄率は、綿標準汚染布が77%、E
/C標準汚染布が18%、綿人工汚染布が22%、E/
C人工汚染布23%であった。漂白率は、綿ワイン汚染
布が66%、綿血液汚染布が46%であった。再汚染率
は、綿白布が0.0%、E/C白布が0.1%であった。
発色性は、本洗浄後が85%、次亜塩素酸ソーダ滴下後
が84%であった。 比較例4 第1槽における予備洗浄を行うことなく、第2槽、第3
槽の本洗浄と第4槽、第5槽の濯ぎのみを実施例5と同
一条件で行って、病院寝具と上記(1)〜(5)のテスト布
を洗濯し、洗浄性、漂白性、再汚染防止法及び発色性を
評価した。洗浄率は、綿標準汚染布が75%、E/C標
準汚染布が19%、綿人工汚染布が23%、E/C人工
汚染布20%であった。漂白率は、綿ワイン汚染布が6
8%、綿血液汚染布が45%であった。再汚染率は、綿
白布が0.1%、E/C白布が0.2%であった。発色性
は、本洗浄後が58%、次亜塩素酸ソーダ滴下後が60
%であった。 比較例5 第1槽における予備洗浄を行わず、第2槽、第3槽の本
洗浄において次亜塩素酸ソーダ(有効塩素12重量%)
の代わりに35重量%−過酸化水素水を用いた以外は、
実施例5と同様にして、病院寝具と上記(1)〜(5)のテ
スト布を洗濯し、洗浄性、漂白性、再汚染防止法及び発
色性を評価した。洗浄率は、綿標準汚染布が77%、E
/C標準汚染布が18%、綿人工汚染布が21%、E/
C人工汚染布22%であった。漂白率は、綿ワイン汚染
布が55%、綿血液汚染布が35%であった。再汚染率
は、綿白布が0.0%、E/C白布が0.1%であった。
発色性は、本洗浄後が86%、次亜塩素酸ソーダ滴下後
が63%であった。実施例5及び比較例4〜5の結果
を、第2表に示す。
[0011] The state of contamination marks on the object to be washed appears most remarkably in the b value as an index of yellow to green, and also in the L value as an index of brightness. Looking at the results of Examples 1 and 2 and Comparative Examples 1 and 2 using sodium hypochlorite which is a chlorine-based bleaching agent, the examples in which the pre-cleaning was performed using citric acid or oxalic acid were performed after the main cleaning. In Comparative Example 1 where pre-cleaning was not performed, the b-value after the main cleaning was 9.78, and the pre-cleaning was performed using acetic acid, whereas the b value of the sample was as low as 2.53 and 2.26. In Comparative Example 2, the b-value after the main cleaning was 9.04, which was all high, and strong coloration of the central spot portion of the test cloth of Comparative Example was visually observed. Also, the L value is higher in the example than in the comparative example, and it can be seen that the test cloth of the example is cleaned to be brighter than the test cloth of the comparative example. By dropping sodium hypochlorite, the spot value was bleached in both the Examples and Comparative Examples to reduce the b value. However, the b values of the test cloths of Comparative Examples were still as large as 6.59 and 6.10, and It can be seen that contaminants that are not bleached even by the dropping of sodium chlorate remain. Further, the results of Examples 3 and 4 and Comparative Example 3 using hydrogen peroxide as an oxygen bleaching agent show that the b value after the main cleaning was -0.32 and -0.4.
3 and 1.09, which are low, and a remarkable difference is not visually observed, but when sodium hypochlorite is dropped, Examples
In both the comparative examples, the b value of the spot portion was large, and especially the b value of the test cloth of the comparative example was 5.31 and the yellowing was visually observed, indicating that the contaminants remained without being removed. I understand. Example 5 When washing hospital bedding using a 5-tub continuous washing machine with a load of 50 kg, the following test cloths (1) to (5) were simultaneously put into the washing machine to perform washing. , Bleaching property, re-staining prevention property and coloring property were evaluated. The test cloth used in this test was prepared as follows. (1) Standard contaminated cloth Cotton cloth or E / C cloth (polyester / cotton = 65/35)
To which 0.2% owf of tallow, 0.9% owf of liquid paraffin, and 0.03% owf of carbon are adhered. (2) Artificial contamination cloth Cotton cloth or E / C cloth (polyester / cotton = 65/35)
0.2% owf. Of tallow fatty acid, 0.2% owf. Of beef tallow, 0.07% owf. Of cholesterol, 0.15% ow of 51 ° F wax
f, carbon 0.01% owf, Kanto loam layer 0.7% owf,
Cloth with 0.07% owf iron oxide. (3) Bleaching test cloth Cotton wine stained cloth [EMPA] and cotton blood stained cloth [E
MPA). (4) Redeposition prevention test cloth Cotton white cloth and E / C white cloth (polyester / cotton = 65/3)
5). (5) Color developing test cloth 5% by weight of chlorhexidine gluconate in the center of cotton cloth
0.12 ml of the aqueous solution is deposited in the form of a spot,
Cloth dried for 0 minutes. The evaluation was performed by the following method. In addition, the reflectance was measured at 550 nm using a colorimeter [Murakami Color Research Laboratory, CM-53D]. (1) Detergency The reflectance of cotton and E / C standard contaminated cloth and artificial contaminated cloth before and after cleaning and the reflectance of cotton and E / C white cloth are measured, and the cleaning rate is calculated by the following equation. Cleaning rate (%) = {(D′−D) / (WD)} × 100 where W is the reflectance of the white cloth, D is the reflectance of the contaminated cloth before cleaning, and D ′ is the contaminated cloth after cleaning. Is the reflectance. (2) Bleaching property The reflectance before and after washing the cotton wine-contaminated cloth and the cotton blood-contaminated cloth and the reflectance of the cotton white cloth are measured, and the bleaching rate is obtained by the following equation. Bleaching rate (%) = {(D′−D) / (WD)} × 100 where W is the reflectance of the white cloth, D is the reflectance of the contaminated cloth before cleaning, and D ′ is the contaminated cloth after cleaning. Is the reflectance. (3) Anti-re-contamination property The reflectance of the cotton and the E / C white cloth before and after washing is measured, and the anti-re-contamination rate is obtained by the following formula. Recontamination rate (%) = {(W−W ′) / W} × 100 where W is the reflectance of the white cloth before cleaning, and W ′ is the reflectance of the white cloth after cleaning. (4) Color-forming property The reflectance of the central spot of the color-forming test cloth after the main washing and the spot of the central part of the cloth after the main washing 0.08 ml of a 12% by weight aqueous solution of sodium hypochlorite were dropped. , 80 ° C
The reflectance was measured for the spot portion of the cloth dried for 30 minutes under the conditions described above, and the color development (%) was calculated as a percentage of the reflectance of the cotton white cloth.
And The color development at the center spot of the color development test cloth before washing was 86%. Oxalic acid and water are added to the first tub of a 5-tub continuous washing machine.
Hospital bedding and each test cloth, which were to be washed, were added so as to have a wf concentration, and preliminarily washed at 28 ° C. for 6 minutes.
In the second and third tanks, sodium hypochlorite (effective chlorine 12
Wt%), phosphorus-free powder alkaline builder [Nichika Chemical
Nikka Miracle Builder Co., Ltd.), phosphorus-free powder detergent [Nichika Chemical Co., Ltd., Siroc AN-55] and water at a concentration of 0.32% ow of sodium hypochlorite (effective chlorine 12% by weight).
f, the concentration of phosphorus-free powdered alkaline builder is 0.08% ow
f. Put the phosphorus-free powder detergent in a concentration of 0.16% owf, put in the pre-washed object to be washed, perform main washing twice at 60 ° C. for 6 minutes each, and further, in the fourth tank And rinsing twice in the fifth tank, and then using a sheet roll at 180 ° C. for 3 hours.
Dry for 0 seconds. The cleaning rate was 77% for the standard cotton cloth and E
/ C standard stain cloth 18%, cotton artificial stain cloth 22%, E /
C: 23% of artificially stained cloth. The bleaching rate was 66% for cotton wine stained cloth and 46% for cotton blood stained cloth. The recontamination rate was 0.0% for cotton white cloth and 0.1% for E / C white cloth.
The color development was 85% after the main washing and 84% after the sodium hypochlorite was dropped. Comparative Example 4 The second tank and the third tank were not cleaned in the first tank.
Only the main cleaning of the tank and the rinsing of the fourth and fifth tanks were performed under the same conditions as in Example 5, and the hospital bedding and the test cloths (1) to (5) were washed, and the washing property, bleaching property, The recontamination prevention method and color development were evaluated. The cleaning rate was 75% for the cotton standard stained cloth, 19% for the E / C standard stained cloth, 23% for the cotton artificially stained cloth, and 20% for the E / C artificially stained cloth. The bleaching rate is 6 for cotton-contaminated cloth.
8%, 45% cotton blood stained cloth. The recontamination rate was 0.1% for cotton white cloth and 0.2% for E / C white cloth. The coloring was 58% after the main washing and 60% after the sodium hypochlorite was dropped.
%Met. Comparative Example 5 Without preliminary cleaning in the first tank, sodium hypochlorite (effective chlorine 12% by weight) in the main cleaning in the second and third tanks.
Except that 35% by weight-hydrogen peroxide solution was used instead of
In the same manner as in Example 5, the hospital bedding and the test cloths (1) to (5) were washed, and the cleaning property, the bleaching property, the recontamination prevention method, and the coloring property were evaluated. The cleaning rate was 77% for the standard cotton cloth and E
/ C standard stained cloth 18%, artificial cotton stained cloth 21%, E /
C was artificially stained cloth 22%. The bleaching rate was 55% for cotton wine-contaminated cloth and 35% for cotton blood-contaminated cloth. The recontamination rate was 0.0% for cotton white cloth and 0.1% for E / C white cloth.
The color development was 86% after the main washing, and 63% after the sodium hypochlorite was dropped. Table 2 shows the results of Example 5 and Comparative Examples 4 and 5.

【0012】[0012]

【表2】 [Table 2]

【0013】第2表の結果から、シュウ酸を含む水溶液
を用いて予備洗浄し、次亜塩素酸ソーダを含む洗浄水を
用いて本洗浄を行った実施例5では、良好な洗浄性、漂
白性及び再汚染防止性が維持され、本洗浄後及び次亜塩
素酸ソーダ滴下後の発色性の値が洗浄前の発色性の値と
ほとんど変わらないことから、ジグルコン酸クロルヘキ
シジンに起因する着色が生じていないことが分かる。こ
れに対して、予備洗浄を行うことなく、次亜塩素酸ソー
ダを含む洗浄水を用いて本洗浄を行った比較例4では、
本洗浄において漂白剤により変色し、発色性の値が低く
なり、次亜塩素酸ソーダを滴下しても発色性の値は回復
しない。また、予備洗浄を行うことなく、過酸化水素を
含む洗浄水を用いて本洗浄を行った比較例5では、本洗
浄後の発色性の値は洗浄前の発色性の値と同じで、中央
のスポット部分に着色を生じていないが、次亜塩素酸ソ
ーダを滴下することにより着色することからジグルコン
酸クロルヘキシジンが除去されずに残存していることが
分かる。
From the results shown in Table 2, it can be seen from Example 5 that the pre-cleaning was carried out using an aqueous solution containing oxalic acid and the main cleaning was carried out using cleaning water containing sodium hypochlorite. The coloring property after main washing and after dropping of sodium hypochlorite is almost the same as the coloring property before washing, and coloring due to chlorhexidine digluconate occurs. You can see that it is not. On the other hand, in Comparative Example 4 in which main cleaning was performed using cleaning water containing sodium hypochlorite without performing preliminary cleaning,
In the main washing, the color is changed by the bleaching agent, and the value of the coloring property is lowered. Even if sodium hypochlorite is dropped, the value of the coloring property is not recovered. In Comparative Example 5 in which the main cleaning was performed using the cleaning water containing hydrogen peroxide without performing the preliminary cleaning, the value of the coloring property after the main cleaning was the same as the value of the coloring property before the cleaning. Although no coloring was caused in the spot portion, it can be seen that chlorhexidine digluconate remains without being removed since coloring is performed by dropping sodium hypochlorite.

【0014】[0014]

【発明の効果】本発明の洗浄方法によれば、殺菌消毒剤
のグルコン酸クロルヘキシジンが付着した病院寝具類に
ついても、良好な洗浄性、漂白性及び再汚染防止性を確
保し、かつグルコン酸クロルヘキシジンに起因する着色
を防止し、延いては、再洗い枚数を減らし、作業性、経
済性の面で寄与することができる。
According to the cleaning method of the present invention, even for hospital bedding to which chlorhexidine gluconate as a disinfectant / disinfectant has adhered, good cleaning properties, bleaching properties and anti-recontamination properties are ensured, and chlorhexidine gluconate is ensured. Can be prevented, and the number of rewashing can be reduced, which contributes to workability and economy.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】病院寝具類を、多価カルボン酸又はオキシ
カルボン酸を含む水溶液で予備洗浄したのち、漂白剤、
アルカリビルダー及び洗剤を含む水溶液で本洗浄するこ
とを特徴とする病院寝具類の洗浄方法。
1. Preliminary cleaning of hospital bedding with an aqueous solution containing a polycarboxylic acid or an oxycarboxylic acid, followed by a bleaching agent,
A method for cleaning hospital bedding, comprising: main cleaning with an aqueous solution containing an alkali builder and a detergent.
【請求項2】多価カルボン酸又はオキシカルボン酸が、
シュウ酸、マロン酸、コハク酸、乳酸、リンゴ酸、酒石
鹸又はクエン酸である請求項1記載の病院寝具類の洗浄
方法。
2. The method according to claim 1, wherein the polycarboxylic acid or oxycarboxylic acid is
The method for cleaning hospital bedding according to claim 1, which is oxalic acid, malonic acid, succinic acid, lactic acid, malic acid, tartar soap or citric acid.
JP3470098A 1998-02-17 1998-02-17 Washing of hospital bedclothes Pending JPH11229271A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3470098A JPH11229271A (en) 1998-02-17 1998-02-17 Washing of hospital bedclothes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3470098A JPH11229271A (en) 1998-02-17 1998-02-17 Washing of hospital bedclothes

Publications (1)

Publication Number Publication Date
JPH11229271A true JPH11229271A (en) 1999-08-24

Family

ID=12421653

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3470098A Pending JPH11229271A (en) 1998-02-17 1998-02-17 Washing of hospital bedclothes

Country Status (1)

Country Link
JP (1) JPH11229271A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002167596A (en) * 2000-12-01 2002-06-11 Lion Corp Cleaning performance reinforcement composition, production method therefor, and cleaning method therewith
WO2003014458A1 (en) * 2001-08-10 2003-02-20 Henkel Kommanditgesellschaft Auf Aktien Washing method
JP2003105390A (en) * 2001-09-28 2003-04-09 Lion Corp Pretreatment composition for mud-stained clothes, method of washing mud-stained clothes and detergent for washing mud-stained clothes
WO2013116734A1 (en) * 2012-02-01 2013-08-08 Gurtler Industries, Inc. Composition and method for removing stains derived from chlorhexidine gluconate
JP2015529515A (en) * 2012-08-20 2015-10-08 エコラボ ユーエスエー インコーポレイティド How to wash textile goods

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002167596A (en) * 2000-12-01 2002-06-11 Lion Corp Cleaning performance reinforcement composition, production method therefor, and cleaning method therewith
WO2003014458A1 (en) * 2001-08-10 2003-02-20 Henkel Kommanditgesellschaft Auf Aktien Washing method
JP2003105390A (en) * 2001-09-28 2003-04-09 Lion Corp Pretreatment composition for mud-stained clothes, method of washing mud-stained clothes and detergent for washing mud-stained clothes
WO2013116734A1 (en) * 2012-02-01 2013-08-08 Gurtler Industries, Inc. Composition and method for removing stains derived from chlorhexidine gluconate
US9228158B2 (en) 2012-02-01 2016-01-05 Gurtler Industries, Inc. Composition and method for removing stains derived from chlorhexidine gluconate
JP2015529515A (en) * 2012-08-20 2015-10-08 エコラボ ユーエスエー インコーポレイティド How to wash textile goods
US10253281B2 (en) 2012-08-20 2019-04-09 Ecolab Usa Inc. Method of washing textile articles
US10995305B2 (en) 2012-08-20 2021-05-04 Ecolab Usa Inc. Method of washing textile articles
US11773350B2 (en) 2012-08-20 2023-10-03 Ecolab Usa Inc. Method of washing textile articles

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