JPH0627043B2 - Disinfectant composition - Google Patents

Disinfectant composition

Info

Publication number
JPH0627043B2
JPH0627043B2 JP60202884A JP20288485A JPH0627043B2 JP H0627043 B2 JPH0627043 B2 JP H0627043B2 JP 60202884 A JP60202884 A JP 60202884A JP 20288485 A JP20288485 A JP 20288485A JP H0627043 B2 JPH0627043 B2 JP H0627043B2
Authority
JP
Japan
Prior art keywords
inorganic peroxide
weight
bactericidal
cationic surfactant
acetic acid
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 - Lifetime
Application number
JP60202884A
Other languages
Japanese (ja)
Other versions
JPS6263504A (en
Inventor
徹治 岩崎
祐一 日置
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP60202884A priority Critical patent/JPH0627043B2/en
Publication of JPS6263504A publication Critical patent/JPS6263504A/en
Publication of JPH0627043B2 publication Critical patent/JPH0627043B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 <産業上の利用分野> 本発明は殺菌剤組成物に関する。更に詳しくは木材の防
腐、製紙工程での防腐など各種産業分野での防腐に優れ
た効果を発揮し、あるいは家庭などで常時湿気をおびた
トイレ、風呂場、台所等で繁殖しやすいカビに対し優れ
た殺菌効果を発揮する殺菌剤組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION <Industrial field of application> The present invention relates to a fungicide composition. More specifically, for molds that exhibit excellent effects in various industrial fields, such as wood preservative and papermaking process preservative, or molds that easily grow in households such as toilets, bathrooms, and kitchens that are constantly humid. The present invention relates to a bactericidal composition that exhibits an excellent bactericidal effect.

<従来技術およびその問題点> 殺菌剤成分として従来から殺菌活性を有する陽イオン性
界面活性剤が使用されている。それらの化合物として例
えばアルキルジメチルベンジルアンモニウム塩、置換ベ
ンザルコニウム塩、ベンゼトニウム塩、ジアルキルジメ
チルアンモニウム塩などがある。
<Prior Art and Problems Thereof> A cationic surfactant having bactericidal activity has been conventionally used as a bactericidal component. Examples of these compounds include alkyldimethylbenzylammonium salt, substituted benzalkonium salt, benzethonium salt, dialkyldimethylammonium salt and the like.

殺菌剤は各種分野で使用されている。例えば木材防腐の
分野、製紙工程での防腐、即ちスライムコントロールの
分野、あるいは家庭の台所、トイレ、風呂場などの防カ
ビの分野などである。
Bactericides are used in various fields. For example, it is in the field of wood preserving, in the paper manufacturing process, that is, in the field of slime control, or in the field of antifungal in home kitchens, toilets, bathrooms, and the like.

しかしながら、殺菌剤成分としてよく知られている陽イ
オン性界面活性剤も上記のような分野では必ずしも十分
満足する効果を発揮するものではなかつた。即ち、木材
防腐においては木材内部への浸透性が悪く、表面塗布処
理では木材の表面加工により塗布面が除かれ殺菌力が著
しく低下する。又、製紙工程における防腐、即ちスライ
ムコントロールにおいては、微小のセルロース繊維へ陽
イオン性界面活性剤が吸着されるため殺菌力が低下す
る。更にまた、家庭での防カビにおいては対象とする壁
面等は“ホコリ”や“スス”などが付着しておりこれも
殺菌力の低下の原因となりやすい。
However, a cationic surfactant well known as a bactericidal component has not always exerted a sufficiently satisfactory effect in the above fields. That is, in wood preservative, the permeability into the interior of wood is poor, and in the surface coating treatment, the coated surface is removed by the surface treatment of the wood, and the bactericidal power is significantly reduced. Further, in the preservative in the paper making process, that is, in slime control, the cationic surfactant is adsorbed to the minute cellulose fibers, so that the bactericidal power is lowered. Furthermore, in the case of mildew prevention at home, "dust" and "soot" are attached to the target wall surface and the like, which also tends to cause a decrease in sterilizing power.

このような理由で、陽イオン性界面活性剤は比較的安価
で入手容易であるにも拘らず、殺菌剤として広範囲に使
われていなかつた。
For this reason, cationic surfactants have not been used extensively as bactericides, despite being relatively cheap and readily available.

<問題点を解決するための手段> そこで本発明者は、陽イオン性界面活性剤の殺菌効力を
高めるべく鋭意研究した結果、陽イオン性界面活性剤と
無機過酸化物および無機過酸化物の活性化剤として多価
アルコールの酢酸エステルを併用することにより、著し
く殺菌活性が高められると共に、上記のような欠点が解
消されることを見い出し本発明を完成した。
<Means for Solving Problems> Therefore, as a result of earnest studies to enhance the bactericidal effect of the cationic surfactant, the present inventor has found that the cationic surfactant, the inorganic peroxide and the inorganic peroxide are The inventors have found that the use of an acetic acid ester of a polyhydric alcohol as an activator in combination can remarkably enhance the bactericidal activity and eliminate the above drawbacks, and thus completed the present invention.

即ち、本発明は陽イオン性界面活性剤、無機過酸化物お
よび無機過酸化物の活性化剤として多価アルコールの酢
酸エステルを必須成分として含有し、陽イオン性界面活
性剤1重量部に対し、無機過酸化物 0.1〜10重量部、多
価アルコールの酢酸エステル 0.1〜10重量部の割合であ
ることを特徴とする殺菌剤組成物を提供するものであ
る。
That is, the present invention contains a cationic surfactant, an inorganic peroxide and an acetic acid ester of a polyhydric alcohol as an activator of the inorganic peroxide as an essential component, and 1 part by weight of the cationic surfactant is used. The present invention provides a bactericidal composition, characterized in that the proportion of the inorganic peroxide is 0.1 to 10 parts by weight and the amount of acetic acid ester of polyhydric alcohol is 0.1 to 10 parts by weight.

本発明に用いられる陽イオン性界面活性剤としては殺菌
活性を有するものであれば特に限定されず、例えばアル
キルジメチルベンジルアンモニウム塩、置換ベンザルコ
ニウム塩、ベンゼトニウム塩、ジアルキルジメチルアン
モニウム塩などのモノカチオン化合物のほか、N−アル
キル−N,N,N′,N′,N′−ペンタメチル−プロ
ピレンアンモニウム塩などのポリカチオン化合物が挙げ
られる。
The cationic surfactant used in the present invention is not particularly limited as long as it has bactericidal activity, and examples thereof include monocations such as alkyldimethylbenzylammonium salt, substituted benzalkonium salt, benzethonium salt and dialkyldimethylammonium salt. In addition to the compounds, polycationic compounds such as N-alkyl-N, N, N ', N', N'-pentamethyl-propylene ammonium salts can be mentioned.

無機過酸化物としては、過炭酸ナトリウム、過硼酸ナト
リウム、過酸化トリポリリン酸ナトリウム、過酸化ピロ
リン酸ナトリウム、過酸化ケイ酸ナトリウム等が挙げら
れる。
Examples of the inorganic peroxide include sodium percarbonate, sodium perborate, sodium peroxytripolyphosphate, sodium peroxypyrophosphate, sodium peroxysilicate and the like.

無機過酸化物の活性化剤としては、グルコースペンタア
セテート、グルコーステトラアセテート、フラクトース
ペンタアセテート、シユークロースオクタアセテート、
ソルビタンテトラアセテート、ソルビトールヘキサアセ
テート、マンニツトヘキサアセテート、アンニタンテト
ラアセテート、キシリツトペンタアセテート、キシリタ
ントリアセテート、ペンタエリスリトールテトラアセテ
ート等の多価アルコールの酢酸エステルが使用される。
As the inorganic peroxide activator, glucose pentaacetate, glucose tetraacetate, fructose pentaacetate, sucrose octaacetate,
Acetic acid esters of polyhydric alcohols such as sorbitan tetraacetate, sorbitol hexaacetate, mannitol hexaacetate, annitane tetraacetate, xylitopentaacetate, xylitane triacetate and pentaerythritol tetraacetate are used.

本発明の殺菌剤組成物においては、貯蔵安定性および殺
菌効果等の点から、陽イオン性界面活性剤1重量部に対
し、無機過酸化物を0.1 〜10重量部、活性化剤として多
価アルコールの酢酸エステルを 0.1〜10重量部の範囲で
使用する。更に無機過酸化物と上記活性化剤の配合割合
(重量比)は10/1〜1/10が好ましい。
In the bactericidal composition of the present invention, from the viewpoint of storage stability and bactericidal effect, 0.1 to 10 parts by weight of an inorganic peroxide is used per 1 part by weight of a cationic surfactant, and a polyvalent activating agent is used. The acetic acid ester of alcohol is used in the range of 0.1 to 10 parts by weight. Further, the mixing ratio (weight ratio) of the inorganic peroxide and the activator is preferably 10/1 to 1/10.

本発明の殺菌剤組成物は通常、粉体、顆粒、錠剤等の固
形物として製剤され、使用に当り、水に希釈し施用され
る。その時の濃度は対象物によつても異なるが、通常5
0〜1000 ppmである。
The bactericidal composition of the present invention is usually formulated as a solid substance such as powder, granules and tablets, and is diluted with water before use. The concentration at that time varies depending on the target object, but is usually 5
0 to 1000 ppm.

勿論、陽イオン性界面活性剤、無機過酸化物および無機
過酸化物の活性化剤として多価アルコールの酢酸エステ
ルをそれぞれ別個に製剤し、使用するに当り、それらを
一緒に水に希釈して施用することも本発明の組成物の使
用態様に含まれるものである。
Of course, cationic surfactants, inorganic peroxides, and acetic acid esters of polyhydric alcohols as the activators of the inorganic peroxides are separately formulated, and when they are used, they are diluted together in water. Applying is also included in the usage of the composition of the present invention.

<作用・効果> 本発明の殺菌剤組成物が各種用途例えば木材の防腐、製
紙工程でのスライムコントロール、家庭での防カビ等に
関し、陽イオン性界面活性剤単独では従来得られなかつ
た顕著な殺菌効果を発揮する機作については必ずしも明
確ではないが、無機過酸化物と多価アルコールの酢酸エ
ステルから生じる有機過酸と陽イオン性界面活性剤との
共役効果により細菌などの細胞膜に不可逆的な変性を起
こさせることによるものと考えられる。
<Action / Effects> The bactericidal composition of the present invention has various advantages such as preserving wood, controlling slime in the paper making process, and preventing mildew at home. The mechanism of exerting the bactericidal effect is not clear, but it is irreversible to the cell membrane of bacteria due to the coupling effect of the organic peracid generated from the inorganic peroxide and the acetate ester of polyhydric alcohol and the cationic surfactant. It is thought that this is due to causing such degeneration.

<実施例> 次に本発明の殺菌剤組成物を各種分野の殺菌に用いた実
施例を挙げて具体的に説明するが、本発明の殺菌剤組成
物はこれら実施例の用途に限定されるものではない。
<Examples> Next, the bactericidal composition of the present invention will be specifically described with reference to Examples used for sterilization in various fields, but the bactericidal composition of the present invention is limited to the use of these examples. Not a thing.

実施例1 ヒノキの辺材を3cm×3cm×3cmの立方体状に切りと
り、本発明品を種々の濃度に希釈した液に60分間浸漬
した木片を標品Aとする。又別に上記浸漬処理した木片
の表面から2mmの深さに正確に切りとつた木片を標品B
とする。標品A,Bに木材腐朽菌であるカワラタケを接
種し3カ月後の無処理木片に体する腐朽木片の重量減少
を測定し防腐効果を百分率であらわした。
Example 1 Japanese cypress sapwood was cut into cubes of 3 cm × 3 cm × 3 cm, and the wood pieces obtained by dipping the present invention product in various concentrations for 60 minutes were designated as Sample A. Separately, a piece of wood precisely cut into a depth of 2 mm from the surface of the piece of wood subjected to the immersion treatment is prepared as a standard B.
And Specimens A and B were inoculated with the wood-rotting fungus Kawaratake, and the weight loss of the decayed wood pieces on the untreated wood pieces after 3 months was measured and the antiseptic effect was expressed as a percentage.

実施例2 セルロース濃度2%白水を30℃14日間ポンプにて循
環させ経日的に白水を殺菌済みピペツトで0.1mlと
り、殺菌済みイオン交換水10ml中に希釈しその希釈液
を0.2mlとり、肉エキス培地に塗布し、27℃6日間
培養し、平板シヤーレー中の菌コロニー数を数えること
により殺菌効力を測定した。
Example 2 White water having a cellulose concentration of 2% was circulated by a pump at 30 ° C. for 14 days, and 0.1 ml of white water was daily taken with a sterilized pipette, diluted with 10 ml of sterilized ion-exchanged water, and the diluted solution was 0.2 ml. The bactericidal effect was measured by applying the solution to a meat extract medium, culturing at 27 ° C. for 6 days, and counting the number of bacterial colonies in the plate Shearley.

実施例3 風呂場の環境を想定して、3cm×3cmのモルタル壁チツ
プを風呂場の残り水に24時間浸漬し、その後とり出し
黒カビ(Aspergilus niger)の胞子懸濁液を散布し、2
7℃90%相対湿度下にて10日間培養する(モルタル
壁チツプ上には黒カビが、一面に繁殖しているものを使
用する。)。その後薬液を調製し、チツプあたり0.2
ml散布し更に3日間同一条件にて培養する。その後下記
の評価法にて薬液の効力を判定した。
Example 3 Assuming the environment of a bathroom, a 3 cm × 3 cm chip of mortar wall is immersed in the remaining water in the bathroom for 24 hours, and then taken out and sprayed with a spore suspension of Aspergilus niger.
Incubate at 7 ° C. and 90% relative humidity for 10 days (use black mold on the surface of the mortar wall chip, which is propagated all over the mold). After that, prepare the drug solution and add 0.2 per chip.
Disperse ml and incubate for 3 days under the same conditions. Then, the efficacy of the drug solution was determined by the following evaluation method.

評価基準 Evaluation criteria

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】陽イオン性界面活性剤、無機過酸化物およ
び無機過酸化物の活性化剤として多価アルコールの酢酸
エステルを必須成分として含有し、陽イオン性界面活性
剤1重量部に対し、無機過酸化物 0.1〜10重量部、多価
アルコールの酢酸エステル 0.1〜10重量部の割合である
ことを特徴とする殺菌剤組成物。
1. A cationic surfactant, an inorganic peroxide, and an acetic acid ester of a polyhydric alcohol as an activator of the inorganic peroxide as an essential component, and 1 part by weight of the cationic surfactant. A disinfectant composition comprising 0.1 to 10 parts by weight of an inorganic peroxide and 0.1 to 10 parts by weight of an acetic acid ester of a polyhydric alcohol.
【請求項2】無機過酸化物と多価アルコールの酢酸エス
テルの配合割合(重量比)が10/1〜1/10である特許
請求の範囲第1項記載の殺菌剤組成物。
2. The disinfectant composition according to claim 1, wherein the mixing ratio (weight ratio) of the inorganic peroxide and the acetic acid ester of a polyhydric alcohol is 10/1 to 1/10.
JP60202884A 1985-09-13 1985-09-13 Disinfectant composition Expired - Lifetime JPH0627043B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60202884A JPH0627043B2 (en) 1985-09-13 1985-09-13 Disinfectant composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60202884A JPH0627043B2 (en) 1985-09-13 1985-09-13 Disinfectant composition

Publications (2)

Publication Number Publication Date
JPS6263504A JPS6263504A (en) 1987-03-20
JPH0627043B2 true JPH0627043B2 (en) 1994-04-13

Family

ID=16464796

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60202884A Expired - Lifetime JPH0627043B2 (en) 1985-09-13 1985-09-13 Disinfectant composition

Country Status (1)

Country Link
JP (1) JPH0627043B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7390432B2 (en) 1998-06-30 2008-06-24 Sandia Corporation Enhanced formulations for neutralization of chemical, biological and industrial toxants
ES2203377T3 (en) 1999-06-30 2004-04-16 Kao Corporation VIRUCIDE AND SPORTS COMPOUND.
US20110177145A1 (en) * 2009-07-27 2011-07-21 E.I. Du Pont De Nemours And Company In situ preparation of peracid-based removable antimicrobial coating compositions and methods of use
AU2010281409B2 (en) * 2009-07-27 2014-08-14 The Chemours Company Fc, Llc Enzymatic in situ preparation of peracid-based removable antimicrobial coating compositions and methods of use
JP2012219069A (en) * 2011-04-11 2012-11-12 Neos Co Ltd Method for controlling mold, and liquid mold-controlling agent composition

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2574424B1 (en) * 1984-12-12 1987-01-16 Interox PROCESS FOR ACTIVATION OF HYDROGEN PEROXIDE IN WASHING OR DISINFECTING BATHS, SOLID WASHING AND DISINFECTING COMPOSITIONS AND USE OF SUCH COMPOSITIONS IN BATHS FOR WASHING OR DISINFECTING TEXTILES

Also Published As

Publication number Publication date
JPS6263504A (en) 1987-03-20

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