JPS60146807A - Fungicide - Google Patents

Fungicide

Info

Publication number
JPS60146807A
JPS60146807A JP137784A JP137784A JPS60146807A JP S60146807 A JPS60146807 A JP S60146807A JP 137784 A JP137784 A JP 137784A JP 137784 A JP137784 A JP 137784A JP S60146807 A JPS60146807 A JP S60146807A
Authority
JP
Japan
Prior art keywords
fungi
agent
boric acid
fungicide
hydrogen peroxide
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
JP137784A
Other languages
Japanese (ja)
Inventor
Kimio Tanji
丹治 紀美男
Takashi Sakamaki
坂巻 喬
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.)
Nippon Peroxide Co Ltd
Original Assignee
Nippon Peroxide 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 Nippon Peroxide Co Ltd filed Critical Nippon Peroxide Co Ltd
Priority to JP137784A priority Critical patent/JPS60146807A/en
Publication of JPS60146807A publication Critical patent/JPS60146807A/en
Pending legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:A fungicide which contains hydrogen peroxide and boric acid, thus having fungi-proof as well as fungicidal activities and inhibiting the regeneration of fungi. CONSTITUTION:The objective agent contains 1-6%, preferably 3-6% of hydrogen peroxide and 0.5-3.5% of boric acid. When the fungicide is applied and let stand, it develops fungicidal effect and the boric acid penetrates into and stays in the treated places to keep fungi-proof effect and inhibit the regeneration of fungi. Preferably, a thickener is combined with the agent so that the agent may not flow down, especially an acrylic acid polymer is added and the pH is adjusted to 4-5.5. It is suitably used to prevent fungi and mildew from growing on walls, floors and ceilings of e.g., bathrooms.

Description

【発明の詳細な説明】 本発明は、浴室、床、壁および天井等に発生するカビを
過酸化水素および硼酸を含有する製剤で殺菌し、更には
、長期間に渡ってカビの再発生を防止するととに関する
DETAILED DESCRIPTION OF THE INVENTION The present invention sterilizes mold that grows in bathrooms, floors, walls, ceilings, etc. with a preparation containing hydrogen peroxide and boric acid, and furthermore, prevents the regrowth of mold over a long period of time. Regarding prevention.

従来の殺カビ剤としては、塩素系、特に4〜6チの次亜
塩素酸塩を含有する製剤が市販されているが、該製剤は
、激しい塩素臭を放出するため、臭気が部屋全体に充満
し、頭痛や吐気を催させしめる。そのため、該製剤の使
用は、特定の場所、例えば浴室等、すぐに水洗できる場
所に限定されていた。仁のように、核製剤は、その臭気
、または、該製剤の残留による処理部位の変色のために
否応なしK、処理後、速やかに水で洗い落さなければな
らないため、殺カビ力はあっても、防カビ力は全く期待
できない。また、該製剤は、強い酸化作用を有するため
、金属類を発錆せしめたり、作業者の衣類を損傷せしめ
゛るおそれがある。
As conventional fungicides, preparations containing chlorine, especially 4 to 6 hypochlorites, are commercially available, but these preparations emit a strong chlorine odor, causing the odor to spread throughout the room. It becomes full, causing headaches and nausea. Therefore, the use of this preparation has been limited to specific locations, such as bathrooms, where it can be easily washed with water. Nucleic preparations are unavoidable due to their odor or discoloration of the treated area due to the residue of the preparations, and because they must be washed off with water immediately after treatment, they have little fungicidal power. However, you can't expect any anti-mold ability at all. Furthermore, since the preparation has a strong oxidizing effect, it may cause rusting of metals or damage the clothing of workers.

本発明者等は、無臭の薬剤で殺菌力のある過酸化水素に
注目し、鋭意、検討した結果、過酸化水素とホウ酸を併
用した製剤は、救カピカだけでなく、長期間に渡って、
防カビ力があることを見出し、本発明を完成したヶ 即ち、本発明は、過酸化水素および、硼酸を倉本発明剤
が、殺カビカ罠加えて防カビカを有するのは、本発明剤
は、従来品と異なり、塗布後核剤を拭きとる必要がない
から、核剤の成分の一つである硼酸が処理部位に浸透し
、残留するためと考えられる。
The present inventors focused on hydrogen peroxide, which is an odorless drug and has bactericidal properties, and as a result of intensive study, we found that a formulation containing hydrogen peroxide and boric acid was not only effective, but also effective for a long period of time. ,
They found that it has antifungal properties and completed the present invention.That is, the present invention has hydrogen peroxide and boric acid. Unlike conventional products, there is no need to wipe off the nucleating agent after application, so it is thought that boric acid, one of the components of the nucleating agent, penetrates into the treated area and remains.

本発明剤の成分である過酸化水素の濃度は、6チを越え
ると劇物に該当するし、また、使用時手指に痛覚を受け
る場合もあるので、1〜6チ好ましくは、3〜6%であ
り、硼酸の濃度は、0.5〜3.5チである。
If the concentration of hydrogen peroxide, which is a component of the present agent, exceeds 6%, it is classified as a deleterious substance, and the hands and fingers may feel pain when using it, so the concentration of hydrogen peroxide is preferably 1 to 6%, preferably 3 to 6%. %, and the concentration of boric acid is 0.5 to 3.5%.

本発明剤の使用方法は、単にカビ発生個所に、本発明剤
を塗布し、そのまま放置すればよい(q#別な場合を除
き、本発明剤は拭きとる必要はない)のであるが、カビ
の発生個所は、種々であシ、壁や天井等の場合、本発明
剤を塗布しても、本発明剤はその効果が発揮される前に
、流れ落ちてしまうため、好ましい実施態様としては、
本発明剤に適当な増粘剤を配合することが好ましい。増
粘剤としては、CMC,ヒドロキシグロビルメチルセル
ロース ポリアクリル酸ノーダ、アルギン酸ソーダおよ
びアクリル酸重合体等が上げられるが、増粘剤の種類に
よっては、本発明剤の粘度が経時的に変化(粘度が低下
)してしまう・ため、最も好ましい増粘剤としては、ア
クリル酸重合体が上げられる。更K、該粘度は、本発明
剤のPHK影響されるため、本発明剤は、PH3〜6、
好ましくは4〜5.5に調整されるべきである。
The method of using the present invention agent is to simply apply the present invention agent to the area where mold has grown and leave it as it is (unless otherwise specified, there is no need to wipe off the present invention agent). There are various places where this occurs, such as walls and ceilings, and even if the present invention agent is applied, the present invention agent will wash off before its effect is exerted. Therefore, as a preferred embodiment,
It is preferable to incorporate a suitable thickener into the agent of the present invention. Examples of thickeners include CMC, hydroxyglobil methylcellulose polyacrylic acid, sodium alginate, and acrylic acid polymers, but depending on the type of thickener, the viscosity of the present agent changes over time (viscosity Therefore, the most preferred thickener is an acrylic acid polymer. Moreover, since the viscosity is affected by the PHK of the present agent, the present agent has a pH of 3 to 6,
Preferably it should be adjusted to 4-5.5.

尚、本発明剤の処理部位への浸透性を高める目的で、ア
ニオン系あるいはノニオン系界面活性剤を本発明剤に配
合すると効果的であり、又、本発明剤の成分の一つであ
る過酸化水素の安定剤として、8−オキシキノリン、各
種リン酸塩等の各種安定剤を配合することKより、本発
明剤の貯蔵安定性を改善することができる。
In addition, for the purpose of increasing the permeability of the present agent to the treated area, it is effective to add an anionic or nonionic surfactant to the present agent. The storage stability of the agent of the present invention can be improved by incorporating various stabilizers such as 8-oxyquinoline and various phosphates as stabilizers for hydrogen oxide.

本発明剤は、スプレー方式でどんな細部にも、手を全く
汚さず塗布でき、かつ、塗布後は、そのtま放置すれば
殺カビ、され、更には、防カビ力も保持されるもので、
簡易かつ安全な殺カビ剤となる。
The agent of the present invention can be applied to any detail by spray method without getting your hands dirty at all, and after application, if you leave it for a while, it will kill mold, and furthermore, it will retain its anti-mold ability.
It is a simple and safe fungicide.

以下に本発明を実施例で説明する。The present invention will be explained below using examples.

参考例 過酸化水素6%、硼酸3%、8−オキシキノリン150
Ppmの混合液に各々の増粘剤を加えPH5,5にNa
OHで調整し、増粘剤の評1価を行った。
Reference example Hydrogen peroxide 6%, boric acid 3%, 8-oxyquinoline 150
Add each thickener to the Ppm mixture and adjust the pH to 5.5 with Na.
Adjustment was made with OH, and a first evaluation of the thickener was performed.

第1表 *1 重合度 2700〜7500 *2 商品名[ハイビスワコ−105J(和光化成■品
)として市販 *31力月後の粘度安定性(視覚による判定)実施例1 増粘剤として参考例墓5のアクリル酸重合体を用いて下
記の組成物を製造し、Ht Ot の安定性及び浴室の
天井(材質:シージングボード)のカビ除去を試みた。
Table 1 *1 Degree of polymerization 2700-7500 *2 Product name [Commercially available as Hibiswako-105J (Wako Kasei product) *Viscosity stability after 31 months (visual judgment) Example 1 Reference example as a thickener The following composition was prepared using the acrylic acid polymer No. 5, and an attempt was made to improve the stability of Ht Ot and to remove mold from a bathroom ceiling (material: sheathing board).

NaOHPH5,5 *4 花王アトラス社製 アニオン界面活性剤カビの除
去試験は、比較例1として上記の組成物の中の硼酸を除
いた物、また比較例2として市販されている次亜塩素酸
ソーダ(有効塩素4チ)の′カビ取り剤を取り上けた。
NaOHPH5,5 *4 Manufactured by Kao Atlas Co., Ltd. The anionic surfactant mold removal test was conducted using the above composition with boric acid removed as Comparative Example 1, and commercially available sodium hypochlorite as Comparative Example 2. (available chlorine: 4 t)' mold remover.

結果は第2表のごとくであったが、比較例2は粘稠性が
ないために液が流れ落ちてしまい、思うような処理がで
きず、5途中で断念した。
The results were as shown in Table 2, but in Comparative Example 2, the liquid ran down due to lack of viscosity, and the desired treatment could not be performed, so the treatment was abandoned halfway through.

(注)回数とは、カビ発生部全面にスプレーで薬剤を塗
布し、その後その表面がよく乾燥した時、その表面をよ
く観察し、カビかのこっている時は、ふたたびスプレー
で塗布する。その回数をいう。
(Note) The number of times refers to spraying the chemical over the entire surface of the mold-infested area, then observing the surface carefully when it has dried thoroughly, and spraying again if mold is present. The number of times.

尚、 H,0,の安定性は95℃水浴中で液温か上昇後
15〜20分間加温し、その際のH20t の分解をガ
ス発生量で判定する方法であるが、これによると分解は
全く見られず、安定性は、著しく優れていることが言え
る。
The stability of H,0, is determined by heating it in a 95°C water bath for 15 to 20 minutes after the liquid temperature rises, and determining the decomposition of H20t by the amount of gas generated at that time. It can be said that the stability is extremely excellent.

実施例2゜ 実施例1と同組成物で押入れの壁(材質、ベニヤ板)の
カビ除去を試みた。比較例3として、同組成物中の硼酸
を除いたもの、又比較例4として、市販されている次亜
塩素酸ソーダ(有効塩素4.0チ)のカビ取り剤を取り
上げた。結果は、第3表の通りであった。
Example 2 An attempt was made to remove mold from the wall of a closet (material: plywood) using the same composition as in Example 1. As Comparative Example 3, the same composition without boric acid was used, and as Comparative Example 4, a commercially available mold remover of sodium hypochlorite (available chlorine: 4.0 H) was used. The results were as shown in Table 3.

Claims (1)

【特許請求の範囲】 1、 過酸化水素および硼酸を含有することを特徴とす
る防カビカを有する殺カビ剤。 2、増粘剤としてアクリル酸重合体を含有する特許請求
の範囲第1項記載の殺カビ剤。 3、Pl−1範囲が3〜6の特許請求の範囲第1.2項
記載の殺カビ剤。
[Scope of Claims] 1. A fungicide having a fungicide characterized by containing hydrogen peroxide and boric acid. 2. The fungicide according to claim 1, which contains an acrylic acid polymer as a thickener. 3. The fungicide according to claim 1.2, having a Pl-1 range of 3 to 6.
JP137784A 1984-01-10 1984-01-10 Fungicide Pending JPS60146807A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP137784A JPS60146807A (en) 1984-01-10 1984-01-10 Fungicide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP137784A JPS60146807A (en) 1984-01-10 1984-01-10 Fungicide

Publications (1)

Publication Number Publication Date
JPS60146807A true JPS60146807A (en) 1985-08-02

Family

ID=11499793

Family Applications (1)

Application Number Title Priority Date Filing Date
JP137784A Pending JPS60146807A (en) 1984-01-10 1984-01-10 Fungicide

Country Status (1)

Country Link
JP (1) JPS60146807A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61158907A (en) * 1985-01-07 1986-07-18 Kao Corp Mildew-removing agent composition
US4988500A (en) * 1989-09-29 1991-01-29 The Procter & Gamble Company Oral compositions
JP2001503768A (en) * 1996-11-13 2001-03-21 ザ、プロクター、エンド、ギャンブル、カンパニー Disinfecting composition for spray and method for disinfecting surface using the same
WO2003059069A1 (en) * 2002-01-18 2003-07-24 Novartis Ag Methods for preserving ophthalmic solutions and preserved ophtalmic solutions

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61158907A (en) * 1985-01-07 1986-07-18 Kao Corp Mildew-removing agent composition
US4988500A (en) * 1989-09-29 1991-01-29 The Procter & Gamble Company Oral compositions
JP2001503768A (en) * 1996-11-13 2001-03-21 ザ、プロクター、エンド、ギャンブル、カンパニー Disinfecting composition for spray and method for disinfecting surface using the same
WO2003059069A1 (en) * 2002-01-18 2003-07-24 Novartis Ag Methods for preserving ophthalmic solutions and preserved ophtalmic solutions

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