JPH07100767B2 - Antifungal bactericidal paint composition - Google Patents

Antifungal bactericidal paint composition

Info

Publication number
JPH07100767B2
JPH07100767B2 JP2219011A JP21901190A JPH07100767B2 JP H07100767 B2 JPH07100767 B2 JP H07100767B2 JP 2219011 A JP2219011 A JP 2219011A JP 21901190 A JP21901190 A JP 21901190A JP H07100767 B2 JPH07100767 B2 JP H07100767B2
Authority
JP
Japan
Prior art keywords
antifungal
weight
bactericidal
composition
paint
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 - Fee Related
Application number
JP2219011A
Other languages
Japanese (ja)
Other versions
JPH04103501A (en
Inventor
茂斗志 吉田
政司 吉田
Original Assignee
ミルドゥ産業株式会社
茂斗志 吉田
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 ミルドゥ産業株式会社, 茂斗志 吉田 filed Critical ミルドゥ産業株式会社
Priority to JP2219011A priority Critical patent/JPH07100767B2/en
Publication of JPH04103501A publication Critical patent/JPH04103501A/en
Publication of JPH07100767B2 publication Critical patent/JPH07100767B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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、防カビ殺菌塗料組成物に関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial field of application> The present invention relates to a fungicide bactericidal coating composition.

<従来の技術> 建築物、特に台所、風呂場等に発生するカビが人体にも
影響を及ぼすことは既に明らかにされており、従来より
カビを防止する防カビ剤については種々研究がなされて
いる。
<Prior Art> It has already been clarified that molds that occur in buildings, particularly kitchens and bathrooms, affect the human body, and various studies have been conducted on mold inhibitors that prevent molds. There is.

しかしながら、従来の防カビ剤の多くは、カビに対して
殺菌効果を有する薬品等の検討又は一般にカビの発生す
る温度、湿度、栄養分、酸素等の条件を抑制する方法の
研究がなされているにすぎない。即ち、最終的に発生す
るカビに対しての防止効果又は殺菌効果を有する防カビ
剤の開発が大部分であって、カビが発生する以前の微生
物が建築物等に付着する点について検討された防カビ剤
については知られていないのが現状である。
However, many of the conventional fungicides have been investigated such as chemicals having a bactericidal effect against fungi, or generally, methods for suppressing the conditions such as temperature, humidity, nutrients, oxygen, etc. in which fungi are generated. Only. That is, most of the development of antifungal agents having a preventive effect or a bactericidal effect against the fungus finally generated, was examined on the point that the microorganisms before the fungus adheres to the building etc. At present, there is no known antifungal agent.

また従来の防カビ剤において、噴霧又は塗布等を行っ
て、被処理物に付着させ使用する親水性の防カビ剤で
は、該被処理物に対する密着性が少ないために、長期に
わたる防カビ効果が期待できない。更に通常の防カビ剤
は、殺菌効果が少ないために、予じめ被処理物の下地を
殺菌処理しなければならず、作業が煩雑化するという欠
点がある。また疏水性の防カビ剤も知られているが、該
疏水性の防カビ剤では、例えば水を多く使用する場所に
発生するシュードモナス(Pseudomonas)菌等のグラム
陰性菌には効果がないという欠点がある。
Further, in the conventional antifungal agent, spraying or coating is performed, and a hydrophilic antifungal agent that is used by adhering to the object to be treated has little adhesion to the object to be treated, and thus has a long-term antifungal effect. I can't expect. Further, since ordinary fungicides have a small bactericidal effect, there is a drawback that the base of the object to be treated has to be sterilized in advance and the work becomes complicated. Hydrophobic antifungal agents are also known, but the hydrophobic antifungal agent has a drawback that it is ineffective against Gram-negative bacteria such as Pseudomonas bacteria which occur in places where much water is used. There is.

一方更にまた、塗料と混合して優れた効果を示す防カビ
剤としては、ジクロロフルアニド等が知られている。し
かしながら、従来、塗料と防カビ剤との混合物は、貯蔵
安定性が乏しいため、被処理物に塗布する直前に混合す
る必要性があり、また塗布時に均一に混合されていない
場合には、塗布後剥離等が生じるという欠点がある。
On the other hand, dichlorofluanid and the like are known as antifungal agents which show excellent effects when mixed with a paint. However, conventionally, a mixture of a paint and an antifungal agent has poor storage stability, so it is necessary to mix it immediately before applying it to the object to be treated, and when it is not uniformly mixed at the time of application, it is necessary to apply it. There is a drawback that post-peeling occurs.

<発明が解決しようとする課題> 本発明の目的は、殺菌作用及び防カビ作用を同時に備
え、且つ被処理物に対して優れた接着性を有し、長期に
わたり防カビ効果を得ることができる防カビ殺菌塗料組
成物を提供することにある。
<Problems to be Solved by the Invention> An object of the present invention is to have a bactericidal action and an antifungal action at the same time, and to have excellent adhesiveness to an object to be treated, and to obtain an antifungal effect for a long period of time. An object of the present invention is to provide a fungicidal germicidal coating composition.

本発明の更に別の目的は、貯蔵安定性に優れた防カビ殺
菌塗料組成物を提供することにある。
Still another object of the present invention is to provide a fungicidal antibacterial coating composition having excellent storage stability.

<課題を解決するための手段> 本発明によれば、防カビ剤及びβ−フェノキシエタノー
ルを含むカビの発生防止及び殺菌作用を有する防カビ殺
菌組成物と、塗料と、前記防カビ殺菌組成物及び前記塗
料を硬化時に被処理物から離脱させずに、且つ得られる
塗膜に撥水性を付与する撥水剤とを含むことを特徴とす
る防カビ殺菌塗料組成物が提供される。
<Means for Solving the Problems> According to the present invention, an antifungal bactericidal composition having an antifungal agent and a fungicidal action containing β-phenoxyethanol and having a bactericidal action, a coating, and the antifungal bactericidal composition and There is provided a fungicidal disinfectant coating composition comprising a water repellent agent that imparts water repellency to an obtained coating film without allowing the coating material to separate from the object to be treated during curing.

以下本発明を更に詳細に説明する。The present invention will be described in more detail below.

本発明に用いる防カビ殺菌組成物において、必須の成分
として含有するβ−フェノキシエタノールは、防カビ殺
菌塗料組成物中に混合される各種成分に対し、溶媒とし
て作用し、且つ例えば従来の殺菌剤に対して強い耐性を
示すことが知られている緑膿菌に対しても優れた殺菌作
用及び不快臭に対する消臭作用を備えた安全性の高いグ
リコールエーテル類の一種であり、しかも該防カビ殺菌
組成物と塗料とを混合する際に優れた相溶性を示す物質
である。該β−フェノキシエタノールの配合割合は、防
カビ殺菌塗料組成物中に好ましくは1〜10重量%、特に
好ましくは2〜5重量%の範囲である。前記配合割合が
1重量%未満の場合には、菌に対して優れた殺菌作用を
示さず、更には塗料を混合する際に相溶性が低下するの
で好ましくない。また10重量%を超える場合は、乾燥性
が悪く、更には粘度が過大に増幅し、作業性が著しく低
下するので好ましくない。
In the antifungal bactericidal composition used in the present invention, β-phenoxyethanol contained as an essential component acts on various components mixed in the antifungal bactericidal coating composition as a solvent, and, for example, to a conventional bactericide. It is a kind of highly safe glycol ether having excellent bactericidal action against Pseudomonas aeruginosa, which is known to have strong resistance to deodorant and deodorizing action against unpleasant odor, It is a substance that exhibits excellent compatibility when the composition and paint are mixed. The blending ratio of the β-phenoxyethanol is preferably 1 to 10% by weight, and particularly preferably 2 to 5% by weight in the antifungal bactericidal coating composition. If the blending ratio is less than 1% by weight, excellent bactericidal action against bacteria is not exhibited, and further, compatibility is deteriorated when mixing paints, which is not preferable. On the other hand, if it exceeds 10% by weight, the drying property is poor, the viscosity is excessively increased, and the workability is remarkably reduced, which is not preferable.

本発明に用いる防カビ殺菌組成物において、必須の成分
として含有する防カビ剤は、人体に対する毒性がなく、
且つカビに対する発育防止効果及び/又は殺菌効果を有
する公知の防カビ剤であれば、特に限定されるものでは
なく、例えば殺菌成分、細菌又は眞菌(カビ)の発育を
阻止する成分を、溶剤に溶解した公知の防菌、防カビ剤
等を用いることができる。前記殺菌成分、細菌又は眞菌
(カビ)の発育を阻止する成分としては、2−(4−チ
アゾリル)ベンツイミダゾール、N,N−ジメチル−N′
−フェニル−N′−(フルオロジクロロメチルチオ)ス
ルホアミド、1−[(ジヨードメチル)スルホニル]−
4−メチルベンゼン、ジクロロフルアニド、ジクロロフ
ェニル及びこれらの混合物等から成る群より選択される
公知の安全性が確認されている化合物を好ましく用いる
ことができる。該成分の使用量は、各成分の最低有効濃
度以上であればよく、防カビ殺菌塗料組成物に対して0.
3〜5重量%の範囲で用いることができ、特に好ましく
は、2−(4−チアゾリル)ベンツイミダゾールの場合
0.3〜1重量%、N,N−ジメチル−N′−フェニル−N′
−(フルオロジクロロメチルチオ)スルホアミドの場合
1〜2重量%、1−[(ジヨードメチル)スルホニル]
−4−メチルベンゼン、ジクロロフェニル又はジクロロ
フルアニドの場合0.3〜2重量%であるのが望ましい。
この際0.3重量%未満の場合には、所望の殺菌又は発育
阻止効果が得られない恐れがあるので好ましくない。
In the antifungal bactericidal composition used in the present invention, the antifungal agent contained as an essential component has no toxicity to the human body,
And, if it is a known antifungal agent having a growth-preventing effect and / or bactericidal effect against mold, it is not particularly limited, for example, a bactericidal component, a component that inhibits the growth of bacteria or fungi (mold), a solvent. Well-known antibacterial and antifungal agents dissolved in can be used. As the bactericidal component, a component for inhibiting the growth of bacteria or fungi (mold), 2- (4-thiazolyl) benzimidazole, N, N-dimethyl-N '
-Phenyl-N '-(fluorodichloromethylthio) sulfoamide, 1-[(diiodomethyl) sulfonyl]-
A publicly known and confirmed safe compound selected from the group consisting of 4-methylbenzene, dichlorofluanide, dichlorophenyl and mixtures thereof can be preferably used. The amount of the component used may be at least the minimum effective concentration of each component, and is 0.
It can be used in the range of 3 to 5% by weight, and particularly preferably in the case of 2- (4-thiazolyl) benzimidazole.
0.3-1% by weight, N, N-dimethyl-N'-phenyl-N '
1-2% by weight in the case of-(fluorodichloromethylthio) sulfoamide, 1-[(diiodomethyl) sulfonyl]
In the case of -4-methylbenzene, dichlorophenyl or dichlorofluoranide, it is preferably 0.3 to 2% by weight.
At this time, if it is less than 0.3% by weight, the desired sterilization or growth inhibition effect may not be obtained, which is not preferable.

本発明に用いる防カビ殺菌組成物において、必要に応じ
て含有させることができる第4級アンモニウム塩は、静
電気の発生を防止し、且つ微生物に対して細菌効果を有
する成分である。該第4級アンモニウム塩は、帯電防止
作用及び細菌作用を有し、且つ防カビ細菌組成物中の他
の成分と相溶性を示すものであれば特に限定されるもの
ではなく、例えば、オクチルトリメチルアンモニウムク
ロライド、デシルトリメチルアンモニウムクロライド、
ドデシルトリメチルアンモニウムクロライド、テトラデ
シルトリメチルアンモニウムクロライド、ヘキサデシル
トリメチルアンモニウムクロライド、オクタデシルトリ
メチルアンモニウムクロライド、オクタデセニルトリメ
チルアンモニウムクロライド、オクタデカジエニルトリ
メチルアンモニウムクロライド等のアルキルトリメチル
アンモニウム塩;ジオクチルトリメチルアンモニウムク
ロライド、ジデシルトリメチルアンモニウムクロライ
ド、ジドデシルトリメチルアンモニウムクロライド、ジ
テトラデシルトリメチルアンモニウムクロライド、ジヘ
キサデシルトリメチルアンモニウムクロライド、ジオク
タデシルトリメチルアンモニウムクロライド、ジオクタ
デセニルトリメチルアンモニウムクロライド、ジオクタ
デカジエニルトリメチルアンモニウムクロライド等のジ
アルキルジメチルアンモニウム塩等を好ましく挙げるこ
とができ、使用に際しては、単独若しくは混合物として
用いることができる。また市販品を用いることも可能で
あり、例えば商品名「ARQUD C−50」,「ARQUD S−
50」,「アーモスタット310」,「アーモスタット410」
(ライオンアクゾ株式会社製)等を好適に使用すること
ができる。前記第4級アンモニウム塩の配合割合は、防
カビ殺菌塗料組成物中に10重量%以下、特に1〜5重量
%の範囲で含有するのが望ましい。
The quaternary ammonium salt that can be contained as necessary in the antifungal bactericidal composition used in the present invention is a component that prevents the generation of static electricity and has a bacterial effect on microorganisms. The quaternary ammonium salt is not particularly limited as long as it has an antistatic action and a bacterial action and is compatible with other components in the antifungal bacterial composition, and for example, octyltrimethyl. Ammonium chloride, decyltrimethylammonium chloride,
Alkyltrimethylammonium salts such as dodecyltrimethylammonium chloride, tetradecyltrimethylammonium chloride, hexadecyltrimethylammonium chloride, octadecyltrimethylammonium chloride, octadecenyltrimethylammonium chloride, octadecadienyltrimethylammonium chloride; dioctyltrimethylammonium chloride, dioctyltrimethylammonium chloride Decyltrimethylammonium chloride, didodecyltrimethylammonium chloride, ditetradecyltrimethylammonium chloride, dihexadecyltrimethylammonium chloride, dioctadecyltrimethylammonium chloride, dioctadecenyltrimethylammonium chloride, dioctadecadienyl trimethyl Can be preferably exemplified Le ammonium chloride dialkyl dimethyl ammonium salts such as chloride, etc., in use, it can be used alone or as a mixture. It is also possible to use a commercially available product, for example, product names “ARQUD C-50” and “ARQUD S-
50 "," Armostat 310 "," Armostat 410 "
(Manufactured by Lion Akzo Co., Ltd.) and the like can be preferably used. The content of the quaternary ammonium salt in the antifungal bactericidal coating composition is preferably 10% by weight or less, and more preferably 1 to 5% by weight.

本発明に用いる防カビ殺菌組成物を調製するには、前記
β−フェノキシエタノールと、防カビ剤と、必要に応じ
て第4級アンモニウム塩とを、例えばイソプロパノー
ル、エタノール等の殺菌、消毒のための溶剤及び/又は
キシレン、キシロール、アセトン、ミネラルスピリット
等の有機溶剤に、好ましくは28〜45℃の加熱状態で溶解
・混合することにより得ることができる。この際前記溶
剤は必らずしも使用する必要はなく、好ましくは防カビ
殺菌組成物に対して0〜96重量%の範囲で用いることが
できる。
To prepare the antifungal bactericidal composition used in the present invention, the β-phenoxyethanol, an antifungal agent, and optionally a quaternary ammonium salt, for example, sterilization of isopropanol, ethanol, etc., for disinfection It can be obtained by dissolving and mixing in a solvent and / or an organic solvent such as xylene, xylol, acetone and mineral spirit, preferably in a heated state at 28 to 45 ° C. At this time, it is not always necessary to use the solvent, and preferably it can be used in the range of 0 to 96% by weight based on the antifungal sterilizing composition.

本発明に用いる撥水剤は、例えば木材、コンクリート、
モルタル、ブロック、レンガ、素焼タイル、プラスチッ
ク等の被処理物に塗布した際に、内面に深く浸透し、溶
剤の蒸発後は被処理物の毛管壁及び表面に沿ってゲル層
を形成することにより、優れた耐候性及び耐汚染性を有
する防水効果を付与するものとして知られた材料を用い
ることができる。例えばエポキシ樹脂、ポリアミド樹脂
等の防水成分と溶剤との混合物(商品名「ケミストッ
プ」(三井石化産資株式会社製)等)、シラン系の撥水
剤、例えばジメチルシリコーンオイル、メチルハイドロ
ジエンポリシロキサン、メチルフェニルシリコーンオイ
ル等の公知の撥水剤を挙げることができる(商品名「KF
96L」、「KF99」、「KP360」、「KF96」、「KF96H」、
「KF69」、「KF92」、「KC89」、「TSF437」、「TSF48
4」、「TSF483」(以上信越化学工業株式会社製)
等)。このような作用を示すことが知られた撥水剤を本
発明の防カビ殺菌塗料組成物に配合することによって、
撥水剤が前記防カビ殺菌組成物の分子に付着して、被処
理物に塗布した後に、時間の経過と共に生ずる前記防カ
ビ殺菌組成物の剥離を防止し、且つ得られる塗膜に撥水
性を付与することができる。また撥水剤の防カビ殺菌塗
料組成物への混合は、前記防カビ殺菌組成物中のβ−フ
ェノキシエタノールの共存により容易に行うことができ
る。
Water repellent used in the present invention, for example, wood, concrete,
When applied to mortar, blocks, bricks, unglazed tiles, plastics, etc., it penetrates deeply into the inner surface, and after evaporation of the solvent forms a gel layer along the capillary wall and surface of the object to be treated. Therefore, a material known to impart a waterproof effect having excellent weather resistance and stain resistance can be used. For example, a mixture of a waterproof component such as an epoxy resin and a polyamide resin and a solvent (trade name "Chemist" (manufactured by Mitsui Kasansan Co., Ltd.)), a silane-based water repellent such as dimethyl silicone oil, methylhydrogen poly Known water repellents such as siloxane and methylphenyl silicone oil can be mentioned (trade name "KF
96L "," KF99 "," KP360 "," KF96 "," KF96H ",
"KF69", "KF92", "KC89", "TSF437", "TSF48"
4 "," TSF483 "(Made by Shin-Etsu Chemical Co., Ltd.)
etc). By incorporating a water repellent known to exhibit such an action into the antifungal bactericidal coating composition of the present invention,
A water repellent adheres to the molecules of the antifungal sterilizing composition, prevents peeling of the antifungal bactericidal composition that occurs over time after being applied to an object to be treated, and makes the resulting coating film water repellent. Can be given. Further, the mixing of the water repellent with the antifungal sterilizing coating composition can be easily carried out by coexistence of β-phenoxyethanol in the antifungal sterilizing composition.

撥水剤の含有割合は、防カビ殺菌塗料組成物全体に対し
て、2〜50重量%であるのが好ましく、特に2〜20重量
%とするのが望ましい。該含有割合が2重量%未満の場
合には、前述の撥水剤の効果が得られず、また50重量%
を超える場合には、防カビ殺菌塗料組成物への混合を十
分行うことができないので好ましくない。
The content of the water repellent is preferably 2 to 50% by weight, and particularly preferably 2 to 20% by weight, based on the entire antifungal sterilizing coating composition. When the content ratio is less than 2% by weight, the above-mentioned effect of the water repellent cannot be obtained, and the content is 50% by weight.
If it exceeds, it is not preferable because it cannot be sufficiently mixed with the antifungal sterilizing coating composition.

本発明の防カビ殺菌塗料組成物に用いる塗料としては、
通常建築物等に使用する公知の塩化ビニル系以外の油性
又は水性塗料等であれば良く、具体的には例えば、酢酸
ビニル系塗料、合成樹脂エマルジョン塗料、アクリル樹
脂エマルジョン塗料、アルキット樹脂塗料等を好ましく
挙げることができる。また塗料の含有割合は、防カビ殺
菌塗料組成物全体に対して、好ましくは10〜95重量%、
特に好ましくは70〜90重量%の範囲であるのが望まし
い。
The paint used in the antifungal sterilizing paint composition of the present invention,
Any oil-based or water-based paint other than the known vinyl chloride-based paint that is usually used for buildings and the like may be used, and specifically, for example, vinyl acetate-based paint, synthetic resin emulsion paint, acrylic resin emulsion paint, alkite resin paint, etc. It can be preferably mentioned. The content ratio of the coating material is preferably 10 to 95% by weight, based on the entire antifungal sterilizing coating composition.
It is particularly preferable that the range is 70 to 90% by weight.

本発明の防カビ殺菌塗料組成物を調製するには、例えば
まず前述の防カビ殺菌組成物を溶解・混合して調製した
後、好ましくは28〜45℃に加熱して塗料に混合させ、次
いで撥水剤を添加して溶解混合することにより得る方法
又は予め撥水剤を、前述の防カビ殺菌組成物に含有させ
ておき、次いで塗料と好ましくは28〜45℃に加熱して混
合する方法等により得ることができる。得られた本発明
の防カビ殺菌塗料組成物は、β−フェノキシエタノール
を含有するので、撥水剤を低温で溶解させることがで
き、しかも長期間にわたり安定に保存することができ
る。
To prepare the antifungal bactericidal coating composition of the present invention, for example, first, after preparing by dissolving and mixing the antifungal bactericidal composition described above, preferably heated to 28 ~ 45 ° C. to be mixed into the paint, then Method obtained by adding a water repellent and dissolving and mixing, or a water repellent is previously contained in the antifungal sterilizing composition, then a method of heating and mixing at 28 to 45 ℃ preferably And the like. Since the obtained antifungal bactericidal coating composition of the present invention contains β-phenoxyethanol, the water repellent can be dissolved at a low temperature and can be stably stored for a long period of time.

本発明の防カビ殺菌塗料組成物を塗装するには、通常の
塗料と同様に被処理物に対してハケ塗り又は噴霧処理等
をすることにより行うことができる。
The antifungal bactericidal coating composition of the present invention can be applied by brushing or spraying the object to be treated in the same manner as in ordinary paints.

<発明の効果> 本発明の防カビ殺菌塗料組成物は、β−フェノキシエタ
ノール及び撥水剤を有するので、防カビ剤成分と塗料成
分との相溶性に優れ、被処理物に対して優れた接着性を
有しており、長期にわたる防カビ効果を期待することが
できる。
<Effects of the Invention> The antifungal bactericidal coating composition of the present invention has β-phenoxyethanol and a water repellent, and therefore has excellent compatibility between the antifungal agent component and the coating component, and excellent adhesion to the object to be treated. It has properties and can be expected to have a long-term antifungal effect.

<実施例> 以下本発明を実施例により更に詳細に説明するが、本発
明はこれらに限定されるものではない。
<Examples> The present invention will be described in more detail with reference to Examples below, but the present invention is not limited thereto.

製造例1 β−フェノキシエタノール20重量部、イソプロピルアル
コール970重量部、2−(4−チアゾリル)ベンツイミ
ダゾール4重量部及びジクロロフルアニド6重量部を常
温で溶解・混合し、防カビ殺菌組成物を調製した。
Production Example 1 20 parts by weight of β-phenoxyethanol, 970 parts by weight of isopropyl alcohol, 4 parts by weight of 2- (4-thiazolyl) benzimidazole and 6 parts by weight of dichlorofluanid are dissolved and mixed at room temperature to prepare an antifungal composition. did.

製造例2 β−フェノキシエタノール60重量部を、イソプロピルア
ルコール500重量部とキシレン275重量部の混合液に添加
し、35℃にて加熱重合した。次いで、2−(4−チアゾ
リル)ベンツイミダゾール6重量部と、ジクロロフルア
ニド14重量部と、ジクロロフェニル5重量部とを添加混
合した後、撥水剤として知られたアクリル樹脂等の数種
類の防水成分と溶剤とからなる商品名「ケミストップ」
(三井石産資株式会社製)120重量部と、第4アンモニ
ウム塩として「アーカードC50」(ライオン株式会社
製)20重量部とを添加混合して防カビ殺菌組成物と撥水
剤との混合物を調製した。
Production Example 2 60 parts by weight of β-phenoxyethanol was added to a mixed solution of 500 parts by weight of isopropyl alcohol and 275 parts by weight of xylene, and heat-polymerized at 35 ° C. Then, 6 parts by weight of 2- (4-thiazolyl) benzimidazole, 14 parts by weight of dichlorofluanid and 5 parts by weight of dichlorophenyl were added and mixed, and then several kinds of waterproof components such as acrylic resin known as a water repellent agent were used. Product name "Chemistop" consisting of solvent and solvent
120 parts by weight (manufactured by Mitsui Sangyo Co., Ltd.) and 20 parts by weight of "Arcard C50" (manufactured by Lion Co., Ltd.) as a quaternary ammonium salt are added and mixed to obtain a mixture of a fungicide-proof composition and a water repellent. Was prepared.

実施例1 イソプロピルアルコール520重量部に、キシレン190重量
部とβ−フェノキシエタノール100重量部とを混合し、5
0℃にて加温した後、2−(4−チアゾリル)ベンツイ
ミダゾール10重量部と、ジクロロフルアニド25重量部
と、ジクロロフェニル25重量部とを溶解・混合して防カ
ビ殺菌組成物を調製した。次いで得られた防カビ殺菌組
成物に、常温撥水剤であるジメチルシリコンオイル(商
品名「KC89」)120重量部及びメチルフェニルシリコン
オイル(商品名「KP 360」)10重量部(以上、信越化
学工業株式会社製)を添加混合し、得られた組成物200
重量部を、アクリル系合成塗料(商品名「シントップGP
P4−401」神東塗料株式会社製)800重量部に添加し
て、30分間、均一相に成るように攪拌し、防カビ殺菌塗
料組成物を調製した。得られた組成物は、塗料中に防カ
ビ殺菌組成物が均一に溶解されたものであった。
Example 1 520 parts by weight of isopropyl alcohol was mixed with 190 parts by weight of xylene and 100 parts by weight of β-phenoxyethanol, and 5
After heating at 0 ° C., 10 parts by weight of 2- (4-thiazolyl) benzimidazole, 25 parts by weight of dichlorofluanid, and 25 parts by weight of dichlorophenyl were dissolved and mixed to prepare an antifungal bactericidal composition. . Then, 120 parts by weight of dimethyl silicone oil (trade name "KC89") which is a water-repellent agent at room temperature and 10 parts by weight of methylphenyl silicone oil (trade name "KP 360") (above, Shin-Etsu) Chemical Industry Co., Ltd.) was added and mixed to obtain the composition 200.
By weight, acrylic synthetic paint (trade name "Shintop GP
P4-401 "(manufactured by Shinto Paint Co., Ltd.) was added to 800 parts by weight and stirred for 30 minutes so as to form a uniform phase, to prepare an antifungal bactericidal paint composition. The composition obtained was one in which the antifungal bactericidal composition was uniformly dissolved in the paint.

実施例2 既にカビの発生が認められる水を大量に使用する食品工
場の壁及び天井を、次亜塩素酸ナトリウムを含む除カビ
液で洗浄した後、実施例1で調製した防カビ殺菌塗料組
成物を、220g/m2の割合で塗布した。また比較として、
β−フェノキシエタノールを含まない市販の防カビ塗料
(商品名「浴室用カビ止め塗料」アサヒペン株式会社
製)を同様な条件で塗布し、カビの発生状態を観察し
た。その結果を表1に示す。尚市販の防カビ塗料では、
カビの発生と共に塗料の剥離も認められた。
Example 2 After the walls and ceiling of a food factory that uses a large amount of water in which mold has already been generated are washed with a mold removal solution containing sodium hypochlorite, the mold bactericidal paint composition prepared in Example 1 The product was applied at a rate of 220 g / m 2 . For comparison,
A commercially available antifungal paint containing no β-phenoxyethanol (trade name “Bathroom antifungal paint” manufactured by Asahi Pen Co., Ltd.) was applied under the same conditions, and the mold generation state was observed. The results are shown in Table 1. In addition, in the commercially available anti-mold paint,
Along with the generation of mold, peeling of the paint was also recognized.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭60−232161(JP,A) 特開 昭60−1102(JP,A) 特開 昭50−82233(JP,A) ─────────────────────────────────────────────────── ─── Continuation of front page (56) References JP-A-60-232161 (JP, A) JP-A-60-1102 (JP, A) JP-A-50-82233 (JP, A)

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】防カビ剤及びβ−フェノキシエタノールを
含むカビの発生防止及び殺菌作用を有する防カビ殺菌組
成物と、塗料と、前記防カビ殺菌組成物及び前記塗料を
硬化時に被処理物から離脱させずに、且つ得られる塗膜
に撥水性を付与する撥水剤とを含むことを特徴とする防
カビ殺菌塗料組成物。
1. A fungicidal sterilizing composition containing a fungicide and β-phenoxyethanol for preventing the generation of fungi and having a bactericidal action, a paint, and the fungicidal sterilizing composition and the paint are separated from an object to be treated during curing. A fungicidal sterilizing coating composition comprising a water-repellent agent which imparts water repellency to a coating film obtained without being applied.
【請求項2】前記防カビ殺菌組成物が、第4級アンモニ
ウム塩を含むことを特徴とする請求項第1記載の防カビ
殺菌塗料組成物。
2. The antifungal bactericidal coating composition according to claim 1, wherein the antifungal bactericidal composition contains a quaternary ammonium salt.
JP2219011A 1990-08-22 1990-08-22 Antifungal bactericidal paint composition Expired - Fee Related JPH07100767B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2219011A JPH07100767B2 (en) 1990-08-22 1990-08-22 Antifungal bactericidal paint composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2219011A JPH07100767B2 (en) 1990-08-22 1990-08-22 Antifungal bactericidal paint composition

Publications (2)

Publication Number Publication Date
JPH04103501A JPH04103501A (en) 1992-04-06
JPH07100767B2 true JPH07100767B2 (en) 1995-11-01

Family

ID=16728863

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2219011A Expired - Fee Related JPH07100767B2 (en) 1990-08-22 1990-08-22 Antifungal bactericidal paint composition

Country Status (1)

Country Link
JP (1) JPH07100767B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002030830A1 (en) * 2000-10-12 2002-04-18 Moltec Co., Ltd. Method of circulating water in circulatory water tank system and liquid compositions for sterilizing and disinfecting circulatory water tank system
JP2002121595A (en) * 2000-10-12 2002-04-26 Morutetsuku:Kk Washing method for circulation-type water tank system, and detergent composition for circulation-type water tank system
JP2008222696A (en) * 2007-03-08 2008-09-25 Morutetsuku:Kk Antimicrobial deodorant composition and manufacturing method of antimicrobial deodorant

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5319653B2 (en) * 1973-11-27 1978-06-22
GB8311144D0 (en) * 1983-04-25 1983-06-02 Dearborn Chemicals Ltd Biocide
JPS60232161A (en) * 1984-04-28 1985-11-18 日本ケミコ−ト化成株式会社 Oil film type antiseptic deodorant

Also Published As

Publication number Publication date
JPH04103501A (en) 1992-04-06

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