JPH0761921B2 - Anti-algal and anti-mildew formulation - Google Patents

Anti-algal and anti-mildew formulation

Info

Publication number
JPH0761921B2
JPH0761921B2 JP25284590A JP25284590A JPH0761921B2 JP H0761921 B2 JPH0761921 B2 JP H0761921B2 JP 25284590 A JP25284590 A JP 25284590A JP 25284590 A JP25284590 A JP 25284590A JP H0761921 B2 JPH0761921 B2 JP H0761921B2
Authority
JP
Japan
Prior art keywords
algal
organic solvent
formulation
dimethylformamide
water
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
JP25284590A
Other languages
Japanese (ja)
Other versions
JPH04134001A (en
Inventor
祐二 柳田
年弘 松本
満 中山
Original Assignee
ナガセ化成工業株式会社
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 ナガセ化成工業株式会社 filed Critical ナガセ化成工業株式会社
Priority to JP25284590A priority Critical patent/JPH0761921B2/en
Publication of JPH04134001A publication Critical patent/JPH04134001A/en
Publication of JPH0761921B2 publication Critical patent/JPH0761921B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、均一な溶液としての防藻防黴製剤に関する。TECHNICAL FIELD OF THE INVENTION The present invention relates to antialgal and antifungal formulations as a homogeneous solution.

従来の技術 従来、製紙、化学、金属加工等における冷却水やプロセ
ス水等として多量の水が用いられているが、これら用水
系には微生物の増殖によるスライムが発生しやすく、例
えば、冷却水系では、熱交換器の伝熱効果の低下等の種
々の弊害の原因となつている。また、特に、工業用冷却
用水においては、藻類の発生も多い。このような藻類の
発生も、管を閉塞し、伝熱効率を低下させる。
BACKGROUND ART Conventionally, a large amount of water has been used as cooling water or process water in papermaking, chemistry, metal processing, etc., but slimes due to the growth of microorganisms are easily generated in these water systems, and for example, in cooling water systems. This is a cause of various harmful effects such as a reduction in heat transfer effect of the heat exchanger. Further, especially in industrial cooling water, algae are often generated. The generation of such algae also clogs the tube and reduces the heat transfer efficiency.

更に、微生物や藻類は、水性塗料、溶剤型塗料、コーキ
ング剤、紙塗工液、捺染糊、樹脂ペースト、皮革製品、
樹脂成形品等の原材料や製品にも発生し、生産性を損な
い、また、製品品質を劣化させる。
In addition, microorganisms and algae are water-based paints, solvent-based paints, caulking agents, paper coating liquids, printing pastes, resin pastes, leather products,
It also occurs in raw materials and products such as resin molded products, impairing productivity and degrading product quality.

そこで、従来、種々の防藻剤や防黴剤を用水や原材料、
製品等の所要の対象に加えて、防藻防黴がなされてい
る。しかし、殆どの防藻剤や防黴剤は、水不溶性又は難
溶性の粉末又は液体であるので、通常は、それぞれ乳剤
等の製剤として用いられているが、その分散性、特に、
用水やエマルジヨンのような水系に対する分散性は尚、
不十分である。また、対象が溶剤型塗料や樹脂のような
ときも、一般に、溶解性が小さく、分散性は不十分であ
る。また、粉末の薬剤を直接に塗料等に分散させたとき
は、長時間静置したときに薬剤が沈降しやすい。
Therefore, in the past, various algal and antifungal agents were used for water and raw materials,
In addition to the required objects such as products, anti-algal and anti-mildew is used. However, most of the antialgae and antifungal agents are water-insoluble or sparingly soluble powders or liquids, and thus are usually used as preparations such as emulsions, but their dispersibility, particularly,
Dispersibility in water systems such as water and emulsion is still
Is insufficient. Also, when the object is a solvent-based paint or resin, the solubility is generally small and the dispersibility is insufficient. Further, when a powdered drug is directly dispersed in a paint or the like, the drug tends to settle when left standing for a long time.

しかも、従来、殆どの場合、防藻剤と防黴剤とは、相互
の相溶性が低く、且つ、共通の溶剤が見当たらないの
で、防藻剤と防黴剤とを共に含む溶液状の製剤は、従
来、知られておらず、かかる製剤が強く要望されてい
る。
Moreover, conventionally, in most cases, the antialgal agent and the antifungal agent have low compatibility with each other and no common solvent is found. Therefore, a formulation in a solution form containing both the antialgal agent and the antifungal agent. Has not hitherto been known, and there is a strong demand for such a formulation.

発明が解決しようとする課題 本発明は、上記した要望に応えるためになされたもので
あつて、防藻剤と防黴剤とを共に含む溶液状の製剤を提
供することを目的とする。
DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention The present invention has been made in order to meet the above-mentioned needs, and an object thereof is to provide a solution-form preparation containing both an antialgal agent and a fungicide.

課題を解決するための手段 本発明による防藻防黴製剤は、2−メチルチオ−4−t
−ブチルアミノ−6−シクロプロピルアミノ−s−トリ
アジンと共に、2−n−オクチル−4−イソチアゾリン
−3−オン又は4−クロルフエニル−3−ヨードプロパ
ルギルホルマールとをジメチルホルムアミドをフタル酸
ジエステル、脂肪族二塩基酸ジエステル、リン酸トリエ
ステル、グリコールエステル及びエポキシ脂肪酸エステ
ルから選ばれる少なくとも1種のエステル化合物とアミ
ド、ケトン及びエーテルから選ばれる少なくとも1種の
有機溶剤とからなる混合溶剤に溶解してなることを特徴
とする。
Means for Solving the Problems The antialgal and antifungal preparation according to the present invention comprises 2-methylthio-4-t
-Butylamino-6-cyclopropylamino-s-triazine together with 2-n-octyl-4-isothiazolin-3-one or 4-chlorophenyl-3-iodopropargylformal with dimethylformamide phthalate diester, aliphatic diester. Dissolved in a mixed solvent consisting of at least one ester compound selected from basic acid diesters, phosphoric acid triesters, glycol esters and epoxy fatty acid esters and at least one organic solvent selected from amides, ketones and ethers. Is characterized by.

従来、知られている防藻剤は、前述したように、殆どが
水不溶性若しくは難溶性である。本発明においても、こ
のように水不溶性若しくは難溶性の防藻剤として、2−
メチルチオ−4−t−ブチルアミノ−6−シクロプロピ
ルアミノ−s−トリアジンが用いられる。この化合物を
有効成分とする防藻剤は、チバ・ガイギー社製イルガロ
ール1051(登録商標)としてよく知られている。
Most of the conventionally known algae inhibitors are water-insoluble or sparingly soluble, as described above. Also in the present invention, as such a water-insoluble or sparingly soluble anti-algal agent, 2-
Methylthio-4-t-butylamino-6-cyclopropylamino-s-triazine is used. An anti-algal agent containing this compound as an active ingredient is well known as Irgalol 1051 (registered trademark) manufactured by Ciba-Geigy.

また、従来、知られている防黴剤も、前述したように、
殆どが水不溶性若しくは難溶性であつて、本発明におい
ては、このように、水不溶性若しくは難溶性である防黴
剤として、2−n−オクチル−4−イソチアゾリン−3
−オンが用いられる。この化合物を有効成分とする防黴
剤は、例えば、ローム・アンド・ハース社製スケンM−
8(登録商標)としてよく知られている。また、4−ク
ロルフエニル−3−ヨードプロパルギルホルマールも本
発明において藻ことができる防黴剤の有用な例である。
この化合物を有効成分とする防黴剤は、ナガセ化成工業
(株)製IF−1000Sとして知られている。
In addition, conventionally known fungicides, as described above,
Most of them are water-insoluble or sparingly soluble, and in the present invention, 2-n-octyl-4-isothiazoline-3 is thus used as a mildewproofing agent which is water-insoluble or sparingly soluble.
-On is used. An antifungal agent containing this compound as an active ingredient is, for example, Sken M-, manufactured by Rohm and Haas Company.
8 (registered trademark). In addition, 4-chlorophenyl-3-iodopropargylformal is also a useful example of a fungicide that can be algae in the present invention.
A fungicide containing this compound as an active ingredient is known as IF-1000S manufactured by Nagase Kasei Co., Ltd.

本発明においては、上記したような水不溶性若しくは難
溶性の防藻剤及び防黴剤の共通溶剤として、脂肪族二塩
基酸ジエステル、リン酸トリエステル、グリコールエス
テル及びエポキシ脂肪酸エステルから選ばれる少なくと
も1種のエステル化合物とアミド、ケトン及びエーテル
から選ばれる少なくとも1種の有機溶剤とからなる混合
溶剤が用いられる。
In the present invention, at least one selected from aliphatic dibasic acid diesters, phosphoric acid triesters, glycol esters and epoxy fatty acid esters as a common solvent for the above water-insoluble or sparingly soluble algae-proofing agents and fungicides. A mixed solvent composed of one kind of ester compound and at least one kind of organic solvent selected from amide, ketone and ether is used.

特に、溶剤として上記エステル化合物を単独で用いれ
ば、防藻剤及び防黴剤を同時にそれに溶解させ難い場合
があるが、本発明に従って、上記エステル化合物と共に
上記有機溶剤を用いることによって、防藻剤と防黴剤と
を同時にこれらに容易に溶解させることができる。
In particular, if the ester compound alone is used as a solvent, it may be difficult to simultaneously dissolve the algae-proofing agent and the mildew-proofing agent therein, but according to the present invention, by using the organic solvent together with the ester compound, the algae-proofing agent And the fungicide can be easily dissolved in these at the same time.

上記エステル類は樹脂工業の分野において可塑剤として
知られている物質であつて、本発明においては、例え
ば、フタル酸ジブチル、フタル酸ジオクチル、アジピン
酸ジ(2−エチルヘキシル)、リン酸トリメチル、リン
酸トリ(2−エチルヘキシル)、アジピン酸と1,3−ブ
チレングリコールとのポリエステル、エポキシ化大豆油
等が好適に用いられる。
The above-mentioned esters are substances known as plasticizers in the field of resin industry, and in the present invention, for example, dibutyl phthalate, dioctyl phthalate, di (2-ethylhexyl) adipate, trimethyl phosphate, phosphorus Tri (2-ethylhexyl) acid, a polyester of adipic acid and 1,3-butylene glycol, epoxidized soybean oil and the like are preferably used.

また、上記有機溶剤は、特に限定されるものではない
が、特に、ジメチルホルムアミド、ジメチルアセトアミ
ド、N−メチル−2−ピロリドン等のアミド類、シクロ
ヘキサノン等のケトン類、テトラヒドロフラン等のエー
テル類が好ましく用いられる。これら以外にも、例え
ば、ブチルセロソルブ、プロピレングリコール、テルペ
ン類、2,2,4−トリメチルペンタン−1,3−ジオールモノ
イソブチレート等も溶剤として用いることができる。
Further, the organic solvent is not particularly limited, but amides such as dimethylformamide, dimethylacetamide, N-methyl-2-pyrrolidone, ketones such as cyclohexanone, ethers such as tetrahydrofuran are preferably used. To be Other than these, for example, butyl cellosolve, propylene glycol, terpenes, 2,2,4-trimethylpentane-1,3-diol monoisobutyrate and the like can be used as the solvent.

本発明による製剤は、通常、防藻剤5〜20重量部、防黴
剤10〜30重量部、有機溶剤20〜40重量部及び可塑剤35〜
55重量部からなる。
The formulation according to the present invention usually comprises 5 to 20 parts by weight of an antialgal agent, 10 to 30 parts by weight of antifungal agent, 20 to 40 parts by weight of an organic solvent and 35 to
It consists of 55 parts by weight.

本発明による製剤の製造に際しては、界面活性剤を必要
としない。
No surfactant is required in the preparation of the formulations according to the invention.

発明の効果 本発明による防藻防黴製剤は、それぞれ水不溶性若しく
は難溶性の防藻剤である2−メチルチオ−4−t−ブチ
ルアミノ−6−シクロプロピルアミノ−s−トリアジン
と、防黴剤である2−n−オクチル−4−イソチアゾリ
ン−3−オン又は4−クロルフエニル−3−ヨードプロ
パルギルホルマールとが可塑剤と有機溶剤とからなる混
合物に均一に溶解してなる油性の溶液状の製剤であるの
で、多くの適用対象にすぐれた分散性を有する。
EFFECTS OF THE INVENTION The antialgal and antifungal formulation according to the present invention comprises 2-methylthio-4-t-butylamino-6-cyclopropylamino-s-triazine, which is a water-insoluble or sparingly soluble antialgal agent, and a fungicide. 2-n-octyl-4-isothiazolin-3-one or 4-chlorophenyl-3-iodopropargylformal is uniformly dissolved in a mixture of a plasticizer and an organic solvent to prepare an oily solution. Therefore, it has excellent dispersibility for many applications.

例えば、適用対象が溶剤型塗料や樹脂成形品のときは、
本発明による製剤が油性の溶液であることから、それら
への親和性にすぐれ、分散が非常に容易である。また、
安定な分散状態が長期間にわたって保持される。他方、
適用対象がエマルジョンン系のときは、製剤の配合量
は、通常、少量であるので、容易に分散され、しかも、
製剤自体は、水不溶性若しくは難溶性のままであるの
で、耐水性が高く、例えば、塗料塗膜や樹脂成形品にお
いて防藻及び防黴の効果が長期間にわたつて保持され
る。
For example, if the target is solvent-based paint or resin molded product,
Since the preparation according to the present invention is an oily solution, it has excellent affinity for them and is very easy to disperse. Also,
A stable dispersion state is maintained for a long period of time. On the other hand,
When the application target is an emulsion type, the amount of the formulation is usually small, so that it is easily dispersed, and
Since the formulation itself remains insoluble or sparingly soluble in water, it has high water resistance, and for example, the algae-proofing and mildew-proofing effects are retained over a long period of time in a paint film or a resin molded product.

更に、本発明の製剤によれば、適用対象に防藻剤と防黴
剤とを一括して同時に配合することができる。
Furthermore, according to the formulation of the present invention, the algae-proofing agent and the mildew-proofing agent can be simultaneously added to the application target at once.

実施例 以下に実施例を挙げて本発明を説明する 実施例1 イルガロール1051の粉末10重量部をジメチルホルムアミ
ド25重量部に溶解させ、これにスケンM−8(プロピレ
ングリコール溶液、有効成分45%)20重量部とフタル酸
ジブチル45重量部とを加えて、均一な溶液を製剤として
得た。
EXAMPLES Hereinafter, the present invention will be described with reference to Examples. Example 1 10 parts by weight of powder of Irgalol 1051 was dissolved in 25 parts by weight of dimethylformamide, and Sken M-8 (propylene glycol solution, active ingredient 45%) was added thereto. 20 parts by weight and 45 parts by weight of dibutyl phthalate were added to obtain a uniform solution as a preparation.

上記において、有機溶剤として、ジメチルアセトアミ
ド、N−メチル−2−ピロリドン、シクロヘキサノン又
はテトラヒドロフランを用いた場合にも、同様にして、
溶液状の製剤を得た。
In the above, when dimethylacetamide, N-methyl-2-pyrrolidone, cyclohexanone or tetrahydrofuran is used as the organic solvent, similarly,
A solution formulation was obtained.

実施例2 イルガロール1051の粉末10重量部をジメチルホルムアミ
ド25重量部に溶解させ、これに液体であるIF−1000S20
重量部とフタル酸ジブチル45重量部とを加えて、均一な
溶液を製剤として得た。
Example 2 10 parts by weight of powder of Irgalol 1051 was dissolved in 25 parts by weight of dimethylformamide, and a liquid IF-1000S20 was added thereto.
By weight, 45 parts by weight of dibutyl phthalate were added to obtain a uniform solution as a formulation.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】2−メチルチオ−4−t−ブチルアミノ−
6−シクロプロピルアミノ−s−トリアジンと共に、2
−n−オクチル−4−イソチアゾリン−3−オン又は4
−クロルフエニル−3−ヨードプロパルギルホルマール
とをジメチルホルムアミドをフタル酸ジエステル、脂肪
族二塩基酸ジエステル、リン酸トリエステル、グリコー
ルエステル及びエポキシ脂肪酸エステルから選ばれる少
なくとも1種のエステル化合物とアミド、ケトン及びエ
ーテルから選ばれる少なくとも1種の有機溶剤とからな
る混合溶剤に溶解してなることを特徴とする防藻防黴製
剤。
1. 2-Methylthio-4-t-butylamino-
2 with 6-cyclopropylamino-s-triazine
-N-octyl-4-isothiazolin-3-one or 4
-Chlorophenyl-3-iodopropargyl formal, dimethylformamide, phthalic acid diester, aliphatic dibasic acid diester, phosphoric acid triester, glycol ester and epoxy fatty acid ester, and at least one ester compound and amide, ketone and ether. An anti-algal and anti-fungal formulation characterized by being dissolved in a mixed solvent comprising at least one organic solvent selected from
【請求項2】有機溶剤がジメチルホルムアミド、ジメチ
ルアセトアミド、N−メチル−2−ピロリドン及びシク
ロヘキサノンから選ばれる少なくとも1種であることを
特徴とする請求項第1項記載の防藻防黴製剤。
2. The anti-algal fungicide formulation according to claim 1, wherein the organic solvent is at least one selected from dimethylformamide, dimethylacetamide, N-methyl-2-pyrrolidone and cyclohexanone.
【請求項3】エステル化合物がフタル酸ジブチルであ
り、有機溶剤がジメチルホルムアミドである請求項1又
は2記載の防藻防黴製剤。
3. The antialgal and antifungal preparation according to claim 1, wherein the ester compound is dibutyl phthalate and the organic solvent is dimethylformamide.
JP25284590A 1990-09-21 1990-09-21 Anti-algal and anti-mildew formulation Expired - Lifetime JPH0761921B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25284590A JPH0761921B2 (en) 1990-09-21 1990-09-21 Anti-algal and anti-mildew formulation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25284590A JPH0761921B2 (en) 1990-09-21 1990-09-21 Anti-algal and anti-mildew formulation

Publications (2)

Publication Number Publication Date
JPH04134001A JPH04134001A (en) 1992-05-07
JPH0761921B2 true JPH0761921B2 (en) 1995-07-05

Family

ID=17242986

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25284590A Expired - Lifetime JPH0761921B2 (en) 1990-09-21 1990-09-21 Anti-algal and anti-mildew formulation

Country Status (1)

Country Link
JP (1) JPH0761921B2 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5707929A (en) * 1995-05-08 1998-01-13 Troy Chemical Corporation Biocidal compositions comprising mixtures of haloproynyl compounds and sulfur containing triazines
JPH09235491A (en) * 1996-03-01 1997-09-09 Takeda Chem Ind Ltd Antialgal coating material
NZ335586A (en) * 1996-10-25 2000-08-25 Monsanto Co Composition and method for treating plants with exogenous chemicals
JP4849743B2 (en) * 2001-06-26 2012-01-11 日本エンバイロケミカルズ株式会社 Industrial composition
DE10237264A1 (en) * 2002-08-14 2004-03-04 Schülke & Mayr GmbH Aqueous dispersion with fungicidal and algicidal effects
JP6412751B2 (en) * 2014-09-18 2018-10-24 日本曹達株式会社 Composition

Also Published As

Publication number Publication date
JPH04134001A (en) 1992-05-07

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