JPS62402A - Fungicidal composition - Google Patents
Fungicidal compositionInfo
- Publication number
- JPS62402A JPS62402A JP13928485A JP13928485A JPS62402A JP S62402 A JPS62402 A JP S62402A JP 13928485 A JP13928485 A JP 13928485A JP 13928485 A JP13928485 A JP 13928485A JP S62402 A JPS62402 A JP S62402A
- Authority
- JP
- Japan
- Prior art keywords
- parts
- tetrahalogenated
- isophthalonitrile
- water
- components
- 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.)
- Granted
Links
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、主に産業上の用水関係で発生する微生物障害
の防止及び一般産業用製品の微生物障害の防止に使用す
る殺菌組成物に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a sterilizing composition used mainly for preventing microbial damage occurring in industrial water supply and for preventing microbial damage to general industrial products.
製紙工程の白水系や化学工場の冷却水系では用水に混入
した有機物を栄養源として微生物が増殖し、不快臭の発
生、スライムの発生と剥離による製品の品質の低下、清
掃のための連続操業の停止、及び冷却効率の低下などの
トラブルを引き起し多大な損害を受ける。また、一般の
産業製品においてもその原料組成や製品の保管条件によ
り微生物の障害は多く発生しその防除は重要なこととな
っている。In the white water system of the paper manufacturing process and the cooling water system of chemical plants, microorganisms grow using organic matter mixed in the water as a nutrient source, causing unpleasant odors, deterioration of product quality due to slime generation and peeling, and the need for continuous operation for cleaning. This causes troubles such as shutdowns and reduced cooling efficiency, resulting in significant damage. In addition, in general industrial products, microbial damage often occurs depending on the raw material composition and storage conditions of the product, and its control is important.
従来これらの防除対策として有機水銀剤を中心とした金
属系化合物を使用していたが、その強い人畜毒性と環境
汚染の問題から近年は非金属系の薬剤が多(知られ、使
用もされている。Conventionally, metallic compounds, mainly organic mercury agents, have been used as control measures for these diseases, but due to their strong toxicity to humans and animals and environmental pollution, in recent years non-metallic compounds have become more popular (known and used). There is.
例えば2,2−ジブロモ−2−シアノアセトアミド(以
下ジプロミドと称する。)は、特公昭42−1o3a6
号公報明細書で抗微生物剤として知られ、2−ブロモ−
2−ニトロプロパン−1,3−ジオール(以下プロノポ
ールと称する。)も特公昭40−8917号公報明細書
で抗微生物剤として公知°である。更にテトラハロゲン
化イソフタロニトリルも農園芸分野に棲息する有害生物
撲滅剤として有効なことが知られている(%公昭41−
11358号公報明細書)。For example, 2,2-dibromo-2-cyanoacetamide (hereinafter referred to as dipromide) is
Known as an antimicrobial agent in the specification of the publication, 2-bromo-
2-Nitropropane-1,3-diol (hereinafter referred to as Pronopol) is also known as an antimicrobial agent in Japanese Patent Publication No. 8917/1983. Furthermore, tetrahalogenated isophthalonitrile is also known to be effective as an exterminator for pests inhabiting the agricultural and horticultural fields (% Kosho 41-
11358 publication specification).
しかし、これらの薬剤はいずれも単独で使用する場合は
問題を生ずる。これは、クロロミド及びプロノポールは
微生物の中でも糸状菌に対する効力が低い為で、糸状菌
を主体とするトラブルの生じやすい古紙原料の製紙工場
では充分な効力は得られない。またテトラハロゲン化イ
ソフタロニトリルは、クロロミドやプロノポールとは異
なり微生物の中で糸状菌に対しては卓効を示すが細菌に
対しては効力が充分でない。However, both of these drugs pose problems when used alone. This is because chloromide and pronopol have low efficacy against filamentous fungi among microorganisms, and cannot be sufficiently effective in paper mills that use used paper raw materials that are prone to troubles mainly caused by filamentous fungi. Furthermore, unlike chloromide and pronopol, tetrahalogenated isophthalonitrile is highly effective against filamentous fungi among microorganisms, but is not sufficiently effective against bacteria.
本発明は、前述したクロロミド・プロノポールの欠点を
補い、更に強力で安全な薬剤を開発すべく鋭意研究を重
ねた結果、テトラハロゲン化f:/7タロニトリルをク
ロロミド又はプロノポールと併用することにより単独で
の使用では推定出来ない驚くべき効果、すなわち、単独
の使用での特徴的性質が単に相加されたものでなく、そ
れぞれの単剤の弱点が補強され、かつ相乗的に作用する
ことを見出した。As a result of intensive research aimed at compensating for the above-mentioned drawbacks of chloromide and pronopol and developing a more powerful and safe drug, the present invention has been developed by using tetrahalogenated f:/7 talonitrile in combination with chloromide or pronopol. We discovered a surprising effect that cannot be estimated from the use of single agents, that is, the characteristic properties of each agent are not simply additive, but the weak points of each agent are reinforced and act synergistically. .
〔問題点を解決するための手段〕
本発明の殺菌組成物はテトラハロゲン化イソフタロニト
リルとクロロミド又はプロノポールを有効成分として含
有してなる。[Means for Solving the Problems] The sterilizing composition of the present invention contains tetrahalogenated isophthalonitrile and chloromide or pronopol as active ingredients.
本発明で使用するテトラハロゲン化イソフタロニトリル
としては次の化合物が挙げられろ。Examples of the tetrahalogenated isophthalonitrile used in the present invention include the following compounds.
テトラクロロイソフタロニトリル(以下TPNと云う)
。Tetrachloroisophthalonitrile (hereinafter referred to as TPN)
.
5−クロロ−2,4,6−ドリフルオロイソフクロニト
リル(以下CFPNと云う)。5-chloro-2,4,6-drifluoroisofucronitrile (hereinafter referred to as CFPN).
本発明の殺菌組成物に於いてテトラハロゲン化イソフタ
ロニトリルとクロロミドはプロノポールした場合に有効
な効果が得られる。製剤形態としては、溶剤、界面活性
剤、固体増量剤、その他補助剤を添加して水溶性液剤、
乳化性液剤、水相剤、粒剤、フロアブル斉II−として
使用するのが好ましい。In the germicidal composition of the present invention, an effective effect can be obtained when tetrahalogenated isophthalonitrile and chloromide are combined with pronopol. Forms of preparation include water-soluble liquid preparations with the addition of solvents, surfactants, solid fillers, and other adjuvants.
It is preferable to use it as an emulsifiable liquid, an aqueous phase agent, a granule, or a flowable formulation.
水溶性液剤として製剤する場合は、有効成分テトラハロ
ゲン化イソフタロニトリル・クロロミド・プロノポール
を充分に浴解し、水との相溶性のある溶剤を使用する。When preparing a water-soluble solution, the active ingredients tetrahalogenated isophthalonitrile, chloromide, and pronopol are sufficiently dissolved in a bath, and a solvent that is compatible with water is used.
この溶剤として、N、N−ジメチルホルムアミド等のア
ミド類、エチレングリコール、ジエチレングリコール、
ポリエチレングリコール、ポリプロピレングリコール、
ポリエチレングリコールモノメチルエーテル等の多価ア
ルコールとその誘導体、アセトン、イソホロン、シクロ
ヘキサノン等のケトン類、ジメチルスルホキシド等が挙
げられ、それぞれを単独又は混合して使用することが出
来る。また、水中又は製品中への分散性を高める目的で
界面活性剤を添加する場合は、アニオン系界面活性剤、
ノニオン系界面活性剤、これらの併用などを使用する溶
剤及び使用法によって選択適用する。As this solvent, amides such as N,N-dimethylformamide, ethylene glycol, diethylene glycol,
polyethylene glycol, polypropylene glycol,
Examples include polyhydric alcohols such as polyethylene glycol monomethyl ether and their derivatives, ketones such as acetone, isophorone, and cyclohexanone, and dimethyl sulfoxide, and each can be used alone or in combination. In addition, when adding a surfactant for the purpose of increasing dispersibility in water or in the product, anionic surfactants,
Nonionic surfactants and their combinations are selected and applied depending on the solvent used and the method of use.
乳化性液剤として製剤する場合は、ベンゼン、キシレン
、溶油等の炭緩水素類、1+L1−) !Jクロルエタ
ン等のハロゲン化炭化水素類等ノ溶剤、界面活性剤を加
える。乳化に必要な界面活性剤としては、アニオン系、
ノニオン系、アニオン−ノニオン混合などを使用する溶
剤によって選択適用する。When preparing as an emulsifiable liquid, benzene, xylene, hydrocarbons such as dissolved oil, 1+L1-)! Add a solvent such as a halogenated hydrocarbon such as J chloroethane, and a surfactant. Surfactants necessary for emulsification include anionic,
It is applied selectively depending on the solvent used, such as nonionic, anion-nonionic mixture, etc.
水和剤、粒剤、フロアブル剤として製剤する場合はクレ
ー、炭酸カルシウム、ホワイトカーボン等の固体増量剤
と界面活性剤を配合した後微粉砕し、それぞれの剤型に
製剤する。When preparing as wettable powders, granules, and flowable preparations, solid extenders such as clay, calcium carbonate, and white carbon, and surfactants are blended, then finely ground, and formulated into the respective dosage forms.
尚、本発明の有効成分は、混合した製剤として使用する
のが簡便であるが使用上の都合や安定性の上から個別に
単独で製剤し使用時において成分比が1:4〜4:1に
なるよう調製すれば混合製剤と何ら変わることのない効
果が得られる。Although it is convenient to use the active ingredients of the present invention as a mixed preparation, for convenience of use and stability, it is preferable to formulate them individually and at a component ratio of 1:4 to 4:1 at the time of use. If prepared in such a way, the same effect as a mixed preparation can be obtained.
次にこれらの実施例を挙げて本発明について説明する。 Next, the present invention will be described with reference to these examples.
実施例1
TPNS部、クロロミド15部とポリエチレングリコー
ル七ツメチルエーテル80部を混合してなる水溶性液剤
を得た。Example 1 A water-soluble liquid preparation was obtained by mixing TPNS, 15 parts of chloramide, and 80 parts of polyethylene glycol 7-methyl ether.
実施例2
CFPNl 0部、クロロミド10部、ツルポール23
64(東邦化学工業■製界面活性剤)5部、ポリエチレ
ングリコ−ルナ200 25部、キシレン50部を混合
してなる乳化性成剤を得た。Example 2 0 parts of CFPNl, 10 parts of chloramide, 23 parts of Tsurpol
An emulsifying agent was obtained by mixing 5 parts of 64 (surfactant manufactured by Toho Chemical Industry Co., Ltd.), 25 parts of polyethylene glycol Luna 200, and 50 parts of xylene.
実施例3
TPNl 5部、ジプロミド5部、ツルポール800人
(東邦化学工業■製界面活性剤)5部、ポリエチレング
リコールモノメチルエーテル15部、キシレン60部を
混合してなる乳化性液剤を得た。Example 3 An emulsifying liquid preparation was obtained by mixing 5 parts of TPNl, 5 parts of dipromide, 5 parts of Tsurpol 800 (a surfactant manufactured by Toho Chemical Industry Co., Ltd.), 15 parts of polyethylene glycol monomethyl ether, and 60 parts of xylene.
実施例4
CFPNB部、ジプロミド12部、デモールN(花王石
鹸器)製)2部、カープレックスナ80(塩野義製薬■
製ホワイトカーボン)2部、クニライトφ250(国峰
鉱化工業■製)5部、クレー71部を混合し粉砕してな
る水相剤を得た。Example 4 CFPNB part, Dipromide 12 parts, Demol N (manufactured by Kao Soapware) 2 parts, Carplexna 80 (Shionogi & Co., Ltd.)
A water phase agent was obtained by mixing and pulverizing 2 parts of Kunilite φ250 (manufactured by Kunimine Mineraka Kogyo) and 71 parts of clay.
実施例5
TPNl 0部、プロノポール10部、ポリエチレング
リコ−77モノメチル工−テ2ノ80部を混合してなる
水溶性液剤を得た。Example 5 A water-soluble liquid preparation was obtained by mixing 0 parts of TPNl, 10 parts of Pronopol, and 80 parts of polyethylene glyco-77 monomethyl-te2.
実施例6
CFPN 4部、プロノポール16部、ポリエチレング
リコールモノメチルエーテル40部、シクロヘキサノン
40部を混合してなる水溶性液剤を得た。Example 6 A water-soluble liquid preparation was obtained by mixing 4 parts of CFPN, 16 parts of Pronopol, 40 parts of polyethylene glycol monomethyl ether, and 40 parts of cyclohexanone.
実施例7
TPN8部、プロノポール12部、ツルポール800A
(東邦化学工業■製界面活性剤)5部、シクロへキサノ
ン10部、キシレン65部を混合してなる乳化性液剤を
得た。Example 7 TPN 8 parts, Pronopol 12 parts, Tsurupol 800A
An emulsifying liquid preparation was obtained by mixing 5 parts of surfactant (manufactured by Toho Chemical Industry ■), 10 parts of cyclohexanone, and 65 parts of xylene.
実施例8
CFPNJ部、プロノポール16部、デモールN(花王
石鹸■製界面活性剤)2部、カープレックスφ80(塩
野義製薬■製ホワイトカーボン)2部、クニライト÷2
50−(国峰鉱化工業■製)5部、クレー71部を混合
し粉砕してなる水相剤を得た。Example 8 Part CFPNJ, 16 parts of Pronopol, 2 parts of Demol N (surfactant manufactured by Kao Soap ■), 2 parts of Carplex φ80 (white carbon manufactured by Shionogi & Co., Ltd.), Kunilite ÷ 2
50- (manufactured by Kunimine Mineraka Kogyo ■) and 71 parts of clay were mixed and ground to obtain an aqueous phase agent.
本発明の殺菌組成物は、産業上有害な微生物に対し糸状
菌、細菌を問わず広範囲に抗菌力を有し、またその作用
濃度は予想出来ない低濃度である。The sterilizing composition of the present invention has antibacterial activity over a wide range of industrially harmful microorganisms, regardless of whether they are filamentous fungi or bacteria, and its effective concentration is unexpectedly low.
本発明の殺菌組成物は、主に産業上の用水関係、例えば
製紙工程、工業用冷却水系、ビル等の空調用冷却水系な
ど水を多量に使用する系での微生物障害防止剤として、
更には建築用の水性塗料、製紙工場における紙塗工用塗
料、金属加工油剤、澱粉、カゼインなどの糊料等の一段
産業用製品の微生物障害防止剤として使用することが出
来る。The sterilizing composition of the present invention is mainly used as an agent for preventing microbial damage in systems that use a large amount of water, such as industrial water systems, such as paper manufacturing processes, industrial cooling water systems, and cooling water systems for air conditioning in buildings.
Furthermore, it can be used as an agent for preventing microbial damage in one-stage industrial products such as water-based paints for construction, paper coating paints in paper mills, metal processing oils, and thickeners such as starch and casein.
次に本発明の殺菌組成物の効果を試験例を挙げて説明す
る。Next, the effects of the sterilizing composition of the present invention will be explained by giving test examples.
試験例1 下記の試験法にてスライム発生の程度を測定した。Test example 1 The degree of slime generation was measured using the following test method.
試験法:縦20(:!IL1横30の、深さ20口のガ
ラス製水槽に、温度調節装置、攪拌機、温度計を設置し
、スライム量測定板として幅5ぼ、長さ20口、厚さL
5C!nのラワン材を2枚縦に取り付けた。この槽に製
紙工程より採取した白水(パルプ濃度0.11% )
10 tを入れ、これに第1表に示す供試薬剤を白水に
対し有効成分で1 ppm になるように添加した。7
日後にスライム付着板に付着したスライムの重量を測定
し、効果を判定した。第1表に7日後のスライム重量を
殺菌組成物の組成と共に示す。表中のスライム重量は2
枚の測定板に付着したスライム量の平均値である。Test method: A temperature control device, a stirrer, and a thermometer were installed in a glass water tank measuring 20 mm in length (:! IL 1 and 30 mm in width and 20 holes in depth), and a slime amount measuring plate was placed in a glass tank measuring 20 mm in width, 20 mm in length, and 20 mm in thickness. L
5C! Two sheets of n lauan material were attached vertically. White water collected from the paper manufacturing process (pulp concentration 0.11%) is placed in this tank.
10 t of water was added thereto, and the test chemicals shown in Table 1 were added to the white water so that the amount of active ingredients was 1 ppm. 7
After 1 day, the weight of the slime attached to the slime attachment plate was measured and the effectiveness was determined. Table 1 shows the slime weight after 7 days, together with the composition of the disinfectant composition. The slime weight in the table is 2
This is the average value of the amount of slime attached to the measurement plates.
第 1 表
試験例2
酢酸ビニール系合成樹脂エマルジョン塗料(酢酸ビニー
ル樹脂、濃度45チ)に、同じエマルジョン塗料の腐敗
したものを種菌として1チ添加したものを試料とし、こ
れを4区分に分けて第2表に示す薬剤をそれぞれ有効成
分としてs o ppm添加し、35℃で密閉保存した
。Table 1 Test Example 2 A vinyl acetate synthetic resin emulsion paint (vinyl acetate resin, concentration 45 cm) was prepared by adding 1 g of the same rotten emulsion paint as an inoculum, and this was divided into 4 categories. So ppm of each of the drugs shown in Table 2 was added as an active ingredient, and the mixture was stored sealed at 35°C.
1週間ごとに菌数の測定を行なったのち腐敗エマルジョ
ン1チを追加し、35℃で保存を続けた。その結果を第
2表に示す。After measuring the number of bacteria every week, 1 ml of spoiled emulsion was added and continued to be stored at 35°C. The results are shown in Table 2.
第 2 表Table 2
Claims (1)
モ−2−シアノアセトアミド、又は2−ブロモ−2−ニ
トロプロパン−1,3−ジオールを有効成分として含有
することを特徴とする殺菌組成物。A sterilizing composition comprising tetrahalogenated isophthalonitrile and 2,2-dibromo-2-cyanoacetamide or 2-bromo-2-nitropropane-1,3-diol as active ingredients.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13928485A JPH06682B2 (en) | 1985-06-26 | 1985-06-26 | Industrial sterilization composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13928485A JPH06682B2 (en) | 1985-06-26 | 1985-06-26 | Industrial sterilization composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62402A true JPS62402A (en) | 1987-01-06 |
JPH06682B2 JPH06682B2 (en) | 1994-01-05 |
Family
ID=15241696
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13928485A Expired - Lifetime JPH06682B2 (en) | 1985-06-26 | 1985-06-26 | Industrial sterilization composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH06682B2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63264504A (en) * | 1987-04-17 | 1988-11-01 | Shinto Paint Co Ltd | Industrial mildewproofing composition |
JPS6461402A (en) * | 1987-08-29 | 1989-03-08 | Somar Corp | Industrial microbicide |
JPH01211507A (en) * | 1988-02-17 | 1989-08-24 | Paamakemu Asia:Kk | Slime controlling agent for manufacturing paper |
JPH08169803A (en) * | 1995-08-14 | 1996-07-02 | Somar Corp | Industrial germicidal composition |
CN105344255A (en) * | 2015-11-24 | 2016-02-24 | 深圳市裕麟环境工程有限公司 | Preparation method for tubular microporous filtering film |
-
1985
- 1985-06-26 JP JP13928485A patent/JPH06682B2/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63264504A (en) * | 1987-04-17 | 1988-11-01 | Shinto Paint Co Ltd | Industrial mildewproofing composition |
JPS6461402A (en) * | 1987-08-29 | 1989-03-08 | Somar Corp | Industrial microbicide |
JPH01211507A (en) * | 1988-02-17 | 1989-08-24 | Paamakemu Asia:Kk | Slime controlling agent for manufacturing paper |
JPH08169803A (en) * | 1995-08-14 | 1996-07-02 | Somar Corp | Industrial germicidal composition |
CN105344255A (en) * | 2015-11-24 | 2016-02-24 | 深圳市裕麟环境工程有限公司 | Preparation method for tubular microporous filtering film |
Also Published As
Publication number | Publication date |
---|---|
JPH06682B2 (en) | 1994-01-05 |
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S531 | Written request for registration of change of domicile |
Free format text: JAPANESE INTERMEDIATE CODE: R313531 |
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R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
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EXPY | Cancellation because of completion of term |