JPH04297401A - Industrial antimicrobial composition - Google Patents
Industrial antimicrobial compositionInfo
- Publication number
- JPH04297401A JPH04297401A JP8625591A JP8625591A JPH04297401A JP H04297401 A JPH04297401 A JP H04297401A JP 8625591 A JP8625591 A JP 8625591A JP 8625591 A JP8625591 A JP 8625591A JP H04297401 A JPH04297401 A JP H04297401A
- Authority
- JP
- Japan
- Prior art keywords
- antibacterial
- industrial
- present
- composition
- glutaraldehyde
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 40
- 230000000845 anti-microbial effect Effects 0.000 title abstract 4
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 claims abstract description 12
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims abstract description 11
- 230000000844 anti-bacterial effect Effects 0.000 claims description 48
- 239000004480 active ingredient Substances 0.000 claims description 4
- 239000004816 latex Substances 0.000 abstract description 10
- 229920000126 latex Polymers 0.000 abstract description 10
- 244000005700 microbiome Species 0.000 abstract description 7
- 229920002472 Starch Polymers 0.000 abstract description 5
- 239000000853 adhesive Substances 0.000 abstract description 5
- 230000001070 adhesive effect Effects 0.000 abstract description 5
- 239000008107 starch Substances 0.000 abstract description 5
- 235000019698 starch Nutrition 0.000 abstract description 5
- 239000005018 casein Substances 0.000 abstract description 4
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 abstract description 4
- 235000021240 caseins Nutrition 0.000 abstract description 4
- 239000002184 metal Substances 0.000 abstract description 4
- 239000000049 pigment Substances 0.000 abstract description 4
- 230000002421 anti-septic effect Effects 0.000 abstract description 3
- 239000000498 cooling water Substances 0.000 abstract description 3
- 239000004599 antimicrobial Substances 0.000 abstract description 2
- 238000004321 preservation Methods 0.000 abstract description 2
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 239000010730 cutting oil Substances 0.000 abstract 1
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 230000001473 noxious effect Effects 0.000 abstract 1
- 239000003242 anti bacterial agent Substances 0.000 description 13
- 241000894006 Bacteria Species 0.000 description 11
- 230000000694 effects Effects 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 229960003887 dichlorophen Drugs 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 6
- 229940079593 drug Drugs 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
- 230000002195 synergetic effect Effects 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 230000000813 microbial effect Effects 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000003755 preservative agent Substances 0.000 description 4
- 230000002335 preservative effect Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000012085 test solution Substances 0.000 description 4
- 244000063299 Bacillus subtilis Species 0.000 description 3
- 235000014469 Bacillus subtilis Nutrition 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 3
- 230000001954 sterilising effect Effects 0.000 description 3
- 238000004659 sterilization and disinfection Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- KANAPVJGZDNSCZ-UHFFFAOYSA-N 1,2-benzothiazole 1-oxide Chemical class C1=CC=C2S(=O)N=CC2=C1 KANAPVJGZDNSCZ-UHFFFAOYSA-N 0.000 description 2
- JLHMJWHSBYZWJJ-UHFFFAOYSA-N 1,2-thiazole 1-oxide Chemical class O=S1C=CC=N1 JLHMJWHSBYZWJJ-UHFFFAOYSA-N 0.000 description 2
- NWPCFCBFUXXJIE-UHFFFAOYSA-N 2-(hydroxymethylamino)ethanol Chemical compound OCCNCO NWPCFCBFUXXJIE-UHFFFAOYSA-N 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 2
- 241000193830 Bacillus <bacterium> Species 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 230000000843 anti-fungal effect Effects 0.000 description 2
- 229940121375 antifungal agent Drugs 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011115 styrene butadiene Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- GKVTXWYBIQNZOS-UHFFFAOYSA-M 1-(4-ethylphenyl)-3-(4-phenylphenyl)-6,7,8,9-tetrahydro-5h-imidazo[1,2-a]azepin-4-ium;bromide Chemical compound [Br-].C1=CC(CC)=CC=C1N1C(CCCCC2)=[N+]2C(C=2C=CC(=CC=2)C=2C=CC=CC=2)=C1 GKVTXWYBIQNZOS-UHFFFAOYSA-M 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- -1 glycol ethers Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は新規な工業用抗菌組成物
、さらに詳しくは、工業分野における障害微生物に対し
、広いpH範囲において、安定して優れた抗菌活性を示
す工業用抗菌組成物に関するものである。[Field of Industrial Application] The present invention relates to a novel industrial antibacterial composition, and more particularly to an industrial antibacterial composition that stably exhibits excellent antibacterial activity over a wide pH range against harmful microorganisms in the industrial field. It is something.
【0002】0002
【従来の技術】従来、工業用抗菌剤は、工業製品の障害
微生物、例えば細菌、カビ、酵母、藻類などによって引
き起こされる腐敗やカビの発生などのいわゆる微生物災
害を防止するために、種々の分野において幅広く用いら
れている。例えば紙パルプ工場におけるスライムコント
ロールや、塗料、接着剤、デンプンやカゼインなどの糊
料、顔料、ラテックス、金属加工油のような油剤などの
防菌・防カビに、さらには木材、建材、皮革、繊維、フ
ィルム、被覆電線、電気通信機器などの防菌・防カビな
どに使用されている。しかしながら、このような工業分
野における微生物処理において、酸性からアルカリ性に
至る広いpH範囲で有効に作用する抗菌剤は極めて少な
いのが実状である。アルカリ性側で特に高い抗菌活性を
示す薬剤としては、例えば2−(ヒドロキシメチルアミ
ノ)エタノール及び第四級アンモニウム塩が知られてい
るが、前者の2−(ヒドロキシメチルアミノ)エタノー
ルは酸性側では著しく抗菌活性が低下するという欠点が
あり、一方、後者の第四級アンモニウム塩は発泡障害を
生じたり、微細物質やパルプなどに吸着して抗菌活性が
失われやすく、安定した微生物処理をするには使いにく
いという欠点を有している。また、代表的な工業用抗菌
剤としては、例えばハロゲン化イソチアゾロン、ベンゾ
イソチアゾロン、ブロモニトロアルコール系などの薬剤
が挙げられるが、これらの抗菌剤は酸性側では抗菌活性
は高いものの、アルカリ性側では抗菌活性が著しく低下
するため、安定した微生物処理がしにくいという問題が
ある。このような事情から、従来、処理対象の工業製品
のpHにより、使用する企業あるいは薬剤を提供する企
業側で、抗菌剤の種類を使いわけているが、この場合、
煩雑さを免れないという問題が生じる。ところで、工業
製品の障害微生物の中で、細菌であるバチルス属菌種は
薬剤に対する抵抗性が強く、抗菌剤処理がしにくい代表
的な菌であることが知られている。本菌種は生育の不適
な環境になると、外界から影響を受けにくい胞子の状態
に形態を変えて存在することができ、その結果薬剤に対
する抵抗性が強くなる。従来、このような菌が存在する
工業製品に対しては、例えばハロゲン化イソチアゾロン
、ベンゾイソチアゾロン、ブロモニトロアルコール系な
どの薬剤の添加量を増加させて対処しているのが現状で
ある。他方、バチルス菌に対して、グルタルアルデヒド
及び2,2’−メチレンビス(4−クロロフェノール)
(以下、ダイクロロフェンと略称する)が優れた抗菌活
性を示すことは知られているが、両薬剤ともpHにより
活性が著しく影響を受けるという欠点を有している。[Prior Art] Conventionally, industrial antibacterial agents have been used in various fields to prevent so-called microbial disasters such as spoilage and mold growth caused by harmful microorganisms such as bacteria, mold, yeast, and algae in industrial products. It is widely used in For example, slime control in paper and pulp factories, antibacterial and antifungal applications such as paints, adhesives, thickeners such as starch and casein, pigments, latex, and oils such as metal processing oil, as well as wood, building materials, leather, etc. It is used for antibacterial and antifungal purposes in textiles, films, coated wires, telecommunications equipment, etc. However, in the microbial treatment in the industrial field, the reality is that there are very few antibacterial agents that act effectively in a wide pH range from acidity to alkalinity. For example, 2-(hydroxymethylamino)ethanol and quaternary ammonium salts are known as agents that exhibit particularly high antibacterial activity in alkaline conditions, but the former 2-(hydroxymethylamino)ethanol exhibits particularly high antibacterial activity in acidic conditions. The latter quaternary ammonium salts have the disadvantage of decreasing antibacterial activity, and on the other hand, the latter quaternary ammonium salts tend to cause foaming problems and adsorb to fine substances and pulp, resulting in loss of antibacterial activity, making it difficult to achieve stable microbial treatment. It has the disadvantage of being difficult to use. In addition, typical industrial antibacterial agents include halogenated isothiazolones, benzisothiazolones, and bromonitroalcohol-based agents, but although these antibacterial agents have high antibacterial activity in acidic conditions, they have no antibacterial activity in alkaline conditions. There is a problem in that it is difficult to perform stable microbial treatment because the activity is significantly reduced. For these reasons, conventionally, the company using the antibacterial agent or the company providing the agent uses different types of antibacterial agents depending on the pH of the industrial product being treated.
The problem arises that complexity cannot be avoided. By the way, among the microorganisms that cause problems in industrial products, it is known that Bacillus species, which are bacteria, are typical bacteria that have strong resistance to drugs and are difficult to treat with antibacterial agents. When this type of fungus becomes in an unsuitable environment for growth, it can change its form to a spore state that is less susceptible to external influences, and as a result, it becomes more resistant to drugs. Conventionally, industrial products containing such bacteria have been dealt with by increasing the amount of chemicals such as halogenated isothiazolones, benzisothiazolones, and bromonitroalcohols. On the other hand, against Bacillus bacteria, glutaraldehyde and 2,2'-methylenebis(4-chlorophenol)
(hereinafter abbreviated as dichlorofen) is known to exhibit excellent antibacterial activity, but both drugs have the drawback that their activity is significantly affected by pH.
【0003】0003
【発明が解決しようとする課題】本発明はこのような事
情のもとで、工業分野における障害微生物に対し、広い
pH範囲において、安定して優れた抗菌活性を示す工業
用抗菌組成物を提供することを目的としてなされたもの
である。[Problems to be Solved by the Invention] Under these circumstances, the present invention provides an industrial antibacterial composition that stably exhibits excellent antibacterial activity over a wide pH range against harmful microorganisms in the industrial field. It was done for the purpose of
【0004】0004
【課題を解決するための手段】本発明者は前記の好まし
い性質を有する工業用抗菌組成物を開発すべく鋭意研究
を重ねた結果、特定の2種の抗菌剤を組み合わせること
により、その相乗効果によって工業分野における障害微
生物に対し、広いpH範囲において、安定して優れた抗
菌活性を示すことを見い出し、この知見に基づいて本発
明を完成するに至った。すなわち、本発明は、グルタル
アルデヒドとダイクロロフェンとを、重量比1:20な
いし20:1の割合で有効成分として含有して成る工業
用抗菌組成物を提供するものである。以下、本発明を詳
細に説明する。[Means for Solving the Problems] As a result of intensive research to develop an industrial antibacterial composition having the above-mentioned preferable properties, the present inventor has found that by combining two specific antibacterial agents, the synergistic effect can be achieved. It was discovered that the antimicrobial agent stably exhibits excellent antibacterial activity in a wide pH range against harmful microorganisms in the industrial field, and based on this knowledge, the present invention was completed. That is, the present invention provides an industrial antibacterial composition containing glutaraldehyde and dichlorophene as active ingredients in a weight ratio of 1:20 to 20:1. The present invention will be explained in detail below.
【0005】本発明の工業用抗菌組成物はグルタルアル
デヒドとダイクロロフェンとを有効成分とするものであ
って、その配合割合は重量比1:20ないし20:1、
好ましくは1:10ないし10:1の範囲で選ぶことが
必要である。この配合割合が前記範囲を免脱すると本発
明の効果が十分に発揮されず、本発明の目的が達せられ
ない。また、本発明の抗菌組成物には、本発明の目的が
損なわれない範囲で、所望に応じ従来公知の他の工業用
殺菌剤を配合することができる。The industrial antibacterial composition of the present invention contains glutaraldehyde and dichlorophene as active ingredients, with a weight ratio of 1:20 to 20:1;
It is necessary to select the ratio preferably in the range of 1:10 to 10:1. If this blending ratio falls outside of the above range, the effects of the present invention will not be fully exhibited and the objectives of the present invention will not be achieved. Furthermore, other conventionally known industrial disinfectants may be blended into the antibacterial composition of the present invention as long as the purpose of the present invention is not impaired.
【0006】本発明組成物の製剤形態については特に制
限はなく、例えば溶剤に溶解させた液剤、粒子として水
に分散させたフロアブル剤、あるいは合成樹脂などへ練
り込んだ固型剤などとして利用できる。溶剤に溶解させ
て液剤とする場合、該溶剤としては、例えばジエチレン
グリコールモノメチルエーテル、エチレングリコールモ
ノメチルエーテルなどのグリコールエーテル類、エチレ
ングリコール、プロピレングリコール、ジエチレングリ
コール、ジプロピレングリコール、ポリエチレングリコ
ールなどのグリコール類、さらにはジメチルホルムアミ
ド、ジメチルスルホキシド、水などが挙げられる。これ
らの溶剤は1種用いてもよいし、2種以上を組み合わせ
て用いてもよい。There are no particular restrictions on the formulation form of the composition of the present invention, and it can be used, for example, as a liquid solution dissolved in a solvent, a flowable agent dispersed in water as particles, or a solid agent kneaded into a synthetic resin. . When dissolved in a solvent to form a liquid agent, examples of the solvent include glycol ethers such as diethylene glycol monomethyl ether and ethylene glycol monomethyl ether, glycols such as ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, and polyethylene glycol; Examples include dimethylformamide, dimethyl sulfoxide, and water. These solvents may be used alone or in combination of two or more.
【0007】本発明の抗菌組成物はこのようにグルタル
アルデヒドとダイクロロフェンとを組み合わせることに
より、その相乗効果によって、広いpH範囲において、
安定して優れた抗菌活性を発揮することができる。本発
明組成物の適用分野については、工業用抗菌剤を適用で
きる分野であればよく、特に制限はないが、一般に冷却
水系や紙パルプ工場におけるスライムコントロール用、
デンプン、カゼインなどの防腐用、ラテックス、顔料、
接着剤、塗料などの製品の防腐用、さらには金属加工油
使用系での防腐用などに好適に用いられる。[0007] The antibacterial composition of the present invention thus combines glutaraldehyde and dichlorophene, and due to their synergistic effect, the antibacterial composition of the present invention has
It can stably exhibit excellent antibacterial activity. The field of application of the composition of the present invention is not particularly limited as long as it can be used as an industrial antibacterial agent, but it is generally used for slime control in cooling water systems and pulp and paper factories,
Preservatives such as starch and casein, latex, pigments,
It is suitably used for preservative purposes in products such as adhesives and paints, and in systems that use metal processing oils.
【0008】本発明の抗菌組成物の添加量は、該組成物
が適用される対象物の種類により適宜選ばれるが、通常
対象物が紙パルプ抄紙系の場合、すなわちスライムコン
トロール剤として用いる場合には、両成分の合計量が1
〜100μg/mlになるように、またその他の分野に
用いる場合には10〜3,000μg/mlになるよう
に選ぶのがよい。また、添加方法としては、両成分をそ
れぞれ所定の割合で添加してもよいし、あらかじめ両成
分を所定の割合で配合してなるものを添加してもよい。[0008] The amount of the antibacterial composition of the present invention to be added is appropriately selected depending on the type of object to which the composition is applied. is, the total amount of both components is 1
It is preferable to select a concentration of 100 to 100 μg/ml, or 10 to 3,000 μg/ml when used in other fields. Further, as for the addition method, both components may be added in predetermined proportions, or a mixture of both components in predetermined proportions may be added.
【0009】[0009]
【実施例】次に実施例により本発明をさらに詳細に説明
するが、本発明はこれらの例によってなんら限定される
ものではない。EXAMPLES Next, the present invention will be explained in more detail with reference to examples, but the present invention is not limited to these examples in any way.
【0010】実施例1〜9、比較例1、2以下に示す組
成の抗菌組成物を調製した。Examples 1 to 9 and Comparative Examples 1 and 2 Antibacterial compositions having the compositions shown below were prepared.
【0011】[0011]
【0012】比較例3
抗菌組成物としてケーソン886(ローム&ハース社製
、商品名、有効成分14wt%)を用意した。Comparative Example 3 Caisson 886 (manufactured by Rohm & Haas, trade name, active ingredient: 14 wt%) was prepared as an antibacterial composition.
【0013】比較例4
抗菌組成物として2−ブロモ−2−ニトロ−1,3−プ
ロパンジオール単独から成るものを用意した。Comparative Example 4 An antibacterial composition consisting of 2-bromo-2-nitro-1,3-propanediol alone was prepared.
【0014】試験例1
スチレン−ブタジエン系エマルジョンラテックス腐敗液
より分離同定したグラム陽性細菌であるバチルス・ズブ
チリスの胞子懸濁液に対する殺菌効果を調べた。すなわ
ち、腐敗していない前記ラテックスをあらかじめ以下に
示すpHに調整しておき、これに所定の抗菌組成物を抗
菌剤として100μg/ml添加したのち、生菌数を寒
天平板法で測定した。なお、比較のため、薬剤無添加の
場合についても同様に試験を行った。結果を次に示す。Test Example 1 The bactericidal effect on a spore suspension of Bacillus subtilis, a Gram-positive bacterium isolated and identified from a styrene-butadiene emulsion latex spoilage liquid, was investigated. That is, the uncorrupted latex was adjusted in advance to the pH shown below, and after adding 100 μg/ml of a predetermined antibacterial composition as an antibacterial agent thereto, the number of viable bacteria was measured by the agar plate method. For comparison, a similar test was also conducted in the case where no drug was added. The results are shown below.
【0015】
生菌数(個/ml) 抗菌組成物種類
pH5.5 pH7.0
pH10.0 実施例2 9
.0×102 3.2×102 2.0×10
実施例5 5.5×10 5.
0×10 1.3×102 実施例8
10以下 3.1×10 3
.5×103 比較例1 3.8
×105 4.6×104 8.5×102
比較例2 7.0×10 1.0
×103 3.9×105 比較例3
3.3×104 7.3×104 4.1
×105 比較例4 6.6×1
04 9.5×104 3.5×105
無添加 7.1×105 7.3×
105 4.5×105[0015]
Number of viable bacteria (number/ml) Type of antibacterial composition pH 5.5 pH 7.0
pH 10.0 Example 2 9
.. 0×102 3.2×102 2.0×10
Example 5 5.5×10 5.
0×10 1.3×102 Example 8
10 or less 3.1×10 3
.. 5×103 Comparative example 1 3.8
×105 4.6×104 8.5×102
Comparative example 2 7.0×10 1.0
×103 3.9×105 Comparative example 3
3.3×104 7.3×104 4.1
×105 Comparative example 4 6.6×1
04 9.5×104 3.5×105
No additives 7.1×105 7.3×
105 4.5×105
【0016】以上の結果から、バチルス・ズブチリスの
胞子に対してグルタルアルデヒドはpH10のアルカリ
性側で、ダイクロロフェンはpH5.5の酸性側でかな
りの殺菌効果を示すことが分かる。また、両成分を併用
した本発明の抗菌組成物は、相乗的に殺菌効果を示すと
ともに、広いpH範囲で安定して効果を示すことが分か
る。該ラテックス腐敗液は、バチルス・ズブチリスが優
占菌種であったことから推察して、本発明の抗菌組成物
が工業製品の防腐に優れた効果を示すことが示唆される
。From the above results, it can be seen that glutaraldehyde has a significant bactericidal effect on Bacillus subtilis spores at an alkaline pH of 10, and dichlorophene has a significant bactericidal effect at an acidic pH of 5.5. Furthermore, it can be seen that the antibacterial composition of the present invention using both components in combination exhibits a synergistic bactericidal effect and exhibits stable effects over a wide pH range. Inferred from the fact that Bacillus subtilis was the dominant bacterial species in the latex spoilage fluid, it is suggested that the antibacterial composition of the present invention exhibits an excellent effect in preserving industrial products.
【0017】試験例2
エマルジョンラテックスを用いた防腐試験により、本発
明の抗菌組成物の防腐効果を確認した。すなわち、スチ
レン−ブタジエン系エマルジョンラテックス(pH9.
0)と所定の抗菌組成物とを含む試験液(抗菌剤100
μg/ml)に、該ラテックスを腐敗させて得られた菌
を試験液中の菌数が106個/mlになるように2週間
に1度の頻度で添加し、30℃で静置保存して7日目に
生菌数を測定した。防腐効果は試験液中の菌数が菌添加
7日後に103個/ml以下になることを基準として、
腐敗阻止日数を調べた。なお、薬剤無添加の場合につい
ても同様に試験を行った。結果を以下に示す。Test Example 2 The antiseptic effect of the antibacterial composition of the present invention was confirmed by an antiseptic test using emulsion latex. That is, styrene-butadiene emulsion latex (pH 9.
0) and a predetermined antibacterial composition (antibacterial agent 100
Microbes obtained by rotting the latex were added once every two weeks to 106 microbes/ml in the test solution, and stored at 30°C. The number of viable bacteria was measured on the seventh day. The preservative effect is based on the fact that the number of bacteria in the test solution is 103 cells/ml or less 7 days after adding the bacteria.
We investigated the number of days to prevent corruption. Note that the same test was conducted in the case where no drug was added. The results are shown below.
【0018】[0018]
【0019】以上の結果から、グルタルアルデヒド及び
ダイクロロフェンをそれぞれ単独で使用する場合に比べ
て、本発明の抗菌組成物は相乗的な効果により、長期間
にわたり、効果を持続することが分かる。
試験例3
紙パルプ工場で層間接着剤として使用している2wt%
リン酸エステル化デンプンスラリー(pH6.0)に、
所定の抗菌組成物を抗菌剤が200μg/mlになるよ
うに添加し、30℃で7日間静置保存後、試験液のpH
低下及び臭気から腐敗程度を測定することにより、防腐
に有効な抗菌剤の最小濃度を求めた。結果を次に示す。From the above results, it can be seen that the antibacterial composition of the present invention maintains its effect for a long period of time due to the synergistic effect, compared to when glutaraldehyde and dichlorophene are used alone. Test Example 3 2wt% used as an interlayer adhesive in a pulp and paper factory
Phosphate esterified starch slurry (pH 6.0),
Add the specified antibacterial composition so that the antibacterial agent concentration is 200 μg/ml, and after storing it for 7 days at 30°C, the pH of the test solution
The minimum concentration of antibacterial agent effective for preservation was determined by measuring the degree of decay based on deterioration and odor. The results are shown below.
【0020】[0020]
【0021】以上の結果から、グルタルアルデヒド及び
ダイクロロフェンをそれぞれ単独で使用する場合に比べ
て、本発明の抗菌組成物は低濃度で防腐効果を発揮する
ことが分かる。From the above results, it can be seen that the antibacterial composition of the present invention exhibits a preservative effect at a lower concentration than when glutaraldehyde and dichlorophene are used alone.
【0022】試験例4
コート原紙を抄造している製紙工場の白水(pH8.0
)に、所定の抗菌組成物を抗菌剤が30μg/mlにな
るように添加し、30℃で60分間振とうしたのち、試
験液中の生菌数を寒天平板法で測定し、殺菌率を求めた
。なお薬剤無添加の場合についても同様に試験を行った
。結果を次に示す。Test Example 4 White water (pH 8.0) from a paper mill manufacturing coated base paper
), a predetermined antibacterial composition was added so that the antibacterial agent concentration was 30 μg/ml, and after shaking at 30°C for 60 minutes, the number of viable bacteria in the test solution was measured by the agar plate method, and the sterilization rate was determined. I asked for it. Note that the same test was conducted in the case where no drug was added. The results are shown below.
【0023】[0023]
【0024】以上の結果から、本発明の抗菌組成物によ
れば、極めて高い殺菌率で殺菌処理しうることが分かる
。From the above results, it can be seen that the antibacterial composition of the present invention can perform sterilization treatment with an extremely high sterilization rate.
【0025】試験例5
実施例5の抗菌組成物を、コート原紙を抄造している製
紙工場に適用した。すなわち、実施例5の抗菌組成物を
、マシンチェストに1日3回の頻度で抗菌剤量30μg
/ml、各30分間注入し、スライム処理を行った。処
理効果は操業中の製品紙切れ回数と停止時における系内
のスライム発生状態から評価した。Test Example 5 The antibacterial composition of Example 5 was applied to a paper mill manufacturing coated base paper. That is, the antibacterial composition of Example 5 was applied to a machine chest in an amount of 30 μg three times a day.
/ml was injected for 30 minutes each, and the slime treatment was performed. The treatment effect was evaluated from the number of times the product was cut during operation and the state of slime generation in the system when the system was stopped.
【0026】本工場では、比較例3に示す薬剤を同一添
加量用い、同様の方法でスライム処理を実施していたが
、操業開始2週間でスライムに起因した紙切れが多発し
、停止後系内にはスライムの生成が観察された。これに
対し、実施例5の抗菌組成物による処理では、紙切れの
発生がなく、1か月間の連続操業ができ、また操業停止
時に系内にスライムの発生が認められず、良好な処理効
果が得られた。[0026] At this factory, slime treatment was carried out in the same manner using the same additive amount of the chemical shown in Comparative Example 3, but within two weeks of operation, there were many paper breaks due to slime, and after the system was stopped, Slime formation was observed. On the other hand, in the treatment using the antibacterial composition of Example 5, there was no paper breakage, continuous operation was possible for one month, no slime was observed in the system when the operation was stopped, and a good treatment effect was achieved. Obtained.
【0027】[0027]
【発明の効果】本発明の工業用抗菌組成物はグルタルア
ルデヒドとダイクロロフェンとを組み合わせたものであ
って、その相乗効果により、工業分野における障害微生
物に対し、広いpH範囲において安定して優れた抗菌活
性を示す。該工業用抗菌組成物は、例えば冷却水系や紙
パルプ工場におけるスライムコントロール用、デンプン
、カゼインなどの防腐用、ラテックス、顔料、接着剤、
塗料などの製品の防腐用、さらには金属加工油使用系で
の防腐用などに好適に用いられる。Effects of the Invention The industrial antibacterial composition of the present invention is a combination of glutaraldehyde and dichlorophene, and due to their synergistic effect, it is stable and excellent against harmful microorganisms in the industrial field over a wide pH range. It exhibits antibacterial activity. The industrial antibacterial composition is used, for example, for slime control in cooling water systems and paper and pulp factories, for preservatives such as starch and casein, latex, pigments, adhesives,
It is suitably used for preservative purposes in products such as paints, and in systems that use metal processing oils.
Claims (1)
ビス(4−クロロフェノール)とを、重量比1:20な
いし20:1の割合で有効成分として含有して成る工業
用抗菌組成物。1. An industrial antibacterial composition comprising glutaraldehyde and 2,2'-methylenebis(4-chlorophenol) as active ingredients in a weight ratio of 1:20 to 20:1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8625591A JPH04297401A (en) | 1991-03-26 | 1991-03-26 | Industrial antimicrobial composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8625591A JPH04297401A (en) | 1991-03-26 | 1991-03-26 | Industrial antimicrobial composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04297401A true JPH04297401A (en) | 1992-10-21 |
Family
ID=13881716
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8625591A Pending JPH04297401A (en) | 1991-03-26 | 1991-03-26 | Industrial antimicrobial composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04297401A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996004343A1 (en) * | 1994-08-04 | 1996-02-15 | Daikin Industries, Ltd. | Aqueous fluoropolymer dispersion |
-
1991
- 1991-03-26 JP JP8625591A patent/JPH04297401A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996004343A1 (en) * | 1994-08-04 | 1996-02-15 | Daikin Industries, Ltd. | Aqueous fluoropolymer dispersion |
US5750606A (en) * | 1994-08-04 | 1998-05-12 | Daikin Industries, Ltd. | Aqueous fluorine-containing polymer dispersion |
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