JPH0469303A - Antifungal agent for wood - Google Patents

Antifungal agent for wood

Info

Publication number
JPH0469303A
JPH0469303A JP17914390A JP17914390A JPH0469303A JP H0469303 A JPH0469303 A JP H0469303A JP 17914390 A JP17914390 A JP 17914390A JP 17914390 A JP17914390 A JP 17914390A JP H0469303 A JPH0469303 A JP H0469303A
Authority
JP
Japan
Prior art keywords
wood
concentration
effect
antifungal
antifungal agent
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
JP17914390A
Other languages
Japanese (ja)
Inventor
Yoshiaki Nakamura
嘉明 中村
Sumihiro Katsu
勝 純宏
Takatsune Takeuchi
竹内 孝常
Hironobu Hamashita
濱下 浩信
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.)
TOYO MOKUZAI BOUFU KK
Nara Prefecture
Original Assignee
TOYO MOKUZAI BOUFU KK
Nara Prefecture
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 TOYO MOKUZAI BOUFU KK, Nara Prefecture filed Critical TOYO MOKUZAI BOUFU KK
Priority to JP17914390A priority Critical patent/JPH0469303A/en
Publication of JPH0469303A publication Critical patent/JPH0469303A/en
Pending legal-status Critical Current

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  • Chemical And Physical Treatments For Wood And The Like (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To obtain the subject antifungal agent showing a high effect in a low concentration by blending 2,4,5,6-(tetrachloroisophthalonitrile) with a compound such as methylene bisthiocyanate or 3-iode-2-propionyl-n-butylcarbanate. CONSTITUTION:An antifungal agent for wood prepared by blending 2,4,5,6-(tetrachloroisophthalonitrile) with one or more compounds selected from methylene bisthiocyanate, 3-iode-2-propionyl-n-butylcarbamate and 2- methoxycarbonylaminobenzimidazole. If each of the above-mentioned compounds is used separately, no sufficient effect is obtained without using it in a high concentration. If using the above-mentioned compounds in combination, a high antifungal effect is obtained in a low total concentration due to an additive effect.

Description

【発明の詳細な説明】[Detailed description of the invention] 【産業上の利用分野】[Industrial application field]

本発明は、木材にかびが発生することを防ぐために用い
られる防かび剤に関するものである。
The present invention relates to a fungicide used to prevent mold from forming on wood.

【従来の技術】[Conventional technology]

木材のかび発生を防止するための薬剤として、従来から
2.4,5.6−(テトラクロロイソ7タロ二トリル)
がその代表的なものとして提供されている。そしてこの
薬剤を所定の濃度で水に分散乃至溶解させることによっ
て木材防かび剤を調製し、木材を木材防かび剤に浸漬し
たり、ある(11土木材に木材防かび剤を塗布したり散
布したりして、防かび処理に供されている。
2.4,5.6-(tetrachloroiso7talonitrile) has been used as a chemical to prevent the growth of mold on wood.
is provided as a representative example. Then, a wood fungicide is prepared by dispersing or dissolving this chemical in water at a predetermined concentration, and the wood is dipped in the wood fungicide, or the wood is coated or sprayed with the wood fungicide. It is used for anti-fungal treatment.

【発明が解決しようとする課題] しかし、二の薬剤は、低濃度では防かび効果カイ十分で
はなく、防かび効果を十分に得るには高濃度で使用しな
ければならず、コスト等の面で満足することができない
ものであった。 本発明は上記の点に鑑みて為されたものであり、低濃度
の配合で高い防かび効果を得ることができる木材防かび
剤を提供することを目的とするものである。 【!I題を解決するための手段1 本発明に係る木材防かび剤は、2,4,5.6−(テト
ラクロロイソ7りロニトリル)に、メチレンとスチオシ
アネートと、3−ヨード−2−プロピニアしn−プチル
カーパネートと、2−メトキシカルボニルアミ/ベンズ
イミダゾールの三種のうち少なくとも一種を配合して成
ることを特徴とする特許ある。 以下本発明の詳細な説明する。 本発明において2.4,5.6−(テトラクロロイソフ
タロニトリル)−以下TCI PNと略称−は必須の薬
剤として使用される。また本発明においてメチレンビス
チオシアネート−以下MBTCと略称−と、3−ヨード
−2−プロピニル−〇−プチルカーバネートー以下IP
BCと略称−と、2−メトキシカルボニルアミ7ペンズ
イミグゾールー以下MERGALと略称−の三種の薬剤
は選択的に使用される。すなわち、TCI PNにMB
TCとIPBCとMERGALのうち一種もしくは二種
、あるいは三種を配合することによって、本発明に係る
木材防かび剤を調製することができる。TCIPN単独
では、またMBTCやIPBCやMERGAL単独では
、高濃度で使用しないと十分な防かび効果を得ることが
できないが、TCI PNにMBTCやIPBCやME
RGALを組み合わせて用いると、これらの相乗作用で
、全体として低い濃度で高い防かび効果を得ることがで
きるのである。 TCIPNと、MBTCやIPBCやMERGALの配
合濃度は、対象とするかびの種類等に応じて適宜設定さ
れるものであり、特に制限されるものではない。 【実施例】 以下本発明tX施例によって例証する。 11九七 TCIPNを0.14重量%(以下%と略記)の濃度で
、IPBCを第1表に示す濃度でそれぞれ水に溶解させ
ることによって、木材防かび剤を調製した。 この防かび剤について防かび性能の試験をおこなった。 試験は日本木材保存協会の試験法に基づいておこなった
。すなわち、ブナ木片を試験体として用い、この試験体
を木材防かび剤の溶液に3分間浸漬し、次いで乾燥した
後にこの試験体を寒天培地の上に置いて菌糸の懸濁液を
塗布し、これを4週間放置した後に、肉眼観察をするこ
とによって試験をおこなった。結果を第1表に示す。 表においてc階欅ごとのモ均評価値jの欄のAIは^5
perH+l1us niger、A2はPenici
lliuw funiculosum、A3はRh1z
opus javanicus、 A 4は^ureo
bas+dium pullulans、 A 5はG
liocladium virenSの各菌種を示す。 また平均評価値は、各菌種の発生状態を、菌が全く発生
しない状態を0、試験体の上面の面積の1/3以上に発
生した状態を3としてθ〜3の数値で評価し、9個の試
験体について評価した数値の平均値として算出したもの
である。さらに表においてSはA1〜A5の平均評価値
の合計値、Dは被害値を示すものであり、無処理試験体
のS=S。 処理試験体のS=S、とすると 被害値D =(S 、/S 、)X 100で算出され
る。この被害値りの数値が小さい程防かび効果が高いと
いうことを評価することができるものであり、−数的に
Dが30以下であれば実用的な防かび性能を具備してい
ると判断することができる。 定量jLL TCr PNのみを第2表に示す濃度で水に分散させろ
ことによって、木材防かび削を調製した。 この防かび剤について同様にして防かび性能の試験をお
こなった。結果を第2表に示す。 比較例2 IPBCのみを第3表に示す濃度で水に分散させること
によって、木材防かび剤を調製した。この防かび剤につ
いて同様にして防かび性能の試験実施例1における第1
表のNolにみちれるように、TCIPNo、14%と
IPBCo、025%の濃度の木材防かび剤はD=9.
3の数値を得ることがでさたのに対して、TCI PN
やIPBCを単独で使用する場合、同様なり値を得るに
は、比較例1における第2表のようにTCI PNの濃
度を0.7%程度に調整する必要があり、また比較例2
における第3表のようにIPBCの濃度を0.15%以
上に調整する必要があり、実施例1のものは低濃度のT
CIPNで高い防かび効果が得られることが確認される
。 友1町影 TCI PNを0.14重量%の濃度で、MBTCを#
S4表に示す濃度でそれぞれ水に分散させることによっ
て、木材防かび剤を調製した。この防かゾ剤について同
様に防かび性能の試験をおこなった。結果を第4表に示
す。 ル上1」ユ MBTCのみを第2表に示す濃度で水に分散させること
によって、木材防かび剤を調製した。この防がゾ剤につ
いて同様にして防がび性能の試験をおこなった。結果を
t!I453に示す。 (以下余白) 実施例2における第4表のNo2にみられるように、T
CIPNo、14%とMBTCo、06%の濃度の木材
防かぴ剤はD=18の数値を得ることができたのに対し
て、TCI PNやMBTCを単独で使用する場合、同
様なり値を得るには、比較例1における第2表のように
TCI PNの濃度を0.35%近くに調整する必要が
あり、また比較例3における#45表のようにMBTC
の濃度を0.25%近くに調整する必要があり、実施例
2のものは低濃度のTCIPNで高い防かび効果が得ら
れることが確認される。 111影 TCI PNを0.14重量%の濃度で、MERGAL
を第6表に示す濃度でそれぞれ水に分散させることによ
って、木材防かび剤を調製した。この防かび剤について
同様に防かび性能の試験をおこなった。結果を#liS
表に示す。 雌1外上 MERGALのみを第7表に示す濃度で水に分散させる
ことによって、木材防かび剤を調製した。 この防かび剤について同様にして防かび性能の試叉施例
3における第6表のNolにみられるように、TCIP
No、14%とMERGALo。 1%の濃度の木材防かび削はD=12.7の数値を得る
ことができたのに対して、TCI PNやMERGAL
を単独で使用する場合、同様なり値を得るには、比較例
1における第2表のようにTCIPNの濃度を0.35
%程度にll!整する必要があり、また比較例4におけ
る第7表のようにMERGALの濃度を0.4%以上に
ll!整する必要があり、実施例3のものは低濃度のT
CI PNで高い防かび効果があることが確認される。 ■発明の効果】 上述のように本発明は、2,4,5.6−(テトラクロ
ロイン7りロニトリル)(こ、メチレンビスチオシアネ
ートと、3−ヨード−2−プロピニル−〇−ブチルカー
バネートと、2−メトキシカルボニル7ミ/ペンズイミ
グゾールの三種のうち少なくとも一種を配合したもので
あり、これらの組み合わせによる相乗作用で防かび性能
が高まり、2,4,5゜6−(テトラクロロイソ7タロ
二トリル)を低い濃度で用いても木材にかびが発生する
ことを防ぐ効果を高く得ることができるものである。
[Problems to be Solved by the Invention] However, the second drug does not have sufficient antifungal effect at low concentrations, and must be used at high concentrations to obtain sufficient antifungal effects, resulting in cost and other issues. I couldn't be satisfied with that. The present invention has been made in view of the above points, and it is an object of the present invention to provide a wood fungicide that can obtain a high fungicide effect even when mixed at a low concentration. [! Means for Solving Problem I 1 The wood fungicide according to the present invention contains 2,4,5,6-(tetrachloroiso7lyronitrile), methylene, sthiocyanate, and 3-iodo-2-propynia. There is a patent which is characterized in that it is a mixture of n-butyl carpanate and at least one of the three types of 2-methoxycarbonyl amide/benzimidazole. The present invention will be explained in detail below. In the present invention, 2,4,5,6-(tetrachloroisophthalonitrile) - hereinafter abbreviated as TCI PN - is used as an essential drug. In addition, in the present invention, methylene bisthiocyanate (hereinafter abbreviated as MBTC) and 3-iodo-2-propynyl-〇-butyl carbonate (hereinafter referred to as IP) are used.
Three drugs are selectively used: BC (abbreviation) and 2-methoxycarbonylamide 7penzimiguzole (hereinafter abbreviated as MERGAL). i.e. MB to TCI PN
The wood fungicide according to the present invention can be prepared by blending one, two, or three of TC, IPBC, and MERGAL. TCIPN alone, MBTC, IPBC, or MERGAL alone cannot provide sufficient antifungal effect unless used at high concentrations;
When RGAL is used in combination, a high antifungal effect can be obtained at a low overall concentration due to their synergistic action. The concentration of TCIPN, MBTC, IPBC, and MERGAL is appropriately set depending on the type of mold to be treated, and is not particularly limited. [Example] The present invention will be illustrated by the tX example below. Wood fungicides were prepared by dissolving 1197TCIPN in water at a concentration of 0.14% by weight (hereinafter abbreviated as %) and IPBC at the concentrations shown in Table 1, respectively. A test for the antifungal performance of this antifungal agent was conducted. The test was conducted based on the test method of the Japan Wood Preservation Association. That is, using a piece of beech wood as a test specimen, this test specimen was immersed in a solution of a wood fungicide for 3 minutes, and then, after drying, the specimen was placed on an agar medium and a suspension of mycelium was applied. After leaving this for 4 weeks, a test was conducted by visually observing it. The results are shown in Table 1. In the table, the AI in the column of mo average evaluation value j for each c-level keyaki is ^5
perH+l1us niger, A2 is Penici
lliuw funiculosum, A3 is Rh1z
opus javanicus, A4 is ^ureo
bas+dium pullulans, A 5 is G
Each species of liocladium virenS is shown. In addition, the average evaluation value is evaluated as a numerical value of θ ~ 3 for the state of occurrence of each bacterial species, with 0 being a state in which no bacteria occur and 3 being a state in which bacteria have occurred on 1/3 or more of the area of the upper surface of the test piece. It was calculated as the average value of the numerical values evaluated for nine test specimens. Further, in the table, S indicates the total value of the average evaluation values of A1 to A5, D indicates the damage value, and S=S for the untreated test specimen. If S=S of the treated specimen, the damage value D is calculated as follows: D=(S,/S,)X100. It is possible to evaluate that the smaller the numerical value of this damage value is, the higher the mold prevention effect is.-If D is 30 or less, it is judged that it has practical mold prevention performance. can do. Wood anti-mildew shavings were prepared by dispersing only quantitative jLL TCr PN in water at the concentrations shown in Table 2. The antifungal performance of this antifungal agent was tested in the same manner. The results are shown in Table 2. Comparative Example 2 A wood fungicide was prepared by dispersing only IPBC in water at the concentrations shown in Table 3. This fungicide was similarly tested for fungibility performance in Example 1.
As shown in No. 1 in the table, the wood fungicide with a concentration of TCIPNo, 14% and IPBCo, 025% has D=9.
It was possible to obtain a value of 3, whereas TCI PN
When using or IPBC alone, in order to obtain the same value, it is necessary to adjust the concentration of TCI PN to about 0.7% as shown in Table 2 in Comparative Example 1, and also in Comparative Example 2.
As shown in Table 3, it is necessary to adjust the concentration of IPBC to 0.15% or more, and in Example 1, a low concentration of T
It is confirmed that CIPN has a high antifungal effect. Tomo 1 Town Shadow TCI PN at a concentration of 0.14% by weight, MBTC #
Wood fungicides were prepared by dispersing each in water at the concentrations shown in Table S4. The fungicidal performance of this antifouling agent was similarly tested. The results are shown in Table 4. Wood fungicides were prepared by dispersing only MBTC in water at the concentrations shown in Table 2. The antifungal performance of this anti-corrosion agent was tested in the same manner. T the results! I453. (Left below) As seen in No. 2 of Table 4 in Example 2, T
A wood fungicide with a concentration of CIP No. 14% and MBTCo 0.6% was able to obtain a value of D = 18, whereas when using TCI PN or MBTC alone, a similar value was obtained. In order to
It is necessary to adjust the concentration of TCIPN to nearly 0.25%, and it is confirmed that a high antifungal effect can be obtained with a low concentration of TCIPN in Example 2. 111 Shadow TCI PN at a concentration of 0.14% by weight, MERGAL
Wood fungicides were prepared by dispersing each of the following in water at the concentrations shown in Table 6. This fungicide was similarly tested for its antifungal performance. #liS the result
Shown in the table. A wood fungicide was prepared by dispersing only MERGAL (Female 1) in water at the concentrations shown in Table 7. As shown in No. 6 of Table 6 in Example 3, TCIP
No, 14% and MERGALo. Wood mold-proofing with a concentration of 1% was able to obtain a value of D = 12.7, whereas TCI PN and MERGAL
When using TCIPN alone, to obtain a similar value, the concentration of TCIPN should be adjusted to 0.35 as shown in Table 2 in Comparative Example 1.
About %ll! Also, as shown in Table 7 in Comparative Example 4, the concentration of MERGAL must be set to 0.4% or more! In Example 3, a low concentration of T was used.
It is confirmed that CI PN has a high antifungal effect. ■Effects of the Invention As described above, the present invention provides 2,4,5,6-(tetrachloroin-7-trilonitrile) (methylene bisthiocyanate and 3-iodo-2-propynyl-〇-butyl carbonate). and 2-methoxycarbonyl 7-mi/penzimigsol, and the synergistic effect of these combinations increases the fungicidal performance, and 2,4,5゜6-(tetrachloro Iso7talonitrile) can be highly effective in preventing the growth of mold on wood even when used at a low concentration.

Claims (1)

【特許請求の範囲】[Claims] (1)2,4,5,6−(テトラクロロイソフタロニト
リル)に、メチレンビスチオシアネートと、3−ヨード
−2−プロピニル−n−ブチルカーバネートと、2−メ
トキシカルボニルアミノベンズイミダゾールの三種のう
ち少なくとも一種を配合して成ることを特徴とする木材
防かび剤。
(1) Three types of 2,4,5,6-(tetrachloroisophthalonitrile), methylene bisthiocyanate, 3-iodo-2-propynyl-n-butyl carbonate, and 2-methoxycarbonylaminobenzimidazole A wood fungicide characterized by containing at least one of the above.
JP17914390A 1990-07-05 1990-07-05 Antifungal agent for wood Pending JPH0469303A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17914390A JPH0469303A (en) 1990-07-05 1990-07-05 Antifungal agent for wood

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17914390A JPH0469303A (en) 1990-07-05 1990-07-05 Antifungal agent for wood

Publications (1)

Publication Number Publication Date
JPH0469303A true JPH0469303A (en) 1992-03-04

Family

ID=16060727

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17914390A Pending JPH0469303A (en) 1990-07-05 1990-07-05 Antifungal agent for wood

Country Status (1)

Country Link
JP (1) JPH0469303A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5607727A (en) * 1995-03-14 1997-03-04 Isk Biosciences Corporation Composition and method for controlling brown stain in wood
WO2000070953A1 (en) * 1999-05-24 2000-11-30 Creanova, Inc. Synergistic composition of biocides
AU757579B2 (en) * 1999-05-24 2003-02-27 Isp Investments Inc. Synergistic composition of biocides
JP2007106693A (en) * 2005-10-13 2007-04-26 Sumika Enviro-Science Co Ltd Wood protecting composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5607727A (en) * 1995-03-14 1997-03-04 Isk Biosciences Corporation Composition and method for controlling brown stain in wood
WO2000070953A1 (en) * 1999-05-24 2000-11-30 Creanova, Inc. Synergistic composition of biocides
AU757579B2 (en) * 1999-05-24 2003-02-27 Isp Investments Inc. Synergistic composition of biocides
JP2007106693A (en) * 2005-10-13 2007-04-26 Sumika Enviro-Science Co Ltd Wood protecting composition

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