JPH04244003A - Fungicide for wood - Google Patents

Fungicide for wood

Info

Publication number
JPH04244003A
JPH04244003A JP1097691A JP1097691A JPH04244003A JP H04244003 A JPH04244003 A JP H04244003A JP 1097691 A JP1097691 A JP 1097691A JP 1097691 A JP1097691 A JP 1097691A JP H04244003 A JPH04244003 A JP H04244003A
Authority
JP
Japan
Prior art keywords
wood
drug
fungicide
remaining
trichlorophenol
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.)
Withdrawn
Application number
JP1097691A
Other languages
Japanese (ja)
Inventor
Yoshiaki Sukai
与志明 須貝
Hiroshi Ueda
洋 上田
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.)
Lomb & Haasu Japan Kk
ZAIENSU KK
Xyence Corp
Original Assignee
Lomb & Haasu Japan Kk
ZAIENSU KK
Xyence Corp
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 Lomb & Haasu Japan Kk, ZAIENSU KK, Xyence Corp filed Critical Lomb & Haasu Japan Kk
Priority to JP1097691A priority Critical patent/JPH04244003A/en
Priority to MYPI92000113A priority patent/MY108690A/en
Priority to NZ24139392A priority patent/NZ241393A/en
Publication of JPH04244003A publication Critical patent/JPH04244003A/en
Withdrawn legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To provide a new antifungal agent having a large synergistic effect, capable of exhibiting an extremely large antifungal effect at a small dose and used for wood. CONSTITUTION:The subject agent contains 4,5-dichloro-2-n-octyl-4-isothiazolon-3- one and 2,4,6-trichlorophenol as active ingredients.

Description

【発明の詳細な説明】[Detailed description of the invention]

【0001】0001

【産業上の利用分野】本発明は、かび発生による木材の
劣化を防止するための木材用防かび剤に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a fungicide for wood to prevent deterioration of wood due to mold growth.

【0002】0002

【従来の技術】2,4,6‐トリクロルフェノール(以
下、TCPということがある)は、従来から木材用防か
び剤として知られている薬剤であるが、抗菌スペクトル
が限られていること、および使用時の濃度が低いときは
効力が弱く、逆に濃度が高過ぎるときは種々の薬害が発
生するという問題がある。また4,5‐ジクロル‐2‐
n‐オクチル‐4‐イソチアゾリン‐3‐オン(以下、
DOIOということがある)は、高価であって、有効濃
度での使用は経済的でないという欠点があった。
[Prior Art] 2,4,6-Trichlorophenol (hereinafter sometimes referred to as TCP) is a chemical that has been known as a fungicide for wood, but its antibacterial spectrum is limited. There is also a problem that when the concentration at the time of use is low, the efficacy is weak, and on the other hand, when the concentration is too high, various chemical harms occur. Also, 4,5-dichloro-2-
n-octyl-4-isothiazolin-3-one (hereinafter referred to as
DOIO) has the disadvantage that it is expensive and uneconomical to use at effective concentrations.

【0003】0003

【発明が解決しようとする課題】本発明は、従来の木材
用防かび剤がその有効性とコストとの面で不満足なもの
であったことに鑑み、このような欠点のない新規の木材
用防かび剤を提供することを目的としたものである。
[Problems to be Solved by the Invention] In view of the fact that conventional wood fungicides have been unsatisfactory in terms of effectiveness and cost, the present invention has been made to develop a new wood fungicide that does not have these drawbacks. The purpose is to provide a fungicide.

【0004】0004

【課題を解決するための手段】かかる本発明の目的は、
4,5‐ジクロル‐2‐n‐オクチル‐4‐イソチアゾ
リン‐3‐オンと2,4,6‐トリクロルフェノールと
を有効成分として含有することを特徴とする木材用防か
び剤によって達成される。そして更に、かかる木材用防
かび剤において、4,5‐ジクロル‐2‐n‐オクチル
‐4‐イソチアゾリン‐3‐オンと2,4,6‐トリク
ロルフェノールとを重量比で1:200乃至1:2の範
囲内で含有することによって、いずれか単独の薬剤より
も優れた相乗的な防かび効果が発揮される。
[Means for Solving the Problems] The purpose of the present invention is to
This is achieved by a wood fungicide characterized by containing 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one and 2,4,6-trichlorophenol as active ingredients. Furthermore, in such a wood fungicide, 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one and 2,4,6-trichlorophenol are mixed in a weight ratio of 1:200 to 1: By containing within the range of 2, a synergistic antifungal effect superior to that of either agent alone can be exhibited.

【0005】[0005]

【実施例】縦3cm×横3cm×厚さ0.6cmのパー
ティクルボードを第1表に示したような配合の薬剤液に
それぞれ3分間浸漬し、薬液の付着量が200〜250
g/m2 の範囲となるような試験体をそれぞれ5個ず
つ作成した。このような試験体を充分に風乾し、シャー
レ内に設けたPDA寒天培地上にポリエチレン製ネット
を敷き、その上に前記の試験体を置いて、別途PDA寒
天培地上で培養した下記に示すかびから調製した混合胞
子懸濁液をそれぞれ2mlずつスプレーした。それぞれ
のシャーレには蓋をし、26℃の恒温器中で1か月培養
したのち試験体表面のかびの発生程度を観察し、下記の
評価方法に従って薬剤の効力の評価を行なった。
[Example] A particle board measuring 3 cm in length x 3 cm in width x 0.6 cm in thickness was immersed for 3 minutes in each chemical solution having the composition shown in Table 1, and the adhesion amount of the chemical solution was 200-250.
Five test specimens each having a range of g/m2 were prepared. After thoroughly air-drying such a test specimen, a polyethylene net was placed on a PDA agar medium set in a petri dish, and the above-mentioned test specimen was placed on top of the polyethylene net, and the mold shown below was separately cultured on a PDA agar medium. 2 ml of the mixed spore suspension prepared from above was sprayed on each of the test tubes. Each petri dish was covered with a lid and cultured for one month in a constant temperature chamber at 26°C. The degree of mold growth on the surface of the specimen was observed, and the efficacy of the drug was evaluated according to the evaluation method described below.

【表1】                         第
  1  表  (重量部)  ──────────
──────────────────────── 
   薬剤    TCP    DOIO    N
aOH    SAA    水      合計  
─────────────────────────
─────────    A      1.0  
      0.1          0.2   
     0.4      残      100 
    B      1.0        0.0
5         0.2        0.4 
     残      100     C    
  2.0        0.1         
 0.4        0.4      残   
   100     D      2.0    
    0.05         0.4     
   0.4      残      100   
  E      1.0        0.01 
        0.2        0.4   
   残      100     F      
1.0        0.005        0
.2        0.4      残     
 100     G      0.5      
  0.1          0.1       
 0.4      残      100     
H      0.5        0.05   
      0.1        0.4     
 残      100     I      0.
2        0.1          0.0
5       0.4      残      1
00     J*     2.0       ─
─          0.4        0.4
      残      100     K*  
   1.0       ──          
0.2        0.4      残    
  100     L*     0.5     
  ──          0.1        
0.4      残      100     M
*     ──       0.1       
   ──       0.4      残   
   100     N*     ──     
  0.05         ──       0
.4      残      100   ────
─────────────────────────
─────TCP  :2,4,6‐トリクロルフェノ
ールDOIO:4,5‐ジクロル‐2‐n‐オクチル‐
4‐イソチアゾリン‐3‐オン NaOH:水酸化ナトリウム SAA  :ノニオン系界面活性剤 *       :比較例
[Table 1] Table 1 (Parts by weight) ──────────
────────────────────────
Drug TCP DOIO N
aOH SAA Water Total
──────────────────────────
────────── A 1.0
0.1 0.2
0.4 remaining 100
B 1.0 0.0
5 0.2 0.4
100 C remaining
2.0 0.1
0.4 0.4 Remaining
100D 2.0
0.05 0.4
0.4 remaining 100
E 1.0 0.01
0.2 0.4
100F left
1.0 0.005 0
.. 2 0.4 remaining
100G 0.5
0.1 0.1
0.4 remaining 100
H 0.5 0.05
0.1 0.4
Remaining 100 I 0.
2 0.1 0.0
5 0.4 remaining 1
00 J* 2.0 ─
─ 0.4 0.4
100K left*
1.0 ---
0.2 0.4 Remaining
100 L* 0.5
─ 0.1
0.4 remaining 100M
*──0.1
─ 0.4 remaining
100 N*──
0.05 --- 0
.. 4 100 remaining ────
──────────────────────────
─────TCP: 2,4,6-trichlorophenol DOIO: 4,5-dichloro-2-n-octyl-
4-isothiazolin-3-one NaOH: Sodium hydroxide SAA: Nonionic surfactant*: Comparative example

【0006】供試かび アスペルギルス  ニガー  (Aspergillu
s niger )トリコデルマ  ビリダ  (Tr
ichoderma viride)アウレオバシヂウ
ム  ブルランス  (Aureobasidium 
pullulans ) ペニシルム  シトリウム  (Penicillum
 citrioum )リゾプス  ニグリカンス  
(Rhizopus nigricans)
[0006] Test mold Aspergillus niger
s niger) Trichoderma virida (Tr.
ichoderma viride) Aureobasidium bullans (Aureobasidium
pullulans ) Penicillum citrium ( Penicillum
citrium) Rhizopus nigricans
(Rhizopus nigricans)

【0007
】評価方法 かびの発生した試験体に、次の基準に従ってそれぞれ被
害値の点数を付け、5個の合計点数を求めてその薬剤処
理試験体の被害度Xとした。
0007
[Evaluation Method] Each mold-infested specimen was given a damage value score according to the following criteria, and the total score of the five was calculated to determine the degree of damage X for the chemical-treated specimen.

【0008】             被害値の判断基準:  ──
─────────────────────────
─      0:試験体の表面にかび発生が認められ
ない      1:  〃    側面のみにかび発
生が認められる      2:  〃    上面の
 1/3 以下に    〃      3:  〃 
   上面の 1/3 以上に    〃  ────
────────────────────────
[0008] Criteria for determining damage value: ---
──────────────────────────
─ 0: No mold growth is observed on the surface of the test specimen. 1: Mold growth is observed only on the side surfaces. 2: 〃 On 1/3 or less of the top surface. 〃 3: 〃
More than 1/3 of the top surface 〃 ────
────────────────────────


0009】更に、無処理試験体についても同様な試験を
行なって被害度X0 を求め、薬剤処理試験体の被害度
Xと無処理試験体の被害度X0 とから、下記の式に従
って各薬剤の防かび指数を算出した。
[
[0009]Furthermore, a similar test was conducted on the untreated test specimen to determine the degree of damage X0, and from the damage degree The mold index was calculated.

【式1】[Formula 1]

【0010】こうして得た試験の結果を第2表に示すが
、これらの結果をみると、TCPの1.0部(薬剤K*
 )はDOIOの0.1部(薬剤M* )と、またTC
Pの0.5部(薬剤L* )はDOIOの0.05部(
薬剤N* )と、それぞれ同等の効果を現すことがわか
る。更に、薬剤J* と薬剤M* との1:1混合組成
に相当する薬剤Bが、また、薬剤K* と薬剤M* と
の1:1混合組成に相当する薬剤Hが、いずれも対応す
る比較例の薬剤と比べて極めて優れた相乗効果を現すこ
ともわかる。
The results of the test thus obtained are shown in Table 2, and these results show that 1.0 part of TCP (drug K*
) is 0.1 part of DOIO (drug M*) and also TC
0.5 part of P (drug L*) is 0.05 part of DOIO (
It can be seen that each drug has the same effect as the drug N*). Furthermore, drug B, which corresponds to a 1:1 mixed composition of drug J* and drug M*, and drug H, which corresponds to a 1:1 mixed composition of drug K* and drug M*, both correspond. It can also be seen that it exhibits an extremely superior synergistic effect compared to the comparative drug.

【表2】                          
     第  2  表      ───────
───────────────────────  
        薬剤      試験体の被害値  
    被害度      防かび指数      ─
─────────────────────────
────          A          
0,0,0,0,1             1  
           93          B 
         0,0,1,1,1       
      3             80   
       C          0,0,0,0
,0             0         
   100          D        
  0,0,0,0,1             1
             93          
E          0,0,1,1,2     
        4             73 
         F          1,2,2
,2,3            10       
      33          G      
    0,1,1,2,2            
 6             60        
  H          0,0,0,1,1   
          2             8
7          I          1,1
,2,3,3            10     
        33          J*   
      1,2,2,2,2          
   9             40      
    K*         2,2,2,3,3 
           12            
 20          L*         2
,2,3,3,3            13   
          13          M* 
        2,2,2,3,3        
    12             20    
      N*         2,2,3,3,
3            13          
   13        ───        3
,3,3,3,3            15   
          −−      ───────
───────────────────────  
      ───  :薬剤無処理の場合
[Table 2]
Table 2 ────────
────────────────────────
Drug Damage value of test specimen
Damage level Mold prevention index ─
──────────────────────────
──── A
0,0,0,0,1 1
93B
0,0,1,1,1
3 80
C 0,0,0,0
,0 0
100D
0,0,0,0,1 1
93
E 0,0,1,1,2
4 73
F 1, 2, 2
,2,3 10
33 G
0,1,1,2,2
6 60
H 0,0,0,1,1
2 8
7 I 1,1
,2,3,3 10
33 J*
1, 2, 2, 2, 2
9 40
K* 2, 2, 2, 3, 3
12
20 L* 2
,2,3,3,3 13
13 M*
2, 2, 2, 3, 3
12 20
N* 2, 2, 3, 3,
3 13
13 ─── 3
,3,3,3,3 15
−− ───────
────────────────────────
─── : Without chemical treatment

【0011
0011
]

【発明の効果】本発明の木材用防かび剤は、従来から知
られていたが効果や経済性などの面で実用上で問題のあ
った薬剤を配合することにより、大きな相乗効果を発揮
させることができたもので、少量の使用で極めて高い防
かび効果を得ることができる特長がある。
[Effects of the Invention] The wood fungicide of the present invention exhibits a great synergistic effect by combining chemicals that have been known in the past but had problems in practical use in terms of effectiveness and economy. It has the feature of being able to obtain extremely high antifungal effects even when used in small amounts.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】  4,5‐ジクロル‐2‐n‐オクチル
‐4‐イソチアゾリン‐3‐オンと2,4,6‐トリク
ロルフェノールとを有効成分として含有することを特徴
とする、木材用防かび剤。
[Claim 1] A fungicide for wood, characterized by containing 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one and 2,4,6-trichlorophenol as active ingredients. agent.
【請求項2】  4,5‐ジクロル‐2‐n‐オクチル
‐4‐イソチアゾリン‐3‐オンと2,4,6‐トリク
ロルフェノールとを重量比で1:200乃至1:2の範
囲内で含有することを特徴とする、請求項1に記載の木
材用防かび剤。
Claim 2: Contains 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one and 2,4,6-trichlorophenol in a weight ratio of 1:200 to 1:2. The wood fungicide according to claim 1, characterized in that:
JP1097691A 1991-01-31 1991-01-31 Fungicide for wood Withdrawn JPH04244003A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP1097691A JPH04244003A (en) 1991-01-31 1991-01-31 Fungicide for wood
MYPI92000113A MY108690A (en) 1991-01-31 1992-01-24 Mildewproofing agent for timber
NZ24139392A NZ241393A (en) 1991-01-31 1992-01-24 Mildewproofing composition for timber comprising a mixture of 4,5-dichloro-2n-octyl-4-isothiazolin-3-one and 2,4,6-trichlorophenol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1097691A JPH04244003A (en) 1991-01-31 1991-01-31 Fungicide for wood

Publications (1)

Publication Number Publication Date
JPH04244003A true JPH04244003A (en) 1992-09-01

Family

ID=11765193

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1097691A Withdrawn JPH04244003A (en) 1991-01-31 1991-01-31 Fungicide for wood

Country Status (3)

Country Link
JP (1) JPH04244003A (en)
MY (1) MY108690A (en)
NZ (1) NZ241393A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004509137A (en) * 2000-09-19 2004-03-25 バイエル アクチェンゲゼルシャフト Combinations of active substances for protecting animal skin and leather
MD3966C2 (en) * 2008-09-30 2010-05-31 Институт Химии Академии Наук Молдовы Process for insectofungicization and hydrophobization of age-old wood articles of art

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004509137A (en) * 2000-09-19 2004-03-25 バイエル アクチェンゲゼルシャフト Combinations of active substances for protecting animal skin and leather
MD3966C2 (en) * 2008-09-30 2010-05-31 Институт Химии Академии Наук Молдовы Process for insectofungicization and hydrophobization of age-old wood articles of art

Also Published As

Publication number Publication date
NZ241393A (en) 1994-04-27
MY108690A (en) 1996-10-31

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