JP2003277207A - Antifungal and anti-discoloring-fungus composition for wood - Google Patents

Antifungal and anti-discoloring-fungus composition for wood

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Publication number
JP2003277207A
JP2003277207A JP2002084673A JP2002084673A JP2003277207A JP 2003277207 A JP2003277207 A JP 2003277207A JP 2002084673 A JP2002084673 A JP 2002084673A JP 2002084673 A JP2002084673 A JP 2002084673A JP 2003277207 A JP2003277207 A JP 2003277207A
Authority
JP
Japan
Prior art keywords
antifungal
discoloring
effectiveness
wood
exhibits
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
Application number
JP2002084673A
Other languages
Japanese (ja)
Other versions
JP4194070B2 (en
Inventor
Kazuhide Fujimoto
和秀 藤本
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.)
Sumika Enviro Science Co Ltd
Original Assignee
Shinto Fine Co Ltd
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 Shinto Fine Co Ltd filed Critical Shinto Fine Co Ltd
Priority to JP2002084673A priority Critical patent/JP4194070B2/en
Publication of JP2003277207A publication Critical patent/JP2003277207A/en
Application granted granted Critical
Publication of JP4194070B2 publication Critical patent/JP4194070B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

<P>PROBLEM TO BE SOLVED: To solve the problem that there is a demand for a further effective antifungal and anti-discoloring-fungus agent because discoloring bacteria outside the conventional antifungal spectra emerges in spite of attempts of combining various antifungal agents or to stabilize antifungal spectra, the enhancement of effectiveness, etc. <P>SOLUTION: It has been found out that when combining the three compounds of 4,5-dichloro-2-n-octylisothiazolin-3-one, methyl 2-benzimidazolecarbamate and methylenebisthiocyanate as the active ingredient, the combination exhibits improved antifungal effectiveness as compared with the case in which they are used singly or in the form of a two-component mix, and exhibits an excellent effectiveness also against wood discoloring fungi. It has been further found out that when 3-iodo-2-propynylbutyl carbamate is added to the above three compounds, the resultant antifungal agent exhibits markedly improved antifungal effectiveness and exhibits effectiveness also against wood discoloring fungi. <P>COPYRIGHT: (C)2004,JPO

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、木材に発生するカ
ビや変色菌を防ぐために用いられる木材防カビ防変色菌
組成物に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a wood-mold anti-mildew and anti-coloring fungus composition used to prevent mold and tarnishing bacteria from occurring in wood.

【0002】[0002]

【従来の技術】従来、木材用防カビ剤としてハロゲン化
フェノール化合物や有機錫化合物が多く利用されてき
た。しかしながらこれらの化合物は急性及び慢性毒性が
強く、また比較的難分解性であることから蓄積による二
次公害の懸念があり、これらの木材防カビ剤は使用に適
さなくなってきた。このため、より安全性の高い木材防
カビ剤の開発が盛んに行われるようになり3-ヨード-2-
プロピニルブチルカーバメート(以下IPBCと略す)など
の化合物が提供されており、木材におけるカビの発生を
防止するために添加されることが多い。しかしながらIP
BCのみの単一成分の使用では、効力を有する微生物の種
が限られるなどの理由で十分な効力が得られず、薬剤の
使用量が増え、コストも高くなることが多い。また、4,
5-ジクロロ-2-n-オクチルイソチアゾリン-3-オン(以
下COITと略す)及び2-ベンズイミダゾールカルバミン酸
メチル(以下BCMと略す)は安全性の高い工業用の防カ
ビ剤として知られているが、単独に適用した場合には微
生物の抵抗性がしばしば生じるため、適用濃度をかなり
高くしなければ十分な効力を得ることができず、防カビ
剤としては著しく適正を欠いていた。
2. Description of the Related Art Conventionally, halogenated phenol compounds and organotin compounds have been widely used as antifungal agents for wood. However, since these compounds have strong acute and chronic toxicity and are relatively hard to decompose, there is concern about secondary pollution due to accumulation, and these wood fungicides have become unsuitable for use. Therefore, the development of safer antifungal agents for wood has been actively conducted. 3-Iodo-2-
Compounds such as propynyl butyl carbamate (hereinafter abbreviated as IPBC) have been provided, and are often added to prevent the formation of mold on wood. However IP
The use of a single component of BC alone does not provide sufficient efficacy due to the limited number of species of microorganisms having efficacy, the amount of drug used is often increased, and the cost is often high. Also, 4,
5-Dichloro-2-n-octylisothiazolin-3-one (hereinafter abbreviated as COIT) and methyl 2-benzimidazole carbamate (hereinafter abbreviated as BCM) are known as highly safe industrial fungicides. However, when it is applied alone, resistance of microorganisms often occurs, and therefore, sufficient efficacy cannot be obtained unless the application concentration is considerably high, and it is remarkably lacking as an antifungal agent.

【0003】[0003]

【発明が解決しようとする課題】このため各種防カビ剤
を組み合わせ、防カビスペクトルの安定化や防カビ効力
の増強などが試みられているが、通常はいずれか一方の
効果の発現に留まるか、相加的な効果しか得られないの
が実情である。例えば特開昭63−41405号には上
記IPBCに1,4-ビス-(2-エチルヘキシル)スルホコハク
酸ナトリウムを安定剤として使用する方法、さらに特開
平2−164803号には、上記IPBCとベンズイミダゾ
ール系化合物を合剤にする方法が提案されている。ま
た、特開平3−251508号にはベンズイミダゾール
系化合物とイソチアゾリン系化合物を合剤にする方法、
さらに特開平7−133205号にはCOITとIPBCを合剤
にする方法が提案されている。しかしながら、木材上に
発生する真菌はカビの他、変色菌があり、最近、変色菌
による被害も多く見られるようになった。そこで、これ
らに対しても効果をもった更なる広い抗菌スペクトルの
薬剤が望まれていた。
For this reason, attempts have been made to combine various antifungal agents to stabilize the antifungal spectrum and enhance the antifungal effect. Usually, either one of the effects will be manifested. The reality is that only additive effects can be obtained. For example, JP-A-63-41405 discloses a method in which sodium 1,4-bis- (2-ethylhexyl) sulfosuccinate is used as a stabilizer in the IPBC, and JP-A-2-164803 discloses the IPBC and benzimidazole. There has been proposed a method of using a system compound as a mixture. Further, JP-A-3-251508 describes a method of using a mixture of a benzimidazole compound and an isothiazoline compound,
Further, JP-A-7-133205 proposes a method of combining COIT and IPBC. However, fungi occurring on wood include fungi and discoloring fungi, and recently, many damages by discoloring fungi have been observed. Therefore, a drug having a broader antibacterial spectrum that is effective against these substances has been desired.

【0004】[0004]

【課題を解決するための手段】本発明者は、前記効力不
足を補う木材防カビ防変色菌組成物に関し、鋭意研究を
重ねた結果、有効成分としてCOITとBCMとメチレンビス
チオシアネート(以下、MBTCと略す)の3種を組み合わ
せた場合、それぞれ単独あるいは2種合剤で用いた場合
と比較して飛躍的に防カビ効力が増大し、かつ、変色菌
にも有効になることを見出した。さらに本発明組成物に
IPBCを加えることにより防カビ防変色菌効力が増大する
ことを見出し本発明を完成した。すなわち、本発明はCO
ITとBCMとMBTCの3種、あるいはIPBCとCOITとBCMとMBTC
の4種を有効成分として含有することを特徴とする木材
用防カビ防変色菌組成物である。
[Means for Solving the Problems] The present inventor has conducted extensive studies as to a composition for anti-mold and anti-mildew wood that compensates for the lack of efficacy. It was found that the antifungal effect is dramatically increased and the antifungal agent is effective against discoloring bacteria when compared with the case of using them alone or as a mixture of two kinds. Further in the composition of the present invention
The present invention has been completed by finding that the addition of IPBC enhances the efficacy of antifungal and anti-tarnish bacteria. That is, the present invention
Three types of IT, BCM and MBTC, or IPBC, COIT, BCM and MBTC
The antifungal and anti-tarnish composition for wood is characterized by containing the following 4 kinds as an active ingredient.

【0005】[0005]

【発明の実施の形態】本発明の木材用防カビ組成物は使
用目的に応じて直接適用することもできるが、一般的に
は油剤、乳剤、ペースト剤、懸濁剤などの剤型として使
用する。製剤化する場合に用いる極性溶媒としては、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、トリエチレングリコール、ジプロピレング
リコール、へキシレングリコール、ポリエチレングリコ
ールなどのグリコール系溶剤、ジエチレングリコールモ
ノメチルエーテル、ジエチレングリコールモノエチルエ
ーテル、ジエチレングリコールモノブチルエーテルなど
のグリコールエーテル系溶剤、イソプロピルアルコー
ル、エタノールなどのアルコール系溶剤、ジメチルアセ
トアミド、ジメチルスルホキシド、γ−ブチロラクト
ン、メチルエチルケトンまたは水などの溶媒が使用でき
る。これらは、単独で用いても良いし、2種以上を組み
合わせても良い。
BEST MODE FOR CARRYING OUT THE INVENTION The antifungal composition for wood of the present invention can be directly applied depending on the purpose of use, but it is generally used as a formulation such as an oil, an emulsion, a paste and a suspension. To do. The polar solvent used in the case of formulation, glycol solvents such as ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, dipropylene glycol, hexylene glycol, polyethylene glycol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol mono A glycol ether solvent such as butyl ether, an alcohol solvent such as isopropyl alcohol and ethanol, a solvent such as dimethylacetamide, dimethyl sulfoxide, γ-butyrolactone, methyl ethyl ketone or water can be used. These may be used alone or in combination of two or more.

【0006】非極性溶媒としては、フタル酸ジオクチ
ル、フタル酸ジイソノニルなどの可塑剤、キシロール、
トルエン、イソホロン、フェニルキシリルエタン、ジエ
チレングリコールモノブチルエーテルアセテート、プロ
ピレンカーボネート、流動パラフィン、灯油、椰子油、
菜種油、綿実油、ヒマシ油または、大豆油などの溶媒が
使用できる。これらは、単独で用いても良いし、2種以
上を組み合わせても良い。また、極性溶媒と非極性溶媒
を2種以上組み合わせてもよい。界面活性剤は使用して
も使用しなくてもよく、使用する場合は、非イオン界面
活性剤、陰イオン界面活性剤、陽イオン界面活性剤、両
イオン界面活性剤のいずれを用いてもかまわない。
Examples of the nonpolar solvent include plasticizers such as dioctyl phthalate and diisononyl phthalate, xylol,
Toluene, isophorone, phenylxylylethane, diethylene glycol monobutyl ether acetate, propylene carbonate, liquid paraffin, kerosene, palm oil,
Solvents such as rapeseed oil, cottonseed oil, castor oil or soybean oil can be used. These may be used alone or in combination of two or more. Further, two or more kinds of polar solvent and non-polar solvent may be combined. The surfactant may or may not be used, and when it is used, any of a nonionic surfactant, an anionic surfactant, a cationic surfactant and a zwitterionic surfactant may be used. Absent.

【0007】非イオン系界面活性剤として例えばポリオ
キシエチレンアルキルフェニルエーテル、ポリオキシエ
チレンスチリルフェニルエーテル、ポリオキシエチレン
アルキルエーテル、ソルビタン脂肪酸エステル、ポリオ
キシエチレンソルビタン脂肪酸エステルなどが挙げら
れ、陰イオン系界面活性剤としてアルキルベンゼン硫酸
塩、ポリオキシエチレンアルキルエーテル硫酸塩、ポリ
オキシエチレンアルキルフェニルエーテル硫酸塩、ジア
ルキルスルホコハク酸塩などが挙げられ、陽イオン系界
面活性剤では脂肪族アミン塩およびその4級アンモニウ
ム塩などが挙げられ、両イオン系界面活性剤ではベタイ
ン型界面活性剤、アミノカルボン酸塩などが挙げられる
が、これらに限定されない。
Examples of nonionic surfactants include polyoxyethylene alkyl phenyl ether, polyoxyethylene styryl phenyl ether, polyoxyethylene alkyl ether, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, and the like. Examples of the activator include alkylbenzene sulfate, polyoxyethylene alkyl ether sulfate, polyoxyethylene alkylphenyl ether sulfate, and dialkyl sulfosuccinate. As the cationic surfactant, aliphatic amine salt and its quaternary ammonium salt are used. Examples of amphoteric surfactants include, but are not limited to, betaine surfactants and aminocarboxylic acid salts.

【0008】また、これらの非イオン系界面活性剤、陰
イオン系界面活性剤、陽イオン系界面活性剤および両イ
オン系界面活性剤は1種を単独に用いても2種以上を併
用してもよい。本発明組成物中における有効成分の含有
割合は特に限定されるものではないが、BCMとCOITの配
合比率は重量比で10:1〜1:10、好ましくは5:
1〜1:5であり、BCMとCOITの合計量と、MBTCとの配
合比率は重量比で10:1〜1:10、好ましくは5:
1〜1:5、BCMとCOITとMBTCの合計量と、IPBCとの配
合比率は重量比で10:1〜1:10、好ましくは5:
1〜1:5である。また他の防カビ剤、殺菌剤、殺虫
剤、防錆剤、劣化防止剤などを配合して使用することも
可能である。
These nonionic surfactants, anionic surfactants, cationic surfactants and amphoteric surfactants may be used alone or in combination of two or more. Good. The content ratio of the active ingredient in the composition of the present invention is not particularly limited, but the mixing ratio of BCM and COIT is 10: 1 to 1:10, preferably 5 :.
It is 1 to 1: 5, and the mixing ratio of the total amount of BCM and COIT and MBTC is 10: 1 to 1:10 by weight ratio, preferably 5:
1 to 1: 5, the total amount of BCM, COIT, and MBTC, and the blending ratio of IPBC is 10: 1 to 1:10 by weight, preferably 5:
It is 1 to 1: 5. It is also possible to mix and use other fungicides, bactericides, insecticides, rust preventives, deterioration inhibitors and the like.

【0009】[0009]

【実施例】次に本発明の実施例及び比較例を挙げて説明
するが、本発明はこれらに限定されるものではない。以
下に示した配合比率はすべて重量%である。
EXAMPLES Examples and comparative examples of the present invention will be described below, but the present invention is not limited thereto. All of the compounding ratios shown below are% by weight.

【0010】実施例1〜3、比較例1〜11の木材用防
カビ防変色菌組成物を表1に示す。比較例1、3、4、
5、7、9は、表1に示す配合比率で常温において通常
の攪拌によって防カビ防変色菌組成物を得た。また、実
施例1、2、3、比較例2,6,8,10,11は、表
1に示す配合で混合し、直径1mmのガラスビーズと混
合し約15分間粉砕し、金網でろ別することによって防
カビ防変色菌分散組成物を得た。
Table 1 shows the fungicidal and anti-tarnish fungus compositions for wood of Examples 1 to 3 and Comparative Examples 1 to 11. Comparative Examples 1, 3, 4,
Nos. 5, 7 and 9 were anti-fungal and anti-tarnish fungi compositions with the mixing ratios shown in Table 1 at room temperature by ordinary stirring. In addition, Examples 1, 2, 3 and Comparative Examples 2, 6, 8, 10, and 11 were mixed in the composition shown in Table 1, mixed with glass beads having a diameter of 1 mm, pulverized for about 15 minutes, and filtered with a wire mesh. As a result, a mold-proof and anti-tarnish disperse composition was obtained.

【0011】[0011]

【表1】 *1:ポリオキシエチレンスチリルフェニルエーテル *2:プロピレングリコール【table 1】 * 1: Polyoxyethylene styryl phenyl ether * 2: Propylene glycol

【0012】試験例1 木材の防カビ試験 水で規定濃度となるように希釈した実施例及び比較例の
木材用防カビ防変色菌組成物の溶液中にベイマツ辺材
(2cm×5cm×0.3cm)を30秒浸漬した後風乾す
る。この試験片をポテトデキストロース寒天培地(以
下、PDA培地とする)上に載せ、カビの混合胞子懸濁
液1mlをふりかけて温度26℃、湿度95%で28日間
培養した。供試菌としては、Aspergillus niger、Penic
illium funiculosum、Aureobasidium pullulans、Glioc
ladium virens、Cladosporium cladosporioides及びNeu
rospora sp.を用いた。結果を表2に示す。ただし、カビ
生育の程度の表示は次の判定基準によった。
Test Example 1 Antifungal test of wood Dilute the bay pine sapwood (2 cm x 5 cm x 0. 3 cm) for 30 seconds and then air dried. This test piece was placed on a potato dextrose agar medium (hereinafter referred to as PDA medium), and 1 ml of a mixed spore suspension of mold was sprinkled on the medium and cultured at a temperature of 26 ° C. and a humidity of 95% for 28 days. As the test bacteria, Aspergillus niger, Penic
illium funiculosum, Aureobasidium pullulans, Glioc
ladium virens, Cladosporium cladosporioides and Neu
rospora sp. was used. The results are shown in Table 2. However, the indication of the degree of mold growth was based on the following criteria.

【0013】−:試験片にカビの生育を全く認めない。 +:試験片の側面にカビの発育が認められる。 ++:試験片上のカビの発育部分の面積が全面積の1/
3未満である。 +++:試験片上のカビの発育部分の面積が全面積の1
/3以上である
-: No mold growth is observed on the test piece. +: Mold growth is recognized on the side surface of the test piece. ++: The area of mold growth on the test piece is 1 / of the total area
It is less than 3. ++: The area of mold growth on the test piece is 1 of the total area
/ 3 or more

【0014】試験例2 木材の防変色菌試験 シャーレにPDA培地を固化させた上にエチレンオキサ
イドガス滅菌された無処理のベイマツ(餌木)を置く。こ
れに木材変色菌Ceratocystis sp.の胞子懸濁液2mlを滴
下し、26℃、相対湿度90%で2週間前培養した。一方、
試験片は水で規定濃度となるように希釈した実施例及び
比較例の木材用防カビ防変色菌組成物の溶液中にベイマ
ツ辺材(2cm×5cm×0.3cm)を30秒浸漬した後風
乾する。前培養後、菌が生育した餌木の上に薬剤処理さ
れた試験体を載せ、26℃、相対湿度90%で28日間培養
した。結果を表2に示す。ただし、変色菌生育の程度の
表示は次の判定基準によった。
Test Example 2 Test for anti-discoloring bacterium of wood A non-treated bay pine (bait tree) sterilized with ethylene oxide gas is placed on a petri dish in which the PDA medium is solidified. 2 ml of a spore suspension of the wood discoloring fungus Ceratocystis sp. Was added dropwise thereto, and precultured at 26 ° C. and 90% relative humidity for 2 weeks. on the other hand,
After dipping the test piece into a solution of the antifungal and discoloration fungal composition for wood of Examples and Comparative Examples diluted with water to a specified concentration for 30 seconds, pine sapwood (2 cm × 5 cm × 0.3 cm) was soaked Air dry. After the pre-culture, the drug-treated test body was placed on the bait tree on which the fungus had grown, and cultured at 26 ° C. and 90% relative humidity for 28 days. The results are shown in Table 2. However, the indication of the degree of growth of the color-changing bacterium was based on the following criteria.

【0015】−:試験片に変色菌の生育を全く認めな
い。 +:試験片の側面に変色菌の発育が認められる。 ++:試験片上の変色菌の発育部分の面積が全面積の1
/3未満である。 +++:試験片上の変色菌の発育部分の面積が全面積の
1/3以上である。
-: No growth of discoloring bacteria is observed on the test piece. +: Growth of discoloring bacteria is recognized on the side surface of the test piece. ++: The area of the part where the discoloring bacteria develop on the test piece is 1 of the total area
It is less than / 3. +++: The area of the developing portion of the discoloring bacterium on the test piece is 1/3 or more of the total area.

【0016】[0016]

【表2】 表2の結果から明らかなように、本発明組成物は比較例
に比べ、カビ及び変色菌に対して著しい効力が認められ
た。
[Table 2] As is clear from the results in Table 2, the composition of the present invention was found to be significantly more effective against fungi and discoloration bacteria than the comparative examples.

【0017】[0017]

【発明の効果】本発明組成物は木材に発生するカビや変
色菌に対し高い防カビ防変色菌効力を示し、木材用防カ
ビ防変色菌剤として好適である。
INDUSTRIAL APPLICABILITY The composition of the present invention exhibits a high fungicidal and anti-discoloring bacterium effect against fungi and discoloring fungi generated on wood, and is suitable as a fungicide and anti-discoloring agent for wood.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 4,5-ジクロロ-2-n-オクチルイソチアゾ
リン-3-オン、2-ベンズイミダゾールカルバミン酸メチ
ル及びメチレンビスチオシアネートを含有することを特
徴とする木材防カビ防変色菌組成物。
1. A wood fungicidal and discoloration preventive composition comprising 4,5-dichloro-2-n-octylisothiazolin-3-one, methyl 2-benzimidazole carbamate and methylenebisthiocyanate.
【請求項2】 3-ヨード-2-プロピニルブチルカーバメ
ートを有効成分を併用することを特徴とする請求項1に
記載の木材防カビ防変色菌組成物。
2. The anti-mold and anti-tarnish composition for wood according to claim 1, wherein 3-iodo-2-propynylbutyl carbamate is used in combination with the active ingredient.
JP2002084673A 2002-03-26 2002-03-26 Anti-fungal discoloration composition for wood Expired - Fee Related JP4194070B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2002084673A JP4194070B2 (en) 2002-03-26 2002-03-26 Anti-fungal discoloration composition for wood

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Cited By (4)

* Cited by examiner, † Cited by third party
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JP2007191437A (en) * 2006-01-19 2007-08-02 Nippon Soda Co Ltd Antiseptic or antifungal agent composition and method for producing antiseptic or antifungal dried wood
JP2015003863A (en) * 2013-06-19 2015-01-08 住化エンバイロメンタルサイエンス株式会社 Wood anti-microbial composition
CN106135273A (en) * 2015-03-17 2016-11-23 王海山 A kind of preparation method of the bactericide suppressing growth of fusarium
CN108605970A (en) * 2018-03-21 2018-10-02 广东省石油与精细化工研究院 A kind of composite type mouldproof agent and its methods for making and using same for Wet-White Leather Manufacture technique

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007191437A (en) * 2006-01-19 2007-08-02 Nippon Soda Co Ltd Antiseptic or antifungal agent composition and method for producing antiseptic or antifungal dried wood
JP2015003863A (en) * 2013-06-19 2015-01-08 住化エンバイロメンタルサイエンス株式会社 Wood anti-microbial composition
CN106135273A (en) * 2015-03-17 2016-11-23 王海山 A kind of preparation method of the bactericide suppressing growth of fusarium
CN108605970A (en) * 2018-03-21 2018-10-02 广东省石油与精细化工研究院 A kind of composite type mouldproof agent and its methods for making and using same for Wet-White Leather Manufacture technique
CN108605970B (en) * 2018-03-21 2020-10-27 广东省石油与精细化工研究院 Composite mildew preventive for white wet leather making process and preparation and application methods thereof

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