JP5649154B2 - Wood preservative treatment method - Google Patents

Wood preservative treatment method Download PDF

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JP5649154B2
JP5649154B2 JP2008225369A JP2008225369A JP5649154B2 JP 5649154 B2 JP5649154 B2 JP 5649154B2 JP 2008225369 A JP2008225369 A JP 2008225369A JP 2008225369 A JP2008225369 A JP 2008225369A JP 5649154 B2 JP5649154 B2 JP 5649154B2
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JP2010058351A (en
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太博 重村
太博 重村
庸介 馬場
庸介 馬場
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SC Environmental Science Co Ltd
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Description

本発明は、合板や単板積層材に従来よりも少ない薬剤量で確実に防蟻効果を付与できる木材保存剤処理方法に関するものである。 The present invention relates to a wood preservative treatment method that can reliably impart an anti-ant effect to a plywood or a veneer laminate with a smaller amount of medicine than before.

従来合板や単板積層材の防蟻処理は、その単板接着剤層に薬剤混入されてきた(特許文献1)。また、接着剤に用いるホルムアルデヒドが防虫の一端を担っていた(ホルムアルデヒド自体が防虫効果を示す)。有機フェノール系薬剤を添加して防蟻効果を上げることもされている(特許文献2)。しかしながら、近年シックハウスやVOCの問題から低ホルムアルデヒドの接着剤が用いられるようになりまた合板や単板積層材が住宅などの構造材として使用されるようになり、強度を増したり、製造効率を上げたりするために合板や単板積層材を構成する単板の厚みが増してきたため、薬剤添加量を増しても十分な薬剤効果を得られにくくなっていた。さらに、接着剤の性能へ影響を与えない接着剤への薬剤添加量には限界があり、また薬剤コスト面からも困難な状況となっていた。
特開平9−136304号公報 特開2000−192001号公報
Conventionally, the ant-proofing treatment for plywood or single-plate laminate has been mixed with chemicals in the single-plate adhesive layer (Patent Document 1). Moreover, the formaldehyde used for the adhesive agent played a part of the insect repellent (formaldehyde itself shows an insect repellent effect). An organic phenolic agent is also added to increase the ant protection effect (Patent Document 2). However, in recent years, low formaldehyde adhesives have been used due to the problems of sick houses and VOCs, and plywood and veneer laminates have been used as structural materials for homes, increasing strength and increasing production efficiency. For this reason, since the thickness of the single plate constituting the plywood or the single plate laminated material has increased, it has been difficult to obtain a sufficient drug effect even if the amount of the drug added is increased. Furthermore, there is a limit to the amount of drug added to the adhesive that does not affect the performance of the adhesive, and the situation is difficult from the viewpoint of drug cost.
JP-A-9-136304 JP 2000-192001 A

本発明は、合板もしくは単板積層材の単板接着剤中へ殺虫組成物を添加し、さらにその表層に殺虫組成物を塗布もしくは吹き付けもしくは浸漬処理することにより、従来よりも少ない薬剤添加量で、高い木材保存性能を付与し、シロアリなどの木材加害害虫から木材表層および内部を保護する事を目的とする。 In the present invention, an insecticidal composition is added into a single-plate adhesive of a plywood or a single-plate laminated material, and further, an insecticidal composition is applied, sprayed or dipped onto the surface layer, thereby reducing the amount of drug added compared to the conventional one. The purpose is to provide high wood preservation performance and protect the wood surface and inside from wood-damaging insects such as termites.

本発明者は、前記課題を解決するために鋭意研究した結果、合板または単板積層材の接着剤中に殺虫組成物を混入し、さらに合板または単板積層材表層に殺虫組成物を処理することで従来よりも使用する薬剤量が少なくても十分な防蟻効力を得ることが可能となった合板または単板積層材およびその保存剤処理方法に関するものである。 As a result of diligent research to solve the above problems, the present inventor mixed an insecticidal composition into the adhesive of the plywood or veneer laminate, and further processed the insecticidal composition on the surface of the plywood or veneer laminate. Thus, the present invention relates to a plywood or veneer laminate capable of obtaining a sufficient ant-repellent effect even when a smaller amount of chemical is used than before, and a preservative treatment method thereof.

すなわち、本発明は、20度における水溶解度が100mg/L以上の殺虫組成物を混入した接着剤を用いて、厚みが1.8mm以上の針葉樹単板を3層以上接着し、さらに20度における水溶解度が100mg/L以下の殺虫組成物を配合した木材保存剤を塗布、吹付けまたは浸漬処理することで、飢餓状態にあるイエシロアリの職蟻150頭と兵蟻15頭を投入したプラスチック容器内に、21日後間静置後も表層単板をそのイエシロアリ群に食害を受けない合板および単板積層材に高い木材保存効果を付与することを特徴とする合板または単板積層材またはその木材保存処理方法に関する発明である。 That is, the present invention uses an adhesive mixed with an insecticidal composition having a water solubility at 20 ° C. of 100 mg / L or more to bond three or more layers of softwood veneer having a thickness of 1.8 mm or more, and further at 20 ° C. Applying, spraying, or dipping a wood preservative containing an insecticidal composition with a water solubility of 100 mg / L or less to the inside of a plastic container filled with 150 ant termite ants and 15 soldier ants In addition, the plywood or veneer laminate or the wood preservation thereof is characterized by imparting a high wood preserving effect to the plywood and veneer laminate that are not damaged by the termite group even after standing for 21 days. The invention relates to a processing method.

本発明による木材保存処理合板および単板積層材は、飢餓状態にあるイエシロアリの職蟻150頭と兵蟻15頭を投入したプラスチック容器内に、21日後間静置後も表層単板をそのイエシロアリ群に食害を受けない。 The wood-preserving plywood and veneer laminate according to the present invention is obtained by placing the surface layer veneer in a plastic container in which 150 termite ants and 15 soldier ants in a starved state are placed, and after standing for 21 days. No damage to the group.

本発明には一般式(1)、
または、一般式(2)
(式中Aは6−クロロ−3−ピリジル基、2−クロロ−5−チアゾリル基、テトラヒドロフラン−2−イル基、テトラヒドロフラン−3−イル基、5−メチルテトラヒドロフラン−3−イル基、3−ピリジル基、6−ブロモ−3−ピリジル基、3−シアノフェニル基、2−メチル−5−チアゾリル基、2−フェニル−5−チアゾリル基または2−ブロモ−5−チアゾリル基を表し、R1は水素原子、メチル基、エチル基、ホルミル基またはアセチル基を表し、R2はメチル基、アミノ基、メチルアミノ基、N,N―ジメチルアミノ基、エチルアミノ基、N,N―ジエチルアミノ基、N―メチル−N−エチルアミノ基、1−ピロリジニル基、(6−クロロ−3−ピリジル)メチルアミノ基またはN―メチル−N−(6−クロロ−3−ピリジル)メチルアミノ基を表し、Xは窒素原子またはCH基を表し、Yはシアノ基、ニトロ基またはトリフルオロアセチル基を表し、ZはNH基またはイオウ原子を表し、nは2または3を表す)で示され、20度における水への溶解度が100mg/L以上である殺虫組成物を用いることができる。
In the present invention, the general formula (1),
Or general formula (2)
(In the formula, A represents 6-chloro-3-pyridyl group, 2-chloro-5-thiazolyl group, tetrahydrofuran-2-yl group, tetrahydrofuran-3-yl group, 5-methyltetrahydrofuran-3-yl group, 3-pyridyl group. Group, 6-bromo-3-pyridyl group, 3-cyanophenyl group, 2-methyl-5-thiazolyl group, 2-phenyl-5-thiazolyl group or 2-bromo-5-thiazolyl group, R1 represents a hydrogen atom Represents a methyl group, an ethyl group, a formyl group or an acetyl group, and R2 represents a methyl group, an amino group, a methylamino group, an N, N-dimethylamino group, an ethylamino group, an N, N-diethylamino group, an N-methyl- N-ethylamino group, 1-pyrrolidinyl group, (6-chloro-3-pyridyl) methylamino group or N-methyl-N- (6-chloro-3-pyridyl) me Tilamino group, X represents a nitrogen atom or CH group, Y represents a cyano group, a nitro group or a trifluoroacetyl group, Z represents an NH group or a sulfur atom, and n represents 2 or 3. An insecticidal composition having a solubility in water at 20 degrees of 100 mg / L or more can be used.

合板または単板積層材の表層に処理する殺虫組成物は20度における水溶解度が100mg/L未満の殺虫組成物で良く、または混合してもよい。例えば、フェニトロチオン、フェンチオン、ダイアジノン、クロルピリホス、ジクロルボス、プロペタンホスなどの有機リン系化合物、カルバリル、フェノブカルブ、プロポキスルなどのカーバメート系化合物、アレスリン、プラレトリン、フタルスリン、フェノトリン、シフェノトリン、ペルメトリン、エンペントリン、イミプロトリン、ビフェントリン、シペルメトリン、フェンバレレート、トラロメトリン、エトフェンプロクス、シラフルオフェン及びそれらの光学異性体や幾何異性体などのピレスロイド系化合物、フィプロニルなどのフェニルピラゾール系化合物、インドキサカルブなどのオキサダイアジン系化合物、ピリプロキシフェン、フェノキシカルブ、ジフルベンズロン、クロルフルアズロン、ビストリフルロン、シロマジンなどの昆虫成長調節剤、その他の殺虫剤などが挙げられる。 The insecticidal composition treated on the surface of the plywood or veneer laminate may be an insecticidal composition having a water solubility at 20 degrees of less than 100 mg / L, or may be mixed. For example, organophosphorus compounds such as fenitrothion, fenthion, diazinon, chlorpyrifos, dichlorvos, propetanephos, carbamate compounds such as carbaryl, fenobucarb, propoxur, allethrin, praretrin, phthalthrin, phenothrin, ciphenothrin, permethrin, empentrin, imiprotolin, Cypermethrin, fenvalerate, tralomethrin, etofenprox, silafluophene and pyrethroid compounds such as optical isomers and geometric isomers thereof, phenylpyrazole compounds such as fipronil, oxadiazine compounds such as indoxacarb, pyriproxy Fen, Phenoxycarb, Diflubenzuron, Chlorfluazuron, Bistrifluron, Shiromagi Insect growth regulators such as, and other insecticides like.

合板または単板積層材表層が腐朽されないように、合板または単板積層材の接着剤中、及び合板または単板積層材の表層に処理する殺虫組成物に防腐剤を添加、処理してもよく、例えば、3−ヨード−2−プロピニル−N−ブチルカーバメート、パラクロフェニル−3−ヨードプロパギルホルマール、3−ジヨード−2−プロペニルエチルカーボナートなどの有機ヨード系化合物、シプロコナゾール((2RS,3RS)−2−(4−クロロフェニル)−3−シクロプロピル−1−(1H−1,2,4−トリアゾール−1−イル)ブタン−2−オール)、ヘキサコナゾール((RS)−2−(2,4−ジクロロフェニル)−1−(1H−1,2,4−トリアゾール−1−イル)ヘキサン−2−オール)、プロピコナゾール((RS)−1−[2−(2,4−ジクロロフェニル)−4−プロピル−1,3−ジオキソラン−2−イルメチル]−1H−1,2,4−トリアゾール)、テブコナゾール((RS)−1−p−クロロフェニル−4,4−ジメチル−3−(1H−1,2,4−トリアゾール−1−イルメチル)ペンタン−3−オール)、イプコナゾール((1RS,2SR,5RS;1RS,2SR,5SR)−2−(4−クロロベンジル)−5−イソプロピル−1−(1H−1,2,4−トリアゾール−1−イルメチル)−1−シクロペンタノール)、アザコナゾール(1−[[2−(2,4−ジクロロフェニル)−1,3−ジオキソラン−2−イル]メチル]−1H−1,2,4−トリアゾール)、エポキシコナゾール((2RS,3SR)−1−[3−(2−クロロフェニル)−2,3−エポキシ−2−(4−フルオロフェニル)プロピル]−1H−1,2,4−トリアゾール)、メトコナゾール((1RS,5RS,1RS,5SR)−5−(4−クロロベンジル)−2,2−ジメチル−1−(1H−1,2,4−トリアゾール−1−イルメチル)シクロペンタノール)、テトラコナゾール((RS)−2−(2,4−ジクロロフェニル)−3−(1H−1,2,4−トリアゾール−1−イル)プロピル−1,1,2,2−テトラフルオロエチルエーテル)、ペンコナゾール(1−(2,4−ジクロロ−β−プロピルフェネチル)−1H−1,2,4−トリアゾール)、トリアジメフォン(1−(4−クロロフェノキシ)−3,3−ジメチル−1−(1H−1,2,4−トリアゾール−1−イル)ブタン−2−オン)、ビテルタノール(1−(ビフェニル−4−イルオキシ)−3,3−ジメチル−1−(1H−1,2,4−トリアゾール−1−イル)ブタン−2−オール)、ミクロブタニル(2−p−クロロフェニル−2−(1H−1,2,4−トリアゾール−1−イルメチル)ヘキサンニトリル)、ジニコナゾール((E)−(RS)−1−(2,4−ジクロロフェニル)−4,4−ジメチル−2−(1H−1,2,4−トリアゾール−1−イル)ペント−1−エン−3−オール)、ジフェノコナゾール(シス,トランス−3−クロロ−4−[4−メチル−2−(1H−1,2,4−トリアゾール−1−イルメチル)−1,3−ジオキソラン−2−イル]フェニル−4−クロロフェニルエーテル)、イミベンコナゾール(4−クロロベンジル−N−(2,4−ジクロロフェニル)−2−(1H−1,2,4−トリアゾール−1−イル)チオアセタミデート)、トリアジメノール((1RS,2RS,1RS,2SR)−1−(4−クロロフェノキシ−3,3−ジメチル−1−(1H−1,2,4−トリアゾール−1−イル)ブタン−2−オール)等のトリアゾール系化合物を用いることができ、単独もしくは二種類以上を用いても良い。 In order to prevent the plywood or veneer laminate surface from being spoiled, preservatives may be added and treated in the pestwood or veneer laminate adhesive and the insecticidal composition treated on the plywood or veneer laminate. Organic iodine compounds such as 3-iodo-2-propynyl-N-butyl carbamate, parachlorophenyl-3-iodopropargyl formal, 3-diiodo-2-propenyl ethyl carbonate, cyproconazole ((2RS , 3RS) -2- (4-chlorophenyl) -3-cyclopropyl-1- (1H-1,2,4-triazol-1-yl) butan-2-ol), hexaconazole ((RS) -2 -(2,4-dichlorophenyl) -1- (1H-1,2,4-triazol-1-yl) hexan-2-ol), propiconazole ((RS) -1- [ -(2,4-dichlorophenyl) -4-propyl-1,3-dioxolan-2-ylmethyl] -1H-1,2,4-triazole), tebuconazole ((RS) -1-p-chlorophenyl-4,4 -Dimethyl-3- (1H-1,2,4-triazol-1-ylmethyl) pentan-3-ol), ipconazole ((1RS, 2SR, 5RS; 1RS, 2SR, 5SR) -2- (4-chlorobenzyl) ) -5-isopropyl-1- (1H-1,2,4-triazol-1-ylmethyl) -1-cyclopentanol), azaconazole (1-[[2- (2,4-dichlorophenyl) -1,3 -Dioxolan-2-yl] methyl] -1H-1,2,4-triazole), epoxiconazole ((2RS, 3SR) -1- [3- (2-chloropheny ) -2,3-epoxy-2- (4-fluorophenyl) propyl] -1H-1,2,4-triazole), metconazole ((1RS, 5RS, 1RS, 5SR) -5- (4-chlorobenzyl) -2,2-dimethyl-1- (1H-1,2,4-triazol-1-ylmethyl) cyclopentanol), tetraconazole ((RS) -2- (2,4-dichlorophenyl) -3- ( 1H-1,2,4-triazol-1-yl) propyl-1,1,2,2-tetrafluoroethyl ether), penconazole (1- (2,4-dichloro-β-propylphenethyl) -1H-1 , 2,4-triazole), triazimephone (1- (4-chlorophenoxy) -3,3-dimethyl-1- (1H-1,2,4-triazol-1-yl) butan-2-o ), Vitertanol (1- (biphenyl-4-yloxy) -3,3-dimethyl-1- (1H-1,2,4-triazol-1-yl) butan-2-ol), microbutanyl (2-p- Chlorophenyl-2- (1H-1,2,4-triazol-1-ylmethyl) hexanenitrile), diniconazole ((E)-(RS) -1- (2,4-dichlorophenyl) -4,4-dimethyl-2) -(1H-1,2,4-triazol-1-yl) pent-1-en-3-ol), difenoconazole (cis, trans-3-chloro-4- [4-methyl-2- (1H-1) , 2,4-triazol-1-ylmethyl) -1,3-dioxolan-2-yl] phenyl-4-chlorophenyl ether), imibenconazole (4-chlorobenzyl-N- ( , 4-dichlorophenyl) -2- (1H-1,2,4-triazol-1-yl) thioacetamidate), triazimenol ((1RS, 2RS, 1RS, 2SR) -1- (4-chlorophenoxy) Triazole compounds such as -3,3-dimethyl-1- (1H-1,2,4-triazol-1-yl) butan-2-ol) can be used, and even if one or more kinds are used. good.

合板又は単板積層材表層に処理する薬剤には、木材変色菌や木材上に発生する各種黴類に有効な防黴剤を併用しても良い。有効な防黴剤としては、例えば、チアベンダゾール(TBZ)、メチルベンズイミダゾール−2−カルバメイト、メチル−1−(ブチルカルバモイル)ベンズイミダゾール−2−カルバメイトなどのイミダゾール系化合物、N(トリクロロメチルチオ)フタルイミドなどのフタルイミド系化合物、N−ニトロソシクロヘキシルヒドロオキシルアミンアルミニウムなどのスファミド系化合物、2,4,5,6−テトラクロルイソフタロニトリルなどのニトリル系化合物、2−(チオシアノメチルチオ)ベンゾチアゾールなどのベンゾチアゾール系化合物、メチレンビスチオシアネートなどのチオシアネート系化合物等を用いることができ、単独もしくは二種類以上を用いても良い。 As the chemical agent to be processed on the surface layer of the plywood or the veneer laminate, an antifungal agent effective for wood discoloring bacteria and various kinds of moss generated on wood may be used in combination. Effective antifungal agents include, for example, imidazole compounds such as thiabendazole (TBZ), methylbenzimidazole-2-carbamate, methyl-1- (butylcarbamoyl) benzimidazole-2-carbamate, N (trichloromethylthio) phthalimide, etc. Phthalimide compounds, sulfamide compounds such as N-nitrosocyclohexylhydroxylamine aluminum, nitrile compounds such as 2,4,5,6-tetrachloroisophthalonitrile, benzoates such as 2- (thiocyanomethylthio) benzothiazole Thiazole compounds, thiocyanate compounds such as methylene bis thiocyanate, and the like can be used alone or in combination of two or more.

本発明の合板および単板積層材製造時に、上記ネオニコチノイド系化合物および防腐剤または/および防黴剤を接着剤に混合する場合、それらの有効成分をそのまま用いても良いが、通常製剤化して用いる。製剤の種類は特に限定されないが、扱いやすさの点から液状の製剤が好ましい。液状の製剤としては、水溶剤、乳剤、油剤、フロアブル剤等を挙げることができるが、これらの製剤に限定されない。上記製剤は通常の農薬の製剤と同様の方法で調製することができる。さらに、接着剤に混合した時の安定化や製剤自体の安定化のために一般の細菌に有効な防腐剤、安定剤、酸化防止剤、キレート剤、防錆剤、消泡剤、pH調節剤等を添加しても良い。また、殺虫・防蟻スペクトルの拡大のために他の殺虫剤を混合しても良い。 When mixing the neonicotinoid compound and the preservative or / and antifungal agent into the adhesive at the time of producing the plywood and veneer laminate of the present invention, those active ingredients may be used as they are, but they are usually formulated. Use. Although the kind of formulation is not particularly limited, a liquid formulation is preferable from the viewpoint of ease of handling. Examples of liquid preparations include aqueous solvents, emulsions, oils, flowables and the like, but are not limited to these preparations. The above-mentioned preparation can be prepared in the same manner as an ordinary agricultural chemical preparation. Furthermore, preservatives, stabilizers, antioxidants, chelating agents, rust preventives, antifoaming agents, and pH regulators that are effective for general bacteria to stabilize when mixed with adhesives and the preparation itself Etc. may be added. In addition, other insecticides may be mixed in order to expand the insecticidal / anticidal spectrum.

次に実施例により、さらに詳細に説明するが、本発明はこれらによって限定されるものではない。 EXAMPLES Next, although an Example demonstrates in detail, this invention is not limited by these.

(実施例1)
フェノール樹脂(株式会社サンベーク社製、ユーロイドPL−255)100重量部、小麦粉9.4重量部、炭酸カルシウム14.0重量部に、表1記載濃度になるように適当な溶媒に溶解したジノテフラン(一般式(1)において、R1が水素原子、R2がメチルアミノ基、Xが窒素原子、Yがニトロ基、Aがテトラヒドロフラン−3−イル基で示される化合物)を0.1重量部混合したものを、縦30cm横30cm厚さが3mmのラジアータパイン単板を芯板とし、縦30cm横30cm厚さ1.8mmのラジアータパイン単板へ、薬剤添加量が表1の処理量になるように接着剤を接着層に塗布して3層の合板にした。これを10kg/cmで60分間冷圧し、30分放置後9kg/m、128℃で4分間熱圧した。
作成した合板を、縦3cm、横3cmの大きさに切断した。この合板表層にエバーウッド乳剤PC30W(住化エンビロサイエンス社製、有効成分ペルメトリン6%)を水で30倍希釈した薬液を110g/mになるように処理した。
Example 1
Dinotefuran (100% by weight of phenol resin (manufactured by Sunbake Co., Ltd., Euroid PL-255), 9.4 parts by weight of flour, and 14.0 parts by weight of calcium carbonate dissolved in an appropriate solvent so as to have the concentrations shown in Table 1 ( In general formula (1), a compound in which 0.1 part by weight of R1 is a hydrogen atom, R2 is a methylamino group, X is a nitrogen atom, Y is a nitro group, and A is a tetrahydrofuran-3-yl group) Adhering to a radiusata pine veneer 30 cm in length 30 cm in width 30 cm in thickness and 1.8 mm in thickness so that the amount of drug added is the treatment amount shown in Table 1. The agent was applied to the adhesive layer to form a three-layer plywood. This was cold-pressed at 10 kg / cm 2 for 60 minutes, allowed to stand for 30 minutes, and then hot-pressed at 9 kg / m 2 and 128 ° C. for 4 minutes.
The prepared plywood was cut into a size of 3 cm in length and 3 cm in width. This plywood surface layer was treated with a chemical solution obtained by diluting Everwood Emulsion PC30W (manufactured by Sumika Enviro Science Co., Ltd., active ingredient permethrin 6%) with water 30 times to 110 g / m 2 .

(実施例2)
実施例1の接着剤の調製で殺虫組成物をイミダクロプリドにしたもので合板を作成した。
(Example 2)
A plywood was made from the preparation of the adhesive of Example 1 using imidacloprid as the insecticidal composition.

(実施例3)
実施例1の接着剤の調製で殺虫組成物をクロチアニジンにして、合板表層にトレボン乳剤(三井化学社製、エトフェンプロックス20%)を水で100倍希釈した薬液を110g/mになるように処理した。
Example 3
In the preparation of the adhesive of Example 1, the insecticidal composition was clothianidin, and a chemical solution obtained by diluting Trebon emulsion (Mitsui Chemicals, Etofenprox 20%) 100 times with water on the plywood surface layer to 110 g / m 2 was obtained. Processed.

(比較例1)
実施例1の接着剤の調製で殺虫組成物をフィプロニルにしたもので合板を作成した。
(Comparative Example 1)
A plywood was made of fipronil as the insecticidal composition in the preparation of the adhesive of Example 1.

(比較例2)
実施例1の接着剤の調製で殺虫組成物をクロルフェナピルにして、合板表層にトレボン乳剤(三井化学株式会社製、エトフェンプロックス20%)を水で100倍希釈した薬液を110g/mになるように処理した。
(Comparative Example 2)
In the preparation of the adhesive of Example 1, the insecticidal composition was changed to chlorfenapyr, and a chemical solution obtained by diluting Trebon emulsion (Mitsui Chemical Co., Ltd., Etofenprox 20%) 100 times with water on the plywood surface layer was 110 g / m 2 . Was processed as follows.

(比較例3及び4)
実施例1の接着剤の調製は殺虫組成物をジノテフラン及びイミダクロプリドにして、合板表層にバリアード顆粒水和剤(バイエルクロップサイエンス社製、有効成分チアクロプリド30%)を水で100倍希釈した薬液を110g/mになるように処理した。
(Comparative Examples 3 and 4)
The adhesive of Example 1 was prepared by using dinotefuran and imidacloprid as the insecticidal composition, and 110 g of a chemical solution obtained by diluting 100 times of water with a hydrated granule wettable powder (manufactured by Bayer Crop Science, 30% active ingredient thiacloprid) on the plywood surface layer. I was treated to be / m 2.

(比較例5)
実施例1の接着剤の調製で殺虫組成物をクロチアニジンにして、モスピラン水溶剤(日本農薬社製、有効成分アセタミプリド20%)を水で100倍希釈した薬液を110g/mになるように処理した。
(Comparative Example 5)
In the preparation of the adhesive of Example 1, the insecticidal composition was clothianidin, and a chemical solution obtained by diluting Mospiran aqueous solvent (produced by Nippon Agricultural Chemicals Co., Ltd., active ingredient acetamiprid 20%) 100 times with water was treated to 110 g / m 2. did.

(比較例6〜8)
実施例1〜3の接着剤に薬剤混入した合板に、合板表層の薬剤添加を行わなかった。
(Comparative Examples 6-8)
The chemical | medical agent addition of the plywood surface layer was not performed to the plywood which mixed the chemical | medical agent in the adhesive agent of Examples 1-3.

(比較例9〜11)
接着剤の調製で、薬剤を添加せずに作成した合板表層に、この合板表層にエバーウッド乳剤PC30Wを水で30倍希釈した薬液及びトレボン乳剤(三井化学社製、エトフェンプロックス20%)を水で100倍希釈した薬液を330g/mになるように処理した。また、表面にも薬剤処理しないものを比較例11とした。
(Comparative Examples 9-11)
In the preparation of the adhesive, on the plywood surface layer prepared without adding any chemicals, a chemical solution obtained by diluting Everwood Emulsion PC30W 30 times with water and Trebon emulsion (Mitsui Chemicals Co., Ltd., Etofenprox 20%) was added to the plywood surface layer. A chemical solution diluted 100 times with water was treated to 330 g / m 2 . In addition, Comparative Example 11 was used in which no chemical treatment was applied to the surface.

(試験例 木材防蟻効力試験)
実施例1〜3及び比較例1〜11で作成した合板について、防蟻効力試験を行った。試験は日本工業規格の木材保存剤の性能試験方法及び性能基準(JIS K1571:2004)を参考にして下記の通り実施した。
(Test example: Wood ant protection test)
About the plywood created in Examples 1-3 and Comparative Examples 1-11, the ant-proof effect test was done. The test was carried out as follows with reference to the performance test method and performance standard (JIS K1571: 2004) of the wood preservative of Japanese Industrial Standard.

<供試虫>
イエシロアリ Coptotermes formosanus SHIRAKI
<Test insect>
Termite Copttermes formosanus SHIRAKI

<耐候操作>
薬液を処理した各木材片を5個1組として500ml容量のビーカーにいれ、その中に木材片容積の10倍のイオン交換水を注ぎ、木材片が浮かび上がらないように適当なおもりを載せ水面下に沈める。マグネチックスターラを用い水温25±3℃で回転子を1分間に400から450回転させ、8時間攪拌した後、直ちに軽く試験体の表層の水切りを行う。続いて60±2℃の循環式乾燥器中に16時間静置し、揮発分を揮散させる。以上の操作を交互に10回繰り返した。
耐候操作が終わった後、温度60±2度で48時間乾燥させた。
<Weatherproof operation>
Put each piece of wood treated with chemicals into a beaker with a capacity of 500 ml, pour ion exchange water 10 times the volume of the piece of wood, and place an appropriate weight so that the piece of wood does not float up below the surface of the water. Sink into. Using a magnetic stirrer, the rotor is rotated from 400 to 450 per minute at a water temperature of 25 ± 3 ° C., stirred for 8 hours, and immediately drained off the surface layer of the test specimen. Then, it is left still in a circulating dryer at 60 ± 2 ° C. for 16 hours to volatilize volatile matter. The above operation was repeated 10 times alternately.
After the weathering operation was completed, drying was performed at a temperature of 60 ± 2 degrees for 48 hours.

<試験方法>
耐候操作を行った試料を1個ずつ、プラスチック容器内に試料を置き、その上からイエシロアリの職蟻150頭と兵蟻15頭を投入し、21日間放置した。その後木材片を温度60±2℃で48時間乾燥させたのち、目視で合板表面の食害度を表2のように判定した。結果を表3に示す。
<Test method>
One sample subjected to weathering operation was placed in a plastic container one by one, and 150 termite ants and 15 soldier ants were put on it, and left for 21 days. Thereafter, the wood pieces were dried at a temperature of 60 ± 2 ° C. for 48 hours, and then the degree of damage on the surface of the plywood was visually determined as shown in Table 2. The results are shown in Table 3.

本発明の木材処理方法は、合板または単板積層材の接着剤中に防蟻剤を混入し、さらに合板または単板積層材表層に防蟻剤を処理することで従来よりも使用する薬材量が少なくても十分な防蟻効力を得ることが可能となった。 The wood treatment method of the present invention is a chemical material that is used more than before by mixing an ant protection agent in the adhesive of a plywood or veneer laminate and further processing the ant inhibitor on the surface layer of the plywood or veneer laminate. Even if the amount is small, it is possible to obtain a sufficient ant protection effect.

Claims (3)

20度における水への溶解度が100mg/L以上である殺虫組成物を混入した接着剤を用いて、厚みが1.8mm以上の針葉樹単板を3層以上接着し、さらに20度における水への溶解度が100mg/L以下である殺虫組成物を配合した木材保存剤を塗布、吹付けまたは浸漬処理された合板または単板積層材で、耐候操作を行った後に、飢餓状態にあるイエシロアリの職蟻150頭と兵蟻15頭を投入したプラスチック容器内に、21日間静置後も表層単板をそのイエシロアリ群に食害を受けないことを特徴とする合板または単板積層材の木材害虫用木材保存剤処理方法。 Using an adhesive mixed with an insecticidal composition having a solubility in water at 20 ° C of 100 mg / L or more, three or more layers of softwood veneer with a thickness of 1.8 mm or more were adhered, and further, water at 20 ° C. A termite ant ant in a starved state after a weathering operation on a plywood or veneer laminate that has been coated, sprayed or dipped with a wood preservative containing an insecticidal composition having a solubility of 100 mg / L or less Plywood or plywood laminate wood pest preservation, characterized in that the surface layer veneer will not be damaged by the termite group even after standing for 21 days in a plastic container containing 150 heads and 15 soldier ants Agent treatment method. 請求項1に記載の20度における水への溶解度が100mg/L以上である殺虫組成物が、一般式(1)、
または、一般式(2)
(式中Aは6−クロロ−3−ピリジル基、2−クロロ−5−チアゾリル基、テトラヒドロフラン−2−イル基、テトラヒドロフラン−3−イル基、5−メチルテトラヒドロフラン−3−イル基、3−ピリジル基、6−ブロモ−3−ピリジル基、3−シアノフェニル基、2−メチル−5−チアゾリル基、2−フェニル−5−チアゾリル基または2−ブロモ−5−チアゾリル基を表し、R1は水素原子、メチル基、エチル基、ホルミル基またはアセチル基を表し、R2はメチル基、アミノ基、メチルアミノ基、N,N―ジメチルアミノ基、エチルアミノ基、N,N―ジエチルアミノ基、N―メチル−N−エチルアミノ基、1−ピロリジニル基、(6−クロロ−3−ピリジル)メチルアミノ基またはN―メチル−N−(6−クロロ−3−ピリジル)メチルアミノ基を表し、Xは窒素原子またはCH基を表し、Yはシアノ基、ニトロ基またはトリフルオロアセチル基を表し、ZはNH基またはイオウ原子を表し、mは0または1、nは2または3を表す)で示される殺虫組成物であることを特徴とする合板または単板積層材の木材害虫用木材保存剤処理方法。
The insecticidal composition having a solubility in water at 20 degrees according to claim 1 of 100 mg / L or more is represented by the general formula (1),
Or general formula (2)
(In the formula, A represents 6-chloro-3-pyridyl group, 2-chloro-5-thiazolyl group, tetrahydrofuran-2-yl group, tetrahydrofuran-3-yl group, 5-methyltetrahydrofuran-3-yl group, 3-pyridyl group. Group, 6-bromo-3-pyridyl group, 3-cyanophenyl group, 2-methyl-5-thiazolyl group, 2-phenyl-5-thiazolyl group or 2-bromo-5-thiazolyl group, R1 represents a hydrogen atom Represents a methyl group, an ethyl group, a formyl group or an acetyl group, and R2 represents a methyl group, an amino group, a methylamino group, an N, N-dimethylamino group, an ethylamino group, an N, N-diethylamino group, an N-methyl- N-ethylamino group, 1-pyrrolidinyl group, (6-chloro-3-pyridyl) methylamino group or N-methyl-N- (6-chloro-3-pyridyl) Represents a tilamino group, X represents a nitrogen atom or a CH group, Y represents a cyano group, a nitro group or a trifluoroacetyl group, Z represents an NH group or a sulfur atom, m is 0 or 1, n is 2 or And pest board or veneer laminated material for treating wood pests for wood pests.
請求項1または2に記載の20度における水への溶解度が100mg/L以下である殺虫組成物が、ピレスロイド系化合物であることを特徴とする合板または単板積層材の木材害虫用木材保存剤処理方法。

The wood preservative for wood pests of plywood or veneer laminate, wherein the insecticidal composition having a solubility in water at 20 degrees of 100 mg / L or less according to claim 1 or 2 is a pyrethroid compound Processing method.

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