JP5688557B2 - Insect control method for wooden building materials - Google Patents
Insect control method for wooden building materials Download PDFInfo
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- JP5688557B2 JP5688557B2 JP2010214085A JP2010214085A JP5688557B2 JP 5688557 B2 JP5688557 B2 JP 5688557B2 JP 2010214085 A JP2010214085 A JP 2010214085A JP 2010214085 A JP2010214085 A JP 2010214085A JP 5688557 B2 JP5688557 B2 JP 5688557B2
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- 239000004566 building material Substances 0.000 title claims description 20
- 238000000034 method Methods 0.000 title claims description 19
- 241000238631 Hexapoda Species 0.000 title claims description 6
- 239000000077 insect repellent Substances 0.000 claims description 22
- 239000002023 wood Substances 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 17
- 239000000853 adhesive Substances 0.000 claims description 16
- 239000011120 plywood Substances 0.000 claims description 16
- 239000011248 coating agent Substances 0.000 claims description 12
- 238000000576 coating method Methods 0.000 claims description 12
- YKBZOVFACRVRJN-UHFFFAOYSA-N dinotefuran Chemical compound [O-][N+](=O)\N=C(/NC)NCC1CCOC1 YKBZOVFACRVRJN-UHFFFAOYSA-N 0.000 claims description 12
- 241000607479 Yersinia pestis Species 0.000 claims description 11
- 230000035515 penetration Effects 0.000 claims description 9
- 230000003405 preventing effect Effects 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
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- XUNYDVLIZWUPAW-UHFFFAOYSA-N (4-chlorophenyl) n-(4-methylphenyl)sulfonylcarbamate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)OC1=CC=C(Cl)C=C1 XUNYDVLIZWUPAW-UHFFFAOYSA-N 0.000 description 1
- WCXDHFDTOYPNIE-RIYZIHGNSA-N (E)-acetamiprid Chemical compound N#C/N=C(\C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-RIYZIHGNSA-N 0.000 description 1
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- CFRPSFYHXJZSBI-DHZHZOJOSA-N (E)-nitenpyram Chemical compound [O-][N+](=O)/C=C(\NC)N(CC)CC1=CC=C(Cl)N=C1 CFRPSFYHXJZSBI-DHZHZOJOSA-N 0.000 description 1
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 description 1
- JZLWSRCQCPAUDP-UHFFFAOYSA-N 1,3,5-triazine-2,4,6-triamine;urea Chemical compound NC(N)=O.NC1=NC(N)=NC(N)=N1 JZLWSRCQCPAUDP-UHFFFAOYSA-N 0.000 description 1
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 1
- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 description 1
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- PNVJTZOFSHSLTO-UHFFFAOYSA-N Fenthion Chemical compound COP(=S)(OC)OC1=CC=C(SC)C(C)=C1 PNVJTZOFSHSLTO-UHFFFAOYSA-N 0.000 description 1
- 239000005899 Fipronil Substances 0.000 description 1
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- 241000219492 Quercus Species 0.000 description 1
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 1
- 241000545593 Scolytinae Species 0.000 description 1
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- 239000005941 Thiamethoxam Substances 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
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- YASYVMFAVPKPKE-UHFFFAOYSA-N acephate Chemical compound COP(=O)(SC)NC(C)=O YASYVMFAVPKPKE-UHFFFAOYSA-N 0.000 description 1
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
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- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
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- 229960005286 carbaryl Drugs 0.000 description 1
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 235000019693 cherries Nutrition 0.000 description 1
- UISUNVFOGSJSKD-UHFFFAOYSA-N chlorfluazuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC(C=C1Cl)=CC(Cl)=C1OC1=NC=C(C(F)(F)F)C=C1Cl UISUNVFOGSJSKD-UHFFFAOYSA-N 0.000 description 1
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 1
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- 230000000593 degrading effect Effects 0.000 description 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 1
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- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 1
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- ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 1
- DIRFUJHNVNOBMY-UHFFFAOYSA-N fenobucarb Chemical compound CCC(C)C1=CC=CC=C1OC(=O)NC DIRFUJHNVNOBMY-UHFFFAOYSA-N 0.000 description 1
- HJUFTIJOISQSKQ-UHFFFAOYSA-N fenoxycarb Chemical compound C1=CC(OCCNC(=O)OCC)=CC=C1OC1=CC=CC=C1 HJUFTIJOISQSKQ-UHFFFAOYSA-N 0.000 description 1
- 229940013764 fipronil Drugs 0.000 description 1
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- VBCVPMMZEGZULK-NRFANRHFSA-N indoxacarb Chemical compound C([C@@]1(OC2)C(=O)OC)C3=CC(Cl)=CC=C3C1=NN2C(=O)N(C(=O)OC)C1=CC=C(OC(F)(F)F)C=C1 VBCVPMMZEGZULK-NRFANRHFSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000002949 juvenile hormone Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
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- 238000004519 manufacturing process Methods 0.000 description 1
- YNKFZRGTXAPYFD-UHFFFAOYSA-N n-[[2-chloro-3,5-bis(trifluoromethyl)phenyl]carbamoyl]-2,6-difluorobenzamide Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1Cl YNKFZRGTXAPYFD-UHFFFAOYSA-N 0.000 description 1
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- 150000008048 phenylpyrazoles Chemical class 0.000 description 1
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- NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
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- 229960005199 tetramethrin Drugs 0.000 description 1
- CXBMCYHAMVGWJQ-UHFFFAOYSA-N tetramethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-UHFFFAOYSA-N 0.000 description 1
- HOKKPVIRMVDYPB-UHFFFAOYSA-N thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=NC#N)SCC1 HOKKPVIRMVDYPB-UHFFFAOYSA-N 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
Landscapes
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Building Environments (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
本発明は住宅その他の建築に使用される木質建材に関するものであり、特に乾材害虫による虫害を予防する防虫性の優れた木質建材の食害防止方法に関する発明である。 The present invention relates to a wooden building material used in houses and other buildings, and more particularly to a method for preventing damage to a wooden building material having excellent insecticidal properties to prevent insect damage caused by dry material pests.
近年、住宅その他の建築に使用される木質建材の低ホルムアルデヒド化対策が盛んに叫ばれており、合板基材やそれを使用した木質床板等において遊離のホルムアルデヒドが削減されている。それに従ってヒラタキクイムシなどの害虫にとっては生息し易くなってきた。 In recent years, measures for reducing formaldehyde in wooden building materials used in houses and other buildings have been actively sought, and free formaldehyde has been reduced in plywood base materials and wooden floorboards using the same. Accordingly, it has become easier to inhabit pests such as the larvae.
従来から行われてきた防虫処理方法に防虫合板の使用があった。防虫合板は、合板は木材の単板を貼り合わせる接着剤に防虫剤を混入し製造するものである。接着剤中に混入する方法では合板を構成する木質単板の厚み方向の中心部付近まで薬剤が達しにくく、確実な防虫効果が得られにくかった。 Insect repellent treatment has been used in the past to use insect repellent plywood. Insect repellent plywood is manufactured by mixing an insect repellent into an adhesive that bonds a single veneer of wood. In the method of mixing in the adhesive, it is difficult for the medicine to reach the vicinity of the center in the thickness direction of the wood veneer constituting the plywood, and it is difficult to obtain a reliable insect-proof effect.
また、大量に防虫剤を使用すると作業性が低下し、また、薬剤使用量が増え、経済的に不利となる。上記理由より、限られた薬剤使用量、処理条件のなかで的確に木質建材の表面貫通を防止する効果を向上させるかが大きな課題となっていた。 In addition, when a large amount of insect repellent is used, workability is reduced and the amount of medicine used is increased, which is economically disadvantageous. For the above reasons, it has become a major issue to improve the effect of preventing the surface penetration of the wooden building materials accurately within the limited amount of medicine used and the processing conditions.
木質床板、木質壁板、木質建具または階段板などの木質建材を作製するにあたり、その品質や作業性を低下させず、最低限の薬剤使用で最大の防虫効果を上げることが、本発明の課題である。 It is an object of the present invention to increase the maximum insect repellent effect by using a minimum amount of chemicals without degrading the quality and workability in producing a wooden building material such as a wooden floor board, a wooden wall board, a wooden fitting or a staircase board. It is.
上記課題を解決するため、木材基材の表面に被覆物を付着させて製造する木質建材において、木質基材と被覆物を付着させる接着剤に防虫剤を混入するによって上記課題を解決したものである。 In order to solve the above-mentioned problem, in a wooden building material manufactured by attaching a coating to the surface of a wood substrate, the above problem is solved by mixing an insect repellent into an adhesive that adheres the wooden substrate and the coating. is there.
本発明により、効率良く安価にしかも高い貫通防止効果を持った木質建材の防虫方法を提供することが可能となる。 According to the present invention, it is possible to provide a method for preventing insects of a wooden building material which is efficient and inexpensive and has a high penetration preventing effect.
本発明の木質建材の食害防止方法について以下詳しく述べる。 The method for preventing damage to wooden building materials of the present invention will be described in detail below.
本発明に用いられる25℃における水溶解度が100ppm以上である殺虫組成物としては、(RS)−1−メチル−2−ニトロ−3−(テトラヒドロ−3−フリルメチル)グアニジン(一般名、ジノテフラン)、1−(6−クロロ−3−ピリジルメチル)−N−ニトロイミダゾリジン−2−イリデンアミン(一般名、イミダクロプリド)、(E)−N−〔(6−クロロ−3−ピリジニル)メチル〕N`−シアノ−N−メチルエタンイミダミド(一般名、アセタミプリド)、3−(2−クロロ−1,3−チアゾール−5−イルメチル)−5−メチル−N−ニトロ−1,3,5−オキサジアジナン−4−イリデンアミン(チアメトキサム)、(E)−1−(2−クロロ−1,3−チアゾール−5−イルメチル)−3−メチル−2−ニトログアニジン(一般名、クロチアニジン)、3−(6−クロロ−3−ピリジルメチル)−1,3−チアゾリジン−2−イリデンシアナミド(一般名、チアクロプリド)、N−((6−クロロ−3−ピリジニル)メチル)−N−エチル−N‘−メチル−2−ニトロ−1,1−エチンジアミン(一般名、ニテンピラム)などのネオニコチノイド系化合物、アセフェート、メチダチオン、ジメトエート等の有機リン系化合物、メトルカルブ、メソミル等のカーバメート系化合物、ホウ酸などが挙げられる。特に、(RS)−1−メチル−2−ニトロ−3−(テトラヒドロ−3−フリルメチル)グアニジン(一般名、ジノテフラン)が特に好ましい。 The insecticidal composition having a water solubility at 25 ° C. of 100 ppm or more used in the present invention includes (RS) -1-methyl-2-nitro-3- (tetrahydro-3-furylmethyl) guanidine (generic name, dinotefuran). 1- (6-chloro-3-pyridylmethyl) -N-nitroimidazolidin-2-ylideneamine (generic name, imidacloprid), (E) -N-[(6-chloro-3-pyridinyl) methyl] N〕 -cyano -N-methylethaneimidamide (generic name, acetamiprid), 3- (2-chloro-1,3-thiazol-5-ylmethyl) -5-methyl-N-nitro-1,3,5-oxadiazinane-4- Irideneamine (thiamethoxam), (E) -1- (2-chloro-1,3-thiazol-5-ylmethyl) -3-methyl-2-nitroguani (Generic name, clothianidin), 3- (6-chloro-3-pyridylmethyl) -1,3-thiazolidine-2-ylidenecyanamide (generic name, thiacloprid), N-((6-chloro-3-pyridinyl) ) Methyl) -N-ethyl-N′-methyl-2-nitro-1,1-ethynediamine (generic name, nitenpyram) and other neonicotinoid compounds, organic phosphorus compounds such as acephate, metidathion, dimethoate, metorcarb, Carbamate compounds such as mesomil, boric acid and the like can be mentioned. In particular, (RS) -1-methyl-2-nitro-3- (tetrahydro-3-furylmethyl) guanidine (generic name, dinotefuran) is particularly preferable.
本発明の防虫剤は、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、製剤自体の安定化や、処理時の薬液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、防虫スペクトルの拡大のために他の防虫剤を混合しても良い。 Although the active ingredient may be used as it is for the insect repellent of the present invention, it is usually used after being formulated. 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 inhibitors, antifoaming agents, pH regulators, etc. effective for general bacteria to stabilize the formulation itself and stabilize the chemicals during processing May be added. Moreover, you may mix another insect repellent for expansion of an insect repellent spectrum.
または25℃における水溶解度が100ppm未満の殺虫組成物を混合してもよい。
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。
Or you may mix the insecticidal composition whose water solubility in 25 degreeC is less than 100 ppm.
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.
対象とする木質基材は、合板や無垢木材、LVL、MDF、パーティクルボード、OSBボードであれば良い。より好ましくは、合板や無垢木材が良い。その木質基材の表面に被覆物を付着させ、基材と被覆物の間に防虫層を設ける。 The target wood substrate may be plywood, solid wood, LVL, MDF, particle board, or OSB board. More preferably, plywood or solid wood is good. A covering is attached to the surface of the wooden substrate, and an insect repellent layer is provided between the substrate and the covering.
防虫層は、被覆物を付着させる為の接着剤などに混入したり、基材や被覆物の表面に薬剤を塗布したり、基材や被覆物自体を薬液に浸漬させる方法がある。特に、基材と被覆物を付着させる接着剤に混入する方法が好ましい。 The insect repellent layer includes a method of mixing in an adhesive for attaching a covering, applying a drug on the surface of the base or covering, or immersing the base or covering itself in a chemical solution. In particular, a method of mixing in an adhesive for adhering the base material and the coating is preferable.
防虫薬剤としては、ネオニコチノイド系の化合物が使用できるが、この限りではない。木質基材と被覆物間の防虫剤の存在量は、1m2あたり0.0025g以上で存在することが好ましい。防虫薬剤は、もちろんこれら以外であってもよいし、処理条件もその薬剤に適する方法を適宜選択すればよい。薬剤処理方法として、木質基材への処理、被覆物への処理及び接着剤への混入が挙げられるが、特に、接着剤に混合する方法が好ましい。 Neonicotinoid compounds can be used as insect repellents, but are not limited thereto. The abundance of the insect repellent between the wooden substrate and the covering is preferably 0.0025 g or more per 1 m 2 . Of course, the insect repellent may be other than these, and the treatment conditions may be appropriately selected from methods suitable for the agent. Examples of the chemical treatment method include treatment on a wooden substrate, treatment on a coating, and mixing in an adhesive, and a method of mixing with an adhesive is particularly preferable.
基材や被覆物の表面に薬剤を処理する場合は、基材や被覆物自体を薬剤の溶液中に浸漬してもよいし吹きつけ塗布や、刷毛塗り、ロ−ル塗布であっても良い。塗布、吹きつけの場合の塗布量はウエットで約10〜400g/m2程度でよい。防虫薬剤は、もちろんこれら以外であってもよいし、処理条件もその薬剤に適する方法を適宜選択すればよい。 When treating the surface of the substrate or coating, the substrate or the coating itself may be immersed in a solution of the drug, or spray coating, brush coating, or roll coating may be used. . The application amount in the case of application and spraying may be about 10 to 400 g / m 2 by wet. Of course, the insect repellent may be other than these, and the treatment conditions may be appropriately selected from methods suitable for the agent.
被覆物を付着させる接着剤は、通常の木工用接着剤が使用できる。例えば、酢酸ビニル樹脂接着剤、ユリア樹脂接着剤、メラミン樹脂接着剤、ユリアメラミン樹脂接着剤、変性シリコーン、その他が使用できる。接着条件は、接着剤の接着条件に従えばよい。接着剤、製造条件は、もちろんこれら以外であってもよい。 As an adhesive for attaching the covering, an ordinary woodworking adhesive can be used. For example, vinyl acetate resin adhesive, urea resin adhesive, melamine resin adhesive, urea melamine resin adhesive, modified silicone, and others can be used. The bonding conditions may follow the bonding conditions of the adhesive. Of course, the adhesive and the production conditions may be other than these.
以上詳述した木質基材としてその上に被覆物を付着させて木質建材とする。この時の被覆物は、例えばナラ、ケヤキ、サクラ、ブナなどの木材、その他の木質化粧単板や、合板、LVLなどの他、塩化ビニルフィルム、オレフィン樹脂フィルム、金属箔、合成樹脂成型品、合成木材、紙、布などが使用できる。特に、ブナなどの木材や、防虫合板以外の合板、オレフィン樹脂製の被覆物が好ましい。 As a wood base material described in detail above, a covering is attached thereon to obtain a wood building material. The covering at this time is, for example, wood such as oak, zelkova, cherry blossom, beech, etc., other wooden decorative veneers, plywood, LVL, etc., vinyl chloride film, olefin resin film, metal foil, synthetic resin molded product, Synthetic wood, paper, cloth, etc. can be used. In particular, wood such as beech, plywood other than insect-proof plywood, and an olefin resin coating are preferable.
〔実施例1〕
木質単板(樹種はブナ、厚み0.3mm)の片面に、ジノテフランをN−メチルピロリドンで所定濃度に希釈し、この希釈液を100g/m2になるように塗布した。つぎに、合板(ラワン、5プライ)の表面に木工用ボンド(コニシ社製、酢酸ビニル樹脂)で、上述の単板を薬剤処理面を合板側となるように付着させて試験体とした。
[Example 1]
Dinotefuran was diluted to a predetermined concentration with N-methylpyrrolidone on one side of a wood veneer (tree species is beech, thickness 0.3 mm), and this diluted solution was applied to 100 g / m 2 . Next, the above-mentioned veneer was adhered to the surface of the plywood (Lawan, 5 ply) with a woodworking bond (manufactured by Konishi Co., Ltd., vinyl acetate resin) so that the drug-treated surface was on the plywood side to obtain a test body.
〔実施例2〕
合板(ラワン、5プライ)の片面に、ジノテフランをN−メチルピロリドンで所定濃度に希釈し、100g/m2になるように塗布した。この合板の薬剤処理面に、木質単板(樹種はブナ、厚み0.3mm)を木工用ボンド(コニシ社製、酢酸ビニル樹脂)で付着させ試験体とした。
[Example 2]
Dinotefuran was diluted with N-methylpyrrolidone to a predetermined concentration on one side of a plywood (Lawan, 5 ply) and applied to 100 g / m 2 . A wood veneer (tree species is beech, thickness 0.3 mm) was attached to the chemical treatment surface of this plywood with a bond for woodworking (made by Konishi Co., Ltd., vinyl acetate resin) to prepare a test specimen.
〔実施例3〕
合板(ラワン、5プライ)の片面に、ジノテフランをN−メチルピロリドンで所定濃度に希釈し、規定濃度となるように木工用ボンド(コニシ社製、酢酸ビニル樹脂)に添加し、良く混合した後、400g/m2になるように塗布し、木質単板(樹種はブナ、厚み0.3mm)を付着させ、試験体を作成した。
Example 3
On one side of plywood (Lawan, 5 ply), dinotefuran is diluted with N-methylpyrrolidone to a predetermined concentration, added to a woodworking bond (made by Konishi, vinyl acetate resin) to a specified concentration, and mixed well , 400 g / m 2 , and a wood veneer (tree species is beech, thickness 0.3 mm) was attached to prepare a test specimen.
〔比較例1〕
実施例1のジノテフランをペルメトリン(25℃での水溶解度が100ppm未満)に変え、試験体を作成した。
[Comparative Example 1]
Dinotefuran of Example 1 was changed to permethrin (water solubility at 25 ° C. is less than 100 ppm) to prepare a test specimen.
〔比較例2〕
実施例1のジノテフランをシラフルオフェン(25℃での水溶解度が100ppm未満)に変え、試験体を作成した。
[Comparative Example 2]
Dinotefuran Example 1 Sila off Ruofen (water solubility at 25 ° C. of less than 100 ppm) changed to, to prepare a test body.
〔比較例3〕
実施例3のジノテフランをペルメトリンに変え、試験体を作成した。
[Comparative Example 3]
A test specimen was prepared by replacing dinotefuran of Example 3 with permethrin.
〔比較例4〕
実施例5のジノテフランをペルメトリンに変え、試験体を作成した。
[Comparative Example 4]
A test specimen was prepared by replacing dinotefuran of Example 5 with permethrin.
〔比較例5〕
実施例1の単板の薬剤処理面を合板側と反対側となるように付着させて試験体とした。
[Comparative Example 5]
The test piece was prepared by adhering the drug-treated surface of the veneer of Example 1 to the side opposite to the plywood side.
〔比較例6〕
実施例3の木質単板を付着させずに、試験体を作成した。
[Comparative Example 6]
A specimen was prepared without attaching the wood veneer of Example 3.
〔防虫性能試験方法〕
所定濃度となるように防虫剤を木質基材と被覆物間に存在させた試験体である実施例1〜6、および比較例1〜4の基材部の側面に孔を開け、そこにヒラタキクイムシ幼虫を1頭ずつ入れ、人工飼料粉末で埋めた後、アルミ栓をしたものをプラスチックカップ内に入れ、恒温室内で4ヶ月静置し、成虫となって脱出した際にできる脱出孔の発生の有無について観察した。結果を表1に示す。
[Insect repellent performance test method]
A hole is made in the side surface of the base material portion of Examples 1 to 6 and Comparative Examples 1 to 4 which are test bodies in which an insect repellent is present between the wood base material and the covering so as to have a predetermined concentration. Place the bark beetle larvae one by one, bury them with artificial feed powder, put the aluminum stopper in a plastic cup, and let it stand in a temperature-controlled room for 4 months. The presence or absence of was observed. The results are shown in Table 1.
本発明の乾材害虫による貫通防止性能を有する木質建材は、害虫によって食害を受けやすい木質基材等を被覆物で被覆する際に、木質基材と被覆物の間に防虫剤を存在させることで、乾材害虫が被覆物を貫通することを防止する方法であり、効率良く安価にしかも高い貫通防止効果を持った木質建材の防虫方法を提供することが可能となる。 The wood building material having the ability to prevent penetration by pests of the dry material according to the present invention should have an insect repellent between the wood base material and the covering material when covering the wood base material and the like that are easily damaged by the pests with the covering material. Thus, it is a method for preventing dry material pests from penetrating the coating, and it is possible to provide an insect control method for wooden building materials that is efficient and inexpensive and has a high penetration prevention effect.
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