JP6896268B2 - How to protect outdoor wood-based materials and wood-based materials protected by that method - Google Patents

How to protect outdoor wood-based materials and wood-based materials protected by that method Download PDF

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JP6896268B2
JP6896268B2 JP2017077221A JP2017077221A JP6896268B2 JP 6896268 B2 JP6896268 B2 JP 6896268B2 JP 2017077221 A JP2017077221 A JP 2017077221A JP 2017077221 A JP2017077221 A JP 2017077221A JP 6896268 B2 JP6896268 B2 JP 6896268B2
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加藤 圭一
圭一 加藤
聖世 鈴木
聖世 鈴木
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三商株式会社
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本発明は、屋外用木質材料の保護方法及びその方法により保護された木質材料に関する。 The present invention relates to a method for protecting an outdoor wood-based material and a wood-based material protected by the method.

従来、屋外で使用される木質材料の保護方法としては、木質材料の表面に木材保護塗料を塗付する方法があり、木材保護塗料としては、(a)木材防腐防カビ剤と、(b)木材防虫剤と、(c)塗膜形成成分と、(d)赤色酸化鉄、黄色酸化鉄およびカーボンブラックからなる群から選ばれる少なくとも1種の顔料と、(e)溶剤と、を含有することを特徴としたもの(例えば、特許文献1参照。)や、合成樹脂、添加剤を配合し、トルエン、キシレン等の刺激臭〜悪臭のある溶剤成分を含有する油性溶剤を用いた木材用塗料組成物において、溶剤成分としてリモネンが該組成物の全重量中5重量%以上(好ましくは5〜30重量%)配合されてなるものがある(例えば、特許文献2参照。)。 Conventionally, as a method of protecting a wood material used outdoors, there is a method of applying a wood protective paint on the surface of the wood material, and the wood protective paint includes (a) a wood antiseptic and antifungal agent and (b). It contains a wood insect repellent, (c) a coating film-forming component, (d) at least one pigment selected from the group consisting of red iron oxide, yellow iron oxide and carbon black, and (e) a solvent. (For example, see Patent Document 1), or a wood-based paint composition using an oil-based solvent containing a synthetic resin and an additive and containing a solvent component having a pungent odor to a foul odor such as toluene and xylene. In some products, limonene is blended as a solvent component in an amount of 5% by weight or more (preferably 5 to 30% by weight) based on the total weight of the composition (see, for example, Patent Document 2).

また、リグノセルロースについて、脱ヘミセルロース処理をなすことにより、変色原因であるヘミセルロースやリグニンおよび抽出成分の一部を除去または減少させ、リグノセルロースの耐候性を向上させる。さらに、脱ヘミセルロース処理をなすことにより、紫外線吸収剤や紫外線安定化剤等の抗紫外線材とリグノセルロース材とのグラフト重合反応を促進させる方法がある(例えば、特許文献3参照。)。 Further, by dehemicellulose treatment of lignocellulosic, hemicellulose and lignin which are the causes of discoloration and a part of the extracted component are removed or reduced, and the weather resistance of lignocellulosic is improved. Further, there is a method of accelerating the graft polymerization reaction between an anti-ultraviolet material such as an ultraviolet absorber or an ultraviolet stabilizer and a lignocellulosic material by performing a dehemicellulose treatment (see, for example, Patent Document 3).

しかし、これらの木材保護塗料による木質材料の保護方法は、顔料や染料等の着色剤を使用するものにあっては、保護したい木質材料の木目や色調等の外観が木質材料本来の外観と大きく異なってしまうという課題があった。また、透明な木材保護塗料を使用する方法にあっては、長期にわたり屋外で曝露すると、経時的に塗膜が劣化して剥離する等の外観に急激な変化が生ずるという課題があった。リグノセルロースについて、脱ヘミセルロース処理をなすことにより、変色原因であるヘミセルロースやリグニンおよび抽出成分の一部を除去または減少させ、リグノセルロースの耐候性を向上させる。さらに、脱ヘミセルロース処理をなすことにより、紫外線吸収剤や紫外線安定化剤等の抗紫外線材とリグノセルロース材とのグラフト重合反応を促進させる方法にあっては製造工程が複雑で特殊な設備を必要とするという課題があった。 However, in the method of protecting wood materials with these wood protective paints, when using colorants such as pigments and dyes, the appearance of the wood materials to be protected, such as the grain and color tone, is larger than the original appearance of the wood materials. There was a problem that it would be different. Further, in the method of using a transparent wood protective paint, there is a problem that when exposed outdoors for a long period of time, the coating film deteriorates over time and the appearance is suddenly changed such as peeling. By dehemicellulose treatment of lignocellulosic, hemicellulose and lignin which are the causes of discoloration and a part of the extracted components are removed or reduced, and the weather resistance of lignocellulosic is improved. Furthermore, the manufacturing process is complicated and special equipment is required for the method of promoting the graft polymerization reaction between the anti-ultraviolet material such as an ultraviolet absorber or an ultraviolet stabilizer and the lignocellulosic material by performing the dehemicellulose treatment. There was a problem of

特開2005−145909号公報Japanese Unexamined Patent Publication No. 2005-145909 特開2009−167310号公報JP-A-2009-167310 特開2002−283306号公報JP-A-2002-283306

解決しようとする課題は、建築物等に用いられる木質材料であって、該木質材料の木目や色調等の外観の大きな変化を伴わず長期にわたって自然な劣化をさせる木質材料の簡易な保護方法を提供する点である。 The problem to be solved is a simple protection method for wood-based materials used for buildings, etc., which naturally deteriorates over a long period of time without major changes in appearance such as grain and color tone of the wood-based materials. It is a point to provide.

本発明は、屋外で使用される木質材料であって、該木質材料の表面に紫外線吸収剤及び光安定化剤を含有し結合材を含有しない木材表面保護剤を塗付した後に、撥水剤を塗付して乾燥させることを最も主要な特徴とする。 The present invention is a wood-based material used outdoors, and a water-repellent agent is applied to the surface of the wood-based material after applying a wood surface protectant containing an ultraviolet absorber and a light stabilizer and not containing a binder. The most important feature is to apply and dry.

本発明の屋外用木質材料の保護方法によれば、塗付・乾燥という簡易な方法により、保護したい木質材料の外観の大きな変化を伴わず長期にわたって自然な劣化をさせることができるという利点がある。 According to the method for protecting an outdoor wood-based material of the present invention, there is an advantage that a simple method of coating and drying can cause natural deterioration for a long period of time without a large change in the appearance of the wood-based material to be protected. ..

本発明の屋外用木質材料の保護方法は、該木質材料の表面に紫外線吸収剤及び光安定化剤を含有し結合材を含有しない木材表面保護剤を塗付した後に、撥水剤を塗付して乾燥させることにより行われる。 The method for protecting an outdoor wood-based material of the present invention is to apply a water-repellent agent to the surface of the wood-based material after applying a wood surface-protecting agent containing an ultraviolet absorber and a light stabilizer and not containing a binder. It is done by drying.

前記木質材料はスギ、カラマツ、ヒノキ、イチイ等の針葉樹やサクラ、ケヤキ、ブナ、クヌギ、ナラ等の広葉樹をそのまま使用するものばかりでなく、これらの天然木を工業的に加工した合板、単板積層板(LVL)、集成材、直交集成板(クロス・ラミネイティド・ティンバー、CLT)等を含む。 The wood-based materials are not only those that use coniferous trees such as cedar, pine, hinoki, and ichii, and broad-leaved trees such as cherry, zelkova, beech, kunugi, and nara as they are, but also plywood and single board that are industrially processed from these natural trees. Includes laminated boards (LVL), laminated lumber, orthogonal laminated boards (Cross Laminated Timber, CLT) and the like.

前記木材表面保護剤は紫外線吸収剤及び光安定化剤を含有しており、かつ結合材を含有しないことが必要である。 It is necessary that the wood surface protectant contains an ultraviolet absorber and a light stabilizer and does not contain a binder.

前記木材表面保護剤は木質材料の表面に塗付することが必要である。 The wood surface protectant needs to be applied to the surface of the wood material.

前記紫外線吸収剤は、2-(2‘−ヒドロキシ−5’−メチルフェニル)ベンゾトリアゾール、2−(2‘-ヒドロキシ−3’−tert−ブチル−5‘−メチルフェニル)−5−クロロベンゾトリアゾール、2−(2’−ヒドロキシ−3‘,5’−ジ−tert−アミルフェニル)ベンゾトリアゾール、2−(2‘−ヒドロキシ−5’−tert−オクチルフェニル)ベンゾトリアゾール、2,2‘−メチレンビス[6−(2H−ベンゾトリアゾール−2−イル)−4−tert−オクチルフェノール]、6−(2−ベンゾトリアゾリル)−4−tert−オクチル−6’−tert−ブチル−4‘−メチル−2,2’−メチレンビスフェノール、2−(2H−ベンソトリアゾール−2−イル)−4,6−ビス(1−メチル−1−フェニルエチル)フェノール、2,2‘−メチレンビス[6−(2H−ベンゾトリアゾール−2−イル)−4−(1,1,3,3−テトラメチルブチル)フェノール]、2−メチレンビス[6−(2H−ベンゾトリアゾール−2−イル)−4−(1,1,3,3−テトラメチルブチル)フェノール]、2−(2H−ベンゾトリアゾール−2−イル)−p−クレゾール、2−(5−クロロ−2H−ベンゾトリアゾール−2−イル)−6−tert−ブチル−4−メチルフェノール等のベンゾトリアゾール系紫外線吸収剤、2−(4,6−ジフェニル−1,3,5−トリアジン−2−イル)−5−[2−(2−エチルヘキサノイロキシ)エトキシ]フェノール、2,4,6−トリス(2−ヒドロキシ−4−ヘキシロキシ−3−メチルフェニル)−1,3,5−トリアジン等のトリアジン系紫外線吸収剤、[2−ヒドロキシ−4−(オクチロキシ)フェニル](フェニル)メタノン等のベンゾフェノン系紫外線吸収剤、ベンゾエート系紫外線吸収剤、酸化鉄、酸化チタン等が挙げられる。これらはそのまま用いても良いし、水、アルコール、有機溶剤等で希釈して用いても良い。これらのうち、油溶性の紫外線吸収剤を用いることが好ましく、トリアジン系紫外線吸収剤を用いることがより好ましく、2−(4,6−ビス(2,4ジメチルフェニル)−1,3,5−トリアジン−2−イル)−5−ヒドロキシフェニル,トオキシラン「(C10−C16主としてC12−C13アルキルオキシ)メチル]オキシランとの反応生成物、ベンゼンプロパン酸・3−(2H−ベンゾトリアゾール−2−イル)−5−(1,1−ジメチルエチル)−4−ヒドロキシ・C7−9側鎖及び直鎖アルキルエステル、2,4,6−トリス(2−ヒドロキシ−4−ヘキシロキシ−3−メチルフェニル)−1,3,5−トリアジンを用いることが最も好ましい。特に2−(4,6−ビス(2,4ジメチルフェニル)−1,3,5−トリアジン−2−イル)−5−ヒドロキシフェニル,トオキシラン「(C10−C16主としてC12−C13アルキルオキシ)メチル]オキシランとの反応生成物及びベンゼンプロパン酸・3−(2H−ベンゾトリアゾール−2−イル)−5−(1,1−ジメチルエチル)−4−ヒドロキシ・C7−9側鎖及び直鎖アルキルエステルは無色透明であるため、木材に塗付した際の外観変化が最も小さい。 The ultraviolet absorbers are 2- (2'-hydroxy-5'-methylphenyl) benzotriazole and 2- (2'-hydroxy-3'-tert-butyl-5'-methylphenyl) -5-chlorobenzotriazole. , 2- (2'-Hydroxy-3', 5'-di-tert-amylphenyl) benzotriazole, 2- (2'-hydroxy-5'-tert-octylphenyl) benzotriazole, 2,2'-methylenebis [6- (2H-benzotriazole-2-yl) -4-tert-octylphenol], 6- (2-benzotriazolyl) -4-tert-octyl-6'-tert-butyl-4'-methyl- 2,2'-Methylenebisphenol, 2- (2H-benzotriazole-2-yl) -4,6-bis (1-methyl-1-phenylethyl) phenol, 2,2'-methylenebis [6- (2H) -Benzotriazole-2-yl) -4- (1,1,3,3-tetramethylbutyl) phenol], 2-methylenebis [6- (2H-benzotriazole-2-yl) -4- (1,1) , 3,3-Tetramethylbutyl) phenol], 2- (2H-benzotriazole-2-yl) -p-cresol, 2- (5-chloro-2H-benzotriazole-2-yl) -6-tert- Benzotriazole-based ultraviolet absorbers such as butyl-4-methylphenol, 2- (4,6-diphenyl-1,3,5-triazine-2-yl) -5- [2- (2-ethylhexanoyloxy) Triazine-based UV absorbers such as ethoxy] phenol, 2,4,6-tris (2-hydroxy-4-hexyloxy-3-methylphenyl) -1,3,5-triazine, [2-hydroxy-4- (octyloxy) ) Phenyl] (phenyl) Metanon and other benzophenone-based ultraviolet absorbers, benzoate-based ultraviolet absorbers, iron oxide, titanium oxide and the like can be mentioned. These may be used as they are, or may be diluted with water, alcohol, an organic solvent or the like before use. Of these, it is preferable to use an oil-soluble ultraviolet absorber, more preferably a triazine-based ultraviolet absorber, and 2- (4,6-bis (2,4 dimethylphenyl) -1,3,5- Triazine-2-yl) -5-hydroxyphenyl, tooxylan "(C10-C16 mainly C12-C13 alkyloxy) methyl] Reaction product with oxylan, benzenepropanoic acid 3- (2H-benzotriazole-2-yl) -5- (1,1-dimethylethyl) -4-hydroxy C7-9 side chain and linear alkyl ester, 2,4,6-tris (2-hydroxy-4-hexyloxy-3-methylphenyl) -1 , 3,5-Triazine is most preferred, especially 2- (4,6-bis (2,4 dimethylphenyl) -1,3,5-triazine-2-yl) -5-hydroxyphenyl, tooxylan " Reaction product with (C10-C16 mainly C12-C13 alkyloxy) methyl] oxylane and benzenepropanoic acid 3- (2H-benzotriazole-2-yl) -5- (1,1-dimethylethyl) -4- Since the hydroxy C7-9 side chain and the linear alkyl ester are colorless and transparent, the change in appearance when applied to wood is the smallest.

前記光安定化剤としては例えば、ビス(2,2,6,6−テトラメチル−4−ピペリジル)セバケート、ビス(1,2,2,6,6−ペンタメチル−4−ピペリジル)セバケート、テトラキス(1,2,2,6,6−ペンタメチル−4−ピペリジル) ブタン−1,2,3,4−テトラカルボキシレート、テトラキス(2,2,6,6−テトラメチル−4−ピペリジル) ブタン−1,2,3,4−テトラカルボキシレート、ビス(1,2,2,6,6−ペンタメチル−4−ピペリジル) セバケート、ビス(2,2,6,6−テトラメチル−4−ピペリジル) セバケート、ビス(1−ウンデカノキシ−2,2,6,6−テトラメチルピペリジン−4−イル)カルボネート、1,2,2,6,6−ペンタメチル−4−ピペリジルメタクリレート、2,2,6,6−テトラメチル−4−ピペリジルメタクリレート、ビス(1,2,2,6,6−ペンタメチル−4−ピペリジル)[[3,5−ビス(1,1−ジメチルエチル)−4−ヒドロキシフェニル]メチル]ブチルマロネート等のヒンダードアミン系光安定剤等が挙げられる。これらはそのまま用いても良いし、水、アルコール、有機溶剤等で希釈して用いても良い。これらのうち、油溶性の光安定化剤を用いることが好ましく、ビス(1,2,2,6,6−ペンタメチル−4−ピペリジル)セバケート、メチル1,2,2,6,6−ペンタメチル-4-ピペリジルセバケート等のセバケートヒンダードアミン系光安定剤を用いることがより好ましい。 Examples of the photostabilizer include bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, and tetrakis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate. 1,2,2,6,6-pentamethyl-4-piperidyl) butane-1,2,3,4-tetracarboxylate, tetrakis (2,2,6,6-tetramethyl-4-piperidyl) butane-1 , 2,3,4-tetracarboxylate, bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, Bis (1-undecanoxy-2,2,6,6-tetramethylpiperidine-4-yl) carbonate, 1,2,2,6,6-pentamethyl-4-piperidyl methacrylate, 2,2,6,6-tetra Methyl-4-piperidyl methacrylate, bis (1,2,2,6,6-pentamethyl-4-piperidyl) [[3,5-bis (1,1-dimethylethyl) -4-hydroxyphenyl] methyl] butylmalo Examples thereof include hindered amine-based light stabilizers such as Nate. These may be used as they are, or may be diluted with water, alcohol, an organic solvent or the like before use. Of these, it is preferable to use an oil-soluble light stabilizer, bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, methyl 1,2,2,6,6-pentamethyl-. It is more preferable to use a sebacate hindered amine-based light stabilizer such as 4-piperidyl sebacate.

前記紫外線吸収剤及び光安定化剤は併用して用いることが必要である。紫外線吸収剤と光安定化剤を併用することにより木質材料の木目や色調等の外観の変化を抑制することができる。 It is necessary to use the ultraviolet absorber and the light stabilizer in combination. By using an ultraviolet absorber and a light stabilizer in combination, changes in appearance such as grain and color tone of wood-based materials can be suppressed.

前記紫外線吸収剤及び光安定化剤はアルコール中に溶解することが好ましい。紫外線吸収剤及び光安定化剤をアルコール中に溶解することにより、紫外線吸収剤及び光安定化剤を木質材料の表面により深く浸透させることができる。 The UV absorber and light stabilizer are preferably dissolved in alcohol. By dissolving the UV absorber and the light stabilizer in alcohol, the UV absorber and the light stabilizer can be deeply penetrated into the surface of the wood material.

前記紫外線吸収剤の塗付量は好ましくは2〜50g/mであり、より好ましくは3〜25g/mであり、最も好ましくは5〜20g/mである。 The amount of the ultraviolet absorber applied is preferably 2 to 50 g / m 2, more preferably 3 to 25 g / m 2 , and most preferably 5 to 20 g / m 2 .

前記光安定化剤の塗付量は好ましくは0.2〜20g/mであり、より好ましくは1.5〜15g/mであり、最も好ましくは5〜10g/mである。 The amount of the light stabilizer applied is preferably 0.2 to 20 g / m 2 , more preferably 1.5 to 15 g / m 2 , and most preferably 5 to 10 g / m 2 .

前記紫外線吸収剤と光安定化剤とは混合して用いることが好ましい。両者を混合して用いることにより単独で別々に塗付した場合に比べて屋外耐久性(耐変色性)に優れる。 It is preferable to use the ultraviolet absorber and the light stabilizer as a mixture. By using both in combination, the outdoor durability (discoloration resistance) is superior as compared with the case where they are individually applied separately.

前記光安定化剤100質量部に対する紫外線吸収剤の混合比は好ましくは300質量部以上、より好ましくは500質量部以上、最も好ましくは、800質量部以上である。紫外線吸収剤及び光安定化剤の塗付量よりも紫外線吸収剤と光安定化剤との混合比の方が木質材料の屋外耐久性(特に色調の変化)に及ぼす影響は大きく、前記の比率で混合したときに最も屋外耐久性に優れる。 The mixing ratio of the ultraviolet absorber to 100 parts by mass of the light stabilizer is preferably 300 parts by mass or more, more preferably 500 parts by mass or more, and most preferably 800 parts by mass or more. The mixing ratio of the UV absorber and the light stabilizer has a greater effect on the outdoor durability (particularly the change in color tone) of the wood material than the amount of the UV absorber and the light stabilizer applied. It has the best outdoor durability when mixed with.

前記紫外線吸収剤及び光安定化剤の合計100質量部に対するアルコールは好ましくは20〜500質量部であり、より好ましくは50〜300質量部であり、最も好ましくは80〜200質量部である。 The alcohol content is preferably 20 to 500 parts by mass, more preferably 50 to 300 parts by mass, and most preferably 80 to 200 parts by mass with respect to 100 parts by mass of the total of the ultraviolet absorber and the light stabilizer.

前記アルコールは炭素数1〜5であることが好ましく、1〜3であることがより好ましい。炭素数1〜5のアルコールとしては例えば、メタノール(炭素数1)、エタノール、エチレングリコール(炭素数2)、プロパノール、イソプロピルアルコール、プロピレングリコール(炭素数3)、ブタノール(炭素数4)、ペンタノール(炭素数5)等が挙げられる。アルコールの炭素数が1〜5であることにより紫外線吸収剤及び光安定化剤を木材表面に深く浸透させることができる。また、前記アルコールは水で希釈して用いても良い。 The alcohol preferably has 1 to 5 carbon atoms, and more preferably 1 to 3 carbon atoms. Examples of alcohols having 1 to 5 carbon atoms include methanol (1 carbon atom), ethanol, ethylene glycol (2 carbon atoms), propanol, isopropyl alcohol, propylene glycol (3 carbon atoms), butanol (4 carbon atoms), and pentanol. (5 carbon atoms) and the like. Since the alcohol has 1 to 5 carbon atoms, the ultraviolet absorber and the light stabilizer can be deeply penetrated into the wood surface. Further, the alcohol may be diluted with water before use.

前記結合材は紫外線吸収剤及び光安定化剤を木質材料表面に固着させるためのものであり、例えば、合成樹脂、グラフト重合を生じさせるモノマー等が挙げられる。本発明は前記結合材を含有しないことが必要である。 The binder is for fixing an ultraviolet absorber and a light stabilizer to the surface of a wood-based material, and examples thereof include synthetic resins and monomers that cause graft polymerization. The present invention needs to be free of the binder.

前記撥水剤を塗付することにより、木質材料への水の浸入を抑制し、該木質材料のひび割れや変形を抑制することができる。 By applying the water-repellent agent, it is possible to suppress the infiltration of water into the wood-based material and suppress the cracking and deformation of the wood-based material.

前記撥水剤は紫外線吸収剤及び光安定化剤を木質材料の表面に塗付した後に、塗付されることが必要である。このように構成することにより、紫外線吸収剤及び光安定化剤の水(例えば雨水等)による溶出を抑制することができるため、木質材料の長期耐久性(特に耐変色性)に優れる。 The water repellent needs to be applied after the ultraviolet absorber and the light stabilizer are applied to the surface of the wood material. With such a configuration, the elution of the ultraviolet absorber and the light stabilizer with water (for example, rainwater) can be suppressed, so that the long-term durability (particularly discoloration resistance) of the wood material is excellent.

前記撥水剤はシリコーン樹脂等のシリコーン系撥水剤、シランモノマー、シランダイマー等のシラン系撥水剤、フッ素樹脂などのフッ素系撥水剤等が挙げられる。これらのうち、フッ素系撥水剤を用いることが好ましく、パーフロロアルキル基を有するフッ素系撥水剤を用いることがより好ましい。これらはそのまま用いても良いし、水やアルコール、有機溶剤等で希釈あるいは乳化して用いても良い。パーフロロアルキル基を有するフッ素系撥水剤の例を[化1]に示す。 Examples of the water repellent include silicone-based water repellents such as silicone resins, silane-based water repellents such as silane monomers and silane dimers, and fluororesin-based water repellents such as fluororesins. Of these, it is preferable to use a fluorine-based water repellent, and it is more preferable to use a fluorine-based water repellent having a perfluoroalkyl group. These may be used as they are, or may be diluted or emulsified with water, alcohol, an organic solvent or the like. An example of a fluorine-based water repellent having a perfluoroalkyl group is shown in [Chemical Formula 1].

Figure 0006896268

ここで、R、R、Rはアルキル基、C13はパーフルオロアルキル基、X,Yは非フッ素側鎖である。パーフルオロ基の炭素数及びフッ素数は任意である。
Figure 0006896268

Here, R 1 , R 2 , and R 3 are alkyl groups, C 6 F 13 is a perfluoroalkyl group, and X and Y are non-fluorine side chains. The number of carbon atoms and the number of fluorines of the perfluoro group are arbitrary.

前記パーフルオロアルキル基はアルキル基の水素の一部または全部をフッ素で置き換えたアルキル基をいう。これらのうち、アルキル基の水素全部をフッ素で置き換えたアルキル基であることが好ましく、アルキル基の炭素数が2〜10であることがより好ましく、アルキル基の炭素数が5〜8であることが最も好ましい。 The perfluoroalkyl group refers to an alkyl group in which part or all of hydrogen in the alkyl group is replaced with fluorine. Of these, an alkyl group in which all hydrogen of the alkyl group is replaced with fluorine is preferable, the number of carbon atoms of the alkyl group is more preferably 2 to 10, and the number of carbon atoms of the alkyl group is 5 to 8. Is the most preferable.

前記パーフルオロアルキル基を有するモノマー単位以外の部分は(メタ)アクリル骨格であることが好ましい。パーフルオロアルキル基を有するモノマー単位以外の部分は(メタ)アクリル骨格であることにより耐候性に優れる。 The portion other than the monomer unit having a perfluoroalkyl group is preferably a (meth) acrylic skeleton. Since the portion other than the monomer unit having a perfluoroalkyl group is a (meth) acrylic skeleton, it has excellent weather resistance.

前記撥水剤の塗付量は不揮発分換算で好ましくは1〜50g/mであり、より好ましくは2〜35g/mであり、最も好ましくは5〜15g/mである。 The amount of the water repellent applied is preferably 1 to 50 g / m 2 in terms of non-volatile content, more preferably 2 to 35 g / m 2, and most preferably 5 to 15 g / m 2 .

前記撥水剤を塗付した後に親水化剤を塗付しても良い。このように構成することにより、屋外で使用された場合に木質材料の表面に付着した汚れが雨水によって流されやすくなるため、耐汚染性に優れる。 After applying the water repellent agent, a hydrophilic agent may be applied. With such a configuration, when used outdoors, dirt adhering to the surface of the wood-based material is easily washed away by rainwater, so that it is excellent in stain resistance.

前記親水化剤は任意に用いることができる。例えば、コロイダルシリカ溶液、ケイ酸ナトリウム、ケイ酸カリウム等のケイ酸化合物、アルコキシシリケート、第四級アンモニウム塩、第四級アンモニウム塩含有ポリマー等が挙げられる。 The hydrophilic agent can be used arbitrarily. For example, a colloidal silica solution, a silicic acid compound such as sodium silicate and potassium silicate, an alkoxysilicate, a quaternary ammonium salt, a quaternary ammonium salt-containing polymer and the like can be mentioned.

前記親水化剤は水溶液の形態で用いることが好ましい。水溶液の形態で用いることにより、木材表面に塗付されている紫外線吸収剤及び光安定化剤を溶解流出させることなく表面を親水化することができる。 The hydrophilic agent is preferably used in the form of an aqueous solution. By using it in the form of an aqueous solution, the surface can be made hydrophilic without dissolving and flowing out the ultraviolet absorber and the light stabilizer coated on the wood surface.

以上のように構成された紫外線吸収剤、光安定化剤及び撥水剤は以下のように用いられる。
始めに、紫外線吸収剤としての2,4,6−トリス(2−ヒドロキシ−4−ヘキシロキシ−3−メチルフェニル)−1,3,5−トリアジンと、光安定化剤としてのビス(1,2,2,6,6−ペンタメチル−4−ピペリジル)セバケート、メチル1,2,2,6,6−ペンタメチル-4-ピペリジルセバケートとを紫外線吸収剤150質量部、光安定化剤100質量部の比率でアルコールとしてのイソプロピルアルコール400質量部中に溶解させ、木材表面保護剤としての紫外線吸収剤・光安定化剤混合溶液とする。
The ultraviolet absorber, light stabilizer and water repellent configured as described above are used as follows.
First, 2,4,6-tris (2-hydroxy-4-hexyloxy-3-methylphenyl) -1,3,5-triazine as an ultraviolet absorber and bis (1,2) as a light stabilizer. , 2,6,6-pentamethyl-4-piperidyl) sebacate, methyl 1,2,2,6,6-pentamethyl-4-piperidyl sebacate with 150 parts by mass of UV absorber and 100 parts by mass of light stabilizer. It is dissolved in 400 parts by mass of isopropyl alcohol as an alcohol in a ratio to prepare a mixed solution of an ultraviolet absorber and a light stabilizer as a wood surface protectant.

続いて、前記木材表面保護剤を木質材料としての幅200mm、長さ1000mm、厚さ20mmのスギ製材の表面に塗付量44g/mで塗付し、16時間室温で放置して乾燥させた後に、撥水剤としてのパーフロロアルキル基を有するフッ素系撥水剤(アルキル基の炭素数6、フッ素数13、パーフロロアルキル基以外はアクリル骨格及びメタクリル骨格)を水に乳化した乳化液(不揮発分40%)を塗付量100g/mで塗付して乾燥させる。 Subsequently, the wood surface protective agent is applied to the surface of a cedar lumber having a width of 200 mm, a length of 1000 mm, and a thickness of 20 mm as a wood material at an application amount of 44 g / m 2 , and left at room temperature for 16 hours to dry. After that, an emulsion obtained by emulsifying a fluorine-based water repellent having a perfluoroalkyl group as a water repellent (alkyl group having 6 carbon atoms, 13 fluorines, acrylic skeleton and methacryl skeleton other than perfluoroalkyl group) in water. (Non-volatile content 40%) is applied at an application amount of 100 g / m 2 and dried.

前記木質材料はスギに限らず、任意に設定することができる。例えばスギ、カラマツ、ヒノキ、イチイ等の針葉樹やサクラ、ケヤキ、ブナ、クヌギ、ナラ等の広葉樹等が挙げられる。 The wood-based material is not limited to sugi, and can be set arbitrarily. Examples thereof include coniferous trees such as Sugi, larch, cypress and Japanese yew, and broad-leaved trees such as cherry, zelkova, beech, oak and oak.

前記木質材料は製剤に限らず任意に設定することができる。例えば、合板、単板積層板(LVL)、集成材、直交集成板(クロス・ラミネイティド・ティンバー、CLT)等が挙げられる。 The wood-based material is not limited to the formulation and can be arbitrarily set. For example, plywood, single plate laminated board (LVL), laminated lumber, orthogonal laminated board (cross laminated timber, CLT) and the like can be mentioned.

前記乾燥は自然乾燥でも良いし、熱風や遠赤外線などを用いた強制乾燥でも良い。 The drying may be natural drying or forced drying using hot air, far infrared rays, or the like.

前記木材表面保護剤には通常の塗料に用いる添加剤を用いることができる。例えば、防腐剤、消泡剤、pH調整剤、凍結防止剤、防藻剤、増粘剤等が挙げられる。 As the wood surface protective agent, additives used in ordinary paints can be used. For example, preservatives, antifoaming agents, pH adjusters, antifreeze agents, algae preventive agents, thickeners and the like can be mentioned.

前記撥水剤はそのまま用いても良いし、アルコールや有機溶剤で溶解させて用いても良いし、水等に乳化して塗付しても良い。 The water repellent may be used as it is, dissolved in alcohol or an organic solvent, or emulsified in water or the like and applied.

以上のようにして表面処理された乾燥させたスギ製材は建築物の外壁として用いられる。 The dried sugi lumber surface-treated as described above is used as the outer wall of the building.

前記木質材料としてのスギ製材は建築物の外壁以外にも風雨や日光にさらされる環境であれば、本発明の効果を有する。例えば、ウッドデッキ、柱材、梁材、軒材、縁側材、こけら葺き、とくさ葺き、とち葺き等の屋根材、カーポート、塀、窓枠、サッシ、柵、看板等の建築材料、橋梁等の土木材料、屋外競技場やキャンプ場などの野外で使用される椅子、机等の家具、自動車や電車等の車両の内外装、電柱、靴、鞄、眼鏡等が挙げられる。また、内装であっても日光と水の影響を受ける部位であれば任意に用いることができる。例えば、床(特に窓際)、内壁、ブラインド等が挙げられる。 The sugi lumber as a wood-based material has the effect of the present invention as long as it is exposed to wind, rain and sunlight in addition to the outer wall of the building. For example, wood decks, pillars, beams, eaves, verandas, moss-roofing, tokusa-roofing, tochi-roofing and other roofing materials, carports, fences, window frames, sashes, fences, signboards and other building materials, bridges. Civil engineering materials such as, chairs used outdoors such as outdoor stadiums and campgrounds, furniture such as desks, interior and exterior of vehicles such as automobiles and trains, electric poles, shoes, bags, glasses, etc. Further, even if it is an interior, it can be arbitrarily used as long as it is a part affected by sunlight and water. For example, floors (especially near windows), inner walls, blinds and the like.

以上のようにして構成された木質材料としてのスギ製材は、特殊な設備がなくとも建築現場で塗装することにより製造することができ、建築物の外壁材として使用されても木目や色調等の急激な外観の変化を伴わず、吸水によるひび割れが少なく、長期にわたってゆっくりと劣化させることができる。 Sugi lumber as a wood-based material constructed as described above can be manufactured by painting at a construction site without special equipment, and even if it is used as an outer wall material of a building, the grain and color tone, etc. It is not accompanied by a sudden change in appearance, has few cracks due to water absorption, and can be slowly deteriorated over a long period of time.

以下、実施例と比較例を挙げて本発明を説明する。試験は50mm×150mm×厚さ10mmのスギ製材の表面に木材表面保護剤を塗付し、常温16時間放置した後に撥水剤を塗付して常温でさらに16時間放置して試験体とした。続いて試験体をJIS K5600−7−6:2002に規定されている塗料一般試験方法−第7部:塗膜の長期耐久性−第6節:屋外暴露耐候性に準拠して、水平面に対して45度の角度で地面から45cmの高さに設置して南面に向け6ヶ月間及び18ヶ月間屋外で曝露した。曝露場所は岐阜県岐阜市である。評価は未曝露の試験体と外観を比較することにより行い、外観の変化がほとんどないものを◎、灰化には至っていないが外観変化があるものを○、やや色調の変化があるもの及び塗膜の浮きが生じているものを△、外観が灰化しているもの及び塗膜がはがれているものを×とした。また、18ヶ月間の屋外曝露が終了した試験体について、同じ仕様で再塗装を行って塗り替え適性を評価した。塗り替えが容易で外観変化が小さいものを〇、塗り替えは容易だが外観変化が生じたものを△、塗り替え時に旧塗膜の剥離が必要であったものを×とした。試験に使用した木材表面保護剤、撥水剤、親水化剤の組成及び試験の結果を表1に示す。 Hereinafter, the present invention will be described with reference to Examples and Comparative Examples. In the test, a wood surface protective agent was applied to the surface of a sugi lumber of 50 mm × 150 mm × 10 mm in thickness, and after leaving it at room temperature for 16 hours, a water repellent was applied and left at room temperature for another 16 hours to prepare a test piece. .. Subsequently, the test piece was subjected to the general paint test method specified in JIS K5600-7-6: 2002-Part 7: Long-term durability of the coating film-Section 6: Outdoor exposure and weather resistance in accordance with the horizontal surface. It was installed at a height of 45 cm from the ground at an angle of 45 degrees and exposed outdoors for 6 months and 18 months toward the south surface. The exposed place is Gifu City, Gifu Prefecture. The evaluation was performed by comparing the appearance with the unexposed test piece, and those with almost no change in appearance were evaluated as ◎, those that had not been incinerated but had a change in appearance were ○, those with a slight change in color and painted. Those in which the film was lifted were marked with Δ, those in which the appearance was incinerated and those in which the coating film was peeled off were marked with x. In addition, the test specimens that had been exposed to the outdoors for 18 months were repainted with the same specifications to evaluate the repainting suitability. Those that were easy to repaint and had a small change in appearance were marked with 〇, those that were easy to repaint but had a change in appearance were marked with Δ, and those that required peeling of the old coating film at the time of repainting were marked with x. Table 1 shows the compositions of the wood surface protectant, water repellent, and hydrophilic agent used in the test and the test results.

なお、表中でUVA/HALSとあるのは紫外線吸収剤の質量をヒンダードアミン系光安定化剤の質量で割った質量比を示す。また、表中で紫外線吸収剤Aは2-(4,6−ビス(2,4−ジメチルフェニル)−1,3,5−トリアジン−2−イル)−5−ヒドロキシフェニル,トオキシラン「(C10−C16主としてC12−C13アルキルオキシ)メチル]オキシランとの反応生成物であり、紫外線吸収剤Bはベンゼンプロパン酸・3−(2H−ベンゾトリアゾール−2−イル)−5−(1,1−ジメチルエチル)−4−ヒドロキシ・C7−9側鎖及び直鎖アルキルエステルであり、紫外線吸収剤Cは2−(2,4−ジヒドロキシフェニル)−4,6−ビス−(2,4−ジメチルフェニル)−1,3,5−トリアジンと(2−エチルヘキシル)−グリシド酸エステルの反応生成物であり、光安定化剤Aはビス(1,2,2,6,6−ぺンタメチル−4−ピぺリジル)セバケートであり、光安定化剤Bはデカン二酸ビス(2,2,6,6−テトラメチル−1−(オクチルオキシ)−4−ピペリジニル)エステル、1,1−ジメチルエチルヒドロペルオキシドとオクタンの反応生成物である。 In the table, UVA / HALS indicates the mass ratio of the mass of the ultraviolet absorber divided by the mass of the hindered amine-based light stabilizer. In the table, the ultraviolet absorber A is 2- (4,6-bis (2,4-dimethylphenyl) -1,3,5-triazine-2-yl) -5-hydroxyphenyl, tooxylan "(C10-). C16 is mainly a reaction product with C12-C13 alkyloxy) methyl] oxylane, and the ultraviolet absorber B is benzenepropanoic acid, 3- (2H-benzotriazole-2-yl) -5- (1,1-dimethylethyl). ) -4-Hydroxy ・ C7-9 side chain and linear alkyl ester, and the ultraviolet absorber C is 2- (2,4-dihydroxyphenyl) -4,6-bis- (2,4-dimethylphenyl)- It is a reaction product of 1,3,5-triazine and (2-ethylhexyl) -glycidate, and the photostabilizer A is bis (1,2,2,6,6-pentamethyl-4-piperidyl). ) Sevacate, the photostabilizer B is bisdecanoate (2,2,6,6-tetramethyl-1- (octyloxy) -4-piperidinyl) ester, 1,1-dimethylethylhydroperoxide and octane. Reaction product of.

Figure 0006896268
Figure 0006896268

Claims (1)

木質材料の表面に木材表面保護剤を塗付した後に、撥水剤を塗付して乾燥させる屋外用木質材料の保護方法であって、前記木材表面保護材が、光安定化剤及び紫外線吸収剤の濃度の合計が17質量%〜57質量%のアルコール溶液であり、前記アルコール溶液は光安定化剤に対して質量比3〜20倍の紫外線吸収剤を含有し結合材を含有しないことを特徴とする屋外用木質材料の保護方法。
A method for protecting an outdoor wood-based material in which a wood surface-protecting agent is applied to the surface of the wood-based material and then a water-repellent agent is applied and dried. The total concentration of the agents is an alcohol solution of 17% by mass to 57% by mass, and the alcohol solution contains an ultraviolet absorber having a mass ratio of 3 to 20 times the mass ratio of the light stabilizer and does not contain a binder. A characteristic method of protecting wood-based materials for outdoor use.
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