JPH06143205A - Manufacture of fungiproof wooden material - Google Patents

Manufacture of fungiproof wooden material

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Publication number
JPH06143205A
JPH06143205A JP32114592A JP32114592A JPH06143205A JP H06143205 A JPH06143205 A JP H06143205A JP 32114592 A JP32114592 A JP 32114592A JP 32114592 A JP32114592 A JP 32114592A JP H06143205 A JPH06143205 A JP H06143205A
Authority
JP
Japan
Prior art keywords
resin
wood
weight
parts
agent
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.)
Pending
Application number
JP32114592A
Other languages
Japanese (ja)
Inventor
Junji Murakami
淳司 村上
Takao Murahashi
隆雄 村橋
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.)
Aica Kogyo Co Ltd
Original Assignee
Aica Kogyo 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 Aica Kogyo Co Ltd filed Critical Aica Kogyo Co Ltd
Priority to JP32114592A priority Critical patent/JPH06143205A/en
Publication of JPH06143205A publication Critical patent/JPH06143205A/en
Pending legal-status Critical Current

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  • Chemical And Physical Treatments For Wood And The Like (AREA)

Abstract

PURPOSE:To inhibit fungal propagation of wooden material and to improve physical properties of its surface such as surface hardness, flaw resistance, etc. CONSTITUTION:Wooden material is impregnated with a treatment which is loaded with 10-30 pts.wt. of low shrinking agent and 0.5-1.0 pts.wt. of fungistat against 100 pts.wt. of solid content of resin fluid which consists of resin for wood-plastic composite, and, then, the material is heat-treated. Melamine resin, unsaturated polyester resin or, etc., is used as the resin for wood-plastic composite, and vinyl acetate or methyl methacrylate is used as low shrinking agent. As the fungistat, benzimidazole group compounds e.g. 2-(4-thiazoline) benzimidazole is used, and as a heat-treat, hot air is used and a flat press, etc., is used.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は、木材の改質に関し、特
に防かび性木質材の製法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to the modification of wood, and more particularly to a method for producing antifungal wood materials.

【0002】[0002]

【従来の技術】従来より、建築用内・外装材として、木
質材を用いたテ−ブル、カウンタ−、ドアは広く使用さ
れており、とりわけ近年においては、木質材資源を有効
に利用し、木質材の持つ種々の欠点を補うため数多くの
改質が講じられている。中でも施工後や保管中に木材に
発生するかびは、製品の外観を損なうばかりでなく、成
形加工用の素材として適用できない場合もあって、
(1)防かび剤を塗装用の塗料中に分散させた後、木質
材の表面に塗工する、(2)木質材に合成樹脂を注入し
てWPC化する、(3)防かび剤を水溶液中に分散させ
た薬剤を木材に含浸させる、(4)無機系の抗菌剤を合
成樹脂中に分散させ木質材内部に注入してWPC化す
る、等の手段が広く一般に用いられている。
2. Description of the Related Art Conventionally, as an interior / exterior material for construction, a table, a counter, and a door made of wood have been widely used. In recent years, in particular, wood resources have been effectively utilized, Numerous modifications have been made to compensate for the various drawbacks of wood materials. Above all, mold that occurs on wood after construction and during storage not only impairs the appearance of the product, but may not be applicable as a material for molding processing,
(1) Disperse the antifungal agent in the paint for coating and then apply it on the surface of the wood material. (2) Inject synthetic resin into the wood material to form WPC. (3) Add the antifungal agent. Means such as impregnating wood with a drug dispersed in an aqueous solution and (4) dispersing an inorganic antibacterial agent in a synthetic resin and injecting it into a wood material to form WPC are widely used.

【0003】[0003]

【本発明が解決しようとする課題】しかしながら、
(1)木質材の表面に塗工する方法においては、塗膜表
面においては、防かび性が有効に作用するものの、塗膜
より下の木質材に至るまでの傷が生じた場合はその効果
は激減する。また、(2)合成樹脂を木質材内部に注入
することによってもかなりの防かび性を付与させること
もできるが、高分子量の合成樹脂が浸入されにくい細胞
壁に時としてかびが発生することがあり、完全にかびを
防ぎえるものではない。また、(3)防かび剤のみを水
溶液中に分散させた薬剤を木質材に含浸させる方法は、
合成樹脂を注入したものに比べて表面硬度を向上させに
くい。さらに、(4)無機系の抗菌剤を合成樹脂中に分
散させ木質材内部に注入する方法は無機系の抗菌剤の粒
子が木材の細胞内部まで注入されにくいとういう欠点を
有しており、いずれも充分な防かび効果が得られにくい
ものとなっていた。
[Problems to be Solved by the Invention]
(1) In the method of coating on the surface of the wood material, the fungus-proof property works effectively on the surface of the coating film, but when scratches up to the wood material below the coating film occur, its effect Is drastically reduced. Further, (2) by injecting a synthetic resin into the wood material, it is possible to impart a considerable antifungal property, but a mold may sometimes be generated in the cell wall where the high molecular weight synthetic resin is difficult to penetrate. , Cannot completely prevent mold. Further, (3) a method of impregnating a wood material with a chemical in which only an antifungal agent is dispersed in an aqueous solution is
It is difficult to improve the surface hardness compared to the one injected with synthetic resin. Further, (4) the method of dispersing an inorganic antibacterial agent in a synthetic resin and injecting it into a wood material has a drawback that particles of the inorganic antibacterial agent are difficult to inject into the cells of wood. In all cases, it was difficult to obtain a sufficient antifungal effect.

【0004】[0004]

【課題を解決するための手段】本発明は、かかる状況に
鑑み検討されたものであって、WPC用樹脂からなる樹
脂液の固形分100重量部に対して、低収縮化剤を10
〜30重量部と、防かび剤を0.5〜1.0重量部添加
した処理剤を、木質材に注入し、しかる後、加熱処理す
ることことによって、前記の課題を解決することができ
る。以下、本発明について詳細に説明する。
SUMMARY OF THE INVENTION The present invention has been made in consideration of the above situation, and a shrinkage reducing agent is added in an amount of 10 parts by weight with respect to 100 parts by weight of a solid content of a resin liquid containing a WPC resin.
The above-mentioned problems can be solved by injecting a treatment agent containing 30 to 30 parts by weight and 0.5 to 1.0 parts by weight of a fungicide into a wood material, and then performing heat treatment. . Hereinafter, the present invention will be described in detail.

【0005】本発明に用いるWPC用樹脂としては、メ
ラミン樹脂、ジアリルフタレ−ト樹脂、不飽和ポリエス
テル樹脂、ポリウレタン樹脂、ポリメタクリル酸メチル
樹脂など、木質材のWPC化に使用される樹脂が適用で
き、必要に応じて、硬化剤、水、有機溶剤、架橋剤など
を添加して、樹脂液としたもので、木質材の材種、とり
わけ密度や厚みにより、適宜粘度調整される。
As the WPC resin used in the present invention, resins used for WPC conversion of wood materials such as melamine resin, diallyl phthalate resin, unsaturated polyester resin, polyurethane resin and polymethylmethacrylate resin can be applied. If necessary, a curing agent, water, an organic solvent, a cross-linking agent, etc. are added to form a resin liquid, and the viscosity is appropriately adjusted depending on the wood material type, particularly the density and thickness.

【0006】メラミン樹脂としては、メラミンとホルマ
リンをアルカリ触媒の存在下で縮合反応させたものや、
アセトグアナミン、ベンゾグアナミンなどのグアナミン
とメラミンとホルマリンをアルカリ触媒の存在下で縮合
反応させたグアナミン変性メラミン樹脂や、粉末状のメ
ラミン樹脂を水に溶解したものが適用できる。
As the melamine resin, melamine and formalin are subjected to a condensation reaction in the presence of an alkali catalyst,
A guanamine-modified melamine resin obtained by condensation reaction of guanamine such as acetoguanamine and benzoguanamine, melamine and formalin in the presence of an alkali catalyst, or a melamine resin in powder form dissolved in water can be applied.

【0007】ジアリルフタレ−ト樹脂、ポリウレタン樹
脂、ポリメタクリル酸メチルとしては、各々、常法によ
り、ジアリルフタレ−トモノマ−を部分重合させたも
の、イソシアネ−トとアルコ−ルを縮重合させたもの、
メタクリル酸メチルを重合させたものが適用できる。
The diallyl phthalate resin, the polyurethane resin and the polymethyl methacrylate are each a partially polymerized diallyl phthalate monomer, a polycondensed isocyanate and an alcohol by a conventional method.
What polymerized methyl methacrylate can be applied.

【0008】不飽和ポリエステル樹脂としては、従来公
知の技術により多塩基酸と多価アルコ−ルを用いて脱水
縮合させたものが適用でき、多塩基酸としては、無水マ
レイン酸、フマル酸、無水フタル酸、イソフタル酸、テ
レフタル酸、イタコン酸などが挙げられ、多価アルコ−
ルとしては、エチレングリコ−ル、プロピレングリコ−
ル、ネオペンチルグリコ−ル、ジエチレングリコ−ル、
ジプロピレングリコ−ル、ブチレングリコ−ルなどが挙
げられる。
As the unsaturated polyester resin, those obtained by dehydration condensation using a polybasic acid and a polyhydric alcohol according to a conventionally known technique can be applied. Examples of the polybasic acid include maleic anhydride, fumaric acid, and anhydride. Phthalic acid, isophthalic acid, terephthalic acid, itaconic acid, etc.
Examples of the ethylene glycol, propylene glycol
, Neopentyl glycol, diethylene glycol,
Examples include dipropylene glycol and butylene glycol.

【0009】低収縮剤としては、例えば、酢酸ビニ−
ル、アクリル酸、アクリル酸メチル、アクリルアミド、
アクリルニトリル、スチレン、メタクリル酸メチル、メ
タクリルアミドなどのポリマ−などが挙げられ、WPC
用樹脂の硬化収縮を考慮し、必要に応じて、適宜選択し
て用いることができる。これは、WPC用樹脂の硬化収
縮にともなう表層部でのクラックや干割れの発生を防止
するためのもので、添加量は、WPC用樹脂からなる樹
脂液の固形分100重量部に対して、10〜30重量部
とするのが望ましい。上限を超えると、防かび性木質材
となった場合の表面物性、とりわけ表面硬度が劣りやす
く、下限に満たないとWPC用樹脂の硬化収縮を抑制し
にくく、反りを生じやすい。
Examples of the low shrinkage agent include vinyl acetate.
, Acrylic acid, methyl acrylate, acrylamide,
Polymers such as acrylonitrile, styrene, methyl methacrylate, methacrylamide, and the like, WPC
In consideration of curing shrinkage of the resin for use, it can be appropriately selected and used as necessary. This is to prevent the occurrence of cracks and cracks in the surface layer portion due to the curing shrinkage of the WPC resin, and the addition amount is 100 parts by weight of the solid content of the resin liquid containing the WPC resin. The amount is preferably 10 to 30 parts by weight. If the upper limit is exceeded, the surface properties of the antifungal wood material, especially the surface hardness, will be poor, and if the lower limit is not reached, it will be difficult to suppress the curing shrinkage of the WPC resin and warp will occur easily.

【0010】防かび剤としては、有機イオウ系化合物、
有機スズ系化合物、クロロフェニ−ル系化合物、ベンツ
イミダゾ−ル系化合物などが挙げられるが、安全性、効
果の面から従来より工業用殺菌剤として知られている、
ベンツイミダゾ−ル系化合物、例えば、2−(4−チア
ゾリル)ベンツイミダゾ−ル、2−ベンツイミダゾ−ル
カルバミン酸メチル、フェノフラゾ−ル、1−(ブチル
カルバモイル)−2−ベンツイミダゾ−ルカルバミン酸
メチルなどを用いるのが好ましい。使用に際しては、こ
れらのベンツイミダゾ−ル系化合物の内1種以上を有機
溶剤、例えばメチルエチルケトン、エチルセルソルブ等
に界面活性剤を適宜添加して、溶解したものを用い、前
述のWPC用樹脂からなる樹脂液、及び低収縮剤と相溶
性があり、WPC用樹脂が硬化する際に発生する反応熱
によって分解しないものを適宜選択して用いることがで
きる。
Antifungal agents include organic sulfur compounds,
Examples include organic tin compounds, chlorophenyl compounds, benzimidazole compounds, etc., which have been conventionally known as industrial fungicides in terms of safety and effects.
Benzimidazole-based compounds, for example, 2- (4-thiazolyl) benzimidazole, methyl 2-benzimidazolecarbamate, fenofrazol, 1- (butylcarbamoyl) -2-benzimidazolecarbamate, etc. Is preferably used. At the time of use, one or more of these benzimidazole-based compounds are dissolved in an organic solvent such as methyl ethyl ketone or ethyl cellosolve by appropriately adding a surfactant, and used as the WPC resin. A resin liquid that is compatible with the resin liquid and the low-shrinking agent and that is not decomposed by the reaction heat generated when the WPC resin is cured can be appropriately selected and used.

【0011】ベンツイミダゾ−ル系化合物の添加量は、
樹脂液の固形分100重量部に対して、固形分換算値で
0.3〜2.0重量部、より望ましくは、0.5〜1.
0重量部とするのが好ましく、ベンツイミダゾ−ル系化
合物の添加量が上限を超えると、WPC用樹脂の硬化を
阻害しやすくなるとともに、紫外線を照射した際の変
色、いわゆる耐光性が劣り、また、下限に満たないと十
分な防かび性が得られにくい。
The amount of benzimidazole compound added is
With respect to 100 parts by weight of the solid content of the resin liquid, 0.3 to 2.0 parts by weight, more preferably 0.5 to 1.
It is preferably 0 part by weight, and when the addition amount of the benzimidazole-based compound exceeds the upper limit, curing of the WPC resin is likely to be hindered, and discoloration upon irradiation with ultraviolet rays, so-called light resistance is poor, Also, if the lower limit is not satisfied, it is difficult to obtain sufficient antifungal properties.

【0012】木質材としては、原材、スライスド単板、
集成材などが挙げられ、具体的には、カバ、ブナ、ラワ
ン、ポプラ、カポ−ル、ナラ、セン、タモ、ケヤキなど
の広葉樹材、スギ、アカマツ、カラマツ、ヒノキ、ツ
ガ、ヒバ、エノキ、アカガシなどの針葉樹材、ゴムノキ
集成材、LVL(Laminated VeneerL
umber)など例示しうるが、これらに限定するもの
ものではない。
Wood materials include raw materials, sliced veneer,
Examples include hardwood, beech, beech, rawan, poplar, capole, oak, sen, duck, zelkova, etc., cedar, red pine, larch, cypress, hemlock, hiba, enoki, Softwood materials such as red oak, laminated lumber, LVL (Laminated Veneer L)
However, the present invention is not limited to these.

【0013】処理剤は、スプレ−による吹き付けや、フ
ロ−コ−タ−による塗布などで木質材の表面を処理して
もさしつかえないが、木質材内部により多く浸透させる
という観点から注入法が望ましく、例えば、浸漬法、減
圧注入、加圧注入、あるいは、これらの注入法を組み合
わせた方法が適用できる。混合樹脂液の含浸量として
は、木質材100に対して、15〜120%とするのが
望ましい。下限に満たないと、防かび性が得られにく
く、また、上限を超えると飽和状態になり、経済的にも
不利となる。
The treating agent may be used even if the surface of the wood material is treated by spraying with a spray or coating with a flow coater. However, the injection method is preferable from the viewpoint of allowing more penetration into the wood material. For example, a dipping method, reduced pressure injection, pressure injection, or a method combining these injection methods can be applied. The impregnated amount of the mixed resin liquid is preferably 15 to 120% with respect to the wood material 100. If it is less than the lower limit, it is difficult to obtain antifungal property, and if it exceeds the upper limit, it becomes saturated, which is economically disadvantageous.

【0014】WPC用樹脂を硬化させる手段としては、
加熱処理、例えば、熱風加熱、赤外線加熱、遠赤外線加
熱、マイクロ波加熱が挙げられるが、これらに限定する
ものではない。加熱温度、加熱時間は、熱硬化性樹脂が
充分に硬化し、木質材が損傷しない程度であればよく、
加熱処理の条件は、混合樹脂液の組成、硬化剤によって
多少異なるが、概ね、80〜140℃、0.1〜8時間
とするのが望ましい。
As means for curing the WPC resin,
Examples of the heat treatment include, but are not limited to, hot air heating, infrared heating, far infrared heating, and microwave heating. The heating temperature and the heating time may be such that the thermosetting resin is sufficiently cured and the wood material is not damaged,
The conditions of the heat treatment are slightly different depending on the composition of the mixed resin liquid and the curing agent, but it is preferably about 80 to 140 ° C. and 0.1 to 8 hours.

【0015】さらに、平板プレス、連続プレスなどを用
いて、加熱と同時に加圧してもよく、この場合は、WP
C用樹脂の硬化が促進され、強度的にも優れたものとな
る。加圧する際の圧力としては、樹脂の硬化を促進し、
木質材が損傷しない程度とするのが望ましく、5〜20
kg/cm2の条件が適する。
Further, a flat plate press, a continuous press or the like may be used to apply pressure simultaneously with heating. In this case, WP is used.
The curing of the C resin is promoted, and the strength becomes excellent. As the pressure when pressurizing, accelerate the curing of the resin,
It is desirable that it does not damage the wood material.
The condition of kg / cm 2 is suitable.

【0016】[0016]

【作用】本発明の防かび性木質材の製法は、WPC用樹
脂が浸入されにくい木質材組織の細胞壁に防かび剤、特
にベンツイミダゾ−ル系化合物が浸入し、定着すること
によって高い防かび効果が得られる。また、WPC用樹
脂を硬化させることによって、木質材がプラスチック化
され、従ってベンツイミダゾ−ル系化合物の木質材組織
からの揮散や、溶脱を防ぐことができる。
The method for producing an antifungal woody material of the present invention has a high antifungal effect by allowing an antifungal agent, particularly a benzimidazole compound, to infiltrate and fix the cell wall of the woody tissue in which the resin for WPC is hard to enter. The effect is obtained. Further, by curing the resin for WPC, the wood material is made into a plastic, and therefore it is possible to prevent volatilization and leaching of the benzimidazole-based compound from the wood material structure.

【0017】また、必要に応じて、低収縮剤を併用する
ことによって、表層部でのWPC用樹脂の硬化収縮が抑
制されるため、クラック、干割れ等を防止することがで
きる。よって、水分や菌糸の浸入を防ぐことができ、か
びの発生を著しく抑制することができる。
Further, if necessary, a low-shrinking agent is used in combination, so that the curing shrinkage of the WPC resin in the surface layer portion is suppressed, so that cracking, cracking and the like can be prevented. Therefore, it is possible to prevent the infiltration of water and mycelia, and it is possible to significantly suppress the generation of mold.

【0018】さらに、WPC用樹脂を加熱硬化させる手
段として、熱圧プレスを用いることにより、木質材表面
が圧密化され、表面硬度を向上させることができる。
Furthermore, by using a hot press as a means for heating and curing the WPC resin, the surface of the wood material is compacted and the surface hardness can be improved.

【0019】[0019]

【実施例】以下、実施例、及び比較例を挙げてより詳細
に説明する。 実施例1 WPC用樹脂として、2−ヒドロキシエチルメタアクリ
レート(ライトエステルHO 共栄社油脂化学工業製)
を用い、これに重合開始剤として過酸化ベンゾイルを添
加して樹脂液(A)を得た。しかる後、酢酸ビニ−ルポ
リマ−、及び2−(4−チアゾリル)ベンツイミダゾ−
ルをエチルセルソルブに溶解した2−(4−チアゾリ
ル)ベンツイミダゾ−ル溶液を、樹脂液(A)の固形分
100重量部に対して、固形分換算値でそれぞれ、12
重量部、0.6重量部添加して処理剤(a)を得た。次
いで、含水率7.6%のゴムノキに、処理剤(a)を含
浸量が16.6%となるように減圧加圧注入した後、1
20℃、8時間の条件で加熱硬化させ、実施例1の防か
び性木質材を得た。
EXAMPLES Hereinafter, examples and comparative examples will be described in more detail. Example 1 As a resin for WPC, 2-hydroxyethyl methacrylate (light ester HO manufactured by Kyoeisha Yushi-Kagaku Kogyo)
Was used and benzoyl peroxide was added as a polymerization initiator thereto to obtain a resin liquid (A). Then, vinyl acetate polymer and 2- (4-thiazolyl) benzimidazole
2- (4-thiazolyl) benzimidazole solution in which ethyl is dissolved in ethyl cellosolve was added to the resin liquid (A) in an amount of 12 in terms of the solid content based on 100 parts by weight of the solid content.
The treating agent (a) was obtained by adding 0.6 part by weight. Then, the treatment agent (a) was injected under reduced pressure and pressure into a rubber tree having a water content of 7.6% so that the impregnation amount was 16.6%, and then 1
The mold-resistant woody material of Example 1 was obtained by heating and curing it at 20 ° C. for 8 hours.

【0020】実施例2 処理剤(a)を含水率8.1%のセセンドックに含浸量
が15.9%となるように減圧加圧注入した後、120
℃、8時間の条件で加熱硬化させ、実施例2の防かび性
木質材を得た。
Example 2 The treating agent (a) was injected under reduced pressure and pressure into a sesendoc with a water content of 8.1% so that the impregnation amount was 15.9%, and then 120
The composition was heat-cured at 8 ° C. for 8 hours to obtain the fungicidal wood material of Example 2.

【0021】実施例3 処理剤(a)を含水率7.2%のゴムノキに、含浸量が
16.0%となるように減圧加圧注入した後、熱盤の表
面温度が140℃、圧力が20kg/cm2、時間が20
分の条件で、加圧を伴わせながら加熱硬化させ、実施例
3の防かび性木質材を得た。
Example 3 The treating agent (a) was injected under reduced pressure and pressure into a rubber tree having a water content of 7.2% so that the impregnation amount was 16.0%. 20 kg / cm 2 , time 20
The mold-resistant woody material of Example 3 was obtained by heating and curing under pressure for minutes.

【0022】実施例4 WPC用樹脂として、不飽和ポリエステル樹脂(DIC
−CS101 大日本インキ工業株式会社製)を用い、
これにスチレンモノマ−、及び硬化剤を加えて樹脂液
(B)を得た。しかる後、実施例1で用いた、酢酸ビニ
−ルポリマ−、及び2−(4−チアゾリル)ベンツイミ
ダゾ−ル溶液を、樹脂液(B)の固形分100重量部に
対して、固形分換算値でそれぞれ20重量部、0.6重
量部添加して処理剤(b)を得た。次いで、含水率7.
1%のゴムノキに、処理剤(b)を含浸量が15.9%
となるように減圧加圧注入した後、120℃、8時間の
条件で加熱硬化させ、実施例4の防かび性木質材を得
た。
Example 4 As a resin for WPC, an unsaturated polyester resin (DIC
-CS101 manufactured by Dainippon Ink and Machinery Co., Ltd.,
A styrene monomer and a curing agent were added to this to obtain a resin liquid (B). Then, the vinyl acetate polymer and the 2- (4-thiazolyl) benzimidazole solution used in Example 1 were converted into solid content based on 100 parts by weight of the solid content of the resin liquid (B). 20 parts by weight and 0.6 parts by weight were added to obtain a treating agent (b). Then, water content 7.
The amount of impregnated treatment agent (b) in 1% of rubber tree is 15.9%
The mixture was injected under reduced pressure and pressure so as to obtain the following, and then heat-cured at 120 ° C. for 8 hours to obtain the mold-resistant woody material of Example 4.

【0023】実施例5 処理剤(b)を含水率8.2%のセセンドックに含浸量
が15.7%となるように減圧加圧注入した後、120
℃、8時間の条件で加熱硬化させ、実施例5の防かび性
木質材を得た。
Example 5 The treating agent (b) was injected under reduced pressure and pressure into a Sesendoc with a water content of 8.2% so that the impregnation amount was 15.7%, and then 120
The mold-proof wood material of Example 5 was obtained by heating and curing under conditions of 8 ° C. and 8 hours.

【0024】実施例6 処理剤(b)を含水率7.0%のゴムノキに、含浸量が
16.7%となるように減圧加圧注入した後、熱盤の表
面温度が140℃、圧力が20kg/cm2、時間が20
分の条件で加圧を伴わせながら加熱硬化させ、実施例6
の防かび性木質材を得た。
Example 6 The treatment agent (b) was injected under reduced pressure and pressure into a rubber tree having a water content of 7.0% so that the impregnation amount was 16.7%. 20 kg / cm 2 , time 20
Example 6 was carried out by heat curing while applying pressure under the condition of minutes.
The mold-resistant woody material was obtained.

【0025】実施例7 樹脂液(B)の固形分100重量部に対して、ポリメタ
クリル酸メチル、及び実施例1で用いた2−(4−チア
ゾリル)ベンツイミダゾ−ル溶液を、固形分換算値でそ
れぞれ28重量部、0.6重量部添加して処理剤(c)
を得た。次いで、含水率7.1%のゴムノキに、処理剤
(c)を含浸量が15.9%となるように減圧加圧注入
した後、120℃、8時間の条件で加熱硬化させ、実施
例7の防かび性木質材を得た。
Example 7 Polymethylmethacrylate and the 2- (4-thiazolyl) benzimidazole solution used in Example 1 were converted into solid content based on 100 parts by weight of the solid content of the resin liquid (B). Value of 28 parts by weight and 0.6 parts by weight of treating agent (c)
Got Then, after injecting the treating agent (c) into the rubber tree having a water content of 7.1% under reduced pressure and pressure so that the impregnation amount becomes 15.9%, it was heated and cured under the conditions of 120 ° C. and 8 hours. Mold-free woody material of No. 7 was obtained.

【0026】実施例8 処理剤(c)を含水率7.1%のゴムノキに、含浸量が
18.6%となるように減圧加圧注入した後、熱盤の表
面温度が140℃、圧力が20kg/cm2、時間が20
分の条件で加圧を伴わせながら加熱硬化させ、実施例8
の防かび性木質材を得た。
Example 8 The treatment agent (c) was injected under reduced pressure and pressure into a rubber tree having a water content of 7.1% so that the impregnation amount was 18.6%. 20 kg / cm 2 , time 20
Example 8 was carried out by heat curing while applying pressure under the condition of minutes.
The mold-resistant woody material was obtained.

【0027】比較例1 樹脂液(A)を、実施例1と同質のゴムノキに、含浸量
が17.7%となるように減圧加圧注入した後、実施例
1と同様の条件で加熱硬化させ、比較例1の処理木材を
得た。
Comparative Example 1 The resin liquid (A) was injected into a rubber tree of the same quality as in Example 1 under reduced pressure and pressure so that the impregnation amount was 17.7%, and then heat curing was performed under the same conditions as in Example 1. The treated wood of Comparative Example 1 was obtained.

【0028】比較例2 樹脂液(B)の固形分100重量部に対して、酢酸ビニ
−ルポリマ−、及び実施例1で用いた2−(4−チアゾ
リル)ベンツイミダゾ−ル溶液を、固形分換算値でそれ
ぞれ7.0重量部、0.2重量部添加して処理剤(d)
を得た。次いで、含水率7.3%のゴムノキに、処理剤
(d)を含浸量が14.3%となるように減圧加圧注入
した後、120℃、8時間の条件で加熱硬化させ、比較
例2の処理木材を得た。
Comparative Example 2 Vinyl acetate polymer and the 2- (4-thiazolyl) benzimidazole solution used in Example 1 were added to 100 parts by weight of the solid content of the resin liquid (B) to obtain a solid content. Treated agent (d) by adding 7.0 parts by weight and 0.2 part by weight, respectively, in converted value
Got Then, the treatment agent (d) was injected under reduced pressure and pressure into a rubber tree having a water content of 7.3% so that the impregnation amount was 14.3%, and then heat-cured at 120 ° C. for 8 hours to obtain a comparative example. 2 treated wood was obtained.

【0029】比較例3 樹脂液(B)の固形分100重量部に対して、酢酸ビニ
−ルポリマ−、及び実施例1で用いた2−(4−チアゾ
リル)ベンツイミダゾ−ル溶液を、固形分換算値でそれ
ぞれ7.0重量部、2.0重量部添加して処理剤(e)
を得た。次いで、含水率7.3%のゴムノキに、処理剤
(e)を含浸量が15.0%となるように減圧加圧注入
した後、120℃、8時間の条件で加熱硬化させ、比較
例3の処理木材を得た。
Comparative Example 3 Vinyl acetate polymer and the 2- (4-thiazolyl) benzimidazole solution used in Example 1 were added to 100 parts by weight of the solid content of the resin liquid (B) to obtain a solid content. Treated agent (e) by adding 7.0 parts by weight and 2.0 parts by weight as converted values, respectively.
Got Then, the treating agent (e) was injected under reduced pressure and pressure into a rubber tree having a water content of 7.3% so that the impregnation amount became 15.0%, and then heat-cured at 120 ° C. for 8 hours to obtain a comparative example. A treated wood of 3 was obtained.

【0031】比較例4 樹脂液(B)の固形分100重量部に対して、酢酸ビニ
−ルポリマ−、及び実施例1で用いた2−(4−チアゾ
リル)ベンツイミダゾ−ル溶液を、固形分換算値でそれ
ぞれ35重量部、0.2重量部添加して処理剤(f)を
得た。次いで、含水率7.4%のゴムノキに、処理剤
(f)を含浸量が15.8%となるように減圧加圧注入
した後、120℃、8時間の条件で加熱硬化させ、比較
例4の処理木材を得た。
Comparative Example 4 The vinyl acetate polymer and the 2- (4-thiazolyl) benzimidazole solution used in Example 1 were added to 100 parts by weight of the solid content of the resin liquid (B) to obtain a solid content. The conversion agent was added in an amount of 35 parts by weight and 0.2 parts by weight, respectively, to obtain a treating agent (f). Then, the treatment agent (f) was injected under reduced pressure and pressure into a rubber tree having a water content of 7.4% so that the impregnation amount was 15.8%, and then heat-cured at 120 ° C. for 8 hours to obtain a comparative example. A treated wood of 4 was obtained.

【0032】比較例5 樹脂液(B)の固形分100重量部に対して、酢酸ビニ
−ルポリマ−、及び実施例1で用いた2−(4−チアゾ
リル)ベンツイミダゾ−ル溶液を、固形分換算値でそれ
ぞれ35重量部、2.0重量部添加して処理剤(g)を
得た。次いで、含水率6.8%のゴムノキに、処理剤
(g)を含浸量が15.8%となるように減圧加圧注入
した後、120℃、8時間の条件で加熱硬化させ、比較
例5の処理木材を得た。
Comparative Example 5 A vinyl acetate polymer and the 2- (4-thiazolyl) benzimidazole solution used in Example 1 were added to 100 parts by weight of the solid content of the resin liquid (B) to obtain a solid content. The treating agent (g) was obtained by adding 35 parts by weight and 2.0 parts by weight in terms of converted values. Then, the treatment agent (g) was injected under reduced pressure and pressure into a rubber tree having a water content of 6.8% so that the impregnated amount was 15.8%, and then heat-cured at 120 ° C. for 8 hours to obtain a comparative example. A treated wood of 5 was obtained.

【0033】比較例6 実施例1で用いた2−(4−チアゾリル)ベンツイミダ
ゾ−ル溶液を蒸留水100重量部に対して、固形分換算
値で1.0重量部を溶解させて殺菌性水溶液を得た。つ
ぎに、含水率6.6%のゴムノキに、殺菌性水溶液を減
圧加圧注入した後、加熱乾燥させて比較例6の処理木材
を得た。
Comparative Example 6 The 2- (4-thiazolyl) benzimidazole solution used in Example 1 was dissolved in 100 parts by weight of distilled water in an amount of 1.0 parts by weight in terms of solid content to disinfect. An aqueous solution was obtained. Next, a bactericidal aqueous solution was injected under reduced pressure and pressure into a rubber tree having a water content of 6.6%, followed by heating and drying to obtain treated wood of Comparative Example 6.

【0034】比較例7 未処理のゴムノキを比較例7の未処理木材とした。Comparative Example 7 Untreated rubber tree was used as the untreated wood of Comparative Example 7.

【0035】評価結果を表1に示す。The evaluation results are shown in Table 1.

【表1】 [Table 1]

【0036】評価方法は、以下の通りとした。防かび性
については、400cm2(縦20cm×横20c
m)、厚み28mmの試験片の表面にナイフにて、深さ
1.0〜1.8mmの傷を碁盤目状につけた後、この上
に水を含ませた布を被せ、しかる後、温度40℃、相対
湿度90%の恒温恒湿槽に10日間放置した後、取り出
して目視にてかびの発生の有無を確認した。かびの発生
のなかったものを〇、傷を付けた部分にかびが発生した
ものを△、全面にかびが発生したものを×とした。
The evaluation method was as follows. For mold resistance, 400 cm 2 (length 20 cm x width 20 c
m), the surface of the test piece having a thickness of 28 mm was cut with a knife to make a scratch with a depth of 1.0 to 1.8 mm in a grid pattern, and then a cloth soaked with water was covered thereon, and then the temperature was measured. After leaving it in a thermo-hygrostat at 40 ° C. and a relative humidity of 90% for 10 days, it was taken out and visually checked for the presence of mold. The case where no mold was generated was evaluated as ◯, the case where mold was generated in the scratched part was evaluated as Δ, and the case where mold was generated on the entire surface was evaluated as x.

【0037】表面ブリネル硬さについては、JISZ2
117に基づき、表面に直径10mmの鋼球を1/πm
m圧入した時の硬さを測定した。単位:[kgf/mm
2
Regarding the surface Brinell hardness, JISZ2
Based on 117, a steel ball with a diameter of 10 mm is 1 / πm on the surface.
The hardness at the time of press-fitting was measured. Unit: [kgf / mm
2 ]

【0038】反りについては、長さ1000mm、巾4
50mm、厚み28mmの試験片を作成し、恒温恒湿槽
にて40℃−90%(相対湿度)−48時間、引き続
き、40℃−30%(相対湿度)−48時間の条件で処
理した後の凹反り方向の反りを測定し、0.1以上〜
0.5mm未満のものを〇、0.5以上〜1.0mm未
満のものを△、1.0mm以上のものを×とした。
Regarding the warp, the length is 1000 mm and the width is 4
After preparing a test piece having a thickness of 50 mm and a thickness of 28 mm and treating it in a thermo-hygrostat at 40 ° C.-90% (relative humidity) -48 hours and subsequently at 40 ° C.-30% (relative humidity) -48 hours. Measure the warp in the concave warp direction of 0.1 or more ~
Those having a length of less than 0.5 mm were evaluated as ◯, those having a value of 0.5 to less than 1.0 mm were evaluated as Δ, and those having a value of 1.0 mm or more were evaluated as x.

【0039】耐光性については、JISK6902に基
づき、紫外線に48時間照射した後、JISZ8722
に基づき、色差(ΔE)を測定した。
Regarding the light resistance, according to JIS K6902, after irradiating with ultraviolet rays for 48 hours, JIS Z8722
Then, the color difference (ΔE) was measured.

【0040】[0040]

【発明の効果】本発明の製法によれば、木質材に、熱に
対して高い安定性を示すベンツイミダゾ−ル系化合物
と、WPC用樹脂と、必要に応じて、低収縮剤を添加し
た処理剤を注入し、加熱処理することによって、こうじ
かび、黒かび、青かびなどのかびの繁殖を抑制すること
ができ、しかも、表面硬度、耐傷性などの表面物性の向
上をはかることができる。
According to the production method of the present invention, a benzimidazole-based compound exhibiting high stability to heat, a resin for WPC, and, if necessary, a low-shrinking agent are added to a wood material. By injecting a treatment agent and heat-treating, it is possible to suppress the growth of mold such as mildew, black mold, and blue mold, and to improve surface physical properties such as surface hardness and scratch resistance.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 WPC用樹脂からなる樹脂液の固形分1
00重量部に対して、低収縮化剤を10〜30重量部
と、防かび剤を0.5〜1.0重量部添加した処理剤
を、木質材に注入し、しかる後、加熱処理することを特
徴とする防かび性木質材の製法。
1. A solid content 1 of a resin liquid comprising a WPC resin.
A treating agent containing 10 to 30 parts by weight of a shrinkage reducing agent and 0.5 to 1.0 parts by weight of an antifungal agent is added to 00 parts by weight of wood and then heat-treated. A method for producing an antifungal wood material characterized by the following.
【請求項2】 防かび剤がベンツイミダゾ−ル系化合物
であることを特徴とする請求項1記載の防かび性木質材
の製法。
2. The method for producing an antifungal wood material according to claim 1, wherein the antifungal agent is a benzimidazole compound.
【請求項3】 加熱処理が加圧操作を伴うものであるこ
とを特徴とする請求項1、又は2記載の防かび性木質材
の製法。
3. The method for producing a fungicidal wood material according to claim 1, wherein the heat treatment is accompanied by pressurizing operation.
JP32114592A 1992-11-04 1992-11-04 Manufacture of fungiproof wooden material Pending JPH06143205A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32114592A JPH06143205A (en) 1992-11-04 1992-11-04 Manufacture of fungiproof wooden material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32114592A JPH06143205A (en) 1992-11-04 1992-11-04 Manufacture of fungiproof wooden material

Publications (1)

Publication Number Publication Date
JPH06143205A true JPH06143205A (en) 1994-05-24

Family

ID=18129309

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32114592A Pending JPH06143205A (en) 1992-11-04 1992-11-04 Manufacture of fungiproof wooden material

Country Status (1)

Country Link
JP (1) JPH06143205A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09169011A (en) * 1995-12-19 1997-06-30 Tomiyasu Honda Decorative panel
JPH09174514A (en) * 1995-12-27 1997-07-08 Jiyuuken Sangyo:Kk Surface reinforcing method of wood
WO1997047399A1 (en) * 1995-04-12 1997-12-18 Nippon Eisei Center Co., Ltd. Method of creating a barrier to wood materials and wooden structures from attack by humidity, fungi and insects
EP1048422A3 (en) * 1999-04-19 2001-12-05 Rohm And Haas Company Compositions for the treatment of wood
WO2008132060A1 (en) * 2007-04-27 2008-11-06 Lanxess Deutschland Gmbh Active ingredient formulations containing 2-thiazole-4yl-1h-benzoimidazol (thiabendazole or tbz) for the production of wpc
CN107471363A (en) * 2017-09-19 2017-12-15 阜南县金威工艺品有限公司 A kind of method for lifting timber wire-drawing effect

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997047399A1 (en) * 1995-04-12 1997-12-18 Nippon Eisei Center Co., Ltd. Method of creating a barrier to wood materials and wooden structures from attack by humidity, fungi and insects
JPH09169011A (en) * 1995-12-19 1997-06-30 Tomiyasu Honda Decorative panel
JPH09174514A (en) * 1995-12-27 1997-07-08 Jiyuuken Sangyo:Kk Surface reinforcing method of wood
EP1048422A3 (en) * 1999-04-19 2001-12-05 Rohm And Haas Company Compositions for the treatment of wood
WO2008132060A1 (en) * 2007-04-27 2008-11-06 Lanxess Deutschland Gmbh Active ingredient formulations containing 2-thiazole-4yl-1h-benzoimidazol (thiabendazole or tbz) for the production of wpc
AU2008244387B2 (en) * 2007-04-27 2011-09-29 Lanxess Deutschland Gmbh Active ingredient formulations containing 2-thiazole-4yl-1H-benzoimidazol (thiabendazole or TBZ) for the production of WPC
CN107471363A (en) * 2017-09-19 2017-12-15 阜南县金威工艺品有限公司 A kind of method for lifting timber wire-drawing effect

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