JPH06247815A - Boric acid composition and wood-preserving agent - Google Patents

Boric acid composition and wood-preserving agent

Info

Publication number
JPH06247815A
JPH06247815A JP5031756A JP3175693A JPH06247815A JP H06247815 A JPH06247815 A JP H06247815A JP 5031756 A JP5031756 A JP 5031756A JP 3175693 A JP3175693 A JP 3175693A JP H06247815 A JPH06247815 A JP H06247815A
Authority
JP
Japan
Prior art keywords
boric acid
wood
weight
chitosan
acid composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP5031756A
Other languages
Japanese (ja)
Other versions
JPH0764883B2 (en
Inventor
Tomonori Kobayashi
智紀 小林
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.)
TOYO MOKUZAI BOUFU KK
Original Assignee
TOYO MOKUZAI BOUFU KK
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 TOYO MOKUZAI BOUFU KK filed Critical TOYO MOKUZAI BOUFU KK
Priority to JP5031756A priority Critical patent/JPH0764883B2/en
Publication of JPH06247815A publication Critical patent/JPH06247815A/en
Publication of JPH0764883B2 publication Critical patent/JPH0764883B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To maintain the potencies of boric acid, such as antimicrobial force, an insecticidal force and a flame-resistant effect over a long period on the surface of wood treated therewith. CONSTITUTION:A boric acid composition is prepared from a boric acid-chitosan complex and used as a wood-preserving agent. The boric acid is stabilized by the adhesive property of the chitosan to wood, and can be adhered to the wood.

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、ほう酸組成物、及びこ
のほう酸組成物を主成分とする木材保存剤に関するもの
である。
TECHNICAL FIELD The present invention relates to a boric acid composition and a wood preservative containing the boric acid composition as a main component.

【0002】[0002]

【従来の技術】ほう酸は強い殺菌力や殺虫力を有してお
り、従来より合板等に発生するヒラタキクイムシの予防
・駆除や、木材に発生するシロアリ駆除等のために使用
されている。またほう酸は高い難燃効果を有するために
木材用難燃剤としても広く使用されている。そしてほう
酸による木材の処理は、ほう酸を水等に溶解してスプレ
ーするかあるいは注入するなどしておこなわれるのが一
般的である。
BACKGROUND OF THE INVENTION Boric acid has a strong bactericidal activity and insecticidal activity, and has been conventionally used for the prevention and control of flat beetles that occur on plywood and the like, and the control of termites that occur on wood. Boric acid is also widely used as a flame retardant for wood because it has a high flame retardant effect. The treatment of wood with boric acid is generally carried out by dissolving boric acid in water or the like and spraying or injecting it.

【0003】[0003]

【発明が解決しようとする課題】しかしほう酸は水溶性
のために、木材に処理しても使用場所によっては水によ
って溶出してしまい、特に住宅の屋外面、屋外建造物、
屋外遊具等など雨水等の作用を受け易い場所では、ほう
酸による効力を長期に亘って保持することができないと
いう問題があった。
However, since boric acid is water-soluble, even if it is treated on wood, it will be eluted by water depending on the place of use, especially on the outdoor surface of houses, outdoor structures,
There has been a problem that the effect of boric acid cannot be maintained for a long period of time in a place such as an outdoor playground that is easily affected by rainwater.

【0004】本発明は上記の点に鑑みてなされたもので
あり、ほう酸の持つ殺菌力や殺虫力、難燃効果などの効
力を長期に亘って処理木材の表面で保持させることがで
きるほう酸組成物及び木材保存剤を提供することを目的
とするものである。
The present invention has been made in view of the above points, and boric acid composition capable of retaining the sterilizing power, insecticidal power, flame retardant effect and the like of boric acid on the surface of treated wood for a long period of time. The object is to provide a product and a wood preservative.

【0005】[0005]

【課題を解決するための手段】本発明に係るほう酸組成
物は、ほう酸とキトサンの錯体から成ることを特徴とす
るものである。このほう酸組成物は、ほう酸1重量部に
対してキトサンを0.1〜0.5重量部及び酸を0.5
重量部未満含むものとして調製することができる。
The boric acid composition according to the present invention is characterized by comprising a complex of boric acid and chitosan. This boric acid composition contains 0.1 to 0.5 parts by weight of chitosan and 0.5 parts by weight of acid per 1 part by weight of boric acid.
It can be prepared as containing less than parts by weight.

【0006】また本発明に係るほう酸組成物は、ほう酸
とキトサンの錯体及び多価アルコールから成ることを特
徴とするものである。このほう酸組成物は、ほう酸1重
量部に対してキトサンを0.1〜0.5重量部及び酸を
0.5重量部未満、多価アルコールを1〜1.5重量部
含むものとして調製することができる。
The boric acid composition according to the present invention is characterized in that it comprises a complex of boric acid and chitosan and a polyhydric alcohol. This boric acid composition is prepared as 0.1 to 0.5 parts by weight of chitosan, less than 0.5 parts by weight of acid, and 1 to 1.5 parts by weight of polyhydric alcohol per 1 part by weight of boric acid. be able to.

【0007】また多価アルコールとしては、分子内にア
ミノ酸を有する多価アルコールを用いることができる。
さらに本発明に係る木材保存剤は、これらのほう酸組成
物から成ることを特徴とするものである。以下、本発明
を詳細に説明する。
As the polyhydric alcohol, a polyhydric alcohol having an amino acid in the molecule can be used.
Furthermore, the wood preservative according to the present invention is characterized by comprising these boric acid compositions. Hereinafter, the present invention will be described in detail.

【0008】キトサンは、カニやエビ等の甲殻類や昆虫
類などの外殻に豊富に含有される多糖類の一種であるキ
チンを脱アセチル化することによって得られるものであ
り、その化学構造の骨格は木材の繊維成分であるセルロ
ースに非常に類似した天然高分子物質である。このキト
サンは一部の菌類に対して抗菌効果があることから食品
や化粧品類の保存剤として使用されている。またキトサ
ンは上記のようにセルロースに非常に類似した化学骨格
構造を有するために繊維類との固着性に優れており、こ
の性質を利用して抗菌繊維の製造に使用されたり、繊維
柔軟剤に応用されたりしている。本発明においてキトサ
ンとしては脱アセチル化率が50〜90%程度のものが
好ましく、また分子量は500以上であれば特に制限さ
れることなく使用することができるが、できれば分子量
50000以下の低分子のものが望ましく、特に分子量
20000以下のものがさらに好ましい。
[0008] Chitosan is obtained by deacetylating chitin, which is one of the polysaccharides abundantly contained in the shells of crustaceans such as crabs and shrimps and the shells of insects, and has a chemical structure of The skeleton is a natural polymeric material very similar to cellulose, which is a fiber component of wood. This chitosan is used as a preservative for foods and cosmetics because it has an antibacterial effect against some fungi. Further, chitosan has a chemical skeleton structure very similar to that of cellulose as described above, and therefore has excellent adhesiveness to fibers, and this property is used for the production of antibacterial fibers or as a fabric softener. It has been applied. In the present invention, chitosan having a deacetylation rate of about 50 to 90% is preferable, and if the molecular weight is 500 or more, it can be used without particular limitation, but if possible, it is preferably a low molecular weight compound having a molecular weight of 50,000 or less. Those having a molecular weight of 20,000 or less are more preferable.

【0009】そして本発明は、このキトサンにほう酸を
反応させ、ほう酸とキトサンの錯体としてほう酸組成物
を調製したものである。このようにほう酸をキトサンの
錯体にすることによって、木材へのキトサンの高い固着
性から、木材にほう酸を安定して固着させることができ
るものである。このほう酸とキトサンの錯体から成るほ
う酸組成物は、ほう酸1重量部に対してキトサンを0.
1〜0.5重量部、及び酸を0.5重量部未満含むもの
として調製することができる。キトサンは水に溶けない
が、酸の存在で塩をつくって水に溶解し、このように水
に溶解させた状態でキトサンとほう酸とは容易に反応し
て錯体を形成する。従ってほう酸とキトサンの錯体から
成るほう酸組成物を調製するにあたっては酸を用いるこ
とが好ましいのである。しかし場合によっては酸は必ず
しも使用する必要はなく、酸を使用しない場合もある。
この酸としては、酢酸、蟻酸、乳酸、クエン酸、アジピ
ン酸、酒石酸、シュウ酸等の有機酸や、塩酸等の無機酸
を用いることができる。有機酸はほぼ例外なく使用する
ことができ、無機酸も大部分のものは使用することがで
きるが、硫酸は使用することができない。
In the present invention, boric acid is reacted with this chitosan to prepare a boric acid composition as a complex of boric acid and chitosan. By using boric acid as a chitosan complex in this way, boric acid can be stably fixed to wood because of the high adhesion of chitosan to wood. This boric acid composition comprising a complex of boric acid and chitosan has a chitosan content of 0.1 parts by weight per 1 part by weight of boric acid.
It can be prepared as containing 1 to 0.5 parts by weight and less than 0.5 parts by weight of acid. Although chitosan is not soluble in water, it forms a salt in the presence of an acid and dissolves in water, and in such a state of being dissolved in water, chitosan easily reacts with boric acid to form a complex. Therefore, it is preferable to use an acid when preparing a boric acid composition comprising a complex of boric acid and chitosan. However, depending on the case, it is not always necessary to use the acid, and there is a case where the acid is not used.
As this acid, organic acids such as acetic acid, formic acid, lactic acid, citric acid, adipic acid, tartaric acid, oxalic acid, and inorganic acids such as hydrochloric acid can be used. Almost all organic acids can be used, and most inorganic acids can be used, but sulfuric acid cannot be used.

【0010】また本発明では、ほう酸とキトサンの錯体
及び多価アルコールから成るほう酸組成物として調製す
ることもできる。多価アルコールを配合することによっ
てほう酸の溶解性を高め、ほう酸組成物を安定化するこ
とができるものである。多価アルコールとしては特に限
定されないものあり、例えばエチレングリコール、ジエ
チレングリコール、ポリエチレングリコール、ポリエチ
レングリコールメタクリレート、プロピレングリコー
ル、グリセリン等を挙げることができるが、特にポリエ
チレングリコールは木材の寸法安定化作用に優れている
ために望ましい。ポリエチレングリコールを用いる場
合、その分子量は400以上のものが望ましく、作業性
よりして特に分子量400〜2000のものがより好ま
しい。
Further, in the present invention, a boric acid composition composed of a complex of boric acid and chitosan and a polyhydric alcohol can be prepared. By adding a polyhydric alcohol, the solubility of boric acid can be increased and the boric acid composition can be stabilized. The polyhydric alcohol is not particularly limited, and examples thereof include ethylene glycol, diethylene glycol, polyethylene glycol, polyethylene glycol methacrylate, propylene glycol, and glycerin. Among them, polyethylene glycol is particularly excellent in the dimensional stabilizing action of wood. Desirable for. When polyethylene glycol is used, its molecular weight is preferably 400 or more, more preferably 400 to 2000 in terms of workability.

【0011】このほう酸とキトサンの錯体及び多価アル
コールから成るほう酸組成物は、ほう酸1重量部に対し
てキトサンを0.1〜0.5重量部、酸を0.5重量部
未満、多価アルコールを1〜1.5重量部含むものとし
て調製することができる。多価アルコールとしてはポリ
エチレングリコールなど上記したものを使用することが
できるが、本発明では分子内にアミノ基を有する多価ア
ルコールを用いることがより好ましい。アミノ基を有す
る多価アルコールとしては、例えばトリエタノールアミ
ンを使用することができる。このように分子内にアミノ
基を有する多価アルコールを用いると、ほう酸と、キト
サンと、分子内にアミノ基を有する多価アルコールの三
者が反応し、水を媒体として錯体を形成するために、水
溶性でしかも安定した粘性液体としてほう酸組成物を調
製することができるものである。ほう酸に対するキトサ
ンや酸、分子内にアミノ基を有する多価アルコールの配
合量は上記と同じであるが、ほう酸1重量部に対してキ
トサン0.2〜0.3重量部、有機酸0.2〜0.3重
量部、分子内にアミノ基を有する多価アルコール1.1
〜1.2重量部の配合がより好ましい。またほう酸とキ
トサンが反応する初期に水が必要であるために、ほう酸
1重量部に対して水3〜5重量部を配合するのが好まし
い。
This boric acid composition comprising a complex of boric acid and chitosan and a polyhydric alcohol comprises 0.1 to 0.5 parts by weight of chitosan, less than 0.5 parts by weight of acid, and polyhydric alcohol per 1 part by weight of boric acid. It can be prepared as containing 1 to 1.5 parts by weight of alcohol. As the polyhydric alcohol, those described above such as polyethylene glycol can be used, but in the present invention, it is more preferable to use a polyhydric alcohol having an amino group in the molecule. As the polyhydric alcohol having an amino group, for example, triethanolamine can be used. When a polyhydric alcohol having an amino group in the molecule is thus used, boric acid, chitosan, and a polyhydric alcohol having an amino group in the molecule react with each other to form a complex with water as a medium. The boric acid composition can be prepared as a water-soluble and stable viscous liquid. The amount of chitosan or acid with respect to boric acid and the polyhydric alcohol having an amino group in the molecule is the same as above, but 0.2 to 0.3 parts by weight of chitosan and 0.2 parts by weight of organic acid per 1 part by weight of boric acid. ~ 0.3 parts by weight, polyhydric alcohol having an amino group in the molecule 1.1
It is more preferable that the amount is 1.2 parts by weight. Further, since water is required at the initial stage of the reaction between boric acid and chitosan, it is preferable to add 3 to 5 parts by weight of water to 1 part by weight of boric acid.

【0012】本発明に係るほう酸組成物は、例えば次の
ような方法で容易に製造することができる。もちろん、
次の方法に限定されるものでないのはいうまでない。ま
ず、キトサンを有機酸の水溶液に添加して60〜80℃
で攪拌しながら完全に溶解させ、次に攪拌しながら徐々
にほう酸を加えて75〜85℃でほぼ溶解させ、最後に
75〜85℃に予め加熱した分子内にアミノ基を有する
多価アルコールを添加して75〜85℃で完全に溶解さ
せることによって、ほう酸組成物を調製することができ
る。
The boric acid composition according to the present invention can be easily produced, for example, by the following method. of course,
It goes without saying that the method is not limited to the following method. First, add chitosan to an aqueous solution of organic acid, and add 60 to 80 ° C.
Completely dissolve it with stirring, and then gradually add boric acid with stirring to dissolve it substantially at 75 to 85 ° C. Finally, add a polyhydric alcohol having an amino group in the molecule preheated to 75 to 85 ° C. The boric acid composition can be prepared by adding and completely dissolving at 75 to 85 ° C.

【0013】上記のようにして調製されるほう酸組成物
は、木材保存剤として使用することができる。本発明に
係るこの木材保存剤は、木材に塗布したり、あるいは加
圧等して注入することによって、ほう酸の作用で、木材
がシロアリ、キクイムシ、ヒラタキクイムシ等から受け
る食害や、木材腐朽菌類から受ける腐朽、黴類から受け
る変色を防止することができると共に、火災等による木
材の燃焼、あるいは水分の吸脱による寸法変化および割
れ等の被害を妨ぐことができるものである。またほう酸
はキトサンと錯体を形成しているために、木材へのキト
サンの高い固着性によってほう酸を安定して木材に固着
させることができるものであり、雨水等の作用によって
ほう酸が木材から洗い流されてしまうこと等を防ぐこと
ができ、ほう酸による木材の保存効果を長期に亘って維
持することができるものである。
The boric acid composition prepared as described above can be used as a wood preservative. This wood preservative according to the present invention is applied to wood, or by injecting under pressure or the like, by the action of boric acid, wood receives damage from termites, bark beetles, flat beetles and the like, and from wood decay fungi. It is possible to prevent the decay and the discoloration caused by the fungi, and also to prevent the damage such as the dimensional change and the crack due to the burning of the wood due to the fire or the absorption and desorption of the moisture. In addition, since boric acid forms a complex with chitosan, boric acid can be stably adhered to wood due to the high adhesion of chitosan to wood, and boric acid is washed away from wood by the action of rainwater. It is possible to prevent the wood from being destroyed, and the preservation effect of wood by boric acid can be maintained for a long time.

【0014】[0014]

【実施例】以下、本発明を実施例によって例証する。 (実施例1)無水酢酸3gに水62.5gを加えて65
℃に加熱し、そこにキトサン(脱アセチル化度87%、
平均分子量約48000)3gを加えて完全に溶解させ
た。次にこれにほう酸15gを加えて75℃に加熱しつ
つ攪拌することによってほぼ溶解させた。最後に、予め
75℃に加熱したトリエタノールアミン16.5gを加
え、完全に溶解させてほう酸組成物を得た。このほう酸
組成物は、粘稠な液体であり、長時間放置しても沈澱等
が生じることはなかった。また任意の割合で水によって
希釈することができるものであった。
EXAMPLES The present invention will now be illustrated by examples. (Example 1) 62.5 g of water was added to 3 g of acetic anhydride to obtain 65
After heating to ℃, chitosan (deacetylation degree 87%,
3 g of average molecular weight of about 48,000) was added and completely dissolved. Next, 15 g of boric acid was added thereto, and the mixture was heated to 75 ° C. and stirred to substantially dissolve it. Finally, 16.5 g of triethanolamine preheated to 75 ° C. was added and completely dissolved to obtain a boric acid composition. The boric acid composition was a viscous liquid and did not cause precipitation or the like even when left for a long time. Further, it could be diluted with water at an arbitrary ratio.

【0015】(実施例2)無水酢酸4gに水62gを加
えて65℃に加熱し、そこにキトサン(脱アセチル化度
87%、平均分子量約48000)4gを加えて完全に
溶解させた。次にこれにほう酸10gを加えて75℃に
加熱しつつ攪拌することによってほぼ溶解させた。最後
に、予め75℃に加熱したポリエチレングリコール20
gを加え、完全に溶解させてほう酸組成物を得た。この
ほう酸組成物は、粘稠な液体であり、長時間放置しても
沈澱等が生じることはなかった。また任意の割合で水に
よって希釈することができるものであった。
(Example 2) 62 g of water was added to 4 g of acetic anhydride and heated to 65 ° C., and 4 g of chitosan (deacetylation degree 87%, average molecular weight about 48,000) was added thereto and completely dissolved. Next, 10 g of boric acid was added thereto, and the mixture was almost dissolved by stirring while heating to 75 ° C. Finally, polyethylene glycol 20 preheated to 75 ° C
g was added and completely dissolved to obtain a boric acid composition. The boric acid composition was a viscous liquid and did not cause precipitation or the like even when left for a long time. Further, it could be diluted with water at an arbitrary ratio.

【0016】(実施例3)無水酢酸4gに水73gを加
えて65℃に加熱し、そこにキトサン(脱アセチル化度
87%、平均分子量約48000)8gを加えて完全に
溶解させた。次にこれにほう酸15gを加えて75℃に
加熱しつつ攪拌することによって完全に溶解させ、ほう
酸組成物を得た。このほう酸組成物は、粘稠な液体であ
り、長時間放置しても沈澱等が生じることはなかった。
また任意の割合で水によって希釈することができるもの
であった。
(Example 3) 73 g of water was added to 4 g of acetic anhydride and heated to 65 ° C., and 8 g of chitosan (deacetylation degree 87%, average molecular weight about 48,000) was added thereto and completely dissolved. Next, 15 g of boric acid was added to this, and the mixture was completely dissolved by stirring while heating at 75 ° C. to obtain a boric acid composition. The boric acid composition was a viscous liquid and did not cause precipitation or the like even when left for a long time.
Further, it could be diluted with water at an arbitrary ratio.

【0017】(実施例4)ポリエチレングリコール(平
均分子量600)50gに水10gを加えて85℃に加
熱し、そこにほう酸を10g加え、さらに直ちにキトサ
ン(脱アセチル化度87%、平均分子量約48000)
3gを加えて90℃で加熱しつつ攪拌することによって
完全に溶解させ、最後に水27gを加えてほう酸組成物
を得た。このほう酸組成物は、粘稠な液体であり、長時
間放置しても沈澱等が生じることはなかった。また任意
の割合で水によって希釈することができるものであっ
た。
Example 4 10 g of water was added to 50 g of polyethylene glycol (average molecular weight 600) and heated to 85 ° C., 10 g of boric acid was added thereto, and immediately chitosan (deacetylation degree 87%, average molecular weight about 48,000). )
3 g was added and completely dissolved by stirring while heating at 90 ° C. Finally, 27 g of water was added to obtain a boric acid composition. The boric acid composition was a viscous liquid and did not cause precipitation or the like even when left for a long time. Further, it could be diluted with water at an arbitrary ratio.

【0018】(耐候試験)実施例1で得られたほう酸組
成物を水で希釈してほう酸の濃度が0.2重量%、0.
4重量%、0.6重量%、1.0重量%の木材保存剤を
調製した。この木材保存剤を2cm×2cm×1cmの
寸法に作成したスギ辺材に減圧注入して試験材を作成し
た。各試験材の注入量を表1のほう酸吸収量の欄に示
す。この試験材を常温の水(水量は試験材総容量の10
倍量)中に8時間浸漬して攪拌することによって溶脱処
理したのち、40℃のオーブン中に16時間入れて揮散
処理をする操作をおこない(この溶脱処理と揮散処理の
操作を耐候操作という)、この耐候操作を10回繰り返
しておこなって各試験材中のほう酸の残存量を測定し
た。ほう酸の残存量の測定は各操作回数毎におこない、
結果を表1に示す。
(Weather resistance test) The boric acid composition obtained in Example 1 was diluted with water so that the concentration of boric acid was 0.2% by weight,
4 wt%, 0.6 wt%, 1.0 wt% wood preservatives were prepared. This wood preservative was injected under reduced pressure into cedar sapwood prepared to have dimensions of 2 cm × 2 cm × 1 cm to prepare test materials. The injection amount of each test material is shown in the column of boric acid absorption amount in Table 1. This test material is cooled to room temperature with water (the amount of water is 10% of the total volume of the test material).
After leaching treatment by immersing in (double volume) for 8 hours and stirring, put into an oven at 40 ° C for 16 hours to perform volatilization treatment (this leaching treatment and volatilization treatment operation is called weatherproof operation) The weathering operation was repeated 10 times to measure the residual amount of boric acid in each test material. The remaining amount of boric acid is measured for each number of operations,
The results are shown in Table 1.

【0019】また比較のために、ほう酸を水で希釈して
濃度が0.4重量%、0.6重量%の木材保存剤(比較
例1)を調製し、同様にしてスギ辺材に減圧注入して試
験材を作成すると共に、耐候操作をおこなってほう酸の
残存量を測定した。結果を表1に示す。
For comparison, a wood preservative having a concentration of 0.4% by weight and 0.6% by weight (Comparative Example 1) was prepared by diluting boric acid with water, and similarly depressurized to cedar sapwood. A test material was prepared by injection, and weathering operation was performed to measure the residual amount of boric acid. The results are shown in Table 1.

【0020】[0020]

【表1】 [Table 1]

【0021】表1にみられるように、ほう酸を水に溶解
して木材保存剤として使用した比較例1のものでは、ほ
う酸の溶脱は著しく発生するが、ほう酸のキトサン錯体
で調製した木材保存剤を使用した実施例1のものでは、
ほう酸の溶脱がかなり抑制されていることが確認され
る。 (防腐効力試験)上記(耐候試験)で作成した実施例1
及び比較例1の試験材を用い、各試験材にオオウズラタ
ケ(褐色腐朽菌:TYP)及びカワラタケ(白色腐朽
菌:COV)を植え、防腐効力を試験した。試験は上記
「耐候試験」における耐候操作をおこなわない試験材
と、耐候操作を10回おこなった試験材についてそれぞ
れ実施した。防腐効力の試験はJIS A 9102に
基づいておこない、試験材の重量減少率を測定した。ま
た比較のために、ほう酸による処理をおこなわない試験
材についてもおこない、同様にして重量減少率を測定し
た。これらの結果を表2に示す。
As shown in Table 1, in Comparative Example 1 in which boric acid was dissolved in water and used as a wood preservative, leaching of boric acid occurred remarkably, but a wood preservative prepared with a chitosan complex of boric acid. In Example 1 using
It is confirmed that the leaching of boric acid is considerably suppressed. (Preservative efficacy test) Example 1 prepared in the above (weather resistance test)
Also, using the test material of Comparative Example 1, the test materials were planted with Pleurotus ostreatus (brown rot fungus: TYP) and Kawaratake (white rot fungus: COV) to test the antiseptic effect. The test was carried out on each of the test materials that were not subjected to the weather resistance operation in the above “weather resistance test” and the test materials that were subjected to the weather resistance operation 10 times. The test of antiseptic effect was conducted based on JIS A 9102, and the weight reduction rate of the test material was measured. For comparison, a test material not treated with boric acid was also tested, and the weight reduction rate was measured in the same manner. The results are shown in Table 2.

【0022】[0022]

【表2】 [Table 2]

【0023】表2にみられるように、比較例1のもので
は耐候操作をしない試験材に比べて耐候操作をした試験
材の重量減少率が大きく高まっており、ほう酸の溶脱で
防腐効力は著しく低下しているが、実施例1のものでは
耐候操作をしない試験材と耐候操作をした試験材の間で
の重量減少率に有意な差がみられず、ほう酸の溶脱が抑
制されて防腐効力が保持されていることが確認される。
As can be seen from Table 2, in Comparative Example 1, the weight loss rate of the test material subjected to the weathering operation is significantly higher than that of the test material not subjected to the weathering operation, and the antiseptic effect is remarkable due to the leaching of boric acid. However, in Example 1, there is no significant difference in the weight reduction rate between the test material that is not weather-proofed and the test material that is weather-proofed, and the leaching of boric acid is suppressed, and the antiseptic effect is suppressed. Is confirmed to be held.

【0024】(寸法安定試験)実施例2で得たほう酸組
成物を水で希釈してほう酸の濃度が0.4重量%、0.
6重量%の木材保存剤を調製した。この木材保存剤を5
cm×5cm×20cmの寸法に作成した含水率50%
のスギ辺材に減圧注入して、ほう酸吸収量が2.9kg
/m3 、4.2kg/m3 の試験材を作成した。この各
試験材及び処理をおこなわない試験材を風通しの良い屋
外に放置したところ、木材保存剤を注入した試験材は未
処理の試験材に比べて木口の割れ発生が極めて少ないも
のであった。
(Dimensional stability test) The boric acid composition obtained in Example 2 was diluted with water so that the concentration of boric acid was 0.4% by weight,
A 6% by weight wood preservative was prepared. 5 of this wood preservative
50% water content created in dimensions of cm x 5 cm x 20 cm
Injected under reduced pressure into Japanese cedar sapwood, boric acid absorption is 2.9kg
/ M 3, to prepare a test material of 4.2kg / m 3. When each of the test materials and the test material not subjected to the treatment were left outdoors with good ventilation, the test material into which the wood preservative was injected had very few cracks in the wood mouth as compared with the untreated test material.

【0025】(防蟻効力試験)実施例1で得たほう酸組
成物を水で希釈してほう酸の濃度が0.4重量%、0.
6重量%の木材保存剤を調製し、この木材保存剤を1c
m×1cm×2cmの寸法に作成したアカマツ辺材に減
圧注入して試験材を作成した。また比較のために、ほう
酸を水で希釈して濃度が0.4重量%、0.6重量%の
木材保存剤(比較例1)を調製し、同様にしてスギ辺材
に減圧注入して試験材を作成した。そして上記「耐候試
験」における耐候操作をおこなわない試験材と、耐候操
作を10回おこなった試験材をそれぞれ用い、これを底
部に歯科用石膏を5mmの厚みに敷詰めた直径10cm
×高さ5cmの円筒の中央に設置し、イエシロアリの職
蟻150頭、兵蟻15頭を投入後、湿潤脱脂綿の上に置
いて(社)日本木材保存協会規格第11号(1)に基づ
いて食害試験をおこない、試験材の重量減少率を測定し
た。また比較のために、ほう酸による処理をおこなわな
い試験材についてもおこない、同様にして重量減少率を
測定した。これらの結果を表3に示す。
(Termite control test) The boric acid composition obtained in Example 1 was diluted with water so that the concentration of boric acid was 0.4% by weight,
Prepare 6% by weight of wood preservative and add 1 c of this wood preservative
A test material was prepared by injecting under reduced pressure into Japanese red pine sapwood prepared to have dimensions of m × 1 cm × 2 cm. For comparison, a wood preservative having a concentration of 0.4% by weight and 0.6% by weight (comparative example 1) was prepared by diluting boric acid with water, and was similarly vacuum-injected into cedar sapwood. A test material was created. A test material not subjected to the weather resistance operation in the above-mentioned "weather resistance test" and a test material subjected to the weather resistance operation 10 times were used, and a dental plaster having a thickness of 5 mm and a diameter of 10 cm.
× Installed in the center of a cylinder with a height of 5 cm, after inserting 150 termite termite workers and 15 soldier ants, place them on wet absorbent cotton (Company) based on Japan Wood Preservation Association Standard No. 11 (1) A feeding damage test was performed to measure the weight loss rate of the test material. For comparison, a test material not treated with boric acid was also tested, and the weight reduction rate was measured in the same manner. The results are shown in Table 3.

【0026】[0026]

【表3】 [Table 3]

【0027】表3にみられるように、比較例1のもので
は耐候操作をしない試験材に比べて耐候操作をした試験
材の重量減少率が大きく高まっており、ほう酸の溶脱で
防蟻効力は著しく低下しているが、実施例1のものでは
耐候操作をしない試験材と耐候操作をした試験材の間で
の重量減少率に有意な差がみられず、ほう酸の溶脱が抑
制されて防蟻効力が保持されていることが確認される。
As can be seen from Table 3, in Comparative Example 1, the weight reduction rate of the test material subjected to the weathering operation was significantly higher than that of the test material not subjected to the weathering operation, and the termite-proof effect was obtained by the leaching of boric acid. Although it is remarkably reduced, in Example 1, there is no significant difference in the weight reduction rate between the test material which is not weather-proofed and the test material which is weather-proofed, and the leaching of boric acid is suppressed, and It is confirmed that the ant effect is maintained.

【0028】(野外防蟻・防腐効力試験)実施例3及び
実施例4で得たほう酸組成物を水で希釈してほう酸濃度
が0.1重量%、0.2重量%、0.4重量%、0.6
重量%の木材保存剤を調製した。この木材保存剤を3c
m×3cm×35cmの先端を尖らせたアカマツ辺材杭
に加圧注入して、ほう酸吸収量が0.7kg/m2
0.8kg/m2 、1.1kg/m2 、2.4kg/m
2 、2.6kg/m2 、3.4kg/m2 、3.7kg
/m2 の試験材を作製した。この各試験材及び処理をお
こなわない試験材を鹿児島県日置郡吹上町吹上浜のクロ
マツ林内のイエシロアリ営巣周辺に30cmの深さまで
埋設して野外試験をおこなった。また比較のために、ほ
う酸を水で希釈して濃度が0.1重量%、0.2重量
%、0.6重量%の木材保存剤(比較例2)を調製し、
同様にアカマツ辺材に加圧注入して試験材を作成すると
共に、同様に野外試験をおこなった。野外試験の評価結
果を表4の「被害状況」の欄に示す。被害状況の評価
は、5本の試験材に次のように点数を与えてその平均値
を出すことによっておこなった。 0点:試験材表面に食痕や腐朽がない。 1点:試験材表面に軽い食痕あるいは腐朽がある。 2点:試験材表面に明らかな食害あるいは腐朽がある。 3点:試験材表面の食害あるいは腐朽が内部まで進行し
ている。 4点:試験材全体が食害あるいは腐朽を受けている。 5点:試験材が食害あるいは腐朽によって破壊されてい
る。
(Field ant / preservative efficacy test) The boric acid compositions obtained in Examples 3 and 4 were diluted with water to give boric acid concentrations of 0.1% by weight, 0.2% by weight and 0.4% by weight. %, 0.6
A wt% wood preservative was prepared. 3c of this wood preservative
It was injected under pressure into a red pine sapwood pile with a sharp tip measuring mx 3 cm x 35 cm, and the amount of boric acid absorbed was 0.7 kg / m 2 ,
0.8 kg / m 2 , 1.1 kg / m 2 , 2.4 kg / m
2 , 2.6 kg / m 2 , 3.4 kg / m 2 , 3.7 kg
A test material of / m 2 was prepared. Field tests were conducted by burying each of the test materials and the test material not subjected to the treatment up to a depth of 30 cm around the nesting of the termite nests in the black pine forest at Fukiagehama, Fukiage-cho, Hioki-gun, Kagoshima Prefecture. For comparison, boric acid was diluted with water to prepare wood preservatives (Comparative Example 2) having concentrations of 0.1% by weight, 0.2% by weight, and 0.6% by weight,
Similarly, a test material was prepared by injecting pressure into Japanese pine sapwood, and a field test was conducted in the same manner. The evaluation results of the field test are shown in the "damage situation" column of Table 4. The damage condition was evaluated by giving scores to the five test materials as follows and calculating the average value. 0 points: No scratches or decay on the surface of the test material. 1 point: There is a slight dent or decay on the surface of the test material. 2 points: There is obvious food damage or decay on the surface of the test material. 3 points: Eating damage or decay on the surface of the test material has progressed to the inside. 4 points: The entire test material is damaged by food or decay. 5 points: The test material is destroyed by food damage or decay.

【0029】[0029]

【表4】 [Table 4]

【0030】表4にみられるように、比較例2のものは
1年目さらに2年目と被害が大きくなっており、ほう酸
の溶脱で防蟻・防腐効力は著しく低下しているが、実施
例3及び実施例4のものではほう酸の溶脱が抑制されて
防蟻・防腐効力が保持されていることが確認される。
As shown in Table 4, the damage of Comparative Example 2 was large in the first year and then in the second year, and the ant-preservation and antiseptic effects were remarkably lowered by the leaching of boric acid. In Examples 3 and 4, it is confirmed that the leaching of boric acid is suppressed and the ant / preservative efficacy is maintained.

【0031】[0031]

【発明の効果】上記のように、ほう酸のキトサン錯体か
らなるほう酸組成物の木材保存剤は、ほう酸の作用で害
虫による食害や、木材腐朽菌類による腐朽、黴類による
変色等を防止することができると共に木材の燃焼や水分
の吸脱による寸法変化の被害を妨ぐことができるもので
あり、しかも木材へのキトサンの高い固着性によってほ
う酸を安定して木材に固着させることができ、ほう酸に
よるこれら木材の保存効果を長期に亘って維持すること
ができるものである。
As described above, the wood preservative of the boric acid composition comprising the chitosan complex of boric acid can prevent feeding damage by pests due to the action of boric acid, decay by wood-destroying fungi, discoloration by fungi, etc. It is possible to prevent damage of dimensional change due to burning of wood and absorption and desorption of water, and moreover, due to the high sticking property of chitosan to wood, boric acid can be stably stuck to wood. The preservation effect of these woods can be maintained for a long period of time.

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 ほう酸とキトサンの錯体から成ることを
特徴とするほう酸組成物。
1. A boric acid composition comprising a complex of boric acid and chitosan.
【請求項2】 ほう酸1重量部に対してキトサンを0.
1〜0.5重量部、及び酸を0.5重量部未満含むこと
を特徴とする請求項1に記載のほう酸組成物。
2. Chitosan is added to 1 part by weight of boric acid.
The boric acid composition according to claim 1, which comprises 1 to 0.5 parts by weight and less than 0.5 parts by weight of the acid.
【請求項3】 ほう酸とキトサンの錯体及び多価アルコ
ールから成ることを特徴とするほう酸組成物。
3. A boric acid composition comprising a complex of boric acid and chitosan and a polyhydric alcohol.
【請求項4】 ほう酸1重量部に対してキトサンを0.
1〜0.5重量部、及び酸を0.5重量部未満、多価ア
ルコールを1〜1.5重量部含むことを特徴とする請求
項3に記載のほう酸組成物。
4. Chitosan is added to 1 part by weight of boric acid.
The boric acid composition according to claim 3, comprising 1 to 0.5 parts by weight, less than 0.5 parts by weight of the acid, and 1 to 1.5 parts by weight of the polyhydric alcohol.
【請求項5】 多価アルコールとして分子内にアミノ酸
を有する多価アルコールを用いることを特徴とする請求
項3又は4に記載のほう酸組成物。
5. The boric acid composition according to claim 3, wherein a polyhydric alcohol having an amino acid in the molecule is used as the polyhydric alcohol.
【請求項6】 請求項1乃至5のいずれかに記載のほう
酸組成物から成る木材保存剤。
6. A wood preservative comprising the boric acid composition according to claim 1.
JP5031756A 1993-02-22 1993-02-22 Boric acid compound, boric acid composition, production method thereof, and wood preservative Expired - Lifetime JPH0764883B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5031756A JPH0764883B2 (en) 1993-02-22 1993-02-22 Boric acid compound, boric acid composition, production method thereof, and wood preservative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5031756A JPH0764883B2 (en) 1993-02-22 1993-02-22 Boric acid compound, boric acid composition, production method thereof, and wood preservative

Publications (2)

Publication Number Publication Date
JPH06247815A true JPH06247815A (en) 1994-09-06
JPH0764883B2 JPH0764883B2 (en) 1995-07-12

Family

ID=12339872

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5031756A Expired - Lifetime JPH0764883B2 (en) 1993-02-22 1993-02-22 Boric acid compound, boric acid composition, production method thereof, and wood preservative

Country Status (1)

Country Link
JP (1) JPH0764883B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11217310A (en) * 1997-11-25 1999-08-10 Takeda Chem Ind Ltd Preservative for timber
US6669903B2 (en) 2000-11-13 2003-12-30 Michio Hayashi Bactericidal or bacteriostatic method
US8747539B2 (en) 2009-02-20 2014-06-10 Uniboard Canada Inc. Chitosan-based adhesives and uses thereof
US9693563B2 (en) 2013-08-20 2017-07-04 3M Innovative Properties Company Boron-silane polyether complex
CN111136747A (en) * 2020-01-20 2020-05-12 河北大学 Bio-based flame-retardant reed woven product and preparation method thereof

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11217310A (en) * 1997-11-25 1999-08-10 Takeda Chem Ind Ltd Preservative for timber
US6669903B2 (en) 2000-11-13 2003-12-30 Michio Hayashi Bactericidal or bacteriostatic method
US8747539B2 (en) 2009-02-20 2014-06-10 Uniboard Canada Inc. Chitosan-based adhesives and uses thereof
US9693563B2 (en) 2013-08-20 2017-07-04 3M Innovative Properties Company Boron-silane polyether complex
CN111136747A (en) * 2020-01-20 2020-05-12 河北大学 Bio-based flame-retardant reed woven product and preparation method thereof
CN111136747B (en) * 2020-01-20 2021-04-20 河北大学 Bio-based flame-retardant reed woven product and preparation method thereof

Also Published As

Publication number Publication date
JPH0764883B2 (en) 1995-07-12

Similar Documents

Publication Publication Date Title
US4622248A (en) Preservative composition for wood
AU2009349905B2 (en) Biocidal composition for wood, method for wood treatment, and wood produced thereby
CN101323121A (en) Modified chitosan metal composite wood preservative and method for producing the same
JP2010005875A (en) Antifungal agent for bamboo or the like and antifungal method
US6319431B1 (en) Preservative and fire retardant composition and combination and process
CA2708180A1 (en) Wood-treating composition and method with monocarboxylic acid and chelating agent dissolved in liquid aqueous vehicle
JP2009522298A (en) Ibuprofen complexes as wood preservatives
JP2009522299A (en) Tropolone complexes as wood preservatives.
JP2009522297A (en) Tungstate and molybdate wood preservatives
EP0175771A1 (en) Preservative composition for wood
JPH06247815A (en) Boric acid composition and wood-preserving agent
US20080131666A1 (en) Penetration improvement of copper amine solutions into dried wood by addition of carbon dioxide
KR102260276B1 (en) Wood preservation composition
JPS58163605A (en) Conserving agent for wood
KR102335785B1 (en) Composition for preserving wood containing natural materials
JPS5925308A (en) Agent for controlling insect and termite for woody material, and method for treating woody material
CN107030821B (en) A kind of preparation method of the special mildew removing agents of alkalescence timber
JPH1017426A (en) Antiseptic, insect-proofing and termite-proofing agent
Husaini et al. Smart polymer composites for wood protection
AU9417198A (en) A preservative and fire retardant composition and combination and process
George Comparative Analysis of Select Sustainable Wood Preservative Systems for Heritage Conservation: A Termite Resistance Laboratory Testing Program on Radiata Pine
US7179327B2 (en) Wood treatment process and chemical composition
JPS6191109A (en) Antiseptic composition
CN107160508A (en) A kind of mildew removing agents for alkaline timber
JPS636521B2 (en)

Legal Events

Date Code Title Description
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 19960109