JPH04278303A - Manufacture of resin treated ligneous material - Google Patents
Manufacture of resin treated ligneous materialInfo
- Publication number
- JPH04278303A JPH04278303A JP6803491A JP6803491A JPH04278303A JP H04278303 A JPH04278303 A JP H04278303A JP 6803491 A JP6803491 A JP 6803491A JP 6803491 A JP6803491 A JP 6803491A JP H04278303 A JPH04278303 A JP H04278303A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- wood
- acid
- ligneous material
- ligneous
- 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
Links
- 239000000463 material Substances 0.000 title claims abstract description 44
- 229920005989 resin Polymers 0.000 title claims abstract description 38
- 239000011347 resin Substances 0.000 title claims abstract description 38
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000005011 phenolic resin Substances 0.000 claims abstract description 42
- 239000002253 acid Substances 0.000 claims abstract description 18
- 229920001568 phenolic resin Polymers 0.000 claims abstract description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 17
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000002023 wood Substances 0.000 claims description 49
- 239000007864 aqueous solution Substances 0.000 claims description 15
- 239000010875 treated wood Substances 0.000 claims description 11
- 238000010438 heat treatment Methods 0.000 claims description 9
- 210000002421 cell wall Anatomy 0.000 abstract description 10
- 238000004040 coloring Methods 0.000 abstract description 4
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 abstract description 3
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 abstract description 3
- 229940092714 benzenesulfonic acid Drugs 0.000 abstract description 3
- 238000002156 mixing Methods 0.000 abstract description 2
- 239000007788 liquid Substances 0.000 description 12
- 238000002347 injection Methods 0.000 description 7
- 239000007924 injection Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000006103 coloring component Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 241000894007 species Species 0.000 description 3
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 230000003834 intracellular effect Effects 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- 239000010876 untreated wood Substances 0.000 description 2
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
- JIRHAGAOHOYLNO-UHFFFAOYSA-N (3-cyclopentyloxy-4-methoxyphenyl)methanol Chemical compound COC1=CC=C(CO)C=C1OC1CCCC1 JIRHAGAOHOYLNO-UHFFFAOYSA-N 0.000 description 1
- 235000007173 Abies balsamea Nutrition 0.000 description 1
- 241000218685 Tsuga Species 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000000051 modifying effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
Landscapes
- Chemical And Physical Treatments For Wood And The Like (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は寸法安定性、耐久性、耐
汚染性、加工性等に優れ、且つ木材本来の外観を呈する
樹脂処理木質材の製造方法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a resin-treated wood material that has excellent dimensional stability, durability, stain resistance, workability, etc., and exhibits the appearance of wood.
【0002】0002
【従来の技術】従来から、木質材の細胞壁内の微細な空
隙にフェノール樹脂液を注入、充填して木質材のもつ欠
点である寸法安定性、強度等の改善を図った、改質した
フェノール樹脂注入処理木質材が知られている。[Prior Art] Modified phenol has traditionally been used to improve dimensional stability, strength, etc., which are the shortcomings of wood, by injecting and filling phenolic resin liquid into the fine voids in the cell walls of wood. Resin injection treated wood materials are known.
【0003】0003
【発明が解決しようとする課題】しかしながら、従来の
フェノール樹脂注入処理木質材の製造方法によれば、フ
ェノール樹脂や木材の発色成分が着色し、又、木材の熱
劣化や注入樹脂の伸縮の相違や木材の収縮によって脆弱
になり、割れや反りが発生すると共に硬化樹脂と木材細
胞壁面との間に隙間が生じ、汚染物質が浸入し易くなる
という問題点を有する。[Problems to be Solved by the Invention] However, according to the conventional method for producing wood materials injected with phenolic resin, the coloring components of the phenol resin and wood become colored, and there is also a difference in thermal deterioration of the wood and expansion and contraction of the injected resin. The problem is that the wood becomes brittle due to shrinkage, cracks and warping occur, and gaps are created between the cured resin and the wood cell wall surface, making it easier for contaminants to enter.
【0004】そのため、種々の触媒によりフェノール樹
脂硬化条件の緩和を図ろうとした場合、木質材に注入す
るフェノール樹脂液が凝集や高粘度化して木質材の微細
な空隙に浸透せず、改質効果が小さかったり、触媒によ
り木質材が汚染されるといった問題点があった。[0004] Therefore, when attempting to relax the curing conditions of phenolic resin using various catalysts, the phenol resin liquid injected into the wood material aggregates and becomes highly viscous, preventing it from penetrating into the fine pores of the wood material, resulting in a reduction in the modification effect. There were problems such as the catalyst was small and the wood material was contaminated by the catalyst.
【0005】本発明はこのような問題点に鑑みてなされ
たもので、フェノール樹脂の注入、硬化に際し殆ど着色
されず、木材本来の外観が維持されると共に脆弱になら
ず、切削性、軽量性、寸法安定性、耐久性、耐汚染性等
の総合的に優れた物性を発揮する樹脂処理木質材の製造
方法を提供するものである。[0005] The present invention was made in view of the above problems, and has a structure in which the phenolic resin is injected and cured with almost no coloration, the original appearance of the wood is maintained, the wood does not become brittle, and it has excellent cutting properties and light weight. The present invention provides a method for producing a resin-treated wood material that exhibits comprehensively excellent physical properties such as dimensional stability, durability, and stain resistance.
【0006】[0006]
【課題を解決するための手段】上記目的を達成するため
に本発明の樹脂処理木質材の製造方法は、トルエンスル
フォン酸、ベンゼンスルフォン酸、ホウ酸、リン酸等の
酸を添加しているとともにpH3〜7に調整した不揮発
分40重量%以下のフェノール樹脂水溶液を木質材に含
浸し、木質材を樹脂硬化可能な温度に加熱して水分を揮
散させると共に樹脂を硬化させることにより、木質材へ
の樹脂液の浸透を容易にしたものである。[Means for Solving the Problems] In order to achieve the above object, the method for producing resin-treated wood materials of the present invention includes adding acids such as toluenesulfonic acid, benzenesulfonic acid, boric acid, and phosphoric acid. By impregnating wood with a phenolic resin aqueous solution with a non-volatile content of 40% by weight or less and adjusting the pH to 3 to 7, and heating the wood to a temperature at which the resin can be cured, the water is evaporated and the resin is cured. This makes it easier for the resin liquid to penetrate.
【0007】[0007]
【作用】フェノール樹脂水溶液を不揮発分40%以下と
し、且つ有機酸を添加してもpH3〜7としているので
、水が樹脂の縮重合反応を抑制して処理液である該フェ
ノール樹脂水溶液の粘度増大を防止し、親水性である木
質材の細胞壁などに処理液が容易に浸入する。又、pH
を3以上にしているので、木質材の酸による汚染も防止
できる。そして、酸を添加したフェノール樹脂水溶液は
、木質材への注入後、加熱されることで水分が揮散する
と共にフェノール樹脂の高粘度化が始まる。さらに、加
熱されることにより樹脂は硬化するが、pH7以下であ
ればフェノール樹脂の濃色化や木材の発色が防止され、
処理木材が着色されることがなく、脆弱化も防げる。[Action] Since the non-volatile content of the phenolic resin aqueous solution is 40% or less, and the pH is kept at 3 to 7 even when an organic acid is added, water suppresses the condensation reaction of the resin and reduces the viscosity of the phenolic resin aqueous solution, which is the treatment liquid. The treatment solution easily penetrates into the cell walls of wood materials, which are hydrophilic. Also, pH
Since it is set to 3 or more, acid contamination of wood materials can also be prevented. After the phenol resin aqueous solution to which an acid has been added is injected into the wood material, it is heated to evaporate water and the phenol resin begins to increase in viscosity. Furthermore, the resin hardens when heated, but if the pH is below 7, darkening of the phenol resin and coloring of the wood will be prevented.
The treated wood will not be colored and will not become brittle.
【0008】[0008]
【実施例】次に、本発明の実施例を詳しく述べると、適
量の水の添加によって不揮発分が1〜40重量%の濃度
に調整されたフェノール樹脂水溶液に、適量の酸を添加
してpH3〜7の注入処理液を作製する。なお、酸とし
ては、トルエンスルフォン酸、ベンゼンスルフォン酸、
フェノールスルフォン酸、キシレンスルフォン酸、シュ
ウ酸、ホウ酸、リン酸等の酸を使用することができ、酸
だけではpH3未満になる場合、ゲル化を防ぐため水酸
化ナトリウム、水酸化カリウムなどのアルカリ金属水酸
化物やジメチルアミンなどのアミン類等を混合してpH
3〜7に調整する。[Example] Next, to describe an example of the present invention in detail, an appropriate amount of acid was added to an aqueous phenol resin solution whose nonvolatile content was adjusted to a concentration of 1 to 40% by weight by adding an appropriate amount of water. 7. Prepare the injection treatment solution. In addition, as acids, toluenesulfonic acid, benzenesulfonic acid,
Acids such as phenol sulfonic acid, xylene sulfonic acid, oxalic acid, boric acid, phosphoric acid, etc. can be used, and if the pH is less than 3 with acids alone, an alkali such as sodium hydroxide, potassium hydroxide, etc. can be used to prevent gelation. Adjust the pH by mixing metal hydroxides and amines such as dimethylamine.
Adjust to 3-7.
【0009】次いで、処理液を木質材中に注入する。こ
の注入方法は、減圧、加圧注入法によって行うが、浸漬
によって行ってもよく、木質材内に合成樹脂水溶液が均
一に注入、含浸するように材の形状や寸法、浸透性、樹
種に適した方法、条件を適宜に選択すればよい。又、注
入処理される木質材としては角材や板材、中空材等の厚
い製材品、集成材、合板、単板のような薄板等のいずれ
であってもよく、その樹種も特に限定されない。[0009] Next, the treatment liquid is injected into the wood material. This injection method is carried out by reduced pressure or pressure injection, but it can also be carried out by immersion, which is suitable for the shape and size of the wood, permeability, and tree species so that the synthetic resin aqueous solution is evenly injected and impregnated into the wood. The method and conditions may be selected as appropriate. Furthermore, the wood material to be injected may be any of thick sawn timber products such as square timber, board timber, and hollow timber, laminated timber, plywood, and thin boards such as veneer, and the species of the wood is not particularly limited.
【0010】このような適宜な注入手段を用いて、木質
材に処理液を注入すると、フェノール樹脂水溶液には多
量の水が存在していると共にpH3〜7に調整している
ので、注入前や注入時には該水によって処理液中の酸と
フェノール樹脂との高粘度化が抑制され、処理液のポッ
トライフを長くすると共に親水性である木質材の細胞壁
中などに処理液が容易に浸入する。なお、pH3未満に
なると樹脂の高粘度化が生じるだけでなく木質材の変色
が生じて好ましくない。又、pH7を越えると処理木質
材の変色や脆弱化が生じて好ましくない。When the treatment solution is injected into wood using such an appropriate injection means, the phenol resin aqueous solution contains a large amount of water and has been adjusted to pH 3 to 7, so it is difficult to At the time of injection, the water suppresses the increase in viscosity of the acid and phenol resin in the treatment liquid, prolonging the pot life of the treatment liquid, and allowing the treatment liquid to easily penetrate into the cell walls of the hydrophilic wood material. In addition, if the pH is less than 3, not only the viscosity of the resin increases, but also discoloration of the wood material occurs, which is not preferable. Moreover, if the pH exceeds 7, the treated wood material may become discolored or brittle, which is not preferable.
【0011】木質材に処理液を注入したのち、この樹脂
注入木質材を熱風ドライヤーによって加熱する。なお、
加熱、乾燥手段としては高周波加熱や熱板等を用い減圧
乾燥手段を採用してもよい。このように処理液を加熱す
ると、木材中の処理液に含まれる大半の水が主として木
質材の細胞内腔などのおおきな空隙から材外へ放出され
て樹脂が充填されない空隙部(細胞内腔)が形成される
一方、細胞壁内の小さな空隙には樹脂が充填される。After injecting the treatment liquid into the wood material, the resin-infused wood material is heated with a hot air dryer. In addition,
As the heating and drying means, high frequency heating, a hot plate, etc. may be used, and reduced pressure drying means may be employed. When the treatment solution is heated in this way, most of the water contained in the treatment solution in the wood is released out of the wood mainly through large cavities such as the cell cavities of the wood, resulting in voids (intracellular cavities) that are not filled with resin. is formed, while small voids within the cell wall are filled with resin.
【0012】この際、酸を混在させている処理液が水分
の除去によってその酸性度が高められるが、フェノール
樹脂との反応を円滑に行わせるためにはpH3未満まで
低下させる。このように処理液中の水分の除去によるp
Hの低下によって酸と樹脂との反応が徐々に開始され、
フェノール樹脂の高粘度化が始まり、樹脂液の流出が少
なくなる。[0012] At this time, the acidity of the treatment liquid containing an acid is increased by removing water, but in order to smoothly carry out the reaction with the phenol resin, the pH is lowered to less than 3. In this way, the p
The reaction between the acid and the resin starts gradually due to the decrease in H.
The viscosity of the phenol resin begins to increase, and the outflow of resin liquid decreases.
【0013】次いで、フェノール樹脂の硬化を40〜1
50 ℃で数分〜数時間に亘って行う。なお、このよう
な樹脂硬化処理は、減圧下では120℃以下の処理条件
によって完全に硬化する。この際、加熱処理を実施して
pH3未満でフェノール樹脂の硬化反応を行うと、木質
材の発色成分の着色や脆弱化が抑制される共にフェノー
ル樹脂の濃色化が防止される。Next, the phenol resin was cured at a temperature of 40 to 1
This is carried out at 50°C for several minutes to several hours. In addition, in such resin curing treatment, the resin is completely cured under a treatment condition of 120° C. or lower under reduced pressure. At this time, if the heat treatment is performed and the curing reaction of the phenol resin is performed at a pH of less than 3, the coloring and brittleness of the coloring component of the wood material are suppressed, and the phenol resin is prevented from becoming darker in color.
【0014】その結果、木質材内の大きな空隙部である
細胞内腔には樹脂が殆ど充填されなくて中空となり、且
つ該細胞壁内の小さな空隙部に樹脂が注入、硬化されて
天然木材の外観をそのまゝ維持した色合いの処理木材が
得られる。なお、酸の存在によってフェノール樹脂の分
子構造が変わり、フェノール樹脂のもつ黄色味が減じら
れて淡色化するので、濃色化が防止される。As a result, the cell cavities, which are large cavities within the wood, are hardly filled with resin and become hollow, and the resin is injected into the small cavities within the cell walls and hardened, giving the appearance of natural wood. The result is treated wood with a color that maintains its original color. Note that the presence of an acid changes the molecular structure of the phenol resin, reducing the yellow tinge of the phenol resin and making it lighter in color, thereby preventing darkening.
【0015】なお、木質材の空隙部内に対する樹脂充填
率が高くなると、フェノール樹脂による着色やコストア
ップ等の弊害が生じるので、あくまでもフェノール樹脂
水溶液の濃度が上記40重量%以下の範囲内で濃度の調
整を行うものである。[0015] If the resin filling rate in the voids of the wood material becomes high, problems such as coloring and cost increase due to the phenol resin will occur, so it is important to keep the concentration of the phenol resin aqueous solution within the above range of 40% by weight or less. It is for making adjustments.
【0016】又、下記の試験結果からも明らかなように
、比重が 0.3 〜0.5 の樹種の木質材であっ
ても濃度が10〜25重量%のフェノール樹脂水溶液を
注入すれば寸法安定性等の改質効果を図ることができる
ので、樹脂注入性の悪い木質材や比重が0.8の高い木
質材でも、40重量%濃度のフェノール樹脂水溶液を注
入すれば、寸法安定性や耐汚染性の改善を図ることがで
きるものである。[0016] Furthermore, as is clear from the test results below, even if the wood species of the tree has a specific gravity of 0.3 to 0.5, the dimensions can be improved by injecting a phenolic resin aqueous solution with a concentration of 10 to 25% by weight. Modifying effects such as stability can be achieved, so even with wood materials with poor resin injectability or wood materials with a high specific gravity of 0.8, by injecting a phenol resin aqueous solution with a concentration of 40%, the dimensional stability and stability can be improved. This makes it possible to improve stain resistance.
【0017】次に、本発明の具体的な実施例および実験
例を示す。
実施例 1
厚さ8mm、幅10cm、長さ1mのベイツガ単板に、
パラトルエンスルフォン酸0.5 重量%を添加してp
H5に調整した樹脂不揮発分10重量%のフェノール樹
脂水溶液を40トールの減圧下で30分、5Kg/cm
2の加圧下で30分、減圧・加圧注入を行った。次いで
、この樹脂注入単板を60℃の熱風ドライヤー内におい
て加熱して水分を除去した後、105 ℃の熱風ドライ
ヤー中で12時間、注入樹脂を反応硬化させた。こうし
て得られた処理単板は、従来のフェノール樹脂特有の赤
身や焼けが消失して処理前の色調をそのまゝ維持した外
観を呈するものであった。また、この処理単板を45日
間屋外暴露しても汚れが殆ど目立たなく、耐汚染性の優
れたものであった。Next, specific examples and experimental examples of the present invention will be shown. Example 1 A hemlock veneer with a thickness of 8 mm, a width of 10 cm, and a length of 1 m,
By adding 0.5% by weight of para-toluenesulfonic acid, p
A phenolic resin aqueous solution with a resin non-volatile content of 10% by weight adjusted to H5 was heated at 5Kg/cm for 30 minutes under a reduced pressure of 40 torr.
Decompression/pressure injection was carried out for 30 minutes under the pressure of 2. Next, this resin-injected veneer was heated in a hot air dryer at 60°C to remove moisture, and then the injected resin was reacted and cured in a hot air dryer at 105°C for 12 hours. The thus obtained treated veneer had an appearance in which the redness and burnt characteristic of conventional phenolic resins disappeared and the color tone before treatment was maintained. Furthermore, even when this treated veneer was exposed outdoors for 45 days, stains were hardly noticeable and it had excellent stain resistance.
【0018】比較例 1
実施例1において、パラトルエンスルフォン酸の添加量
を0.05%とし、pH7.5に調整し、硬化温度を1
50 ℃にした他は実施例1と同様の操作を行って比較
例1を得た。
こうして得られた処理単板は赤色化していた。Comparative Example 1 In Example 1, the amount of para-toluenesulfonic acid added was 0.05%, the pH was adjusted to 7.5, and the curing temperature was set to 1.
Comparative Example 1 was obtained by performing the same operation as in Example 1 except that the temperature was 50°C. The treated veneer thus obtained had a red color.
【0019】実験例 1
実施例1及び比較例1を無処理材とともに気乾状態及び
水注入状態で衝撃曲げ強さを測定し、脆弱性の防止効果
を実験した。その結果、次に示す表1から明らかなよう
に比較例は無処理木材の1/2に脆弱化したにも拘わら
ず実施例1は無処理材同等の靱性を有することがわかっ
た。従って、従来から角欠けが生じ易かったフェノール
樹脂処理木材の欠点を大幅に改善できることがわかった
。Experimental Example 1 The impact bending strength of Example 1 and Comparative Example 1 together with the untreated material was measured in an air-dried state and in a water-injected state, and the effect of preventing brittleness was tested. As a result, as is clear from Table 1 below, although the Comparative Example was weakened to 1/2 that of the untreated wood, the Example 1 was found to have the same toughness as the untreated wood. Therefore, it has been found that the defects of phenolic resin-treated wood, which has conventionally been prone to corner chipping, can be significantly improved.
【0020】[0020]
【表1】[Table 1]
【0021】[0021]
【発明の効果】以上のように本発明の樹脂処理木質材の
製造方法によれば、酸を添加しているともにpH3〜7
に調整した不揮発分40重量%以下のフェノール樹脂水
溶液を木質材に含浸し、該木質材を樹脂硬化可能な温度
に加熱して水分を揮散させると共に樹脂を硬化させるこ
とを特徴とするものであるから、pH3〜7に調整し且
つフェノール樹脂水溶液には多量の水が存在しているの
で、酸が存在しても低粘度を保持し、木質材の細胞壁内
の小さな空隙部にまで容易に該フェノール樹脂水溶液を
含浸させることができるばかりでなく、この含浸処理後
に加熱することでフェノール樹脂の高粘度化が開始され
てフェノール樹脂を細胞壁内の微細な空隙部等から流出
しにくい状態で硬化させることができるものである。Effects of the Invention As described above, according to the method for producing resin-treated wood materials of the present invention, acid is added and the pH is 3 to 7.
This method is characterized by impregnating a wooden material with an aqueous solution of phenolic resin having a non-volatile content of 40% by weight or less and heating the wooden material to a temperature at which the resin can be cured to volatilize water and cure the resin. Since the pH is adjusted to 3 to 7 and a large amount of water is present in the phenol resin aqueous solution, it maintains a low viscosity even in the presence of acids and easily penetrates into the small voids in the cell walls of wood materials. Not only can it be impregnated with an aqueous solution of phenolic resin, but heating after this impregnation treatment starts to increase the viscosity of the phenol resin, hardening it in a state that makes it difficult for the phenol resin to flow out from minute voids in the cell wall. It is something that can be done.
【0022】さらに、加熱することで、酸の存在によっ
て硬化温度、時間等のフェノール樹脂硬化条件を緩和で
き、木質材の発色成分の着色や靱性の低下が抑制される
共に上記酸によってフェノール樹脂の濃色化を防止する
ことができる。また、処理液を作製する際に、酸を添加
させてもフェノール樹脂水溶液が多量の水によって処理
前に縮重合するのを防止され、ポットライフの維持や粘
度の調整なども容易となる。又、加熱により水分の揮散
と樹脂の硬化を行うものであるから、同一の設備により
連続的に作業を行うことができるものである。Furthermore, by heating, the presence of an acid can ease the curing conditions of the phenol resin, such as curing temperature and time, suppressing the coloration of the coloring component of the wood material and the decrease in toughness, and the acid also suppresses the curing conditions of the phenol resin. Darkening can be prevented. In addition, even if an acid is added when preparing a treatment liquid, the phenol resin aqueous solution is prevented from condensation polymerization by a large amount of water before treatment, making it easier to maintain pot life and adjust viscosity. Furthermore, since the method uses heating to volatilize water and harden the resin, it is possible to perform the work continuously using the same equipment.
【0023】従って、木質材の細胞壁に注入、硬化した
フェノール樹脂によって木質材に対する水分や汚染物質
の浸入を阻止することができ、寸法安定性や耐汚染性、
防腐防虫性の向上を図ることができる。さらに、木質材
には細胞内腔等の大きな空隙が残存して多孔質となるも
のであるから、該空隙を樹脂により充填する従来の樹脂
処理木質材の製造方法のように着色を防止でき、天然木
質材本来のもつ外観を維持して優れた化粧性を発揮する
木質材が得られると共に、切削性、軽量性においても優
れた木質材を製造できる。[0023] Therefore, the phenol resin injected into the cell walls of the wood material and cured can prevent moisture and contaminants from entering the wood material, improving dimensional stability, stain resistance, and
It is possible to improve the antiseptic and insect repellent properties. Furthermore, since the wood material remains porous with large voids such as intracellular cavities, it is possible to prevent discoloration unlike the conventional manufacturing method of resin-treated wood materials in which the voids are filled with resin. It is possible to obtain a wood material that maintains the original appearance of natural wood materials and exhibits excellent cosmetic properties, and also to produce a wood material that is excellent in cutability and lightness.
Claims (1)
に調整した不揮発分40重量%以下のフェノール樹脂水
溶液を木質材に含浸し、該木質材を樹脂硬化可能な温度
に加熱して水分を揮散させると共に樹脂を硬化させるこ
とを特徴とする樹脂処理木質材の製造方法。[Claim 1] Contains an acid and has a pH of 3 to 7.
A resin-treated wood characterized by impregnating a wooden material with a phenolic resin aqueous solution with a non-volatile content of 40% by weight or less and heating the wood to a temperature at which the resin can be cured to volatilize water and cure the resin. Method of manufacturing wood.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6803491A JPH04278303A (en) | 1991-03-06 | 1991-03-06 | Manufacture of resin treated ligneous material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6803491A JPH04278303A (en) | 1991-03-06 | 1991-03-06 | Manufacture of resin treated ligneous material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04278303A true JPH04278303A (en) | 1992-10-02 |
Family
ID=13362113
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6803491A Pending JPH04278303A (en) | 1991-03-06 | 1991-03-06 | Manufacture of resin treated ligneous material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04278303A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001181552A (en) * | 1999-12-22 | 2001-07-03 | Chugoku Marine Paints Ltd | Aqueous stain composition and process for coloring substrate using this composition |
JP2020172589A (en) * | 2019-04-10 | 2020-10-22 | ケミプロ化成株式会社 | Woody member protectant, and surface-treated woody member |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4942807A (en) * | 1972-09-06 | 1974-04-22 | ||
JPH0281603A (en) * | 1988-09-20 | 1990-03-22 | Daiken Trade & Ind Co Ltd | Manufacture of reformed lumber |
-
1991
- 1991-03-06 JP JP6803491A patent/JPH04278303A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4942807A (en) * | 1972-09-06 | 1974-04-22 | ||
JPH0281603A (en) * | 1988-09-20 | 1990-03-22 | Daiken Trade & Ind Co Ltd | Manufacture of reformed lumber |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001181552A (en) * | 1999-12-22 | 2001-07-03 | Chugoku Marine Paints Ltd | Aqueous stain composition and process for coloring substrate using this composition |
JP2020172589A (en) * | 2019-04-10 | 2020-10-22 | ケミプロ化成株式会社 | Woody member protectant, and surface-treated woody member |
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