JPS63109002A - Improved woody material - Google Patents
Improved woody materialInfo
- Publication number
- JPS63109002A JPS63109002A JP25616386A JP25616386A JPS63109002A JP S63109002 A JPS63109002 A JP S63109002A JP 25616386 A JP25616386 A JP 25616386A JP 25616386 A JP25616386 A JP 25616386A JP S63109002 A JPS63109002 A JP S63109002A
- Authority
- JP
- Japan
- Prior art keywords
- wood
- wood material
- hardness
- impregnation
- resin
- 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 description 74
- 239000002023 wood Substances 0.000 claims description 81
- 239000003973 paint Substances 0.000 claims description 32
- 239000011248 coating agent Substances 0.000 claims description 17
- 238000000576 coating method Methods 0.000 claims description 17
- 239000002904 solvent Substances 0.000 claims description 15
- 229920001477 hydrophilic polymer Polymers 0.000 claims description 13
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- 239000000919 ceramic Substances 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 3
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 claims description 2
- 239000004814 polyurethane Substances 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 238000005470 impregnation Methods 0.000 description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 25
- 229920005989 resin Polymers 0.000 description 21
- 239000011347 resin Substances 0.000 description 21
- 229920000642 polymer Polymers 0.000 description 16
- 239000000243 solution Substances 0.000 description 14
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
- 229920001587 Wood-plastic composite Polymers 0.000 description 12
- 239000011155 wood-plastic composite Substances 0.000 description 12
- 229920003002 synthetic resin Polymers 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 238000001723 curing Methods 0.000 description 8
- 238000005498 polishing Methods 0.000 description 8
- 238000007654 immersion Methods 0.000 description 7
- 239000000057 synthetic resin Substances 0.000 description 7
- 238000010521 absorption reaction Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 238000010422 painting Methods 0.000 description 5
- -1 polytetrafluoroethylene Polymers 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000002952 polymeric resin Substances 0.000 description 4
- 241000218645 Cedrus Species 0.000 description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- 235000000405 Pinus densiflora Nutrition 0.000 description 3
- 240000008670 Pinus densiflora Species 0.000 description 3
- 229920002125 Sokalan® Polymers 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000012046 mixed solvent Substances 0.000 description 3
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 239000004584 polyacrylic acid Substances 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000218691 Cupressaceae Species 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 230000002087 whitening effect Effects 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 235000007173 Abies balsamea Nutrition 0.000 description 1
- 244000283070 Abies balsamea Species 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- 241001070941 Castanea Species 0.000 description 1
- 235000014036 Castanea Nutrition 0.000 description 1
- 240000000731 Fagus sylvatica Species 0.000 description 1
- 235000010099 Fagus sylvatica Nutrition 0.000 description 1
- 241000549546 Fraxinus spaethiana Species 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 241000219492 Quercus Species 0.000 description 1
- 241000736892 Thujopsis dolabrata Species 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000002648 azanetriyl group Chemical group *N(*)* 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229940116333 ethyl lactate Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000013035 low temperature curing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 235000019462 natural additive Nutrition 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 1
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
Landscapes
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Rod-Shaped Construction Members (AREA)
- Laminated Bodies (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔技術分野〕
この発明は、木材−プラスチック複合体を得るためのW
P C(Wood Plastic Combina
tionまたはWood Plastic CoI@p
ositeの略)加工を利用した改質木質材料に関する
ものである。[Detailed Description of the Invention] [Technical Field] The present invention relates to a method for obtaining a wood-plastic composite.
PC (Wood Plastic Combina)
tion or Wood Plastic CoI@p
This relates to a modified wood material that utilizes processing (abbreviation for osite).
従来より、木質材料の表面性能の改良、すなわち、美装
、耐汚染性、耐候性、耐防腐性などを目的として、各種
の水性塗料、油性塗料、繊維素塗料、天然手封脂塗料、
合成樹脂塗料、うるし塗料などを木質材料の表面に塗装
する処理が行なわれている。Traditionally, various water-based paints, oil-based paints, cellulose paints, natural hand-sealing paints,
The surface of wood materials is treated with synthetic resin paint, lacquer paint, etc.
一方、木質材料に合成樹脂の七ツマ−または初期重合物
、あるいはこれらにポリエステル樹脂等を組み合せた重
合性樹脂を含浸させ、木材中で重合硬化させて得られる
木材−プラスチック複合体は通常の木質材料に比べて耐
摩耗性、耐水性、耐候性、強度、寸法安定性等が優れる
ために、これらの性能付与を目的として樹脂含浸処理が
行なわれている。On the other hand, a wood-plastic composite obtained by impregnating a wooden material with a synthetic resin, an initial polymer, or a polymeric resin obtained by combining these with polyester resin, etc., and polymerizing and curing it in the wood is made of ordinary wood. Since it has superior abrasion resistance, water resistance, weather resistance, strength, dimensional stability, etc. compared to other materials, resin impregnation treatment is performed for the purpose of imparting these properties.
i!!l常の木質材料への塗装は、塗料の木質材料への
i着性能が大きな問題点となり、これを改善するために
、木理、木目等を検査する素地調査あるいは研磨などに
よる素地調整を経て、捨て塗り、研磨、目止め、研磨、
下塗り、VFg、中塗り、研磨、上塗り、(研磨)、麿
きなどの塗装と研磨を組み合せた複雑な工程を経て行な
われている。しかし、木質材料素地が改良された形とな
っていないために、特に水分の影響下にある場合は、そ
の水分によって木質材料が寸法変化などの変形を生じ、
木質材料素地と塗膜の界面に変形による歪が発生し、塗
膜の密着性は水分の影響度に比例して劣化する。i! ! When painting wood-based materials, a major problem is the adhesion of the paint to the wood-based material. , disposable coating, polishing, sealing, polishing,
It is done through a complex process that combines painting and polishing, such as undercoating, VFg, intermediate coating, polishing, topcoating, polishing, and polishing. However, because the wood material base is not in an improved shape, especially when it is under the influence of moisture, the moisture may cause deformation of the wood material such as dimensional changes.
Strain occurs due to deformation at the interface between the wood material base and the paint film, and the adhesion of the paint film deteriorates in proportion to the degree of influence of moisture.
これらの改善のために、上記の木材−プラスチック複合
体と組み合せ、これによって木質材料素地を変形の少な
い形にして、塗膜の密着性を上げることが行なわれてい
る。In order to improve these, it is being combined with the above-mentioned wood-plastic composite to make the wood material substrate into a shape with less deformation and improve the adhesion of the coating film.
しかし、重合性樹脂と重合開始剤を予め減圧または加圧
等の操作方法によって木材中に含浸し、加熱して重合硬
化させる従来の木材−プラスチック複合体では、その重
合硬化によって重合性樹脂の硬化に伴なう硬化収縮が発
生し、木材中に注入された硬化樹脂体と木材組織との間
に隙間が生じる。このため、水分がこの隙間内に浸入し
、その部分が白く見える現象(白化)が生じ、また寸法
変化(それに伴なう歪による塗膜の劣化)も出て来るか
ら耐水性が劣化する。このような素地との組み合せでは
、たとえ塗装によって表面性能を改良しても、これらの
影響から特に水分影響下の高い部分では塗膜密着性の大
巾な改良は望めなかった。However, in conventional wood-plastic composites in which a polymerizable resin and a polymerization initiator are impregnated into wood in advance by operating methods such as reduced pressure or pressurization, and then polymerized and cured by heating, the polymerizable resin is cured by the polymerization and curing. As a result, curing shrinkage occurs, and a gap is created between the cured resin body injected into the wood and the wood structure. As a result, water enters into these gaps, causing the area to appear white (whitening), and dimensional changes (deterioration of the coating film due to accompanying distortion) to occur, resulting in deterioration of water resistance. In combination with such a substrate, even if the surface performance was improved by painting, it was not possible to expect a significant improvement in the adhesion of the paint film due to these effects, especially in areas that are highly affected by moisture.
また、加熱による重合硬化には均一な一定時間の加熱操
作が必要であり、材料の厚さ、重合開始剤の量などの一
定条件を保持しなければ完全硬化に至らない、この時、
未反応の重合性樹脂が特に単量体の形で残存した場合、
得られる木材−プラスチック複合体は未反応物の浸出や
塗膜への浸入によって著しく塗膜性能を劣化させる問題
も生じる。このように、耐水性、耐候性を主たる目的と
して使用する部分では、現状の組み合せでは問題があり
、高耐久性の改質木質材料が切望されている。In addition, polymerization curing by heating requires a uniform heating operation for a certain period of time, and complete curing cannot be achieved unless certain conditions such as the thickness of the material and the amount of polymerization initiator are maintained.
If unreacted polymeric resin remains, especially in the form of monomers,
The resulting wood-plastic composite also has the problem of significantly deteriorating coating film performance due to unreacted substances leaching out or penetrating into the coating film. As described above, in parts where water resistance and weather resistance are the main objectives, there are problems with the current combinations, and highly durable modified wood materials are desperately needed.
更に、これら木材−プラスチック複合体は通常120%
以上の含浸率((ff1合性…脂i![1/木材重1)
X100)になり、非常に硬度が高く、プラスチック感
の強いものとなり、木質材料本来の木質感(木肌、暖か
味、やわらか味、風合い等)が消失した形となる。Furthermore, these wood-plastic composites are typically 120%
or more impregnation rate ((ff1 combination... fat i! [1/wood weight 1)
X100), it has extremely high hardness and a strong plastic feel, and the original wood texture (wood skin, warmth, soft taste, texture, etc.) of the wood material has disappeared.
この発明の目的は、木質材料が本来有する木質感(大味
、風合い等)を損なうことなく、耐汚染性、耐薬品性、
耐候性、耐水性などの木質材料表面の性能の高耐久化を
図った改質木質材料を提供することである。The purpose of this invention is to provide stain resistance, chemical resistance, and
An object of the present invention is to provide a modified wood material that has improved surface performance such as weather resistance and water resistance.
この発明の改質木質材料は、溶剤可溶型の親水性ポリマ
ーをその溶剤と共に含浸し乾燥させてなる木質材料に高
耐候性塗料を塗布してなるものである。The modified wood material of this invention is made by coating a highly weather resistant paint on a wood material impregnated with a solvent-soluble hydrophilic polymer and dried.
この発明によれば、親水性ポリマーを含浸させた木質材
料の高耐久性(寸法安定性、耐吸水性)と、この木質材
料の表面に塗布した高耐候性塗料の有する高耐候性、耐
汚染性、耐薬品性などの性情とが総合的に付与、合致さ
れた形となり、木質感を残したままで耐久性にきわめて
すぐれたものになる。According to this invention, the high durability (dimensional stability, water absorption resistance) of a wood material impregnated with a hydrophilic polymer, and the high weather resistance and stain resistance of a highly weather resistant paint applied to the surface of this wood material. The result is a shape that is comprehensively given and matched to properties such as hardness and chemical resistance, resulting in an extremely durable product that retains its woody feel.
従って、この発明の木質材料は通常の壁材、床材、天井
材等としての用途はもちろん、耐水性。Therefore, the wood material of this invention can be used not only as ordinary wall materials, floor materials, ceiling materials, etc., but also has water resistance.
耐腐朽性が要求される浴室の壁、天井、窓枠、換気口等
の施工部材や浴槽にも好適に保用することができる。It can be suitably maintained in bathroom walls, ceilings, window frames, ventilation openings, and other construction parts that require rot resistance, as well as bathtubs.
木質材料としては、住宅等の建築材料として従来より広
く使用されている松、杉、桧、ツガ、ヒバなどの針葉樹
、あるいはナラ、ブナ、クモ、シオジなどの広葉樹の無
垢材、合板、集成材である。Wood materials include softwood such as pine, cedar, cypress, hemlock, and hiba, which have been widely used as building materials for houses, and solid wood, plywood, and laminated wood such as oak, beech, spider, and shioji. It is.
また、これらの木質材料に含浸する親水性ポリマーとし
ては、たとえばポリアクリル酸エステル、ポリメタクリ
ル酸エステル、ポリアクリル酸アミド、ポリメタクリル
酸アミド、ポリビニルアルコール、ポリ酢酸ビニル、ポ
リアクリル酸ポリウレタン、ポリエチレンイミン、セル
ロース314体、などであって、その分子構造内に、:
c=o (カルボニル基) 、−OH(水酸基) 、−
CO−NH−(アミド基) 、−COOH(カルボキシ
ル基)、【
−N−(アミノ基、イミノ基、ニトリロ基)、−O−(
エーテル基)などの極性基を有したものがあげられ、こ
れらを単独あるいは2種以上の混合物、あるいはこれら
の共重合体または他のモノマーやオリゴマー、プレポリ
マー、ポリマーとの共重合体である。また、平均分子量
は含浸性から5万以下であることが望ましい、それぞれ
の親水性ポリマーと相溶性の良い溶剤とその溶媒として
選定し単独あるいは混合溶媒として溶解する。Hydrophilic polymers that can be impregnated into these wood materials include, for example, polyacrylic acid ester, polymethacrylic acid ester, polyacrylic acid amide, polymethacrylic acid amide, polyvinyl alcohol, polyvinyl acetate, polyacrylic acid polyurethane, and polyethylene imine. , cellulose 314 bodies, etc., whose molecular structure includes:
c=o (carbonyl group), -OH (hydroxyl group), -
CO-NH- (amide group), -COOH (carboxyl group), [ -N- (amino group, imino group, nitrilo group), -O-(
Examples include those having a polar group such as ether group), and these may be used alone or in mixtures of two or more, or copolymers thereof, or copolymers with other monomers, oligomers, prepolymers, and polymers. In addition, it is desirable that the average molecular weight is 50,000 or less from the viewpoint of impregnating properties.Select a solvent that has good compatibility with each hydrophilic polymer and dissolve it alone or as a mixed solvent.
溶剤としては、たとえば、メタノール、n−ブチルアル
コールなどのアルコール類、酢酸エチル、酢酸n−ブチ
ル、乳酸エチルなどのエステル類、ジオキサンなどのエ
ーテル類、トルエン、キシレンなどの炭化水素類あるい
はアセトン、メチルエチルケトンなどのケトン類などで
ある。希釈濃度は含浸性、作業性などから50%以下が
好ましい。Examples of solvents include alcohols such as methanol and n-butyl alcohol, esters such as ethyl acetate, n-butyl acetate, and ethyl lactate, ethers such as dioxane, hydrocarbons such as toluene and xylene, or acetone and methyl ethyl ketone. and other ketones. The dilution concentration is preferably 50% or less from the viewpoint of impregnating properties and workability.
また、必要に応して着色剤、N然剤、防黴剤などの添加
物を添加してもよい、この溶解した親木性ポリマー溶液
を木質材料に含浸する。Furthermore, the dissolved wood-philic polymer solution, to which additives such as colorants, natural additives, and fungicides may be added as necessary, is impregnated into the wood material.
含浸方法としては、常圧下でポリマー溶液内に木質材料
を浸漬する常圧浸漬法の他、減圧下で木質材料をポリマ
ー溶液に浸漬し、ついで常圧または加圧下で浸漬する減
圧常圧法または減圧加圧法などがいずれも採用可能であ
り、目的とする含浸度合いあるいは木質材料の種類など
により適宜選択する。常圧含浸法の場合、ポリマー溶液
内に木質材料を数時間以上浸漬する必要がある。また減
圧下での浸漬は木質材料を減圧釜に入れて減圧(たとえ
ば10トール以下で1時間以上排気)を行なったのち、
釜内にポリマー溶液を注入して行なう、樹脂液の注入後
、釜内を常圧にもどし、そのまま数時間以上浸漬を続行
するか、あるいは加圧して浸漬を行なう、また、含浸操
作にあたっては、木質材料をあらかじめよく乾燥(平衡
含水率以下)させておくことが好ましい。Impregnation methods include the normal pressure immersion method, in which the wood material is immersed in the polymer solution under normal pressure, and the reduced pressure normal pressure method or reduced pressure, in which the wood material is immersed in the polymer solution under reduced pressure, and then immersed under normal pressure or increased pressure. Any method such as a pressurization method can be adopted, and the method is appropriately selected depending on the desired degree of impregnation or the type of wood material. In the case of the atmospheric pressure impregnation method, it is necessary to immerse the wood material in the polymer solution for several hours or more. In addition, for soaking under reduced pressure, the wood material is placed in a vacuum pot and the pressure is reduced (e.g., evacuated at 10 torr or less for more than 1 hour).
The polymer solution is injected into the pot. After the resin solution is injected, the pressure inside the pot is returned to normal pressure, and the immersion is continued for several hours or more, or the immersion is carried out under pressure. Also, during the impregnation operation, It is preferable to thoroughly dry the wood material (below the equilibrium moisture content) in advance.
親水性ポリマーの含浸量は、これによって木質材料の硬
度が決定されるために重要であり、目的とする最適の硬
度が得られるように含浸量を定める必要がある。この場
合、親水性合成樹脂ポリマーを含浸した木質材料に末法
や木の風合いを残す為には、硬度をバーコール硬度で4
0以下に保持することが必要となる。すなわち、木質材
料が本来有する木質感(末法、風合い、素材感)が消失
してしまった従来の木材−プラスチック複合材の硬度が
50〜90であるのに対して、この硬度を40以下に保
持できれば、木質材料が本来有する木質感は損なわれず
、また合成樹脂ポリマーを含浸させているために、反り
、ねじれがなく、割れに<<、汚れが付きに<<、耐水
性が向上し腐りにくいなど、木質材料の欠点を排除でき
る。また、親水性合成tM脂ポリマー自体の性質あるい
は木質材料の種類にもよるが、含浸率としては、5〜5
0%が適当であり、この範囲であればバーコール硬度を
40以下に保持できる。The amount of hydrophilic polymer impregnated is important because it determines the hardness of the wood material, and it is necessary to determine the amount of impregnation so that the desired optimum hardness can be obtained. In this case, in order to retain the finish and wood texture of the wood material impregnated with the hydrophilic synthetic resin polymer, the hardness must be set to 4 on the Barcoll scale.
It is necessary to keep it below 0. In other words, while the hardness of conventional wood-plastic composite materials, which have lost the wood feel (finishing, texture, texture) inherent in wood materials, is 50 to 90, this hardness is maintained at 40 or less. If possible, the original wood feel of the wood material will not be impaired, and since it is impregnated with a synthetic resin polymer, it will not warp or twist, and will be resistant to cracks, stains, water resistance, and rot resistance. This eliminates the drawbacks of wood materials. In addition, depending on the properties of the hydrophilic synthetic tM fat polymer itself or the type of wood material, the impregnation rate is 5 to 5.
0% is appropriate, and within this range, Barcol hardness can be maintained at 40 or less.
含浸操作を終えた後、溶媒を揮発又は蒸発させ親水性合
成樹脂ポリマーを固化させる。揮発または蒸発方法とし
ては、風乾法、温風や熱風の雰囲気で行なう強制乾燥法
、減圧下で行なう減圧乾燥法、またはこれらを組み合せ
たものなどがあるが、親水性合成樹脂ポリマーが溶媒と
共に溶出しない様に徐々に揮発または蒸発させることが
好ましい。After the impregnation operation is completed, the solvent is volatilized or evaporated to solidify the hydrophilic synthetic resin polymer. Volatilization or evaporation methods include air drying, forced drying in a warm air or hot air atmosphere, vacuum drying under reduced pressure, or a combination of these methods, but the hydrophilic synthetic resin polymer is eluted together with the solvent. It is preferable to gradually volatilize or evaporate to prevent
この様にして得られた木材−プラスチック複合化による
改質木質材料は、親水性ポリマーの有する極性基により
木材組織との高い親和性(具体的にはセルロースの一〇
H基との結合)が得られ、固化に伴なう収縮での親木性
ポリマーと木材組織との隙間の発生は全く見られない、
したがって従来の白化現象は生じなくなる。また、木材
中に注入された親水性合成樹脂ポリマーは、木材組織内
の導管あるいは仮導管の壁面部をコーティングし、各種
の壁孔(ピント)をふさいだ形を形成している為に寸法
変化に寄与する。木材1)1胞壁への水分の浸入は防止
され、寸法安定性は非常に良い値を示す、一方、親水性
ポリマー溶液に直接触れた改質木材の表面、側面、裏面
、木口部の各表層部はその内部より高い含浸率となるた
め、それらの部分からの水の浸入は阻止される結果、吸
水性能は高く、吸水率は低い値を示す、従って、通常の
重合性樹脂を注入、硬化してなる木材−プラスチッり複
合体に比べ、寸法安定性で約2倍、吸水性で1.5〜2
.0倍の効果がある。The modified wood material obtained through the wood-plastic composite obtained in this way has a high affinity with wood tissue (specifically, bonding with the 10H group of cellulose) due to the polar groups of the hydrophilic polymer. As a result, no gaps are observed between the wood-philic polymer and the wood structure due to shrinkage during solidification.
Therefore, the conventional whitening phenomenon does not occur. In addition, the hydrophilic synthetic resin polymer injected into the wood coats the walls of the conduits or tracheids in the wood tissue, forming a shape that blocks various wall holes (pinto), resulting in dimensional changes. Contribute to Wood 1) 1 Moisture infiltration into the cell wall is prevented and the dimensional stability shows very good values.On the other hand, the surface, side, back, and end of the modified wood that came into direct contact with the hydrophilic polymer solution Since the surface layer has a higher impregnation rate than the interior, water intrusion from those areas is prevented, resulting in high water absorption performance and low water absorption rate. Therefore, when injecting ordinary polymeric resin, Compared to a hardened wood-plastic composite, it has approximately twice the dimensional stability and 1.5 to 2 times more water absorption.
.. It is 0 times more effective.
さらに5〜50%の含浸率であるから、改質木質材料の
切削加工性は良好で、従来の木質材料と同様の加工性が
ある。また、従来の重合硬化体タイプで問題となる残存
モノマーの悪臭や浸出の心配はポリマータイプのために
全くない。Furthermore, since the impregnation rate is 5 to 50%, the cutting workability of the modified wood material is good, and the workability is similar to that of conventional wood materials. Furthermore, since it is a polymer type, there is no concern about the odor or leaching of residual monomers, which is a problem with conventional polymer cured product types.
このようにして処理されて得られた木材−プラスチック
複合体である木質材料の表面にフッ素樹脂系塗料あるい
はアクリル系塗料、ウレタン系、シリコーン系、セラミ
ック系塗料などの高耐候性塗料をコーティングする。目
的とする木質感を保持するためには、塗布量はできるだ
け低いほうがよいが、耐汚染性、耐候性など性能の面か
ら40μ以下、なかんづく20〜30μの膜厚が好まし
い、また、出来れば、高耐候性塗料はつや消しタイプが
好ましく、とりわけ7分つや以下のつや消しタイプのも
のが望ましい。The surface of the wood material, which is a wood-plastic composite thus obtained, is coated with a highly weather-resistant paint such as a fluororesin paint, an acrylic paint, a urethane paint, a silicone paint, or a ceramic paint. In order to maintain the desired wood texture, the amount of coating should be as low as possible, but from the viewpoint of performance such as stain resistance and weather resistance, a film thickness of 40 μ or less, especially 20 to 30 μ, is preferable, and if possible, The highly weather-resistant paint is preferably a matte type, and particularly a matte type with a gloss level of 7 minutes or less is particularly desirable.
高耐候性塗料は、木材−プラスチック複合体の表面に研
磨処理後あるいは直接にスプレーガン、ロールコータ、
フローコーターなどの塗装機器あるいははけ塗りなどに
よって塗布する。場合によっては下塗り、中塗り、上塗
りなどのように、研磨との組み合せで多層に塗布するこ
ともあるが通常は1〜2回の塗布で十分である。塗装後
は塗料の性質あるいは環境の度合いにより常温放置、加
温、乾燥などの操作によって塗膜を形成させる。Highly weather-resistant paints can be applied to the surface of wood-plastic composites after polishing or directly using spray guns, roll coaters, etc.
Apply using painting equipment such as a flow coater or by brushing. In some cases, multiple layers may be applied in combination with polishing, such as undercoat, intermediate coat, top coat, etc., but usually one or two coats is sufficient. After painting, a coating film is formed by leaving it at room temperature, heating, drying, etc. depending on the properties of the paint or the level of the environment.
目的とする木質感を保持するためには、出来れば常温硬
化タイプもしくは50℃以下の低温硬化タイプでそれ以
上の加熱を必要としないものの方が好ましい、また、塗
膜の硬度も低い方が良く、具体的には鉛IE+!度で6
H以下のものが好ましく、その様な性能を付与、調整さ
れた高耐候性塗料を使用するのが望ましい。In order to maintain the desired wood texture, it is preferable to use a room-temperature curing type or a low-temperature curing type below 50°C that does not require further heating, and the lower the hardness of the coating, the better. , specifically lead IE+! 6 degrees
H or less is preferable, and it is desirable to use a highly weather resistant paint that has been imparted and adjusted with such performance.
このようにして得られた改質木質材料は、木質材料の高
耐水性と表面塗装の高耐候性、耐汚染性、耐薬品性など
の性能が総合的に付与、合致された形となり高耐久性材
料となる。The modified wood material obtained in this way has a comprehensive combination of properties such as the high water resistance of the wood material and the high weather resistance, stain resistance, and chemical resistance of the surface coating, and is highly durable. It becomes a sexual material.
次に実施例をあげてこの発明の改質木質材料を説明する
。Next, the modified wood material of the present invention will be explained with reference to Examples.
実施例1;木質材料(米松柾目板、厚み×巾×長さ一3
0x30x60 (鶴)、含水率14.0%)を減圧含
浸釜内に入れ、釜内を10トール以下に排気減圧したの
ち、ポリウレタン樹脂、(平均分子1)7.500)の
メチルエチルケトン溶液(ポリウレタン樹脂濃度40.
0%)を注入した。ついで、釜内を常圧にもどし、浸漬
した状態を保ちながら、18時間浸漬を行なった。その
後、含浸釜より木質材料を取り出し、65℃の温風乾燥
機内に55時間保持して、溶媒(メチルエチルケトン)
を揮発させた。その結果、樹脂含浸率は40.2〜44
.4%で、バーコール硬度は33.0であった。Example 1; Wooden material (Japanese pine straight grain board, thickness x width x length 13
0x30x60 (Tsuru), water content 14.0%) was placed in a vacuum impregnation pot, the pressure inside the pot was evacuated to 10 torr or less, and then a methyl ethyl ketone solution (polyurethane resin Concentration 40.
0%) was injected. Then, the pressure inside the pot was returned to normal pressure, and immersion was carried out for 18 hours while maintaining the immersion state. After that, the wood material was taken out from the impregnation pot and kept in a hot air dryer at 65°C for 55 hours to remove the solvent (methyl ethyl ketone).
evaporated. As a result, the resin impregnation rate was 40.2 to 44
.. 4%, the Barcol hardness was 33.0.
これにフッ素樹脂(ルミフロンLF200、旭硝子#l
製)を20μの膜厚となるように塗布した。Add to this fluororesin (Lumiflon LF200, Asahi Glass #l)
Co., Ltd.) was applied to a film thickness of 20 μm.
室温放置10日間後、塗膜の硬度を測定すると、鉛筆硬
度で3Hであり、未処理品に近い木質の風合いを残した
ものであった。After being left at room temperature for 10 days, the hardness of the coating film was measured and was found to be 3H on a pencil hardness, retaining a woody texture similar to that of an untreated product.
実施例2:木質材料(米杉柾目板、厚み×巾×長さ一3
0x30x60 (m) 、含水率15.7%)を減圧
含浸釜内に入れ、釜内を5トール以下に排気減圧したの
ち、酢酸ビニル樹脂(平均分子量43.0OQ)を(メ
タノール;キシレン−75=25)の混合溶媒で28.
0%に希釈した溶液を注入した。ついで、釜内を常圧に
もどし、さらに15〜17−/−に加圧して9時間加圧
含浸した。その後、含浸釜より木質材料を取り出し、8
5℃の熱風乾燥機内に65時間保持し溶媒を揮発させた
。Example 2: Wooden material (straight grained rice cedar board, thickness x width x length 13
0x30x60 (m), water content 15.7%) was placed in a vacuum impregnation pot, and the pressure inside the pot was evacuated to 5 torr or less, and then vinyl acetate resin (average molecular weight 43.0OQ) was added to (methanol; xylene-75= 28. with the mixed solvent of 25).
A solution diluted to 0% was injected. Then, the pressure inside the pot was returned to normal pressure, and the pressure was further increased to 15 to 17-/- for 9 hours of pressure impregnation. After that, take out the wood material from the impregnation pot and
The solution was kept in a hot air dryer at 5° C. for 65 hours to volatilize the solvent.
その結果、樹脂含浸率は38.0〜44.2%であった
。またバーコール硬度は20.4であった。As a result, the resin impregnation rate was 38.0 to 44.2%. Moreover, the barcol hardness was 20.4.
これに、アクリルウレタン系塗料(UA−13、三洋化
成工業領製)を25μ塗布した。室温放置14日間後、
塗膜の硬度は鉛筆硬度で2Hであり、風合が未処理品に
近いものであった。To this, 25 μm of acrylic urethane paint (UA-13, manufactured by Sanyo Chemical Industries) was applied. After 14 days at room temperature,
The hardness of the coating film was 2H on a pencil hardness scale, and the texture was close to that of an untreated product.
実施例3:木質材料(米松柾目板、厚みX巾×長さ一3
0X30X60 (B) 、含水率12.8%)を減圧
含浸釜内に入れ、釜内を7.oトール以下に排気減圧し
たのち、ポリメチルメタクリレート樹脂(平均分子量4
1.000)の酢酸メチル溶液(ポリメチルメタクリレ
ート樹脂濃度35.0%)を注入した。ついで釜内を常
圧にもどし、更に1゜〜12駄/−に加圧して、12時
間加圧含浸した。Example 3: Wooden material (Japanese pine straight grain board, thickness x width x length 13
0X30X60 (B), water content 12.8%) was placed in a vacuum impregnation pot, and the inside of the pot was heated to 7. After reducing the exhaust pressure to below o torr, polymethyl methacrylate resin (average molecular weight 4
1.000) of methyl acetate solution (polymethyl methacrylate resin concentration 35.0%) was injected. Then, the pressure inside the pot was returned to normal pressure, and the pressure was further increased to 1° to 12°/- for 12 hours of pressure impregnation.
その後含浸釜より木質材料を取り出し、80℃熱風乾燥
機内に50時間保持して溶媒(酢酸エチル)を揮発させ
た。その結果、樹脂含浸率は30.5〜36.4%であ
った。またバーコール硬度は27.0であった。Thereafter, the wood material was taken out from the impregnation pot and kept in a hot air dryer at 80° C. for 50 hours to volatilize the solvent (ethyl acetate). As a result, the resin impregnation rate was 30.5 to 36.4%. Moreover, the barcol hardness was 27.0.
これに、セラミック系塗料(グラス力、リボール社m)
を膜厚15μでコーティングした。室温で20日後、塗
膜の硬度は鉛筆硬度で5Hであった。このものは、若干
硬い感じはあるが、まだ木質の肌合いを残したものであ
った。In addition, ceramic paint (Glass Power, Reball Co., Ltd.)
was coated with a film thickness of 15μ. After 20 days at room temperature, the hardness of the coating film was 5H on a pencil hardness scale. Although this item felt a little hard, it still had a woody feel to it.
実施例4:実施例1の木質基材を#180のサンディン
グベーパで軽くサンディングし、ポリウレタン樹脂塗料
(ポリウラツクNa200 C,四面塗料@製)を15
μ塗布し、硬化後、#240のサンディングを行ない、
さらに同様の塗料を10μ塗布した。硬化処理(40℃
で60分)後の硬度は鉛筆硬度でIHであり、木質の風
合いを残したものであった。Example 4: The wood base material of Example 1 was lightly sanded with #180 sanding vapor, and a polyurethane resin paint (Polyuratsuku Na200 C, manufactured by Yotsuya Paint@) was applied for 15 minutes.
Apply μ, and after curing, sand with #240.
Furthermore, 10μ of the same paint was applied. Hardening treatment (40℃
After 60 minutes), the hardness was IH in terms of pencil hardness, and a woody texture remained.
この発明によれば、親水性ポリマーを含浸させた木質材
料の高耐水性(寸法安定性、耐吸水性)と、この木質材
料の表面に塗布した高耐候性塗料の有する高耐候性、耐
汚染性、耐栗品性などの性情とが総合的に付与、合致さ
れた形となり、木質感を残したままで耐久性にきわめて
すぐれたものになるという効果がある。According to this invention, the high water resistance (dimensional stability, water absorption resistance) of a wood material impregnated with a hydrophilic polymer, and the high weather resistance and stain resistance of a highly weather resistant paint applied to the surface of this wood material. The result is a shape that is comprehensively given and matched with properties such as hardness and chestnut resistance, and has the effect of being extremely durable while retaining its wood feel.
この発明ではフッ素系等の高耐候性塗料を木質材料の表
面に塗布したが、木質材料に含浸する溶剤可溶型の親水
性ポリマーにフッ素樹脂を添加して溶剤と共に木質材料
に含浸し乾燥して、溶剤を除去するようにしてもよい、
この場合も、木質材料の硬度(バーコール硬度)は40
以下とし、前記親水性ポリマーとフッ素樹脂との含浸量
は木質材料100重量部に対して5〜50重量部とする
のが好ましい。In this invention, a highly weather-resistant paint such as a fluorine-based paint is applied to the surface of the wood material, but a fluororesin is added to a solvent-soluble hydrophilic polymer that is impregnated into the wood material, and the material is impregnated with a solvent and dried. The solvent may be removed by
In this case as well, the hardness of the wood material (Barcol hardness) is 40
The amount of impregnation of the hydrophilic polymer and fluororesin is preferably 5 to 50 parts by weight per 100 parts by weight of the wood material.
かかる場合も、前記と同様に木質材料の木質感を残した
ままで、耐汚染性、耐薬品性、耐水性、耐候性、撥水性
などの性能を付与向上させることができる。ちなみに、
通常の重合性樹脂を注入、硬化してなる。木材−プラス
チック複合体に比べ、寸法安定性で約2.5倍、吸水性
で1.0〜3.0倍の効果がある。In such a case as well, it is possible to impart and improve performances such as stain resistance, chemical resistance, water resistance, weather resistance, and water repellency while retaining the woody feel of the wood material, as described above. By the way,
It is made by injecting and curing ordinary polymeric resin. Compared to wood-plastic composites, it is about 2.5 times more effective in dimensional stability and 1.0 to 3.0 times more effective in water absorption.
ここで、使用する木質材料、親水性ポリマーおよび溶剤
は前記と同じである。フッ素樹脂としては、ポリテトラ
フルオロエチレン、ポリクロルトリフルオロエチレン、
ポリフッ化ビニル、フッ化ビニリデン、ヘキサフルオロ
プロピレン−テトラフルオロエチレン共重合体、クロル
トリフルオロエチレンーフフ化ビニリデン共重合体など
があげられるが、他の樹脂との相溶性がなく、通常はパ
ウダーの形で混入しなければならないなどの問題があり
、使用範囲は限定される。それゆえ、好ましくはパーフ
ルオロアルキル基を有するアクリレート樹脂あるいはこ
れと他のモノマーとの共m合物などからなる。パーフル
オロアルキル化合物の形となったものが良い、このパー
フルオロアルキル化合物は、パーフルオロアルキル基の
疎水性、疎油性と他の樹脂側の親油性、親水性の両方の
特性を持つため、添加する樹脂体あるいは溶媒とは親水
性、親油性基の効果によって相溶性が良く、樹脂体、固
化後は樹脂体の表面側でCF3基が均一に配向された形
となり、耐汚染性、耐候性、耐水性などの特徴を発揮す
る。したがって、このような含フツ素化合物を選定する
のが望ましい、さらに、必要に応じて着色剤、難燃剤、
防黴剤などの添加物を添加してもよい。Here, the wood material, hydrophilic polymer and solvent used are the same as described above. Examples of fluororesins include polytetrafluoroethylene, polychlorotrifluoroethylene,
Examples include polyvinyl fluoride, vinylidene fluoride, hexafluoropropylene-tetrafluoroethylene copolymer, and chlorotrifluoroethylene-vinylidene fluoride copolymer, but they are not compatible with other resins and are usually used in powder form. There are problems such as having to mix it in the form of a liquid, which limits its range of use. Therefore, it preferably consists of an acrylate resin having a perfluoroalkyl group or a co-compound of this and other monomers. It is best to use a perfluoroalkyl compound in the form of a perfluoroalkyl compound.This perfluoroalkyl compound has both the hydrophobic and oleophobic properties of the perfluoroalkyl group and the lipophilic and hydrophilic properties of other resins. It has good compatibility with the resin body or solvent due to the effects of hydrophilic and lipophilic groups, and after solidification, the CF3 groups are uniformly oriented on the surface side of the resin body, resulting in stain resistance and weather resistance. , exhibits characteristics such as water resistance. Therefore, it is desirable to select such a fluorine-containing compound, and if necessary, colorants, flame retardants,
Additives such as antifungal agents may be added.
次に参考例をあげて説明する。Next, a reference example will be given and explained.
参考例1:木質材料(米松板目板、厚み×巾×長さ一3
0X30X60 (鶴)、含水率14.1%)を減圧含
浸釜内に入れ、釜内を10トール以下に排気減圧したの
ち、ポリウレタン樹脂(平均分子1)18.000)の
メチルエチルケトン溶液(ポリウレタン樹脂濃度40.
5%)に、フッ素系樹脂(サーフロン3382、旭硝子
■製)を0.2%添加した溶液を注入した。ついで釜内
を常圧にもどし、浸漬した状態を保ちながら25時間浸
漬を行なった。その後、含浸釜より取り出し70℃の温
風乾燥機内に60時間保持して、溶媒(メチルエチルケ
トン)を揮発させた。その結果、樹脂含浸率は、40.
0〜45.0%でバーコール硬度30.2であった。Reference example 1: Wooden material (Japanese pine board, thickness x width x length 13
0 x 30 40.
A solution containing 0.2% of a fluororesin (Surflon 3382, manufactured by Asahi Glass ■) was injected into the sample. Then, the inside of the pot was returned to normal pressure, and immersion was continued for 25 hours while maintaining the immersion state. Thereafter, it was taken out from the impregnation pot and kept in a hot air dryer at 70° C. for 60 hours to volatilize the solvent (methyl ethyl ketone). As a result, the resin impregnation rate was 40.
The Barcol hardness was 30.2 at 0% to 45.0%.
参考例2:木質材料(米杉板目板、厚み×巾×長さ一3
0x30x60 (鶴)、含水率15.2%)を減圧含
浸釜内に入れ、釜内を5トール以下に排気減圧したのち
、ポリ酢酸ビニル樹脂(平均分子量41.000)をメ
タノール:キシレンが80:20の混合溶媒で29.0
9,6に希釈した溶液にフッ素系樹脂であるパーフルオ
ロアルキルEO付加物(サーフロンS−145、旭硝子
■製)を0.5%添加した溶液を注入した。ついで、釜
内を常圧にもどし、更に15〜17−/−に加圧して、
10時間加圧含浸した。その後、含浸釜より取り出し、
85℃熱風乾燥機内に50時間保持し、溶媒を揮発させ
た。その結果樹脂含浸率は39.2〜44.4%であつ
た。又、バーコール硬度が21.0であった。Reference example 2: Wooden material (rice cedar grain board, thickness x width x length 13
0x30x60 (Tsuru), water content 15.2%) was placed in a vacuum impregnation pot, the pressure inside the pot was evacuated to 5 torr or less, and polyvinyl acetate resin (average molecular weight 41.000) was mixed with methanol: xylene in a proportion of 80: 29.0 with 20 mixed solvents
A solution in which 0.5% of a perfluoroalkyl EO adduct (Surflon S-145, manufactured by Asahi Glass ■), which is a fluororesin, was added was injected into the solution diluted to 9.6. Next, the pressure inside the pot was returned to normal pressure, and the pressure was further increased to 15 to 17-/-.
Impregnation was carried out under pressure for 10 hours. After that, take it out from the impregnation pot,
It was kept in a hot air dryer at 85° C. for 50 hours to volatilize the solvent. As a result, the resin impregnation rate was 39.2 to 44.4%. Further, the barcol hardness was 21.0.
参考例3:木質材料(米桧板目板、厚み×巾×長さ一3
QX30X60 (鶴)、含水率12.4%)を減圧含
浸釜内に入れ釜内を7.0トール以下に排気減圧したの
ち、ポリメチルメタクリレート樹脂(平均分子138.
000)の酢酸エチル溶液(ポリメチルメタクリレート
樹脂濃度32.0%)にフッ素系樹脂(サーフロン51
01、旭硝子■製)を1.0%添加した溶液を注入した
、ついで釜内を常圧にもどし、更にlO〜12kg/a
Jに加圧して、9時間加圧含浸した。その後、含浸釜よ
り取り出し、80℃熱風乾燥機内に45時間保持して溶
媒(酢酸エチル)を揮発させた。その結果、樹脂含浸率
は、32.5〜38.0%であった。また、バーコール
硬度は29.3であった。Reference example 3: Wooden material (Japanese cypress board, thickness x width x length 13
QX30X60 (Tsuru), water content 12.4%) was placed in a vacuum impregnation pot and the pressure inside the pot was evacuated to below 7.0 Torr, and then polymethyl methacrylate resin (average molecular weight 138.
Fluorine-based resin (Surflon 51
01, manufactured by Asahi Glass ■) was injected into the pot, and then the inside of the pot was returned to normal pressure, and further 10 ~ 12 kg/a was added.
Pressure was applied to J and impregnated under pressure for 9 hours. Thereafter, it was taken out from the impregnation pot and kept in a hot air dryer at 80° C. for 45 hours to volatilize the solvent (ethyl acetate). As a result, the resin impregnation rate was 32.5 to 38.0%. Moreover, the barcol hardness was 29.3.
Claims (4)
浸し乾燥させてなる木質材料に高耐候性塗料を塗布して
なる改質木質材料。(1) A modified wood material made by coating a wood material with a highly weather resistant paint on a wood material made by impregnating a solvent-soluble hydrophilic polymer with the solvent and drying it.
硬度(バーコール硬度)が40以下である特許請求の範
囲第(1)項記載の改質木質材料。(2) The modified wood material according to claim (1), wherein the wood material base material impregnated with the hydrophilic polymer has a hardness (Barcol hardness) of 40 or less.
度(鉛筆硬度)を6H以下にした特許請求の範囲第(1
)項記載の改質木質材料。(3) The coating amount of the highly weather-resistant paint is 40μ or less, and the coating film hardness (pencil hardness) is 6H or less.
) The modified wood material described in section 2.
シリコーン系、セラミック系である特許請求の範囲第(
1)項記載の改質木質材料。(4) The highly weather resistant paint is fluorine-based, polyurethane-based,
Claim No. 1 (which is silicone-based or ceramic-based)
Modified wood material described in section 1).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25616386A JPS63109002A (en) | 1986-10-27 | 1986-10-27 | Improved woody material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25616386A JPS63109002A (en) | 1986-10-27 | 1986-10-27 | Improved woody material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63109002A true JPS63109002A (en) | 1988-05-13 |
Family
ID=17288779
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25616386A Pending JPS63109002A (en) | 1986-10-27 | 1986-10-27 | Improved woody material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63109002A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0423674A2 (en) * | 1989-10-20 | 1991-04-24 | Dr. Wolman GmbH | Wood preservative containing polymeric nitrogen compounds |
JPH04118204A (en) * | 1990-04-25 | 1992-04-20 | Hyogo Izumi | Manufacture of composite wood using heating steam |
JPH04100803U (en) * | 1991-02-07 | 1992-09-01 | 段谷産業株式会社 | durable plywood |
-
1986
- 1986-10-27 JP JP25616386A patent/JPS63109002A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0423674A2 (en) * | 1989-10-20 | 1991-04-24 | Dr. Wolman GmbH | Wood preservative containing polymeric nitrogen compounds |
JPH04118204A (en) * | 1990-04-25 | 1992-04-20 | Hyogo Izumi | Manufacture of composite wood using heating steam |
JPH04100803U (en) * | 1991-02-07 | 1992-09-01 | 段谷産業株式会社 | durable plywood |
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