JPH03130104A - Production of acetylated fiber plate - Google Patents
Production of acetylated fiber plateInfo
- Publication number
- JPH03130104A JPH03130104A JP26983189A JP26983189A JPH03130104A JP H03130104 A JPH03130104 A JP H03130104A JP 26983189 A JP26983189 A JP 26983189A JP 26983189 A JP26983189 A JP 26983189A JP H03130104 A JPH03130104 A JP H03130104A
- Authority
- JP
- Japan
- Prior art keywords
- organic fiber
- acetylated
- adhesive
- curing
- acetic anhydride
- 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
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 41
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 11
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims abstract description 65
- 239000000853 adhesive Substances 0.000 claims abstract description 19
- 230000001070 adhesive effect Effects 0.000 claims abstract description 19
- 239000002253 acid Substances 0.000 claims abstract description 9
- 238000006243 chemical reaction Methods 0.000 claims abstract description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
- 239000011094 fiberboard Substances 0.000 claims description 22
- 238000007664 blowing Methods 0.000 claims description 5
- 230000000397 acetylating effect Effects 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 11
- 239000000203 mixture Substances 0.000 abstract description 4
- 238000010521 absorption reaction Methods 0.000 abstract description 3
- 241000218691 Cupressaceae Species 0.000 abstract description 2
- 235000008331 Pinus X rigitaeda Nutrition 0.000 abstract description 2
- 235000011613 Pinus brutia Nutrition 0.000 abstract description 2
- 241000018646 Pinus brutia Species 0.000 abstract description 2
- 241000219000 Populus Species 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract description 2
- 244000146553 Ceiba pentandra Species 0.000 abstract 1
- 235000003301 Ceiba pentandra Nutrition 0.000 abstract 1
- 241000218631 Coniferophyta Species 0.000 abstract 1
- 240000005109 Cryptomeria japonica Species 0.000 abstract 1
- 238000005187 foaming Methods 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 31
- 238000006640 acetylation reaction Methods 0.000 description 9
- 239000006227 byproduct Substances 0.000 description 8
- 229920002522 Wood fibre Polymers 0.000 description 7
- 239000002025 wood fiber Substances 0.000 description 7
- 230000021736 acetylation Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000012295 chemical reaction liquid Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011121 hardwood Substances 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000011122 softwood Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- PNVPNXKRAUBJGW-UHFFFAOYSA-N (2-chloroacetyl) 2-chloroacetate Chemical compound ClCC(=O)OC(=O)CCl PNVPNXKRAUBJGW-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241001070941 Castanea Species 0.000 description 1
- 235000014036 Castanea Nutrition 0.000 description 1
- 241000218645 Cedrus Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000008577 Pinus radiata Nutrition 0.000 description 1
- 241000218621 Pinus radiata Species 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
Landscapes
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Dry Formation Of Fiberboard And The Like (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明はアセチル化繊維板の製造方法に関し、特に寸法
安定性に優れたアセチル化繊維板を製造することのでき
る新規な方法に関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a method for producing an acetylated fiberboard, and particularly to a novel method capable of producing an acetylated fiberboard with excellent dimensional stability.
〈従来技術〉
従来より各種の針葉樹又は広葉樹材をチップにした後解
繊して得られる有機質繊維を圧縮成形することにより有
機質繊維板を製造することが知られている。<Prior Art> It has been known to manufacture organic fiberboards by compression molding organic fibers obtained by cutting various softwood or hardwood materials into chips and defibrating them.
しかしながら、有機質繊維中への水分の吸湿・吸水及び
その乾燥に伴って有機質繊維板が膨張又は収縮するため
に寸法安定性に欠け、その影響によって反りや割れが生
じ、またこの水分の浸透に伴って汚染物質が入り込むこ
とから繊維板の内部から腐食が生じる等の問題を有して
いた。However, as the organic fiberboard expands or contracts as moisture absorbs and dries into the organic fibers, it lacks dimensional stability, causing warping and cracking. This has led to problems such as corrosion occurring from inside the fiberboard due to contaminants entering the fiberboard.
この問題を解決するだめの方法として、木繊維マットに
無水酢酸を被覆し、密封空間において加熱することによ
り木繊維マットをアセチル化し、副生物の酢酸及び残留
無水酢酸を除去して成るアセチル化有機質繊維マットを
製造し、このマットを加熱圧締することにより熱可塑性
繊維板を製造することが提案されている(特表昭57−
501915号公報)。As a final method to solve this problem, an acetylated organic material is produced by coating a wood fiber mat with acetic anhydride, acetylating the wood fiber mat by heating it in a sealed space, and removing the by-product acetic acid and residual acetic anhydride. It has been proposed to produce a thermoplastic fiberboard by producing a fiber mat and heat-pressing this mat (Japanese Patent Publication No. 1987-
501915).
〈発明が解決しようとする課題〉
上記した熱可塑性繊維板の製造方法によれば、無処理の
繊維板に比べて、水分の吸収に伴う繊維板の膨張を防止
する効果が向上されるが、本発明者の実験によれば長時
間浸水に対する耐水性は必ずしも十分に満足できるもの
ではなかった。またこの方法によって製造される繊維板
は、アセチル化木繊維マットを接着剤を用いずに単に加
熱圧締することにより得られるものであるため、加熱圧
締の際にその温度、圧力及び時間等の加熱圧締条件を厳
密にコントロールする必要があり操作が煩雑である。<Problems to be Solved by the Invention> According to the method for manufacturing a thermoplastic fiberboard described above, the effect of preventing expansion of the fiberboard due to moisture absorption is improved compared to an untreated fiberboard. According to the inventor's experiments, the water resistance against long-term immersion was not necessarily fully satisfactory. In addition, the fiberboard manufactured by this method is obtained by simply heating and pressing an acetylated wood fiber mat without using an adhesive, so the temperature, pressure, time, etc. It is necessary to strictly control the heating and compacting conditions, making the operation complicated.
く課題を解決するための手段〉
このような現状に鑑み、本発明者は、水分の吸収・放出
に対する寸法安定性に優れた有機質繊維板を工業的に製
造する方法を提供すべく鋭意研究を重ねた結果、本発明
を完成するに至った。Means for Solving the Problems> In view of the current situation, the present inventor has conducted extensive research in order to provide a method for industrially manufacturing organic fiberboard with excellent dimensional stability against moisture absorption and release. As a result of repeated efforts, the present invention was completed.
すなわち本発明は、有機質繊維に酢酸無水物を含浸させ
て反応させることにより該有機質繊維中の水酸基をアセ
チル化し、このアセチル化された有機質繊維に酸の存在
により硬化が促進される接着剤を添加し、更に熱風によ
り風送した後、7オーミングを行い、熱圧成形して成る
ことを特徴とするアセチル化繊維板の製造方法である。That is, the present invention acetylates the hydroxyl groups in the organic fiber by impregnating the organic fiber with acetic anhydride and causing the reaction, and then adding an adhesive whose curing is accelerated by the presence of an acid to the acetylated organic fiber. This method of manufacturing an acetylated fiberboard is characterized in that the fiberboard is further blown with hot air, subjected to 7 ohming, and then hot-press molded.
本発明において用いる有機質繊維としては、例えば松、
杉、桧等の針葉樹、またはラワン、カポール、栗、ポプ
ラ等の広葉樹材のチ・ノブを常法に従って解繊し、含水
率20%以下好ましくは10%以下に乾燥して得られる
有機質繊維が好適に用いられる。この有機質繊維は長さ
1〜30mm、直径2〜300μ程度のものが大半を占
める。この有機質繊維は導管及び仮導管又は細胞が束に
なったような形をしており、繊維外周部の細胞壁は引き
裂かれたり割れ目を生じたりしているものが多い。Examples of organic fibers used in the present invention include pine,
Organic fibers obtained by defibrating chi-nobu of softwood such as cedar, cypress, or hardwood such as lauan, capor, chestnut, poplar, etc. according to a conventional method and drying to a moisture content of 20% or less, preferably 10% or less. Suitably used. Most of these organic fibers have a length of 1 to 30 mm and a diameter of 2 to 300 μm. These organic fibers are shaped like a bundle of conduits, tracheids, or cells, and the cell walls around the fiber periphery are often torn or cracked.
本発明に従いアセチル化処理された繊維板を製造するに
は、上記有機質繊維を、無触媒下で又は触媒として例え
ば酢酸ナトリウムや酢酸カリウム等の酢酸金属塩水溶液
を含浸させ乾燥させた後、無水酢酸、無水クロル酢酸等
の酢酸無水物反応液槽中に浸漬する。次いで、酢酸無水
物を含浸した有機質繊維を反応液槽から取り出し又は反
応液槽から酢酸無水物を排出することにより、有機質繊
維に対し約50〜80重量%の酢酸無水物を含浸させる
。酢酸無水物の含浸方法としては、有機質繊維に酢酸無
水物を噴霧等により添加して混合含浸させることによっ
ても良い。In order to produce the acetylated fiberboard according to the present invention, the above-mentioned organic fibers are impregnated with an aqueous solution of metal acetate such as sodium acetate or potassium acetate without any catalyst or as a catalyst, dried, and then dried with acetic anhydride. , immersed in an acetic anhydride reaction solution bath such as chloroacetic anhydride. Next, the organic fiber impregnated with acetic anhydride is taken out from the reaction liquid tank or the acetic anhydride is discharged from the reaction liquid tank, thereby impregnating the organic fiber with about 50 to 80% by weight of acetic anhydride. As a method for impregnating acetic anhydride, it is also possible to add acetic anhydride to organic fibers by spraying or the like, and mix and impregnate the organic fibers.
このようにして酢酸無水物が含浸された有機質繊維を、
別の反応器中或は混合器中で70〜150℃で数分乃至
数時間加熱し、副生物の酢酸を除去しながら反応させる
ことにより、有機質繊維中の水酸基をアセチル基と置換
したアセチル化繊維を売ることができる。この際アセチ
ル化に伴う重量増加率は約15〜25%である。アセチ
ル化反応が終了した時点では、副生物の酢酸は殆ど系外
に排出されており、未反応の無水酢酸が残留している。Organic fibers impregnated with acetic anhydride in this way are
Acetylation in which hydroxyl groups in organic fibers are replaced with acetyl groups by heating in a separate reactor or mixer at 70 to 150°C for several minutes to several hours and reacting while removing by-product acetic acid. You can sell textiles. At this time, the weight increase rate due to acetylation is about 15 to 25%. At the end of the acetylation reaction, most of the by-product acetic acid has been discharged from the system, and unreacted acetic anhydride remains.
この残留している未反応の無水酢酸(及び若干量の酢酸
)を除去することなく混合器(ブレンダー)に投入し、
酸の存在により硬化が促進される接着剤として尿素樹脂
系接着剤又はフェノール系接着剤を添加混合する。これ
によってアセチル化された有機質繊維の一本一本に接着
剤が十分に付着される。接着剤の添加量は有機質繊維に
対して2〜15重量%であることが好ましく、またその
樹脂率は30〜60%であることが好ましい。This remaining unreacted acetic anhydride (and some amount of acetic acid) is put into a mixer (blender) without being removed,
A urea resin adhesive or a phenol adhesive is added and mixed as an adhesive whose curing is accelerated by the presence of an acid. As a result, the adhesive is sufficiently attached to each acetylated organic fiber. The amount of adhesive added is preferably 2 to 15% by weight based on the organic fiber, and the resin percentage is preferably 30 to 60%.
一般に低樹脂率の方が有機質繊維に対して均一に混入す
ることができる。有機質繊維に添加された接着剤は酸の
存在により硬化が促進されるタイプのものであるため、
アセチル化処理後に残留する酢酸無水物(及び若干量の
副生物である酢酸)の存在によって添加後徐々に硬化す
る。Generally, the lower the resin ratio, the more uniformly the resin can be mixed into the organic fibers. The adhesive added to organic fibers is of a type whose curing is accelerated by the presence of acid.
Gradual hardening occurs after addition due to the presence of acetic anhydride (and some by-product acetic acid) remaining after the acetylation process.
接着剤を付着されたアセチル化有機質繊維は次いで熱風
ダクト中に投入され、風送乾燥される。The acetylated organic fibers to which the adhesive has been attached are then placed into a hot air duct and dried by blowing air.
この際の風送速度は一般に約15〜20m/秒であるが
、有機質繊維の比重、送り量、前後の工程の処理能力等
によって広範な範囲に互って適宜調整されるものである
。この熱風による風送で有機質繊維は6〜8%の水分量
にまで乾燥される。The air blowing speed at this time is generally about 15 to 20 m/sec, but it can be appropriately adjusted within a wide range depending on the specific gravity of the organic fiber, the feeding amount, the processing capacity of the previous and subsequent steps, etc. The organic fibers are dried to a moisture content of 6 to 8% by blowing with this hot air.
乾燥された有機質繊維は通常の方法で7オーミングされ
、一定厚さの繊維マットとされた後、ホットプレスに挿
入される。ホットプレスによる熱圧成形時に、添加され
た接着剤が更に強固に硬化して、所望のアセチル化有機
質繊維板が得られる。The dried organic fibers are subjected to 7 ohms in a conventional manner to form a fiber mat of a constant thickness, and then inserted into a hot press. During hot press molding, the added adhesive is further hardened to obtain the desired acetylated organic fiberboard.
〈作用〉
有機質繊維のアセチル化処理において若干量の副生物で
ある酢酸と相当量の酢酸無水物とが残留するが、アセチ
ル化繊維に対して酸の存在により硬化が促進されるタイ
プの接着剤を添加するため、該接着剤の硬化がこれら酢
酸及び酢酸無水物の働きによって促進される。従ってこ
れら酢酸及び酢酸無水物を除去する必要がない。<Function> A small amount of acetic acid, which is a by-product, and a considerable amount of acetic anhydride remain in the acetylation process of organic fibers, but this is a type of adhesive whose curing is accelerated by the presence of acid on acetylated fibers. The curing of the adhesive is accelerated by the action of acetic acid and acetic anhydride. Therefore, there is no need to remove acetic acid and acetic anhydride.
〈実施例〉
ラジアータパインのチップを160℃、 7kg/cm
2で3分間煮沸し、デフアイブレーター式リファイナー
で解繊した後、乾燥した木繊維を液体無水酢酸反応液槽
に2分間浸漬した後、反応液槽から取り出し、過剰の無
水酢酸を木繊維から5分間に互って排出した。この木繊
維に対して120°Cで副生物の酢酸を排出しながら1
時間加熱反応させてアセチル化処理を行った。反応終了
後50’Cまで冷却し、ブレングー中において、樹脂固
形分45%の尿素樹脂系接着剤を繊維に対して6%添加
混合した。次いで熱風ダクト中に投入し風送しながら水
分量6〜8%まで乾燥した。乾燥した木繊維を常法に従
って7オーミングし、125°0で6分間熱圧締するこ
とにより、5mm厚のアセチル化有機質繊維板を得た。<Example> Radiata pine chips at 160℃, 7kg/cm
2 for 3 minutes, defibrated using a defibrator refiner, and then immersed the dried wood fibers in a liquid acetic anhydride reaction tank for 2 minutes, and then removed from the reaction tank to remove excess acetic anhydride from the wood fibers. They were drained alternately for 5 minutes. This wood fiber is heated at 120°C while emitting the by-product acetic acid.
Acetylation treatment was performed by heating and reacting for a period of time. After the reaction was completed, the mixture was cooled to 50'C, and a urea resin adhesive having a resin solid content of 45% was added and mixed in an amount of 6% to the fibers in a blender. Next, it was placed in a hot air duct and dried to a moisture content of 6 to 8% while blowing air. The dried wood fibers were subjected to 7 ohms according to a conventional method and heat-pressed at 125°0 for 6 minutes to obtain an acetylated organic fiberboard with a thickness of 5 mm.
このアセチル化有機質繊維板は長期間の浸水に対しても
極めて優れた耐水性を示し、寸法安定性が良好なもので
あった。This acetylated organic fiberboard exhibited extremely excellent water resistance even when immersed in water for a long period of time, and had good dimensional stability.
〈発明の効果〉
本発明方法によれば、繊維板製造のための接着剤として
酸の存在により硬化が促進されるタイプのものが用いら
れているため、アセチル化反応により副生ずる酢酸及び
残留酢酸無水物を該接着剤の硬化剤として有効利用する
ことができる。従ってアセチル化反応後の反応副生物及
び残留物の除去工程を必要とせず、製造効率に優れてい
る。しかも繊維板の加熱成形において、加熱による硬化
機構に加えて上記酸による硬化促進機能が付加されるの
で、硬化反応が促進される。更に本発明方法は従来の繊
維板の製造工程中にアセチル化処理工程を付加するだけ
で実施可能であり、工業的に極めて有用である。<Effects of the Invention> According to the method of the present invention, since a type of adhesive whose curing is accelerated by the presence of acid is used as an adhesive for manufacturing fiberboard, acetic acid and residual acetic acid produced as by-products due to the acetylation reaction are The anhydride can be effectively used as a curing agent for the adhesive. Therefore, there is no need for a step for removing reaction by-products and residues after the acetylation reaction, resulting in excellent production efficiency. Moreover, in thermoforming the fiberboard, in addition to the curing mechanism by heating, the curing accelerating function by the acid is added, so that the curing reaction is accelerated. Furthermore, the method of the present invention can be implemented by simply adding an acetylation treatment step to the conventional fiberboard manufacturing process, and is extremely useful industrially.
Claims (1)
ことにより該有機質繊維中の水酸基をアセチル化し、こ
のアセチル化された有機質繊維に酸の存在により硬化が
促進される接着剤を添加し、更に熱風により風送した後
、フォーミングを行い、熱圧成形して成ることを特徴と
する、アセチル化繊維板の製造方法。(1) acetylating the hydroxyl groups in the organic fiber by impregnating the organic fiber with acetic anhydride and causing the reaction; adding an adhesive whose curing is accelerated by the presence of an acid to the acetylated organic fiber; A method for producing an acetylated fiberboard, which comprises further blowing with hot air, followed by forming and thermopressing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26983189A JPH0677921B2 (en) | 1989-10-16 | 1989-10-16 | Method for producing acetylated fiberboard |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26983189A JPH0677921B2 (en) | 1989-10-16 | 1989-10-16 | Method for producing acetylated fiberboard |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03130104A true JPH03130104A (en) | 1991-06-03 |
JPH0677921B2 JPH0677921B2 (en) | 1994-10-05 |
Family
ID=17477788
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP26983189A Expired - Fee Related JPH0677921B2 (en) | 1989-10-16 | 1989-10-16 | Method for producing acetylated fiberboard |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0677921B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06198610A (en) * | 1993-01-08 | 1994-07-19 | Yamaha Corp | Preparation of wooden fibrous material |
US6723766B1 (en) | 1999-06-10 | 2004-04-20 | Yamaha Corporation | Method for manufacturing ligneous material |
JP2019518635A (en) * | 2016-06-23 | 2019-07-04 | トライコヤ テクノロジーズ エルティーディーTricoya Technologies Ltd | Cooling of acetylated wood elements |
-
1989
- 1989-10-16 JP JP26983189A patent/JPH0677921B2/en not_active Expired - Fee Related
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06198610A (en) * | 1993-01-08 | 1994-07-19 | Yamaha Corp | Preparation of wooden fibrous material |
US6723766B1 (en) | 1999-06-10 | 2004-04-20 | Yamaha Corporation | Method for manufacturing ligneous material |
JP2019518635A (en) * | 2016-06-23 | 2019-07-04 | トライコヤ テクノロジーズ エルティーディーTricoya Technologies Ltd | Cooling of acetylated wood elements |
US11697221B2 (en) | 2016-06-23 | 2023-07-11 | Tricoya Technologies Ltd | Cooling acetylated wood elements |
Also Published As
Publication number | Publication date |
---|---|
JPH0677921B2 (en) | 1994-10-05 |
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