JPS62225303A - Manufacture of improved woody-material small piece - Google Patents
Manufacture of improved woody-material small pieceInfo
- Publication number
- JPS62225303A JPS62225303A JP6895286A JP6895286A JPS62225303A JP S62225303 A JPS62225303 A JP S62225303A JP 6895286 A JP6895286 A JP 6895286A JP 6895286 A JP6895286 A JP 6895286A JP S62225303 A JPS62225303 A JP S62225303A
- Authority
- JP
- Japan
- Prior art keywords
- wood
- reaction
- strips
- reaction solution
- raw
- 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 23
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 239000002023 wood Substances 0.000 claims description 67
- 239000000376 reactant Substances 0.000 claims description 8
- 238000005520 cutting process Methods 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000002344 surface layer Substances 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 description 40
- 239000003795 chemical substances by application Substances 0.000 description 12
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 9
- 239000012295 chemical reaction liquid Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000002994 raw material Substances 0.000 description 7
- 239000010876 untreated wood Substances 0.000 description 7
- -1 organic acid halides Chemical class 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- 235000013312 flour Nutrition 0.000 description 4
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000010875 treated wood Substances 0.000 description 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 239000005639 Lauric acid Substances 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000007385 chemical modification Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012374 esterification agent Substances 0.000 description 2
- 238000006266 etherification reaction Methods 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 239000011094 fiberboard Substances 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 235000019260 propionic acid Nutrition 0.000 description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical compound FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VGJBOZZPXZVBBI-UHFFFAOYSA-N O=C1C=CC(C=C2N=C(C=C3N=C(C=C4N=CC=C4)C=C3)C=C2)=N1 Chemical compound O=C1C=CC(C=C2N=C(C=C3N=C(C=C4N=CC=C4)C=C3)C=C2)=N1 VGJBOZZPXZVBBI-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000008050 dialkyl sulfates Chemical class 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
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) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
産業上の利用分野
本発明は耐湿性5防腐防虫性、熱可塑性、成形性を付与
した木質材細片、例えば、フェノール樹脂。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention is directed to wood strips, such as phenolic resins, which are endowed with moisture resistance, antiseptic properties, thermoplasticity, and moldability.
ユリア樹脂、メラミン樹脂等の熱硬化性樹脂や塩化ビニ
ル、ポリエステル樹脂等の熱可塑性樹脂の充填材やファ
イバーボード等の原料、土壌改良材として用いられる粉
状、繊維状、フレーク状の改質された木質材細片の製造
方法に関する。Thermosetting resins such as urea resin and melamine resin, thermoplastic resins such as vinyl chloride and polyester resin, and modified powders, fibers, and flakes used as fillers and raw materials for fiberboard, and as soil conditioners. The present invention relates to a method for producing wood strips.
従来技術とその問題点
従来、木質材細片に熱可塑性を付与して樹脂と混合して
用いることが特開昭56−135552号公報にて提案
されている。PRIOR ART AND THEIR PROBLEMS Conventionally, it has been proposed in Japanese Patent Laid-Open No. 135552/1983 to impart thermoplasticity to wood strips and use the mixture with a resin.
しかしながら、開示されているような木粉を反応液に接
触させて処理する方法は、工業的には、木質材細片を反
応器に仕込み、この反応器に反応液を反応液貯槽から供
給し、反応終了後、反応液をくり返し使用するために前
記反応液を前記反応液貯槽に回収するとともに、処理し
た木質材細片より余剰の反応液を脱液し、洗浄する必要
があるが、木質材細片間に反応液が保持されやすく、P
水性か悪い。このため、反応液の回収作業に手間がかか
るとともに、反応液の回収率が低く、また、反応後に行
う改質木質材細片の洗浄にも手間がかかった。However, the disclosed method of treating wood flour by bringing it into contact with a reaction liquid is industrially performed by charging wood chips into a reactor and supplying the reaction liquid to the reactor from a reaction liquid storage tank. After the reaction is completed, it is necessary to collect the reaction solution into the reaction solution storage tank for repeated use, as well as drain the excess reaction solution from the treated wood strips and wash them. The reaction liquid is easily retained between the material strips, and P
Water-based or bad. For this reason, it took time and effort to recover the reaction solution, the recovery rate of the reaction solution was low, and it also took time and effort to wash the modified wood strips after the reaction.
しかム、前記反応液中に混入した木質材細片の微粉が配
管のバルブ部分等に目詰まりしてバルブ等の操作を妨げ
るおそれがあった。However, there was a risk that the fine powder of wood chips mixed in the reaction solution would clog the valve portion of the piping, thereby interfering with the operation of the valve and the like.
さらに、木質材細片は嵩高いため、同一重量の木質材原
材と比較すると、体積が大きくなる。このため、同一重
量の木質材細片を改質するには、作業回数を多くするか
、反応器の容積を大きくする必要があり、多大の労力、
設備費が必要であるという問題点があった。Furthermore, since the wood strips are bulky, they have a larger volume compared to the same weight of raw wood material. Therefore, in order to modify wood chips of the same weight, it is necessary to increase the number of operations or increase the volume of the reactor, which requires a great deal of labor and effort.
There was a problem that equipment costs were required.
一方、改質された木質材細片と無処理木質材細片とを混
合して用いることが、特開昭58−174699号公報
記載にて提案されているが、この方法では両者を計量し
て混合しなければならず、生産工数が多くなるという問
題点があった。On the other hand, it has been proposed in JP-A-58-174699 to use a mixture of modified wood strips and untreated wood strips, but this method requires both to be weighed. There was a problem in that the number of production steps was increased because it had to be mixed by
発明の構成
本発明は、前記問題点を解決する手段として、板状、ブ
ロック状、デツプ状の木質材原材の少なくとも表層部に
その木質材成分中の水酸基と反応しうる反応体を接触さ
せて化学的に修飾した後、前記木質材原材を細片化する
ようにしたものである。Structure of the Invention The present invention, as a means to solve the above-mentioned problems, involves contacting at least the surface layer of a wood raw material in the form of a plate, block, or depression with a reactant capable of reacting with the hydroxyl groups in the wood component. After chemically modifying the raw wood material, the raw wood material is cut into pieces.
木質材原材としては、木材単板、薄板、小角材。Wood raw materials include wood veneers, thin boards, and small square timbers.
小割材、木材チップ、丸太、角材を切削、小割りあるい
は塊状に破砕してなるものがあげられる。These include items made by cutting, cutting, cutting, or crushing small pieces of lumber, wood chips, logs, and square lumber into small pieces or chunks.
木質材成分中の水酸基と反応しうる反応体としては、例
えば、エステル化剤およびエーテル化剤のほか、イソシ
アネート類(例えば、メチルイソシアネート、エヂルイ
ソシアネートなど)を挙げることができる。Examples of reactants that can react with the hydroxyl groups in the wood component include esterifying agents and etherifying agents, as well as isocyanates (eg, methyl isocyanate, edyl isocyanate, etc.).
エステル化剤としては有機酸無水物(例えば酢酸、プロ
ピオン酸、酪酸等の無水物)、有機酸ハロゲン化物(例
えば前記の酸の他、カプロン酸、ラウリン酸、ステアリ
ン酸およびメタクリル酸等のハロゲン化物、特にこれら
の塩化物)、および有機酸無水物と脂肪酸との混合物(
例えば無水トリフルオル酢酸または無水クロル酢酸等と
、例えばプロピオン酸、カプロン酸またはラウリン酸等
との混合物)などを挙げることができる。これらのエス
テル化剤は単独で、あるいは2種以上混合して使用する
ことができる。Esterifying agents include organic acid anhydrides (for example, anhydrides such as acetic acid, propionic acid, butyric acid, etc.), organic acid halides (for example, in addition to the above acids, halides such as caproic acid, lauric acid, stearic acid, and methacrylic acid). , especially their chlorides), and mixtures of organic acid anhydrides and fatty acids (
Examples include mixtures of trifluoroacetic anhydride or chloroacetic anhydride, and propionic acid, caproic acid, lauric acid, etc.). These esterifying agents can be used alone or in combination of two or more.
前記エステル化剤には、木質材成分との反応を促進する
ための触媒および/または、エステル化剤の木質材細胞
膜内への浸透を促進するための溶剤を添加しておくこと
ができる。このような触媒としては硫酸、過塩素酸、尿
素=硫安、脂肪酸塩およびビリノンなどが、溶剤として
はベンゼン、トルエン、ジメヂルホルムアミドおよび四
酸化二窒素−ノメヂルホルムアミドなどが挙げられ、さ
らに各々2種またはそれ以上の混合物として用いてらよ
い。A catalyst for promoting the reaction with the wood component and/or a solvent for promoting the penetration of the esterifying agent into the wood cell membrane may be added to the esterifying agent. Examples of such catalysts include sulfuric acid, perchloric acid, urea (ammonium sulfate), fatty acid salts, and bilinone, and examples of solvents include benzene, toluene, dimedylformamide, and dinitrogen tetroxide-nomedylformamide, and each It may be used as a seed or a mixture of more than one.
これらの触媒および/または溶剤は、エステル化剤と混
合するか、前記エステル化剤で処理する而の木質材原材
に予め含浸させておいてもよい。These catalysts and/or solvents may be mixed with an esterifying agent or impregnated in advance into the wood material to be treated with the esterifying agent.
次に、エーテル化剤としては、例えば、エヂレンオキサ
イド、プロピレンオキサイド等の1.2=エポキシド、
塩化メヂル、塩化エヂル等のハロゲン化アルキル、塩化
ベンジル等の芳香族ハロゲン化物、ジメチル硫酸等のジ
アルキル硫酸、モノクロル酢酸等のα−ハロゲン酸、シ
アン化ビニル等の陰性基で活性化されたビニル化合物、
ホルムアルデヒド等のアルデヒドなどを用いることがで
きる。Next, as the etherification agent, for example, 1.2=epoxide such as ethylene oxide and propylene oxide;
Alkyl halides such as medyl chloride and edyl chloride, aromatic halides such as benzyl chloride, dialkyl sulfates such as dimethyl sulfate, α-halogen acids such as monochloroacetic acid, and vinyl compounds activated with negative groups such as vinyl cyanide. ,
Aldehydes such as formaldehyde can be used.
エーテル化剤の場合も、エステル化剤の場合と同様、触
媒(例えば、水酸化ナトリウムの如きアルカリ触媒)や
溶剤(例えば、エステル化剤の場合に使用されるものと
同様の溶剤)を適宜添加することができ、エーテル化剤
で処理する前の木質材原材に予めこれらを含浸させてお
くことが好ましい。In the case of an etherification agent, as in the case of an esterification agent, a catalyst (for example, an alkaline catalyst such as sodium hydroxide) and a solvent (for example, a solvent similar to that used in the case of an esterification agent) are added as appropriate. It is preferable to impregnate the wood material in advance with the etherifying agent before treating it with the etherifying agent.
反応体を木質材原材に接触させるには、例えば木質材原
材を反応体中に浸漬するか、あるいは反応体を気化せし
め、これに木質材原材を晒らせばよい。また、このよう
な方法を減圧下、加圧下あるいは威圧加圧法により行い
、木質材原材に対する反応体の含浸を促進させることが
できる。In order to bring the reactant into contact with the raw wood material, for example, the raw wood material may be immersed in the reactant, or the reactant may be vaporized and the raw wood material may be exposed to this. In addition, such a method can be carried out under reduced pressure, under increased pressure, or by a forced pressure method to promote impregnation of the reactant into the wood raw material.
化学的修飾は木質材原材を反応液と共に加熱し、前記反
応液中の官能基を木質材成分中の水酸基に反応させるこ
とにより達成される。反応後は、残存する反応液を直接
に、又は、中和して木質材外に洗浄、除去して乾燥する
。Chemical modification is achieved by heating the wood material together with a reaction solution and causing the functional groups in the reaction solution to react with the hydroxyl groups in the wood component. After the reaction, the remaining reaction solution is washed or removed from the wood material either directly or by neutralization, and then dried.
前記化学修飾の程度は触媒の有無、触媒の種類。The degree of chemical modification depends on the presence or absence of a catalyst and the type of catalyst.
反応体の種類1反応時間、木質材原材の大きさにより異
なる。Type of reactant 1 Reaction time varies depending on the size of the wood material.
通常、反応率は反応前の乾燥木質材原材の重量をベース
にし、反応処理後、乾燥した化学修飾木質材原材の重量
増加率で示す。Usually, the reaction rate is based on the weight of the dry raw wood material before the reaction, and is expressed as the weight increase rate of the dry chemically modified raw wood material after the reaction treatment.
例えば、反応液に無水酢酸を用いて熱可塑性や溶融性を
付与したい時に、硫酸やピリジンの様な木材の結晶領域
を膨潤させて結晶域中の木材成分までアセチル化する必
要があるので、アセチル化反応率は40〜70%になる
。For example, when using acetic anhydride to impart thermoplasticity or meltability to the reaction solution, it is necessary to swell the crystalline region of wood with sulfuric acid or pyridine and acetylate the wood components in the crystalline region. The conversion reaction rate will be 40 to 70%.
一方、前記無水酢酸を用いても、無触媒や酢酸ナトリウ
ム等の酢酸塩触媒の場合、木材の非晶領域のみをアセチ
ル化するので、非晶領域中の木材成分中の水酸基を概ね
アセチル基に置換しても反応率は約30%である。On the other hand, even if acetic anhydride is used, in the case of no catalyst or an acetate catalyst such as sodium acetate, only the amorphous region of the wood is acetylated, so most of the hydroxyl groups in the wood components in the amorphous region are converted to acetyl groups. Even with substitution, the reaction rate is about 30%.
前述の如く、最大の反応率を見出して適宜変化させると
、木質材原材中の化学修飾処理部分と無処理部分との略
比率を調整することができるので、後述する細片化工程
1回で、改質された木質材細片と無処理木質材細片との
混合物をつくることができる。As mentioned above, by finding the maximum reaction rate and changing it appropriately, it is possible to adjust the approximate ratio of the chemically modified part and the untreated part in the raw wood material, so it is possible to adjust the approximate ratio of the chemically modified part and the untreated part in the wood raw material. A mixture of modified wood strips and untreated wood strips can be made.
更に、前記反応液を再使用するため、又、余剰の反応液
が木質材内に残ると臭気が問題になるとともに、改質さ
れた木質材細片を利用して行なう接着やその他の化学反
応に悪影響を与えるので、これらを防止するため、反応
処理後に余剰の反応液を減圧にて脱液1回収する。Furthermore, because the reaction solution is reused, odor becomes a problem if excess reaction solution remains in the wood, and adhesives and other chemical reactions using the modified wood strips are difficult. In order to prevent this, the excess reaction solution is removed and recovered under reduced pressure after the reaction treatment.
尚、化学的に修飾した木質材原材には、改質された合板
やLVLの製造中に出る廃材も含まれる。Note that chemically modified wood raw materials include modified plywood and waste materials produced during the production of LVL.
化学的に修飾した木質材原材を細片化する手段としては
、ローラーミル、ボールミル等の粉砕機による粉砕、フ
レーカ−、シェービングマシン等の切削機による切削、
クラッシャー等の破砕機による破砕、パルパー、リファ
イナーによる繊維化が採用できる。Means for cutting chemically modified wood raw materials into pieces include crushing with a crusher such as a roller mill or ball mill, cutting with a cutting machine such as a flaker or shaving machine,
Crushing using a crusher such as a crusher, and fiberization using a pulper or refiner can be used.
前記細片化による木質材細片の形状としては、粉状、繊
維状およびフレーク状などの細片(削片、薄片、破砕片
、粉砕片)があげられる。The shape of the wood material fragments obtained by the above-mentioned fragmentation includes powder-like, fibrous-like, and flake-like fragments (shavings, thin pieces, crushed pieces, and pulverized pieces).
前述の操作により得られる改質された木質l細片の用途
は、従来の無処理木質材細片と同様であり、例えば、フ
ェノール樹脂やアミノ樹脂の充填材として用いると、成
形性や耐水性の良好な成形品が得られる。The uses of the modified wood strips obtained by the above-mentioned operation are the same as those of conventional untreated wood strips. A molded product with good quality can be obtained.
又、前記処理木質材細片をパーティクルボードの表層材
として用いると、耐水性が向上するとともに、表面の平
滑性が向上する。Further, when the treated wood strips are used as a surface layer material of particle board, water resistance and surface smoothness are improved.
更に、反応率を調整して得た無処理材混合木質材細片を
抄造して得られるファイバーボードは、優れた耐腐朽性
3寸法安定性を有する。Furthermore, the fiberboard obtained by paper-making the untreated wood mixed wood strips obtained by adjusting the reaction rate has excellent rot resistance and three-dimensional stability.
実施例1
3jIJ!厚の木質材単板を5重量%の酢酸ナトリウム
水溶液に浸漬、含浸させて乾燥し、この木質材単板を反
応容器である反応釜に仕込み、前記木質材単板内に無水
酢酸からなる反応液を加圧、注入し、余剰の反応液を反
応釜から脱液8回収し、加熱温度120℃で30分間反
応させて木質材単板を改質した後、この木質材単板に残
存する反応液を脱液、除去し、さらに、洗浄、乾燥して
反応率(重量増加率)25%のアセデル化処理木質材単
板を得た。そして、このアセデル化処理木質材単板をク
ラッシャーにて破砕し、更に、ボールミルにて粉砕して
+00メツシユの大きさのアセデル化処理木質材細片を
得た。Example 1 3jIJ! A thick wood veneer is immersed in a 5% by weight aqueous sodium acetate solution, impregnated and dried, and this wood veneer is placed in a reaction pot, which is a reaction vessel, and a reaction mixture consisting of acetic anhydride is added to the wood veneer. The liquid is pressurized and injected, the excess reaction liquid is removed from the reaction pot, and the remaining reaction liquid is removed from the reaction vessel. After reacting at a heating temperature of 120°C for 30 minutes to modify the wood veneer, the remaining reaction liquid remains in the wood veneer. The reaction solution was deliquified and removed, and further washed and dried to obtain an acedelized wood veneer with a reaction rate (weight increase rate) of 25%. The acedelized wood veneer was then crushed using a crusher and further crushed using a ball mill to obtain acedelized wood strips having a size of +00 mesh.
本実施例においては、回収した反応液に新しい反応液を
補給しないでも20回くり返して利用でき、優れた回収
率を有することが確認できた。In this example, it was confirmed that the collected reaction solution could be used 20 times without replenishing new reaction solution, and had an excellent recovery rate.
実施例1をユリア樹脂に乾燥重量比で1.5倍混合し、
成形したところ、表面平滑で成形性良好な成型品が得ら
れた。Example 1 was mixed with urea resin in a dry weight ratio of 1.5 times,
When molded, a molded product with a smooth surface and good moldability was obtained.
これは、100メツシユの木粉をアセデル化処理して用
いたものと同程度の成形性であり、無処理本粉を用いた
ものに比べ平滑性、光沢、白色度において優れているこ
とが確認できる。It has been confirmed that this has the same moldability as that made using 100 mesh wood flour treated with acedel, and is superior in smoothness, gloss, and whiteness compared to that made using untreated wood flour. can.
実施例2
実施例1の反応時間を5分間にしたところ反応率10%
のアセチル化処理単板を得た。更に、同様の操作により
+00メツシユの木粉を得た。これを選別したところ処
理木質材細片と無処理木質材細片との混在が確認できた
。Example 2 When the reaction time of Example 1 was changed to 5 minutes, the reaction rate was 10%.
An acetylated veneer was obtained. Furthermore, +00 mesh wood flour was obtained by the same operation. When this was sorted, it was confirmed that treated wood strips and untreated wood strips were mixed together.
発明の効果
以上の説明から明らかなように、本発明によれば、反応
液の脱液工程において胛水性が良好であるので、反応液
の回収作業が容易になるとともに、回収率が高まり、反
応液をくり返し使用できる。Effects of the Invention As is clear from the above explanation, according to the present invention, the water retention property is good in the step of removing the reaction solution, which facilitates the recovery work of the reaction solution, increases the recovery rate, and improves the reaction rate. The liquid can be used repeatedly.
又、処理材の洗浄ら容易になる。Additionally, cleaning of the treated material becomes easier.
しかし、反応液に木質材の微粉が混入しにくいので、反
応釜等の配管やバルブに目詰まりが生じにくくなり、メ
インテナンスが容易になる。However, since fine wood particles are less likely to be mixed into the reaction solution, the piping and valves of the reaction vessel are less likely to become clogged, making maintenance easier.
さらに、木質材原材は木質材細片のように嵩高くないの
で、−回の作業で多量の改質木質材細片を得ることがで
きる。特に、木質材原材の表層部だけを化学的に修飾し
て反応率を適宜調整すれば、改質木質材細片と無処理木
質材細片とが混在するものを一回の作業で得られるので
、生産工数を減少させることができ、生産性が高くなる
という効果がある。Furthermore, since the raw wood material is not as bulky as the wood strips, a large amount of modified wood strips can be obtained in one operation. In particular, if only the surface layer of raw wood material is chemically modified and the reaction rate is adjusted appropriately, a mixture of modified wood chips and untreated wood chips can be obtained in one operation. This has the effect of reducing production man-hours and increasing productivity.
Claims (1)
くとも表層部にその木質材成分中の水酸基と反応しうる
反応体を接触させて化学的に修飾した後、前記木質材原
材を細片化することを特徴とする改質された木質材細片
の製造方法。(1) After chemically modifying at least the surface layer of a wood material in the form of a plate, block, or chip with a reactant capable of reacting with the hydroxyl group in the wood component, the wood material is A method for producing modified wood strips, the method comprising cutting into strips.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6895286A JPS62225303A (en) | 1986-03-26 | 1986-03-26 | Manufacture of improved woody-material small piece |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6895286A JPS62225303A (en) | 1986-03-26 | 1986-03-26 | Manufacture of improved woody-material small piece |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62225303A true JPS62225303A (en) | 1987-10-03 |
Family
ID=13388510
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6895286A Pending JPS62225303A (en) | 1986-03-26 | 1986-03-26 | Manufacture of improved woody-material small piece |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62225303A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001096511A (en) * | 1999-09-30 | 2001-04-10 | Yamaha Corp | Method for modification of wood element |
JP2007216438A (en) * | 2006-02-15 | 2007-08-30 | Forestry & Forest Products Research Institute | Wood modifying method |
KR20140073540A (en) * | 2011-09-28 | 2014-06-16 | 타이탄 우드 리미티드 | Panels of medium density fibreboard |
-
1986
- 1986-03-26 JP JP6895286A patent/JPS62225303A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001096511A (en) * | 1999-09-30 | 2001-04-10 | Yamaha Corp | Method for modification of wood element |
JP2007216438A (en) * | 2006-02-15 | 2007-08-30 | Forestry & Forest Products Research Institute | Wood modifying method |
JP4686775B2 (en) * | 2006-02-15 | 2011-05-25 | 独立行政法人森林総合研究所 | Method for modifying wood |
KR20140073540A (en) * | 2011-09-28 | 2014-06-16 | 타이탄 우드 리미티드 | Panels of medium density fibreboard |
JP2014531348A (en) * | 2011-09-28 | 2014-11-27 | チタン ウッド リミテッド | Medium density fiberboard panel |
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