JPS5811575A - Water-resistant adhesive - Google Patents
Water-resistant adhesiveInfo
- Publication number
- JPS5811575A JPS5811575A JP10917381A JP10917381A JPS5811575A JP S5811575 A JPS5811575 A JP S5811575A JP 10917381 A JP10917381 A JP 10917381A JP 10917381 A JP10917381 A JP 10917381A JP S5811575 A JPS5811575 A JP S5811575A
- Authority
- JP
- Japan
- Prior art keywords
- water
- dialdehyde
- gum
- polyvinyl alcohol
- isocyanate compound
- 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
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は耐水性に優れた接着剤に関するものであり、特
に木材や紙の11層に好適な接着剤を提供するものであ
る・
元来、木材等の接着剤には、zリア樹騙、メクζン樹騙
、フェノール411騰、レゾルクツ−に樹−等のホルマ
リン系1lj11が多く使用されている。Detailed Description of the Invention The present invention relates to an adhesive with excellent water resistance, and provides an adhesive particularly suitable for 11 layers of wood and paper. Formalin-based 1lj11 such as Zria Judama, Meku ζn Judama, Phenol 411 Teng, and Resolkutsu ni Ju- are often used.
これらの本kMリン系樹虐緩清剤には、憾(少息のホル
ムアルデk)″が未反応の状−で*#L?#’す、それ
が大気中に揮散してI11職^を与えたり、皮膚に炎症
な起こす等の停書を招(lII系となっている。These kM phosphorus-based tree detoxifiers contain unreacted formalde, which evaporates into the atmosphere and causes I11 jobs. If you give it too much, it may cause irritation to your skin, etc., which may lead to suspension.
そこで、ホルマリ/を使用しないiitw剤とし【、イ
ソブチレンと無水マレイン酸の共重合偶膿**剤や水性
ビ品ルウレタンIM!着剤等がII角され、−一にこれ
らの**剤がll!用されている。Therefore, we decided to use an IITW agent that does not use formali, such as a copolymerized pus** agent of isobutylene and maleic anhydride, and a water-based vinyl urethane IM! The adhesive etc. are squared, and these ** agents are ll! It is used.
しかし、これらの接着剤は二すア樹騙II舗lI4に比
べて価格が島(、また遣膜性がよいため優潰層が乾−し
て螢看不真を起こしやすいという性質を有し、使用11
1に接着条件を厳しく管鳳する必要が生ずる等の欠点が
あるため、広く一般に普及するまでKMっていない。However, these adhesives are more expensive than Nisu-Ajudama II-4 (and also have good film-forming properties, so the adhesive layer tends to dry out and cause flaking). , use 11
1 has drawbacks such as the need for strict adhesive bonding conditions, so it has not been commercialized until it is widely used.
41に、水性ピJWkクレ17g層剤は、インクア半一
ト化會豐が金属と良好なR’IQ性を有するため熱圧時
に熱板に付層する等の閾1があり、実用化への大会な障
害になプている。41, the water-based PJWK 17g layer agent has good R'IQ properties with metals, so there is a threshold 1 such as layering on the hot plate during hot pressing, so it is difficult to put it into practical use. The tournament has become a major obstacle.
水性ビニルウレタン豪着剤は、−紋に、ポリビニルアル
コールと水性クテックスを含む水#疲にイソシアネート
化會物を−1して#凝されるもので、これkよりインシ
アネート基がボリビJLkアルコールの水酸基と反応し
てクレタy曽會を生じ鍜僑構造をとるために耐水性能が
向上すると言われている。The water-based vinyl urethane adhesive is made by adding an isocyanate compound to water containing polyvinyl alcohol and water-based Cutex, and from this, the incyanate group is added to the water containing polyvinyl alcohol and water-based Cutex. It is said that water resistance is improved because it reacts with hydroxyl groups to form Creta-yellow-like structures and takes on a hollow structure.
しかしながら、*llKは、ポリビニルアルコールが存
在しなくても、イソシアネート化合1が均一に分款して
いれば、はば同一の耐水接着性−が得られることから、
ポリビニルアルコールはイソシアネート化會智を均一に
分数するための乳化剤的役割りを1にたしているに過ぎ
ないと4考えられる。However, *IIK shows that even if polyvinyl alcohol is not present, if the isocyanate compound 1 is uniformly distributed, the same water-resistant adhesion can be obtained.
It is believed that polyvinyl alcohol only plays the role of an emulsifier for uniformly dividing the isocyanate.
また、インシアネート化會物は水が存在すると、水と反
応し″cm素化合書な生じ、さらに、その尿素化曾智と
イソシアネートが反応してビニレット−會を生じ、果備
構造が形成されていく。In addition, in the presence of water, the incyanate reacts with water to form a cm compound, and further, the urea reacts with the isocyanate to form a vinylet-like structure, forming a monomer structure. To go.
従って、イソシアネート化合1は水と反応する比率が高
いので、このインシアネート化合書なポリビニルアルコ
ールと反応させるためには多量Km加する必要がある。Therefore, since the isocyanate compound 1 has a high reaction ratio with water, it is necessary to add a large amount of Km in order to cause the inocyanate compound to react with polyvinyl alcohol.
しかしながら、イソノ化合−ト化合書の添加量を多くす
ると、置板等を劇造する鏝の感圧時Km層剤が弐幽に浸
出し【熱板に付着しやすくなり、その結果、作業性な着
しく低下してしまう。However, when the amount of isono-compound added is increased, the Km layer agent leaches out when the pressure is sensitive to the trowel used to dramatically create the plate, etc. [It becomes easier to adhere to the hot plate, and as a result, the workability is reduced. It will drop slowly.
熱板への付着はイン7アネート化曾豐の11瀘な威らす
ことによりて錦上できるが、イソシアネート化合−を賦
らすと蟻橋反応が十分に進まず、満足すべき耐水接層性
能が得られない。Adhesion to the hot plate can be achieved by applying an in7anate compound, but if an isocyanate compound is added, the dovetail reaction does not proceed sufficiently, resulting in a satisfactory water-resistant adhesive layer. Performance cannot be obtained.
本発明者らは、このような矛盾を解決する万f&につ1
櫨々研究したIm巣、ダル;−ス単位騨の50〜100
%がジアルデヒド単位#に転化したポリサッカライドな
配合することにより、イノ7アネート化合物を多jiK
*JElせ 、ずと4優れた耐水優着性簡が得られる
ことな見出した。The inventors have proposed a number of ways to resolve such contradictions.
I've researched a lot, and there are 50 to 100 units.
By blending the polysaccharide with % converted to dialdehyde units, the ino7anate compound can be converted into polysaccharide.
*JEL SE has discovered that it is possible to obtain a sheet with excellent water resistance and adhesion properties.
すなわち、本発明は、水#性會JiKA分子を含む水−
液に、ダルコース単位群の50〜10口Nがジアルデヒ
ド単位−に転化されたボ菅ナツカフィドおよび/または
その一導体とインシアネート系化合豐またはイノシアネ
ート系重合物とを配合して祷られる耐水性**削で、こ
れによりポリビニルアルコールの水酸基とインシアネー
ト基の蝋橋反応、ポリサッカ2イドの水酸基とイソシア
ネート基との反応、ポリビニルアルコールやポ曽ナツカ
ツィドの水酸基とアルデヒド基との架橋反応、さらにイ
ノシアネート化會愉が水と反応して生じた尿素化會吻と
アルデヒド基との反応等が平列的Kmこり、優れた耐水
装着性能が発揮されるものである。That is, the present invention provides a water-based compound containing water-based JiKA molecules.
Water resistance achieved by blending bosuga natucapide in which 50 to 10 units of the dulcose unit group are converted into dialdehyde units and/or its conductor and an inocyanate compound or an inocyanate polymer. By cutting the hydroxyl group of polyvinyl alcohol and inocyanate group, the reaction of the hydroxyl group of polysaccharide and isocyanate group, the crosslinking reaction of the hydroxyl group of polyvinyl alcohol and porcelain and aldehyde group, and furthermore The reaction between the inocyanate group and the aldehyde group, which is generated by the reaction of the inocyanate group with water, causes a parallel Km reaction, which results in excellent water-resistant mounting performance.
従って、本発−の豪看剤は、イソシアネート化會吻の1
1iJII量が少量でよく、また、そのために陽圧時に
おける島黴への付着をなくすことができる。Therefore, the advanced drug of the present invention is suitable for the first part of the isocyanation process.
The amount of 1iJII may be small, and therefore adhesion to island mold during positive pressure can be eliminated.
本発明の優層剤に用いられる水*a會成^分子としては
、ポリビニルアルコールおよび/またはその一導体がM
隣的に−1また礪々の晶質のものが入手しやすいという
点でも、WK3iIましいが、そのはかにポリアクリル
ア建ド、ポリアクリル−またはそのアルカリ塩類、ポリ
ビニルピロリドン、ポリエチレンイミン、α−オVフィ
ンと無水マレイン酸との共重合響またはそのアルカリ塩
類等のごとき水浴性酋成蟲分子も使用でき、また、それ
らの中から選ばれた24以上な編付したものでも差支え
ない。As the water *a association^ molecules used in the superior layer agent of the present invention, polyvinyl alcohol and/or one conductor thereof is M
Adjacent to -1, WK3iI is also preferable in that it is easy to obtain many crystalline products, but it is far more preferable to use polyacrylic acid, polyacrylic acid, or its alkali salts, polyvinylpyrrolidone, polyethyleneimine, Water bathing molecules such as a copolymer of α-V fin and maleic anhydride or alkali salts thereof can also be used, and 24 or more knitted molecules selected from them may also be used.
また、本発明でいプポリサツカライドとは1反応に必要
な一優したヒドロキシル1なイする−のであれが従来か
ら用いられているポリサッカライドの如何なる−のでも
よいが、通常便用されるものとしては、と54ろこし、
馬−IF、f#ai、小麦、米、サゴ、タピオカ、ツル
ガム等のごとき1lIllI源から得られる#粉、アラ
ビアガム、トラガカ/トガム、グアガム、ローカストビ
ーンガム等のごとき天然より處するガム質、セルロース
、デキストリン、アルギン、イヌリンの中から選ばれた
1櫨ま1こは211以上の重合物等がある。In addition, the polysaccharide used in the present invention refers to the primary hydroxyl required for one reaction, so it may be any conventionally used polysaccharide, but it may be any polysaccharide that is commonly used. As for things, 54 rokoshi,
Horse-IF, f#ai, #flour obtained from sources such as wheat, rice, sago, tapioca, turgid gum, etc., natural gums such as gum arabic, tragaca/togum, guar gum, locust bean gum, etc.; There are polymers of 211 or more selected from cellulose, dextrin, algin, and inulin.
また、ダルコース単位群の50〜100Xがジアルデヒ
ド単位群に転化したポリサッカライドとは、通常、これ
らのポリサッカ2イドを逼璽り木酸またはその塩で旭1
することにより、これらポリサッカ2イドが有するグル
コース単位−の50〜100Xをジアルデヒド単位群に
転化させた−のである。In addition, polysaccharide in which 50 to 100X of the dulcose unit group is converted to a dialdehyde unit group is usually referred to as a polysaccharide in which these polysaccharides are entrapped and treated with Asahi 1 with wood acid or its salt.
By doing so, 50 to 100X of the glucose units possessed by these polysaccharides were converted into dialdehyde units.
この−、ジアルデヒド単位−への転化の割合は50〜1
00%−遣轟であるが、なかで−70〜100%転化し
た−のがrLL性に優れており、耐水接着性簡な十分脅
憚す ゛る意味で41に好ましい。The rate of conversion to -, dialdehyde units - is 50 to 1
00% conversion, but 41 is preferable in the sense that 70 to 100% conversion is excellent in rLL properties and has easy water-resistant adhesion and is sufficiently threatening.
また、本II@でいうポリサッカ2イド#導体とは、前
記したポリサッカライドのエステル化書、エーテル化書
、グツ7ト化物、酸化書のほか、#素、値生1等により
て@虐することにより部分分解もしくは再配列した−の
等がある。In addition, the polysaccharide #conductor referred to in Book II@ refers to the above-mentioned polysaccharide esterification book, etherification book, gutsu7to compound, oxidation book, as well as # element, value production 1, etc. There may be partial decomposition or rearrangement of - and so on.
さらに、本発明において使用するイソ7アネート系化會
吻またはその重曹1は、−Vフレメンな−るものであれ
ば例でもよく、例えば、トリレンジイソシアネート、ジ
フエエルメタンジイノシアネート、へ1?ナメチレ/ジ
イソVアネート、dfクリデ7ジイノシアネート、ナツ
メV/ジイソシアネート等の1ソシア専−トル合一およ
びこれらイソシアネート化會書とインシアネートj&に
対してrk4&な水嵩をMする化合吻との!LL12が
遍蟻である。Furthermore, the iso7anate-based compound or its sodium bicarbonate used in the present invention may be any of -V-Flemen, for example, tolylene diisocyanate, difermethane diinocyanate, and H-1? The combination of 1 socia-specific compounds such as Namethyle/diiso V anate, df Clide 7 diinocyanate, Jujube V/diisocyanate, etc., and the combination of these isocyanate formulas and a compound that increases the water volume of rk4& for inocyanate j&! LL12 is an ant.
本発明の耐水性**剤は、通常、1〜50重量%一度の
水−憔金成島分子水M波100皿agに周し、ダルコー
ス単位群の50〜100+Xがジアルデしド単位−に転
化されたポリサッカライドおよび/またはその締導体を
1〜50重量部、好ましくは1〜sO重重廊を粉末状の
まままたは水1w液の状態で趣え、さらにイソシアネー
ト系化合書の1〜50重量部、好ましくは1〜10重j
isを攪拌しながら加え、均一な分款状−とする方法に
よって開運される。The water-resistant ** agent of the present invention is usually 1 to 50% by weight once passed through a 100 plate ag of Narushima molecular water M wave, and 50 to 100+X of the darcose unit group is converted to dialde unit -. 1 to 50 parts by weight of the polysaccharide and/or its conductor, preferably 1 to 50% by weight, as a powder or in a solution of 1 wt of water, and 1 to 50 parts by weight of an isocyanate compound. , preferably 1 to 10 times
It is prepared by adding is while stirring and making it into uniform crumbs.
さらに、この接着剤に対して小威験、大虞看、低温属鮨
大!看、と5もろこしを、米を等のごとき置物粉を増量
剤として加えたり、メルI、クレー、ベントナイト、巌
鍛マダネンウム、 mailカルシウム、石と5、二酸
化ケイ素、値−バリウム、本旨、ヤン」Lクルを威幹等
のごと1充填剤を任意に龜1してもよい。In addition, this adhesive has a small test, a large warning, and a low-temperature sushi large! Add 5 sorghum, rice, etc. as a bulking agent, mel I, clay, bentonite, gantennium, mail calcium, stone 5, silicon dioxide, value - barium, main purpose, yang. You may optionally add 1 filler to 1 filler per weight.
また、必要に応じ℃、ステレノブタジェンラバー2テツ
タス、アクljaニトリルブタジエンラパークテツクス
、り■−ルン2パーラテックス、イソグレン?/(−2
?2クス、天然ゴムラテックス等のごとき水性ラテック
スあるいはそれらのカルボ中シル化*咎、従来公知の水
性2テツIスな任意の濾−一することもできる。In addition, if necessary, ℃, Stereobutadiene Rubber 2 Tetsutas, Acrylja Nitrile Butadiene Rapaque Tetsu, Ri■-Run 2 Per Latex, Isogrene? /(-2
? It is also possible to use any conventionally known aqueous latex, such as aqueous latex, natural rubber latex, etc., or carboxylates thereof.
不角−の優潰肩を用いて木材や紙を接層した場合、優看
愉を長時間冷水に&潰しても、また煮沸水中に4啼閾〜
72時間凌績して一剥−することがなく、優れた耐水*
*m*度が帰られるのみならず、合板等を潰遣する一〇
鵬圧時K11fi剤の浸出に基づ<S板への付着をなく
すことができる。When wood or paper is layered using Fukkaku's excellent crushing shoulder, even if it is submerged in cold water for a long time and crushed, it will not last until 4 hours in boiling water.
Excellent water resistance that lasts for 72 hours without peeling*
Not only can the *m* degree be reduced, but also the adhesion to the <S board can be eliminated based on the leaching of the K11fi agent when crushing plywood, etc.
次に本発明の夷纏例な示す。Next, an example of implementation of the present invention will be shown.
夷膳iqt
■ホリヒニルアルコール(bJLククレ51、PVA−
117)の10′IILム鳥水−波、■イノブチレン・
無水マレイ/ml共重會mjil(dりyvs、I80
RAM−Q4 )F)ア/4にエクム塩の10重盪X水
m*、■ポリエチレンイぜ/の1031皿%水−液(日
本績媒化宇工業1組P−1000)、■N−メチロール
アクリルアンド重含金t14整して過嘘−アン彎二りム
α2tを1え60℃で2時間反応して員造した−の)、
七各々100重量部とり、それらの各々に、ジアルデに
ド#11(日本カーリットα属、カルメス5号、ジアル
デヒド転化率80%)’)場末5重量部、炭酸カルシウ
ム(白石工業α顧、ホワイトンP−40)40重創り小
麦看(日清勇看ル展、赤化)5重量部、およびジ7エエ
ルメI/シイyクアネート系の簾會−(日本ポリウレタ
ン1員、ミリオ専−IMR)5重量部を攪拌しながら1
え、櫓−に晶會して本発明の耐水11に緩層層を得た・
−万、対照として、ジアルデLドIIl#I#′kII
Ii遍しなか9たほかは夷jII例1と同様にして磯着
剤を得た。Izen iqt ■ Holihinyl alcohol (bJL Kukure 51, PVA-
117) 10'IIL M Chosui-Nami, ■ Inobutyren・
Malay anhydride/ml co-polymerized mjil (dyvs, I80
RAM-Q4) F) A/4 10x water m* of Ecum salt, ■1031 plate% water solution of polyethylene oxide (Nippon Kai Kogyo 1 set P-1000), ■N- Methylol acrylic and heavy metal-containing T14 were prepared by reacting 2T at 60°C for 2 hours to create a structure).
Take 100 parts by weight of each of 7, and add to each of them 5 parts by weight of dialdehyde #11 (Japan Carlit α, Carmes No. 5, dialdehyde conversion rate 80%), 5 parts by weight of calcium carbonate (Shiraishi Kogyo α, white) P-40) 40 parts by weight of heavy wheat (Nissin Yukan Le Exhibition, Red), and 5 parts by weight of Di7 Elume I/Ciy Quanate series (Japan Polyurethane 1 member, Mirio Sen-IMR) 5 1 part by weight while stirring
Eh, a loose layer was obtained in the water resistant 11 of the present invention by crystallization on the turret.
-10,000, as a control, Gialde L de IIl#I#'kII
An isoadhesive agent was obtained in the same manner as in Example 1 except for the difference between I and II.
このよ5にして得られた各lIj剤を台々厚さz5■の
ラワ/*@の両画に111m11層轟たりlS0f/w
tの開会で塗付し、その麿付−上に厚Sα8■の2ワン
率at繊一方向が亙いに直交するように慮ね會すせて1
0即/−の圧力で20分関仮圧−した。Each of the lIj agents obtained in step 5 was layered in 111 m and 11 layers on both sides of Rawa/*@ with a thickness of z5■ lS0f/w
Apply it at the opening of t, and then apply a 2-one rate at fiber with a thickness of Sα8mm on top of it, making sure that one direction is perpendicular to the other.
Temporary pressure was applied for 20 minutes at a pressure of 0/-.
その後、120CK保ったホットブレスに挿入し【8穆
/−の圧力で15分間熱圧して試料音板を製造した。Thereafter, it was inserted into a hot press maintained at 120 CK and hot pressed for 15 minutes at a pressure of 8 m/- to produce a sample tone plate.
このよ5KL?4られた試料音板をj1@下に1透間装
置した後、JA11m合板嵐暢の試験機に従りて豪雪*
*を一定した。Is this 5KL? After placing the test sample sound plate 4 under the J1 @ 1-hole device, heavy snow was applied according to the JA11m plywood Arannobu testing machine.
* was kept constant.
七の線系を次真に示す。The line system of seven is shown below.
なお、4)試料金板とも熱圧時に熱板へ付着すること+
1全くなかつたO
9−
α纒、ネワイトンP−40)40重鰍鵠、ヘキナメテレ
ンジイノVア卑−ト(試薬)5富量跡を1えてよく晶脅
し、耐水tiii着剤を得た。In addition, 4) Both the sample plate and the sample plate should not adhere to the hot plate during hot pressure.
1 completely free of O 9-alpha, Newton P-40) 40 heavy porcupines, hekinametelenediino V-a-base (reagent) 5 traces of richness were thoroughly crystallized, and a water-resistant tiii adhesive was obtained. .
一方、対雇として、ジアルデヒド鹸看を龜1しなかりた
ほかは実施912と同様にして接着剤を得た。On the other hand, an adhesive was obtained in the same manner as in Example 912, except that the dialdehyde solution was not added.
このよ5Kして碍られた各豪層剤な厚さ25−の2ワン
単板の1111kK111着層蟲たり150F/Itの
割合で塗付し、その愈付自上に厚さα8■のフワン率板
を線繊方向が亙いに直交するよ5に1ね會b(て10#
f/−の圧力で20分間開圧締した。Apply the 1111kK111 adhesion layer of 25-thick 2-inch veneer to the layer of 1111kK111 at a rate of 150F/It, and apply a layer of α8mm thick to the surface of the 5K layer. Set the ratio plate so that the fiber directions are perpendicular to each other.
Open clamping was carried out for 20 minutes at a pressure of f/-.
その優、120℃に憬りたホットブレスに挿入して84
/−の圧力で15分間熱圧して賦糾置板&負遺した。That Yuu inserts it into the hot breath that has cooled to 120℃ and 84
It was hot-pressed for 15 minutes at a pressure of /- and then placed on a plate.
この試料合板を富内に1遍14mIILc伏、JAal
lll會IN規格の試験流に疵コ(磯着羞度を一菫した
。This sample plywood was placed in Tominai once with 14 mIILc, and JAal
There were some flaws in the test flow of the llll meeting IN standard.
その績糸を次表に示す。The yarns are shown in the table below.
集線p4五
1ソプチレン・黒水マレイノ鐘共重會111Jil(K
Aタフレ顧、IIOBAM −Q6 )のアyモエクム
塩の5重量%水s*ioo東慮Sに、ジアルデヒド澱粉
の30重量X水fII痕(日亭カーリットa員、カルメ
スO−5>20真量−、スチレンプ!ジエノクパークテ
ツタス(a本命JilEコAKKJIl、−y s *
φ0692 )50重量鄭、タルタ30重量博、Hよび
クルR威1110重量i11を1えて均一に1會し、さ
らに、トラレンジイソシアネート(試瘍)5重量Ilを
−1して均一になるまで攪拌を続は本発明の耐水性−着
剤を得た。Collection line p451 Soptyren/Kurosui Mareino Kane Joint Society 111 Jil (K
Add 5% water by weight of Aymoecum salt (IIOBAM-Q6) to 30% water by weight of dialdehyde starch (IIOBAM-Q6) and add 30% by weight of dialdehyde starch Quantity -, styrenep! Dienok parktetutus (a favorite JilEko AKKJIl, -y s *
φ0692) Add 50 weight of Zheng, Tarta 30 weight of H, H and Kururu Rwei 1110 weight of i11 and mix uniformly.Furthermore, add 5 weight of Tolene diisocyanate (sample) -1 and stir until uniform. Next, a water-resistant adhesive of the present invention was obtained.
一方、対癩として、ジアルデヒド澱樹を*mLなかりた
はかはIIJII儒5と同機にして曇看Mな慢た。On the other hand, as an anti-leprosy drug, I was arrogant to use dialdehyde starch at the same time as IIJII Yu 5.
このよ5Kして傅られたI!着剤を厚さ10■のカバ材
に150F/wt(片自)の−會で麿付し、さらに厚さ
10■onパ材を重ね會b−tて慮1下、10峙/−の
圧力で6Q分間圧−した。I was defeated by this 5K! The adhesive was applied to birch wood with a thickness of 10 cm at a rate of 150 F/wt (one side), and then a layer of birch wood with a thickness of 10 cm was layered at a rate of 150 F/wt (one side). Pressure was applied for 6Q minutes.
II層1lk1遍関麿内に装置してからJIB、K−4
852に準じてff1llせん−II瘤領さを一定した
。JIB, K-4 after installing the equipment in the II layer 1lk1
In accordance with 852, the ff1ll-II aneurysm area was made constant.
その1111j&を次表に示す。The 1111j& is shown in the following table.
以上の細事から本発明の接着剤は耐水擬着性能が開成と
優れていることがわかるFrom the above details, it can be seen that the adhesive of the present invention has excellent water-resistant adhesion performance.
Claims (2)
ス単位#050〜100%がジアルデヒド単位#に転化
されたポ9+ツカフィトおよび/またはそO#4体と、
イノシアネート系化會物または1ノシアネ一訃畢重會物
とt配食して成る耐水性接着剤。(1) In the water that meets the water #I11 chemical molecules, a po9+tukaphyte and/or its O #4 body in which 50 to 100% of glucose units #0 are converted to dialdehyde units #,
A water-resistant adhesive formed by adding an inocyanate compound or a heavy compound of inocyanate.
その#導体、ポリアタリルア(ド、ポリアクリル鑓ま=
はそのアルカリ塩舗、ポ2リビニルピロνドン、ポ9罵
テレンイミン、α−オレフィンと無水マレイノ鏡との共
重合1またはそのア**’)#1事の中から選ばれた1
sまたは2櫨以上の1會吻である特軒−求の聰噛才(1
)項記−の耐水**2a剤・(2) ポνナツカツイド
がと5もろこし、馬鈴薯、t−1小麦、米、?ゴ、タピ
オカ、ンルガム等のごと電植411Il−から萄られる
#粉、アラビアガム、トクガカントガム、ダアガム、ロ
ーカストビーンガ五等のごとき天然より處するガム質、
セルロース、デ中ストリノ、アルギン、イメリンの中か
ら迩ばれた16117:は2種以上の墨會1である骨#
vn求の11層才(1)項または才(2)at起義の耐
水性接着剤。(2) One molecule of water is the conductor of polyvinyl alcohol, and polyacrylic is the conductor of polyvinyl alcohol.
Copolymerization of alkali salts, polyvinyl pyro νdone, polyteleneimine, α-olefins and anhydrous maleino mirrors 1 or 1 selected from #1
s or 1 proboscis of 2 or more proboscises - Tokuken no Sokakusai (1
)Waterproof **2a agent in item - (2) Potato 5 sorghum, potato, t-1 wheat, rice, ? Powder grown from electroplants such as gourd, tapioca, and gum, gum arabic, gum arabic, gum daa, locust bean gum, etc.
16117: is a bone # that is a combination of two or more types of cellulose, detrino, algin, and imeline.
A water-resistant adhesive based on 11 layers of vn (1) or (2) at.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10917381A JPS5811575A (en) | 1981-07-13 | 1981-07-13 | Water-resistant adhesive |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10917381A JPS5811575A (en) | 1981-07-13 | 1981-07-13 | Water-resistant adhesive |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5811575A true JPS5811575A (en) | 1983-01-22 |
JPS6110510B2 JPS6110510B2 (en) | 1986-03-29 |
Family
ID=14503501
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10917381A Granted JPS5811575A (en) | 1981-07-13 | 1981-07-13 | Water-resistant adhesive |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5811575A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6531323B1 (en) | 1999-01-28 | 2003-03-11 | Fuji Photo Film Co., Ltd. | Agglutination assay method and element in a dry system |
US7166476B2 (en) | 2000-08-29 | 2007-01-23 | Kyowa Medex Co., Ltd. | Highly reproducible agglutination immunoassay method and reagents |
KR100714986B1 (en) * | 2001-05-02 | 2007-05-09 | 박준석 | Door Flame |
JP2008545042A (en) * | 2005-07-01 | 2008-12-11 | アクゾ ノーベル コーティングス インテルナショナール ベー.ファオ. | Adhesive composition and method |
WO2010137532A1 (en) | 2009-05-29 | 2010-12-02 | チッソ株式会社 | Detection method and quantification method of detection target |
US8815518B2 (en) | 2006-06-30 | 2014-08-26 | Jnc Corporation | Kit for detection/quantification of analyte, and method for detection/quantification of analyte |
CN115584237A (en) * | 2022-11-01 | 2023-01-10 | 西南林业大学 | Biomass wood adhesive and preparation method and application thereof |
-
1981
- 1981-07-13 JP JP10917381A patent/JPS5811575A/en active Granted
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6531323B1 (en) | 1999-01-28 | 2003-03-11 | Fuji Photo Film Co., Ltd. | Agglutination assay method and element in a dry system |
US7166476B2 (en) | 2000-08-29 | 2007-01-23 | Kyowa Medex Co., Ltd. | Highly reproducible agglutination immunoassay method and reagents |
KR100714986B1 (en) * | 2001-05-02 | 2007-05-09 | 박준석 | Door Flame |
JP2008545042A (en) * | 2005-07-01 | 2008-12-11 | アクゾ ノーベル コーティングス インテルナショナール ベー.ファオ. | Adhesive composition and method |
US8815518B2 (en) | 2006-06-30 | 2014-08-26 | Jnc Corporation | Kit for detection/quantification of analyte, and method for detection/quantification of analyte |
WO2010137532A1 (en) | 2009-05-29 | 2010-12-02 | チッソ株式会社 | Detection method and quantification method of detection target |
CN115584237A (en) * | 2022-11-01 | 2023-01-10 | 西南林业大学 | Biomass wood adhesive and preparation method and application thereof |
CN115584237B (en) * | 2022-11-01 | 2023-11-28 | 西南林业大学 | Biomass wood adhesive and preparation method and application thereof |
Also Published As
Publication number | Publication date |
---|---|
JPS6110510B2 (en) | 1986-03-29 |
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