JPS59106932A - Method of rapid bonding of solid substance - Google Patents
Method of rapid bonding of solid substanceInfo
- Publication number
- JPS59106932A JPS59106932A JP21548382A JP21548382A JPS59106932A JP S59106932 A JPS59106932 A JP S59106932A JP 21548382 A JP21548382 A JP 21548382A JP 21548382 A JP21548382 A JP 21548382A JP S59106932 A JPS59106932 A JP S59106932A
- Authority
- JP
- Japan
- Prior art keywords
- binder
- solid substance
- water
- spreaded
- base plate
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/302—Water
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Dry Formation Of Fiberboard And The Like (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は弾性または剛性結合体を得るため、粉状、粒状
またはそれらの混合固形物をバインダーによシ急速に結
合する方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for rapidly bonding powdered, granular or mixed solids with a binder in order to obtain elastic or rigid bonds.
分子末端にイソシアネート基を有するプレポリマー及び
有機ポリイソシアネートは空気中の湿気と反応して樹脂
状またはゴム状となシ、またインシアネート基は加硫ゴ
ム、ポリウレタン樹脂などの粉砕物、木屑、砂等広範囲
にわたる有機及び無機系固形物の表面活性点と反応し強
固に接着する。Prepolymers and organic polyisocyanates that have an isocyanate group at the end of the molecule react with moisture in the air and become resinous or rubbery. It reacts with the active sites on the surface of a wide range of organic and inorganic solid materials, and forms a strong bond.
1−
従ってこの性質をバインダーとして利用した例としてハ
、タイヤ、クッション、シート、バンパーのようなゴム
、塩化ビニル、ポリウレタン等からなる高分子成形品の
破砕物、木屑、コルク粉、もみがら、砂、その他の粉状
または粒状固形物を接着し、得られた弾性または剛性結
合体は床材、テニスコート、競技場、歩道などの舗装材
として使用されている。1- Therefore, as an example of using this property as a binder, c. Rubber such as tires, cushions, seats, bumpers, crushed polymer molded products made of vinyl chloride, polyurethane, etc., wood chips, cork powder, rice husk, sand. , and other powdered or granular solids, and the resulting elastic or rigid composites are used as paving materials for flooring, tennis courts, stadiums, sidewalks, etc.
これらのイソシアネート系バインダーを使用して前記粉
状、粒状またはその混合固形物を接着させる方法と尤で
は、これらの固形物をバインダーと混合し、固形物衣直
にバインダーをできるだけ均一に付着させた稜、基盤上
に広げ展圧するいわゆる現場施工法か、またはこれを型
に入れプレス成形して舗装材を製造するいわゆる予備成
形法による。A method of adhering the powdered, granular, or mixed solid materials using these isocyanate-based binders involves mixing these solid materials with a binder and adhering the binder as uniformly as possible to the solid material. There is a so-called on-site construction method in which the paving material is spread and pressed onto the ridge or base, or a so-called preforming method in which the paving material is manufactured by placing it in a mold and press-forming it.
この現場施工法においては、付着物が硬化し使用できる
ようになるには一般に12時間以上を要するため、工事
の際には施工場所の使用を一定期間休まねばならない。In this on-site construction method, it generally takes 12 hours or more for the deposit to harden and become usable, so the construction site must be closed for a certain period of time during construction.
この点は運動施設の運営上2− 重大な問題となるため改善を強く要望されていた。This point is important for the management of sports facilities. Improvements were strongly requested as this was a serious problem.
本発明者らはインシアネート系バインダーの可使時間を
十分保持したまま、施工稜の硬化を急速に進行させる方
法について種々検討を行った結果本発明に到達した。The present inventors conducted various studies on a method for rapidly progressing the hardening of the construction ridge while maintaining a sufficient pot life of the incyanate binder, and as a result, the present invention was arrived at.
即ち、本発明は次の通シである。That is, the present invention is as follows.
分子末端にインシアネート基を有するプレポリマー、有
機ポリインシアネートまたはこれらの混合物からなるバ
インダーを、粉状または粒状の固形物に付着させ、基盤
上に拡げ、展圧し硬化させるに際し、水の存在下で展圧
することを特徴とする該固形物の急速結合方法。A binder consisting of a prepolymer, an organic polyincyanate, or a mixture thereof having an incyanate group at the molecular end is attached to a powder or granular solid, spread on a substrate, spread under pressure, and cured in the presence of water. A method for rapidly bonding solid materials, characterized by applying pressure.
本発明はバインダーの付着した粉状、粒状またはそれら
の混合固形物に水を添加した後、プレス例えば常温また
は加熱ロールによシ展圧することによシ始めて目的を達
し得るのであって、水を散布せずに加熱ロールで展圧し
た場合には硬化速度が遅い。The purpose of the present invention can be achieved only by adding water to a powder, granule, or solid mixture thereof to which a binder is attached, and then applying pressure by pressing, for example, at room temperature or with a heated roll. If the adhesive is rolled out using a heated roll without being sprayed, the curing speed will be slow.
本発明において使用する水は、ノ(インダー中のインシ
アネート基に対し一般に大過剰に使用する。The water used in the present invention is generally used in large excess relative to the incyanate groups in the inder.
水の添加は、バインダーの付着した固形物を基盤上に拡
げる前または拡げた後に行う。Water is added before or after the solid material to which the binder is attached is spread on the substrate.
水には必要に応じ触媒を添加することもできる。A catalyst can also be added to the water if necessary.
その際使用する触媒は例えばトリエチレンジアミン、ビ
スジメチルアミノエチルエーテル、ジブチル錫ジラウレ
ート、オクタン酸銀々ど通常のウレタン用触媒ならば何
れでもよい。The catalyst used in this case may be any common catalyst for urethane, such as triethylene diamine, bisdimethylaminoethyl ether, dibutyltin dilaurate, and silver octoate.
また例挙する加熱ロールを使用する場合にはその温度は
110℃までが適当で、これよシ高い場合にはバインダ
ーが分解する危険がある。Further, when using the heating roll mentioned above, it is appropriate that the temperature be up to 110°C; if the temperature is higher than this, there is a risk that the binder will decompose.
ウレタン系舗装材料を施工する場合は通常15℃以上の
気温を必要とし、冬期は施工が困難である。然るに本発
明の方法によれば、10℃以下の気温例えば5℃におい
ても急速硬化が行えるため、冬期においても施工ができ
ることは大きな特徴である。When constructing urethane-based paving materials, a temperature of 15°C or higher is usually required, making construction difficult in winter. However, according to the method of the present invention, rapid curing can be performed even at a temperature of 10° C. or lower, for example, 5° C., so a major feature is that construction can be performed even in winter.
本発明のバインダーに使用する有機ポリイソシアネート
は、2.4−)リレンジイソシアネート、2.6−)リ
レンジイソシアネート、この両インシアネートの80/
20または65/35重量比の混合物、ジフェニルメタ
ンジイソシアネート、特公昭38−4576など従来公
知の種々の方法で液状化したいわゆる液状ジフェニルメ
タンジイソシアネート、トリレンジイソシアネートの粗
製物、ポリメチレンポリフェニルポリインシアネート(
ジフェニルメタンジイソシアネートの粗製物)寿ど従来
公知の芳香族ポリイソシアネート、ジシクロヘキシルメ
タンジイノシアネート、イソホロンジイソシアネートな
ど従来公知の脂肪族イソシアネートの一種又は二種以上
の混合物である。The organic polyisocyanates used in the binder of the present invention include 2.4-) lylene diisocyanate, 2.6-) lylene diisocyanate, and 80% of both incyanates.
20 or 65/35 weight ratio mixture, diphenylmethane diisocyanate, so-called liquid diphenylmethane diisocyanate liquefied by various conventionally known methods such as Japanese Patent Publication No. 38-4576, crude product of tolylene diisocyanate, polymethylene polyphenyl polyinsyanate (
(crude product of diphenylmethane diisocyanate) It is one or a mixture of two or more of conventionally known aliphatic isocyanates such as aromatic polyisocyanate, dicyclohexylmethane diinocyanate, and isophorone diisocyanate.
これらのポリイソシアネートは本発明の分子末端にイン
シアネート基を有するプレポリマーの製造にも使用し得
る。These polyisocyanates can also be used in the production of prepolymers having inocyanate groups at the molecular ends of the present invention.
これらのポリイソシアネートと反応しポリウレタンプレ
ポリマーを製造する際に使用するボリオールハクリセリ
ン、トリメチロールプロパン、ペンタエリスリトール等
の多価アルコール類、水、エチレングリコール、プロピ
レングリコール、グリセリン、ペンタエリスリトール、
ソルビット、蔗糖等の多価アルコールにプロピレンオキ
サイド5−
又はプロピレンオキサイドとエチレンオキサイドとを付
加重合して得たポリエーテルポリオール類、ポリテトラ
メチレンエーテルグリコール類、ポリカプロラクトンポ
リオール類、ポリエチレンアジペートのようなポリエス
テルポリオール類、ポリブタジェンポリオール類、ひま
し油のようなヒドロキシル基を含む高級脂肪酸のエステ
ル類、ポリエーテルポリオールまたはポリエステルポリ
オールにビニルモノマーをグラフトして得たポリマーポ
リオール類である。Polyhydric alcohols, water, ethylene glycol, propylene glycol, glycerin, pentaerythritol, polyols used when producing polyurethane prepolymers by reacting with these polyisocyanates, such as polyacrycerin, trimethylolpropane, and pentaerythritol.
Polyesters such as polyether polyols, polytetramethylene ether glycols, polycaprolactone polyols, and polyethylene adipate obtained by addition polymerization of propylene oxide 5- or propylene oxide and ethylene oxide to polyhydric alcohols such as sorbitol and sucrose. These are polyols, polybutadiene polyols, esters of higher fatty acids containing hydroxyl groups such as castor oil, and polymer polyols obtained by grafting vinyl monomers onto polyether polyols or polyester polyols.
分子末端にイソシアネート基を有するポリウレタンプレ
ポリマーを製造する際にはポリインシアネートとポリオ
ールをNC010H当量比1・5−10、反応温度60
−130℃で公知の方法により反応させる。反応に当っ
てはジブチル錫ジラウレートなどの公知の触媒を使用し
ても差支えない。When producing a polyurethane prepolymer having an isocyanate group at the molecular end, the polyincyanate and polyol are mixed at a NC010H equivalent ratio of 1.5-10 and a reaction temperature of 60.
The reaction is carried out at -130°C by a known method. In the reaction, a known catalyst such as dibutyltin dilaurate may be used.
またバインダーを固形物に付着させ、基盤上に拡げ、展
圧するまでの可使時間を延長し、作業をやシ易くするた
めに有機酸ノ・2イドをバインダーに対し0.1−10
重量%添加することもできる。In addition, in order to extend the pot life until the binder is attached to a solid material, spread on a substrate, and rolled out, and to make the work easier, organic acid 2-ide is added to the binder at a concentration of 0.1-10%.
It can also be added in weight percent.
6−
このバインダーの粘度が高すぎる場合には、アセトン、
メチルエチルケトン、酢酸エチル、トルエン、などの溶
剤を添加することができ、また必要に応じて充填剤、着
色剤などを添加することもできる。6- If the viscosity of this binder is too high, acetone,
Solvents such as methyl ethyl ketone, ethyl acetate, toluene, etc. can be added, and fillers, colorants, etc. can also be added as necessary.
固形物とバインダーの混合比率は99/1〜60/40
重量比が好ましく、とくに9515〜75/25重量比
が推奨される。The mixing ratio of solids and binder is 99/1 to 60/40
A weight ratio of 9515 to 75/25 is particularly recommended.
本発明を適用するには、先づ所定量のバインダーと固形
物とを十分混合する。バインダーの付着した固形物にさ
らに水を加えて混合し基盤上に拡げるか、またはバイン
ダーの付着した固形物を基例えば口〜ルで展圧すれば、
付着物は数10分〜3時間で硬化完了し、施工面は直ち
に使用を開始することができる。従って本発明の方法に
よれば、運動施設の舗装工事を夜間実施し翌日は朝から
通常通シ舗装面を使用することができる。To apply the present invention, first, a predetermined amount of binder and solid material are thoroughly mixed. If water is added to the solid material to which the binder is attached, the mixture is mixed and spread on the substrate, or the solid material to which the binder is attached is spread on the substrate, for example, by using a mouth-roll.
The deposit is completely cured in several tens of minutes to three hours, and the applied surface can be used immediately. Therefore, according to the method of the present invention, paving work for an athletic facility can be carried out at night, and the paved surface can be used normally from the morning on the next day.
舗装面の硬化度はJIS K−6401に準拠し一定の
高さから鋼球を落下させ、そのはね返り距離と一7=
落下距離との比率%によシ測定する。このはね返シ比率
が20%以上に達すれば舗装面は使用できる。The degree of hardening of a pavement surface is determined by dropping a steel ball from a certain height in accordance with JIS K-6401, and measuring the ratio of the bounce distance to the falling distance (%). If this repulsion ratio reaches 20% or more, the paved surface can be used.
実施例1
ンクリコールとより製造したインシアネート基を有量7
.2重量%のプレポリマー。三井日曹ウレタン株式会社
製品)と粒子の大きさ1〜3mmからなるタイヤゴムチ
ップとを1:4の重量比で攪拌機を用いて混合し、チッ
プの表面にバインダーを均一に付着させた。Example 1 An amount of 7 incyanate groups produced from glycol and
.. 2% by weight prepolymer. Mitsui Nisso Urethane Co., Ltd. product) and tire rubber chips having a particle size of 1 to 3 mm were mixed at a weight ratio of 1:4 using a stirrer, and the binder was uniformly adhered to the surface of the chips.
バインダー中のイソシアネートに対し16倍当量の水を
この付着物に添加し良く混合した後、30±1℃、相対
湿度70±10%の室内で平板上にならした。Water in an amount equivalent to 16 times the amount of isocyanate in the binder was added to this deposit, mixed well, and then smoothed onto a flat plate in a room at 30±1° C. and relative humidity of 70±10%.
次にこれを30℃のロールで展圧した場合の硬化時間は
1.5時間であった。 また100℃の加熱ロールで展
圧した場合の硬化時間は0.5時間であった。100℃
のロールで展圧した場合の硬化8−
後の物性は、100%モジュラス13 kf/am”、
引張強さ14 kW/crr?、伸び130%、引裂強
さ11 kW/cm であった。Next, when this was rolled out using a roll at 30° C., the curing time was 1.5 hours. Further, the curing time was 0.5 hours when the film was rolled out using a heated roll at 100°C. 100℃
The physical properties after curing are 100% modulus 13 kf/am" when rolled with a roll of
Tensile strength 14 kW/crr? , elongation was 130%, and tear strength was 11 kW/cm.
実施例2
実施例1で得た付着物と水との混合物を5±1℃、相対
湿度70±10%の室内で平板の上にならした。Example 2 The mixture of deposits and water obtained in Example 1 was leveled on a flat plate in a room at 5±1° C. and relative humidity 70±10%.
次にこれを5℃のロールで展圧した場合の硬化時間は3
時間であった。硬化後の物性は100%モジュラス10
kf/cm” 、引張シ強さ10 kf/cm−伸び
100%、引裂強さ8 kW/cmであった。Next, when this is rolled out with a roll at 5℃, the curing time is 3
It was time. Physical properties after curing are 100% modulus 10
kf/cm'', tensile strength 10 kf/cm-elongation 100%, and tear strength 8 kW/cm.
比較例1
実施例1において水の添加を行わずに100℃に加熱し
たロールで展圧し、硬化時間を測定したところ、7時間
であった。この舗装面の物性を測定した結果、引張強さ
5 kf/cm” 、引裂強さ5kf/cmとなシ強度
不足であった。Comparative Example 1 In Example 1, rolling pressure was applied using a roll heated to 100° C. without adding water, and the curing time was measured and found to be 7 hours. As a result of measuring the physical properties of this paved surface, the tensile strength was 5 kf/cm" and the tear strength was 5 kf/cm", indicating that the strength was insufficient.
実施例3
実施例1と同じバインダーとポリウレタンエラストマー
のチップを1:4の重量比で攪拌機を用9−
イテ混合し、バインダーをチップの表面に均一に付着さ
せた。この混合物を23±1℃、相対湿度70±10%
の室内で平板の上に15mmの厚さにならし、その上に
水を7.7当量散布した。その後100℃に加熱したロ
ールで展圧し、硬化時間を測定したところ、3時間であ
った。Example 3 The same binder and polyurethane elastomer chips as in Example 1 were mixed at a weight ratio of 1:4 using a stirrer for 9 cycles to uniformly adhere the binder to the surface of the chips. This mixture was heated at 23±1℃ and relative humidity 70±10%.
The mixture was leveled to a thickness of 15 mm on a flat plate in a room, and 7.7 equivalents of water was sprinkled thereon. Thereafter, it was rolled out using a roll heated to 100° C., and the curing time was measured to be 3 hours.
硬化後の物性は100%モジュラス13 kf/cm”
、引張強さ19 kf/cm”、伸び180%、引裂強
さ16 kW/cmであったう
特許出願人
三井日1ウレタン株式会社
10−Physical properties after curing are 100% modulus 13 kf/cm”
, tensile strength of 19 kf/cm", elongation of 180%, and tear strength of 16 kW/cm.
Claims (1)
機ポリイソシアネートまたはこれらの混合物からなるバ
インダーを、粉状または粒状の固形物に付着させ、基盤
上に拡げ、展圧し硬化させるに際し、水の存在下で展圧
することを特徴とする該固形物の急速結合方法。A binder made of a prepolymer, an organic polyisocyanate, or a mixture thereof having an incyanate group at the molecular end is attached to a powder or granular solid, spread on a substrate, spread under pressure, and cured in the presence of water. A method for rapidly bonding solid materials, characterized by applying pressure.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21548382A JPS59106932A (en) | 1982-12-10 | 1982-12-10 | Method of rapid bonding of solid substance |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21548382A JPS59106932A (en) | 1982-12-10 | 1982-12-10 | Method of rapid bonding of solid substance |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS59106932A true JPS59106932A (en) | 1984-06-20 |
Family
ID=16673125
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP21548382A Pending JPS59106932A (en) | 1982-12-10 | 1982-12-10 | Method of rapid bonding of solid substance |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59106932A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6322840A (en) * | 1986-07-14 | 1988-01-30 | Dai Ichi Kogyo Seiyaku Co Ltd | Production of sheet and molding |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54149785A (en) * | 1978-05-12 | 1979-11-24 | Bayer Ag | Method of making elastic laminate * and binder therefor |
| JPS5529550A (en) * | 1978-08-24 | 1980-03-01 | Dainippon Ink & Chem Inc | Reclamation of thermosetting resin wastes |
-
1982
- 1982-12-10 JP JP21548382A patent/JPS59106932A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54149785A (en) * | 1978-05-12 | 1979-11-24 | Bayer Ag | Method of making elastic laminate * and binder therefor |
| JPS5529550A (en) * | 1978-08-24 | 1980-03-01 | Dainippon Ink & Chem Inc | Reclamation of thermosetting resin wastes |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6322840A (en) * | 1986-07-14 | 1988-01-30 | Dai Ichi Kogyo Seiyaku Co Ltd | Production of sheet and molding |
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