JPS60258276A - Water-resistant elastic adhesive - Google Patents

Water-resistant elastic adhesive

Info

Publication number
JPS60258276A
JPS60258276A JP11276284A JP11276284A JPS60258276A JP S60258276 A JPS60258276 A JP S60258276A JP 11276284 A JP11276284 A JP 11276284A JP 11276284 A JP11276284 A JP 11276284A JP S60258276 A JPS60258276 A JP S60258276A
Authority
JP
Japan
Prior art keywords
water
adhesive
component
ethylene
present
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
Application number
JP11276284A
Other languages
Japanese (ja)
Inventor
Seiroku Sasauchi
笹内 清六
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
KINDAI CHISUI CENTER KK
Original Assignee
KINDAI CHISUI CENTER KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by KINDAI CHISUI CENTER KK filed Critical KINDAI CHISUI CENTER KK
Priority to JP11276284A priority Critical patent/JPS60258276A/en
Publication of JPS60258276A publication Critical patent/JPS60258276A/en
Pending legal-status Critical Current

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  • Adhesives Or Adhesive Processes (AREA)

Abstract

PURPOSE:To provide the titled adhesive consisting of the first liquid composed of an ethylene-vinyl acetate copolymer emulsion and the second liquid composed of a polyisocyanate compound, suitable for the production of an elastic mat, the base of a TATAMI mat, etc. having high air permeability and water resistance, and available at a low cost. CONSTITUTION:The objective adhesive can be prepared by mixing (A) an ethylene-vinyl actate copolymer with (B) a polyisocyanate compound in the presence of a proper amount of water. The adhesive is applied to or mixed with an adhered and heated at 140-160 deg.C to obtain a bonded product. The sum of the solid content of the component A and the component B is preferably 40-60(wt)% of the mixture, and the content of water is preferably 60-40%. The weight ratio of the component B to the component A is preferably 0.3-0.6 to 1.

Description

【発明の詳細な説明】 本発明はもみ殻や、コルク細片などの疎水性の微細な粒
子を原料として通気性、耐水性の弾性マット、又は畳床
等を成形するに好適な耐水性および弾性に優れた接着剤
に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides water-resistant and water-resistant materials suitable for molding breathable, water-resistant elastic mats, tatami floors, etc. using hydrophobic fine particles such as rice husks and cork pieces as raw materials. It relates to adhesives with excellent elasticity.

従来、もみ殻のような微細な粒子を原料として。Traditionally, fine particles such as rice husks are used as raw materials.

畳床あるいはじゅうたん下マットなどの耐水性と弾性に
すぐれたマットを成形する場合、適用される接着剤の性
能及びコストには厳しい条件がめられ、今日までこれに
対応出来る接着剤は知られていない。
When molding mats with excellent water resistance and elasticity, such as tatami floor or carpet undermats, strict requirements are placed on the performance and cost of the adhesive used, and to date no adhesive is known that can meet these requirements. .

もみ殻は1本来、疎水性で、腐りにくい特性を有してい
るが、これを圧縮成形して畳床として使用する場合、そ
の形状保持に使用される接着剤には優れた耐水性がめら
れる。即ち、もみ殻を用いて畳床を作製する場合、その
保有する空隙に大気中の湿気が吸収され、時には浸水が
生じたりするため、使用される接着剤は耐水性にすぐれ
たものであることが要求されるが、この耐水性の点から
、従来の尿素系接着剤や酢酸ビニル系接着剤は一般に不
適当である。また、畳床には独特の触感を伴う腰の強い
弾性が要求されるが、この弾性の点から、フェノール樹
脂系や尿素樹脂系の熱硬化性接着剤は不適当である。更
に、もみ殻を用いた畳床の場合、その通気性を保持する
ためには、成形に際し、圧縮比を大にすることができず
、圧縮比はある限定された範囲に保持することが必要で
あるが、この場合には、もみ殻相互の接触密度が小さく
なるため、使用される接着剤にはそれだけ強力な接着力
がめられる。
Rice husks are naturally hydrophobic and do not rot easily, but when compression molded and used as tatami flooring, the adhesive used to hold the shape must have excellent water resistance. . In other words, when making tatami floors using rice husks, moisture in the atmosphere is absorbed by the voids in the tatami mats, which can sometimes lead to water seepage, so the adhesive used must be highly water resistant. However, from the viewpoint of water resistance, conventional urea-based adhesives and vinyl acetate-based adhesives are generally unsuitable. Furthermore, tatami floors are required to have strong elasticity with a unique tactile feel, and from this elasticity point of view, thermosetting adhesives based on phenol resins or urea resins are unsuitable. Furthermore, in the case of tatami floors made from rice husks, in order to maintain their breathability, the compression ratio cannot be increased during molding, and the compression ratio must be kept within a certain limited range. However, in this case, since the contact density between the rice husks is reduced, the adhesive used must have a stronger adhesive force.

一般に、耐水性、弾性に優れ、かつ接着力の強力な接着
剤としては、イソシアネート系、ゴム系、エポキシ樹脂
系の接着剤があるが、これらのものはいずれもコストが
高く、もみ殻畳床作製のような大量処理には適しない上
、粘度が高いために微細粒子に均一な濡れを生じさせる
ことが困難であるという欠点を有する。
In general, there are isocyanate-based, rubber-based, and epoxy resin-based adhesives that have excellent water resistance, elasticity, and strong adhesion, but these are all expensive and do not work well on rice husk tatami floors. It is not suitable for large-scale processing such as manufacturing, and has the disadvantage that it is difficult to uniformly wet fine particles due to its high viscosity.

本発明者は、前記のような事情に鑑み、もみ殻畳床作製
用に好適な接着剤を開発′すべく鋭意研究を重ねた結果
1本発明を完成するに到った。
In view of the above-mentioned circumstances, the present inventor has conducted extensive research to develop an adhesive suitable for making rice husk tatami floors, and has finally completed the present invention.

即ち、本発明によれば、エチレン−酢酸とニル系共重合
体エマルジョンからなる第1液と、ポリイソシアネート
系化合物からなる第2液とから構成される耐水性、弾性
接着剤が提供される。
That is, according to the present invention, there is provided a water-resistant, elastic adhesive comprising a first liquid consisting of an ethylene-acetic acid and nyl-based copolymer emulsion and a second liquid consisting of a polyisocyanate-based compound.

本発明で用いるエチレン−酢酸ビニル系共重合体エマル
ジョンとしては、市販の各種のものが適用され、例えば
、デンカEVAテックス(電気化学工業−社製)等が用
いられる。この場合、共重合体成分には、必要に応じ、
他の成分、例えば、アクリル酸、マレイン酸、フマル酸
等が含まれていてもよい。またポリイソシアネート系化
合物としては、例えば、通常の2個以上のインシアネー
ト基(NGO)を有するインシアネート系化合物、例え
ば、トリレンジイソシアネート(TDI)、ジフェニル
メタンジイソシアネート(MDI)、トリフェニルメタ
ントリイソシアネート(TTI)等が挙げられる。
As the ethylene-vinyl acetate copolymer emulsion used in the present invention, various commercially available emulsions can be used, such as Denka EVA Tex (manufactured by Denki Kagaku Kogyo Co., Ltd.). In this case, the copolymer component may include, if necessary,
Other ingredients such as acrylic acid, maleic acid, fumaric acid, etc. may also be included. Examples of polyisocyanate compounds include ordinary incyanate compounds having two or more incyanate groups (NGO), such as tolylene diisocyanate (TDI), diphenylmethane diisocyanate (MDI), and triphenylmethane triisocyanate ( TTI), etc.

本発明の場合、これらのポリイソシアネート系化合物は
、ポリオールを用いてプレポリマー化したプレポリマー
の形で用いることができる。本発明の場合、このポリイ
ソシアネート系化合物としては、イソシアネート系接着
剤成分として市販されている各種の製品をそのまま用い
ることができる。
In the case of the present invention, these polyisocyanate compounds can be used in the form of a prepolymer prepared using a polyol. In the case of the present invention, various products commercially available as isocyanate adhesive components can be used as they are as the polyisocyanate compound.

本発明の接着剤は、エチレン−酢酸ビニル系共重合体エ
マルジョンを主体にし、これにポリイソシアネート系化
合物を組合せたものである。本発明の接着剤は、使用に
際し、両者を混合して、混合物の形で適用される。この
場合、混合物の組成は、混合物中、エチレン−酢酸ビニ
ル系共重合体(エマルジョン中の固形分)とポリイソシ
アネート系化合物との合計量が30〜80重量%、好ま
しくは40〜60重景%、及び水分が70〜20重量%
、好ましくは60〜40重量%になるよう調節するのが
よい。
The adhesive of the present invention is mainly composed of an ethylene-vinyl acetate copolymer emulsion, which is combined with a polyisocyanate compound. In use, the adhesive of the present invention is applied in the form of a mixture by mixing both. In this case, the composition of the mixture is such that the total amount of the ethylene-vinyl acetate copolymer (solid content in the emulsion) and the polyisocyanate compound is 30 to 80% by weight, preferably 40 to 60% by weight. , and water content is 70-20% by weight.
, preferably adjusted to 60 to 40% by weight.

また、ポリイソシアネート系化合物は、エチレン−酢酸
ビニル系共重合体1重量部に対し、0.1〜0.8重量
部、好ましくは0.3〜0.6重量部の割合で用いるの
がよい。本発明において、エチレン−酢酸ビニル系共重
合体エマルジョンにポリイソシアネート系化合物を添加
する場合、水分量の調節は任意に行うことができ、例え
ば、′ポリイソシアネート系化合物に適量の水を混合し
、この混合物をエチレン−酢酸ビニル系共重合体エマル
ジ5ンに添加混合する方法や、エチレン−酢酸ビニル系
共重合体エマルジョンに水を加え、これにポリイソシア
ネート系化合物を添加混合する方法等を採用することが
できる。
The polyisocyanate compound is preferably used in an amount of 0.1 to 0.8 parts by weight, preferably 0.3 to 0.6 parts by weight, per 1 part by weight of the ethylene-vinyl acetate copolymer. . In the present invention, when adding a polyisocyanate compound to the ethylene-vinyl acetate copolymer emulsion, the water content can be adjusted arbitrarily.For example, 'mixing an appropriate amount of water with the polyisocyanate compound, A method of adding and mixing this mixture to an ethylene-vinyl acetate copolymer emulsion, a method of adding water to an ethylene-vinyl acetate copolymer emulsion, and adding and mixing a polyisocyanate compound thereto, etc. are adopted. be able to.

本発明の接着剤は、長時間を必要とする運搬や保存にお
いては、2液性接着剤として適用され、現場において混
合して用いるのが好ましい。
The adhesive of the present invention is preferably applied as a two-component adhesive during transportation or storage that requires a long period of time, and mixed on site.

本発明の接着剤は、熱架橋型の接着剤であり、対象物に
塗布又は混合した後、120〜180℃、好ましくは1
40〜160℃程度に加熱することにより、接着物を得
ることができる。
The adhesive of the present invention is a thermally crosslinkable adhesive, and after being applied or mixed onto an object, the adhesive is heated to a temperature of 120 to 180 °C, preferably 1
An adhesive can be obtained by heating to about 40 to 160°C.

本発明の接着剤は、従来のものとは異なり、耐水性及び
弾性にすぐれ、しかも安価であるため、殊に、もみ殻の
ような弾性に富む微粒子を原料とし、これから耐水性及
び弾性に富む成形品を得る場合の接着剤として好適であ
る。本発明の接着剤を用いてもみ殻から畳床を得るには
、本発明の接着剤をもみ殻に混和した後、これを多孔加
圧板を用いて上下より加圧し、上下多孔加圧板の一方か
ら他方の多孔加圧に熱風を流通させればよい。この場合
、熱風の温度は140〜150℃程度でよい。
Unlike conventional adhesives, the adhesive of the present invention has excellent water resistance and elasticity, and is inexpensive. In particular, the adhesive of the present invention is made from highly elastic fine particles such as rice husks, and is made from highly elastic particles such as rice husks. It is suitable as an adhesive for obtaining molded products. In order to obtain a tatami floor from rice husks using the adhesive of the present invention, the adhesive of the present invention is mixed with rice husks, and then pressure is applied from above and below using porous pressure plates. Hot air may be passed from the hole to the other porous pressurizer. In this case, the temperature of the hot air may be about 140 to 150°C.

次に、本発明を実施例によりさらに詳細に説明する。Next, the present invention will be explained in more detail with reference to Examples.

実施例1 市販のエチレン−酢酸ビニル共重合体エマルジョン(以
下EVAという)〔商品名:デンカEVA # 60(
電気化学工業製造品)、固形分55%、粘度(cps)
 2500、pH4,5) 200gに、ポリイソシア
ネート〔商品名:コロネートc−3o53(日本ポリウ
レタン製品)、NGO含有量29.4%、粘度240c
p/25℃〕50gと水50gの混合液を配合し、これ
をもみ殻11Q(見かけ比重約0.1)に混和し、熱風
吹抜型試験機(30cm X 30cm、プレス圧力3
kg/c+#)にて5cm厚(畳床規格寸法)に圧縮(
圧縮地組2.2)L、一方の多孔加圧板より他方の多孔
加圧板に熱風(温度140°C1風力0.3kg/cJ
)を5NM37時の風量で約30分間吹き抜けさせて成
形した。次に、耐水試験のため、この成形品を冷水中に
3時間浸漬し、引き上げたが、成形品の容積(4500
cc)に対し空隙への浸水量は約2100ccであり、
水の放出速度は約20分にて1700ccであり1.こ
れを常温で2日間放置すると、含水量は試験開始前の1
50ccとなったが、この間、接着樹脂被膜の崩壊、溶
解或いは溶失を検出せず、また、成形品のふくれ、くず
れなどの変形を生じず、さらに部分的剥離も生じなかっ
た。
Example 1 Commercially available ethylene-vinyl acetate copolymer emulsion (hereinafter referred to as EVA) [trade name: Denka EVA #60 (
manufactured by Denki Kagaku Kogyo), solid content 55%, viscosity (cps)
2500, pH 4,5) 200g, polyisocyanate [Product name: Coronate C-3O53 (Japan Polyurethane Products), NGO content 29.4%, viscosity 240c
p/25℃] and 50 g of water, mixed with rice husk 11Q (apparent specific gravity approximately 0.1), and tested in a hot air blow-out type tester (30 cm x 30 cm, press pressure 3).
Compressed (kg/c+#) to a thickness of 5cm (standard tatami floor dimensions)
Compression ground assembly 2.2) L, hot air (temperature 140°C 1 wind force 0.3 kg/cJ) is applied from one porous pressure plate to the other porous pressure plate.
) was molded by blowing through it for about 30 minutes at an air volume of 5NM and 37 hours. Next, for a water resistance test, this molded product was immersed in cold water for 3 hours and taken out, but the volume of the molded product (4500
cc), the amount of water infiltrating into the void is approximately 2100cc,
The water release rate is 1700cc in about 20 minutes, and 1. If this is left at room temperature for 2 days, the water content will decrease to 1
During this period, no collapse, melting, or dissolution of the adhesive resin coating was detected, and no deformation such as blistering or collapse of the molded product occurred, and no partial peeling occurred.

また、この成形品を乾燥後、再度60℃の温水に3時間
浸漬して引き上げたが、この場合にも殆んど前記の場合
と同様に変化を示さなかった。
Further, after drying, this molded product was immersed in warm water at 60° C. for 3 hours and then pulled out, but in this case as well, almost no change was observed as in the above case.

比較例 実施例1で示したEVA300gをもみ殻11Qに混和
し熱風吹抜型試験機(実施例1と同機)にて5cmに圧
縮Ll&tt(120°C15C15N時)ヲ30分間
吹キ抜ケサセて成形した。得られた成形品は実施例1と
同様に通気性、弾性のある堅固な形状外観を呈したが、
これを耐水試験のため冷水に浸漬したところ、僅か15
分にて接着樹脂被膜は水に溶解して流失し、もみ殻に対
する圧縮力、接着力は失われてふくらみ、30分後には
完全に崩壊した。
Comparative Example 300 g of EVA shown in Example 1 was mixed with rice husk 11Q and compressed to 5 cm using a hot air blow-out test machine (same machine as in Example 1) (120°C, 15C, 15N) for 30 minutes. . The obtained molded product had a strong shape and appearance with air permeability and elasticity as in Example 1, but
When this was immersed in cold water for a water resistance test, it was only 15
Within minutes, the adhesive resin coating was dissolved in water and washed away, lost its compressive force and adhesive force to the rice husks, swelled, and completely disintegrated after 30 minutes.

実施例2 実施例1で示したEVA3600gに実施例1で示した
ポリイソシアネート900gと水900gの混合液を配
合攪拌して、もみがら190Qに混和し、熱風吹抜型実
物大試験機(91cm X 182cm)にて5cm厚
に圧縮し、一方の多孔加圧板より他方の多孔加圧板に熱
風(140°C1C11O0N/時)を30分間吹き抜
けさせて成形した。得られた成形品を実施例1と同様に
耐水試験した結果、実施例1と殆んど同様で抜群の耐水
性を示した。
Example 2 A mixed solution of 3600 g of EVA shown in Example 1, 900 g of polyisocyanate shown in Example 1, and 900 g of water was mixed and stirred, mixed with rice husks 190Q, and heated in a full-scale hot air blower type tester (91 cm x 182 cm). ) and molded by blowing hot air (140°C1C11O0N/hour) through one porous pressure plate to the other porous pressure plate for 30 minutes. The obtained molded product was subjected to a water resistance test in the same manner as in Example 1, and as a result, it showed excellent water resistance, almost the same as in Example 1.

7″: #・“2″局′°I得f″+″″■創;!9 
+、・品であり、JIS規格は設定されていないが、こ
れをフオームポリスチレンサンドウィッチ畳床の規格を
準用し、これに規定する曲げ試験によるたわみ量、及び
局部試験による局部圧縮量を測定した。
7″: #・“2″ station′°I get f″+″″■create;! 9
Although the product is a +,・ product and there is no JIS standard set, the standard for foam polystyrene sandwich tatami flooring was applied mutatis mutandis, and the amount of deflection by the bending test specified therein and the amount of local compression by the local test were measured.

その結果を次表に示す。The results are shown in the table below.

なお、試験品の寸法は、規格品(91W)と同じ寸法の
長さ182cm、幅91cm、厚さ5cmである。
The dimensions of the test product are the same as the standard product (91W): length 182 cm, width 91 cm, and thickness 5 cm.

表−1 また、本発明の接着剤の場合、EVA、ポリイソシアネ
ート及び水の混合によって、発泡し容積を増加(約30
%)するが、これにより大量微細の粒子に成分の均一な
濡れを充分与える利点がある上、加熱温度についても、
実施例1で示したポリイソシアネートを単独で使用する
場合、反応させるための加熱温度は160°C〜180
 ’Cを必要とするのに対し、本発明の接着剤の場合は
140″C〜150℃で完全に反応し、本発明の接着剤
は、熱エネルギー的にも有利である。
Table 1 In addition, in the case of the adhesive of the present invention, by mixing EVA, polyisocyanate, and water, it foams and increases in volume (approximately 30
%), but this has the advantage of sufficiently uniformly wetting the ingredients to a large amount of fine particles, and the heating temperature is also
When the polyisocyanate shown in Example 1 is used alone, the heating temperature for reaction is 160°C to 180°C.
'C, whereas the adhesive of the present invention reacts completely at 140''C to 150°C, and the adhesive of the present invention is also advantageous in terms of thermal energy.

特許出願人 近代地水センター株式会社代理人弁理士池
浦敏明
Patent applicant: Toshiaki Ikeura, patent attorney, Kindai Jisui Center Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] (1)エチレン−酢酸ビニル系共重合体エマルジョンか
らなる第1液と、ポリイソシアネート系化合物からなる
第2液とから構成される耐水性、弾性接着剤。
(1) A water-resistant, elastic adhesive composed of a first liquid consisting of an ethylene-vinyl acetate copolymer emulsion and a second liquid consisting of a polyisocyanate compound.
JP11276284A 1984-06-01 1984-06-01 Water-resistant elastic adhesive Pending JPS60258276A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11276284A JPS60258276A (en) 1984-06-01 1984-06-01 Water-resistant elastic adhesive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11276284A JPS60258276A (en) 1984-06-01 1984-06-01 Water-resistant elastic adhesive

Publications (1)

Publication Number Publication Date
JPS60258276A true JPS60258276A (en) 1985-12-20

Family

ID=14594888

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11276284A Pending JPS60258276A (en) 1984-06-01 1984-06-01 Water-resistant elastic adhesive

Country Status (1)

Country Link
JP (1) JPS60258276A (en)

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4922436A (en) * 1972-06-22 1974-02-27
JPS5069142A (en) * 1973-10-08 1975-06-09
JPS5076143A (en) * 1973-10-08 1975-06-21
JPS5333251A (en) * 1976-09-09 1978-03-29 Nippon Synthetic Chem Ind Co Ltd:The Crosslinkable composition
JPS5679119A (en) * 1979-11-30 1981-06-29 Kuraray Co Ltd Crosslinkable composition
JPS5730775A (en) * 1980-07-31 1982-02-19 Dainippon Ink & Chem Inc Adhesive composition
JPS5785871A (en) * 1980-11-17 1982-05-28 Sumitomo Chem Co Ltd Adhesive composition for decorative plywood
JPS5823868A (en) * 1982-03-01 1983-02-12 Kuraray Co Ltd Adhesive composition

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4922436A (en) * 1972-06-22 1974-02-27
JPS5069142A (en) * 1973-10-08 1975-06-09
JPS5076143A (en) * 1973-10-08 1975-06-21
JPS5333251A (en) * 1976-09-09 1978-03-29 Nippon Synthetic Chem Ind Co Ltd:The Crosslinkable composition
JPS5679119A (en) * 1979-11-30 1981-06-29 Kuraray Co Ltd Crosslinkable composition
JPS5730775A (en) * 1980-07-31 1982-02-19 Dainippon Ink & Chem Inc Adhesive composition
JPS5785871A (en) * 1980-11-17 1982-05-28 Sumitomo Chem Co Ltd Adhesive composition for decorative plywood
JPS5823868A (en) * 1982-03-01 1983-02-12 Kuraray Co Ltd Adhesive composition

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