JPS6279217A - Production of shock-absorbing foam - Google Patents

Production of shock-absorbing foam

Info

Publication number
JPS6279217A
JPS6279217A JP60219496A JP21949685A JPS6279217A JP S6279217 A JPS6279217 A JP S6279217A JP 60219496 A JP60219496 A JP 60219496A JP 21949685 A JP21949685 A JP 21949685A JP S6279217 A JPS6279217 A JP S6279217A
Authority
JP
Japan
Prior art keywords
polyol
foam
component
tackifier
oxyalkylene
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
Application number
JP60219496A
Other languages
Japanese (ja)
Other versions
JPH0610239B2 (en
Inventor
Takayoshi Ishino
石野 卓由
Shizuo Yamazaki
山崎 静男
Masahiko Fuyumuro
昌彦 冬室
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.)
Achilles Corp
Original Assignee
Achilles Corp
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 Achilles Corp filed Critical Achilles Corp
Priority to JP60219496A priority Critical patent/JPH0610239B2/en
Publication of JPS6279217A publication Critical patent/JPS6279217A/en
Publication of JPH0610239B2 publication Critical patent/JPH0610239B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

PURPOSE:To obtain the titled light-weight foam having sound-absorbing property as well as vibration-damping property and having excellent heat-resistance, by using a specific polyether polyol as a polyol component and using specific amounts of a plasticizer and a tackifier soluble in the polyol component. CONSTITUTION:The objective foam can be produced by compounding (A) a mixed polyol composed of (i) >=10wt% poly(oxyalkylene)diol having an average molecular weight of 1,000-3,000 and (ii) a poly(oxyalkylene)triol having an average molecular weight of 2,000-6,000 with (B) 25-200pts.(wt.) (based on 100pts. of the component A) of a tackifier soluble in the component A, (C) 0.25-2pts. (based on 1pt. of the component B) of a plasticizer (e.g. phthalic acid ester), (D) an organic isocyanate, (E) a foaming agent, (F) a catalyst and (G) a foam stabilizer and reacting and foaming the mixture e.g. by one-shot process.

Description

【発明の詳細な説明】 (産業上の利用分野) この発明は、自動車、電車、航空機などの「輸送車輛」
や工場、機械、住宅などの時(二振動を伴う騒音を低減
させる防音材として使用する@撃吸収性7オームの製造
方法に関する。
[Detailed Description of the Invention] (Industrial Application Field) This invention is applicable to "transport vehicles" such as automobiles, trains, and airplanes.
This article relates to a method of manufacturing @shock absorbing 7 ohm material, which is used as a soundproofing material to reduce noise accompanied by vibrations in factories, machinery, houses, etc.

(従来の技術〉 軟質ポリウレタンフォームは、連通セル製造を有するた
め書=多孔質型吸音材として広く使用されているがダン
ピング(制振ン性能が小さく、振動音を伴う発生音に対
する防音材としては不十分であった。そのため制振性能
を向上させるため(二充填剤やアスファルトヲ添加し密
度を高める方法が行なわれたがコストアップになること
と、7オ一ム自体の物性低下をまね、く次めや加工時の
アスファルト汚染が生じるため実用上野1しくなかつ次
(Prior art) Flexible polyurethane foam is widely used as a porous sound-absorbing material because it has continuous cell manufacturing, but it has low damping performance and is not suitable as a sound-insulating material for noise generated with vibration noise. Therefore, in order to improve the damping performance (adding filler or asphalt to increase the density), it increased the cost and imitated the deterioration of the physical properties of the 7-ohm itself. Because asphalt contamination occurs during processing and machining, it is difficult to put into practical use.

一方割振材としては各種のゴム状物質や熱可塑性樹脂に
充填剤を添加し、質量の大きいゴム状シートが使用さ几
ているが、重量があり、コストも高く、また吸音性能が
ない大きな欠点がめった。このためこnらを解消すべく
吸音性能t−’Nする軟質ポリウレタンフォーム(=良
好な割振性能を付与するべく、ポリオールの種類や整泡
剤、ポリイソシアネートなどの使用原料そのものを種々
選択することによって吸音性能金有し、しかも制振性能
も有する軟質ポリウレタンフォームも開発されている。
On the other hand, rubber-like sheets with a large mass, which are made by adding fillers to various rubber-like substances or thermoplastic resins, are used as damping materials, but these have the major disadvantages of being heavy, expensive, and lacking in sound-absorbing properties. I was disappointed. Therefore, in order to solve these problems, a flexible polyurethane foam with sound absorption performance t-'N (= in order to give good vibration distribution performance, various types of polyols, foam stabilizers, polyisocyanates, and other raw materials used should be selected) A flexible polyurethane foam has been developed that has not only sound absorption performance but also vibration damping performance.

(発明が解決しようとする問題点) 使用原料の選択により吸音性能及び割振性能を併有する
軟質ポリウレタンフォームが得られたが、ポリマーは温
度変化に伴い物性変化がおこるものであり、こうして得
られた衝撃吸収性7オームも例外ではなく温度上昇に伴
い伸びや引張り強さなどの機械的強度が低下し、熱圧縮
成形などの成形手段において不都合を生じ、又高温雰囲
気中(=おける使用時の衝撃吸収性能の低下を招く欠点
がおった。この発明はこのような点に鑑みなされ念もの
で、高温時においてもなお7オームの物性低下が小さく
、熱圧縮成形加工などに耐え得るような衝撃吸収性7オ
ームを得ることを目的とするものである。
(Problems to be Solved by the Invention) A flexible polyurethane foam that has both sound absorption and vibration damping properties was obtained by selecting the raw materials used, but the physical properties of polymers change with temperature changes, Shock absorption of 7 ohms is no exception; mechanical strength such as elongation and tensile strength decreases as the temperature rises, causing inconveniences in molding methods such as thermocompression molding. This invention had the disadvantage of causing a decrease in absorption performance.This invention was developed in consideration of these points, and was developed to create a shock absorbing material that has a small decrease in physical properties of 7 ohm even at high temperatures and can withstand thermal compression molding. The purpose is to obtain a resistance of 7 ohms.

(問題点を解決するための手段〉 すなわちこの発明はポリオール、有機イソシアネート、
発泡剤、触媒、整泡剤などから軟質ポリウレタンフォー
ム全製造する1:際し。
(Means for solving the problem) In other words, this invention uses polyol, organic isocyanate,
1: For the complete production of flexible polyurethane foam from blowing agents, catalysts, foam stabilizers, etc.

(1)ポリオールとして平均分子量が1OOO〜300
0のポリ(オキシアルキレン)ジオールと平均分子量が
2000〜6000のポリ(オキシアルキレン)トリオ
ールとの混合ポリオールであり、ジオールが全ポリオー
ルに対して10重量%以上であるポリエーテル系ポリオ
ールを使用し。
(1) The average molecular weight as a polyol is 100 to 300
0 poly(oxyalkylene) diol and a poly(oxyalkylene) triol having an average molecular weight of 2,000 to 6,000, and a polyether polyol in which the diol accounts for 10% by weight or more based on the total polyol.

(2)ポリオールに溶解する粘着付与剤をポリオール1
001:対して25〜200重全部使用し。
(2) Add a tackifier that dissolves in polyol to polyol 1
001: 25 to 200 weights are used.

(′!I)可塑剤′f:粘着付与剤1(二対して025
〜2使用する、 ことを特徴とする衝撃吸収性7オームの製造方法である
('!I) Plasticizer'f: Tackifier 1 (025 for 2
A method for manufacturing a shock-absorbing 7 ohm, characterized in that: -2 is used.

ポリオールはポリマーの耐熱性を決定するうえで重要な
要素となるものであり、侍に重要な物性である伸び率が
摂氏80℃においても100%以上を保持させる耐熱性
を有するものとして前記ポリオールの組成でこれを達成
することを見い出した。
Polyol is an important element in determining the heat resistance of polymers, and the polyol is said to have heat resistance that allows the elongation rate, which is an important physical property for Samurai, to maintain 100% or more even at 80 degrees Celsius. We have found that this can be achieved with a composition.

ポリ(オキシアルキレンンジオールは2個の活性水素含
有化合物にエチレンオキシド、プロピレンオキシドなど
を単独または2種以上をランダムもしくはブロック付加
した形の製造を有する平均分子量1000〜3000の
化合物でるる。2個の活性水素含有化合物としてr;水
、エチレングリコール、プロピレングリコール、フチレ
ンゲリコール、ヘキシレングリコールなどを挙げること
ができる。
Poly(oxyalkylene diol) is a compound with an average molecular weight of 1,000 to 3,000, which is produced by adding ethylene oxide, propylene oxide, etc. alone or in random or block form to two active hydrogen-containing compounds. Examples of the active hydrogen-containing compound include water, ethylene glycol, propylene glycol, ethylene glycol, hexylene glycol, and the like.

ポリ(オキシアルキレン〕トリオールは3個の活性水素
含有化合物にエチレンオキシド、プロピレンオキシド、
プチレ/オキシドなどを単独もしくはブロック付加した
形の製造を有する平均分子量2000〜6000の化合
物である。3個の活性水素含有化合物としてはグリセリ
ン、トリメチロールプロパンなどがある。
Poly(oxyalkylene) triols contain three active hydrogen-containing compounds: ethylene oxide, propylene oxide,
It is a compound with an average molecular weight of 2,000 to 6,000, which can be produced singly or in the form of a block addition of petite/oxide, etc. Examples of the three active hydrogen-containing compounds include glycerin and trimethylolpropane.

粘着付与剤は得られたフオームに粘着性全付与して7オ
ームの圧、縮侵の回復を遅くし、7オームに割振性能を
与える。この発明においては粘着付与剤はポリオールに
溶解するものであることが必要不可欠でるる。非溶解で
あると混合原料のタンクストレージ段階で相分離を起し
たり、製品の品質が不均一になったり、発泡状態が不安
定になったり、発泡原液の粘度が上昇したりして製造上
や品質上好ましくない。粘着付与剤はポリオール100
重量部に対して25〜200重量部の範囲で添加する。
The tackifier imparts tackiness to the resulting foam, slowing down recovery from 7 ohm compression, shrinkage, and providing 7 ohm splitting performance. In this invention, it is essential that the tackifier be soluble in the polyol. If undissolved, phase separation may occur during tank storage of mixed raw materials, product quality may become uneven, the foaming state may become unstable, and the viscosity of the foaming stock solution may increase, resulting in production problems. It is unfavorable in terms of quality. Tackifier is polyol 100
It is added in an amount of 25 to 200 parts by weight.

添加量が少ないとフオームの粘着性が不十分となり、圧
縮後の回復時間が短かく割振効果が期待できない。添加
量が増加していくにつれて。
If the amount added is small, the adhesiveness of the foam will be insufficient, the recovery time after compression will be short, and no distribution effect can be expected. As the amount added increases.

系の粘度が増大し、ワンショットによる発泡が難しくな
シ、又発泡安定性も不安定となるので、200重量部程
度が実用上の限度でらる。
The viscosity of the system increases, making one-shot foaming difficult and foaming stability unstable, so about 200 parts by weight is the practical limit.

この発明で使用できる粘着付与剤としては、高級炭化水
素樹脂の11PTR−6100(三井石油化学工業ン、
水素添加ロジンエステルのエステルガムH(荒用化学工
業)などがあるが、ポリオールに溶解性を有するもので
あればこれに限定されるものではない。粘着付与効果を
有するものでろっても、ポリオールへの溶解性が乏しい
もの、たとえば合成ポリテルペン樹脂のフィントン(三
井石油化学工業)、脂肪族系環状炭化水素樹脂の7・イ
レツツ(三井石油化学工業ン、液状ポリブタジェン、ポ
リブテンなどや、あるいは粘着性:二乏しかったシ臭気
の強いもの、たとえばアスファルト、クマロン樹脂、芳
香族系炭化水素樹脂のベトロジン(三井石油化学工業]
などは好ましくない。
As a tackifier that can be used in this invention, high-grade hydrocarbon resin 11PTR-6100 (Mitsui Petrochemical Co., Ltd.,
Ester Gum H (Arayo Kagaku Kogyo), which is a hydrogenated rosin ester, is available, but it is not limited thereto as long as it is soluble in polyol. Even if they have a tackifying effect, they have poor solubility in polyols, such as the synthetic polyterpene resin Finton (Mitsui Petrochemical Industries) and the aliphatic cyclic hydrocarbon resin 7-Iretsutsu (Mitsui Petrochemical Industries). , liquid polybutadiene, polybutene, etc., or those with a strong odor, such as asphalt, coumaron resin, aromatic hydrocarbon resin Vetrozin (Mitsui Petrochemical Industries)
etc. are not desirable.

可塑剤は釉層付与剤1に対して025〜2の範囲で添加
する。可塑剤の配合比率が多くなりすぎるとフオーム自
体のペタツキが大きく、加工段階での汚染が問題となり
、また圧縮後のフオームの回復時間が短かく割振効果が
期待できない。可塑剤の増加はフオームの難燃性の低下
及び耐熱性の低下を招くので少ない程好まし令番い。し
かしながら、釉層付与剤に粘着性を与えるためには可塑
剤の併用が必要であり、割振性やフオームの発泡安定性
など総体的な見地から決定さt″Lfcものである。
The plasticizer is added in an amount of 0.25 to 2.0 to 1 of the glaze layer imparting agent. If the blending ratio of the plasticizer is too high, the foam itself will become sticky, causing problems with contamination during processing, and the recovery time of the foam after compression will be short, making it impossible to expect an allocation effect. An increase in the amount of plasticizer causes a decrease in the flame retardancy and heat resistance of the foam, so the smaller the amount, the better. However, in order to impart tackiness to the glaze layer imparting agent, it is necessary to use a plasticizer in combination, and t''Lfc is determined from overall viewpoints such as vibration stability and foam stability.

添加量が少なすぎると粘着性が不十分となり、圧縮後の
回復時間が短かく割振効果が期待できない。
If the amount added is too small, the adhesiveness will be insufficient, the recovery time after compression will be short, and no distribution effect can be expected.

またフオームの伸びも小さくなり、熱圧縮成形加工に耐
えられない。
In addition, the elongation of the foam becomes small and it cannot withstand hot compression molding.

使用できる可塑剤としては、フタル酸エステルなどのエ
ステル類、トリクレジルホスフェートなどのリン酸エス
テル類などかめる。トリスクロロエチルホスフェート、
トリスジクロロプロピルホスフェートなどのハロゲン化
リン酸エステルは溶解性が乏しく使用できない。
Examples of plasticizers that can be used include esters such as phthalate esters and phosphate esters such as tricresyl phosphate. trischloroethyl phosphate,
Halogenated phosphate esters such as tris dichloropropyl phosphate have poor solubility and cannot be used.

有機イソシアネートとしては、一般的に軟質ポリウレタ
ンフォームに使用さnるものであり、トリレンジイソシ
アネートの2・4異性体と2・6異性体及びそれらの混
合物などである。
The organic isocyanate is generally used for flexible polyurethane foam, and includes 2.4 isomer, 2.6 isomer and mixtures thereof of tolylene diisocyanate.

発泡剤としては水やフロン−11,メチレンクロリドな
どの低沸点ハロゲン化炭化水素の単独または併用使用が
でき、その他触媒%添加剤は一般に軟質ウレタンフオー
ムに使用さ九るものである。
As the blowing agent, water, low-boiling halogenated hydrocarbons such as Freon-11 and methylene chloride can be used alone or in combination, and other catalyst additives are those generally used for flexible urethane foams.

(実施例及び比較例) 表−1に示す原料配合;二よりワンショット法にて発泡
させて軟質ポリウレタンフォームを裂遺し、得られたフ
オームの密度1反ばつ弾性、ヒステリシスロス、伸び(
25℃及び80℃)、圧縮後の回復時間を測定し1表−
1に示す結果が得られた。
(Examples and Comparative Examples) Raw material formulations shown in Table 1; Foamed by two-way one-shot method to leave flexible polyurethane foam, density 1 of elasticity, hysteresis loss, elongation
25℃ and 80℃), the recovery time after compression was measured and Table 1-
The results shown in 1 were obtained.

(発明の効果) この発明によると、軽量で吸音性能と割振性能ケ兼ね備
えた軟質ポリウレタンフォームからなる衝撃吸収性7オ
ームが得られ、耐熱性(二すぐれ、高温下においても強
度物性の低下が小さく、熱成形加工が可能でおるので他
材料との組合せ加工も可能であり1種々形状の防音材が
得られるので用途の拡大、コストの低下がはかれる。
(Effects of the Invention) According to this invention, it is possible to obtain a shock absorption of 7 ohms made of a lightweight flexible polyurethane foam that has both sound absorption and vibration distribution properties, and has excellent heat resistance (excellent), with little decrease in strength and physical properties even at high temperatures. Since it can be thermoformed, combination processing with other materials is also possible, and soundproofing materials of various shapes can be obtained, expanding the range of uses and reducing costs.

Ya M H与剤はポリオール溶解性であり、従来のワ
ンショット法がそのま一適用でき、製造工程上も全く変
りがないので、経済的であり、しかも粘M付与剤自体の
使用量も比較的少なくて割振性能が得られるのでフオー
ムのコストも低下する。
The Ya M H imparting agent is polyol-soluble, so the conventional one-shot method can be applied as is, and there is no change in the manufacturing process, so it is economical, and the amount of the viscosity M imparting agent itself is also comparable. Since the allocation performance can be obtained with less target, the cost of the form is also reduced.

Claims (1)

【特許請求の範囲】 ポリオール、有機イソシアネート、発泡剤、触媒、整泡
剤などから軟質ポリウレタンフォームを製造するに際し
、 (1)ポリオールとして平均分子量が1000〜300
0のポリ(オキシアルキレン)ジオールと平均分子量が
2000〜6000のポリ(オキシアルキレン)トリオ
ールとの混合ポリオールであり、ジオールが全ポリオー
ルに対して10重量%以上であるポリエーテル系ポリオ
ールを使用し、 (2)ポリオールに溶解する粘着付与剤をポリオール1
00に対して25〜200重量部使用し、(3)可塑剤
を粘着付与剤1に対して0.25〜2使用する ことを特徴とする衝撃吸収性フォームの製造方法。
[Claims] When producing flexible polyurethane foam from polyols, organic isocyanates, blowing agents, catalysts, foam stabilizers, etc., (1) polyols with an average molecular weight of 1000 to 300;
0 poly(oxyalkylene) diol and an average molecular weight of 2000 to 6000 poly(oxyalkylene) triol, using a polyether polyol in which the diol is 10% by weight or more based on the total polyol, (2) Add a tackifier that dissolves in polyol to polyol 1
(3) 0.25 to 200 parts by weight of plasticizer to 1 part of tackifier.
JP60219496A 1985-10-02 1985-10-02 Method of manufacturing shock absorbing foam Expired - Lifetime JPH0610239B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60219496A JPH0610239B2 (en) 1985-10-02 1985-10-02 Method of manufacturing shock absorbing foam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60219496A JPH0610239B2 (en) 1985-10-02 1985-10-02 Method of manufacturing shock absorbing foam

Publications (2)

Publication Number Publication Date
JPS6279217A true JPS6279217A (en) 1987-04-11
JPH0610239B2 JPH0610239B2 (en) 1994-02-09

Family

ID=16736360

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60219496A Expired - Lifetime JPH0610239B2 (en) 1985-10-02 1985-10-02 Method of manufacturing shock absorbing foam

Country Status (1)

Country Link
JP (1) JPH0610239B2 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01280413A (en) * 1988-04-30 1989-11-10 Nhk Spring Co Ltd Cushion body for seat
US6136879A (en) * 1997-10-28 2000-10-24 Tokai Rubber Industries, Ltd. Soft polyurethane foam, method of producing the same and vehicle interior member using the same
JP2002003821A (en) * 2000-06-23 2002-01-09 Toho Chem Ind Co Ltd One-pack foamable hardening urethane based material for stopping water
WO2002050148A3 (en) * 2000-12-20 2002-08-29 Orycle Applic Ltd Polyurethane compositions useful as shock absorbers and a method for their preparation
JP2008239816A (en) * 2007-03-27 2008-10-09 Inoac Corp Flexible polyurethane foam
WO2013161931A1 (en) * 2012-04-26 2013-10-31 モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社 Polyurethane foam composition, and method for producing soft polyurethane foam
JP2021517191A (en) * 2018-03-13 2021-07-15 ダウ グローバル テクノロジーズ エルエルシー Soft polyurethane foam with long recovery time

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01280413A (en) * 1988-04-30 1989-11-10 Nhk Spring Co Ltd Cushion body for seat
US6136879A (en) * 1997-10-28 2000-10-24 Tokai Rubber Industries, Ltd. Soft polyurethane foam, method of producing the same and vehicle interior member using the same
JP2002003821A (en) * 2000-06-23 2002-01-09 Toho Chem Ind Co Ltd One-pack foamable hardening urethane based material for stopping water
US7897652B2 (en) 2000-12-20 2011-03-01 Orycle Applications Ltd. Polyurethane composition useful as shock absorbers and a method for their preparation
WO2002050148A3 (en) * 2000-12-20 2002-08-29 Orycle Applic Ltd Polyurethane compositions useful as shock absorbers and a method for their preparation
JP2004520460A (en) * 2000-12-20 2004-07-08 オライクル アプリケーションズ エルティーディー. Polyurethane compositions suitable for use as shock absorbers and methods for their production
AU2002217383B2 (en) * 2000-12-20 2006-10-05 Orycle Applications Ltd Polyurethane compositions useful as shock absorbers and a method for their preparation
JP2008239816A (en) * 2007-03-27 2008-10-09 Inoac Corp Flexible polyurethane foam
WO2013161931A1 (en) * 2012-04-26 2013-10-31 モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社 Polyurethane foam composition, and method for producing soft polyurethane foam
JP2014114459A (en) * 2012-04-26 2014-06-26 Momentive Performance Materials Inc Method for producing polyurethane foaming composition and flexible polyurethane foam
JPWO2013161931A1 (en) * 2012-04-26 2015-12-24 モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社 Polyurethane foam composition and method for producing flexible polyurethane foam
JP2021517191A (en) * 2018-03-13 2021-07-15 ダウ グローバル テクノロジーズ エルエルシー Soft polyurethane foam with long recovery time
JP2021517189A (en) * 2018-03-13 2021-07-15 ダウ グローバル テクノロジーズ エルエルシー Viscoelastic foam

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