JPS61235418A - Sound-and vibration-proof foam - Google Patents

Sound-and vibration-proof foam

Info

Publication number
JPS61235418A
JPS61235418A JP60076962A JP7696285A JPS61235418A JP S61235418 A JPS61235418 A JP S61235418A JP 60076962 A JP60076962 A JP 60076962A JP 7696285 A JP7696285 A JP 7696285A JP S61235418 A JPS61235418 A JP S61235418A
Authority
JP
Japan
Prior art keywords
foam
polyol
sound
vibration
polyurethane foam
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
JP60076962A
Other languages
Japanese (ja)
Other versions
JPH0725863B2 (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 JP60076962A priority Critical patent/JPH0725863B2/en
Publication of JPS61235418A publication Critical patent/JPS61235418A/en
Publication of JPH0725863B2 publication Critical patent/JPH0725863B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:The title lightweight foam excellent in processability and sound- absorbing and vibration-proof performances, obtained by foaming and organic polyisocyanate and a specified polyol in the presence of a blowing agent, a catalyst, a foam stabilizer, a fluid having a plasticizing effect, etc. CONSTITUTION:The title foam comprising a flexible polyurethane foam is obtained by foaming, by one-shot process, an organic polyisocyanate (A) such as tolylene diisocyanate and at least one polyol (B), such as polyoxyalkylenepolyol of a functionality of 2-3 and an average hydroxyl value of 150-400, in the presence of a blowing agent such as a low-boiling halohydrocarbon, a catalyst such as an amine and 10-100pts.wt. (per 100pts.wt. polyol) fluid having a plasticizing effect (e.g., trisdichloropropyl phosphate).

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は吸音性能と制振性能を兼ね備えた防音性ポリウ
レタンフォームに関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a soundproof polyurethane foam that has both sound absorption and vibration damping performance.

〔従来の技術〕[Conventional technology]

従来、ポリウレタンフォームは連通微細セル構造を有す
るため、優れた多孔質型吸音材料として自動車や事務機
器などの機器や建築物などに広範に利用されている。
Conventionally, polyurethane foam has a continuous fine cell structure and has been widely used as an excellent porous sound-absorbing material in equipment such as automobiles and office equipment, and in buildings.

一般に、自動車や工場の機械類、事務機器などの騒音は
、音源から空気伝達されるだけでなく、自動車のボデー
や機器の櫟いなどが機械的に加振され、そこから音が放
射されている。そのため、これらの騒音防止には吸音材
にて吸音することだけでなく、吸音材自体でボデーや覆
いなどを制振することが必要である。しかしながら、従
来吸音材として用いられているポリウレタンフォームは
振動エネルギー吸収能が小さく、ダンピング性能が低い
ため、上記のような機械振動にともなう騒音を低減させ
る材料としては不十分であった@ 割振材料としては、各種のゴム状物質、熱可塑性樹脂な
どく例えば雲母、カーボンブラック、炭酸カルシウムな
どの充てん剤を添加したものがあるが、コストが高く、
そして重く、また、制振性能は発揮されたとしても吸音
性能を有しているものではなかった。また、ポリウレタ
ンフォームに上記のような充てん剤を添加し、密度を大
きくして遮音性能を向上させる対策がとられているが、
この場合であってもコストの上昇及び物性の低下を招き
、満足できるものではなかった。そのため、吸音性能と
制振性能を兼ね備えた防音材料として、吸音材料と制振
材料を組み合わせた複合体、例えばポリウレタンフォー
ムを後処理し、それにアスファルトを含浸させたフオー
ムやポリウレタンフォームの原料にアスファルトを添加
し、一体発泡させたフオームなどの粘性特性の大きい、
粘弾性発泡体が用いられている現状であった。
In general, noise from automobiles, factory machinery, office equipment, etc. is not only transmitted through the air from the sound source, but also due to the mechanical vibration of the car body and the structure of the equipment, and the sound is radiated from there. There is. Therefore, in order to prevent these noises, it is necessary not only to absorb sound with a sound-absorbing material, but also to dampen the vibration of the body, cover, etc. using the sound-absorbing material itself. However, polyurethane foam, which has traditionally been used as a sound-absorbing material, has a low vibration energy absorption capacity and low damping performance, so it was insufficient as a material to reduce noise caused by mechanical vibrations as described above. There are various rubber-like substances, thermoplastic resins, etc., with fillers such as mica, carbon black, and calcium carbonate added, but they are expensive and
Moreover, it was heavy, and even if it exhibited vibration damping performance, it did not have sound absorption performance. In addition, measures have been taken to add fillers such as those mentioned above to polyurethane foam to increase its density and improve its sound insulation performance.
Even in this case, it resulted in an increase in cost and a decrease in physical properties, resulting in an unsatisfactory result. Therefore, as a soundproofing material that has both sound absorption and vibration damping performance, we use composites that combine sound absorption and vibration damping materials, such as polyurethane foam that is post-treated and impregnated with asphalt, or asphalt as a raw material for polyurethane foam. Foam with high viscosity such as foam that is added and foamed together.
Currently, viscoelastic foam is used.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

上記のように、アスファルト系フオームは吸音性能と制
振性能を兼ね備えているが、熱圧縮成形等の加工時、ア
スファルトによって加工装置が汚染されるなど作業性の
面で非常に能率性に欠け、そして更に、コストが高いと
いう欠点を有している。更に後処理アスファルト7オー
ムは、含浸むらが生じ、均一な品質のものが得にくい。
As mentioned above, asphalt-based foam has both sound absorption and vibration damping performance, but it is extremely inefficient in terms of workability, as processing equipment is contaminated by asphalt during processing such as hot compression molding. Furthermore, it has the disadvantage of high cost. Furthermore, the post-treated asphalt 7 ohm has uneven impregnation, making it difficult to obtain uniform quality.

また、車両等に用いる防音材料としては軽量であること
が望ましいが、上記アスファルトフオームや充てん剤を
添加した各種ゴム、樹脂などは密度が大きく、重いとい
う問題点も有している。
Furthermore, although it is desirable that soundproofing materials used in vehicles be lightweight, the above-mentioned asphalt foams and various rubbers, resins, etc. with fillers added have large densities and have the problem of being heavy.

本発明は上記問題点を解決するためのもので、加工作業
性が良好で、かつ軽量で、吸音性能と割振性能を兼ね備
えた防音性ポリウレタンフォームを提供することを目的
とするものである。
The present invention is intended to solve the above-mentioned problems, and aims to provide a soundproof polyurethane foam that is easy to work with, is lightweight, and has both sound absorption performance and vibration distribution performance.

〔問題点を解決するための手段〕[Means for solving problems]

本発明の防音・割振性7オームは有機ポリインシアネー
トとポリオールとを発泡剤、触媒、整泡剤及び他の添加
剤の存在下にワンシ1ット法により軟質ポリウレタンフ
ォームを製造する際K、 1)ポリオール成分として、2又は5官能で平均水酸基
価150ないし400を有する単独又は2種以上の組み
合わせのポリオキシアルキレンポリオールを使用し; 1i)−i1!l      可塑効果を有する流動体
を前記ポリオール100重量部に対して10ないし10
0重量部; 添加することによって得られたことを特徴とするもので
ある。
The soundproofing/dissonance property of the present invention of 7 ohm is obtained when a flexible polyurethane foam is produced by a one-shot method using an organic polyinsyanate and a polyol in the presence of a blowing agent, a catalyst, a foam stabilizer, and other additives. 1i)-i1!) As the polyol component, a polyoxyalkylene polyol which is di- or penta-functional and has an average hydroxyl value of 150 to 400, used alone or in combination of two or more; 1i)-i1! 10 to 10 parts of a fluid having a plasticizing effect per 100 parts by weight of the polyol
0 parts by weight; is characterized by being obtained by adding.

〔作用〕[Effect]

この場合、ポリオール成分として用いられるポリオキシ
アルキレンポリオールは2又は3官能で、単独又は2種
以上組み合わせて平均水酸基価が150ないし400、
好ましくは20ロ ないし300となるポリオキシアル
キレンポリオールである。
In this case, the polyoxyalkylene polyol used as the polyol component is difunctional or trifunctional, and has an average hydroxyl value of 150 to 400, alone or in combination of two or more,
Preferred is a polyoxyalkylene polyol having a molecular weight of 20 to 300%.

用いることができるこの種のポリオキシアルキレンポリ
オールとしては2ないし3個の活性水素含有化合物K例
えばエチレンオキシド、プロピレンオキシド、エピクロ
ルヒドリンなどを単独付加又は2種以上をランダム若し
くはブロック付加させた構造を有する分子量20口ない
し8000の化合物などを挙げる仁とができる。上記の
2ないし5個の活性水素含有化合物の例とシテハ、水、
エチレングリコール、グロピレングリコール、ブチレン
グリコール、ヘキシレングリコール、グリセリン、トリ
メチロールプロパンたどを挙げることができる。
This type of polyoxyalkylene polyol that can be used includes a molecular weight of 20 having a structure in which two or three active hydrogen-containing compounds K, such as ethylene oxide, propylene oxide, epichlorohydrin, etc. are added singly or in random or block addition of two or more kinds. There are 8,000 compounds that can be found in the mouth. Examples of the above 2 to 5 active hydrogen-containing compounds and Citeha, water,
Examples include ethylene glycol, glopylene glycol, butylene glycol, hexylene glycol, glycerin, and trimethylolpropane.

水酸基価が150未満のポリオールを用いて得られたポ
リウレタンフォームは、圧縮後の戻り時間が短く、また
、ヒステリシスロスの小さい、いわゆる反発の大きい割
振性能に欠けるフオームとなり、更に、このようなポリ
オールに可塑効果を有する流動体を添加すると反発の大
きい制振性能が極めて劣るフオームとなる。一方、水酸
基価が400を超えるポリオールは非常圧反応性が大き
く、一般的な配合では独立気泡の収縮フオームとなりや
すいので、発泡のコントロールが難しく、良好なフオー
ムが得られない。
A polyurethane foam obtained using a polyol with a hydroxyl value of less than 150 has a short return time after compression, and also has a low hysteresis loss, which is a foam that lacks so-called high repulsion distribution performance. Addition of a fluid having a plasticizing effect results in a foam with large repulsion and extremely poor vibration damping performance. On the other hand, polyols with a hydroxyl value exceeding 400 have high emergency pressure reactivity and tend to form a closed-cell contracted foam in a typical formulation, making it difficult to control foaming and making it difficult to obtain a good foam.

また、水酸基価が150〜400のポリオールを用いて
も、可塑効果を有する流動体を添加しないフオームは、
比較的反発の小さい、ヒステリシスの大きいフオームに
はなるが、圧縮後の戻り時間が短く、優れた防音・割振
性能が得られない。
In addition, even if a polyol with a hydroxyl value of 150 to 400 is used, a foam without adding a fluid having a plasticizing effect,
Although this results in a foam with relatively low repulsion and large hysteresis, the return time after compression is short and excellent soundproofing and vibration distribution performance cannot be obtained.

可塑効果を有する流動体は制振性効果があり、その添加
量はポリオールの官能基数と水酸基価の組み合わせくお
いて決定されるが、ポリオール100重量部に対して該
流動体の添加量が10重量部未満では、圧縮後の戻り時
間が短すぎたり、又は戻らない現象が生じ、目的とする
良好な物性が得られない。一方、100重量部を超えて
該流動体を添加する場合目的とする良好なフオーム物性
を得るためには水酸基価の大きいポリオールを用いるこ
とが必要であり、このような水酸基価の大きいポリオー
ルは反応性が高く、独立気泡の収縮フオームとなりやす
く、発泡コントロールが難しい。したがって、可塑効果
を有する流動体は10ないし100重量部、好ましくは
20ないし80重量部添加するとよい。
A fluid with a plasticizing effect has a damping effect, and the amount added is determined by the combination of the number of functional groups and the hydroxyl value of the polyol. If the amount is less than 1 part by weight, the return time after compression may be too short or the return may not return, resulting in failure to obtain desired good physical properties. On the other hand, if more than 100 parts by weight of the fluid is added, it is necessary to use a polyol with a high hydroxyl value in order to obtain the desired foam properties, and such a polyol with a high hydroxyl value may cause reaction. It is difficult to control foaming because it tends to form a closed-cell contracted foam. Therefore, the fluid having a plasticizing effect may be added in an amount of 10 to 100 parts by weight, preferably 20 to 80 parts by weight.

添加できる可塑効果を有する流動体の例としては、トリ
スジクロロプロピルホスフェート、トリスクロログロビ
ルホス7エー)71”+7)ハロゲン化リン酸エステル
類、トリクレジルホスフェート、トリフェニルホスフェ
ート、クレジルジフェニルホスフェートなどのリン酸エ
ステル類及びフタル酸エステル、セバシン酸ポリエステ
ル、アジピン酸ポリエステル、トリメリット酸エステル
などのエステル類などの一般に使用されている可塑剤及
び液状クマロンインデン樹脂、芳香族系炭化水素樹脂な
どの粘性物質などを挙げることができる。
Examples of fluids with a plasticizing effect that can be added include trisdichloropropyl phosphate, trischloroglobyl phosphate 71''+7) halogenated phosphate esters, tricresyl phosphate, triphenyl phosphate, cresyl diphenyl phosphate. Commonly used plasticizers such as phosphoric acid esters and phthalic acid esters, esters such as sebacic acid polyester, adipic acid polyester, trimellitic acid ester, liquid coumaron indene resin, aromatic hydrocarbon resin, etc. Examples include viscous substances.

本発明に使用するインシアネートは特に限定されず、ポ
リウレタンフォームの製造のために一般に使用されてい
るインシアネート、例えばトリレンジイソシアネートの
2,4−異性体若しくは2,6−異性体又はそれらの混
合物、ジフェニルメタンジイソシアネート、ヘキサメチ
レンジイソシアネート、又はナフタレンジイソシアネー
トなどが使用できる。発泡制御の点からトリレンジイソ
シアネートの2.4異性体と2,6−異性体の65:5
5混合物が好ましい。
The incyanate used in the present invention is not particularly limited, and includes incyanates commonly used for the production of polyurethane foam, such as the 2,4-isomer or 2,6-isomer of tolylene diisocyanate, or mixtures thereof. , diphenylmethane diisocyanate, hexamethylene diisocyanate, or naphthalene diisocyanate. From the viewpoint of foaming control, the ratio of 2.4 isomer and 2,6-isomer of tolylene diisocyanate is 65:5.
5 mixture is preferred.

発泡剤は水又はフロン−11、メチレンクロリドなどの
低沸点ハロゲン化炭化水素を単独使用又は併用できる。
As the blowing agent, water or a low boiling point halogenated hydrocarbon such as Freon-11 or methylene chloride can be used alone or in combination.

アミン触媒、整泡剤など他の添加剤は特に限定されず、
ポリウレタンフォームの製造のために一般に使用されて
いるものが使用できる。
Other additives such as amine catalysts and foam stabilizers are not particularly limited.
Those commonly used for the production of polyurethane foams can be used.

本発明のポリウレタンフォームの製造は有機ポリイソシ
アネート、ポリオール、触媒、発泡剤、添加剤などを同
時に混合して発泡させるワンシヲット法により行うのが
合理的、経済的かつ量産可能であるため好ましい。
The polyurethane foam of the present invention is preferably produced by a one-shot method in which an organic polyisocyanate, a polyol, a catalyst, a blowing agent, an additive, etc. are simultaneously mixed and foamed because it is rational, economical, and can be mass-produced.

〔実施例〕〔Example〕

以下実施例並びに比較例にて本発明の詳細な説明する。 The present invention will be explained in detail below using Examples and Comparative Examples.

表に示す配合に基づきポリウレタンフォームを製造した
Polyurethane foam was manufactured based on the formulation shown in the table.

得られた41SIPポリウレタンフオームについて密変
、硬さ、反発弾性、ヒステリシスロス、圧縮後の戻り特
性を測定し、それらの結果を表中和併記する。なお、硬
さ及び反発弾性の測定はJISK6401に基づいて行
った。圧縮後の戻り特性は、得られたフオーム(大きさ
soxsox50m)を鉄板の上に置き、円盤形の鉛の
重り(6に4、直径100鵡)をそのフオームの上に載
せて押しつぶした状態で30秒間放置後、該重りを取り
除き、この時点から元の形状に戻るまでの時間を測定し
た。
The resulting 41SIP polyurethane foam was measured for density change, hardness, impact resilience, hysteresis loss, and return characteristics after compression, and the results are also listed in the table. Note that hardness and impact resilience were measured based on JIS K6401. The return characteristics after compression were determined by placing the obtained foam (size SOXSOX 50 m) on an iron plate, placing a disc-shaped lead weight (4 in 6, diameter 100 m) on top of the foam, and crushing it. After leaving it for 30 seconds, the weight was removed, and the time from this point until it returned to its original shape was measured.

注1)平均分子量700、水酸基価24[lL4のポリ
オキシアルキレ/トリオール 2)平均分子量1500、水酸基価112.2のポリオ
キシアルキレントリオール 3)平均分子量3000、水酸基価5&1のポリオキシ
アルキレントリオール リ 平均分子量400、水酸基価4208のポリオキシ
アルキレントリオール 5)新日本製鉄■クマロンし−20 6)日東粉化工業−NS”100 7)ダブコ33Lv 8)  N−エチルモルホリン 反発弾性は小さい方が好ましく、比較例1及び2がそれ
ぞれ17チ及び45チと大きいのに対し、実施例1〜4
は6〜8チと小さかった。
Note 1) Polyoxyalkylene triol with an average molecular weight of 700 and a hydroxyl value of 24 [lL4] 2) Polyoxyalkylene triol with an average molecular weight of 1500 and a hydroxyl value of 112.2 3) Polyoxyalkylene triol with an average molecular weight of 3000 and a hydroxyl value of 5 & 1 Polyoxyalkylene triol with an average molecular weight of 400 and a hydroxyl value of 4208 5) Nippon Steel ■Kumaronshi-20 6) Nitto Funka Kogyo-NS"100 7) DABCO 33Lv 8) N-Ethylmorpholine The smaller the impact resilience, the better; Comparative Examples 1 and 2 were large at 17 inches and 45 inches, respectively, whereas Examples 1 to 4 were large.
It was small, 6 to 8 inches.

ヒステリシスロスは、大きい方が良く、実施例1〜4は
8五2〜89.6 %と大きく、比較例1も94.5%
と大きいが、比較例2は4&5チと小さかった。圧縮後
の戻り時間は30〜240秒の範囲が防音・割振性能の
ために好ましいが、比較例1は6に4の重量では圧縮さ
れず、強制的に更に加圧して7オームを圧縮すると歪み
が残り、完全に元に戻らず、比較例2Fiすぐに戻って
しまうのに対し、実施例1〜4は52〜152秒かかっ
た。
The larger the hysteresis loss, the better; Examples 1 to 4 are as high as 852 to 89.6%, and Comparative Example 1 is also 94.5%.
However, Comparative Example 2 was small at 4&5 inches. It is preferable for the return time after compression to be in the range of 30 to 240 seconds for soundproofing and vibration isolation performance, but Comparative Example 1 was not compressed at a weight of 6 to 4, and was distorted when further pressure was applied and compressed to 7 ohms. remained and did not completely return to its original state, and returned immediately in Comparative Example 2Fi, whereas Examples 1 to 4 took 52 to 152 seconds.

また、得られたポリウレタンフォームを防音性能の測定
に供した。測定は、20mの厚さの試験用フオームをそ
の上に厚さ5mのポリ塩化ビニルシートを重ねて積層体
とし、それを厚さα8mbの鋼板の上に載置し、100
に保たれた室内で該鋼板に振動音を発生させ、音圧レベ
ルを測定することKより行った。フオームを載置せずに
0.811の鋼板のみで行ったものを基準として結果を
第1図及び第2図に示した。
In addition, the obtained polyurethane foam was subjected to measurement of soundproofing performance. The measurement was carried out by placing a 20 m thick test foam on top of a 5 m thick polyvinyl chloride sheet, placing it on a steel plate with a thickness of α8 mb, and
Vibrating sound was generated on the steel plate in a room maintained at a constant temperature, and the sound pressure level was measured. The results are shown in FIGS. 1 and 2 based on the results obtained using only a 0.811 steel plate without placing the foam.

防音性能は、第1図及び第2図に示したように実施例1
及び2は比較例1に、対して周波数により最高5dB、
実施例5及び4#′i比較例2に対して周波数により最
高4dB優れていた。4?罠、低い周波数域の200〜
a o OHz において実施例1〜4は比較例1及び
2に対して2〜3dB防音性能が優れていた。これは実
施例のポリウレタンフォームが吸音性能に加えて制振性
能を有することを示すものである。
The soundproofing performance of Example 1 was as shown in Figures 1 and 2.
and 2 is up to 5 dB depending on the frequency compared to Comparative Example 1,
It was superior to Example 5 and 4#'i Comparative Example 2 by up to 4 dB depending on the frequency. 4? Trap, low frequency range 200~
At aoOHz, Examples 1 to 4 were superior to Comparative Examples 1 and 2 in soundproofing performance by 2 to 3 dB. This shows that the polyurethane foam of the example has vibration damping performance in addition to sound absorption performance.

〔発明の効果〕〔Effect of the invention〕

以上の結果から明らかなよう罠1本発明のポリウレタン
フォームは、上記したように規定したポリオールと可塑
効果を有する流動体を配合したため、吸音性能に加えて
制振性能を備えた優れた防音・制振材とすることができ
る。しかも、アスファルトを使用しないため、熱圧縮成
形等の加工時に加工装置がアスファルトによ抄汚染され
ることがなく、作業能率の低下を来たすことがない。更
K、充てん剤を使用していないため軽く、車両等への用
途としてはエネルギーの節約にもなり好ましいものであ
る。
As is clear from the above results, the polyurethane foam of the present invention contains the polyol specified above and a fluid having a plasticizing effect. It can be used as a shaking material. Moreover, since asphalt is not used, the processing equipment is not contaminated by asphalt during processing such as hot compression molding, and there is no reduction in work efficiency. It is lightweight because no filler is used, and it is preferable for applications such as vehicles as it saves energy.

更Kまた、本発明のポリウレタンフォームは特別な製造
装置を必要とせず、従来のポリウレタンフォーム製造装
置によりワンショット法により製造できるので量産も可
能であり、安い製造コストで生産でき、また、スクラッ
プの還元使用が可能であるため、資源の有効利用が図れ
る等多くの利点を併有する。
Further, the polyurethane foam of the present invention does not require any special manufacturing equipment, and can be manufactured by a one-shot method using conventional polyurethane foam manufacturing equipment, making it possible to mass produce it at low manufacturing costs. Since it can be reused, it has many advantages such as effective use of resources.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は実施例1及び2と比較例1の防音効果と周波数
の関係を示すグラフ、 第2図は実施例5及び4と比較例2の防音効果と周波数
の関係を示すグラフを表わす。 特許出願人  アキレス株式会社 牙1図 層表#!L H。 牙2図 周哀秋  Hz
FIG. 1 is a graph showing the relationship between the soundproofing effect and frequency of Examples 1 and 2 and Comparative Example 1, and FIG. 2 is a graph showing the relationship between the soundproofing effect and frequency of Examples 5 and 4 and Comparative Example 2. Patent applicant Achilles Co., Ltd. Fang 1 layer table #! LH. Fang 2 illustration Zhou Aiqiu Hz

Claims (1)

【特許請求の範囲】 有機ポリイソシアネートとポリオールとを発泡剤、触媒
、整泡剤及び他の添加剤の存在下にワンショット法によ
り軟質ポリウレタンフォームを製造する際に、 i)ポリオール成分として、2又は3官能で平均水酸基
価150ないし400を有する単独又は2種以上の組み
合わせのポリオキシアルキレンポリオールを使用し; ii)可塑効果を有する流動体を前記ポリオール100
重量部に対して10ないし100重量部;添加すること
によって得られたことを特徴とする防音・制振性フォー
ム。
[Claims] When producing a flexible polyurethane foam by a one-shot method using an organic polyisocyanate and a polyol in the presence of a blowing agent, a catalyst, a foam stabilizer and other additives, i) as a polyol component, 2 or using a trifunctional polyoxyalkylene polyol having an average hydroxyl value of 150 to 400, alone or in combination of two or more; ii) using a fluid having a plasticizing effect as the polyol 100;
10 to 100 parts by weight; a soundproofing/vibration-damping foam characterized by being obtained by adding 10 to 100 parts by weight;
JP60076962A 1985-04-11 1985-04-11 Soundproofing and damping foam manufacturing method Expired - Fee Related JPH0725863B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60076962A JPH0725863B2 (en) 1985-04-11 1985-04-11 Soundproofing and damping foam manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60076962A JPH0725863B2 (en) 1985-04-11 1985-04-11 Soundproofing and damping foam manufacturing method

Publications (2)

Publication Number Publication Date
JPS61235418A true JPS61235418A (en) 1986-10-20
JPH0725863B2 JPH0725863B2 (en) 1995-03-22

Family

ID=13620410

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60076962A Expired - Fee Related JPH0725863B2 (en) 1985-04-11 1985-04-11 Soundproofing and damping foam manufacturing method

Country Status (1)

Country Link
JP (1) JPH0725863B2 (en)

Cited By (2)

* 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
WO1993004103A2 (en) * 1991-08-20 1993-03-04 The Dow Chemical Company Polyurethanes having improved physical properties

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5289199A (en) * 1976-01-21 1977-07-26 Toyo Rubber Chem Ind Co Ltd Production of freely foldable polyurethane foam
JPS5496599A (en) * 1977-12-27 1979-07-31 Monsanto Co Composition for forming rigid polyurethane foam
JPS55144019A (en) * 1979-04-12 1980-11-10 Reeves Bros Inc Manufacture of fire retardant soft polyurethane foam blended with dibromoneopentylglycol and fire retardant plasticizer
JPS5857419A (en) * 1981-09-30 1983-04-05 Bridgestone Corp Vibration damping material

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5289199A (en) * 1976-01-21 1977-07-26 Toyo Rubber Chem Ind Co Ltd Production of freely foldable polyurethane foam
JPS5496599A (en) * 1977-12-27 1979-07-31 Monsanto Co Composition for forming rigid polyurethane foam
JPS55144019A (en) * 1979-04-12 1980-11-10 Reeves Bros Inc Manufacture of fire retardant soft polyurethane foam blended with dibromoneopentylglycol and fire retardant plasticizer
JPS5857419A (en) * 1981-09-30 1983-04-05 Bridgestone Corp Vibration damping material

Cited By (2)

* 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
WO1993004103A2 (en) * 1991-08-20 1993-03-04 The Dow Chemical Company Polyurethanes having improved physical properties

Also Published As

Publication number Publication date
JPH0725863B2 (en) 1995-03-22

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