JPH0448099B2 - - Google Patents

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Publication number
JPH0448099B2
JPH0448099B2 JP4734885A JP4734885A JPH0448099B2 JP H0448099 B2 JPH0448099 B2 JP H0448099B2 JP 4734885 A JP4734885 A JP 4734885A JP 4734885 A JP4734885 A JP 4734885A JP H0448099 B2 JPH0448099 B2 JP H0448099B2
Authority
JP
Japan
Prior art keywords
viscoelastic
crosslinking reaction
damping plate
manufacturing
curing agent
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.)
Expired
Application number
JP4734885A
Other languages
Japanese (ja)
Other versions
JPS61206640A (en
Inventor
Shinya Shimada
Hirobumi Kakimoto
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.)
Hayakawa Rubber Co Ltd
Original Assignee
Hayakawa Rubber Co Ltd
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 Hayakawa Rubber Co Ltd filed Critical Hayakawa Rubber Co Ltd
Priority to JP4734885A priority Critical patent/JPS61206640A/en
Publication of JPS61206640A publication Critical patent/JPS61206640A/en
Publication of JPH0448099B2 publication Critical patent/JPH0448099B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) 本発明は、制振板の製造方法に係り、制振、防
音に優れた性能を有し、特に重量衝撃源即ち、低
周波域の音源に起因する衝撃音の遮断性能を向上
させた制振板の製造方法に関するものである。 (従来技術) 近年、住宅に於る居住性能という観点から、遮
音、結露防止、断熱、害虫防止等が重要視されて
きた。そのうち遮音対策については、技術的困難
さもあつて衝撃音の遮断性能向上対策がクローズ
アツプされて来ている。更に近年、カーペツト、
畳類に於てはダニ等の害虫類が繁殖しやすく、木
質床材が見直されている。しかし乍ら、木質床の
最大の欠点は、スリツパ音を始め、子供の飛びは
ねる音等に起因する衝撃音を遮断する事が非常に
困難である点である。これら衝撃音は不快を感ず
る種類の騒音であり、固体振動の伝播により発生
する騒音のため、床板構造が大きな影響を及ぼす
事が知られている。床衝撃音の遮音性能を評価す
る衝撃源として、「建物の現場における床衝撃音
レベルの測定方法JIS−A−1418」で、ハイヒー
ル靴での歩行や、ナイフの落下を対象と考える力
積の小さい軽量衝撃源と疲び降り音や走り回る音
を対象と考える力積の大きい重量衝撃源とが規定
されている。 軽量衝撃源による遮音性能は、上階で畳床、カ
ーペット等床仕上げ材の使用、又は下階に天井を
増設する事により比較的容易に改善しうるが重量
衝撃源による遮音性能は周波数が低い為、通常床
板の板厚を厚くする方法がとられている。 (発明が解決しようとする課題) 床板の板厚増加は、剛性強化をもたらし、重量
衝撃源に対する遮音性能は向上するが、床板重量
の増加によりこれを支える柱、はり等の建物駆体
自体の強化、床下スペースの減少、住宅の軒高の
増加、居住空間の圧縮を来し、建築コストを含め
デメリツトが大きくなつてしまう。 床板厚の増加による剛性向上とは別に、床板に
高い制振性能を付加して、床板内での振動エネル
ギーの損失を増大させれば床衝撃音の遮断性能も
向上する筈である。しかしながら低周波域で遮音
効果を発揮しなければならない点、重量増を柱、
はり等建物構造体自体の強化が不要である範囲に
抑える必要がある点、既設住宅にも適用し得るも
のである点等の条件を考慮すると技術条件は極め
て難しくなる。 従来制振材として構造部材にシート状タイプの
ものを接着させる、又は、制振塗料を塗布、吹付
け等を行うものがある。しかしながらこれら非拘
束タイプのものは厚みを基板厚の2〜数倍にしな
いと制振効果が小さくなり、且つ、充分な厚みに
するとコスト高になつてしまう。 一方、建物、その他の構造体自体に高い制振性
能を付与する手段として、鋼板の間に粘弾性物質
をはさんだ拘束タイプの制振鋼板が極めて高制振
性能を有することが知られている。 粘弾性物としては、例えば特公昭39−12451号
公報、或いは、特公昭49−34703号公報などに見
られる如き酢酸ビニル、塩化ビニル、アクリルな
どの樹脂と、可塑剤、顔料などからなるプラスチ
ツク系の粘弾性物質やポリイソブチレン、ポリブ
テン、顔料などからなるゴム系の粘弾性物質が公
知であるが、これらの粘弾性物質は熱溶解したも
のを構造部材に粘着させるホツトメルトタイプ
故、建設現場、或いは、工場生産の場合でも通常
100℃以上で溶解させ、塗工する必要があり、木
質板への適用は木質板からの水分等の影響を受け
てふくれの発生等、不具合が発生し易く、又、熱
容量が大でコスト高になるなどにより望ましくな
い。 また従来のものとして、特開昭55−90735号公
報に記載の如く、ウレタンエラストマーを剛直な
板状体に一体発泡形成により同時に接着し、か
つ、ウレタンエラストマー材の基体底面に接する
部分に切欠部を設けたものが知られているが、発
泡体は永久圧縮歪を受け易く、製造当初は振動防
止効果が高くても徐々にその機能が低下し、長期
にわたる振動防止効果を保証できない欠点があ
る。このためにウレタンエラストマーの製造過程
で鎖長延長剤を用いてハードセグメント数を増加
させハードセグメントを多く有する比較的硬いウ
レタンエラストマーを使用し、かつ、基板との接
合面に切欠部を設けバネ定数を低減させるように
しているが、発泡体の振動防止効果の経時劣化を
防止し得ない欠点がある。 (課題を解決するための手段) 本発明は、特に近年、ダニを始めとする害虫に
対しての問題より、カベ紙、カーペツト、及び畳
から木質材への要求が高まり、従来床衝撃音レベ
ルに言うL−55が技術的に非常に困難とされてき
た木質材の衝撃音を緩和し、木質材でのL−55達
成を目的として、従来からの要望や技術的困難を
解決するため詳細な多くの実験の結果なされたも
ので本発明は少くとも未端に水酸基を有する液状
ゴムと、イソシアネート系硬化剤とを必須成分と
し、これを20万cps以下の粘度で混合し、これを
0℃〜80℃の反応温度で架橋反応させて得られた
エラストマーで、且つ架橋反応物が150℃以下の
温度条件下で流動しない無発泡の粘弾性物質A
を、木質系及び/又は無機質系の板材、若しくは
複合板材Bに複数層被着し拘束タイプのA,B多
層構造とする事を特徴とする制振板の製造方法に
あり、重量増が小さくて制振性能に優れ、衝撃音
の遮断性能に優れた制振板を提供するにある。 次に本発明の構成材料について説明する。 粘弾性物質Aとは、未端に水酸基を有する液状
ポリマーとイソシアネート系硬化剤を必須成分と
し、これを20万cps以下の粘度で二液混合し、こ
れを0℃〜80℃の反応温度で架橋反応させて得ら
れたエラストマーで、且つ架橋反応物が150℃以
下の温度条件下で流動しない無発泡の粘弾性体物
質である。 更に詳細に述べると、水酸基未端液状ポリマー
には主鎖をポリブタジエン、水素添加ポリブタジ
エン、ポリブタジエン−ニトリル、ポリブタジエ
ン−スチレン、クロロプレン、イソプレン等とし
た液状ゴムポリオール、ポリエーテルポリオー
ル、ポリエステルポリオール、ウレタンアクリル
ポリオール等があるが、それ等を単独、若しくは
併用して用いる事が出来る。 又、イソシアネート系硬化剤としては、トルイ
レンジイソシアネート、イソホロンジイソシアネ
ート、未端にイソシアネート基を有するプレポリ
マー、及び、それ等のブロツク品を挙げる事が出
来、単独、若しくは併用して用いる事が出来る。
イソシアネート系硬化剤はその配合比率、及び、
粘度等の問題で可塑剤と混合して用いることも出
来るが、可塑剤は脱水処理をしたものである事
と、イソシアネート化合物と反応しない事が必要
である。 上記のことき必須成分のみの組み合わせで本発
明を満足し得る粘弾性物質を得る事もできるが、
コスト面、作業性、物性の点で更に各種の添加剤
を加える事により、幅広い安定した粘弾性物質を
得る事が出来る。 添加剤として、可塑剤、瀝青物、充填剤、その
他を挙げる事が出来る。 次にそれ等の具体例を示す。 可塑剤は粘度を調節し、作業性の調整を行う
事、粘弾性体の物性コントロールを行う事、難燃
性を附与する事等を目的として配合される。 可塑剤の具体例としては、ナフテン酸オイル、
パラフイン系オイル、アロマテイツク系オイル、
ひまし油、綿実油、パインオイル、トール油、フ
タル酸誘導体、イソフタル酸誘導体、アジピン酸
誘導体、マレイン酸誘導体、液状ゴムの管能基を
含まないもの等があり、単独、又は併用して用い
る事が出来る。 瀝青物としては、ストレートアスフアルト、ブ
ロンアスフアルト、タール等があり、所望の粘弾
性体を得る為に、予め粘着性附与樹脂、石油系軟
化剤等で改質して用いる事も出来る。 充填剤は、振動減衰性、遮音性、難燃性に影響
を与え、主剤/硬化剤の配合比率の調整、粘性の
調整、及び配合のコストダウンを計る目的で使用
するものであり、ゴム及び塗料関係で使用される
ものを用いる事が出来る。 その具体例としては、マイカ、グラフアイト、
ヒル石、クレー、タルク等の鱗片状無機粉体、フ
エライト、金属粉、硫酸バリウム、リトポン等の
高比重充填剤、炭酸カルシウム、徴粉シリカ、カ
ーボン、炭酸マグネシウム、水酸化アルミニウ
ム、アスベスト等の汎用充填剤等を、単独、又は
併用して用いる事も出来る。又、三酸化アンチモ
ン、ホウ砂を難燃化を目的として用いる事も出来
る。その他の添加剤として、各種老化防止剤、触
媒、顔料、界面活性剤、防虫、防カビ、カツプリ
ング剤を配合する事も出来る。 上記の如く配合される粘弾性物質Aは、二液混
合作業時の粘度が20万CPS以下であり、架橋反応
物が150℃以下の温度条件下で流動しない粘弾性
物質Aであり、常温、低周波域での力学的損失率
が大きい事が要望される。 又、この粘弾性物質Aは、イソシアネート系硬
化剤により架橋反応を行うが、イソシアネート系
硬化剤の添加量により反応モル比を調節し、架橋
密度をコントロールする事が出来る。その結果、
非常に柔軟な粘弾性物質から硬い粘弾性物質迄得
られるが、本発明に適した反応モル比は、0.5モ
ル〜1.5モルNCO/OHである。 反応モル比が0.5モルNCO/OH以下である場
合は、イソシアネート系硬化剤が不充分である
為、未反応水酸基未端ポリマーが過剰となり、高
温での流動現象、低温でのゴム弾性の不虫が生
じ、振動吸収の温度特性が悪くなつたり、圧縮永
久歪が大きくなつたりする欠点が生じる。又、施
工面では硬化不良が発生する危険性が高まる。 逆に反応モル比が1.5モルNCO/OH以上の場
合、イソシアネート系硬化剤が過剰となり、ゴム
弾性が損なわれて供用温度域、及び低周波域での
制振特性が損なわれる傾向がある。又、施工面で
は余剰イソシアネート系硬化剤の微量水分等との
反応による炭酸ガスの発生に伴う発泡現象が起こ
り易く、粘弾性物質の耐久性に悪影響を及ぼす危
険性があり好ましくない。 尚、水酸基未端液状ゴム100重量部に対するイ
ソシアネート系硬化剤の必要量(反応モル比
1.0NCO/OHの場合)の計算方法は次の様にな
る。 硬化剤必要量=水酸基未端液状ゴムの重量(100)×水
酸基含有率(重量%)/イソシアネート基含有率(重量
%)×NCO/OH ここでNCO/OH=42/17=2.47である。 水酸基含有率とは、水酸基未端液状ゴム中の水
酸基の重量百分率を示す。 イソシアネート基含有率とは、イソシアネート
系硬化剤中のイソシアネート基の重量百分率を示
す。 次に架橋反応条件について述べると、本発明に
適用される粘弾性物質は、常温、若しくは加温時
に液状である、水酸基末端液状ゴムを主成分に含
む主剤と常温で液状であるイソシアネート系硬化
剤とが混合されて架橋反応を行つて得られる物質
であり、その架橋反応を行わせる条件としては、
温度と時間の要因が架橋反応速度に大きく係り、
非流動固体化に至る迄の架橋硬化時間は低温にな
るに従い長くなり、好ましくは、架橋反応温度が
0℃〜80℃の温度範囲である。 次に木質系、及び/又は、無機質系の板材、若
しくは複合板材Bの説明をする。 木質系板材とは、合板、化粧合板、寄木板、コ
ルク板、ラワン板、杉板等、各種の木材単板をそ
の具体例として挙げる事が出来る。 無機質板とは、石綿板、木毛セメント板、ケイ
カル板、ALC板、PC板、コンクリート板等をそ
の具体例として挙げる事が出来る。 複合板材とは、前記木質板材、及び/又は、無
機質板材とその組み合わせはもとより、加硫ゴム
シート、非加硫ゴムシート、塩化ビニルを始めと
するプラスチツクシート、ポリエチレンを始めと
する各種発泡体、ガラス繊維、フエルト等を1
種、又は2種以上併用して積層せしめた物を言
い、これらは制振板取付基材の不陸調整等にも有
効である。 又、木質系、及び/又は、無機質系の板材、若
しくは複合板材Bは必ずしも平板である必要はな
く、目的用途によつて、穴あき板、溝付板、波状
板等の板材であつてもよい。 次に、木質系、及び/又は、無機質の板材、若
しくは複合板材Bと粘弾性物質Aとの組み合わせ
はどの様になつてもよく、粘弾性物質Aは前記板
材Bとの組み合わせにより2層以上となつてもよ
い。 又、粘弾性物質Aの厚みは、1層当り0.5mm〜
10.0mmである事が望ましく、0.5mm以下では衝撃
遮断能力が乏しく、10.0mm以上ではコスト面で不
適当である。 板材Bは性能的、経済的に通常用いられる取扱
い容易な材料でよく、充分な剛性を持ち得る板厚
であればよい。 上記の如く構成された制振板は、床材としての
みならず、天井材、壁材としての応用展開も当然
可能である。 次に、本発明の制振板の実施態様を示すが、本
発明はこれにより何等制限を受けるもではない。 先ず粘弾性物質Aの製造の一態様を示す。 撹拌容器中に反応性液状ゴムを投入し、加熱溶
解したアスフアルト、及び粘着附与樹脂、可塑剤
を投入し、充分均一な溶液となる様に混合した
後、充填剤、老化防止剤、触媒等を適宜添加し、
例えばインクロールの如き混合分散機を用いて充
分均一な溶液として粘弾性物質の主剤を得る。 次に前記方法にて得られた主剤にイソシアネー
ト系硬化剤に加えて充分混合した後、木質系板材
上に塗布し、架橋反応せしめ本発明の制振板を得
た。 次に本発明に用いる粘弾性物質Aの架橋反応例
を、液温と固体化に要する時間の関係にて第1表
に示す。本発明に用いる粘弾性物質Aは、0℃以
下の低温から80℃以上の高温でも架橋反応する
が、0℃以下の低温の場合は架橋反応に要する時
間が長すぎる。又、80℃以上の高温の場合は、木
質系、及び/又は、無機質板材、若しくは複合板
材Bから発生する水蒸気等によるふくれ等の問題
点が発生し易い等の欠点を有するため、0℃〜80
℃での温度範囲で架橋反応を行う事が望ましい。 次に本発明に用いる粘弾性物質Aの配合例を第
2表に示す。 第2表に示した配合例は、何れも本発明に適用
出来る粘弾性物質であるが各々に次の様な特徴を
有する。 配合例1は、低粘度であり、作業性に優れ、温
度変化による衝撃遮断性に差がほとんど生じない
特徴を有する。 配合例2は、粘弾性物質の架橋反応を行わせる
際の主剤と硬化剤の重量比が100:8のタイプで
あり、混合撹拌操作を改善したものである。 配合例3は、特に粘弾性物質のコスト面を重視
した場合の配合例である。このタイプは、加温す
る事により作業性改善、及び架橋反応速度が早い
特徴を有し、工場ライン生産に適するものであ
る。
(Industrial Application Field) The present invention relates to a method for manufacturing a vibration damping plate, which has excellent vibration damping and soundproofing performance, and particularly blocks impact noise caused by heavy impact sources, that is, low frequency sound sources. The present invention relates to a method of manufacturing a damping plate with improved performance. (Prior Art) In recent years, importance has been placed on sound insulation, prevention of dew condensation, heat insulation, prevention of pests, etc. from the perspective of livability in houses. Regarding sound insulation measures, due to technical difficulties, measures to improve the performance of blocking impact noise are attracting attention. Furthermore, in recent years, carpets,
Pests such as mites can easily breed in tatami mats, so wooden flooring materials are being reconsidered. However, the biggest drawback of wooden floors is that it is extremely difficult to block out impact noises caused by the sound of slippers and the sounds of children jumping. These impact noises are a type of noise that makes people feel uncomfortable, and it is known that the structure of the floorboards has a large effect because the noise is generated by the propagation of solid vibrations. As an impact source for evaluating the sound insulation performance of floor impact sound, the ``Method for measuring floor impact sound level in building sites JIS-A-1418'' uses impulse sources that consider walking in high-heeled shoes and falling knives. It defines a small lightweight impact source and a heavy impact source with a large impulse, which is considered to be the sound of falling fatigue and the sound of running around. Sound insulation performance due to light impact sources can be relatively easily improved by using floor finishing materials such as tatami floors or carpets on the upper floors, or by adding ceilings on the lower floors, but sound insulation performance due to heavy impact sources has a low frequency. Therefore, the usual method is to increase the thickness of the floorboard. (Problems to be Solved by the Invention) Increasing the thickness of the floorboards increases the rigidity and improves the sound insulation performance against weight impact sources, but the increase in the weight of the floorboards causes damage to the building structure itself such as columns and beams that support it. This results in reinforcement, a decrease in the space under the floor, an increase in the height of the eaves of the house, and a compression of the living space, which increases the disadvantages including the construction cost. In addition to improving rigidity by increasing the thickness of the floorboard, adding high vibration damping performance to the floorboard and increasing the loss of vibration energy within the floorboard should improve the ability to block floor impact noise. However, the main drawbacks are the need to exhibit sound insulation effects in the low frequency range, and the increased weight.
The technical conditions become extremely difficult when considering conditions such as the need to keep reinforcement of the building structure itself such as beams to a level that is not necessary, and the fact that it can be applied to existing houses as well. Conventionally, as vibration damping materials, there are those in which a sheet-type material is adhered to a structural member, or a damping material is applied or sprayed. However, in these non-restrictive types, the vibration damping effect will be reduced unless the thickness is two to several times the substrate thickness, and if the thickness is made sufficient, the cost will be high. On the other hand, as a means of imparting high vibration damping performance to buildings and other structures themselves, restraint-type vibration damping steel plates in which a viscoelastic substance is sandwiched between steel plates are known to have extremely high vibration damping performance. . Examples of viscoelastic materials include plastics made of resins such as vinyl acetate, vinyl chloride, and acrylic, as well as plasticizers and pigments, as disclosed in Japanese Patent Publication No. 39-12451 and Japanese Patent Publication No. 49-34703. Rubber-based viscoelastic substances made of polyisobutylene, polybutene, pigments, etc. are well known, but because these viscoelastic substances are hot-melt types that are melted and adhered to structural members, they are often used at construction sites, Or, even in the case of factory production,
It must be melted and applied at a temperature of 100°C or higher, and when applied to wood boards, problems such as blistering are likely to occur due to the influence of moisture from the wood boards, and the heat capacity is large, making it expensive. This is undesirable because it causes In addition, as a conventional method, as described in JP-A-55-90735, a urethane elastomer is bonded to a rigid plate-like body at the same time by integral foaming, and a notch is formed in the part of the urethane elastomer material that is in contact with the bottom surface of the base. However, foams are susceptible to permanent compressive strain, and even if they have a high vibration-preventing effect at the beginning of manufacture, their function gradually deteriorates, and the drawback is that long-term vibration-preventing effects cannot be guaranteed. . To this end, we use a relatively hard urethane elastomer that has many hard segments by increasing the number of hard segments using a chain extender during the manufacturing process of the urethane elastomer, and we also create a notch on the bonding surface with the substrate to increase the spring constant. However, there is a drawback that the vibration-preventing effect of the foam cannot be prevented from deteriorating over time. (Means for Solving the Problems) The present invention is designed to solve the problem of floor impact sound levels that have been lower than the conventional floor impact sound levels, especially in recent years when there has been an increasing demand for wooden materials instead of wall paper, carpets, and tatami mats due to problems with pests such as mites. In order to alleviate the impact noise of wood materials, which has been considered to be technically extremely difficult, and to achieve L-55 with wood materials, we have developed detailed information to solve the traditional requests and technical difficulties. The present invention was made as a result of many experiments, and the present invention consists of a liquid rubber having at least an end of hydroxyl groups and an isocyanate curing agent, which are mixed at a viscosity of 200,000 cps or less, and then Non-foaming viscoelastic material A, which is an elastomer obtained by crosslinking reaction at a reaction temperature of ℃ to 80℃, and in which the crosslinking reaction product does not flow under temperature conditions of 150℃ or less
A method for producing a vibration damping plate characterized in that a plurality of layers are applied to a wood-based and/or inorganic-based board material or a composite board B to form a restraint type A and B multilayer structure, and the weight increase is small. To provide a vibration damping plate having excellent vibration damping performance and excellent impact sound blocking performance. Next, the constituent materials of the present invention will be explained. Viscoelastic substance A consists of a liquid polymer with terminal hydroxyl groups and an isocyanate curing agent as essential components, which are mixed together at a viscosity of 200,000 cps or less, and then mixed at a reaction temperature of 0°C to 80°C. It is an elastomer obtained by crosslinking reaction, and the crosslinking reaction product is a non-foaming viscoelastic material that does not flow under temperature conditions of 150°C or lower. More specifically, hydroxyl-terminated liquid polymers include liquid rubber polyols whose main chain is polybutadiene, hydrogenated polybutadiene, polybutadiene-nitrile, polybutadiene-styrene, chloroprene, isoprene, etc., polyether polyols, polyester polyols, urethane acrylic polyols. These can be used alone or in combination. Examples of the isocyanate curing agent include toluylene diisocyanate, isophorone diisocyanate, prepolymers having isocyanate groups at the ends, and block products thereof, which can be used alone or in combination.
The isocyanate curing agent has its blending ratio and
Due to problems such as viscosity, it can be used in combination with a plasticizer, but the plasticizer must be dehydrated and must not react with the isocyanate compound. Although it is possible to obtain a viscoelastic material that satisfies the present invention by combining only the above essential components,
From the viewpoint of cost, workability, and physical properties, a wide variety of stable viscoelastic substances can be obtained by adding various additives. As additives, mention may be made of plasticizers, bituminous substances, fillers, etc. Next, specific examples thereof will be shown. Plasticizers are blended for the purposes of adjusting viscosity and workability, controlling the physical properties of viscoelastic bodies, and imparting flame retardancy. Specific examples of plasticizers include naphthenic acid oil,
Paraffin oil, aromatic oil,
There are castor oil, cottonseed oil, pine oil, tall oil, phthalic acid derivatives, isophthalic acid derivatives, adipic acid derivatives, maleic acid derivatives, and those that do not contain the tubular functional group of liquid rubber, and they can be used alone or in combination. . Bituminous materials include straight asphalt, blown asphalt, tar, etc., and in order to obtain a desired viscoelastic body, they can be used after being modified with a tackifying resin, a petroleum softener, etc. Fillers affect vibration damping properties, sound insulation properties, and flame retardancy, and are used to adjust the blending ratio of the main ingredient/curing agent, adjust viscosity, and reduce the cost of blending. Those used in paints can be used. Specific examples include mica, graphite,
Scale-like inorganic powders such as vermiculite, clay, and talc, high-density fillers such as ferrite, metal powder, barium sulfate, and lithopone, and general-purpose materials such as calcium carbonate, powdered silica, carbon, magnesium carbonate, aluminum hydroxide, and asbestos. Fillers and the like can also be used alone or in combination. Moreover, antimony trioxide and borax can also be used for the purpose of flame retardation. As other additives, various anti-aging agents, catalysts, pigments, surfactants, insect repellents, anti-mold agents, and coupling agents can be added. The viscoelastic substance A blended as described above has a viscosity of 200,000 CPS or less during two-component mixing operation, and the crosslinking reaction product does not flow under temperature conditions of 150°C or less. It is desired that the mechanical loss rate be large in the low frequency range. Further, this viscoelastic substance A undergoes a crosslinking reaction using an isocyanate curing agent, and the crosslinking density can be controlled by adjusting the reaction molar ratio by adjusting the amount of the isocyanate curing agent added. the result,
Although very soft viscoelastic materials to hard viscoelastic materials can be obtained, the reaction molar ratio suitable for the present invention is between 0.5 mol and 1.5 mol NCO/OH. If the reaction molar ratio is less than 0.5 mol NCO/OH, the isocyanate curing agent is insufficient, and unreacted hydroxyl group-terminated polymer becomes excessive, leading to flow phenomena at high temperatures and poor rubber elasticity at low temperatures. This results in drawbacks such as poor vibration absorption temperature characteristics and increased compression set. Furthermore, in terms of construction, there is an increased risk of curing failure. Conversely, when the reaction molar ratio is 1.5 moles NCO/OH or more, the isocyanate curing agent becomes excessive, which tends to impair rubber elasticity and damping properties in the service temperature range and low frequency range. In addition, in terms of construction, a foaming phenomenon is likely to occur due to the generation of carbon dioxide gas due to the reaction of excess isocyanate-based curing agent with trace amounts of moisture, etc., which is undesirable since there is a risk of adversely affecting the durability of the viscoelastic material. The required amount of isocyanate curing agent (reaction molar ratio) per 100 parts by weight of hydroxyl terminated liquid rubber
1.0NCO/OH) is calculated as follows. Required amount of curing agent=weight of hydroxyl-terminated liquid rubber (100) x hydroxyl group content (wt%)/isocyanate group content (wt%) x NCO/OH where NCO/OH = 42/17 = 2.47. The hydroxyl group content refers to the weight percentage of hydroxyl groups in the hydroxyl group-terminated liquid rubber. The isocyanate group content refers to the weight percentage of isocyanate groups in the isocyanate curing agent. Next, regarding the crosslinking reaction conditions, the viscoelastic substance applied to the present invention consists of a main ingredient containing a hydroxyl-terminated liquid rubber that is liquid at room temperature or when heated, and an isocyanate curing agent that is liquid at room temperature. It is a substance obtained by mixing and performing a crosslinking reaction, and the conditions for performing the crosslinking reaction are as follows:
Temperature and time factors greatly affect the crosslinking reaction rate;
The crosslinking curing time required to reach non-fluid solidification becomes longer as the temperature decreases, and preferably the crosslinking reaction temperature is in the temperature range of 0°C to 80°C. Next, wood-based and/or inorganic-based board material or composite board material B will be explained. Specific examples of wood-based board materials include various wood veneers, such as plywood, decorative plywood, parquet board, cork board, lauan board, and cedar board. Specific examples of inorganic boards include asbestos boards, wood wool cement boards, silica boards, ALC boards, PC boards, and concrete boards. Composite board materials include not only the above-mentioned wood board materials and/or inorganic board materials and combinations thereof, but also vulcanized rubber sheets, non-vulcanized rubber sheets, plastic sheets including vinyl chloride, various foams including polyethylene, 1 glass fiber, felt, etc.
It refers to a type or a combination of two or more types laminated together, and these are also effective for adjusting the unevenness of the vibration damping plate mounting base material. In addition, the wood-based and/or inorganic board material or composite board material B does not necessarily have to be a flat board, and may be a perforated board, a grooved board, a corrugated board, etc. depending on the intended use. good. Next, the combination of the wood-based and/or inorganic board material or the composite board B and the viscoelastic substance A may be any combination, and the viscoelastic material A may have two or more layers depending on the combination with the board material B. It may become. In addition, the thickness of the viscoelastic material A is 0.5 mm per layer.
A thickness of 10.0 mm is desirable; if it is less than 0.5 mm, the impact isolation ability is poor, and if it is more than 10.0 mm, it is inappropriate from a cost perspective. The plate material B may be any material that is commonly used in terms of performance and economy and is easy to handle, as long as it has a thickness that provides sufficient rigidity. The damping plate configured as described above can of course be applied not only as a flooring material but also as a ceiling material and a wall material. Next, embodiments of the damping plate of the present invention will be shown, but the present invention is not limited thereto in any way. First, one aspect of the production of viscoelastic material A will be described. Pour the reactive liquid rubber into a stirring container, add the heated and melted asphalt, tackifier resin, and plasticizer, mix to make a sufficiently uniform solution, and then add fillers, anti-aging agents, catalysts, etc. Add as appropriate,
For example, the main ingredient of the viscoelastic substance is obtained as a sufficiently uniform solution using a mixing and dispersing machine such as an ink roll. Next, an isocyanate curing agent was added to the base material obtained in the above method, and the mixture was sufficiently mixed, and then applied onto a wood board to cause a crosslinking reaction, thereby obtaining a vibration damping plate of the present invention. Next, Table 1 shows an example of the crosslinking reaction of the viscoelastic material A used in the present invention in terms of the relationship between the liquid temperature and the time required for solidification. The viscoelastic material A used in the present invention undergoes a crosslinking reaction even at a low temperature of 0°C or lower to a high temperature of 80°C or higher, but the time required for the crosslinking reaction at a low temperature of 0°C or lower is too long. In addition, in the case of high temperatures of 80°C or higher, problems such as blistering due to water vapor generated from wood-based and/or inorganic board materials or composite board material B are likely to occur. 80
It is desirable to carry out the crosslinking reaction in the temperature range of °C. Next, Table 2 shows blending examples of the viscoelastic material A used in the present invention. The formulation examples shown in Table 2 are all viscoelastic substances that can be applied to the present invention, but each has the following characteristics. Formulation Example 1 has characteristics such as low viscosity, excellent workability, and almost no difference in impact insulation properties due to temperature changes. Formulation Example 2 is a type in which the weight ratio of the main agent and curing agent is 100:8 when crosslinking the viscoelastic substance, and the mixing and stirring operation is improved. Formulation example 3 is a combination example in which the cost aspect of the viscoelastic substance is particularly important. This type has the characteristics of improved workability and fast crosslinking reaction rate by heating, and is suitable for factory line production.

【表】【table】

【表】【table】

【表】 次に試験方法について記す。 表3に示す構成をもつて供試体とし、JIS−A
−1418に記される「建築物の現場における床衝撃
音レベルの測定方法」に従い、床衝撃音レベルの
測定を行つた。 尚、第5図に試験設備の概要図を示した。 又、測定結果と「床衝撃音に関する評価の遮音
等級」に照し合わせた評価は、第4表に示した。 次に本発明に適用する水酸基未端液状ゴムとイ
ソシアネート系硬化剤を必須成分とし、且つ、架
橋反応物が150℃以下の温度条件下で流動しない
粘弾性物質Aと木質系、及び/又は、無機質系の
板材、若しくは複合板材Bの構成と制振効果につ
いて第3表、及び第4表に示す。 実施例1は、木質フロアー材を板材Bとし、粘
弾性物質Aを積層した例である。 実施例2は、実施例1にラワン合板とポリエチ
レン発泡シートを積層した例である。 実施例3は、実施例1に更に石綿板とポリエチ
レン発泡シートを積層した例である。 比較例1は、粘弾性物質Aの代わりに加硫ゴム
板を使用した例である。 比較例2は、実施例1〜3に使用した同一の板
材B単独の例である。 比較例3は、実施例3に使用した石綿板単独の
例である。 比較例4は、粘弾性物質Aの厚みが0.5mm以下
の場合の例である。 第4表の結果より、実施例1は木質系板材Bに
粘弾性物質Aを5mm厚で積層して成る制振板であ
り、遮音等級L−55を達成している。 実施例2は、木質系板材Bの間に粘弾性物質A
を3mm厚みで積層し、更にポリエチレンシート、
又はゴムシートを積層して成る制振板であり、遮
音等級L−55を達成している。 実施例3は、木質系板材Bと無機質系板材Bと
の間に粘弾性物質Aを積層し、更にポリエチレン
シート、又はゴムシートを積層して成る制振板で
あり、遮音等級L−55を達成している。 比較例1は、木質系床材Bと加硫ゴム板をクロ
ロプレン系接着剤で積層した制振板であるが、粘
弾性物質Aを積層していない為、本発明の制振板
の製造方法に該当するものではない。 比較例2は、実施例1〜3に表層部として使用
した木質系板材B単独で用いた場合を示したもの
であり、本発明に該当するものではない。 比較例3は、実施例3に使用した無機質系板材
B単独で用いた場合を示したものであり、本発明
に該当するものではない。 比較例4は、実施例1の粘弾性物質Aの厚みが
0.4mmであり、本発明の粘弾性物質Aの厚みの条
件より外れる。 以上の事から、実施例1〜3は何れも遮音等級
L−55を達成しており、粘弾性物質Aを制振板に
適用した事により大幅な改善が出来た。 又、比較例4に於いても遮音性能は充分でない
ものの、相当改善されており、粘弾性物質の衝撃
音の遮断性能の高さを知る事が出来る。 上記の如く、本発明により得られた制振材は木
質系板材に於いて、従来技術では達し得なかつた
遮音等級L−55を達成する事が出来た。 本発明の制振材は床のみに限るものでなく、天
井材、壁材への適用を行う事により、衝撃音の遮
断に対し非常に有効であり、快適な居住空間を得
る事が出来る点で社会への貢献度は大である。
[Table] Next, the test method is described. A specimen with the configuration shown in Table 3 was used, and JIS-A
The floor impact sound level was measured in accordance with the ``Method for measuring floor impact sound level at building sites'' described in 1418. Incidentally, Fig. 5 shows a schematic diagram of the test equipment. Table 4 shows the measurement results and the evaluation based on the "sound insulation grade for evaluation of floor impact noise." Next, a viscoelastic substance A and a wood-based material, which have the hydroxyl-terminated liquid rubber and the isocyanate curing agent as essential components applied to the present invention, and in which the crosslinking reaction product does not flow under temperature conditions of 150°C or lower, and/or Tables 3 and 4 show the structure and damping effect of the inorganic plate material or composite plate material B. Example 1 is an example in which a wooden floor material is used as a board material B, and a viscoelastic material A is laminated thereon. Example 2 is an example in which lauan plywood and a polyethylene foam sheet were laminated on Example 1. Example 3 is an example in which an asbestos board and a polyethylene foam sheet were further laminated on Example 1. Comparative Example 1 is an example in which a vulcanized rubber plate was used instead of the viscoelastic material A. Comparative Example 2 is an example in which the same plate material B used in Examples 1 to 3 is used alone. Comparative Example 3 is an example in which the asbestos board used in Example 3 was used alone. Comparative Example 4 is an example in which the thickness of the viscoelastic material A is 0.5 mm or less. From the results shown in Table 4, Example 1 is a damping plate made by laminating viscoelastic material A to a thickness of 5 mm on wood board B, and achieves a sound insulation grade of L-55. In Example 2, a viscoelastic substance A is placed between wood-based board B.
Laminated with a thickness of 3 mm, and then a polyethylene sheet,
Or, it is a vibration damping plate made of laminated rubber sheets, achieving a sound insulation grade of L-55. Example 3 is a vibration damping plate made by laminating a viscoelastic substance A between a wooden board B and an inorganic board B, and further laminating a polyethylene sheet or a rubber sheet, and has a sound insulation grade of L-55. Achieved. Comparative Example 1 is a damping board made by laminating wood-based flooring material B and a vulcanized rubber board with a chloroprene adhesive, but since the viscoelastic material A is not laminated, the manufacturing method of the damping board of the present invention is not applicable. does not apply. Comparative Example 2 shows the case where the wooden board B used as the surface layer in Examples 1 to 3 was used alone, and does not correspond to the present invention. Comparative Example 3 shows the case where the inorganic plate material B used in Example 3 was used alone, and does not correspond to the present invention. In Comparative Example 4, the thickness of the viscoelastic material A of Example 1 was
The thickness is 0.4 mm, which is outside the thickness condition of the viscoelastic material A of the present invention. From the above, Examples 1 to 3 all achieved the sound insulation grade L-55, and a significant improvement was achieved by applying the viscoelastic material A to the damping plate. Although the sound insulation performance of Comparative Example 4 is not sufficient, it is considerably improved, and it can be seen that the impact sound insulation performance of the viscoelastic material is high. As mentioned above, the damping material obtained by the present invention was able to achieve a sound insulation grade of L-55 in wood-based board materials, which was not possible with the prior art. The vibration damping material of the present invention is not limited to floors only, but can be applied to ceiling materials and wall materials, making it extremely effective in blocking impact noise and creating a comfortable living space. The contribution to society is significant.

【表】【table】

【表】 注:括弧内は、厚みを示す
[Table] Note: Thickness is shown in parentheses.

【表】 依る
[Table] Depends

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

第1図は、板材Bと粘弾性物質Aとの積層を示
す断面構成図であり、第2図は、板材Bで粘弾性
物質Aをサンドイツチし、制振板取付基材面に発
泡ポリエチレンシート、又はゴムシートを積層し
た断面構成図であり、第3図は、板材Bとゴムシ
ート、又は発泡ポリエチレンシートと粘弾性物質
Aとグラスウール、フエルト、又は各種発泡体を
積層した断面構成図であり、第4図は、板材Bと
粘弾性物質Aとを交互に積層した断面構成図であ
り、さらに、第5図は、実験設備の概要図であ
る。 1…制振板取付基材、2…木質系板材、又は無
機質系板材、3…粘弾性物質、4…ゴムシート、
又は発泡ポリエチレンシート、5…グラスウー
ル、又は各種発泡体、又はフエルト。
FIG. 1 is a cross-sectional diagram showing the lamination of plate material B and viscoelastic substance A, and FIG. 2 is a cross-sectional diagram showing the lamination of plate material B and viscoelastic substance A. FIG. , or a sectional configuration diagram of a laminated rubber sheet, and FIG. 3 is a sectional configuration diagram of a laminated plate material B and a rubber sheet, or a foamed polyethylene sheet, a viscoelastic substance A, and glass wool, felt, or various foams. , FIG. 4 is a cross-sectional configuration diagram in which plate material B and viscoelastic material A are alternately laminated, and FIG. 5 is a schematic diagram of the experimental equipment. 1... Damping plate mounting base material, 2... Wooden board material or inorganic board material, 3... Viscoelastic substance, 4... Rubber sheet,
or foamed polyethylene sheet, 5...glass wool, or various foams, or felt.

Claims (1)

【特許請求の範囲】 1 少くとも末端に水酸基を有する液状ゴムと、
イソシアネート系硬化剤とを必須成分とし、これ
を20万cps以下の粘度で混合し、これを0℃〜80
℃の反応温度で架橋反応させて得られたエラスト
マーで、且つ架橋反応物が150℃以下の温度条件
下で流動しない無発泡の粘弾性物質Aを、木質系
及び/又は無機質系の板材、若しくは複合板材B
に複数層被着し拘束タイプのA,B多層構造とす
る事を特徴とする制振板の製造方法。 2 粘弾性物質Aが、二液混合作業の粘度が20万
cps以下であり、架橋反応温度が0℃〜80℃の低
温から中高温で架橋反応させて得られる無発泡の
エラストマーであることを特徴とする特許請求の
範囲第1項記載の制振板の製造方法。 3 粘弾性物質の架橋反応物の厚みが0.5mm〜
10.0mmである事を特徴とする特許請求の範囲第1
項記載の制振板の制造方法。 4 粘弾性物質Aは添加剤として、適量の可塑
剤、瀝青剤、充填剤の何れか1種又は2種以上を
配合して得られる特許請求の範囲第1項記載の制
振板の製造方法。 5 粘弾性物質Aは添加剤として、各種老化防止
剤、触媒、顔料、界面活性剤、防虫剤、防カビ
剤、カツプリング剤の何れか1種又は2種以上を
適量配合して得られる特許請求の範囲第1項記載
の制振板の製造方法。 6 末端に水酸基を有する液状ゴムとイソシアネ
ート系硬化剤との反応モル比は0.5〜1.5モル
NCO/OHである特許請求の範囲第1項記載の制
振板の製造方法。 7 末端に水酸基を有する液状ゴム100重量部に
対するイソシアネート系硬化剤の必要量は 硬化剤必要量=水酸基末端液状ゴムの重量(100)×水
酸基含有率(重量%)/イソシアネート基含有率(重量
%)×NCO/OH ここでNCO/OH=42/17=2.47 である特許請求の範囲第1項記載の制振板の製造
方法。
[Claims] 1. A liquid rubber having at least a hydroxyl group at the end;
An isocyanate curing agent is an essential component, and this is mixed at a viscosity of 200,000 cps or less, and this is heated from 0℃ to 80℃.
A non-foamed viscoelastic material A, which is an elastomer obtained by a crosslinking reaction at a reaction temperature of 150°C and in which the crosslinking reaction product does not flow under a temperature condition of 150°C or less, is used as a wood-based and/or inorganic board material, or Composite board material B
A method for manufacturing a vibration damping plate, characterized in that a plurality of layers are adhered to the plate to form a restraining type A and B multilayer structure. 2 Viscoelastic substance A has a viscosity of 200,000 yen during two-liquid mixing work.
cps or less and is a non-foamed elastomer obtained by crosslinking reaction at a low to medium-high crosslinking reaction temperature of 0°C to 80°C. Production method. 3 The thickness of the crosslinking reaction product of the viscoelastic substance is 0.5 mm ~
Claim 1 characterized in that the diameter is 10.0 mm.
Method of manufacturing the vibration damping plate described in Section 1. 4. The method for manufacturing a damping plate according to claim 1, wherein the viscoelastic substance A is obtained by blending an appropriate amount of one or more of a plasticizer, a bituminous agent, and a filler as an additive. . 5 Viscoelastic substance A is a patent claim obtained by blending appropriate amounts of any one or two or more of various anti-aging agents, catalysts, pigments, surfactants, insect repellents, fungicides, and coupling agents as additives. A method for manufacturing a damping plate according to item 1. 6. The reaction molar ratio between the liquid rubber having a hydroxyl group at the end and the isocyanate curing agent is 0.5 to 1.5 moles.
A method for manufacturing a damping plate according to claim 1, which is NCO/OH. 7 The required amount of isocyanate curing agent for 100 parts by weight of liquid rubber having a hydroxyl group at the end is calculated as follows: Required amount of curing agent = Weight of hydroxyl group-terminated liquid rubber (100) x Hydroxyl group content (wt%) / Isocyanate group content (wt%) )×NCO/OH where NCO/OH=42/17=2.47, the method for manufacturing a damping plate according to claim 1.
JP4734885A 1985-03-12 1985-03-12 Manufacture of vibration-damping board Granted JPS61206640A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4734885A JPS61206640A (en) 1985-03-12 1985-03-12 Manufacture of vibration-damping board

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4734885A JPS61206640A (en) 1985-03-12 1985-03-12 Manufacture of vibration-damping board

Publications (2)

Publication Number Publication Date
JPS61206640A JPS61206640A (en) 1986-09-12
JPH0448099B2 true JPH0448099B2 (en) 1992-08-05

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JP4734885A Granted JPS61206640A (en) 1985-03-12 1985-03-12 Manufacture of vibration-damping board

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Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63274541A (en) * 1987-05-06 1988-11-11 Idemitsu Petrochem Co Ltd Soundproof material

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JPS61206640A (en) 1986-09-12

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