JPH061904A - Vibration-deadening material composition - Google Patents

Vibration-deadening material composition

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Publication number
JPH061904A
JPH061904A JP4185706A JP18570692A JPH061904A JP H061904 A JPH061904 A JP H061904A JP 4185706 A JP4185706 A JP 4185706A JP 18570692 A JP18570692 A JP 18570692A JP H061904 A JPH061904 A JP H061904A
Authority
JP
Japan
Prior art keywords
resin
petroleum
softening point
weight
parts
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
JP4185706A
Other languages
Japanese (ja)
Other versions
JP3177620B2 (en
Inventor
Yuji Takeda
裕二 竹田
Koji Tanaka
浩二 田中
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.)
Tosoh Corp
Original Assignee
Tosoh 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 Tosoh Corp filed Critical Tosoh Corp
Priority to JP18570692A priority Critical patent/JP3177620B2/en
Publication of JPH061904A publication Critical patent/JPH061904A/en
Application granted granted Critical
Publication of JP3177620B2 publication Critical patent/JP3177620B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Vibration Prevention Devices (AREA)

Abstract

PURPOSE:To obtain a composition suitable for automobiles, household electric appliances, having high vibration damping properties by blending an ethylenic copolymer with a hydrocarbon resin, a petroleum-based resin, etc. CONSTITUTION:(A) 100 pts.wt. ethylenic copolymer is blended with (B) 100-300 pts.wt. resinous substance having 90-120 deg.C softening point obtained by blending a hydrocarbon resin having 115-145 deg.C softening point with a resin selected from an aliphatic petroleum resin, an aromatic petroleum resin, an aliphatic aromatic copolymer-based petroleum resin, a terpene-based resin and a coumarone-based resin having 50-100 deg.C softening point obtained by polymerizing 100 pts.wt. raw material oil having 60-90% indene content prepared from distillate having 140-220 deg.C boiling point among cracked petroleum distillate of cracking of petroleums in the presence of 4-10 pts.wt. phenolic compound by using a Friedel- Crafts catalyst.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、制振性能の改良された
制振材に関するもので、自動車、建材、家電機器等、振
動抑制を目的とする分野で幅広く利用できるものであ
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a vibration damping material having improved vibration damping performance, and can be widely used in fields for suppressing vibration, such as automobiles, building materials and home appliances.

【0002】[0002]

【従来の技術】従来より、成形性の向上あるいは軽量化
を目的とした制振材の結合材料としてエチレン系共重合
物を用いることが提案されている(特開昭52−977
02、特開昭54−110256、特開昭61−222
972、特開昭63−295669)。さらに、これら
エチレン系共重合物を配合した制振材の金属板に対する
密着性を向上するために、石油樹脂等を粘着付与樹脂と
して添加することが提案されている(特開昭64−38
446、特開平2−209936)。しかしながら、こ
れら粘着付与樹脂を配合した場合の制振性の向上効果に
ついては、これまでほとんど検討がなされていない。
2. Description of the Related Art Conventionally, it has been proposed to use an ethylene-based copolymer as a binding material for a damping material for the purpose of improving moldability or reducing weight (Japanese Patent Laid-Open No. 52-977).
02, JP-A-54-110256, JP-A-61-222.
972, JP-A-63-295669). Further, it has been proposed to add petroleum resin or the like as a tackifying resin in order to improve the adhesion of the vibration damping material containing these ethylene-based copolymers to the metal plate (JP-A-64-38).
446, JP-A-2-209936). However, almost no studies have been made so far on the effect of improving the vibration damping property when these tackifying resins are blended.

【0003】一方、これら制振材が使用される用途、特
に車両用途等においては更に軽量化が押し進められてき
ているため、より高性能の制振材がのぞまれているもの
の、上記に示した従来の提案では充分な性能を得られな
い。
On the other hand, in applications where these damping materials are used, especially in vehicle applications, further weight reduction is being promoted, so that higher performance damping materials are desired, but as shown above. In addition, the conventional proposal cannot obtain sufficient performance.

【0004】[0004]

【発明が解決しようとする課題】本発明は、高い制振性
能を持つ制振材を提供することを目的とするものであ
る。
SUMMARY OF THE INVENTION An object of the present invention is to provide a damping material having high damping performance.

【0005】[0005]

【課題を解決するための手段】そこで、本発明者は、従
来、粘着付与剤としてのみ利用されていた石油樹脂、天
然樹脂等の熱可塑性樹脂の制振性改良効果に注目し、優
れた制振性能を有する制振材について鋭意検討した結
果、特定の組成物がそれを満足することを見出して本発
明を完成した。
Therefore, the present inventor has paid attention to the effect of improving the damping property of thermoplastic resins such as petroleum resin and natural resin, which have been conventionally used only as tackifiers. As a result of intensive studies on a damping material having a vibration performance, the present invention has been completed by finding that a specific composition satisfies it.

【0006】すなわち、本発明は、 (A)エチレン系共重合物 100重量部及び (B)(イ)石油類の熱分解により得られる分解油留分
のうち、140〜220℃の沸点範囲を有する留分を蒸
留することにより得たインデン含有率60〜90%の原
料油100重量部をフェノール化合物4.0〜10.0
重量部の存在下、フリーデルクラフト型触媒を用いて重
合してなる軟化点115〜145℃の炭化水素樹脂と、
(ロ)軟化点50〜100℃の脂肪族系石油樹脂、芳香
族系石油樹脂、脂肪族芳香族共重合系石油樹脂、ロジン
系樹脂、テルペン系樹脂、クマロン系樹脂のなかから選
ばれる1種または2種以上の樹脂とを混合してなる軟化
点90〜120℃の樹脂状物 100〜300重量部か
らなる制振材組成物に関する。以下、本発明を詳細に説
明する。
That is, according to the present invention, (A) 100 parts by weight of an ethylene-based copolymer and (B) (a) a cracked oil fraction obtained by thermal decomposition of petroleum, having a boiling point range of 140 to 220 ° C. 100 parts by weight of a feedstock oil having an indene content of 60 to 90% obtained by distilling a fraction having
A hydrocarbon resin having a softening point of 115 to 145 ° C. obtained by polymerization using a Friedel-Crafts type catalyst in the presence of parts by weight;
(B) One selected from aliphatic petroleum resins having a softening point of 50 to 100 ° C., aromatic petroleum resins, aliphatic aromatic copolymer petroleum resins, rosin resins, terpene resins, and coumarone resins. Alternatively, the present invention relates to a damping material composition comprising 100 to 300 parts by weight of a resinous material having a softening point of 90 to 120 ° C., which is obtained by mixing two or more kinds of resins. Hereinafter, the present invention will be described in detail.

【0007】本発明において使用される(イ)炭化水素
樹脂とは、石油類の熱分解により得られる分解油留分の
うち140〜220℃の沸点範囲を有する留分を蒸留す
ることにより得た、インデン含有率60〜90%の原料
油100重量部に、フェノール化合物4.0〜10.0
重量部の存在下、フリーデルクラフツ型触媒を用いて重
合して得られる軟化点115〜145℃の芳香族系石油
樹脂である。
The hydrocarbon resin (a) used in the present invention is obtained by distilling a fraction having a boiling point range of 140 to 220 ° C. among cracked oil fractions obtained by thermal decomposition of petroleum. , 100 parts by weight of feedstock oil having an indene content of 60 to 90%, and a phenol compound of 4.0 to 10.0
It is an aromatic petroleum resin having a softening point of 115 to 145 ° C. obtained by polymerization using a Friedel-Crafts type catalyst in the presence of parts by weight.

【0008】ここで、フリーデルクラフツ型触媒として
は、三弗化硼素のエチルエーテル、フェノール、ブチル
エーテル、ブチルアルコール、メチルアルコール等を使
用した錯体触媒が好ましく挙げられる。
Here, the Friedel-Crafts type catalyst is preferably a complex catalyst using boron trifluoride ethyl ether, phenol, butyl ether, butyl alcohol, methyl alcohol or the like.

【0009】また、石油類の熱分解で得られる分解油留
分のうち沸点範囲が140〜220℃の留分には、スチ
レン、α−メチルスチレン、β−メチルスチレン、ビニ
ルトルエン、インデン、ジシクロペンタジエン、エチル
ベンゼン、トリメチルベンゼン、ナフタレン等が含まれ
る。このうち、スチレン、α−メチルスチレン、β−メ
チルスチレン、ビニルトルエン、インデンを重合可能成
分とし、インデン含有率は次式で定義する。 インデン含有率(%)=(B/A)×100 A;重合可能成分含有量(wt%) B;インデン含有量(wt%) 各成分の含有量は、ガスクロマトグラフィー法により分
析した値である。
Of the cracked oil fractions obtained by the thermal cracking of petroleum, those having a boiling point range of 140 to 220 ° C. are styrene, α-methylstyrene, β-methylstyrene, vinyltoluene, indene and diene. Cyclopentadiene, ethylbenzene, trimethylbenzene, naphthalene, etc. are included. Of these, styrene, α-methylstyrene, β-methylstyrene, vinyltoluene, and indene are the polymerizable components, and the indene content is defined by the following formula. Indene content (%) = (B / A) × 100 A; Polymerizable component content (wt%) B; Indene content (wt%) The content of each component is the value analyzed by the gas chromatography method. is there.

【0010】フェノール化合物としては、フェノールあ
るいはクレゾール、キシレノールなどのアルキル置換フ
ェノールが挙げられる。なお、本発明のフェノール化合
物の添加量には、フリーデルクラフト型触媒の一部とし
て添加されるフェノール等の添加量は含まれない。
Examples of the phenol compound include phenol and alkyl-substituted phenols such as cresol and xylenol. The addition amount of the phenol compound of the present invention does not include the addition amount of phenol or the like added as a part of the Friedel-Crafts type catalyst.

【0011】本発明において使用される(ロ)軟化点5
0〜100℃の樹脂としては、脂肪族系石油樹脂、芳香
族系石油樹脂、脂肪族芳香族共重合系石油樹脂、ロジン
系樹脂、テルペン系樹脂、クマロン系樹脂が挙げられ
る。
(B) Softening point 5 used in the present invention
Examples of the resin at 0 to 100 ° C. include aliphatic petroleum resin, aromatic petroleum resin, aliphatic aromatic copolymer petroleum resin, rosin resin, terpene resin, and coumarone resin.

【0012】ロジン系樹脂としては、ロジン、ロジンエ
ステル、水添ロジン、水添ロジンエステル、重合ロジン
等があげられる。テルペン系樹脂としては、合成テルペ
ン樹脂、テルペンフェノール樹脂等があげられる。
Examples of the rosin resin include rosin, rosin ester, hydrogenated rosin, hydrogenated rosin ester and polymerized rosin. Examples of the terpene resin include synthetic terpene resin and terpene phenol resin.

【0013】本発明において使用される(A)エチレン
系共重合物とは、エチレン−アクリル酸メチル、エチレ
ン−アクリル酸エチル、エチレン−酢酸ビニル共重合体
などであり、特にエチレン−酢酸ビニル共重合体が好ま
しい。エチレン−酢酸ビニル共重合体の酢酸ビニル含有
量は25〜50重量部であるものが好ましく、分子量の
目安として用いられているメルトインデックス(MI)
(190℃、加重2160g、10分間にて測定)が1
0〜400g/10分であるものが好ましい。
The ethylene-based copolymer (A) used in the present invention is ethylene-methyl acrylate, ethylene-ethyl acrylate, ethylene-vinyl acetate copolymer and the like, and particularly ethylene-vinyl acetate copolymer. Coalescence is preferred. The ethylene-vinyl acetate copolymer preferably has a vinyl acetate content of 25 to 50 parts by weight, which is a melt index (MI) used as a measure of the molecular weight.
(190 ℃, weighted 2160g, measured at 10 minutes) is 1
It is preferably 0 to 400 g / 10 minutes.

【0014】本発明において使用される(イ)炭化水素
樹脂と、本発明において使用される(ロ)軟化点50〜
100℃の樹脂とを混合してなる(B)樹脂状物は、軟
化点90〜120℃が好ましく、更に好ましくは100
〜115℃である。軟化点が90℃未満の場合は、制振
性能のピークの温度が低くなるため適当でない。また、
軟化点が120℃より高い場合は、制振性能のピークの
温度が高くなるため適当でない。
The hydrocarbon resin (a) used in the present invention and the softening point (b) used in the present invention are from 50 to 50.
The resinous material (B) obtained by mixing with a resin at 100 ° C. preferably has a softening point of 90 to 120 ° C., more preferably 100 ° C.
It is ~ 115 ° C. If the softening point is lower than 90 ° C, the peak temperature of the vibration damping performance will be low, which is not suitable. Also,
When the softening point is higher than 120 ° C., the peak temperature of the vibration damping performance becomes high, which is not suitable.

【0015】更に、本発明において使用される(イ)炭
化水素樹脂と本発明において使用される(ロ)軟化点5
0〜100℃の樹脂とを混合してなる(B)樹脂状物
は、あらかじめ(イ)と(ロ)を混合した後、本発明に
おいて使用される(A)エチレン系共重合物と混練する
という方法に限定されるものではなく、順序、手段につ
いては限定されない。その例としては、(イ)と(A)
とを混練したものと、(ロ)と(B)とを混練したもの
とを予め準備し、それらをさらに混練するといった方
法、あるいは、(イ)(ロ)のいずれかと(A)を混練
した後(イ)(ロ)のもう一方を混練するという方法等
が挙げられる。
Further, the (a) hydrocarbon resin used in the present invention and the (b) softening point 5 used in the present invention.
The (B) resinous material obtained by mixing a resin at 0 to 100 ° C. is mixed with (A) and (B) in advance and then kneaded with the (A) ethylene-based copolymer used in the present invention. However, the order and means are not limited. For example, (a) and (A)
And (B) were prepared in advance and then further kneaded, or either (A) or (B) and (A) were kneaded. Examples include a method of kneading the other of the latter (a) and (b).

【0016】また、本発明の制振材組成物の制振性能を
向上するために、無機充填剤を添加してもよい。例え
ば、マイカ、酸化チタン、カーボンブラック等が挙げら
れる。
Further, an inorganic filler may be added to improve the vibration damping performance of the vibration damping composition of the present invention. Examples thereof include mica, titanium oxide, carbon black and the like.

【0017】[0017]

【実施例】以下、実施例を示すがこれらは一例であって
本発明はその主旨に反しない限り本実施例に限定される
ものではない。
EXAMPLES Examples will be shown below, but these are examples and the present invention is not limited to these examples unless it deviates from the gist thereof.

【0018】尚、試験方法は以下に従った。 試験法 (1)軟化点 JIS K−2207 (2)粘弾性測定 制振性能の評価は、粘弾性測定により行った。一般に、
非拘束タイプで制振材が使用される場合、制振性能は損
失弾性率(E”)の上昇に伴い、また、拘束タイプの場
合は、損失正接(tanδ)の上昇に伴い向上するた
め、高い損失弾性率(E”)若しくは、高い損失正接
(tanδ)を示す組成物が、制振性能高いと判断し
た。 機種;株式会社オリエンテック製 レオバイブロンDD
V−III−EP 条件;昇温速度 2℃/min、周波数 35Hzで測
定。
The test method was as follows. Test method (1) Softening point JIS K-2207 (2) Viscoelasticity measurement The vibration damping performance was evaluated by viscoelasticity measurement. In general,
When the damping material is used in the unrestrained type, the damping performance improves as the loss elastic modulus (E ″) increases, and in the restricted type as the loss tangent (tan δ) increases, A composition exhibiting a high loss elastic modulus (E ″) or a high loss tangent (tan δ) was judged to have high vibration damping performance. Model: Orientec Co., Ltd., Leo Vibron DD
V-III-EP conditions: Measured at a heating rate of 2 ° C./min and a frequency of 35 Hz.

【0019】実施例1 石油類の熱分解により得られる分解油留分のうち140
〜220℃の沸点範囲を有する留分を蒸留することによ
り得たインデン含有率が85%に調整した留分100重
量部にフェノール5重量部を添加して、三弗化硼素エチ
ルエーテルを0.6wt%加えて30℃で3時間重合し
た後、苛性ソーダ水溶液で触媒を除去し、次いで水洗し
て蒸留により未反応油及び低重合物を除去して樹脂
(A)を得た。樹脂(A)の軟化点は130℃であっ
た。このようにして得られた樹脂(A)に対して軟化点
70℃の脂肪族芳香族共重合系石油樹脂(東ソー株式会
社製ペトロタック70)を等量、溶融混練し、軟化点1
02℃の樹脂状物(B)を得た。
Example 1 140 out of cracked oil fractions obtained by thermal cracking of petroleum
5 parts by weight of phenol was added to 100 parts by weight of a fraction having an indene content adjusted to 85% obtained by distilling a fraction having a boiling range of 220 to 220 ° C. After 6 wt% was added and the mixture was polymerized at 30 ° C. for 3 hours, the catalyst was removed with an aqueous solution of caustic soda, followed by washing with water to remove unreacted oil and low-polymerization products to obtain a resin (A). The softening point of the resin (A) was 130 ° C. The resin (A) thus obtained was melt-kneaded with an equal amount of an aliphatic aromatic copolymer petroleum resin (PETROTAC 70 manufactured by Tosoh Corporation) having a softening point of 70 ° C. to obtain a softening point of 1
A resinous material (B) having a temperature of 02 ° C. was obtained.

【0020】このようにして得られた樹脂状物(B)2
00重量部、エチレン−酢酸ビニル共重合体(酢酸ビニ
ル含有量32%、MI 60)100重量部、マイカ
(クラレ製60C)50重量部を溶融混練し、制振材組
成物を調製し評価した結果を表1、図1及び図2に示し
た。
The resinous material (B) 2 thus obtained
00 parts by weight, 100 parts by weight of ethylene-vinyl acetate copolymer (vinyl acetate content 32%, MI 60), and 50 parts by weight of mica (60C manufactured by Kuraray) were melt-kneaded to prepare and evaluate a damping material composition. The results are shown in Table 1 and FIGS. 1 and 2.

【0021】実施例2 実施例1と同様にして得られた樹脂(A)80重量部に
対し、軟化点89℃の脂肪族芳香族共重合系石油樹脂
(東ソー株式会社製 ペトロタック90)120重量部
を、溶融混練し、軟化点105℃の樹脂状物(C)を得
た。このようにして得られた樹脂状物(C)200重量
部、エチレン−酢酸ビニル共重合体(酢酸ビニル含有量
32%、MI 60)100重量部、マイカ(クラレ製
60C)50重量部を溶融混練し、制振材組成物を調製
し評価した結果を表1、図1及び図2に示した。
Example 2 To 80 parts by weight of the resin (A) obtained in the same manner as in Example 1, an aliphatic-aromatic copolymer petroleum resin having a softening point of 89 ° C. (PETROTAC 90 manufactured by Tosoh Corporation) 120 Part by weight was melt-kneaded to obtain a resinous material (C) having a softening point of 105 ° C. 200 parts by weight of the resinous material (C) thus obtained, 100 parts by weight of ethylene-vinyl acetate copolymer (vinyl acetate content 32%, MI 60), and 50 parts by weight of mica (Kuraray 60C) are melted. The results of evaluation by kneading to prepare a vibration damping composition are shown in Table 1, FIG. 1 and FIG.

【0022】比較例1 脂肪族系石油樹脂(トーネックス社製 ESCOREZ
1310 軟化点93℃)(D)100重量部と、エチ
レン−酢酸ビニル共重合体(酢酸ビニル含有量32%、
MI 60)100重量部、マイカ(クラレ製60C)
50重量部を溶融混練し、制振材組成物を調製し評価し
た結果を表1、図1及び図2に示した。
Comparative Example 1 Aliphatic petroleum resin (ESCOREZ manufactured by Tonex Co., Ltd.)
1310 softening point 93 ° C.) (D) 100 parts by weight, ethylene-vinyl acetate copolymer (vinyl acetate content 32%,
MI 60) 100 parts by weight, mica (Kuraray 60C)
50 parts by weight were melt-kneaded to prepare a vibration damping composition, and the evaluation results are shown in Table 1, FIG. 1 and FIG.

【0023】比較例2 テルペン樹脂(ヤスハラケミカル社製 TO−105
軟化点100℃)(E)200重量部と、エチレン−酢
酸ビニル共重合体(酢酸ビニル含有量32%、MI 6
0)100重量部、マイカ(クラレ製60C)50重量
部を溶融混練し、制振材組成物を調製し評価した結果を
表1、図1及び図2に示した。
Comparative Example 2 Terpene resin (TO-105 manufactured by Yasuhara Chemical Co., Ltd.
Softening point 100 ° C.) (E) 200 parts by weight, ethylene-vinyl acetate copolymer (vinyl acetate content 32%, MI 6
0) 100 parts by weight and 50 parts by weight of mica (60C manufactured by Kuraray) were melt-kneaded to prepare a damping material composition, and the evaluation results are shown in Table 1, FIG. 1 and FIG.

【0024】[0024]

【表1】 [Table 1]

【0025】[0025]

【発明の効果】以上述べたとうり、本発明の制振材組成
物は優れた制振性能を示し、自動車、建材、家電機器
等、制振制御を目的とする分野で幅広く利用できる。
Industrial Applicability As described above, the damping material composition of the present invention exhibits excellent damping performance and can be widely used in fields for damping control such as automobiles, building materials and home appliances.

【図面の簡単な説明】[Brief description of drawings]

【図1】実施例及び比較例で得られた組成物の損失弾性
率を示す図。
FIG. 1 is a graph showing loss elastic moduli of compositions obtained in Examples and Comparative Examples.

【図2】実施例及び比較例で得られた組成物の損失正接
を示す図。
FIG. 2 is a graph showing loss tangents of compositions obtained in Examples and Comparative Examples.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C08L 93/04 LSK 7415−4J F16F 15/02 Q 9138−3J ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location C08L 93/04 LSK 7415-4J F16F 15/02 Q 9138-3J

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】(A)エチレン系共重合物 100重量部
及び (B)(イ)石油類の熱分解により得られる分解油留分
のうち、140〜220℃の沸点範囲を有する留分を蒸
留することにより得たインデン含有率60〜90%の原
料油100重量部をフェノール化合物 4.0〜10.
0重量部の存在下、フリーデルクラフト型触媒を用いて
重合してなる軟化点115〜145℃の炭化水素樹脂
と、(ロ)軟化点50〜100℃の脂肪族系石油樹脂、
芳香族系石油樹脂、脂肪族芳香族共重合系石油樹脂、ロ
ジン系樹脂、テルペン系樹脂、クマロン系樹脂の中から
選ばれる1種または2種以上の樹脂とを混合してなる軟
化点90〜120℃の樹脂状物100〜300重量部か
らなる制振材組成物。
1. (A) 100 parts by weight of an ethylene copolymer and (B) (a) a cracked oil fraction obtained by thermal decomposition of petroleum, which has a boiling point range of 140 to 220 ° C. 100 parts by weight of a feedstock oil having an indene content of 60 to 90% obtained by distillation was added to a phenol compound of 4.0 to 10.
A hydrocarbon resin having a softening point of 115 to 145 ° C. obtained by polymerization using a Friedel-Crafts type catalyst in the presence of 0 part by weight, and (b) an aliphatic petroleum resin having a softening point of 50 to 100 ° C.
A softening point of 90-by mixing with one or more resins selected from aromatic petroleum resins, aliphatic aromatic copolymer petroleum resins, rosin resins, terpene resins and coumarone resins. A damping material composition comprising 100 to 300 parts by weight of a resinous material at 120 ° C.
JP18570692A 1992-06-22 1992-06-22 Damping composition Expired - Fee Related JP3177620B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18570692A JP3177620B2 (en) 1992-06-22 1992-06-22 Damping composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18570692A JP3177620B2 (en) 1992-06-22 1992-06-22 Damping composition

Publications (2)

Publication Number Publication Date
JPH061904A true JPH061904A (en) 1994-01-11
JP3177620B2 JP3177620B2 (en) 2001-06-18

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP18570692A Expired - Fee Related JP3177620B2 (en) 1992-06-22 1992-06-22 Damping composition

Country Status (1)

Country Link
JP (1) JP3177620B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005015767A (en) * 2003-06-06 2005-01-20 Tosoh Corp Aromatic petroleum resin for hot melt adhesive, aromatic petroleum resin composition for hot melt adhesive, and hot melt adhesive composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005015767A (en) * 2003-06-06 2005-01-20 Tosoh Corp Aromatic petroleum resin for hot melt adhesive, aromatic petroleum resin composition for hot melt adhesive, and hot melt adhesive composition
JP4581437B2 (en) * 2003-06-06 2010-11-17 東ソー株式会社 Aromatic petroleum resin for hot melt adhesive, aromatic petroleum resin composition for hot melt adhesive, and hot melt adhesive composition

Also Published As

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