JPH03166286A - Elastic sealant composition - Google Patents

Elastic sealant composition

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Publication number
JPH03166286A
JPH03166286A JP30316789A JP30316789A JPH03166286A JP H03166286 A JPH03166286 A JP H03166286A JP 30316789 A JP30316789 A JP 30316789A JP 30316789 A JP30316789 A JP 30316789A JP H03166286 A JPH03166286 A JP H03166286A
Authority
JP
Japan
Prior art keywords
rubber
sebs
phase
weight
softener
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP30316789A
Other languages
Japanese (ja)
Inventor
Katsuaki Sekihara
克章 関原
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.)
Nissin Kogyo Co Ltd
Original Assignee
Nissin Kogyo 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 Nissin Kogyo Co Ltd filed Critical Nissin Kogyo Co Ltd
Priority to JP30316789A priority Critical patent/JPH03166286A/en
Publication of JPH03166286A publication Critical patent/JPH03166286A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Sealing Material Composition (AREA)

Abstract

PURPOSE:To obtain the subject composition giving excellent water-stopping effect and having high heat-resistance, stability and weather-resistance by mixing an SEBS rubber consisting of a specific block copolymer with a rubber softener at a specific ratio. CONSTITUTION:The objective composition is a mixture composed of (A) 15-30wt.% of an SEBS rubber consisting of a block copolymer having PS phase at both terminal phases and a hydrogenated polyolefin phase as the intermediate rubber phase and (B) 70-80wt.% of a rubber softener consisting of one or more substances preferably selected from process oil, straight asphalt having a penetration of >=100 and a liquid resin.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、土木・建築分野に用いる弾性シール材組成物
に関し、詳しくはコンクリートの打継部、セグメントの
接合部、ヒューム管継手、コンクリート製ボックス力ル
パート継手などに使用する弾性に優れた成型シール材ま
たは加熱注入用シール材組成物に関する6のである. [従来の技術1 従来、トンネルなどの構造物を構築するために、複数の
セグメントを接合して所定の構造物としている.このよ
うな構造物には、トンネルのばか各種のケーブルやガス
管、上下水道管などを埋設するヒューム管やコンクリー
ト製ボックス力ルバートなどがある.これらはいずれも
地中に設けられるものであるが、地上に設けられる高架
鉄道や高速道路などら前記構造物に含まれる.これら構
造物のコンクリートの打継ぎおよびセグメントなどの接
合部分の止水は、従来、重要な問題として認識され、幾
多のシール材が提供されている.シール材としては注入
するタイプのものと成型材として使用するちのがある.
注入タイプとしては非加硫ゴム、ゴム化アスファルト、
アスファルトなどの可撓性材料がある.また、成型材と
しては、合成樹脂、加硫ゴム、非加硫ゴムなどのものが
あるが、合成樹脂成型材は,コンクリート打設時に埋込
むもので主に打綿部の止水に使用される.加硫ゴム成型
材は、セグメントの接合部に多く使用されており、最近
では水膨張性と言い、水に反応して膨張し止水効果を増
すタイプのものちある.非加硫ゴム成型材は、それ自体
,粘着性を有し、打継部等に容易に施工できるようにし
た材料であり、吸水して膨張するちのもある.〔発明が
解決しようとする課題〕 従来の注入型シール材は、コンクリートに対する接着性
に優れているものの、弾性に欠けており塑性変形しやす
い、また、加熱溶融して使用するので,非加硫ゴムない
しゴム化アスファルトなどでは熱によってゴムが分解を
受けやすく、ゴム弾性が損なわれることが多い.また、
成型シール材では、合成樹脂.加硫ゴムなど後打のコン
クリートに対する接着性が悪く止水性に欠ける.非加硫
ゴムのものは粘着性があり、コンクリートに対してはよ
く接着するが、弾性に欠けるなどの欠点を有している. 【課題を解決するための手段〕 本発明は、上記の従来技術の欠点を解決するためになさ
れたものである.すなわち、SEBSゴムl5〜30重
量%およびゴム軟化剤70〜85重量%とから成る混合
物を用いたことを特徴とする弾性シール材組成物である
. 本発明に用いられるSEBS(スチレン・エチレン・ブ
チレン・スチレン)ゴムは、スチレン系熱可塑性エラス
トマーと称されるもので、両末端相にボリスチレン相、
ゴム中間相として水素添加型のポリオレフィンをもつブ
ロックコポリマーである.そのボリスチレン末端ブロッ
クとゴム中間ブロックは、互いに相溶することなく2相
構造を形成する.このうち、ボリスチレン相は物理的架
橋点(ドメイン)を形成し,常温で従来の加硫ゴムの架
橋点と同様のはたらきを示し,熱可塑性エラストマーに
ゴム弾性を付与している.該熱可塑性エラストマーをボ
リスチレンのガラス転移点以上に加熱すると、ドメイン
は軟化し流動性を増すが、冷却するとドメインが再現さ
れゴム弾性が示される.このような構造のため加熱加工
を容易に行なうことが可能であり、また物性的にも高い
凝集力、低温での高弾性等数々のすぐれた性質を得るこ
とができる. このようなスチレン系熱可塑性エラストマーとしては、
上記のSEBSゴムのほかにSBS (スチレン・ブタ
ジエン・スチレン)ゴムおよびSIS(スチレン・イソ
ブレン・スチレン)ゴムがあるが.SEBSゴムは、こ
れらと比較して耐候性、耐熱性が非常にすぐれている.
本発明に使用されるゴム軟化剤は、プロセスオイル,ス
トレートアスファルト、および液状樹脂があげられ、こ
れらのうちから単独または併用してSEBSゴムと混合
する.これらのゴム軟化剤は、ゴムに可塑性および粘着
性を付与する目的で使われるものであるが、SEBSゴ
ム15〜30重量%に対しゴム軟化剤70〜85重量%
の配合割合である.SEBSゴムの使用量が15重量%
未満では組成物の軟化点が低く実用的でない.一方、3
0重量%を超えると組成物の粘度が極端に増大し取扱い
上好ましくない.またコストち高くなり過ぎ経済的でな
い. ここでプロセスオイルとは石油の高沸点留分て、飽和ま
たは不活性の不飽和炭化水素から成り、無色から蛍光を
発する濃緑色までの色相をらち、粘度、比重,アニリン
点によって規搦づけされている.大別して、パラフィン
系、ナフテン系、芳香族系の3種類があるが、本発明に
用いるプロセスオイルはこれらの何れでも好適に使用す
ることができる. また、ストレートアスファルトとしては針入度100以
上のものが好ましく、このものは,原油を常圧・減圧蒸
留装置などにかけ、軽質分を除去して得られる瀝青物で
、計人度がlOO〜120.120〜150,150〜
200、および200〜300のものが使用できる. 前記液状樹脂としては、常温で液状の天然系および合成
系の樹脂で,松やにを原料とするテレビン系の液状樹脂
や石油から合成される液状樹脂が、ゴムに粘着性を与え
るものとして好適に用いることができる. 本発明においては、配合コストを引下げ、加工性の改善
やゴムに対する補強効果などを考慮してSEBSに対し
充填剤を配合することが好ましい.この場合、通常SE
BSゴムとゴム軟化剤の混合物100重量部に対して、
充填剤O〜40重量部の範囲で配合される.充填剤の配
合量が40重量部を超えると、コンクリートなどに対す
る接着強さが低下するので実用上好ましくない.使用す
る充填剤としては,炭酸カルシウム、タルク、クレーな
どがあげられるが、何れら好適に使用しつるものである
. 本発明の組成物を製造するには、あらかじめ180〜2
00℃に加熱溶融したゴム軟化剤とSEBSゴムを所定
の割合でホモミキサーなどの高ぜん断撹拌装置で撹拌混
合し、SEBSゴムが完全に溶解した後に充填剤を投入
して均一に混合する.混合物は所定の形状に成型するが
、型枠に流し込むか、押出機で成型してもよい. また混合には、バンバリーミキサーあるいは加圧二−ダ
ーなどを使用して行なうことも可能である. 〔実施例1 次に実施例について説明する. 実施例l SEBSゴム(シェル化学社製、クレイトンG1650
)1.5kg.プロセスオイル(共同石油社製、ソニッ
クプロセスオイルX−140)8.5kgの割合で、プ
ロセスオイルをあらかじめ200℃に加熱しておき、特
殊機化工業社製のT.K.ホモミキサーHV−SL (
最大容量20I2)で撹拌混合し、60分後、SEBS
ゴムが完全に溶解したのを確認してから炭酸カルシウム
3kgを加えて更に10分間撹拌し続け均質な混合物を
得た. この混合物の軟化点は102℃、200℃における粘度
は2100CPS.JISK6854(接着剤のはく離
接着強さ試験方法)によるはく離接着強さは0.62k
gf/cmであった.さらに水圧をかけた時のシール性
能を見るために、道路橋鉄筋コンクリート床版防水層設
計施工資料(社団法人日本道路協会)の防水性試験方法
に準じて、シール剤の接着面に水圧がかかるように試験
体を作成し試験温度20℃、水圧が3kgf/cm”、
加圧時間60分で試験し、漏水の有無を調べた.本実施
例では漏水は全く無かった.実施例2 SEBSゴム2.5kg、プロセスオイル7.5kgを
実施例lと同様にして撹拌混合し、さらにタルク2kg
を加えて混合し均質な混合物を得た. この混合物の性能は第1表に示す通りである.実施例3 SEBSゴム2.5kg.プロセスオイル7.5kgを
実施例1と同様にして撹拌混合して均質な混合物を得た
. この混合物の性能は第1表に示す通りである.実施例4 SEBSゴム2.5kg、針大度150〜200ストレ
ートアスファルト(三菱石油社製)7.5kgの割合で
、アスファルトをあらかじめ200℃に加熱しておき、
T.K.ホモミキサーHV−SLで撹拌混合し、60分
後、SEBSゴムが完全に溶解したのを確認してがら炭
酸カルシウムlkgを加えて更にlO分間撹拌して均質
な混合物を得た. この混合物の性能は第1表に示す通りである.実施例5 SEBSゴム2.5kg、ゴム軟化剤として、プロセス
オイル3.5kg、針入度100〜l20ストレートア
スファルト(三菱石油社製)2kg、テレビン系液状樹
脂(安原油脂社製グイマロン)2kgを使い、これらの
ゴム軟化剤をあらかじめ180℃に加熱しておき、実施
例1と同じように撹拌混合し、さらにタルク3kgを加
えて混合し均質な混合物を得た. この混合物の性能は第1表に示す通りである.実施例6 SEBSゴム3kg、プロセスオイル7kgを実施例l
と同様にして撹拌混合し、さらに炭酸カルシウム4kg
を加えて混合し均質な混合物を得た. この混合物の性能は第1表に示す通りである.比較例1
〜3 第1表の配合欄に示すように、SEBSゴム、プロセス
オイルおよび充填剤の量をそれぞれ本発明の要旨とする
範囲外の数値とし、実施例lと同様にして均質な混合物
をそれぞれ作製した.それぞれの混合物の性能は第1表
に示す通りである. 比較例4 ブチルゴム系のものを用いた従来の成形シール材である
. 以上の如く、SEBSゴムとゴム軟化剤の配合割合でS
EBSゴムがl5重量%未滴になると組成物の軟化点が
100℃以下になり、実用上、直射日光等の影響でダレ
現象の発生が懸念され好ましくない。
[Detailed Description of the Invention] [Industrial Field of Application] The present invention relates to an elastic sealing material composition used in the civil engineering and construction fields, and more specifically, for use in concrete joints, segment joints, Hume pipe joints, concrete joints, etc. No. 6 relates to a molded sealing material with excellent elasticity or a sealing material composition for hot injection used in box-force Rupert joints, etc. [Prior Art 1] Conventionally, in order to construct a structure such as a tunnel, a plurality of segments are joined to form a predetermined structure. Such structures include hume pipes and concrete box rubatos for burying various cables, gas pipes, water and sewage pipes, etc. in tunnels. All of these are installed underground, but they are also included in the above-mentioned structures, such as elevated railways and expressways installed above ground. Water sealing of joints such as concrete joints and segments of these structures has been recognized as an important problem, and a number of sealing materials have been provided. There are two types of sealing materials: those that are injected and those that are used as molding materials.
Injection types include non-vulcanized rubber, rubberized asphalt,
There are flexible materials such as asphalt. In addition, molding materials include synthetic resins, vulcanized rubber, and non-vulcanized rubber, but synthetic resin molding materials are embedded during concrete pouring and are mainly used to stop water in the batting area. Ru. Vulcanized rubber molding materials are often used for segment joints, and recently there is a type called water-swellable, which expands in response to water and increases its water-stopping effect. Non-vulcanized rubber molding material itself has adhesive properties, making it easy to apply to joints, etc., and it also swells when it absorbs water. [Problems to be solved by the invention] Although conventional injection-type sealants have excellent adhesion to concrete, they lack elasticity and are prone to plastic deformation, and because they are used after being heated and melted, they are non-vulcanized. Rubber or rubberized asphalt is easily decomposed by heat, often resulting in loss of rubber elasticity. Also,
For molded sealing materials, synthetic resins are used. It has poor adhesion to post-cast concrete such as vulcanized rubber, and lacks water-stopping properties. Non-vulcanized rubber is sticky and adheres well to concrete, but has drawbacks such as a lack of elasticity. [Means for Solving the Problems] The present invention has been made in order to solve the drawbacks of the above-mentioned prior art. That is, this is an elastic sealing material composition characterized by using a mixture consisting of 5 to 30% by weight of SEBS rubber and 70 to 85% by weight of a rubber softener. The SEBS (styrene-ethylene-butylene-styrene) rubber used in the present invention is called a styrene-based thermoplastic elastomer, and has a polystyrene phase in both terminal phases.
It is a block copolymer with a hydrogenated polyolefin as the rubber intermediate phase. The polystyrene end block and the rubber intermediate block form a two-phase structure without being mutually compatible. Among these, the polystyrene phase forms physical crosslinking points (domains) that function in the same way as crosslinking points in conventional vulcanized rubber at room temperature, giving the thermoplastic elastomer rubber elasticity. When the thermoplastic elastomer is heated above the glass transition point of polystyrene, the domains soften and fluidity increases, but when cooled, the domains reappear and exhibit rubber elasticity. Because of this structure, it can be easily heated and processed, and it also has many excellent physical properties such as high cohesive strength and high elasticity at low temperatures. As such styrene thermoplastic elastomer,
In addition to the SEBS rubber mentioned above, there are SBS (styrene-butadiene-styrene) rubber and SIS (styrene-isoprene-styrene) rubber. SEBS rubber has much better weather resistance and heat resistance than these rubbers.
Rubber softeners used in the present invention include process oil, straight asphalt, and liquid resin, which may be used alone or in combination with the SEBS rubber. These rubber softeners are used for the purpose of imparting plasticity and tackiness to rubber, and 70 to 85% by weight of rubber softeners are used for 15 to 30% by weight of SEBS rubber.
This is the mixing ratio of The amount of SEBS rubber used is 15% by weight.
If it is less than that, the softening point of the composition will be low and it is not practical. On the other hand, 3
If it exceeds 0% by weight, the viscosity of the composition increases extremely, making it unfavorable for handling. Also, the cost is too high and it is not economical. Process oil is a high-boiling fraction of petroleum, consisting of saturated or inert unsaturated hydrocarbons, and has a hue ranging from colorless to fluorescent dark green, and is regulated by viscosity, specific gravity, and aniline point. ing. There are three main types: paraffinic, naphthenic, and aromatic, and any of these can be suitably used in the present invention. In addition, straight asphalt preferably has a penetration value of 100 or more, and this is a bituminous material obtained by subjecting crude oil to normal pressure/vacuum distillation equipment to remove light components, and has a total penetration degree of 100 to 120. .120~150,150~
200 and 200-300 can be used. The liquid resin is a natural or synthetic resin that is liquid at room temperature, such as a turpentine liquid resin made from pine resin or a liquid resin synthesized from petroleum, which is preferably used to impart stickiness to rubber. be able to. In the present invention, it is preferable to incorporate a filler into SEBS in order to reduce compounding costs, improve processability, and have a reinforcing effect on rubber. In this case, usually SE
For 100 parts by weight of the mixture of BS rubber and rubber softener,
The filler is blended in a range of 0 to 40 parts by weight. If the amount of filler added exceeds 40 parts by weight, the adhesive strength to concrete etc. will decrease, which is undesirable from a practical standpoint. Examples of the filler used include calcium carbonate, talc, clay, etc., and any of them are suitable. To produce the composition of the present invention, 180 to 2
A rubber softener heated and melted at 00°C and SEBS rubber are stirred and mixed in a predetermined ratio using a high shear stirring device such as a homomixer, and after the SEBS rubber is completely dissolved, the filler is added and mixed uniformly. The mixture is molded into a predetermined shape, and may be poured into a mold or molded using an extruder. Mixing can also be carried out using a Banbury mixer or a pressure kneader. [Example 1 Next, an example will be explained. Example 1 SEBS rubber (manufactured by Shell Chemical Co., Ltd., Kraton G1650
)1.5kg. Process oil (manufactured by Kyodo Oil Co., Ltd., Sonic Process Oil K. Homo mixer HV-SL (
Stir and mix at maximum capacity 20I2), and after 60 minutes, SEBS
After confirming that the rubber was completely dissolved, 3 kg of calcium carbonate was added and stirring was continued for an additional 10 minutes to obtain a homogeneous mixture. The softening point of this mixture is 102°C, and the viscosity at 200°C is 2100 CPS. Peel adhesive strength according to JISK6854 (adhesive peel adhesive strength test method) is 0.62k
gf/cm. Furthermore, in order to check the sealing performance when water pressure is applied, water pressure was applied to the adhesive surface of the sealant according to the waterproofing test method in the waterproof layer design and construction materials for road bridge reinforced concrete deck slabs (Japan Road Association). A test specimen was created at a test temperature of 20℃ and a water pressure of 3kgf/cm.
A test was conducted with a pressurization time of 60 minutes to check for water leakage. In this example, there was no water leakage at all. Example 2 2.5 kg of SEBS rubber and 7.5 kg of process oil were stirred and mixed in the same manner as in Example 1, and further 2 kg of talc was added.
was added and mixed to obtain a homogeneous mixture. The performance of this mixture is shown in Table 1. Example 3 SEBS rubber 2.5 kg. 7.5 kg of process oil was stirred and mixed in the same manner as in Example 1 to obtain a homogeneous mixture. The performance of this mixture is shown in Table 1. Example 4 Asphalt was preheated to 200°C at a ratio of 2.5 kg of SEBS rubber and 7.5 kg of straight asphalt with a needle size of 150 to 200 (manufactured by Mitsubishi Oil Corporation).
T. K. The mixture was stirred and mixed using a homomixer HV-SL, and after 60 minutes, 1 kg of calcium carbonate was added while confirming that the SEBS rubber had completely dissolved, and the mixture was further stirred for 10 minutes to obtain a homogeneous mixture. The performance of this mixture is shown in Table 1. Example 5 2.5 kg of SEBS rubber, 3.5 kg of process oil as a rubber softener, 2 kg of straight asphalt with a penetration of 100 to 120 (manufactured by Mitsubishi Oil Corporation), and 2 kg of turpentine liquid resin (Guimaron, manufactured by Yasushi Oil Co., Ltd.) were used. These rubber softeners were preheated to 180° C., stirred and mixed in the same manner as in Example 1, and 3 kg of talc was added and mixed to obtain a homogeneous mixture. The performance of this mixture is shown in Table 1. Example 6 3 kg of SEBS rubber and 7 kg of process oil were added to Example 1.
Stir and mix in the same manner as above, and add 4 kg of calcium carbonate.
was added and mixed to obtain a homogeneous mixture. The performance of this mixture is shown in Table 1. Comparative example 1
~3 As shown in the formulation column of Table 1, the amounts of SEBS rubber, process oil, and filler were set to values outside the scope of the present invention, and homogeneous mixtures were prepared in the same manner as in Example 1. did. The performance of each mixture is shown in Table 1. Comparative Example 4 This is a conventional molded seal material using butyl rubber. As mentioned above, the mixing ratio of SEBS rubber and rubber softener
If the EBS rubber is reduced to 15% by weight, the softening point of the composition will be 100° C. or lower, which is undesirable in practical use because there is a fear that sagging may occur under the influence of direct sunlight.

また、SEBSゴムが30重量%を超えると、組成物の
溶融時の粘度が極端に高く、20’O℃における粘度が
sooocps以上となり、特に注入作業などに支障を
生じることがあるとと6に、水圧をかけた時のシール性
ら漏水が生じ適当でない. 更に、SEBSゴムとゴム軟化剤の配合割合が適正であ
ってち、充填剤を配合する場合はその量が、ゴム及びゴ
ム軟化剤の合計量100重量部に対して40重量部を超
えると、はく離接着強さが0.4kgf/cm以下とな
り,また水圧をかけた時のシール性においてら漏水が見
られ好ましくない. なお、比較例4の従来のブチルゴム系のちのは、このゴ
ムが周知のとおり耐候性に劣るため,使用部位が限定さ
れるばかりでなく、著しく高粘度であるため熱溶融型と
しては使用できず成型シール剤としても水圧がかかると
漏水し易い欠点がある. [発明の効果]
In addition, if the SEBS rubber exceeds 30% by weight, the viscosity of the composition when melted will be extremely high, and the viscosity at 20'O ℃ will be more than sooocps, which may cause problems especially in injection work. , Water leakage occurs due to poor sealing properties when water pressure is applied, making it unsuitable. Furthermore, if the blending ratio of SEBS rubber and rubber softener is appropriate, and if a filler is blended, the amount exceeds 40 parts by weight based on 100 parts by weight of the total amount of rubber and rubber softener, The peel adhesion strength was less than 0.4 kgf/cm, and water leakage was observed due to the sealing properties when water pressure was applied, which is undesirable. As is well known, the conventional butyl rubber rubber used in Comparative Example 4 has poor weather resistance, which not only limits the areas in which it can be used, but also has an extremely high viscosity, so it cannot be used as a heat-melting type. Even as a molded sealant, it has the disadvantage that it tends to leak when water pressure is applied. [Effect of the invention]

Claims (1)

【特許請求の範囲】 1、両端末相にポリスチレン相、ゴム中間相として水素
添加型のポリオレフィン相をもつブロックコポリマーで
あるSEBSゴム15〜30重量%およびゴム軟化剤7
0〜85重量%よりなる混合物を用いたことを特徴とす
る弾性シール材組成物。 2、ゴム軟化剤がプロセスオイル、針入度100以上の
ストレートアスファルト、液状樹脂のうち少なくとも1
種類からなる請求項1記載の弾性シール材組成物。
[Claims] 1. 15 to 30% by weight of SEBS rubber, which is a block copolymer having a polystyrene phase as both terminal phases and a hydrogenated polyolefin phase as a rubber intermediate phase, and a rubber softener 7
An elastic sealing material composition characterized by using a mixture consisting of 0 to 85% by weight. 2. The rubber softener is at least one of process oil, straight asphalt with a penetration of 100 or more, and liquid resin.
The elastic sealing material composition according to claim 1, comprising:
JP30316789A 1989-11-24 1989-11-24 Elastic sealant composition Pending JPH03166286A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP30316789A JPH03166286A (en) 1989-11-24 1989-11-24 Elastic sealant composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP30316789A JPH03166286A (en) 1989-11-24 1989-11-24 Elastic sealant composition

Publications (1)

Publication Number Publication Date
JPH03166286A true JPH03166286A (en) 1991-07-18

Family

ID=17917696

Family Applications (1)

Application Number Title Priority Date Filing Date
JP30316789A Pending JPH03166286A (en) 1989-11-24 1989-11-24 Elastic sealant composition

Country Status (1)

Country Link
JP (1) JPH03166286A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0641514A (en) * 1992-07-20 1994-02-15 Nisshin Kogyo Kk Sealing material, method for waterproofing of roof and material subjected to waterproofing
JP2001335640A (en) * 2000-03-24 2001-12-04 Asahi Kagaku Gosei Kk Production method of styrene-based thermoplastic elastomer composition
JP2007270042A (en) * 2006-03-31 2007-10-18 Showa Shell Sekiyu Kk Asphalt composition

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52111918A (en) * 1976-03-16 1977-09-20 Nichireki Chem Ind Co Sealing material
JPS58109576A (en) * 1981-12-23 1983-06-29 Fujikura Ltd Sealing and filling compound
JPS60197784A (en) * 1984-03-19 1985-10-07 Sumitomo Chem Co Ltd Water-swellable composition and water-stopping molding made thereof
JPS6248787A (en) * 1985-08-28 1987-03-03 Iida Sangyo Kk Hot-melt type thermosetting body sealer
JPH01182387A (en) * 1988-01-11 1989-07-20 Bridgestone Corp Sealing material
JPH01190781A (en) * 1988-01-26 1989-07-31 Nitta Gelatin Inc Presealing material for lap joint of external wall of building
JPH01207377A (en) * 1988-02-15 1989-08-21 Sumitomo Electric Ind Ltd Water stopping tape
JPH01217093A (en) * 1988-02-25 1989-08-30 Aica Kogyo Co Ltd Hot-melt type sealing agent for lighting tool

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52111918A (en) * 1976-03-16 1977-09-20 Nichireki Chem Ind Co Sealing material
JPS58109576A (en) * 1981-12-23 1983-06-29 Fujikura Ltd Sealing and filling compound
JPS60197784A (en) * 1984-03-19 1985-10-07 Sumitomo Chem Co Ltd Water-swellable composition and water-stopping molding made thereof
JPS6248787A (en) * 1985-08-28 1987-03-03 Iida Sangyo Kk Hot-melt type thermosetting body sealer
JPH01182387A (en) * 1988-01-11 1989-07-20 Bridgestone Corp Sealing material
JPH01190781A (en) * 1988-01-26 1989-07-31 Nitta Gelatin Inc Presealing material for lap joint of external wall of building
JPH01207377A (en) * 1988-02-15 1989-08-21 Sumitomo Electric Ind Ltd Water stopping tape
JPH01217093A (en) * 1988-02-25 1989-08-30 Aica Kogyo Co Ltd Hot-melt type sealing agent for lighting tool

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0641514A (en) * 1992-07-20 1994-02-15 Nisshin Kogyo Kk Sealing material, method for waterproofing of roof and material subjected to waterproofing
JP2001335640A (en) * 2000-03-24 2001-12-04 Asahi Kagaku Gosei Kk Production method of styrene-based thermoplastic elastomer composition
JP2007270042A (en) * 2006-03-31 2007-10-18 Showa Shell Sekiyu Kk Asphalt composition

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