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JPS6360051B2 - - Google Patents
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JPS6360051B2 - - Google Patents

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Publication number
JPS6360051B2
JPS6360051B2 JP55078151A JP7815180A JPS6360051B2 JP S6360051 B2 JPS6360051 B2 JP S6360051B2 JP 55078151 A JP55078151 A JP 55078151A JP 7815180 A JP7815180 A JP 7815180A JP S6360051 B2 JPS6360051 B2 JP S6360051B2
Authority
JP
Japan
Prior art keywords
liquid polymer
waterproofing material
petroleum resin
parts
weight
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
JP55078151A
Other languages
Japanese (ja)
Other versions
JPS573835A (en
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 filed Critical
Priority to JP7815180A priority Critical patent/JPS573835A/en
Publication of JPS573835A publication Critical patent/JPS573835A/en
Publication of JPS6360051B2 publication Critical patent/JPS6360051B2/ja
Granted legal-status Critical Current

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  • Polyurethanes Or Polyureas (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

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

本発明は、建築用防水材に関し、更に詳しくは
石油樹脂含有ジエン系液状ポリマーを架橋して成
る建築用防水材に関する。 近年、液状ポリマーは、建築材料の分野におい
て接着剤、塗料、シーリング剤および防水材など
各種製品としての用途が開発されており、注目さ
れている。しかしながら、液状ポリマーについて
はその架橋反応性や充填剤による補強作用が充分
解明されているとはいい難い。 これまで、補強剤としてカーボンブラツク、含
水ケイ酸等の充填剤を用いた補強液状ポリマーが
開発され、実用化されつつあるが、この種の充填
剤は、粒子径が数十mμという微粉末の形で使用
される上に、充分な補強効果を得るには3本ロー
ル(ペイントミル)のような特殊混合機を用いて
液状ポリマー中に均一に分散させる必要がある
為、配合物の粘度を著しく上昇させ、加工性を低
下させるという欠点を有している。また、可塑
剤、オイル、アスフアルト等を配合すれば加工性
は向上するが、物性において充分満足しうる液状
ポリマーを得ることができない。 本発明者らは、かかる液状ポリマーの現状に鑑
み、特にその架橋物の物性向上に関し、鋭意研究
を行つた結果、液状ポリマーに補強剤としてある
種の石油樹脂を混合した組成物は、架橋後の物性
が高水準に保たれ、耐アルカリ性、耐熱性の優れ
た建築用防水材を与えることができることを見い
出し、本発明を完成した。 すなわち、本発明の要旨は、反応性活性水素を
有するジエン系液状ポリマーおよび石油樹脂を含
有する液状ポリマー組成物を架橋させた建築用防
水材に存する。 本発明で使用する液状ポリマーは、室温で流動
性を有し、架橋処理により三次元網目構造を形成
して他の架橋ポリマーと同様の物理的特性を示す
重合体である。好ましい液状ポリマーとしては、
分子両末端に水酸基、カルボキシ基、メルカプト
基、アミノ基などの架橋を形成しうる官能基を有
する平均分子量500〜10000のポリブタジエン、ポ
リイソプレン、ポリクロロプレン、ブタジエン/
イソプレン共重合体、アクリロニトリル/ブタジ
エン共重合体、スチレン/ブタジエン共重合体、
エチレン/プロピレン/ブタジエン共重合体およ
びこれらの混合物が例示される。 液状ポリマーの物性を改良するために、必要に
応じて補足的にポリオール、ポリアミン、ポリカ
ルボン酸など、たとえばグリセリン、ポリエチレ
ングリコール、4,4′−メチレン−ビス(2−ク
ロロアニリン)、N,N−ビス(2−ヒドロキシ
プロパノール)アニリン、ポリプロピレングリコ
ール、1,4−ビス(β−ヒドロキシエトキシ)
ベンゼン、ヒドロピバリン酸ネオペンチルグリコ
ールエステルなどを液状ポリマー100重量部当り
0〜50重量部の割合で添加してもよい。 本発明で使用する石油樹脂としては、軟化点60
〜180℃および平均分子量500〜3000、特に軟化点
70〜130℃および平均分子量800〜1500の石油樹脂
が好ましい。 石油樹脂は、石油精製プロセスで得られる特定
留分の重合可能な物質を単離精製することなく樹
脂化したものの総称である。従つて、詳細な組成
を示すことはできないが、その単量体組成からす
ると、たとえばイソプレン、ピペリレン、2−メ
チルブテン−1または2などから成る脂肪族系共
重合体およびたとえばスチレン、ビニルトルエ
ン、α−メチルスチレン、クマロン、インデンな
どから成る芳香族系共重合体に大別される。 また、液状ポリマー組成物には、必要に応じて
粉末充填剤、老化防止剤などの添加物を配合する
ことができる。 粉末充填剤としては、炭酸カルシウム、クレ
ー、タルクなどの無機粉末、着色用顔料などが挙
げられる。配合量は液状ポリマー100重量部に対
して0〜300重量部、好ましくは50〜200重量部で
ある。老化防止剤としては、通常のゴム製品に配
合されるもの、たとえばアミン系およびフエノー
ル系の老化防止剤を使用することができる。これ
らの配合量は、液状ポリマー100部に対して0.1〜
10部が適当である。 本発明で用いる架橋剤としては、トルエンジイ
ソシアネート、4,4′−ジフエニルメタンジイソ
シアネート、キシレンジイソシアネートおよびこ
れらのイソシアネートプレポリマーなどのポリイ
ソシアネート化合物が適当である。この様な架橋
剤は、液状ポリマー100重量部に対して5〜50重
量部の割合で使用する。 架橋反応は、通常加熱することなく常温におい
て行なわれるが、触媒の添加または加熱により架
橋速度を早くすることもできる。 この様な触媒としては、オクテン酸鉛、ナフテ
ン酸コバルト、塩化第二鉄、ジブチルスズジラウ
レートなどの金属化合物、トリエチルアミン、テ
トラメチルエチレンジアミンなどのアミン類など
が好ましく用いられる。この場合、触媒は液状ポ
リマー100重量部に対して0.01〜2.0重量部の割合
で使用するのが好ましい。 本発明で用いられる組成物は、石油樹脂により
補強される為、三本ロールのような特殊混合機を
用いて粉砕する必要もなく、三枚羽のような簡易
混合機により均一に混合でき、製造工程の省力化
にも寄与する。 次に、実施例および比較例を示して本発明を更
に具体的に説明する。なお、実施例中、部とある
のは特記しない限り重量部を表わす。 実施例1〜4および比較例1〜2 まず、第1表に示す各成分から成るポリマー組
成物を調製する。実施例1〜4の組成物はプロペ
ラシヤフト型の混合機により混合し、比較例1〜
2の組成物は三本ロールで混合粉砕して調製し
た。 次いで、第1表に示す架橋剤を所定量添加、混
合し、JIS A6021に準拠してガラス板上に約2.0
mm厚に塗布した後、20℃で14日間養生して物性測
定を行なつた。 架橋物についてアルカリ処理および熱処理を行
い、物性測定を行なつた。 アルカリ処理は、5%苛性ソーダ煮沸水溶液に
4日間浸漬して、また熱処理は、恒温器内に100
℃で168時間静置して行なつた。 結果を第2表に示す。
The present invention relates to a waterproofing material for construction, and more particularly to a waterproofing material for construction made by crosslinking a diene-based liquid polymer containing petroleum resin. In recent years, liquid polymers have been attracting attention as they have been developed for use in various products such as adhesives, paints, sealants, and waterproofing materials in the field of building materials. However, with regard to liquid polymers, their crosslinking reactivity and the reinforcing effect of fillers have not been sufficiently elucidated. Up to now, reinforcing liquid polymers using fillers such as carbon black and hydrated silicic acid have been developed and are being put into practical use as reinforcing agents. In addition, in order to obtain a sufficient reinforcing effect, it is necessary to use a special mixer such as a three-roll (paint mill) to uniformly disperse the liquid polymer, so the viscosity of the compound must be adjusted. It has the disadvantage of significantly increasing the amount of steel and reducing workability. Furthermore, although processability is improved by adding plasticizers, oils, asphalt, etc., it is not possible to obtain liquid polymers with sufficiently satisfactory physical properties. In view of the current state of liquid polymers, the present inventors have conducted extensive research, particularly regarding improving the physical properties of crosslinked products, and have found that a composition in which a liquid polymer is mixed with a certain type of petroleum resin as a reinforcing agent has been developed after crosslinking. The present invention was completed based on the discovery that it is possible to provide a waterproofing material for construction that maintains high physical properties and has excellent alkali resistance and heat resistance. That is, the gist of the present invention resides in a waterproofing material for construction in which a liquid polymer composition containing a diene liquid polymer having reactive active hydrogen and a petroleum resin is crosslinked. The liquid polymer used in the present invention is a polymer that has fluidity at room temperature, forms a three-dimensional network structure through crosslinking treatment, and exhibits physical properties similar to other crosslinked polymers. Preferred liquid polymers include:
Polybutadiene, polyisoprene, polychloroprene, butadiene/with an average molecular weight of 500 to 10,000, which has functional groups capable of forming crosslinks such as hydroxyl, carboxy, mercapto, and amino groups at both ends of the molecule.
Isoprene copolymer, acrylonitrile/butadiene copolymer, styrene/butadiene copolymer,
Examples include ethylene/propylene/butadiene copolymers and mixtures thereof. In order to improve the physical properties of the liquid polymer, polyols, polyamines, polycarboxylic acids, etc., such as glycerin, polyethylene glycol, 4,4'-methylene-bis(2-chloroaniline), N,N -Bis(2-hydroxypropanol)aniline, polypropylene glycol, 1,4-bis(β-hydroxyethoxy)
Benzene, neopentyl glycol hydropivalate, etc. may be added in a proportion of 0 to 50 parts by weight per 100 parts by weight of the liquid polymer. The petroleum resin used in the present invention has a softening point of 60
~180℃ and average molecular weight 500-3000, especially softening point
Petroleum resins with a temperature of 70-130°C and an average molecular weight of 800-1500 are preferred. Petroleum resin is a general term for polymerizable substances from specific fractions obtained in petroleum refining processes that are made into resin without being isolated and purified. Therefore, although the detailed composition cannot be shown, the monomer composition suggests that it is an aliphatic copolymer consisting of isoprene, piperylene, 2-methylbutene-1 or 2, etc., and aliphatic copolymers such as styrene, vinyltoluene, α - It is broadly classified into aromatic copolymers consisting of methylstyrene, coumaron, indene, etc. Additionally, additives such as powder fillers and anti-aging agents can be added to the liquid polymer composition as needed. Examples of powder fillers include inorganic powders such as calcium carbonate, clay, and talc, and coloring pigments. The blending amount is 0 to 300 parts by weight, preferably 50 to 200 parts by weight, per 100 parts by weight of the liquid polymer. As the anti-aging agent, those compounded in ordinary rubber products, such as amine-based and phenol-based anti-aging agents, can be used. The amount of these compounds is 0.1 to 100 parts of liquid polymer.
10 copies is appropriate. As the crosslinking agent used in the present invention, polyisocyanate compounds such as toluene diisocyanate, 4,4'-diphenylmethane diisocyanate, xylene diisocyanate, and isocyanate prepolymers thereof are suitable. Such a crosslinking agent is used in an amount of 5 to 50 parts by weight per 100 parts by weight of the liquid polymer. The crosslinking reaction is usually carried out at room temperature without heating, but the crosslinking rate can also be increased by adding a catalyst or heating. As such catalysts, metal compounds such as lead octenoate, cobalt naphthenate, ferric chloride, and dibutyltin dilaurate, and amines such as triethylamine and tetramethylethylenediamine are preferably used. In this case, the catalyst is preferably used in an amount of 0.01 to 2.0 parts by weight per 100 parts by weight of the liquid polymer. Since the composition used in the present invention is reinforced with petroleum resin, there is no need for pulverization using a special mixer such as a three-roll type, and it can be mixed uniformly with a simple mixer such as a three-blade type. It also contributes to labor saving in the manufacturing process. Next, the present invention will be explained in more detail with reference to Examples and Comparative Examples. In the examples, "parts" refer to parts by weight unless otherwise specified. Examples 1 to 4 and Comparative Examples 1 to 2 First, a polymer composition consisting of each component shown in Table 1 is prepared. The compositions of Examples 1 to 4 were mixed using a propeller shaft type mixer, and the compositions of Comparative Examples 1 to 4 were mixed using a propeller shaft type mixer.
Composition 2 was prepared by mixing and pulverizing with three rolls. Next, a predetermined amount of the crosslinking agent shown in Table 1 is added and mixed, and the crosslinking agent of about 2.0
After coating to a thickness of mm, it was cured at 20°C for 14 days and its physical properties were measured. The crosslinked product was subjected to alkali treatment and heat treatment, and its physical properties were measured. For alkaline treatment, immerse in 5% caustic soda boiling water solution for 4 days, and for heat treatment, immerse in 100℃ in a thermostatic chamber.
The test was carried out by standing at ℃ for 168 hours. The results are shown in Table 2.

【表】【table】

【表】【table】

【表】 第2表から明らかなように、実施例1〜4の架
橋物と比較例1の架橋物を比較すると、石油樹脂
を配合することにより14日間後物性は顕著に改良
されており、石油樹脂配合の良好な結果を示して
いる。比較例1の組成物では、強度、特に引張強
度が小さく、建築用途では使用に耐えない。 また、本発明の液状ポリマー組成物架橋物は、
比較例2の組成物に比べると14日後物性は若干劣
るが、アルカリ処理後および熱処理後の物性は、
非常に優れていることが理解される。 なお、実施例1〜4および比較例1の架橋物は
処理後も外観変化はほとんどなく良好であつた。 本発明は、従来建築用途では強度が弱く実用で
きなかつたジエン系液状ポリマーの欠点を石油樹
脂の配合により解消したものであり、建築用防水
材としての耐水性はもちろん、耐薬品性、耐熱
性、耐久性に優れた材料を提供するものである。
[Table] As is clear from Table 2, when comparing the crosslinked products of Examples 1 to 4 and the crosslinked product of Comparative Example 1, the physical properties were significantly improved after 14 days by adding petroleum resin. It shows good results for petroleum resin formulation. The composition of Comparative Example 1 has low strength, especially tensile strength, and cannot be used in architectural applications. Moreover, the liquid polymer composition crosslinked product of the present invention is
Compared to the composition of Comparative Example 2, the physical properties after 14 days are slightly inferior, but the physical properties after alkali treatment and heat treatment are
It is understood that it is very good. The crosslinked products of Examples 1 to 4 and Comparative Example 1 were in good condition with almost no change in appearance even after treatment. The present invention solves the drawbacks of conventional diene-based liquid polymers, which were too weak to be used for construction purposes due to their low strength and could not be put to practical use, by incorporating petroleum resin, and has not only water resistance as a waterproofing material for construction, but also chemical resistance and heat resistance. , provides a material with excellent durability.

Claims (1)

【特許請求の範囲】 1 反応性活性水素を有するジエン系液状ポリマ
ーおよび石油樹脂を含有する組成物を架橋剤によ
り架橋させたことを特徴とする建築用防水材。 2 ジエン系液状ポリマーの平均分子量が500〜
10000である特許請求の範囲第1項記載の建築用
防水材。 3 石油樹脂の軟化点が60〜180℃および平均分
子量が500〜3000である特許請求の範囲第1項記
載の建築用防水材。 4 組成物がジエン系液状ポリマー100重量部に
対して石油樹脂10〜500部を含有する特許請求の
範囲第1項記載の建築用防水材。 5 架橋剤が二官能性または多官能性イソシアネ
ートである特許請求の範囲第1項記載の建築用防
水材。
[Scope of Claims] 1. A waterproofing material for construction, characterized in that a composition containing a diene liquid polymer having reactive active hydrogen and a petroleum resin is crosslinked with a crosslinking agent. 2 The average molecular weight of the diene liquid polymer is 500~
10,000, the architectural waterproofing material according to claim 1. 3. The waterproofing material for construction according to claim 1, wherein the petroleum resin has a softening point of 60 to 180°C and an average molecular weight of 500 to 3,000. 4. The waterproofing material for construction according to claim 1, wherein the composition contains 10 to 500 parts of petroleum resin per 100 parts by weight of diene liquid polymer. 5. The architectural waterproofing material according to claim 1, wherein the crosslinking agent is a difunctional or polyfunctional isocyanate.
JP7815180A 1980-06-09 1980-06-09 Petroleum resin-containing liquid diene polymer composition and use thereof Granted JPS573835A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7815180A JPS573835A (en) 1980-06-09 1980-06-09 Petroleum resin-containing liquid diene polymer composition and use thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7815180A JPS573835A (en) 1980-06-09 1980-06-09 Petroleum resin-containing liquid diene polymer composition and use thereof

Publications (2)

Publication Number Publication Date
JPS573835A JPS573835A (en) 1982-01-09
JPS6360051B2 true JPS6360051B2 (en) 1988-11-22

Family

ID=13653904

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7815180A Granted JPS573835A (en) 1980-06-09 1980-06-09 Petroleum resin-containing liquid diene polymer composition and use thereof

Country Status (1)

Country Link
JP (1) JPS573835A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH075398B2 (en) * 1987-04-24 1995-01-25 出光石油化学株式会社 Hydrophobic material

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5135171B2 (en) * 1972-05-16 1976-09-30
JPS564576B2 (en) * 1973-09-22 1981-01-30

Also Published As

Publication number Publication date
JPS573835A (en) 1982-01-09

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