JPS58164667A - Waterproofing technique - Google Patents

Waterproofing technique

Info

Publication number
JPS58164667A
JPS58164667A JP4765982A JP4765982A JPS58164667A JP S58164667 A JPS58164667 A JP S58164667A JP 4765982 A JP4765982 A JP 4765982A JP 4765982 A JP4765982 A JP 4765982A JP S58164667 A JPS58164667 A JP S58164667A
Authority
JP
Japan
Prior art keywords
adhesive
ethylene
water
vinyl
dispersion
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
JP4765982A
Other languages
Japanese (ja)
Other versions
JPH0222779B2 (en
Inventor
Takeshi Yuki
健 結城
Takenori Tanaka
田中 偉業
Makoto Shiraishi
誠 白石
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.)
Kuraray Co Ltd
Original Assignee
Kuraray 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 Kuraray Co Ltd filed Critical Kuraray Co Ltd
Priority to JP4765982A priority Critical patent/JPS58164667A/en
Publication of JPS58164667A publication Critical patent/JPS58164667A/en
Publication of JPH0222779B2 publication Critical patent/JPH0222779B2/ja
Granted legal-status Critical Current

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  • Laminated Bodies (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

PURPOSE:To carry out waterproofing easily without deleterious change in working circumstances, by applying a water-base adhesive consisting mainly of an ethylene/vinyl ester copolymer dispersion onto one side of a ground such as concrete or plywood and pressing a waterproof sheet against the adhesive in a highly dried state. CONSTITUTION:A water-base adhesive consisting mainly of an aq. dispersion with a glass transition temp. of -5--40 deg.C, having 5-50wt% ethylene content and 95-50wt% vinyl ester (e.g., vinyl acetate, vinyl propionate) content is applied on one side of a ground comprising concrete or plywood, and a waterproof sheet (e.g., a sheet consisting mainly of ethylene/propylene/diene terpolymer) is pressed against the adhesive in a dryness of 40-100%. There is no fear of deleterious change in working circumstances caused by evaporation of solvents. When dried, waterproofing can be carried out in application onto only one side but not both sides, which are difficult to work, and also in a highly dried state.

Description

【発明の詳細な説明】 本発−はルーフインダ材勢に用いられる**シートを用
い九防水工法Kllする。
DETAILED DESCRIPTION OF THE INVENTION The present invention uses nine waterproofing methods using **sheets used for roof inder materials.

従来構造物における防水工法にはアスファルト防水、モ
ルタル防水、シート防水 m膜防水があるがなかでもシ
ート防水は施工の容墨さ、防水性能において優れている
ことから数多く採用され施工実績も、近年着しく伸びて
いる。
Conventional waterproofing methods for structures include asphalt waterproofing, mortar waterproofing, sheet waterproofing, and m-membrane waterproofing.Among these, sheet waterproofing has been widely adopted due to its ease of construction and excellent waterproof performance, and its construction track record has increased in recent years. It's growing nicely.

ところが従来のシート肪水工法はスラブコンクリート等
の下地と防水シートとO接着には有機溶剤系のりcIc
lプレンゴム系中ブチルゴム系の接着剤を用い、下地と
防水シート両1iK#接着剤を塗布し10011を燥畜
せ九〇ち圧着すゐ必要がある。
However, in the conventional sheet fat water construction method, organic solvent-based glue cIc is used to bond the base material such as slab concrete, the waterproof sheet, and O.
It is necessary to apply 1iK# adhesive to both the base and waterproof sheet using a prene rubber type or butyl rubber type adhesive, dry the 10011, and press it for 90 minutes.

cの九めll011水工法に比べ施工性が容易とは言う
ものの、有機溶剤発散によ抄作業環境を悪化させるとい
うことや作1ml中中煩雑であるという問題点を有して
いえ。
Although it is said to be easier to implement than the water method, it has problems such as deterioration of the papermaking work environment due to organic solvent emission and the complexity of making 1 ml of paper.

このよう&観点から種々の水性接着剤の使用が提案され
ているがまにこれらの水性接着剤は種々の点で問題点を
有している。例えばアクリル系のものは耐アルカリ性、
低温接着性が不充分であり合成ゴム系040は低温接着
性の他耐久性にも欠点がある。防水シートはその耐久性
の良さのためエチレン−プロピレン−ジェンタープリマ
ー(以上EPTと略す)を主成分とし九防水シートが多
様されていゐが、これ嬬低極性、疎水性であるため接着
しにくいものである0特にこ0EPTシートに対しては
上述の水性接着剤では下地への片面塗布では勿論のこと
両面塗布でも光分な接着力が得られないのが実情である
。また最近EPTシートの接着性を改良した接着層つき
シートが販売されているが、アクリル系エマルジョンの
中にはこれに対して接着するものもあるが、乾燥度が高
くなるとタックが失われ圧着できなくなるのが実状であ
る。
From these and other viewpoints, the use of various water-based adhesives has been proposed, but these water-based adhesives have various problems. For example, acrylic products are alkali resistant,
Low-temperature adhesion is insufficient, and synthetic rubber type 040 has drawbacks not only in low-temperature adhesion but also in durability. Tarpaulin sheets are made of ethylene-propylene-genter primer (hereinafter abbreviated as EPT) as its main ingredient due to its good durability, and there are various types of tarpaulin sheets, but these sheets are generally difficult to adhere to because of their low polarity and hydrophobicity. In particular, the fact is that the water-based adhesive described above does not provide sufficient adhesion for EPT sheets, let alone when coated on one side of the substrate, or even when coated on both sides. Recently, sheets with an adhesive layer that have improved the adhesive properties of EPT sheets have been sold, but some acrylic emulsions will adhere to these, but if the degree of dryness is high, the tack will be lost and pressure bonding will not be possible. The reality is that it will disappear.

本発明者らは作業環境を悪化させずEPTを主成分とす
る防水シートを用いて、下地への片面塗布で防水施工を
行う方法について鋭意研究を重ね71!i果、!定範囲
のエチレン−ビニルエステル共重合体分散液を主成分と
する接着剤組成物を用いることが要求性能を満足するこ
とを見出し本発明に到達し九。
The inventors of the present invention have conducted extensive research on a method of waterproofing by applying a single-sided coating to the base using a waterproof sheet containing EPT as its main component without deteriorating the working environment71! i fruit! The inventors have discovered that the required performance can be satisfied by using an adhesive composition containing a certain range of ethylene-vinyl ester copolymer dispersion as a main component, and have thus arrived at the present invention.

すなわち、スラブコンクリ□−トおよび特殊合板からな
る上−地にエチレン含有率5〜50重量饅、ビニルエス
テル含有率5〜50量v1戸ガラス転移 温度が一5℃〜−40℃の水性分散液を主成分とする水
性接着剤組成物を片WJ]Ik布し乾燥度40〜100
饅とし、次いで防水シートを圧着することt”%黴とす
る防水工法である。乾燥すれば作業しK〈い両面塗布、
でなく1片面塗布でしかも乾燥度が高い状態で施工する
ことに41徽がある0こむで乾燥度とは見掛けの乾燥度
のことで、接着剤層は塗布後乾燥すJIK従い乳白色か
ら透明へと変化するが透明になる時点を乾燥jil O
O#IIとする。
That is, an aqueous dispersion with an ethylene content of 5 to 50% by weight and a vinyl ester content of 5 to 50% on a surface made of slab concrete and special plywood and a glass transition temperature of 15°C to -40°C. A piece of water-based adhesive composition mainly composed of
This is a waterproofing method in which the mold is coated and then the waterproof sheet is crimped.Once it dries, the work is done.
It is important to apply the adhesive on one side and in a highly dry state.Dryness refers to the apparent dryness, and the adhesive layer dries after application.According to JIK, the adhesive layer changes from milky white to transparent. The drying time changes to the point where it becomes transparent.
It shall be O#II.

本発明に用いる防水シートは、EPT中プチルゴムシよ
びこれらOII舎物からなる未加硫渥およヒ加硫シート
中、ポリクロロプレンシート、クロルスルホン化ポリエ
チレンシート、エチレン−酢酸ビニル共重合シート、ポ
リ塩化ビニルシート勢や上記合成高分子を主原料としそ
れに基布その他を積層加工し←−ト中基布にアスファル
トを金円□ 浸させたアスファベト系肪水シート等いずれも使゛用可
能であるが耐久性、強度などに優れ九EFT    ’
を主成分とする防水シートが好ましい。
The waterproof sheets used in the present invention include unvulcanized sheets and vulcanized sheets made of EPT butyl rubber, polychloroprene sheets, chlorosulfonated polyethylene sheets, ethylene-vinyl acetate copolymer sheets, polychlorinated sheets, etc. Vinyl sheets and asphalt-based fat-water sheets made by laminating the above-mentioned synthetic polymers as the main raw material and a base fabric and other materials and soaking asphalt in the base fabric can all be used. Nine EFT's with excellent durability and strength
A waterproof sheet containing as a main component is preferable.

本発WAKlN用しうるエチレン−ビニルエステル共重
合体のエチレン含有率は5〜50重量−である。5重量
嚢以下では、ガラス転移温度が一5℃以下でもEFTに
対する接着性が低下し、50重量−をこえると凝集力が
極度に低下し、高温接着力が低下する。を九ビニルエス
テル含有率ハ50〜95重量−に限定される。50重量
−以下では凝集力が低下して高温接着力が低下し、95
重量−をこえると低温接着力が低下する。
The ethylene content of the ethylene-vinyl ester copolymer that can be used for WAKIN of the present invention is 5 to 50% by weight. If the weight is less than 5 weight bags, the adhesiveness to EFT will decrease even if the glass transition temperature is 15° C. or less, and if it exceeds 50 weight bags, the cohesive force will be extremely reduced and the high temperature adhesive strength will be reduced. The vinyl ester content is limited to 50-95% by weight. If the weight is less than 50%, the cohesive force decreases and the high temperature adhesive strength decreases.
If the weight exceeds -, the low-temperature adhesive strength decreases.

本発明に用いられるビニルエステルとしては炭素数2〜
12の脂肪族カルボン酸のビニルエステルで1例えば酢
酸ビニル、プロピオン酸ビニル、ラウリン酸ビニル、平
均炭素数10の第3級カルボン酸ビニル(VeoVa 
10 m シェル社商品名)勢を挙げることができ、I
IIPK酢酸ビニル、プロピオン酸ビニルV@ova 
1 Gおよびこれらの混合系が有効である。
The vinyl ester used in the present invention has 2 or more carbon atoms.
Vinyl esters of 12 aliphatic carboxylic acids, such as vinyl acetate, vinyl propionate, vinyl laurate, and vinyl tertiary carboxylates with an average carbon number of 10 (VeoVa
10 m (Shell company product name)
IIPK vinyl acetate, vinyl propionate V@ova
1 G and mixtures thereof are effective.

さらに、上記2成分が特定範囲内であればこれらと共重
合回期な成分を併用することも可能である。特にアクリ
ル酸エステルが11tL<、プ+ルアクリレート、ヘキ
シルアクリレート、2−エテルヘキシルアクリレート等
が適している0その他、共重合可能な不飽和化合一とし
てはアクリル酸、メタアクリル酸、マレイン酸、フマー
ル酸、クロトン酸、イタコン酸等の不飽和カルボン酸、
メタアクリル駿エステル、N−ビニルピロリドン、アク
リルアミド、2−ヒドロキシエチルアクリレート、N−
メチロールアクリルアミド、グリシジルメタアクリレー
ト、塩化ビニル、ジアリルフタレート、トリアリルシア
ヌレート、エチレングリコールジメタアク°リレート等
があげられる0本発明において使用される水性分散液は
界面活性剤または保験コーイドの存在下で加圧重合して
得られるものであるが、保護コロイドが望ましく、保腫
コロイド単独を大は界面活性剤と併用しても有効である
。保護コロイドとしては、ポリビニルアルコール(以下
Pvムという)が最もすぐれており、平均重合度100
〜4200、ケン化度70〜100モル慢Os分ケン化
物t′#−は完全ケン化物が用いられる他、重合過程で
7クリロニトリル、アクリルアミドやタロンン酸、アク
リル酸、メタアクリル酸、4レイン酸、イタコン酸等の
不飽和カルボン酸やそのアル中ルエステル等を酢酸ビニ
ルと共重合したのち、ケン化したものや、PVAを製造
価、硫酸、リン酸、ホリマリン、尿素、無水マレイン酸
等と反応したものなどいわゆる質性pvAtiFipv
As導体も使用できる0PVA以外の保躾コロイドとし
て無水マレイン酸−イソブチレン共重合体、スチレンの
カルメン酸愛性共重合体、ヒドロ中ジエチルセルローズ
、ヒドロキシグロビルセルローズ等が使用できる。
Furthermore, as long as the above two components are within a specific range, it is also possible to use a component that can be copolymerized together with these two components. Particularly suitable are acrylic acid esters of 11 tL or less, phosphor acrylate, hexyl acrylate, 2-ethylhexyl acrylate, etc. Other copolymerizable unsaturated compounds include acrylic acid, methacrylic acid, maleic acid, fumaric acid, etc. acids, unsaturated carboxylic acids such as crotonic acid and itaconic acid,
Methacrylic ester, N-vinylpyrrolidone, acrylamide, 2-hydroxyethyl acrylate, N-
Examples include methylol acrylamide, glycidyl methacrylate, vinyl chloride, diallyl phthalate, triallyl cyanurate, ethylene glycol dimethacrylate, etc. The aqueous dispersion used in the present invention is prepared in the presence of a surfactant or a safety coid. Although a protective colloid is preferable, it is also effective to use a protective colloid alone or in combination with a surfactant. Polyvinyl alcohol (hereinafter referred to as Pvm) is the best protective colloid, with an average degree of polymerization of 100.
-4200, degree of saponification 70-100 molar Os fraction Saponified product t'#- is completely saponified, and in addition to 7-acrylonitrile, acrylamide, talonic acid, acrylic acid, methacrylic acid, 4-leic acid in the polymerization process. , copolymerization of unsaturated carboxylic acids such as itaconic acid and their esters in alcohol with vinyl acetate and saponification, and reaction of PVA with sulfuric acid, phosphoric acid, formalin, urea, maleic anhydride, etc. So-called qualitative properties such as things pvAtiFipv
As the protective colloid other than OPVA, which can also be used as an As conductor, maleic anhydride-isobutylene copolymer, carmenic acid-loving copolymer of styrene, diethyl cellulose in hydrochloride, hydroxyglobil cellulose, etc. can be used.

界面活性剤としては一般に市販されているアニオン界面
活性剤、ノニオン界面活性剤、カチオン界面活性剤が使
用される。
As the surfactant, commercially available anionic surfactants, nonionic surfactants, and cationic surfactants are used.

重合開始剤は過酸化水素、過硫酸カリウム勢の水溶性無
機過酸化物i九は過硫酸塩、アゾ化合物勢が用いられる
0壇九これらと遺元削の併用によゐレドックス系開始剤
を使用−′□”4こともできる。
The polymerization initiator used is a water-soluble inorganic peroxide such as hydrogen peroxide or potassium persulfate, or a persulfate or an azo compound.A redox type initiator can be created by combining these with oxidation. You can also use −′□”4.

重合方法はビニルエステルを一括して、或いは分割して
、或いは連続的に添加してもよい。
In the polymerization method, the vinyl ester may be added all at once, in portions, or continuously.

本願発明に適用される該共重合体水性分散液のガラス転
移ii*は一5°〜−40’Cに限定される。
The glass transition ii* of the aqueous copolymer dispersion applied to the present invention is limited to -5° to -40'C.

咳転移温度は掬定方法によって値が異なるが、ここで祉
トーシ冒ナルプレイドアナリシス(TBA。
The value of the cough transition temperature varies depending on the scooping method, but here it is determined by TBA.

周波数IH3以下)Kよる値をいう。TBAKついて#
i例えば、日本化学会鍋;f#実験化学講座第19巻、
第904頁(1978年九豐発行)K記載されている0
ガラス転移温度が一5℃よ如高い場合は常温及び低温接
着力が低下しb−40’C以下では鳥温接着力が低下し
不適轟である0特に−1(P〜−35℃の範■が好オし
い〇 本発明の施工方法は、皺エチレンービニルエステル共重
合体水性分歓諌をスラブコンクリート壇九Fi特殊合板
等からなぁ下地に塗布し、乾燥度40〜100参と、な
る壜でオーブンタイムをとp次いで防水シート渣圧着す
ることからなるが、乾、:1・ 織度が40s以下、では成木しにくい下地に対して1、
・、:・・・1 施工vIL後に−が一ヤえ鳩舎接着破壊を起すおそれが
あり40暢以上乾燥して貼合せる必要がある。
Frequency IH3 or lower) refers to the value determined by K. About TBAK#
For example, Chemical Society of Japan Nabe; f#Experimental Chemistry Course Volume 19;
Page 904 (Published by Kufyo in 1978) K listed 0
When the glass transition temperature is higher than 15°C, the adhesive strength at room temperature and low temperature decreases, and when the glass transition temperature is below -40'C, the adhesive strength at bird temperature decreases, making it unsuitable. 〇 The construction method of the present invention is to apply the wrinkled ethylene-vinyl ester copolymer aqueous component to the base material, such as slab concrete platform special plywood, etc., and achieve a dryness of 40 to 100 cm. It consists of oven time in a bottle and then crimping the tarpaulin residue, but when dry: 1. For substrates with a weave of 40 seconds or less, which are difficult to mature, 1.
・、:・・・1 After applying VIL, there is a risk of damage to the adhesive of the pigeon house, so it is necessary to dry it for more than 40 minutes before laminating.

本発明の施工対策は主Kl&水性のあるコンクリート、
モルタル中台ateであるが、lk水性のない断熱材や
防水シート勢の下地に対しても施工可能である。但しそ
の場合は接着剤層を10〇−乾燥させて貼合せる必要が
ある。
The construction measures of the present invention are mainly Kl & water-based concrete,
Although it is made of mortar, it can also be applied to non-water-based insulation materials and waterproof sheets. However, in that case, it is necessary to dry the adhesive layer for 100 minutes before bonding.

本発明の特徴は非極性のEPTを主成分とする防水シー
トを用い、特定の接着剤を使用し特定の条件で防水施工
を1行なうことである。すなわち。
A feature of the present invention is that waterproofing is performed once under specific conditions using a specific adhesive using a waterproof sheet containing non-polar EPT as a main component. Namely.

一般の水性接着剤はEPTK対しては接着剤はおろか剥
離剤になりうるような性質のものが多く、従来からよく
知られ薔いるエチレン−ビニルエステル共重合体水性分
散液も接着性は低い。しかるにガラス転移温度が一5℃
〜−40℃でかつ特定範囲の組成のビニルエステルおよ
びエチレンを主成分とし丸孔化共重合体はEPTK対す
る接着性が着しく高くなり、41に低温接着力が向上す
る。
Most common water-based adhesives have properties that allow them to act as release agents as well as adhesives for EPTK, and even the well-known aqueous ethylene-vinyl ester copolymer dispersion has low adhesive properties. However, the glass transition temperature is 15℃.
The round-hole copolymer mainly composed of vinyl ester and ethylene with a composition in a specific range at ~-40°C exhibits significantly high adhesion to EPTK, and the low-temperature adhesive strength is improved to 41%.

皺襞着剤はエチレンを主成分の一つとして有するためゴ
ム系と異な)1重合中にオリゴマーが合成され、粘着付
与物質も自動的に合成されることにより防水シートに対
する密着性または他の物質に対する密着性が着しく向上
し施工性4良好となる。
The wrinkle adhesive has ethylene as one of its main components, so it is different from rubber-based adhesives. Oligomers are synthesized during one polymerization, and tackifying substances are also automatically synthesized, which improves the adhesion to waterproof sheets and to other substances. The adhesion is improved and the workability is good (4).

さらに、本発明の特徴の一つは、無公害型の水系であり
コンクリート中台板@0下地に対してプライマーを必要
とせず1片面塗布で接着が可能であり施工が筒素化され
ていることは□勿論、耐寒性、耐熱性、耐老化も優れて
いる。
Furthermore, one of the features of the present invention is that it is non-polluting, water-based, and can be bonded to a concrete base plate @ 0 base plate with one single-sided coating without the need for a primer, making it possible to apply it in a single-sided manner. Of course, it also has excellent cold resistance, heat resistance, and aging resistance.

冑本−1に用いる接着剤親戚物には必11に応じて他の
重合体の水性分散液を混合して4よく、例えばン酢駿ビ
ニル系重合体、アクリル蒙アル中ルエステル系共重合体
、オレフィン系重合体、塩化ビニル系重合体、スチレン
−ブタジェン系共重合体等の水性分散Ilが挙けられる
。さらに本願発明の接着剤に#i伽〇一般的に使用され
てい石添加剤、例えば増粘剤、粘着付与剤、可朧剤、消
泡剤、顔料中イソシアネート化合物、フェノール樹脂、
メラミン樹脂、尿素樹脂、エポ中シ化合物勢の架橋剤等
を混合してもよいが、前記の他の重合体水性分散液混合
の場合・と則じく、組成物の性能を低下させない@縦の
量Kilられる。
Adhesives used in Kabumoto-1 may be prepared by mixing aqueous dispersions of other polymers, such as vinyl-based polymers, acrylic, monoalcohol-based copolymers, and aqueous dispersions of other polymers. Examples include aqueous dispersions Il of olefin polymers, vinyl chloride polymers, styrene-butadiene copolymers, and the like. Furthermore, stone additives commonly used in the adhesive of the present invention, such as thickeners, tackifiers, hazy agents, antifoaming agents, isocyanate compounds in pigments, phenolic resins,
A melamine resin, a urea resin, a crosslinking agent such as an Epoxy compound, etc. may be mixed, but as in the case of mixing other polymer aqueous dispersions mentioned above, it is necessary to use a crosslinking agent that does not reduce the performance of the composition. amount of kill.

以r%*細例、比I2例をあげて本発明を具体的Kag
Aするがこれらの例は同等本発明を限定するものではな
い。肯これらの例における「s」及び「慢」は特に断り
のない@t)Fi倉量基準で表わすものとする。
Hereinafter, we will give two examples of detailed examples and ratios to illustrate the present invention.
However, these examples are not intended to limit the invention. ``s'' and ``arrogance'' in these examples are expressed on the basis of @t)Fi storage capacity unless otherwise specified.

実施例1 攪拌機およびジャケット付オートクレーブにイオン交換
水60.3部1重責酸ナトリウム0.2%。
Example 1 In an autoclave with a stirrer and a jacket, 60.3 parts of ion-exchanged water and 0.2% of sodium bisulfate were added.

過硫酸カリウム0.5i1S、PVA(ケン化度88モ
ル嚢、重合度500 ) 2.6f!6.ポリオ中ジエ
チレンノニルフェニルエーテル(エチレンオキシド付加
モル数−30)1.3部を添加し均一に溶解させエチレ
ン圧力を501v/j K加圧し3o+:1’cに調整
し九。
Potassium persulfate 0.5i1S, PVA (saponification degree 88 molar capsules, polymerization degree 500) 2.6f! 6. Add 1.3 parts of diethylene nonylphenyl ether (number of moles of ethylene oxide added - 30) in polyethylene, dissolve uniformly, and apply ethylene pressure to 501 v/j K to adjust the ratio to 3o+:1'c.

メタ重亜硫酸ソーダ0.06部をイオン交換水0.26
部に溶解し、この溶液の1/6をオートクレーブに添加
した。これと同時に酢酸ビニル52.5部を11時間か
けて連続添加し、さらにイオン交換水33.79にポリ
オキシエチレンノニル7エ二・旨。
0.06 parts of sodium metabisulfite and 0.26 parts of ion-exchanged water
1/6 of this solution was added to the autoclave. At the same time, 52.5 parts of vinyl acetate was continuously added over a period of 11 hours, and 7.2 parts of polyoxyethylene nonyl was added to 33.79 parts of ion-exchanged water.

ルエーテル(エチレンオキシド付加モルa−30)1.
3部を溶解した溶液を逐次添加した。酢酸ビニルを添加
すると直ちに重合が開始した。重合中メタ重亜硫酸ナト
リウム溶液の残pを5WAK分けて添加し九〇なお、重
合中適宜少量サンプリングしてブロム滴定法により系内
の酢酸ビニル11度を求め九がいずれも1−以下で6つ
九。を九エチレン圧力は50 IQ/ai 、温度は3
鍍±1℃に酢酸ビニル添加終了オで一定に保持し良。得
られ走水性分散液の安定性は良好で6つ九〇鋏分散液の
組成を第1機に示す。
ether (ethylene oxide addition mole a-30) 1.
A solution containing 3 parts was added sequentially. Polymerization started immediately upon addition of vinyl acetate. During the polymerization, add the remaining p of the sodium metabisulfite solution in 5 WAK portions.During the polymerization, take a small sample as appropriate and use the bromine titration method to determine the vinyl acetate 11 degrees in the system. Nine. 9 ethylene pressure is 50 IQ/ai, temperature is 3
It can be maintained at a constant temperature of ±1°C after adding vinyl acetate. The stability of the hydrotactic dispersion obtained was good, and the composition of the six-scissor dispersion is shown in the first machine.

腋分散液を歩道1[(305w830m、J I S 
−A−5304)にスポンジローラーでs o o t
7iの塗順量で處布し30分のオープンタイムで接着剤
層の見掛は乾燥度が70憾となった。次いでEPT防水
シート(東洋ゴム社l1ll)を圧着し3日養生俵(1
)〜ts+接着力闘定試験を行なつ九。
Armpit dispersion on sidewalk 1 [(305w830m, JIS
-A-5304) with a sponge roller.
The adhesive layer was applied with a coating weight of 7i and the apparent dryness of the adhesive layer was 70 after 30 minutes of open time. Next, an EPT waterproof sheet (Toyo Rubber Co., Ltd.) was crimped and the bales were cured for 3 days (1
) to ts+ conduct the adhesion strength test.

(υ 常繍剥離強縦 20℃において剥−適txoo■/分でオート3::: グラフを用いて90°I11離強度を一定した。(υ Regular embroidery peeling strong vertical Peel at 20°C, auto 3::: The 90°I11 separation strength was determined using a graph.

、11゜ (1)耐水−一強度 20℃6水□道水に1遍間浸漬後湿潤状態で(1)(に
準じて剥離強度を一定しえ。
, 11° (1) Water Resistance--Strength 20°C 6 □ After immersing in tap water for one hour, maintain the peel strength in accordance with (1) (in a wet state).

(1)  ^温りリープ性試験 70℃200tの荷重下での剪断クリープを測定した0
(接着面積;25■xzs■)(句 低温接着性 5℃で前記と同様KEPTと歩道板の接着を行ない5℃
で3日養生後、5℃で90°剥離強度を測定し九〇結果
を第2−に示す。
(1) Warm Leap Test Shear creep was measured under a load of 200 tons at 70°C.
(Adhesion area: 25 x zs)
After curing for 3 days, the 90° peel strength was measured at 5°C and the results are shown in Section 2-.

表よシ明らかなように低温下での接着性も良好であり常
態、耐水強度、高温クリープ性も優れている。
As is clear from the table, it has good adhesion at low temperatures, and is also excellent in normal state, water resistance strength, and high temperature creep properties.

実施例2 実施例と同じオートクレーブに平均重合度1700、ケ
ン化度88 モル−〇 P V A 4.51Bを70
部のイオン交換水に溶解し、エチレン35 kl/j加
圧下、60℃で平均炭素数10の三級カルボン酸のビニ
ルエステル76部と酢酸ビニルを過酸化水素1%水溶液
とロンガリツ)5s水溶液を使用して連続重合した。得
られた水性分散液は安定であった。該分散液の組成を第
1表に示す。を九実施例1と同様に測定した剥離強度を
第2表に示す。
Example 2 In the same autoclave as in Example, 70% of P V A 4.51B with an average degree of polymerization of 1700 and a degree of saponification of 88 mol-0
76 parts of vinyl ester of a tertiary carboxylic acid having an average carbon number of 10 and vinyl acetate were dissolved in 1% aqueous solution of hydrogen peroxide and 5s aqueous solution of Rongarits at 60°C under a pressure of 35 kl/j of ethylene. was used for continuous polymerization. The resulting aqueous dispersion was stable. The composition of the dispersion is shown in Table 1. Table 2 shows the peel strength measured in the same manner as in Example 1.

実施例3 実施例1と同じオートクレーブに平均重合度1700、
ケン化度88モル−のPVA21Bとノニオン活性剤(
ノーポール4001三洋化成■製)2sを70sのイオ
ン交換水に溶解し401v/jのエチレン加圧下、50
℃でアクリ、ル酸0.5部、酢酸ビニル6011.2−
エチルへ中シルアクリレート22sを過硫酸アン七ニウ
ム2慢水溶液を用いて連続重合し九〇得られ走水性分散
液の組成を第1表に、接着性能橢定結果を第2*に示す
Example 3 In the same autoclave as in Example 1, an average polymerization degree of 1700,
PVA21B with a saponification degree of 88 mol- and a nonionic activator (
Norpol 4001 (manufactured by Sanyo Chemical) 2s was dissolved in 70s of ion-exchanged water, and under 401v/j ethylene pressure, 50
Acrylic acid, 0.5 part of phosphoric acid, vinyl acetate 6011.2-
The composition of the hydrotactic dispersion obtained by continuous polymerization of 22s of ethyl silacrylate using an aqueous solution of am7nium persulfate is shown in Table 1, and the results of adhesion performance evaluation are shown in Table 2*.

実施例4 実施例3と同じ重合方法で単量体組成を変えた水性分散
液を得九〇その組成を第111に示す。諌分散液100
mにジプテルフタレー)3sを添加混合し組成物を調製
し接着性能を評価し九。その結果を第2表に示す。
Example 4 An aqueous dispersion with a different monomer composition was obtained using the same polymerization method as in Example 3. The composition is shown in No. 111. Isa dispersion liquid 100
Dipterphthale) 3s was added and mixed to m to prepare a composition, and the adhesive performance was evaluated. The results are shown in Table 2.

実施例5 実施例3と−じ重合方法で単量体組成を変えた水性分散
液を得九〇そ01m1成を第1表に示す。該分散液の接
着性能を第2表に示す〇 実施例6 実施例2のPVA5部に代えてノニオン活性剤(ノニボ
ール200)5鄭を使用する以外は同一の条件で重合し
た。得られた水性分散液の組成を第1t4に示し咳分散
液の接着性能を第2表に示す0実施例7 実施例2のPVA5部に代えてとドロ中ジエチルセルロ
ース1部とノニオン活[1j(ノニポール200)4@
を使用する以外は同一の条件で重合した。得られ九本性
分散液の組成を第1*に示し骸分散液の接着性能を第2
表に示す。
Example 5 An aqueous dispersion having a different monomer composition was obtained by the same polymerization method as in Example 3. The composition of 90 mL of the dispersion is shown in Table 1. The adhesive performance of the dispersion is shown in Table 2. Example 6 Polymerization was carried out under the same conditions except that 5 parts of a nonionic activator (Noniball 200) was used in place of 5 parts of PVA in Example 2. The composition of the obtained aqueous dispersion is shown in Table 1t4 and the adhesion performance of the cough dispersion is shown in Table 2.0 Example 7 In place of 5 parts of PVA in Example 2, 1 part of diethyl cellulose and nonionic active [1j (Nonipole 200) 4@
Polymerization was carried out under the same conditions except that . The composition of the resulting nine-bonded dispersion is shown in 1st*, and the adhesion performance of the carcass dispersion is shown in 2nd.
Shown in the table.

比較例1〜4 実施例と同じ重合方法で単量体組成を変えて重合した。Comparative examples 1 to 4 Polymerization was carried out using the same polymerization method as in the examples, but with different monomer compositions.

得られ九本性分散液の組成を第1表に示す。実施例1と
同じ条件で測定し良接着性能を第2衆に示す。
Table 1 shows the composition of the nine-pronged dispersion obtained. Measurements were made under the same conditions as in Example 1, and good adhesion performance was shown in the second group.

第2表から明らかなようにガラ5ス転移温度が−・ト′
As is clear from Table 2, the glass transition temperature is −・t′
.

5℃〜−40℃の範囲を外れるもの、エチレン含有率が
5重量n以下Oもの、ビニルエステル含有率が50〜9
5重量−の範囲を外れるもの鉱、常騰、耐水、低亀剥離
強II!および高温クリープ性の。
Items outside the range of 5℃ to -40℃, ethylene content of 5wtn or less, vinyl ester content of 50 to 9
Items outside of the 5 weight range, regular rise, water resistance, low peeling strength II! and high temperature creep properties.

いずれかが低いことがわかる。It can be seen that one of them is low.

専:、1:・ 比較例5および実施例8 実施例2で用いた水性分散液を使用して上記の条件で屋
外施工試験を行なった。
Comparative Example 5 and Example 8 An outdoor construction test was conducted using the aqueous dispersion used in Example 2 under the above conditions.

下 地;コンクリート一体にポリマーセメントモルタル
で塗厚5mに塗工したもの 被着材; EPT防水シート〔東洋ゴム■TS−8シー
 ト ] 塗布型; 300 f/m’(wet ) 、接着面構
1mx1m下地にローラーで水性分散液を塗工しオープ
ンタイムをとり見掛けの乾燥度10mと60慢に達した
時点でそれぞれ防水シートを貼合せた。
Base: Concrete integrally coated with polymer cement mortar to a thickness of 5 m Adherent material: EPT waterproof sheet [Toyo Rubber TS-8 sheet] Application type: 300 f/m' (wet), adhesive surface structure The aqueous dispersion was applied to a 1 m x 1 m substrate using a roller, and an open time was taken, and when the apparent dryness reached an apparent dryness of 10 m x 60 m, a waterproof sheet was laminated to each base.

次いで施工直後の降雨を想定して、水性分散液塗工後3
時間後に防水ソート上に散水した。
Next, assuming rainfall immediately after construction, 3 times after applying the aqueous dispersion.
After an hour water was sprinkled on the waterproof sort.

散水24時間後に防水シートの端部を25謹巾に切目を
入れそ云ぞれの防水シート/下地間の接着強度を測定す
ると、乾燥度10%の場合、60*o*eu−tiぞ卆
”“″パ・ “、01V/25“  1でめった。
After 24 hours of watering, we made a 25-wide cut in the edge of the tarpaulin sheet and measured the adhesive strength between the tarpaulin sheet and the substrate.When the degree of dryness was 10%, it was 60*o*eu-ti. """Pa・", 01V/25" I got it in 1.

ポリマー入りセメントモルタルのような吸水性が比較的
小さい′F地にtユ接着剤の乾燥度か低い時点で防水シ
ートを・貼合せると施工後の降雨に対して接着不良をも
たらすおそれがある。
If a waterproof sheet is attached to a substrate with relatively low water absorption, such as polymer-containing cement mortar, when the dryness level of the adhesive is low, there is a risk of poor adhesion due to rainfall after construction.

特許出願人株式会社クラレ 代理人弁塩士本多 騒Patent applicant Kuraray Co., Ltd. Agent Benshio Honda Satoru

Claims (1)

【特許請求の範囲】[Claims] (1)  コンクリートま九は合板等からなる下地に゛
 エチレン含有率5〜50重量−、ビニルエステル含有
率5〜50量饅、ガラス転移温度−50〜−4oQco
水性分散液を主成分とする水性接着剤を塗布し、乾燥度
40〜10011として防水シートを圧着することを特
徴とする防水工法0 (1)  防水シートカエチレンープロピレン−ジェン
ターポリマーを主成分とするシートである特許請求01
11111s1項記載の防水工法。
(1) Concrete is a base made of plywood etc. Ethylene content 5-50% by weight, vinyl ester content 5-50%, glass transition temperature -50--4oQco
Waterproofing method 0 characterized by applying an aqueous adhesive containing an aqueous dispersion as a main component and press-bonding a waterproof sheet with a dryness of 40 to 10011. Patent claim 01 which is a sheet that
The waterproofing method described in Section 11111s1.
JP4765982A 1982-03-24 1982-03-24 Waterproofing technique Granted JPS58164667A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4765982A JPS58164667A (en) 1982-03-24 1982-03-24 Waterproofing technique

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4765982A JPS58164667A (en) 1982-03-24 1982-03-24 Waterproofing technique

Publications (2)

Publication Number Publication Date
JPS58164667A true JPS58164667A (en) 1983-09-29
JPH0222779B2 JPH0222779B2 (en) 1990-05-21

Family

ID=12781379

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4765982A Granted JPS58164667A (en) 1982-03-24 1982-03-24 Waterproofing technique

Country Status (1)

Country Link
JP (1) JPS58164667A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5989378A (en) * 1982-11-11 1984-05-23 Mitsuboshi Belting Ltd Primer for waterproof application

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006036878A (en) * 2004-07-26 2006-02-09 J-Chemical:Kk Aqueous adhesive composition

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5688478A (en) * 1979-12-19 1981-07-17 Kuraray Co Ltd Aqueous contact-adhesive composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5688478A (en) * 1979-12-19 1981-07-17 Kuraray Co Ltd Aqueous contact-adhesive composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5989378A (en) * 1982-11-11 1984-05-23 Mitsuboshi Belting Ltd Primer for waterproof application
JPH0348235B2 (en) * 1982-11-11 1991-07-23 Mitsuboshi Belting Ltd

Also Published As

Publication number Publication date
JPH0222779B2 (en) 1990-05-21

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