JPS63178183A - Adhesive composition for waterproof smeet - Google Patents
Adhesive composition for waterproof smeetInfo
- Publication number
- JPS63178183A JPS63178183A JP821387A JP821387A JPS63178183A JP S63178183 A JPS63178183 A JP S63178183A JP 821387 A JP821387 A JP 821387A JP 821387 A JP821387 A JP 821387A JP S63178183 A JPS63178183 A JP S63178183A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- adhesive
- waterproof
- compsn
- 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.)
- Pending
Links
- 239000000853 adhesive Substances 0.000 title claims abstract description 34
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 34
- 239000000203 mixture Substances 0.000 title claims abstract description 12
- 229920001971 elastomer Polymers 0.000 claims abstract description 17
- 244000043261 Hevea brasiliensis Species 0.000 claims abstract description 13
- 229920003052 natural elastomer Polymers 0.000 claims abstract description 13
- 229920001194 natural rubber Polymers 0.000 claims abstract description 13
- 229920003049 isoprene rubber Polymers 0.000 claims abstract description 10
- 229920002367 Polyisobutene Polymers 0.000 claims abstract description 8
- 229920005549 butyl rubber Polymers 0.000 claims description 9
- 229920005555 halobutyl Polymers 0.000 claims description 7
- 239000003513 alkali Substances 0.000 abstract description 7
- 238000004073 vulcanization Methods 0.000 abstract description 7
- 239000000463 material Substances 0.000 abstract description 6
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 abstract description 3
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 239000000758 substrate Substances 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 229920005556 chlorobutyl Polymers 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000005259 measurement Methods 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000004636 vulcanized rubber Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000010454 slate Substances 0.000 description 3
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- 235000014692 zinc oxide Nutrition 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000004570 mortar (masonry) Substances 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 229920006271 aliphatic hydrocarbon resin Polymers 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229920005557 bromobutyl Polymers 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- AFZSMODLJJCVPP-UHFFFAOYSA-N dibenzothiazol-2-yl disulfide Chemical compound C1=CC=C2SC(SSC=3SC4=CC=CC=C4N=3)=NC2=C1 AFZSMODLJJCVPP-UHFFFAOYSA-N 0.000 description 1
- LMBWSYZSUOEYSN-UHFFFAOYSA-N diethyldithiocarbamic acid Chemical compound CCN(CC)C(S)=S LMBWSYZSUOEYSN-UHFFFAOYSA-N 0.000 description 1
- MZGNSEAPZQGJRB-UHFFFAOYSA-N dimethyldithiocarbamic acid Chemical compound CN(C)C(S)=S MZGNSEAPZQGJRB-UHFFFAOYSA-N 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- 229950004394 ditiocarb Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- -1 n-octane Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000009182 swimming Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- RKQOSDAEEGPRER-UHFFFAOYSA-L zinc diethyldithiocarbamate Chemical compound [Zn+2].CCN(CC)C([S-])=S.CCN(CC)C([S-])=S RKQOSDAEEGPRER-UHFFFAOYSA-L 0.000 description 1
- PGNWIWKMXVDXHP-UHFFFAOYSA-L zinc;1,3-benzothiazole-2-thiolate Chemical compound [Zn+2].C1=CC=C2SC([S-])=NC2=C1.C1=CC=C2SC([S-])=NC2=C1 PGNWIWKMXVDXHP-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【発明の詳細な説明】
〔発明の技術分野〕
本発明は、防水シート用の接着剤に関し、詳しくは、施
工性に優れ、耐アルカリ性の良好な防水シート用接着剤
組成物に関する。DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to an adhesive for a waterproof sheet, and more particularly to an adhesive composition for a waterproof sheet that has excellent workability and good alkali resistance.
防水シートは屋上ルーフィング材あるいは土木用防水材
などとして幅広く用いられており、なかでもエチレン・
プロピレンターポリマー(EPT)を主成分とする加硫
ゴムシートは耐久性、強度などに優れているため特に多
用されている。Tarpaulin sheets are widely used as rooftop roofing materials or waterproof materials for civil engineering, among others, ethylene and
Vulcanized rubber sheets containing propylene terpolymer (EPT) as a main component are particularly widely used because of their excellent durability and strength.
従来、このような防水シート用接着剤としてはクロロプ
レン系の溶剤型接着剤が用いられ一ζきたが、これはア
ルカリ耐性が弱いためクギ穴やシート継目の接着不良か
ら雨水が侵入した際に容易に剥離してしまうという欠点
を持っており、さらに、接着工法においてプライマーを
使用し、かつ下地と防水シート側の両面に接着剤を塗布
する必要があるため作業性が悪いという問題があった。Conventionally, chloroprene-based solvent-based adhesives have been used as adhesives for such waterproof sheets, but because they have low alkali resistance, they are easily damaged when rainwater enters through nail holes or poor adhesion at sheet seams. This method has the disadvantage that it tends to peel off, and it also has the problem of poor workability because it requires the use of a primer in the adhesive method and the need to apply adhesive to both the base and the waterproof sheet side.
本発明は、施工性に優れ、かつ耐アルカリ性が良好であ
る防水シート用接着剤組成物を提供することを目的とす
る。この接着剤組成物は、特に防水シート同士あるいは
防水シートとコンクリート面またはモルタル面との接着
剤として利用される。An object of the present invention is to provide an adhesive composition for a waterproof sheet that has excellent workability and good alkali resistance. This adhesive composition is particularly used as an adhesive between waterproof sheets or between a waterproof sheet and a concrete or mortar surface.
このため、本発明は、ブチルゴム、ハロゲン化ブチルゴ
ム、又はポリイソブチレンゴム85〜30重量部、天然
ゴム又はイソプレンゴム15〜70重量部、および超加
硫促進剤5〜40重量部からなる防水シート用接着剤組
成物を要旨とするものである。Therefore, the present invention provides a waterproof sheet comprising 85 to 30 parts by weight of butyl rubber, halogenated butyl rubber, or polyisobutylene rubber, 15 to 70 parts by weight of natural rubber or isoprene rubber, and 5 to 40 parts by weight of a supervulcanization accelerator. The gist of this paper is an adhesive composition.
以下、本発明の構成につき詳しく説明する。Hereinafter, the configuration of the present invention will be explained in detail.
(11ブチルゴム、ハロゲン化ブチルゴム、又はポリイ
ソブチレンゴム85〜3oit部。(85 to 3 oit parts of 11 butyl rubber, halogenated butyl rubber, or polyisobutylene rubber.
ハロゲン化ブチルゴムとしては塩素化ブチルゴム、臭素
化ブチルゴム等が挙げられる。天然ゴムとの相溶性を考
慮するとブチルゴムよりもむしろハロゲン化ブチルゴム
を用いる方が好ましい。ブチルゴム、ハロゲン化ブチル
ゴム又はポリイソブチレンゴムの配合量は、全ゴム分1
00重量部のうちで85〜30重量部である。85重量
部を越えるとブチルゴムまたはポリイソブチレンゴムが
高温で軟化しているために耐熱性が上がらない。また、
30重量部未満では粘着力が低下し、剥離強度が劣って
くるため85〜30重量部であることが良い。Examples of the halogenated butyl rubber include chlorinated butyl rubber and brominated butyl rubber. Considering compatibility with natural rubber, it is preferable to use halogenated butyl rubber rather than butyl rubber. The amount of butyl rubber, halogenated butyl rubber or polyisobutylene rubber is 1 for the total rubber.
It is 85 to 30 parts by weight out of 00 parts by weight. If the amount exceeds 85 parts by weight, the butyl rubber or polyisobutylene rubber will be softened at high temperatures, and the heat resistance will not improve. Also,
If it is less than 30 parts by weight, the adhesive force will decrease and the peel strength will deteriorate, so it is preferably 85 to 30 parts by weight.
(2)天然ゴム又はイソプレンゴム15〜70重量部。(2) 15 to 70 parts by weight of natural rubber or isoprene rubber.
天然ゴム又はイソプレンゴムのいずれでもよい。配合量
は全ゴム分100重量部のうちで15〜70重量部であ
る。Either natural rubber or isoprene rubber may be used. The blending amount is 15 to 70 parts by weight out of 100 parts by weight of the total rubber content.
(3)超加硫促進剤5〜40重量部。(3) 5 to 40 parts by weight of super vulcanization accelerator.
本発明で使用される超加硫促進剤は、天然ゴムまたはイ
ソプレンゴムを常温において迅速に加硫促進するもので
、例えば、ジメチルジチオカルバミン酸亜鉛、ジエチル
ジチオカルバミン酸亜鉛、ジブチルジチオカルバミン酸
亜鉛、ジメチルジチオカルバミン酸ナトリウム、ジエチ
ルジチオカルバミン酸ナトリウムなどのジチオカルバミ
ン酸金属塩やプチルザントゲン酸亜鉛、イソプロビルザ
ントゲン酸亜鉛、イソプロビルザントゲン酸ナトリウム
などのザントゲン酸金属塩、2−メルカプトベンゾチア
ゾール、ジベンゾチアジルジスルフィドなどのチアゾー
ル系加硫促進剤などが挙げられる。その配合量は全ゴム
分100重量部に対して5〜40重量部で、配合量が5
重量部未満では加硫速度が遅くなり、耐熱性が劣ってく
る。また、40重量部を越えると凝集力が低下し、もろ
くなり接着力が十分でないからである。The super vulcanization accelerator used in the present invention is one that rapidly accelerates the vulcanization of natural rubber or isoprene rubber at room temperature, and examples thereof include zinc dimethyldithiocarbamate, zinc diethyldithiocarbamate, zinc dibutyldithiocarbamate, and dimethyldithiocarbamate. Sodium, metal salts of dithiocarbamates such as sodium diethyldithiocarbamate, metal salts of xanthocarbamates such as zinc butylxanthogenate, zinc isoprobylxanthogenate, sodium isoprobylxanthogenate, 2-mercaptobenzothiazole, dibenzothiazyl disulfide, etc. Examples include thiazole-based vulcanization accelerators. The blending amount is 5 to 40 parts by weight per 100 parts by weight of the total rubber, and the blending amount is 5 to 40 parts by weight.
If the amount is less than 1 part by weight, the vulcanization rate will be slow and the heat resistance will be poor. Moreover, if the amount exceeds 40 parts by weight, the cohesive force decreases, resulting in brittleness and insufficient adhesive force.
本発明においては、イオウを天然ゴムまたはイソプレン
ゴムの加硫剤として用いる。このイオウは、天然ゴムま
たはイソプレンゴム100重量部に対して2重量部程度
使用するのが好ましい。In the present invention, sulfur is used as a vulcanizing agent for natural rubber or isoprene rubber. It is preferable to use about 2 parts by weight of sulfur per 100 parts by weight of natural rubber or isoprene rubber.
また、本発明においては、溶剤を配合する。Further, in the present invention, a solvent is blended.
使用される溶剤としてはブチルゴムおよびハロゲン化ブ
チルゴム、ポリイソブチレンゴム、天然ゴム、イソプレ
ンゴムに対して溶解性の高いものが選択される。例えば
、ベンゼン、トルエン、キシレンなどの芳香族炭化水素
、n−オクタンなどの脂肪族炭化水素などであり、これ
らは単独もしくは2種以上の混合溶媒として用いられる
。これらの溶媒の使用量は、接着剤組成物の固形分が2
0〜30重量%になるように調整される。As the solvent used, one is selected that is highly soluble in butyl rubber, halogenated butyl rubber, polyisobutylene rubber, natural rubber, and isoprene rubber. Examples include aromatic hydrocarbons such as benzene, toluene, and xylene, and aliphatic hydrocarbons such as n-octane, and these solvents may be used alone or as a mixed solvent of two or more. The amount of these solvents used is determined when the solid content of the adhesive composition is 2.
The content is adjusted to 0 to 30% by weight.
さらに、本発明においては、ゴム組成物中に種々の充填
剤を加えることができる。例えば、タレ止めやコストダ
ウンのためにカーボンブラック、金属酸化物、炭酸カル
シウム、タルク、シリカのような無機充填剤や加硫助剤
としての亜鉛華などの混合も可能である。また、粘着付
与剤(タッキファイヤ−)なども初期接着力を与えるた
めに使用することができる。例えば、ロジン及びロジン
誘導体、テルペン系樹脂、脂肪族系炭化水素樹脂、芳香
族系石油樹脂などが有効である。Furthermore, in the present invention, various fillers can be added to the rubber composition. For example, it is possible to mix inorganic fillers such as carbon black, metal oxides, calcium carbonate, talc, and silica, and zinc white as a vulcanization aid to prevent sagging and reduce costs. Additionally, tackifiers and the like can also be used to provide initial adhesive strength. For example, rosin and rosin derivatives, terpene resins, aliphatic hydrocarbon resins, aromatic petroleum resins, and the like are effective.
以下に実施例および比較例を示す。Examples and comparative examples are shown below.
1〜7、 1〜3
下記表1に示す配合内容(重量部)で塩素化ブチルゴム
(クロロブチルラバー1066、エクソン化学)または
ブチルゴム(エッソブチル264、エクソン化学)、ポ
リイソブチレンゴム(Ves ta−nex MML−
100、エクソン化学)と天然ゴム(RSS#1)ある
いはイソプレンゴムにボールIR−2200、日本ゼオ
ン)、 イオウ、カーボンブラック (MA600、三
菱化成工業)をロールで混練した後、さらにジブチルジ
チオカルバミン酸亜鉛(ツクセラーBZ、入内新興化学
工業)、亜鉛華を添加し、トルエンで溶解させ、接着剤
とした。1-7, 1-3 Chlorinated butyl rubber (chlorobutyl rubber 1066, Exxon Chemical), butyl rubber (Essobutyl 264, Exxon Chemical), polyisobutylene rubber (Vesta-nex MML) with the compounding contents (parts by weight) shown in Table 1 below. −
100, Exxon Chemical) and natural rubber (RSS#1) or isoprene rubber, Ball IR-2200, Nippon Zeon), sulfur, and carbon black (MA600, Mitsubishi Chemical Industries) are kneaded with a roll, and then zinc dibutyldithiocarbamate ( Tsukusela BZ, Iriuchi Shinko Kagaku Kogyo) and zinc white were added and dissolved in toluene to make an adhesive.
接着条件:
ここでは防水シートとしてEPTとブチルゴムを主成分
とする加硫ゴムシート(ニスシート、シバタ工業製)を
用い、ゴムシート同士または防水シートとスレート板(
JIS A 5043(F))間において接着試験を行
なった。加硫ゴムシート表面は特に溶剤などで処理する
ことなしに使用した。接着剤はヘラでスレート板あるい
は被着側ゴムシートに350g/n?の塗布量で塗布し
、約15分のオープンタイムをとった後、ゴムシートを
貼り合わせ、ハンドローラで圧着し、室温で1週間放置
後、接着力測定試験を行なった。Adhesion conditions: Here, a vulcanized rubber sheet (varnish sheet, manufactured by Shibata Industries) whose main components are EPT and butyl rubber is used as the waterproof sheet, and the rubber sheets are bonded to each other or the waterproof sheet and the slate board (
An adhesion test was conducted between JIS A 5043 (F)). The surface of the vulcanized rubber sheet was used without being particularly treated with a solvent or the like. Apply 350 g/n of adhesive to the slate board or rubber sheet on the adherend side using a spatula. After approximately 15 minutes of open time, rubber sheets were pasted together and pressed together with a hand roller, and after being left at room temperature for one week, an adhesive force measurement test was conducted.
測定試験; ■ 常態剥離強度。Measurement test; ■Normal peel strength.
剥離角度180’ 、剥離速度200mm/min、測
定温度25℃の条件で測定した。Measurement was carried out under the conditions of a peeling angle of 180', a peeling rate of 200 mm/min, and a measurement temperature of 25°C.
■ 耐アルカリ剥離強度。■Alkali peel strength.
Ca (OH) 2で飽和されたNaOHO,1%溶液
に4日間浸漬させた後、4時間乾燥させ、その後、上記
■に準じて測定した。After 4 days of immersion in a 1% solution of NaOHO saturated with Ca (OH) 2 , it was dried for 4 hours, and then measured according to the above ①.
■ 高温剥離強度。■High temperature peel strength.
60℃の恒温槽中に10分間放置した後、上記■に準じ
て測定した。After being left in a constant temperature bath at 60° C. for 10 minutes, measurements were taken according to the above procedure (①).
以上の結果を表1に示す。なお、比較のために市販のク
ロロプレン系接着剤および表1中に配合を示す塩素化ブ
チルゴム、天然ゴムを単独に使用したものについても同
様の試験を行ない、その結果を示した。表1から、実施
例1〜7のものが比較例1〜3に比し優れていることが
判る。The above results are shown in Table 1. For comparison, similar tests were conducted on commercially available chloroprene adhesives, and those using chlorinated butyl rubber and natural rubber, whose formulations are shown in Table 1, alone, and the results are shown. From Table 1, it can be seen that Examples 1 to 7 are superior to Comparative Examples 1 to 3.
(本頁以下余白)
ス1」0L1u
下記表2に示す配合内容(重量部)で塩素化ブチルゴム
(クロロブチルラバー1066、エクソンケミカル社)
と天然ゴム(RSS jll)、イオウ、カーボンブラ
ック(MA600、三菱化成工業)をロールで混練した
後、亜鉛華とジブチルジチオカルバミン酸亜鉛(ツクセ
ラーBZ、入内新興化学工業)、 またはジメチルジチ
オカルバミン酸亜鉛(ツクセラーPZ、入内新興化学工
業)、 2−メルカプトベンゾチアゾール亜鉛塩(ツク
セラーMZ、入内新興化学工業)を添加し、トルエンで
溶解、接着剤とした。加硫ゴムシートとスレート板との
接着力を実施例1と同様の方法で測定した。この結果を
表2に示す。(Margins below this page) Chlorinated butyl rubber (Chlorobutyl Rubber 1066, Exxon Chemical Company) with the formulation content (parts by weight) shown in Table 2 below.
After kneading with a roll, natural rubber (RSS Jll), sulfur, and carbon black (MA600, Mitsubishi Chemical Industries), zinc white and zinc dibutyldithiocarbamate (Tsukusela BZ, Iriuchi Shinko Kagaku Kogyo) or zinc dimethyldithiocarbamate (Tskusela PZ, Irinai Shinko Kagaku Kogyo) and 2-mercaptobenzothiazole zinc salt (Tsukusela MZ, Iriuchi Shinko Kagaku Kogyo) were added and dissolved in toluene to form an adhesive. The adhesive strength between the vulcanized rubber sheet and the slate plate was measured in the same manner as in Example 1. The results are shown in Table 2.
(本頁以下余白)
表 2
注)*ツクセラーBZ 本章ツクセラーPZ 本市
率ツクセラーに〔発明の効果〕
以上説明したように本発明の接着剤組成物は、従来品の
ようにプライマーを用いなくともよいので接着工法が繁
雑でなく、簡単な下地側−面塗布だけで十分な接着力が
得られ、かつアルカリ中においても高い接着力を保つの
でモルタル面、コンクリート面等のアルカリ耐性に優れ
る。(Margins below this page) Table 2 Note) *Tsukuseller BZ This chapter Tsukseller PZ To this city rate Tsukseller [Effects of the invention] As explained above, the adhesive composition of the present invention does not require the use of a primer like conventional products. The bonding method is not complicated, and sufficient adhesive strength can be obtained by simply applying the adhesive to the base side. Furthermore, it maintains high adhesive strength even in alkali, so it has excellent alkali resistance on mortar surfaces, concrete surfaces, etc.
また、屋上表面などは真夏においては50〜60℃の温
度まで上がるが、そのような温度でもある程度の耐熱接
着力を兼ねそなえているものであるから、屋上ルーフィ
ング材、あるいは池、プール等の土木用防水材の接着剤
として有効に使用できるという利点がある。In addition, rooftop surfaces can reach temperatures of 50 to 60 degrees Celsius in midsummer, and since they have a certain degree of heat-resistant adhesive strength even at such temperatures, they can be used as rooftop roofing materials or in civil engineering works such as ponds and swimming pools. It has the advantage that it can be effectively used as an adhesive for waterproof materials.
Claims (1)
レンゴム85〜30重量部、天然ゴム又はイソプレンゴ
ム15〜70重量部、および超加硫促進剤5〜40重量
部からなる防水シート用接着剤組成物。An adhesive composition for a waterproof sheet comprising 85 to 30 parts by weight of butyl rubber, halogenated butyl rubber, or polyisobutylene rubber, 15 to 70 parts by weight of natural rubber or isoprene rubber, and 5 to 40 parts by weight of a supervulcanization accelerator.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP821387A JPS63178183A (en) | 1987-01-19 | 1987-01-19 | Adhesive composition for waterproof smeet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP821387A JPS63178183A (en) | 1987-01-19 | 1987-01-19 | Adhesive composition for waterproof smeet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63178183A true JPS63178183A (en) | 1988-07-22 |
Family
ID=11686953
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP821387A Pending JPS63178183A (en) | 1987-01-19 | 1987-01-19 | Adhesive composition for waterproof smeet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63178183A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100381910B1 (en) * | 2000-04-17 | 2003-05-01 | 금호산업 주식회사 | For Improving Endurance in TBR Tire Applied Thin Cushion |
-
1987
- 1987-01-19 JP JP821387A patent/JPS63178183A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100381910B1 (en) * | 2000-04-17 | 2003-05-01 | 금호산업 주식회사 | For Improving Endurance in TBR Tire Applied Thin Cushion |
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