JPH07138532A - Adhesive composition for carpet - Google Patents
Adhesive composition for carpetInfo
- Publication number
- JPH07138532A JPH07138532A JP31286893A JP31286893A JPH07138532A JP H07138532 A JPH07138532 A JP H07138532A JP 31286893 A JP31286893 A JP 31286893A JP 31286893 A JP31286893 A JP 31286893A JP H07138532 A JPH07138532 A JP H07138532A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- emulsion
- adhesive
- water
- carpet
- 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 description 55
- 230000001070 adhesive effect Effects 0.000 title claims description 55
- 239000000203 mixture Substances 0.000 title claims description 40
- 229920005989 resin Polymers 0.000 claims abstract description 48
- 239000011347 resin Substances 0.000 claims abstract description 48
- 239000000839 emulsion Substances 0.000 claims abstract description 34
- 239000002245 particle Substances 0.000 claims abstract description 20
- 239000007787 solid Substances 0.000 claims abstract description 15
- 230000009477 glass transition Effects 0.000 claims abstract description 9
- 239000004568 cement Substances 0.000 claims description 23
- 239000006260 foam Substances 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 21
- -1 acrylic ester Chemical class 0.000 abstract description 8
- 239000000178 monomer Substances 0.000 abstract description 8
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract description 6
- 239000011398 Portland cement Substances 0.000 abstract description 3
- 239000002002 slurry Substances 0.000 abstract description 3
- 238000013329 compounding Methods 0.000 abstract 2
- 239000011396 hydraulic cement Substances 0.000 abstract 2
- 239000010410 layer Substances 0.000 description 27
- 206010040844 Skin exfoliation Diseases 0.000 description 16
- 239000012790 adhesive layer Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000002313 adhesive film Substances 0.000 description 7
- 230000005856 abnormality Effects 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 244000025254 Cannabis sativa Species 0.000 description 5
- 229920006026 co-polymeric resin Polymers 0.000 description 5
- 229920001519 homopolymer Polymers 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 239000004570 mortar (masonry) Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- 229920005789 ACRONAL® acrylic binder Polymers 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-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
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000011400 blast furnace cement Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000013530 defoamer Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 238000004078 waterproofing Methods 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 239000011494 foam glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920006327 polystyrene foam Polymers 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、人工芝生と呼ばれるも
のをはじめとする種々のカーペットをコンクリート体等
に接着せしめるのに用いられる接着剤組成物に関するも
のである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an adhesive composition used for adhering various carpets including those called artificial grass to concrete bodies and the like.
【0002】[0002]
【従来の技術】ビルの屋上、ゴルフ場、公園の通路等に
人工芝生と呼ばれるカーペットが敷設されており、かか
るカーペットをコンクリート体等に固定させるにはエポ
キシ樹脂系やウレタン樹脂系の接着剤が使用されてい
る。しかしながら、固定されたこれらの人工芝生を取り
替えるために剥離しようとすると、コンクリート体上に
接着剤が残留したり、或いはコンクリート体等に施され
ていた下地防水層まで破壊したりしてしまう。前者の場
合には、人工芝生を再度接着させようとしても接着でき
ないという問題が生じ、後者の場合には、コンクリート
体等に再度防水層を施工する必要があり、多大の時間、
労力及び経費を必要とするという問題があった。2. Description of the Related Art Carpets called artificial lawns are laid on the roofs of buildings, golf courses, and aisles in parks. To fix such carpets to concrete bodies, epoxy resin or urethane resin adhesives are used. It is used. However, when these fixed artificial lawns are peeled off for replacement, the adhesive remains on the concrete body, or even the base waterproof layer applied to the concrete body or the like is destroyed. In the case of the former, there is a problem that the artificial lawn cannot be adhered even if it is attempted to be adhered again, and in the case of the latter, it is necessary to construct the waterproof layer again on the concrete body, etc.
There was a problem of requiring labor and expense.
【0003】また、人工芝生等を固定するのに釘打ちに
よる方法も考えられるが、防水層が施工されている場合
には、せっかくの防水層に穴をあけてしまうという問題
があった。A method of nailing can be used to fix the artificial lawn or the like, but when the waterproof layer is applied, there is a problem that a hole is made in the waterproof layer.
【0004】[0004]
【発明が解決しようとする課題】本発明は、コンクリー
ト体等に強固に接着でき、しかもカーペットの剥離時に
は下地防水層を破壊することなく、かつ剥離面上に接着
剤が残留していても、その上に再接着できるカーペット
用接着剤組成物を提供しようとするものである。DISCLOSURE OF THE INVENTION The present invention is capable of firmly adhering to a concrete body or the like, and does not destroy the underlying waterproof layer when the carpet is peeled off, and even if the adhesive remains on the peeled surface, It is an object of the present invention to provide a carpet adhesive composition that can be rebonded thereon.
【0005】[0005]
【課題を解決するための手段】本発明者らは、前記の課
題を解決するために種々研究を重ねた結果、下記のカー
ペット用接着剤組成物によりその目的を達成することが
できたものである。Means for Solving the Problems As a result of various studies to solve the above problems, the inventors of the present invention were able to achieve the object by the following adhesive composition for carpet. is there.
【0006】すなわち、本発明のカーペット用接着剤組
成物は、ガラス転移点5℃以下の樹脂の水性エマルジョ
ン、該エマルジョンの樹脂固形分100重量部に対して
水硬性無機質セメント150〜450重量部及び発泡体
粒子20〜160重量部を含有せしめてなることを特徴
とする組成物である。That is, the carpet adhesive composition of the present invention comprises an aqueous emulsion of a resin having a glass transition point of 5 ° C. or lower, and 150 to 450 parts by weight of a hydraulic inorganic cement with respect to 100 parts by weight of the resin solid content of the emulsion. The composition is characterized by containing 20 to 160 parts by weight of foam particles.
【0007】本発明の接着剤組成物に用いられるガラス
転移点5℃以下の樹脂水性エマルジョンは、通常、種々
の不飽和単量体の乳化重合によって容易に得られる。す
なわち、種々のガラス転移点を有するホモ重合体を与え
る種々の不飽和単量体、たとえばアクリル酸2−エチル
ヘキシル(Tg −85℃)〔注;カッコ内の記載は、
アクリル酸2−エチルヘキシルのホモ重合体のガラス転
移点が−85℃であることの略記である。以下同様〕、
アクリル酸n・ブチル(Tg −54℃)、アクリル酸
エチル(Tg −22℃)、塩化ビニリデン(Tg −
18℃)、アクリル酸イソプロピル(Tg −5℃)、
メタクリル酸2エチルヘキシル(Tg−5℃)、アクリ
ル酸n・プロピル(Tg 8℃)、メタクリル酸n・ブ
チル(Tg 20℃)、酢酸ビニル(Tg 30℃)、
アクリル酸(Tg 87℃)、メタクリル酸n・プロピ
ル(Tg 81℃)、スチレン(Tg 100℃)、ア
クリロニトリル(Tg 100℃)、メタクリル酸メチ
ル(Tg 105℃)、メタクリル酸(Tg 130
℃)、無水マレイン酸、イタコン酸(Tg 130
℃)、アクリル酸アミド(Tg 153℃)、メタクリ
ル酸エチル(Tg 65℃)、塩化ビニル(Tg 79
℃)、エチレン及びブタジエンなどから適宜に選ばれた
不飽和単量体の1種又は2種以上を乳化重合させること
により得られる。The resin aqueous emulsion having a glass transition point of 5 ° C. or lower used in the adhesive composition of the present invention is usually easily obtained by emulsion polymerization of various unsaturated monomers. That is, various unsaturated monomers that give homopolymers having various glass transition points, for example, 2-ethylhexyl acrylate (Tg-85 ° C) [Note;
It is an abbreviation that the glass transition point of a homopolymer of 2-ethylhexyl acrylate is -85 ° C. The same applies below],
N-Butyl acrylate (Tg-54 ° C), ethyl acrylate (Tg-22 ° C), vinylidene chloride (Tg-
18 ° C), isopropyl acrylate (Tg-5 ° C),
2-ethylhexyl methacrylate (Tg-5 ° C), n-propyl acrylate (Tg 8 ° C), n-butyl methacrylate (Tg 20 ° C), vinyl acetate (Tg 30 ° C),
Acrylic acid (Tg 87 ° C), n-propyl methacrylate (Tg 81 ° C), styrene (Tg 100 ° C), acrylonitrile (Tg 100 ° C), methyl methacrylate (Tg 105 ° C), methacrylic acid (Tg 130)
℃), maleic anhydride, itaconic acid (Tg 130
° C), acrylic acid amide (Tg 153 ° C), ethyl methacrylate (Tg 65 ° C), vinyl chloride (Tg 79
C.), and one or more kinds of unsaturated monomers appropriately selected from ethylene, butadiene and the like are obtained by emulsion polymerization.
【0008】本発明で用いる樹脂水性エマルジョンはホ
モ重合体であってもよいし、共重合体であってもよい。
なお、前記の樹脂水性エマルジョン調製用の不飽和単量
体にカッコ書きで付記したTg値は、前記のように、そ
のその単量体のホモ重合体のガラス転移点(Tg)をさ
すのであるが、一般に、共重合体のTgは、単量体のホ
モ重合体のTgと単量体の共重合比率から、その概略値
を容易に推測できる。したがって、本発明で使用するガ
ラス転移点5℃以下の樹脂の水性エマルジョンは、かか
る推測される概略値にもとづいてポリマー設計をするこ
とにより、容易に所望のTg値を有する樹脂の水性エマ
ルジョンを製造することができる。The aqueous resin emulsion used in the present invention may be a homopolymer or a copolymer.
The Tg value added in parentheses to the unsaturated monomer for preparing the resin aqueous emulsion is, as described above, the glass transition point (Tg) of the homopolymer of the monomer. However, generally, the Tg of the copolymer can be easily estimated from the Tg of the homopolymer of the monomer and the copolymerization ratio of the monomer. Therefore, the aqueous emulsion of a resin having a glass transition point of 5 ° C. or less used in the present invention can be easily produced by designing a polymer based on the estimated approximate value to easily produce an aqueous emulsion of a resin having a desired Tg value. can do.
【0009】また、本発明で用いる樹脂水性エマルジョ
ンは、2種以上の樹脂エマルジョンの混合物であっても
よいし、さらには樹脂エマルジョンより製造される水再
分散性の樹脂粉末を水性媒体中に再分散せしめて得られ
た樹脂エマルジョン(俗称パウダーエマルジョン)であ
ってもよい。The resin aqueous emulsion used in the present invention may be a mixture of two or more kinds of resin emulsions, and the water-redispersible resin powder produced from the resin emulsion is redispersed in an aqueous medium. It may be a resin emulsion (commonly known as a powder emulsion) obtained by dispersing.
【0010】使用する樹脂エマルジョンの樹脂のガラス
転移点が高くなりすぎると接着剤組成物皮膜が硬くて柔
軟性のないものとなり、歩行性が悪くなるし、弾性を有
する防水層との伸びの差にもとづき、下地防水層の切断
を起したり、接着剤層に割れや剥離が生じたりするし、
さらにはカーペットの剥離時に防水層の剥離を起した
り、防水層に傷が発生したりするし、冬期の接着時には
接着剤組成物の皮膜化が困難になるなどの問題が生じ
る。そのために、Tgが5℃以下、好ましくは−40〜
0℃の樹脂の水性エマルジョンを使用するのである。If the glass transition point of the resin of the resin emulsion used is too high, the adhesive composition film becomes hard and inflexible, resulting in poor walkability and a difference in elongation from the elastic waterproof layer. Based on the above, the waterproof layer may be cut or the adhesive layer may be cracked or peeled off.
Further, there arise problems that the waterproof layer is peeled off when the carpet is peeled off, the waterproof layer is scratched, and it becomes difficult to form the adhesive composition into a film during adhesion in winter. Therefore, Tg is 5 ° C. or less, preferably −40 to
An aqueous emulsion of the resin at 0 ° C is used.
【0011】また、本発明の接着剤組成物に用いられる
水硬性無機質セメントとしては、ポルトランドセメント
と称されるもの(たとえば普通セメント、白色セメン
ト、早強セメント、超早強セメントなど)、混合セメン
トと称されるもの(たとえば高炉セメント、シリカセメ
ント、フライアッシュセメントなど)、その他アルミナ
セメント、水硬性石膏粉末などがあげられるが、一般的
にはポルトランドセメント、特に普通セメント、白色セ
メントが好ましい。The hydraulic inorganic cement used in the adhesive composition of the present invention includes what is called Portland cement (for example, ordinary cement, white cement, early strength cement, super early strength cement, etc.) and mixed cement. Examples thereof include blast furnace cement (eg, blast furnace cement, silica cement, fly ash cement, etc.), alumina cement, hydraulic gypsum powder, etc., but generally Portland cement, especially ordinary cement, and white cement are preferred.
【0012】水硬性無機質セメントは、樹脂水性エマル
ジョンの樹脂固形分100重量部に対して150〜45
0重量部、好ましくは150〜300重量部用いられ
る。セメントの割合が少なすぎると、接着剤皮膜が柔軟
性に富み、歩行感も良好となるが、接着強度、特に水浸
漬時の接着強度が低下する。また、セメントの割合が多
すぎると、接着剤皮膜が柔軟性に乏しくなり、歩行感が
悪くなるばかりでなく、接着強度が大きくなりすぎて、
カーペットの剥離時に下地の防水層を傷つけるようにな
る。The hydraulic inorganic cement is 150 to 45 to 100 parts by weight of the resin solid content of the resin aqueous emulsion.
0 parts by weight, preferably 150 to 300 parts by weight are used. If the proportion of cement is too low, the adhesive film will be flexible and the walking feeling will be good, but the adhesive strength, especially when immersed in water, will be reduced. Also, if the proportion of cement is too large, the adhesive film becomes poor in flexibility, and not only the walking feeling becomes poor, but also the adhesive strength becomes too large,
When the carpet is peeled off, the underlying waterproof layer will be damaged.
【0013】本発明の接着剤組成物に含有せしめる発泡
体粒子は、粒径が好ましくは5〜500μm、より好ま
しくは50〜300μmであり、比重が好ましくは0.
7〜1.2g/cm3 であり、形状が必ずしも球形であ
る必要はない。その発泡体粒子の例としては、たとえば
シラスバルーン、発泡ガラス、発泡シリカなどの無機質
発泡体、ポリエチレン発泡体、ポリプロピレン発泡体、
ポリスチレン発泡体などの有機質発泡体があるが、有機
質発泡体粒子は接着剤組成物中での分散・混合性が劣る
ので、無機質発泡体が好ましい。The foam particles to be contained in the adhesive composition of the present invention have a particle size of preferably 5 to 500 μm, more preferably 50 to 300 μm, and a specific gravity of preferably 0.
It is 7 to 1.2 g / cm 3 , and the shape does not necessarily have to be spherical. Examples of the foam particles, for example, shirasu balloon, foam glass, inorganic foam such as foam silica, polyethylene foam, polypropylene foam,
Although there are organic foams such as polystyrene foams, inorganic foams are preferred because the organic foam particles have poor dispersibility / mixability in the adhesive composition.
【0014】発泡体粒子は接着剤皮膜に適度の柔軟性を
付与し、歩行性を向上させるとともに、カーペットの剥
離時に適度の剥離力で粒子自体が破壊して接着剤層での
剥離を容易ならしめて、下地の防水層が損傷されるのを
防止する作用をさせるのである。発泡体粒子の使用量
は、樹脂水性エマルジョンの樹脂固形分100重量部に
対して20〜160重量部、好ましくは25〜130重
量部である。この発泡体粒子の割合が少なすぎると、接
着剤皮膜の柔軟性は良好となるが、カーペットの剥離時
に下地の防水層に傷をつけやすくなるし、その割合が多
すぎると接着剤皮膜がもろくなり、接着強度が低下す
る。The foam particles impart appropriate flexibility to the adhesive film to improve walkability, and at the same time, when the carpet is peeled off, the particles themselves are destroyed by an appropriate peeling force to facilitate peeling in the adhesive layer. As a result, it acts to prevent the underlying waterproof layer from being damaged. The amount of the foam particles used is 20 to 160 parts by weight, preferably 25 to 130 parts by weight, based on 100 parts by weight of the resin solid content of the resin aqueous emulsion. If the proportion of the foam particles is too small, the flexibility of the adhesive film will be good, but it will be easy to scratch the underlying waterproof layer at the time of peeling the carpet, and if the proportion is too large, the adhesive film will be brittle. And the adhesive strength is reduced.
【0015】本発明の接着剤組成物は、適量の水を含有
せしめた含水スラリーとして使用されるが、その水は樹
脂水性エマルジョンにもとづく水のみであってもよい
が、通常は、さらに追加の水が添加されて使用される。
一般に、水の量が少なすぎると、組成物が流動性に乏し
くなり、塗布等の作業性が悪くなる。また、水の量が多
すぎると、樹脂水性エマルジョンと他の成分との分離を
起し、好ましくないばかりでなく、硬化・乾燥後の接着
剤皮膜に割れが発生したり、収縮が起きたりする。この
接着剤組成物の使用時の水の量は、樹脂固形分100重
量部に対して、通常、100〜200重量部が好まし
い。The adhesive composition of the present invention is used as a water-containing slurry containing an appropriate amount of water. The water may be only water based on the resin aqueous emulsion, but usually, additional water is added. Water is added and used.
In general, if the amount of water is too small, the composition has poor fluidity and the workability such as coating becomes poor. Further, if the amount of water is too large, the resin aqueous emulsion and other components are separated from each other, which is not preferable, and the adhesive film after curing and drying may be cracked or shrink. . The amount of water when the adhesive composition is used is usually preferably 100 to 200 parts by weight with respect to 100 parts by weight of the resin solid content.
【0016】本発明の接着剤組成物には、前記した必須
成分のほかに、必要に応じて種々の添加物を含有せしめ
ることができる。たとえば、炭酸カルシウム、硅砂、タ
ルク、クレー、水酸化アルミニウムなどの無機質体質顔
料を、樹脂水性エマルジョンの樹脂固形分100重量部
に対して400重量部以下、好ましくは300重量部以
下含有せしめることができる。無機質体質顔料の含有割
合が多すぎると、接着剤皮膜が柔軟性に乏しくなり、歩
行性が悪くなる。The adhesive composition of the present invention may contain various additives, if necessary, in addition to the above-mentioned essential components. For example, an inorganic extender pigment such as calcium carbonate, silica sand, talc, clay, or aluminum hydroxide can be contained in an amount of 400 parts by weight or less, preferably 300 parts by weight or less, based on 100 parts by weight of the resin solid content of the resin aqueous emulsion. . If the content ratio of the inorganic extender pigment is too high, the adhesive film becomes poor in flexibility and the walking property becomes poor.
【0017】また、本発明の接着剤組成物には、着色用
の顔料や塗料、各種の繊維粉末、消泡剤、可塑剤、増粘
剤、防カビ剤、減水剤、流動剤、硬化調整剤、湿潤剤、
分散剤、乳化剤、凍結防止剤、難燃剤等を含有せしめる
ことができる。In the adhesive composition of the present invention, pigments and paints for coloring, various fiber powders, antifoaming agents, plasticizers, thickeners, antifungal agents, water reducing agents, flow agents, curing control agents. Agent, wetting agent,
A dispersant, an emulsifier, an antifreezing agent, a flame retardant, etc. can be contained.
【0018】さらに、本発明の接着剤組成物には、場合
によっては、前記の樹脂の水性エマルジョン以外の他の
樹脂の水性エマルジョンを含有せしめることも可能であ
る。しかし、他の樹脂エマルジョンを含有せしめる場合
であっても、前記の樹脂水性エマルジョンの含有量が、
樹脂固形分量で全樹脂固形分量に対して60重量%以上
になるようにする必要がある。Further, the adhesive composition of the present invention can optionally contain an aqueous emulsion of a resin other than the above-mentioned aqueous emulsion of the resin. However, even when containing other resin emulsion, the content of the resin aqueous emulsion is
It is necessary to set the resin solid content to 60% by weight or more based on the total resin solid content.
【0019】本発明の接着剤組成物を用いて、コンクリ
ート体上にカーペット(人工芝生等)を接着する代表的
な方法について述べると、コンクリート体上に、好まし
くは表面に適当な下地防水層を設けたコンクリート体上
に、本発明の接着剤組成物を、湿潤厚さ1〜5mmの接
着剤層が形成されるように塗布する。その塗布は接着剤
組成物を流してコテやローラーで展延させてもよいし、
吹付け塗装で行なってもよい。次いで、その接着剤層上
にカーペットの裏面を重ねて、上から軽く圧接したの
ち、3〜24時間、好ましくは、10〜20時間放置し
て接着剤層を硬化・乾燥させる。硬化・乾燥を速くする
ためには、セメント量をやや多くしてもよいし、速硬性
セメントやアルミナセメントを使用することができる。A typical method of adhering a carpet (artificial grass etc.) onto a concrete body using the adhesive composition of the present invention will be described. An appropriate undercoat waterproof layer is provided on the concrete body, preferably on the surface. On the provided concrete body, the adhesive composition of the present invention is applied so that an adhesive layer having a wet thickness of 1 to 5 mm is formed. For the application, the adhesive composition may be poured and spread with a trowel or roller,
It may be applied by spray painting. Then, the back surface of the carpet is overlaid on the adhesive layer, lightly pressed from above, and left for 3 to 24 hours, preferably 10 to 20 hours to cure and dry the adhesive layer. In order to accelerate the hardening and drying, the amount of cement may be increased a little, and fast-setting cement or alumina cement can be used.
【0020】また、カーペットの剥離の際に、接着剤層
での剥離を確実に行なわせるために、前記の接着剤層中
に合成繊維系のネット、織物、不織布、スパンボンド、
ガラス繊維のネット、織物、不織布、又はこれらのネッ
トや布等に樹脂コーティングを施したものを介在させる
ことができる。また、本発明の接着剤組成物はセメント
系接着剤であるので、接着剤組成物を施用(塗布)する
下地上に多少の水が付着していたり、或いは湿潤状態で
あったりしてもさしつかえがない(従来の二液型エポキ
シ樹脂接着剤の場合には、接着剤を施用する下地は充分
に乾燥させておく必要があった)。When the carpet is peeled off, in order to ensure the peeling at the adhesive layer, the synthetic fiber net, woven fabric, non-woven fabric, spun bond,
It is possible to interpose a glass fiber net, a woven fabric, a non-woven fabric, or these nets or fabrics coated with a resin. Further, since the adhesive composition of the present invention is a cement-based adhesive, it does not matter even if some water is attached to the base to which the adhesive composition is applied (applied) or it is in a wet state. No. (In the case of the conventional two-pack type epoxy resin adhesive, the base to which the adhesive is applied needs to be sufficiently dried).
【0021】[0021]
【実施例】以下に、実施例及び比較例をあげてさらに詳
述する。これらの例において記載の部及び%は、特に付
記しない限り重量基準による。EXAMPLES The present invention will be described in more detail below with reference to Examples and Comparative Examples. Parts and% described in these examples are by weight unless otherwise specified.
【0022】実施例1 下記の組成物を充分に攪拌混合して、防水下地層用の樹
脂モルタルを調製した。 普通セメント 150部 アクロナール S−400 *1 100部 消泡剤 *2 0.5部 水 10部 注: *1・・・ 三菱油化バーディッシェ株式会社商品
名、アクリル酸エステル−スチレン共重合体樹脂エマル
ジョン、樹脂のTgが0℃以下、樹脂固形分56% *2・・・ サンノプコ社商品名 ノプコ8034Example 1 The following compositions were thoroughly mixed with stirring to prepare a resin mortar for a waterproof underlayer. Ordinary cement 150 parts Acronal S-400 * 1 100 parts Defoamer * 2 0.5 parts Water 10 parts Note: * 1 Mitsubishi Yuka Birdishe Co., Ltd. trade name, acrylic ester-styrene copolymer resin emulsion , Tg of resin is 0 ° C or less, resin solid content is 56% * 2 ... San Nopco brand name Nopco 8034
【0023】まず、コンクリート舗道板の表面のほこり
を払い、表面が濡れた状態になるまで水打ちしたのち、
その表面に、上記組成の防水下地層用の樹脂モルタルを
水で容積が倍量になるまで希釈したものを、プライマー
としてローラーで塗布して乾燥させた。First, after dusting the surface of the concrete pavement board and watering it until the surface becomes wet,
A resin mortar for the waterproof underlayer having the above composition was diluted on the surface with water until the volume was doubled, and then applied as a primer with a roller and dried.
【0024】次いで、その乾燥塗布面上に、上記組成の
防水下地層用の樹脂モルタルを、ローラーで湿潤厚さが
それぞれ1mmになるように3回塗り重ねて、硬化・乾
燥厚さが2mmの防水下地層を形成させた。この防水下
地層は20℃で3週間空気中で放置後に測定した剥離強
度が13Kgf/50mm巾であった。Next, a resin mortar for the waterproof underlayer having the above composition was coated on the dried coated surface three times with a roller so that each wet thickness was 1 mm, and the cured and dried thickness was 2 mm. A waterproof underlayer was formed. The waterproof underlayer had a peel strength of 13 Kgf / 50 mm width measured after standing in air at 20 ° C. for 3 weeks.
【0025】また別に、下記の組成物を充分に攪拌混合
して接着剤組成物を調製した。 普通セメント 200部 アクロナール S−400 *1 樹脂固形分として100部 ウイニライト WB−501 *2 60部 水 40部 消泡剤 *3 0.3部 注: *1・・・ 三菱油化バーディッシェ株式会社商品
名、アクリル酸エステル−スチレン共重合体樹脂エマル
ジョン、樹脂のTgが0℃以下、樹脂固形分56% *2・・・ イヂチ化成株式会社商品名、シラス発泡体粒
子、比重0.8〜0.9、粒径130μm *3・・・ サンノプコ社商品名 ノプコ8034Separately, the following compositions were sufficiently stirred and mixed to prepare an adhesive composition. Ordinary cement 200 parts Acronal S-400 * 1 100 parts as resin solids Winilite WB-501 * 2 60 parts Water 40 parts Defoamer * 3 0.3 parts Note: * 1: Mitsubishi Yuka Birdishe Co., Ltd. Name, acrylic ester-styrene copolymer resin emulsion, Tg of the resin is 0 ° C. or less, resin solid content is 56% * 2 ... Idishi Kasei Co., Ltd. trade name, Shirasu foam particles, specific gravity 0.8 to 0. 9, particle size 130 μm * 3 ... San Nopco's trade name Nopco 8034
【0026】前記の下地防水層を形成させた舗道板の該
防水層上に、上記の接着剤組成物のスラリーを湿潤厚さ
約3mmに塗布し、その上に直ちに人工芝生(泉州敷物
株式会社商品名 SAターフ・SA−1、ポリプロピレ
ン糸製、パイル長8mm)の裏面を重ね、軽く上から圧
接したのち、室温(20℃)で10日間放置して接着剤
層を硬化・乾燥させた。A slurry of the above adhesive composition was applied to the waterproof layer of the pavement board having the above-mentioned waterproof layer to a wet thickness of about 3 mm, and an artificial lawn (Senshu Rug Co., Ltd.) was immediately applied thereon. After the back surfaces of the product name SA Turf SA-1 made of polypropylene yarn and having a pile length of 8 mm) were overlapped and lightly pressed from above, the adhesive layer was cured and dried by leaving it at room temperature (20 ° C.) for 10 days.
【0027】得られた接着カーペット(人工芝生)につ
いて、表1及び表2の注に記載の試験方法により試験を
した結果は、剥離強度が6.8Kgf/50mm巾であ
った。また、48時間浸漬後の同剥離強度が5.0Kg
f/50mm巾であり、この場合の剥離面が全く水で濡
れていなかった。また、両剥離とも、接着剤層の破断で
あり、防水層に異常が全く認められなかった。また、折
り曲げ試験の結果も異常が全く認められなかった。The obtained adhesive carpet (artificial grass) was tested by the test method described in the notes of Tables 1 and 2, and the result was that the peel strength was 6.8 Kgf / 50 mm width. The peel strength after immersion for 48 hours is 5.0 kg.
The width was f / 50 mm, and the peeled surface in this case was not wet with water at all. Further, in both peelings, the adhesive layer was broken, and no abnormality was observed in the waterproof layer. Also, no abnormality was found in the bending test results.
【0028】さらに、前記の剥離後の破断面に、前記と
全く同様の方法を用いて人工芝生を再び接着し、同様の
剥離試験を行なったところ、その剥離強度は6.9Kg
f/50mm巾であり、最初の接着時の剥離強度と全く
差が認められなかった。Further, an artificial lawn was adhered again to the fracture surface after peeling using the same method as described above, and a similar peeling test was conducted. The peel strength was 6.9 Kg.
The width was f / 50 mm, and no difference was observed with the peel strength at the time of the first adhesion.
【0029】表1に、実施例1の接着剤組成物の組成及
び接着性能試験結果を摘記した。Table 1 shows the composition of the adhesive composition of Example 1 and the results of the adhesive performance test.
【0030】実施例2〜8 比較例1〜8 接着剤組成物として表1及び表2に記載した各接着剤を
使用し、そのほかは実施例1に記載の方法と同様の方法
を用いて、コンクリート舗道板に下地防水層を形成さ
せ、さらにその上に同様の方法で人工芝生(カーペッ
ト)を接着させた。得られた接着カーペットの接着性能
試験結果は表1及び表2にそれぞれ示すとおりであっ
た。Examples 2 to 8 Comparative Examples 1 to 8 Each of the adhesives listed in Tables 1 and 2 was used as an adhesive composition, and otherwise the same method as that described in Example 1 was used. A base waterproofing layer was formed on a concrete pavement board, and an artificial lawn (carpet) was further adhered to the base waterproofing layer by the same method. The adhesive performance test results of the obtained adhesive carpet are shown in Tables 1 and 2, respectively.
【0031】[0031]
【表1】 [Table 1]
【0032】[0032]
【表2】 [Table 2]
【0033】表1及び表2の注: *1・・・ 三菱油化バーディッシェ株式会社商品名、アク
リル酸エステル−スチレン共重合体樹脂エマルジョン、
樹脂のTgが0℃以下、樹脂固形分56% *2・・・ イヂチ化成株式会社商品名、シラス発泡体粒
子、比重0.8〜0.9、粒径130μm *3・・・ 同和鉱業株式会社商品名 KD−80Notes to Tables 1 and 2: * 1 ... Mitsubishi Yuka Birdiche Co., Ltd. trade name, acrylic ester-styrene copolymer resin emulsion,
Tg of resin is 0 ° C or less, resin solid content is 56% * 2 ... Idishi Kasei Co., Ltd. trade name, Shirasu foam particles, specific gravity 0.8 to 0.9, particle size 130 μm * 3 ... Dowa Mining Co., Ltd. Company product name KD-80
【0034】*4・・・ 舗道板に接着した人工芝生に、巾
50mm×長さ150mmの矩形状に舗道板表面に達す
る深さの傷を付け、その矩形の巾の端部を剥離し、その
剥離端部を持って矩形の長辺の方向に同長辺と45°の
角度になるように引張って剥離をしたときの最大剥離強
度(Kgf/50mm巾)で表わす。なお、水浸漬後の
剥離強度は、前記の傷を付けた試験片を20℃の水中に
48時間浸漬後に取出し、直ちに同様の剥離試験をした
ときの最大剥離強度で表わす。* 4 ... The artificial lawn adhered to the pavement board is scratched in a rectangular shape with a width of 50 mm and a length of 150 mm to reach the surface of the pavement board, and the end of the rectangular width is peeled off. The maximum peel strength (Kgf / 50 mm width) when peeling by pulling the peeled end in the direction of the long side of the rectangle so as to form an angle of 45 ° with the long side, is shown. The peel strength after immersion in water is represented by the maximum peel strength when the above-mentioned scratched test piece was taken out in water at 20 ° C. for 48 hours and then immediately subjected to the same peel test.
【0035】*5・・・ 前記の剥離試験における水浸漬を
しないものの剥離面(これを便宜上「水浸漬前の剥離
面」という)を目視により調べ、下記の基準により評価
する。 ○ :下地防水層に全く異常がなく、剥離面が凹凸がな
く平坦である。 △ :下地防水層に異常がないが、剥離面にやや凹凸が
ある。 × :下地防水層に異常があり、剥離面の凹凸が著し
い。* 5 ... In the above-mentioned peeling test, the peeling surface of the product not soaked in water (this is referred to as "peeling surface before water immersion" for convenience) is visually inspected and evaluated according to the following criteria. ◯: There is no abnormality in the base waterproof layer, and the peeling surface is flat with no unevenness. Δ: There is no abnormality in the undercoat waterproof layer, but the release surface is slightly uneven. ×: There is an abnormality in the waterproof underlayer, and the unevenness of the peeled surface is remarkable.
【0036】*6・・・ テフロン板上に接着剤組成物を湿
潤厚さが3mmになるように流延塗布し、室温で10日
間放置して硬化・乾燥させてから剥離し、得られた硬化
・乾燥接着剤組成物層の試験片(50mm巾×150m
m長さ)を、丸棒(直径20mm)を半ばつつむような
状態に90°折り曲げたときの折り曲げ部分の状態を目
視により調べ、下記の基準で評価する。 ○ :折り曲げ部分に全く異常がない。 △ :折り曲げ部分に多少のクラックがある。 × :折り曲げ部分が割れている。* 6: An adhesive composition was cast-coated on a Teflon plate so that the wet thickness was 3 mm, left at room temperature for 10 days to cure and dry, and then peeled. Hardened / dried adhesive composition layer test piece (50 mm width x 150 m
The length (m length) is visually inspected for the state of the bent portion when the round bar (diameter 20 mm) is bent by 90 ° so as to envelop it halfway, and evaluated according to the following criteria. ○: There is no abnormality in the bent portion. Δ: There are some cracks in the bent portion. X: The bent portion is cracked.
【0037】実施例9 比較例9〜10 接着剤として表3にそれぞれ示す接着剤組成物を使用
し、そのほかは実施例1と全く同様の方法で接着カーペ
ットを製造した。得られた接着カーペットについて実施
例1におけると同様の接着性能の試験をした結果は表3
に示すとおりであった。Example 9 Comparative Examples 9 to 10 Adhesive carpets were produced in the same manner as in Example 1 except that the adhesive compositions shown in Table 3 were used as the adhesive. The obtained adhesive carpet was tested for the same adhesive performance as in Example 1, and the results are shown in Table 3.
It was as shown in.
【0038】[0038]
【表3】 [Table 3]
【0039】表3の注: *1 ・・・三菱油化バーディッシェ株式会社商品名、アク
リル酸エステル・スチレン共重合体樹脂エマルジョン、
樹脂のTgが3℃、樹脂固形分50% *2 ・・・三菱油化バーディッシェ株式会社商品名、アク
リル酸エステル−スチレン共重合体樹脂エマルジョン、
樹脂のTgが15℃、樹脂固形分50% *3 ・・・イヂチ化成株式会社商品名、シラス発泡体粒
子、比重0.8〜0.9、粒径130μmNote to Table 3: * 1 Mitsubishi Yuka Birdiche Co., Ltd. trade name, acrylic ester / styrene copolymer resin emulsion,
Resin Tg is 3 ° C., resin solid content is 50% * 2 Mitsubishi Yuka Birdishe Co., Ltd. trade name, acrylic ester-styrene copolymer resin emulsion,
Resin Tg is 15 ° C., resin solid content is 50% * 3 ... Idiji Kasei Co., Ltd. trade name, Shirasu foam particles, specific gravity 0.8 to 0.9, particle size 130 μm
【0040】実施例10 実施例1における接着剤組成物の塗布時に、下地層上に
ポリプロピレン製二次基布(テザツク社商品名 テバッ
ク−II 8.5P×8(418)BE×WHを重ねてお
いてから接着剤組成物を塗布するように変更し、そのほ
かは実施例1と同様にして接着剤カーペットを製造し、
同様にして剥離強度を測定したところ、剥離強度は実施
例1の場合と同様に6.8Kgf/50mm巾であった
が、この場合には、接着剤層が防水層との境界面で確実
に、均一に剥離でき、剥離面が極めて平坦であったの
で、カーペットの再接着を著しく円滑に行うことができ
た。Example 10 During the application of the adhesive composition in Example 1, a secondary polypropylene base fabric (Tebac-II 8.5Px8 (418) BExWH manufactured by Tesatsk Co., Ltd.) was overlaid on the underlayer. After that, the adhesive composition was changed to be applied, and otherwise an adhesive carpet was produced in the same manner as in Example 1,
When the peel strength was measured in the same manner, the peel strength was 6.8 Kgf / 50 mm width as in the case of Example 1, but in this case, the adhesive layer was surely formed at the interface with the waterproof layer. Since the peeling was possible and the peeling surface was extremely flat, the re-adhesion of the carpet could be remarkably smoothly performed.
【0041】比較例11 下地防水層を形成させるまでは実施例1と全く同様の方
法を用いて得られた舗道板の該下地防水層上に、実施例
1で用いたのと同一の人工芝生を、市販のエポキシ樹脂
系二液型接着剤(コニシ株式会社商品名 コニシボンド
E350R、A液とB液を重量比1:1で混合して使
用、可使用時間20℃で60分)を用い、500g/m
2 の塗布量で貼り合わせ、室温で3週間放置後に実施例
1におけると同様の剥離試験をしたところ、コンクリー
ト舗道板から下地防水層が剥離してしまった(剥離強度
15Kgf/50mm巾)。したがって、この場合に人
工芝生の再接着をさせる場合に、下地防水層を再塗布し
てから、接着剤を塗布して接着させる必要があった。Comparative Example 11 The same artificial lawn as used in Example 1 was formed on the underwater-proof layer of the pavement board obtained by using the same method as in Example 1 until the underwater-proof layer was formed. Using a commercially available epoxy resin two-component adhesive (Konishi Co., Ltd. trade name Konishi Bond E350R, A liquid and B liquid are mixed at a weight ratio of 1: 1 and used, usable time is 60 minutes at 20 ° C.), 500 g / m
After applying the coating amount of 2 and leaving it at room temperature for 3 weeks, the same peeling test as in Example 1 was performed. As a result, the base waterproof layer peeled from the concrete pavement board (peel strength 15 Kgf / 50 mm width). Therefore, in this case, when the artificial lawn is to be re-bonded, it is necessary to re-apply the base waterproof layer and then apply the adhesive to bond the artificial grass.
【0042】また、前記の方法において、接着させる人
工芝生として市販のピノキオサンドS−20(泉州敷物
株式会社商品名、ポリプロピレン糸製、パイル長19m
m)を用い、そのほかは前記と同様の方法で貼合わせ、
得られた接着カーペットを同様の方法で剥離試験をした
ところ、人工芝生の一部がちぎれ、下地防水層上にパイ
ルの付着した接着剤層の一部が残り、そのままではその
上に人工芝生を再接着させることができなかった。In the above-mentioned method, a commercially available Pinocchio Sand S-20 (trade name of Senshu Rug Co., Ltd., polypropylene yarn, pile length 19 m) is used as an artificial lawn to be bonded.
m) is used and the other method is the same as above,
When a peeling test was performed on the obtained adhesive carpet in the same manner, a part of the artificial lawn was torn, and a part of the adhesive layer with the pile adhered remained on the waterproof underlayer, and the artificial lawn was left on it as it was. Could not be re-bonded.
【0043】[0043]
【発明の効果】本発明の接着剤組成物は、人工芝生等の
カーペットをコンクリート体等に強固に接着でき、しか
もセメント量及び発泡体粒子量の調節によって接着剥離
強度を容易に制御できるので、下地防水層を破壊するこ
となく、接着したカーペットを容易に剥離でき、カーペ
ットの再接着が著しく容易である。EFFECT OF THE INVENTION The adhesive composition of the present invention can firmly adhere carpet such as artificial grass to concrete and the like, and can easily control the adhesive peel strength by adjusting the amount of cement and the amount of foam particles. The adhered carpet can be easily peeled off without destroying the underwater waterproof layer, and re-adhesion of the carpet is extremely easy.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 鷹尾 浩樹 大阪府大阪市中央区備後町3丁目1−2 株式会社泉州ストリーム内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Hiroki Takao 3-1-2, Bingo-cho, Chuo-ku, Osaka City, Osaka Prefecture Senshu Stream Co., Ltd.
Claims (1)
ルジョン、該エマルジョンの樹脂固形分100重量部に
対して水硬性無機質セメント150〜450重量部及び
発泡体粒子20〜160重量部を含有せしめてなること
を特徴とするカーペット用接着剤組成物。1. An aqueous emulsion of a resin having a glass transition point of 5 ° C. or less, containing 150 to 450 parts by weight of a hydraulic inorganic cement and 20 to 160 parts by weight of foam particles with respect to 100 parts by weight of a resin solid content of the emulsion. An adhesive composition for carpets, which comprises:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31286893A JPH07138532A (en) | 1993-11-19 | 1993-11-19 | Adhesive composition for carpet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31286893A JPH07138532A (en) | 1993-11-19 | 1993-11-19 | Adhesive composition for carpet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH07138532A true JPH07138532A (en) | 1995-05-30 |
Family
ID=18034408
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP31286893A Pending JPH07138532A (en) | 1993-11-19 | 1993-11-19 | Adhesive composition for carpet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07138532A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09508662A (en) * | 1994-02-11 | 1997-09-02 | ビーエーエスエフ アクチェンゲゼルシャフト | Floor dispersion adhesive |
EP0792926A2 (en) * | 1996-02-28 | 1997-09-03 | Henkel Kommanditgesellschaft auf Aktien | Aqueous dispersion adhesive |
JP2015110727A (en) * | 2013-11-01 | 2015-06-18 | 日本エイアンドエル株式会社 | Adhesive composition |
CN110387203A (en) * | 2018-04-23 | 2019-10-29 | 立邦涂料(中国)有限公司 | A kind of exterior wall ceramic tile backing material |
-
1993
- 1993-11-19 JP JP31286893A patent/JPH07138532A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09508662A (en) * | 1994-02-11 | 1997-09-02 | ビーエーエスエフ アクチェンゲゼルシャフト | Floor dispersion adhesive |
EP0792926A2 (en) * | 1996-02-28 | 1997-09-03 | Henkel Kommanditgesellschaft auf Aktien | Aqueous dispersion adhesive |
EP0792926A3 (en) * | 1996-02-28 | 1999-12-22 | Henkel Kommanditgesellschaft auf Aktien | Aqueous dispersion adhesive |
JP2015110727A (en) * | 2013-11-01 | 2015-06-18 | 日本エイアンドエル株式会社 | Adhesive composition |
CN110387203A (en) * | 2018-04-23 | 2019-10-29 | 立邦涂料(中国)有限公司 | A kind of exterior wall ceramic tile backing material |
CN110387203B (en) * | 2018-04-23 | 2021-04-20 | 立邦涂料(中国)有限公司 | Ceramic tile gum material for external wall |
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