JPH0756016B2 - Adhesive composition having thermoformability - Google Patents
Adhesive composition having thermoformabilityInfo
- Publication number
- JPH0756016B2 JPH0756016B2 JP1332385A JP33238589A JPH0756016B2 JP H0756016 B2 JPH0756016 B2 JP H0756016B2 JP 1332385 A JP1332385 A JP 1332385A JP 33238589 A JP33238589 A JP 33238589A JP H0756016 B2 JPH0756016 B2 JP H0756016B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- adhesive composition
- thermoformability
- present
- glass transition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000853 adhesive Substances 0.000 title claims description 26
- 230000001070 adhesive effect Effects 0.000 title claims description 26
- 239000000203 mixture Substances 0.000 title claims description 26
- 230000009477 glass transition Effects 0.000 claims description 12
- 239000000839 emulsion Substances 0.000 claims description 9
- 239000000178 monomer Substances 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 239000003431 cross linking reagent Substances 0.000 claims description 8
- 229920003002 synthetic resin Polymers 0.000 claims description 7
- 239000000057 synthetic resin Substances 0.000 claims description 7
- 229920006174 synthetic rubber latex Polymers 0.000 claims description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 6
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 5
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 5
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 3
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 3
- 239000002174 Styrene-butadiene Substances 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000001530 fumaric acid Substances 0.000 claims description 3
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 3
- 239000011115 styrene butadiene Substances 0.000 claims description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
- 239000000835 fiber Substances 0.000 description 20
- 229920000126 latex Polymers 0.000 description 7
- 239000004816 latex Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 238000003672 processing method Methods 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- -1 polyethylene Polymers 0.000 description 6
- 229920005992 thermoplastic resin Polymers 0.000 description 6
- 230000007423 decrease Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000004094 surface-active agent 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
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical class O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000013001 point bending Methods 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 102200150779 rs200154873 Human genes 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Reinforced Plastic Materials (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Manufacturing Of Multi-Layer Textile Fabrics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Paper (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、繊維基材または紙に塗布あるいは含浸するこ
とにより、かかる繊維基材または紙に熱成型性を与える
接着剤組成物に関する。TECHNICAL FIELD The present invention relates to an adhesive composition that imparts thermoformability to a fiber base material or paper by coating or impregnating the fiber base material or paper.
繊維基材に熱成型性を付与するために、例えば、自動車
内装用のニードルパンチカーペットおよびタフテッドカ
ーペットは、スチレン−ブタジエン共重合体ラテックス
あるいはエチレン−酢酸ビニル系の樹脂エマルジョンを
主成分とする接着剤組成物を該カーペット裏面に塗布ま
たは含浸加工した後に、ポリエチレン等の熱可塑性樹脂
皮膜を熱融着によって裏打ちする2段加工法が行われて
いる。In order to impart thermoformability to a fiber base material, for example, needle punched carpets and tufted carpets for automobile interiors have an adhesive containing styrene-butadiene copolymer latex or ethylene-vinyl acetate resin emulsion as a main component. A two-step processing method has been performed in which after applying or impregnating the agent composition on the back surface of the carpet, a thermoplastic resin film such as polyethylene is lined by heat fusion.
また、水性プラスチック分散液をカーペット裏面に塗布
することにより持続成型可能なカーペットを得る、いわ
ゆる1段加工法が特開昭53−52776号公報により開示さ
れている。Further, Japanese Patent Application Laid-Open No. 53-52776 discloses a so-called one-step processing method in which a continuously moldable carpet is obtained by applying an aqueous plastic dispersion liquid to the back surface of the carpet.
従来の2段加工法においては、スチレン−ブタジエン共
重合体ラテックスあるいは樹脂の水性エマルジョンから
なる接着剤を塗布または含浸することにより不織布繊維
またはパイル糸を固着せしめ、更に熱可塑性樹脂の皮膜
を裏打ちすることによってカーペットに熱成型性を与え
ているが、この様な2段加工法はカーペットの製造工程
が煩雑となり、このためその改良が望まれていた。In the conventional two-step processing method, the non-woven fabric fiber or pile yarn is fixed by applying or impregnating an adhesive consisting of an aqueous emulsion of styrene-butadiene copolymer latex or resin, and further lining the thermoplastic resin film. This gives the carpet thermoformability, but such a two-step processing method complicates the carpet manufacturing process, and therefore improvement thereof has been desired.
一方、前述の熱可塑性樹脂の皮膜を裏打ちすることなし
に接着剤に熱成型性を付与させる1段加工法では、製品
に求められる硬い風合い(剛性)が不十分であり、剛性
を改良しようとすれば繊維の固着力が低下してしまうと
いう問題があった。On the other hand, in the one-step processing method that imparts thermoformability to the adhesive without backing the thermoplastic resin film, the hard texture (rigidity) required for the product is insufficient, and it is attempted to improve the rigidity. If so, there is a problem that the fixing force of the fiber is reduced.
従って、剛性と繊維の固着力の面において優れた1段加
工用の熱成型性を有する接着剤組成物の開発が望まれて
いた。Therefore, it has been desired to develop an adhesive composition having excellent thermoformability for one-step processing, which is excellent in terms of rigidity and fiber adhesion.
本発明者らは、かかる問題点を解決するために熱成型性
を有する接着剤組成物について鋭意研究を行った結果、
特定のガラス転移点を有する合成樹脂エマルジョン
(A)と特定のガラス転移点を有する合成ゴムラテック
ス(B)をある特定の比率にて混合した混合物に対して
架橋剤および/または加硫剤とを特定の比率で配合して
得られる配合物を接着剤として用いることにより、剛性
および繊維の固着力の面に優れた効果を発現するという
事実を見い出し、本発明を完成するに至った。The present inventors, as a result of intensive studies on an adhesive composition having thermoformability in order to solve such problems,
A synthetic resin emulsion (A) having a specific glass transition point and a synthetic rubber latex (B) having a specific glass transition point are mixed in a specific ratio, and a crosslinking agent and / or a vulcanizing agent are added to the mixture. We have found the fact that by using a compound obtained by compounding in a specific ratio as an adhesive, an excellent effect is exhibited in terms of rigidity and fiber adhesion, and the present invention has been completed.
すなわち、本発明は、固形分重量換算値で、芳香族ビニ
ル系単量体およびアクリル酸、メタクリル酸、イタコン
酸、フマル酸、β−ヒドロキシエチルアクリレート、ア
クリロニトリル、アクリルアミドから選ばれた共重合可
能な他の単量体を共重合させて得られる、80〜120℃の
ガラス転移点を有する合成樹脂エマルジョン(A)30〜
50重量%および0〜50℃のガラス転移点を有するスチレ
ン−ブタジエン系合成ゴムラテックス(B)70〜50重量
%からなる混合物100重量部に対して、架橋剤および/
または加硫剤(C)0.1〜25重量部を配合してなること
を特徴とする熱成型性を有する接着剤組成物を提供する
ものである。That is, the present invention, in terms of solid content weight, is a copolymerizable aromatic vinyl-based monomer and acrylic acid, methacrylic acid, itaconic acid, fumaric acid, β-hydroxyethyl acrylate, acrylonitrile, acrylamide copolymerizable. Synthetic resin emulsion (A) having a glass transition point of 80 to 120 ° C., which is obtained by copolymerizing other monomer
Based on 100 parts by weight of a mixture of 50% by weight and 70 to 50% by weight of a styrene-butadiene synthetic rubber latex (B) having a glass transition point of 0 to 50 ° C., a crosslinking agent and / or
Alternatively, the present invention provides an adhesive composition having thermoformability, which comprises 0.1 to 25 parts by weight of a vulcanizing agent (C).
本発明の接着剤組成物を繊維基材または紙に塗布または
含浸させることにより、優れた剛性を有しかつ繊維の固
着力に優れた繊維基材または含浸紙を容易に得ることが
できる。By applying or impregnating a fiber base material or paper with the adhesive composition of the present invention, a fiber base material or impregnated paper having excellent rigidity and excellent fiber fixing force can be easily obtained.
また、本発明は前述の2段加工法とは異なり、熱可塑性
樹脂皮膜の裏打ちを必要としないことから、カーペット
の製造工程の簡略化、生産性の向上の面においても優れ
ている。Further, unlike the above-described two-step processing method, the present invention does not require lining of the thermoplastic resin film, and is therefore excellent in terms of simplification of the carpet manufacturing process and improvement of productivity.
以下に、本発明を更に詳しく説明する。Hereinafter, the present invention will be described in more detail.
合成樹脂エマルジョン(A) 本発明にて用いられる合成樹脂エマルジョン(A)は、
芳香族ビニル系単量体およびこれと共重合可能な他の単
量体を共重合させて得ることができる。芳香族ビニル系
単量体としては、スチレン、α−メチルスチレン等が挙
げられる。共重合可能な他の単量体としては、アクリル
酸、メタクリル酸、イタコン酸、フマル酸、β−ヒドロ
キシエチルアクリレート、アクリロニトリル、アクリル
アミド等が挙げられる。Synthetic Resin Emulsion (A) The synthetic resin emulsion (A) used in the present invention is
It can be obtained by copolymerizing an aromatic vinyl monomer and another monomer copolymerizable therewith. Examples of the aromatic vinyl-based monomer include styrene and α-methylstyrene. Other copolymerizable monomers include acrylic acid, methacrylic acid, itaconic acid, fumaric acid, β-hydroxyethyl acrylate, acrylonitrile, acrylamide and the like.
(A)のガラス転移点は80〜120℃の範囲にあり、ガラ
ス転移点が80℃未満では剛性が低下する。また120℃を
超えると繊維の固着力が低下する。The glass transition point of (A) is in the range of 80 to 120 ° C, and when the glass transition point is less than 80 ° C, the rigidity is lowered. On the other hand, if the temperature exceeds 120 ° C, the fixing strength of the fibers will be reduced.
合成ゴムラテックス(B) 本発明にて用いられるスチレン−ブタジエン系合成ゴム
ラテックス(B)は、スチレン、ブタジエンを共重合さ
せて得られるものであり、これらモノマーと共重合可能
な不飽和カルボン酸、さらにはアクリロニトリル等を共
重合させたものが好ましい。Synthetic Rubber Latex (B) The styrene-butadiene synthetic rubber latex (B) used in the present invention is obtained by copolymerizing styrene and butadiene, and is an unsaturated carboxylic acid copolymerizable with these monomers, Further, those obtained by copolymerizing acrylonitrile and the like are preferable.
(B)のガラス転移点は0〜50℃の範囲にあり、ガラス
転移点が0℃より低い場合には剛性が低下し、更に50℃
を超えると繊維の固着力が低下する。The glass transition point of (B) is in the range of 0 to 50 ° C, and when the glass transition point is lower than 0 ° C, the rigidity decreases, and further 50 ° C.
If it exceeds, the fixing strength of the fibers will decrease.
ラテックス混合物 本発明にて用いられるラテックス混合物は、合成樹脂エ
マルジョン(A)と合成ゴムラテックス(B)との混合
比率が重量比で(A)/(B)=30〜50/70〜50の範囲
である。Latex mixture In the latex mixture used in the present invention, the mixing ratio of the synthetic resin emulsion (A) and the synthetic rubber latex (B) is in the range of (A) / (B) = 30-50 / 70-50. Is.
(A)の使用比率が30重量%未満では剛性が低下し、50
重量%を超えると繊維の固着力が低下するので好しくな
い。If the usage ratio of (A) is less than 30% by weight, the rigidity will decrease, and
If the content is more than weight%, the fiber's fixing strength is lowered, which is not preferable.
架橋剤または加硫剤(C) 本発明にて用いられる架橋剤または加硫剤としては、亜
鉛華、エポキシ基を有する化合物、ブロックイソシアネ
ート化合物、エチレン尿素化合物、メラミン樹脂、尿素
樹脂、硫黄、過酸化物等が挙げられ、これらを1種もし
くは2種以上用いることができる。Crosslinking Agent or Vulcanizing Agent (C) Examples of the crosslinking agent or vulcanizing agent used in the present invention include zinc white, compounds having an epoxy group, blocked isocyanate compounds, ethyleneurea compounds, melamine resins, urea resins, sulfur and peroxides. Examples thereof include oxides, and these can be used alone or in combination of two or more.
架橋剤または加硫剤(C)はラテックス混合物100重量
部(固形分)に対して0.1〜25重量部用いられる。The crosslinking agent or vulcanizing agent (C) is used in an amount of 0.1 to 25 parts by weight based on 100 parts by weight (solid content) of the latex mixture.
架橋剤または加硫剤が0.1重量部未満では剛性が低下
し、25重量部を超えても剛性の向上は見られず、経済的
に好しくない。If the cross-linking agent or the vulcanizing agent is less than 0.1 parts by weight, the rigidity will decrease, and if it exceeds 25 parts by weight, the rigidity will not be improved, which is not economically preferable.
本発明の接着剤組成物には、酸化防止剤、充填剤、成膜
助剤、難燃剤、増粘剤、界面活性剤などを含むことがで
きる。The adhesive composition of the present invention may contain an antioxidant, a filler, a film forming aid, a flame retardant, a thickener, a surfactant and the like.
本発明の接着剤組成物は、ポリプロピレン、ポリエステ
ル、ナイロン、アクリル、羊毛などの繊維を用いたタフ
テッドカーペット、ニードルパンチカーペットおよび不
織布などの繊維基材または含浸紙に適用される。The adhesive composition of the present invention is applied to a fiber base material or impregnated paper such as tufted carpet, needle punched carpet and nonwoven fabric using fibers such as polypropylene, polyester, nylon, acrylic and wool.
本発明の接着剤組成物を塗布または含浸するに際し、接
着剤を発泡あるいは増粘して用いてもよく、その加工方
法としては、リックロール、絞りロール、吹付けガン、
浸績等が挙げられる。また、繊維基材または紙への含浸
を完全にするためには、塗布または含浸された接着剤組
成物を絞りロールにより圧搾することが好ましい。接着
剤組成物を塗布または含浸した後、加熱により水分を除
去して成型可能な製品を得ることができる。製品を成型
する方法としては加熱後加圧ロールまたはプレス成型機
による成型方法等が挙げられる。When applying or impregnating the adhesive composition of the present invention, the adhesive may be foamed or thickened to be used, and as a processing method thereof, a lick roll, a squeezing roll, a spray gun,
Examples include stealing. Further, in order to completely impregnate the fiber base material or the paper, it is preferable to squeeze the coated or impregnated adhesive composition with a squeezing roll. After applying or impregnating the adhesive composition, the moisture can be removed by heating to obtain a moldable product. Examples of the method for molding the product include a molding method using a pressure roll or a press molding machine after heating.
なお、本発明の接着剤組成物をカーペット裏面に塗布し
た後、ポリエチレン等の熱可塑性樹脂皮膜を熱融着によ
って裏打ちすることを何ら妨げるものではない。It should be noted that the application of the adhesive composition of the present invention to the back surface of the carpet does not hinder the backing of the thermoplastic resin film such as polyethylene by heat fusion.
以下に実施例をあげて本発明を具体的に説明するが、本
発明はこれら実施例によって何ら制限されるものではな
い。The present invention will be specifically described below with reference to examples, but the present invention is not limited to these examples.
尚、実施例中の部および%は断りのない限り全て重量部
および重量%を意味する。All parts and% in the examples mean parts by weight and% by weight, unless otherwise specified.
実施例1〜3および比較例1〜3 ガラス転移温度110℃の合成樹脂エマルジョン(A)
(スチレン/アクリロニトリル/アクリル酸=77/20/
3)とガラス転移温度10℃の合成ゴムラテックス(B)
(スチレン/ブタジエン/アクリロニトリル/アクリル
酸=51/37/10/2)を表−1に示す比率にて混合し、ラテ
ックス混合物を得た。Examples 1 to 3 and Comparative Examples 1 to 3 synthetic resin emulsion (A) having a glass transition temperature of 110 ° C.
(Styrene / acrylonitrile / acrylic acid = 77/20 /
3) and synthetic rubber latex with a glass transition temperature of 10 ° C (B)
(Styrene / butadiene / acrylonitrile / acrylic acid = 51/37/10/2) were mixed at a ratio shown in Table 1 to obtain a latex mixture.
得られたラテックス混合物の各々100部(固形分)に対
して架橋剤(C)としてエチレン尿素化合物を表−1に
示す割合で添加し、更に酸化防止剤1部(スミライザー
S:住友化学工業(株)製)および界面活性剤1部(エマ
ール2FN:花王(株)製)を添加して接着剤組成物を得
た。An ethylene urea compound as a cross-linking agent (C) was added at a ratio shown in Table 1 to 100 parts (solid content) of each of the obtained latex mixtures, and further 1 part of an antioxidant (Sumilyzer).
S: Sumitomo Chemical Co., Ltd.) and 1 part of a surfactant (Emar 2FN: Kao Co., Ltd.) were added to obtain an adhesive composition.
得られた接着剤組成物の各々についてホバートミキサー
にて3倍容量に泡立て、ポリプロピレン、ポリエステル
混紡ニードルパンチカーペットの裏面に300g/m2の塗布
量にて塗布し、内部まで含浸させた。その後、130℃に
て5分間乾燥して得られたカーペット試料を180℃で5
分間加熱した後プレス成型して試験片を得た。得られた
試験片について、剛性および繊維固着力を各々次の測定
方法に基づいて試験した。Each of the obtained adhesive compositions was foamed in a volume of 3 times with a Hobart mixer, coated on the back surface of a polypropylene / polyester needle-punched carpet with a coating amount of 300 g / m 2 , and the interior was impregnated. Then, the carpet sample obtained by drying at 130 ° C for 5 minutes was heated at 180 ° C for 5 minutes.
After heating for a minute, press molding was performed to obtain a test piece. The test pieces thus obtained were tested for rigidity and fiber fixing force based on the following measuring methods.
結果を表−1に示す。The results are shown in Table-1.
剛性:試験片を50mm巾に裁断し、3点曲げ治具を用いて
50mm/minの速度で曲げ、その時の最大荷重(kg)を測定
し、次の基準にて評価した。Rigidity: Cut a test piece into 50 mm width and use a 3-point bending jig
Bending was performed at a speed of 50 mm / min, the maximum load (kg) at that time was measured, and evaluation was performed according to the following criteria.
○:3kg超 △:2〜3kg ×:2kg未満 繊維固着力:カーペット試料の裏面の金属片にて摩擦
し、接着剤の脱落ならびに繊維のピリングの程度を次の
基準に基づき評価した。○: more than 3 kg △: 2-3 kg ×: less than 2 kg Fiber fixing force: Rub on the metal piece on the back surface of the carpet sample, and the degree of peeling of the adhesive and pilling of the fiber was evaluated based on the following criteria.
○:接着剤の脱落がなく、ピリング良好 △:接着剤の脱落が少し有り、ピリングやや不良 ×:接着剤の脱落(粉落ち)が多く、ピリング不良 〔本発明の効果〕 本発明にて得られる接着剤組成物は、優れた剛性と繊維
固着力を同時に発現させることができ、かつ、本発明の
接着剤組成物は熱可塑性樹脂皮膜の裏打ちという2段加
工技術の工程を省略することができ、カーペット製造工
程の簡略化、生産性の向上という効果をも併せて具備し
ている。◯: Adhesive did not fall off and pilling was good. Δ: Adhesive fell off a little and pilling was a little poor. X: Adhesive fell off (powder drop) was large and pilling was bad. [Effect of the present invention] The adhesive composition obtained in the present invention can exhibit excellent rigidity and fiber fixing strength at the same time, and the adhesive composition of the present invention is called a lining of a thermoplastic resin film. The step of the two-step processing technique can be omitted, and the carpet manufacturing process can be simplified and the productivity can be improved.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 D06M 17/00 D21H 19/56 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical display location D06M 17/00 D21H 19/56
Claims (1)
体およびアクリル酸、メタクリル酸、イタコン酸、フマ
ル酸、β−ヒドロキシエチルアクリレート、アクリロニ
トリル、アクリルアミドから選ばれた共重合可能な他の
単量体を共重合させて得られる、80〜120℃のガラス転
移点を有する合成樹脂エマルジョン(A)30〜50重量%
および0〜50℃のガラス転移点を有するスチレン−ブタ
ジエン系合成ゴムラテックス(B)70〜50重量%からな
る混合物100重量部に対して、架橋剤および/または加
硫剤(C)0.1〜25重量部を配合してなることを特徴と
する熱成型性を有する接着剤組成物。1. A copolymerizable compound selected from aromatic vinyl monomers and acrylic acid, methacrylic acid, itaconic acid, fumaric acid, β-hydroxyethyl acrylate, acrylonitrile, and acrylamide in terms of solid content weight. 30 to 50% by weight of a synthetic resin emulsion (A) having a glass transition point of 80 to 120 ° C., obtained by copolymerizing the monomer of
And 100 parts by weight of a mixture of 70 to 50% by weight of a styrene-butadiene synthetic rubber latex (B) having a glass transition point of 0 to 50 ° C., a crosslinking agent and / or a vulcanizing agent (C) of 0.1 to 25 An adhesive composition having thermoformability, which is characterized by containing parts by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1332385A JPH0756016B2 (en) | 1989-12-20 | 1989-12-20 | Adhesive composition having thermoformability |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1332385A JPH0756016B2 (en) | 1989-12-20 | 1989-12-20 | Adhesive composition having thermoformability |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03190987A JPH03190987A (en) | 1991-08-20 |
| JPH0756016B2 true JPH0756016B2 (en) | 1995-06-14 |
Family
ID=18254376
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1332385A Expired - Fee Related JPH0756016B2 (en) | 1989-12-20 | 1989-12-20 | Adhesive composition having thermoformability |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0756016B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09169028A (en) * | 1995-12-20 | 1997-06-30 | Sangyo Gijutsu Kenkyusho:Kk | Paper pellet and granulation thereof |
| JP4752614B2 (en) * | 2006-05-23 | 2011-08-17 | セントラル硝子株式会社 | Fiber coating solution and rubber reinforcing fiber using the same |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0726074B2 (en) * | 1987-01-19 | 1995-03-22 | 住友ダウ株式会社 | Adhesive composition for carpet backing |
-
1989
- 1989-12-20 JP JP1332385A patent/JPH0756016B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH03190987A (en) | 1991-08-20 |
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