JPS63205378A - Adhesive composition for carpet backing - Google Patents
Adhesive composition for carpet backingInfo
- Publication number
- JPS63205378A JPS63205378A JP3660687A JP3660687A JPS63205378A JP S63205378 A JPS63205378 A JP S63205378A JP 3660687 A JP3660687 A JP 3660687A JP 3660687 A JP3660687 A JP 3660687A JP S63205378 A JPS63205378 A JP S63205378A
- Authority
- JP
- Japan
- Prior art keywords
- latex
- component
- styrene
- weight
- mixture
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 42
- 239000000853 adhesive Substances 0.000 title claims abstract description 25
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 25
- 239000004816 latex Substances 0.000 claims abstract description 47
- 229920000126 latex Polymers 0.000 claims abstract description 47
- 239000000178 monomer Substances 0.000 claims abstract description 42
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229920003048 styrene butadiene rubber Polymers 0.000 claims abstract description 13
- 229920005989 resin Polymers 0.000 claims abstract description 11
- 239000011347 resin Substances 0.000 claims abstract description 11
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 9
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 8
- 150000001993 dienes Chemical class 0.000 claims abstract description 8
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229920001577 copolymer Polymers 0.000 claims description 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 238000007334 copolymerization reaction Methods 0.000 abstract 2
- 125000005907 alkyl ester group Chemical group 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 239000000835 fiber Substances 0.000 description 11
- 230000014759 maintenance of location Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 238000003672 processing method Methods 0.000 description 7
- 229920005992 thermoplastic resin Polymers 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- 239000002174 Styrene-butadiene Substances 0.000 description 3
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000011115 styrene butadiene Substances 0.000 description 3
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 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
- 239000004971 Cross linker Substances 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
- 239000004677 Nylon Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 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
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 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
- 230000004927 fusion Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 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
- 229920001778 nylon Polymers 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
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N7/00—Flexible sheet materials not otherwise provided for, e.g. textile threads, filaments, yarns or tow, glued on macromolecular material
- D06N7/0005—Floor covering on textile basis comprising a fibrous substrate being coated with at least one layer of a polymer on the top surface
- D06N7/0036—Floor covering on textile basis comprising a fibrous substrate being coated with at least one layer of a polymer on the top surface characterised by their backing, e.g. secondary backing, back-sizing
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、自動車の内装材として用いられるカーペット
の裏打ち用接着剤組成物に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an adhesive composition for backing carpets used as interior materials for automobiles.
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−ブタジェン共1会体ラテ
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、熱成型性を付与するため
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段加工法により製造されている。Needle-punched carpets and tufted carpets for automobile interiors are manufactured by coating or impregnating the back surface of the carpet with an adhesive composition mainly composed of styrene-butadiene co-monomer latex or ethylene-vinyl acetate resin emulsion. It is manufactured by a two-step processing method in which it is lined with a thermoplastic resin film such as polyethylene by heat fusion in order to impart thermoformability.
これらのカーペットは、裁断され、加熱時のプレス成型
によって自動車の床の型状に合わせて成型され、自動車
に組み込まれる。These carpets are cut, molded to match the shape of the car floor by press molding while heated, and then assembled into the car.
一方、前述の2段加工法とは異なり、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性成
形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。On the other hand, unlike the above-mentioned two-stage processing method, a so-called one-stage processing method is disclosed in JP-A-53-52776, in which a carpet that can be continuously molded is obtained by applying an aqueous plastic dispersion to the back surface of the carpet. ing.
従来の2段加工法においては、スチレン−ブタジェン共
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
なる接着剤全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 nonwoven fibers or pile yarns are fixed by full application or impregnation with an adhesive consisting of a styrene-butadiene copolymer latex or an aqueous emulsion of a resin, and then backed with a thermoplastic resin film. This gives the carpet thermoformability, but such a two-step processing method complicates the carpet manufacturing process, and therefore improvements have 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、熱成
型性およびその型状を保ち得る性能(保型性と呼ばれて
いる)が不十分であり、この熱成型性と保型性を改良し
ようとすれば、繊維の固着力が低下してし捷うという問
題があった。On the other hand, the above-mentioned one-step processing method that imparts thermoformability to the adhesive without backing with a thermoplastic resin film has the ability to maintain thermoformability and its shape (called shape retention). ) is insufficient, and if attempts were made to improve the thermoformability and shape retention, there was a problem that the adhesion of the fibers would decrease and the fibers would unravel.
従って、熱成型性、保型性、繊維の固着力の全ての面に
おいて優れた、1段加工用の裏打ち接着剤組成物の開発
が望1れていた。Therefore, it has been desired to develop a backing adhesive composition for one-stage processing that is excellent in all aspects of thermoformability, shape retention, and fiber adhesion.
本発明者らは、かかる問題点を解決するため、1段加工
用のカーペット裏打ち用接着剤組成物について鋭意研究
を行った結果、従来技術である特開昭53−52776
号で提案されている公知の水性プラスチック分散液およ
び該分散液の混合物を裏打ち用接着剤として用いるより
も、スチレン系ラテックスとスチレン−ブタジェン系共
N曾体ラテックスの混合物であり特定の最低造膜温度を
有し、特定の温度以上にて乾燥した場合に樹脂成分が連
続相を形成する層履層――ラテックス混合物を裏打ち用
接着剤として用いた際に、熱成型性、保型性および繊維
の固着力の全ての面において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0
すなわち本発明は、スチレン系ラテックス(A)とスチ
レン−ブタジェン系共重合体ラテックスCB)の混合物
であって、該混合物が60℃以下の最低造膜温度を有し
、かつ90℃以上で乾燥した場合に樹脂成分が連続相と
なるように調整してなる混合物を主要成分として用いる
ことを特徴とするカーペット裏打ち用接着剤組成物全提
供するものである。In order to solve these problems, the present inventors conducted extensive research on adhesive compositions for carpet lining for one-stage processing, and found that
Rather than using a known aqueous plastic dispersion or a mixture of the dispersion as a backing adhesive as proposed in the above issue, a mixture of a styrenic latex and a styrene-butadiene co-N latex can be used to achieve a specific minimum film formation rate. A layered footwear layer in which the resin component forms a continuous phase when dried above a certain temperature - When a latex mixture is used as a backing adhesive, thermoformability, shape retention and fiber The present invention was completed based on the discovery that styrene latex (A) and styrene-butadiene copolymer latex CB) exhibit excellent effects in all aspects of adhesion. A mixture having a minimum film-forming temperature of 60°C or lower and adjusted so that the resin component becomes a continuous phase when dried at 90°C or higher is used as the main component. A carpet backing adhesive composition is provided.
本発明の接着剤組成物をニードルパンチカーペットまた
はタフテッドカーペットに塗布もし−叫
くは含浸させることにより優れた熱成型性、保型性およ
び繊維固着力を有する自動車用カーペット全容易に得る
ことができる。By applying the adhesive composition of the present invention to needle-punched carpets or tufted carpets, it is possible to easily obtain automotive carpets having excellent thermoformability, shape retention, and fiber adhesion. can.
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-mentioned two-stage processing method, the present invention does not require backing with a thermoplastic resin film, and is therefore excellent in terms of simplifying the carpet manufacturing process and improving productivity.
以下に、本発明を更に詳しく説明する。The present invention will be explained in more detail below.
0スチレン系ラテツクス(A)
本発明にて用いられるスチレン系ラテックス(8は、芳
香族ビニル系単量体を主要成分とし、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、共重合可能な他の単量体としては1.3−ブタジ
ェン、アクリロニトリル、メチルメタクリンート、アク
リル酸、フマル酸、β−ヒドロキシエチルアクリンート
等が挙げられる。0 Styrenic latex (A) Styrenic latex used in the present invention (8 is obtained by copolymerizing an aromatic vinyl monomer as a main component and other monomers that can be copolymerized with this) Aromatic vinyl monomers include styrene, α-methylstyrene, etc., and other copolymerizable monomers include 1,3-butadiene, acrylonitrile, methyl methacrylate, acrylic acid, fumaric acid, Examples include β-hydroxyethyl acrylate.
本発明におけるスチレン系ラテックス(A)は、芳香族
ビニル系単量体70〜100M世襲およびこれと共重合
可能な他の単量体0〜30重量%からなることが好まし
い。The styrenic latex (A) in the present invention preferably comprises 70 to 100M of an aromatic vinyl monomer and 0 to 30% by weight of other monomers copolymerizable therewith.
0スチレン−ブタジェン系共重合体ラテックス(B)本
発明にて用いられるスチレン−ブタジェン系共重合体ラ
テックス(B)は、芳香族ビニル系単量体、脂肪族共役
ジエン系単量体、エチレン系不飽和カルボン酸アルキル
エステル単量体およびこれらと共重合可能な他の単量体
全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、脂肪族
共役ジエン系単量体としては1.3−ブタジェン、2−
メチル−1,3−ブタジェン等が、エチレン系不飽和カ
ルボン酸アルキルエステル単量体としてはメチルメタク
リレート、エチルアクリレート等が、これらと共重合可
能な他の単量体としてはアクリロニトリル、メタクリレ
ートリル、アクリル酸、フマル酸、メタクリル酸、イタ
コン酸、β−ヒドロキシエチルアクリレート等が挙げら
れる。0 Styrene-butadiene copolymer latex (B) The styrene-butadiene copolymer latex (B) used in the present invention contains aromatic vinyl monomers, aliphatic conjugated diene monomers, and ethylene monomers. It can be obtained by copolymerizing all of the unsaturated carboxylic acid alkyl ester monomers and other monomers copolymerizable with them. Examples of aromatic vinyl monomers include styrene and α-methylstyrene, and examples of aliphatic conjugated diene monomers include 1,3-butadiene and 2-
Methyl-1,3-butadiene, etc., ethylenically unsaturated carboxylic acid alkyl ester monomers include methyl methacrylate, ethyl acrylate, etc., and other monomers that can be copolymerized with these include acrylonitrile, methacrylatetril, acrylic. acid, fumaric acid, methacrylic acid, itaconic acid, β-hydroxyethyl acrylate, and the like.
本発明におけるスチレン−ブタジェン系共重合体ラテッ
クスCB)は、芳香族ビニル系単量体10〜79重指部
、脂肪族共役ジエン系単量体1〜40量%、エチレン系
不飽和カルボン酸アルキルエステル単量体1〜40i量
%およびこれらと共重合可能な他の単量体0〜20重量
係か世襲ることが好ましく、脂肪族共役ジエン系単量体
が10〜40M量受であることが更に好筐しい。The styrene-butadiene copolymer latex CB) in the present invention includes 10 to 79 deuteranyl aromatic vinyl monomers, 1 to 40% by weight of aliphatic conjugated diene monomers, and ethylenically unsaturated alkyl carboxylates. It is preferable to inherit 1 to 40 I weight percent of ester monomers and 0 to 20 weight percent of other monomers copolymerizable with these, and 10 to 40 M weight percent of aliphatic conjugated diene monomers. is even better.
0ラテツクス混付物
本発明にて用いられるラテックス混合物は、固形分でス
チレン系ラテックス仏〕30〜90i量部およびスチレ
ン−ブタジェン系共M 、lx体シラテックスB) 1
0〜70:jEt景部からなることが好ましく、スチレ
ン系ラテックス(A)50〜8ON量部およびスチレン
−ブタジェン系共重合体ラテックス(B) 20〜50
重量部からなることが更に好ましい。0 latex mixture The latex mixture used in the present invention has a solid content of styrene latex (30 to 90 parts) and styrene-butadiene (M), lx-form silatex (B) 1
0 to 70: preferably consists of a styrene latex (A) of 50 to 8 parts and a styrene-butadiene copolymer latex (B) of 20 to 50 parts.
More preferably, it consists of parts by weight.
本発明におけるラテックス混合物は、芳香族ビニル系単
量体15〜96fi量%、脂肪族共役ジエン系単量体2
〜70重量%、シアン化ビニル系単量体1〜35重世襲
、エチレン系不飽和カルボン酸アルキルエステル単量体
0.2〜3ON量係およびこれらと共重合可能な他の単
量体0〜20重量%からなることが好ましく、脂肪族共
役ジエン系単量体が10〜200〜20重量部とが更に
好ましい。また、シアン化ビニル系単量体は、スチレン
系ラテックス(A)またはスチレン−ブタジェン系共重
合体ラテックスCB)のどちらか一方のみに用いること
が好捷しい。The latex mixture in the present invention contains 15 to 96 fi amount% of aromatic vinyl monomers and 2% of aliphatic conjugated diene monomers.
~70% by weight, vinyl cyanide monomer 1~35 monomers, ethylenically unsaturated carboxylic acid alkyl ester monomer 0.2~3ON, and other monomers copolymerizable with these 0~ It is preferably 20% by weight, and more preferably 10 to 200 to 20 parts by weight of the aliphatic conjugated diene monomer. Furthermore, it is preferable to use the vinyl cyanide monomer only in either the styrene latex (A) or the styrene-butadiene copolymer latex CB).
本発明のラテックス混合物の最低造膜温度は60℃以下
であるが、60℃を超えると繊維の固着力が低下し、ま
た、ラテックス混合物を90℃以上で乾燥した場会、樹
脂成分が連続相を形成しなければならないが、樹脂成分
が連続相を形成しないと保型性に劣り、好ましくない。The minimum film-forming temperature of the latex mixture of the present invention is 60°C or lower, but if it exceeds 60°C, the adhesion of the fibers will decrease, and if the latex mixture is dried at 90°C or higher, the resin component will form a continuous phase. However, if the resin component does not form a continuous phase, the shape retention property will be poor, which is not preferable.
本発明のスチレン系ラテックス(A)およびスチレン−
ブタジェン系共重合体ラテックス(B)は、公知の方法
により製造される。すなわち一括添加方法、分割添加方
法、連続添加方法、二段重置方法、パワーフィード方法
などが適用できる。Styrenic latex (A) of the present invention and styrene-
The butadiene copolymer latex (B) is produced by a known method. That is, a batch addition method, a divided addition method, a continuous addition method, a two-stage overlapping method, a power feed method, etc. can be applied.
本発明の接着剤組成物には、酸化防止剤、充填剤、難燃
剤、増粘剤、界面活性剤、架橋剤などを含むことができ
る。The adhesive composition of the present invention can contain antioxidants, fillers, flame retardants, thickeners, surfactants, crosslinkers, and the like.
本発明の接着剤組成物が適用できるカーペットとしては
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であり、加熱成型工程を必要と
する自動車用カーペットおよび内装材に適用される。Carpets to which the adhesive composition of the present invention can be applied include polypropylene, polyester, nylon, acrylic,
These are needle punch carpets and tufted carpets that use fibers such as wool, and are applied to automobile carpets and interior materials that require a heat molding process.
以下余白
実施例
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。EXAMPLES Below, the present invention will be specifically explained with reference to examples.
The present invention is not limited in any way by these Examples.
なお、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。Note that all parts and % in the examples mean parts by weight and % by weight unless otherwise specified.
実施例−1
(共重合体ラテックスおよびラテックス混合物の調製)
水100部に、ドデシルベンゼンスルホン酸ソーダ1.
5部を加え溶解させる。これに、表−1に示した単量体
混合物を添加し、さらに1−60℃に保ち乳化重合を行
った。単量体の重合転化率が97%に達した時点で重合
を停止した。Example-1 (Preparation of copolymer latex and latex mixture) 1.0 parts of sodium dodecylbenzenesulfonate was added to 100 parts of water.
Add 5 parts and dissolve. The monomer mixture shown in Table 1 was added to this, and the mixture was further kept at 1-60°C for emulsion polymerization. Polymerization was stopped when the monomer polymerization conversion rate reached 97%.
得られたラテックス中の未反応単量体を減圧により除去
して、共重合体ラテックスA−D’i得た。得られた共
重合体ラテックスを表−2で示した割付で各々混会して
ラテックス混合物(1)。Unreacted monomers in the obtained latex were removed under reduced pressure to obtain copolymer latex A-D'i. The obtained copolymer latexes were mixed in the layout shown in Table 2 to form a latex mixture (1).
(41を得た。これらのラテックス混合物(++ 、
<:+)の最低造膜温度を測定し、結果を衣−2に示し
た。(41 was obtained. These latex mixtures (++,
The minimum film forming temperature of <:+) was measured and the results are shown in Cloth-2.
これらのラテックスを120℃にて乾燥して得られたフ
ィルム全電子顕微鏡にて観察した。The films obtained by drying these latex at 120°C were observed using a total electron microscope.
これより、樹脂成分が連続相を形成していることが確認
された。This confirmed that the resin component formed a continuous phase.
(接着剤組成物の調製)
得られたラテックス混合物(i) 、 (ii)の各々
について、共M合体ラテックス(固形分)100部に対
し、酸化防止剤1部(スミライザーS;住友化学工業■
製)、増粘剤0.3部(アロンA7150;東亜会成化
学工業■製)および界面活性剤1部(エマール2EN;
花王石けん■製)を添加して、固形分47%、粘度20
00 cpsの接着剤組成物■、■を作成した。(Preparation of adhesive composition) For each of the obtained latex mixtures (i) and (ii), 1 part of antioxidant (Sumilyzer S; Sumitomo Chemical Co., Ltd.) was added to 100 parts of co-M combined latex (solid content).
), 0.3 part of thickener (Aron A7150; manufactured by Toa Kaisei Kagaku Kogyo ■), and 1 part of surfactant (Emar 2EN;
Kao Soap (manufactured by Kao Soap) is added to achieve a solid content of 47% and a viscosity of 20.
00 cps adhesive compositions (2) and (2) were prepared.
以下余白
表−2
(試験結果)
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、ポリプロピレンニード
ルパンチカーペットの裏面に150Pr/rn’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について、
成型性、保型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。Margin Table 2 below (Test results) Each of the obtained adhesive compositions ■ and ■ was foamed to 3 times the volume using a Hobart mixer, and applied to the back side of a polypropylene needle punch carpet at a coating amount of 150 Pr/rn'. and impregnated the inside. After that, 130℃
For carpet samples obtained by drying for 5 minutes at
Moldability, shape retention, and fiber adhesion were tested based on the following measurement methods.
結果を表−3に示す。The results are shown in Table-3.
熟成型性:カーベット試料’1130℃のオーブン中に
て5分間加熱し、凸凹状の金
型にてプレスして型付けを施した。Aging moldability: Carvette sample '11 was heated in an oven at 30° C. for 5 minutes and pressed with a convex-concave mold to form a mold.
この型付けした角度を測定し、次の 基準にて評価した。Measure this typed angle and Evaluation was made based on the criteria.
○:80度超(良好)
△エフ5度〜80度(不十分)
×ニア5度未満(苓ま)
保型性:上記成型性試験により成型したカーペット試料
を90℃のオーブン中に
24時間静置し、型付は部の角度を
測定した。この角度の変化を次の基
準にて評価した。○: Over 80 degrees (good) △F 5 degrees to 80 degrees (inadequate) The mold was left to stand and the angle of the part was measured. This change in angle was evaluated based on the following criteria.
O:10度未満(良好)
△:10度〜15度(不十分)
×:15度超 (木さ)
繊維固着カニカーペット試料の裏面を金属片にて摩擦し
、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。O: Less than 10 degrees (good) △: 10 to 15 degrees (inadequate) ×: More than 15 degrees (woodenness) Rub the back side of the fiber-fixed crab carpet sample with a metal piece to prevent the adhesive from falling off and the fibers from falling off. The degree of pilling was evaluated based on the following criteria.
○:接着剤の脱落なく、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
比較例
表−1に示した単量体組成にて、実施例と同様の操作を
行い共重合体ラテックスE、F’i得た。実施例と同様
操作を行いラテックス混合物(11)〜(V)を得た。○: No adhesive falling off, good pilling △: Some adhesive falling off, pilling slightly poor ×: A lot of adhesive falling off (powder falling), pilling poor Comparative example Monomer composition shown in Table-1 The same operations as in Examples were performed to obtain copolymer latexes E and F'i. Latex mixtures (11) to (V) were obtained by performing the same operation as in the example.
得られたラテックス混合物の最低造膜温度を測定し結果
を表−2に示す。ラテックス混合物a+++〜(Vlに
ついて実施例と同様にして電子顕微鏡観察をしたところ
、(11〕と(Vlは樹脂成分が連続相を形成し、0φ
は樹脂成分が連続相を形成していないことがわかった。The minimum film forming temperature of the obtained latex mixture was measured and the results are shown in Table 2. When the latex mixture a+++~(Vl was observed with an electron microscope in the same manner as in the example, it was found that (11) and (Vl) have a resin component forming a continuous phase and 0φ
It was found that the resin component did not form a continuous phase.
実施例と同様操作を行い、接着剤組成物0〜0表−3
〔本発明の効果〕
本発明にて得られる接着剤組成物は、自動車用カーペッ
トに必要な成型性、保型性ならびに繊維の固着力を同時
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。[Effects of the present invention] The adhesive composition obtained by the present invention has excellent moldability, shape retention, and fiber properties necessary for automobile carpets. At the same time, the adhesive composition of the present invention can omit the two-step process of backing with a thermoplastic resin film, simplifying the carpet manufacturing process and increasing productivity. It also has the effect of improvement.
Claims (1)
ン系共重合体ラテックス(B)の混合物であって、該混
合物が60℃以下の最低造膜温度を有し、かつ90℃以
上で乾燥した場合に樹脂成分が連続相となるように調整
してなる混合物を主要成分として用いることを特徴とす
るカーペット裏打ち用接着剤組成物。 2、ラテックス混合物が乾燥重量部換算値で、スチレン
系ラテックス(A)30〜90重量部およびスチレン−
ブタジエン系共重合体ラテックス(B)10〜70重量
部からなることを特徴とする特許請求の範囲第1項記載
のカーペット裏打ち用接着剤組成物。 3、ラテックス混合物が芳香族ビニル系単量体15〜9
6重量%、脂肪族共役ジエン系単量体2〜70重量%、
シアン化ビニル系単量体1〜35重量%、エチレン系不
飽和カルボン酸アルキルエステル単量体0.2〜30重
量%およびこれらと共重合可能な他の単量体0〜20重
量%からなり、かつ(A)または(B)のどちらか一方
のみにシアン化ビニル系単量体を含有することを特徴と
する特許請求の範囲第1項および第2項記載のカーペッ
ト裏打ち用接着剤組成物。[Claims] 1. A mixture of a styrene latex (A) and a styrene-butadiene copolymer latex (B), wherein the mixture has a minimum film forming temperature of 60°C or less, and 90°C An adhesive composition for carpet lining, characterized in that a mixture prepared by adjusting the resin component to form a continuous phase when dried is used as a main component. 2. The latex mixture contains 30 to 90 parts by weight of styrenic latex (A) and styrene based on dry weight parts.
2. The carpet lining adhesive composition according to claim 1, comprising 10 to 70 parts by weight of the butadiene copolymer latex (B). 3. The latex mixture contains aromatic vinyl monomers 15-9
6% by weight, 2 to 70% by weight of aliphatic conjugated diene monomer,
Consisting of 1 to 35% by weight of vinyl cyanide monomer, 0.2 to 30% by weight of ethylenically unsaturated carboxylic acid alkyl ester monomer, and 0 to 20% by weight of other monomers copolymerizable with these. , and contains a vinyl cyanide monomer only in either (A) or (B). .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62036606A JP2521743B2 (en) | 1987-02-19 | 1987-02-19 | Adhesive composition for carpet backing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62036606A JP2521743B2 (en) | 1987-02-19 | 1987-02-19 | Adhesive composition for carpet backing |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63205378A true JPS63205378A (en) | 1988-08-24 |
JP2521743B2 JP2521743B2 (en) | 1996-08-07 |
Family
ID=12474457
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62036606A Expired - Lifetime JP2521743B2 (en) | 1987-02-19 | 1987-02-19 | Adhesive composition for carpet backing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2521743B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02112485A (en) * | 1988-10-18 | 1990-04-25 | Japan Synthetic Rubber Co Ltd | Adhesive for baking of carpet |
JPH03182582A (en) * | 1989-12-12 | 1991-08-08 | Sumitomo Naugatuck Co Ltd | Thermoformable adhesive composition |
JP2002194671A (en) * | 2000-12-21 | 2002-07-10 | Kanegafuchi Chem Ind Co Ltd | Method for preventing dropping off of fiber from napped fiber product |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54131095A (en) * | 1978-03-29 | 1979-10-11 | Nippon Ratetsukusu Kakou Kk | Carpet backing agent with heat moldability and adhesivility |
-
1987
- 1987-02-19 JP JP62036606A patent/JP2521743B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54131095A (en) * | 1978-03-29 | 1979-10-11 | Nippon Ratetsukusu Kakou Kk | Carpet backing agent with heat moldability and adhesivility |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02112485A (en) * | 1988-10-18 | 1990-04-25 | Japan Synthetic Rubber Co Ltd | Adhesive for baking of carpet |
JPH03182582A (en) * | 1989-12-12 | 1991-08-08 | Sumitomo Naugatuck Co Ltd | Thermoformable adhesive composition |
JP2002194671A (en) * | 2000-12-21 | 2002-07-10 | Kanegafuchi Chem Ind Co Ltd | Method for preventing dropping off of fiber from napped fiber product |
Also Published As
Publication number | Publication date |
---|---|
JP2521743B2 (en) | 1996-08-07 |
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