JPH0726327B2 - Adhesive composition for carpet backing - Google Patents
Adhesive composition for carpet backingInfo
- Publication number
- JPH0726327B2 JPH0726327B2 JP63156350A JP15635088A JPH0726327B2 JP H0726327 B2 JPH0726327 B2 JP H0726327B2 JP 63156350 A JP63156350 A JP 63156350A JP 15635088 A JP15635088 A JP 15635088A JP H0726327 B2 JPH0726327 B2 JP H0726327B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- carpet
- adhesive composition
- parts
- monomer
- 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
- 239000000203 mixture Substances 0.000 title claims description 28
- 239000000853 adhesive Substances 0.000 title claims description 27
- 230000001070 adhesive effect Effects 0.000 title claims description 27
- 239000004816 latex Substances 0.000 claims description 22
- 229920000126 latex Polymers 0.000 claims description 22
- 239000000178 monomer Substances 0.000 claims description 22
- 229920001577 copolymer Polymers 0.000 claims description 19
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 12
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 8
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 claims description 6
- 229920002554 vinyl polymer Polymers 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims 1
- 239000000835 fiber Substances 0.000 description 14
- 230000014759 maintenance of location Effects 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 238000003672 processing method Methods 0.000 description 8
- 238000000465 moulding Methods 0.000 description 7
- 229920005992 thermoplastic resin Polymers 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-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 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-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
- 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
- 239000000839 emulsion Substances 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 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
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 238000003856 thermoforming Methods 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
- JNPCNDJVEUEFBO-UHFFFAOYSA-N 1-butylpyrrole-2,5-dione Chemical compound CCCCN1C(=O)C=CC1=O JNPCNDJVEUEFBO-UHFFFAOYSA-N 0.000 description 1
- BQTPKSBXMONSJI-UHFFFAOYSA-N 1-cyclohexylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1CCCCC1 BQTPKSBXMONSJI-UHFFFAOYSA-N 0.000 description 1
- SJLLJZNSZJHXQN-UHFFFAOYSA-N 1-dodecylpyrrole-2,5-dione Chemical compound CCCCCCCCCCCCN1C(=O)C=CC1=O SJLLJZNSZJHXQN-UHFFFAOYSA-N 0.000 description 1
- FBPVUBVZRPURIU-UHFFFAOYSA-N 1-hexylpyrrole-2,5-dione Chemical compound CCCCCCN1C(=O)C=CC1=O FBPVUBVZRPURIU-UHFFFAOYSA-N 0.000 description 1
- KIKBJYQCJJXCBZ-UHFFFAOYSA-N 1-octylpyrrole-2,5-dione Chemical compound CCCCCCCCN1C(=O)C=CC1=O KIKBJYQCJJXCBZ-UHFFFAOYSA-N 0.000 description 1
- NQDOCLXQTQYUDH-UHFFFAOYSA-N 1-propan-2-ylpyrrole-2,5-dione Chemical compound CC(C)N1C(=O)C=CC1=O NQDOCLXQTQYUDH-UHFFFAOYSA-N 0.000 description 1
- 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
- CYLVUSZHVURAOY-UHFFFAOYSA-N 2,2-dibromoethenylbenzene Chemical compound BrC(Br)=CC1=CC=CC=C1 CYLVUSZHVURAOY-UHFFFAOYSA-N 0.000 description 1
- CISIJYCKDJSTMX-UHFFFAOYSA-N 2,2-dichloroethenylbenzene Chemical compound ClC(Cl)=CC1=CC=CC=C1 CISIJYCKDJSTMX-UHFFFAOYSA-N 0.000 description 1
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- GHAZCVNUKKZTLG-UHFFFAOYSA-N N-ethyl-succinimide Natural products CCN1C(=O)CCC1=O GHAZCVNUKKZTLG-UHFFFAOYSA-N 0.000 description 1
- HDFGOPSGAURCEO-UHFFFAOYSA-N N-ethylmaleimide Chemical compound CCN1C(=O)C=CC1=O HDFGOPSGAURCEO-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- YMOONIIMQBGTDU-VOTSOKGWSA-N [(e)-2-bromoethenyl]benzene Chemical compound Br\C=C\C1=CC=CC=C1 YMOONIIMQBGTDU-VOTSOKGWSA-N 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
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000007598 dipping method Methods 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
- 238000001035 drying Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 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
- 238000005470 impregnation Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- SEEYREPSKCQBBF-UHFFFAOYSA-N n-methylmaleimide Chemical compound CN1C(=O)C=CC1=O SEEYREPSKCQBBF-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Passenger Equipment (AREA)
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。TECHNICAL FIELD The present invention relates to an adhesive composition for lining a carpet used as an interior material for automobiles.
〔従来の技術〕 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、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。[Prior Art] Needle-punched carpets and tufted carpets for automobile interiors are manufactured by applying an adhesive composition containing styrene-butadiene copolymer latex or ethylene-vinyl acetate resin emulsion as a main component to the back surface of the carpet or After impregnation, it is manufactured by a two-step processing method in which a thermoplastic resin film such as polyethylene is lined 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 by press molding at the time of heating according to the shape of the floor of the automobile, and then incorporated into the automobile.
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-step processing method, a so-called one-step processing method is disclosed in Japanese Patent Laid-Open No. 53-52776, in which an aqueous plastic dispersion is applied to the back surface of a carpet to obtain a continuously moldable carpet. ing.
〔発明が解決しようとする問題点〕 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。[Problems to be Solved by the Invention] In the conventional two-step processing method, the nonwoven 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. Further, the carpet is provided with thermoformability by backing a film of a thermoplastic resin, 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、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まうという問
題があった。On the other hand, in the one-step processing method for imparting thermoformability to the adhesive without backing the thermoplastic resin film, the thermoformability and the ability to maintain its shape (called shape retention) ) Is not sufficient, and there is a problem that if the thermoformability and the shape-retaining property are to be improved, the fixing force of the fiber is lowered.
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段加工可能な裏打ち接着剤組成物の開
発が望まれていた。Therefore, it has been desired to develop a backing adhesive composition that can be processed in one step and 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
可能な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、
特定の組成から成る共重合体ラテックス(A)および
(B)をある特定の比率にて混合して得られる混合物を
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優れだ効果を発現すると
いう事実を見い出し、本発明を完成するに至った。In order to solve such a problem, the inventors of the present invention have conducted earnest research on a one-step processable adhesive composition for carpet backing, and as a result, have been proposed in Japanese Patent Laid-Open No. 53-52776. Rather than using known aqueous plastic dispersions and mixtures of such dispersions as backing adhesives,
When a mixture obtained by mixing the copolymer latexes (A) and (B) having a specific composition in a specific ratio is used as an adhesive for lining, thermoformability, shape retention and fiber The present invention has been completed by discovering the fact that an excellent effect is exhibited in all aspects of the fixing force.
すなわち、本発明は、マレイミド系単量体3〜70重量
%、芳香族ビニル系単量体30〜97重量%およびこれらと
共重合可能な他の単量体0〜67重量%から構成される共
重合体ラテックス(A)30〜70重量部(固形分重量換算
値)とブタジエン10〜90重量%、スチレン10〜90重量%
およびこれらと共重合可能な他の単量体0〜80重量%か
ら構成される共重合体ラテックス(B)70〜30重量部
(固形分重量換算値)の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を提
供するものである。That is, the present invention comprises 3 to 70% by weight of a maleimide monomer, 30 to 97% by weight of an aromatic vinyl monomer, and 0 to 67% by weight of another monomer copolymerizable therewith. Copolymer latex (A) 30 to 70 parts by weight (solid weight conversion value), butadiene 10 to 90% by weight, styrene 10 to 90% by weight
And a mixture of 70 to 30 parts by weight of a copolymer latex (B) composed of 0 to 80% by weight of another monomer copolymerizable therewith (solid content weight conversion value) as a main component. An adhesive composition for carpet backing 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の裏面に塗布または含浸させる
ことにより、優れた熱成型性および保型性を有し、かつ
繊維の固着力に優れた自動車用カーペットを容易に得る
ことができる。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を必須としないことか
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。By coating or impregnating the adhesive composition of the present invention on the back surface of a needle punched carpet or a tufted carpet, an automobile carpet having excellent thermoformability and shape-retaining property and excellent fiber adhesion is obtained. Can be easily obtained. Further, unlike the above-described two-step processing method, the present invention does not require backing 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.
共重合体ラテックス(A) 本発明にて用いられる共重合体ラテックス(A)は、マ
レイミド系単量体3〜70重量%、芳香族ビニル系単量体
30〜97重量%およびこれらと共重合可能な他の単量体0
〜67重量%から構成される。Copolymer Latex (A) The copolymer latex (A) used in the present invention is a maleimide monomer 3 to 70% by weight, an aromatic vinyl monomer.
30-97% by weight and other monomers copolymerizable therewith
It consists of ~ 67% by weight.
マレイミド系単量体が3重量%未満あるいは70重量%を
超えると保型性が劣る。芳香族ビニル系単量体が30重量
%未満あるいは97重量%を超えると保型性が劣る。If the maleimide-based monomer is less than 3% by weight or more than 70% by weight, the shape retention is poor. If the amount of the aromatic vinyl-based monomer is less than 30% by weight or exceeds 97% by weight, the shape retention is poor.
マレイミド系単量体としては、マレイミド、N−メチル
マレイミド、N−エチルマレイミド、N−イソプロピル
マレイミド、N−ブチルマレイミド、N−ヘキシルマレ
イミド、N−オクチルマレイミド、N−ラウリルマレイ
ミド、N−シクロヘキシルマレイミド、N−フェニルマ
レイミド等が挙げられ、1種又は2種以上用いることが
できる。特にN−フェニルマレイミドが好ましい。As the maleimide-based monomer, maleimide, N-methylmaleimide, N-ethylmaleimide, N-isopropylmaleimide, N-butylmaleimide, N-hexylmaleimide, N-octylmaleimide, N-laurylmaleimide, N-cyclohexylmaleimide, N-phenylmaleimide and the like can be mentioned, and one kind or two or more kinds can be used. N-phenylmaleimide is particularly preferable.
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、クロロスチレン、ジクロロスチレン、ブロモ
スチレン、ジブロモスチレン等が挙げられ、1種又は2
種以上用いることができる。特にスチレン、α−メチル
スチレンが好ましい。Examples of the aromatic vinyl-based monomer include styrene, α-methylstyrene, chlorostyrene, dichlorostyrene, bromostyrene, dibromostyrene, and the like.
More than one species can be used. Particularly, styrene and α-methylstyrene are preferable.
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、メチルメタクリレー
ト、β−ヒドロキシメチルメタクリレート、アクリロニ
トリル、アクリルアミド等が挙げられ、1種又は2種以
上用いることができる。共重合体ラテックス(A)の粒
子径は50〜300nmが好ましく、50〜150nmであることが更
に好ましい。Examples of other copolymerizable monomers include acrylic acid, methacrylic acid, itaconic acid, fumaric acid, methyl methacrylate, β-hydroxymethyl methacrylate, acrylonitrile, acrylamide, etc., and one or more types may be used. it can. The particle size of the copolymer latex (A) is preferably 50 to 300 nm, more preferably 50 to 150 nm.
共重合体ラテックス(B) 本発明にて用いられる共重合体ラテックス(B)は、ブ
タジエン10〜90重量%、スチレン10〜90重量%およびこ
れらと共重合可能な他の単量体0〜80重量%から構成さ
れる。Copolymer Latex (B) The copolymer latex (B) used in the present invention comprises 10 to 90% by weight of butadiene, 10 to 90% by weight of styrene, and 0 to 80% of another monomer copolymerizable therewith. Composed of weight percent.
ブタジエンが10重量%未満では繊維の固着力が劣り、90
重量%を超えると、成型性が劣る。スチレンが10重量%
未満では成型性が劣り、90重量%を超えると繊維の固着
力が劣る。If the butadiene content is less than 10% by weight, the fiber adhesion will be poor and 90
When it exceeds the weight%, the moldability is deteriorated. 10% by weight of styrene
If it is less than 90% by weight, the moldability is poor, and if it exceeds 90% by weight, the fixing strength of the fiber is poor.
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、フマル酸、イタコン酸、メチルメタクリレー
ト、ブチルアクリレート、アクリロニトリル、アクリル
アミド、β−ヒドロキシエチルアクリレート、α−メチ
ルスチレン等が挙げられる。Examples of other copolymerizable monomers include acrylic acid, methacrylic acid, fumaric acid, itaconic acid, methyl methacrylate, butyl acrylate, acrylonitrile, acrylamide, β-hydroxyethyl acrylate, and α-methylstyrene.
共重合体ラテックス(B)の粒子径は50〜300nmである
ことが好ましく、50〜150nmであることが更に好しい。The particle size of the copolymer latex (B) is preferably 50 to 300 nm, more preferably 50 to 150 nm.
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、共重合体ラ
テックス(A)30〜70重量部(固形分重量換算値)およ
び共重合体ラテックス(B)70〜30重量部(固形分重量
換算値)からなる。(A)が30重量部未満では、成型
性、保型性が劣り、70重量部を超えると繊維の固着力が
劣る。(B)が70重量部を超えると成型性、保型性が劣
り、30重量部未満では繊維の固着力が劣る。Latex Mixture The latex mixture used in the present invention is a copolymer latex (A) 30 to 70 parts by weight (solid content weight conversion value) and a copolymer latex (B) 70 to 30 parts by weight (solid content weight conversion value). ) Consists of. When (A) is less than 30 parts by weight, moldability and shape retention are inferior, and when it exceeds 70 parts by weight, the fiber fixing force is inferior. If (B) exceeds 70 parts by weight, moldability and shape retention are inferior, and if it is less than 30 parts by weight, the fiber fixing force is inferior.
本発明の共重合体ラテックス(A)および(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、二段重合方法、パワーフィ
ード方法などが適用できる。The copolymer latexes (A) and (B) of the present invention are produced by a known method. That is, a batch addition method, a divided addition method, a continuous addition method, a two-stage polymerization method, a power feed method and the like 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、架橋剤などを適宜含むことが
できる。The adhesive composition of the present invention may appropriately contain an antioxidant, a filler, a flame retardant, a thickener, a surfactant, a crosslinking agent 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等が挙げられ、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 needle punched carpets and tufted carpets using fibers such as polypropylene, polyester, nylon, acrylic and wool, and for automobiles that require a heat molding step. Applies to carpets and interior materials.
本発明の接着剤組成物を塗布または含浸する方法として
は、接着剤を発泡あるいは増粘して用いてもよく、加工
方法としては、リックロール、絞りロール、吹付けガ
ン、浸漬等が挙げられる。また、カーペットへの含浸を
完全にするためには、塗布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
可能なカーペットが得られる。As a method for applying or impregnating the adhesive composition of the present invention, an adhesive may be foamed or thickened and used, and as a processing method, a lick roll, a squeezing roll, a spray gun, dipping and the like can be mentioned. . Further, in order to completely impregnate the carpet, it is preferable to squeeze the applied adhesive composition with a squeezing roll. After coating or impregnating the adhesive composition, the moisture is removed by heating to obtain a moldable carpet.
カーペットを成型する方法としては、カーペットを加熱
し、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。Examples of the method for molding the carpet include a method of heating the carpet and molding it with a pressure roll or a press molding machine.
本発明の接着剤組成物を用いて得られた自動車用カーペ
ットおよび内装材は、必要に応じて更に、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こと
も可能である。The carpet and interior materials for automobiles obtained by using the adhesive composition of the present invention may further be lined with a thermoplastic resin film such as polyethylene by heat fusion if necessary.
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。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。EXAMPLES Hereinafter, the present invention will be described specifically with reference to Examples.
The present invention is in no way limited by these examples. All parts and% in the examples mean parts by weight and% by weight, unless otherwise specified.
<共重合体ラテックス(A)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t−ドデシルメルカプタン0.2部を
加え乳化させる。<Preparation of copolymer latex (A)> To 100 parts of water, 1.5 parts of sodium dodecylbenzenesulfonate is added and dissolved. The monomer mixture shown in Table 1 is added thereto, and 0.2 part of t-dodecyl mercaptan is further added to emulsify.
次いで過硫酸カリウム0.5部を加え、全体を60℃に保ち
乳化重合を行った。単量体の転化率が97%に達した時点
で重合を停止した。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、共重合体ラテックスA−1〜3
およびA−i、iiを得た。Next, 0.5 part of potassium persulfate was added, and the whole was kept at 60 ° C. to carry out emulsion polymerization. The polymerization was stopped when the conversion of the monomers reached 97%. The unreacted monomer in the obtained latex was removed under reduced pressure to obtain copolymer latex A-1 to 3
And A-i and ii were obtained.
<共重合ラテックス(B)の調製> 表−2に示す量の単量体混合物を使用した以外は共重合
体ラテックス(A)と同様の操作を行い、共重合体ラテ
ックスB−1〜3およびB−i、iiを得た。 <Preparation of Copolymer Latex (B)> The same operations as those for the copolymer latex (A) were performed except that the amounts of the monomer mixtures shown in Table 2 were used, and copolymer latexes B-1 to 3 and B-i and ii were obtained.
実施例1〜3および比較例1〜6 表−3に示すラテックス混合物100部(固形分)に対
し、酸化防止剤(スミライザーS;住友化学工業(株)
製)1部および界面活性剤(エマール2FN;花王石けん
(株)製)1部を添加して、固形分47%の接着剤組成物
を得た。 Examples 1 to 3 and Comparative Examples 1 to 6 With respect to 100 parts (solid content) of the latex mixture shown in Table 3, an antioxidant (SUMILIZER S; Sumitomo Chemical Co., Ltd.)
1 part) and a surfactant (Emar 2FN; manufactured by Kao Soap Co., Ltd.) 1 part were added to obtain an adhesive composition having a solid content of 47%.
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150g/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。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 blended needle punch carpet at a coating amount of 150 g / m 2 , and was impregnated to the inside. After that, 130 ℃
The carpet sample obtained by drying for 5 minutes at
Moldability, shape retention and fiber fixing force were tested based on the following measuring methods.
結果を表−3に示す。The results are shown in Table-3.
熱成型性;カーペット試料を180℃のオーブン中にて5
分間加熱した後、第1図に示す凹凸の金型(A部:90
度)にてプレス成形(1分間)して型付けを施した。こ
の成形品を金型より取り出し、第2図に示すA′部の角
度を測定し、次の基準にて評価した。Thermoformability; Carpet sample in oven at 180 ° C for 5
After heating for a minute, the uneven mold shown in Fig. 1 (A part: 90
And press molding (for 1 minute). This molded product was taken out of the mold and the angle of the A'section shown in FIG. 2 was measured and evaluated according to the following criteria.
○:80度超(良好) △:75〜80度(不十分) ×:75度未満(不良) 保型性;熱成型性評価後、成形品を再度90℃のオーブン
中にて24時間静置。○: More than 80 degrees (good) △: 75 to 80 degrees (insufficient) ×: Less than 75 degrees (poor) Shape retention: After evaluation of thermoformability, the molded product is again stored in an oven at 90 ° C for 24 hours Place
その後オーブンより取り出し第3図に示すA″の角度を
測定した。この角度の変化(A′−A″)を次の基準に
て評価した。After that, it was taken out from the oven and the angle A ″ shown in FIG. 3 was measured. The change in this angle (A′−A ″) was evaluated according to the following criteria.
○:10度未満(良好) △:10〜15度(不十分) ×:15度超(不良) 繊維固着力;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。○: less than 10 degrees (good) △: 10 to 15 degrees (insufficient) ×: more than 15 degrees (poor) Fiber fixing force; rubbing the back side of the carpet sample with a metal piece, dropping off the adhesive and pilling the fiber Was evaluated based on the following criteria.
○:接着剤の脱落がない、又はピリング良好 △:接着剤の脱落が少し有り、又はピリングやや不良 ×:接着剤の脱落(粉落ち)が多い、又はピリング不良 〔本発明の効果〕 本発明にて得られる接着剤組成物は、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。◯: Adhesive did not fall off or pilling was good. Δ: Adhesive fell off a little or pilling was slightly poor. X: Adhesive was dropped off (powder drop) or pilling was bad. [Effects of the present invention] The adhesive composition obtained in the present invention can simultaneously exhibit the moldability, shape retention property, and fiber fixing force required for automobile carpets, and the adhesive composition of the present invention. The product can omit the step of the two-step processing technology of lining the thermoplastic resin film, and also has the effects of simplifying the carpet manufacturing process and improving productivity.
第1図は型付け金型の断面図、第2図は熱成型後のカー
ペットの断面図ならびに第3図は熱成型後のカーペット
を90℃のオーブン中にて24時間静置後のカーペットの断
面図を示す。 イ……金型 ロ……カーペット A……型付け時の角度(90度) A′……熱成型後の角度 A″……90℃オーブン中にて24時間静置後の角度Fig. 1 is a cross-sectional view of the molding die, Fig. 2 is a cross-sectional view of the carpet after thermoforming, and Fig. 3 is a cross-section of the carpet after leaving the thermoformed carpet in an oven at 90 ° C for 24 hours. The figure is shown. B mold ... B carpet A ... angle when mold is attached (90 degrees) A '... angle after thermoforming A''... angle after standing in oven at 90 ° C for 24 hours
───────────────────────────────────────────────────── 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 15/285 15/693 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display location D06M 15/285 15/693
Claims (1)
ビニル系単量体30〜97重量%およびこれらと共重合可能
な他の単量体0〜67重量%から構成される共重合体ラテ
ックス(A)30〜70重量部(固形分重量換算値)とブタ
ジエン10〜90重量%、スチレン10〜90重量%およびこれ
らと共重合可能な他の単量体0〜80重量%から構成され
る共重合体ラテックス(B)70〜30重量部(固形分重量
換算値)の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。1. A copolymer composed of 3 to 70% by weight of a maleimide monomer, 30 to 97% by weight of an aromatic vinyl monomer, and 0 to 67% by weight of another monomer copolymerizable therewith. From 30 to 70 parts by weight of the polymer latex (A) (solid content weight value), 10 to 90% by weight of butadiene, 10 to 90% by weight of styrene, and 0 to 80% by weight of other monomer copolymerizable therewith An adhesive composition for carpet backing, characterized in that a mixture of 70 to 30 parts by weight (converted to a solid content) of the copolymer latex (B) is used as a main component.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63156350A JPH0726327B2 (en) | 1988-06-24 | 1988-06-24 | Adhesive composition for carpet backing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63156350A JPH0726327B2 (en) | 1988-06-24 | 1988-06-24 | Adhesive composition for carpet backing |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH026668A JPH026668A (en) | 1990-01-10 |
| JPH0726327B2 true JPH0726327B2 (en) | 1995-03-22 |
Family
ID=15625837
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63156350A Expired - Fee Related JPH0726327B2 (en) | 1988-06-24 | 1988-06-24 | Adhesive composition for carpet backing |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0726327B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2591105B2 (en) * | 1988-10-18 | 1997-03-19 | 日本合成ゴム株式会社 | Carpet backing adhesive |
| US5378511A (en) * | 1993-03-22 | 1995-01-03 | International Business Machines Corporation | Material-saving resist spinner and process |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4568722A (en) * | 1984-04-20 | 1986-02-04 | Atlantic Richfield Company | Polymer compositions containing styrene/cyanostyrene copolymers |
| JPH0828190B2 (en) * | 1986-08-12 | 1996-03-21 | ソニー株式会社 | Ion beam device |
-
1988
- 1988-06-24 JP JP63156350A patent/JPH0726327B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH026668A (en) | 1990-01-10 |
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