JPH026668A - Adhesive composition for carpet backing - Google Patents
Adhesive composition for carpet backingInfo
- Publication number
- JPH026668A JPH026668A JP15635088A JP15635088A JPH026668A JP H026668 A JPH026668 A JP H026668A JP 15635088 A JP15635088 A JP 15635088A JP 15635088 A JP15635088 A JP 15635088A JP H026668 A JPH026668 A JP H026668A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- copolymer latex
- carpet
- adhesive composition
- styrene
- 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 30
- 239000000853 adhesive Substances 0.000 title claims abstract description 27
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 27
- 239000004816 latex Substances 0.000 claims abstract description 26
- 229920000126 latex Polymers 0.000 claims abstract description 26
- 239000000178 monomer Substances 0.000 claims abstract description 24
- 229920001577 copolymer Polymers 0.000 claims abstract description 21
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 15
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000007787 solid Substances 0.000 claims abstract description 9
- 239000000835 fiber Substances 0.000 abstract description 13
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 abstract description 7
- 229920002554 vinyl polymer Polymers 0.000 abstract description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 4
- -1 polypropylene Polymers 0.000 abstract description 4
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 abstract description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract description 3
- 239000004743 Polypropylene Substances 0.000 abstract description 3
- 229920000728 polyester Polymers 0.000 abstract description 3
- 229920001155 polypropylene Polymers 0.000 abstract description 3
- 230000014759 maintenance of location Effects 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 238000003672 processing method Methods 0.000 description 7
- 238000000465 moulding Methods 0.000 description 6
- 229920005992 thermoplastic resin Polymers 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
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 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
- 230000032683 aging Effects 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
- 239000001530 fumaric acid Substances 0.000 description 2
- 239000000463 material Substances 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
- SEEYREPSKCQBBF-UHFFFAOYSA-N n-methylmaleimide Chemical compound CN1C(=O)C=CC1=O SEEYREPSKCQBBF-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
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 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
- CISIJYCKDJSTMX-UHFFFAOYSA-N 2,2-dichloroethenylbenzene Chemical compound ClC(Cl)=CC1=CC=CC=C1 CISIJYCKDJSTMX-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
- 241000252233 Cyprinus carpio Species 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
- 239000004698 Polyethylene 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
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 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
- 239000000839 emulsion Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000005516 engineering process 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
- 238000000691 measurement method Methods 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229920000573 polyethylene 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
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Landscapes
- Passenger Equipment (AREA)
- Compositions Of Macromolecular Compounds (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.
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。It is molded using press molding to match the shape of the car's floor, and then installed 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58−52776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-58-52776, 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r2 )
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
ーぺ、1・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, nonwoven fibers or pile yarns are fixed by coating or impregnating with an adhesive consisting of a styrene-butadiene copolymer latex or a water-based emulsion of a resin, and then a thermoplastic resin film is applied. However, 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まうという問
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 an attempt is made to improve this thermoformability and shape retention, there is a problem in that the adhesion of the fibers decreases.
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 is excellent in all aspects of thermoformability, shape retention, and fiber adhesion and that can be processed in one step.
本発明者らは、かかる問題点を解決するため、1段加工
可能なカーベン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53−5277
6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■および
(均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。In order to solve these problems, the present inventors conducted intensive research on an adhesive composition for car vent lining that can be processed in one step, and found that
Rather than using a known aqueous plastic dispersion and a mixture of the dispersion as a backing adhesive as proposed in No. 6, a copolymer latex consisting of a specific composition and a mixture of The present invention was completed based on the discovery that when the resulting mixture is used as a backing adhesive, it exhibits excellent effects in all aspects of thermoformability, shape retention, and fiber adhesion. It's arrived.
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式30〜フ0重量部(固形分重
量換算値)とブタジェン10〜90重量%、スチレン1
0〜90重里%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(均
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 is 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 with these monomers. Copolymer latex formula: 30-0 parts by weight (solid content weight equivalent), 10-90% by weight of butadiene, 1 part by weight of styrene
Copolymer latex composed of 0 to 90% by weight and 0 to 80% by weight of other monomers copolymerizable with these (70 to 30 parts by weight (solid content equivalent) as the main component) The present invention provides an adhesive composition for use in carpet backing.
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ち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 applying or impregnating the adhesive composition of the present invention on the back side of a needle-punched carpet or tufted carpet, an automobile carpet with excellent thermoformability and shape retention, and excellent fiber adhesion strength can be obtained. can be obtained easily. Furthermore, unlike the two-stage processing method described above, the present invention does not require backing with a thermoplastic resin film, and is therefore excellent in 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共重合体ラテックス■
本発明にて用いられる共重合体ラテックス式は、マレイ
ミド系単量体3〜70重量%、芳香族ビニル系単量体3
0〜97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。0 copolymer latex■ The copolymer latex formula used in the present invention contains 3 to 70% by weight of maleimide monomer, 3% by weight of aromatic vinyl monomer.
It is composed of 0 to 97% by weight and 0 to 67% by weight of other monomers copolymerizable with these.
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。芳香族ビ一ル系単量体が30
重量%未満あるいは97重量%を超えると保型性が劣る
。Maleimide monomer content is less than 3% by weight or 70% by weight
If it exceeds , the shape retention will be poor. Aromatic vinyl monomer is 30
If it is less than 97% by weight or more than 97% by weight, shape retention will be 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−メチルマレイミド、N−へキシルマレ
イミド、N−オクチルマレイミド、N−ラウリルマレイ
ミド、Nシクロへキシルマレイミド、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。Maleimide monomers include maleimide, N-methylmaleimide, N-ethylmaleimide, N-isopropylmaleimide, N-methylmaleimide, N-hexylmaleimide, N-octylmaleimide, N-laurylmaleimide, N-cyclohexyl Examples include maleimide and N-phenylmaleimide, and one or more types can be used. Particularly preferred is N-phenylmaleimide.
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、ジプ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 monomer include styrene, α-methylstyrene, chlorostyrene, dichlorostyrene, bromostyrene, dipromostyrene, etc.
More than one species can be used. Particularly preferred are styrene and α-methylstyrene.
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フリレート、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への粒子径は
5Q−−3(lQnmが好しく、50〜150nmであ
ることが更に好しい。Other monomers that can be copolymerized include acrylic acid, methacrylic acid, itaconic acid, fumaric acid, methyl methacrylate, β-hydroxymethyl methacrylate, acrylonitrile, acrylamide, etc., and one or more of them may be used. be able to. The particle size of the copolymer latex is preferably 5Q-3 (1Q nm, more preferably 50 to 150 nm).
0共重合体ラテックスの)
本発明にて用いられる共重合体ラテックス(B)は、ブ
タジェン10〜90M量%、スチレン10〜90M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。0 copolymer latex) The copolymer latex (B) used in the present invention contains 10 to 90 M% of butadiene and 10 to 90 M% of styrene.
and other monomers copolymerizable with these 0 to 80% by weight
It consists of
ブタジェンが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 adhesion of the fiber will be poor;
If it exceeds 90% by weight, moldability will be poor. Styrene is 10
If it is less than 90% by weight, the moldability will be poor, and if it exceeds 90% by weight, the adhesion of the fibers will be 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。Other copolymerizable monomers include acrylic acid, methacrylic acid, fumaric acid, itaconic acid, methyl methacrylate, butyl acrylate, acrylonitrile, acrylamide, β-hydroxyethyl acrylate, α-methylstyrene, and the like.
共重合体ラテックス(13)の粒子径は50〜3o。The particle size of the copolymer latex (13) is 50 to 3o.
nmであることが好しく、50〜1501mであること
が更に好しい。It is preferably nm, and more preferably 50 to 1501 m.
0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
テックス式30〜フ0重量部(固形分重量換算値)およ
び共重合体ラテックス(13)70〜30重量部(固形
分重量換算値)からなる。0 latex mixture The latex mixture used in the present invention consists of copolymer latex formula 30 to 0 parts by weight (solid content weight equivalent) and copolymer latex (13) 70 to 30 parts by weight (solid content weight equivalent). ).
八が30%量部未満では、成型性、保型性が劣り、70
重量部を超えるとm維の固着力が劣る。If 8 is less than 30% by weight, moldability and shape retention will be poor, and 70%
If the amount exceeds the weight part, the fixing strength of the m-fibers will be poor.
(均が70重量部を超えると成型性、保型性が劣り、3
0重量部未満では繊維の固着力が劣る。(If the average weight exceeds 70 parts by weight, moldability and shape retention will be poor;
If the amount is less than 0 parts by weight, the adhesion of the fibers will be poor.
本発明の共重合体ラテックス■および0は、公知の方法
により製造される。すなわち−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。Copolymer latexes (1) and (0) of the present invention are produced by known methods. That is, a batch addition method, a divided addition method, a continuous addition method, a two-stage polymerization 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、架橋剤などを適宜含むことが
できる。The adhesive composition of the present invention can 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ラトとしては
、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 punch carpets and tufted carpets using fibers such as polypropylene, polyester, nylon, acrylic, wool, etc., and automotive carpets that require a heat molding process. Applies to carpets and upholstery.
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、吹付はガン
、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, the adhesive may be foamed or thickened, and processing methods include rick roll, squeezing roll, spraying with a gun, dipping, etc. . Further, in order to completely impregnate the carpet, it is preferable to squeeze the applied adhesive composition using a squeezing roll. After applying or impregnating the adhesive composition, 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 heating the carpet and molding it using 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。Carpets and interior materials for automobiles obtained using the adhesive composition of the present invention can be further lined with a thermoplastic resin film such as polyethylene by thermal 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 The present invention will be specifically explained with reference to Examples below.
The present invention is not limited in any way by these Examples. Note that 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への調製〉
水xoo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 to copolymer latex> Add 1.0 parts of sodium dodecylbenzenesulfonate to x0 parts of water.
Add 5 parts and dissolve. To this was added the monomer mixture shown in Table 1, and further added 0.2 t of dodecyl mercaptan.
and emulsify.
次いで過硫酸カリウム0.5部を加え、全体を60°C
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、;iを得た。Next, 0.5 part of potassium persulfate was added and the whole was heated to 60°C.
Emulsion polymerization was carried out while maintaining the temperature. Polymerization was stopped when the monomer conversion rate reached 97%. Unreacted monomers in the obtained latex were removed under reduced pressure to form copolymer latex A.
-1 to 3 and A-i, ;i were obtained.
表−1
〈共重合体ラテツクス(Bl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
体ラテックス八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−1、を得た。Table 1 <Preparation of copolymer latex (Bl)> Copolymer latex B-1 to B-3 were prepared in the same manner as for copolymer latex 8 except that the monomer mixture in the amount shown in Table 2 was used. and B-1 were obtained.
表−2
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。Table 2 Examples 1 to 3 and Comparative Examples 1 to 6 Antioxidant (Sumilizer S; Sumitomo Chemical Co., Ltd.) was added to 100 parts (solid content) of the latex mixture shown in Table 3.
(manufactured by Kao Soap Co., Ltd.) and 1 part of a surfactant (EMAL 2FN; manufactured by Kao Soap Co., Ltd.) were added to obtain an adhesive composition with 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
ル混紡二一ドルパンチカーペソトの裏面に150 (/
/m’の塗布量にて塗布し、内部まで含浸させた。その
後、130°C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 resulting adhesive compositions was whipped to 3 times its volume in a Hobart mixer and applied to the back of a polypropylene/polyester blended 21-dollar punch carpe bag.
/m' coating amount to impregnate the inside. Thereafter, the carpet samples obtained by drying at 130°C for 5 minutes were tested for moldability, shape retention, and fiber fixation strength 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;カーペット試料を180°Cのオーブン中に
て5分間加熱した後、第1図に示す凹凸状の金型(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。Aging moldability: After heating the carpet sample in an oven at 180°C for 5 minutes, it was press-molded (for 1 minute) in a concavo-convex mold (part A: 90°) as shown in Figure 1 for molding. provided. This molded product is taken out from the mold and A' shown in Fig. 2 is
The angle of the part was measured and evaluated based on the following criteria.
○:80度超(良好)
△ニア5〜80度(不十分)
Xニア5度未満(不良)
保型性;熱成型性評価後、成形品を再度90°Cのオー
ブン中にて24時間静置。○: More than 80 degrees (good) △Near 5 to 80 degrees (inadequate) Leave still.
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(AA)を次の基準にて評価し
た。Thereafter, it was taken out of the oven and the angle A shown in FIG. 3 was measured. The change in angle (AA) was evaluated based on the following criteria.
O:10度未満(良好)
△:10〜15度(不十分)
×:15度良好不良)
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。O: Less than 10 degrees (good) △: 10 to 15 degrees (inadequate) ×: 15 degrees (good) The degree of damage was evaluated based on the following criteria.
Q: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
4゜
〔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。Q: No adhesive falling off, or good pilling △: Slight adhesive falling off, or slightly poor pilling ×: Much adhesive falling off (powder falling), or poor pilling 4° [Effects of the present invention] The adhesive composition obtained in the present invention can simultaneously exhibit the moldability, shape retention, and fiber fixing strength required for automobile carpets, and the adhesive composition of the present invention can be used to form a thermoplastic resin film. The two-step process of lining can be omitted, which also has the effect of simplifying the carpet manufacturing process and improving productivity.
第1図は型付は金型の断面図、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°C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
口・・・φ・カーペット
A・・・・・型付は時の角度(90度)A′・・・・・
熟成型後の角度
A“・・・・・90°Cオーブン中にて24時間静置後
の角度Figure 1 is a cross-sectional view of the mold, Figure 2 is a cross-sectional view of the carpet after thermoforming, and Figure 3 is a cross-sectional view of the carpet after thermoforming, after it has been left in an oven at 90°C for 24 hours. A cross-sectional view of the carpet is shown. A... Mold Mouth... φ Carpet A... Mold is attached at an angle (90 degrees) A'...
Angle A after aging mold...Angle after standing in a 90°C oven for 24 hours
Claims (1)
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。A copolymer latex (A ) 30 to 70 parts by weight (solid content weight equivalent), 10 to 90% by weight of butadiene, 10 to 90% by weight of styrene, and 0 to 80% by weight of other monomers copolymerizable with these. An adhesive composition for carpet lining, characterized in that a mixture of 70 to 30 parts by weight (solid content weight equivalent) of a combined 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 true JPH026668A (en) | 1990-01-10 |
JPH0726327B2 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) |
Cited By (2)
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 |
US5378511A (en) * | 1993-03-22 | 1995-01-03 | International Business Machines Corporation | Material-saving resist spinner and process |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6128540A (en) * | 1984-04-20 | 1986-02-08 | アトランテイツク・リツチフイ−ルド・カンパニ− | Polymer composition and manufacture |
JPS6345740A (en) * | 1986-08-12 | 1988-02-26 | Sony Corp | Ion beam device |
-
1988
- 1988-06-24 JP JP63156350A patent/JPH0726327B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6128540A (en) * | 1984-04-20 | 1986-02-08 | アトランテイツク・リツチフイ−ルド・カンパニ− | Polymer composition and manufacture |
JPS6345740A (en) * | 1986-08-12 | 1988-02-26 | Sony Corp | Ion beam device |
Cited By (2)
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 |
US5378511A (en) * | 1993-03-22 | 1995-01-03 | International Business Machines Corporation | Material-saving resist spinner and process |
Also Published As
Publication number | Publication date |
---|---|
JPH0726327B2 (en) | 1995-03-22 |
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