JPS6123316B2 - - Google Patents
Info
- Publication number
- JPS6123316B2 JPS6123316B2 JP53148219A JP14821978A JPS6123316B2 JP S6123316 B2 JPS6123316 B2 JP S6123316B2 JP 53148219 A JP53148219 A JP 53148219A JP 14821978 A JP14821978 A JP 14821978A JP S6123316 B2 JPS6123316 B2 JP S6123316B2
- Authority
- JP
- Japan
- Prior art keywords
- rug
- polymer
- glass transition
- transition point
- heat
- 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
Links
- 229920000642 polymer Polymers 0.000 claims description 31
- 230000009477 glass transition Effects 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 14
- 239000004744 fabric Substances 0.000 claims description 10
- 239000006185 dispersion Substances 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 5
- 238000000465 moulding Methods 0.000 claims description 4
- 239000004815 dispersion polymer Substances 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims 1
- 239000000839 emulsion Substances 0.000 description 9
- 229920001038 ethylene copolymer Polymers 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 230000004927 fusion Effects 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- 238000007493 shaping process Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 229920003002 synthetic resin Polymers 0.000 description 4
- 239000000057 synthetic resin Substances 0.000 description 4
- ZSBRYDJXHOFQMW-UHFFFAOYSA-N chloroethene;ethene;ethenyl acetate Chemical group C=C.ClC=C.CC(=O)OC=C ZSBRYDJXHOFQMW-UHFFFAOYSA-N 0.000 description 3
- HDERJYVLTPVNRI-UHFFFAOYSA-N ethene;ethenyl acetate Chemical group C=C.CC(=O)OC=C HDERJYVLTPVNRI-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- 239000004416 thermosoftening plastic Substances 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-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
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- HGAZMNJKRQFZKS-UHFFFAOYSA-N chloroethene;ethenyl acetate Chemical compound ClC=C.CC(=O)OC=C HGAZMNJKRQFZKS-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000004455 differential thermal analysis Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Description
本発明は織布または不織布からなる敷物のバツ
キング方法に係り、更に詳しくは、敷物の裏面に
ガラス転移点が20〜80℃である重合体の分散液も
しくはそれを主成分とする配合物を部分的あるい
は全面的に塗布したのち、ガラス転移点が0〜15
℃である重合体の分散液もしくはそれを主成分と
する配合物を部分的あるいは全面的に塗布し、乾
燥したのち二次基布を重ね合わせて加熱成型する
ことを特徴とする敷物のバツキング方法であつ
て、その目的とするところは敷物に耐久性を付与
し、また一定の形状を与えることができ、かつ二
次基布との熱圧着性の良好な敷物を得ることにあ
る。
従来より敷物に耐久性を与えるために敷物の裏
面を合成樹脂あるいは合成ゴム等で加工する所謂
バツキング法は、広く採用されているところであ
る。
ところが敷物の用途が拡大され、たとえば自動
車の内装のように床が平担でないところに用いら
れるようになると、床の形状に即して敷物を賦型
することが必要になり、従来のバツキング技術で
はこの要望を満足できなくなつてきている。
また、自動車用敷物では賦型することのできる
性能の他に断熱性、遮音性、弾力性等を与えるた
めに厚手のフエルト状物などの二次基布を効率よ
く賦型と同時に敷物に熱融着できることが要望さ
れている。こうした賦型性、熱融着性を同時に満
足させるためにポリエチレンなどの熱可塑性合成
樹脂による被覆層を敷物の裏面に形成せしめるこ
とが提案されている。しかしこの方法において
は、熱可塑性合成樹脂の被覆に先立つて従来のバ
ツキング法による加工を行わないと敷物のバイル
の抜糸の防止といつた敷物の基本的性能を満たせ
ないという制限がある。
本発明者らはこうした現状に鑑み、従来のバツ
キング加工に加えて熱可塑性合成樹脂で被覆する
という煩雑な二段の工法を簡略化して、簡単に敷
物の耐久性、賦型性および熱融着性の三つの要求
を満足させるバツキング方法を種々研究の結果、
本発明を完成するに至つた。
すなわち本発明は、敷物の裏面にガラス転移点
が20〜80℃である重合体を分散液もしくはそれを
主成分とする配合物を部分的あるいは全面的に塗
布したのち、ガラス転移点が0〜15℃である重合
体の分散液もしくはそれを主成分とする配合物を
部分的あるいは全面的に塗布し、乾燥したのち二
次基布を重ね合わせて加熱成型することからなる
敷物のバツキング方法を提供するものである。
本発明の最も重要な部分は賦型性と熱融着性と
いう相反する要求を満たすためにガラス転移点の
異なる二種の重合体を別々に敷物裏面に塗布し、
バツキングすることにある。
すなわち、賦型させてそれが安定に保持される
には高い軟化点の重合体が望ましく、熱融着には
低い軟化点の重合体が有利であるが、一般には敷
物の繊維の劣化、構造の維持のためには120℃以
下の温度で賦型および熱融着しうることが必要で
あるとされている。こうした熱処理条件下におい
て、賦型性と熱融着性という相反する要求を満た
すには、敷物の裏面にガラス転移点が20〜80℃で
ある硬質重合体とガラス転移点が0〜15℃の軟質
重合体を別々に塗布してバツキングすることが必
要であるということを見出した点に本発明の主要
な特徴が存する。
ここでガラス転移点がこの範囲外であると、た
とえば硬質重合体のガラス転移点が20℃未満であ
ると、賦型した敷物が次第に形状がくずれるた
め、その形状安定性が低下する。一方、ガラス転
移点が80℃を越えると加熱して軟化させて賦型す
るためには高い温度が必要となり、敷物の繊維素
材を損傷することになる。また軟質重合体のガラ
ス転移点が15℃を越えるとフエルト状物などの二
次基布との熱融着性が劣り、ガラス転移点が0℃
未満では賦型効果を低下させるなどの欠点を生
じ、本発明の目的を満足し得ない。
本発明にいうガラス転移点とは重合体の比容
積、比熱、屈折率、熱伝導率、誘電率、弾性係数
などが不連続的に変化する温度であり、簡便には
示差熱分析によつて測定することができる。
本発明に用いる重合体は、ガラス転移点が重要
であつて、その組成自体には特に限定されない
が、ガラス転移点が20〜80℃のいわゆる硬質重合
体としては、酢酸ビニル、スチレン、メタクリル
酸メチル、塩化ビニル等のモノマーを主成分とす
る単独もしくは共重合体が好ましく、例えばポリ
酢酸ビニル、ポリ塩化ビニルエマルジヨン、スチ
レン―アクリル酸エステル、塩化ビニル―アクリ
ル酸エステル、塩化ビニル―酢酸ビニル―エチレ
ン共重合体エマルジヨン等がある。ガラス転移点
が0〜15℃のいわゆる軟質重合体としては、前記
モノマーとエチレン、アクリル酸エステル、ビニ
ルエステルなど共重合したものが好ましく、例え
ば酢酸ビニル―アクリル酸エステル、酢酸ビニル
―エチレン、塩化ビニル―酢酸ビニル―エチレン
共重合体エマルジヨン等がある。
なお、たとえば塩化ビニル―酢酸ビニル―エチ
レン共重合体エマルジヨンなどについては、硬
質、軟質両重合体として両方に例示されている
が、これはその組成比等の差によるものである。
かかる硬軟両質の重合体は、分散液そのままあ
るいは増粘剤、充填剤、着色剤、難燃剤、分散剤
などの各種の添加物を配合してなる配合物として
使用することができる。
本発明に用いる敷物とは、織布または不織布か
らなる敷物で繊維素材としては羊毛、レイヨン、
ポリアクリロニトリル、ポリアミド、ポリエステ
ル、ポリプロピレン、ポリ塩化ビニルなどの天然
もしくは合成繊維が用いられ、敷物の構造として
はとくに限定されないが、一般にタフテツトカー
ペツト、ニードルパンチカーペツトと呼ばれてい
るものである。
前記のガラス転移点の異なる硬軟二種の重合体
の分散液(もしくは配合物)を塗布するにおいて
は、まずはじめに硬質重合体を塗布し、必要によ
り適度に乾燥させたのち、軟質重合体を塗布する
ことが原則である。
塗布方法としては、敷物裏面に硬質重合体を全
面に塗布し、次いでその塗布面に軟質重合体を全
面的に重ね塗りする方法が基本となるが、硬質重
合体あるいは軟質重合体のどちらか一方のみを全
面に塗布し、他方をたとえば縞状あるいは網状に
部分的に塗布することも有効である。もちろんこ
のような場合であつても硬質重合体をはじめに塗
布することが原則である。
本発明において目的とする効果を得るには重合
体の塗布量が重要であり、一般には硬質両重合体
の合計が固形分として100〜1000g/m2の範囲で選
ばれるが、前記二種の重合体の塗布量の配合は、
そのいずれかが二種の合計の30重量%以上である
ことが好ましい。
目的とする敷物の耐久性付与は前記両重合体の
塗布と乾燥によつて得られるが、賦型および二次
基布との熱融着は塗布した敷物を加熱成型するこ
とによつて行われる。即ち前述の両重合体を塗布
および必要により乾燥して得られた敷物を熱風、
赤外線等の方法によつて予め80〜120℃に予熱
後、塗布面に二次基布(フエルトもしくは綿く
ず、ジユートなどを含む)をあて、任意の形状を
もつ冷却された金型にて圧締して形付する方法あ
るいは加熱された金型にて圧締し、圧締した状態
で金型を冷却する方法などの方法によつて賦型お
よび熱融着される。
かくして本発明の方法によつてバツキングされ
た敷物は、耐久性を有し、かつ二次基布を重ねて
圧締することにより任意の安定した形状と二次基
布の強固な一体化がなされる。
以下、本発明を実施例によつて説明する。
実施例 1
ガラス転移点が20℃である塩化ビニル―酢酸ビ
ニル―エチレン共重合体エマルジヨンにポリアク
リル酸ソーダを配合して、固形分が30重量%で粘
度が5000センチポイズの組成物を調整した。
ポリプロピレン繊維をニードルパンチング法に
よつてウエブ状とした目付600g/m2のニードルパ
ンチカーペツトに、上記組成物をロールコーター
法により塗布し、110℃の熱風循環式乾燥機で乾
燥した。このときの上記組成物の塗布量は、固形
分として300g/m2であつた。
次にこのうえにガラス転移点が5℃である酢酸
ビニル―エチレン共重合体エマルジヨンをスプレ
ー法により乾燥固形分として150g/m2塗布し、
110℃の熱風乾燥機中で乾燥した。
かくして得たカーペツトを120℃の熱風中で10
分間予熱したのち、塗布面に綿くずからなるフエ
ルトをあて凹凸の形状をもつ一対の金型で3分間
圧締し、冷却したのち取り出してカーペツトの賦
型性およびフエルト状物との熱融着性能を試験し
た。この結果を第1表に示す。
実施例 2
ガラス転移点が30℃である塩化ビニル―酢酸ビ
ニル―エチレン共重合体エマルジヨンを用いる以
外は実施例1と同様にして配合組成物を調整し、
同様にカーペツトを処理した。
次にガラス転移点が15℃である酢酸ビニル―エ
チレン共重合体エマルジヨンを実施例1と全く同
様に処理し、また得られたカーペツトについても
全く同様にして賦型性および熱融着性について試
験を行つた。
その結果を第1表に示す。
比較例 1〜4
第1表に示すガラス転移点をもつ重合あるいは
共重合体エマルジヨンを用いて実施例1に準じて
同様にカーペツトを処理し、得られたそれぞれの
カーペツトについても全く同様にして賦型性およ
び熱融着性を試験した。
これらの結果を第1表に示す。
The present invention relates to a method for backing a rug made of woven fabric or non-woven fabric, and more specifically, the present invention relates to a method for backing a rug made of woven or non-woven fabric, and more specifically, a dispersion of a polymer having a glass transition point of 20 to 80°C or a blend containing the same as a main component is applied to the back side of the rug. After coating on the target or entire surface, the glass transition point is 0 to 15.
A method for backing a rug, characterized by partially or completely applying a polymer dispersion or a mixture containing it as a main component at a temperature of °C, drying, overlaying a secondary base fabric, and heat-molding. The purpose is to provide a rug that has durability, can be given a certain shape, and has good thermocompression bondability with a secondary base fabric. Conventionally, the so-called buckling method, in which the back side of a rug is treated with synthetic resin or synthetic rubber, has been widely used in order to impart durability to the rug. However, as the uses of rugs expanded and they began to be used in places where the floor was not flat, such as the interior of a car, it became necessary to shape the rug to match the shape of the floor, and the conventional bucking technology It is becoming impossible to satisfy this demand. Furthermore, in addition to the performance that can be formed into automobile rugs, secondary base fabrics such as thick felt-like materials are efficiently formed and heat is applied to the rug at the same time in order to provide heat insulation, sound insulation, elasticity, etc. It is desired that it can be fused. In order to simultaneously satisfy such moldability and heat sealability, it has been proposed to form a covering layer of thermoplastic synthetic resin such as polyethylene on the back surface of the rug. However, this method has a limitation in that it cannot meet the basic performance of the rug, such as preventing thread removal from the rug's vile, unless it is processed by the conventional backing method prior to coating with the thermoplastic synthetic resin. In view of these current circumstances, the present inventors simplified the complicated two-step method of coating with a thermoplastic synthetic resin in addition to the conventional backing process, and easily improved the durability, shapeability, and thermal bonding of rugs. As a result of various studies on banging methods that satisfy the three sexual demands,
The present invention has now been completed. That is, in the present invention, after applying a dispersion of a polymer having a glass transition point of 20 to 80 degrees Celsius or a composition containing the polymer as a main component to the back side of the rug, the glass transition point is 0 to 80 degrees Celsius. A method for backing rugs consists of partially or fully applying a polymer dispersion at 15°C or a blend containing it as a main component, drying, overlaying a secondary base fabric, and heat-molding. This is what we provide. The most important part of the present invention is that two types of polymers with different glass transition points are separately coated on the back side of the rug in order to satisfy the conflicting demands of moldability and heat sealability.
It's about bashing. In other words, a polymer with a high softening point is desirable for shaping and stably holding it, and a polymer with a low softening point is advantageous for heat fusion. In order to maintain this, it is said that it is necessary to be able to form and heat-seal at a temperature of 120°C or less. Under these heat treatment conditions, in order to satisfy the conflicting demands of formability and heat-fusibility, it is necessary to use a hard polymer with a glass transition point of 20 to 80°C on the back side of the rug and a hard polymer with a glass transition point of 0 to 15°C on the back side of the rug. A key feature of the present invention lies in the discovery that separate coating and backing of the soft polymer is necessary. If the glass transition point is outside this range, for example if the glass transition point of the hard polymer is less than 20° C., the shaped rug will gradually lose its shape and its shape stability will decrease. On the other hand, if the glass transition point exceeds 80°C, high temperatures are required to heat, soften, and shape the material, which may damage the fiber material of the rug. Furthermore, if the glass transition point of the soft polymer exceeds 15°C, the thermal adhesion with secondary base fabrics such as felt will be poor, and the glass transition point will be 0°C.
If it is less than this, there will be disadvantages such as a decrease in the imprinting effect, and the object of the present invention cannot be satisfied. The glass transition point in the present invention is the temperature at which the specific volume, specific heat, refractive index, thermal conductivity, dielectric constant, elastic modulus, etc. of a polymer changes discontinuously, and can be easily determined by differential thermal analysis. can be measured. The glass transition point of the polymer used in the present invention is important, and the composition itself is not particularly limited. Examples of so-called hard polymers with a glass transition point of 20 to 80°C include vinyl acetate, styrene, and methacrylic acid. Single or copolymers containing monomers such as methyl and vinyl chloride as main components are preferred, such as polyvinyl acetate, polyvinyl chloride emulsion, styrene-acrylic ester, vinyl chloride-acrylic ester, and vinyl chloride-vinyl acetate. Examples include ethylene copolymer emulsion. The so-called soft polymer having a glass transition point of 0 to 15°C is preferably one copolymerized with the above monomers such as ethylene, acrylic ester, vinyl ester, etc. For example, vinyl acetate-acrylic ester, vinyl acetate-ethylene, vinyl chloride, etc. -Vinyl acetate-ethylene copolymer emulsion, etc. Note that, for example, vinyl chloride-vinyl acetate-ethylene copolymer emulsion is exemplified as both a hard polymer and a soft polymer, but this is due to differences in their composition ratios, etc. Such a hard and soft polymer can be used as a dispersion as it is or as a mixture with various additives such as thickeners, fillers, colorants, flame retardants, and dispersants. The rug used in the present invention is a rug made of woven fabric or non-woven fabric, and the fiber materials include wool, rayon,
Natural or synthetic fibers such as polyacrylonitrile, polyamide, polyester, polypropylene, and polyvinyl chloride are used, and the structure of the rug is not particularly limited, but it is generally called tufted carpet or needle punch carpet. . When applying a dispersion (or mixture) of the above-mentioned hard and soft polymers with different glass transition points, first apply the hard polymer, dry it appropriately if necessary, and then apply the soft polymer. The principle is to do so. The basic application method is to apply a hard polymer to the entire surface of the back of the rug, and then overcoat the coated surface with a soft polymer. It is also effective to apply only one layer to the entire surface and partially apply the other layer, for example, in a striped or mesh pattern. Of course, even in such cases, the principle is to apply the hard polymer first. In order to obtain the desired effect in the present invention, the coating amount of the polymer is important, and generally the total amount of both hard polymers is selected as a solid content in the range of 100 to 1000 g/m 2 . The composition of the amount of polymer applied is as follows:
It is preferable that either of them accounts for 30% or more by weight of the total of the two types. The desired durability of the rug can be obtained by applying and drying the above-mentioned polymers, but shaping and heat fusion with the secondary base fabric are performed by heating and molding the applied rug. . That is, the rug obtained by applying both of the above-mentioned polymers and drying if necessary is heated with hot air,
After preheating to 80 to 120°C using infrared rays or other methods, a secondary base fabric (including felt, cotton shavings, juute, etc.) is applied to the coated surface, and pressure is applied using a cooled mold with an arbitrary shape. Shaping and heat-sealing are performed by methods such as tightening and shaping, or pressing with a heated mold and cooling the mold in the pressed state. Thus, the rug backed by the method of the present invention has durability, and by overlapping and pressing the secondary base fabric, an arbitrary stable shape and a strong integration of the secondary base fabric can be achieved. Ru. Hereinafter, the present invention will be explained with reference to Examples. Example 1 Sodium polyacrylate was blended with a vinyl chloride-vinyl acetate-ethylene copolymer emulsion having a glass transition point of 20°C to prepare a composition having a solid content of 30% by weight and a viscosity of 5000 centipoise. The above composition was applied by a roll coater method to a needle punch carpet having a basis weight of 600 g/m 2 made of polypropylene fibers formed into a web by a needle punching method, and dried in a hot air circulation dryer at 110°C. The coating amount of the above composition at this time was 300 g/m 2 in terms of solid content. Next, a vinyl acetate-ethylene copolymer emulsion having a glass transition point of 5° C. was applied on top of this by a spray method at a dry solid content of 150 g/m 2 .
It was dried in a hot air dryer at 110°C. The thus obtained carpet was heated in hot air at 120℃ for 10 minutes.
After preheating for a few minutes, a felt made of cotton waste is applied to the coated surface and pressed for three minutes using a pair of molds with uneven shapes. After cooling, the carpet is taken out to improve the shapeability of the carpet and the heat fusion with the felt material. Performance tested. The results are shown in Table 1. Example 2 A blended composition was prepared in the same manner as in Example 1 except for using a vinyl chloride-vinyl acetate-ethylene copolymer emulsion with a glass transition point of 30°C,
The carpet was treated in the same way. Next, a vinyl acetate-ethylene copolymer emulsion with a glass transition point of 15°C was treated in exactly the same manner as in Example 1, and the resulting carpet was also tested for formability and heat-fusibility in the same manner. I went there. The results are shown in Table 1. Comparative Examples 1 to 4 Carpets were treated in the same manner as in Example 1 using polymerized or copolymer emulsions having the glass transition points shown in Table 1, and each of the resulting carpets was treated in exactly the same manner. Moldability and heat fusion properties were tested. These results are shown in Table 1.
【表】【table】
Claims (1)
重合体の分散液もしくはそれを主成分とする配合
物を部分的あるいは全面的に塗布したのち、ガラ
ス転移点が0〜15℃である重合体の分散液もしく
はそれを主成分とする配合物を部分的あるいは全
面的に塗布し、乾燥したのち、二次基布を重ね合
わせて加熱成型することを特徴とする敷物のバツ
キング方法。1 After partially or completely applying a dispersion of a polymer with a glass transition point of 20 to 80°C or a compound containing it as a main component to the back side of the rug, the glass transition point is 0 to 15°C. A method for backing a rug, which comprises partially or fully applying a polymer dispersion or a mixture containing the polymer as a main component, drying, overlapping a secondary base fabric, and heat-molding.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14821978A JPS5576173A (en) | 1978-11-29 | 1978-11-29 | Backing method of carpet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14821978A JPS5576173A (en) | 1978-11-29 | 1978-11-29 | Backing method of carpet |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5576173A JPS5576173A (en) | 1980-06-09 |
JPS6123316B2 true JPS6123316B2 (en) | 1986-06-05 |
Family
ID=15447932
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14821978A Granted JPS5576173A (en) | 1978-11-29 | 1978-11-29 | Backing method of carpet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5576173A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57210850A (en) * | 1981-06-20 | 1982-12-24 | Nippon Tokushu Toryo Co Ltd | Molding acoustic material for car and its manufacture |
JPS5971484A (en) * | 1982-10-15 | 1984-04-23 | 三菱油化バーディッシェ株式会社 | Production of heat adhesive carpet |
JPS59192778A (en) * | 1983-04-18 | 1984-11-01 | 池田物産株式会社 | Carpet packing method |
-
1978
- 1978-11-29 JP JP14821978A patent/JPS5576173A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5576173A (en) | 1980-06-09 |
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