JPS6059183A - Manufacture of flooring material having cushioning property - Google Patents

Manufacture of flooring material having cushioning property

Info

Publication number
JPS6059183A
JPS6059183A JP58161642A JP16164283A JPS6059183A JP S6059183 A JPS6059183 A JP S6059183A JP 58161642 A JP58161642 A JP 58161642A JP 16164283 A JP16164283 A JP 16164283A JP S6059183 A JPS6059183 A JP S6059183A
Authority
JP
Japan
Prior art keywords
particles
emulsion
resin
aqueous
weight
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
Application number
JP58161642A
Other languages
Japanese (ja)
Other versions
JPH0114351B2 (en
Inventor
Naoyuki Kato
直行 加藤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Chemical BASF Co Ltd
Original Assignee
Mitsubishi Chemical BASF Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsubishi Chemical BASF Co Ltd filed Critical Mitsubishi Chemical BASF Co Ltd
Priority to JP58161642A priority Critical patent/JPS6059183A/en
Publication of JPS6059183A publication Critical patent/JPS6059183A/en
Publication of JPH0114351B2 publication Critical patent/JPH0114351B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To manufacture a flooring material having excellent cushioning property, and having a backing layer furnished with protruded foamed particles, by coating the back side of the raw fabric of a carpet with an aqueous emulsion of a resin containing expandable polystyrene particles, and heating the coated surface. CONSTITUTION:An aqueous emulsion of a resin containing expandable polystyrene particles having particle diameter of <=1.5mm., preferably 0.2-0.8mm. (containing 10-100pts.wt. of expandable particle based on 100pts.wt. of resin) is applied to the back surface of the raw fabric of a carpet at a rate of 600-1,000g/m<2>, preferably 80-300g/m<2> (solid basis). The coated surface is heated (preferably with hot air of 100-140 deg.C to effect the expansion of the expandable particles and the drying of the aqueous resin emulsion to obtain the backing layer having expanded polystyrene particles protruded from the surface.

Description

【発明の詳細な説明】 本発明はクッションに1・賢れたカーペットに関し、特
に自動車の床敷設材として有用で、ちるカーペットを提
供するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a carpet that is superior to cushioning, and provides a carpet that is particularly useful as a floor covering material for automobiles.

従来、カーペットは敷物原反のパイル糸の抜けを防止す
ると共に形状の安定化のために、スチレン・ブタジェン
ラバーやブタジェン・゛rクリロニトリルラパー等のゴ
ムラテックスや塩化ビニル共重合体、スチレン・アクリ
ル酸アルキルエステル共重合体、酢酸ビニル・アクリル
酸アルキルエステル共重合体、塩化ビニリデン共重合体
、ポリ酢酸ビニル、エチレン・酢酸ビニル共重合体等の
樹脂水性エマルジョン(以下、ラテックスとφ1脂水性
エマルジョンを[樹脂水性エマルジョ=、−,1で代表
して記す)でバッキングが繍こされている。
Traditionally, carpets have been made using rubber latex such as styrene-butadiene rubber, butadiene-crylonitrile wrapper, vinyl chloride copolymer, styrene-butadiene rubber, etc. to prevent the pile threads of the original rug from coming off and to stabilize the shape. Resin aqueous emulsions such as acrylic acid alkyl ester copolymer, vinyl acetate/acrylic acid alkyl ester copolymer, vinylidene chloride copolymer, polyvinyl acetate, ethylene/vinyl acetate copolymer (hereinafter referred to as latex and φ1 fat aqueous emulsion) The backing is embroidered with [Resin aqueous emulsion =, -, 1].

この樹脂水性エマルジョンでバッキングされたカーペッ
トのクッション性を更に向上させる方法とし℃先にこの
樹脂エマルジョンバッキング月の裏面に発泡体シートを
接着したノJ−ペットを我々は提案した(実願昭57−
170656号、同57−195731号参照)。
As a method to further improve the cushioning properties of carpets backed with this resin aqueous emulsion, we previously proposed NoJ-Pet, which was created by bonding a foam sheet to the back side of this resin emulsion backing.
(See No. 170656 and No. 57-195731).

しかし、この方法ではバッキング層形成1淫と発泡体シ
ートの接着工程が必要であるとともに、発f1q体シー
トの折曲による破1與を防止するために、更にこの発泡
体シートに非発泡シートを積層する必要がある。
However, this method requires the steps of forming a backing layer and adhering the foam sheet, and in addition, in order to prevent the foam sheet from breaking due to bending, a non-foam sheet is added to the foam sheet. It is necessary to laminate.

本発明は、先に提案した敷設材のかかる工程の多い製法
をより少ない工程で行うことを目的でなされたものであ
り、バッキング材として発泡性ポリスチレン樹脂粒子を
含有する樹脂水性エマルジョンを用いることによりかか
る課題を解決したものである。
The present invention was made for the purpose of performing the previously proposed manufacturing method of laying material, which requires many steps, in fewer steps, and by using an aqueous resin emulsion containing expandable polystyrene resin particles as a backing material. This problem has been solved.

即ち、本発明は、敷物原反の裏面に、粒径が1.5」以
下の発泡性ポリスチレン粒子を含有する樹脂水性エマル
ジョンを塗布し、次いで塗布面を加熱して前記発泡性ポ
リスチレン粒子の発泡を行うとともに樹脂水性エマルジ
ョンを乾燥させて敷物原反の裏面にポリスチレン発泡体
粒子が突出したバッキング層を形成させることを特徴と
するクッション性を有する敷設材の製造方法を提供する
ものである。
That is, in the present invention, an aqueous resin emulsion containing expandable polystyrene particles having a particle size of 1.5" or less is applied to the back side of an original rug, and then the applied surface is heated to cause the expansion of the expandable polystyrene particles. The present invention provides a method for producing a laying material having cushioning properties, which comprises drying the aqueous resin emulsion to form a backing layer with protruding polystyrene foam particles on the back side of the original rug.

本発明におけるカーベツ、ト用の敷物原反としては任意
のものが用いられ、天然繊維、化学繊維、合成繊維等の
各種繊維を素材とする原反を使用できる。一般には、羊
毛、ナイロン、ポリアクリロニトリル、ポリアセテート
、ポリプロピレン等の繊維を素材として得たニードルパ
ンチカーペットやフラットヤーンで編んだ一次基布土に
パイルを起立させたタフテッドカーペット川原反、前記
ニードルパンチカーペットを一次基布とし、この上にパ
イルを起立させたタフテッドカーペット原反が使用され
る・ これらの中でも自動車内装用には安価なニードルパンチ
カーペットが好ましい。
Any material can be used as the material for carpets and carpets in the present invention, and materials made from various fibers such as natural fibers, chemical fibers, and synthetic fibers can be used. In general, needle-punched carpets made from fibers such as wool, nylon, polyacrylonitrile, polyacetate, and polypropylene, tufted carpets with piles erected on a primary base fabric knitted with flat yarns, and the needle-punched A tufted carpet material is used, in which a carpet is used as a primary base fabric and a pile is made to stand up on top of the carpet.Among these, inexpensive needle punch carpets are preferred for automobile interiors.

次にバッキング材として、パイル糸の係止、ポリスチレ
ン発泡体粒子の接着機能をなす樹脂水性エマルジョンと
しては、ガラス転移点が一65C〜+150℃の樹脂の
水性エマルジョン、例えばポリ酢酸ビニル、塩化ビニル
・塩化ビニリデン共重合体、スチレン・ブタジェン共重
合体ゴム、スチレンφメタクリル酸メチル共重合体、ス
チレン・アクリル酸n−ブチル共重合体、エチレン・酢
IY’Zビニル共重合体、スチレン・アクリル酸n−ブ
チル・アクリル酸共重合体、塩化ビニリデン・アクリロ
ニトリル・アクリル酸共重合体等のラテックス、水性エ
マルジョンの単独並びに混合体が用いられる。
Next, as a backing material, an aqueous resin emulsion that functions to secure the pile threads and adhere the polystyrene foam particles is an aqueous emulsion of a resin with a glass transition temperature of 165°C to +150°C, such as polyvinyl acetate, vinyl chloride, etc. Vinylidene chloride copolymer, styrene/butadiene copolymer rubber, styrene φ methyl methacrylate copolymer, styrene/n-butyl acrylate copolymer, ethylene/acetic acid IY'Z vinyl copolymer, styrene/acrylic acid n -Latices such as butyl/acrylic acid copolymer, vinylidene chloride/acrylonitrile/acrylic acid copolymer, and aqueous emulsions may be used alone or in mixtures.

敷設材の成形性、柔軟性の面からはガラス転移点が20
℃以下の樹脂水性エマルジョン、ラテックスが好ましく
、逆に敷設材に成形性を付与するにはガラス転移点が8
0℃以上の樹脂水性エマルジョンが好ましい。
In terms of formability and flexibility of the laying material, the glass transition point is 20.
Aqueous resin emulsions and latexes with a temperature below
An aqueous resin emulsion having a temperature of 0° C. or higher is preferred.

ガラス転移点が80℃以上の水性エマルジョンとしては
、(a)、ポリメタクリル市n−グロビル(Tg81C
)、ポリスチレン(100℃)、ポリアクリロニトリル
(100℃)、ポリメタクリル酸メチル(105℃)、
ポリメタクリル酸(130℃)、ポリイタコン酸(13
0℃)、ポリアクリルアミド(153℃)等のホモ重合
体の水1’JEエマルジョンの他、(b)、これら重合
体の原料であるビニル単量体50〜100重重%、好ま
しくは65〜95重日%と、曲のビニル単量体、例えば
アクリル酸2−エチルヘキシル(Tg −85℃)、ア
クリル酸n・ブチル(−54’C)、アクリル酸エチル
(−22℃)、アクリル酸イソプロピル(−5℃)、メ
タクリル酸2−エチルヘキシル(−5℃)、アクリル−
酸n・プロピル(8℃)、メタクリル酸n・ブチル(2
0℃)、酢酸ビニル(30℃)、メタクリル酸エチル(
65℃)、塩化ビニル(79℃)等もしくは塩化ビニリ
デン(−18℃)50重量%以下、好ましくは35〜5
重量%との共重合体の水性エマルジョン〔この(b)項
において、()内に示される′vgは、これらビニル単
量体もしくは塩化ビニリデンのホモ重合体のガラス転移
点である〕、(c)、Pgが一ト80〜155℃の樹脂
水性エマルジョン50〜97重旬%、好ましくは55〜
95重骨%と、l’gが一85℃〜+80℃未満の樹脂
水性エマルジョン50〜3重量%、好ましくは45〜5
重量%との混合物等があげられる。
As the aqueous emulsion having a glass transition point of 80°C or higher, (a) polymethacrylic city n-globil (Tg81C
), polystyrene (100°C), polyacrylonitrile (100°C), polymethyl methacrylate (105°C),
Polymethacrylic acid (130°C), polyitaconic acid (13
In addition to water 1'JE emulsions of homopolymers such as (0°C) and polyacrylamide (153°C), (b) 50 to 100% by weight of vinyl monomers, which are raw materials for these polymers, preferably 65 to 95% by weight. % and vinyl monomers such as 2-ethylhexyl acrylate (Tg -85°C), n-butyl acrylate (-54'C), ethyl acrylate (-22°C), isopropyl acrylate ( -5℃), 2-ethylhexyl methacrylate (-5℃), Acrylic-
n-propyl acid (8℃), n-butyl methacrylate (2
0℃), vinyl acetate (30℃), ethyl methacrylate (
65°C), vinyl chloride (79°C), etc. or vinylidene chloride (-18°C) 50% by weight or less, preferably 35-5%
[In this (b) section, 'vg' shown in parentheses is the glass transition point of the vinyl monomer or vinylidene chloride homopolymer], (c ), Pg is 50-97% in aqueous resin emulsion at 80-155°C, preferably 55-97%
Resin aqueous emulsion with 95% heavy bone and l'g of 185°C to less than +80°C 50-3% by weight, preferably 45-5%
% by weight, etc.

水性エマルジョンの樹脂固形分NU I川は通茗20〜
60重量%であり、分散している(fft脂粒子の径け
】0μ(ミクロン)以下、好ましくは0.05〜1.0
μである。
Resin solid content of aqueous emulsion NU Ikawa 20~
60% by weight and dispersed (fft diameter of fat particles) 0 μ (micron) or less, preferably 0.05 to 1.0
μ.

ガラス転移点が20’C以下の樹脂水性エマルジョンと
しては、例えば、 (1)、アクリル酸2−エチルヘキシル、アクリル酸n
−ブチル、アクリル酸エチル、アクリル酸イングロビル
、メタクリル酸2−エチルヘキシル、アクリル酸n−プ
ロピル、メタクリル酸n・ブチル、塩化ビニリデン、エ
チレン、ブタジェンより選ばれた単量体 20〜100重景% (I重量、酢酸ビニル、メタクリル酸エチル、塩化ビニ
ル、メタクリルrffn−フロビル、スチレン、アクリ
ロニトリル、メタクリル酸メチル、アクフノル酸、イタ
コン酸、アクリルアミド、メタクリルアミドより選ばれ
た 80重量%以下 (Il+)−ジアセトンアクリルアミド、無水マレイン
酸、ジエチレングリコールジアクリレートより選ばれた
単量体 0〜5重η% の乳化重合物があげられる。
Examples of aqueous resin emulsions having a glass transition point of 20'C or lower include (1), 2-ethylhexyl acrylate, n-acrylic acid;
- Monomer selected from butyl, ethyl acrylate, inglovir acrylate, 2-ethylhexyl methacrylate, n-propyl acrylate, n-butyl methacrylate, vinylidene chloride, ethylene, butadiene 20-100% (I Weight, 80% by weight or less selected from vinyl acetate, ethyl methacrylate, vinyl chloride, methacryl rffn-flovir, styrene, acrylonitrile, methyl methacrylate, acufunolic acid, itaconic acid, acrylamide, methacrylamide (Il+)-diacetone acrylamide Examples include emulsion polymers containing 0 to 5 weight η% of monomers selected from , maleic anhydride, and diethylene glycol diacrylate.

この水性樹脂エマルジョンに、粒径が1.5.以下、好
ましくは0.2〜0.8門の発泡性ポリスチレン樹脂粒
子を、エマルジョン中の樹脂分100g景部に対し、1
0〜l00Ji景部の割合で配合し、バッキング材とし
て用いる。粒径が1.5r+Imを越えるとエマルジョ
ンとの混和作業性が劣るとともに、発泡性ポリスチレン
粒子がエマルジョンの上部罠移動し、分離しゃすい。い
いかえればバッキング材の作業性および貯蔵安定性が悪
い。また、粒子が大きいとバッキング材の塗工性が低下
しさらに敷物原反にバッキング材を塗布後、原反より発
IF’)性ポリスチレン粒子が脱落しゃすい。
This aqueous resin emulsion has a particle size of 1.5. Hereinafter, preferably 0.2 to 0.8 particles of expandable polystyrene resin are added per 100 g of resin in the emulsion.
It is blended at a ratio of 0 to 100 Ji Keibu and used as a backing material. If the particle size exceeds 1.5r+Im, the workability of mixing with the emulsion will be poor, and the expandable polystyrene particles will trap and move to the upper part of the emulsion and easily separate. In other words, the workability and storage stability of the backing material are poor. In addition, if the particles are large, the coating properties of the backing material will deteriorate, and furthermore, after the backing material is applied to the original rug, the IF')-prone polystyrene particles will easily fall off from the original rug.

かかる発泡性ポリスチレン粒子は、重合開始剤を含有す
るスチレン、必要によりメチルメタクリレート、ビニル
ベンゼン、アクリルK1%のビニル単量体を水に乳化さ
せ、加熱してスチレン等のビニル単量体を重合させ、次
いでこの車合体粒子が分散している懸濁液中にブタン、
ヘプタン等の膨張剤を圧入し、前記重合体粒子中に揮発
性膨張剤を3〜7重R%の割合で含浸させることにより
得られる。また、スチレン等のビニル単量体を懸濁+I
i合する際、前記膨張剤をltf、m液に供給しつつ重
合を行って得ることもできる。
Such expandable polystyrene particles are produced by emulsifying styrene containing a polymerization initiator, optionally methyl methacrylate, vinylbenzene, and 1% vinyl monomer of acrylic K in water, and heating the mixture to polymerize the vinyl monomer such as styrene. Then, butane,
It is obtained by injecting an expanding agent such as heptane under pressure and impregnating the volatile expanding agent into the polymer particles at a ratio of 3 to 7% by weight. In addition, vinyl monomers such as styrene can be suspended + I
It can also be obtained by polymerizing while supplying the swelling agent to the ltf and m liquids during the polymerization.

このバンキング材に、炭酸カルシウム、水酸化アルミニ
ウム、クレイ、タルク、硫酔バリウム、パーライト等の
体質顔料やベンガラ、マラカイトグリーン、酸化チタン
等の顔料、染料を配合することもできる。
Extender pigments such as calcium carbonate, aluminum hydroxide, clay, talc, barium sulfate, perlite, pigments and dyes such as red iron oxide, malachite green, and titanium oxide can also be blended with this banking material.

バッキング材の20℃における粘度は500〜8、+)
 OOセンチポイズであることが塗布の面より好ましい
The viscosity of the backing material at 20℃ is 500-8, +)
OO centipoise is preferable from the viewpoint of coating.

敷物原反へのバッキング材の塗布は、スプレー、はけ、
フオーム塗工機、ロール等を用いて、一般にはロールコ
ータ−を用いて行われる。バッキング材の塗布月は、6
0〜1,1) OOt/rr?(固型分)、好ましくけ
80〜3oop/m”である。
The backing material can be applied to the original rug by spraying, brushing,
This is carried out using a foam coating machine, rolls, etc., generally a roll coater. The month of application of the backing material is 6
0~1,1) OOt/rr? (solid content), preferably 80 to 3 oop/m''.

一般に、バッキング材の総重量は、敷物原反重量の30
〜100重量%(固形分重量)となるように用いる。
Generally, the total weight of the backing material is 30% of the weight of the original rug.
It is used so that it becomes ~100% by weight (solid content weight).

塗布されたエマルジョンの加熱乾燥、および発泡性樹脂
粒子の発泡は任意の方法で行なうことができる・例えば
加熱シリンダー、赤外線加熱様、熱風乾燥機、サクショ
ンドライヤー等を用いることができるが、熱風乾燥機を
使用するのが好ましい。また、乾燥は80〜180℃で
行なうことができるが、繊維劣化防止の面および発泡を
十分に行わしめるために100〜140℃の熱風で行な
うことが好ましい。
Heat drying of the applied emulsion and foaming of the expandable resin particles can be carried out by any method.For example, a heating cylinder, infrared heating, hot air dryer, suction dryer, etc. can be used, but hot air dryer It is preferable to use Although drying can be carried out at 80 to 180°C, it is preferable to dry with hot air at 100 to 140°C in order to prevent fiber deterioration and to ensure sufficient foaming.

この加熱により発泡性ポリスチレン粒子は約5〜50倍
発泡し、粒径が帆5〜4,5圓の発i包体(1)となり
、樹脂エマルジョンが形成した膜(2)により敷物原反
(3)に接着されているとともに、膜(2)面より突出
する(第1図参照)。
As a result of this heating, the expandable polystyrene particles expand approximately 5 to 50 times, forming an expanded i-envelope (1) with a particle size of 5 to 4.5 mm, and a film (2) formed by the resin emulsion forms a rug material. 3) and protrudes from the surface of the membrane (2) (see Figure 1).

従って、本発明の敷設材(4)はかかる発泡1体粒子(
1)の存在ゆえにクッション性が大幅に向上した4、(
教材となっている。
Therefore, the laying material (4) of the present invention has such foamed monolithic particles (
Due to the presence of 1), the cushioning properties have been greatly improved 4, (
It is used as a teaching material.

また、樹脂エマルジョンとじ℃ガラス転移点が80℃以
上の樹脂のエマルジョンを用いたときは、成形性を敷設
材が有するので、パノギング層の1(′シ(2)が溶融
する温度に加熱し、敷設材をプレス成形すれば所望の形
状に敷設材を賦型できる。
In addition, when using a resin emulsion with a glass transition point of 80°C or higher, the laying material has moldability, so it is heated to a temperature at which 1(' and 2) of the panogging layer melts. By press-molding the laying material, the laying material can be shaped into a desired shape.

以下、実施例により本発明を更に詳細に説明するO ニードルパンチカーペットの製造例 15デニール、繊維長的100■のポリプロピレン(融
点164℃)繊維をランダムに積み重ねた繊維マット(
400f/m’)を、15−18−32−3RBの針を
用いて1平方インチ当り50本の割合でニードリングし
℃、厚さ約3■のニードルパンチカーペットを得り。
Hereinafter, the present invention will be explained in more detail with reference to Examples.O Manufacture example of needle punch carpet 15 denier, fiber length 100cm polypropylene (melting point 164°C) fibers randomly stacked together to form a fiber mat (
400 f/m') was needled at a rate of 50 needles per square inch using 15-18-32-3RB needles to obtain a needle punch carpet with a thickness of about 3 cm.

以下の実施例、比較例に用いた敷物原反はこのニードル
パンチカーペットである。
The raw carpet material used in the following Examples and Comparative Examples is this needle punch carpet.

実施例1 ニードルパンチカーペットの裏面に、バッキング材とし
て「スチレン(49重量%)・アクリル酸n〜ブチル(
49重量%)・アクリル酸(2重量%)共重合体の水性
エマルジョン(樹脂粒子径0.1〜0.2ミクロン、固
型分50重挟部、造膜温度20℃)100重量部に、平
均粒径が0.33mの発泡性ポリスチレン粒子(ブタン
5.5%含有)10重挟部を配合し、更に油化バーディ
ッシエ■製増粘剤“ラテコールD″(商品名)を配合し
て25℃における粘度を3.000 cpsに調製した
ものjを用い、これをリッカーローラーで150f/−
(固型分)となるように塗布し、次いでニップロールを
用いてエマルジョンをニードルパンチカーペットに含浸
させた。そして、エマルジョンを含浸させたニードルパ
ンチカーペットを130℃の熱風で10分間加熱して水
分を除去するとともに発泡性ポリスチレン粒子を発泡さ
せ、嵩密度が約0.15f/cd、粒径が0.5〜1.
5鰭のポリスチレン発泡体粒子が樹脂膜を介してニード
ルパンチカーペットの裏面に接着した敷設材を得た。
Example 1 Styrene (49% by weight)/n-butyl acrylate (
49% by weight) and acrylic acid (2% by weight) copolymer aqueous emulsion (resin particle size 0.1 to 0.2 microns, solid content 50 parts, film forming temperature 20°C), By blending 10 times more expandable polystyrene particles (containing 5.5% butane) with an average particle size of 0.33 m, and further blending the thickener "Latechol D" (trade name) manufactured by Yuka Verdissier ■, 25% The viscosity at ℃ was adjusted to 3.000 cps, and it was rolled at 150 f/- with a licker roller.
(solid content), and then the needle punch carpet was impregnated with the emulsion using a nip roll. Then, the needle punch carpet impregnated with the emulsion was heated with hot air at 130°C for 10 minutes to remove moisture and foam the expandable polystyrene particles, with a bulk density of about 0.15 f/cd and a particle size of 0.5 ~1.
A laying material was obtained in which five-fin polystyrene foam particles were adhered to the back side of a needle punch carpet via a resin film.

このもののクッション性を次の方法で評価したところ、
良好であった。
The cushioning properties of this product were evaluated using the following method.
It was good.

評価法: 敷設材に荷重5of/ltlをかけた際の初期の肉厚を
toとし、次に荷重400f/crr?を1分間かけた
際の肉厚をtlとし、この荷重を敗り除き、1′分経過
した時の肉厚をt2としだとき、 2 変形率=(1−−)X100 t。
Evaluation method: The initial wall thickness when a load of 5of/ltl is applied to the laying material is to, then the load is 400f/crr? Let tl be the wall thickness when the load is applied for 1 minute, and let t2 be the wall thickness after 1 minute has passed after this load is removed. 2 Deformation rate = (1--)X100 t.

とじ℃算出し、変形率が小さく、厚み変化率の小さいも
のをクッション性良好とした@実施例2〜3、比較例1 実I!FU51J1において、バッキング材中の樹脂水
性エマルジョンと、発泡性ポリスチレン粒子の配合比を
表1のように変更する他は同様にして敷設材を得、賦型
した。敷設材の性能を同表に示す。
Binding temperature was calculated, and those with a small deformation rate and a small thickness change rate were considered to have good cushioning properties @Examples 2 to 3, Comparative Example 1 Actual I! A laying material was obtained and shaped in the same manner as in FU51J1, except that the blending ratio of the aqueous resin emulsion and expandable polystyrene particles in the backing material was changed as shown in Table 1. The performance of the laying materials is shown in the same table.

なお、参考のためA社製ニードルフェルト“アンゴーフ
ェルト”651111P/rr?目付のクッション性を
同表に示す。
For reference, needle felt "Ango Felt" 651111P/rr? manufactured by Company A is used. The table shows the cushioning properties based on the basis weight.

実施例4 実施例1において、バッキング材としてスチレン(80
1RJt%)・アクリル酸n−ブチル(20重量%)共
重合体の水性エマルジョン(横114t粒径約0,2ミ
クロン、固型分50%)100重量部に発泡性ポリスチ
レン粒子10重量部を配合したものを用いる他は同様に
してクッション性に虐む敷設材を得た。
Example 4 In Example 1, styrene (80%
1RJt%)/n-butyl acrylate (20% by weight) copolymer aqueous emulsion (width 114t particle size approximately 0.2 microns, solid content 50%) 100 parts by weight is blended with 10 parts by weight of expandable polystyrene particles. A laying material with poor cushioning properties was obtained in the same manner, except that the same material was used.

また、この敷設材を120℃に加熱してバッキング層の
樹脂膜を軟化させ、次いで冷却プレス金型を用いて5 
Kg/rfAの圧力を5分間かけて成形し、自動車室内
床用カーペットを製造した。
In addition, this laying material was heated to 120°C to soften the resin film of the backing layer, and then 5
A pressure of Kg/rfA was applied for 5 minutes to form a carpet for an automobile interior floor.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の実施により得られた敷設材の断面図で
ある。 図中、1はポリスチレン発泡体粒子、2は樹脂膜、3は
敷物原反、4は敷設材である。 特許出願人 油化バーディノシエ株式会社代理人 弁理
士 占 川 秀 利 代理人 弁理士 長 谷 正 玖 閉1図 〆4
FIG. 1 is a sectional view of a laying material obtained by implementing the present invention. In the figure, 1 is a polystyrene foam particle, 2 is a resin film, 3 is a rug material, and 4 is a laying material. Patent Applicant Yuka Birdinocie Co., Ltd. Agent Patent Attorney Hidetoshi Utsukawa Agent Patent Attorney Tadashi Hase Kusei 1 Figure 4

Claims (1)

【特許請求の範囲】 1)、敷物原反の裏面に、粒径が1.5簡以下の発泡性
ポリスチレン粒子を含有する樹脂水性エマルジョンを塗
布し、次いで塗布面を加熱して前記発泡体ポリスチレン
粒子の発泡を行うとともに樹脂水性エマルジョンを乾燥
させて敷物原反の裏面にポリスチレン発泡体粒子が突出
したバッキング層を形成させることを特徴とするクッシ
ョン性を有する敷設材の製造方法。 2)、 4fi(脂水性エマルジョンの樹脂分100重
量部に対する発泡性ポリスチレン粒子の割合が、10〜
ioo重量部であることを特徴とする特許請求の範囲第
1項記載の敷設材の製造方法0
[Scope of Claims] 1) An aqueous resin emulsion containing expandable polystyrene particles with a particle size of 1.5 or less is applied to the back side of the original rug, and then the applied surface is heated to remove the expanded polystyrene particles. A method for manufacturing a laying material having cushioning properties, which comprises foaming the particles and drying the aqueous resin emulsion to form a backing layer in which polystyrene foam particles protrude on the back side of an original rug. 2), 4fi (the ratio of expandable polystyrene particles to 100 parts by weight of the resin content of the fat-aqueous emulsion is 10 to
The method for manufacturing a laying material according to claim 1, characterized in that the amount is 100 parts by weight.
JP58161642A 1983-09-02 1983-09-02 Manufacture of flooring material having cushioning property Granted JPS6059183A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58161642A JPS6059183A (en) 1983-09-02 1983-09-02 Manufacture of flooring material having cushioning property

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58161642A JPS6059183A (en) 1983-09-02 1983-09-02 Manufacture of flooring material having cushioning property

Publications (2)

Publication Number Publication Date
JPS6059183A true JPS6059183A (en) 1985-04-05
JPH0114351B2 JPH0114351B2 (en) 1989-03-10

Family

ID=15739060

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58161642A Granted JPS6059183A (en) 1983-09-02 1983-09-02 Manufacture of flooring material having cushioning property

Country Status (1)

Country Link
JP (1) JPS6059183A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62253447A (en) * 1986-04-25 1987-11-05 日本バイリーン株式会社 Skin agent for interior material
EP0270330A2 (en) * 1986-12-02 1988-06-08 Mitsubishi Yuka Badische Co., Ltd. Manufacturing method for a laminated sheet
WO1999035327A3 (en) * 1998-01-12 1999-11-04 Mannington Mills A surface covering backing containing polymeric microspheres and processes of making the same
JP2015048356A (en) * 2013-08-29 2015-03-16 積水化成品工業株式会社 Foamable styrenic resin particle, foamed particle, foam molded body and manufacturing method of foamed particle
CN107672237A (en) * 2017-09-05 2018-02-09 福建金坛实业有限公司 A kind of high imbibition pro-skin hot-wind nonwoven cloth of composite environmental-friendly and its manufacture method

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62253447A (en) * 1986-04-25 1987-11-05 日本バイリーン株式会社 Skin agent for interior material
JPH0611530B2 (en) * 1986-04-25 1994-02-16 日本バイリーン株式会社 Skin material for interior materials
EP0270330A2 (en) * 1986-12-02 1988-06-08 Mitsubishi Yuka Badische Co., Ltd. Manufacturing method for a laminated sheet
WO1999035327A3 (en) * 1998-01-12 1999-11-04 Mannington Mills A surface covering backing containing polymeric microspheres and processes of making the same
JP2015048356A (en) * 2013-08-29 2015-03-16 積水化成品工業株式会社 Foamable styrenic resin particle, foamed particle, foam molded body and manufacturing method of foamed particle
CN107672237A (en) * 2017-09-05 2018-02-09 福建金坛实业有限公司 A kind of high imbibition pro-skin hot-wind nonwoven cloth of composite environmental-friendly and its manufacture method
CN107672237B (en) * 2017-09-05 2019-06-07 福建金坛实业有限公司 A kind of high imbibition pro-skin hot-wind nonwoven cloth of composite environmental-friendly and its manufacturing method

Also Published As

Publication number Publication date
JPH0114351B2 (en) 1989-03-10

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