JPS6328980A - Backing composition of carpet - Google Patents
Backing composition of carpetInfo
- Publication number
- JPS6328980A JPS6328980A JP16886186A JP16886186A JPS6328980A JP S6328980 A JPS6328980 A JP S6328980A JP 16886186 A JP16886186 A JP 16886186A JP 16886186 A JP16886186 A JP 16886186A JP S6328980 A JPS6328980 A JP S6328980A
- Authority
- JP
- Japan
- Prior art keywords
- carpet
- weight
- properties
- composition
- ethylene
- 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 description 37
- 239000004014 plasticizer Substances 0.000 claims description 19
- 229920001038 ethylene copolymer Polymers 0.000 claims description 18
- 229920005989 resin Polymers 0.000 claims description 16
- 239000011347 resin Substances 0.000 claims description 16
- 239000011256 inorganic filler Substances 0.000 claims description 10
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 10
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 9
- 239000000314 lubricant Substances 0.000 claims description 8
- 239000000463 material Substances 0.000 description 32
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 14
- 238000000034 method Methods 0.000 description 13
- 229920001577 copolymer Polymers 0.000 description 11
- 239000005038 ethylene vinyl acetate Substances 0.000 description 11
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 235000010216 calcium carbonate Nutrition 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 229920001971 elastomer Polymers 0.000 description 7
- 229910000019 calcium carbonate Inorganic materials 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 6
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 5
- 239000000945 filler Substances 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- -1 Kuen 1!2 derivatives Chemical class 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000005042 ethylene-ethyl acrylate Substances 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Chemical class C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Chemical class O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000010426 asphalt Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 230000002787 reinforcement Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Chemical class OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 239000005973 Carvone Substances 0.000 description 1
- 239000004593 Epoxy Chemical class 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical compound [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000002723 alicyclic group Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical class C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical class OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 229920006225 ethylene-methyl acrylate Polymers 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 150000002531 isophthalic acids Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000002888 oleic acid derivatives Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical class CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Manufacturing Of Multi-Layer Textile Fabrics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は無機充てん剤を高度に配合された高密度のカー
ペット用裏打ら組成物に関するものである。さらに詳し
くは不飽和カルボン酸変性エチレン共重合体単独または
不飽和カルボン酸変性エチレン共重合体とエチレン共重
合体との混合物、無機充てん剤、可塑剤その他からなる
混練加工性および配合特性に優れたカーペット用裏打ち
組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to high density carpet backing compositions highly loaded with inorganic fillers. More specifically, it consists of an unsaturated carboxylic acid-modified ethylene copolymer alone or a mixture of an unsaturated carboxylic acid-modified ethylene copolymer and an ethylene copolymer, an inorganic filler, a plasticizer, etc. with excellent kneading processability and compounding properties. The present invention relates to carpet backing compositions.
また本発明は首記組成物を加熱溶融状態でカーペットに
裏打ちした自動車用カーペットおよびタイルカーペット
に関するものである。The present invention also relates to automobile carpets and tile carpets, which are lined with the above-mentioned composition in a heated and molten state.
[従来技術および発明が解決しようとする問題点〕自動
車用カーペットは、車内の装飾、保温、吸音効果と遮音
効果を具備した内装材である。自動車用カーペットの裏
打ち材には、カーペットの補強、成形保持性、パイル扱
は防止、収縮防止などのl1lfllが基本的に要求さ
れている。また自動車のエンジン音など苗鉢からの騒音
を下げて、室内の居住性を向上させる要求も高まってき
ており、この目的には遮音性能を付与した裏打ち材が必
要である。遮音効果は裏打ち材の単位面積あたりの質1
貰に比例するため、裏打ち材は高密度で、ある程度の厚
さが必要である。このようにカーペット本来の機能を付
与し、同時に遮音性を付与した裏打ち材が高価な材料を
使用することなしに得られることが望ましい。[Prior Art and Problems to be Solved by the Invention] Automotive carpets are interior materials that provide interior decoration, heat retention, sound absorption, and sound insulation effects. Carpet backing materials for automobiles are basically required to have the following properties: carpet reinforcement, mold retention, prevention of pile handling, and prevention of shrinkage. Additionally, there is an increasing demand for improving indoor comfort by reducing noise from seedling pots, such as the sound of automobile engines, and this purpose requires a lining material with sound insulating properties. The sound insulation effect is determined by the quality of the lining material per unit area.
In order to be proportional to the amount received, the lining material needs to be dense and have a certain thickness. It would be desirable to be able to obtain a backing material that provides the original functions of a carpet and at the same time provides sound insulation properties without using expensive materials.
タイルカーペットは、正方形、長方形、菱形もしくはざ
らに複Mな形状のもので、1枚の面積がたとえばO,O
S〜2Tn、3程度の根状のカーペットであり、これら
を組合わせて用いることにより、隙間を作ることなく床
に敷けるものである。これらのタイルカーペットは通常
のカーペットに比べ、床に並べて固定するだけで簡単に
施工できる利点を有し、またタイルカーベラ1−の形状
、色調などの多くの組合わせで種々の感じのカーペット
にすることができ、補修も容易であるという長所も有し
ている。これらのタイルカーペットは床に敷いた場合、
床に十分密着し歩行時に一部がはがれたりしないことが
必要である。そのための方法として、接着剤もしくは粘
着剤を用いる方法や、釘や鋲でとめる方法などがあるが
、これらの方法は施工が面倒であること、また張り換え
も手間がかかるなどの欠点がある。これらの欠点を改良
したものとして、比較的厚い裏打ち材によりタイルカー
ペットに自重を与え、その自重による固定性(置敷性)
を有したタイルカーペットが知られている。Carpet tiles are square, rectangular, diamond-shaped, or roughly multi-M in shape, and the area of one carpet is, for example, O, O.
It is a root-shaped carpet of about S to 2Tn, 3, and by using these in combination, it can be laid on the floor without creating any gaps. These tile carpets have the advantage of being easier to install than regular carpets by simply arranging them on the floor and fixing them, and can be made into carpets with a variety of textures by combining many shapes, colors, etc. It also has the advantage of being easy to repair. When these carpet tiles are laid on the floor,
It is necessary that it adheres well to the floor and that part of it does not come off when walking. Methods for this include using adhesives or adhesives, and fastening with nails or rivets, but these methods have drawbacks such as being troublesome to install and requiring time and effort to re-upholster. As an improvement over these shortcomings, a relatively thick backing material gives the tile carpet its own weight, and its own weight provides stability (placeability).
Tile carpets with
またこの裏打ち材は、タイルカーペットに糸扱は防止性
、寸法安定性、および弾力性等の諸性能を付与する目的
も兼ねている。したがってタイルカーペットの裏打ち材
は、一般のカーペット用尖打ち材の要求性状を満足しな
ければならないことはもちろんであり、ざらに置くだけ
で安定できる置敷性をも有していなければならない。ま
た高価な材料を使用することなしに、この置敷性を付与
しなければならない。This backing material also serves the purpose of imparting various properties to the tile carpet, such as yarn handling resistance, dimensional stability, and elasticity. Therefore, the backing material for tile carpets must not only satisfy the required properties of general carpet lining materials, but also have the ability to be placed stably by simply placing it on a rough surface. Furthermore, this ease of placement must be provided without using expensive materials.
従来、カーペットの裏打ち材としては、ゴムラテックス
系、エラストマー系、合成樹脂系およびアスファルト系
などが知られている。これらはたとえば特公昭46−3
839号公報、特公昭48−201991)公報、特公
昭48−3455G号公報、特公昭52−17851号
公報および特公昭53−4525号公報などに開示され
ている。Conventionally, known carpet backing materials include rubber latex, elastomer, synthetic resin, and asphalt. For example, these are
It is disclosed in Japanese Patent Publication No. 839, Japanese Patent Publication No. 48-201991), Japanese Patent Publication No. 3455G of Sho 48, Japanese Patent Publication No. 17851 of Sho 52, and Japanese Patent Publication No. 4525 of Sho 53.
しかしなから、これら従来より公知の裏打ち材をカーペ
ット基材に用いた場合には、県央は防止性が十分でなく
カーペットのパイル原糸に「はつれ」が生じ易い。ある
いは裏打ち材の十分な厚みが得られないとか、カーペッ
ト表地に裏打ち材の色相がしみ出すとかなどのほか、タ
イルカーペットとして寸法安定性、置敷性が不十分であ
り、また自動車用カーペットとしての補強性、成形保持
性、連名性などが不十分であり、必ずしも満足な結果が
得られていない。However, when these conventionally known backing materials are used as carpet base materials, they do not have sufficient preventive properties and tend to cause "fraying" in the pile fibers of the carpet. In addition, the backing material may not be thick enough, the color of the backing material may seep into the outer surface of the carpet, and the dimensional stability and placement of the tile carpet may be insufficient, and the reinforcement required for an automobile carpet may be insufficient. However, the properties such as properties such as durability, mold retention, and jointness are insufficient, and satisfactory results are not always obtained.
またさらに、エヂレンー酢酸ビニル共重合体く以下EV
^と略す)に代表されるオレフィン−極性上ツマー共重
合体に無機充てん剤を配合した組成物も公知である。し
かしなから、無機充てん剤の配合旦が多くなるにつれて
、均一な配合物を得るには困難を伴ない、均一な配合物
が得られたとしても硬さが増加してもろいものとなり、
引張特性、低温特性が劣ってくる。さらに軟化温度、流
動温度が急上昇して加工性が低下し、カーペットへの裏
打ち加工条件がきびしくなるなど多くの欠点があった。Furthermore, EV of Edylene-vinyl acetate copolymer
Also known are compositions in which an inorganic filler is blended with an olefin-polar supramid copolymer represented by (abbreviated as ^). However, as the amount of inorganic fillers added increases, it becomes difficult to obtain a uniform composition, and even if a uniform composition is obtained, the hardness increases and the composition becomes brittle.
Tensile properties and low temperature properties deteriorate. Furthermore, there were many other drawbacks, such as the softening temperature and flow temperature rising rapidly, resulting in lower workability and stricter conditions for lining carpets.
したがって、このような配合物はカーペット用裏打ち材
としては好ましい材料ではなかった。Therefore, such formulations were not preferred materials for carpet backing.
これらを改良するために、EVA 、充てん剤、可塑剤
の組合せた組成物(特[;1田755−71734号公
報、特開昭56−53141号公報、特開昭56−79
033号公報等) 、EVA 、充てん剤、可塑剤、エ
ラストマー(ゴム)の組合せた組成物(特開昭56−1
22847@公報、特開昭57−59942号公報等)
が考案され、組成物の混練性、加工性、配合物物性があ
る程度改良された。しかし配合された可塑剤等に基因す
る物性の低下が大きく、すなわち配合物の引張特性、引
裂特性、および耐熱性の低下があって、これを裏打ちし
たカーペットは補強性、成形保持性、寸法安定性、耐久
性等が不十分であり、より′−層の改善が望まれていた
。In order to improve these problems, compositions containing EVA, fillers, and plasticizers have been developed.
033, etc.), EVA, a filler, a plasticizer, and an elastomer (rubber) composition (Unexamined Japanese Patent Publication No. 56-1)
22847@publication, Japanese Unexamined Patent Publication No. 57-59942, etc.)
was devised, and the kneading properties, processability, and physical properties of the composition were improved to some extent. However, the physical properties of the blended plasticizer etc. are greatly reduced, that is, the tensile properties, tear properties, and heat resistance of the blend are reduced, and the carpet backed with this has poor reinforcing properties, mold retention properties, and dimensional stability. The strength and durability were insufficient, and further improvement of the '-layer was desired.
[問題点を解決するための手段]
本発明の目的はカーペット用裏打ち材の要求性状を満足
し、かつ前記従来法の欠点を改良した裏打ち材を提供す
ることにある。特に本発明は前記自動車用カーペットお
よびタイルカーペットに好適な天打ち材を提供すること
にある。[Means for Solving the Problems] An object of the present invention is to provide a carpet backing material that satisfies the required properties of a carpet backing material and that improves the drawbacks of the conventional methods. In particular, it is an object of the present invention to provide a ceiling material suitable for the above-mentioned automobile carpets and tile carpets.
カーペット用裏打ち組成物として、混練性、加工性、低
温特性を良くするために配合する可塑剤、軟化剤、粘着
付与樹脂、滑剤により配合物の引張・特性、引裂特性、
および耐熱性の低下を引き起こしていたが、これらの可
塑剤、軟化剤、粘着付与樹脂、滑剤を除くことなく、前
記項目の低下を起こさないような材料について、鋭意検
討を進めた結果、不飽和カルボン酸変性エチレン共重合
体の配合が好ましいことを見い出した。すなわち、本発
明は
(a) 不飽和カルボン酸および/またはその誘導体
によって変性されたエチレン共重合体5〜75重f%
(b) 無機充てん剤20〜85重量%(c) 可
塑剤、軟化剤、粘着付与樹脂、滑剤から這ばれた1種ま
たは2種以上の混合物1〜20重量%
とからなるカーペット用裏打ち組成物である。また、
(a) 不飽和カルボン酸および/またはその誘導体
によって変性されたエチレン共重合体1〜75重量%
(b) エチレン共重合体75〜1重量%(c)
無機充てん剤20〜85重量%(d) 可塑剤、軟化
剤、粘着付与樹脂、滑剤から選ばれた1種または2種以
上の混合物1〜20重旦%
とからなるカーペット用裏打ち組成物である。As a carpet backing composition, the tensile properties, tear properties,
However, as a result of intensive research into materials that would not cause the deterioration of the above items without removing these plasticizers, softeners, tackifier resins, and lubricants, we found that unsaturated It has been found that blending a carboxylic acid-modified ethylene copolymer is preferable. That is, the present invention comprises (a) 5-75% by weight of an ethylene copolymer modified with an unsaturated carboxylic acid and/or its derivative (b) 20-85% by weight of an inorganic filler (c) Plasticizer, softener This is a carpet backing composition comprising 1 to 20% by weight of a mixture of one or more of a tackifying resin, a tackifying resin, and a lubricant. Also, (a) 1 to 75% by weight of an ethylene copolymer modified with an unsaturated carboxylic acid and/or a derivative thereof (b) 75 to 1% by weight of an ethylene copolymer (c)
A carpet backing composition comprising 20 to 85% by weight of an inorganic filler (d) and 1 to 20% by weight of a mixture of one or more of two or more selected from plasticizers, softeners, tackifying resins, and lubricants. .
本発明でいうエチレン共重合体とは、エチレンとプロピ
レン、ブテンなどのα−オレフィンとの共重合体(α−
オレフィンの共重合割合は50重量%以下)、エチレン
と酢酸ビニル、アクリル酸メチル、アクリル酸エチル、
アクリル酸、メタクリル酸メチル、メタクリル酸エチル
、メタクリル酸、−酸化炭素、あるいはこれらの2種以
上との共重合体をいう。好ましい共重合体はエチレン−
酢酸ビニル共重合体、エチレン−アクリル酸メチル共重
合体、エチレン−アクリル酸エチル共重合体、エチレン
−アクリル酸エチル−アクリル酸共重合体、エチレン−
アクリル醒エチルー酢酸ビニル共重合体などであり、特
にエチレン−酢酸ビニル共重合体(EVA)およびエチ
レン−アクリル酸エチル共重合体(以下[E^と略す)
が好ましい。In the present invention, the ethylene copolymer refers to a copolymer of ethylene and an α-olefin such as propylene or butene (α-
Copolymerization ratio of olefin is 50% by weight or less), ethylene and vinyl acetate, methyl acrylate, ethyl acrylate,
It refers to acrylic acid, methyl methacrylate, ethyl methacrylate, methacrylic acid, carbon oxide, or a copolymer of two or more of these. A preferred copolymer is ethylene-
Vinyl acetate copolymer, ethylene-methyl acrylate copolymer, ethylene-ethyl acrylate copolymer, ethylene-ethyl acrylate-acrylic acid copolymer, ethylene-
Acrylic-vinyl acetate copolymer, etc., especially ethylene-vinyl acetate copolymer (EVA) and ethylene-ethyl acrylate copolymer (hereinafter abbreviated as [E^)]
is preferred.
これらの共重合体は極性モノマー含有量が5〜40重量
%、特に10〜35重量%であることが望ましい。極性
モノマー含有量がこの範囲を越える場合は、組成物の硬
さが低下し引張強度が小さくなるとともに耐熱性が劣る
ため好ましくない。また極性モノマー含有量がこの範囲
より少ない場合には、組成物の硬さが増大し、もろくな
って柔軟性がなくなり伸びが減少するとともに低温特性
の脆化温度が上昇して好ましくない。These copolymers preferably have a polar monomer content of 5 to 40% by weight, particularly 10 to 35% by weight. If the polar monomer content exceeds this range, it is not preferable because the hardness of the composition decreases, the tensile strength decreases, and the heat resistance deteriorates. If the content of the polar monomer is less than this range, the hardness of the composition increases, the composition becomes brittle, loses flexibility, and elongation decreases, and the embrittlement temperature of low-temperature properties increases, which is undesirable.
これらの共重合体のメルトインデックスは0.1〜40
0であり、好ましくは0.1〜150で特に好ましくは
0.2〜50である。メルトインデックスがこの範囲を
越える場合には、耐熱性、引張強度、脆化温度などの物
性が劣り好ましくない。メルトインデックスがこの範囲
より小さい場合は配合性、加工性が低下して好ましくな
い。The melt index of these copolymers is 0.1-40
0, preferably 0.1-150, particularly preferably 0.2-50. If the melt index exceeds this range, physical properties such as heat resistance, tensile strength, and embrittlement temperature will be poor, which is not preferable. If the melt index is smaller than this range, blendability and processability will deteriorate, which is undesirable.
本発明で用いられる不飽和カルボン酸および/またはそ
の誘導体によって変性されたエチレン共重合体とは、前
記のエチレン共重合体を、炭素数が10以下であり、少
なくとも1個の二重結合を有するーj2基カルボン!I
!(たとえばアクリル酸、メタクリル酸)、炭素数15
以下で少なくとも1個の二重結合を有する二基基カルボ
ン11i(たとえばマレインlSり、ならびにその二基
基カルボン酸の無水物(たとえば無水マレイン酸、無水
ハイミック酸)を用いて変性されたものである。これら
のうち無水マレイン酸によって変性されたエチレン共重
合体が最も好ましく用いられる。The ethylene copolymer modified with an unsaturated carboxylic acid and/or its derivative used in the present invention refers to the ethylene copolymer having 10 or less carbon atoms and at least one double bond. Suru j 2 group carvone! I
! (e.g. acrylic acid, methacrylic acid), carbon number 15
Hereinafter, diradical carboxylates 11i with at least one double bond (e.g. maleic acid) and those modified using dicarboxylic acid anhydrides (e.g. maleic anhydride, hymic anhydride) are used. Of these, ethylene copolymers modified with maleic anhydride are most preferably used.
前記不飽和カルボン酸変性エチレン共重合体の製法とし
ては、一般には有機過酸化物の存在下でエチレン共重合
体と前記不飽和カルボン酸とを反応させることによって
得られるものであり、溶液法、懸濁法、溶融法等の公知
の方法が用いられる。前記不飽和カルボン酸の反応率(
含有率)は0、01〜10重閣%、好ましくは0.02
〜5重給%のものが用いられる。この不飽和カルボン酸
の反応率が0.01重量%未満では使用効果が乏しく、
10重槌%を越えると変色が著しくまた残菌未反応不飽
和カルボン酸による刺激臭があって好ましくない。The method for producing the unsaturated carboxylic acid-modified ethylene copolymer is generally obtained by reacting an ethylene copolymer with the unsaturated carboxylic acid in the presence of an organic peroxide, and includes a solution method, Known methods such as suspension method and melting method are used. The reaction rate of the unsaturated carboxylic acid (
content) is 0.01-10%, preferably 0.02
~5% by weight is used. If the reaction rate of this unsaturated carboxylic acid is less than 0.01% by weight, the effect of use is poor;
If it exceeds 10% by weight, discoloration will be significant and there will be a pungent odor due to residual bacteria and unreacted unsaturated carboxylic acid, which is not preferable.
本発明に用いる無機充てん剤はゴムやプラスチックに用
いられる充てん剤を使用することができる。この充てん
剤はたとえば「便覧・ゴム・プラスチック配合薬品」
(ラバーダイジェスト社、昭和49年光行)の第11項
および第12項に記載されているようなものである。具
体的には炭酸カルシウム類、クレー類、シリカ類、アル
ミナ類、タルク類、硫酸バリウム、硫酸カルシウム、亜
1aa12カルシウム、亜鉛基、カーボンブラック、水
酸化アルミニウム、水酸化マグネシウムなどである。こ
れら無磯充てん剤の配合量は20〜85千m%、好まし
くは40〜85重量%、最も好ましくは50〜85重量
%である。この範囲を越える場合は組成物の硬さが非常
に大きくなり、もろくなって実用に供し得ない。またこ
の範囲より少ない場合には本発明の目的にそわないため
前記範囲内に止めることが好ましい。As the inorganic filler used in the present invention, fillers used for rubber and plastics can be used. This filler is, for example, ``handbook, rubber, and plastic compounded chemicals.''
(Rubber Digest Co., Ltd., Mitsuyuki, 1972), Sections 11 and 12. Specifically, they include calcium carbonates, clays, silicas, aluminas, talcs, barium sulfate, calcium sulfate, sub-1aa12 calcium, zinc groups, carbon black, aluminum hydroxide, magnesium hydroxide, and the like. The blending amount of these non-porous fillers is 20 to 85,000 m%, preferably 40 to 85% by weight, and most preferably 50 to 85% by weight. If it exceeds this range, the hardness of the composition will become extremely large and it will become brittle and cannot be put to practical use. Further, if it is less than this range, it is not suitable for the purpose of the present invention, so it is preferable to keep it within the above range.
また本発明に用いる可塑剤、軟化剤、粘着付与樹脂、滑
剤は前記「便覧・ゴム・プラスチック配合薬品」の第8
項、第9項、第10項および第15項に記載されている
ようなものである。具体的には、フタル酸誘導体、イソ
フタル酸誘導体、テトラヒドロフタル酸誘導体、アジピ
ン酸Lj 6体、アゼラインPrt誘導体、セバシン!
誘導体、マレイン酸誘導体、フマルIS!2誘導体、ト
リメリット酸誘導体、くえん1!2誘導体、オレイン酸
誘導体、ステアリン酸誘導体、リシノール酸誘導体、グ
リセリン誘導体、エポキシ誘導体、重合形可塑剤等の可
塑剤、鉱物油、植物油等の軟化剤、クマロン樹脂、フェ
ノール樹脂、デルベン系樹脂、シクロペンタジェン樹脂
、脂肪族系、脂環族系および芳香族系炭化水素からなる
石油樹脂、ロジンおよびロジン誘導体、これらの水素添
加樹脂等の粘着付与樹脂、パラフィンワックス、マイク
ロクリスタリンワックス、ポリエチレンワックス、非晶
性ポリプロピレン、アスファルト等の滑剤である。上記
の材料は、本発明の組成物を混合する際の混線性を向上
し、力−ベツ1−への夷打ち加工に際して流れを改善す
るとともに、カーペットへの接着性を良くする作用があ
り、また裏打ちしたカーペットの柔軟性を向上する働き
がある。これらの材料の配合量は1〜20重梼%であり
、好ましくは2〜16重M%である。この範囲を越える
場合には配合物の物性低下がむしろ著しくなって好まし
くなく、またこの範囲をV14たない場合には配合効果
が現われない。Furthermore, the plasticizers, softeners, tackifying resins, and lubricants used in the present invention are listed in the 8th section of the "Handbook of Rubber and Plastic Compounded Chemicals" above.
as described in Sections 9, 10 and 15. Specifically, phthalic acid derivatives, isophthalic acid derivatives, tetrahydrophthalic acid derivatives, adipic acid Lj 6, azelain Prt derivatives, sebacin!
Derivatives, maleic acid derivatives, fumar IS! 2 derivatives, trimellitic acid derivatives, Kuen 1!2 derivatives, oleic acid derivatives, stearic acid derivatives, ricinoleic acid derivatives, glycerin derivatives, epoxy derivatives, plasticizers such as polymeric plasticizers, softeners such as mineral oil and vegetable oil, Tackifying resins such as coumaron resin, phenolic resin, derubene resin, cyclopentadiene resin, petroleum resins consisting of aliphatic, alicyclic and aromatic hydrocarbons, rosin and rosin derivatives, hydrogenated resins of these, Lubricants such as paraffin wax, microcrystalline wax, polyethylene wax, amorphous polypropylene, and asphalt. The above-mentioned materials have the effect of improving the crosstalk property when mixing the composition of the present invention, improving the flow during the punching process on the bed, and improving the adhesion to the carpet. It also works to improve the flexibility of the carpet backing. The blending amount of these materials is 1 to 20% by weight, preferably 2 to 16% by weight. If it exceeds this range, the physical properties of the blend will deteriorate rather significantly, which is undesirable, and if it does not fall within this range, the blending effect will not appear.
このほか必要により酸化防止剤、帯電防止剤、顔料など
を0.01〜5.0重量%配合することができる。In addition, 0.01 to 5.0% by weight of an antioxidant, an antistatic agent, a pigment, etc. may be added if necessary.
本発明の組成物はニーダ−、ブラベンダー、バンバリー
、ロール等のミキサー、−軸および二軸混練機によって
配合することができる。たとえば(a)不飽和カルボン
酸および/またはその誘導体によって変性されたエチレ
ン共重合体、(b)無機充てん剤、(c)可塑剤、軟化
剤、粘着付与樹脂、滑剤、また必要あらば(d)エチレ
ン共重合体のそれぞれの必要量をミキ丈−に添加するが
、これらの添加順序は制約されない。加熱温度は100
〜200℃好ましくは110〜180℃、配合時間は5
〜40m i n好ましくは8〜30m i nで十分
均一に混合される。配合物はそのあと押出機などにより
100〜220℃で押し出し、パウダー、ベレット、
フィルム、シートなどに成形することができる。また配
合後直ちにフィルム状またはシート状に押し出してカー
ペット基材に直接裏打ち加工することができる。あらか
じめパウダー状に調製した配合物は、カーペット基材の
裏面に均一に貼布したのち加熱浸漬することによって裏
打ちすることができる。The composition of the present invention can be compounded using mixers such as kneaders, Brabenders, Banburys, rolls, and screw and twin-screw kneaders. For example, (a) ethylene copolymers modified with unsaturated carboxylic acids and/or derivatives thereof, (b) inorganic fillers, (c) plasticizers, softeners, tackifying resins, lubricants, and if necessary (d ) The required amount of each of the ethylene copolymers is added in the desired amount, but the order of addition is not restricted. Heating temperature is 100
~200℃, preferably 110~180℃, blending time 5
-40min, preferably 8-30min, to ensure sufficient uniformity of mixing. The compound is then extruded using an extruder at 100 to 220°C to form powder, pellet,
It can be formed into films, sheets, etc. Immediately after blending, it can be extruded into a film or sheet and can be directly lined onto a carpet substrate. A mixture prepared in advance in powder form can be applied uniformly to the back side of a carpet substrate and then heated and dipped for lining.
ベレット状に成形した配合物は、押出機などによってフ
ィルム状またはシート状に押し出して、カーペット基材
に裏打ち加工することができる。The pellet-formed compound can be extruded into a film or sheet using an extruder or the like to line a carpet substrate.
またフィルム、シートに成形した配合物は、このフrル
ム、シートおよびカーペット基材を加熱もしくは接着剤
を用いて張り合わせることによって裏打ち加工をするこ
とができる。このようにカーペット基材に裏打ちされた
上に、必要あらばざらに織布、不織布、プラスチックフ
ィルム、紙、フェルトなどを積層することができる。Further, the composition formed into a film or sheet can be lined by laminating the film, sheet, and carpet base material together by heating or using an adhesive. On the backing of the carpet base material in this way, woven fabric, non-woven fabric, plastic film, paper, felt, etc. can be laminated as necessary.
本発明の組成物が裏打ち材として使用できるカーペット
基材は、織カーペット、編カーペット、タフテッドカー
ペット、ニードルバンチカーペット、人工芝などであり
、特にタフテッドカーベラ1〜に好ましく使用できる。Carpet base materials for which the composition of the present invention can be used as a backing material include woven carpets, knitted carpets, tufted carpets, needle bunch carpets, artificial grass, etc., and it can be particularly preferably used for tufted carberas 1 to 1.
これらのカーペット基材にラテックス系のプレコート処
理、EVA系ホットメルトタイプ接着剤によるプレコー
ト処理、低密度ポリエチレンのフィルムプレコート処理
などをされたものも使用できる。It is also possible to use these carpet base materials that have been precoated with latex, EVA hot-melt adhesive, low-density polyethylene film, or the like.
本発明の組成物は自動車用カーペット、タイルカーペッ
トの裏打ち材として用いることができる。The composition of the present invention can be used as a backing material for automobile carpets and tile carpets.
[実 施 例]
以下、本発明を実施例によって詳述するが、本発明の要
旨を逸脱しない限り、これらの実施例のみに限定される
ものではない。[Examples] Hereinafter, the present invention will be explained in detail with reference to Examples, but the present invention is not limited to these Examples unless it departs from the gist of the present invention.
なお、この明細書を通して温度は仝て℃であり、部およ
び%は特記しない限り重量基準である。Throughout this specification, temperatures are expressed in °C, and parts and percentages are by weight unless otherwise specified.
実施例 1〜3
溶融法によって作製された無水マレイン酸変性エチレン
−酢酸ビニル共重合体(以下HAn化[■^と略す)
、EVA 、炭酸カルシウム、可塑剤および軟化剤の所
定量を電気加熱式加圧ニーダ−で150℃、30分間混
練し配合物を得た。熱いうちにこれをロールシーテイン
グして冷却し、シートカッターを用いて細断した。これ
を押出機でTダイから200℃でシート状に押出し、タ
フテッドカーペット基材の裏面に広げ、水冷ニップロー
ル間を通して裏打ちした。得られた配合物および裏打ち
カーペットの物性は表1に示したとおり良好であった。Examples 1 to 3 Maleic anhydride-modified ethylene-vinyl acetate copolymer produced by a melting method (hereinafter referred to as HAn [abbreviated as ■^)]
, EVA, calcium carbonate, a plasticizer, and a softener were kneaded in an electrically heated pressure kneader at 150° C. for 30 minutes to obtain a blend. This was roll sheeted while hot, cooled, and shredded using a sheet cutter. This was extruded into a sheet at 200° C. through a T-die using an extruder, spread on the back side of a tufted carpet base material, and passed between water-cooled nip rolls for lining. The physical properties of the resulting blend and backing carpet were good as shown in Table 1.
比較例1〜2
EVA 、炭酸カルシウム、可塑剤の所定量を電気加熱
式加圧ニーダ−で150℃、30分間混練し、これを直
ちにロールシーテイング冷却し、シートカッターで細断
した。これを押出機でTダイから200℃でシート状に
押出しカーペットに裏打ちした。この物性は表1に示し
たように、引張強度、伸び率、引裂強度、折り曲げ性に
劣っていた。Comparative Examples 1 to 2 Predetermined amounts of EVA, calcium carbonate, and plasticizer were kneaded at 150° C. for 30 minutes in an electrically heated pressure kneader, immediately cooled by roll sheeting, and shredded with a sheet cutter. This was extruded into a sheet at 200° C. from a T-die using an extruder and lined with a carpet. As shown in Table 1, the physical properties were poor in tensile strength, elongation, tear strength, and bendability.
実施例 4〜7
溶融法によって作製した無水マレイン酸変性エヂレンー
アクリル酸エチル共重合体(HAn化EE^)、[Eへ
、炭酸カルシウム、可塑剤および軟化剤の所定はを用い
、実施例1と同じ方法で実施し、表2に示したとおり良
好であった。Examples 4 to 7 A maleic anhydride-modified edylene-ethyl acrylate copolymer (HAn-based EE^) prepared by a melting method was prepared using [E, calcium carbonate, a plasticizer, and a softening agent in specified amounts. It was carried out in the same manner as in 1, and the results were good as shown in Table 2.
比較例 3
比較例1においてEVAに替えてEEAを用いたほかは
同様に行ない、その結果を表2に示した。引張強度、伸
び率、引裂強度、折り曲げ性に劣っていた。Comparative Example 3 The same procedure as in Comparative Example 1 was performed except that EEA was used instead of EVA. The results are shown in Table 2. It was inferior in tensile strength, elongation, tear strength, and bendability.
実施例 8〜9
溶融法によって作製したHAn化EE^、EvA、炭酸
カルシウム、粘着付与樹脂の所定量を用い、実施例1と
同じ方法で実施し、表3に示したとおり、良好であった
。Examples 8 to 9 It was carried out in the same manner as in Example 1 using predetermined amounts of HAnified EE^, EvA, calcium carbonate, and tackifying resin prepared by the melting method, and as shown in Table 3, the results were good. .
比較例 4
比較例1において、EVAに替えてEEA 、可塑剤に
替えて粘着付与樹脂の所定量を用いたほかは同様に行い
、その結果を表3に示した。引張強度、引裂強度、折り
曲げ性に劣っていた。Comparative Example 4 Comparative Example 1 was carried out in the same manner as in Comparative Example 1, except that EEA was used instead of EVA and a predetermined amount of tackifying resin was used instead of the plasticizer. The results are shown in Table 3. It was inferior in tensile strength, tear strength, and bendability.
実施例 10
溶融法によって作製した無水マレイン酸変性エチレン−
プロピレン共重合体(HAn化EP) 、[:E^、炭
酸カルシウム、可塑剤の所定量を用い、実施例1と同じ
方法で実施し、表3に示したとおり良好であった。Example 10 Maleic anhydride-modified ethylene produced by melting method
The experiment was carried out in the same manner as in Example 1 using the predetermined amounts of propylene copolymer (HAnized EP), [:E^, calcium carbonate, and plasticizer, and the results were good as shown in Table 3.
比較例 5
エチレン−プロピレン共重合体(EP) 、EEA、炭
酸カルシウム、可塑剤の所定♀を用い、比較例1と同じ
方法で実施し、この結果を表3に示した。Comparative Example 5 The same method as in Comparative Example 1 was conducted using ethylene-propylene copolymer (EP), EEA, calcium carbonate, and a specified ♀ plasticizer, and the results are shown in Table 3.
引張強度、伸び率、引裂強度、折り曲げ性に劣っていた
。It was inferior in tensile strength, elongation, tear strength, and bendability.
[発明の効果1
本発明のカーペット用裏打ち組成物は、不飽和カルボン
酸および/またはその誘導体によって変性されたエチレ
ン共重合体を配合したことにより、配合物の引張強度、
伸び率、引裂強度、折り曲げ性が改善されるとともに、
場合によっては、軟化点、ぜい化温度も良くなり、これ
をカーペットに裏打ちすると、自動車用カーペットにあ
っては、抜糸強度、引張強度、成形保)4性が向上し、
タイルカーペットにあっても同様の効果が得られるもの
である。[Effects of the Invention 1] The carpet backing composition of the present invention has improved tensile strength and
In addition to improving elongation, tear strength, and bendability,
In some cases, the softening point and embrittlement temperature are also improved, and when carpet is lined with this material, the removal strength, tensile strength, and moldability properties of automotive carpets are improved.
A similar effect can be obtained with carpet tiles.
Claims (2)
体によって変性されたエチレン共重合体5〜75重量% (b)無機充てん剤 20〜85重量% (c)可塑剤、軟化剤、粘着付与樹脂、滑剤から選ばれ
た1種または2種以上の混合物1〜20重量% とからなるカーペット用裏打ち組成物。(1) (a) 5-75% by weight of ethylene copolymer modified with unsaturated carboxylic acid and/or its derivatives (b) 20-85% by weight of inorganic filler (c) Plasticizer, softener, tackifier A carpet lining composition comprising 1 to 20% by weight of one or more mixtures of resins and lubricants.
体によって変性されたエチレン共重合体1〜75重量% (b)エチレン共重合体75〜1重量% (c)無機充てん剤20〜85重量% (d)可塑剤、軟化剤、粘着付与樹脂、滑剤から選ばれ
た1種または2種以上の混合物1〜20重量% とからなるカーペット用裏打ち組成物。(2) (a) 1 to 75% by weight of ethylene copolymer modified with unsaturated carboxylic acid and/or its derivatives (b) 75 to 1% by weight of ethylene copolymer (c) 20 to 85% by weight of inorganic filler % (d) A carpet backing composition comprising 1 to 20% by weight of one or a mixture of two or more selected from plasticizers, softeners, tackifying resins, and lubricants.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61168861A JP2514802B2 (en) | 1986-07-17 | 1986-07-17 | Carpet backing composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61168861A JP2514802B2 (en) | 1986-07-17 | 1986-07-17 | Carpet backing composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6328980A true JPS6328980A (en) | 1988-02-06 |
JP2514802B2 JP2514802B2 (en) | 1996-07-10 |
Family
ID=15875918
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61168861A Expired - Lifetime JP2514802B2 (en) | 1986-07-17 | 1986-07-17 | Carpet backing composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2514802B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995014806A1 (en) * | 1993-11-24 | 1995-06-01 | E.I. Du Pont De Nemours And Company | A method for making tufted nylon or polyester pile carpets and carpets prepared therefrom |
WO1998038376A1 (en) * | 1997-02-28 | 1998-09-03 | Shaw Industries, Inc. | Carpet, carpet backings and methods |
EP0753404A3 (en) * | 1995-07-11 | 1999-12-01 | Basf Aktiengesellschaft | Method for producing multilayer materials using an adhesion promoter |
US9376769B2 (en) | 1997-02-28 | 2016-06-28 | Columbia Insurance Company | Homogeneously branched ethylene polymer carpet backsizing compositions |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4856992A (en) * | 1971-11-02 | 1973-08-10 | ||
JPS5225195A (en) * | 1975-08-13 | 1977-02-24 | Sumitomo Chemical Co | Composition for carpet backing |
JPS5468497A (en) * | 1977-11-04 | 1979-06-01 | Japan Synthetic Rubber Co Ltd | Latex composition for carpet backing |
JPS5898479A (en) * | 1981-12-01 | 1983-06-11 | 日本石油化学株式会社 | New carpet lining material |
-
1986
- 1986-07-17 JP JP61168861A patent/JP2514802B2/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4856992A (en) * | 1971-11-02 | 1973-08-10 | ||
JPS5225195A (en) * | 1975-08-13 | 1977-02-24 | Sumitomo Chemical Co | Composition for carpet backing |
JPS5468497A (en) * | 1977-11-04 | 1979-06-01 | Japan Synthetic Rubber Co Ltd | Latex composition for carpet backing |
JPS5898479A (en) * | 1981-12-01 | 1983-06-11 | 日本石油化学株式会社 | New carpet lining material |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995014806A1 (en) * | 1993-11-24 | 1995-06-01 | E.I. Du Pont De Nemours And Company | A method for making tufted nylon or polyester pile carpets and carpets prepared therefrom |
EP0753404A3 (en) * | 1995-07-11 | 1999-12-01 | Basf Aktiengesellschaft | Method for producing multilayer materials using an adhesion promoter |
WO1998038376A1 (en) * | 1997-02-28 | 1998-09-03 | Shaw Industries, Inc. | Carpet, carpet backings and methods |
WO1998038375A3 (en) * | 1997-02-28 | 1998-12-03 | Shaw Ind Inc | Carpet, carpet backings and methods |
US9376769B2 (en) | 1997-02-28 | 2016-06-28 | Columbia Insurance Company | Homogeneously branched ethylene polymer carpet backsizing compositions |
Also Published As
Publication number | Publication date |
---|---|
JP2514802B2 (en) | 1996-07-10 |
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