JPH02203816A - Manufacture of carpet - Google Patents
Manufacture of carpetInfo
- Publication number
- JPH02203816A JPH02203816A JP2256989A JP2256989A JPH02203816A JP H02203816 A JPH02203816 A JP H02203816A JP 2256989 A JP2256989 A JP 2256989A JP 2256989 A JP2256989 A JP 2256989A JP H02203816 A JPH02203816 A JP H02203816A
- Authority
- JP
- Japan
- Prior art keywords
- carpet
- copolymer resin
- ethylene copolymer
- sheet
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 229920001038 ethylene copolymer Polymers 0.000 claims abstract description 35
- 229920005989 resin Polymers 0.000 claims abstract description 35
- 239000011347 resin Substances 0.000 claims abstract description 35
- 239000002313 adhesive film Substances 0.000 claims abstract description 21
- 239000011521 glass Substances 0.000 claims abstract description 18
- 239000011256 inorganic filler Substances 0.000 claims abstract description 18
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 18
- 239000011342 resin composition Substances 0.000 claims abstract description 9
- 238000000034 method Methods 0.000 claims description 18
- 239000004745 nonwoven fabric Substances 0.000 claims description 16
- 238000003825 pressing Methods 0.000 claims description 7
- 239000000203 mixture Substances 0.000 abstract description 14
- 239000004744 fabric Substances 0.000 abstract description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract description 10
- 239000005977 Ethylene Substances 0.000 abstract description 10
- 230000001070 adhesive effect Effects 0.000 abstract description 9
- -1 vinyl compound Chemical class 0.000 abstract description 6
- 239000000853 adhesive Substances 0.000 abstract description 5
- 229920001577 copolymer Polymers 0.000 abstract description 5
- 229920002554 vinyl polymer Polymers 0.000 abstract description 5
- 239000004711 α-olefin Substances 0.000 abstract description 5
- 238000010438 heat treatment Methods 0.000 abstract description 3
- 238000002844 melting Methods 0.000 abstract description 2
- 230000008018 melting Effects 0.000 abstract description 2
- 239000000463 material Substances 0.000 description 23
- 239000010410 layer Substances 0.000 description 16
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 14
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 9
- 239000005038 ethylene vinyl acetate Substances 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 229910000019 calcium carbonate Inorganic materials 0.000 description 7
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 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
- 239000004743 Polypropylene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 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
- 238000005520 cutting process Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- 229920003318 Keldax® Polymers 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- 229920003298 Nucrel® Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products 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 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 229920006271 aliphatic hydrocarbon resin Polymers 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
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 229920006272 aromatic hydrocarbon resin Polymers 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 150000001734 carboxylic acid salts Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 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
- 159000000003 magnesium salts Chemical class 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 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
- 239000002952 polymeric resin Substances 0.000 description 1
- 150000003097 polyterpenes Chemical class 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 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
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Floor Finish (AREA)
- Carpets (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、環境温度の変化に対して、良好な寸法安定性
を示すカーペットの製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for manufacturing a carpet that exhibits good dimensional stability against changes in environmental temperature.
[従来の技術]
カーペットは、基本的には、カーペット原反とその裏面
に形成された裏打ち材とから構成されている。このよう
な裏打ち材として、従来、塩化ビニル樹脂やアスファル
トを主成分とし、これに無機充填剤や可塑剤等を配合し
たものが用いられてきた。しかしながら、塩化ビニル樹
脂ベースのものは、火災時に、発煙量が多いという欠点
があり、またアスファルトベースのものは、臭気や強度
の弱さが問題となって新しい代替裏打ち材の開発が望ま
れていた。[Prior Art] Carpets basically consist of a carpet material and a backing material formed on the back surface thereof. Conventionally, as such a backing material, a material containing vinyl chloride resin or asphalt as a main component and blending an inorganic filler, a plasticizer, etc. therewith has been used. However, vinyl chloride resin-based backing materials have the disadvantage of producing a large amount of smoke in the event of a fire, and asphalt-based backing materials have problems with odor and low strength, so the development of new alternative backing materials is desired. Ta.
こうした新しい代替裏打ち材として、塩化ビニル樹脂ベ
ースのものよりも、火災時における発煙量が少なく、ま
た無毒、無臭で強度も大きい無機充填剤配合エチレン共
重合樹脂組成物を用いるものが注目され、検討され始め
てきた。As a new alternative backing material, one using an ethylene copolymer resin composition containing an inorganic filler, which produces less smoke in the event of a fire, is non-toxic, odorless, and has greater strength than a vinyl chloride resin-based one, has attracted attention and is being studied. It's starting to happen.
[発明が解決しようとする課題]
しかしながら、このような裏打ち材を用い、単純な構成
のカーペットを製造した場合、寸法安定性が必ずしも良
好でないため、とくにタイルカーペット用としては満足
すべきものとはならなかった。[Problems to be Solved by the Invention] However, when a carpet with a simple structure is manufactured using such a backing material, the dimensional stability is not necessarily good, so it is not satisfactory especially for tile carpets. There wasn't.
ところで、タイルカーペットは、小型平板状のカーペッ
トで一般には一辺が30〜50cm程度の方形のものが
多い。タイルカーペットは通常のカーペットに比較して
、取扱いや敷設施工が容易である上に、汚れ等による部
分的な取り替えも簡単に行うことができるという利点が
ある。さらに、数種のタイルカーペットの色、形状等を
組合せることにより、種々の模様を現出させることがで
きるという長所等もあることから、最近急速に使用され
るようになってきた。このタイルカーペットは、壁から
壁まで完全に敷きつめるという施工法がほとんどであり
、このため気温差等による寸法変化を極力低減させない
と、例えば、冬場に施工したものが夏場に膨張して浮き
上ったり、あるいは夏場に施工したものが冬場に収縮し
て隙間ができる等のトラブルを生ずるおそれがあった。By the way, tile carpets are small, flat carpets, and are generally rectangular with a side of about 30 to 50 cm. Tile carpets have the advantage that they are easier to handle and install than regular carpets, and can also be easily replaced due to dirt or the like. Furthermore, it has the advantage of being able to create various patterns by combining the colors, shapes, etc. of several types of tile carpets, and has recently come to be used rapidly. Most of these carpet tiles are installed by completely laying them from wall to wall. Therefore, unless dimensional changes due to temperature differences are minimized, for example, carpet tiles installed in the winter may expand and float in the summer. Otherwise, there was a risk that something constructed in the summer would shrink in the winter, causing problems such as gaps being formed.
このような欠点を改良するために、例えば、特開昭61
−49886号公報には、カーペット原反と裏打ち材の
間に熱に対して線膨張係数の小さい網目状の基布を用い
る方法が示されている。しかしながら、本発明者らの検
討によれば、この公共重合樹脂系熱接着フィルム
(b)ガラス不織布
(c)溶融押出しされたシート状の無機充填剤配合エチ
レン共重合樹脂組成物を、この順序に重ね合せ、該シー
トの熱間時に押圧し、該シートの熱間時に押圧して一体
化させることを特徴とするカーペットの製造方法が提供
される。In order to improve such drawbacks, for example, Japanese Patent Application Laid-Open No. 61
Japanese Patent No. 49886 discloses a method of using a mesh-like base fabric with a small coefficient of linear expansion against heat between the original carpet material and the backing material. However, according to the studies of the present inventors, this public polymer resin thermal adhesive film (b) glass nonwoven fabric (c) melt-extruded sheet-like inorganic filler-containing ethylene copolymer resin composition was added in this order. A method for manufacturing a carpet is provided, which comprises stacking the sheets together, pressing the sheets together while they are hot, and pressing the sheets together while they are hot.
本発明においては、カーペット原反としては天然繊維、
合成繊維、再生繊維等種々の素材から製造されるものが
使用できる。より具体的には、麻、綿、羊毛等の天然繊
維、ポリプロピレン、ポリアミド、ポリエステル、ポリ
アクリロニトリル、ポリ塩化ビニリデン等の合成繊維等
からなるタフテッドカーペットやニードルパンチカーペ
ット等を例示することができる。これらカーペット原反
裏面にはSBRラテックス処理等のプレコート処理が行
われていてもよい。In the present invention, the carpet material includes natural fibers,
Those manufactured from various materials such as synthetic fibers and recycled fibers can be used. More specifically, examples include tufted carpets and needle punch carpets made of natural fibers such as linen, cotton, and wool, and synthetic fibers such as polypropylene, polyamide, polyester, polyacrylonitrile, and polyvinylidene chloride. The back surface of these carpet raw materials may be subjected to a precoating treatment such as SBR latex treatment.
本発明においては、カーペット原反の裏面とガラス不織
布(b)を強固に接着させるために、目付量が10〜2
00g/m2のエチレン共重合樹脂層に開示されている
ような、開孔度の大きい網目状の基布を用いた場合には
、寸法安定性が充分満足しつるものにはならないことを
認めた。さらに、特開昭61−19887号公報によれ
ば、裏打ち材層を2層に分け、その間に熱に対して線膨
張係数の小さい中間基布を設ける方法を提案している。In the present invention, in order to firmly adhere the back side of the carpet material and the glass nonwoven fabric (b), the basis weight is 10 to 2.
It was recognized that when using a mesh-like base fabric with a large degree of porosity, such as the one disclosed for the ethylene copolymer resin layer of 00 g/m2, the dimensional stability would not be sufficiently satisfied and the material would not hang. . Furthermore, Japanese Patent Application Laid-Open No. 19887/1987 proposes a method in which the backing material layer is divided into two layers and an intermediate base fabric having a small linear expansion coefficient against heat is provided between them.
しかしながらこの方法では、裏打ち材を2度にわたって
カーペット基材に積層する必要があり、装置、操作両面
からみて経済的に不利な方法であった。However, this method requires the backing material to be laminated twice on the carpet base material, which is economically disadvantageous in terms of both equipment and operation.
本発明者らは、従来技術における前述の欠点を改善し、
寸法安定性及び強度の優れたカーペット、とりわけタイ
ルカーペットを経済的に製造する方法につき検討を行っ
た。その結果、エチレン共重合樹脂系熱接着フィルムと
ガラス不織布を用いて、所望のカーペットを一段階で製
造しうる方法を見出すに至った。The present inventors have improved the above-mentioned shortcomings in the prior art,
We investigated methods for economically producing carpets with excellent dimensional stability and strength, especially tile carpets. As a result, we have discovered a method for manufacturing a desired carpet in one step using an ethylene copolymer resin thermal adhesive film and a glass nonwoven fabric.
[課題を解決するための手段]
本発明によれば、カーペット原反の裏面に、(a)目付
量が10〜200g/m2のエチレン系熱接着フィルム
(a)が用いられる。このエチレン共重合樹脂は、エチ
レンを主成分として、これにα−オレフィンや極性ビニ
ル化合物等を共重合成分とするものであって、後記(c
)成分の溶融押出シートの保有する熱により溶融し、接
着剤としての働きをなすものである。より具体的には、
前記α−オレフィンとしては、プロピレン、1−ブテン
、1−ペンテン、1−ヘキセン、1−ヘプテン、1−オ
クテン、1−デセン、4−メチル−1−ペンテン等、ま
た極性ビニル化合物としては、酢酸ビニル、プロピオン
酸ビニル等のビニルエステル、アクリル酸、メタクリル
酸、フマル酸、無水マレイン酸のような不飽和カルボン
酸、またはその無水物、これらのナトリウム塩、カリウ
ム塩、リチウム塩、マグネシウム塩、亜鉛塩、アンモニ
ウム塩のような、不飽和カルボン酸塩、アクリル酸メチ
ル、アクリル酸エチル、アクリル酸イソブチル、アクリ
ル酸n−ブチル、メタクリル酸メチル、メタクリル酸グ
リシジルのような不飽和カルボン酸エステル等を例示す
ることができこれら共重合成分は、勿論2種以上共重合
されていてもよい。これら共重合成分は、ランダム共重
合されたものであってもよく、またグラフト共重合され
たものであってもよい。[Means for Solving the Problems] According to the present invention, an ethylene-based thermal adhesive film (a) having a basis weight of 10 to 200 g/m2 is used on the back side of the original carpet. This ethylene copolymer resin has ethylene as its main component and copolymerized components such as α-olefin and polar vinyl compounds.
) is melted by the heat possessed by the melt-extruded sheet of the component, and functions as an adhesive. More specifically,
Examples of the α-olefin include propylene, 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene, 1-decene, 4-methyl-1-pentene, etc., and the polar vinyl compound includes acetic acid. Vinyl, vinyl esters such as vinyl propionate, unsaturated carboxylic acids such as acrylic acid, methacrylic acid, fumaric acid, maleic anhydride, or their anhydrides, their sodium salts, potassium salts, lithium salts, magnesium salts, zinc Examples include unsaturated carboxylic acid salts such as salts and ammonium salts, unsaturated carboxylic acid esters such as methyl acrylate, ethyl acrylate, isobutyl acrylate, n-butyl acrylate, methyl methacrylate, and glycidyl methacrylate. Of course, two or more of these copolymerizable components may be copolymerized. These copolymerization components may be randomly copolymerized or graft copolymerized.
エチレン−α−オレフィン共重合樹脂にあっては、エチ
レンが80〜95モル%程度含有しているものが好まし
く、また、エチレン−極性ビニル化合物共重合体にあっ
ては、エチレンが55〜95重量%のものが好ましい。The ethylene-α-olefin copolymer resin preferably contains about 80 to 95 mol% of ethylene, and the ethylene-polar vinyl compound copolymer preferably contains 55 to 95 mol% of ethylene. % is preferred.
これら共重合体樹脂はまた、2種類以上併用してもよい
。Two or more of these copolymer resins may also be used in combination.
カーペットやガラス繊維に対する接着性あるいはフィル
ムの生産性の観点からみて、好ましいエチレン共重合樹
脂は、エチレン−極性ビニル化合物共重合体、とりわけ
エチレン−酢酸ビニル共重合体であり、そのエチレン含
量として70〜95重量%のものである。また、190
℃、2160g荷重で測定したメルトフローレートが0
.1〜200g/10分、とくに1〜100g/10分
のものが好適である。From the viewpoint of adhesion to carpets and glass fibers or film productivity, preferred ethylene copolymer resins are ethylene-polar vinyl compound copolymers, especially ethylene-vinyl acetate copolymers, with an ethylene content of 70 to 70%. It is 95% by weight. Also, 190
The melt flow rate measured at ℃ and 2160g load is 0.
.. 1 to 200 g/10 minutes, particularly 1 to 100 g/10 minutes, is suitable.
す、その目付量が10〜300g/rrr1とくに30
〜150 glrd程度のものを用いるのが好ましい。The basis weight is 10 to 300g/rrr1, especially 30
It is preferable to use one having a weight of about 150 glrd.
目付量が少なすぎると、寸法安定性良好なものが得られ
ず、また反対に目付量が多すぎると、カーペットが剛直
になりすぎる傾向があるので適当な範囲のものを選択使
用すべきである。If the basis weight is too low, it will not be possible to obtain a product with good dimensional stability, and on the other hand, if the basis weight is too high, the carpet will tend to become too rigid, so one should select and use a carpet within an appropriate range. .
特開昭61−19886号公報に開示されている方法で
は、裏打ち材を通過させるために必要な開孔度を有する
網目上の基布が用いられているがこのような開孔度の大
きい開孔処理を施した不織布を用いたり、あるいは織布
を用いたりしたのでは、寸法安定性の優れたカーペット
を得ることができない。In the method disclosed in Japanese Patent Application Laid-Open No. 19886/1986, a mesh-like base fabric having a degree of opening necessary for passing the backing material is used. If a nonwoven fabric treated with holes or a woven fabric is used, a carpet with excellent dimensional stability cannot be obtained.
本発明においては、シート状に溶融押出しされた(c)
成分の接着性および(c)成分の保有する熱によって溶
融した(a)成分の接着性を利用して、カーペットを構
成する各層を一体化するので、(c)成分がガラス不織
布を通り抜ける必要はなく、本発明において用いるガラ
ス不織布は、逆に開孔度が小さく、カーペットの成形時
に、これらエチレン共重合樹脂には、熱接着性等を改良
する目的で、脂肪族系炭化水素樹脂、脂環族系炭化水素
樹脂、芳香族系炭化水素樹脂、ポリテルペン系樹脂、ロ
ジン類、スチレン系樹脂等の粘着付与剤を、例えば25
重量%までの量で配合して用いてもよい。さらに、フィ
ルムのスリップ性を改良するためのスリップ剤、その地
番種添加剤を配合することができる。In the present invention, (c) is melt-extruded into a sheet shape.
The layers constituting the carpet are integrated by utilizing the adhesive properties of the components and the adhesive properties of component (a) melted by the heat possessed by component (c), so there is no need for component (c) to pass through the glass nonwoven fabric. On the contrary, the glass nonwoven fabric used in the present invention has a small porosity, and when forming a carpet, these ethylene copolymer resins are mixed with aliphatic hydrocarbon resins and alicyclic resins for the purpose of improving thermal adhesion. For example, a tackifier such as a group hydrocarbon resin, an aromatic hydrocarbon resin, a polyterpene resin, a rosin, a styrene resin, etc.
They may be used in amounts up to % by weight. Furthermore, a slip agent and a lot number additive for improving the slip properties of the film can be blended.
熱接着フィルムは、その目付量が5〜200g/ゴ、好
ましくは15〜100 g/rrlとなる量で用いられ
る。目付量が上記範囲より少ないと、カーペット原反と
ガラス不織布の間の接着力が充分でな(、またその目付
量が多(なりすぎると、(c)成分の溶融押出シートの
保有する熱によって充分に溶融せず、接着剤として機能
し難(なる。The thermal adhesive film is used in an amount such that its basis weight is 5 to 200 g/rrl, preferably 15 to 100 g/rrl. If the basis weight is less than the above range, the adhesion between the carpet material and the glass nonwoven fabric will not be sufficient (and if the basis weight is too large, the heat retained by the melt-extruded sheet of component (c) will It does not melt sufficiently and has difficulty functioning as an adhesive.
本発明においては、カーペットに寸法安定性を付与する
ため、ガラス不織布(b)が用いられる。ガラス不織布
は、ガラス繊維を任意の方向に一定の厚みに積み重ね、
凝結剤で固めたものであ(c)成分が実質的に(a)成
分側まで通り抜けないものであるべきであり、実質的に
開孔処理は施されていない。このような開孔度の小さい
ガラス不織布を用いるので、製造されたカーペットの寸
法安定性は著しく向上する。 本発明においては、裏打
ち材として無機充填剤配合エチレン共重合樹脂組成物が
用いられる。この目的に使用されるエチレン共重合樹脂
は、(a)成分で説明したエチレン共重合樹脂と同様の
ものが使用できる。In the present invention, a glass nonwoven fabric (b) is used to impart dimensional stability to the carpet. Glass nonwoven fabric is made by stacking glass fibers in any direction to a certain thickness.
It should be solidified with a coagulant so that component (c) will not substantially pass through to the component (a) side, and substantially no hole-opening treatment will be performed. By using such a glass nonwoven fabric with a small degree of porosity, the dimensional stability of the manufactured carpet is significantly improved. In the present invention, an ethylene copolymer resin composition containing an inorganic filler is used as the backing material. The ethylene copolymer resin used for this purpose can be the same as the ethylene copolymer resin explained for component (a).
と(にT−ダイ等を用いてシート状に押出す際に、とく
に優れた成形性を保つために、そのメルトフローレート
は1〜150g/10分、とくに1〜50g/10分程
度のものが好ましい。また経済性、無機充填剤との混和
性、柔軟性、耐寒性等の観点から、エチレン共重合樹脂
として、エチレン−酢酸ビニル共重合体を使用するのが
よい。(In order to maintain particularly excellent formability when extruding into a sheet using a T-die etc., the melt flow rate is 1 to 150 g/10 minutes, especially 1 to 50 g/10 minutes. It is preferable to use an ethylene-vinyl acetate copolymer as the ethylene copolymer resin from the viewpoints of economy, miscibility with inorganic fillers, flexibility, cold resistance, etc.
該共重合体として好適なものは、上記性質及び耐熱性等
を考慮すると酢酸ビニル含量が10〜40重量%程度の
ものを用いるのが好ましい。勿論、このようなエチレン
酢酸ビニル共重合体の一部、例えば、半量以下を他のエ
チレン共重合樹脂、例えば、エチレン−α−オレフィン
共重合体やエチレンー不飽和カルボン酸共重合体等で置
き換えることができる。The copolymer preferably has a vinyl acetate content of about 10 to 40% by weight, considering the above properties and heat resistance. Of course, a part of such ethylene-vinyl acetate copolymer, for example, half or less, can be replaced with other ethylene copolymer resin, such as ethylene-α-olefin copolymer or ethylene-unsaturated carboxylic acid copolymer. Can be done.
エチレン共重合樹脂に混練される無機充填剤としては、
炭酸カルシウム、硫酸バリウム、シリカ、タルク、クレ
イ、雲母、水酸化マグネシウム、水酸化アルミニウム等
が用いられる。これらは、コストダウン、重量性付与、
寸法安定性等の目的で使用されるものであって、コスト
あるいはエチレン共重合樹脂との混和性の点からみて、
とくに炭酸カルシウムが好適である。上記目的を達成す
るため、無機充填剤の使用量は、エチレン共重合体樹脂
組成物中、少なくとも20重量%以上、好ましくは30
重量%以上とするのが望ましいが、あまり配合量を増や
しすぎるとシート成形性が悪くなるので、80重量%以
下とするのが望ましい。Inorganic fillers to be kneaded into ethylene copolymer resin include:
Calcium carbonate, barium sulfate, silica, talc, clay, mica, magnesium hydroxide, aluminum hydroxide, etc. are used. These are cost reduction, weight addition,
It is used for the purpose of dimensional stability etc., and from the point of view of cost or miscibility with ethylene copolymer resin,
Particularly suitable is calcium carbonate. In order to achieve the above object, the amount of inorganic filler used in the ethylene copolymer resin composition is at least 20% by weight, preferably 30% by weight.
It is desirable that the amount be at least 80% by weight, but if the amount is increased too much, the sheet formability will deteriorate, so it is desirable that the amount be 80% by weight or less.
エチレン共重合樹脂は、組成物中、20〜80重量%、
とくに30〜80重量%とするのがよい無機充填剤のマ
スターバッチを作り、このベレットとエチレン共重合樹
脂をT−ダイ押出加工時に直接任意の比率でトライブレ
ンドする事により、使用する方法がある。The ethylene copolymer resin is 20 to 80% by weight in the composition,
There is a method of using it by making a master batch of inorganic filler, which is preferably 30 to 80% by weight, and tri-blending this pellet and ethylene copolymer resin directly at an arbitrary ratio during T-die extrusion processing. .
シート成形は、T−ダイ押出機によって行われる。この
際、シートの目付量は、タイルカーペット用には重量性
を付与し、歩行時に動かないようにするため、1kg/
r&以上とするのが好ましいが、あまり目付量を大きく
すると剛直になりすぎ、施工性が悪くなるので、5kg
/n−r以下とするのがよい。Sheet forming is performed by a T-die extruder. At this time, the basis weight of the sheet is 1 kg/1 kg for tile carpets to give it weight and prevent it from moving when walking.
It is preferable to set it to r& or more, but if the area weight is too large, it will become too rigid and workability will deteriorate, so 5kg
It is preferable to set it to /nr or less.
本発明においては、カーペット原反裏面に、前記エチレ
ン共重合樹脂系熱接着フィルム、ガラス不織布及び溶融
押出しされたシート状の無機充填剤配合エチレン共重合
樹脂系組成物をこの順序に重ね合せ、溶融押出しされた
上記シートの熱間時に押圧し、該シートおよび該シート
の保有する熱によるエチレン共重合樹脂系熱接着フィル
ムの溶融接着作用によりカーペットを構成する各層を一
体化させるものである。抑圧一体化は、圧着ローが、無
機充填剤との配合を容易にするため、あるいは組成物の
シート成形性を改良するために、先に例示したような粘
着付与剤、ワックス、低分子量オレフィン重合体、液状
可塑剤、油等を、エチレン共重合樹脂の一部に替えて使
用することができる。これらの加工性改善用添加剤は、
例えば、組成物全体の20重量%以下の量で使用される
。In the present invention, the ethylene copolymer resin thermal adhesive film, the glass nonwoven fabric, and the melt-extruded sheet-like ethylene copolymer resin composition containing an inorganic filler are superimposed on the back side of the original carpet in this order, and then melted. The extruded sheet is pressed while hot, and the layers constituting the carpet are integrated by the melting adhesive action of the sheet and the ethylene copolymer resin thermal adhesive film caused by the heat possessed by the sheet. Suppressing integration is a process in which the crimping row is injected with tackifiers, waxes, and low molecular weight olefins, such as those exemplified above, in order to facilitate blending with inorganic fillers or to improve the sheet formability of the composition. A liquid plasticizer, oil, etc. can be used in place of a part of the ethylene copolymer resin. These additives for improving processability are
For example, it is used in an amount of up to 20% by weight of the total composition.
エチレン共重合樹脂組成物には、また、各種安定剤、難
燃付与剤、顔料等の添加剤を適宜配合することができる
。The ethylene copolymer resin composition may also contain additives such as various stabilizers, flame retardants, pigments, and the like.
エチレン共重合樹脂に無機充填剤をブレンドする方法に
は、とくに制限はない。カレンダーロール、バンバリー
ミキサ−、ヘンシェルミキサー、2軸混練機等で、直接
、粉末状の無機充填剤と、エチレン共重合樹脂をブレン
ドする事により、ベレット状のエチレン共重合樹脂と無
機充填剤の配合組成物を作成し、これを用いて、T−ダ
イ押出加工する方法。また、粉末状の無機充填剤と前記
加工性改善用添加剤とをバンバリーミキサ−12軸混練
機等を用いて混合してベレット状の高濃度ルを通すこと
によって、好適に行われる。この際、熱接着フィルムが
溶融されること、及び各層が抑圧により互いに接着して
一体化するような条件を選定する必要がある。そのため
には、押圧部における上記押出しシートが軟化状態にあ
る温度、例えば100〜200℃に維持するとともに、
圧着ロールを線圧2〜10Kg/crrrの如き条件を
保てばよい。There are no particular limitations on the method of blending the inorganic filler with the ethylene copolymer resin. By directly blending the powdered inorganic filler and ethylene copolymer resin using a calender roll, Banbury mixer, Henschel mixer, twin-screw kneader, etc., the pellet-shaped ethylene copolymer resin and inorganic filler are blended. A method of preparing a composition and performing T-die extrusion processing using the composition. It is also suitably carried out by mixing the powdered inorganic filler and the processability improving additive using a Banbury mixer, 12-screw kneader, etc., and passing the mixture through a pellet-shaped high-concentration tube. At this time, it is necessary to select conditions such that the thermal adhesive film is melted and the layers are bonded to each other and integrated by compression. For this purpose, the extruded sheet in the pressing part is maintained at a temperature at which it is in a softened state, for example, 100 to 200°C, and
The pressure roll may be maintained at a linear pressure of 2 to 10 kg/crrr.
本発明においては、溶融押出シートの熱間時にカーペッ
トを構成する各層を重ねあわせて押圧することにより、
該シートの溶融接着性を利用し、かつ該シートが保有す
る熱によりエチレン系熱接着フィルムを溶融させて接着
剤として利用して、これらを同時に一体化するので、1
段でカーペットを製造することができる。 このような
1段のプロセスの代りに、エチレン系熱接着フィルムを
予めカーペット原反裏面にコートしておく方法をとるの
は、工程が複雑になるばかりか、カーペットにテンショ
ンがかかり、却って寸法安定性を悪くすることになるの
で好ましい方法とはいえな上記の如く、押圧一体化した
後は、必要に応じ冷却後、所望形状に切断することによ
りタイルカーペットを製造することができる。In the present invention, by overlapping and pressing the layers constituting the carpet while the melt-extruded sheet is hot,
Utilizing the melt adhesive properties of the sheet, and using the heat possessed by the sheet to melt the ethylene-based thermal adhesive film and use it as an adhesive, these are integrated at the same time.
Carpets can be manufactured in stages. Instead of such a one-step process, applying a method in which the back side of the carpet material is coated with an ethylene-based thermal adhesive film not only complicates the process, but also puts tension on the carpet, making it more difficult to maintain its dimensional stability. Although this is not a preferable method because it will impair the properties, after pressing and integrating as described above, a tile carpet can be produced by cooling if necessary and cutting into a desired shape.
[実施例]
以下に実施例及び比較例によって本発明を具体的に説明
する。[Example] The present invention will be specifically explained below using Examples and Comparative Examples.
実施例1
ポリエチレンワックス(以下PEWAXと略す。)(密
度0.93g/ctrl、分子量4000)10部と、
アタクティックボリプロピレン(以下APPと略す。)
(密度0.87g/crtf、分子量30000)10
部、ステアリン酸カルシウム0.2部及び炭酸カルシウ
ム80部とを、バンバリーミキサ−を用いて温度125
℃の条件下で、溶融混合した後、溶融混合物を押出機を
通して、排出する事によってペレット化し、ベレット状
の高濃度炭酸カルシウムの配合物を得た。(以下CaC
0,MBと略す。)次いで、エバフレックスP3307
(三井・デュポンポリケミカル■製X500mmの寸
法に裁断した後、以下に示す物性の評価を行った。Example 1 10 parts of polyethylene wax (hereinafter abbreviated as PEWAX) (density 0.93 g/ctrl, molecular weight 4000),
Atactic polypropylene (hereinafter abbreviated as APP)
(density 0.87g/crtf, molecular weight 30000) 10
1 part, 0.2 parts of calcium stearate, and 80 parts of calcium carbonate at a temperature of 125 parts using a Banbury mixer.
After melt-mixing under conditions of 0.degree. C., the molten mixture was pelletized by passing through an extruder and discharging to obtain a pellet-shaped blend of high concentration calcium carbonate. (hereinafter CaC
It is abbreviated as 0,MB. ) Then Evaflex P3307
(Mitsui DuPont Polychemical ■) After cutting into a size of 500 mm, the following physical properties were evaluated.
(1)寸法安定性 タイルカーペットのタテ方向(T
−グイシートの流れ方向)、ヨコ方向(T−ダイシート
の流れ方向に対して直角方向)に、それぞれ23℃に於
いて、3本ずつ標準線を弓き、0.05mm単位まで、
寸法を実測する。この後、60℃の熱風循環式乾燥機内
に2時間放置し、その後、非イオン活性剤0.1%を含
む20℃の水の中に浸漬する。2時間後、水中より取出
し、水切りした後、60℃の乾燥機で、24時間乾燥さ
せた試験片を標準状態に24時間放置し、寸法を測定す
る。未処理時の寸法と、処理後の寸法の変化を%で表示
する。(1) Dimensional stability Vertical direction (T
- Draw three standard lines in each direction (direction of flow of T-die sheet) and horizontal direction (direction perpendicular to the direction of flow of T-die sheet) at 23°C to the nearest 0.05 mm.
Measure the dimensions. Thereafter, it is left in a hot air circulation dryer at 60° C. for 2 hours, and then immersed in water at 20° C. containing 0.1% of a nonionic activator. After 2 hours, the specimen was taken out of the water, drained, dried in a dryer at 60° C. for 24 hours, left in standard conditions for 24 hours, and its dimensions were measured. Displays the change in dimensions between untreated dimensions and dimensions after treatment as a percentage.
(2)抜糸強度
通常の引張試験機を用いて23℃、引張速度200mm
/minの条件下で、パイルの抜糸強度を測定した。(2) Stitch removal strength Using a normal tensile tester at 23°C and a tensile speed of 200 mm
The thread removal strength of the pile was measured under the condition of /min.
これらの評価結果を表−1に示す。These evaluation results are shown in Table-1.
尚、熱接着フィルム層を第1層、T−グイシーEVA、
酢酸ビニル含量33重量%、M、F、R30g/10分
)40重量部と、Ca COsMB60重量部とをトラ
イブレンドして得た混合物を巾700mmのT−グイを
備えた65mm押出機(L/D=24)を用いて、T−
グイ温度150°Cの加工条件で、巾600mm、目付
量2.6kg/r&の炭酸カルシウム含有EVAのシー
トを成形し、さらに該シートが冷却固化する前に、T−
グイ上方より、カーペット原反(ナイロンパイル、第1
基布)と、通常のT−グイフィルム成形法によって作成
されたエバフレックスP。In addition, the first layer of thermal adhesive film layer is T-Guicy EVA,
A mixture obtained by tri-blending 40 parts by weight of vinyl acetate (33% by weight, 30 g/10 min) of M, F, R and 60 parts by weight of CaCOsMB was heated in a 65 mm extruder (L/ D=24), T-
A sheet of calcium carbonate-containing EVA with a width of 600 mm and a basis weight of 2.6 kg/r was formed under the processing conditions of a temperature of 150°C, and before the sheet was cooled and solidified, T-
From above, the carpet material (nylon pile, 1st
(base fabric) and Evaflex P created by the normal T-gui film molding method.
1905 (三井・デュポン ポリケミカル■製EVA
、酢酸ビニル含量19重量%、M、 F、 R2,5g
/10分)の目付量30g/ゴのフィルムと、ガラス不
織布(目付量45 g/rf)とが重ね合された3層構
成体を、ガラス不織布面が、炭酸カルシウム含有EVA
のシート面と接触するように、送り込んで、タイルカー
ペットの原反を作成した。1905 (Mitsui DuPont Polychemical ■EVA
, vinyl acetate content 19% by weight, M, F, R2.5g
A three-layer structure in which a film with a basis weight of 30 g/rf (20 min.) and a glass nonwoven fabric (10 min.
The raw material for carpet tiles was created by feeding the carpet so that it was in contact with the sheet surface of the carpet.
さらに、タイルカーペットの原反な500mmト層を第
2層とした。Furthermore, a 500 mm thick layer of original tile carpet was used as a second layer.
実施型λ
実施例1に於いて、熱接着フィルムの目付量を100g
/rrrにした以外は、実施例1と全く同様にしてカー
ペットを製造し、評価を行った。この結果を表−1に示
す。Implementation type λ In Example 1, the basis weight of the thermal adhesive film was 100g.
A carpet was manufactured and evaluated in exactly the same manner as in Example 1, except that the ratio was changed to /rrr. The results are shown in Table-1.
実施伝旦
実施例1に於いて、熱接着フィルムの種類をエバフレッ
クスV−340(三井・デュポンポリケミカル■製EV
A、酢酸ビニル含量10wt%M、F、R1,9g/1
0分)に変えた以外は、実施例1と全(同様にしてカー
ペットを製造し、評価を行った。この結果を表−1に示
す。In Implementation Example 1, the type of thermal adhesive film was Evaflex V-340 (EV manufactured by Mitsui DuPont Polychemicals).
A, vinyl acetate content 10wt% M, F, R1,9g/1
A carpet was manufactured and evaluated in the same manner as in Example 1, except that the heating time was changed to 0 minutes). The results are shown in Table 1.
実施型A
実施例1に於いて、熱接着フィルムの種類をエチレン−
メタクリル酸共重合樹脂、ニュクレル925(三井・デ
ュポン ポリケミカル■製、M、F、R25g/10分
、メタクリル酸含量15wt%)に変更した以外は、実
施例1と全(同様にしてカーペットを製造し、評価を行
った。Embodiment A In Example 1, the type of thermal adhesive film was changed to ethylene-
A carpet was produced in the same manner as in Example 1, except that the methacrylic acid copolymer resin was changed to Nucrel 925 (Mitsui DuPont Polychemical ■, M, F, R 25 g/10 min, methacrylic acid content 15 wt%). and conducted an evaluation.
この結果を表−1に示す。The results are shown in Table-1.
実施桝互
実施例1に於いて、熱接着フィルムの種類を、エチレン
−エチルアクリレート共重合樹脂、エバフレックス・E
EA A702 (三井・デュポンポリケミカル■製
、M、F、R5g/10分エチルアクリレート含量19
wt%)に変更した以外は、実施例1と全く同様にして
カーペットを製造し、評価を行った。この結果を表−1
に示す。In Example 1, the type of thermal adhesive film was ethylene-ethyl acrylate copolymer resin, Evaflex E
EA A702 (manufactured by Mitsui DuPont Polychemical ■, M, F, R 5g/10 minutes Ethyl acrylate content 19
A carpet was manufactured and evaluated in exactly the same manner as in Example 1, except that the ratio was changed to (wt%). Table 1 shows the results.
Shown below.
実施例負
実施例−1に於いて、熱接着フィルムの種類をエバフレ
ックスV−34085wt%と、炭化水素系粘着剤 F
TR−6100(三井石油化学工業■製、軟化点97℃
)15wt%からなる配合組成物に変更した以外は、実
施例1と全く同様にしてカーペットを製造し、評価を行
った。この結果を表−1に示す。Example In negative example-1, the type of thermal adhesive film was Evaflex V-34085wt%, and the hydrocarbon adhesive F
TR-6100 (manufactured by Mitsui Petrochemical Industries, Ltd., softening point 97°C
) A carpet was produced and evaluated in exactly the same manner as in Example 1, except that the blended composition was changed to 15 wt%. The results are shown in Table-1.
実施例1
実施例1に於いて、ガラス不織布の種類を、目付量20
0 g/dのものに変更した以外は、実施例と全く同様
にしてカーペットを製造し、評価を行った。この結果を
表−1に示す。Example 1 In Example 1, the type of glass nonwoven fabric was changed to a basis weight of 20.
A carpet was manufactured and evaluated in exactly the same manner as in the example except that the carpet was changed to 0 g/d. The results are shown in Table-1.
実施例1
実施例1に於いて第2層のEVAとCaC0゜MBの比
率を、EVA、60 w t% CaCO3MB 4
0wt%に変更した以外は、実施例1と全(同様にして
カーペットを製造し、評価を行った。この結果を表−1
に示す。Example 1 In Example 1, the ratio of EVA and CaCO3MB in the second layer was changed to EVA, 60 wt% CaCO3MB4
A carpet was manufactured and evaluated in the same manner as in Example 1, except that the content was changed to 0 wt%.The results are shown in Table 1.
Shown below.
実施例旦
実施例1に於いて、第2層をEVAとプロセスオイルと
炭酸カルシウムの混合物であるKeldax6826
(米国1)upont社製、炭酸カルシウム含量72w
t%、M、F、R,3g/10分)を用いた以外は、実
施例1と全(同様にしてカーペットを製造し、評価を行
った。この結果を表−1に示す。Example In Example 1, the second layer was Keldax 6826, which is a mixture of EVA, process oil, and calcium carbonate.
(USA 1) Manufactured by Upont, calcium carbonate content 72w
A carpet was manufactured and evaluated in the same manner as in Example 1, except that t%, M, F, R, 3 g/10 min) was used. The results are shown in Table 1.
比較例よ
実施例1に於いて、第1層を用いない以外は、実施例1
と全く同様にしてカーペットを製造し、評価を行っ。こ
の結果を表−2に示す。Comparative Example Example 1 except that the first layer is not used.
Carpets were manufactured and evaluated in exactly the same manner. The results are shown in Table-2.
比較例λ
実施例1に於いて、第1層を、高圧法低密度ポリエチレ
ン(三井石油工業■製ミラソンM−68(M、F、R2
3g/10分、密度0.916g/arrr・・以下L
DPEと略す。)に変更した以外は、実施例1と全く同
様にしてカーペットを製造し、評価を行った。この結果
を表−2に示す。Comparative Example λ In Example 1, the first layer was made of high-pressure low-density polyethylene (Mirason M-68 (M, F, R2 manufactured by Mitsui Oil Industries, Ltd.)).
3g/10 minutes, density 0.916g/arrr...less than L
It is abbreviated as DPE. ) A carpet was manufactured and evaluated in exactly the same manner as in Example 1, except for changing to . The results are shown in Table-2.
比較例λ
実施例1に於いて、ガラス不織布を用いない以外は、実
施例1と全く同様にしてカーペットを製造し、評価を行
った。この結果を表−2に示す。Comparative Example λ In Example 1, a carpet was manufactured and evaluated in exactly the same manner as in Example 1, except that the glass nonwoven fabric was not used. The results are shown in Table-2.
以下余白
來
[発明の効果]
本発明によれば、溶融押出しされた無機充填剤配合エチ
レン共重合樹脂組成物のシート上にカーペット原反、エ
チレン系熱接着フィルムおよびガラス不織布を重ね合わ
せ、上記シートの熱間時に押圧するだけの簡単な操作で
、寸法安定性、強度、層間接着性等が良好なタイルカー
ペットを製造することができる。[Effects of the Invention] According to the present invention, a carpet raw material, an ethylene-based thermal adhesive film, and a glass nonwoven fabric are superimposed on a sheet of a melt-extruded inorganic filler-containing ethylene copolymer resin composition, and the above-mentioned sheet is A tile carpet with good dimensional stability, strength, interlayer adhesion, etc. can be manufactured by a simple operation of pressing the carpet while it is hot.
Claims (1)
合樹脂系熱接着フィルム (b)ガラス不織布 (c)溶融押出しされたシート状の無機充填剤配合エチ
レン共重合樹脂組成物 をこの順序に重ね合せ、該シートの熱間時に押圧して一
体化させることを特徴とするカーペットの製造方法。[Claims] 1. On the back side of the original carpet (a) an ethylene copolymer resin thermal adhesive film with a basis weight of 10 to 200 g/m^2, (b) a glass nonwoven fabric, and (c) a melt-extruded sheet. A method for manufacturing a carpet, which comprises stacking the inorganic filler-containing ethylene copolymer resin compositions in this order and pressing the sheets together while they are hot.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1022569A JPH084549B2 (en) | 1989-02-02 | 1989-02-02 | Carpet manufacturing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1022569A JPH084549B2 (en) | 1989-02-02 | 1989-02-02 | Carpet manufacturing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02203816A true JPH02203816A (en) | 1990-08-13 |
JPH084549B2 JPH084549B2 (en) | 1996-01-24 |
Family
ID=12086508
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1022569A Expired - Lifetime JPH084549B2 (en) | 1989-02-02 | 1989-02-02 | Carpet manufacturing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH084549B2 (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5776579U (en) * | 1980-10-29 | 1982-05-12 | ||
JPS6399811A (en) * | 1986-10-15 | 1988-05-02 | 東洋リノリユ−ム株式会社 | Tile carpet and its production |
-
1989
- 1989-02-02 JP JP1022569A patent/JPH084549B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5776579U (en) * | 1980-10-29 | 1982-05-12 | ||
JPS6399811A (en) * | 1986-10-15 | 1988-05-02 | 東洋リノリユ−ム株式会社 | Tile carpet and its production |
Also Published As
Publication number | Publication date |
---|---|
JPH084549B2 (en) | 1996-01-24 |
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