JPH0120260B2 - - Google Patents
Info
- Publication number
- JPH0120260B2 JPH0120260B2 JP61144590A JP14459086A JPH0120260B2 JP H0120260 B2 JPH0120260 B2 JP H0120260B2 JP 61144590 A JP61144590 A JP 61144590A JP 14459086 A JP14459086 A JP 14459086A JP H0120260 B2 JPH0120260 B2 JP H0120260B2
- Authority
- JP
- Japan
- Prior art keywords
- layer
- carpet
- fiber
- weight
- fibers
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000835 fiber Substances 0.000 claims description 110
- 239000010410 layer Substances 0.000 claims description 49
- 239000000839 emulsion Substances 0.000 claims description 34
- 239000011230 binding agent Substances 0.000 claims description 33
- 238000002844 melting Methods 0.000 claims description 26
- 230000008018 melting Effects 0.000 claims description 25
- 229920005989 resin Polymers 0.000 claims description 25
- 239000011347 resin Substances 0.000 claims description 25
- 239000004745 nonwoven fabric Substances 0.000 claims description 23
- 229920005992 thermoplastic resin Polymers 0.000 claims description 23
- 239000002344 surface layer Substances 0.000 claims description 18
- 238000004519 manufacturing process Methods 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 238000000465 moulding Methods 0.000 claims description 6
- 230000035515 penetration Effects 0.000 claims description 6
- 230000009477 glass transition Effects 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 3
- 238000010030 laminating Methods 0.000 claims 1
- -1 polypropylene Polymers 0.000 description 16
- 239000004743 Polypropylene Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 229920001155 polypropylene Polymers 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 8
- 238000000034 method Methods 0.000 description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 description 5
- 239000005020 polyethylene terephthalate Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 229920002647 polyamide Polymers 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 229920002994 synthetic fiber Polymers 0.000 description 3
- 239000012209 synthetic fiber 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
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene 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
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- BWHLPLXXIDYSNW-UHFFFAOYSA-N ketorolac tromethamine Chemical compound OCC(N)(CO)CO.OC(=O)C1CCN2C1=CC=C2C(=O)C1=CC=CC=C1 BWHLPLXXIDYSNW-UHFFFAOYSA-N 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 238000004080 punching Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- JETSKDPKURDVNI-UHFFFAOYSA-N [C].[Ca] Chemical compound [C].[Ca] JETSKDPKURDVNI-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 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
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pentâ4âenâ2âone Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Carpets (AREA)
- Laminated Bodies (AREA)
- Manufacturing Of Multi-Layer Textile Fabrics (AREA)
- Nonwoven Fabrics (AREA)
Description
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ãŠæçšãªã«ãŒãããã®è£ææ¹æ³ã«é¢ãããDETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for lining carpets useful as interior materials for automobiles and rugs in homes.
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èç¹ã®ç±å¯å¡æ§æš¹èçµæãš100ã170âã®èç¹ãæ
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Non-woven fiber mats impregnated with an aqueous resin emulsion are used as floor carpets for automobiles, and non-woven webs made of mixed fibers of a thermoplastic resin composition with a high melting point and a resin fiber binder with a melting point of 100 to 170°C are used as resin in the emulsion. Alternatively, carpets that are heated to a temperature higher than the melting point of a resin fiber binder and then press-molded into the shape of an automobile floor are known.
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ããããã¡ã«ãå€ãçšããŠæ¥çãããŠããã These carpets lack luxury on their own, and also lack performance in terms of rigidity, elasticity, and moldability, so fibers are raised in a loop shape on a polypropylene flat sane cloth base fabric on the surface of the carpet. The tufted carpet for the surface layer is attached using a hot melt agent.
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ãã This tufted carpet is expensive and is used as an interior material for luxury cars, but for cars for the general public, the surface layer is plain needle-punch carpet, which is coated with high-melting point fibers and a resin fiber binder. The backing nonwoven fabric web made of mixed fibers of The fibers are sufficiently intertwined with the plain carpet for the surface layer and the web for the backing layer by performing needling to a depth of 100 mm).Then, the fibers are heated to melt the fiber binder and fix the fibers to form the plain carpet for the surface layer. A method has been proposed for manufacturing an inexpensive moldable multilayer carpet by integrating the PET and backing web.
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ãã This is not practical because the peel strength of the plain carpet A layer for the surface layer is weak at 0.25 kg/5 cm width, so after needling, a water-based resin emulsion is applied from the backing web side and squeezed to coat the emulsion close to the surface layer. A method has been implemented in which the surface layer and the backing web are integrated by heating and melting the binder and emulsion resin.
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ãã®ã§ããã The peel strength of the fibers of Plain Carpet A is as high as about 5 kg/5 cm, which is sufficient for practical use.
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This practical multi-layer carpet has a high needling density of about 70 to 90 needles/cm 2 and a second
As the needle penetrates into the carpet up to the 2nd part of the 3rd to 4th barb (12 to 15 mm) shown in the figure, many thick needle marks remain on the surface of the plain type surface carpet, and many fibers of the carpet layer fall to the lower layer side. The carpet will be removed, and the carpet will become thinner and its appearance will be spoiled. However, this increases the bond (strength) between the upper and lower layers, making it more practical.
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æäŸãããã®ã§ããã The present invention aims to improve this appearance, and
The present invention provides a multilayer carpet with practically sufficient fibers fixed therein.
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In the present invention, the back surface of the nonwoven carpet A for the surface layer has a basis weight of 6 to 200 g/m 2 and a melting point of 90 g/m2.
Water-permeable nonwoven fabric B made of a thermoplastic resin fiber binder with a temperature of ~200°C, followed by 15 to 50% by weight of a thermoplastic resin fiber binder with a melting point of 95 to 200°C, which is 40°C or more higher than the melting point of the fiber binder. A superimposed backing web C in which a fiber mat consisting of 85 to 50% by weight of synthetic fibers or natural fibers having a melting point is needled is needled from the nonwoven carpet A side for the surface layer to form a nonwoven carpet A, water permeable. After intertwining the fibers of each layer of the nonwoven fabric B and the backing web C, an aqueous emulsion of a thermoplastic resin with a glass transition point of 80°C or higher is applied from the backing web C side to form the surface carpet A layer. After the emulsion resin is impregnated to the extent that it does not penetrate, the fibers of the nonwoven carpet A for the surface layer do not melt in the solidified or unsolidified state of the emulsion resin, and the fiber binder of the nonwoven fabric B, the fiber binder of the web C, and the emulsion resin do not melt. The present invention provides a method for manufacturing a moldable multi-layer carpet, which is characterized in that the thermoplastic resin is heated to a temperature higher than the melting temperature and then compressed to bond and mold the respective layers.
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ãããèµ·æ¯ç¶ã®ãã®ã¯äœ¿çšã§ããªãã€ãã Adhesion of facing carpet A and backing web C is as follows:
Conventionally, needle punching involves fiber entanglement between the upper and lower layers, which requires sufficient needle density and penetration (needling depth), and due to the needle structure,
70 to 100 needles/cm 2 for alternating needling,
The depth is 12 to 15 mm, and a large amount of the fibers of the facing carpet are guided to the lower layer, and it is difficult to reduce the amount of fibers due to the loss of facing fibers, and there are needle holes and uneven surfaces due to needling on the surface. It lingers forever. For this reason, only the plain type was used, and the raised type could not be used.
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ïŒããŒãã局ã«éããã°è¯ãããšã«ãªãã In the present invention, in order to solve this problem, a nonwoven fabric B layer made of a thermoplastic resin fiber binder is placed between the facing carpet A and the backing web C.
Since C is used to bond C and C, temporary needling from the A side is sufficient until A and C are bonded by heat, so the needle density should be as low as possible to reduce fiber loss in the A layer. , and from the structure of the needle, it is sufficient that the first barb reaches the C layer.
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ã®åã¿ããè¶ããªãç¯å²ã§ååã§ããã However, since a large needle mark remains when the needle penetration is large, the appearance of the needle penetration has a greater influence than the needle density. For this reason, the needle density is lower than the normal range, less than 100 needles/ cm2 , preferably 25 to 50 needles/cm2.
cm 2 , the penetration is within the range where the first barb reaches the C layer and does not penetrate the C layer.
6mm + (A layer + B layer + C layer)
It is sufficient that the thickness does not exceed .
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ã®ããŒãã«ãã³ãã«ãŒãããã䜿çšã§ããã(Nonwoven fabric carpet for surface layer) The nonwoven fabric carpet A for the surface layer is mainly made of plain fibers obtained from fibers such as western wool, nylon, polyacrylonitrile, polyacetate, and polyethylene terephthalate, which have a higher melting point than the fiber binders of layers B and C. Although a type of needle punch carpet is used, a raised needle punch carpet can also be used in the present invention.
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æ¥ããå°ãç¹ç¶å±€ãéæåºæ¥ãã The basis weight of this needle punch type carpet A is 100 to 500 g/m 2 . Generally 200g/m 2
However, in the present invention, since there is less migration from the facing layer to the lower layer due to needling, fewer fiber layers can be achieved than in the past.
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ã®ã§ããã(Nonwoven fabric of fiber binder) Nonwoven fabric B of thermoplastic resin fiber binder is made of fibers such as polyethylene, polypropylene, linear polyester, polyamide, polyethylene/polypropylene laminate fibers, etc., and has a melting point of 90 to 200°C, preferably 90 to 170°C. , 6~ obtained by intertwining 2~12 denier resin fibers by the spunpond method.
It is breathable and has a basis weight of 200 g/m 2 , preferably 20 to 60 g/m 2 , and a wall thickness of 5 to 500 microns.
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ãã In addition, this fiber binder is made by melting pellets of resin such as polypropylene, polyester, polyamide, etc. using an extruder and extruding them in a continuous shape through a die with many thin holes, which is then carried by the wind so that the individual fibers do not converge. It may also be produced by drawing it out, depositing it on a screen below the die, and pulling it off with a winder.
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ã¬ãŒãåãä»ããŠè²©å£²ãããŠããã Such fiber binder nonwoven fabric B has many gaps through which water can pass, and is manufactured by Diabond Industries.
Mitsui Petrochemical Co., Ltd.'s Meltron W product name is PAY-200, PAS-200 for polyamide-based products, ES-500 for polyester-based products, and Y7 for ethylene-acetic acid copolymer-based products. Syntex PK is a polypropylene-based product from Kogyo Co., Ltd.
103, PK-106, PK-404, PK-408, etc. Polyethylene-based products are available under Admel's product names, and similar non-woven fabrics are available from Kureha Sen'i Co., Ltd.
DYNAC product name LNS-0000, LNS-2000,
It is sold with grade names such as ES-00, B-1000, B-2000, and B-3000.
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ããäžç¹åžãšãããã®ã§ãè¯ãã Alternatively, polypropylene fibers may be made into a nonwoven fabric by needle punching or the like.
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ã§ããã(Backing material) The backing material web C contains 15 to 50% by weight of a thermoplastic resin fiber binder with a melting point of 90 to 200°C, and synthetic or natural fibers having a melting point 40°C or more higher than the melting point of the thermoplastic resin. This web is obtained by needling a fiber mat consisting of 85 to 50% by weight of fibers, and is manufactured by a known nonwoven fabric manufacturing method. i.e. 1.2~300 denier, fiber length 25~
15-50% by weight of a 150 mm thermoplastic resin fiber binder; 15-50% by weight of a 1.2-300 denier thermoplastic resin fiber binder with a fiber length of 25-150 mm;
1.2 to 300 denier, fiber length 25 to 150 mm synthetic fibers and/or 85 to 50% by weight of natural fibers are sufficiently mixed and opened and supplied to a web forming device, and a card is formed from the mixed fibers. The web (fiber mat) is obtained by stacking the web (fiber mat) so that it has the desired fiber weight, and is temporarily fixed by needling in the vertical direction to entangle the fibers.
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ã®ãšãªãã The fiber binder is used in a proportion of 15 to 50% by weight, preferably 20 to 40% by weight of the fiber mat weight. If it is less than 15% by weight, the contribution to improving the rigidity and dimensional stability of the carpet obtained by press molding will be small. On the other hand, if it exceeds 50% by weight, it becomes like resin felt, hard and brittle with impaired fiber texture.
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æ¯çãçšããããã In addition, the raw material for the synthetic fiber, which is the other fiber that substantially constitutes the fiber mat, has a melting point that is 40°C or more, preferably 70°C or more higher than the melting point of the thermoplastic resin fiber binder such as polyethylene terephthalate or polyamide. A thermoplastic resin having a Further, as natural fibers, cotton, linen, wool, etc. are used.
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ã€åæ§ãäžååã§ããã The fiber weight of the backing material web C is 300 to 2000 g/
m 2 , preferably 500 to 1000 g/m 2 . Since this backing material web C layer contains thermoplastic resin fibers, it exhibits thermoformability, but it is difficult to obtain a sharp shape and has insufficient rigidity.
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ç±å¯å¡æ§æš¹èãæããããã(Thermoplastic resin aqueous emulsion) The thermoplastic resin used in the emulsion applied to and impregnated into the stacked carpets to provide molding and rigidity has a glass transition point of 80°C or higher, preferably 100°C or higher.
At 180°C, the particle size is between 0.01 and 5 microns.
Specifically, lower ester copolymers of styrene and acrylic acid (ester has 2 to 6 carbon atoms), lower ester copolymers of methacrylate and acrylic acid,
Vinylidene chloride copolymer (vinylidene chloride content is
85% by weight or more) and thermoplastic resins such as styrene/diene copolymers.
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ãã Optimally, (a) polyn-propyl methacrylate (Tg 81°C),
Polystyrene (100â), polyacrylonitrile (100â), polymethyl methacrylate (105â),
In addition to aqueous emulsions of homopolymers such as polymethacrylic acid (130°C), polyitaconic acid (130°C), and polyacrylamide (153°C), (b) vinyl monomer 50, which is the raw material for these polymers.
-100% by weight, preferably 65-95% by weight, and other vinyl monomers such as 2-ethylhexyl acrylate (Tg 85°C), n-butyl acrylate (-54°C), ethyl acrylate (-22°C). ), isopropyl acrylate (-5â), 2-ethylhexyl methacrylate (-5â), n-propyl acrylate (8â), n-butyl methacrylate (20â), vinyl acetate (30â), acrylic acid t
-Butyl (45â), 2-hydroxyethyl methacrylate (55â), ethyl methacrylate (65
), isobutyl methacrylate (67â), vinyl chloride (79â), etc. or vinylidene chloride (-18â), etc.
°C) Aqueous emulsion of a copolymer with 50% by weight or less, preferably 35 to 5% by weight (c) Resin aqueous emulsion with Tg of +80 to 155°C 50
~97% by weight, preferably 55-95% by weight, Tg
Resin water-based emulsion 50 with a temperature of -85 to less than +80â
-3% by weight, preferably 45-5% by weight, and the like. Fillers such as calcium carbon, iron oxide, ferrite, barium sulfate, etc. may be blended into this emulsion to give the obtained nonwoven fabric a sense of weight, and fillers such as low-density polyethylene or polystyrene may be added to give moldability. It is also possible to blend a powder of a low melting point resin such as ethylene/vinyl acetate copolymer.
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ãã«ã¯æåœ¢æ§ãšåæ§ãä»äžãããã The means for applying and impregnating the emulsion onto the fiber mat of the stacked carpet include a licker roll, a squeezing roll, a spray gun, dipping and the like. Generally, the applied emulsion is squeezed by squeezing rolls to completely impregnate the fiber mat with the emulsion. The emulsion is applied from the side of the fiber matte web C for backing. The fiber mats coated and impregnated with emulsion are heated to 80-250â to remove moisture.
A multilayer needle punch carpet with bonded fibers is produced. During this heating and drying process, some of the resin particles in the emulsion remain in the fiber mat in a particulate state, and some form a film that strengthens the intertwining of the fibers and also strengthens the fiber mat of the carpet. is given moldability and rigidity.
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100éééšã®å²åã§çšããããã The aqueous thermoplastic resin emulsion contains 10 to 10 parts by weight of the resin solids in the emulsion, based on 100 parts by weight of the fibers in layer A, layer B, and layer C of the carpet.
It is used in a proportion of 100 parts by weight.
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ããããšãšãã«æåœ¢ãè¡ãã(Backing method) To back the carpet A with the web C, use the nonwoven fabric B made of resin fiber binder as an adhesive and overlap them between the two, and then use the needle 1 to apply the web C to the carpet A for the surface layer. 20-50
at a rate of 25 to 50 strands/cm 2 , preferably from 25 to 50 strands/cm 2 , and
The depth of the needle 1 is within the total thickness of each layer A, B, and C + 6 mm, for example, 7 to 9 mm (see Figure 1) to lightly entangle the fibers in each layer, and then The backing web C side is impregnated with a resin aqueous emulsion and heated to 90 to 220°C, preferably 100 to 160°C to dry the water, and the fiber binder resin of nonwoven fabric B, the fiber binder resin of web C, and the emulsion resin are is melted and compressed using a press molding machine or a pressure cooling roll, and the layers A, B, and C are bonded and integrated to complete the lining and are also molded.
ãã®äžäœåã®å Žåãèãã«ãŒããããäœãæ
ãåºæ¬ãšããŠäœ¿çšãããŸããã€ãŠïŒ¡ãšïŒ¢ã®è€å
äœããšéããããŒããªã³ã°ããŠæ¥åããããšã
è¯ãã In the case of this integration, it is also good to use B as a base when making a thin carpet A, and to first overlap the composite of A and B with C and join them by needling.
åããŠãšã局ã®çé¢ã«ç±å¯å¡æ§ç¹ç¶éãå¢ã
ããåºæ¬ãšããŠããããããšïŒ£ã®ç©å±€äœãåŸ
ãã®ã¡ãããã«ïŒ¡ãéãããŠãããŒããªã³ã°æ¥å
ããã®ãè¯ãã Alternatively, it is also possible to increase the amount of thermoplastic fibers on one side of the web layer C or to obtain a laminate of B and C in advance using B as a base, and then overlay A on this and perform needling bonding.
ïŒå¹æïŒ
æ¬çºæã®è€å±€ã«ãŒãããã¯æåœ¢å¯èœã§ãããç¹
ç¶ã®åºå®ã匷åïŒå¥é¢åŒ·åºŠçŽ7.5KgïŒïŒcmå¹
ïŒã§
ããããã¬ãŒã³äžŠã³ã«èµ·æ¯ç¶ããŒãã«ãã³ãã«ãŒ
ãããã䜿çšã§ããå€èгã«åªããéæ°æ§ãåæ§ã«
ãåªããã(Effects) The multilayer carpet of the present invention can be molded, has strong fiber fixation (peel strength approximately 7.5 kg/5 cm width), can be used with plain or brushed needle punch carpet, has an excellent appearance, and has excellent ventilation. It also has excellent strength and rigidity.
宿œäŸ ïŒ
15ãããŒã«ãç¹ç¶é·85ã120mmã®ããªãšãã¬ã³
ãã¬ãã¿ã¬ãŒãïŒèç¹264âïŒç¹ç¶ã«ãŒããã©ã³
ãã ã«ç©ã¿éããç¹ç¶ããã150ïœïŒm2ãçŽ æãš
ãããã¬ãŒã³ã¿ã€ãã®ããŒãã«ãã³ãã«ãŒããã
ã®è£é¢ã«ãäžäºç³æ²¹ååŠå·¥æ¥(æ ª)補ããªãããã¬
ã³ç¹ç¶ãã€ã³ããŒè£œäžç¹åžïŒ¢âã·ã³ããã¯ã¹PKâ
100ïŒåååãç®ä»30ïœïŒm2ãç¹ç¶åŸïŒãããŒã«ïŒ
ããæŽã«ãã®äžç¹åžïŒ¢ã®äžã«åŸè¿°ã®ããã«ããŠè£œ
é ããããŒãã«ã«ãŒããããããªããŠãšããé
ãåããèŠããã®åããçŽ12mmã®äžå±€ç©å±€äœãåŸ
ããExample 1 Mitsui Oil Co., Ltd. was applied to the back side of a plain type needle punch carpet A made of fiber mat 150 g/m 2 randomly stacked with polyethylene terephthalate (melting point 264°C) fiber cards of 15 denier and fiber length 85 to 120 mm. Polypropylene fiber binder nonwoven fabric B âSyntex PKâ manufactured by Kagaku Kogyo Co., Ltd.
100 (Product name, basis weight 30g/m 2 , fiber diameter 3 denier)
A web C made of a needle carpet produced as described below was further superimposed on the nonwoven fabric B to obtain a three-layer laminate having an apparent thickness of about 12 mm.
ã€ãã§ããã®ç©å±€äœã®è¡šå±€ã«ãŒãããåŽã
ããïŒcm2åœã25æ¬ãç©å±€äœãžã®éå
¥æ·±ãïŒmmã®å²
åã§ããŒããªã³ã°ããåå±€ã®ç¹ç¶åå¿ã®çµ¡ã¿åã
ãè¡ã€ãã Then, needling was carried out from the surface carpet A side of this laminate at a rate of 25 fibers per cm 2 and a penetration depth of 8 mm into the laminate to entangle the fibers in each layer.
ãã®åŸããã®ç©å±€äœã®è£æçšãŠãšãåŽããã
ã¬ã©ã¹è»¢ç§»ç¹ã90âã®ã¹ãã¬ã³ã»ã¢ã¯ãªã«é
žãã
ã«å
±éåäœã®æ°Žæ§ãšãã«ãžãšã³ã130ïœïŒm2ïŒåº
ååïŒã®å²åã§å¡åžãå§æŸããŠãŠãšãã®1/2ã®
æ·±ããŸã§å«æµžãããã€ãã§80âã§ä¹Ÿç¥ããŠæ°Žåã
é€å»ããåŸãæŽã«ãã®ç©å±€äœã190âã«å ç±ããŠ
äžç¹åžïŒ¢ãšãŠãšãã®ããªãããã¬ã³ç¹ç¶ãã€ã³
ããŒäžŠã³ã«ãšãã«ãžãšã³ã®å
±éåäœæš¹èãæº¶èã
ããã®ã¡ããã¬ã¹æåœ¢æ©ãçšããŠå å§æåœ¢ããé
åã«å¿ å®ãªåå±€ãäžäœåããåã¿çŽ9.5mmã®æ·èš
æãåŸãã Then, from the backing web C side of this laminate,
An aqueous emulsion of styrene-butyl acrylate copolymer with a glass transition point of 90°C is applied at a rate of 130g/m 2 (solid content) and squeezed to impregnate the web C to a depth of 1/2. After drying at â to remove moisture, this laminate was further heated to 190â to melt the polypropylene fiber binder of nonwoven fabric B and web C, and the copolymer resin of the emulsion, and then using a press molding machine. By pressure molding, we obtained a laying material with a thickness of approximately 9.5 mm in which each layer was integrated, faithful to the mold.
ãã®æ·èšæã®è¡šå±€å€ã®é穎ã¯ç®ç«ãããå¹³æ»ã§
å€èгã¯è¯å¥œã§ã衚局çšç¹ç¶ã®å¥é¢åŒ·åºŠã¯7.5KgïŒ
ïŒcmå¹
ã§ãã€ãããã®ãã®ã®äžã«500ïœè·éãã®
ããŠæ©èãã¹ããè¡ãªã€ãŠãããŒãªã³ã°ã¯çããª
ãã€ãã The needle holes in the surface layer agent of this laying material are not noticeable, it is smooth and has a good appearance, and the peel strength of the surface layer fiber is 7.5 kg/
It was 5cm wide. Even when a 500g load was placed on this product and an abrasion test was performed, no peeling occurred.
ããŒãã«ã«ãŒãããã®è£œé æ³
15ãããŒã«ãç¹ç¶é·çŽ100mmã®ååããªããã
ã¬ã³ïŒèç¹164âïŒç¹ç¶ãã€ã³ããŒ20ïŒ
ãš15ãã
ãŒã«ãç¹ç¶é·75ã125mmã®ååããªãšãã¬ã³ãã¬
ãã¿ã¬ãŒãïŒèç¹264âïŒç¹ç¶80ïŒ
ã®æ··åç¹ç¶å±
ãã©ã³ãã ã«ç©ã¿éããç¹ç¶ãããïŒ700ïœïŒm2ïŒ
ãã15â18â32â3RBã®éãçšããŠïŒå¹³æ¹ã»ã³
ãåœã100æ¬ã®å²åã§ããŒããªã³ã°ããèåçŽ7.1
mmãèŠæå¯åºŠ0.10ïœïŒcm3ã®ããŒãã«ã«ãŒããã
ãåŸããManufacturing method for Needle Carpet C A mixed fiber of 20% recycled polypropylene (melting point 164°C) fiber binder of 15 denier and approximately 100 mm fiber length and 80% recycled polyethylene terephthalate (melting point 264°C) fiber of 15 denier and fiber length 75 to 125 mm. Fiber mat (700g/m 2 ) made by stacking waste randomly
was needled using 15-18-32-3RB needles at a rate of 100 needles per square centimeter, and the wall thickness was approximately 7.1 mm.
mm, needle carpet C with apparent density 0.10g/ cm3
I got it.
æ¯èŒäŸ ïŒ
宿œäŸïŒã«ãããŠãç¹ç¶ãã€ã³ããŒè£œäžç¹åžïŒ¢
ãçšããããã€ãç©å±€äœããšïŒ£ããžã®ããŒããª
ã³ã°ã70æ¬ïŒcm2ãéå
¥æ·±ã14mmãšããä»ã¯åæ§ã«
ããŠåŸãæ·èšæã®ç©æ§ã¯æ¬¡ã®ããã§ãã€ããComparative Example 1 In Example 1, fiber binder nonwoven fabric B
The physical properties of the laying material obtained in the same manner were as follows, except that the laminates [A and C] were needled at a rate of 70 needles/cm 2 and at a depth of 14 mm.
å€èгâãã¬ãŒã³ã«ãŒãããã®è¡šå±€ã«ã¯éè·¡ã
ã¯ã€ãããšç®ç«ã€ã Appearance - Needle marks are clearly visible on the surface of plain carpet A.
局ã®å¥é¢åŒ·åºŠâ0.25KgïŒïŒcmå¹
ãæ°Žæ§ãšãã«ãžãšã³ã嫿µžããŠãªãå Žåã
ã â5.5KgïŒïŒcmå¹
ãæ°Žæ§ãšãã«ãžãšã³ã嫿µžããå Žåã
èãŸããæ§â500ïœè·éãã®ããŠã®ãŸãããã¹
ãã§å®¹æã«ããŒãªã³ã°çããã Peel strength of layer A - 0.25Kg/5cm width [When not impregnated with water-based emulsion] -5.5Kg/5cm width [When impregnated with water-based emulsion] Resistance - resistance test with a 500g load Peeling occurs easily.
第ïŒå³ã¯æ¬çºæã®ããŒããªã³ã°ã®ç¶æ
ã瀺ãæ
é¢å³ã§ããã第ïŒå³ã¯ããŒãã«ã®å¹³é¢å³ã§ããã
FIG. 1 is a sectional view showing the needling state of the present invention, and FIG. 2 is a plan view of the needle.
Claims (1)
éãïŒã200ïœïŒm2ã§ãã€ãŠãèç¹ã90ã200âã®
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ç¶ãã€ã³ããŒã15ã50ééïŒ ãšã該ç¹ç¶ãã€ã³ã
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ïŒmmãã©ã¹ããèå以äžã§ããããšãç¹åŸŽãšãã
ç¹èš±è«æ±ã®ç¯å²ç¬¬ïŒé èšèŒã®è£œé æ¹æ³ã ïŒ ç±å¯å¡æ§æš¹èæ°Žæ§ãšãã«ãžãšã³ã¯ãã«ãŒãã
ãã®ïŒ¡å±€ã局ããã³ïŒ£å±€ã®ç¹ç¶ééã®å100é
ééšã«å¯Ÿãããšãã«ãžãšã³äžã®æš¹èåºååéã§10
ã100éééšã®å²åã§çšããããããšãç¹åŸŽãšã
ãç¹èš±è«æ±ã®ç¯å²ç¬¬ïŒé èšèŒã®è£œé æ¹æ³ã ïŒ è¡šå±€çšã®äžç¹åžã«ãŒãããã®ç¹ç¶ç®ä»éã
100ã500ïœïŒm2ã§ãããè£æçšãŠãšãã®ç¹ç¶ç®
ä»éã300ã2000ïœïŒm2ã§ããããšãç¹åŸŽãšãã
ç¹èš±è«æ±ã®ç¯å²ç¬¬ïŒé èšèŒã®è£œé æ¹æ³ã[Claims] 1. On the back side of the nonwoven carpet A for the surface layer, a water permeable nonwoven fabric B having a basis weight of 6 to 200 g/m 2 and a thermoplastic resin fiber binder having a melting point of 90 to 200°C.
, followed by 15-50% by weight of a thermoplastic resin fiber binder with a melting point of 95-200°C, and 85-50% by weight of synthetic or natural fibers having a melting point 40°C or more higher than the melting point of the fiber binder. The backing web C, which is made by needling fiber mats, is needled from the surface nonwoven carpet A side to entangle the fibers in each layer of the nonwoven carpet A, the water-permeable nonwoven fabric B, and the backing web C. After laminating, an aqueous emulsion of a thermoplastic resin with a glass transition point of 80°C or higher is applied from the backing web C side, and the emulsion resin is impregnated to the extent that it does not penetrate the surface carpet A layer. When the resin is in a solidified or unsolidified state, the fibers of nonwoven carpet A for the surface layer do not melt, and the fiber binder of nonwoven fabric B, the fiber binder of web C, and the thermoplastic resin of the emulsion are heated to a temperature higher than that at which they are melted, and then compressed. A method for producing a moldable multi-layer carpet, which comprises bonding and molding each layer. 2. The manufacturing method according to claim 1, wherein the needle density during needling is 20 to 100 needles/cm 2 . 3 The depth of penetration of the needle tip into the overlapped carpet exceeds the thickness of layer A, layer B, and layer C plus 6 mm plus the thickness of layer A, layer B, and layer C. 2. The manufacturing method according to claim 1, wherein the thickness is less than or equal to . 4. The aqueous thermoplastic resin emulsion has a resin solid content of 10 parts by weight per 100 parts by weight of the fibers in layer A, layer B, and layer C of the carpet.
2. The manufacturing method according to claim 1, wherein the amount is 100 parts by weight. 5 The fiber weight of nonwoven carpet A for the surface layer is
100 to 500 g/m 2 , and the fiber basis weight of the backing web C is 300 to 2000 g/m 2 .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61144590A JPS6392765A (en) | 1986-06-20 | 1986-06-20 | Method of manufacturing moldable multi-layer carpet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61144590A JPS6392765A (en) | 1986-06-20 | 1986-06-20 | Method of manufacturing moldable multi-layer carpet |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6392765A JPS6392765A (en) | 1988-04-23 |
| JPH0120260B2 true JPH0120260B2 (en) | 1989-04-14 |
Family
ID=15365618
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61144590A Granted JPS6392765A (en) | 1986-06-20 | 1986-06-20 | Method of manufacturing moldable multi-layer carpet |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6392765A (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0730709Y2 (en) * | 1989-11-11 | 1995-07-12 | æ±æŽçŽ¡çžŸæ ªåŒäŒç€Ÿ | Vehicle seat |
| DE59707081D1 (en) * | 1997-01-13 | 2002-05-23 | Quadrant Plastic Composites Ag | THERMOPLASTICALLY DEFORMABLE COMPOSITE BODY |
| US6786988B1 (en) | 2001-02-14 | 2004-09-07 | Mohawk Brands Inc. | Use of waste carpet as filler |
| US7045590B2 (en) | 2001-02-14 | 2006-05-16 | Mohawk Brands, Inc. | Use of waste carpet as filler |
| JPWO2004058014A1 (en) * | 2002-12-26 | 2006-04-27 | 氞倧åå·¥æ ªåŒäŒç€Ÿ | Laying mat excellent in sound absorbing and water imperviousness and manufacturing method thereof |
| US6814826B1 (en) | 2003-03-03 | 2004-11-09 | Mohawk Brands, Inc. | Use of waste carpet as backing filler for floor coverings |
-
1986
- 1986-06-20 JP JP61144590A patent/JPS6392765A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6392765A (en) | 1988-04-23 |
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