JP7633800B2 - Tatami mat - Google Patents
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- JP7633800B2 JP7633800B2 JP2020203455A JP2020203455A JP7633800B2 JP 7633800 B2 JP7633800 B2 JP 7633800B2 JP 2020203455 A JP2020203455 A JP 2020203455A JP 2020203455 A JP2020203455 A JP 2020203455A JP 7633800 B2 JP7633800 B2 JP 7633800B2
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- resin
- twisted yarn
- tatami
- bundle
- uniaxially stretched
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- 229920005989 resin Polymers 0.000 claims description 62
- 239000011347 resin Substances 0.000 claims description 62
- 229920005992 thermoplastic resin Polymers 0.000 claims description 29
- 239000003063 flame retardant Substances 0.000 claims description 19
- 238000010438 heat treatment Methods 0.000 claims description 19
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 14
- 239000003242 anti bacterial agent Substances 0.000 claims description 13
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- 238000000576 coating method Methods 0.000 claims description 12
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- 239000000835 fiber Substances 0.000 claims description 6
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
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- 229920001577 copolymer Polymers 0.000 description 8
- 229920001155 polypropylene Polymers 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 238000009941 weaving Methods 0.000 description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
- 229910052794 bromium Inorganic materials 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
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- 244000025254 Cannabis sativa Species 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
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- 235000015429 Mirabilis expansa Nutrition 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 239000003429 antifungal agent Substances 0.000 description 3
- 229940121375 antifungal agent Drugs 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 235000006708 antioxidants Nutrition 0.000 description 3
- 239000004566 building material Substances 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000002781 deodorant agent Substances 0.000 description 3
- 239000012757 flame retardant agent Substances 0.000 description 3
- 229920001903 high density polyethylene Polymers 0.000 description 3
- 239000004700 high-density polyethylene Substances 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 229910021645 metal ion Inorganic materials 0.000 description 3
- 235000013536 miso Nutrition 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- 239000011342 resin composition Substances 0.000 description 3
- 235000014347 soups Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 2
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 244000195452 Wasabia japonica Species 0.000 description 2
- 235000000760 Wasabia japonica Nutrition 0.000 description 2
- ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- 235000009120 camo Nutrition 0.000 description 2
- 235000005607 chanvre indien Nutrition 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229910052570 clay Inorganic materials 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000011487 hemp Substances 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000001023 inorganic pigment Substances 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 229920000092 linear low density polyethylene Polymers 0.000 description 2
- 239000004707 linear low-density polyethylene Substances 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
- 239000001095 magnesium carbonate Substances 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 2
- 239000000347 magnesium hydroxide Substances 0.000 description 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 229920001179 medium density polyethylene Polymers 0.000 description 2
- 239000004701 medium-density polyethylene Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000000052 vinegar Substances 0.000 description 2
- 235000021419 vinegar Nutrition 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 240000005109 Cryptomeria japonica Species 0.000 description 1
- 241000218691 Cupressaceae Species 0.000 description 1
- 229920001651 Cyanoacrylate Polymers 0.000 description 1
- 235000011511 Diospyros Nutrition 0.000 description 1
- 244000236655 Diospyros kaki Species 0.000 description 1
- 239000004609 Impact Modifier Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- PMSNFNRNIGPRQJ-UHFFFAOYSA-N [Cr](=O)(=O)([O-])[O-].[Mo+4].[Cr](=O)(=O)([O-])[O-] Chemical compound [Cr](=O)(=O)([O-])[O-].[Mo+4].[Cr](=O)(=O)([O-])[O-] PMSNFNRNIGPRQJ-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 235000016720 allyl isothiocyanate Nutrition 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 150000001556 benzimidazoles Chemical class 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 150000001565 benzotriazoles Chemical class 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 description 1
- 235000005487 catechin Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229950001002 cianidanol Drugs 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- NLCKLZIHJQEMCU-UHFFFAOYSA-N cyano prop-2-enoate Chemical class C=CC(=O)OC#N NLCKLZIHJQEMCU-UHFFFAOYSA-N 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
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- 238000010030 laminating Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
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- 150000005527 organic iodine compounds Chemical class 0.000 description 1
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- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- 239000004306 orthophenyl phenol Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000002728 pyrethroid Substances 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 0.000 description 1
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- 229910052709 silver Inorganic materials 0.000 description 1
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- 238000003892 spreading Methods 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
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- 230000037303 wrinkles Effects 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Floor Finish (AREA)
Description
本発明は、畳表に関する。 The present invention relates to tatami coverings.
日本家屋における床材として広く使用されている畳は畳床の表面に畳表を積層することにより構成されている。畳表は天然いぐさを横糸とし、綿糸や麻糸を縦糸とし引き目織りや目積織りにより製織することにより製造されてきたが、天然いぐさは害虫が発生する、機械的強度が低い、高価格である、供給量が少ない等の欠点を有していた。 Tatami mats, which are widely used as flooring in Japanese houses, are made by laminating a tatami surface onto the surface of a tatami floor. Tatami surface mats are made by weaving natural rush as the weft and cotton or hemp thread as the warp using a hikime weave or meseki weave method, but natural rush has drawbacks such as being prone to pests, having low mechanical strength, being expensive, and being in limited supply.
そのため、最近は紙や種々の熱可塑性樹脂フィルムを材料とした人工いぐさが(例えば、特許文献1、2、3参照。)が提案されている。これら人工いぐさは、紙や可塑性樹脂を材料とする工業製品であるから、害虫が発生しない、低価格である、供給が安定している、機械的強度やクッション性等が優れている等の長所を有していた。更に、防ダニ剤、防カビ剤、消臭剤、抗菌剤、難燃剤、VOC吸着剤、遠赤外線放射剤、マイナスイオン放射剤等の機能性物質を人工いぐさの周囲に塗布して機能性を向上させた人工いぐさ(例えば、特許文献4参照。)も提案されている。 Recently, therefore, artificial rushes made from paper or various thermoplastic resin films have been proposed (see, for example, Patent Documents 1, 2, and 3). These artificial rushes are industrial products made from paper and plastic resin, and therefore have the advantages of being pest-free, low-cost, stable in supply, and excellent mechanical strength and cushioning. Furthermore, artificial rushes have been proposed that have been coated with functional substances such as anti-mite agents, anti-fungal agents, deodorants, antibacterial agents, flame retardants, VOC adsorbents, far-infrared emitters, and negative ion emitters to improve their functionality (see, for example, Patent Document 4).
しかしながら、縦糸としては、依然として綿糸や麻糸が使用されている。これら縦糸は吸水性及び保水性が優れており、横糸として熱可塑性樹脂製の人工いぐさが製織されている畳表においては、吸水性及び保水性小さい人工いぐさを使用しているにもかかわらず畳表としての吸水性及び保水性が優れていた。そのため畳表上に味噌汁、コーヒー等をこぼした場合、容易にふき取ることができず、畳表の表面に長いこと残存したり、汚れがついたりするという、クリーン性、耐汚染性が小さいという欠点があった。 However, cotton and hemp threads are still used as warp threads. These warp threads have excellent water absorption and water retention, and tatami mats made of artificial rush woven from thermoplastic resin as weft threads have excellent water absorption and water retention properties as tatami mats, despite the use of artificial rush, which has low water absorption and water retention properties. Therefore, if miso soup, coffee, etc. is spilled on the tatami mat, it cannot be easily wiped off, and it remains on the surface of the tatami mat for a long time or leaves a stain, which is a drawback in that it has low cleanability and stain resistance.
又、畳表は家屋における建築材料であるから、最近はより優れた難燃性、火がついても短時間で消火しうる防炎性、抗菌性等の機能が要求されるようになってきている。 In addition, since tatami mats are a building material for houses, there has been a recent demand for better flame retardancy, flame resistance that allows fires to be extinguished quickly even if they catch fire, antibacterial properties, etc.
本発明の目的は、上記問題点に鑑み、クリーン性、耐汚染性の優れた畳表を提供することにある。又、異なる目的は、難燃性、火がついても短時間で消火しうる防炎性、抗菌性等の優れた畳表を提供することにある。 In view of the above problems, the object of the present invention is to provide a tatami surface that is excellent in cleanability and stain resistance. Another object is to provide a tatami surface that is excellent in flame retardancy, flame resistance that allows fire to be extinguished in a short time even if it catches fire, antibacterial properties, etc.
即ち、本発明は、
[1]300~2000デニールの熱可塑性樹脂単繊維2~10本が撚られてなる樹脂系撚糸を縦糸とし、いぐさを横糸として製織されていることを特徴とする畳表、
[2]熱可塑性樹脂がポリプロピレン系樹脂又はポリエステル系樹脂であることを特徴とする上記[1]記載の畳表、
[3]熱可塑性樹脂単繊維に、更に、難燃剤及び/又は抗菌剤が練り込まれていることを特徴とする上記[1]又は[2]記載の畳表、
[4]いぐさが人工いぐさであることを特徴とする上記[1]~[3]のいずれか1項記載の畳表、
[5]人工いぐさが、オレフィン系樹脂及び無機充填剤よりなる一軸延伸フィルムを紐状に結束し、得られた結束体を該結束体の直径より狭い空隙部を有する加熱部材の空隙部中を通過させることにより、該結束体の一軸延伸フィルムを互いに不規則且つ部分的に融着結束させると共に、該結束体の表面に融着被膜を形成することにより得られた人工いぐさであることを特徴とする上記[4]記載の畳表、及び、
[6]一軸延伸フィルムに、更に、難燃剤及び/又は抗菌剤が練り込まれていることを特徴とする上記[5]記載の畳表
に関する。
That is, the present invention provides:
[1] A tatami mat lining characterized by being woven using a resin-based twisted yarn formed by twisting 2 to 10 thermoplastic resin single fibers having a denier of 300 to 2000 as a warp thread and igusa as a weft thread.
[2] The tatami mat according to the above [1], characterized in that the thermoplastic resin is a polypropylene-based resin or a polyester-based resin.
[3] The tatami mat according to [1] or [2] above, characterized in that a flame retardant and/or an antibacterial agent is further kneaded into the thermoplastic resin monofilament;
[4] The tatami mat according to any one of the above [1] to [3], characterized in that the rush is artificial rush.
[5] The tatami covering described in [4] above, characterized in that the artificial rush is obtained by bundling uniaxially oriented films made of olefin resin and inorganic filler into a string shape, and passing the resulting bundle through a gap in a heating element having a gap narrower than the diameter of the bundle, thereby irregularly and partially fusing and binding the uniaxially oriented films of the bundle and forming a fused coating on the surface of the bundle; and
[6] The tatami covering according to the above [5], further comprising a flame retardant and/or an antibacterial agent kneaded into the uniaxially stretched film.
本発明の畳表の構成は上述の通りであり、クリーン性及び耐汚染性が優れている。又、難燃性、火がついても短時間で消化しうる防炎性、抗菌性等が優れている。 The tatami mat of the present invention has the above-mentioned structure, and is excellent in cleanliness and stain resistance. It also has excellent flame retardancy, flame resistance that allows fire to be extinguished in a short time even if it catches fire, antibacterial properties, etc.
本発明の畳表は、300~2000デニールの熱可塑性樹脂単繊維2~10本が撚られてなる樹脂系撚糸を縦糸とし、いぐさを横糸として製織されていることを特徴とする。 The tatami mat of the present invention is characterized by being woven using resin-based twisted yarns made by twisting 2 to 10 thermoplastic resin monofilaments having a denier of 300 to 2000 as the warp yarns and rush as the weft yarns.
上記熱可塑性樹脂は、熱可塑性を有する任意の樹脂が使用可能であり、例えば、ポリプロピレン樹脂、エチレン-プロピレン共重合体などのポリプロピレン系樹脂、高密度ポリエチレン樹脂、中密度ポリエチレン樹脂、低密度ポリエチレン樹脂、直鎖状低密度ポリエチレン樹脂、エチレン-1-ブテン共重合体、エチレン―1-ペンテン共重合体、エチレン―1-ヘキセン共重合体などのエチレン系樹脂、その他のオレフィン系樹脂、ポリエステル系樹脂、アクリル系樹脂、ウレタン系樹脂等が挙げられ、ポリプロピレン系樹脂及びポリエステル系樹脂が好ましい。 The above thermoplastic resin can be any resin having thermoplastic properties, for example, polypropylene resins such as ethylene-propylene copolymers, high-density polyethylene resins, medium-density polyethylene resins, low-density polyethylene resins, linear low-density polyethylene resins, ethylene-1-butene copolymers, ethylene-1-pentene copolymers, ethylene-1-hexene copolymers, and other olefin resins, polyester resins, acrylic resins, urethane resins, etc., with polypropylene resins and polyester resins being preferred.
上記樹脂系撚糸は、熱可塑性樹脂単繊維が撚られてなる樹脂系撚糸であり、熱可塑性樹脂単繊維は熱可塑性樹脂を押出成形した単なる糸状の繊維である。熱可塑性樹脂単繊維の太さは細くなると、撚った際に水の吸水量や保水量が多くなり、味噌汁、コーヒー等をこぼした場合、長時間こぼれたままで放置すると、樹脂系撚糸まで含浸し、容易にふき取ることができず、クリーン性、耐汚染性が小さくなる。又、太くなると撚るのが困難なると共に撚られた樹脂系撚糸が太くなり、畳表の縦糸として使用できなくなるので300~2000デニールである。 The resin twisted yarn is a resin twisted yarn made by twisting thermoplastic resin monofilaments, and the thermoplastic resin monofilaments are simply thread-like fibers formed by extrusion molding of thermoplastic resin. If the thickness of the thermoplastic resin monofilaments is thin, they will absorb and retain more water when twisted, and if miso soup, coffee, or the like is spilled and left for a long time, it will soak into the resin twisted yarn and will not be easy to wipe off, resulting in poor cleanability and stain resistance. Also, if the thickness is thick, it will be difficult to twist and the twisted resin twisted yarn will be thick, making it impossible to use as a warp thread for tatami mats, so the denier is 300 to 2000.
撚られている熱可塑性樹脂単繊維の本数は、少なくなると機械的強度が小さくなり、多くなると撚られた樹脂系撚糸は味噌汁、コーヒー等をこぼした場合、長時間こぼれたままで放置すると、樹脂系撚糸まで含浸し、容易にふき取ることができず、クリーン性、耐汚染性が小さくなると共に太くなりすぎて、製織が困難となり、畳表の縦糸として使用できなくなる。従って、撚られる熱可塑性樹脂単繊維の本数は2~10本であり、好ましくは3~5本である。又、樹脂系撚糸の太さは、特に限定されないが、畳表の縦糸であるから1000~5000デニールが好ましい。 If the number of twisted thermoplastic resin single fibers is small, the mechanical strength will be low, and if the number is large, if miso soup, coffee, etc. is spilled on the twisted resin-based twisted yarn and left for a long time, the spill will soak into the resin-based twisted yarn and it will not be easy to wipe off, and the cleanability and stain resistance will be reduced, and the yarn will become too thick, making it difficult to weave and unable to use as the warp thread for tatami mat facings. Therefore, the number of twisted thermoplastic resin single fibers is 2 to 10, and preferably 3 to 5. There is no particular limit to the thickness of the resin-based twisted yarn, but since it is the warp thread for tatami mat facings, 1000 to 5000 denier is preferable.
尚、上記熱可塑性樹脂単繊維が撚られてなる樹脂系撚糸とは、複数の熱可塑性樹脂単繊維のみが撚られてなる樹脂系撚糸であり、綿糸、麻糸等の天然糸が混合されて撚られた混合撚糸は含まない。 The resin-based twisted yarn formed by twisting the above-mentioned thermoplastic resin monofilaments refers to a resin-based twisted yarn formed by twisting only a plurality of thermoplastic resin monofilaments, and does not include mixed twisted yarns formed by mixing and twisting natural yarns such as cotton yarns and linen yarns.
畳表は家屋における建築材料であるからより優れた難燃性や火がついても短時間で消火し得る防炎性が優れているが好ましい。本発明の畳表はいぐさを横糸とし上記樹脂系撚糸を縦糸として製織されているので、畳表の難燃性や防炎性を向上させるには火がついたり高温にさらされた際に縦糸が溶断され横糸がバラバラになるのが好ましい。これは横糸がバラバラになると横糸間に隙間が発生し延焼せず消火されるからである。 Because tatami mats are building materials for houses, they are preferably flame-retardant and have excellent flame resistance so that even if a fire does catch, the fire can be extinguished in a short time. The tatami mats of the present invention are woven using rush grass as the weft and the above-mentioned resin-based twisted yarn as the warp, so in order to improve the flame resistance and flame resistance of the tatami mats, it is preferable that the warp melts and the weft breaks apart when the tatami mat catches fire or is exposed to high temperatures. This is because if the weft breaks apart, gaps will form between the weft threads, preventing the fire from spreading and allowing the fire to be extinguished.
従って、樹脂系撚糸は溶融し切断された後又は同時に収縮すると、樹脂系撚糸は切断面の上下に間隙ができると共に切断面に位置する横糸は樹脂系撚糸が融着して切断面上下に引っ張られ上下に間隙ができるので樹脂系撚糸は加熱収縮性を有するのが好ましく、加熱収縮率は3%以上であるのが好ましい。 Therefore, when the resin-based twisted yarn shrinks after melting and cutting or at the same time, gaps are created above and below the cut surface of the resin-based twisted yarn, and the weft yarn located at the cut surface is pulled above and below the cut surface as the resin-based twisted yarn melts and creates gaps above and below. Therefore, it is preferable that the resin-based twisted yarn has heat shrinkability, and the heat shrinkage rate is preferably 3% or more.
尚、加熱収縮率は樹脂系撚糸を60℃の雰囲気下、無負荷で6時間加熱した際の収縮比率であり、下記式により計算される。
加熱収縮率(%)=(加熱前の樹脂系撚糸の長さ-加熱後の樹脂系撚糸の長さ)×100/加熱前の樹脂系撚糸の長さ
The heat shrinkage rate is the shrinkage ratio when the resin twisted yarn is heated in an atmosphere of 60° C. for 6 hours without load, and is calculated by the following formula.
Heat shrinkage rate (%) = (length of resin-based twisted yarn before heating - length of resin-based twisted yarn after heating) x 100 / length of resin-based twisted yarn before heating
樹脂系撚糸に加熱収縮性を付与する方法は、従来公知の任意の方法が採用されてよく、例えば、撚る前の熱可塑性樹脂単繊維を一軸延伸する等方法が挙げられる。 Any conventionally known method may be used to impart heat shrinkability to the resin-based twisted yarn, such as uniaxially stretching a thermoplastic resin monofilament before twisting.
畳表の難燃性、火がついても短時間で消火しうる防炎性、抗菌性等を向上させるために熱可塑性樹脂単繊維に、難燃剤及び/又は抗菌剤が添加されるのが好ましい。又、難燃剤及び/又は抗菌剤は熱可塑性樹脂単繊維の表面に塗布したのでは経時により剥離除去され効果が低下するので、熱可塑性樹脂単繊維に練り込まれているのが好ましい。 In order to improve the flame retardancy of the tatami mat, its flame resistance so that even if it catches fire it can be extinguished in a short time, its antibacterial properties, etc., it is preferable to add a flame retardant and/or an antibacterial agent to the thermoplastic resin monofilament. Also, if the flame retardant and/or antibacterial agent is applied to the surface of the thermoplastic resin monofilament, it will peel off and be removed over time, reducing its effectiveness, so it is preferable to knead it into the thermoplastic resin monofilament.
上記難燃剤としては、従来から熱可塑性樹脂成型品の成形に使用されている公知の任意の難燃剤が使用可能であり、例えば、グラファイト系難燃剤、メラミン系化合物やグアニジン系化合物などの窒素系難燃剤、赤リン系難燃剤、リン酸アンモニウムなどのリン系難燃剤、シリコン系難燃剤、臭素系難燃剤等が挙げられ、臭素系難燃剤が好ましい。 The flame retardant may be any known flame retardant that has been conventionally used in the molding of thermoplastic resin molded products. Examples of the flame retardant include graphite-based flame retardants, nitrogen-based flame retardants such as melamine-based compounds and guanidine-based compounds, red phosphorus-based flame retardants, phosphorus-based flame retardants such as ammonium phosphate, silicon-based flame retardants, and bromine-based flame retardants, with bromine-based flame retardants being preferred.
上記抗菌剤としては、従来公知の任意の抗菌剤が使用可能であり、例えば、抗菌作用を有する金属(例えば、銀、亜鉛、銅等)や金属イオンを無機系担体に担持させた無機系の金属イオン化合物(例えば、東亜合成社製、商品名「ノバロン」)、ニトリル系化合物、ピリジン系化合物、ハロアルキルチオ系化合物、有機ヨード系化合物、チアゾール系化合物、ベンズイミダゾール化合物、わさび成分(アリルイソチオシアネート)等が挙げられ、亜鉛系金属イオン化合物が好ましい。 As the antibacterial agent, any conventionally known antibacterial agent can be used, for example, inorganic metal ion compounds in which antibacterial metals (e.g., silver, zinc, copper, etc.) or metal ions are supported on an inorganic carrier (e.g., product name "Novalon" manufactured by Toa Gosei Co., Ltd.), nitrile compounds, pyridine compounds, haloalkylthio compounds, organic iodine compounds, thiazole compounds, benzimidazole compounds, wasabi components (allyl isothiocyanate), etc. are listed, and zinc-based metal ion compounds are preferred.
又、更に、熱可塑性樹脂単繊維に防ダニ剤、防カビ剤、消臭剤、無機充填剤、着色剤等が必要に応じて練り込まれていてもよい。 Furthermore, anti-mite agents, anti-fungal agents, deodorants, inorganic fillers, colorants, etc. may be kneaded into the thermoplastic resin monofilaments as necessary.
上記防ダニ剤としては、例えば、ピレスロイド系化合物、有機リン系化合物、カーバメイト系化合物等が挙げられ、上記防カビ剤としては、例えば、柿渋、木酢液、ヒノキ精油、ヒバ精油、ワサビ、カテキン、木酢液などの天然物、チアベンダゾール、ジフェニル、オルトフェニルフェノールなどの有機化合物、酸化チタンなどの無機化合物等が挙げられ、又、上記消臭剤としては、例えば、木炭、竹炭、活性炭、備長炭などの炭素材料や、シリカ、アルミナ、ゼオライト等が挙げられる。 Examples of the above-mentioned anti-mite agents include pyrethroid compounds, organophosphorus compounds, carbamate compounds, etc., and examples of the above-mentioned anti-mold agents include natural products such as persimmon tannin, wood vinegar, cypress essential oil, Japanese cedar essential oil, wasabi, catechin, wood vinegar, etc., organic compounds such as thiabendazole, diphenyl, orthophenylphenol, and inorganic compounds such as titanium oxide, etc., and examples of the above-mentioned deodorants include carbon materials such as charcoal, bamboo charcoal, activated charcoal, and binchotan charcoal, as well as silica, alumina, zeolite, etc.
上記無機充填剤としては、例えば、炭酸カルシウム、炭酸マグネシウム、酸化アルミニウム、酸化マグネシウム、酸化チタン、水酸化マグネシウム、タルク、マイカ、クレー等が挙げられる。 Examples of the inorganic fillers include calcium carbonate, magnesium carbonate, aluminum oxide, magnesium oxide, titanium oxide, magnesium hydroxide, talc, mica, clay, etc.
上記着色剤としては、例えば、アゾ系、フタロシアニン系、スレン系、染料レーキ系等の有機顔料、酸化物系、クロム酸モリブデン系、硫化物・セレン化物系、フェロシアン化物系等の無機顔料等が挙げられる。 Examples of the colorants include organic pigments such as azo, phthalocyanine, threne, and dye lake pigments, and inorganic pigments such as oxide, molybdenum chromate, sulfide/selenide, and ferrocyanide pigments.
更に、必要に応じて、フェノール系抗酸化剤、芳香族アミン系酸化防止剤等の酸化防止剤、サリチル酸エステル系、ベンゾフェノン系、ベンゾトリアゾール系、シアノアクリレート系等の紫外線吸収剤、ヒンダードアミン系の光安定剤、カチオン系、非イオン系等の帯電防止剤、衝撃改良剤等が練り込まれていてもよい。 Furthermore, if necessary, antioxidants such as phenol-based antioxidants and aromatic amine-based antioxidants, ultraviolet absorbers such as salicylic acid esters, benzophenones, benzotriazoles, and cyanoacrylates, hindered amine-based light stabilizers, cationic and nonionic antistatic agents, impact modifiers, etc. may be kneaded into the composition.
上記いぐさは天然いぐさでも紙や熱可塑性樹脂から製造された人工いぐさでもよいが、オレフィン系樹脂及び無機充填剤よりなる一軸延伸フィルムを紐状に結束し、得られた結束体を該結束体の直径より狭い空隙部を有する加熱部材の空隙部中を通過させることにより、該結束体の一軸延伸フィルムを互いに不規則且つ部分的に融着結束させると共に、該結束体の表面に融着被膜を形成することにより得られた人工いぐさが好ましい。 The rush mentioned above may be natural rush or artificial rush made from paper or thermoplastic resin, but artificial rush obtained by bundling uniaxially stretched film made of olefin resin and inorganic filler into a string shape and passing the resulting bundle through the gap of a heating element having a gap narrower than the diameter of the bundle, thereby irregularly and partially fusing and binding the uniaxially stretched film of the bundle together and forming a fused coating on the surface of the bundle, is preferred.
上記いぐさの太さは、特に限定されないが、一般に直径0.5~5mmであり、0.8~3mmが好ましい。又、人工いぐさは緻密であると重くなると共に硬くなり、断熱性、耐衝撃性、遮蔽性等が低下するので、15~50%の空隙率を有するのが好ましい。 There are no particular restrictions on the thickness of the rush, but it is generally 0.5 to 5 mm in diameter, with 0.8 to 3 mm being preferable. Furthermore, if artificial rush is dense, it will become heavy and hard, reducing its insulation, impact resistance, shielding properties, etc., so it is preferable for it to have a porosity of 15 to 50%.
尚、空隙率とは、人工いぐさ中に存在する、空気を有する気泡の体積比率である。気泡は独立気泡のみならず連続気泡であってもよく、連続気泡は人工いぐさの外部に連通していてもよい。 The porosity is the volume ratio of air bubbles that are present in the artificial rush. The bubbles may be not only closed bubbles but also open bubbles, and the open bubbles may be connected to the outside of the artificial rush.
上記一軸延伸フィルムは、オレフィン系樹脂及び無機充填剤よりなる樹脂フィルムを一軸延伸したフィルムである。 The uniaxially stretched film is a resin film made of an olefin resin and an inorganic filler that is uniaxially stretched.
上記オレフィン系樹脂としては、例えば、高密度ポリエチレン樹脂、中密度ポリエチレン樹脂、低密度ポリエチレン樹脂、直鎖状低密度ポリエチレン樹脂、ポリプロピレン樹脂、エチレン-プロピレン共重合体、エチレン-1-ブテン共重合体、エチレン―1-ペンテン共重合体、エチレン―1-ヘキセン共重合体等が挙げられ、高密度ポリエチレン樹脂及びポリプロピレン樹脂が好ましい。 Examples of the olefin resin include high-density polyethylene resin, medium-density polyethylene resin, low-density polyethylene resin, linear low-density polyethylene resin, polypropylene resin, ethylene-propylene copolymer, ethylene-1-butene copolymer, ethylene-1-pentene copolymer, ethylene-1-hexene copolymer, etc., with high-density polyethylene resin and polypropylene resin being preferred.
上記無機充填剤としては、例えば、炭酸カルシウム、炭酸マグネシウム、酸化アルミニウム、酸化マグネシウム、酸化チタン、水酸化マグネシウム、タルク、マイカ、クレー等が挙げられる。 Examples of the inorganic fillers include calcium carbonate, magnesium carbonate, aluminum oxide, magnesium oxide, titanium oxide, magnesium hydroxide, talc, mica, clay, etc.
樹脂フィルム中に無機充填剤が含有されていると、樹脂フィルムを一軸延伸した際に、含まれる無機充填剤を核として一軸延伸フィルム中に空隙が形成され、軽量になり、断熱性、クッション性等が向上するので、熱可塑性樹脂100重量部に対し10~50重量部の無機充填剤が添加されているのが好ましい。 If the resin film contains an inorganic filler, when the resin film is uniaxially stretched, voids are formed in the uniaxially stretched film with the inorganic filler as a nucleus, making the film lighter and improving its heat insulation and cushioning properties, so it is preferable to add 10 to 50 parts by weight of inorganic filler to 100 parts by weight of thermoplastic resin.
又、畳表の難燃性、火がついても短時間で消火しうる防炎性、抗菌性等を向上させるために上記樹脂フィルムに、難燃剤及び/又は抗菌剤が添加されるのが好ましい。熱可塑性樹脂単繊維の表面に塗布したのでは経時により剥離除去され効果が低下するので、上記樹脂フィルムに練り込まれているのが好ましい。 In addition, it is preferable to add a flame retardant and/or antibacterial agent to the resin film in order to improve the flame retardancy of the tatami mat, the flame resistance so that even if a fire is started, it can be extinguished in a short time, and the antibacterial properties. If applied to the surface of the thermoplastic resin monofilament, the agent will peel off and be removed over time, reducing its effectiveness, so it is preferable to knead the agent into the resin film.
上記難燃剤及び抗菌剤は前記の通りであり、更に、前記防ダニ剤、防カビ剤、消臭剤、着色剤等が必要に応じて練り込まれていてもよい。 The flame retardant and antibacterial agent are as described above, and furthermore, the above-mentioned anti-mite agent, anti-fungal agent, deodorizer, colorant, etc. may be kneaded in as necessary.
上記樹脂フィルムの製造方法は、従来公知の任意の製造方法が採用可能であり、例えば、上記オレフィン系樹脂及び無機充填剤等よりなる樹脂組成物を押出法、Tダイ法、キャスティング法、カレンダー法、インフレーション法、プレス法等の製膜法が挙げられる。 The resin film can be produced by any conventionally known production method, such as extrusion, T-die, casting, calendaring, inflation, pressing, or other film-forming methods using a resin composition made of the olefin resin and inorganic filler.
上記一軸延伸フィルムは、上記樹脂フィルムを一軸延伸したものであり、一軸延伸方法は、従来公知の任意の方法が採用されればよく、例えば、ロール一軸延伸法、ゾーン一軸延伸法等が挙げられる。 The uniaxially stretched film is the resin film uniaxially stretched. Any conventionally known method may be used for the uniaxial stretching, such as roll uniaxial stretching and zone uniaxial stretching.
一軸延伸温度は、低くなると均一に延伸できず、高くなると樹脂フィルムが溶融切断するので、延伸する樹脂フィルムのオレフィン系樹脂の「融点-60℃」~融点の範囲が好ましく、より好ましくは、オレフィン系樹脂の「融点-50℃」~「融点-5℃」である。 If the uniaxial stretching temperature is too low, the film will not be stretched uniformly, and if it is too high, the resin film will melt and break, so the temperature is preferably in the range of "melting point - 60°C" to the melting point of the olefin resin in the resin film to be stretched, and more preferably "melting point - 50°C" to "melting point - 5°C" of the olefin resin.
一軸延伸倍率は、倍率が低くなると機械的強度が低下し大きくなると硬くなっていぐさとしての風合いが低下するので2~10倍が好ましい。又、上記一軸延伸フィルムの厚さは5~20μmが好ましい。 The uniaxial stretching ratio is preferably 2 to 10 times, because a lower ratio reduces the mechanical strength, and a higher ratio makes the material hard and reduces the texture of the rush. The thickness of the uniaxially stretched film is preferably 5 to 20 μm.
上記結束体は、上記一軸延伸フィルムを紐状に結束することにより形成される。結束方法は特に限定されず、例えば、上記一軸延伸フィルムを一軸延伸方向に沿って折り畳んで結束する方法、細幅の上記一軸延伸フィルムを撚糸状に撚り合わす方法、細幅の上記一軸延伸フィルムを組紐状に組み合わせる方法等が挙げられ、折り畳んで結束する方法が好ましい。 The bundle is formed by bundling the uniaxially stretched film into a string. The bundling method is not particularly limited, and examples include a method of folding the uniaxially stretched film along the uniaxial stretching direction and bundling it, a method of twisting narrow uniaxially stretched films into a twisted thread, and a method of combining narrow uniaxially stretched films into a braided string, and the folding and bundling method is preferred.
次に、上記結束体を、結束体の直径より狭い空隙部を有する加熱部材の空隙部中を通過させることにより、上記一軸延伸フィルムを互いに不規則に融着収束させると共に表面に融着被膜を形成することにより人工いぐさが得られる。 Next, the bundle is passed through the gap of a heating element having a gap narrower than the diameter of the bundle, causing the uniaxially stretched films to irregularly fuse and converge with each other and form a fused coating on the surface, resulting in artificial rush.
上記加熱部材は、加熱可能であり、結束体の直径より狭く且つ、結束体を通過させることが可能な狭い空隙部を有するものであればよいが、結束体を狭い空隙を通過させることにより、上記一軸延伸フィルムを互いに不規則に融着収束させると共に表面に融着被膜を形成するのであるから、空隙部の直径は結束体の直径の40~90%が好ましい。又、空隙部の断面形状は、得ようとする人工いぐさの断面形状と略同一であればよく、例えば、円形、楕円形、四角形、六角形、八角形等が好ましい。 The heating element may be any member capable of heating, narrower than the diameter of the bundle, and having a narrow gap through which the bundle can pass. However, since the uniaxially stretched film is irregularly fused and converged to each other by passing the bundle through the narrow gap, and a fused coating is formed on the surface, it is preferable that the diameter of the gap is 40 to 90% of the diameter of the bundle. The cross-sectional shape of the gap may be approximately the same as the cross-sectional shape of the artificial rush to be obtained, and for example, a circle, ellipse, square, hexagon, octagon, etc. are preferable.
又、空隙部の出口付近に、形成された融着被膜にしわや貫通孔が形成されるように突起が形成されていてもよい。形成された融着被膜に貫通孔が形成されると、融着被膜内の空隙部が外気と連通され、吸湿性、断熱性等がより向上するので好ましい。 In addition, protrusions may be formed near the exit of the gap so that wrinkles or through holes are formed in the formed fused coating. If through holes are formed in the formed fused coating, the gaps in the fused coating are connected to the outside air, which is preferable as it further improves moisture absorption, heat insulation, etc.
上記加熱部材の加熱温度は、結束体を加熱部材の空隙部中を通過させることにより、上記一軸延伸フィルムを互いに不規則に融着結束させると共に表面に融着被膜を形成するのであるから、上記一軸延伸フィルムのオレフィン系樹脂の融点以上であり、好ましくは、オレフィン系樹脂の「融点+100℃」~「融点+150℃」である。 The heating temperature of the heating element is equal to or higher than the melting point of the olefin resin of the uniaxially stretched film, and is preferably between the melting point + 100°C and the melting point + 150°C of the olefin resin, since the bundle is passed through the gap of the heating element to irregularly fuse and bind the uniaxially stretched films together and form a fused coating on the surface.
結束体を加熱部材の空隙部中を通過させる速度は、遅くなると一軸延伸フィルムの融着率が高くなって、空隙率が減少して、重くなると共に硬くなり、逆に早くなると表面に融着被膜が形成しにくくなるので、加熱温度にもよるが、一般に、15~75m/分が好ましい。 If the speed at which the bundle is passed through the gap in the heating element is slow, the fusion rate of the uniaxially stretched film will increase, the void ratio will decrease, and the bundle will become heavier and harder. Conversely, if the speed is fast, it will be difficult to form a fused coating on the surface. Although this depends on the heating temperature, a speed of 15 to 75 m/min is generally preferred.
本発明の畳表は、上記樹脂系撚糸を縦糸とし、いぐさを横糸として製織されているが、製織方法は特に限定されず、従来公知の任意の製織方法が可能であり、例えば、引き目織、目積織り、平織、綾織等が挙げられる。 The tatami mat of the present invention is woven using the above-mentioned resin-based twisted yarn as the warp and rush as the weft, but the weaving method is not particularly limited and any conventionally known weaving method can be used, such as hikime weave, meseki weave, plain weave, and twill weave.
又、畳表においては、機械的強度が向上するように、互いに隣り合ういぐさは互いに密着して製織され、互いに隣り合う縦糸は、従来の畳表と同様に、2~30mm間隔で製織されているのが好ましい。 In addition, in order to improve the mechanical strength of the tatami facing, adjacent rushes are woven in close contact with each other, and adjacent warp threads are preferably woven at intervals of 2 to 30 mm, as in conventional tatami facings.
次に、本発明の実施例を説明するが、本発明は実施例に限定されるものではない。 Next, we will explain examples of the present invention, but the present invention is not limited to these examples.
熱可塑性樹脂単繊維の製造
表1に示した所定量のポリプロピレン樹脂(密度0.9g/cm3、融点155~165℃)、ポリエステル樹脂、臭素系難燃剤(大日精化工業社製、商品名「ダイフネン」)及び亜鉛系抗菌剤(東亜合成社製、商品名「ノバロン」)よりなる樹脂組成物を一軸混錬押出機に供給し210℃で溶融混錬押出して、表1に示すデニールの熱可塑性樹脂単繊維(1)、(2)、(3)及び(4)を得た。
A resin composition consisting of a polypropylene resin (density 0.9 g/cm 3 , melting point 155-165° C.), a polyester resin, a bromine-based flame retardant (manufactured by Dainichiseika Chemicals Mfg. Co., Ltd., product name "Daifuunen") and a zinc-based antibacterial agent (manufactured by Toa Gosei Co., Ltd., product name "Novalon") in the prescribed amounts shown in Table 1 was fed to a single-screw kneading extruder and melt-kneaded and extruded at 210° C. to obtain thermoplastic resin single fibers (1), (2), (3) and (4) having the deniers shown in Table 1.
樹脂系撚糸の製造
上記熱可塑性樹脂単繊維(1)、(2)、(3)及び(4)をそれぞれ5本束ねて撚ることにより2500デニールの樹脂系撚糸(1)及び(2)並びに5000デニールの樹脂系撚糸(3)及び(4)を得た。又、樹脂系撚糸(1)2本と550デニールの綿糸3本束ねて撚ることにより2650デニールの混合撚糸を得た。
Manufacture of resin twisted yarns Five each of the thermoplastic resin monofilaments (1), (2), (3) and (4) were bundled and twisted to obtain 2500 denier resin twisted yarns (1) and (2) and 5000 denier resin twisted yarns (3) and (4). Also, two resin twisted yarns (1) and three 550 denier cotton yarns were bundled and twisted to obtain a 2650 denier mixed twisted yarn.
撚糸の吸水・保水性試験
得られた長さ10mの上記樹脂系撚糸(1)及び(4)並びに混合撚糸を25℃、湿度50%の雰囲気下で2時間以上調整した後、1時間水に浸漬した。浸漬後、取り出して、25℃、湿度50%の雰囲気下で乾燥し、表2に示した所定の乾燥時間ごとに撚糸の重量を測定し、結果を表2に示した。尚、水浸漬前の撚糸の重量を0とし、所定の乾燥時間ごとの撚糸の重量増加率を%で示した。
Water absorption and water retention test of twisted yarn The above-mentioned resin-based twisted yarns (1) and (4) and the mixed twisted yarn, each having a length of 10 m, were conditioned for at least 2 hours in an atmosphere of 25°C and 50% humidity, and then immersed in water for 1 hour. After immersion, the yarns were taken out and dried in an atmosphere of 25°C and 50% humidity, and the weight of the twisted yarn was measured at each predetermined drying time shown in Table 2, and the results are shown in Table 2. The weight of the twisted yarn before immersion in water was set to 0, and the weight increase rate of the twisted yarn at each predetermined drying time was shown in %.
加熱収縮率
得られた長さ10cmの上記樹脂系撚糸(1)及び(4)並びに混合撚糸を60℃に設定されたギアオーブンに供給し、無負荷で6時間加熱して加熱収縮率を測定し、結果を表2に示した。
Heat shrinkage rate The above resin-based twisted yarns (1) and (4) and the mixed twisted yarn having a length of 10 cm were fed into a gear oven set at 60° C. and heated for 6 hours without load to measure the heat shrinkage rate. The results are shown in Table 2.
(実施例1~4、比較例1、2)
人工いぐさの製造
ポリプロピレン樹脂(密度0.9g/cm3、融点155~165℃)100重量部、炭酸カルシウム27重量部及びアゾ系無機顔料2.0重量部並びに表3に示した所定量の臭素系難燃剤(大日精化工業社製、商品名「ダイフネン」)及び亜鉛系抗菌剤(東亜合成社製、商品名「ノバロン」)よりなる樹脂組成物をスクリュー70mmの一軸混錬押出機に供給して210℃で混錬押出して厚さ100μmのポリプロピレン樹脂フィルムを得た。
(Examples 1 to 4, Comparative Examples 1 and 2)
Manufacturing of artificial rush
A resin composition consisting of 100 parts by weight of polypropylene resin (density 0.9 g/cm 3 , melting point 155 to 165°C), 27 parts by weight of calcium carbonate, 2.0 parts by weight of an azo-based inorganic pigment, and the prescribed amounts of a bromine-based flame retardant (manufactured by Dainichiseika Chemicals Mfg. Co., Ltd., product name "Daifuunen") and a zinc-based antibacterial agent (manufactured by Toa Gosei Co., Ltd., product name "Novalon") shown in Table 3 was fed into a single-screw kneading extruder with a 70 mm screw and kneaded and extruded at 210°C to obtain a polypropylene resin film having a thickness of 100 μm.
得られたポリプロピレン樹脂フィルムを120℃に設定された熱板方式の一軸延伸装置に供給し、5倍に延伸して、厚さ20μmの一軸延伸フィルムを得た。得られた一軸延伸フィルムを一軸延伸方向に折り畳んで、直径2.0mmの貫通孔を通過させ紐状に成形した直径2.0mmの結束体を得た。得られた直径2.0mmの結束体を直径1.0mmの断面円形の空隙部を有する加熱部材に供給し、空隙部を65m/分の速度で通過させて人工いぐさ(1)、(2)、(3)及び(4)を得た。 The obtained polypropylene resin film was fed to a hot plate type uniaxial stretching device set at 120°C and stretched 5 times to obtain a uniaxially stretched film with a thickness of 20 μm. The obtained uniaxially stretched film was folded in the uniaxial stretching direction and passed through a through hole with a diameter of 2.0 mm to obtain a bundle formed into a string shape with a diameter of 2.0 mm. The obtained bundle with a diameter of 2.0 mm was fed to a heating element having a circular cross-sectional gap with a diameter of 1.0 mm, and passed through the gap at a speed of 65 m/min to obtain artificial rush (1), (2), (3) and (4).
加熱部材は300℃に加熱されており、空隙部の出口付近に高さ0.05mmで先の尖った突起が45度間隔に8本立設されていた。得られた人工いぐさは、テープ状体が部分的に融着されていると共に表面に融着被膜が形成され、融着被膜にはランダムに貫通孔や凹凸が形成されていた。又、得られた人工いぐさは黒色であり、その直径は約1.1mm、空隙率は33%であった。又、人工いぐさ(1)、(2)、(3)及び(4)をJIS K7127に準拠し、チャック間距離200mm、引張速度300mm/minで機械的特性を測定したところ、長さ方向の破断強度は9.5~9.8Nであり、破断伸度は9~11%であった。 The heating element was heated to 300°C, and eight pointed protrusions, 0.05 mm high, were installed at 45° intervals near the exit of the gap. The resulting artificial rush had the tape-shaped body partially fused and a fused coating formed on the surface, with random through-holes and irregularities formed in the fused coating. The resulting artificial rush was black, had a diameter of approximately 1.1 mm, and a porosity of 33%. The mechanical properties of artificial rushes (1), (2), (3), and (4) were measured in accordance with JIS K7127 at a chuck distance of 200 mm and a tensile speed of 300 mm/min. The breaking strength in the longitudinal direction was 9.5-9.8 N, and the breaking elongation was 9-11%.
畳表の製造
表4及び5に示した所定の人工いぐさを横糸とし、撚糸を縦糸とし、縦糸の間隔4mm及び横糸の打ち込み数は90本/10cmに設定し、表4及び5に示した所定の製織方法で製織して畳表を得た。
Manufacturing of Tatami Coverings The specified artificial rush shown in Tables 4 and 5 was used as the weft, twisted yarn was used as the warp, the interval between the warp threads was set to 4 mm, and the weft thread count was set to 90 threads/10 cm. The tatami coverings were obtained by weaving using the specified weaving method shown in Tables 4 and 5.
又、比較例2として、天然いぐさを横糸とし、上記樹脂系撚糸(2)を縦糸とし、縦糸の間隔4mm、横糸の打ち込み数は90本/10cmに設定し、引き目織で製織して畳表を得た。 In Comparative Example 2, natural rush was used as the weft and the resin-based twisted yarn (2) was used as the warp, the interval between the warp threads was set to 4 mm, and the weft thread count was set to 90 threads/10 cm. The tatami mat was woven using a hikime weave method.
得られた畳表を切断して、3枚の試料を作成し、消防法施行規則第4条「じゅうたん」に準拠して燃焼試験を行い、残炎時間及び炭化長さを測定し、結果を表4及び5に示した。又、残炎時間20秒以下で炭化長さが10cm以下のものを総合評価○とし、それ以上の点が1か所でもあれば×とした。 The resulting tatami mat was cut into three samples, which were then subjected to a combustion test in accordance with Article 4 of the Fire Service Act Enforcement Regulations (Carpets), measuring the afterflame time and char length, with the results shown in Tables 4 and 5. Those with an afterflame time of 20 seconds or less and a char length of 10 cm or less were given an overall rating of ○, and those with even one point greater than this were given an ×.
又、JIS Z2801-2012に準拠して抗菌性の評価を行い、抗菌活性値2,0以上を示した場合、〇とし、それ以下の場合は×とした。得られた結果を表4及び5に示した。結果を表4及び5に示した。 In addition, antibacterial properties were evaluated in accordance with JIS Z2801-2012, and antibacterial activity values of 2.0 or more were marked as ◯, and values below that were marked as ×. The results are shown in Tables 4 and 5. The results are shown in Tables 4 and 5.
実施例1、4及び比較例1、2で得られた畳表を10×10cmに切断して正方形の試料を作成し、前記撚糸の吸水・保水性試験で行ったと同様にして吸水・保水性試験を行い、結果を表5に示した。 The tatami mats obtained in Examples 1 and 4 and Comparative Examples 1 and 2 were cut into square samples of 10 x 10 cm, and water absorption and water retention tests were carried out in the same manner as in the water absorption and water retention tests for the twisted yarn, and the results are shown in Table 5.
本発明の畳表はクリーン性、耐汚染性等が優れていると共に、難燃性、火がついても短時間で消火しうる防炎性、抗菌性等効果を適宜付与することができるので、建築部材として好適に使用できる。 The tatami mat of the present invention has excellent cleanability and stain resistance, and can be appropriately imparted with flame retardancy, flame resistance that allows fire to be extinguished in a short time even if it catches fire, antibacterial properties, etc., making it suitable for use as a building material.
Claims (5)
加熱収縮率は樹脂系撚糸を60℃の雰囲気下、無負荷で6時間加熱した際の収縮比率であり、
加熱収縮率(%)=(加熱前の樹脂系撚糸の長さ-加熱後の樹脂系撚糸の長さ)×100 /(加熱前の樹脂系撚糸の長さ) The tatami covering is woven using a resin-based twisted yarn formed by twisting 3 to 5 thermoplastic resin single fibers having a denier of 500 to 1000 as a warp yarn and an artificial rush as a weft yarn, and is characterized in that the heat shrinkage rate of the resin-based twisted yarn calculated by the following formula is 3% or more.
The heat shrinkage rate is the shrinkage ratio when the resin twisted yarn is heated in an atmosphere of 60° C. for 6 hours without load.
Heat shrinkage rate (%) = (length of resin-based twisted yarn before heating - length of resin-based twisted yarn after heating) x 100 / (length of resin-based twisted yarn before heating)
5. The tatami mat according to claim 4, wherein a flame retardant and/or an antibacterial agent is further kneaded into the uniaxially stretched film.
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| JP3135831U (en) | 2007-03-23 | 2007-10-04 | 三橋 昭司郎 | Deodorant, antibacterial, antifungal effect yarn woven tatami mat |
| JP2009013640A (en) | 2007-07-04 | 2009-01-22 | Sekisui Seikei Ltd | Warp for tatami facing |
| WO2017149914A1 (en) | 2016-03-01 | 2017-09-08 | 積水成型工業株式会社 | Anisotropic tatami mat face |
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| JPH03180532A (en) * | 1989-12-09 | 1991-08-06 | Unitika Ltd | Warp for tatami facing |
| JPH08284039A (en) * | 1995-04-07 | 1996-10-29 | Nissho Kk | Multiple rush and artificial tatami mat surface |
| JPH08284380A (en) * | 1995-04-17 | 1996-10-29 | Toray Ind Inc | Artificial tatami mat |
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| JP3135831U (en) | 2007-03-23 | 2007-10-04 | 三橋 昭司郎 | Deodorant, antibacterial, antifungal effect yarn woven tatami mat |
| JP2009013640A (en) | 2007-07-04 | 2009-01-22 | Sekisui Seikei Ltd | Warp for tatami facing |
| WO2017149914A1 (en) | 2016-03-01 | 2017-09-08 | 積水成型工業株式会社 | Anisotropic tatami mat face |
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