JP5019426B2 - Standing blanket with reduced aldehyde emission - Google Patents
Standing blanket with reduced aldehyde emission Download PDFInfo
- Publication number
- JP5019426B2 JP5019426B2 JP2006318606A JP2006318606A JP5019426B2 JP 5019426 B2 JP5019426 B2 JP 5019426B2 JP 2006318606 A JP2006318606 A JP 2006318606A JP 2006318606 A JP2006318606 A JP 2006318606A JP 5019426 B2 JP5019426 B2 JP 5019426B2
- Authority
- JP
- Japan
- Prior art keywords
- fabric
- resin
- amount
- carpet
- pile yarn
- 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.)
- Active
Links
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 title 1
- 239000004744 fabric Substances 0.000 claims description 49
- 150000001875 compounds Chemical class 0.000 claims description 28
- 229920000768 polyamine Polymers 0.000 claims description 24
- 229920005989 resin Polymers 0.000 claims description 23
- 239000011347 resin Substances 0.000 claims description 23
- 229910021331 inorganic silicon compound Inorganic materials 0.000 claims description 19
- 239000011230 binding agent Substances 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 10
- 239000004745 nonwoven fabric Substances 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 10
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 30
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 27
- 239000000835 fiber Substances 0.000 description 24
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 18
- 150000001299 aldehydes Chemical class 0.000 description 18
- 235000012239 silicon dioxide Nutrition 0.000 description 15
- 239000000377 silicon dioxide Substances 0.000 description 15
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 10
- 230000001877 deodorizing effect Effects 0.000 description 9
- 239000007789 gas Substances 0.000 description 9
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- -1 adipic acid dihydrazide compound Chemical class 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229920006026 co-polymeric resin Polymers 0.000 description 4
- 238000001514 detection method Methods 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 230000007935 neutral effect Effects 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- 241000219146 Gossypium Species 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000004332 deodorization Methods 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
- 239000011342 resin composition Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 229920003048 styrene butadiene rubber Polymers 0.000 description 3
- 244000025254 Cannabis sativa Species 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
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 235000009120 camo Nutrition 0.000 description 2
- 235000005607 chanvre indien Nutrition 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 239000011487 hemp Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229910021426 porous silicon Inorganic materials 0.000 description 2
- 238000003672 processing method Methods 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-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 1
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- KLIYQWXIWMRMGR-UHFFFAOYSA-N buta-1,3-diene;methyl 2-methylprop-2-enoate Chemical compound C=CC=C.COC(=O)C(C)=C KLIYQWXIWMRMGR-UHFFFAOYSA-N 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- RPOCFUQMSVZQLH-UHFFFAOYSA-N furan-2,5-dione;2-methylprop-1-ene Chemical compound CC(C)=C.O=C1OC(=O)C=C1 RPOCFUQMSVZQLH-UHFFFAOYSA-N 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 208000008842 sick building syndrome Diseases 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 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
- 239000002562 thickening agent Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 238000009732 tufting Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Carpets (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
本発明は、カーペット等の立毛布帛から放散する微量なアルデヒドガス類を吸着除去し、室内空気の汚染を防ごうとするものである。 The present invention intends to prevent the contamination of indoor air by adsorbing and removing a small amount of aldehyde gas diffused from a napped fabric such as carpet.
近年製造されるカーペット等の立毛布帛は、リサイクルされた材料を使用することが多くなってきており、これらリサイクル原料は様々な使用履歴があり、不純物等の混入を完全に防いで管理しリサイクルすることは不可能とされている。そのため、見た目には特に問題のない材料であっても、これらのリサイクル原料で製造されるカーペット等の繊維布帛からは、極微量ではあるが、アルデヒドガス類の放散が確認されることもあり、問題視されてきている。また、近年建設される住宅は、気密性が著しく向上しており、たとえ極微量なガスであっても、人体に影響を与え、シックハウス症候群を引き起こす原因の一つになっているとも言われている。 In recent years, raised fabrics such as carpets are increasingly used recycled materials, and these recycled materials have various usage histories, and are managed and recycled with complete prevention of contamination. It is considered impossible. Therefore, even if it is a material that does not have a particular problem in appearance, from the fiber fabric such as carpet manufactured with these recycled raw materials, although it is a very small amount, the emission of aldehyde gases may be confirmed, It has been regarded as a problem. Houses constructed in recent years have significantly improved airtightness, and even a trace amount of gas is said to affect the human body and cause sick house syndrome. Yes.
このような問題に対応するため、エアコンや空気清浄機等を使った消臭、脱臭、集塵が行なわれるようになり、フィルタ−等によって空気中のアルデヒドガスや臭い、塵等を捕集する方法が提案されている。 In order to deal with such problems, deodorization, deodorization and dust collection using air conditioners and air purifiers will be carried out, and aldehyde gas, odor, dust etc. in the air will be collected by filters etc. A method has been proposed.
特許文献1においては、アジピン酸ジヒドラジド化合物がアルデヒド類を吸着する吸着剤としたカ−ペットが提案されている。特許文献2においては、繊維表面にチタンとケイ素を含む複合酸化物と、アルデヒド消臭組成物としてヒドラジド系化合物または窒素含有複素環化合物を含むものが、樹脂により付着させた繊維構造物が開示されている。また、出願人は特許文献3、特許文献4において、ヒドラジン誘導体から選択された1種以上の化合物と、多孔質無機物質から選択された1種以上の化合物と、金属酸化物から選択された1種以上の化合物とからなる消臭組成物が、バインダー樹脂によって繊維層に担持した消臭布帛を開示している。これらの技術は、ヒドラジン等の消臭組成物を繊維等に浸漬、噴霧、印刷等の方法で塗布して担持させたり、バッキング層に混入するものであって、ある程度のアルデヒド類の消臭効果を発揮するものではあるが、そのいずれもが空気中にあるアルデヒド類の消臭効果を目的に提案されているものであって、本願のように自ら発生する微量のアルデヒド類の放散を抑えるようなものは今だ提案されていない。
本発明は、かかる技術的背景に鑑みてなされたものであって、住宅や自動車の室内、電車、旅客機等の室内に使用される布帛から発生するアルデヒドガスの拡散を極力防止して、室内空気をクリーンな状態に維持することを目的としている。 The present invention has been made in view of such a technical background, and it is possible to prevent diffusion of aldehyde gas generated from fabrics used in houses, automobiles, trains, passenger airplanes, etc. The goal is to keep it clean.
本発明者らは、このような課題を解決するために鋭意検討の結果、ポリアミン化合物を担持した無機ケイ素化合物を立毛布帛のパイル糸及び/またはバッキング層に固着することにより、立毛布帛から発生するアルデヒド類の拡散を低減することができることを見出し本発明に到達した。前記目的を達成するために、本発明は以下の手段を提供する。 As a result of intensive studies to solve such problems, the present inventors have generated the napped fabric by fixing the inorganic silicon compound carrying the polyamine compound to the pile yarn and / or the backing layer of the napped fabric. It has been found that diffusion of aldehydes can be reduced, and the present invention has been reached. In order to achieve the above object, the present invention provides the following means.
[1]ポリアミン化合物を担持した無機ケイ素化合物を、バインダー樹脂を介してパイル糸に固着及び/またはバッキング層に混入したことに特徴のある立毛布帛。 [1] A raised fabric characterized in that an inorganic silicon compound carrying a polyamine compound is fixed to a pile yarn and / or mixed into a backing layer through a binder resin.
[2]前記ポリアミン化合物を担持した無機ケイ素化合物の粒径が10nm〜100μmで、0.2〜10.0g/m2(乾燥重量)パイル糸に固着及び/またはバッキング樹脂に混入したことに特徴のある前項1に記載の立毛布帛。 [2] The inorganic silicon compound carrying the polyamine compound has a particle size of 10 nm to 100 μm, and is fixed to 0.2 to 10.0 g / m 2 (dry weight) pile yarn and / or mixed with a backing resin. The napped fabric according to item 1 above.
[3]前記立毛布帛が再生原料を使用したモケット、不織布、またはカ−ペットであることに特徴のある前項1又は2に記載の立毛布帛。 [3] The raised fabric according to item 1 or 2, characterized in that the raised fabric is a moquette, nonwoven fabric, or carpet using a recycled material.
[1]の発明によれば、ポリアミン化合物を担持した無機ケイ素化合物を、バインダー樹脂を介してパイル糸に固着及び/またはバッキング層に混入しているので、立毛布帛から発生する極微量のアルデヒド類の中性ガスを効率よく効果的に除去する立毛布帛とすることができる。また、バインダー樹脂を介してパイル糸に固着及び/またはバッキング層に混入しているので、洗濯にも十分耐えることのできる立毛布帛とすることができる。 According to the invention of [1], since the inorganic silicon compound carrying the polyamine compound is fixed to the pile yarn and / or mixed in the backing layer via the binder resin, a very small amount of aldehydes generated from the napped fabric It is possible to make a napped fabric that efficiently and effectively removes neutral gas. Moreover, since it adheres to the pile yarn via the binder resin and / or is mixed in the backing layer, it is possible to obtain a napped fabric that can sufficiently withstand washing.
[2]の発明によれば、前記ポリアミン化合物を担持した無機ケイ素化合物の粒径が10nm〜100μmで、0.2〜10.0g/m2(乾燥重量)パイル糸に固着及び/またはバッキング樹脂に混入しているので、ざらつき感がなく、持続して立毛布帛の風合を良好に保ったまま、立毛布帛から発生する極微量のアルデヒド類の中性ガスを効率よく効果的に除去する立毛布帛とすることができる。 According to the invention of [2], the inorganic silicon compound carrying the polyamine compound has a particle diameter of 10 nm to 100 μm and is fixed to the pile yarn and / or a backing resin of 0.2 to 10.0 g / m 2 (dry weight). Napped to effectively remove the trace amount of neutral aldehydes generated from the napped fabric without any roughness and maintaining a good texture of the napped fabric. It can be a fabric.
[3]の発明によれば、前記立毛布帛が再生原料を使用したモケット、不織布、またはカ−ペットであっても、立毛布帛から発生する極微量のアルデヒド類の中性ガス拡散が押さえられ、室内空気が汚染されるのを防ぐことができる。 According to the invention of [3], even if the raised fabric is a moquette, non-woven fabric, or carpet using a recycled material, neutral gas diffusion of a trace amount of aldehydes generated from the raised fabric is suppressed, Indoor air can be prevented from being contaminated.
次に、この発明に係る立毛布帛の一実施形態について説明する。この実施形態の立毛布帛としては特に限定されず、例えば、立毛不織布、カーペット、モケットのような立毛布帛等を挙げることができる。立毛布帛を形成する繊維についても特に限定されず、ポリエステル繊維、ポリアミド繊維、ポリプロピレン繊維、アクリル繊維、レ−ヨン繊維等の繊維からなるもの等を好適に使用でき、その他麻、綿、羊毛等の天然繊維からなるもの等も使用できる。中でもリサイクルによって再生した繊維からは、極微量のアルデヒド類の中性ガスが発生することがあり、これらの再生繊維に対して、本発明は効果的である。 Next, an embodiment of the napped fabric according to the present invention will be described. The raised fabric of this embodiment is not particularly limited, and examples thereof include a raised fabric such as a raised nonwoven fabric, a carpet, and a moquette. The fibers forming the napped fabric are not particularly limited, and those made of fibers such as polyester fibers, polyamide fibers, polypropylene fibers, acrylic fibers, rayon fibers, etc. can be suitably used, and other hemp, cotton, wool, etc. Those made of natural fibers can also be used. Among them, a very small amount of neutral gas of aldehydes may be generated from fibers regenerated by recycling, and the present invention is effective for these regenerated fibers.
また、本発明において、ポリアミン化合物を担持した無機ケイ素化合物としては、例えば多孔質二酸化ケイ素、ケイ酸アルミニウム等にポリアミン化合物を担持したものが挙げられる。ポリアミン化合物は、分子内に第一級アミノ基を一個以上有している化合物であれば脂肪族アミン、芳香族アミン、脂環式アミンのいずれも使用でき、例えばジエチレントリアミン、テトラエチレンペンタミン等が挙げられる。ポリアミン化合物を担持する方法としては、例えばポリアミン化合物の水溶液を作成し、この水溶液中に多孔質二酸化ケイ素を浸漬し、これを加熱焼成することによってポリアミン化合物を担持した二酸化ケイ素化合物を得ることが出来る。 In the present invention, examples of the inorganic silicon compound carrying a polyamine compound include those carrying a polyamine compound on porous silicon dioxide, aluminum silicate, or the like. As the polyamine compound, any one of aliphatic amine, aromatic amine, and alicyclic amine can be used as long as it has one or more primary amino groups in the molecule. For example, diethylenetriamine, tetraethylenepentamine, etc. Can be mentioned. As a method for supporting a polyamine compound, for example, an aqueous solution of a polyamine compound is prepared, porous silicon dioxide is immersed in this aqueous solution, and this is heated and fired to obtain a silicon dioxide compound supporting the polyamine compound. .
前記ポリアミン化合物を担持した無機ケイ素化合物の粒径は10nm〜100μmであるのが好ましい。平均粒径が10nm〜100μmであるので、パイル部に担持したとき、ざらつき感を受けることなく、風合も良好な立毛布帛を得ることができる。中でも、平均粒径は10nm〜10μmにするのが好ましく、特に好ましくは10nm〜5μm以下である。 The particle size of the inorganic silicon compound carrying the polyamine compound is preferably 10 nm to 100 μm. Since the average particle diameter is 10 nm to 100 μm, it is possible to obtain a raised fabric having a good texture without receiving a feeling of roughness when it is carried on a pile portion. Among them, the average particle diameter is preferably 10 nm to 10 μm, and particularly preferably 10 nm to 5 μm.
前記ポリアミン化合物を担持した無機ケイ素化合物の塗布量は0.2〜10.0g/m2(乾燥重量)とするのが好ましい。0.2g/m2未満では十分なアルデヒド類の除去性能が得られなくなるので好ましくない。また、10.0g/m2を超えてもアルデヒド類の除去性能の向上はなく、徒にコストを増大することになり好ましくない。 The coating amount of the inorganic silicon compound carrying the polyamine compound is preferably 0.2 to 10.0 g / m 2 (dry weight). Less than 0.2 g / m 2 is not preferable because sufficient aldehyde removal performance cannot be obtained. Moreover, even if it exceeds 10.0 g / m < 2 >, the removal performance of aldehydes will not be improved, and the cost will increase undesirably.
前記ポリアミン化合物を担持した無機ケイ素化合物の塗布方法は、まず前記ポリアミン化合物を担持した無機ケイ素化合物とバインダ−樹脂を水に分散させた水分散液からなる処理液を調合する。この時、ポリアミン化合物を担持した無機ケイ素化合物とバインダ−樹脂を可能な限り分散させることが好ましく、バインダ−樹脂については、水との間でエマルジョン状態を形成することがより好ましい。また、調合の際予め先にポリアミン化合物を担持した無機ケイ素化合物を水に分散させておいてから、バインダ−樹脂を分散するのが、より均一に分散させるのに好ましい。 The coating method of the inorganic silicon compound carrying the polyamine compound is prepared by first preparing a treatment liquid comprising an aqueous dispersion in which the inorganic silicon compound carrying the polyamine compound and a binder resin are dispersed in water. At this time, it is preferable to disperse the inorganic silicon compound carrying the polyamine compound and the binder resin as much as possible, and it is more preferable that the binder resin forms an emulsion state with water. In addition, it is preferable to disperse the binder resin after dispersing the inorganic silicon compound carrying the polyamine compound in water in advance before the preparation.
前記バインダ−樹脂は、どのような樹脂でも使用することができる。例えば、自己架橋型アクリル樹脂、メタアクリル樹脂、ウレタン樹脂、シリコン樹脂、グリオキザ−ル樹脂、酢酸ビニル樹脂、塩化ビニリデン樹脂、ブタジエン樹脂、メラミン樹脂、エポキシ樹脂、アクリル−シリコン共重合体樹脂、エチレン−酢酸ビニル共重合体樹脂、イソブチレン無水マレイン酸共重合体樹脂、エチレン−スチレン−アクリレート−メタアクリレ−ト共重合体樹脂などが挙げられる。これらの樹脂を2種類以上混合してバインダ−樹脂としてもよい。 As the binder resin, any resin can be used. For example, self-crosslinking acrylic resin, methacrylic resin, urethane resin, silicone resin, glyoxal resin, vinyl acetate resin, vinylidene chloride resin, butadiene resin, melamine resin, epoxy resin, acrylic-silicone copolymer resin, ethylene- Examples thereof include vinyl acetate copolymer resin, isobutylene maleic anhydride copolymer resin, and ethylene-styrene-acrylate-methacrylate copolymer resin. Two or more of these resins may be mixed to form a binder resin.
また、前記処理液には、分散剤や、増粘剤などの各種添加剤を、各種特性向上のため配合してもよい。こうして得られる処理液をカ−ペットやモケット等の立毛布帛に塗布させる。この塗布する手段としては、特に限定されるものではないが、例えばスプレ−法、浸漬法、コ−ティング法、パディング法等が挙げられる。塗布する時期は、カ−ペットの場合、パイル糸、基布、バッキング層それぞれ単体の状態でもよいし、基布にパイル糸を殖設した表皮層の形態で処理液を塗布してもよいし、表皮層とバッキング層と接着一体化した形態で塗布してもよい。また、前記ポリアミン化合物を担持した無機ケイ素化合物をバッキング剤に混入し、スプレ−やロ−ラ−コ−ティングで塗布してバッキング層としてもよい。 Moreover, you may mix | blend various additives, such as a dispersing agent and a thickener, with the said process liquid for various characteristic improvement. The treatment liquid thus obtained is applied to a raised fabric such as a carpet or a moquette. The means for applying is not particularly limited, and examples thereof include a spray method, a dipping method, a coating method, and a padding method. In the case of carpet, the application time may be a single state of the pile yarn, the base fabric, and the backing layer, or the treatment solution may be applied in the form of a skin layer in which the pile yarn is laid on the base fabric. The skin layer and the backing layer may be applied in an integrated form. Alternatively, the backing layer may be formed by mixing an inorganic silicon compound carrying the polyamine compound in a backing agent and applying the mixture by spraying or roller coating.
上記のように、処理液を付与した後に乾燥させるが、乾燥手段としては、加熱処理する方法が乾燥効率から好ましい。加熱処理温度は、100〜180℃とするのが好ましい。この温度での加熱処理によって、ポリアミン化合物を担持した無機ケイ素化合物の固着性をより高め、持続耐久性を一層向上させることができる。 As described above, the treatment liquid is applied and then dried. As a drying means, a heat treatment method is preferable from the viewpoint of drying efficiency. The heat treatment temperature is preferably 100 to 180 ° C. By the heat treatment at this temperature, the sticking property of the inorganic silicon compound carrying the polyamine compound can be further increased, and the sustained durability can be further improved.
一般に布帛には、消臭性能以外に、難燃、防虫、防汚等の各種機能性を付与すべく加工が施されることが多く、その加工を加えることにより、立毛布帛表面のPH値が酸性側に振れたり、塩基性に振れたりして消臭効果の低下を招くことがある。本発明においては、本加工を施す前の布帛表面のPH値を6〜8に保つことが大切で、各種機能性を付与する加工によって布帛表面のPH値が酸性側に振れたり、塩基性に振れた場合には、りん酸塩やクエン酸等の水溶液に浸漬して中和処理するのが好ましい。立毛布帛表面のPH値を6〜8に調整した後で消臭加工を施すことにより、消臭効率のよい立毛布帛とすることができる。 In general, the fabric is often processed to impart various functionalities such as flame retardancy, insect repellency, and antifouling in addition to the deodorizing performance. By adding the processing, the PH value of the surface of the napped fabric is increased. The deodorizing effect may be deteriorated by swinging to the acidic side or basic. In the present invention, it is important to maintain the pH value of the fabric surface before the main processing at 6 to 8, and the PH value of the fabric surface may be shifted to the acidic side or become basic due to various functionalities. In the case of shaking, it is preferably neutralized by immersing in an aqueous solution of phosphate, citric acid or the like. By adjusting the PH value of the surface of the napped fabric to 6 to 8 and then applying a deodorizing process, a napped fabric with good deodorizing efficiency can be obtained.
また、バッキング層5は、図1のように、パイル糸2が使用中に抜けないように基布3に固定するものであり、樹脂組成物やゴム組成物であれば特に限定されないが、例えば樹脂組成物の樹脂成分としてはアクリル系、ウレタン系、ポリ塩化ビニル、ポリエチレン、ポリプロピレン、エチレン−酢酸ビニル共重合体(EVA)等の樹脂が挙げられる。ゴム組成物のゴム成分としてはSBR(スチレン−ブタジエンゴム)、NBR(アクリロニトリル−ブタジエンゴム)、MBR(メチルメタクリレート−ブタジエンゴム)あるいは天然ゴム等が挙げられる。これらの樹脂組成物やゴム組成物からなるバッキング剤にポリアミン化合物を担持した無機ケイ素化合物を混入し、立毛布帛の裏面に塗布し乾燥すればよい。塗布方法としてはロールコーティング法、スプレーコーティング法等を挙げることができる。 Further, as shown in FIG. 1, the backing layer 5 is fixed to the base fabric 3 so that the pile yarn 2 does not come off during use, and is not particularly limited as long as it is a resin composition or a rubber composition. Examples of the resin component of the resin composition include resins such as acrylic, urethane, polyvinyl chloride, polyethylene, polypropylene, and ethylene-vinyl acetate copolymer (EVA). Examples of the rubber component of the rubber composition include SBR (styrene-butadiene rubber), NBR (acrylonitrile-butadiene rubber), MBR (methyl methacrylate-butadiene rubber), and natural rubber. What is necessary is just to mix the inorganic silicon compound which carry | supported the polyamine compound in the backing agent which consists of these resin composition and rubber composition, and it apply | coats to the back surface of a napped fabric, and dries. Examples of the coating method include a roll coating method and a spray coating method.
ポリアミン化合物を担持した無機ケイ素化合物7の塗布量は、パイル糸2及び/またはバッキング層5に0.2〜10.0g/m2(乾燥重量)とするのが好ましい。0.2g/m2未満では十分なアルデヒド類の除去性能が得られなくなるので好ましくない。また、10.0g/m2を超えてもアルデヒド類の除去性能の向上はなく、徒にコストを増大することになり好ましくない。 The coating amount of the inorganic silicon compound 7 supporting the polyamine compound is preferably 0.2 to 10.0 g / m 2 (dry weight) on the pile yarn 2 and / or the backing layer 5. Less than 0.2 g / m 2 is not preferable because sufficient aldehyde removal performance cannot be obtained. Moreover, even if it exceeds 10.0 g / m < 2 >, the removal performance of aldehydes will not be improved, and the cost will increase undesirably.
また、バッキング層5の下側に、バッキング層の保護や、さらなるクッション性、防音性の付与を目的に、織布や不織布からなる2nd基布6を貼着させてもよい。形態としては、テープヤーン等からなる織基布や、スパンボント不織布、ニードルパンチ不織布、ウォターパンチ不織布等を挙げられる。前記2nd基布6の素材としては、どのような素材のものでもよく、例えば、ポリエステル系繊維、ポリアミド系繊維、ポリオレフィン系繊維等の熱可塑性繊維、またこれら各繊維の複合化繊維、アセテート等の半合成繊維、レーヨン等の再生繊維、麻、綿等の天然繊維、あるいはこれらの混綿したものが挙げられ、またこれら各種繊維のリサイクル品であっても使用することができる。 In addition, a 2nd base fabric 6 made of a woven fabric or a non-woven fabric may be attached to the lower side of the backing layer 5 for the purpose of protecting the backing layer and providing further cushioning properties and soundproofing properties. Examples of the form include a woven base fabric made of tape yarn and the like, a spunbond nonwoven fabric, a needle punched nonwoven fabric, and a water punch nonwoven fabric. The material of the 2nd base fabric 6 may be any material, for example, thermoplastic fibers such as polyester fibers, polyamide fibers and polyolefin fibers, and composite fibers of these fibers, acetates and the like. Examples thereof include semi-synthetic fibers, regenerated fibers such as rayon, natural fibers such as hemp and cotton, and mixed cottons of these, and even recycled products of these various fibers can be used.
<実施例1>
この発明の一実施例として、カーペットの使用材料、加工方法、試験評価方法を列記する。
<使用材料および加工方法>
基布・・・ポリエステルのスパンボンド不織布(通常の1st基布 目付110g/m2 見かけ厚みが0.3mm)
パイル糸・・・2600デシテックスの原着ポリエステル糸。
タフティング機・・・1/8カット機
タフト規格・・・30ステッチ/10cm パイル長8ミリ パイル目付け780g/m2
バッキング層・・・SBRラテックスをローラーコーティングし、120℃の条件下で10分間乾燥した。(塗布量260g/m2乾燥重量)
2nd基布・・・ポリエステル再生繊維のニードルパンチ不織布(目付410g/m2 見かけ厚みが8mm)
消臭加工・・・ジエチレントリアミンを担持した平均粒径10μmの二酸化ケイ素(東亞合成株式会社製NS231)20質量部を80質量部の水に加えた後、攪拌機により攪拌を行ない、分散液を得た。この分散液にさらに10質量部のアクリルシリコン系バインダー樹脂(固形分25%)を加え、良く攪拌して均一な処理液を得た。次に、バッキング層を塗布する前に、パイル糸にこの処理液を10g/m2塗布しバッキング層の乾燥と同時に乾燥し、ジエチレントリアミンを担持した二酸化ケイ素を1.8g/m2(乾燥重量)担持した。
<Example 1>
As an embodiment of the present invention, materials used for carpets, processing methods, and test evaluation methods are listed.
<Materials used and processing methods>
Base fabric: polyester spunbonded nonwoven fabric (ordinary 1st base fabric, basis weight 110 g / m 2 and apparent thickness 0.3 mm)
Pile yarn: 2600 decitex original polyester yarn.
Tufting machine ... 1/8 cut machine
Tuft Standard: 30 stitches / 10 cm, pile length 8 mm, pile weight 780 g / m 2
Backing layer: SBR latex was roller-coated and dried at 120 ° C. for 10 minutes. (Application amount 260 g / m 2 dry weight)
2nd base fabric: Needle-punched non-woven fabric of polyester recycled fiber (410 g / m 2 per unit weight, apparent thickness 8 mm)
Deodorization processing: 20 parts by mass of silicon dioxide having an average particle diameter of 10 μm carrying NS, which was supported by diethylenetriamine, was added to 80 parts by mass of water, and then stirred with a stirrer to obtain a dispersion. . 10 parts by mass of an acrylic silicon binder resin (solid content 25%) was further added to this dispersion, and the mixture was stirred well to obtain a uniform treatment liquid. Next, before applying the backing layer, 10 g / m 2 of this treatment solution was applied to the pile yarn and dried simultaneously with the drying of the backing layer, and 1.8 g / m 2 (dry weight) of silicon dioxide carrying diethylenetriamine. Supported.
<試験評価方法>
内容量10Lの袋内に、10cm角に裁断した試料片を入れ、窒素ガスを一定量封入後60〜65℃で二時間加熱した後、捕集管に前記袋内のガスを採取し、高速液体クロマトグラフィーにて定量分析して、アルデヒド類の放散量を測定した。ホルムアルデヒトの放散量は0.5μg/unit以下を、アセトアルデヒトの放散量は0.5μg/unit以下を合格とした。実施例1でのホルムアルデヒトの放散量は0.10μg/unit、アセトアルデヒトの放散量は0.15μg/unitで合格であった。
<Test evaluation method>
A sample piece cut into a 10 cm square is placed in a 10 L inner bag, and after a certain amount of nitrogen gas is sealed and heated at 60-65 ° C. for 2 hours, the gas in the bag is collected in a collecting tube, Quantitative analysis was performed by liquid chromatography to measure the amount of aldehydes emitted. The amount of formaldehyde released was 0.5 μg / unit or less, and the amount of acetaldehyde was 0.5 μg / unit or less. In Example 1, the emission of formaldehyde was 0.10 μg / unit, and the emission of acetaldehyde was 0.15 μg / unit.
<実施例2>
実施例1において、ジエチレントリアミンを担持した二酸化ケイ素の平均粒径を20nmとした以外は実施例1と同様にしてカーペットを得た。ホルムアルデヒトの放散量は検出限界以下、アセトアルデヒトの放散量は0.05μg/unitで合格であった。
<Example 2>
A carpet was obtained in the same manner as in Example 1 except that the average particle size of silicon dioxide carrying diethylenetriamine was 20 nm. The amount of formaldehyde released was below the detection limit, and the amount of acetonitrile released was 0.05 μg / unit.
<実施例3>
実施例1において、ジエチレントリアミンを担持した平均粒径10μmの二酸化ケイ素を、パイル糸に0.2g/m2バッキング層に0.1g/m2(乾燥重量)担持した以外は実施例1と同様にしてカーペットを得た。ホルムアルデヒトの放散量は0.28μg/unit、アセトアルデヒトの放散量は0.34μg/unitで合格であった。
<Example 3>
In Example 1, silicon dioxide having an average particle diameter of 10 μm carrying diethylenetriamine was carried out in the same manner as in Example 1 except that 0.2 g / m 2 was supported on the pile yarn by 0.1 g / m 2 (dry weight). And got a carpet. The amount of formaldehyde released was 0.28 μg / unit, and the amount of acetoaldehyde released was 0.34 μg / unit.
<実施例4>
実施例1において、パイル糸にジエチレントリアミンを担持した二酸化ケイ素を8g/m2(乾燥重量)担持した以外は実施例1と同様にしてカーペットを得た。ホルムアルデヒトの放散量は検出限界以下、アセトアルデヒトの放散量は0.09μg/unitで合格であった。
<Example 4>
A carpet was obtained in the same manner as in Example 1 except that 8 g / m 2 (dry weight) of silicon dioxide carrying diethylenetriamine was carried on the pile yarn. The amount of formaldehyde released was below the detection limit, and the amount of acetonitrile released was 0.09 μg / unit.
<実施例5>
実施例1において、パイル糸にジエチレントリアミンを担持した二酸化ケイ素を担持しないで、バッキング層に1.8g/m2(乾燥重量)担持した以外は実施例1と同様にしてカーペットを得た。ホルムアルデヒトの放散量は0.12μg/unit、アセトアルデヒトの放散量は0.22μg/unitで合格であった。
<Example 5>
A carpet was obtained in the same manner as in Example 1 except that in the pile yarn, silicon dioxide carrying diethylenetriamine was not carried on the pile yarn, but 1.8 g / m 2 (dry weight) was carried on the backing layer. The amount of formaldehyde released was 0.12 μg / unit, and the amount of acetonitrile released was 0.22 μg / unit.
<実施例6>
実施例1において、ジエチレントリアミンを担持した二酸化ケイ素をパイル糸に4g/m2、バッキング層に4g/m2(乾燥重量)担持した以外は実施例1と同様にしてカーペットを得た。ホルムアルデヒトの放散量は検出限界以下、アセトアルデヒトの放散量は0.02μg/unitで合格であった。
<Example 6>
A carpet was obtained in the same manner as in Example 1 except that silicon dioxide supporting diethylenetriamine was supported on the pile yarn at 4 g / m 2 and the backing layer at 4 g / m 2 (dry weight). The amount of formaldehyde released was below the detection limit, and the amount of acetonitrile released was 0.02 μg / unit.
<実施例7>
実施例1において、ジエチレントリアミンを担持した二酸化ケイ素に替えてテトラエチレンペンタミンを担持した二酸化ケイ素とした以外は実施例1と同様にしてカーペットを得た。ホルムアルデヒトの放散量は0.11μg/unit、アセトアルデヒトの放散量は0.14μg/unitで合格であった。
<Example 7>
A carpet was obtained in the same manner as in Example 1 except that silicon dioxide carrying tetraethylenepentamine was used instead of silicon dioxide carrying diethylenetriamine. The amount of formaldehyde released was 0.11 μg / unit, and the amount of acetonitrile released was 0.14 μg / unit.
<比較例1>
実施例1において、パイル糸とバッキング層共にジエチレントリアミンを担持した二酸化ケイ素を担持しないようにした以外は実施例1と同様にしてカーペットを得た。ホルムアルデヒトの放散量は0.58μg/unit、アセトアルデヒトの放散量は0.69μg/unitで不合格であった。
<Comparative Example 1>
In Example 1, a carpet was obtained in the same manner as in Example 1 except that neither the pile yarn nor the backing layer supported silicon dioxide supporting diethylenetriamine. The amount of formaldehyde consumed was 0.58 μg / unit, and the amount of acetaldehyde was 0.69 μg / unit, which was unacceptable.
<比較例2>
実施例1において、ジエチレントリアミンを担持した二酸化ケイ素をパイル糸に6g/m2、バッキング層に6g/m2(乾燥重量)担持した以外は実施例1と同様にしてカーペットを得た。ホルムアルデヒトの放散量は検出限界以下、アセトアルデヒトの放散量は0.02μg/unitで合格であったが、担持量を増加しただけの効果が得られるものではなかった。
<Comparative example 2>
A carpet was obtained in the same manner as in Example 1 except that silicon dioxide supporting diethylenetriamine was supported on a pile yarn at 6 g / m 2 and the backing layer was supported at 6 g / m 2 (dry weight). The amount of formaldehyde released was below the detection limit and the amount of acetonitrile released was 0.02 μg / unit, which was acceptable. However, the effect of only increasing the loading was not obtained.
<比較例3>
実施例1において、ジエチレントリアミンを担持した二酸化ケイ素の平均粒径を120μmとした以外は実施例1と同様にしてカーペットを得たが、表面風合にざらつき感があり、好ましい商品とはならなかった。
<Comparative Example 3>
In Example 1, a carpet was obtained in the same manner as in Example 1 except that the average particle diameter of silicon dioxide carrying diethylenetriamine was 120 μm, but the surface texture was rough and did not become a preferred product. .
1・・・カ−ペット
2・・・パイル糸
3・・・基布
4・・・表皮層
5・・・バッキング層
6・・・2nd基布
7・・・ポリアミン化合物を担持した無機ケイ素化合物
DESCRIPTION OF SYMBOLS 1 ... Carpet 2 ... Pile thread 3 ... Base fabric 4 ... Skin layer 5 ... Backing layer 6 ... 2nd base fabric 7 ... Inorganic silicon compound which carry | supported polyamine compound
Claims (3)
An inorganic silicon compound carrying a polyamine compound is fixed to and / or backing to a pile yarn via a binder resin on a fabric whose PH value on the surface of the fabric is maintained at 6 to 8 before being mixed into the fixing and / or backing layer. A raised fabric characterized by being mixed in the layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006318606A JP5019426B2 (en) | 2006-11-27 | 2006-11-27 | Standing blanket with reduced aldehyde emission |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006318606A JP5019426B2 (en) | 2006-11-27 | 2006-11-27 | Standing blanket with reduced aldehyde emission |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2008132007A JP2008132007A (en) | 2008-06-12 |
JP5019426B2 true JP5019426B2 (en) | 2012-09-05 |
Family
ID=39557285
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006318606A Active JP5019426B2 (en) | 2006-11-27 | 2006-11-27 | Standing blanket with reduced aldehyde emission |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP5019426B2 (en) |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0928778A (en) * | 1995-07-14 | 1997-02-04 | Mitsubishi Rayon Co Ltd | Deodorant and deodorant fiber and its production |
JPH0967767A (en) * | 1995-08-29 | 1997-03-11 | Kanebo Ltd | Fiber product having deodorizing property |
JP3765147B2 (en) * | 1997-02-17 | 2006-04-12 | 東レ株式会社 | Deodorant molded product and method for producing the same |
JP3885326B2 (en) * | 1997-12-04 | 2007-02-21 | 東亞合成株式会社 | Deodorant fiber |
JP2000136481A (en) * | 1998-11-04 | 2000-05-16 | Toray Ind Inc | Fabric and bags |
JP2003052800A (en) * | 2001-08-21 | 2003-02-25 | Toagosei Co Ltd | Deodorant composition suitable for deodorization of sulfur-base malodor |
JP4395876B2 (en) * | 2002-12-27 | 2010-01-13 | 日本絨氈株式会社 | Tile carpet |
-
2006
- 2006-11-27 JP JP2006318606A patent/JP5019426B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
JP2008132007A (en) | 2008-06-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4917047B2 (en) | Deodorant fabric and method for producing the same | |
US6335075B1 (en) | Carpet having deodorant properties | |
JP2009285164A (en) | Deodorizing composition and deodorizing fabric with deodorizing composition | |
JP2008255507A (en) | Deodorant fabric | |
JP2014000292A (en) | Deodorant composition and deodorant fabric | |
JP4981441B2 (en) | Carpet and manufacturing method thereof | |
JP2008206802A (en) | Deodorant antibacterial carpet | |
JP5411516B2 (en) | Interior materials for vehicles | |
JP2009221621A (en) | Deodorant fabric and method for producing the same | |
JP5515692B2 (en) | Skin material | |
JP5019426B2 (en) | Standing blanket with reduced aldehyde emission | |
JP2006204603A (en) | Deodorant carpet | |
JP2013051993A (en) | Deodorizing composition and deodorizing cloth having the deodorizing composition adhering thereto | |
EP0962584A1 (en) | Fabric having deodorizing function and method of deodorizing fabric | |
JP2000354535A (en) | Deodorant carpet and its manufacture | |
JP2009153670A (en) | Deodorant sheet | |
JP2008054898A (en) | Antiallergenic carpet and its manufacturing method | |
JP2003310725A (en) | Method for preventing lowering of adsorption action of porous body, deodorizing sheet, product equipped therewith and manufacturing method for deodorizing sheet | |
JP2021098340A (en) | Skin material and method for producing the same, and interior material | |
JP2005198684A (en) | Deodorant carpet | |
JP2004208769A (en) | Tile carpet | |
JP2014042728A (en) | Method for manufacturing deodorant carpet, and deodorant carpet | |
EP4252903A1 (en) | Volatile organic compounds (voc) reducing patch for treating automotive parts | |
JP2009028207A (en) | Deodorant sheet and its production method, deodorant, and air filter | |
JP2000014520A (en) | Deodorant carpet |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20091120 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20120316 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20120512 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20120607 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20120607 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5019426 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20150622 Year of fee payment: 3 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |