JPH0534981B2 - - Google Patents
Info
- Publication number
- JPH0534981B2 JPH0534981B2 JP62161195A JP16119587A JPH0534981B2 JP H0534981 B2 JPH0534981 B2 JP H0534981B2 JP 62161195 A JP62161195 A JP 62161195A JP 16119587 A JP16119587 A JP 16119587A JP H0534981 B2 JPH0534981 B2 JP H0534981B2
- Authority
- JP
- Japan
- Prior art keywords
- deodorizing
- fibers
- copper
- nonwoven fabric
- component
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 230000001877 deodorizing effect Effects 0.000 claims description 40
- 239000004745 nonwoven fabric Substances 0.000 claims description 30
- 239000000463 material Substances 0.000 claims description 14
- 239000005749 Copper compound Substances 0.000 claims description 7
- 229910019142 PO4 Inorganic materials 0.000 claims description 7
- 230000002378 acidificating effect Effects 0.000 claims description 7
- 150000001880 copper compounds Chemical class 0.000 claims description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 6
- 239000010452 phosphate Substances 0.000 claims description 6
- 239000000835 fiber Substances 0.000 description 28
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 6
- 235000021317 phosphate Nutrition 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 5
- -1 inorganic acid salts Chemical class 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 229910000365 copper sulfate Inorganic materials 0.000 description 3
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 2
- QTMDXZNDVAMKGV-UHFFFAOYSA-L copper(ii) bromide Chemical compound [Cu+2].[Br-].[Br-] QTMDXZNDVAMKGV-UHFFFAOYSA-L 0.000 description 2
- HWDGVJUIHRPKFR-UHFFFAOYSA-I copper;trisodium;18-(2-carboxylatoethyl)-20-(carboxylatomethyl)-12-ethenyl-7-ethyl-3,8,13,17-tetramethyl-17,18-dihydroporphyrin-21,23-diide-2-carboxylate Chemical compound [Na+].[Na+].[Na+].[Cu+2].N1=C(C(CC([O-])=O)=C2C(C(C)C(C=C3C(=C(C=C)C(=C4)[N-]3)C)=N2)CCC([O-])=O)C(=C([O-])[O-])C(C)=C1C=C1C(CC)=C(C)C4=N1 HWDGVJUIHRPKFR-UHFFFAOYSA-I 0.000 description 2
- 238000004332 deodorization Methods 0.000 description 2
- 235000019820 disodium diphosphate Nutrition 0.000 description 2
- GYQBBRRVRKFJRG-UHFFFAOYSA-L disodium pyrophosphate Chemical compound [Na+].[Na+].OP([O-])(=O)OP(O)([O-])=O GYQBBRRVRKFJRG-UHFFFAOYSA-L 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 229940079841 sodium copper chlorophyllin Drugs 0.000 description 2
- 235000013758 sodium copper chlorophyllin Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical compound [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 description 1
- 229910021589 Copper(I) bromide Inorganic materials 0.000 description 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 1
- 229910021595 Copper(I) iodide Inorganic materials 0.000 description 1
- 229910021590 Copper(II) bromide Inorganic materials 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- RAOSIAYCXKBGFE-UHFFFAOYSA-K [Cu+3].[O-]P([O-])([O-])=O Chemical compound [Cu+3].[O-]P([O-])([O-])=O RAOSIAYCXKBGFE-UHFFFAOYSA-K 0.000 description 1
- NUSORQHHEXCNQC-UHFFFAOYSA-N [Cu].N1C(C=C2N=C(C=C3NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 Chemical compound [Cu].N1C(C=C2N=C(C=C3NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 NUSORQHHEXCNQC-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000019804 chlorophyll Nutrition 0.000 description 1
- 229930002875 chlorophyll Natural products 0.000 description 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229940116318 copper carbonate Drugs 0.000 description 1
- 229940108925 copper gluconate Drugs 0.000 description 1
- BWFPGXWASODCHM-UHFFFAOYSA-N copper monosulfide Chemical compound [Cu]=S BWFPGXWASODCHM-UHFFFAOYSA-N 0.000 description 1
- 229940120693 copper naphthenate Drugs 0.000 description 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 1
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 1
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 description 1
- NKNDPYCGAZPOFS-UHFFFAOYSA-M copper(i) bromide Chemical compound Br[Cu] NKNDPYCGAZPOFS-UHFFFAOYSA-M 0.000 description 1
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 description 1
- LSXDOTMGLUJQCM-UHFFFAOYSA-M copper(i) iodide Chemical compound I[Cu] LSXDOTMGLUJQCM-UHFFFAOYSA-M 0.000 description 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 1
- SVOAENZIOKPANY-CVBJKYQLSA-L copper;(z)-octadec-9-enoate Chemical compound [Cu+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O SVOAENZIOKPANY-CVBJKYQLSA-L 0.000 description 1
- WMYBXRITVYIFCO-UHFFFAOYSA-N copper;2-hydroxybutanedioic acid Chemical compound [Cu].OC(=O)C(O)CC(O)=O WMYBXRITVYIFCO-UHFFFAOYSA-N 0.000 description 1
- RLSHUBNQSDLPAG-UHFFFAOYSA-L copper;2-oxopentanedioate Chemical compound [Cu+2].[O-]C(=O)CCC(=O)C([O-])=O RLSHUBNQSDLPAG-UHFFFAOYSA-L 0.000 description 1
- FSQAIQPPCOCRAX-UHFFFAOYSA-L copper;2-oxopropanoate Chemical compound [Cu+2].CC(=O)C([O-])=O.CC(=O)C([O-])=O FSQAIQPPCOCRAX-UHFFFAOYSA-L 0.000 description 1
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
- FSHOIESIOHHWIA-UHFFFAOYSA-L copper;4-hydroxy-3,4-dioxobutanoate Chemical compound [Cu+2].OC(=O)C(=O)CC([O-])=O.OC(=O)C(=O)CC([O-])=O FSHOIESIOHHWIA-UHFFFAOYSA-L 0.000 description 1
- GEZOTWYUIKXWOA-UHFFFAOYSA-L copper;carbonate Chemical compound [Cu+2].[O-]C([O-])=O GEZOTWYUIKXWOA-UHFFFAOYSA-L 0.000 description 1
- YXKOWHMCBBEJPS-UHFFFAOYSA-L copper;oxaldehydate Chemical compound [Cu+2].[O-]C(=O)C=O.[O-]C(=O)C=O YXKOWHMCBBEJPS-UHFFFAOYSA-L 0.000 description 1
- UVVWIYVATLQAFM-UHFFFAOYSA-I copper;tripotassium;18-(2-carboxylatoethyl)-20-(carboxylatomethyl)-12-ethenyl-7-ethyl-3,13,17-trimethyl-8-(oxidomethylidene)-17,18-dihydroporphyrin-21-ide-2-carboxylate Chemical compound [K+].[K+].[K+].[Cu+2].C1=C([N-]2)C(C)=C(C([O-])=O)C2=C(CC([O-])=O)C(C(C2C)CCC([O-])=O)=NC2=CC(C(=C2C=C)C)=NC2=CC\2=NC1=C(CC)C/2=C\[O-] UVVWIYVATLQAFM-UHFFFAOYSA-I 0.000 description 1
- 229960003280 cupric chloride Drugs 0.000 description 1
- 235000019855 cupric citrate Nutrition 0.000 description 1
- 239000011641 cupric citrate Substances 0.000 description 1
- 229960004643 cupric oxide Drugs 0.000 description 1
- 229940045803 cuprous chloride Drugs 0.000 description 1
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 description 1
- 229940112669 cuprous oxide Drugs 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- PEVJCYPAFCUXEZ-UHFFFAOYSA-J dicopper;phosphonato phosphate Chemical compound [Cu+2].[Cu+2].[O-]P([O-])(=O)OP([O-])([O-])=O PEVJCYPAFCUXEZ-UHFFFAOYSA-J 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 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
- 239000000049 pigment Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006306 polyurethane fiber Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- STDMRMREKPZQFJ-UHFFFAOYSA-H tricopper;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Cu+2].[Cu+2].[Cu+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O STDMRMREKPZQFJ-UHFFFAOYSA-H 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Description
(産業上の利用分野)
本発明は脱臭材に関し、更に詳しくは、脱臭を
目的としたフイルター、マスク、おむつ、寝具の
シーツなどに好適な脱臭材に関する。
(従来の技術)
従来、脱臭材は、脱臭剤単体で液体あるいは粉
末の状態のまま、室内消臭剤として噴霧又は散布
して使用されることが多いが、また、各種基材に
含浸、担持するなど他の材料とを組合わせた形で
も使用される。
しかして、各種基材のなかでも、不織布は、各
種繊維及びバインダーよりなる多孔質の繊維集合
体であり、通気性、吸収性がよいことから、フイ
ルターや各種衛生材料に用いられているものであ
り、脱臭剤と組合わせて多彩な用途が期待できる
材料である。
このため、不織布と各種脱臭剤との組合せが検
討されており、例えば、特開昭62−33854号公報
には、金属フタロシアニンを担持させた繊維を用
いた消臭性不織布が開示されている。しかしなが
ら、この不織布の場合、脱臭性能を有する化合物
を繊維に導入するために長時間を要するため生産
性に問題があつたり、また、着色や脱臭効率の点
から、脱臭性能を有する化合物の導入量も最大20
%程度までに限られており、脱臭効果の大きさに
限界がある。
(発明が解決しようとする問題点)
本発明者らは前記問題点を解決すべく鋭意研究
を重ねた結果、酸性リン酸塩及び銅化合物よりな
る脱臭性成分を不織布に担持させることにより、
脱臭効率及び持続性に優れた脱臭材が簡便に製造
できることを見出し、この知見に基いて本発明を
完成するに至つた。
(問題点を改良するための手段)
かくして本発明によれば、不織布に(A)酸性リン
酸塩及び(B)銅化合物よりなる脱臭性成分を担持さ
せてなることを特徴とする脱臭材が提供される。
本発明において使用される(A)成分の酸性リン酸
塩は、酸性を有するリン酸塩をいい、具体例とし
ては、リン酸二水素塩、リン酸一水素塩、酸性ピ
ロリン酸塩、酸性メタリン酸塩などが挙げられ
る。かかる塩の種類としては、例えば、ナトリウ
ム、カリウム、カルシウム、アルミニウム、亜鉛
及びアンモニウム塩等が挙げられ、なかでも水溶
性の塩が好ましい。これらの酸性リン酸塩は、一
種類で、あるいは二種類以上を混合して、使用す
ることができる。
本発明に用いられる(B)成分の銅化合物は、無機
酸塩、有機酸塩、水酸化物、硫化物、錯体、酸化
物のいずれでもよく、その具体例として、例え
ば、硫酸銅、硝酸銅、塩化第一銅、塩化第二銅、
臭化第一銅、臭化第二銅、沃化第一銅、炭酸銅、
水酸化第二銅、硫化第二銅、シアン化銅、酢酸
銅、クエン酸第二銅、グルコン酸銅、リンゴ酸
銅、グリオキシル酸銅、2−ケトグルタル酸銅、
ピルビン酸銅、オキサロ酢酸銅、酸性リン酸銅、
ピロリン酸銅、銅クロロフイル、銅クロロフイリ
ンナトリウム、銅クロロフイリンカリウム、フタ
ロシアニン銅、銅ポルフイリン、酸化第一銅、酸
化第二銅、オレイン酸銅、ナフテン酸銅などが例
示される。これらの銅化合物の内、コストや入手
の容易性からは無機酸塩が、安全性の面からは錯
体が好ましい。
なお、本発明においては、上記銅化合物が酸性
リン酸銅である場合には、別途(A)成分を加えなく
とも、銅化合物と(A)成分を含んでいるものと理解
すべきである。
本発明における(A)成分と(B)成分との比は、目的
物の要求性能に応じ適宜選択しうるが、通常は(A)
成分100重量部に対し(B)成分が0.01〜200重量部、
好ましくは0.02〜50重量部、さらに好ましくは
0.05〜20重量部の範囲である。(B)成分の量が過度
に少ないと脱臭性能に劣る場合があり、逆に過度
に多いと毒性の面で好ましくない場合がある。
又、本発明の効果を損なわない範囲であれば、
他の消臭剤、脱臭剤、殺菌剤、防カビ剤、吸着剤
等と併用したり、顔料、着色剤、安定剤、酸化防
止剤等の各種添加剤を必要に応じ添加することが
できる。
本発明に用いられる不織布を構成する繊維の種
類は、特に制限されるものではなく、天然繊維、
再生繊維、合成繊維、半合成繊維のいずれでもよ
い。具体例としては、例えば木綿、麻、レーヨ
ン、パルプなどのセルロース系繊維、例えば羊
毛、絹などの蛋白質系繊維、ポリエステル系繊
維、ポリアミド系繊維、ポリアクリル系繊維、ポ
バール系繊維、ポリオレフイン系繊維、ポリウレ
タン系繊維、ポリ塩化ビニル系繊維などが挙げら
れる。またガラス繊維、金属繊維、炭素繊維、繊
維状活性炭、石綿繊維などの無機繊維であつても
よい。また、これらの繊維の繊維長、繊維径も限
定されない。これらの繊維は、一種類だけを用い
てもよく、また、二種類以上の組合せで使用して
もよい。
本発明に用いられる不織布は、乾式、湿式ある
いはその他の方法のいずれの製法で作られたもの
でもよく、目的に応じて適宜選択される。繊維の
目付量も、また、特に限定されない。
本発明における不織布に対する脱臭性成分の担
持量は、目的物の要求性能によつて適宜選択し得
るが、不織布を構成する繊維100重量部に対して
通常、0.5〜500重量部の範囲である。担持量が少
なすぎると脱臭性能に劣る場合があり、担持量が
過度に多いときは、不織布の風合を損ねることが
あり、また、経済的ではない。
脱臭性成分の不織布への担持方法は、特に限定
されるものではなく、予め脱臭性成分を担持させ
た繊維を、不織布を構成する繊維の少なくも一部
として用いて、不織布を作製する方法、できあが
つた不織布に脱臭性成分をスプレーあるいはデイ
ツピングなどにより担持させる方法、あるいは、
不織布作製時に用いるバインダーエマルジヨン等
の中に溶融ないし分散させて不織布作製と同時に
担持させる方法などがある。
また、本発明の(A)及び(B)脱臭性成分の担持の順
序は、いずれか一方を担持させたのち、他方を担
持させてもよく、また、両成分を同時に担持させ
てもよい。
また、脱臭性成分を担持させるときに、バイン
ダーを用いることは必ずしも必要ではないが、バ
インダーを用いることにより、脱臭性成分の担持
量を多くすることができる。バインダーの種類
は、特に限定されるものではないが、カルボキシ
ル基又はスルホン酸基を含有する重合体のラテツ
クスが好適である。
(発明の効果)
かくして本発明によれば、従来技術に比較して
脱臭性及び脱臭性能の持続性に優れた脱臭材を得
ることができる。この脱臭材は脱臭を目的とした
フイルター、マスク、おむつ、寝具のシーツなど
に用いる不織布として有用である。
(実施例)
以下に実施例を挙げて本発明をさらに具体的に
説明する。なお、参考例、実施例及び比較例中の
部および%は特に断りのないかぎり重量基準であ
る。
参考例 1
繊維径4.5デニールのビスコースレーヨン繊維
を、ウエツパーを用いて、目付量100g/m2のラ
ンダムウエツブにした。このウエツブに酸性ピロ
リン酸ナトリウム100部、硫酸銅1部、カルボキ
シル変性スチレンブタジエンラテツクス200部
(日本ゼオン株式会社製、LX415A、TS43%)及
び水より調製した固形分10%の水溶液をスプレー
したのち、乾燥することを繰返して、第一表に示
す脱臭性成分担持量を有する不織布()〜
()を得た。
参考例 2
繊維径2.5デニールのポリエステル繊維からな
るスパンボンド型不織布(目付量:50g/m2)
を、酸性ピロリン酸ナトリウム100部、硫酸銅1
部、他の脱臭剤としてのスチレン−無水マレイン
酸共重合体(アーコケミカルカンパニー製、
SMA1000A)50部、カルボキシル変性スチレン
ブタジエンラテツクス(日本ゼオン株式会社製、
LX415A、TS43%)300部及び水より調製した固
形分10%の水溶液に含浸させた。所望の目付量に
なるように過剰の水溶液を絞りロールで除去した
のち、乾燥して脱臭性成分50g/m2を含有する不
織布()を得た。
参考例 3
硫酸銅1部及びスチレン−無水マレイン酸共重
合体50部に代えて、銅クロロフイリンナトリウム
5部及び粉末状活性炭10部を用いる他は参考例2
と同様にして脱臭性成分50g/m2を含有する不織
布()を得た。
参考例 4
特開昭62−33854の実施例2の方法に従つて、
約7重量%の鉄フタロシアニンテトラカルボン酸
が担持されたナイロン不織布()を得た。
実施例 1
参考例1〜4で得られた不織布()〜()
1gを、アンモニア0.7mgを含む空気で充たされ
た100ml三角フラスコに入れて密栓したのち、1
時間後に、ガスクロマトグラフイーにより気相部
分のアンモニア濃度を測定して、脱臭率を算出し
た。結果を第一表(1回目の欄)に示す。
実施例 2
アンモニア脱臭性能の持続性を調べるため、実
施例1で用いた不織布について、実施例1の操作
を繰返した(2回目)。得られた不織布について
さらに同じ操作を繰返した(3回目)。この結果
を第一表に合せて示す。
(Field of Industrial Application) The present invention relates to a deodorizing material, and more particularly to a deodorizing material suitable for filters, masks, diapers, bedding sheets, etc. for the purpose of deodorizing. (Prior Art) Conventionally, deodorizing materials have often been used as indoor deodorizers by spraying or scattering them in a liquid or powder state, but they have also been used by impregnating or supporting various substrates. It is also used in combination with other materials such as Among various base materials, nonwoven fabrics are porous fiber aggregates made of various fibers and binders, and are used in filters and various sanitary materials because of their good breathability and absorbency. It is a material that can be expected to have a variety of uses when combined with deodorizers. For this reason, combinations of nonwoven fabrics and various deodorizing agents have been studied. For example, Japanese Patent Application Laid-Open No. 62-33854 discloses a deodorizing nonwoven fabric using fibers carrying metal phthalocyanine. However, in the case of this nonwoven fabric, it takes a long time to introduce the compound with deodorizing performance into the fibers, which causes problems in productivity. also up to 20
%, and there is a limit to the magnitude of the deodorizing effect. (Problems to be Solved by the Invention) As a result of intensive research by the present inventors to solve the above-mentioned problems, the present inventors found that by supporting a deodorizing component consisting of acidic phosphate and a copper compound on a nonwoven fabric,
It was discovered that a deodorizing material with excellent deodorizing efficiency and durability can be easily produced, and based on this knowledge, the present invention was completed. (Means for Improving the Problems) Thus, according to the present invention, there is provided a deodorizing material comprising a nonwoven fabric supporting a deodorizing component consisting of (A) an acidic phosphate and (B) a copper compound. provided. The acidic phosphate as component (A) used in the present invention refers to a phosphate having acidity, and specific examples thereof include dihydrogen phosphate, monohydrogen phosphate, acid pyrophosphate, and acidic metal phosphate. Examples include acid salts. Examples of such salts include sodium, potassium, calcium, aluminum, zinc, and ammonium salts, and among these, water-soluble salts are preferred. These acidic phosphates can be used alone or in combination of two or more. The copper compound as component (B) used in the present invention may be any of inorganic acid salts, organic acid salts, hydroxides, sulfides, complexes, and oxides, and specific examples include copper sulfate, copper nitrate, etc. , cuprous chloride, cupric chloride,
Cuprous bromide, cupric bromide, cuprous iodide, copper carbonate,
Cupric hydroxide, cupric sulfide, copper cyanide, copper acetate, cupric citrate, copper gluconate, copper malate, copper glyoxylate, copper 2-ketoglutarate,
Copper pyruvate, copper oxaloacetate, copper acid phosphate,
Examples include copper pyrophosphate, copper chlorophyll, sodium copper chlorophyllin, potassium copper chlorophyllin, copper phthalocyanine, copper porphyrin, cuprous oxide, cupric oxide, copper oleate, and copper naphthenate. Among these copper compounds, inorganic acid salts are preferred from the viewpoint of cost and availability, and complexes are preferred from the viewpoint of safety. In addition, in the present invention, when the copper compound is acidic copper phosphate, it should be understood that the copper compound and component (A) are included even if component (A) is not separately added. The ratio of component (A) to component (B) in the present invention can be appropriately selected depending on the required performance of the target product, but usually (A)
Component (B) is 0.01 to 200 parts by weight per 100 parts by weight,
Preferably 0.02 to 50 parts by weight, more preferably
It ranges from 0.05 to 20 parts by weight. If the amount of component (B) is too small, the deodorizing performance may be poor, whereas if it is too large, it may be unfavorable in terms of toxicity. In addition, as long as it does not impair the effects of the present invention,
It can be used in combination with other deodorizers, deodorants, bactericides, fungicides, adsorbents, etc., and various additives such as pigments, colorants, stabilizers, antioxidants, etc. can be added as necessary. The type of fibers constituting the nonwoven fabric used in the present invention is not particularly limited, and includes natural fibers,
Any of recycled fibers, synthetic fibers, and semi-synthetic fibers may be used. Specific examples include cellulose fibers such as cotton, hemp, rayon, and pulp, protein fibers such as wool and silk, polyester fibers, polyamide fibers, polyacrylic fibers, poval fibers, polyolefin fibers, Examples include polyurethane fibers and polyvinyl chloride fibers. Inorganic fibers such as glass fibers, metal fibers, carbon fibers, fibrous activated carbon, and asbestos fibers may also be used. Furthermore, the fiber length and fiber diameter of these fibers are not limited. These fibers may be used alone or in combination of two or more types. The nonwoven fabric used in the present invention may be produced by any of dry, wet, or other methods, and is appropriately selected depending on the purpose. The basis weight of the fibers is also not particularly limited. The amount of the deodorizing component supported on the nonwoven fabric in the present invention can be appropriately selected depending on the required performance of the object, but is usually in the range of 0.5 to 500 parts by weight based on 100 parts by weight of the fibers constituting the nonwoven fabric. If the supported amount is too small, the deodorizing performance may be poor, and if the supported amount is too large, the texture of the nonwoven fabric may be impaired and it is not economical. The method of supporting the deodorizing component on the nonwoven fabric is not particularly limited, and includes a method of producing a nonwoven fabric using fibers that have previously supported the deodorizing component as at least some of the fibers constituting the nonwoven fabric; A method of supporting a deodorizing component on the finished nonwoven fabric by spraying or dipping, or
There is a method of melting or dispersing it in a binder emulsion or the like used when producing a nonwoven fabric and supporting it simultaneously with the production of the nonwoven fabric. Further, the order of supporting the deodorizing components (A) and (B) of the present invention may be such that either one is supported and then the other is supported, or both components may be supported simultaneously. Further, when supporting the deodorizing component, it is not necessarily necessary to use a binder, but by using a binder, the amount of the deodorizing component supported can be increased. The type of binder is not particularly limited, but a polymer latex containing a carboxyl group or a sulfonic acid group is suitable. (Effects of the Invention) Thus, according to the present invention, it is possible to obtain a deodorizing material that has superior deodorizing properties and durability of deodorizing performance compared to the prior art. This deodorizing material is useful as a nonwoven fabric for use in filters, masks, diapers, bedding sheets, etc. for the purpose of deodorizing. (Example) The present invention will be described in more detail with reference to Examples below. Note that parts and percentages in Reference Examples, Examples, and Comparative Examples are based on weight unless otherwise specified. Reference Example 1 Viscose rayon fibers with a fiber diameter of 4.5 denier were made into a random web with a basis weight of 100 g/m 2 using a wet cloth. After spraying an aqueous solution of 10% solid content prepared from 100 parts of sodium acid pyrophosphate, 1 part of copper sulfate, 200 parts of carboxyl-modified styrene-butadiene latex (manufactured by Nippon Zeon Co., Ltd., LX415A, TS 43%) and water on this web, , drying is repeated to obtain a nonwoven fabric () having the amount of deodorizing component supported as shown in Table 1.
I got (). Reference example 2 Spunbond nonwoven fabric made of polyester fibers with a fiber diameter of 2.5 denier (fabric weight: 50 g/m 2 )
, 100 parts of sodium acid pyrophosphate, 1 part of copper sulfate
Styrene-maleic anhydride copolymer (manufactured by Arco Chemical Company,
SMA1000A) 50 parts, carboxyl-modified styrene-butadiene latex (manufactured by Nippon Zeon Co., Ltd.,
It was impregnated with an aqueous solution with a solid content of 10% prepared from 300 parts of LX415A, TS43%) and water. After removing the excess aqueous solution with a squeezing roll so as to obtain a desired basis weight, it was dried to obtain a nonwoven fabric containing 50 g/m 2 of a deodorizing component. Reference Example 3 Reference Example 2 except that 5 parts of sodium copper chlorophyllin and 10 parts of powdered activated carbon were used instead of 1 part of copper sulfate and 50 parts of styrene-maleic anhydride copolymer.
A nonwoven fabric containing 50 g/m 2 of deodorizing components was obtained in the same manner as above. Reference Example 4 According to the method of Example 2 of JP-A No. 62-33854,
A nylon nonwoven fabric (2) was obtained in which approximately 7% by weight of iron phthalocyanine tetracarboxylic acid was supported. Example 1 Nonwoven fabrics () to () obtained in Reference Examples 1 to 4
After putting 1 g into a 100 ml Erlenmeyer flask filled with air containing 0.7 mg of ammonia and sealing it,
After a period of time, the ammonia concentration in the gas phase was measured by gas chromatography, and the deodorization rate was calculated. The results are shown in Table 1 (first column). Example 2 In order to examine the sustainability of ammonia deodorizing performance, the operation of Example 1 was repeated for the nonwoven fabric used in Example 1 (second time). The same operation was repeated for the obtained nonwoven fabric (third time). The results are also shown in Table 1.
【表】
第一表より本発明の脱臭材が、アンモニアの脱
臭性及び脱臭性能の持続性に優れていることが分
る。
実施例 3
参考例1〜4で得られた不織布()〜()
各1gを、メチルメルカプタン0.02mgを含む空気
で充たされた100ml三角フラスコに入れて密栓し
たのち、1時間後に、ガスクロマトグラフイーに
より気相部分のメチルメルカプタン濃度を測定し
て、脱臭率を算出した。結果を第二表(1回目の
欄)に示す。
実施例 4
メチルメルカプタン脱臭性能の持続性を調べる
ため、実施例3で用いた不織布について、実施例
3の操作を繰返した(2回目)。得られた不織布
についてさらに同じ操作を繰返した(3回目)。
この結果を第二表に合せて示す。[Table] From Table 1, it can be seen that the deodorizing material of the present invention is excellent in ammonia deodorizing ability and sustainability of deodorizing performance. Example 3 Nonwoven fabrics () to () obtained in Reference Examples 1 to 4
After putting 1 g of each into a 100 ml Erlenmeyer flask filled with air containing 0.02 mg of methyl mercaptan and sealing it, the methyl mercaptan concentration in the gas phase was measured by gas chromatography after 1 hour, and the deodorization rate was calculated. did. The results are shown in Table 2 (first column). Example 4 In order to examine the sustainability of methyl mercaptan deodorizing performance, the operation of Example 3 was repeated (second time) using the nonwoven fabric used in Example 3. The same operation was repeated for the obtained nonwoven fabric (third time).
The results are also shown in Table 2.
【表】【table】
【表】
第二表より本発明の脱臭材が、メチルメルカプ
タンの脱臭性及び脱臭性能の持続性に優れている
ことが分る。Table 2 shows that the deodorizing material of the present invention is excellent in deodorizing properties of methyl mercaptan and in maintaining deodorizing performance.
Claims (1)
なる脱臭性成分を担持させてなることを特徴とす
る脱臭材。1. A deodorizing material comprising a nonwoven fabric carrying a deodorizing component consisting of (A) an acidic phosphate and (B) a copper compound.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62161195A JPS645551A (en) | 1987-06-30 | 1987-06-30 | Deodorizing material |
| US07/118,884 US4906462A (en) | 1986-11-14 | 1987-11-10 | Deodorant composition and deodorant composite material |
| US07/397,512 US4983441A (en) | 1986-11-14 | 1989-08-23 | Deodorant composition and deodorant composite material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62161195A JPS645551A (en) | 1987-06-30 | 1987-06-30 | Deodorizing material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS645551A JPS645551A (en) | 1989-01-10 |
| JPH0534981B2 true JPH0534981B2 (en) | 1993-05-25 |
Family
ID=15730391
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62161195A Granted JPS645551A (en) | 1986-11-14 | 1987-06-30 | Deodorizing material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS645551A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006526423A (en) * | 2003-06-06 | 2006-11-24 | ボルダック・ルルー・インコーポレイテッド | Sterilization air filter |
| US7422577B2 (en) * | 2003-06-27 | 2008-09-09 | Hollister Incorporated | Lubricating deodorant for ostomy pouches |
| JP5412055B2 (en) * | 2008-05-15 | 2014-02-12 | 安積濾紙株式会社 | Method for producing aqueous copper phosphate solution and method for producing deodorizing material |
-
1987
- 1987-06-30 JP JP62161195A patent/JPS645551A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS645551A (en) | 1989-01-10 |
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