JPH01238866A - Deodorizer - Google Patents
DeodorizerInfo
- Publication number
- JPH01238866A JPH01238866A JP63066995A JP6699588A JPH01238866A JP H01238866 A JPH01238866 A JP H01238866A JP 63066995 A JP63066995 A JP 63066995A JP 6699588 A JP6699588 A JP 6699588A JP H01238866 A JPH01238866 A JP H01238866A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- ferrous
- basic compound
- compound
- salt
- 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.)
- Pending
Links
- 230000001877 deodorizing effect Effects 0.000 claims abstract description 43
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000000203 mixture Substances 0.000 claims abstract description 22
- 150000007514 bases Chemical class 0.000 claims abstract description 19
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 claims abstract description 18
- 235000015165 citric acid Nutrition 0.000 claims abstract description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 11
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims abstract description 8
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000011975 tartaric acid Substances 0.000 claims abstract description 8
- 235000002906 tartaric acid Nutrition 0.000 claims abstract description 8
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 7
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims abstract description 7
- 239000011976 maleic acid Substances 0.000 claims abstract description 7
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims abstract description 7
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims abstract description 6
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims abstract description 6
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229960005070 ascorbic acid Drugs 0.000 claims abstract description 6
- 239000001630 malic acid Substances 0.000 claims abstract description 6
- 235000011090 malic acid Nutrition 0.000 claims abstract description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims abstract description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract 6
- 239000002211 L-ascorbic acid Substances 0.000 claims abstract 3
- 235000000069 L-ascorbic acid Nutrition 0.000 claims abstract 3
- 239000000463 material Substances 0.000 claims description 21
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 3
- 239000002781 deodorant agent Substances 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract description 26
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 abstract description 22
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 abstract description 16
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 abstract description 14
- 229910000037 hydrogen sulfide Inorganic materials 0.000 abstract description 14
- 229910021529 ammonia Inorganic materials 0.000 abstract description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 12
- 239000007789 gas Substances 0.000 abstract description 11
- 238000000034 method Methods 0.000 abstract description 10
- 239000011790 ferrous sulphate Substances 0.000 abstract description 8
- 235000003891 ferrous sulphate Nutrition 0.000 abstract description 8
- 229910000359 iron(II) sulfate Inorganic materials 0.000 abstract description 8
- 229910052742 iron Inorganic materials 0.000 abstract description 7
- -1 methylmerptan Chemical compound 0.000 abstract description 7
- 235000019645 odor Nutrition 0.000 abstract description 6
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract description 5
- 238000004332 deodorization Methods 0.000 abstract description 5
- 239000002253 acid Substances 0.000 abstract description 4
- 238000006243 chemical reaction Methods 0.000 abstract description 4
- 229910001448 ferrous ion Inorganic materials 0.000 abstract description 3
- 235000011007 phosphoric acid Nutrition 0.000 abstract description 3
- 150000003839 salts Chemical class 0.000 abstract description 3
- 230000003647 oxidation Effects 0.000 abstract description 2
- 238000007254 oxidation reaction Methods 0.000 abstract description 2
- IMBKASBLAKCLEM-UHFFFAOYSA-L ferrous ammonium sulfate (anhydrous) Chemical compound [NH4+].[NH4+].[Fe+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O IMBKASBLAKCLEM-UHFFFAOYSA-L 0.000 abstract 1
- 150000002505 iron Chemical class 0.000 abstract 1
- 238000012423 maintenance Methods 0.000 abstract 1
- 230000001629 suppression Effects 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 description 22
- 230000000052 comparative effect Effects 0.000 description 13
- 239000004745 nonwoven fabric Substances 0.000 description 11
- 230000000694 effects Effects 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 229920005830 Polyurethane Foam Polymers 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- IDCBOTIENDVCBQ-UHFFFAOYSA-N TEPP Chemical compound CCOP(=O)(OCC)OP(=O)(OCC)OCC IDCBOTIENDVCBQ-UHFFFAOYSA-N 0.000 description 6
- 239000011496 polyurethane foam Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 5
- 230000007774 longterm Effects 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 3
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 3
- 235000011130 ammonium sulphate Nutrition 0.000 description 3
- 239000011668 ascorbic acid Substances 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000012229 microporous material Substances 0.000 description 2
- 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 2
- 239000011148 porous material Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 235000010265 sodium sulphite Nutrition 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 229960002089 ferrous chloride Drugs 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 150000008040 ionic compounds Chemical class 0.000 description 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 1
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 1
- 239000010871 livestock manure Substances 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、消臭材に関するものであり、さらに詳しくは
、四人悪臭成分であるアンモニア、トリメチルアミン、
メチルメルカプタン、硫化水素などに対して、優れた消
臭効果を示す消臭材に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a deodorizing material, and more specifically, the present invention relates to a deodorizing material that contains four malodorous components such as ammonia, trimethylamine,
This invention relates to a deodorizing material that exhibits excellent deodorizing effects against methyl mercaptan, hydrogen sulfide, and the like.
[従来の技術]
従来、悪臭ガスの除去法としては、香料でマスキングす
る感覚的脱臭法、クエン酸、マレイン酸などを主成分と
した物質と化学的に反応させ除去する化学的脱臭法、活
性炭、ゼオライトなどの微多孔物質による物理的脱臭法
などが知られている。[Prior art] Conventional methods for removing malodorous gases include a sensory deodorization method that masks the gas with fragrance, a chemical deodorization method that removes it by chemically reacting with a substance whose main ingredients are citric acid, maleic acid, etc., and activated carbon. , physical deodorization methods using microporous materials such as zeolite are known.
しかしながら、これらの方法においては、十分な脱臭効
果が得られないのが現状である。たとえば、香料でマス
キングする方法は本質的な除去でないため、刺激の強い
臭気に対しては効果はない。However, the current situation is that these methods do not provide a sufficient deodorizing effect. For example, masking methods with fragrances do not essentially remove odors, so they are not effective against strong odors.
クエン酸、マレイン酸などを主成分とした物質による方
法は、除去できる悪臭成分がアンモニア、アミン類など
に限られている。また、活性炭、ゼオライトなどの微多
孔物質による方法は、多種ガスに対して比較的有効であ
るが、吸着容量が限られており、またアンモニアに対し
ては効果がほとんど見られないという欠点がある。Methods using substances mainly composed of citric acid, maleic acid, etc. can only remove malodorous components such as ammonia and amines. In addition, methods using microporous materials such as activated carbon and zeolite are relatively effective for a variety of gases, but have the disadvantage of limited adsorption capacity and little effect on ammonia. .
一方、特公昭61−113091号公報に提案されてい
る硫酸第一鉄と、[−アスコルビン酸化合物による脱臭
方法は、アンモニア、トリメチルアミンに対しては、効
果が認められるが、メチルメルカプタン、硫化水素など
の含イオウ化合物に対しては、効果が不十分であり、ま
た空気中に長期間放置すると脱臭能力が低下するという
問題がある。On the other hand, the deodorizing method using ferrous sulfate and [-ascorbic acid compound proposed in Japanese Patent Publication No. 61-113091 is effective against ammonia and trimethylamine, but it is effective against methyl mercaptan, hydrogen sulfide, etc. There is a problem that the effect is insufficient for sulfur-containing compounds, and the deodorizing ability decreases when left in the air for a long period of time.
また、特開昭61−258078号公報に提案されてい
る金属フタロシアニンによる脱臭方法は、効果の長期持
続性に優れているが、基材に担持させにくいという問題
があった。Further, the deodorizing method using metal phthalocyanine proposed in JP-A No. 61-258078 has excellent long-term sustainability of the effect, but has the problem that it is difficult to support the metal phthalocyanine on the base material.
本発明者らは、これらの問題点を改善した消臭材を先に
出願したが、それなりの改善効果は認められるものの、
なお十分満足すべき状態に至っていない。The present inventors have previously applied for a deodorizing material that has improved these problems, but although some improvement effects have been recognized,
However, the situation has not yet reached a fully satisfactory state.
[発明が解決しようとしている課題]
、 本発明は、上述した従来技術の欠点を改良し、ア
ンモニア、硫化水素、メチルメルブタン、トリメチルア
ミンの四人悪臭成分などに対し、優れた消臭効果を有す
る消臭材を提供することを目的とするものである。[Problems to be Solved by the Invention] The present invention improves the drawbacks of the prior art described above, and has an excellent deodorizing effect against the four malodorous components of ammonia, hydrogen sulfide, methyl merbutane, and trimethylamine. The purpose is to provide a deodorizing material.
[課題を解決するための手段]
上記本発明の目的は、第一鉄塩と、クエン酸、酒石酸、
マレイン酸1.リンゴ酸、リン酸、[−アスコルビン酸
の中から選ばれた少なくとも一種の化合物からなる組成
物と塩基性化合物から構成される消臭材によって達成さ
れる。[Means for Solving the Problems] The object of the present invention is to combine ferrous salts, citric acid, tartaric acid,
Maleic acid 1. This is achieved by a deodorizing material composed of a basic compound and a composition composed of at least one compound selected from malic acid, phosphoric acid, and [-ascorbic acid.
以下、本発明の詳細な説明する。The present invention will be explained in detail below.
本発明で言う第一鉄塩とは、悪臭ガスと化学的に反応し
消臭する成分であり、その具体例としては、硫酸第一鉄
、@酸第−鉄アンモニウム、塩化第一鉄、硝酸第一鉄な
どを挙げることができる。The ferrous salt referred to in the present invention is a component that chemically reacts with malodorous gas to deodorize it, and specific examples thereof include ferrous sulfate, ferrous ammonium @acid, ferrous chloride, and nitric acid. Examples include first iron.
これらは、単独であっても、混合物であってもよい。第
一鉄塩は通常0.01〜1モル10水溶液として調整さ
れる。These may be used alone or in a mixture. The ferrous salt is usually prepared as a 0.01 to 1 molar aqueous solution.
また本発明で言うクエン酸、酒石酸、リンゴ酸、マレイ
ン酸、リン酸、[−アスコルビン酸は第一鉄イオンと化
学的反応により、鉄イオンの酸化抑制、活性状態維持に
有効に作用するとともに、中和反応によりそれ自体が悪
臭を消臭する成分でもある。In addition, the citric acid, tartaric acid, malic acid, maleic acid, phosphoric acid, and [-ascorbic acid referred to in the present invention act effectively to suppress the oxidation of iron ions and maintain the active state through chemical reactions with ferrous ions. It is also a component that eliminates bad odors through a neutralization reaction.
これらの化合物の中で、カルボキシル基を有する化合物
は、カルボキシル基の一部または全部がアで使用するこ
ともできる。該化合物は人体に無害であり、環境汚染す
ることなく、かつ工業的に安価な化合物であるという利
点がある。この中でも、特にクエン酸、酒石酸、マレイ
ン酸、リンゴ酸が消臭効果を発揮する。Among these compounds, compounds having a carboxyl group can also be used in which part or all of the carboxyl group is a. This compound has the advantage that it is harmless to the human body, does not pollute the environment, and is industrially inexpensive. Among these, citric acid, tartaric acid, maleic acid, and malic acid particularly exhibit deodorizing effects.
これらの化合物(A)は第一鉄塩(B)に対し、(A)
/(B)=0.003/1〜2/1(モル1モル)、好
ましくは0.01/1〜1.5/1(モル1モル)の範
囲が第一鉄イオンの長期安定化、消臭効果の長期持続の
点から好ましい。These compounds (A) differ from ferrous salt (B) in (A)
/(B)=0.003/1 to 2/1 (1 mole), preferably 0.01/1 to 1.5/1 (1 mole) for long-term stabilization of ferrous ions, It is preferable from the viewpoint of long-term deodorizing effect.
また、必要に応じて第三成分として硫酸塩およびまたは
亜硫酸塩を用いると効果はさらに発揮される。また消臭
効果の長期持続性、消臭原液付与成形品の白色度および
固着性などの点でも効果を助長する。これらの具体例と
しては、水溶性塩であればよく、特に限定されないが、
中でも硫酸アンモニウム、硫酸ナトリウム、亜硫酸アン
モニウム、亜硫酸ナトリウム、硫酸カリウムなどが挙げ
られる。硫酸塩、亜硫酸塩(C)は、第一鉄塩(B)に
対して、(C,)/ (B)=0.05/1〜10/1
(モル1モル)、好ましくは0.1/1〜5/1(モル
1モル)がよい。Further, if necessary, a sulfate and/or a sulfite may be used as a third component to further enhance the effect. It also enhances the deodorizing effect in terms of long-term sustainability, whiteness and adhesion of the molded product to which the deodorizing stock solution has been applied. Specific examples of these include water-soluble salts and are not particularly limited;
Among them, ammonium sulfate, sodium sulfate, ammonium sulfite, sodium sulfite, potassium sulfate, etc. can be mentioned. Sulfate and sulfite (C) are (C,)/(B)=0.05/1 to 10/1 relative to ferrous salt (B)
(1 mol), preferably 0.1/1 to 5/1 (1 mol).
一方、本発明で言う塩基性化合物は、メチルメルカプタ
ン、硫化水素などの含イオン化合物と第一鉄塩の反応を
促進させるものであり、またそれ自体が反応し消臭する
成分でもある。具体例としては、水溶液において、水酸
イオンを出す物質または水溶液が塩基性を有する物質す
なわち、弱酸と強塩基からなる塩が挙げられる。たとえ
ば、水酸化ナトリウム、水酸化カリウム、水酸化カルシ
ウム、水酸化アルミニウム、水酸化バリウム、炭酸ナト
リウム、炭酸水素ナトリウム、酢酸ナトリウムなどが挙
げられるが、特に限定されるものではない。On the other hand, the basic compound referred to in the present invention is one that promotes the reaction between an ionic compound such as methyl mercaptan or hydrogen sulfide and a ferrous salt, and is also a component that reacts itself to deodorize. Specific examples include a substance that releases hydroxyl ions in an aqueous solution or a substance whose aqueous solution has basicity, that is, a salt consisting of a weak acid and a strong base. Examples include, but are not limited to, sodium hydroxide, potassium hydroxide, calcium hydroxide, aluminum hydroxide, barium hydroxide, sodium carbonate, sodium hydrogen carbonate, and sodium acetate.
また、本発明でいう担持体としては、紙類、編織物類、
不織布類、人工多孔材、オガクズなどが挙げられる。中
でも特に人工多孔質が好ましい。In addition, the carrier mentioned in the present invention includes papers, knitted fabrics,
Examples include nonwoven fabrics, artificial porous materials, and sawdust. Among these, artificial porosity is particularly preferred.
人工多孔材としては、ポリスチレン、ポリウレタン、ポ
リエチレンなどからなる発泡シートがある。Examples of artificial porous materials include foam sheets made of polystyrene, polyurethane, polyethylene, and the like.
一方、前記組成物を担持体に付着させるに際しては、原
液そのまま、あるいは数倍〜数百倍に希釈して、含浸、
散布、噴霧方式などにより付着させるとよい。また、前
記組成物を蒸発乾固などにより粒状にし、コーティング
方式にて付着させてもよい。もちろん、担持体の片面あ
るいは両面の一部または全体に付着せしめてよい。なお
、担持体は、前記組成物のみから構成されていてもよい
。On the other hand, when attaching the composition to a carrier, the composition may be used as it is, or diluted several times to several hundred times, and then impregnated.
It is best to apply it by spreading, spraying, etc. Alternatively, the composition may be made into granules by evaporation to dryness or the like, and may be applied by a coating method. Of course, it may be attached to part or all of one or both sides of the carrier. Note that the carrier may be composed only of the above composition.
また、付着量としては、該担持体に対し、固型分として
0.1〜500重量%が好ましく、さらに好ましくは、
1〜200重量%がよい。0.1重量%未満では消臭効
果が不十分で、500重ω%を越えると、前記組成物の
保持面から好ましくない。In addition, the amount of adhesion is preferably 0.1 to 500% by weight as a solid content, more preferably,
It is preferably 1 to 200% by weight. If it is less than 0.1% by weight, the deodorizing effect is insufficient, and if it exceeds 500% by weight, it is not preferred from the viewpoint of retention of the composition.
また、塩基性化合物を担持体に付着させるに際しては、
通常、0.01〜30%水溶液にて含浸、散布、噴霧方
式などにより付着せしめるとよい。In addition, when attaching the basic compound to the carrier,
Usually, it is preferable to apply the adhesive by impregnating, spraying, spraying, etc. with a 0.01 to 30% aqueous solution.
粒状で用いる際には、コーティング方式にて付着せしめ
る。この場合も担持体は、塩基性化合物のみから構成さ
れていてもよい。When used in granular form, it is applied using a coating method. In this case as well, the carrier may be composed only of the basic compound.
本発明消臭材の好ましい態様は、前記組成物含有担持体
と塩基性化合物含有担持体が、積層または包含構造を有
するものである。積層構造の好ましい具体例としては、
(1)前記組成物含有のシート状担持体と塩基性化合物
含有のシート状担持体が積層状。In a preferred embodiment of the deodorizing material of the present invention, the composition-containing carrier and the basic compound-containing carrier have a laminated or inclusive structure. Preferred specific examples of the laminated structure include: (1) A sheet-like carrier containing the composition and a sheet-like carrier containing a basic compound are laminated.
(2)前記組成物含有のシート状担持体と塩基性化合物
が積層状。(2) A sheet-like carrier containing the composition and a basic compound are layered.
(3〉前記組成物と塩基性化合物のシート状担持体が積
層状。(3) The sheet-like carrier of the composition and the basic compound is laminated.
などの構造を有しているものを挙げることができるがこ
れに限定されるものではない。Examples include, but are not limited to, those having the following structure.
また包含構造の具体例としては、
(1)前記組成物含有のシート状担持体が、塩基性化合
物を包含している形態。Further, specific examples of the inclusion structure include: (1) A form in which the sheet-like carrier containing the composition includes a basic compound.
(2)塩基性化合物含有のシート状担持体が、前記組成
物を包含している形態。(2) A form in which the basic compound-containing sheet-like carrier contains the composition.
などの構造を有しているものを挙げることができる。Examples include those having the following structure.
上記のように、前記組成物と塩基性化合物を所定の態様
で用いることにより、両者の活性状態が十分に維持でき
、また相乗効果も出現し、多種悪臭ガスに対して優れた
消臭性能を示す。また、該消臭材は、フィルター類に特
に効果を発揮する。As mentioned above, by using the composition and the basic compound in a predetermined manner, the active state of both can be sufficiently maintained, and a synergistic effect also appears, resulting in excellent deodorizing performance against various malodorous gases. show. Moreover, the deodorizing material is particularly effective for filters.
以下、実施例を挙げて詳細に説明する。Hereinafter, it will be explained in detail by giving examples.
[実施例]
実施例1
硫酸第一鉄0.4モル/Q、クエン酸0.4モル/α、
硫酸アンモニウム0.5モル/Qになるように水溶液を
調整した。この水溶液にポリエチレンテレフタレートよ
りなる目付105C]/mのテトロン不織布を浸漬し、
100%絞りになるようにパッドし、110℃で5分間
乾燥した。不織布への付着量は20.4%であった。(
鉄分の付着量は2.2%である)。一方、水酸化ナトリ
ウム1.5%水溶液に上記と同一のテトロン不織布を浸
漬し、100%絞りになるようにパッドし、120℃で
5分間乾燥した。この両者処理品を積層状に重ね合わし
、周囲を融着した。[Example] Example 1 Ferrous sulfate 0.4 mol/Q, citric acid 0.4 mol/α,
The aqueous solution was adjusted so that the ammonium sulfate content was 0.5 mol/Q. A Tetron nonwoven fabric made of polyethylene terephthalate and having a basis weight of 105 C]/m is immersed in this aqueous solution,
It was padded so that it was 100% squeezed and dried at 110° C. for 5 minutes. The amount of adhesion to the nonwoven fabric was 20.4%. (
The adhesion amount of iron is 2.2%). On the other hand, the same Tetron nonwoven fabric as above was immersed in a 1.5% sodium hydroxide aqueous solution, padded so that it was 100% squeezed, and dried at 120° C. for 5 minutes. These two treated products were stacked on top of each other and the periphery was fused.
比較例A
硫酸第一鉄0.4モル/α、クエンvi0.4モル/、
11.硫酸ナトリウム0.5モル/rLになるように水
溶液を調整した。この水溶液に実施例1と同一のテトロ
ン不織布を浸漬し、100%絞りになるようにパッドし
、110℃で5分間乾燥した。Comparative example A ferrous sulfate 0.4 mol/α, citric acid vi 0.4 mol/,
11. The aqueous solution was adjusted to have a sodium sulfate content of 0.5 mol/rL. The same Tetron nonwoven fabric as in Example 1 was immersed in this aqueous solution, padded so that it was 100% squeezed, and dried at 110° C. for 5 minutes.
不織布への付着量は20.5%であった(鉄分の付着間
は2.2%である)。The amount of adhesion to the nonwoven fabric was 20.5% (the amount of iron adhesion was 2.2%).
比較例B
水酸化ナトリウム2.0%水溶液に実施例1と同一のテ
トロン不織布を浸漬し、100%絞りになるようにパッ
ドし、120℃で5分間乾燥した。Comparative Example B The same Tetron nonwoven fabric as in Example 1 was immersed in a 2.0% sodium hydroxide aqueous solution, padded to 100% reduction, and dried at 120° C. for 5 minutes.
このようにして得られた消臭材を目付41q/尻のテト
ロン不織イhで覆い、アンモニア、トリメチルアミン、
メチルメルカプタン、硫化水素に対する消臭効果を調べ
た。評価は次のように行った。The deodorizing material thus obtained was covered with Tetron non-woven material having a fabric weight of 41q/h, and ammonia, trimethylamine,
The deodorizing effect on methyl mercaptan and hydrogen sulfide was investigated. The evaluation was performed as follows.
各種悪臭成分を有する試薬を1%水溶液になるように調
整し、その水溶液1r11flを採取し、1000dの
三角フラスコに入れた。1時間放置俊、20cmの各消
臭材を三角フラスコ内に吊るし、10分後の残菌ガス濃
度をガス検知機にて測定した。Reagents containing various malodorous components were adjusted to a 1% aqueous solution, and 1r11fl of the aqueous solution was collected and placed in a 1000 d Erlenmeyer flask. After leaving it for 1 hour, each 20 cm of deodorizing material was suspended in an Erlenmeyer flask, and the residual bacteria gas concentration was measured with a gas detector after 10 minutes.
なお、硫化水素については、鶏糞を三角フラスコ内で醗
酵させ硫化水素の成分を同様に測定した。Regarding hydrogen sulfide, chicken manure was fermented in an Erlenmeyer flask and the hydrogen sulfide component was measured in the same manner.
得られた結果を表1に示す。The results obtained are shown in Table 1.
これからもわかるように、本実施例のものは、各種悪臭
成分すべてに対し、優れた消臭効果を有する。比較例A
のものは、−窓効果は認められるが、メチルメルカプタ
ン、硫化水素に対する消臭効果が不十分であり、また比
較例Bのものは、消臭効果が不十分であり、特にアンモ
ニア、トリメチルアミンに対しては効果は、はとんど見
られなかった。As can be seen from this, the product of this example has an excellent deodorizing effect against all of the various malodorous components. Comparative example A
- Although the window effect was observed, the deodorizing effect of Comparative Example B was insufficient against methyl mercaptan and hydrogen sulfide, and the deodorizing effect of Comparative Example B was insufficient, especially against ammonia and trimethylamine. However, the effect was rarely seen.
実施例2
硫酸第一鉄0.5モル10、酒石酸0.5モル/a、亜
硫酸アンモニウム0.5モル/Qになるように水溶液を
調整した。この水溶液に厚さ3trunよりなるポリウ
レタンフォームを浸漬し、300%絞りになるようにパ
ッドし、100℃で5分間乾燥した。ポリウレタンフォ
ームへの付着aは66.9%であった。(鉄分の付着量
は8,4%である)。一方、炭酸ナトリウム2.0%水
溶液に上記と同一のポリウレタンフォームを浸漬し、3
00%絞りになるようにパッドし、100℃で5分間乾
燥した。この両者処理品を積層状に重ね合わし、周囲を
融着した。Example 2 An aqueous solution was adjusted to contain 0.5 mol/Q of ferrous sulfate, 0.5 mol/a of tartaric acid, and 0.5 mol/Q of ammonium sulfite. A polyurethane foam having a thickness of 3 trun was immersed in this aqueous solution, padded to a 300% reduction, and dried at 100° C. for 5 minutes. Adhesion a to polyurethane foam was 66.9%. (The amount of iron deposited is 8.4%). On the other hand, the same polyurethane foam as above was immersed in a 2.0% sodium carbonate aqueous solution.
It was padded to a 00% reduction and dried at 100° C. for 5 minutes. These two treated products were stacked on top of each other and the periphery was fused.
比較例C,D
硫酸第一鉄0.5モル/Q、酒石酸0.5モル10、、
亜硫酸ナトリウム0.5モル/Qになるように水溶液を
調整し、この水溶液に実施例2と同一のポリウレタンフ
ォームを浸漬し、300%絞りになるようにパッドし、
100℃で5分間乾燥した。ポリウレタンフォームへの
付着口は66゜5%であった。(鉄分の付着量は8.4
%である)[比較例C]。また、炭酸ナトリウム5%水
溶液に実施例2と同一のポリウレタンフォームを浸漬し
、300%絞りになるようにパッドし、100℃で5分
間乾燥した[比較例D]。Comparative Examples C, D Ferrous sulfate 0.5 mol/Q, tartaric acid 0.5 mol 10,
An aqueous solution was adjusted to have a sodium sulfite concentration of 0.5 mol/Q, the same polyurethane foam as in Example 2 was immersed in this aqueous solution, and padded to a 300% reduction.
It was dried at 100°C for 5 minutes. Adhesion to polyurethane foam was 66.5%. (The amount of iron attached is 8.4
%) [Comparative Example C]. Further, the same polyurethane foam as in Example 2 was immersed in a 5% sodium carbonate aqueous solution, padded to a 300% aqueous solution, and dried at 100° C. for 5 minutes [Comparative Example D].
このようにして得られた消臭材を目付41g/麓のテト
ロン不織布で覆い、実施例1と同様に消臭効果を調べた
。得られた結果を表2に示す。The deodorizing material thus obtained was covered with a Tetron nonwoven fabric having a basis weight of 41 g/foot, and the deodorizing effect was examined in the same manner as in Example 1. The results obtained are shown in Table 2.
表2からもわかるように、本実施例のものは、すべての
悪臭ガスに対し、優れた消臭効果を有する。一方、比較
例Cのものは、アンモニア、トリメチルアミンに対して
は、優れた消臭効果を有するが、メチルメルカプタン、
硫化水素に対して、消臭効果が不十分で、比較例りのも
のは、アンモニア、トリメチルアミンに対して効果がほ
とんど見られなかった。As can be seen from Table 2, the sample of this example has an excellent deodorizing effect on all malodorous gases. On the other hand, Comparative Example C has an excellent deodorizing effect against ammonia and trimethylamine, but has an excellent deodorizing effect against methyl mercaptan and
The deodorizing effect was insufficient against hydrogen sulfide, and the comparative example showed almost no effect against ammonia and trimethylamine.
実施例3
硫酸第一鉄0.5モル/a、クエン酸0.5モル/α、
硫酸アンモニウム0.5モル/Qからなる水溶液を蒸発
乾固し、粒状物を得た。一方、ポリアミドよりなる目付
65C1/TItのナイロン不織布を水酸化カルシウム
1.0%水溶液に浸漬し、100%絞りになるようにパ
ッドし、100℃で5分間乾燥した。しかるのち、かか
るナイロン不織布を袋状に縫製し、その中にほぼ満杯に
なるように前記粒状物を入れた。Example 3 Ferrous sulfate 0.5 mol/a, citric acid 0.5 mol/α,
An aqueous solution containing 0.5 mol/Q of ammonium sulfate was evaporated to dryness to obtain granules. On the other hand, a nylon nonwoven fabric made of polyamide and having a basis weight of 65C1/TIt was immersed in a 1.0% calcium hydroxide aqueous solution, padded to a 100% aqueous solution, and dried at 100° C. for 5 minutes. Thereafter, the nylon nonwoven fabric was sewn into a bag, and the granules were placed in the bag until it was almost full.
一方、比較例として、ポリアミドよりなる目付65q/
TIlのナイロン不織布を袋状に縫製し、その中に実施
例3で得た粒状組成物をほぼ満杯になるように入れた(
比較例E)。On the other hand, as a comparative example, a fabric weight of 65q/
A nylon nonwoven fabric of TIl was sewn into a bag shape, and the granular composition obtained in Example 3 was placed in the bag until it was almost full (
Comparative Example E).
このようにして得られた包含形態の消臭材について、実
施例1と同様に消臭効果を調べた。The deodorizing effect of the thus obtained deodorizing material in the inclusion form was investigated in the same manner as in Example 1.
本実施例のものは、アンモニア、トリメチルアミン1.
エチルメルカプタン、硫化水素のすべての悪臭ガスに対
して、優れた消臭効果を示した。In this example, ammonia, trimethylamine 1.
It showed excellent deodorizing effects against all malodorous gases such as ethyl mercaptan and hydrogen sulfide.
一方、比較例Eのものは、アンモニア、トリメチルアミ
ンに対しては、優れた消臭効果を示したが、メチルメル
カプタン、硫化水素に対しては0、満足した効果が得ら
れなかった、。On the other hand, Comparative Example E showed an excellent deodorizing effect against ammonia and trimethylamine, but had no satisfactory effect against methyl mercaptan and hydrogen sulfide.
ただし、ili位はppmでめ金。However, the illi position is in ppm.
[発明の効果]
本発明の消臭材は、アンモニア、トリメチルアミン、メ
ヂルメル力ブタン、硫化水素などの四人悪臭成分を含む
数多くの悪臭ガスに対して、優れた消臭効果を発揮する
。また活性炭のような物理的吸着でなく、化学的に反応
し、消臭するため効果持続性に優れる。[Effects of the Invention] The deodorizing material of the present invention exhibits an excellent deodorizing effect against many malodorous gases containing four malodorous components such as ammonia, trimethylamine, methylbutane, and hydrogen sulfide. In addition, it has excellent long-lasting effects because it deodorizes by chemically reacting rather than physically adsorbing it like activated carbon.
さらに、本発明の消臭材は、トイレ、老人居室、病室な
どに適するが、特に空気清浄機、掃除殿などに用いられ
るフィルター類にとくに効果を特徴する
特許出願人 東し株式会社Further, the deodorizing material of the present invention is suitable for toilets, elderly living rooms, hospital rooms, etc., but is particularly effective for filters used in air purifiers, cleaning rooms, etc. Patent applicant Toshi Co., Ltd.
Claims (5)
ン酸、リン酸、L−アスコルビン酸の中から選ばれた少
なくとも一種の化合物から成る組成物と、塩基性化合物
から構成されることを特徴とする消臭材。(1) A composition consisting of a ferrous salt, at least one compound selected from citric acid, tartaric acid, malic acid, maleic acid, phosphoric acid, and L-ascorbic acid, and a basic compound. A deodorizing material featuring:
亜硫酸塩を含有する請求項(1)記載の消臭材。(2) The deodorant material according to claim (1), wherein the composition contains a sulfate and/or a sulfite as a third component.
、(2)記載の消臭材。(3) Claim (1) in which the composition is contained in a carrier.
, (2) The deodorant material described in (2).
1)記載の消臭材。(4) Claim in which the basic compound is contained in the carrier (
1) Deodorizing material described.
層または包含構造を有する請求項(1)〜(4)記載の
消臭材。(5) The deodorizing material according to any one of (1) to (4), wherein the composition-containing carrier and the basic compound-containing carrier have a laminated or inclusive structure.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63066995A JPH01238866A (en) | 1988-03-18 | 1988-03-18 | Deodorizer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63066995A JPH01238866A (en) | 1988-03-18 | 1988-03-18 | Deodorizer |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01238866A true JPH01238866A (en) | 1989-09-25 |
Family
ID=13332096
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63066995A Pending JPH01238866A (en) | 1988-03-18 | 1988-03-18 | Deodorizer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01238866A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007282797A (en) * | 2006-04-14 | 2007-11-01 | Kao Corp | Deodorant composition |
JP2007282799A (en) * | 2006-04-14 | 2007-11-01 | Kao Corp | Deodorant composition |
JP2007289221A (en) * | 2006-04-21 | 2007-11-08 | Kao Corp | Deodorant composition |
WO2010088064A3 (en) * | 2009-01-30 | 2010-12-02 | Elc Management Llc | Preservation of ergothioneine |
WO2011118749A1 (en) * | 2010-03-25 | 2011-09-29 | 東レ株式会社 | Deodorant fiber structure |
US8933245B2 (en) | 2009-01-30 | 2015-01-13 | Elc Management Llc | Preservation of ergothioneine |
-
1988
- 1988-03-18 JP JP63066995A patent/JPH01238866A/en active Pending
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007282797A (en) * | 2006-04-14 | 2007-11-01 | Kao Corp | Deodorant composition |
JP2007282799A (en) * | 2006-04-14 | 2007-11-01 | Kao Corp | Deodorant composition |
JP2007289221A (en) * | 2006-04-21 | 2007-11-08 | Kao Corp | Deodorant composition |
WO2010088064A3 (en) * | 2009-01-30 | 2010-12-02 | Elc Management Llc | Preservation of ergothioneine |
EP2391362A2 (en) * | 2009-01-30 | 2011-12-07 | ELC Management LLC | Preservation of ergothioneine |
US8410156B2 (en) | 2009-01-30 | 2013-04-02 | Elc Management, Llc | Preservation of ergothioneine |
US8933245B2 (en) | 2009-01-30 | 2015-01-13 | Elc Management Llc | Preservation of ergothioneine |
EP2391362A4 (en) * | 2009-01-30 | 2015-03-18 | Elc Man Llc | Preservation of ergothioneine |
WO2011118749A1 (en) * | 2010-03-25 | 2011-09-29 | 東レ株式会社 | Deodorant fiber structure |
CN102822411A (en) * | 2010-03-25 | 2012-12-12 | 东丽株式会社 | Deodorant fiber structure |
JPWO2011118749A1 (en) * | 2010-03-25 | 2013-07-04 | 東レ株式会社 | Deodorant fiber structure |
JP2015180788A (en) * | 2010-03-25 | 2015-10-15 | 東レ株式会社 | deodorant fiber structure |
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