JPH0620539B2 - Deodorant - Google Patents
DeodorantInfo
- Publication number
- JPH0620539B2 JPH0620539B2 JP62203535A JP20353587A JPH0620539B2 JP H0620539 B2 JPH0620539 B2 JP H0620539B2 JP 62203535 A JP62203535 A JP 62203535A JP 20353587 A JP20353587 A JP 20353587A JP H0620539 B2 JPH0620539 B2 JP H0620539B2
- Authority
- JP
- Japan
- Prior art keywords
- deodorant
- peroxide
- acid
- examples
- same manner
- 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 - Lifetime
Links
- 239000002781 deodorant agent Substances 0.000 title claims description 38
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 18
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims description 11
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 9
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 7
- 239000004343 Calcium peroxide Substances 0.000 claims description 5
- LHJQIRIGXXHNLA-UHFFFAOYSA-N calcium peroxide Chemical compound [Ca+2].[O-][O-] LHJQIRIGXXHNLA-UHFFFAOYSA-N 0.000 claims description 5
- 235000019402 calcium peroxide Nutrition 0.000 claims description 5
- 150000002978 peroxides Chemical class 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
- XXQBEVHPUKOQEO-UHFFFAOYSA-N potassium superoxide Chemical compound [K+].[K+].[O-][O-] XXQBEVHPUKOQEO-UHFFFAOYSA-N 0.000 claims description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 239000011651 chromium Substances 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 claims description 2
- 229910052732 germanium Inorganic materials 0.000 claims description 2
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 239000011733 molybdenum Substances 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 claims description 2
- 229910052709 silver Inorganic materials 0.000 claims description 2
- 239000004332 silver Substances 0.000 claims description 2
- 229960001922 sodium perborate Drugs 0.000 claims description 2
- 229940045872 sodium percarbonate Drugs 0.000 claims description 2
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 claims description 2
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 claims description 2
- 229910052712 strontium Inorganic materials 0.000 claims description 2
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 claims description 2
- 229910052718 tin Inorganic materials 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 239000010936 titanium Substances 0.000 claims description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 239000010937 tungsten Substances 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- 230000001877 deodorizing effect Effects 0.000 description 20
- 238000000034 method Methods 0.000 description 18
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical compound O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 description 14
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 235000019645 odor Nutrition 0.000 description 10
- 239000007789 gas Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000004155 Chlorine dioxide Substances 0.000 description 7
- 235000019398 chlorine dioxide Nutrition 0.000 description 7
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000010813 municipal solid waste Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000003463 adsorbent Substances 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000010865 sewage Substances 0.000 description 4
- 238000001179 sorption measurement Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 229910001919 chlorite Inorganic materials 0.000 description 3
- 229910052619 chlorite group Inorganic materials 0.000 description 3
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 3
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 3
- 244000144972 livestock Species 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 229910021529 ammonia Inorganic materials 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
- 239000010794 food waste Substances 0.000 description 2
- 230000000873 masking effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 108010082455 Sebelipase alfa Proteins 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000002144 chemical decomposition reaction Methods 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 1
- 229940041615 kanuma Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Treating Waste Gases (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は悪臭成分を吸着、分解する脱臭剤に関するもの
であり、生ごみ、冷蔵庫、トイレ、病院、ホテル、家畜
飼育場、汚水処理場その他の脱臭に広く利用できる。TECHNICAL FIELD The present invention relates to a deodorant that adsorbs and decomposes malodorous components, such as kitchen garbage, refrigerators, toilets, hospitals, hotels, livestock farms, sewage treatment plants, and others. Widely used for deodorizing.
(従来の技術) 悪臭の発生源は日常生活の中での生ごみ、冷蔵庫、トイ
レ等から、一般の生産工場、家畜飼育場、汚水処理場等
に至るまで多岐にわたって存在する。また、病院、ホテ
ル、レストラン等悪臭とは言わないまでも特有の臭いを
持つところも多い。これら悪臭の原因物質としては、ア
ンモニア、メルカプタン類、硫化物、アミン類、アセト
アルデヒド等が注目されているが、実際にはさらに複雑
であり、これらの物質に限定されない。近年これら悪臭
を除去する技術に対する要望が高まるにつれ、悪臭除去
技術の研究が盛んとなり、例えば次のように種々の方法
が提案されている。(Prior Art) Sources of offensive odors are diverse, ranging from food waste, refrigerators, toilets, etc. in daily life to general production plants, livestock farms, sewage treatment plants, etc. Also, there are many places in hospitals, hotels, restaurants, etc. that have a unique, if not stinking, odor. Ammonia, mercaptans, sulfides, amines, acetaldehyde and the like have been attracting attention as substances causing these malodors, but they are actually more complicated and are not limited to these substances. In recent years, as the demand for a technique for removing these malodors has increased, research on the malodor removing technique has become popular, and various methods have been proposed, for example, as follows.
(1)悪臭よりも強力な芳香性の物質を発散させて悪臭を
なくすマスキング法 (2)活性炭その他の吸着剤を使用して悪臭原因物質を吸
着させる吸着法 (3)悪臭原因物質を酸、アルカリで中和して除去する
酸、アルカリ中和法 (4)悪臭原因物質を化学的に分解させる化学的酸化還元
法 (発明が解決しようとする問題点) しかしながら、上述の方法には、それぞれ重大な欠点が
存在する。例えば、マスキング法は本質的な方法とは言
えない。吸着法は飽和吸着量の関係から吸着量に限りが
あり、強力な悪臭には対応できない。酸、アルカリ中和
法は中和できる物質に限られ、適応できる臭いが限定さ
れる。化学的分解法は最も期待できる技術と考えられる
が、現在までのところ十分な能力を有するものは見あた
らない。その中で、二酸化塩素ガスの酸化力を利用する
方法がいくつか提案されている。例えば、特公昭48−
32079には亜塩素酸塩水溶液を塩基性吸着剤に吸着
させて安定化し、これを固体酸性粉末と混合して二酸化
塩素ガスを発生させる方法が開示されている。また、特
開昭60−161307には、亜塩素酸塩水溶液を多孔
性無機担体に含浸させた二酸化塩素ガス発生組成物が開
示されている。しかし、二酸化塩素ガスを発生させる方
法は、その発生量をコントロールすることが難しく、未
使用保存中にも分解し、しかも亜塩素酸塩がすべて分解
すれば効力は消失する。また、使用場所によっては二酸
化塩素ガスの発生が好ましくない場合もある。一方、特
開昭58−36619、特開昭57−1441等には、
リン酸類を活性炭等の担体に担持させた脱臭剤が開示さ
れている。しかしながら、本発明者等の検討によれば、
これらは塩基性悪臭物質にはある程度効果があるもの
の、全ての悪臭物質の処理には問題がある。(1) Masking method to eliminate a bad odor by emitting an aromatic substance that is stronger than a bad odor (2) Adsorption method to adsorb a bad odor causing substance using activated carbon or other adsorbents (3) An acid causing a bad odor causing substance Acid for neutralization and removal with alkali, alkali neutralization method (4) Chemical redox method for chemically decomposing malodorous substances (problems to be solved by the invention) There are serious drawbacks. For example, the masking method is not an essential method. The adsorption method has a limited adsorption amount due to the saturated adsorption amount and cannot cope with a strong malodor. The acid and alkali neutralization methods are limited to substances that can be neutralized, and the applicable odors are limited. The chemical decomposition method is considered to be the most promising technology, but so far no one has sufficient capacity. Among them, some methods of utilizing the oxidizing power of chlorine dioxide gas have been proposed. For example, Japanese Patent Publication 48-
32079 discloses a method in which a chlorite aqueous solution is adsorbed on a basic adsorbent to be stabilized, and this is mixed with solid acidic powder to generate chlorine dioxide gas. Further, JP-A-60-161307 discloses a chlorine dioxide gas generating composition in which a porous inorganic carrier is impregnated with an aqueous chlorite solution. However, in the method of generating chlorine dioxide gas, it is difficult to control the amount of generation, and it decomposes even during unused storage, and the efficacy disappears if all chlorite is decomposed. Further, depending on the place of use, the generation of chlorine dioxide gas may not be preferable. On the other hand, JP-A-58-36619 and JP-A-57-1441 disclose that
A deodorant in which phosphoric acid is supported on a carrier such as activated carbon is disclosed. However, according to the study by the present inventors,
Although they have some effect on basic malodorous substances, they are problematic in treating all malodorous substances.
これら上述の方法はそれぞれ一応の脱臭効果を示し、実
際に応用されているが、上述のような欠点からその技術
的改良が強く望まれている。Although each of these above-mentioned methods has a deodorizing effect to some extent and is actually applied, its technical improvement is strongly desired due to the above-mentioned drawbacks.
本発明の目的とするところは、従来法の欠点を克服しう
る汎用性があり、強力で寿命の長い脱臭剤を提供するこ
とにある。It is an object of the present invention to provide a deodorant which is versatile, strong and has a long life, which can overcome the drawbacks of the conventional methods.
(問題点を解決するための手段) 本発明者等はこのような背景から、生ごみ、冷蔵庫、ト
イレの悪臭から家畜飼育場、ごみ処理場、汚水処理場等
の悪臭まで種々の悪臭を吸着分解する高活性な脱臭剤に
ついて検討した結果、リン酸、亜リン酸、次亜リン酸か
ら選ばれた少なくとも一種と特定の過酸化物の少なくと
も一種および/または特定元素の酸化物の少なくとも一
種とからなる組成物が酸性、塩基性を問わず種々の悪臭
成分を分解する高い能力を有しており、従来になく安定
かつ高活性な脱臭剤であることを見出し、本発明を完成
するに至った。(Means for Solving Problems) Against this background, the present inventors adsorb various malodors from malodors such as garbage, refrigerators and toilets to livestock farms, garbage treatment plants, sewage treatment plants and the like. As a result of studying a highly active deodorant that decomposes, at least one selected from phosphoric acid, phosphorous acid and hypophosphorous acid, and at least one specific peroxide and / or at least one specific element oxide. The composition consisting of has a high ability of decomposing various malodorous components regardless of acidity and basicity, and found that it is a deodorant which is stable and highly active, and has completed the present invention. It was
すなわち、本発明はリン酸、亜リン酸、次亜リン酸から
選ばれた少なくとも一種と過酸化カルシウム、過酸化ナ
トリウム、過酸化カリウム、過ホウ酸ナトリウム、過炭
酸ナトリウム、過硫酸カリウム、過酸化水素の群から選
ばれた少なくとも一種および/または鉄、コバルト、ニ
ツケル、チタン、ジルコニウム、バナジウム、クロム、
モリブデン、タングステン、マンガン、銅、銀、亜鉛、
ゲルマニウム、錫、鉛、マグネシウム、ストロンチウム
の群から選ばれた元素の酸化物の少なくとも一種とから
なる脱臭剤に関する。特徴とするところは本剤使用中二
酸化塩素のようなガスの発生はなく、酸性、中性、塩基
性物質を問わず種々の悪臭成分を分解し、しかも長期間
使用あるいは保存しても、その効力が変わらないことで
ある。That is, the present invention is at least one selected from phosphoric acid, phosphorous acid, hypophosphorous acid and calcium peroxide, sodium peroxide, potassium peroxide, sodium perborate, sodium percarbonate, potassium persulfate, peroxide At least one selected from the group of hydrogen and / or iron, cobalt, nickel, titanium, zirconium, vanadium, chromium,
Molybdenum, tungsten, manganese, copper, silver, zinc,
The present invention relates to a deodorant comprising at least one oxide of an element selected from the group of germanium, tin, lead, magnesium and strontium. The feature is that no gas such as chlorine dioxide is generated during the use of this drug, it decomposes various malodorous components regardless of acidic, neutral or basic substances, and even if it is used or stored for a long period of time, its The effect is unchanged.
以下、本発明を詳細に説明する。Hereinafter, the present invention will be described in detail.
本発明で使用されるリン酸、亜リン酸、次亜リン酸(以
下、「リン酸等」という)とは、これらの酸、酸無水
物、を含む。これらは、それ自体の脱臭能力は大きくな
いが、上述の通り、これに特定の過酸化物及び/又は特
定の酸化物を共存させると、その脱臭能力は飛躍的に増
大する。The phosphoric acid, phosphorous acid and hypophosphorous acid (hereinafter referred to as “phosphoric acid etc.”) used in the present invention include these acids and acid anhydrides. These do not have a large deodorizing capacity by themselves, but as described above, the coexistence of a specific peroxide and / or a specific oxide dramatically increases the deodorizing capacity.
前記の特定の過酸化物及び/又は酸化物の脱臭剤中に占
める割合は任意であるが、好ましくは0.1〜90重量パ
ーセント、更に好ましくは0.1〜60重量パーセントで
ある。The ratio of the above-mentioned specific peroxide and / or oxide in the deodorant is arbitrary, but is preferably 0.1 to 90% by weight, more preferably 0.1 to 60% by weight.
本発明の脱臭剤は通常用いられる多孔性の担体に担持あ
るいは混合することができる。好ましい担体としては、
シリカ、アルミナ、シリカアルミナ、天然ゼオライト、
合成ゼオライト、ケイソウ土、活性炭、鹿沼土、粘土鉱
物等を挙げることができるが、特にこれらに限定される
ことはなく、通常用いられる担体、吸着剤であればいず
れも使用可能である。脱臭剤中に占める担体の割合は任
意であるが、好ましくは10〜90重量パーセント、更
に好ましくは30〜70重量パーセントである。The deodorant of the present invention can be supported or mixed on a commonly used porous carrier. The preferred carrier is
Silica, alumina, silica-alumina, natural zeolite,
Examples thereof include synthetic zeolite, diatomaceous earth, activated carbon, Kanuma soil, clay minerals, etc., but are not particularly limited thereto, and any commonly used carrier or adsorbent can be used. The proportion of the carrier in the deodorant is arbitrary, but is preferably 10 to 90 weight percent, more preferably 30 to 70 weight percent.
本発明の脱臭剤に使用する原料は特に限定されない。通
常入手し得るものが使用でき、調製によって最終的に好
ましい化合形態になるものであれば、いずれの原料も使
用できる。調製法も特に限定されない。例えば、リン酸
等の水溶液をその他の成分原料と混合した後、乾燥、必
要に応じて焼成するなどの方法によって調製することが
できる。The raw material used for the deodorant of the present invention is not particularly limited. What is normally available can be used, and any raw material can be used as long as it can be finally obtained in a preferable compounded form by the preparation. The preparation method is also not particularly limited. For example, it can be prepared by a method of mixing an aqueous solution of phosphoric acid or the like with other component raw materials, followed by drying and, if necessary, firing.
本発明の脱臭剤は固体状脱臭剤として使用する以外に、
水溶液として液状脱臭剤としても使用することができ
る。その場合リン酸等と過酸化物合計の濃度は特に制限
はないが、好ましくは1〜50重量パーセントの範囲で
ある。The deodorant of the present invention is used as a solid deodorant,
It can also be used as an aqueous solution as a liquid deodorant. In that case, the total concentration of phosphoric acid and the like is not particularly limited, but is preferably in the range of 1 to 50 weight percent.
本発明の脱臭剤の使用方法は特に限定されない。上述の
通り、本発明の脱臭剤は、その形態として液状、固体状
いずれの状態でも用いることができる為、その応用範囲
は広い。例えば、粒状、ペレツト状に成形して、通気性
を有する袋、容器等に充填して冷蔵庫、トイレ等に使用
できる。あるいは悪臭ガスを強制的に本発明の脱臭剤の
層に通じて処理することも可能である。包装材料、壁紙
等の住宅材料等に塗布あるいは混合して使用することも
可能である。さらに悪臭発生源である例えば生ごみ、汚
泥等に直接散布することも可能である。The method of using the deodorant of the present invention is not particularly limited. As described above, the deodorant of the present invention can be used in either a liquid state or a solid state, so that its application range is wide. For example, it can be used in a refrigerator, a toilet, etc. by molding it into a granular or pellet shape and filling it into a bag, container or the like having air permeability. Alternatively, the malodorous gas can be forcibly passed through the layer of the deodorant of the present invention for treatment. It is also possible to use by coating or mixing with packaging materials, housing materials such as wallpaper, and the like. Furthermore, it is also possible to spray directly on the source of offensive odors, such as garbage and sludge.
本発明の脱臭剤による脱臭機構は明らかでないが、主体
は触媒作用によるものと考えられる。従って、吸着剤や
二酸化塩素発生剤と異なり、長期間の使用が可能であ
る。また、活性が高いために強い悪臭に対しても短時間
で効くという長所を有している。Although the deodorizing mechanism by the deodorant of the present invention is not clear, it is considered that the main component is the catalytic action. Therefore, unlike the adsorbent and the chlorine dioxide generator, it can be used for a long period of time. In addition, since it has high activity, it has an advantage that it is effective against a strong odor in a short time.
(実施例) 以下、実施例を挙げて本発明を更に具体的に説明する
が、本発明はこれらの実施例によって限定されるもので
はない。(Examples) Hereinafter, the present invention will be described more specifically with reference to Examples, but the present invention is not limited to these Examples.
実施例1 50%次亜リン酸水溶液25g、三二酸化鉄25gおよ
び粒状シリカアルミナ(アルミナ含量28wt.%)50
gを混練して均一に混合し、110℃で乾燥して脱臭剤
を得た。Example 1 25 g of 50% aqueous solution of hypophosphorous acid, 25 g of iron sesquioxide and 50 granular silica alumina (alumina content 28 wt.%) 50
g was kneaded, uniformly mixed, and dried at 110 ° C. to obtain a deodorant.
得られた脱臭剤1gをあらかじめ調製されたメチルメル
カプタン1000ppm、硫化水素500ppm、アンモニア
500ppmを含む被検ガス500mと共にポリエチレン容
器に密封し、それぞれの濃度変化を測定した。結果を第
一表に示した。尚、三者の濃度が0になった時点で実際
に無臭であることを確認した。1 g of the obtained deodorant was sealed in a polyethylene container together with 500 m of a test gas containing 1000 ppm of methyl mercaptan, 500 ppm of hydrogen sulfide, and 500 ppm of ammonia, which had been prepared in advance, and each concentration change was measured. The results are shown in Table 1. It was confirmed that the odor was actually odorless when the concentrations of the three became zero.
実施例2〜11 実施例1と同様にして、第一表に示す組成の脱臭剤を得
た。それぞれについて実施例1と同様に脱臭効果を調べ
た。結果を第一表に示した。Examples 2 to 11 In the same manner as in Example 1, deodorants having the compositions shown in Table 1 were obtained. For each of them, the deodorizing effect was examined in the same manner as in Example 1. The results are shown in Table 1.
実施例12〜18 実施例1と同様にして、第二表に示す組成の脱臭剤を得
た。それぞれについて実施例1と同様に脱臭効果を調べ
た。 Examples 12 to 18 In the same manner as in Example 1, deodorants having the compositions shown in Table 2 were obtained. For each of them, the deodorizing effect was examined in the same manner as in Example 1.
結果を第二表に示した。The results are shown in Table 2.
実施例19 50%次亜リン酸水溶液50g粉末活性炭50gに添加
し、混合した後、更に過酸化カルシウム25gを加え
て、均一に混合し、110℃で乾燥して脱臭剤を得た。 Example 19 After adding 50 g of 50% aqueous solution of hypophosphorous acid to 50 g of powdered activated carbon and mixing, 25 g of calcium peroxide was further added and uniformly mixed, and dried at 110 ° C. to obtain a deodorant.
得られた脱臭剤について、実施例1と同様にその脱臭効
果を調べた。結果を第三表に示した。The deodorizing effect of the obtained deodorizing agent was examined in the same manner as in Example 1. The results are shown in Table 3.
実施例20〜21 実施例19において、次亜リン酸の代わりに50%亜リ
ン酸水溶液50gおよび50%リン酸水溶液50gとし
た以外は同様にして第三表に示す組成の脱臭剤を得た。
それぞれについて実施例1と同様に脱臭効果を調べた。
結果を第三表に示した。Examples 20 to 21 In Example 19, the deodorant having the composition shown in Table 3 was obtained in the same manner except that 50 g of a 50% phosphorous acid aqueous solution and 50 g of a 50% phosphoric acid aqueous solution were used instead of the hypophosphorous acid. .
For each of them, the deodorizing effect was examined in the same manner as in Example 1.
The results are shown in Table 3.
比較例1〜3 実施例19〜21において、過酸化カルシウムを加えな
い以外は全く同様にして第四表に示す組成物を得た。そ
れぞれについて実施例1と同様に脱臭効果を調べ、その
結果を第四表に示した。 Comparative Examples 1 to 3 Compositions shown in Table 4 were obtained in exactly the same manner as in Examples 19 to 21 except that calcium peroxide was not added. For each of them, the deodorizing effect was examined in the same manner as in Example 1, and the results are shown in Table 4.
実施例22 50%次亜リン酸水溶液50g、過酸化ナトリウム25
gおよび活性炭50gを少量の水の存在下に混練して均
一に混合し、110℃で乾燥して脱臭剤を得た。得られ
た脱臭剤について実施例1と同様に脱臭効果を調べた。
結果を第五表に示した。 Example 22 50 g 50% aqueous solution of hypophosphorous acid, 25 sodium hydroxide
g and 50 g of activated carbon were kneaded in the presence of a small amount of water, uniformly mixed, and dried at 110 ° C. to obtain a deodorant. The deodorizing effect of the obtained deodorizing agent was examined in the same manner as in Example 1.
The results are shown in Table 5.
実施例23〜26 実施例22と同様にして第五表に示す組成の脱臭剤を
得、実施例1と同様の操作で、その脱臭効果を調べた。
結果を第五表に示した。Examples 23 to 26 In the same manner as in Example 22, deodorizing agents having the compositions shown in Table 5 were obtained, and the deodorizing effect was examined by the same operation as in Example 1.
The results are shown in Table 5.
実施例27 50%次亜リン酸水溶液20gを粉末活性炭40gに添
加し、混合した後、更に、酸化亜鉛20gおよび過酸化
カルシウム20gを加えて、均一に混合し、110℃で
乾燥して脱臭剤を得、実施例1と同様の操作で、その脱
臭効果を調べた。結果を第六表に示した。 Example 27 20 g of 50% aqueous solution of hypophosphorous acid was added to 40 g of powdered activated carbon and mixed, and then 20 g of zinc oxide and 20 g of calcium peroxide were further added, mixed uniformly and dried at 110 ° C. to remove the deodorant. Then, the deodorizing effect was examined by the same operation as in Example 1. The results are shown in Table 6.
実施例28〜31 実施例27と同様にして第六表に示す組成の脱臭剤を
得、同様にその脱臭効果を調べた。結果を第六表に示し
た。Examples 28 to 31 In the same manner as in Example 27, deodorizing agents having the compositions shown in Table 6 were obtained, and the deodorizing effect was examined in the same manner. The results are shown in Table 6.
実施例32 実施例1〜18において、次亜リン酸の代りにリン酸又
は亜リン酸を用い、その他は実施例1〜18と同様にし
て脱臭剤を得、それぞれについて実施例1と同様に脱臭
効果を調べたところ、それぞれ実施例1〜18とほぼ同
様な結果が得られた。 Example 32 In Examples 1 to 18, phosphorous acid or phosphorous acid was used in place of hypophosphorous acid, and the deodorant was obtained in the same manner as in Examples 1 to 18 except that the same as in Example 1. When the deodorizing effect was examined, almost the same results as in Examples 1 to 18 were obtained.
実施例33〜34 下水処理に使用した汚泥の脱水ケーキ(含水率80%)
100gを2のガラス瓶にいれ、これに実施例27お
よび28で得られた脱臭剤2gをそれぞれふりかけ、密
閉して30℃に放置し、24時間後の硫化水素とメチル
メルカプタンの濃度を測定した。脱臭剤を用いない場合
は、それぞれ200ppmおよび100ppmであったのに対
し、脱臭剤を用いた場合はいずれもそれぞれ1ppm以下
であった。Examples 33 to 34 Dewatered cake of sludge used for sewage treatment (water content 80%)
100 g was placed in a glass bottle 2 and 2 g of the deodorant obtained in each of Examples 27 and 28 was sprinkled on each, sealed and left at 30 ° C. After 24 hours, the concentrations of hydrogen sulfide and methyl mercaptan were measured. When the deodorant was not used, it was 200 ppm and 100 ppm, respectively, whereas when the deodorant was used, it was 1 ppm or less in each case.
実施例35 実施例28で調製した脱臭剤10gを紙袋にパツクし、
生ごみの入った内容積30のポリバケツのふたの裏側
に固定した。その結果、生ごみ臭は消失し、その効果は
3カ月を経過しても変わらなかった。Example 35 10 g of the deodorant prepared in Example 28 was packed in a paper bag,
It was fixed to the back side of the lid of a poly bucket with an internal volume of 30 containing garbage. As a result, the smell of food waste disappeared, and the effect did not change even after 3 months.
実施例36 実施例29で調製した脱臭剤20gを紙袋にパツクし、
冷蔵庫に置いたところ、脱臭効果が認められ、その効果
は3カ月を経過しても変わらなかった。Example 36 20 g of the deodorant prepared in Example 29 was packed in a paper bag,
When placed in the refrigerator, a deodorizing effect was recognized, and the effect did not change even after 3 months.
実施例37 50%次亜リン酸水溶液100mと30%過酸化水素
水溶液100mを混合し、これに脱イオン水200m
を加えて液状脱臭剤を得た。Example 37 100m of 50% aqueous solution of hypophosphorous acid and 100m of 30% aqueous solution of hydrogen peroxide were mixed and mixed with 200m of deionized water.
Was added to obtain a liquid deodorant.
実施例33において、脱臭剤2gの代わりに得られた液
状脱臭剤20mを散布して同様の実験を行った。その
結果、24時間後の硫化水素、メチルメルカプタンの濃
度はそれぞれ5ppm以下であった。The same experiment was performed by spraying 20 m of the liquid deodorant obtained in place of 2 g of the deodorant in Example 33. As a result, the concentrations of hydrogen sulfide and methyl mercaptan after 24 hours were each 5 ppm or less.
(発明の効果) 本発明の脱臭剤は悪臭成分を速やかに分解する。しかも
長期間の使用が可能であり、また、極めて高濃度の悪臭
まで処理可能であり、脱臭剤として広く利用することが
できる。(Effects of the Invention) The deodorant of the present invention rapidly decomposes malodorous components. In addition, it can be used for a long period of time, and it can treat an extremely high concentration of malodor, and can be widely used as a deodorant.
Claims (1)
た少なくとも一種と過酸化カルシウム、過酸化ナトリウ
ム、過酸化カリウム、過ホウ酸ナトリウム、過炭酸ナト
リウム、過硫酸カリウム、過酸化水素の群から選ばれた
少なくとも一種および/または鉄、コバルト、ニッケ
ル、チタン、ジルコニウム、バナジウム、クロム、モリ
ブデン、タングステン、マンガン、銅、銀、亜鉛、ゲル
マニウム、錫、鉛、マグネシウム、ストロンチウムの群
から選ばれた元素の酸化物の少なくとも一種とからなる
脱臭剤。1. At least one selected from phosphoric acid, phosphorous acid and hypophosphorous acid, and calcium peroxide, sodium peroxide, potassium peroxide, sodium perborate, sodium percarbonate, potassium persulfate, and peroxide. At least one selected from the group of hydrogen and / or iron, cobalt, nickel, titanium, zirconium, vanadium, chromium, molybdenum, tungsten, manganese, copper, silver, zinc, germanium, tin, lead, magnesium, strontium A deodorant comprising at least one oxide of a selected element.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62203535A JPH0620539B2 (en) | 1986-12-02 | 1987-08-18 | Deodorant |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61-285913 | 1986-12-02 | ||
JP28591386 | 1986-12-02 | ||
JP62203535A JPH0620539B2 (en) | 1986-12-02 | 1987-08-18 | Deodorant |
CA000611140A CA1334628C (en) | 1986-08-26 | 1989-09-12 | Ethylene removal agent, postharvest preservation agent and deodorant |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63258644A JPS63258644A (en) | 1988-10-26 |
JPH0620539B2 true JPH0620539B2 (en) | 1994-03-23 |
Family
ID=27168462
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62203535A Expired - Lifetime JPH0620539B2 (en) | 1986-12-02 | 1987-08-18 | Deodorant |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0620539B2 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2574159B2 (en) * | 1987-08-28 | 1997-01-22 | 日本ゼオン株式会社 | Deodorant |
US20080099375A1 (en) * | 2006-10-30 | 2008-05-01 | Exxonmobil Research And Engineering Company | Process for adsorption of sulfur compounds from hydrocarbon streams |
JP2010131565A (en) * | 2008-12-08 | 2010-06-17 | Toyota Central R&D Labs Inc | Sulfur-based gas removing material and method for producing the same |
JP6371102B2 (en) * | 2014-04-24 | 2018-08-08 | 日揮触媒化成株式会社 | Metal-supported molded article, its production method, adsorptive desulfurization catalyst, adsorptive desulfurization method, hydrogen production method, and fuel cell system |
CN114177934B (en) * | 2021-12-28 | 2024-01-16 | 华夏碧水环保科技股份有限公司 | Treatment method of coking ammonia distillation wastewater and heterogeneous Fenton catalyst used in treatment method |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4931875B2 (en) | 2008-07-16 | 2012-05-16 | リンナイ株式会社 | Cooker |
JP5939180B2 (en) | 2013-03-15 | 2016-06-22 | ブラザー工業株式会社 | Information processing apparatus, relay server, information relay method, information relay program, and communication system |
JP6115732B2 (en) | 2013-04-04 | 2017-04-19 | パナソニックIpマネジメント株式会社 | Imaging system |
-
1987
- 1987-08-18 JP JP62203535A patent/JPH0620539B2/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4931875B2 (en) | 2008-07-16 | 2012-05-16 | リンナイ株式会社 | Cooker |
JP5939180B2 (en) | 2013-03-15 | 2016-06-22 | ブラザー工業株式会社 | Information processing apparatus, relay server, information relay method, information relay program, and communication system |
JP6115732B2 (en) | 2013-04-04 | 2017-04-19 | パナソニックIpマネジメント株式会社 | Imaging system |
Also Published As
Publication number | Publication date |
---|---|
JPS63258644A (en) | 1988-10-26 |
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