JP2002001105A - Deodorizing composition - Google Patents
Deodorizing compositionInfo
- Publication number
- JP2002001105A JP2002001105A JP2000190239A JP2000190239A JP2002001105A JP 2002001105 A JP2002001105 A JP 2002001105A JP 2000190239 A JP2000190239 A JP 2000190239A JP 2000190239 A JP2000190239 A JP 2000190239A JP 2002001105 A JP2002001105 A JP 2002001105A
- Authority
- JP
- Japan
- Prior art keywords
- deodorizing
- titanium dioxide
- iron hydroxide
- deodorizing composition
- hydrogen sulfide
- 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.)
- Granted
Links
- 230000001877 deodorizing effect Effects 0.000 title claims abstract description 35
- 239000000203 mixture Substances 0.000 title claims abstract description 29
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 51
- 235000014413 iron hydroxide Nutrition 0.000 claims abstract description 24
- NCNCGGDMXMBVIA-UHFFFAOYSA-L iron(ii) hydroxide Chemical compound [OH-].[OH-].[Fe+2] NCNCGGDMXMBVIA-UHFFFAOYSA-L 0.000 claims abstract description 24
- 239000004408 titanium dioxide Substances 0.000 claims abstract description 21
- 238000000034 method Methods 0.000 claims abstract description 17
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 9
- 150000002505 iron Chemical class 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 238000001035 drying Methods 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- 239000010936 titanium Substances 0.000 claims description 4
- 238000005406 washing Methods 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 2
- 230000001678 irradiating effect Effects 0.000 claims 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 abstract description 22
- 229910000037 hydrogen sulfide Inorganic materials 0.000 abstract description 18
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract description 10
- 229910021529 ammonia Inorganic materials 0.000 abstract description 5
- 229910052742 iron Inorganic materials 0.000 abstract description 5
- 150000003839 salts Chemical class 0.000 abstract description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- 239000000843 powder Substances 0.000 description 17
- 239000000243 solution Substances 0.000 description 14
- 239000002002 slurry Substances 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 239000002244 precipitate Substances 0.000 description 9
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- 239000004570 mortar (masonry) Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 230000032683 aging Effects 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- -1 acetaldehyde, amines Chemical class 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000011941 photocatalyst Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 102100032566 Carbonic anhydrase-related protein 10 Human genes 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 101000867836 Homo sapiens Carbonic anhydrase-related protein 10 Proteins 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- JZQOJFLIJNRDHK-CMDGGOBGSA-N alpha-irone Chemical compound CC1CC=C(C)C(\C=C\C(C)=O)C1(C)C JZQOJFLIJNRDHK-CMDGGOBGSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 230000001699 photocatalysis Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000012256 powdered iron Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Catalysts (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、硫化水素、アンモ
ニア、ホルマリン、アセトアルデヒド、アミン類、メル
カプタン類等の悪臭成分を除去あるいは低減するための
脱臭組成物及びそれを用いる脱臭方法に関する。The present invention relates to a deodorizing composition for removing or reducing malodorous components such as hydrogen sulfide, ammonia, formalin, acetaldehyde, amines and mercaptans, and a deodorizing method using the same.
【0002】[0002]
【従来の技術及び発明が解決しようとする課題】空気中
に含まれる硫化水素、メルカプタン類、アンモニア、ア
ルデヒド類等の悪臭成分を除去、脱臭する方法について
は様々な方法が提案されている。活性炭を用いて吸着、
脱臭する方法は、そのひとつとして有効であるが、脱臭
性能はすべての悪臭成分に対して優れているわけではな
く、また吸着が飽和になったときに効果が著しく低下す
る問題があった。2. Description of the Related Art Various methods have been proposed for removing and deodorizing malodorous components such as hydrogen sulfide, mercaptans, ammonia and aldehydes contained in air. Adsorption using activated carbon,
The deodorizing method is effective as one of the methods, but the deodorizing performance is not excellent for all the malodorous components, and there is a problem that the effect is remarkably reduced when the adsorption becomes saturated.
【0003】特開平10−43593にはα水酸化鉄と
γ水酸化鉄を含有する複合水酸化鉄が硫化水素の除去剤
として提案されているが、この複合水酸化鉄はアンモニ
ア等のガスに対しては脱臭能が低く、硫化水素に対して
も脱臭能は十分とは言えない。また、この組成物を調製
する際には水酸化物沈殿のスラリーを10日間撹拌を続
けて熟成を行う必要があるという問題があった。Japanese Patent Application Laid-Open No. Hei 10-43593 proposes a composite iron hydroxide containing α-iron hydroxide and γ-iron hydroxide as a hydrogen sulfide removing agent. Deodorizing ability is low for hydrogen sulfide, and deodorizing ability for hydrogen sulfide is not sufficient. Further, when preparing this composition, there is a problem that it is necessary to continue stirring and ripen the slurry of the hydroxide precipitate for 10 days.
【0004】一方、二酸化チタン等の光触媒を用いた悪
臭の除去に関しても多くの提案がなされている。二酸化
チタンが紫外線等の光エネルギーによって有機物を酸化
分解することを利用したものである。しかし、分解する
速度は比較的遅く、悪臭成分の濃度が高い場合には脱臭
効果が得られにくい欠点があった。また光の照射がない
場合には分解反応が起こらない等、脱臭剤としては不十
分であった。On the other hand, many proposals have been made regarding the removal of offensive odor using a photocatalyst such as titanium dioxide. It utilizes the fact that titanium dioxide oxidizes and decomposes organic substances by light energy such as ultraviolet rays. However, the decomposition rate is relatively slow, and when the concentration of the malodorous component is high, the deodorizing effect is hardly obtained. In addition, when there is no light irradiation, the decomposition reaction does not occur.
【0005】[0005]
【課題を解決するための手段】本発明者らは、このよう
な課題を解決するため、鋭意研究の結果、3価の鉄塩よ
り調製した水酸化鉄と二酸化チタンを含有させた組成物
が、高い脱臭性能と脱臭性能の持続力を有することを見
いだし、本発明を完成させた。すなわち本発明は、3価
の鉄塩より調製した水酸化鉄と二酸化タンを含有するこ
とを特徴とする脱臭組成物を提供するものである。これ
までの二酸化チタンの脱臭力に関しては、光触媒性能を
利用したものであるが、本発明では紫外線等の光を照射
しなくても高い脱臭性能を示す。Means for Solving the Problems The present inventors have conducted intensive studies to solve such problems, and as a result, have found that a composition containing iron hydroxide and titanium dioxide prepared from a trivalent iron salt has been developed. The present invention has been found to have high deodorizing performance and sustainability of deodorizing performance. That is, the present invention provides a deodorizing composition comprising iron hydroxide and tan dioxide prepared from a trivalent iron salt. The deodorizing power of conventional titanium dioxide utilizes photocatalytic performance, but the present invention exhibits high deodorizing performance without irradiation with light such as ultraviolet rays.
【0006】[0006]
【発明の実施の形態】本発明の脱臭組成物における3価
の鉄塩は、硫酸塩、硝酸塩、塩化物塩、臭化物塩、ヨウ
化物塩、クエン酸塩等いずれの塩を用いても差し支えな
いが、塩化物塩が好ましい。水酸化鉄は、3価の鉄塩の
水溶液を撹拌しながらアルカリを添加し、pHを上昇さ
せることによって調製する。pHは、4〜13の範囲で
調製することが可能であり、好ましくはpH4〜9が良
い。水酸化鉄を調製する際に添加するアルカリはアンモ
ニア水、水酸化ナトリウム水溶液、水酸化カリウム水溶
液等いずれを用いても差し支えないが、水酸化ナトリウ
ムが好ましい。水溶液中の鉄塩の濃度は、1〜100g
/Lの範囲で可能であるが、好ましくは20〜50g/
Lで行われる。3価の鉄塩から調製した水酸化鉄は、ほ
とんどがβ水酸化鉄として存在していると考えられ、乾
燥後には一部が酸化鉄に変化していると考えられる。BEST MODE FOR CARRYING OUT THE INVENTION The trivalent iron salt in the deodorizing composition of the present invention may be any salt such as sulfate, nitrate, chloride, bromide, iodide and citrate. However, chloride salts are preferred. Iron hydroxide is prepared by adding an alkali while stirring an aqueous solution of a trivalent iron salt to increase the pH. The pH can be adjusted in the range of 4 to 13, and preferably 4 to 9. As the alkali to be added when preparing iron hydroxide, any of ammonia water, aqueous sodium hydroxide solution, aqueous potassium hydroxide solution and the like may be used, but sodium hydroxide is preferred. The concentration of iron salt in the aqueous solution is 1 to 100 g
/ L, but preferably 20 to 50 g / L.
L. It is considered that most of the iron hydroxide prepared from the trivalent iron salt is present as β-iron hydroxide, and partly changed to iron oxide after drying.
【0007】二酸化チタンはアナターゼ型、ルチル型、
ブルカイト型のいずれでも差し支えないが、アナターゼ
型が好ましい。一般に光触媒として市販されているもの
が使用可能である。[0007] Titanium dioxide is anatase type, rutile type,
The brookite type may be used, but the anatase type is preferred. Generally, commercially available photocatalysts can be used.
【0008】水酸化鉄と二酸化チタンの混合方法につい
ては、水酸化鉄を調製したスラリー液に二酸化チタン粉
末を添加し、ろ過、水洗、乾燥を行う方法、3価の鉄塩
の水溶液に二酸化チタン粉末を添加、分散させてからp
Hを調整し水酸化鉄を生成させる方法、水酸化鉄粉末と
二酸化チタン粉末を混合させる方法等が可能で、いずれ
の方法で混合しても良い。水酸化鉄スラリーまたは二酸
化チタン粉末を混合した水酸化鉄スラリーを脱水する方
法としては、吸引濾過器または遠心濾過装置を用いる方
法や、静置した後に上澄み液を除去する方法等いずれの
方法でも差し支えない。混合した脱臭組成物を乾燥させ
る方法及び条件に特に制限はないが、50〜150℃の
範囲の温度で加温しながら乾燥させることが好ましい。
水酸化鉄と二酸化チタンの混合比は、Fe:Tiが1:
9〜80:20が良く、好ましくは5:95〜50:5
0が良い。[0008] As to the method of mixing iron hydroxide and titanium dioxide, a method of adding titanium dioxide powder to a slurry liquid prepared with iron hydroxide, followed by filtration, washing with water and drying is performed by adding titanium dioxide to an aqueous solution of a trivalent iron salt. After adding and dispersing the powder, p
A method of adjusting H to produce iron hydroxide, a method of mixing iron hydroxide powder and titanium dioxide powder, and the like are possible, and any method may be used. As a method for dehydrating the iron hydroxide slurry mixed with the iron hydroxide slurry or the titanium dioxide powder, any method such as a method using a suction filter or a centrifugal filtration device or a method of removing the supernatant after standing still may be used. Absent. The method and conditions for drying the mixed deodorizing composition are not particularly limited, but it is preferable to dry while heating at a temperature in the range of 50 to 150 ° C.
The mixing ratio of iron hydroxide and titanium dioxide is such that Fe: Ti is 1:
9-80: 20 is good, preferably 5: 95-50: 5
0 is good.
【0009】本発明の脱臭組成物は、粉体そのもので脱
臭剤として使用することが可能であるが、粉末状ではそ
の取り扱いにおいて粉立ちの問題があるため、造粒して
用いるか、金属、ガラス、セラミックス、紙、プラスチ
ック、木材等の基質に担持あるいは塗布して使用するこ
とも可能である。コーティング剤として使用する場合に
はバインダー等の樹脂と混合することも可能である。ま
たアルミナ、タルク、クレー、炭酸カルシウム等のフィ
ラーを混合して使用することも可能である。The deodorizing composition of the present invention can be used as a deodorant in the form of a powder itself. However, in the case of a powder, there is a problem of dusting in the handling, so that the powder may be used after granulation or use of metal or metal. It is also possible to use it by supporting or coating it on a substrate such as glass, ceramics, paper, plastic, and wood. When used as a coating agent, it can be mixed with a resin such as a binder. It is also possible to use a mixture of fillers such as alumina, talc, clay and calcium carbonate.
【0010】本発明の脱臭組成物によって除去される悪
臭成分には、硫化水素、アンモニア、ホルマリン、アセ
トアルデヒド、アミン類、メルカプタン類が挙げられ
る。The malodor components removed by the deodorizing composition of the present invention include hydrogen sulfide, ammonia, formalin, acetaldehyde, amines, and mercaptans.
【0011】[0011]
【実施例】本発明を実施例、試験例により更に詳しく説
明するが、本発明がこれらによって限定されるものでは
ない。The present invention will be described in more detail with reference to Examples and Test Examples, but the present invention is not limited by these.
【0012】[0012]
【実施例1〜3】塩化第二鉄(FeCl3・6H2O)
20gを蒸留水400gに溶解した。この場合の溶液の
pHは約1.5であった。次に、この溶液にpHが約8.
5になるまで水酸化ナトリウム水溶液(10重量%)を
徐々に滴下し、濃茶色の水酸化鉄沈殿のスラリーを得
た。2時間熟成後ろ過し、110℃の乾燥機中に入れ、
乾燥させた。乾燥後、乳鉢を用いて粉砕を行い粉末の水
酸化鉄を得た。この水酸化鉄とアナターゼ型光触媒用二
酸化チタン(タイノックA-100:多木化学工業株式会社
製)を表1に示す重量比で混合し、実施例1〜3を得
た。[Examples 1-3] Ferric chloride (FeCl 3 · 6H 2 O)
20 g was dissolved in 400 g of distilled water. The pH of the solution in this case was about 1.5. Next, a pH of about 8.
An aqueous sodium hydroxide solution (10% by weight) was gradually added dropwise until the pH reached 5. A dark brown iron hydroxide precipitate slurry was obtained. After aging for 2 hours, it is filtered and put in a dryer at 110 ° C.
Let dry. After drying, it was pulverized using a mortar to obtain powdered iron hydroxide. This iron hydroxide and titanium dioxide for an anatase type photocatalyst (Tynoc A-100: manufactured by Taki Chemical Industry Co., Ltd.) were mixed at the weight ratio shown in Table 1 to obtain Examples 1 to 3.
【0013】[0013]
【表1】 [Table 1]
【0014】[0014]
【実施例4】塩化第二鉄(FeCl3・6H2O)20
gを蒸留水400gに溶解した。この場合の溶液のpH
は約1.5であった。次に、この溶液にpHが約7.0
になるまで水酸化ナトリウム水溶液(10重量%)を徐
々に滴下し、濃茶色の水酸化鉄沈殿のスラリーを得た。
続いてこのスラリー液に二酸化チタン(多木化学工業株
式会社製タイノックA−100(アナターゼ型))62
gを加え、十分に攪拌した後、更に水酸化ナトリウム溶
液(10重量%)を攪拌しながらpHが約8.5になる
まで滴下して薄茶色の沈殿を得た。2時間熟成後、この
沈殿を吸引濾過し、水洗後、30℃以下で乾燥した。こ
れを乳鉢で100ミクロン以下まで粉砕して、FeとT
iが1:9の重量比で混合されている粉体の脱臭組成物
を得た。Example 4 Ferric chloride (FeCl 3 .6H 2 O) 20
g was dissolved in 400 g of distilled water. PH of the solution in this case
Was about 1.5. Next, a pH of about 7.0 was added to this solution.
An aqueous solution of sodium hydroxide (10% by weight) was gradually added dropwise until a slurry of a dark brown iron hydroxide precipitate was obtained.
Subsequently, titanium dioxide (Tynoc A-100 (anatase type) manufactured by Taki Chemical Industry Co., Ltd.) is added to the slurry liquid 62.
g was added thereto, and the mixture was sufficiently stirred. Then, a sodium hydroxide solution (10% by weight) was further added dropwise with stirring until the pH became about 8.5 to obtain a light brown precipitate. After aging for 2 hours, the precipitate was filtered by suction, washed with water and dried at 30 ° C. or lower. This is crushed in a mortar to 100 microns or less, and Fe and T
A powdered deodorizing composition in which i was mixed at a weight ratio of 1: 9 was obtained.
【0015】[0015]
【実施例5】実施例4において二酸化チタン(多木化学
工業株式会社製タイノックA−100(アナターゼ
型))28gを加えたものを調製し、同様にFeとTi
が2:8の重量比で混合されている粉体の脱臭組成物を
得た。Fifth Embodiment In Example 4, 28 g of titanium dioxide (Tynoc A-100 (anatase type) manufactured by Taki Kagaku Kogyo KK) was added, and Fe and Ti were similarly prepared.
Was obtained at a weight ratio of 2: 8 to obtain a powdery deodorizing composition.
【0016】[0016]
【実施例6】実施例4において二酸化チタン(多木化学
工業株式会社製タイノックA−100(アナターゼ
型))28gを加えたものを調製し、水洗後110℃の
乾燥機中で乾燥させた。乳鉢で100ミクロン以下まで
粉砕し、FeとTiが2:8の重量比で混合されている
粉体の脱臭組成物を得た。Example 6 A product prepared by adding 28 g of titanium dioxide (Tynoc A-100 (anatase type) manufactured by Taki Chemical Industry Co., Ltd.) in Example 4 was prepared, washed with water and dried in a drier at 110 ° C. The powder was pulverized to 100 microns or less in a mortar to obtain a powdery deodorizing composition in which Fe and Ti were mixed at a weight ratio of 2: 8.
【0017】[0017]
【比較例1】塩化第二鉄(FeCl3・6H2O)20
gを蒸留水400gに溶解した。この場合の溶液のpH
は約1.5であった。次に、この溶液にpHが約8.5に
なるまで水酸化ナトリウム溶液(10重量%)を徐々に
滴下し、濃茶色の水酸化鉄沈殿のスラリーを得た。2時
間熟成後ろ過し、室温で乾燥させた。これを乳鉢で10
0ミクロン以下まで粉砕して粉体を得た。Comparative Example 1 Ferric chloride (FeCl 3 .6H 2 O) 20
g was dissolved in 400 g of distilled water. PH of the solution in this case
Was about 1.5. Next, a sodium hydroxide solution (10% by weight) was gradually added dropwise to the solution until the pH reached about 8.5, and a dark brown iron hydroxide precipitate slurry was obtained. After aging for 2 hours, the mixture was filtered and dried at room temperature. Put this in a mortar for 10
A powder was obtained by pulverizing the powder to 0 micron or less.
【0018】[0018]
【比較例2】塩化第二鉄(FeCl3・6H2O)20
gを蒸留水400gに溶解した。この場合の溶液のpH
は約1.5であった。次に、この溶液にpHが約8.5に
なるまで水酸化ナトリウム溶液(10重量%)を徐々に
滴下し、濃茶色の水酸化鉄沈殿のスラリーを得た。続い
てこのスラリー液に酸化亜鉛63gを加え、十分に攪拌
した後、更に水酸化ナトリウム溶液(10重量%)を攪
拌しながらpHが約8.5になるまで滴下して薄茶色の
沈殿を得た。2時間熟成後、この沈殿を吸引濾過し、3
0℃以下で乾燥した。これを乳鉢で100ミクロン以下
まで粉砕してFeとZnが1:9の重量比で混合されて
いる粉体の脱臭組成物を得た。Comparative Example 2 Ferric chloride (FeCl 3 .6H 2 O) 20
g was dissolved in 400 g of distilled water. PH of the solution in this case
Was about 1.5. Next, a sodium hydroxide solution (10% by weight) was gradually added dropwise to the solution until the pH reached about 8.5, and a dark brown iron hydroxide precipitate slurry was obtained. Subsequently, 63 g of zinc oxide was added to the slurry solution, and the mixture was sufficiently stirred. Then, while stirring a sodium hydroxide solution (10% by weight), the pH was dropped to about 8.5 to obtain a pale brown precipitate. Was. After aging for 2 hours, the precipitate was filtered off with suction.
It was dried at 0 ° C. or lower. This was ground in a mortar to 100 microns or less to obtain a powdery deodorizing composition in which Fe and Zn were mixed at a weight ratio of 1: 9.
【0019】[0019]
【比較例3】比較例2に用いた酸化亜鉛の代わりにアル
ミナ粉末を用いて同様に調製し、FeとAlが1:9の
重量比で混合されている粉体の脱臭組成物を得た。Comparative Example 3 A powdery deodorizing composition was prepared in the same manner as in Comparative Example 2 except that alumina powder was used instead of zinc oxide, and Fe and Al were mixed at a weight ratio of 1: 9. .
【0020】[0020]
【比較例4】二酸化チタン(多木化学工業株式会社製タ
イノックA−100(アナターゼ型))の粉末を比較例
4とした。Comparative Example 4 A powder of titanium dioxide (Tynoc A-100 (anatase type) manufactured by Taki Chemical Industry Co., Ltd.) was used as Comparative Example 4.
【0021】[0021]
【試験例1】実施例1〜5及び比較例1〜4の粉末10
0mgを内容積2500mlのガラス製三角フラスコに
入れ、活栓付きゴム栓にて密封した。次にシリンジを使
って硫化水素ガスを三角フラスコ内に濃度300ppm
になるように注入した。この時点から1時間後の三角フ
ラスコ内の硫化水素濃度を硫化水素用検知管(株式会社
ガステック製)にて測定した。結果を表2に示した。Test Example 1 Powder 10 of Examples 1 to 5 and Comparative Examples 1 to 4
0 mg was placed in a 2500 ml glass Erlenmeyer flask, and sealed with a stoppered rubber stopper. Next, use a syringe to introduce 300 ppm of hydrogen sulfide gas into the Erlenmeyer flask.
Was injected so that One hour after this point, the concentration of hydrogen sulfide in the Erlenmeyer flask was measured using a hydrogen sulfide detector tube (manufactured by Gastec Corporation). The results are shown in Table 2.
【0022】[0022]
【表2】 [Table 2]
【0023】[0023]
【試験例2】実施例4〜6及び比較例1及び4の粉体1
00mgを内容積2500mlのガラス製三角フラスコ
に入れ、活栓付きゴム栓にて密封した。次にシリンジを
使って硫化水素ガスを三角フラスコ内に濃度3000p
pmになるように注入した。定期的に三角フラスコ内の
硫化水素濃度を硫化水用検知管(株式社ガステック製)
にて測定し、もしも24時間以内にほぼ0ppmになっ
たことが確認された場合には、更に濃度3000ppm
になるよう新たに硫化水素ガスを添加した。これを硫化
水素ガス濃度が変化しなくなるまで継続し、粉体の硫化
水素に対する除去性能を求めた。結果を表3に示した。Test Example 2 Powder 1 of Examples 4 to 6 and Comparative Examples 1 and 4
00 mg was placed in a 2500-ml glass Erlenmeyer flask, and sealed with a stoppered rubber stopper. Next, use a syringe to introduce hydrogen sulfide gas into the Erlenmeyer flask at a concentration of 3000p.
pm. Periodically detects the concentration of hydrogen sulfide in an Erlenmeyer flask for water sulfide (Gastec Co., Ltd.)
If it was confirmed that the concentration was almost 0 ppm within 24 hours, the concentration was further increased to 3000 ppm.
The hydrogen sulfide gas was newly added so as to become. This was continued until the hydrogen sulfide gas concentration did not change, and the performance of removing the powder from hydrogen sulfide was determined. The results are shown in Table 3.
【0024】[0024]
【表3】 [Table 3]
【0025】[0025]
【試験例3】実施例6及び比較例4の粉末100mgを
内容積2500mlのガラス製三角フラスコに入れ、活
栓付きゴム栓にて密封した。次にシリンジを使って硫化
水素ガスを三角フラスコ内に濃度3000ppmになる
ように注入し、それぞれ室内と屋外(太陽光照射)に置
いた。この時点から、表4記載の時点で三角フラスコ内
の硫化水素濃度を検知管(株式会社ガステック製)にて
測定した。結果を表4に示した。Test Example 3 100 mg of the powders of Example 6 and Comparative Example 4 were placed in a 2500 ml glass Erlenmeyer flask and sealed with a rubber stopper with a stopcock. Next, hydrogen sulfide gas was injected into the Erlenmeyer flask using a syringe so as to have a concentration of 3000 ppm, and was placed indoors and outdoors (sunlight irradiation), respectively. From this point on, the concentration of hydrogen sulfide in the Erlenmeyer flask was measured at the point described in Table 4 using a detector tube (manufactured by Gastec Corporation). The results are shown in Table 4.
【0026】[0026]
【表4】 [Table 4]
【0027】[0027]
【発明の効果】本発明の脱臭組成物は二酸化チタンと水
酸化鉄を含有するもので、硫化水素、アンモニア、ホル
マリン、アセトアルデヒド、アミン類、メルカプタン類
等の悪臭成分を簡易に、しかも長期にわたって吸着、除
去が可能となる。The deodorizing composition of the present invention contains titanium dioxide and iron hydroxide, and easily and stably adsorbs malodorous components such as hydrogen sulfide, ammonia, formalin, acetaldehyde, amines and mercaptans for a long time. , Can be removed.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) B01J 20/30 B01D 53/36 J 23/745 ZABH 35/02 B01J 23/74 301A Fターム(参考) 4C080 AA07 BB02 CC02 CC04 CC05 CC08 HH05 JJ03 JJ04 KK08 LL03 MM02 NN01 NN03 4D048 AA01 AA03 AA05 AA08 AA19 AA22 AB03 BA07X BA13X BA36X BA42X BB01 EA01 4G066 AA13A AA23B AA27B AA39A CA02 CA25 CA27 CA29 CA52 DA03 FA02 FA03 FA05 FA21 FA34 FA36 FA37 4G069 AA02 AA08 AA09 BB05C BB06A BB06B BC50A BC50B BC66A BC66B BC66C CA10 CA17 EA02Y EB18Y FA01 FB06 FB31 FB57 FC02 FC07 FC08 ──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) B01J 20/30 B01D 53/36 J23 / 745 ZABH 35/02 B01J 23/74 301A F-term (Reference) 4C080 AA07 BB02 CC02 CC04 CC05 CC08 HH05 JJ03 JJ04 KK08 LL03 MM02 NN01 NN03 4D048 AA01 AA03 AA05 AA08 AA19 AA22 AB03 BA07X BA13X BA36X BA42X BB01 EA01 4G066 AA13A AA23B AA37 CAA FAA FAA FAA BB05C BB06A BB06B BC50A BC50B BC66A BC66B BC66C CA10 CA17 EA02Y EB18Y FA01 FB06 FB31 FB57 FC02 FC07 FC08
Claims (5)
チタンを、重量比でFe:Ti=1:99〜80:20
の範囲の比率で含有することを特徴とする脱臭組成物1. An iron hydroxide prepared from a trivalent iron salt and titanium dioxide in a weight ratio of Fe: Ti = 1: 99 to 80:20.
Deodorizing composition characterized by containing at a ratio in the range of
チタンを混合し、脱水、水洗して製造した組成物を含有
することを特徴とする請求項1記載の脱臭組成物2. The deodorizing composition according to claim 1, comprising a composition prepared by mixing titanium dioxide with iron hydroxide prepared from a trivalent iron salt, dehydrating and washing with water.
チタンを混合し、脱水、水洗した後、50〜150℃以
下の温度で加温して乾燥させて製造した組成物を含有す
ることを特徴とする請求項1または2記載の脱臭組成物3. A composition prepared by mixing titanium dioxide with iron hydroxide prepared from a trivalent iron salt, dehydrating and washing with water, and then heating and drying at a temperature of 50 to 150 ° C. or less. The deodorizing composition according to claim 1 or 2, wherein
特徴とする脱臭方法4. A deodorizing method comprising using the deodorizing composition according to claim 1.
用いることを特徴とする脱臭方法5. A deodorizing method comprising irradiating the deodorizing composition according to claim 1 with light.
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004105958A (en) * | 2002-08-30 | 2004-04-08 | Sk Kaken Co Ltd | Method for manufacturing porous photocatalyst composite powder |
JP2014516766A (en) * | 2011-04-14 | 2014-07-17 | クローノス インターナショナル インコーポレイテッド | Method for producing titanium dioxide-based photocatalyst |
JP2016189964A (en) * | 2015-03-31 | 2016-11-10 | 住化エンバイロメンタルサイエンス株式会社 | Deodorization composition and manufacturing method of deodorization composition |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6379659A (en) * | 1986-09-22 | 1988-04-09 | 村上 哲夫 | Deodorant and its production |
JPH01218635A (en) * | 1988-02-29 | 1989-08-31 | Hitachi Ltd | Deodorizing agent, its manufacturing method, deodorizing method, deodorizing apparatus and refrigeration cycle apparatus with said deodorizing apparatus |
JPH07303835A (en) * | 1994-02-07 | 1995-11-21 | Ishihara Sangyo Kaisha Ltd | Titanium oxide for photocatalyst, and manufacture of the same |
-
2000
- 2000-06-23 JP JP2000190239A patent/JP4539936B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6379659A (en) * | 1986-09-22 | 1988-04-09 | 村上 哲夫 | Deodorant and its production |
JPH01218635A (en) * | 1988-02-29 | 1989-08-31 | Hitachi Ltd | Deodorizing agent, its manufacturing method, deodorizing method, deodorizing apparatus and refrigeration cycle apparatus with said deodorizing apparatus |
JPH07303835A (en) * | 1994-02-07 | 1995-11-21 | Ishihara Sangyo Kaisha Ltd | Titanium oxide for photocatalyst, and manufacture of the same |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004105958A (en) * | 2002-08-30 | 2004-04-08 | Sk Kaken Co Ltd | Method for manufacturing porous photocatalyst composite powder |
JP2014516766A (en) * | 2011-04-14 | 2014-07-17 | クローノス インターナショナル インコーポレイテッド | Method for producing titanium dioxide-based photocatalyst |
JP2016189964A (en) * | 2015-03-31 | 2016-11-10 | 住化エンバイロメンタルサイエンス株式会社 | Deodorization composition and manufacturing method of deodorization composition |
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