JP2647756B2 - Method for producing composition having air cleaning power - Google Patents

Method for producing composition having air cleaning power

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Publication number
JP2647756B2
JP2647756B2 JP3120473A JP12047391A JP2647756B2 JP 2647756 B2 JP2647756 B2 JP 2647756B2 JP 3120473 A JP3120473 A JP 3120473A JP 12047391 A JP12047391 A JP 12047391A JP 2647756 B2 JP2647756 B2 JP 2647756B2
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JP
Japan
Prior art keywords
iron
hydroxide
aqueous solution
composition
performance
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
Application number
JP3120473A
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Japanese (ja)
Other versions
JPH04346831A (en
Inventor
多美夫 野田
洋三 竹村
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Steel Corp
Original Assignee
Nippon Steel Corp
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Filing date
Publication date
Application filed by Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP3120473A priority Critical patent/JP2647756B2/en
Publication of JPH04346831A publication Critical patent/JPH04346831A/en
Application granted granted Critical
Publication of JP2647756B2 publication Critical patent/JP2647756B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
  • Treating Waste Gases (AREA)
  • Separation Of Gases By Adsorption (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Food Preservation Except Freezing, Refrigeration, And Drying (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明はNH3やH2S等に代表さ
れる悪臭ガス類を含有する汚染空気を浄化する空気清浄
化材に関し、この空気清浄化材は、例えば家庭用の脱臭
剤として用いることができる。
The present invention relates to an air-cleaning material to clean the polluted air containing malodorous gases typified by NH 3 and H 2 S or the like, the air cleaning member, for example deodorizing household It can be used as an agent.

【0002】[0002]

【従来の技術】空気中の悪臭ガスに対しては、活性炭を
用いる吸着法や、他の香料を用いるマスキング法や、臭
気を化学反応させる化学的方法で除去、あるいは不快感
の軽減が行われている。しかし、活性炭を用いる吸着法
は脱臭性能が短期間で劣化するという問題があり、他の
香料を用いるマスキング法では香料が新たな不快感を与
えることがあり、根本的な解決策とならない。化学反応
をさせる化学的方法では例えばオゾンにより、悪臭ガス
を酸化分解する方法等があるが、過剰なオゾンが人体に
有害であるために新たな害を引き起こす。即ち、悪臭ガ
スとちょうど反応してくれる化学物質の量を制御するこ
とが困難なために不要な化学物質を発生させることにな
り、根本的な解決と成りがたい。
2. Description of the Related Art Offensive odor gases in the air are removed by an adsorption method using activated carbon, a masking method using other fragrances, or a chemical method of chemically reacting odors, or reducing the discomfort. ing. However, the adsorption method using activated carbon has a problem that the deodorizing performance deteriorates in a short period of time, and the masking method using other fragrances may give a new discomfort to the fragrances, which is not a fundamental solution. As a chemical method for causing a chemical reaction, for example, there is a method of oxidizing and decomposing a malodorous gas by using ozone. However, since excess ozone is harmful to a human body, it causes new harm. That is, since it is difficult to control the amount of the chemical substance that just reacts with the odorous gas, an unnecessary chemical substance is generated, which is hardly a fundamental solution.

【0003】それらの問題点を解決する技術として、繊
維学会誌(繊維と工業)Vol.42,No.12(198
6)、P18〜26には、第一鉄化合物とアスコルビン
酸とを水溶液状態で反応させて得られた錯体化合物が窒
素化合物系臭気ガスに対して脱臭力を有することが述べ
られている。しかし、本発明者等の知見では、この錯体
化合物は硫黄化合物系の臭気ガスに対する脱臭力が弱い
という問題点がある。また本発明者等の知見によれば、
この錯体化合物は脱臭力が比較的短期間で劣化するとい
う問題点もあった。
As a technique for solving these problems, a journal of the Textile Society of Japan (Textile and Industry), Vol. 42, No. 12 (198)
6), pages 18 to 26, describe that a complex compound obtained by reacting a ferrous compound with ascorbic acid in an aqueous solution has a deodorizing power against nitrogen compound-based odor gas. However, according to the findings of the present inventors, there is a problem that this complex compound has a weak deodorizing power against a sulfur compound-based odor gas. According to the findings of the present inventors,
This complex compound also has a problem that the deodorizing power deteriorates in a relatively short period of time.

【0004】本発明者等は、鉄、マンガン等の金属にア
スコルビン酸等を接触させてできる反応生成物を未反応
の鉄、マンガン等と共存させた組成物を発明し、先に特
願平1−280776号で特許出願した。この組成物は
安価に製造できるし、空気清浄力の劣化が極めて小さ
く、従来技術の問題点を解決するものであった。
The present inventors have invented a composition in which a reaction product obtained by contacting a metal such as iron or manganese with ascorbic acid or the like coexists with unreacted iron or manganese or the like. A patent application was filed under No. 1-280776. This composition can be manufactured at low cost, and the deterioration of the air cleaning power is extremely small, thereby solving the problems of the prior art.

【0005】[0005]

【発明が解決しようとする課題】本発明者は、特願平1
−280776号の組成物を更に広範囲に研究して成し
たもので、更に簡潔な工程で新たな空気清浄力を有する
材料の提供を課題としている。特に、脱CH3SH速度
の改善、及び脱CH3SH性能を長期間にわたって発揮
する脱臭材が望まれている。
SUMMARY OF THE INVENTION The present inventor has disclosed in Japanese Patent Application No. Hei.
No. 280776, which has been obtained by further extensive research, and aims to provide a material having a new air cleaning power in a simpler process. Particularly, deodorizing material exhibiting a long period of time improved de-CH 3 SH speed, and the de-CH 3 SH performance is desired.

【0006】[0006]

【課題を解決するための手段】本発明は、硫酸鉄または
塩酸鉄または水酸化鉄を使って、2価または3価または
両方の鉄イオンを含む水溶液を製造し、該水溶液に鉄ま
たは鉄合金を接触させて酸化雰囲気に放置して反応させ
酸化第一鉄または水酸化第一鉄を形成した後、その生成
物に硫化水素を吸着させ、硫化鉄を形成せしめることを
特徴とする空気清浄力を有する組成物の製造方法であ
る。また、請求項1の水溶液にL−アスコルビン酸、没
食子酸、タンニン酸から選ばれる少なくとも一種類の有
機酸を共存させ、水酸化カルシウム、水酸化ナトリウ
ム、水酸化カリウム等の塩基性物質を添加し、pHを2
〜11に調整したことを特徴とする空気清浄力を有する
組成物の製造方法である。
According to the present invention, there is provided iron sulfate or iron sulfate.
Using iron chloride or iron hydroxide, divalent or trivalent or
An aqueous solution containing both iron ions is produced, and the aqueous solution is
Or an iron alloy is brought into contact and left in an oxidizing atmosphere to react.
After the formation of ferrous oxide or ferrous hydroxide, its formation
Adsorb hydrogen sulfide on the material and form iron sulfide
A method for producing a composition having a characteristic air cleaning power.
You. Further, aqueous L- ascorbic acid of claim 1, gallic acid, the coexistence of at least one organic acid selected from tannic acid, added water calcium oxide, sodium hydroxide, a basic substance such as potassium hydroxide And adjust the pH to 2
A method for producing a composition having air cleaning power, characterized in that the composition was adjusted to ~ 11.

【0007】[0007]

【作用】本発明者等の研究によれば、NH3や(CH3)3
N等の窒素系ガスは酸と金属の反応生成物である金属錯
体や酸化鉄に非常に良く吸着するが、H2Sガスは吸着
力が弱い。その一つの解決方法は、本発明者等が特願昭
63−273195号に記述しているような金属錯体に
固体塩基を配する方法である。しかし、その後の研究
で、H2S等の酸性ガスの吸着力の強い物質は金属鉄が
水溶液に溶解して生成する水酸化第一鉄及び酸化第一鉄
であることを突き止めた。一般に酸化鉄がH2Sの分解
作用を有することは知られているが、常温では反応速度
が遅く、200℃以上の雰囲気に保つ必要がある。し
か、水酸化第一鉄や酸化第一鉄は常温でもH2Sの分解
速度が極めて速く、脱臭材として充分に活用できること
が発明者等の研究により明らかになった。
According to the study of the present inventors, NH 3 and (CH 3 ) 3
A nitrogen-based gas such as N adsorbs very well to a metal complex or an iron oxide which is a reaction product of an acid and a metal, whereas an H 2 S gas has a weak adsorbing power. One solution is to dispose a solid base on a metal complex as described in Japanese Patent Application No. 63-273195 by the present inventors. However, in subsequent studies, it was determined that the substances having strong adsorption power for acidic gas such as H 2 S were ferrous hydroxide and ferrous oxide formed by dissolving metallic iron in an aqueous solution. It is generally known that iron oxide has an H 2 S decomposing action, but the reaction rate is slow at room temperature, and it is necessary to keep the atmosphere at 200 ° C. or higher. However, studies by the inventors have revealed that ferrous hydroxide and ferrous oxide have an extremely high decomposition rate of H 2 S even at room temperature and can be sufficiently utilized as a deodorizing material.

【0008】しかし、一般に水酸化第一鉄や酸化第一鉄
は大気中に放置することにより簡単にマグネタイト、ヘ
マタイト、ゲーサイト等に酸化が進み、常温でのH2
分解性能を無くしてしまうので実用的な材料を作るため
には、酸化第一鉄を効率良く生成させることと、更には
生成した酸化第一鉄が酸化第二鉄に酸化が進んでしまわ
ないように安定化する方法が必要である。また、酸化第
一鉄のみでは脱NH3性能、脱CH3SH性能が無いの
で、他の材料との共存を成立させる条件も必要となる。
However, in general, ferrous hydroxide and ferrous oxide are easily oxidized to magnetite, hematite, goethite, etc. by leaving them in the air, and H 2 S at room temperature.
In order to make a practical material because it loses decomposition performance, it is necessary to efficiently produce ferrous oxide and furthermore, to prevent the generated ferrous oxide from oxidizing to ferric oxide There is a need for a method of stabilization. Further, since ferrous oxide alone does not have NH 3 removal performance or CH 3 SH removal performance, conditions for establishing coexistence with other materials are also required.

【0009】脱H2S性能が良くなると脱CH3SH性能
も良くなるのは−SH基のHがH2Sと同様な性質を持
つためと考えられる。従って水酸化第一鉄、酸化第一鉄
を効果的に生成せしめることが有効であることが推察で
きる。しかし、脱H2S性能が良いことが脱CH3SH性
能も良いことの充分条件ではないことが、本発明者等の
研究で判明した。例えば、鉄とL−アスコルビン酸水溶
液を空気中で接触させ、生成した錯塩と鉄の共存物を1
50℃で24時間加熱処理した反応生成物は酸化第一鉄
を含み、極めて脱H2S性能が良いが脱CH3SH性能が
やや劣る。脱CH3SH性能を改善するために種々の対
策を調査研究した結果、2価または3価の鉄イオンを含
む水溶液のpHを2〜11に調整し、その水溶液を金属
鉄と接触させて大気中で放置乾燥させると効率良く鉄表
面に酸化第一鉄が生じ、極めて脱H2S性能の優れた組
成物が生じる。
[0009] de H 2 S performance and is improved de-CH 3 SH performance of even better is -SH group H is considered to have properties similar to H 2 S. Therefore, it can be inferred that it is effective to effectively produce ferrous hydroxide and ferrous oxide. However, studies by the present inventors have revealed that good H 2 S removal performance is not a sufficient condition for good CH 3 SH removal performance. For example, iron and an aqueous solution of L-ascorbic acid are brought into contact with each other in the air, and the resulting complex salt and iron coexist
The reaction product heat-treated at 50 ° C. for 24 hours contains ferrous oxide, and has extremely good H 2 S removal performance but slightly inferior CH 3 SH performance. As a result of researching and studying various measures to improve the de-CH 3 SH performance, the pH of an aqueous solution containing divalent or trivalent iron ions was adjusted to 2 to 11, and the aqueous solution was brought into contact with metallic iron to form an atmosphere. When left to dry in a medium, ferrous oxide is efficiently formed on the iron surface, and a composition having extremely excellent H 2 S removal performance is formed.

【0010】pHが低過ぎると鉄と酸の錯体が過剰に生
成し、保護膜を形成してしまうため、酸化第一鉄、水酸
化第一鉄の形成が抑えられ窒素化合物系の悪臭除去能力
は高まるが硫化水素の除去能力が低下する。逆にpHが
高過ぎると酸化第一鉄、水酸化第一鉄の形成が多くなり
硫化水素の除去能力は高まるが窒素化合物系の悪臭除去
能力は弱まる。従って、総合的な空気清浄力を持たせる
ためにはpHを2〜11に調整する必要がある。
[0010] If the pH is too low, the complex of iron and acid is excessively formed and a protective film is formed. Therefore, the formation of ferrous oxide and ferrous hydroxide is suppressed, and the nitrogen compound-based odor removing ability is suppressed. But the ability to remove hydrogen sulfide decreases. Conversely, if the pH is too high, the formation of ferrous oxide and ferrous hydroxide increases and the ability to remove hydrogen sulfide increases, but the odor removing ability of the nitrogen compound system decreases. Therefore, it is necessary to adjust the pH to 2 to 11 in order to have comprehensive air cleaning power.

【0011】pHの最適点は水溶液中の鉄イオン濃度、
2価と3価の比率、接触させる金属鉄の組成によって変
化する要素を持っている。また、水溶液と金属鉄、合金
鉄類を反応させる雰囲気温度、湿度、酸素分圧によって
も最適なpHは変化するが、pHを上記範囲に制御すれ
ば実用的には問題の無い脱臭能力を有する組成物が得ら
れる。それらの組成物の特性を更に研究した結果、それ
らに硫化水素が吸着すると、硫化水素を吸着させる前の
組成物に比較して極めて脱CH3SH性能の優れた組成
物に変化することを突き止めた。
The optimum point of the pH is the concentration of iron ions in the aqueous solution,
It has factors that change depending on the ratio of divalent to trivalent and the composition of the metallic iron to be brought into contact. In addition, although the optimum pH varies depending on the ambient temperature, humidity, and oxygen partial pressure at which the aqueous solution reacts with metallic iron and ferroalloys, if the pH is controlled within the above range, there is practically no problem in deodorizing ability. A composition is obtained. As a result of further study of the properties of these compositions, they found that when hydrogen sulfide was adsorbed on them, the composition changed to a composition with extremely excellent CH 3 SH performance compared to the composition before adsorbing hydrogen sulfide. Was.

【0012】また、水溶液にL−アスコルビン酸、没食
子酸、タンニン酸から選ばれる少なくとも一種類の有機
酸を共存させ、中和剤として水酸化カルシウム、水酸化
ナトリウム等を使用すると脱NH3性能を良くする鉄錯
(鉄合金錯体を含む)と酸化第一鉄が同時に形成し、
脱NH3、脱(CN33N、脱H2S性能の全てに優れた
材料を製造できることを突き止めた。また、それにH2
Sを吸着させると脱NH3、脱(CN33N、脱H2S性
能を維持しながら、更に脱CH3SH性能が飛躍的に向
上することも突き止めた。
[0012] In addition, L- ascorbic acid, death diet aqueous solution
At least one kind of organic acid selected from citric acid and tannic acid
When an acid coexists and calcium hydroxide, sodium hydroxide, or the like is used as a neutralizing agent, an iron complex (including an iron alloy complex) and ferrous oxide that improve the deNH 3 performance are simultaneously formed,
It has been found that a material excellent in all of the NH 3 removal, the (CN 3 ) 3 N, and the H 2 S removal performance can be produced. In addition, H 2
It has also been found that when S is adsorbed, the CH 3 SH performance is dramatically improved while maintaining the NH 3 , (CN 3 ) 3 N, and H 2 S performance.

【0013】更に、そのようにして製造した材料は金属
鉄が共存することによって性能が長期間維持できるこ
と、かつ金属鉄または硫化鉄の表面を鉄錯体、酸化鉄、
硫化鉄が覆う構造を形成することによってより長期間に
わたって脱臭性能を維持できることを突き止め、本発明
を完成させるに至った。
Further, the material thus produced can maintain its performance for a long time due to the coexistence of metallic iron, and the surface of metallic iron or iron sulfide has an iron complex, iron oxide,
The inventors have found that the formation of the structure covered with iron sulfide can maintain the deodorizing performance for a longer period of time, and have completed the present invention.

【0014】硫化水素を吸着させることによる脱CH3
SH性能の改善効果のメカニズムは充分には解明できて
いないが、脱硫化水素性能は繰り返し使用しても劣化が
殆ど見られないこと、硫化水素吸着後の組成物の分析結
果より吸着した硫化水素は大半が分解していること、脱
臭フィルターの残留硫黄分が吸着した硫化水素の硫黄分
にほぼ匹敵する量であることから推定して、この組成物
に硫化鉄が生じてCH3SHの吸着性能を大幅に改善し
ているものと考えられる。次に本発明の実施例について
述べる。
Removal of CH 3 by adsorbing hydrogen sulfide
Although the mechanism of the effect of improving the SH performance has not been fully elucidated, the hydrogen sulfide desorbing performance shows almost no deterioration even after repeated use. Is estimated to be mostly decomposed and that the residual sulfur content of the deodorizing filter is almost equal to the sulfur content of the adsorbed hydrogen sulfide. This composition produces iron sulfide and adsorbs CH 3 SH. It is considered that the performance has been greatly improved. Next, examples of the present invention will be described.

【0015】[0015]

【実施例】目の粗さが20PPIのウレタンフォームに、
10μアンダーの微細銑鉄粉末を塗着して非酸化雰囲気
で1150℃×2時間焼成して鉄多孔体を製造した。一
部の鉄多孔体には20μアンダーの微細硫化鉄粉末、ま
たは酸化コバルト微細粉末を混合して約10%の硫黄を
含有する鉄多孔体製造して使用した。1個のサイズは約
90mm×80mm×10mmで重量は約40gであっ
た。
[Example] Urethane foam with a coarseness of 20 PPI
A fine pig iron powder of 10 μm under was applied and fired at 1150 ° C. for 2 hours in a non-oxidizing atmosphere to produce a porous iron body. Some iron porous bodies were mixed with a fine iron sulfide powder of under 20 μm or a fine powder of cobalt oxide to produce and use an iron porous body containing about 10% sulfur. One piece was about 90 mm x 80 mm x 10 mm and weighed about 40 g.

【0016】その鉄多孔体を硫酸第一鉄、硫酸第二鉄、
塩化第一鉄、塩化第二鉄、タンニン酸、L−アスコルビ
ン酸、Ca(OH)2粉末、水酸化ナトリウムを適宜組合
せ混合して製造した水溶液に浸漬し、大気中で約2週間
乾燥させた。同一の水溶液で2枚の脱臭フィルターを製
造しておき、各1枚についてはそのまま脱臭性能を評価
し、各1枚についてはH2Sを予め100cc吸着させ
て24時間放置してから脱臭性能を評価した。具体的な
配合比については代表的な例を表1に示し、それらに対
応した水溶液のpHとそれぞれの脱臭性能評価結果につ
いては表2に示した。
The iron porous material is made of ferrous sulfate, ferric sulfate,
It was immersed in an aqueous solution produced by appropriately mixing and mixing ferrous chloride, ferric chloride, tannic acid, L-ascorbic acid, Ca (OH) 2 powder, and sodium hydroxide, and dried in the air for about 2 weeks. . Two deodorizing filters were manufactured using the same aqueous solution, and the deodorizing performance of each one was evaluated as it was. For each one, 100 cc of H 2 S was adsorbed in advance and allowed to stand for 24 hours. evaluated. Table 1 shows typical examples of specific mixing ratios, and Table 2 shows the pH of the aqueous solution corresponding to them and the results of evaluating the deodorizing performance.

【0017】[0017]

【表1】 [Table 1]

【0018】[0018]

【表2】 [Table 2]

【0019】脱臭性能は40リツトルの密封容器に40
0リットル/分の送風能力を持つ循環ファンを設置し、
図1に示した要領でNH3、(CH3)3N、H2S、CH3
SHの除去性能を調べた。初期値はNH3は1000p
pm、(CH3)3Nは100ppm、H2Sは500pp
m、CH3SHは50ppmに設定して各10分後〜3
0分後の残存濃度を測定し除去率を脱臭率として求め
た。脱CH3SH性能はH2Sの吸着により大幅に改善さ
れ、他の脱臭性能は殆ど影響を受けていない。その後の
繰り返し脱CH3SH試験でも改善効果が持続すること
が確認できた。
The deodorizing performance is 40 liters in a sealed container.
Install a circulation fan with a blowing capacity of 0 liters / minute,
As shown in FIG. 1, NH 3 , (CH 3 ) 3 N, H 2 S, CH 3
The SH removal performance was examined. The initial value is NH 3 is 1000p
pm, (CH 3 ) 3 N is 100 ppm, H 2 S is 500 pp
m and CH 3 SH were set to 50 ppm, and after 10 minutes,
The residual concentration after 0 minute was measured, and the removal rate was determined as the deodorization rate. The CH 3 SH performance was greatly improved by the adsorption of H 2 S, and the other deodorization performance was hardly affected. In the subsequent repeated CH 3 SH test, it was confirmed that the improvement effect was maintained.

【0020】[0020]

【発明の効果】本発明により、脱CH3SH性能の高い
空気清浄化物、脱臭フィルターが製造できる。
According to the present invention, an air-purified product and a deodorizing filter having high CH 3 SH performance can be manufactured.

【図面の簡単な説明】[Brief description of the drawings]

図1は脱臭性能を評価する試験装置の構造を示す説明図
である。
FIG. 1 is an explanatory view showing the structure of a test device for evaluating the deodorizing performance.

【符号の説明】[Explanation of symbols]

1:密閉容器、 2:循環ファン、 3:脱臭フィルタ
ー、 4:ガス導入口、 5:ガスサンプル採取口、
6:ガス循環の方向。
1: closed container, 2: circulation fan, 3: deodorizing filter, 4: gas inlet, 5: gas sampling port,
6: Direction of gas circulation.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 B01D 53/38 B01D 53/34 116D 53/77 (56)参考文献 特開 平4−219136(JP,A) 特開 平4−220257(JP,A) 特開 平4−235736(JP,A) 特開 平4−219137(JP,A) 特開 平3−174216(JP,A) 特開 昭55−34164(JP,A) 特開 昭62−254840(JP,A)──────────────────────────────────────────────────の Continuation of the front page (51) Int.Cl. 6 Identification number Agency reference number FI Technical display location B01D 53/38 B01D 53/34 116D 53/77 (56) References JP-A-4-219136 (JP) JP-A-4-220257 (JP, A) JP-A-4-235736 (JP, A) JP-A-4-219137 (JP, A) JP-A-3-174216 (JP, A) JP 55-34164 (JP, A) JP-A-62-254840 (JP, A)

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】硫酸鉄または塩酸鉄または水酸化鉄を使っ
て、2価または3価または両方の鉄イオンを含む水溶液
を製造し、該水溶液に鉄または鉄合金を接触させて酸化
雰囲気に放置して反応させ酸化第一鉄または水酸化第一
鉄を形成した後、その生成物に硫化水素を吸着させ、硫
化鉄を形成せしめることを特徴とする空気清浄力を有す
る組成物の製造方法。
1. Use iron sulfate, iron chloride or iron hydroxide
Aqueous solution containing divalent or trivalent or both iron ions
Oxidized by contacting iron or iron alloy with the aqueous solution
Leave it in the atmosphere and let it react to ferrous oxide or hydroxide
After forming iron, the product adsorbs hydrogen sulfide and
A method for producing a composition having air cleaning power, characterized in that iron fossil is formed .
【請求項2】請求項1の水溶液にL−アスコルビン酸、
没食子酸、タンニン酸から選ばれる少なくとも一種類の
有機酸を共存させ、水酸化カルシウム、水酸化ナトリウ
ム、水酸化カリウム等の塩基性物質を添加し、pHを2
〜11に調整したことを特徴とする空気清浄力を有する
組成物の製造方法。
2. The aqueous solution according to claim 1, wherein L-ascorbic acid is added to the aqueous solution.
At least one of gallic acid and tannic acid
Organic hydroxide, calcium hydroxide, sodium hydroxide
And a basic substance such as potassium hydroxide to adjust the pH to 2
A process for producing a composition having air cleaning power, characterized in that the composition is adjusted to ~ 11 .
JP3120473A 1991-05-24 1991-05-24 Method for producing composition having air cleaning power Expired - Lifetime JP2647756B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3120473A JP2647756B2 (en) 1991-05-24 1991-05-24 Method for producing composition having air cleaning power

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3120473A JP2647756B2 (en) 1991-05-24 1991-05-24 Method for producing composition having air cleaning power

Publications (2)

Publication Number Publication Date
JPH04346831A JPH04346831A (en) 1992-12-02
JP2647756B2 true JP2647756B2 (en) 1997-08-27

Family

ID=14787047

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3120473A Expired - Lifetime JP2647756B2 (en) 1991-05-24 1991-05-24 Method for producing composition having air cleaning power

Country Status (1)

Country Link
JP (1) JP2647756B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101404974B (en) * 2006-03-22 2013-12-25 高砂香料工业株式会社 Deodorant composition
JP5101557B2 (en) * 2009-04-10 2012-12-19 花王株式会社 Deodorants
CA2744780C (en) * 2011-06-23 2014-01-14 Willard E. Wood A material and method for absorbing unwanted or target substances from a gas or vapor phase
JP7380182B2 (en) * 2019-12-20 2023-11-15 東ソー株式会社 Hydrogen sulfide scavenger

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2652023B1 (en) * 1989-06-16 1991-10-31 Air Liquide CONTINUOUS CASTING DISTRIBUTOR OF STEEL.

Also Published As

Publication number Publication date
JPH04346831A (en) 1992-12-02

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