JPH07812A - Production of air purifier - Google Patents

Production of air purifier

Info

Publication number
JPH07812A
JPH07812A JP5165924A JP16592493A JPH07812A JP H07812 A JPH07812 A JP H07812A JP 5165924 A JP5165924 A JP 5165924A JP 16592493 A JP16592493 A JP 16592493A JP H07812 A JPH07812 A JP H07812A
Authority
JP
Japan
Prior art keywords
clay mineral
layered clay
silicic acid
hydrazine
air
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
Application number
JP5165924A
Other languages
Japanese (ja)
Other versions
JP2949455B2 (en
Inventor
Tamio Noda
多美夫 野田
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
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP5165924A priority Critical patent/JP2949455B2/en
Publication of JPH07812A publication Critical patent/JPH07812A/en
Application granted granted Critical
Publication of JP2949455B2 publication Critical patent/JP2949455B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Treating Waste Gases (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)

Abstract

PURPOSE:To remove CH3CHO(acetaldehyde), a main component of tobacco smoke. CONSTITUTION:The subject air purifier is produced by a method wherein a double salt of an Al metal salt and N2H4 is on the supported surface of particles of a laminar clay mineral based on silicate with a specific surface area of 50m<2>/g min. The laminar clay mineral based on silicate is treated previously using an acid so that the mineral is allowed to bleed out. The laminar clay mineral based on silicate is thermally treated at 400 deg. to 700 deg.C in advance.

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、タバコの臭いの主成分
であるCH3CHO(アセトアルデヒド)を除去する空
気清浄化物の製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing an air-purified product which removes CH 3 CHO (acetaldehyde) which is a main component of tobacco odor.

【0002】本発明の空気清浄化物は、例えば、家庭用
の脱臭剤、乗物の脱臭剤あるいは空気調整装置に内蔵す
る脱臭剤として用いることができる。
The air-purified product of the present invention can be used, for example, as a household deodorant, a vehicle deodorant, or a deodorant incorporated in an air conditioner.

【0003】[0003]

【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。
2. Description of the Related Art Odorous gas in the air is removed by an adsorption method using activated carbon, a masking method using another fragrance, or a chemical method of chemically reacting an odor, or reducing discomfort. ing.

【0004】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、また可燃性の為
火災の原因となりやすい欠点がある。
However, the adsorption method using activated carbon has a problem that the deodorizing performance is deteriorated in a short period of time, and it is flammable, which causes a fire.

【0005】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。
Masking methods using other fragrances are not a fundamental solution because the fragrance may give new discomfort.

【0006】化学反応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為に新たな害を引き起こ
す。
As a chemical method of chemically reacting, for example, there is a method of oxidizing and decomposing a malodorous gas with ozone, but excessive ozone is harmful to the human body and causes new harm.

【0007】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為に不要な化学物
質を発生させることになり、根本的な解決と成りがた
い。
That is, since it is difficult to control the amount of the chemical substance that reacts with the malodorous gas, an unnecessary chemical substance is generated, and it is difficult to achieve a fundamental solution.

【0008】特に、タバコの臭いの主成分であるCH3
CHOの除去については活性炭でもとれ難く、特開昭5
6―53744号のように活性炭に化学反応性の高いア
ニリンを添着させて除去性能を改善したり、特開昭56
―95319号のようにフェニルヒドラジンと化学反応
させて除去する等様々な対策が採られてきたが、本発明
者等の知見によれば化学反応性物質自体の悪臭が問題と
なったり、化学物質の活性維持が困難で寿命が短い等の
弱点があり根本的な解決とは成りがたかった。
In particular, CH 3 which is the main component of cigarette odor
For removal of CHO, activated carbon is difficult to remove.
As in 6-53744, aniline having a high chemical reactivity is attached to activated carbon to improve the removal performance, and JP-A-56-56
Although various countermeasures such as chemical reaction with phenylhydrazine to remove the same have been adopted as in No. 95319, the present inventors have found that the odor of the chemically reactive substance itself becomes a problem, It is difficult to maintain the activity of the syrup and has a weakness such as a short life.

【0009】本発明者等は特に脱CH3CHO速度の改
善、及び脱CH3CHO性能を長期間にわたって発揮す
る脱臭剤を発明し、先に特願平04―018173号で
提案した。即ち、金属塩とヒドラジンの複塩を製造する
ものである。
The present inventors have invented a deodorizing agent which improves the de-CH 3 CHO rate and exerts the de-CH 3 CHO performance for a long period of time, and has previously proposed it in Japanese Patent Application No. 04-018173. That is, a double salt of a metal salt and hydrazine is produced.

【0010】ヒドラジンは還元力の強い反応性の高い物
質であり、また自己分解性も強く自然にNH3やN2、H
2O等に分解あるいは酸化されてしまう物質であるが金
属塩との複塩とすることにより化学的に安定性を増し、
より強い活性を持つガス類と反応するまでヒドラジンが
安定していることができる。
[0010] Hydrazine is a highly reactive substance having a strong reducing power, and also has a strong self-decomposability and naturally NH 3 , N 2 , and H.
Although it is a substance that decomposes or oxidizes into 2 O etc., its chemical stability is increased by using a double salt with a metal salt,
The hydrazine can be stable until it reacts with more active gases.

【0011】より強い活性を持つガス類としてはCH3
CHO等のアルデヒド類があり、ヒドラジンとの化学吸
着力が強いため複塩に取り込まれてしまい空気の清浄化
が可能となる。
CH 3 is a gas having stronger activity.
There are aldehydes such as CHO, and since they have strong chemical adsorption with hydrazine, they are taken into double salts and the air can be cleaned.

【0012】上記金属塩とヒドラジンとの複塩を効果的
に働かせる為には比表面積を大きく保つ必要があり、担
体としては鎖状珪酸マグネシウムを始めとする層状粘土
鉱物が優れていることも見出した。
It has been found that the specific surface area must be kept large in order to effectively work the double salt of the above metal salt and hydrazine, and that layered clay minerals such as chain magnesium silicate are excellent as carriers. It was

【0013】これら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改
善するものであった。
These compositions can be manufactured at low cost, and the deterioration of the air cleaning power is extremely small, and the problems of the prior arts have been solved.

【0014】しかし、担持体である、例えば、鎖状珪酸
マグネシウムの安定的な入手については若干の不安があ
った。
However, there was some concern about the stable availability of the carrier, for example, chain-shaped magnesium silicate.

【0015】鎖状珪酸マグネシウム自体は天然の粘土鉱
物であり合成粘土等に比較すればはるかに安価である
が、国内では工業的に採算の合う産地は発見されておら
ず、輸入に頼らざるを得ない粘土鉱物であることから、
日本国内でも安定的に入手できる担持体材料が望まれて
いた。
[0015] Chain-shaped magnesium silicate itself is a natural clay mineral and is much cheaper than synthetic clay, but no industrially profitable production area has been found in Japan, and it is necessary to rely on imports. Because it is a clay mineral that you do not get,
A carrier material that can be stably obtained in Japan has been desired.

【0016】また、上記金属塩とヒドラジンとの複塩を
用いて、脱臭性能の高い脱臭剤を安価に製造するために
はバインダーを添加することなく成形、保形できること
が必須となる。
Further, in order to inexpensively produce a deodorant having a high deodorizing performance by using the double salt of the above metal salt and hydrazine, it is essential that the compound can be molded and shaped without adding a binder.

【0017】上記金属塩とヒドラジンの混合水溶液と層
状粘土鉱物を混練成形後に乾燥処理を施した脱臭剤の成
形体は、特定雰囲気下において上記条件を満足するもの
であったが、水蒸気による結露が発生すると成形体が崩
壊してしまうという解膠特性を解決することが望まれて
いた。
The deodorant moldings obtained by kneading and molding the mixed aqueous solution of the metal salt and hydrazine and the layered clay mineral and then performing the drying treatment satisfy the above conditions under a specific atmosphere, but dew condensation due to water vapor occurs. It was desired to solve the deflocculating property that the molded body collapses when it occurs.

【0018】[0018]

【発明が解決しようとする課題】本発明は、担持体とし
ての組成物の種類を拡大し、一層の安定的な原料の入手
ルートを確保すると共に、温度、湿度の変化に対して広
範囲に対応できる材料の提供を目的としている。
DISCLOSURE OF THE INVENTION The present invention expands the types of compositions as a carrier, secures a more stable route of obtaining raw materials, and copes with a wide range of changes in temperature and humidity. The purpose is to provide materials that can.

【0019】[0019]

【課題を解決するための手段】本発明は、比表面積が5
0m2/g以上の、珪酸を主体とする層状粘土鉱物の粒
子表面に、Alの金属塩とN24の複塩を担持すること
を特徴とする空気清浄化物の製造方法である。
The present invention has a specific surface area of 5
A method for producing an air-purified product, characterized in that a metal salt of Al and a double salt of N 2 H 4 are carried on the surface of particles of a layered clay mineral mainly composed of silicic acid of 0 m 2 / g or more.

【0020】また本発明は、上記珪酸を主体とする層状
粘土鉱物を、予め酸による溶出処理をすることを特徴と
する請求項1記載の空気清浄化物の製造方法である。
Further, the present invention is the method for producing an air-purified product according to claim 1, wherein the layered clay mineral mainly composed of silicic acid is previously subjected to an elution treatment with an acid.

【0021】また本発明は、上記珪酸を主体とする層状
粘土鉱物を、予め400℃〜700℃に加熱処理するこ
とを特徴とする請求項1又は2記載の空気清浄化物の製
造方法である。
Further, the present invention is the method for producing an air-purified product according to claim 1 or 2, wherein the layered clay mineral mainly composed of silicic acid is preheated to 400 to 700 ° C.

【0022】[0022]

【作用】上記各種金属塩ヒドラジン複塩の担持体として
様々な粘土鉱物について評価を行ったところ、Alの金
属塩ヒドラジン複塩を選択使用することにより、該複塩
の化学的安定性を阻害することなく空気清浄化物として
の性能を発揮させる担持体としての機能に共通する特徴
として、N2吸着法測定による比表面積が50m2/g以
上と大きく、ミクロ構造体として見た表層が珪酸ででき
ている層状粘土鉱物が使用できることを見出し、本発明
を完成させるに到った。
When various clay minerals were evaluated as a carrier of the above various metal salt hydrazine double salts, the chemical stability of the metal salt of Al was inhibited by selectively using the metal hydrazine double salt of Al. The characteristics common to the function as a carrier that exerts the performance as an air purifying substance without any special feature are that the specific surface area measured by N 2 adsorption method is as large as 50 m 2 / g or more, and the surface layer seen as a microstructure is made of silicic acid. It has been found that the layered clay minerals used can be used, and the present invention has been completed.

【0023】上記珪酸を主体とする層状粘土鉱物の粒子
の比表面積は組成物の種類によって異なっており、該層
状粘土鉱物の粒子表面にAlの金属塩ヒドラジン複塩を
担持させることでそれぞれ脱臭性能は発現するものの、
実用的なレベルでの脱臭性能を発現させるためには、そ
の比表面積を50m2/g以上とすることが必須とな
り、比表面積は大きくなる程より高い脱臭性能が得られ
る。
The specific surface area of the particles of the layered clay mineral mainly composed of silicic acid varies depending on the kind of the composition, and the deodorizing performance is respectively improved by supporting the metal salt hydrazine double salt of Al on the particle surface of the layered clay mineral. Is expressed,
In order to express the deodorizing performance at a practical level, it is essential that the specific surface area is 50 m 2 / g or more, and the larger the specific surface area, the higher the deodorizing performance can be obtained.

【0024】上記珪酸を主体とする層状粘土鉱物には不
可避的に珪酸以外の金属酸化物が介在しており、表層に
介在する珪酸以外の金属酸化物、具体的には鉄、アルミ
ニウム、マグネシウムはAlの金属塩ヒドラジン複塩の
安定性を損なう作用を持っている。
The layered clay mineral mainly composed of silicic acid inevitably contains metal oxides other than silicic acid, and the metal oxides other than silicic acid existing in the surface layer, specifically iron, aluminum and magnesium, are It has a function of impairing the stability of the metal salt of hydrazine double salt of Al.

【0025】特に、鉄酸化物のヒドラジンに対する影響
が大きく、例えば、鉱物粒子の表面に鉄酸化物が5%以
上顕在すると、その量に応じてヒドラジンが消費されて
しまう。
In particular, the influence of iron oxides on hydrazine is great, and for example, when iron oxides of 5% or more appear on the surface of mineral particles, hydrazine is consumed depending on the amount.

【0026】従って、鉱物粒子の表面に顕在する鉄酸化
物量は5%未満に低減することが望ましい。
Therefore, it is desirable to reduce the amount of iron oxide manifested on the surface of the mineral particles to less than 5%.

【0027】アルミニウム酸化物、マグネシウム酸化物
のヒドラジンに対する影響は鉄酸化物より小さいが、鉱
物粒子の表面に顕在するアルミニウム酸化物量は25%
未満、マグネシウム酸化物量は30%未満に低減するこ
とが望ましい。
The effect of aluminum oxide and magnesium oxide on hydrazine is smaller than that of iron oxide, but the amount of aluminum oxide manifested on the surface of mineral particles is 25%.
Less, and the amount of magnesium oxide is desirably reduced to less than 30%.

【0028】上記したように層状粘土鉱物の粒子表層に
介在する珪酸以外の金属酸化物の介在量は少ない程、ヒ
ドラジンの消耗が抑制されるものであるが、その組成物
の産地、種類によってまちまちである。
As described above, the smaller the amount of metal oxides other than silicic acid present in the surface layer of the particles of the layered clay mineral, the more the consumption of hydrazine is suppressed, but it varies depending on the origin and type of the composition. Is.

【0029】本発明は上記珪酸を主体とする層状粘土鉱
物を、予め酸、例えば、硫酸による溶出処理をすること
によって、表層部に介在する珪酸を溶出することなく、
鉄、アルミニウム、マグネシウム等の不純金属酸化物を
溶出、除去するので、上記複塩の脱臭性能を持続性を改
善できた。
According to the present invention, the layered clay mineral mainly composed of silicic acid is preliminarily subjected to an elution treatment with an acid, for example, sulfuric acid, so that silicic acid existing in the surface layer portion is not eluted.
Since the impure metal oxides such as iron, aluminum and magnesium are eluted and removed, the deodorizing performance of the above double salt can be improved.

【0030】上記珪酸を主体とする層状粘土鉱物の酸に
よる不純金属酸化物の溶出処理は、容器に所定量の層状
粘土鉱物と1〜2Nの硫酸水溶液を装入した後、攪拌し
て充分混合し、例えば、24時間静置することによっ
て、該粘土粒子の表層部に介在する鉄、アルミニウム、
マグネシウム等の金属酸化物が溶出できる。
In the elution treatment of the impure metal oxide with the acid of the layered clay mineral mainly composed of silicic acid, the container is charged with a predetermined amount of the layered clay mineral and an aqueous solution of 1 to 2N, and then stirred and sufficiently mixed. Then, for example, by allowing it to stand for 24 hours, iron, aluminum intervening in the surface layer of the clay particles,
Metal oxides such as magnesium can be eluted.

【0031】また、上記珪酸を主体とする層状粘土鉱物
の酸による溶出処理によって、該鉱物の粒子の表層に形
成されるミクロのクレータは該粒子の比表面積を増すの
で、酸による溶出処理時間を調節することによって上記
層状粘土鉱物の比表面積を任意に改善できる。
In addition, since the micro craters formed on the surface layer of the particles of the mineral increase the specific surface area of the particles by the elution treatment of the layered clay mineral mainly composed of silicic acid with the acid, the elution time with the acid is increased. By adjusting, the specific surface area of the layered clay mineral can be arbitrarily improved.

【0032】例えば、タルクの粒子の比表面積は約30
2/gであるが、上記酸処理を24時間行うことによ
って50m2/g以上に高めることができるものであ
る。かかる粒子群を担持体とする空気清浄化物の脱臭性
能は確実に高まる。
For example, the specific surface area of talc particles is about 30.
is a m 2 / g, in which the acid treatment can be increased to more than 50 m 2 / g by performing 24 hours. The deodorizing performance of an air-purified product having such a particle group as a carrier is certainly enhanced.

【0033】また本発明は、上記珪酸を主体とする層状
粘土鉱物を、予め400℃〜700℃に加熱処理するの
で、結晶水を分解逸散でき、該粒子とAlの金属塩とヒ
ドラジンの混合水溶液とを混練、成形後の水和反応およ
び上記複塩そのもののバインダー効果による結合が進
み、その結果、その後、水と接触しても崩壊が起こらな
いものと推定できる。
Further, according to the present invention, since the layered clay mineral mainly composed of silicic acid is preheated to 400 to 700 ° C., the water of crystallization can be decomposed and dissipated, and the particles, the metal salt of Al and hydrazine are mixed. It can be presumed that the hydration reaction after the kneading with the aqueous solution, the hydration reaction after the molding, and the binding due to the binder effect of the double salt itself proceed, and as a result, the disintegration does not occur even when the water is subsequently contacted.

【0034】この層状粘土鉱物の加熱処理において、い
ま一つ重要なことは該鉱物の再結晶、焼結に至らない温
度とすることであり、このことによって、鉱物粒子の比
表面積を小さくするという問題が解消できる。
In the heat treatment of this layered clay mineral, another important thing is to set the temperature at which the recrystallization and sintering of the mineral are not reached, and this makes it possible to reduce the specific surface area of the mineral particles. The problem can be resolved.

【0035】上記珪酸を主体とする層状粘土鉱物の加熱
による結晶水の分解温度及び再結晶、焼結温度は鉱物の
組成によって異なるので、組成毎に加熱温度を選択す
る。
Since the decomposition temperature, recrystallization and sintering temperature of the water of crystallization by heating the layered clay mineral mainly composed of silicic acid differ depending on the composition of the mineral, the heating temperature is selected for each composition.

【0036】この加熱温度が400℃未満になると、鉱
物の結晶水が充分に分解されないため、上記水和反応に
よる結合力が小さく、水と接触した際に、成形体の崩壊
がおきる。
When the heating temperature is lower than 400 ° C., the water of crystallization of minerals is not sufficiently decomposed, so that the binding force due to the hydration reaction is small and the molded product collapses when contacted with water.

【0037】逆に、加熱温度が700℃を越えると結晶
水の分解は完全に進行するが、再結晶が進んで該粒子の
比表面積が小さくなり、脱臭剤の担持効果が低減する。
On the contrary, if the heating temperature exceeds 700 ° C., the water of crystallization is completely decomposed, but the recrystallization proceeds to reduce the specific surface area of the particles, and the effect of supporting the deodorant is reduced.

【0038】[0038]

【実施例1】タルク、カオリナイト、セピオライト、ベ
ントナイト、活性ベントナイト、モンモリロナイト、活
性モンモリロナイト、アルミナ、活性アルミナ、シリカ
ゲル、合成ゼオライト、コージェライト、ジルコニア、
チタニア等の鉱物微粉末に硫酸アルミニウムとヒドラジ
ンの混合水溶液を混ぜて混練し、厚さ1mmの板状に成
形して100℃で6時間、室温で2週間乾燥した後、ア
セトアルデヒドの平衡濃度吸着容量を測定した。
Example 1 Talc, kaolinite, sepiolite, bentonite, activated bentonite, montmorillonite, activated montmorillonite, alumina, activated alumina, silica gel, synthetic zeolite, cordierite, zirconia,
Mineral fine powder such as titania is mixed with a mixed aqueous solution of aluminum sulfate and hydrazine, kneaded, molded into a plate with a thickness of 1 mm, and dried at 100 ° C for 6 hours and at room temperature for 2 weeks, and then the acetaldehyde equilibrium concentration adsorption capacity Was measured.

【0039】硫酸アルミニウムとヒドラジンの混合水溶
液の濃度はアルミニウムイオン0.5モル/l、ヒドラ
ジン0.5モル/l、硫酸イオン0.75モル/lで鉱
物粉末と水溶液の配合比は板状に成形しやすい粘土とし
鉱物の種類によって変えたがその比率は100gの粉末
に対して水溶液が100〜150ccであった。
The concentration of the mixed aqueous solution of aluminum sulfate and hydrazine was 0.5 mol / l of aluminum ion, 0.5 mol / l of hydrazine and 0.75 mol / l of sulfate ion, and the mixing ratio of the mineral powder and the aqueous solution was plate-like. The clay was made to be easy to mold and varied depending on the type of mineral, but the ratio was 100 to 150 cc of the aqueous solution to 100 g of powder.

【0040】それぞれの乾燥した板を乳鉢で粉砕し、1
00μ以下の粉末として評価試料とし、図1に示すよう
に、テドラーパックを使ってCH3CHOの平衡濃度吸
着容量の評価を行った。
Crush each dried plate in a mortar and
A powder having a size of 00 μ or less was used as an evaluation sample, and the equilibrium concentration adsorption capacity of CH 3 CHO was evaluated using a Tedlar pack as shown in FIG.

【0041】本来の平衡濃度吸着容量は一定濃度のCH
3CHOを含む空気を一定体積だけ評価試料とともにテ
ドラーパックに封入し、48時間後のCH3CHO残留
濃度を測定するものであり、残留濃度、即ち平衡到達濃
度が1ppm〜200ppm程度の広範囲になるように
色々な試料重量の試験を繰り返すのが普通である。
The original equilibrium concentration adsorption capacity is a constant concentration of CH.
Air containing 3 CHO is enclosed in a Tedlar pack together with the evaluation sample in a fixed volume, and the residual concentration of CH 3 CHO after 48 hours is measured. The residual concentration, that is, the equilibrium reached concentration is in the wide range of 1 ppm to 200 ppm. It is common to repeat the test with various sample weights.

【0042】今回は評価を簡便に行う為、テドラーパッ
クに封入する空気の体積を5 l、CH3CHOの初期濃
度を2000ppm、評価試料の投入重量を0.1gと
0.2gと0.5gの3種類に限定し、48時間後の残
留濃度で評価した。
In order to make the evaluation simple, this time, the volume of the air enclosed in the Tedlar pack was 5 liters, the initial concentration of CH 3 CHO was 2000 ppm, and the weight of the evaluation sample was 0.1 g, 0.2 g, and 0.5 g. It was limited to 3 types and evaluated by the residual concentration after 48 hours.

【0043】第1表に評価鉱物のN2吸着法による比表
面積、主要鉱物組成を示した。また、第2表にはCH3
CHOの吸着容量の評価結果を示した。
Table 1 shows the specific surface area and the main mineral composition of the evaluated minerals by the N 2 adsorption method. In addition, Table 3 shows CH 3
The evaluation results of the adsorption capacity of CHO are shown.

【0044】この表より鎖状珪酸マグネシウム以外の鉱
物でも比表面積が大きく、珪酸を主体とする鉱物では極
めて高いCH3CHO吸着容量を示すことが判った。
From this table, it was found that minerals other than chain-like magnesium silicate also have a large specific surface area, and minerals mainly containing silicic acid show extremely high CH 3 CHO adsorption capacity.

【0045】[0045]

【表1】 [Table 1]

【0046】[0046]

【表2】 [Table 2]

【0047】[0047]

【実施例2】活性ベントナイト、モンモリロナイト、活
性モンモリロナイト、セピオライト等の鉱物微粉末を大
気雰囲気下で300℃〜900℃にそれぞれ3時間保持
した後冷却した。
Example 2 Mineral fine powders of activated bentonite, montmorillonite, activated montmorillonite, sepiolite and the like were kept at 300 ° C. to 900 ° C. for 3 hours in an air atmosphere and then cooled.

【0048】それぞれの粉末に硫酸アルミニウムとヒド
ラジンの混合水溶液を混ぜて混練し、厚さ1mmの板状
に成形して100℃で6時間、室温で2週間乾燥した
後、アセトアルデヒドの平衡濃度吸着容量を測定した。
Each powder was mixed with a mixed aqueous solution of aluminum sulfate and hydrazine, kneaded, molded into a plate having a thickness of 1 mm, dried at 100 ° C. for 6 hours and at room temperature for 2 weeks, and then the acetaldehyde equilibrium concentration adsorption capacity was obtained. Was measured.

【0049】硫酸アルミニウムとヒドラジンの混合水溶
液の濃度はアルミニウムイオン0.5モル/l、ヒドラ
ジン0.5モル/l、硫酸イオン0.75モル/lで鉱
物粉末と水溶液の配合比は板状に延ばしやすい粘土とし
鉱物の種類によって変えたがその比率は100gの粉末
に対して水溶液が80〜130ccであった。
The concentration of the mixed aqueous solution of aluminum sulfate and hydrazine was 0.5 mol / l of aluminum ion, 0.5 mol / l of hydrazine and 0.75 mol / l of sulfate ion, and the mixing ratio of the mineral powder and the aqueous solution was plate-like. The clay was made to be easily spread and varied depending on the type of mineral, but the ratio was 80 to 130 cc of the aqueous solution to 100 g of the powder.

【0050】それぞれの鉱物については比較の為に、加
熱処理を行わないものも同様の薬液処理を行い、評価試
料を製作した。
For comparison, each mineral was subjected to the same chemical treatment for those not subjected to the heat treatment to produce evaluation samples.

【0051】それぞれの乾燥した板を乳鉢で粉砕し、1
00μ以下の粉末として評価試料とし、テドラーパック
を使ってCH3CHOの平衡濃度吸着容量の評価を行う
とともに、板状品を水中に投入し、崩壊状態を調査し
た。
Crush each dried plate in a mortar and
Using a Tedlar pack, the equilibrium concentration adsorption capacity of CH 3 CHO was evaluated, and the plate-like product was put into water to investigate the state of collapse.

【0052】本来の平衡濃度吸着容量は一定濃度のCH
3CHOを含む空気を一定体積だけ評価試料とともにテ
ドラーパックに封入し、48時間後のCH3CHO残留
濃度を測定するものであり、残留濃度、即ち平衡到達濃
度が1ppm〜200ppm程度の広範囲になるように
色々な試料重量の試験を繰り返すのが普通である。
The original equilibrium concentration adsorption capacity is a constant concentration of CH.
Air containing 3 CHO is enclosed in a Tedlar pack together with the evaluation sample in a fixed volume, and the residual concentration of CH 3 CHO after 48 hours is measured. The residual concentration, that is, the equilibrium reached concentration is in the wide range of 1 ppm to 200 ppm. It is common to repeat the test with various sample weights.

【0053】今回は評価を簡便に行う為、テドラーパッ
クに封入する空気の体積を5 l、CH3CHOの初期濃
度を2000ppm、評価試料の投入重量を0.1gと
0.2gと0.5gの3種類に限定し、48時間後の残
留濃度で評価した。
In order to make the evaluation simple, this time, the volume of air enclosed in the Tedlar pack was 5 liters, the initial concentration of CH 3 CHO was 2000 ppm, and the weight of the evaluation sample was 0.1 g, 0.2 g, and 0.5 g. It was limited to 3 types and evaluated by the residual concentration after 48 hours.

【0054】第3表に評価鉱物のCH3CHOの吸着容
量の評価結果と水中に投入した時の崩壊現象を示した。
Table 3 shows the evaluation results of the adsorption capacity of CH 3 CHO as the evaluation mineral and the disintegration phenomenon when it was put into water.

【0055】この表より加熱処理の無いもの、300℃
以下の加熱処理では水との接触で成形体の崩壊が起きる
こと、400℃〜700℃の加熱処理では水との接触で
成形体の崩壊が起きない上に、CH3CHO吸着容量で
も非加熱処理品と比較して遜色が無いことが判る。
From this table, no heat treatment, 300 ° C
In the following heat treatment, the molded body collapses on contact with water, and in the heat treatment at 400 ° C to 700 ° C, the molded body does not collapse on contact with water, and the CH 3 CHO adsorption capacity does not cause heating. It can be seen that it is comparable to the processed product.

【0056】また、800℃以上の加熱処理では水との
接触により、崩壊が起こらないもののCH3CHO吸着
容量では劣化が認められることが明らかである。
Further, it is clear that in the heat treatment at 800 ° C. or higher, the CH 3 CHO adsorption capacity is deteriorated by the contact with water, although the decomposition does not occur.

【0057】[0057]

【表3】 [Table 3]

【0058】[0058]

【発明の効果】本発明により、脱CH3CHO性能が高
い空気清浄化物を安価に安定的に製造できる。
EFFECTS OF THE INVENTION According to the present invention, it is possible to inexpensively and stably produce an air-purified product having high CH 3 CHO removal performance.

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

【図1】脱臭性能を評価する試験方法を示す説明図。FIG. 1 is an explanatory view showing a test method for evaluating deodorizing performance.

【符号の説明】[Explanation of symbols]

1 テドラーパック 2 粉末試料 3 ガス導入口兼ガス濃度検知口 1 Tedlar pack 2 Powder sample 3 Gas inlet and gas concentration detection port

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 比表面積が50m2/g以上の、珪酸を
主体とする層状粘土鉱物の粒子表面に、Alの金属塩と
24の複塩を担持することを特徴とする空気清浄化物
の製造方法。
1. An air cleaner comprising a metal salt of Al and a double salt of N 2 H 4 supported on the surface of particles of a layered clay mineral mainly composed of silicic acid having a specific surface area of 50 m 2 / g or more. Method for producing compound.
【請求項2】 上記珪酸を主体とする層状粘土鉱物を、
予め酸による溶出処理をすることを特徴とする請求項1
記載の空気清浄化物の製造方法。
2. The layered clay mineral containing silicic acid as a main component,
The elution treatment with an acid is carried out in advance.
A method for producing the air-purified product described.
【請求項3】 上記珪酸を主体とする層状粘土鉱物を、
予め400℃〜700℃に加熱処理することを特徴とす
る請求項1又は2記載の空気清浄化物の製造方法。
3. The layered clay mineral containing silicic acid as a main component,
The method for producing an air-purified product according to claim 1 or 2, wherein heat treatment is performed in advance at 400 ° C to 700 ° C.
JP5165924A 1993-06-14 1993-06-14 Manufacturing method of air-purified material Expired - Lifetime JP2949455B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5165924A JP2949455B2 (en) 1993-06-14 1993-06-14 Manufacturing method of air-purified material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5165924A JP2949455B2 (en) 1993-06-14 1993-06-14 Manufacturing method of air-purified material

Publications (2)

Publication Number Publication Date
JPH07812A true JPH07812A (en) 1995-01-06
JP2949455B2 JP2949455B2 (en) 1999-09-13

Family

ID=15821602

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Application Number Title Priority Date Filing Date
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Country Link
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006028366A (en) * 2004-07-16 2006-02-02 Nippon Kasei Chem Co Ltd Formaldehyde scavenger and woody material
JP2006116442A (en) * 2004-10-22 2006-05-11 Nihon Funen Co Ltd Formaldehyde absorbent composition and its use
JP2007054328A (en) * 2005-08-25 2007-03-08 Sinanen Zeomic Co Ltd Deodorant and deodorant resin composition
WO2015046417A1 (en) * 2013-09-27 2015-04-02 東洋紡株式会社 Aldehyde removal material
US12011122B2 (en) 2020-08-31 2024-06-18 Lg Electronics Inc. Drying apparatus

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006028366A (en) * 2004-07-16 2006-02-02 Nippon Kasei Chem Co Ltd Formaldehyde scavenger and woody material
JP2006116442A (en) * 2004-10-22 2006-05-11 Nihon Funen Co Ltd Formaldehyde absorbent composition and its use
JP2007054328A (en) * 2005-08-25 2007-03-08 Sinanen Zeomic Co Ltd Deodorant and deodorant resin composition
WO2015046417A1 (en) * 2013-09-27 2015-04-02 東洋紡株式会社 Aldehyde removal material
JPWO2015046417A1 (en) * 2013-09-27 2017-03-09 東洋紡株式会社 Aldehyde removal material
US12011122B2 (en) 2020-08-31 2024-06-18 Lg Electronics Inc. Drying apparatus

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