JP2002159852A - Active carbon fiber for removing malodorous gas and air cleaning sheet - Google Patents

Active carbon fiber for removing malodorous gas and air cleaning sheet

Info

Publication number
JP2002159852A
JP2002159852A JP2000361167A JP2000361167A JP2002159852A JP 2002159852 A JP2002159852 A JP 2002159852A JP 2000361167 A JP2000361167 A JP 2000361167A JP 2000361167 A JP2000361167 A JP 2000361167A JP 2002159852 A JP2002159852 A JP 2002159852A
Authority
JP
Japan
Prior art keywords
activated carbon
carbon fiber
amount
phosphoric acid
aromatic amino
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2000361167A
Other languages
Japanese (ja)
Inventor
Takashi Nogi
崇志 野木
Shigeaki Sawada
重明 澤田
Masayoshi Matsumoto
優美 松本
Kana Tokunaga
加奈 徳永
Keiichi Asami
圭一 浅見
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.)
Unitika Ltd
Original Assignee
Unitika Ltd
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 Unitika Ltd filed Critical Unitika Ltd
Priority to JP2000361167A priority Critical patent/JP2002159852A/en
Publication of JP2002159852A publication Critical patent/JP2002159852A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide an active carbon fiber for removing malodorous gases which has a high capacity of removing lower aldehydes and basic gases and a high rate of removing such gases and to provide an air cleaning sheet using the same. SOLUTION: There is provided an active carbon fiber carrying an aromatic amino acid salt and phosphoric acid, wherein the amount of the aromatic amino acid salt carried is 7-30 mass %, the amount of the phosphoric acid carried is such that the ratio of the number of moles of the phosphoric acid carried to the number of moles of the aromatic amino acid salt carried is 0.05-1.0, and the specific surface area of the active carbon fiber carrying them is 300-1,000 m2/g.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は、室内空間や車内の
空間に存在する、特にたばこ臭に含まれるアセトアルデ
ヒドや、家具、建材等から発生するホルムアルデヒド等
の低級アルデヒド類と、アンモニア等の塩基性ガスを効
率よく除去できる悪臭ガス除去用活性炭繊維、及びその
活性炭繊維を主成分とする空気浄化シートに関するもの
である。
The present invention relates to a basic aldehyde such as acetaldehyde or formaldehyde generated from furniture, building materials, etc., which is present in an indoor space or a space inside a vehicle, particularly from a tobacco smell. The present invention relates to an activated carbon fiber for removing odorous gas, which can efficiently remove gas, and an air purification sheet containing the activated carbon fiber as a main component.

【0002】[0002]

【従来の技術】従来より、たばこの煙等を含有する空気
を浄化するには、アセトアルデヒド類の除去が大きな課
題とされてきた。このアセトアルデヒドの除去を目的と
して、多孔質体に有機アミン化合物等を添着した低級ア
ルデヒド除去材が知られており、特公昭60−5409
5号公報や特開平7−80292号公報には、アミン化
合物としてアニリン、トルイジン等を添着した活性炭が
開示されている。しかし、これらのアミン化合物は本来
劇薬であり、人のいる空間の空気浄化に用いるには安全
や衛生上好ましくなく、また、満足のいく除去効果を示
すものでもなかった。
2. Description of the Related Art Conventionally, removal of acetaldehyde has been a major issue in purifying air containing tobacco smoke and the like. For the purpose of removing acetaldehyde, a lower aldehyde removing material in which an organic amine compound or the like is attached to a porous body is known, and Japanese Patent Publication No. Sho 60-5409 is known.
No. 5 and JP-A-7-80292 disclose activated carbon to which aniline, toluidine, or the like is attached as an amine compound. However, these amine compounds are inherently powerful drugs, and are not preferable in terms of safety and hygiene when used for air purification in a space where people are present, and have not exhibited a satisfactory removal effect.

【0003】また、特公昭60−54095号公報に
は、セピオライト、活性炭等の多孔性担体に、芳香族ア
ミノ酸又は芳香族アミノ酸の塩を担持した低級アルデヒ
ド類の除去剤が提案されている。しかし、これらの除去
剤は、低級アルデヒドの除去能は有するものの、たばこ
の煙中に含まれるアンモニアのような塩基性物質の除去
にはほとんど効果がないという欠点を有していた。
In addition, Japanese Patent Publication No. 60-54095 proposes a remover for lower aldehydes in which an aromatic amino acid or a salt of an aromatic amino acid is supported on a porous carrier such as sepiolite or activated carbon. However, although these removing agents have the ability to remove lower aldehydes, they have the drawback that they have little effect on removing basic substances such as ammonia contained in cigarette smoke.

【0004】[0004]

【解決しようとする課題】本発明は、上記の問題を解決
し、低級アルデヒド類と塩基性ガスの除去量が大きく、
かつ、除去速度の速い悪臭ガス除去用活性炭繊維と、そ
の活性炭繊維を主成分とする空気浄化シートを提供する
ことを技術的な課題とするものである。
SUMMARY OF THE INVENTION The present invention solves the above-mentioned problems and has a large removal amount of lower aldehydes and basic gas.
Another object of the present invention is to provide an activated carbon fiber for removing odorous gas having a high removal rate and an air purification sheet containing the activated carbon fiber as a main component.

【0005】[0005]

【課題を解決するための手段】本発明者らは、上記の課
題を達成するために鋭意検討した結果、特定の薬剤を特
定量で担持させた活性炭繊維は、低級アルデヒド類と塩
基性ガスの除去量が多く、かつ、除去速度が速いことを
見出して本発明に到達した。すなわち、本発明は、次の
構成をその要旨とするものである。 (1) 芳香族アミノ酸の塩とリン酸が担持された活性炭繊
維において、芳香族アミノ酸の塩の担持量が7〜30質
量%、リン酸の担持量が芳香族アミノ酸の塩のモル数に
対するリン酸のモル数の比が0.05〜1.0となる量
であり、担持後の活性炭繊維の比表面積が300〜10
00m2 /gであることを特徴とする悪臭ガス除去用活
性炭繊維。 (2) 上記(1) 記載の活性炭繊維と熱融着性繊維を主成分
とし、熱融着性繊維の融着又は軟化で所定の形態を保持
してなるシートであって、上記(1) 記載の活性炭繊維の
含有率が40質量%以上であることを特徴とする空気浄
化用シート。
Means for Solving the Problems The inventors of the present invention have conducted intensive studies to achieve the above-mentioned object, and as a result, activated carbon fibers carrying a specific agent in a specific amount have been prepared from lower aldehydes and basic gas. The inventors have found that the removal amount is large and the removal rate is high, and the present invention has been reached. That is, the present invention has the following configuration as its gist. (1) In an activated carbon fiber carrying a salt of an aromatic amino acid and phosphoric acid, the amount of the salt of the aromatic amino acid is 7 to 30% by mass, and the amount of phosphoric acid is phosphorus relative to the number of moles of the salt of the aromatic amino acid. The molar ratio of the acid is an amount that becomes 0.05 to 1.0, and the specific surface area of the activated carbon fiber after loading is 300 to 10
Activated carbon fiber for removing odorous gas, characterized by having a water content of 00 m 2 / g. (2) A sheet comprising the activated carbon fiber and the heat-fusible fiber according to the above (1) as main components, and maintaining a predetermined form by fusing or softening the heat-fusible fiber, wherein the sheet (1) An air purification sheet, wherein the content of the activated carbon fiber described in the above is 40% by mass or more.

【0006】[0006]

【発明の実施の形態】以下、本発明について詳細に説明
する。本発明の悪臭ガス除去用活性炭繊維は、活性炭繊
維を基材とし、芳香族アミノ酸の塩とリン酸を担持させ
たものである。活性炭繊維は、通常の粒状活性炭に比べ
るとその外表面積、比表面積共に大きいので、空間中に
存在するガス成分との接触効率が高く、吸着速度を速め
ることができる。
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail. The activated carbon fiber for removing offensive odor gas of the present invention has activated carbon fiber as a base material and carries a salt of an aromatic amino acid and phosphoric acid. Activated carbon fibers have a larger outer surface area and a larger specific surface area than ordinary granular activated carbon, so that the efficiency of contact with gas components existing in the space is high and the adsorption speed can be increased.

【0007】本発明では、活性炭繊維に芳香族アミノ酸
の塩とリン酸を担持させることにより、低級アルデヒド
類と塩基性ガスの除去能を付与するが、その担持量は芳
香族アミノ酸の塩の担持量が7〜30質量%(芳香族ア
ミノ酸の塩とリン酸を担持した悪臭ガス除去用活性炭繊
維全体の7〜30質量%)、リン酸の担持量は芳香族ア
ミノ酸の塩のモル数に対するリン酸のモル数の比が0.
05〜1.0となる量であることが必要である。
In the present invention, the activated carbon fiber is loaded with an aromatic amino acid salt and phosphoric acid to provide the ability to remove lower aldehydes and basic gases. The amount is 7 to 30% by mass (7 to 30% by mass of the entire activated carbon fiber for removing malodorous gas carrying an aromatic amino acid salt and phosphoric acid), and the amount of phosphoric acid is phosphorus relative to the number of moles of the aromatic amino acid salt. The molar ratio of the acid is 0.
It is necessary that the amount is in the range of 0.5 to 1.0.

【0008】芳香族アミノ酸としては、o−アミノ安息
香酸、m−アミノ安息香酸、p−アミノ安息香酸、アミ
ノアセトアニリド、アミノサリチル酸等があるが、例え
ばp−アミノ安息香酸はそのアミノ基と低級アルデヒド
類が脱水反応し、シッフ塩基を形成して低級アルデヒド
類を固定化するが、化学的に不安定であり、反応性も高
いことから分解もされやすく、元の状態に戻ってしまう
と低級アルデヒド類の除去量が低下する。
The aromatic amino acids include o-aminobenzoic acid, m-aminobenzoic acid, p-aminobenzoic acid, aminoacetanilide, aminosalicylic acid and the like. For example, p-aminobenzoic acid has its amino group and lower aldehyde. The dehydration reaction forms a Schiff base to immobilize the lower aldehyde, but it is chemically unstable and highly reactive, so it is easily decomposed. The amount of removal of the class decreases.

【0009】この反応を安定化させ、低級アルデヒド類
の除去量を高めるには塩、好ましくは酸性塩にすること
が有効であることを見い出し、さらにリン酸が存在する
ことにより触媒的な作用が働き、脱水縮合反応が進んで
空気中に含まれる微量の低級アルデヒド類も完全に除去
することが可能となる。
In order to stabilize this reaction and increase the removal amount of lower aldehydes, it has been found that it is effective to use a salt, preferably an acidic salt, and furthermore, the presence of phosphoric acid has a catalytic effect. The dehydration / condensation reaction proceeds, and a trace amount of lower aldehydes contained in the air can be completely removed.

【0010】芳香族アミノ酸を酸性塩にするには、硝
酸、硫酸、塩酸、リン酸等の一般的な酸を用いることが
できるが、担持させる酸と、芳香族アミノ酸を酸性塩化
させる酸は同一の酸であることが好ましく、硝酸、硫酸
は活性炭繊維へのダメージが大きく、塩酸は揮発性が高
いことから、用いる酸としてはリン酸が好適であり、除
去量、除去速度の点からも芳香族アミノ酸のリン酸塩と
リン酸を担持させたものが最も好ましい。
In order to convert an aromatic amino acid into an acidic salt, a common acid such as nitric acid, sulfuric acid, hydrochloric acid or phosphoric acid can be used, but the acid to be carried and the acid to acidify the aromatic amino acid are the same. Since acid is preferred, nitric acid and sulfuric acid have a large damage to activated carbon fiber, and hydrochloric acid has high volatility. Therefore, phosphoric acid is suitable as an acid to be used. Those carrying a phosphate and phosphoric acid of an aromatic amino acid are most preferred.

【0011】本発明では、芳香族アミノ酸の塩の担持量
を7〜30質量%とすることで十分な低級アルデヒドの
除去量を確保することができるが、さらに好ましくは9
〜25質量%である。芳香族アミノ酸の塩が7質量%よ
り少ないと、低級アルデヒドの除去量が少なく、逆に3
0質量%より多くなると、後述するように芳香族アミノ
酸の塩のモル数とリン酸のモル数の比が0.05〜1.
0となるようにリン酸も担持させなければならいことか
ら、担持後の比表面積が小さくなりすぎ、活性炭繊維の
吸着力が弱まることで低級アルデヒドの除去量が逆に下
がり、除去速度も低下する。
In the present invention, a sufficient amount of lower aldehyde can be removed by controlling the amount of the salt of the aromatic amino acid to be 7 to 30% by mass.
2525% by mass. When the amount of the aromatic amino acid salt is less than 7% by mass, the removal amount of the lower aldehyde is small.
When the amount is more than 0% by mass, the ratio of the number of moles of the salt of the aromatic amino acid to the number of moles of the phosphoric acid is 0.05 to 1.
Since phosphoric acid must be supported so as to be 0, the specific surface area after the support is too small, and the adsorption power of the activated carbon fiber is weakened, so that the removal amount of the lower aldehyde is reduced and the removal rate is also reduced. .

【0012】また、リン酸の担持量は芳香族アミノ酸の
塩のモル数に対するリン酸のモル数の比が0.05〜
1.0となる量であることが必要であり、芳香族アミノ
酸の塩の担持量に対してリン酸量が多くなりすぎると、
触媒としての機能が失われてしまい、低級アルデヒド類
の除去量が低下する。芳香族アミノ酸の塩とリン酸のそ
れぞれの担持量には適切な量的関係が存在しており、リ
ン酸量はモル数に換算して、芳香族アミノ酸の塩のモル
数とリン酸のモル数の比率が0.05〜1.0、好まし
くは0.1〜0.8となる範囲でなければ低級アルデヒ
ド類の除去量、除去速度を高く維持することができな
い。ここで言う比率は、芳香族アミノ酸の塩のモル数を
1とした時のリン酸のモル数であり、計算式は(リン酸
モル数)/(芳香族アミノ酸の塩のモル数)となる。
Further, the amount of phosphoric acid supported is preferably such that the ratio of the number of moles of phosphoric acid to the number of moles of the salt of the aromatic amino acid is 0.05 to 0.05.
It is necessary that the amount is 1.0, and if the amount of phosphoric acid is too large relative to the amount of the salt of the aromatic amino acid carried,
The function as a catalyst is lost, and the removal amount of lower aldehydes decreases. There is an appropriate quantitative relationship between the amount of the aromatic amino acid salt and the amount of phosphoric acid carried, and the amount of phosphoric acid is converted into the number of moles, and the number of moles of the aromatic amino acid salt and the number of moles of phosphoric acid are converted. Unless the ratio of numbers is in the range of 0.05 to 1.0, preferably 0.1 to 0.8, the removal amount and removal rate of lower aldehydes cannot be kept high. The ratio mentioned here is the number of moles of phosphoric acid when the number of moles of the salt of the aromatic amino acid is 1 and the calculation formula is (moles of phosphoric acid) / (moles of the salt of the aromatic amino acid). .

【0013】さらに、芳香族アミノ酸の塩とリン酸を担
持させた後の活性炭繊維の比表面積も非常に重要であ
る。芳香族アミノ酸の塩と低級アルデヒド類が反応する
ことで低級アルデヒド類が除去されるが、その前に活性
炭繊維が低級アルデヒド類を吸着し、活性炭繊維の細孔
内にある芳香族アミノ酸の塩のところまで導かなければ
芳香族アミノ酸の塩との反応は起こらない。活性炭繊維
の細孔が埋まってしまうほどの担持は、低級アルデヒド
類の除去量、除去速度を下げてしまうどころか、全く除
去できなくなることさえある。
Further, the specific surface area of the activated carbon fiber after supporting the salt of aromatic amino acid and phosphoric acid is also very important. The lower aldehydes are removed by the reaction of the salt of the aromatic amino acid with the lower aldehyde.Before that, the activated carbon fiber adsorbs the lower aldehyde, and the salt of the aromatic amino acid in the pores of the activated carbon fiber is removed. If it is not guided to the point, the reaction with the salt of the aromatic amino acid does not occur. Carrying such that the pores of the activated carbon fibers are buried may not only reduce the removal amount and removal rate of the lower aldehydes, but may even make it impossible to remove them at all.

【0014】したがって、本発明では、担持後の活性炭
繊維の比表面積が300〜1000m2 /g、好ましく
は350〜800m2 /gであることが必要である。こ
の比表面積が300m2 /g未満では、活性炭繊維によ
る低級アルデヒド類の吸着が起こり難くなり、1000
2 /gを超えると、芳香族アミノ酸の塩やリン酸の担
持量を満足することが困難となる。
[0014] Therefore, in the present invention, a specific surface area of 300~1000m 2 / g, the activated carbon fiber after carrying preferably required to be 350~800m 2 / g. When the specific surface area is less than 300 m 2 / g, the adsorption of lower aldehydes by activated carbon fibers becomes difficult, and
If it exceeds m 2 / g, it is difficult to satisfy the amount of salt of aromatic amino acid or phosphoric acid supported.

【0015】低級アルデヒド類の除去量を高めるには、
芳香族アミノ酸の酸性塩の担持量を増加させればある程
度可能となるが、いかに除去量が高くても空気浄化シー
トとして用いるためには除去速度が速くなければ実用に
は至らない。本発明では、除去速度を速くするために比
表面積の高い活性炭繊維を使用し、担持後の比表面積を
高くすることで、活性炭繊維の持つ速い物理吸着能力を
そのまま保存させ、活性炭繊維の細孔内にある芳香族ア
ミノ酸の塩のところまで低級アルデヒド類を素早く導
き、芳香族アミノ酸の塩とリン酸を前記比率で担持させ
るでその反応速度を速め、アセトアルデヒド等の低級ア
ルデヒド類の除去速度を非常に速くすることが可能とな
る。また、リン酸も担持させていることから、アセトア
ルデヒド等の低級アルデヒド類だけではなく、アンモニ
アのような塩基性のガスも含んだような複合臭の場合で
も、その両方を除去することが可能であり、非常に優れ
た悪臭ガス除去材となる。さらに、担持後の活性炭繊維
の比表面積が300〜1000m2 /gであることか
ら、物理吸着能も十分に有しており、酢酸等のガスの吸
着量も高く、一般的にたばこ臭と呼ばれる臭気成分のア
セトアルデヒド、アンモニア、酢酸の3成分のガスを本
発明の悪臭ガス除去用活性炭繊維や空気浄化シートのみ
で全て除去することが可能である。
In order to increase the removal amount of lower aldehydes,
It is possible to some extent if the amount of the acidic salt of the aromatic amino acid is increased, but no matter how high the amount of removal, it is not practical unless the removal rate is high for use as an air purification sheet. In the present invention, activated carbon fibers having a high specific surface area are used to increase the removal rate, and by increasing the specific surface area after loading, the fast physical adsorption ability of the activated carbon fibers is preserved as it is, and the pores of the activated carbon fibers are reduced. The lower aldehydes are quickly led to the salt of the aromatic amino acid present therein, and the reaction rate is increased by supporting the salt of the aromatic amino acid and phosphoric acid in the above-described ratio, and the removal rate of the lower aldehydes such as acetaldehyde is extremely increased. It is possible to be faster. In addition, since phosphoric acid is also supported, it is possible to remove not only lower aldehydes such as acetaldehyde but also complex odors containing a basic gas such as ammonia. Yes, it is a very excellent odor gas remover. Further, since the activated carbon fiber after loading has a specific surface area of 300 to 1000 m 2 / g, it has a sufficient physical adsorption capacity and a high adsorption amount of gas such as acetic acid, which is generally called tobacco smell. It is possible to remove all of the three components of the odor components, acetaldehyde, ammonia and acetic acid, using only the activated carbon fiber for removing odorous gas and the air purification sheet of the present invention.

【0016】なお、活性炭繊維に担持されている、芳香
族アミノ酸の塩とリン酸の担持量は、有機元素分析によ
り測定することができる。すなわち、担持された活性炭
繊維そのものを有機元素分析することで、活性炭繊維中
に存在する窒素とリンを定量し、窒素の割合から芳香族
アミノ酸の量を、リンの割合からリン酸の量をそれぞれ
算出することで、それぞれの担持量が求められる。
The amount of the salt of the aromatic amino acid and the amount of the phosphoric acid carried on the activated carbon fiber can be measured by organic element analysis. That is, by carrying out organic elemental analysis of the supported activated carbon fiber itself, nitrogen and phosphorus present in the activated carbon fiber are quantified, and the amount of aromatic amino acid is determined from the ratio of nitrogen, and the amount of phosphoric acid is determined from the ratio of phosphorus. By carrying out the calculations, the respective supported amounts are obtained.

【0017】次に、本発明の悪臭ガス除去用活性炭繊維
の製法例について説明する。前記のように、芳香族アミ
ノ酸の塩とリン酸を担持した後の活性炭繊維の比表面積
を300〜1000m2 /gとするためには、比表面積
が700m2 /g以上の活性炭繊維に担持させることが
好ましい。担持前の活性炭繊維の比表面積が700m2
/gより小さいと、担持後の比表面積を300m2 /g
以上とするには担持量が少なくなりすぎ、低級アルデヒ
ド類の除去量や除去速度が低下する。
Next, an example of a method for producing the activated carbon fiber for removing offensive odor gas of the present invention will be described. As described above, the specific surface area of the activated carbon fiber after carrying salt and phosphoric acid in an aromatic amino acid in order to 300~1000m 2 / g, the specific surface area is supported above the activated carbon fiber 700 meters 2 / g Is preferred. Activated carbon fiber before loading has a specific surface area of 700 m 2
/ G, the specific surface area after loading is 300 m 2 / g.
In order to achieve the above, the supported amount becomes too small, and the removal amount and removal rate of lower aldehydes decrease.

【0018】本発明では、活性炭繊維の比表面積に応じ
て、担持後の比表面積が300〜1000m2 /g残る
ように、好ましくは350〜800m2 /gの比表面積
が残るように芳香族アミノ酸の塩を7〜30質量%から
選択して担持させ、さらにリン酸を、芳香族アミノ酸の
塩のモル数とリン酸のモル数の比が0.05〜1.0と
なる量担持させることで、低級アルデヒド類に対して非
常に優れた除去速度と大きい除去量を示す本発明の悪臭
ガス除去用活性炭繊維を得ることができる。
In the present invention, depending on the specific surface area of the activated carbon fibers, as the specific surface area after carrying the 300~1000m 2 / g remain, preferably an aromatic amino acid to remain a specific surface area of 350~800m 2 / g Is supported by selecting from 7 to 30% by mass of a salt of phosphoric acid, and phosphoric acid is further carried in such an amount that the ratio of the number of moles of the salt of the aromatic amino acid to the number of moles of the phosphoric acid is 0.05 to 1.0. Thus, the activated carbon fiber for removing offensive odor gas of the present invention, which shows a very excellent removal rate and a large removal amount for lower aldehydes, can be obtained.

【0019】また、芳香族アミノ酸の酸性塩、例えばp
−アミノ安息香酸は、リン酸溶液中にp−アミノ安息香
酸を添加すると、リン酸塩化して溶液中に溶解していく
ので、その温度に対する飽和量に近い量を溶解させた
後、液温を下げてp−アミノ安息香酸リン酸塩の結晶物
として析出させ、取り出すことができる。この析出した
p−アミノ安息香酸リン酸塩を水に溶解させ、その水溶
液中に活性炭繊維を浸漬させて吸着させれば、p−アミ
ノ安息香酸リン酸塩を担持させることができる。さら
に、この担持量に合わせてリン酸を活性炭繊維にシャワ
ーリング等で担持させれば、本発明の悪臭ガス除去用活
性炭繊維とすることができる。
Also, acidic salts of aromatic amino acids such as p
-Addition of p-aminobenzoic acid to a phosphoric acid solution causes phosphorylation and dissolution of the aminobenzoic acid in the phosphoric acid solution. And precipitated as a crystal of p-aminobenzoic acid phosphate, and can be taken out. The precipitated p-aminobenzoic acid phosphate is dissolved in water, and the activated carbon fiber is immersed and adsorbed in the aqueous solution to support the p-aminobenzoic acid phosphate. Further, if phosphoric acid is supported on the activated carbon fiber by showering or the like in accordance with the amount of the supported carbon, the activated carbon fiber for removing offensive odor gas of the present invention can be obtained.

【0020】また、リン酸溶液にp−アミノ安息香酸を
溶解させる際、リン酸を過剰にしておけば、p−アミノ
安息香酸リン酸塩とリン酸の混合溶液ができる。この
時、p−アミノ安息香酸とリン酸の比率を調整しておけ
ば、この溶液中に活性炭繊維を浸漬させると、p−アミ
ノ安息香酸リン酸塩とリン酸を同時に担持させることも
できる。
When dissolving p-aminobenzoic acid in a phosphoric acid solution, a mixed solution of phosphoric acid salt of p-aminobenzoic acid and phosphoric acid can be prepared by making phosphoric acid excessive. At this time, if the ratio of p-aminobenzoic acid and phosphoric acid is adjusted, if the activated carbon fiber is immersed in this solution, p-aminobenzoic acid phosphate and phosphoric acid can be supported at the same time.

【0021】次に、本発明の空気浄化シートについて説
明する。本発明の空気浄化シートは、前記した芳香族ア
ミノ酸の塩とリン酸を担持したた悪臭ガス除去用活性炭
繊維と熱融着性繊維を主成分とし、熱融着性繊維の融着
又は軟化で所定の形態を保持したシートであり、前記活
性炭繊維の含有率が40質量%以上を占めているもので
ある。空気浄化シートとして用いるには、室内用空気清
浄器、車載用空気清浄器等の風量やガスと活性炭繊維の
接触効率の点から、空気浄化シート中の活性炭繊維量が
40質量%以上、好ましくは50質量%以上ないと、除
去量、除去率ともに低下する。また、空気浄化シートの
目付も、同様に除去量、除去率の点から60g/m2
上が好ましい。
Next, the air purification sheet of the present invention will be described. The air purifying sheet of the present invention comprises, as main components, the above-mentioned activated carbon fiber for removing malodorous gas carrying the salt of the aromatic amino acid and phosphoric acid and the heat-fusible fiber, and the heat-fusible fiber is fused or softened. A sheet having a predetermined form, wherein the content of the activated carbon fibers accounts for 40% by mass or more. In order to use as an air purifying sheet, the amount of activated carbon fiber in the air purifying sheet is 40% by mass or more, preferably from the viewpoint of the air volume of an indoor air purifier, an in-vehicle air purifier or the like, and the contact efficiency between gas and activated carbon fiber. If it is not more than 50% by mass, both the removal amount and the removal rate decrease. Similarly, the basis weight of the air purification sheet is preferably 60 g / m 2 or more from the viewpoint of the removal amount and the removal rate.

【0022】活性炭繊維とともに本発明の空気浄化シー
トを構成する熱融着性繊維は、接触している活性炭繊維
を接触点においてのみ、重合体の溶融の融着又は軟化に
より接着することができる。熱融着性繊維の構成は単一
成分、複数成分からなる複合繊維のいずれでもよいが、
鞘成分に低融点重合体を、芯成分に高融点重合体を配し
た芯鞘複合繊維の場合、鞘成分は熱融着による繊維間の
接着を行うが、芯成分は付与された熱量により熱的劣化
や不定型化することがないので、空気浄化シートを構成
する繊維の一つとなり、シートの機械的性能を向上させ
ることから特に好ましく、その他の二成分系複合繊維も
同様の理由から好適である。
The heat fusible fibers constituting the air purification sheet of the present invention together with the activated carbon fibers can adhere the activated carbon fibers which are in contact with each other only at the contact points by melt fusion or softening of the polymer. The configuration of the heat-fusible fiber may be any of a single component and a composite fiber composed of a plurality of components,
In the case of a core-sheath composite fiber in which a low-melting polymer is disposed in the sheath component and a high-melting polymer is disposed in the core component, the sheath component bonds the fibers by heat fusion, but the core component is heated by the applied heat. It is one of the fibers constituting the air purifying sheet because it does not deteriorate or become irregular, and is particularly preferable because it improves the mechanical performance of the sheet.Other bicomponent composite fibers are also preferable for the same reason. It is.

【0023】また、この熱融着性繊維に用いられる重合
体は、繊維形成性、熱融着性、耐薬品性の観点から、ポ
リアミド系、ポリエステル系、ポリオレフィン系重合体
が好ましく、代表的には、ナイロン6、ナイロン46、
ナイロン66等のポリアミド系重合体、ポリエチレンテ
レフタレ−ト、ポリブチレンテレフタレ−ト、イソフタ
ル酸共重合ポリエチレンテレフタレ−ト、ポリ乳酸等の
ポリエステル系重合体や、ポリエチレン、ポリプロピレ
ン等のポリオレフィン系重合体、そして、これら重合体
のブレンド物や、これら重合体同士の共重合体からなる
ものも含まれ、本発明の効果を阻害しない範囲で、艶消
し剤、顔料、防炎剤、消泡剤、帯電防止剤、酸化防止
剤、紫外線吸収剤等の任意の添加剤が添加されていても
よい。
The polymer used for the heat-fusible fiber is preferably a polyamide-based, polyester-based, or polyolefin-based polymer from the viewpoints of fiber-forming properties, heat-fusing properties, and chemical resistance. Is nylon 6, nylon 46,
Polyester polymers such as polyamide 66 such as nylon 66, polyethylene terephthalate, polybutylene terephthalate, polyethylene terephthalate copolymerized with isophthalic acid, and polylactic acid; and polyolefin-based polymers such as polyethylene and polypropylene. Coalesce, and blends of these polymers, and those comprising copolymers of these polymers are also included, as long as the effects of the present invention are not impaired, matting agents, pigments, flame retardants, defoamers Optional additives such as an antistatic agent, an antioxidant, and an ultraviolet absorber may be added.

【0024】本発明の空気浄化シートは、前記のように
悪臭ガス除去用活性炭繊維と熱融着性繊維を主成分とす
るものであるが、悪臭ガス除去用活性炭繊維と熱融着性
繊維のみで構成してもよく、あるいは本発明の効果を損
なわない範囲で他の繊維やパルプ等を含有させてもよ
い。
The air purifying sheet of the present invention is mainly composed of the activated carbon fiber for removing odorous gas and the heat fusible fiber as described above, but only the activated carbon fiber for removing odorous gas and the heat fusible fiber. Or other fibers or pulp may be contained as long as the effects of the present invention are not impaired.

【0025】次に、本発明の空気浄化シートの製法例に
ついて説明する。まず、前記した悪臭ガス除去用活性炭
繊維と熱融着性繊維を所定の重量比にて混綿した後、ラ
ンダムカード、パラレルカード等のカード機を用い活性
炭繊維と熱融着性繊維からなる不織ウェブを形成する。
なおこの際、目付に応じてクロスラッパー等により不織
ウェブをクロスラップさせ、ニードルパンチ装置により
機械的に繊維の三次元交絡を生じさせて一体化した不織
ウェブを形成する方法も採用することができる。
Next, an example of a method for producing the air purification sheet of the present invention will be described. First, the activated carbon fiber for removing odorous gas and the heat-fusible fiber are mixed at a predetermined weight ratio, and then a non-woven fabric composed of the activated carbon fiber and the heat-fusible fiber using a card machine such as a random card or a parallel card. Form the web.
At this time, a method of cross-lapping the non-woven web with a cross wrapper or the like according to the basis weight and mechanically generating three-dimensional entanglement of the fibers with a needle punch device to form an integrated non-woven web is also adopted. Can be.

【0026】このようにして形成した活性炭繊維からな
る不織ウェブを、熱融着性繊維の融点又は軟化点温度以
上、(融点又は軟化点+40)℃未満の温度に設定した
乾燥機中を通過させることで、活性炭繊維と熱融着性繊
維との間に熱融着又は軟化による繊維間固定を生じさせ
てシート化することにより、目的とする空気浄化シート
を得る。その際、カレンダーロールでシートの厚みを調
整することもできる。
The thus formed non-woven web of activated carbon fibers is passed through a dryer set at a temperature equal to or higher than the melting point or softening point of the heat-fusible fiber and lower than (melting point or softening point +40) ° C. By doing so, an inter-fiber fixation between the activated carbon fiber and the heat-fusible fiber is caused by heat fusion or softening to form a sheet, thereby obtaining an intended air purification sheet. At that time, the thickness of the sheet can be adjusted with a calender roll.

【0027】このようにして得られた空気浄化シートを
空気浄化用として用いる際には、エレクトレット化され
た不織布シート等を張り合わせることで除塵効果を付与
することも可能であり、空気浄化と除塵を兼ね合わせた
空気清浄器等に好適なフィルターとすることができる。
また、フィルター形状は、平板シートと波形シートを交
互に重ね合わせたコルゲート形状でも、シートをプリー
ツ状に折り曲げた形状のものでも、単にシートを平板と
して使用したものでも、フィルターとして有効に作用さ
せることができる。
When the air purification sheet thus obtained is used for air purification, a dust removing effect can be imparted by laminating an electretized nonwoven fabric sheet or the like. And a filter suitable for an air purifier or the like that combines the above.
In addition, the filter shape can be a corrugated shape in which a flat sheet and a corrugated sheet are alternately overlapped, a shape in which the sheet is folded in a pleated shape, or a shape in which the sheet is simply used as a flat plate, to effectively act as a filter. Can be.

【0028】[0028]

【実施例】次に、本発明を実施例により具体的に説明す
る。なお、本発明は、これらの実施例によって何ら限定
されるものではない。なお、実施例における各物性値
は、次の方法で測定した。 (1) 単位重量当たりのアセトアルデヒド吸着量 試料を、アセトアルデヒド濃度100ppm、ガス容量
3Lのテドラーバック中に24時間静置し、24時間後
のアセトアルデヒド濃度を測定し、測定した値から単位
重量当たりのアセトアルデヒド吸着量を求めた。 (2) アセトアルデヒドの吸着速度 アセトアルデヒド濃度20ppm、ガス容量20Lのテ
ドラーバック内のガスを、ポンプを使い、7L/分のガ
ス流量で試料を入れたガラスカラム中を通過させ、出て
きたガスをもう一度テドラーバック内に戻す循環通気を
行い、アセトアルデヒドの減衰濃度を測定して、測定し
た値から単位時間当たりのアセトアルデヒド吸着量を求
めた。上記(1)(2)において、アセトアルデヒド濃度は、
FIDガス検出器を備えたYanaco製G3810ガ
スクロマトグラフィを用いて測定した。 (3) 単位重量当たりのアンモニア吸着量 アンモニア濃度100ppm、ガス容量3Lのテドラー
バック中に試料を24時間静置し、24時間後のアンモ
ニア濃度を測定し、測定した値から単位重量当たりのア
ンモニア吸着量を求めた。 (4) アンモニアの吸着速度 アンモニア濃度20ppm、ガス容量20Lのテドラー
バック内のガスをポンプを使い、7L/minのガス流
量で、試料を入れたガラスカラム中を通過させ、出てき
たガスをもう一度テドラーバック内に戻す循環通気を行
い、アンモニアの減衰濃度を測定し、測定した値から単
位時間当たりのアンモニア吸着量を求めた。上記(3)(4)
において、アンモニアのガス濃度は北川式ガス検知管で
測定した。 (5) 比表面積 カンターソーブ社製オートシックス自動ガス吸着装置を
用い、低温窒素吸着法でBET多点法による相対圧0.
3で測定した。
Next, the present invention will be described in detail with reference to examples. Note that the present invention is not limited by these examples. In addition, each physical property value in an Example was measured by the following method. (1) Acetaldehyde adsorption amount per unit weight The sample was allowed to stand in a Tedlar bag having an acetaldehyde concentration of 100 ppm and a gas volume of 3 L for 24 hours, and the acetaldehyde concentration after 24 hours was measured, and the acetaldehyde adsorption per unit weight was determined from the measured value. The amount was determined. (2) Acetaldehyde adsorption rate The gas in the Tedlar bag having an acetaldehyde concentration of 20 ppm and a gas volume of 20 L was passed through a glass column containing a sample at a gas flow rate of 7 L / min using a pump, and the gas that came out was again Tedlar bag. The inside of the container was circulated and the acetaldehyde decay concentration was measured, and the amount of acetaldehyde adsorbed per unit time was determined from the measured value. In the above (1) and (2), the acetaldehyde concentration is
Measurements were made using a Yanaco G3810 gas chromatography equipped with a FID gas detector. (3) Ammonia adsorption amount per unit weight The sample was allowed to stand for 24 hours in a Tedlar bag having an ammonia concentration of 100 ppm and a gas capacity of 3 L, and the ammonia concentration after 24 hours was measured. From the measured value, the ammonia adsorption amount per unit weight was measured. I asked. (4) Ammonia adsorption rate The gas in the Tedlar bag having an ammonia concentration of 20 ppm and a gas capacity of 20 L was passed through the glass column containing the sample at a gas flow rate of 7 L / min using a pump, and the gas that came out was again Tedlar bag. Circulation ventilation was performed to return the inside of the chamber, and the attenuation concentration of ammonia was measured, and the ammonia adsorption amount per unit time was determined from the measured value. Above (3) (4)
In, the gas concentration of ammonia was measured with a Kitagawa gas detector tube. (5) Specific surface area Using a Cantersorb Auto Six automatic gas adsorption apparatus, the relative pressure was determined by the BET multipoint method using a low-temperature nitrogen adsorption method.
3 was measured.

【0029】実施例1 比表面積1200m2 /gの活性炭繊維にp−アミノ安
息香酸リン酸塩とリン酸を、p−アミノ安息香酸リン酸
塩が13.4質量%、リン酸はp−アミノ安息香酸リン
酸塩とのモル数比で0.74となる量を浴比1:50と
した浸漬法で担持させ、担持後の活性炭繊維の比表面積
を800m2 /gとした悪臭ガス除去用活性炭繊維(試
料)を作製した。この試料を用い、単位重量当たりのア
セトアルデヒド吸着量、アセトアルデヒドの吸着速度、
単位重量当たりのアンモニア吸着量及びアンモニアの吸
着速度を測定した。
Example 1 Activated carbon fibers having a specific surface area of 1200 m 2 / g were provided with p-aminobenzoic acid phosphate and phosphoric acid, p-aminobenzoic acid phosphate at 13.4% by mass, and phosphoric acid as p-amino acid. For the removal of malodorous gas, the activated carbon fiber was supported by an immersion method with a bath ratio of 1:50 in an amount of 0.74 in molar ratio with benzoic acid phosphate, and the specific surface area of the supported carbon fiber was 800 m 2 / g. Activated carbon fiber (sample) was produced. Using this sample, acetaldehyde adsorption amount per unit weight, acetaldehyde adsorption rate,
The amount of ammonia adsorbed per unit weight and the adsorption rate of ammonia were measured.

【0030】実施例2 p−アミノ安息香酸リン酸塩の担持量を20質量%、リ
ン酸の担持量をp−アミノ安息香酸リン酸塩のモル数比
で0.16となる量とし、担持後の活性炭繊維の比表面
積を700m2 /gとした以外は、実施例1と同様にし
て試料を作製し、各物性値を測定した。
Example 2 The supported amount of p-aminobenzoic acid phosphate was set to 20% by mass, and the supported amount of phosphoric acid was set to 0.16 in molar ratio of p-aminobenzoic acid phosphate. Samples were prepared in the same manner as in Example 1 except that the specific surface area of the activated carbon fiber was 700 m 2 / g, and the physical properties were measured.

【0031】実施例3 比表面積800m2 /gの活性炭繊維を用い、p−アミ
ノ安息香酸リン酸塩の担持量を14.5質量%、リン酸
の担持量をp−アミノ安息香酸リン酸塩のモル数比で
0.21となる量とし、担持後の活性炭繊維の比表面積
を350m2 /gとした以外は、実施例1と同様にして
試料を作製し、各物性値を測定した。
Example 3 Using activated carbon fiber having a specific surface area of 800 m 2 / g, the loading of p-aminobenzoic acid phosphate was 14.5% by mass, and the loading of phosphoric acid was p-aminobenzoic acid phosphate. And the physical properties were measured in the same manner as in Example 1 except that the molar ratio was 0.21 and the specific surface area of the activated carbon fiber after loading was 350 m 2 / g.

【0032】実施例4 比表面積1700m2 /gの活性炭繊維を用い、p−ア
ミノ安息香酸リン酸塩の担持量を25.0質量%、リン
酸の担持量をp−アミノ安息香酸リン酸塩のモル数比で
0.22となる量とし、担持後の活性炭繊維の比表面積
を850m2 /gとした以外は、実施例1と同様にして
試料を作製し、各物性値を測定した。
Example 4 Using activated carbon fibers having a specific surface area of 1700 m 2 / g, the amount of p-aminobenzoic acid phosphate supported was 25.0% by mass, and the amount of phosphoric acid supported was p-aminobenzoic acid phosphate. A sample was prepared in the same manner as in Example 1 except that the molar ratio was 0.22, and the specific surface area of the activated carbon fiber after loading was 850 m 2 / g, and the physical properties were measured.

【0033】実施例5 比表面積1200m2 /gの活性炭繊維にp−アミノ安
息香酸リン酸塩とリン酸を、p−アミノ安息香酸リン酸
塩が13.4質量%、リン酸はp−アミノ安息香酸リン
酸塩とのモル数比で0.74となる量を浸漬法で担持さ
せ、担持後の比表面積が800m2 /gである悪臭ガス
除去用活性炭繊維Aを作成した。次いで、上記で得られ
た悪臭ガス除去用活性炭繊維Aと、芯成分がポリエチレ
ンテレフタレート、鞘成分がイソフタル酸共重合ポリエ
ステル(融点110℃)からなる芯鞘複合繊維Bとをパ
ラレルカードを用いて質量比(A:B)が70:30と
なる不織ウェブを形成した後、クロスラッパーにより不
織ウェブをクロスラップさせ、ニードルパンチ装置によ
り機械的に繊維の三次元交絡を生じさせて一体化した不
織ウェブを作成した。さらに、この不織ウェブを、(鞘
成分の融点+30)℃の温度で乾燥機中を通過させ、活
性炭繊維と熱融着性繊維とを熱融着による繊維間固定を
生じさせ、目付100g/m2 の空気浄化シートとし、
このシートの各物性値を測定した。実施例1〜5で得ら
れた結果を表1に示す。
Example 5 Activated carbon fibers having a specific surface area of 1200 m 2 / g were mixed with p-aminobenzoic acid phosphate and phosphoric acid, p-aminobenzoic acid phosphate at 13.4% by mass, and phosphoric acid as p-amino acid. An amount of 0.74 in terms of mole ratio with respect to benzoic acid phosphate was carried by an immersion method to prepare activated carbon fiber A for removing odorous gas having a specific surface area of 800 m 2 / g after carrying. Next, the activated carbon fiber A for removing malodorous gas obtained above and the core-sheath composite fiber B whose core component is made of polyethylene terephthalate and whose sheath component is made of isophthalic acid copolymerized polyester (melting point 110 ° C.) are mass-processed using a parallel card. After forming a nonwoven web having a ratio (A: B) of 70:30, the nonwoven web was cross-wrapped by a cross wrapper, and mechanically three-dimensionally entangled with a needle punch device to be integrated. Created a non-woven web. Further, the nonwoven web is passed through a dryer at a temperature of (melting point of the sheath component + 30) ° C., and the activated carbon fiber and the heat-fusible fiber are fixed to each other by heat-sealing. and air purifying sheet m 2,
The physical properties of this sheet were measured. Table 1 shows the results obtained in Examples 1 to 5.

【0034】比較例1 実施例1と同じ活性炭繊維を用い、同様の方法でp−ア
ミノ安息香酸を10質量%となる量、浸漬法で担持さ
せ、担持後の活性炭繊維の比表面積を800m2/gと
した試料を作製し、各物性値を測定した。
Comparative Example 1 The same activated carbon fiber as in Example 1 was used, and p-aminobenzoic acid was loaded in a similar manner to an amount of 10% by mass by an immersion method. The activated carbon fiber after loading had a specific surface area of 800 m 2. / G sample was prepared, and each physical property value was measured.

【0035】比較例2 p−アミノ安息香酸リン酸塩の担持量を40質量%、リ
ン酸の担持量をp−アミノ安息香酸リン酸塩とのモル数
比で1.2となる量とし、担持後の活性炭繊維の比表面
積を200m2 /gとした以外は、実施例1と同様にし
て試料を作製し、各物性値を測定した。
Comparative Example 2 The amount of p-aminobenzoic acid phosphate carried was 40% by mass, and the amount of phosphoric acid carried was 1.2 in terms of molar ratio with p-aminobenzoic acid phosphate. A sample was prepared in the same manner as in Example 1 except that the specific surface area of the activated carbon fiber after loading was 200 m 2 / g, and each physical property value was measured.

【0036】比較例3 p−アミノ安息香酸リン酸塩の担持量を10質量%、リ
ン酸の担持量をp−アミノ安息香酸リン酸塩とのモル数
比で2.5となる量とし、担持後の活性炭繊維の比表面
積を400m2 /gとした以外は、実施例1と同様にし
て試料を作製し、各物性値を測定した。
Comparative Example 3 The supported amount of p-aminobenzoic acid phosphate was 10% by mass, and the supported amount of phosphoric acid was 2.5 such that the molar ratio with respect to p-aminobenzoic acid phosphate was 2.5. Samples were prepared in the same manner as in Example 1, except that the specific surface area of the activated carbon fiber after loading was 400 m 2 / g, and the physical properties were measured.

【0037】比較例4 比表面積が400m2 /gの市販の粒状活性炭を用い、
p−アミノ安息香酸リン酸塩の担持量を10質量%、リ
ン酸の担持量をp−アミノ安息香酸リン酸塩とのモル数
比で0.8となる量とし、担持後の活性炭の比表面積を
100m2 /gとした以外は、実施例1と同様にして試
料を作製し、各物性値を測定した。
Comparative Example 4 A commercially available granular activated carbon having a specific surface area of 400 m 2 / g was used.
The supported amount of p-aminobenzoic acid phosphate was 10% by mass, and the supported amount of phosphoric acid was 0.8 such that the molar ratio with respect to p-aminobenzoic acid phosphate was 0.8. A sample was prepared in the same manner as in Example 1 except that the surface area was changed to 100 m 2 / g, and each physical property value was measured.

【0038】比較例5 比表面積1700m2 /gの活性炭繊維を用い、p−ア
ミノ安息香酸リン酸塩の担持量を25.0質量%、リン
酸の担持量をp−アミノ安息香酸リン酸塩とのモル数比
で0.01となる量とし、担持後の活性炭繊維の比表面
積を850m2/gとした以外は、実施例1と同様にし
て試料を作製し、各物性値を測定した。比較例1〜5で
得られた結果を表2に示す。
Comparative Example 5 Using activated carbon fiber having a specific surface area of 1700 m 2 / g, the loading amount of p-aminobenzoic acid phosphate was 25.0% by mass, and the loading amount of phosphoric acid was p-aminobenzoic acid phosphate. A sample was prepared and the physical properties were measured in the same manner as in Example 1 except that the molar ratio with respect to the amount was 0.01, and the specific surface area of the activated carbon fiber after loading was 850 m 2 / g. . Table 2 shows the results obtained in Comparative Examples 1 to 5.

【0039】[0039]

【表1】 [Table 1]

【0040】[0040]

【表2】 [Table 2]

【0041】表1、2から明らかなように、実施例1〜
5で得られた悪臭ガス除去用活性炭繊維や空気浄化シー
トは、アセトアルデヒドとアンモニアのいずれも吸着量
が高く、吸着速度も速く、悪臭ガス除去用素材として優
れていた。これに対して、比較例1〜5のものは、アセ
トアルデヒド及びアンモニア両方とも吸着量が高く、吸
着速度も速いものはなく、低級アルデヒド類と塩基性ガ
スを含有する悪臭ガスの除去用素材としては劣るもので
あった。
As is clear from Tables 1 and 2, Examples 1 to
The activated carbon fiber for removing odor gas and the air purification sheet obtained in 5 had a high adsorption amount of both acetaldehyde and ammonia, a high adsorption speed, and were excellent as a material for removing odor gas. On the other hand, those of Comparative Examples 1 to 5 have high adsorption amounts of both acetaldehyde and ammonia, and none of them have a high adsorption speed, and are used as materials for removing malodorous gas containing lower aldehydes and basic gas. It was inferior.

【0042】実施例6 実施例5の空気浄化シートを用い、酢酸の吸着能力を評
価した。測定は、酢酸濃度100ppm、ガス容量3L
のテドラーバック中に試料を24時間静置し、24時間
後の酢酸濃度を北川式ガス検知管で測定し、測定値から
単位重量当たりの酢酸吸着量を求めた。また、吸着速度
は、酢酸濃度50ppm、ガス容量20Lのテドラーバ
ック内のガスを、ポンプを使い、7L/minのガス流
量で試料を入れたガラスカラム中を通過させ、出てきた
ガスをもう一度テドラーバック内に戻す循環通気を行
い、酢酸の減衰濃度を測定し、測定した値から単位時間
当たりの酢酸吸着量を求めた。得られた結果を表3に示
すが、酢酸に対して良好な吸着能力と吸着速度を有して
いた。
Example 6 Using the air purification sheet of Example 5, the acetic acid adsorption capacity was evaluated. The measurement was performed with an acetic acid concentration of 100 ppm and a gas volume of 3 L.
The sample was allowed to stand for 24 hours in a Tedlar bag, and the acetic acid concentration after 24 hours was measured with a Kitagawa gas detector tube, and the acetic acid adsorption amount per unit weight was determined from the measured value. The adsorption speed was such that the gas in the Tedlar bag having an acetic acid concentration of 50 ppm and a gas capacity of 20 L was passed through a glass column containing a sample at a gas flow rate of 7 L / min using a pump, and the gas that had come out was once again placed in the Tedlar bag. The circulating aeration was carried out, and the decay concentration of acetic acid was measured, and the acetic acid adsorption amount per unit time was determined from the measured value. The obtained results are shown in Table 3, and showed that the acetic acid had good adsorption capacity and adsorption speed.

【0043】[0043]

【表3】 [Table 3]

【0044】[0044]

【発明の効果】本発明の悪臭ガス除去用活性炭繊維は、
悪臭ガス、特にアセトアルデヒド等の低級アルデヒド類
とアンモニア等の塩基性ガスの除去量がいずれも高く、
かつ、その除去速度も速いものである。このように、単
一の素材で低級アルデヒド類と塩基性ガス、両方の悪臭
成分を除去できるので、この活性炭繊維を主成分とする
本発明の空気浄化シートは、室内用、車載用を問わず、
空気清浄器ほぼ全般の分野でフィルターとして好適なも
のである。
The activated carbon fiber for removing offensive odor gas of the present invention comprises:
The removal amount of malodorous gas, especially lower aldehydes such as acetaldehyde and basic gas such as ammonia are both high,
In addition, the removal speed is high. As described above, the lower aldehydes and the basic gas, both of which are offensive odor, can be removed by a single material, so that the air purification sheet of the present invention containing this activated carbon fiber as a main component can be used indoors or in vehicles. ,
The air purifier is suitable as a filter in almost all fields.

─────────────────────────────────────────────────────
────────────────────────────────────────────────── ───

【手続補正書】[Procedure amendment]

【提出日】平成13年3月12日(2001.3.1
2)
[Submission date] March 12, 2001 (2001.3.1.
2)

【手続補正1】[Procedure amendment 1]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0003[Correction target item name] 0003

【補正方法】変更[Correction method] Change

【補正内容】[Correction contents]

【0003】また、特公平4−39368号公報には、
セピオライト、活性炭等の多孔性担体に、芳香族アミノ
酸又は芳香族アミノ酸の塩を担持した低級アルデヒド類
の除去剤が提案されている。しかし、これらの除去剤
は、低級アルデヒドの除去能は有するものの、たばこの
煙中に含まれるアンモニアのような塩基性物質の除去に
はほとんど効果がないという欠点を有していた。
Further, Japanese Patent Publication No. 4-39368 discloses that
A remover for lower aldehydes in which an aromatic amino acid or a salt of an aromatic amino acid is supported on a porous carrier such as sepiolite or activated carbon has been proposed. However, although these removing agents have the ability to remove lower aldehydes, they have the drawback that they have little effect on removing basic substances such as ammonia contained in cigarette smoke.

【手続補正2】[Procedure amendment 2]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0044[Correction target item name] 0044

【補正方法】変更[Correction method] Change

【補正内容】[Correction contents]

【0044】[0044]

【発明の効果】本発明の悪臭ガス除去用活性炭繊維は、
悪臭ガス、特にアセトアルデヒド等の低級アルデヒド類
とアンモニア等の塩基性ガス及び酢酸の除去量がいずれ
も高く、かつ、その除去速度も速いものである。このよ
うに、単一の素材で低級アルデヒド類と塩基性ガス及び
酢酸の三成分の悪臭成分を除去できるので、この活性炭
繊維を主成分とする本発明の空気浄化シートは、室内
用、車載用を問わず、空気清浄器ほぼ全般の分野でフィ
ルターとして好適なものである。
The activated carbon fiber for removing offensive odor gas of the present invention comprises:
The removal amount of the odorous gas, particularly the lower aldehydes such as acetaldehyde, the basic gas such as ammonia, and the acetic acid are all high, and the removal rate is high. Thus, lower aldehydes and basic gas and
Since the three odor components of acetic acid can be removed, the air purification sheet of the present invention containing this activated carbon fiber as a main component is suitable as a filter in almost all fields of air purifiers regardless of whether it is for indoor use or vehicle use. It is.

───────────────────────────────────────────────────── 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) B01D 53/04 B01D 53/04 A D06M 13/342 D06M 13/342 // D06M 101:40 101:40 (72)発明者 徳永 加奈 京都府宇治市宇治小桜23番地 ユニチカ株 式会社中央研究所内 (72)発明者 浅見 圭一 京都府宇治市宇治小桜23番地 ユニチカ株 式会社中央研究所内 Fターム(参考) 4C080 AA05 CC12 HH09 JJ05 JJ06 MM01 MM05 MM18 NN05 4D012 BA03 CA09 CA10 CB03 CE03 CG03 CG04 4G066 AA05B AA05C AA50B AA50D AB27B AB27D AC23C BA03 BA16 BA26 CA02 CA29 CA52 DA03 FA12 FA37 4L033 AA09 AB01 AC15 BA53 DA04──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification code FI Theme coat ゛ (Reference) B01D 53/04 B01D 53/04 A D06M 13/342 D06M 13/342 // D06M 101: 40 101: 40 ( 72) Inventor Kana Tokunaga 23 Uji Kozakura, Uji City, Kyoto Prefecture, Unitika Central Research Laboratory (72) Inventor Keiichi Asami 23 Uji Kozakura Uji City, Kyoto Prefecture Unitika Central Research Laboratory F term 4C080 AA05 CC12 HH09 JJ05 JJ06 MM01 MM05 MM18 NN05 4D012 BA03 CA09 CA10 CB03 CE03 CG03 CG04 4G066 AA05B AA05C AA50B AA50D AB27B AB27D AC23C BA03 BA16 BA26 CA02 CA29 CA52 DA03 FA12 FA37 4L033 AA09 DA

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 芳香族アミノ酸の塩とリン酸が担持され
た活性炭繊維において、芳香族アミノ酸の塩の担持量が
7〜30質量%、リン酸の担持量が芳香族アミノ酸の塩
のモル数に対するリン酸のモル数の比が0.05〜1.
0となる量であり、担持後の活性炭繊維の比表面積が3
00〜1000m2 /gであることを特徴とする悪臭ガ
ス除去用活性炭繊維。
1. In an activated carbon fiber carrying an aromatic amino acid salt and phosphoric acid, the amount of the aromatic amino acid salt carried is 7 to 30% by mass, and the amount of phosphoric acid carried is the number of moles of the aromatic amino acid salt. The molar ratio of phosphoric acid to 0.05 to 1.
And the specific surface area of the activated carbon fiber after loading is 3
Activated carbon fiber for removing odorous gas, characterized by having a molecular weight of from 00 to 1000 m 2 / g.
【請求項2】 請求項1記載の活性炭繊維と熱融着性繊
維を主成分とし、熱融着性繊維の融着又は軟化で所定の
形態を保持したシートであって、請求項1記載の活性炭
繊維の含有率が40質量%以上であることを特徴とする
空気浄化用シート。
2. A sheet comprising the activated carbon fiber and the heat-fusible fiber according to claim 1 as main components, and maintaining a predetermined shape by fusing or softening the heat-fusible fiber. An air purification sheet, wherein the content of activated carbon fibers is 40% by mass or more.
JP2000361167A 2000-11-28 2000-11-28 Active carbon fiber for removing malodorous gas and air cleaning sheet Pending JP2002159852A (en)

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Country Link
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Publication number Priority date Publication date Assignee Title
WO2009031248A1 (en) * 2007-09-05 2009-03-12 Daicel Chemical Industries, Ltd. Composition containing amino compound and silica gel, and tobacco filter
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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009031248A1 (en) * 2007-09-05 2009-03-12 Daicel Chemical Industries, Ltd. Composition containing amino compound and silica gel, and tobacco filter
CN101623582B (en) * 2009-07-30 2011-09-28 上海交通大学 Device for indicating and removing formaldehyde
WO2011040577A1 (en) * 2009-09-30 2011-04-07 株式会社 キャタラー Adsorbent material and method for producing same
JP5504274B2 (en) * 2009-09-30 2014-05-28 株式会社キャタラー Adsorbent and method for producing the same
JP2014073439A (en) * 2012-10-03 2014-04-24 Kao Corp Gas adsorbent
JP5728113B1 (en) * 2014-07-25 2015-06-03 ユニチカ株式会社 Adsorbent
CN106310874A (en) * 2015-06-17 2017-01-11 中国石油化工股份有限公司 Absorbent for trapping carbon dioxide
CN111971075A (en) * 2018-03-30 2020-11-20 尤尼吉可株式会社 Deodorizing material, method for producing the same, deodorizing method, and deodorizing sheet
CN111971075B (en) * 2018-03-30 2022-09-30 尤尼吉可株式会社 Deodorizing material, method for producing the same, deodorizing method, and deodorizing sheet
CN110013832A (en) * 2019-03-18 2019-07-16 贵州万峰湖智慧水产科技有限公司 A kind of cultivation water process carbon fiber modifying material and preparation method thereof
CN110013832B (en) * 2019-03-18 2022-03-04 广州誉隆智慧科技有限公司 Carbon fiber modified material for aquaculture water treatment and preparation method thereof
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