JPH0338212A - Air filter - Google Patents

Air filter

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Publication number
JPH0338212A
JPH0338212A JP1173324A JP17332489A JPH0338212A JP H0338212 A JPH0338212 A JP H0338212A JP 1173324 A JP1173324 A JP 1173324A JP 17332489 A JP17332489 A JP 17332489A JP H0338212 A JPH0338212 A JP H0338212A
Authority
JP
Japan
Prior art keywords
parts
deodorizer
air filter
fungal agent
sheet material
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
JP1173324A
Other languages
Japanese (ja)
Other versions
JP2954236B2 (en
Inventor
Yasuo Yokoi
横井 保夫
Michio Kashima
道夫 加島
Kenji Ichikawa
賢治 市川
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP1173324A priority Critical patent/JP2954236B2/en
Publication of JPH0338212A publication Critical patent/JPH0338212A/en
Application granted granted Critical
Publication of JP2954236B2 publication Critical patent/JP2954236B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
  • Treating Waste Gases (AREA)
  • Filtering Materials (AREA)

Abstract

PURPOSE:To manufacture an air filter for cleaning inside a room or a car by adhering a deodorizer or an anti-fungal agent to a sheet material constituted of a breathing material. CONSTITUTION:An air filter made of a sheet material constituted of a breathing material to which a deodorizer or an anti-fungal agent is adhered is manufactured. As for a solid adsorbent as the deodorizer, alumina group, aluminosilicate group or silica group adsorbent such as active carbon and seolite, zinc silicate, sepiolite, Crystpearl(R) or the like as well as anion exchange resin, amphoteric ion exchange resin or the like can be used. As for the anti-fungal agent, amino acid metallic salt 2,4,4-trichloro-2-hydroxydiphenyl ether, or Vinylzene(R) or the like is used. Said deodorizer or anti-fungal agent is used individually or by mixing together and used by the process of immersing, spraying or the like to a sheet material (synthetic fiber or vegetable fiber such as loofah).

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明はエアーフィルターに関する。[Detailed description of the invention] [Industrial application field] The present invention relates to air filters.

[従来の技術] 従来、自動車や家庭等に使用される空調用のエアーフィ
ルターは除塵を目的とし、あるいは除塵の他に脱臭を目
的としている。
[Prior Art] Conventionally, air filters for air conditioning used in automobiles, homes, etc. are intended to remove dust, or to deodorize in addition to dust removal.

[発明が解決しようとする課題] 近年室内あるいは車内をクリーンにすることが望まれ、
そのために除塵と脱臭の他に滅菌を行なうことが要求さ
れている。そこで本発明は係る目的のためのフィルター
を提供するものである。
[Problem to be solved by the invention] In recent years, it has become desirable to keep the interior of a car or a car clean.
Therefore, in addition to dust removal and deodorization, sterilization is required. Therefore, the present invention provides a filter for this purpose.

[:JR題を解決するための手段] 上記の課題を解決するために次の構成とする。[:Means for solving JR problems] In order to solve the above problems, the following configuration is adopted.

即ち、通気性素材よりなるシート材にllG1臭剤及び
抗菌剤を付着してなるエアーフィルターである。
That is, the air filter is made by adhering the llG1 odor agent and antibacterial agent to a sheet material made of a breathable material.

前記シート材は合成WANや植物繊維としてヘチマやヤ
シのtlrHをシート状に加工したものである。
The sheet material is made by processing synthetic WAN or vegetable fibers such as loofah or palm tlrH into a sheet shape.

また前記1151臭剤となる固体吸着剤としては活性炭
及びゼオライト、珪酸亜鉛、セビオライト、クリスバー
ル、シリカゲル、カオリン等のアルミナ系、アルミノシ
リケート系、シリカ系@着剤の他に陽イオン交換樹脂、
陰イオン交換樹脂、両性イオン交換樹脂等がある。
In addition, the solid adsorbents used as the 1151 odorant include activated carbon, zeolite, zinc silicate, Seviolite, Crisbar, silica gel, kaolin, and other alumina-based, aluminosilicate-based, and silica-based adsorbents, as well as cation exchange resins,
There are anion exchange resins, amphoteric ion exchange resins, etc.

好ましい固体吸着剤としてはMO,Zn、Aj)、Si
などを主成分として固体*Uや固体酸及び各種金属のリ
ン酸塩を主成分として固体塩基や固体酸がある。
Preferred solid adsorbents include MO, Zn, Aj), Si
There are solid bases and solid acids containing phosphates of various metals as main components.

Mq、Zn、AI、Siなどを主成分とする[i’、1
体塩基としてはMaO−Al  O−nH2O。
The main components are Mq, Zn, AI, Si, etc. [i', 1
The body base is MaO-Al O-nH2O.

3 ZnO−At  O−nH2O,等がある。3 ZnO-At, O-nH2O, etc.

3 そして、固定酸としてはAl2O3・9Si02”n口
20.2Mgo・6SiO2・0口201等がある。
3. Examples of fixed acids include Al2O3.9Si02''n20.2Mgo.6SiO2.0201.

また、条件によっては両性を示すものとしてAI  O
−nH2O。
Also, depending on the conditions, AIO
-nH2O.

3 z、5Mao−A I  O−nH2O。3 z, 5Mao-A I O-nH2O.

3 A   I   (OH)      −NaHCO3
、2MqO−6SiOaj1口、O1 2 AI O−Na 0・2CO−0口、023  2  
  3 などがある。
3 A I (OH) -NaHCO3
, 2MqO-6SiOaj 1 mouth, O1 2 AI O-Na 0.2CO-0 mouth, 023 2
3 etc.

各秤金属のリンm塩を主成分としたリンm塩の中には酸
型としてBPO、Z「(HPO4)2、Zr     
(トIPO)     、  AIPO4、OCP、H
344 P1 塩基型としてに3PO4、Na3PO4、両性型として
βTCP、LiNa  PO、Li4 2MePO4の三つのタイプがある。
Among the phosphorus m-salts whose main components are phosphorus m-salts of various scale metals, there are acid forms such as BPO, Z'(HPO4)2, and Zr.
(ToIPO), AIPO4, OCP, H
344 P1 There are three base types: 3PO4 and Na3PO4, and amphoteric types: βTCP, LiNa PO, and Li4 2MePO4.

これらのうち好ましい固体リン酸塩としてはCaHPO
1Ca (PO〉 、Ca2P24  3  42 07、Ca4 〈PO4〉20.0PC1Ca1゜(P
O4)6X2  (X=OローF−CI)、Zr(口P
O)  ・H20ST t (HP 04 ) 22 020、H5(口PO4)2−H20、Ge(口PO)
  ・口 0.Rb(口PO)  ・口242    
2               4205Mg口PO
、(LiPO)  、Rb(P4          
 3n O)  、(KPO)  、(NaPO3)。等3n 
          3n のリンm塩がある。また、脱臭機構が活性炭ように吸着
作用でなく、触媒作用等による反応であるリン酸系化合
物、金a酸化物を主剤とし、これに担体を組み合わせた
無機系の固体l112臭剤がある(日本犬i1(株〉装
面品名KAYAMAX)。
Among these, the preferred solid phosphate is CaHPO
1Ca (PO> , Ca2P24 3 42 07, Ca4 <PO4> 20.0PC1Ca1゜(P
O4) 6X2 (X=OlowF-CI), Zr(mouth P
O) ・H20ST t (HP 04 ) 22 020, H5 (mouth PO4) 2-H20, Ge (mouth PO)
・Mouth 0. Rb (mouth PO) ・mouth 242
2 4205Mg port PO
, (LiPO) , Rb(P4
3nO), (KPO), (NaPO3). etc. 3n
There is a phosphorus m salt of 3n. In addition, there are inorganic solid l112 odorants whose deodorizing mechanism is not adsorption like activated carbon, but a reaction based on catalytic action.The main ingredients are phosphoric acid compounds and gold a oxide, and these are combined with a carrier (Japanese). Inu i1 Co., Ltd. Product name: KAYAMAX).

抗菌剤としては、アミノ酸金属塩や2−4−4トリクロ
ロ−2−ハイドロキシジフェニールエテル等であり、ま
たプラスチックに発生するカビの防止剤としてバイナジ
ン、ブリベントールやチアベンダゾール等である。
Examples of antibacterial agents include amino acid metal salts and 2-4-4 trichloro-2-hydroxydiphenyl ether, and agents for preventing molds that occur on plastics include vinazine, briventol, and thiabendazole.

なお上記の脱臭剤と抗菌剤及びこれらを接着させるため
の接着剤の組成は次の如くである。即ち、lt2臭剤と
して、固体酸を0〜100%、活性炭を0〜100%の
範囲で固体酸と活性炭を単独あるいは混合物として5〜
60部、抗菌剤を0.01〜2部1.接着剤10〜90
部の範囲で組成を構成する。
The compositions of the above deodorizing agent, antibacterial agent, and adhesive for bonding these are as follows. That is, as an lt2 odorant, solid acid and activated carbon may be used in a range of 0 to 100% and activated carbon in a range of 0 to 100%, either alone or as a mixture.
60 parts, 0.01 to 2 parts of antibacterial agent1. Adhesive 10-90
The composition consists of a range of parts.

そして、脱臭剤を単独あるいは抗菌剤と混合してシート
材に浸漬又は吹き付けによって、あるいは脱臭剤を単独
あるいは抗菌剤を混合したもの、あるいは2種類以上の
固体酸と活性炭を組合せたものをそれぞれシート材に部
分的に捺染め又は吹き付けて作る。
Then, the deodorizer alone or mixed with an antibacterial agent is soaked or sprayed onto the sheet material, or the deodorizer alone or mixed with an antibacterial agent, or a combination of two or more types of solid acids and activated carbon is applied to the sheet material. It is made by partially printing or spraying the material.

ここで前記の接着剤の特質としては接着力があり、被膜
の伸びがよく、折り曲げても亀裂の入らないことが望ま
しい。また、加工後は仕上風合がよく、耐洗)a性、耐
油性があることが必要である。
Here, it is preferable that the above-mentioned adhesive has adhesive strength, has good film elongation, and does not crack even when bent. In addition, after processing, it is necessary to have a good finish, wash resistance (a), and oil resistance.

この目的に使用できる接着剤としては天然ゴムラテック
ス、S B Rラテックス、8Bラテツクス、NBRラ
テックス、NRラテックス、MBRラテックスス、MB
ラテックス、クロロブレンゴムラテックス、ネオプレン
ラテックス、ブチルゴムラテックス、ポリイソプレンラ
テックス、塩化ビニルラテックス、塩化ビニリデンラテ
ックス、酢ビラテックス、アクリル酸エステルラテック
ス等があげられる。
Adhesives that can be used for this purpose include natural rubber latex, SBR latex, 8B latex, NBR latex, NR latex, MBR latex, MB
Examples include latex, chloroprene rubber latex, neoprene latex, butyl rubber latex, polyisoprene latex, vinyl chloride latex, vinylidene chloride latex, acetic acid vinyl latex, and acrylic acid ester latex.

これらのうち好ましいものはアクリル酸エステル系ラテ
ックスでメチルアクリレート、エチルアクリレート、ブ
チルアクリレート、2エチルへキシルアクリレート、ア
クリル酸、アクリルアマイドなとの単独又は共重合体が
用いられる。
Among these, preferred are acrylic ester latexes, such as single or copolymers of methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, acrylic acid, and acrylamide.

また、これらにスチレン、メタアクリル酸メチルや酢ビ
、塩ビ等を共重合させることにより、適当な柔軟性、接
着力、強度、耐水性等が付与できる。
Further, by copolymerizing these with styrene, methyl methacrylate, vinyl acetate, vinyl chloride, etc., appropriate flexibility, adhesive strength, strength, water resistance, etc. can be imparted.

更に8度な要求に対しては反応性高分子による分子間及
び分子内架橋によるポリマーのグラフト化、三次元化を
行ない耐洗濯性、耐溶剤性、防シワ性、バネ弾性、屈撓
性、接着力の増強等の特性を付与することができる。
Furthermore, in response to the 8 degrees requirement, we graft polymers and make them three-dimensional by intermolecular and intramolecular cross-linking using reactive polymers to improve wash resistance, solvent resistance, wrinkle resistance, spring elasticity, flexibility, Properties such as enhanced adhesive strength can be imparted.

主な反応性七ノマーとしてはカルボキシル基を有するも
の、アミド及びイミノ基を有するもの、エポキシ基を有
するもの、ヒドロキシル基を有するものなどが有効であ
る。
As the main reactive heptanomers, those having a carboxyl group, those having an amide and imino group, those having an epoxy group, those having a hydroxyl group, etc. are effective.

これらの反応基を有する反応性アクリレート系ラテック
スは耐溶剤性、耐洗濯性、弾性付与、強度上界、耐熱性
の向上及びIl雑等の基材との反応による密着性の向上
等の特徴を与えることができる。
Reactive acrylate latex with these reactive groups has characteristics such as solvent resistance, washing resistance, elasticity, upper limit of strength, improved heat resistance, and improved adhesion by reaction with base materials such as Il and other materials. can give.

また、アクリル酸エステルにジビニルベンゼン、ジビニ
ルスルホン、アクリル酸アリル、クロトン酸ビニルなど
を加えて乳化重合させると内部架橋し、弾性体ゴム状物
質となって不織布等にバネ弾性屈撓性、耐老化性、耐薬
品性、耐溶剤性、を付与することができる。
In addition, when divinylbenzene, divinyl sulfone, allyl acrylate, vinyl crotonate, etc. are added to acrylic acid ester and emulsion polymerized, it internally crosslinks and becomes an elastic rubber-like substance that can be used as a nonwoven fabric with spring elastic flexibility and aging resistance. properties, chemical resistance, and solvent resistance.

(A)次に各種試料を作り脱臭性能を比較する。(A) Next, various samples are prepared and their deodorizing performance is compared.

(試料1) (a)活性炭(ヤシガラ系)  25部(b)固体!!
2(ラサ工業(株)型打品名KD211 主成分 珪酸
亜鉛〉   25部(C)アクリルエマルジョン(新中
村化学(株)製造の樹脂分50%の接着剤商品名FX−
34)100部 (d)抗菌剤〈N−ステアロイル−し−グルタミンl!
12銀〉  0.5部 (e)水  55部 (f)エチレングリコール  10部 以上(a)〜(f)の成分を充分に混練りする。
(Sample 1) (a) Activated carbon (coconut shell type) 25 parts (b) Solid! !
2 (Rasa Kogyo Co., Ltd. molding product name KD211 Main component: zinc silicate) 25 parts (C) Acrylic emulsion (Adhesive with 50% resin content manufactured by Shin Nakamura Chemical Co., Ltd. Product name FX-
34) 100 parts (d) Antibacterial agent <N-stearoyl-glutamine!
12 Silver> 0.5 parts (e) Water 55 parts (f) Ethylene glycol 10 parts or more The components (a) to (f) are thoroughly kneaded.

そして、混練した物100部と架橋剤(新中村化学(株
)装面品名MEG)5部を加えて更に混合する。この混
合物に厚み0.5センチで縦、横が25センチのエアー
フィルター用の不織布(重量10グラム〉を浸漬し、ゴ
ムロール等で絞ってエアーフィルターのlff1が59
グラムの物を得た。
Then, 100 parts of the kneaded material and 5 parts of a crosslinking agent (product name: MEG, manufactured by Shin-Nakamura Chemical Co., Ltd.) are added and further mixed. A non-woven fabric for an air filter (weighing 10 grams) with a thickness of 0.5 cm and a length and width of 25 cm was dipped in this mixture, and it was squeezed with a rubber roll etc. until the lff1 of the air filter was 59.
Got a gram of stuff.

このフィルターを温度100〜120℃の熱風で約20
分間予備乾燥し、そして温度140〜150℃の熱風で
約3分乾燥して重量33グラムの試料を得た。
This filter is heated with hot air at a temperature of 100 to 120℃ for about 20 minutes.
The sample was pre-dried for 3 minutes and then dried with hot air at a temperature of 140-150C for about 3 minutes to obtain a sample weighing 33 grams.

(試料2) (a)固体wI(ラサ工業(株)装面品名KD211)
50部 (b)アクリルエマルジョン(新中村化学(株)vJ造
の樹脂分50%の接着剤商品名FX−34>100部 (C)抗菌剤(チアベンダゾール〈メルク社製〉)  
0.5部 (d)水  50部 (e)エチレングリコール  10部 以上(a)〜(e)の成分を充分に混練りする。
(Sample 2) (a) Solid wI (Rasa Kogyo Co., Ltd. mounting product name KD211)
50 parts (b) Acrylic emulsion (Adhesive with 50% resin content manufactured by Shin Nakamura Kagaku Co., Ltd. vJ) Product name FX-34 > 100 parts (C) Antibacterial agent (thiabendazole <manufactured by Merck & Co., Ltd.>)
0.5 parts (d) Water 50 parts (e) Ethylene glycol 10 parts or more Components (a) to (e) are thoroughly kneaded.

そして、混練した物98部と架橋剤(新中村化学(株)
装面品名MEG)5部を加えて更に混合する。この混合
物を試料1と同様の方法で加工処理をして試料を得る。
Then, 98 parts of the kneaded material and a crosslinking agent (Shin Nakamura Chemical Co., Ltd.)
Add 5 parts of MEG) and mix further. This mixture is processed in the same manner as Sample 1 to obtain a sample.

(試料3) (a)活性炭(A7シガラ系)50部部(1))アクリ
ルエマルジョン(新中村化学(株〉製造の樹脂分50%
の接着剤商品名FX−34)008IS (C)抗菌剤(N−ステアロイル−し一グルタミン1S
lI2銀)  0.5部 (d)水  60部 (e)エチレングリコール  10部 以上(a)〜(e)の成分を充分に混練りする。
(Sample 3) (a) Activated carbon (A7 Cigarette type) 50 parts (1)) Acrylic emulsion (resin content 50% manufactured by Shin Nakamura Chemical Co., Ltd.)
Adhesive product name FX-34) 008IS (C) Antibacterial agent (N-stearoyl-glutamine 1S
lI2 Silver) 0.5 parts (d) Water 60 parts (e) Ethylene glycol 10 parts or more The components (a) to (e) are thoroughly kneaded.

そして、混練した物102部と架橋剤(新中村化学(株
)装面品名MEG)5部を加えて更に混合する。そして
、混練した物98部と架橋剤(新中村化学〈株〉装面品
名MEG)5部を加えて更に混合する。この混合物を試
料1と同様の方法で加工処理をして試料を得る。
Then, 102 parts of the kneaded material and 5 parts of a crosslinking agent (product name: MEG, manufactured by Shin Nakamura Chemical Co., Ltd.) were added and further mixed. Then, 98 parts of the kneaded material and 5 parts of a crosslinking agent (product name: MEG, manufactured by Shin Nakamura Chemical Co., Ltd.) were added and further mixed. This mixture is processed in the same manner as Sample 1 to obtain a sample.

(試料4) (a)固体酸(KO211(うl+工業(株〉)25部 (b)固体脱臭剤(日本火薬(株)装面品名KAYAM
AX  DR−301)   2−5部(C)アクリル
エマルジョン(新中村化学(株)製造の樹脂分50%の
接着剤商品名FX−34)25部 (d)抗菌剤(ブリベントール(西独バイエル社)) 
  0.5部 (e)水  60部 (f)エチレングリコール  10部 以上(a)〜(f)の成分を充分に混練りする。
(Sample 4) (a) 25 parts of solid acid (KO211 (Ul+ Kogyo Co., Ltd.)) (b) Solid deodorizer (Nippon Kapowder Co., Ltd. Product name: KAYAM
AX DR-301) 2-5 parts (C) Acrylic emulsion (Adhesive with 50% resin content manufactured by Shin-Nakamura Chemical Co., Ltd. Trade name FX-34) 25 parts (d) Antibacterial agent (Briventol (West German Bayer AG) )
0.5 parts (e) Water 60 parts (f) Ethylene glycol 10 parts or more Components (a) to (f) are thoroughly kneaded.

そして、混練した物102部と架橋剤(新中村化学(株
〉装面品名MEG)5部を加えて更に混合する。そして
、混練した物98部と架橋剤(新中村化学(株>’IJ
商品名MEG)5部を加えて更に混合する。この混合物
を試料1と同様の方法で加■処理をして試料を得る。
Then, 102 parts of the kneaded product and 5 parts of a crosslinking agent (Shin Nakamura Chemical Co., Ltd., MEG) are added and mixed further.98 parts of the kneaded product and a crosslinking agent (Shin Nakamura Chemical Co., Ltd., product name: MEG) are added and mixed.
Add 5 parts of the product (trade name: MEG) and mix further. This mixture is processed in the same manner as Sample 1 to obtain a sample.

上記で得た試料1〜4について図に示す装置で脱臭テス
トを行なった。なお図において通気流量は11/分とし
ホルダーのエフ−フィルターの通気面積は20cjであ
る。また試料がブランクとはホルダーにエアーフィルタ
ーを挿入しないで行なったものである。なお15度測定
は検知管を使用した。
A deodorization test was conducted on Samples 1 to 4 obtained above using the apparatus shown in the figure. In the figure, the ventilation flow rate is 11/min, and the ventilation area of the F-filter of the holder is 20cj. Also, a blank sample is one that was conducted without inserting an air filter into the holder. Note that a detection tube was used for the 15 degree measurement.

脱臭結果 上記試験結果から試料1〜4はいずれも優れた脱臭効果
のあることが認められる。
Deodorizing Results From the above test results, it is recognized that Samples 1 to 4 all have excellent deodorizing effects.

(B)次に抗菌性能の比較について記載する。(B) Next, a comparison of antibacterial performance will be described.

各種微生物の菌液をエアーフィルターの試料片(5部厘
×50)の表面に一様に接種し、菌は37℃で0,6及
び240「、カビは25℃で0.24及び480「保存
後に測定した。
Bacterial solutions of various microorganisms were uniformly inoculated onto the surface of an air filter sample piece (5 parts x 50), and the bacteria were 0.6 and 240" at 37°C, and the mold was 0.24 and 480" at 25°C. Measured after storage.

なお試料1−1.1−2.1−3.1−4は上記試料1
において、抗菌剤の塑を夫々0.2部、0.5部、1.
0部、2.5部で製造したものである。又表中の対照は
各試料に接種したものと同量の菌液をシャーレに分注し
て保存したものである。
Note that sample 1-1.1-2.1-3.1-4 is the same as sample 1 above.
In , the antibacterial agent was added to 0.2 parts, 0.5 parts, and 1 part, respectively.
0 parts and 2.5 parts. The control in the table was obtained by dispensing the same amount of bacterial solution as that inoculated into each sample into petri dishes and storing it.

黄色ブドウ球菌 黒麹機 上記から明らかなように、タラトスボリウムを除く黄色
ブドウ球菌、大腸菌及び黒麹機のいずれも減少している
As is clear from the above, Staphylococcus aureus, Escherichia coli, and black malt, except for Talatosborium, have all decreased.

[考案の効果] 本考案のエアーフィルターによれば、脱臭剤の他に抗菌
剤を付着してなるものであるため、従来のエアーターに
よる除塵及び脱臭の他に滅菌効能を有する。
[Effects of the Invention] The air filter of the present invention has an antibacterial agent attached to it in addition to a deodorizing agent, so it has a sterilization effect in addition to the dust removal and deodorization by conventional air filters.

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

図面は脱臭試験を行なった装置の系統図。 The drawing is a system diagram of the equipment that conducted the deodorization test.

Claims (1)

【特許請求の範囲】[Claims] 通気性素材よりなるシート材に脱臭剤及び抗菌剤を付着
してなるエアーフィルター。
An air filter made by adhering a deodorizer and antibacterial agent to a sheet material made of breathable material.
JP1173324A 1989-07-05 1989-07-05 Manufacturing method of air filter Expired - Fee Related JP2954236B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1173324A JP2954236B2 (en) 1989-07-05 1989-07-05 Manufacturing method of air filter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1173324A JP2954236B2 (en) 1989-07-05 1989-07-05 Manufacturing method of air filter

Publications (2)

Publication Number Publication Date
JPH0338212A true JPH0338212A (en) 1991-02-19
JP2954236B2 JP2954236B2 (en) 1999-09-27

Family

ID=15958323

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1173324A Expired - Fee Related JP2954236B2 (en) 1989-07-05 1989-07-05 Manufacturing method of air filter

Country Status (1)

Country Link
JP (1) JP2954236B2 (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05261142A (en) * 1992-03-19 1993-10-12 Hinomaru Nenryo Kogyo Kk Humidity conditioning article incorporating anti-fungal function
EP0718011A1 (en) * 1994-12-21 1996-06-26 Kwangyeon Lee Wool filter for dustproof mask and manufacturing method thereof
JPH09308679A (en) * 1996-05-21 1997-12-02 Kuraray Chem Corp Adsorptive material
JP2000342668A (en) * 1999-06-07 2000-12-12 Toagosei Co Ltd Deodorant sheet
JP2002523207A (en) * 1998-08-20 2002-07-30 エクストラクシヨン・システムズ・インコーポレーテツド Filter using porous strongly acidic polymer
JP2003504175A (en) * 1999-07-08 2003-02-04 エム、ハー、べー、フィルトラツィオーン、ゲゼルシヤフト ミツト ベシユレンクテル ハフツング ウント コンパニー コマンディートゲゼルシャフト Biodestructive filter media for gas filtration
ES2228247A1 (en) * 2003-04-08 2005-04-01 Jose Luis Alonso Iglesias Fabrication of preservatives for fresh animal and vegetable foodstuffs comprises incorporation of activated carbon in dough, with addition of permanganate salt
US7922791B2 (en) 2006-07-13 2011-04-12 Entegris, Inc. Filtering system for a semiconductor processing tool
WO2011055893A1 (en) * 2009-11-03 2011-05-12 Lg Electronics Inc. Air cleaning filter comprising protein deactivating agent and process for producing same
JP2012061401A (en) * 2010-09-15 2012-03-29 Kinki Univ Method of manufacturing dust collection filter using loofah being natural material
WO2023121487A1 (en) * 2021-12-21 2023-06-29 Pąprowicz, Jan Filtering and absorbing material for filtration and removal of pollutants from the air, particularly chemical pollutants harmful to health and unpleasant odors

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05261142A (en) * 1992-03-19 1993-10-12 Hinomaru Nenryo Kogyo Kk Humidity conditioning article incorporating anti-fungal function
EP0718011A1 (en) * 1994-12-21 1996-06-26 Kwangyeon Lee Wool filter for dustproof mask and manufacturing method thereof
JPH09308679A (en) * 1996-05-21 1997-12-02 Kuraray Chem Corp Adsorptive material
JP2002523207A (en) * 1998-08-20 2002-07-30 エクストラクシヨン・システムズ・インコーポレーテツド Filter using porous strongly acidic polymer
JP2000342668A (en) * 1999-06-07 2000-12-12 Toagosei Co Ltd Deodorant sheet
JP2003504175A (en) * 1999-07-08 2003-02-04 エム、ハー、べー、フィルトラツィオーン、ゲゼルシヤフト ミツト ベシユレンクテル ハフツング ウント コンパニー コマンディートゲゼルシャフト Biodestructive filter media for gas filtration
ES2228247A1 (en) * 2003-04-08 2005-04-01 Jose Luis Alonso Iglesias Fabrication of preservatives for fresh animal and vegetable foodstuffs comprises incorporation of activated carbon in dough, with addition of permanganate salt
ES2228247B1 (en) * 2003-04-08 2006-06-01 Jose Luis Alonso Iglesias PROCEDURE FOR THE MANUFACTURE OF NEW PRODUCTS FOR APPLICATION IN THE CONSERVATION OF FRESH FOODS OF ANIMAL AND VEGETABLE ORIGIN, AND PURIFICATION OF ENVIRONMENTS THROUGH AIR CONDITIONING FACILITIES.
US7922791B2 (en) 2006-07-13 2011-04-12 Entegris, Inc. Filtering system for a semiconductor processing tool
WO2011055893A1 (en) * 2009-11-03 2011-05-12 Lg Electronics Inc. Air cleaning filter comprising protein deactivating agent and process for producing same
US8609027B2 (en) 2009-11-03 2013-12-17 Lg Electronics Inc. Air cleaning filter comprising protein deactivating agent and process for producing same
JP2012061401A (en) * 2010-09-15 2012-03-29 Kinki Univ Method of manufacturing dust collection filter using loofah being natural material
WO2023121487A1 (en) * 2021-12-21 2023-06-29 Pąprowicz, Jan Filtering and absorbing material for filtration and removal of pollutants from the air, particularly chemical pollutants harmful to health and unpleasant odors

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