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JPS58122022A - Body and implement for absorbing harmful gas - Google Patents

Body and implement for absorbing harmful gas

Info

Publication number
JPS58122022A
JPS58122022A JP57003482A JP348282A JPS58122022A JP S58122022 A JPS58122022 A JP S58122022A JP 57003482 A JP57003482 A JP 57003482A JP 348282 A JP348282 A JP 348282A JP S58122022 A JPS58122022 A JP S58122022A
Authority
JP
Japan
Prior art keywords
harmful gas
absorbing
chemicals
materials
gas
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
JP57003482A
Other languages
Japanese (ja)
Inventor
Tadaichi Nishikawa
奥村正利
Masatoshi Okumura
吉田雅幸
Masayuki Yoshida
西川唯一
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.)
Shin Nisson Kako Co Ltd
Original Assignee
Shin Nisson Kako Co 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 Shin Nisson Kako Co Ltd filed Critical Shin Nisson Kako Co Ltd
Priority to JP57003482A priority Critical patent/JPS58122022A/en
Publication of JPS58122022A publication Critical patent/JPS58122022A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To improve the effective rate of consumption of absorbing chemicals and the rate of absorption by depositing said chemicals in the internal spaces of porous materials without substantially closing said internal spaces. CONSTITUTION:Open-celled materials of organics such as urethane foam or inorganics such as calcined vermiculite are used, and acidic materials such as sulfamic acid, malic acid, or the like are used as absorbing chemicals in order to absorb alkaline gases and alkaline materials such as NaOH, K2CO3 or the like are used in order to absorb acidic gases. The liquid prepd. by dissolving or suspending the absorbing chemicals in water or a suitable solvent is impregnated into the open-celled materials which are then dried. The resultant open-celled materials deposited with the absorbing chemicals are packaged with films having fine holes which have gas permeability but prohibit the permeation of liquid at high density, whereby a harmful gas absorbing body is obtained. In the case of absorbing several kinds of harmful gases simultaneously, >=2 kinds of the harmful gas absorbing bodies differing in the adsorbing chemicals are combined and are contained in a perforated vessel.

Description

【発明の詳細な説明】 従来有害ガス吸収体としては活性縦、フミン酸、酸性ト
リポリン酸アルミニウムあるいにゼオライトなどの吸着
剤を透気性のシートで包装したものが用いられている。
DETAILED DESCRIPTION OF THE INVENTION Conventionally, harmful gas absorbers have been used in which an adsorbent such as active fiber, humic acid, acidic aluminum tripolyphosphate, or zeolite is packaged in an air-permeable sheet.

これらの吸収体は吸着剤の物理的性5iLを利用したも
のであるが、他方敵性物質、アルカリ性物質あるいは反
応性二重結合を有する低分子f4!1JJXなどを吸収
剤と(。
These absorbers utilize the physical properties of adsorbents, but on the other hand, adsorbents such as hostile substances, alkaline substances, or low-molecular-weight f4!1JJX having reactive double bonds are used as adsorbents.

て使用し、有害ガスを化学的に吸収する試みも行われて
いる。
Attempts are also being made to chemically absorb harmful gases by using them.

本発明はこの化学的な吸収を効果的に行うことを目的と
するものであって、 (1)  有害ガス吸収桑剤tm持する連続多孔性物質
を透気性シートにて包装し九有Wガス吸収体において、
連続多孔性物質の内部空間を実質的に閉塞することなく
有害ガス吸収薬剤が該空間内に担持されていることを特
徴とする有害ガス吸収体。
The purpose of the present invention is to effectively perform this chemical absorption. In the absorber,
A harmful gas absorber characterized in that a harmful gas absorbing agent is supported within the internal space of a continuous porous material without substantially blocking the space.

(2〕  透気性シートが透気性ではあるが液体は透さ
ないシートであることよりなる特許請求の軛i8第1項
の有害ガス吸収体。
(2) The harmful gas absorber according to Paragraph 1 of Claim i8, wherein the air permeable sheet is a sheet that is permeable to air but not permeable to liquids.

であり、さらにこれらの有害ガス吸収体を有効に使用す
るため、 (3)異なる種類の有害ガス吸収薬剤を用いた前項(1
)の有害ガス吸収体を各々1個以上即ち合tt211以
上を有孔容器内に収納し九ことを特徴とする有害ガス吸
収用具。
In addition, in order to use these harmful gas absorbers effectively, (3) the above (1) using different types of harmful gas absorbing agents
1.) A harmful gas absorbing device, characterized in that one or more of each of the harmful gas absorbers (tt211 or more) are housed in a perforated container.

(4)a気性シートが透気性ではあるが液体は通さない
シートであることよりなる前項の有害ガス吸収用具。
(4) The harmful gas absorbing device according to the preceding item, wherein the gas-permeable sheet is permeable but impermeable to liquids.

(5)芳香剤又は透気性シートに包装された活性炭を有
孔容器に収納した前3及び4項記載の有害ガス昧収用臭
(5) The noxious gas-containing odor described in items 3 and 4 above, in which an aromatic agent or activated carbon packaged in an air-permeable sheet is housed in a perforated container.

である。It is.

本発明におiて連続多孔性物質はその倣細な内部空間内
に有害ガス吸収薬剤を担持しているのであるが、その担
持の状態はガス吸収薬剤が薄膜状になって連続多孔性物
質の内S表面【4j1覆しているかあるいは極めてIi
#な収状筐たは結晶の形で内部空間内に存在しているも
ので6って、有害ガス吸収薬剤によって連続多孔性物質
の内部空間が実質的に閉塞されることがなく、従ってそ
れは本来通気性を保持している。このような形lIIを
とることによって有害ガス吸収薬剤はその有効消費率が
着しく大になシ、且つ吸収速度も著しく向上するのであ
る。
In the present invention, the continuous porous material supports the harmful gas absorbing agent in its narrow internal space, and the gas absorbing agent becomes a thin film in the continuous porous material. S surface [4j1 is overturned or extremely Ii
6, the internal space of the continuous porous material is not substantially blocked by the harmful gas-absorbing agent, and therefore it is It retains its inherent breathability. By adopting such a form III, the effective consumption rate of the harmful gas absorbing agent is significantly increased, and the absorption rate is also significantly improved.

本発明に使用する連続多孔性物質としては、NJばウレ
タンフオーム、コーンコブミール、ふすま、おが″〈ず
、パルプ、バガス、もみがら、落花生から等の有機物系
多孔質、あるいは焼成バーミキュライト、焼成ノ母−ラ
イト、シリカゲル、微粉シリカ、セラミックフィルター
、粒状活性炭、スラグ等の無機物事多孔質が刺網できる
が、これらのみに限られるものではなi0本発v4にお
いて使用する有害ガス吸収薬剤とt、テUアンモニア、
トリメチルアイ/の加電アルカリ性ガスを吸収する丸め
には、例えばスル7アイン畝、シんご酸、仁はく鈑、乳
酸、酒石酸、くえん敵、蓚酸、酸性懺瞭ソー〆、敵性リ
ン緻ソーダなどの如き同体の酸性−質を用いることがで
きるが、これらのみVC@られるものではない。硫化水
素、メルカプタンなどの如き敵性ガスのためには苛性ソ
ーダ、苛性カリ、水酸化リチウム、炭酸ソーダ、畿識カ
リ、消石灰、ヘキサメチレンテトラミンなどの如き固体
のアルカリ性物質を用いることがで纏るが、これらのみ
に限られるものではない。またグリオキプールを用いる
ことによりアルデヒドと付加体を作るアンモニア、メチ
ルアミンの如曹愚臭を吸収させることができ、マレイン
酸液で硫化水素の如暑二重結合に付加する患臭物質を、
を九トリグリセリドなどによってメチルアミン、アンモ
ニア、メルカプタンなどを除去することもできる。
Continuous porous materials used in the present invention include organic porous materials such as NJ urethane foam, corncob meal, bran, sawdust, pulp, bagasse, rice husks, and peanuts, or calcined vermiculite and calcined wood. Porous inorganic materials such as matrix light, silica gel, finely divided silica, ceramic filters, granular activated carbon, and slag can be used as gill nets, but are not limited to these. TeU ammonia,
For example, trimethyl eye/rolling which absorbs the charged alkaline gas includes: suru 7 ain ridge, sinic acid, nickel, lactic acid, tartaric acid, sulfuric acid, oxalic acid, acidic acidic acid, hostile phosphorus soda. It is possible to use similar acidic substances such as, but these are not the only ones that can be VC@. For hostile gases such as hydrogen sulfide and mercaptans, solid alkaline substances such as caustic soda, caustic potash, lithium hydroxide, soda carbonate, slaked lime, hexamethylenetetramine, etc. can be used. It is not limited to only. In addition, by using glyokypur, it is possible to absorb the odor of ammonia and methylamine that form adducts with aldehydes, and with maleic acid solution, it is possible to absorb odor-causing substances that add to the double bond of hydrogen sulfide.
Methylamine, ammonia, mercaptan, etc. can also be removed by triglyceride, etc.

これらの有害ガス吸収薬剤を連続多孔性物質の内s!2
間に担持させるには、有害ガス吸収薬剤を水あるいは適
烏な溶剤に靜解した俗wLるるいは液中に懸濁したS濁
液の過菫を連続多孔性物質に含浸させ、次で退室の方法
で乾−させる。
These harmful gas-absorbing agents are contained in continuous porous materials! 2
In order to support the harmful gas absorbing agent in water or a suitable solvent, a continuous porous material is impregnated with a slurry of S suspension in water or a suitable solvent. Leave to dry by leaving the room.

このようにして得られる有害ガス吸収薬剤が担持され九
連続多孔性物質を包装するための通気性を有するシート
としては通常の鰍、布あるいは不織布などが使用される
が、また透気性を有するにもかかわらず液体會透過する
ことのないきわめて微細な孔を高!Ifに有するフィル
ム、例えばデュポン社製の「°タイベック」あるいは徳
山曹達■製のl’N?Rシート」、槓水化宇■製の「セ
ルボア」などを使用すれは内部の有害ガス吸収薬剤が水
分などを吸収して液体化してもその液体が外部に漏出す
ることがなく、筐九包装の外部が水で濡れてもその水が
円部に浸入するおそれがないので極めて好都合である。
As a breathable sheet for packaging the nine-continuously porous material on which the harmful gas-absorbing agent obtained in this way is supported, ordinary fabric, cloth, or non-woven fabric is used. Despite this, it has extremely fine pores that do not allow liquid to pass through! If the film you have, for example, "°Tyvek" manufactured by DuPont or l'N manufactured by Tokuyama Soda ■? When using products such as ``R Sheet'' and ``Celboa'' manufactured by Kansui Chemical, even if the harmful gas-absorbing agent inside absorbs water and becomes liquid, the liquid will not leak outside, and the packaging will be easier. Even if the outside of the ring gets wet with water, there is no risk of the water entering the circular part, which is extremely convenient.

本発明におけるV!ガス吸収粂剤を内包する数種の有害
ガス吸収体を、有害ガス吸収薬剤の異なる211以上組
合せて収納し九有孔容器(例、tばJILm、グラスチ
ックあるいは金属板などで造られるネット容器或は籠等
)は、数種類の有害ガス【同時に吸収するための吸収用
具として有効でめヤ、さらに活性炭を通気性シートで包
装した包鋏物をも組合せて有孔容器に収納したものは化
学的には吸収されにくい有害ガスtおも成分として含有
する混合有害ガスを効果的に吸収するのに有利である。
V in the present invention! A 9-perforated container (e.g., TBA JILm, a net container made of plastic or metal plate, etc.) in which several types of harmful gas absorbers containing gas absorbing agents are stored in combinations of 211 or more different harmful gas absorbing agents. (or baskets, etc.) are effective as absorption devices for simultaneously absorbing several types of harmful gases.In addition, a combination of activated carbon wrapped in a breathable sheet and stored in a perforated container is a chemical In particular, it is advantageous for effectively absorbing mixed harmful gases that are contained as main components of harmful gases that are difficult to absorb.

また活性炭包装物の代りに芳香剤會有孔容器内に共存さ
せれば有害ガスの吸収除去と同時に積境内に芳香を与え
ることができる。ま九「タイベック」、l’−NIIF
Rシート」あるいは「セルポア」などを包装材料として
使用した本発明の吸収体は乾燥剤と共存させて使用する
ことも可能である。
Furthermore, if an aromatic agent is placed in a perforated container instead of an activated carbon package, it is possible to absorb and remove harmful gases and at the same time impart a fragrance to the interior of the container. Maku "Tyvek", l'-NIIF
The absorbent material of the present invention using "R Sheet" or "Cellpore" as a packaging material can also be used in coexistence with a desiccant.

本発明の有害ガス吸収体あるい鉱有害ガス吸収用臭を使
用する意義のある空間としては工業用品としては、例え
は薬品包装容器の上部空間、精密機械の工場出荷時の包
装内の空間、食品原料包輪容器の空間、集品庫内の空間
、工X室円の空間などがある。また家庭用品として使用
する対象空間としては冷蔵犀内、台所戸棚、食品収納庫
、納戸、押入れ、@I!所、物置、洋服ダンス、ロッカ
ー、地下室、ペット飼w室、ペット権送容器勢がある。
The spaces in which the harmful gas absorber or mineral harmful gas absorbing odor of the present invention is meaningful include, for example, the upper space of a drug packaging container, the space inside the factory packaging of a precision machine, There is a space for food raw material wrapping containers, a space inside the collection warehouse, and a space for the factory X room. In addition, the target spaces for use as household goods include refrigerators, kitchen cupboards, food storage, storerooms, closets, and @I! There are storage areas, storage rooms, wardrobes, lockers, basements, pet rooms, and pet storage facilities.

更に水産加工業、曽*na工l All加工集において
も、工程中、貯賊中、輸送中において本発明品を使用す
べき空間が多極存在する。
Furthermore, in the seafood processing industry and all processing industries, there are many spaces in which the products of the present invention should be used during processing, storage, and transportation.

これらの有害ガスが発生しあるいは涌貿する空間内に本
発明の有害ガス吸収体あるいはV壺ガス吸収用具を吊し
、あるいは平面的VctIt〈ことにより、その空間内
の対象有害ガスを経満的且つ有効に吸収除去することが
できるのである。
By suspending the harmful gas absorber or V-bottle gas absorbing device of the present invention in a space where these harmful gases are generated or flowing, or by applying a planar VctIt, the target harmful gases in the space can be absorbed in a timely manner. Moreover, it can be effectively absorbed and removed.

以下の実施例に本発明に基く、いくつかの実用例を述べ
るが、本発明の内容はこれらに限られるものではない。
Although some practical examples based on the present invention will be described in the following examples, the content of the present invention is not limited thereto.

実施例1 焼成バーミキュライトZoo hとりんご#45−水浴
液toOK4tスチーム加熱式減圧可能なグラスライニ
ング製コニカルブレンダ−兼ドライヤーに入れ、80℃
に加熱しつつ2時間回転させて均一に混和する。
Example 1 Calcined vermiculite Zoo h and apple #45 - Water bath liquid to OK 4t Place in a steam-heated decompressible glass-lined conical blender/dryer and heat to 80°C.
Mix evenly by rotating for 2 hours while heating.

次にこO装置を真空ポンプに接続し、100−Hfの減
圧に保ちつつスチーム加熱し内壁温度を110℃に上昇
させ3時間回転しつつ乾燥させたこの乾燥物tiii漉
まで冷却した後取り出してドラム缶VC密閉保存した。
Next, the O device was connected to a vacuum pump, heated with steam while maintaining a reduced pressure of 100-Hf, the inner wall temperature was raised to 110°C, and the dried product was dried while rotating for 3 hours. After cooling to a third strainer, the dried product was taken out. Stored in a sealed VC drum.

このなかから500fをとυMPRシート製駿に詰めて
口部をヒートシールして密閉してアルカリ性ガス吸収体
を製造した。
From this, 500f was packed into a υMPR sheet shell, and the mouth was heat-sealed to make an alkaline gas absorber.

心積2 dの密閉室にアンモニアガスを吹込んでそのl
lI[t 1000 pPn+とし、このなかに上記の
吸収体を吊しガス検知管で1時間毎にアンモニアst’
tsa+定した所第1表に示す如く急速なアンモーフ1
11度の減少を示した。これは対照として同一条件で試
験し良、粒状酸性トリボIJ @緻アルミニウムに比べ
格段の速さである。
Ammonia gas is blown into a closed chamber with a central product of 2 d, and the l
lI [t 1000 pPn+, suspend the above absorber in it, and add ammonia st' every hour using a gas detection tube.
tsa + rapid unmorph 1 as shown in Table 1
It showed a decrease of 11 degrees. This was tested under the same conditions as a control, and was much faster than Granular Acidic Tribo IJ @ Dense Aluminum.

第1!! 残存アンモニアガス#Il!度陶この包装体
をバットに平に置き水100011.1゜かけて1日静
置したが、水に対する酸分の浴出は検出されなかった。
1st! ! Residual ammonia gas #Il! This package was placed flat on a vat and poured with 100011.1° of water and allowed to stand for one day, but no acid was detected in the water.

実施例2 焼成バーミキュライト100Kfと20−石灰乳100
TI4を実施例1と同一の方法により均一に混和したの
ち乾燥して、酸性ガス吸収剤t−得る。この吸収剤15
0 klを「タイベック」製袋に充填した後入れ口をヒ
ートシールして密閉した。
Example 2 Calcined vermiculite 100Kf and 20-lime milk 100
TI4 is mixed uniformly in the same manner as in Example 1 and then dried to obtain an acidic gas absorbent t-. This absorbent 15
After filling a "Tyvek" bag with 0 kl, the opening was heat-sealed to seal it.

容積2ootのポリエチレン内輪ドラム缶に塩化水素ガ
スを吹込んでその幽寂を10001)Pmとしこのなか
に上記の吸収体を吊し、ガス検知管で塩化水素ガスを測
定した。その結果は第211に示す如く急速な敏濃度の
減少を示し友。
Hydrogen chloride gas was blown into a polyethylene inner drum with a capacity of 2 oots, the atmosphere was set to 10001) Pm, the above-mentioned absorber was suspended therein, and hydrogen chloride gas was measured with a gas detection tube. The results showed a rapid decrease in concentration as shown in Figure 211.

第  2  表 筐九本実施例の吸収体をバットに入れ水10CCを上か
らかけ、l&夜放置したが、アルカリ分の溶出は認めら
れなかった。
Table 2 Case 9 The absorbent material of this example was placed in a vat, 10 cc of water was poured over it, and it was left to stand overnight, but no alkaline content was observed to elute.

実m例3 コーンコブミール100 Klとへキサメチレンテトラ
ミンの50−水溶液1001i1 ’iブレード回転式
混和機に入れ、1時間混和した。これを回転式コニカル
乾燥機に入れて100■Hfの減圧下、ジャケットをス
チームにて栃℃に加熱し乾燥し死後、室温まで冷却し、
酸性ガス吸収体を得九。
Example 3 A 50-aqueous solution of 100 Kl of corn cob meal and hexamethylenetetramine was placed in a 1001l1'i blade rotary mixer and mixed for 1 hour. This was placed in a rotary conical dryer and under reduced pressure of 100 ■ Hf, the jacket was heated to Tochi °C with steam and dried, and after death, it was cooled to room temperature.
Obtain an acid gas absorber.

1     この吸収剤の150 fをセルポア製袋に
rI!i閉じた。
1 Put 150 f of this absorbent into a Cellpore bag. i closed.

200 tのドラム缶に硫化水嵩ガスを尋人してその*
[會1000 PI)mとし、この中に上記の吸収体を
吊し、ガス検知管で1時間毎に硫化水素〃ス鎖*t−醐
定したところ表3に示す如く急速な像化水嵩ガスII反
の減少を示した。
A 200 ton drum was filled with sulfide water gas.
[1000 PI) m, the above-mentioned absorber was suspended therein, and the hydrogen sulfide gas chain*t was determined every hour using a gas detection tube. II showed a decrease in resistance.

第  3  表 また、本実施例の吸収体をパットに入れ、水10CCを
上からかけlJi夜放置したが、アルカリ分の溶出は認
められなかった。
Table 3 Also, the absorbent material of this example was placed in a pad, 10 cc of water was poured over it, and it was left overnight, but no alkaline content was observed to elute.

実施例4 炭酸カリウムの50%水溶液50〜と焼成パーミキュラ
イ)50Kfを実施例1と同様の方法により均一に混和
したのち乾燥、冷却してこれを50fづつNFRシート
製袋に密閉して酸性ガス吸収体を得た。
Example 4 50 ~ 50% aqueous solution of potassium carbonate and 50 Kf of calcined permiculite were mixed uniformly in the same manner as in Example 1, then dried, cooled, and each 50 f was sealed in an NFR sheet bag to absorb acid gas. I got a body.

一方、509にのくえん酸I水溶液50縁と焼成パーミ
キュライ)50Jill前記と同一にしてアルカリ性ガ
ス吸収体tl!友。
On the other hand, 509 citric acid I aqueous solution 50 edges and calcined permiculite) 50 Jill the same as above and alkaline gas absorber tl! friend.

上記緻性ガス吸収体l駿とアルカリ性ガス吸収体1袋と
粒状活性炭50tt紙袋に充填したもの1袋とをポリス
チレン襄多孔成11f器に入れ、多機能の有害ガス吸収
用具を製造した。
The above-mentioned dense gas absorber, one bag of alkaline gas absorber, and one bag filled with a 50 tt paper bag of granular activated carbon were placed in a polystyrene 11F vessel to produce a multifunctional harmful gas absorbing device.

これを家庭量大製冷蔵g (400t )内に設置し友
ところ表4に示す如くアンモニア、ア建/拳及び硫化水
素、メルカプタフ類の鎖度は大幅に減少した。
This was installed in a large-scale household refrigeration unit (400 tons), and as shown in Table 4, the degree of chaining of ammonia, carbon dioxide, hydrogen sulfide, and mercaptaf was significantly reduced.

第4表 悪臭ガス11度(ppm ) ま九、臭覚的にも全く臭気を感じさせなかりた。Table 4 Malodorous gas 11 degrees (ppm) Also, from an olfactory standpoint, I didn't notice any odor at all.

実施例5 実施例3における酸性ガス吸収体1袋と、アルカリ性ガ
ス吸収体1袋と、マスキング香料l〇−をシート状ノf
ルプ20fK@浸させ、NFRシートに@閉したものと
をポリプロピレン製多孔成型容器に入れ、多機能の悪臭
ガス吸収芳香用具t−製造した。これを運動遇手用の汗
果がはけしく出ているロッカーに入れ、−夜装置した所
、翌朝はマスキング香料臭のみしか感じられなかった。
Example 5 One bag of acidic gas absorber and one bag of alkaline gas absorber in Example 3, and masking fragrance l〇- were put into sheet form.
A multi-functional foul-smelling gas-absorbing fragrance tool was manufactured by soaking the sample in a 20fK loop and closing it with an NFR sheet in a polypropylene porous molded container. I put this in my sweat-prone sports locker and put it in at night, and the next morning I could only smell the masking fragrance.

実施例6 実施例5に述べた悪臭ガス吸収芳香用J1.を家庭用コ
ンポスト製造品のふたの内側に吊しておいた所、為時間
後、マスキング香料臭のみしか感じられなかった。
Example 6 J1. for malodorous gas absorbing fragrance described in Example 5. When I hung it inside the lid of a household compost product, after a while, I could only smell the masking scent.

手続補正書 昭和58年4月14日 特許庁長官 若杉 和犬 殿 1、事件の表示 昭和57年特許願第003482号 2、発明の名称 有害ガス吸収体及び用具 3、補正する者 事件との関係   特許出願人 東京都北区浮間3丁目1番60号 新日曹化工株式会社 代表者  中 山   要 4、代理人 8100東京都千代田区大手町2丁目2番1号日本曹達
株式会社内 (1)明細書の第3真下から第3行目の1芳香剤」の前
に1前記(1)または(2)の有害ガス吸収体と共に」
を挿入する。
Procedural amendment April 14, 1980 Director of the Patent Office Kazuinu Wakasugi 1. Indication of the case 1982 Patent Application No. 003482 2. Name of the invention Noxious gas absorber and device 3. Person making the amendment Relationship to the case Patent applicant: 3-1-60 Ukima, Kita-ku, Tokyo Representative: Kaname Nakayama 4, Agent: 8100 Nippon Soda Co., Ltd., 2-2-1 Otemachi, Chiyoda-ku, Tokyo (1) In the 3rd line from the bottom of the specification, in front of 1. ``Fragrance agent'', 1. Together with the harmful gas absorber described in (1) or (2) above.''
Insert.

(2)明細書の第7頁第8行目の最後の「お」を削除す
る。
(2) Delete the last "o" on page 7, line 8 of the specification.

(3)明細書の第10頁最下行の1塩化水素ガス」のつ
ぎに「濃度」を挿入する。
(3) Insert "concentration" next to "hydrogen monochloride gas" on the bottom line of page 10 of the specification.

Claims (5)

【特許請求の範囲】[Claims] (1)  有害ガス吸収薬剤を担持する連続多孔性物質
を透気性シートにて包装した有害ガス吸収体において、
連続多孔性物質の内部空間上実質的に閉墨することなく
有害ガス吸収薬剤が鎮窒関内に担持されていることt%
黴とする有害ガス吸収体。
(1) In a harmful gas absorber in which a continuous porous material supporting a harmful gas absorbing agent is wrapped in an air-permeable sheet,
The harmful gas-absorbing agent is supported in the quenching chamber without substantially closing the internal space of the continuous porous material.t%
Harmful gas absorber that turns into mold.
(2)透気性シートが透気性ではめるが液体は透さない
シートであることよシなる特許請求の範B農1項の有害
ガス吸収体。
(2) The harmful gas absorber according to Claim B, Paragraph 1, wherein the air permeable sheet is a sheet that is air permeable but impermeable to liquids.
(3)連続多孔性物質の内部空間を実質的に閉寵するこ
となく有害ガス吸収薬剤が骸空関内に担持され九多孔性
物質を透気性シートにて包装した有害ガス吸収体を、異
なる種類の有害ガス吸収薬剤につき各々1個以上有孔容
器内に収納し喪ことを41黴とする有害ガス吸収用具。
(3) A harmful gas absorber in which a harmful gas absorbing agent is supported in the skeleton without substantially enclosing the internal space of the continuous porous material, and the nine-porous material is packaged with an air permeable sheet, A harmful gas absorbing device containing one or more of each type of harmful gas absorbing agent in a perforated container.
(4)透気性シートが透気性ではあるが歌詠は通さない
シー トでるることよりなる%W!f請求の範囲第3X
Jlの有害ガス吸収用共。
(4) The air-permeable sheet is air-permeable but does not allow the song to pass through.%W! fClaim No. 3X
For Jl's harmful gas absorption.
(5)芳香剤又は透気性シートに包装された活性炭を有
孔容器内に収納した特許請求の範囲第3項又は特許請求
の範囲@4積配躯の有害ガス吸収用具。
(5) A noxious gas absorption device according to Claim 3 or Claims@4-pack arrangement, in which an aromatic agent or activated carbon packaged in an air-permeable sheet is housed in a perforated container.
JP57003482A 1982-01-14 1982-01-14 Body and implement for absorbing harmful gas Pending JPS58122022A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57003482A JPS58122022A (en) 1982-01-14 1982-01-14 Body and implement for absorbing harmful gas

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57003482A JPS58122022A (en) 1982-01-14 1982-01-14 Body and implement for absorbing harmful gas

Publications (1)

Publication Number Publication Date
JPS58122022A true JPS58122022A (en) 1983-07-20

Family

ID=11558550

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57003482A Pending JPS58122022A (en) 1982-01-14 1982-01-14 Body and implement for absorbing harmful gas

Country Status (1)

Country Link
JP (1) JPS58122022A (en)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62299266A (en) * 1986-06-20 1987-12-26 セ−レン株式会社 Washable deodorizing body and its production
JPS6379663A (en) * 1986-09-24 1988-04-09 エヌオーケー株式会社 Composite deodorizing material
JPS63194663A (en) * 1987-02-06 1988-08-11 ハリマセラミック株式会社 Deodorizing member of respiration protector
WO2006084008A1 (en) * 2005-02-02 2006-08-10 Global Research Technologies, Llc Removal of carbon dioxide from air
WO2007016271A2 (en) * 2005-07-28 2007-02-08 Global Research Technologies, Llc Removal of carbon dioxide from air
US7708806B2 (en) 2006-10-02 2010-05-04 Global Research Technologies, Llc Method and apparatus for extracting carbon dioxide from air
US7993432B2 (en) 2006-03-08 2011-08-09 Kilimanjaro Energy, Inc. Air collector with functionalized ion exchange membrane for capturing ambient CO2
US8491705B2 (en) 2009-08-19 2013-07-23 Sunho Choi Application of amine-tethered solid sorbents to CO2 fixation from air
US8894747B2 (en) 2007-05-21 2014-11-25 Peter Eisenberger System and method for removing carbon dioxide from an atmosphere and global thermostat using the same
US9028592B2 (en) 2010-04-30 2015-05-12 Peter Eisenberger System and method for carbon dioxide capture and sequestration from relatively high concentration CO2 mixtures
US9227153B2 (en) 2007-05-21 2016-01-05 Peter Eisenberger Carbon dioxide capture/regeneration method using monolith
US9266051B2 (en) 2005-07-28 2016-02-23 Carbon Sink, Inc. Removal of carbon dioxide from air
US9427726B2 (en) 2011-10-13 2016-08-30 Georgia Tech Research Corporation Vapor phase methods of forming supported highly branched polyamines
US9433896B2 (en) 2010-04-30 2016-09-06 Peter Eisenberger System and method for carbon dioxide capture and sequestration
US9527747B2 (en) 2008-02-19 2016-12-27 Carbon Sink, Inc. Extraction and sequestration of carbon dioxide
US9616375B2 (en) 2007-04-17 2017-04-11 Carbon Sink, Inc. Capture of carbon dioxide (CO2) from air
US9908080B2 (en) 2007-05-21 2018-03-06 Peter Eisenberger System and method for removing carbon dioxide from an atmosphere and global thermostat using the same
US9925488B2 (en) 2010-04-30 2018-03-27 Peter Eisenberger Rotating multi-monolith bed movement system for removing CO2 from the atmosphere
US11059024B2 (en) 2012-10-25 2021-07-13 Georgia Tech Research Corporation Supported poly(allyl)amine and derivatives for CO2 capture from flue gas or ultra-dilute gas streams such as ambient air or admixtures thereof
US11737398B2 (en) 2018-02-16 2023-08-29 Carbon Sink, Inc. Fluidized bed extractors for capture of CO2 from ambient air

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JPS5155790A (en) * 1974-11-11 1976-05-17 Rodo Daijin Anmonia mataha chitsusoganjujukienkijokinokyuchakujokyohoho
JPS5263882A (en) * 1975-11-21 1977-05-26 Mitsubishi Heavy Ind Ltd Acivated carbon for deodorization
JPS5312789A (en) * 1976-07-23 1978-02-04 Taiyo Kaken Co Collecting agents for basic nasty smell ingredients
JPS5395891A (en) * 1977-02-01 1978-08-22 Taiyo Kaken Co Animal smell removing method
JPS546766U (en) * 1977-06-17 1979-01-17
JPS54152687A (en) * 1978-05-24 1979-12-01 Unitika Ltd Adsorbent
JPS54155188A (en) * 1978-05-29 1979-12-06 Unitika Ltd Special adsorbent

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Publication number Priority date Publication date Assignee Title
JPS5155790A (en) * 1974-11-11 1976-05-17 Rodo Daijin Anmonia mataha chitsusoganjujukienkijokinokyuchakujokyohoho
JPS5263882A (en) * 1975-11-21 1977-05-26 Mitsubishi Heavy Ind Ltd Acivated carbon for deodorization
JPS5312789A (en) * 1976-07-23 1978-02-04 Taiyo Kaken Co Collecting agents for basic nasty smell ingredients
JPS5395891A (en) * 1977-02-01 1978-08-22 Taiyo Kaken Co Animal smell removing method
JPS546766U (en) * 1977-06-17 1979-01-17
JPS54152687A (en) * 1978-05-24 1979-12-01 Unitika Ltd Adsorbent
JPS54155188A (en) * 1978-05-29 1979-12-06 Unitika Ltd Special adsorbent

Cited By (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62299266A (en) * 1986-06-20 1987-12-26 セ−レン株式会社 Washable deodorizing body and its production
JPS6379663A (en) * 1986-09-24 1988-04-09 エヌオーケー株式会社 Composite deodorizing material
JPH0696036B2 (en) * 1986-09-24 1994-11-30 エヌオーケー株式会社 Composite deodorant material
JPS63194663A (en) * 1987-02-06 1988-08-11 ハリマセラミック株式会社 Deodorizing member of respiration protector
US7655069B2 (en) 2005-02-02 2010-02-02 Global Research Technologies, Llc Removal of carbon dioxide from air
WO2006084008A1 (en) * 2005-02-02 2006-08-10 Global Research Technologies, Llc Removal of carbon dioxide from air
WO2007016271A3 (en) * 2005-07-28 2007-03-22 Global Res Technologies Llc Removal of carbon dioxide from air
US10010829B2 (en) 2005-07-28 2018-07-03 Carbon Sink, Inc. Removal of carbon dioxide from air
WO2007016271A2 (en) * 2005-07-28 2007-02-08 Global Research Technologies, Llc Removal of carbon dioxide from air
US9266051B2 (en) 2005-07-28 2016-02-23 Carbon Sink, Inc. Removal of carbon dioxide from air
US9205372B2 (en) 2006-03-08 2015-12-08 Carbon Sink, Inc. Air collector with functionalized ion exchange membrane for capturing ambient CO2
US10150112B2 (en) 2006-03-08 2018-12-11 Carbon Sink, Inc. Air collector with functionalized ion exchange membrane for capturing ambient CO2
US7993432B2 (en) 2006-03-08 2011-08-09 Kilimanjaro Energy, Inc. Air collector with functionalized ion exchange membrane for capturing ambient CO2
US9266052B2 (en) 2006-10-02 2016-02-23 Carbon Sink, Inc. Method and apparatus for extracting carbon dioxide from air
US7708806B2 (en) 2006-10-02 2010-05-04 Global Research Technologies, Llc Method and apparatus for extracting carbon dioxide from air
US9861933B2 (en) 2006-10-02 2018-01-09 Carbon Sink, Inc. Method and apparatus for extracting carbon dioxide from air
US9616375B2 (en) 2007-04-17 2017-04-11 Carbon Sink, Inc. Capture of carbon dioxide (CO2) from air
US8894747B2 (en) 2007-05-21 2014-11-25 Peter Eisenberger System and method for removing carbon dioxide from an atmosphere and global thermostat using the same
US9908080B2 (en) 2007-05-21 2018-03-06 Peter Eisenberger System and method for removing carbon dioxide from an atmosphere and global thermostat using the same
US9227153B2 (en) 2007-05-21 2016-01-05 Peter Eisenberger Carbon dioxide capture/regeneration method using monolith
US9555365B2 (en) 2007-05-21 2017-01-31 Peter Eisenberger System and method for removing carbon dioxide from an atmosphere and global thermostat using the same
US9527747B2 (en) 2008-02-19 2016-12-27 Carbon Sink, Inc. Extraction and sequestration of carbon dioxide
US8491705B2 (en) 2009-08-19 2013-07-23 Sunho Choi Application of amine-tethered solid sorbents to CO2 fixation from air
US9630143B2 (en) 2010-04-30 2017-04-25 Peter Eisenberger System and method for carbon dioxide capture and sequestration utilizing an improved substrate structure
US9433896B2 (en) 2010-04-30 2016-09-06 Peter Eisenberger System and method for carbon dioxide capture and sequestration
US9878286B2 (en) 2010-04-30 2018-01-30 Peter Eisenberger System and method for carbon dioxide capture and sequestration
US9925488B2 (en) 2010-04-30 2018-03-27 Peter Eisenberger Rotating multi-monolith bed movement system for removing CO2 from the atmosphere
US9975087B2 (en) 2010-04-30 2018-05-22 Peter Eisenberger System and method for carbon dioxide capture and sequestration from relatively high concentration CO2 mixtures
US9028592B2 (en) 2010-04-30 2015-05-12 Peter Eisenberger System and method for carbon dioxide capture and sequestration from relatively high concentration CO2 mixtures
US10413866B2 (en) 2010-04-30 2019-09-17 Peter Eisenberger System and method for carbon dioxide capture and sequestration
US10512880B2 (en) 2010-04-30 2019-12-24 Peter Eisenberger Rotating multi-monolith bed movement system for removing CO2 from the atmosphere
US9427726B2 (en) 2011-10-13 2016-08-30 Georgia Tech Research Corporation Vapor phase methods of forming supported highly branched polyamines
US11059024B2 (en) 2012-10-25 2021-07-13 Georgia Tech Research Corporation Supported poly(allyl)amine and derivatives for CO2 capture from flue gas or ultra-dilute gas streams such as ambient air or admixtures thereof
US11737398B2 (en) 2018-02-16 2023-08-29 Carbon Sink, Inc. Fluidized bed extractors for capture of CO2 from ambient air

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