JPH0566819B2 - - Google Patents

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Publication number
JPH0566819B2
JPH0566819B2 JP62161860A JP16186087A JPH0566819B2 JP H0566819 B2 JPH0566819 B2 JP H0566819B2 JP 62161860 A JP62161860 A JP 62161860A JP 16186087 A JP16186087 A JP 16186087A JP H0566819 B2 JPH0566819 B2 JP H0566819B2
Authority
JP
Japan
Prior art keywords
deodorizing
carrier
chloride
component
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP62161860A
Other languages
Japanese (ja)
Other versions
JPS645552A (en
Inventor
Shinji Ekuma
Suketoshi Yamanaka
Hideo Nishikawa
Tasaku Ishida
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.)
Shiraimatsu Shinyaku KK
Original Assignee
Shiraimatsu Shinyaku KK
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 Shiraimatsu Shinyaku KK filed Critical Shiraimatsu Shinyaku KK
Priority to JP62161860A priority Critical patent/JPS645552A/en
Publication of JPS645552A publication Critical patent/JPS645552A/en
Publication of JPH0566819B2 publication Critical patent/JPH0566819B2/ja
Granted legal-status Critical Current

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  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

産業上の利用分野 本発明は、すぐれた消臭作用を有する担持体に
関するものである。 従来の技術 多孔性を有する担体に植物から分離される消臭
成分を担持させた消臭剤または消臭材について、
本出願人はすでに以下に列挙するような出願を行
つている。 特開昭57−6657号公報および特開昭57−
66757号公報:ツバキ科植物からの抽出物を素
焼材に担持させた消臭材。 特開昭59−96号公報:ツバキ科植物から分離
した成分を織布、不織布をはじめとする繊維製
品に担持させた消臭性繊維製品。 実開昭59−70719号公報:内部が多孔性物質、
外皮が通気性包装材からなる多重構造体の内部
または外皮の少なくとも一方にツバキ科植物抽
出分または留分を含浸させたフイルター。 実開昭61−150031号公報:多数枚の薄葉シー
トを積層一体化した拡巾自在のハンカム材にツ
バキ科植物乾留分などの消臭剤を添着した消臭
構造物。 本出願人にかかる出願以外にも、多孔性を有す
る担体に植物から分離される消臭成分を担持させ
た消臭剤または消臭材について、多数の出願があ
る。一例をあげると、特開昭51−27882号公報に
は、種々の植物からの抽出物の加水分解物をシリ
カゲル、ケイ藻土、バーミキユライト、炭素粒、
軽石粒、レンガ細片などに含浸させた空気浄化剤
について開示がある。 発明が解決しようとする問題点 しかしながら、多孔性を有する担体に植物から
分離される消臭成分を担持させた消臭剤または消
臭材は、これを空調機のフイルターなどの目的に
用いると、使用当初は所期の消臭効果を奏しえて
も、使用中に消臭効果が変動または低下したり、
気候によつて消臭効果が変動または低下すること
があつた。 本発明者らは、担体に担持させた植物由来の消
臭成分の消臭効果が雰囲気の湿度の影響を受ける
のではないかとの考えに基いて種々検討を行つた
結果、本発明を見出すに至つた。 問題点を解決するための手段 本発明は「多孔性を有する担体(A)に、植物から
抽出または乾留により分離された消臭成分(B)を、
潮解性または高吸湿性を有する化合物(C)と共に担
持させてなる消臭性担持体。」をその要旨とする
ものである。 以下、本発明を詳細に説明する。 多孔性を有す担体(A)としては、繊維、繊維塊、
繊維束、織布、不織布、編物、繊維製品、パル
プ、紙、紙製品(段ボール、ハニカム等)などの
繊維系担体(無機繊維、鉱物繊維を含む);シリ
カ、アルミナ、ゼオライト、パーライト、粘土鉱
物、素焼、セラミツクス、金属、ガラスなどの粒
子、破砕片、成形物、焼結物等からなる無機質系
担体;プラスチツクス粒子、発泡プラスチツクス
などのプラスチツクス系担体;もみ殻、ソバ殻、
オガクズ、これらの焼成物などの天然物系担体;
などがあげられる。「多孔性を有する」とは、担
体自身が多孔性である場合と、担体間に無数の空
隙を有する場合との双方を含む。 消臭成分(B)としては、各種の植物、たとえば、
ツバキ科植物、シソ科植物、クスノキ科植物、フ
トモモ科植物、キキヨウ科植物、アオイ科植物な
どの植物から抽出または乾留により分離される消
臭成分が用いられる。殊に、茶、山茶花、椿、サ
カキ、モツコクなどのツバキ科植物の主として葉
部を減圧下に乾留し、20mmHgの場合で180〜200
℃で沸騰して留出する乾留分の消臭力が特に大き
いので、この乾留分を用いることが特に好まし
い。 潮解性または高吸湿性を有する化合物(C)として
は、空気中の水分によつて潮解性を示すか、空気
中の水分を強く吸収する性質を示す塩類、酸類、
アルカリ類などが用いられ、特に潮解性または高
吸湿性を有する塩類が実用的である。 このような化合物(C)の具体例としては、塩化リ
チウム、粗製塩化ナトリウム、粗製塩化カリウ
ム、塩化カルシウム、塩化マグネシウム、塩化マ
グネシウムアンモニウム、塩化マグネシウムナト
リウム、塩化マグネシウムカリウム、塩化マンガ
ン、塩化マンガンカリウム、塩化アンチモン、塩
化コバルトアンモニウム、塩化亜鉛、塩化鉄、塩
化ビスマス、塩化ベリリウム、塩化ニツケル、塩
化ニツケルアンモニウム、塩化銅、塩化クロム;
臭化リチウム、臭化ベリリウム、臭化カルシウ
ム、臭化亜鉛、臭化銅、臭化鉄、臭化コバルト、
臭化カドミウム;ヨウ化リチウム、ヨウ化ナトリ
ウム、ヨウ化マグネシウム、ヨウ化カルシウム、
ヨウ化鉄、ヨウ化ニツケル;亜硝酸ナトリウム、
亜硝酸カリウム、亜硝酸マグネシウム;硝酸アン
モニウム、硝酸リチウム、硝酸ナトリウム、硝酸
カルシウム、硝酸ベリリウム、硝酸マグネシウ
ム、硝酸マンガン、硝酸セリウム、硝酸セリウム
アンモニウム、硝酸鉄、硝酸銅;塩素酸リチウ
ム、塩素酸カルシウム、塩素酸マグネシウム、塩
素酸亜鉛、塩素酸カドミウム、塩素酸コバルト、
塩素酸銅;炭酸カリウム;硫酸リチウム、硫酸亜
鉛アンモニウム、硫酸アンチモン、硫酸鉄、硫酸
カドミウムアンモニウム;チオ硫酸アンモニウ
ム;リン酸カリウム;亜リン酸アンモニウム、亜
リン酸カリウム、亜リン酸ヒドラジニウム;次亜
リン酸ナトリウム、次亜リン酸カリウム;過マン
ガン酸ナトリウム、過マンガン酸カルシウム、過
マンガン酸ストロンチウム、過マンガン酸マグネ
シウム、過マンガン酸亜鉛;リン酸;水酸化ナト
リウム、水酸化カリウム;などがあげられ、目
的、用途、使用環境等に合せて適当なものを選択
する。2種以上の併用も可能である。 なお、化合物(C)に代えて高吸水性樹脂を用いて
も、消臭作用の改善効果は小さい。 多孔性を有する担体(A)に対する消臭成分(B)の担
持量は、担体(A)の種類、消臭成分(B)の種類によつ
て最適範囲が大きく相違するので一慨に決められ
ないが、消臭成分(B)として消臭効果の大きいツバ
キ科植物の乾留分を用いた場合で、たとえば0.01
〜10重量%である。 多孔性を有する担体(A)に対する潮解性または高
吸湿性を有する化合物(C)の担持量も、担体(A)の種
類、消臭成分(B)の種類、化合物(C)の種類によつて
最適範囲が大きく相違するので一慨に決められな
いが、担体(A)に対して0.1〜50重量%の範囲から
選択することが多い。 担体(A)に消臭成分(B)および化合物(C)を担持させ
る方法としては、消臭成分(B)を含む溶液に化合物
(C)またはそれを含む溶液を混合し、この混合溶液
を担体(A)に塗布、含浸、噴霧等の手段により付着
させ、ついで乾燥する方法が採用される。消臭成
分(B)を含む溶液と化合物(C)を含む溶液とを別個に
担体(A)に担持させることも可能ではあるが、担持
操作が2段階になること、消臭成分(B)と化合物(C)
とが担体(A)上で分離して担持されるおそれがある
ことなどの点で、消臭成分(B)と化合物(C)の混合物
を担体(A)に担持させる方法に比しては不利とな
る。 本発明の担持体は、空調機、空気清浄機、脱臭
機、送・排風機用のフイルター、冷蔵庫用の消臭
剤または消臭材、室内または車内の消臭剤または
消臭材などとして有用である。 作 用 本発明の担持体を臭気成分を含む雰囲気と接触
させると、雰囲気中の臭気成分は担体(A)に担持さ
れている植物由来の消臭成分(B)によつて捕捉され
る。この場合、担体(A)は化合物Cにより湿潤状態
にあるため臭気成分が付着しやすい状態にあり、
消臭成分(B)による臭気成分の捕捉が加速される。 そして消臭成分(B)は化合物(C)により水分で湿潤
した状態に保たれているので、消臭成分(B)の消臭
能力が最大限に発揮される状態において、捕捉さ
れた臭気成分が分解または包接され、無臭化され
る。 一般的に、乾燥により乾化した植物由来の消臭
剤は消臭能力が減じるのであるが、本発明の担持
体を用いると、担体(A)の表面で消臭成分(B)により
いわばミクロな湿式処理がなされることになるの
である。 実施例 次に実施例をあげて本発明をさらに説明する。
以下「%」とあるのは重量%である。 担体(A) 多孔性を有する担体(A)として、陶石、白雲母お
よび木節粘土を原料として酸化雰囲気下に温度
950℃で焼成した直径2〜4mmの素焼粒子(A−
1)を準備した。 消臭成分(B) 茶葉粉末を20mmHgの減圧下に乾留し、温度180
〜200℃にて沸騰して留出してくる留出分をプロ
ピレングリコール中に受け、乾留分の20%プロピ
レングリコール溶液を得た。この溶液を水で10倍
に稀釈して消臭成分含有液(B−1)となした。 化合物(C) 潮解性または高吸湿性を有する化合物(C)とし
て、塩化リチウム(C−1)、粗製塩化ナトリウ
ム(C−2)、塩化カルシウム(C−3)を準備
した。 吸湿性試験 上述の消臭成分含有液(B−1)に塩化リチウ
ム(C−1)、粗製塩化ナトリウム(C−2)、塩
化カルシウム(C−3)をそれぞれ5%、10%、
15%添加した溶液に、素焼粒子(A−1)を投入
し、ついで引き上げて60℃で12時間乾燥し、試験
に供した。 比較のため、消臭成分含有液(B−1)に素焼
粒子(A−1)を投入、乾燥した場合についても
試験に供した。 上記の乾燥後の担持体を室内に放置して、1〜
48時間にわたつて重量変化を測定した。 吸湿性試験の結果を第1〜3図に示す。第1図
は塩化リチウム(C−1)を用いた場合、第2図
は粗製塩化ナトリウム(C−2)を用いた場合、
第3図は塩化カルシウム(C−3)を用いた場合
である。各図において0%とあるのは、消臭成分
含有液(B−1)のみを担持し、化合物(C)を担持
しなかつた場合を意味する。 第1〜3図から、化合物(C)の担持により、それ
を担持しなかつた場合に比し相当量の重量増加が
認められ、その吸湿効果が確認された。 消臭試験 上述の消臭成分含有液(B−1)に塩化リチウ
ム(C−1)、粗製塩化ナトリウム(C−2)、塩
化カルシウム(C−3)をそれぞれ15%添加した
溶液に、素焼粒子(A−1)投入し、ついで引き
上げて60℃で12時間乾燥した。乾留分の担持量は
ネツトで0.04%、(C−1)、(C−2)、(C−3)
の担持量はいずれも3%であつた。 得られた担持体500gを網体内に充填してフイ
ルターとなし、1m3の密閉容器内の空調機にセツ
トした。 密閉容器内にアンモニアを30ppm濃度に添加
し、2.0m/secの風速で空調液を作動し、密閉容
器内に残存する残留アンモニアの濃度を検知管に
て経時的に測定した。 同様に、密閉容器内にトリメチルアミンを
33ppm濃度に添加し、2.0m/secの風速で空調機
を作動し、密閉容器内に残存する残留トリメチル
アミンの濃度を検知管にて経時的に測定した。 比較例として、消臭成分含有液(B−1)に素
焼粒子(A−1)を投入、乾燥した場合について
も同様の実験を行つた。 また参考例として、化合物(C)に代えて少量のア
クリル系高吸水性樹脂(D−1)を用いた場合に
ついても実験を行つた。 臭気成分としてアンモニアを用いた場合の結果
を第1表に、臭気成分としてトリメチルアミンを
用いた場合の結果を第2表に示す。
INDUSTRIAL APPLICATION FIELD The present invention relates to a carrier having an excellent deodorizing effect. BACKGROUND ART Regarding deodorants or deodorizing materials in which a porous carrier supports deodorizing ingredients separated from plants,
The applicant has already filed the applications listed below. JP-A-57-6657 and JP-A-57-
Publication No. 66757: A deodorizing material in which an extract from a plant of the Camellia family is supported on a clay material. JP-A-59-96: A deodorizing textile product in which a component separated from a plant of the Camellia family is supported on textile products such as woven fabrics and non-woven fabrics. Utility Model Application Publication No. 59-70719: Porous material inside,
A filter in which at least one of the inside or the outer skin of a multilayer structure whose outer skin is made of an air-permeable packaging material is impregnated with an extract or distillate from a plant of the Camellia family. Utility Model Application No. 61-150031: A deodorizing structure in which a deodorizing agent such as the dry distillate of a plant of the Camellia family is attached to an expandable handkerchief material made by laminating and integrating a large number of thin sheets. In addition to the applications filed by the present applicant, there are numerous applications regarding deodorants or deodorizing materials in which deodorizing components separated from plants are supported on porous carriers. For example, Japanese Patent Application Laid-Open No. 51-27882 discloses that hydrolysates of extracts from various plants are mixed with silica gel, diatomaceous earth, vermiculite, carbon grains,
There is a disclosure regarding an air purifying agent impregnated with pumice grains, brick pieces, etc. Problems to be Solved by the Invention However, when a deodorant or deodorizing material in which a porous carrier carries a deodorizing component separated from plants is used for purposes such as filters in air conditioners, Even if the desired deodorizing effect is achieved at the beginning of use, the deodorizing effect may change or decrease during use.
The deodorizing effect sometimes varied or decreased depending on the climate. The present inventors conducted various studies based on the idea that the deodorizing effect of a plant-derived deodorant component supported on a carrier may be affected by the humidity of the atmosphere, and as a result, they discovered the present invention. I've reached it. Means for Solving the Problems The present invention is based on the following technology: ``A deodorant component (B) extracted from plants or separated by carbonization is added to a porous carrier (A).
A deodorizing carrier supported together with a deliquescent or highly hygroscopic compound (C). ” is its gist. The present invention will be explained in detail below. As the porous carrier (A), fibers, fiber lumps,
Fiber-based carriers (including inorganic fibers and mineral fibers) such as fiber bundles, woven fabrics, non-woven fabrics, knitted fabrics, textile products, pulp, paper, paper products (cardboard, honeycomb, etc.); silica, alumina, zeolite, perlite, clay minerals Inorganic carriers consisting of particles, crushed pieces, molded products, sintered products, etc. of unglazed ceramics, ceramics, metals, glass, etc.; Plastic carriers such as plastic particles, foamed plastics; Rice husks, buckwheat husks,
Natural product carriers such as sawdust and baked products of these;
etc. "Having porosity" includes both the case where the carrier itself is porous and the case where there are countless voids between the carriers. As the deodorizing ingredient (B), various plants such as
Deodorizing ingredients extracted or separated by carbonization from plants such as Camellia, Lamiaceae, Lauraceae, Myrtaceae, Cucumberaceae, and Malvaceae are used. In particular, the leaves of plants of the Camellia family, such as tea, sasanqua, camellia, sakaki, and motsukoku, are carbonized under reduced pressure to produce a concentration of 180 to 200
It is particularly preferable to use a dry distillate that is boiled at a temperature of 0.degree. C. and has a particularly high deodorizing power. Examples of deliquescent or highly hygroscopic compounds (C) include salts, acids, which exhibit deliquescent properties when exposed to moisture in the air, or which exhibit the property of strongly absorbing moisture in the air;
Alkalies and the like are used, and deliquescent or highly hygroscopic salts are particularly practical. Specific examples of such compounds (C) include lithium chloride, crude sodium chloride, crude potassium chloride, calcium chloride, magnesium chloride, ammonium magnesium chloride, sodium magnesium chloride, potassium magnesium chloride, manganese chloride, potassium manganese chloride, chloride Antimony, cobalt ammonium chloride, zinc chloride, iron chloride, bismuth chloride, beryllium chloride, nickel chloride, nickel ammonium chloride, copper chloride, chromium chloride;
Lithium bromide, beryllium bromide, calcium bromide, zinc bromide, copper bromide, iron bromide, cobalt bromide,
Cadmium bromide; lithium iodide, sodium iodide, magnesium iodide, calcium iodide,
Iron iodide, nickel iodide; sodium nitrite,
Potassium nitrite, magnesium nitrite; ammonium nitrate, lithium nitrate, sodium nitrate, calcium nitrate, beryllium nitrate, magnesium nitrate, manganese nitrate, cerium nitrate, ammonium cerium nitrate, iron nitrate, copper nitrate; lithium chlorate, calcium chlorate, chloric acid Magnesium, zinc chlorate, cadmium chlorate, cobalt chlorate,
Copper chlorate; potassium carbonate; lithium sulfate, zinc ammonium sulfate, antimony sulfate, iron sulfate, cadmium ammonium sulfate; ammonium thiosulfate; potassium phosphate; ammonium phosphite, potassium phosphite, hydrazinium phosphite; hypophosphorous acid Sodium, potassium hypophosphite; sodium permanganate, calcium permanganate, strontium permanganate, magnesium permanganate, zinc permanganate; phosphoric acid; sodium hydroxide, potassium hydroxide; etc. , select the appropriate one according to the purpose, usage environment, etc. A combination of two or more types is also possible. Note that even if a super absorbent resin is used in place of compound (C), the effect of improving the deodorizing effect is small. The amount of the deodorizing component (B) supported on the porous carrier (A) cannot be determined uniformly because the optimal range varies greatly depending on the type of carrier (A) and the type of deodorizing component (B). However, if the dry distillate fraction of Camelliaaceae plants, which has a large deodorizing effect, is used as the deodorizing ingredient (B), for example, 0.01
~10% by weight. The amount of the deliquescent or highly hygroscopic compound (C) supported on the porous carrier (A) also depends on the type of carrier (A), the type of deodorizing component (B), and the type of compound (C). Although the optimum range cannot be definitively determined as it varies greatly, it is often selected from the range of 0.1 to 50% by weight based on the carrier (A). A method for supporting the deodorizing component (B) and the compound (C) on the carrier (A) is to add the compound to a solution containing the deodorizing component (B).
A method is employed in which (C) or a solution containing the same is mixed, this mixed solution is applied to the carrier (A) by means such as coating, impregnating, or spraying, and then drying. Although it is possible to separately support the solution containing the deodorizing component (B) and the solution containing the compound (C) on the carrier (A), the loading operation requires two steps, and the solution containing the deodorizing component (B) and compound (C)
Compared to the method of supporting a mixture of the deodorizing component (B) and the compound (C) on the carrier (A), it It will be disadvantageous. The carrier of the present invention is useful as a filter for an air conditioner, an air cleaner, a deodorizer, a blower/exhaust fan, a deodorizing agent or deodorizing material for a refrigerator, a deodorizing agent or deodorizing material for indoor or car interiors, etc. It is. Effect When the carrier of the present invention is brought into contact with an atmosphere containing odor components, the odor components in the atmosphere are captured by the plant-derived deodorizing component (B) supported on the carrier (A). In this case, the carrier (A) is in a wet state due to compound C, so the odor component is likely to adhere to it.
The capture of odor components by the deodorizing component (B) is accelerated. Since the deodorizing component (B) is kept moist with water by the compound (C), the captured odor components is decomposed or included and becomes odorless. Generally, the deodorizing ability of plant-derived deodorants is reduced by drying, but when the carrier of the present invention is used, the deodorizing component (B) is applied to the surface of the carrier (A) in a microscopic manner. This means that wet processing is required. Examples Next, the present invention will be further explained with reference to Examples.
Hereinafter, "%" means % by weight. Support (A) Porous support (A) is made of pottery stone, muscovite, and kibushi clay as raw materials and heated under an oxidizing atmosphere at a temperature.
Unglazed particles (A-
1) was prepared. Deodorizing ingredient (B) Tea leaf powder is carbonized under reduced pressure of 20mmHg and heated to 180℃.
The distillate that boiled at ~200°C was collected in propylene glycol to obtain a 20% solution of the dry distillate in propylene glycol. This solution was diluted 10 times with water to obtain a deodorizing component-containing liquid (B-1). Compound (C) As a deliquescent or highly hygroscopic compound (C), lithium chloride (C-1), crude sodium chloride (C-2), and calcium chloride (C-3) were prepared. Hygroscopicity test Lithium chloride (C-1), crude sodium chloride (C-2), and calcium chloride (C-3) were added to the above deodorizing component-containing liquid (B-1) at 5% and 10%, respectively.
Unglazed particles (A-1) were added to a solution containing 15% of the mixture, then pulled out, dried at 60°C for 12 hours, and subjected to a test. For comparison, a test was also conducted in which the unglazed particles (A-1) were added to the deodorizing component-containing liquid (B-1) and dried. The above dried carrier was left indoors, and
Weight changes were measured over 48 hours. The results of the hygroscopicity test are shown in Figures 1-3. Figure 1 shows the case when lithium chloride (C-1) is used, and Figure 2 shows the case when crude sodium chloride (C-2) is used.
FIG. 3 shows the case using calcium chloride (C-3). In each figure, 0% means that only the deodorizing component-containing liquid (B-1) was supported and the compound (C) was not supported. From FIGS. 1 to 3, it was observed that by supporting Compound (C), a considerable weight increase was observed compared to the case where Compound (C) was not supported, and its hygroscopic effect was confirmed. Deodorizing test A solution in which 15% each of lithium chloride (C-1), crude sodium chloride (C-2), and calcium chloride (C-3) were added to the above-mentioned deodorizing component-containing liquid (B-1) was unglazed. Particles (A-1) were added, then taken out and dried at 60°C for 12 hours. The supported amount of dry distillate is 0.04% in net, (C-1), (C-2), (C-3)
The supported amount was 3% in all cases. 500 g of the obtained carrier was filled into a mesh body to form a filter, and the filter was set in an air conditioner in a 1 m 3 airtight container. Ammonia was added to a concentration of 30 ppm in a sealed container, the air conditioning fluid was operated at a wind speed of 2.0 m/sec, and the concentration of residual ammonia remaining in the sealed container was measured over time using a detection tube. Similarly, store trimethylamine in a closed container.
The concentration of residual trimethylamine remaining in the sealed container was measured over time using a detection tube by adding the solution to a concentration of 33 ppm and operating the air conditioner at a wind speed of 2.0 m/sec. As a comparative example, a similar experiment was conducted in which unglazed particles (A-1) were added to the deodorizing component-containing liquid (B-1) and dried. As a reference example, an experiment was also conducted in which a small amount of acrylic superabsorbent resin (D-1) was used in place of compound (C). Table 1 shows the results when ammonia was used as the odor component, and Table 2 shows the results when trimethylamine was used as the odor component.

【表】【table】

【表】 担体(A)として坪量74g/m2のポリエステル−レ
イヨン混抄不織布(A−2))を用い、これに上
述消臭成分含有液(B−1)に塩化リチウム(C
−1)、粗製塩化ナトリウム(C−2)、塩化カル
シウム(C−3)をそれぞれ10%添加した溶液を
噴霧し、ついで60℃で12時間乾燥した。乾留分の
担持量はネツトで0.2%、(C−1)、(C−2)、
(C−3))の担持量はいずれも10%であつた。 得られた担持体40gをフイルターとして上述の
1m3の密閉容器にセツトし、上記と同様の消臭試
験を行つた。 比較例として、不織布(A−2)に消臭成分含
有液(B−1)を噴霧、乾燥した場合についても
同様の実験を行つた。 臭気成分としてアンモニアを用いた場合の結果
を第3表に、臭気成分としてトリメチルアミンを
用いた場合の結果を第4表に示す。
[Table] A polyester-rayon blend nonwoven fabric (A-2) with a basis weight of 74 g/m 2 was used as the carrier (A), and lithium chloride (C
-1), a solution containing 10% each of crude sodium chloride (C-2) and calcium chloride (C-3) was sprayed thereon, and then dried at 60°C for 12 hours. The supported amount of carbonized distillate is 0.2% in net, (C-1), (C-2),
The supported amount of (C-3)) was 10% in all cases. 40 g of the obtained carrier was set as a filter in the above-mentioned 1 m 3 airtight container, and the same deodorization test as above was conducted. As a comparative example, a similar experiment was conducted in which the deodorizing component-containing liquid (B-1) was sprayed onto the nonwoven fabric (A-2) and dried. Table 3 shows the results when ammonia was used as the odor component, and Table 4 shows the results when trimethylamine was used as the odor component.

【表】【table】

【表】 発明の効果 本発明の担持体、すなわち、担体(A)に植物由来
の消臭成分(B)と共に化合物(C)を担持させた担持体
を消臭剤または消臭材として用いると、消臭成分
の乾固による消臭能力の低下が防止され、単に担
体(A)に消臭成分(B)を担持させた場合に比し、雰囲
気中のの臭気がすみやかに除去されると共に、消
臭性能も大きく向上する。しかも、使用中に消臭
効果が変動または低下したり、気候によつて消臭
効果が変動または低下したりすることがなく、常
に安定した消臭能力が持続的に発揮される。
[Table] Effects of the Invention When the carrier of the present invention, that is, a carrier in which the compound (C) is supported together with the plant-derived deodorizing component (B) on the carrier (A), is used as a deodorant or a deodorizing material. , the deodorizing ability is prevented from decreasing due to drying of the deodorizing component, and the odor in the atmosphere is quickly removed compared to when the deodorizing component (B) is simply supported on the carrier (A). , the deodorizing performance is also greatly improved. Furthermore, the deodorizing effect does not fluctuate or decrease during use, nor does it fluctuate or decrease depending on the climate, so that a stable deodorizing ability is constantly exhibited.

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

第1〜3図は、吸湿性試験の結果を示したグラ
フであり、第1図は塩化リチウムを用いた場合、
第2図は粗製塩化ナトリウムを用いた場合、第3
図は塩化カルシウムを用いた場合である。
Figures 1 to 3 are graphs showing the results of the hygroscopicity test, and Figure 1 shows the results when lithium chloride was used.
Figure 2 shows that when crude sodium chloride is used, the third
The figure shows the case using calcium chloride.

Claims (1)

【特許請求の範囲】 1 多孔性を有する担体(A)に、植物から抽出また
は乾留により分離された消臭成分(B)を、潮解性ま
たは高吸湿性を有する化合物(C)と共に担持させて
なる消臭性担持体。 2 化合物(C)が、潮解性または高吸湿性を有する
塩類である特許請求の範囲第1項記載の担持体。 3 消臭成分(B)が、ツバキ科植物の乾留分である
特許請求の範囲第1項記載の担持体。
[Claims] 1. A deodorizing component (B) extracted from plants or separated by carbonization is supported on a porous carrier (A) together with a deliquescent or highly hygroscopic compound (C). A deodorizing carrier. 2. The carrier according to claim 1, wherein the compound (C) is a salt having deliquescent property or high hygroscopicity. 3. The carrier according to claim 1, wherein the deodorizing component (B) is a dry distillate of a plant belonging to the Camellia family.
JP62161860A 1987-06-29 1987-06-29 Deodorizing carrier Granted JPS645552A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62161860A JPS645552A (en) 1987-06-29 1987-06-29 Deodorizing carrier

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62161860A JPS645552A (en) 1987-06-29 1987-06-29 Deodorizing carrier

Publications (2)

Publication Number Publication Date
JPS645552A JPS645552A (en) 1989-01-10
JPH0566819B2 true JPH0566819B2 (en) 1993-09-22

Family

ID=15743335

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62161860A Granted JPS645552A (en) 1987-06-29 1987-06-29 Deodorizing carrier

Country Status (1)

Country Link
JP (1) JPS645552A (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5942323A (en) * 1995-01-27 1999-08-24 Purafil, Inc. Fiber filter and methods of use thereof
EP0774264A1 (en) * 1995-11-20 1997-05-21 Espo, Ltd. Air purifying agent and air purifying method
JP4230558B2 (en) * 1998-03-11 2009-02-25 株式会社エルブ Antibacterial ceramics and manufacturing method thereof
JP2001149718A (en) * 1999-11-24 2001-06-05 Katsumi Matsumoto Filter for air cleaner and its manufacturing method
JP4601102B2 (en) * 1999-11-24 2010-12-22 勝美 松本 air purifier
JP4665067B2 (en) * 2000-01-11 2011-04-06 株式会社白元 Solid humidity control material
JP2001311048A (en) * 2000-02-22 2001-11-09 Erubu:Kk Functional coating composition and cover

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62290462A (en) * 1986-06-10 1987-12-17 日清製粉株式会社 Deodorant containing metal phthalocyanine as constitutional component

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62290462A (en) * 1986-06-10 1987-12-17 日清製粉株式会社 Deodorant containing metal phthalocyanine as constitutional component

Also Published As

Publication number Publication date
JPS645552A (en) 1989-01-10

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