JPH0124508B2 - - Google Patents

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Publication number
JPH0124508B2
JPH0124508B2 JP58230895A JP23089583A JPH0124508B2 JP H0124508 B2 JPH0124508 B2 JP H0124508B2 JP 58230895 A JP58230895 A JP 58230895A JP 23089583 A JP23089583 A JP 23089583A JP H0124508 B2 JPH0124508 B2 JP H0124508B2
Authority
JP
Japan
Prior art keywords
deodorizing
activated carbon
liquid
ethanol
extract
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
Application number
JP58230895A
Other languages
Japanese (ja)
Other versions
JPS60122566A (en
Inventor
Masaaki Sano
Yukiteru Myamoto
Jiro Kawachi
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.)
NITSUSHIN KORYO KK
Original Assignee
NITSUSHIN KORYO 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 NITSUSHIN KORYO KK filed Critical NITSUSHIN KORYO KK
Priority to JP58230895A priority Critical patent/JPS60122566A/en
Publication of JPS60122566A publication Critical patent/JPS60122566A/en
Publication of JPH0124508B2 publication Critical patent/JPH0124508B2/ja
Granted legal-status Critical Current

Links

Description

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

本発明はツバキ科及び/又はクスノキ科植物の
生葉又は乾燥葉に存在する消臭効果を有する成分
をエタノールを使用して加熱抽出して、その抽出
エキスを活性炭素などの吸着剤で脱色、精製した
黄色の処理液を有効成分として含有する消臭剤か
又は脱色精製した処理液を除去した後の残渣活性
炭、酸性白土、珪藻土よりなる消臭剤に関するも
のである。 本出願人はさきに田辺製薬株式会社と共同して
特公昭58―18098号の発明をしたが、この先願発
明による消臭剤は濃緑色〜濃褐色を有する着色固
形物をそのまま有効成分として含有するため極め
て着色が強く、しかも水に対する溶解性が悪ため
消臭対照物によつては使用制限を受ける欠点があ
る。 本発明はこの欠点を補ぎない、広範囲に使用可
能であり、しかも水に対する溶解性がよく、着色
が少なく、酸性、アルカリ性の悪臭物質に対して
も消臭効果の大なる消臭剤を得ることを目的とす
るものである。そのため本発明者は先願発明の消
臭剤に含有される着色原因成分及び水に不溶の成
分と考えられる葉緑素、樹脂及び精油成分を除去
することにより目的が達成されるとの考えの下に
鋭意研究した結果、これらの除去剤として活性炭
素、酸性白土、珪藻土等が除去効果も高く、操作
が簡便で、効率的であり、しかも消臭成分を分離
した残渣活性炭素、酸性白土、珪藻土が酸性及び
アルカリ性の悪臭物質に対して、消臭効果の優れ
ていることを見付け、本発明を完成するに至つた
もので、本発明の第1発明はツバキ科の植物又
は/及びクスノキ科の植物の生葉又は乾燥葉1部
に対してエタノール4〜10部を使用して2〜10時
間熱抽出を行ない得られた抽出物を活性炭素、酸
性白土又は珪藻土等を使用して脱色処理を行な
い、得られた液状の処理物を有効成分として含有
する消臭剤であり、その第2発明は上記脱色処理
を行ない液状の処理物を分離した残渣として得ら
れる粗製の消臭有効成分を含有する活性炭素、酸
性白土、珪藻土を消臭用に供する消臭剤を提供す
るものである。 従来から活性炭素自体が吸着効果があるため各
種脱臭剤として使用されていた。 しかしながら活性炭素の吸着作用には悪臭成分
の消臭に対して選択性があり、高温よりも低温で
消臭効果が高く、代表的な酸性悪臭成分である硫
化水素、メルカプタン系の悪臭に対しては、吸着
能力が高いが、アルカリ性側の悪臭成分であるア
ンモニア、トリメチルアミン等の悪臭、特にアン
モニアについては脱臭効果が劣る欠点がある。ま
た水の存在においてもその脱臭効果が低下するの
である。 本発明の消臭有効成分を分離した粗製の消臭有
効成分を含有する残渣活性炭素、酸性白土又は珪
藻土をそのまゝ消臭剤として使用する場合本来の
活性炭素等の酸性悪臭成分に対する消臭効果と共
にアルカリ性悪臭成分に対する消臭効果をも兼ね
備え、著しい広範囲の消臭作用を有し、しかも水
の存在においても、また高温においても従来の活
性炭素自体等よりも高い消臭効果を有するのであ
る。 本発明の脱色処理方法は例えば緑茶の乾燥葉末
1部に対して、エタノール4〜10部を使用し、2
〜10時間熱抽出を行ない、得られた抽出液を濃縮
して約30%の抽出物を含む粗製の抽出溶液が得ら
れる。この30%抽出物溶液に対してエタノール、
水の単独またはそれらの混合溶液、および食品添
加物規格の活性炭素を抽出物1部に対して0.3〜
3.0部を加えて、10〜60分間程度、室温もしくは
加熱下に撹拌することによつて行なうことが好ま
しい。 脱色処理後は活性炭素を別して液を採取
し、この有効成分を含有する液(消臭原液剤と
いう。)および別した粗製の抽出物を含む残渣
活性炭素を有効成分とする消臭剤(以下消臭粉末
剤という。)が得られる。酸性白土、珪藻土の場
合も同様である。 (A) 上記により得られた消臭原液剤を使用する場
合は (イ) 低級アルコール、含水低級アルコールおよ
び多価アルコール、含水多価アルコール等で
希釈を行ない、得られた消臭液剤を悪臭発生
場所に散布する。 (ロ) 食品関係には直接配合し、よく混合する。 (ハ) 香粧類には直接配合する。 (ニ) 消臭、脱臭器の消臭成分として用いる。 (ホ) 医薬品等の悪臭を消臭する場合は粉末とし
て常法により顆粒剤または錠剤に成型して包
装乃至は貯蔵容器内に別封する。 (B) または消臭粉末剤を使用する場合は、 (イ) 冷蔵庫及び吸湿剤としては適当な形に成型
して単独またはヤシガラ活性炭の1部として
用いる。 (ロ) 生理用品、靴の敷皮、空調関係には直接配
合する。 (ハ) 工場排液処理槽に直接添加する。 (ニ) 薫製に用いる薫剤の一成分として配合す
る。 (C) 本発明の消臭液剤および消臭粉末剤の使用例
を下記に示すが、使用例はこれのみに限定され
るものではない。 尚%はすべて重量%である。 使用例1 (消臭スプレー) エタノール 50% ジクロロジフルオロメタン 48 実施例5の消臭液剤 2 100% 使用例2 (ペツト消臭液剤) エタノール 10% 香 料 0.01 実施例5の消臭液剤 2 水 残 100.0% 使用例3 (キヤンデイ) 砂 糖 50% 水あめ 34 有機酸 1 香 料 0.2 実施例5の消臭液剤 0.5 水 残 100.0% 使用例4 (ドリンク) 砂 糖 12 % ハチミツ 1 ドリンクベース 0.3 香 料 0.1 実施例5の消臭液剤 1.0 水 残 100.0% 使用例5 (錠剤) 乳 糖 65部 デキストリン 10 タルク 5 実施例2の消臭原液剤 20 水 適量 100部 使用例6 (冷蔵車用) ヤシガラ活性炭 70% 実施例6の消臭用顆粒 30 100% 使用例7 (靴の敷皮) 活性炭 80% 実施例4の消臭粉末剤 20 100% 本発明者の研究によると、本発明の消臭作用は
フラバノール、フラボノール類及びアミノ酸、有
機酸、糖類その他の高分子化合物を含む多数の成
分により付加作用、中和反応作用および包接作用
等の複合作用により消臭作用を奏するのである。 残渣活性炭素による消臭粉末剤においては、本
来の活性炭素の吸着作用をも合せ奏することは前
記した通りである。 次に実施例によつて本発明を説明する。 実施例1 (有効成分の抽出) 茶乾燥葉末100gとエタノール900gを抽出器に
仕込み、4時間還流を行なう。抽出液より原料残
渣を去し、液を濃縮して、30%の熱抽出物を
含む抽出溶液100gを得た。 実施例2 (有効成分の脱色処理) 実施例1で得た粗製の30%抽出物溶液35g、エ
タノール30g、精製水40gおよび活性炭素15gを
容器に加え、30分間70〜80℃で加熱後、同じく撹
拌を30分間行なう。 その後吸引にて過を行ない、残渣を新たなエ
タノールで洗浄して残渣を別し、有効成分5%
を含有する黄色の透明な液(消臭原液剤)を得
た。 この消臭原液剤の1000倍アルコール溶液は紫外
線吸収スペクトルで275±2mμに極大吸収を示す。 実施例 3 実施例1で得た粗製の30%抽出物溶液30g、エ
タノール70gおよび活性炭素12gを容器に加え
て、実施例2と同じ操作を行ない、有効成分6%
を含有する黄色の透明な液(消臭原液剤)を得
た。 実施例 4 実施例2で別された残渣を乾燥して粗製の抽
出物を有効成分として約5%含有する活性炭素粉
末(消臭粉末剤)20gを得た。 実施例 5 実施例2で得た液(消臭原液剤)50部をプロ
ピレングリコール、グリセリン、エタノールまた
はそれらの混合物によつて稀釈して種々の用途に
使用される液状消臭剤を得た。 実施例 6 実施例4で得た消臭粉末剤10部に対して、ポリ
ビニルピロリドン10%含水エタノール溶液5〜10
部を用いて練り合した後、造粒機を用いて成型す
ることにより顆粒状の消臭剤を得た。 実施例7 (本発明消臭剤の消臭効果試験) 実施例5で得た消臭液剤について消臭効果を測
定した。 (1) 悪臭成分 (a) 30%トリメチルアミン水溶液 (b) ベンジルメルカプタン (2) 試験方法 (a) トリメチルアミン水溶液36mg (b) ベンジルメルカプタン12mg をそれぞれの容器に取り、消臭液剤1gを加えて
密封容器内でよく混合する。 その後(a)、(b)それぞれの密封容器内の空気分を
注射器で取り出し、ガスクロマトグラフに注入す
る。同様に空試験を行ない、クロマトグラフの面
積値を100として除去率を求めた。 (a) トリメチルアミン除去率 80.3% (b) ベンジルメルカプタン除去率 73.1% 尚、ガスクロマトグラフの測定条件は下記の通
りである。
The present invention heat-extracts components with a deodorizing effect that are present in fresh or dried leaves of plants of the Camellia family and/or Lauraceae family using ethanol, and decolorizes and purifies the extracted extract with an adsorbent such as activated carbon. The present invention relates to a deodorizer containing a yellow treatment liquid as an active ingredient, or a deodorizer made of activated carbon, acid clay, or diatomaceous earth, which is the residue after removing the decolorized and purified treatment liquid. The present applicant previously made an invention in Japanese Patent Publication No. 58-18098 in collaboration with Tanabe Seiyaku Co., Ltd., but the deodorant according to this earlier invention contains a colored solid having a dark green to dark brown color as an active ingredient. Therefore, it is extremely colored, and its solubility in water is poor, so it has the drawback of being limited in its use depending on the deodorizing substance. The present invention aims to provide a deodorant that does not compensate for this drawback, can be used over a wide range of areas, has good solubility in water, has little coloration, and has a great deodorizing effect against acidic and alkaline malodorous substances. The purpose is to Therefore, the present inventor believes that the objective can be achieved by removing the coloring-causing components and the chlorophyll, resin, and essential oil components that are considered to be water-insoluble components contained in the deodorant of the prior invention. As a result of intensive research, we have found that activated carbon, acid clay, diatomaceous earth, etc. have a high removal effect, are easy to operate, and are efficient. The present invention was completed by discovering that it has an excellent deodorizing effect on acidic and alkaline malodorous substances, and the first invention of the present invention is a plant of the Camellia family and/or a plant of the Lauraceae family. 1 part of fresh or dried leaves is subjected to heat extraction for 2 to 10 hours using 4 to 10 parts of ethanol, and the resulting extract is decolorized using activated carbon, acid clay, diatomaceous earth, etc. The second invention is a deodorizing agent containing the obtained liquid treated product as an active ingredient, and the second invention is an active deodorizing agent containing a crude deodorizing active ingredient obtained as a residue after performing the above decolorization treatment and separating the liquid treated product. The present invention provides a deodorizing agent that uses carbon, acid clay, and diatomaceous earth for deodorizing purposes. Activated carbon itself has traditionally been used as a deodorizing agent because it has an adsorption effect. However, the adsorption effect of activated carbon is selective for deodorizing malodorous components, and the deodorizing effect is higher at low temperatures than at high temperatures, and it is effective against the malodors of hydrogen sulfide and mercaptan, which are typical acidic malodorous components. Although it has a high adsorption capacity, it has the disadvantage that its deodorizing effect is poor for alkaline malodor components such as ammonia and trimethylamine, especially ammonia. The deodorizing effect is also reduced in the presence of water. When the residual activated carbon, acid clay, or diatomaceous earth containing the crude deodorizing active ingredient from which the deodorizing active ingredient of the present invention is separated is used as a deodorizing agent, the deodorization of the acidic malodorous components such as the original activated carbon etc. It also has a deodorizing effect on alkaline malodorous components, and has a remarkable wide-ranging deodorizing effect, and even in the presence of water and at high temperatures, it has a higher deodorizing effect than conventional activated carbon itself. . The decolorization treatment method of the present invention uses, for example, 4 to 10 parts of ethanol to 1 part of dried green tea leaf powder, and
Thermal extraction is carried out for ~10 hours and the resulting extract is concentrated to obtain a crude extract solution containing about 30% extract. Ethanol for this 30% extract solution,
A solution of water alone or a mixture thereof, and activated carbon according to food additive standards at 0.3 to 1 part of extract.
It is preferable to carry out this by adding 3.0 parts and stirring for about 10 to 60 minutes at room temperature or under heating. After the decolorization process, the activated carbon is separated and the liquid is collected, and the liquid containing this active ingredient (hereinafter referred to as deodorizing stock solution) and the separated crude extract are collected. ) is obtained. The same applies to acid clay and diatomaceous earth. (A) When using the deodorizing stock solution obtained as above, (a) Dilute with lower alcohol, hydrous lower alcohol, polyhydric alcohol, hydrous polyhydric alcohol, etc., and use the obtained deodorizing liquid to generate a bad odor. Spray in place. (b) Add directly to food-related products and mix thoroughly. (c) Add directly to cosmetics. (d) Used as a deodorizing ingredient in deodorizers and deodorizers. (e) When deodorizing the bad odor of pharmaceuticals, etc., form the powder into granules or tablets using a conventional method and seal them separately in a package or storage container. (B) Or when using a deodorant powder, (a) As a refrigerator and moisture absorbent, mold it into an appropriate shape and use it alone or as part of coconut shell activated carbon. (b) Contain directly in sanitary products, shoe pads, and air conditioning products. (c) Add directly to the factory wastewater treatment tank. (d) It is blended as a component of a smoke agent used in smoking. (C) Usage examples of the deodorizing liquid and deodorant powder of the present invention are shown below, but the usage examples are not limited thereto. All percentages are by weight. Usage example 1 (Deodorizing spray) Ethanol 50% Dichlorodifluoromethane 48 Deodorant liquid of Example 5 2 100% Usage example 2 (PET deodorizing liquid) Ethanol 10% Fragrance 0.01 Deodorant liquid of Example 5 2 Water Residual 100.0% Usage example 3 (Candy) Sugar 50% Starch syrup 34 Organic acid 1 Flavor 0.2 Deodorant liquid of Example 5 0.5 Water Remaining 100.0% Usage example 4 (Drink) Sugar 12% Honey 1 Drink base 0.3 Flavor 0.1 Deodorant liquid of Example 5 1.0 Water Balance 100.0% Usage example 5 (tablet) Lactose 65 parts Dextrin 10 Talc 5 Deodorizing stock solution of Example 2 20 Water Appropriate amount 100 parts Usage example 6 (For refrigerated cars) Coconut shell activated carbon 70 % Deodorizing granules of Example 6 30 100% Usage example 7 (shoe padding) Activated carbon 80% Deodorant powder of Example 4 20 100% According to the inventor's research, the deodorizing effect of the present invention is The deodorizing effect is achieved through the combined effects of addition, neutralization reaction, and clathration of a large number of components including flavanols, flavonols, amino acids, organic acids, saccharides, and other polymeric compounds. As mentioned above, the deodorizing powder using residual activated carbon also has the adsorption effect of the original activated carbon. Next, the present invention will be explained with reference to Examples. Example 1 (Extraction of active ingredients) 100 g of dried tea leaf powder and 900 g of ethanol were placed in an extractor and refluxed for 4 hours. The raw material residue was removed from the extract and the liquid was concentrated to obtain 100 g of an extract solution containing 30% hot extract. Example 2 (Decolorization treatment of active ingredients) 35 g of the crude 30% extract solution obtained in Example 1, 30 g of ethanol, 40 g of purified water, and 15 g of activated carbon were added to a container, and after heating at 70 to 80 ° C. for 30 minutes, Stirring was continued for 30 minutes. After that, it was filtered by suction, the residue was washed with fresh ethanol, the residue was separated, and 5% of the active ingredient was removed.
A yellow transparent liquid (deodorizing stock solution) containing the following was obtained. A 1000 times alcoholic solution of this deodorizing stock solution shows maximum absorption at 275±2 mμ in the ultraviolet absorption spectrum. Example 3 The same operation as in Example 2 was carried out by adding 30 g of the crude 30% extract solution obtained in Example 1, 70 g of ethanol, and 12 g of activated carbon to a container to obtain a solution containing 6% of the active ingredient.
A yellow transparent liquid (deodorizing stock solution) containing the following was obtained. Example 4 The residue separated in Example 2 was dried to obtain 20 g of activated carbon powder (deodorant powder) containing about 5% of the crude extract as an active ingredient. Example 5 50 parts of the liquid (deodorizing stock solution) obtained in Example 2 was diluted with propylene glycol, glycerin, ethanol or a mixture thereof to obtain a liquid deodorant used for various purposes. Example 6 For 10 parts of the deodorant powder obtained in Example 4, 5 to 10 parts of a 10% aqueous ethanol solution of polyvinylpyrrolidone was added.
After kneading the mixture using a granulator, a granular deodorant was obtained by molding the mixture using a granulator. Example 7 (Test on deodorizing effect of the deodorant of the present invention) The deodorizing effect of the deodorant liquid obtained in Example 5 was measured. (1) Malodorous components (a) 30% trimethylamine aqueous solution (b) Benzyl mercaptan (2) Test method (a) Trimethylamine aqueous solution 36 mg (b) Place 12 mg of benzyl mercaptan in each container, add 1 g of deodorizing liquid, and seal the container. Mix well inside. Then, use a syringe to remove the air from each sealed container (a) and (b) and inject it into a gas chromatograph. A blank test was conducted in the same manner, and the removal rate was determined by setting the area value of the chromatograph as 100. (a) Trimethylamine removal rate: 80.3% (b) Benzyl mercaptan removal rate: 73.1% The measurement conditions for the gas chromatograph are as follows.

【表】【table】

【表】 実施例8 (本発明消臭粉末剤と従来の活性炭と
の消臭比較試験) 実施例4で得た消臭粉末剤を用いて、脱色行程
で使用する活性炭との消臭能力を比較した。 悪臭成分―アンモニア28%水溶液 試験方法 アンモニア(2g)、消臭粉末剤(5g)およ
び0.5N HCl10mlをそれぞれの一定容器に充填す
る。 各容器を接続して、100cm3/分の空気を送入し、
アンモニアガスを消臭粉末剤部に吸着させ、未吸
着のアンモニアガスを検出部である0.5N HCl試
液に吸収させる。 検出部のHClを指示薬としてメチルオレンジを
用いて0.5N NaOHで逆滴定を行ない、各時間ご
とのアンモニアの重量を算出した。 同様に活性炭(5g)を用いて試験を行なつ
た。除去率はブランクテストを100として求めた。 その結果を第1表に示した。
[Table] Example 8 (Comparative test on deodorizing the deodorizing powder of the present invention and conventional activated carbon) Using the deodorizing powder obtained in Example 4, the deodorizing ability of the activated carbon used in the decolorization process was evaluated. compared. Malodorous components - Ammonia 28% aqueous solution test method Fill ammonia (2 g), deodorizing powder (5 g) and 10 ml of 0.5N HCl into each container. Connect each container and introduce air at 100cm 3 /min.
Ammonia gas is adsorbed by the deodorizing powder part, and unadsorbed ammonia gas is absorbed by the 0.5N HCl test solution which is the detection part. Back titration was performed with 0.5N NaOH using HCl in the detection part as an indicator and methyl orange, and the weight of ammonia was calculated at each time point. A test was similarly conducted using activated carbon (5 g). The removal rate was determined by setting the blank test as 100. The results are shown in Table 1.

【表】 第1表の結果より、本発明の消臭粉末剤は従来
の活性炭素のみよりアンモニア除去率が著しく優
れていることを示す。
[Table] The results in Table 1 show that the deodorizing powder of the present invention is significantly superior in ammonia removal rate to conventional activated carbon alone.

Claims (1)

【特許請求の範囲】 1 ツバキ科又は/及びクスノキ科の植物の生葉
又は乾燥葉1部に対してエタノール4〜10部を使
用して2〜10時間熱抽出を行ない、その抽出物を
活性炭素、酸性白土又は珪藻土等を使用して脱色
処理を行ない、得られた液状部分の処理物を有効
成分として含有してなる消臭剤。 2 ツバキ科又は/及びクスノキ科の植物の生葉
又は乾燥葉1部に対してエタノール4〜10部を使
用して2〜10時間熱抽出を行ないその抽出物を活
性炭素、酸性白土又は珪藻土を使用して脱色処理
を行ない、処理物の液状部分を分離して得られた
残渣の活性炭素、酸性白土又は珪藻土よりなる消
臭剤。
[Scope of Claims] 1. Heat extraction is performed for 2 to 10 hours using 4 to 10 parts of ethanol to 1 part of fresh or dried leaves of plants of the Camellia family and/or Lauraceae family, and the extract is extracted with activated carbon. A deodorizing agent containing as an active ingredient a treated liquid portion obtained by decolorizing using acid clay, diatomaceous earth, or the like. 2 Heat extraction is performed for 2 to 10 hours using 4 to 10 parts of ethanol to 1 part of fresh or dried leaves of plants of the Camellia family and/or Lauraceae family, and the extract is extracted using activated carbon, acid clay, or diatomaceous earth. A deodorizer made of activated carbon, acid clay, or diatomaceous earth, which is the residue obtained by decolorizing the treated product and separating the liquid part.
JP58230895A 1983-12-06 1983-12-06 Deodorant Granted JPS60122566A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58230895A JPS60122566A (en) 1983-12-06 1983-12-06 Deodorant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58230895A JPS60122566A (en) 1983-12-06 1983-12-06 Deodorant

Publications (2)

Publication Number Publication Date
JPS60122566A JPS60122566A (en) 1985-07-01
JPH0124508B2 true JPH0124508B2 (en) 1989-05-11

Family

ID=16914977

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58230895A Granted JPS60122566A (en) 1983-12-06 1983-12-06 Deodorant

Country Status (1)

Country Link
JP (1) JPS60122566A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20190048159A (en) * 2017-10-30 2019-05-09 한국생산기술연구원 Decolorized gelite deodorant and method for producing the same

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63292963A (en) * 1987-05-26 1988-11-30 Teijin Ltd Deodorizing material
JPH0761353B2 (en) * 1987-09-08 1995-07-05 ライオン株式会社 Liquid deodorant composition
JPH01153377U (en) * 1988-04-11 1989-10-23
JP2006045461A (en) * 2004-08-09 2006-02-16 Tsubaki:Kk Cleanser

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57203445A (en) * 1981-06-11 1982-12-13 Lion Corp Production of deodorant substance

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57203445A (en) * 1981-06-11 1982-12-13 Lion Corp Production of deodorant substance

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20190048159A (en) * 2017-10-30 2019-05-09 한국생산기술연구원 Decolorized gelite deodorant and method for producing the same

Also Published As

Publication number Publication date
JPS60122566A (en) 1985-07-01

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