JPH02239865A - Production of deodorizer - Google Patents
Production of deodorizerInfo
- Publication number
- JPH02239865A JPH02239865A JP1061232A JP6123289A JPH02239865A JP H02239865 A JPH02239865 A JP H02239865A JP 1061232 A JP1061232 A JP 1061232A JP 6123289 A JP6123289 A JP 6123289A JP H02239865 A JPH02239865 A JP H02239865A
- Authority
- JP
- Japan
- Prior art keywords
- extraction
- solvent
- polar solvent
- executed
- subjected
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 241001092080 Hydrangea Species 0.000 claims abstract description 13
- 239000000284 extract Substances 0.000 claims abstract description 9
- 239000002798 polar solvent Substances 0.000 claims abstract description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 241000220151 Saxifragaceae Species 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims abstract description 5
- 239000002781 deodorant agent Substances 0.000 claims description 22
- 235000014486 Hydrangea macrophylla Nutrition 0.000 claims description 12
- 241000196324 Embryophyta Species 0.000 claims description 10
- 241001647091 Saxifraga granulata Species 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims 1
- 230000001877 deodorizing effect Effects 0.000 abstract description 17
- 238000000605 extraction Methods 0.000 abstract description 16
- 239000007788 liquid Substances 0.000 abstract description 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract description 9
- 239000002904 solvent Substances 0.000 abstract description 9
- 238000000034 method Methods 0.000 abstract description 8
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 abstract description 8
- 239000000843 powder Substances 0.000 abstract description 5
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 abstract description 4
- 229910021529 ammonia Inorganic materials 0.000 abstract description 4
- 239000002994 raw material Substances 0.000 abstract description 4
- 239000000706 filtrate Substances 0.000 abstract description 3
- 150000002576 ketones Chemical class 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract 3
- 238000004332 deodorization Methods 0.000 abstract 1
- 238000010298 pulverizing process Methods 0.000 abstract 1
- 230000008719 thickening Effects 0.000 abstract 1
- 235000019645 odor Nutrition 0.000 description 11
- 238000001179 sorption measurement Methods 0.000 description 9
- 239000007787 solid Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- 230000000873 masking effect Effects 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000000419 plant extract Substances 0.000 description 2
- 238000000967 suction filtration Methods 0.000 description 2
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- 241000272814 Anser sp. Species 0.000 description 1
- 240000001548 Camellia japonica Species 0.000 description 1
- 241000218641 Pinaceae Species 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000206609 Porphyra Species 0.000 description 1
- 244000171263 Ribes grossularia Species 0.000 description 1
- 235000002357 Ribes grossularia Nutrition 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012496 blank sample Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229930002875 chlorophyll Natural products 0.000 description 1
- 235000019804 chlorophyll Nutrition 0.000 description 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
- 235000018597 common camellia Nutrition 0.000 description 1
- 230000009918 complex formation Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
Landscapes
- Medicines Containing Plant Substances (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、植物抽出成分より得られる消臭剤の製造方法
に関するものである。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a method for producing a deodorant obtained from plant extract components.
く従来技術〉
今日、悪臭事象は極めて複雑であり、その発生源は工場
、飲食店、汚水処理場から、家庭内にいたっては、冷蔵
庫、便所、また車内など、実に様々である。発生する臭
気も微量成分が多種混合されて悪臭となっている場合が
ほとんどである。従来、異臭・悪臭除去の手法としては
臭気成分を多孔質表面へ物理吸着させて除去する方法、
これらを化学的結合による吸着や反応により除去する方
法、悪臭成分よりも強い芳香をもつものにより、悪臭を
怒しさせなくする方法などが知られている。Prior Art Today, bad odor events are extremely complex and come from a wide variety of sources, from factories, restaurants, and sewage treatment plants to homes such as refrigerators, toilets, and even cars. In most cases, the odor generated is a mixture of various trace components. Conventionally, methods for removing foreign odors and malodors include methods of physically adsorbing odor components onto porous surfaces and removing them;
Methods of removing these substances through adsorption or reaction through chemical bonds, and methods of using substances with a stronger aroma than the malodorous components to make the malodor less intense are known.
しかしながら、物理吸着による方法では、吸着剤自身が
短時間のうちに飽和状態に達してしまうという欠点があ
り、化学吸着による方法では、悪臭物質に対する選択性
が大きく、複合臭気よりなる実際の悪臭事象には適さな
いという欠点がある。However, methods using physical adsorption have the disadvantage that the adsorbent itself reaches a saturated state in a short period of time, while methods using chemical adsorption have a high selectivity for malodorous substances and are used in actual malodor events consisting of complex odors. The disadvantage is that it is not suitable for
マスキングによる方法は悪臭事象を覆い隠す芳香成分が
、必ずしも使用者の嗜好に合わなかったり、マスキング
剤の臭気が強ければ、かえって不快の原因になるという
欠点がある。The masking method has the disadvantage that the aromatic component that masks the malodor event does not necessarily suit the taste of the user, or that if the masking agent has a strong odor, it may even cause discomfort.
〈発明が解決しようとする課題〉
本発明は、上述の問題点を解決すべく発明されたもので
あり、消臭成分自身の臭気は弱く、かつ種々の有臭物質
に対して効果を有し、特にアンモニア、トリメチルアミ
ン、メチルメルカブタンに対して著しい効果を有する消
臭剤を提供せんとするものである。<Problems to be Solved by the Invention> The present invention was invented to solve the above-mentioned problems, and the deodorant component itself has a weak odor and is effective against various odorous substances. The object of the present invention is to provide a deodorant that is particularly effective against ammonia, trimethylamine, and methylmercabutane.
く課題を解決するための手段〉
すなわち、本発明はユキノシタ科植物、詳しくはアジサ
イ属植物の葉または花びらの生物もしくは乾燥物を、極
性溶媒を用いて抽出を行い、得られた抽出物を有効成分
とする消臭剤の製造方法である。Means for Solving the Problems> That is, the present invention extracts living organisms or dried products of leaves or petals of plants of the family Saxifrage family, specifically plants of the genus Hydrangea, using a polar solvent, and effectively uses the obtained extract. This is a method for producing a deodorant as an ingredient.
極性溶媒としては、水、低級アルコール、ケトン類等の
親水性溶媒があげられるが、望ましくは極性溶媒が混合
物であって、例えば、水とエタノールを1:4で混合し
た溶媒を用いて抽出を施す。Examples of polar solvents include hydrophilic solvents such as water, lower alcohols, and ketones. Preferably, the polar solvents are a mixture. For example, extraction may be performed using a mixture of water and ethanol at a ratio of 1:4. give
必要に応じて、該抽出液を遠心分離器にかけて不溶分を
除去し、かつ溶媒も除去して有効消臭成分を得る消臭剤
の製造方法である。If necessary, the extract is centrifuged to remove insoluble matter and the solvent is also removed to obtain an effective deodorizing component.
ここで言うユキノシタ科の植物としては、ユキノシタ属
、アラシグサ属、ネコノメソウ属、ウツギ属、スグリ属
、アジサイ属等がある。この中で比較的入手しやすいア
ジザイ属の種名をあげると、アジサイ、コアジサイ、ガ
クアジサイ、ベニガク、ヤマアジサイ、タマアジサイ等
がある。The plants of the Saxifrage family mentioned here include the genus Saxifrage, the genus Arachigusa, the genus Porphyra, the genus Deutschia, the genus Gooseberry, and the genus Hydrangea. Among them, species of the genus hydrangea that are relatively easy to obtain include hydrangea, little hydrangea, hydrangea, rosy hydrangea, mountain hydrangea, and red hydrangea.
該消臭物質を得る方法としては、上記原料を60゜Cに
設定したオーブン中で水分を除去、乾燥させた後、ミキ
サーを用いてこれをパウダー化する。The deodorizing substance is obtained by removing moisture from the raw material in an oven set at 60°C, drying it, and then powdering it using a mixer.
このパウダー1gに対しておよそ20m2の割合で上記
溶媒を加え、60゜Cにて1時間温抽出ののち、15〜
24時間の室温抽出を施す。ろ過し、残渣にさらに同様
の溶媒を加えて60゜C、1時間の温抽出ののちに分離
ろ過し、ろ液を先に分離した抽出液と合わせてロータリ
ーエバボレーター等により濃縮作業を行なう。濃縮液を
遠心分離器にかけて固型物と溶解分とを分離ののち、溶
解分のみをメスフラスコにて、水を用いて一定濃度に希
釈ののち消臭液が得られる。さらにこの消臭液を減圧下
において乾燥させて消臭固型物を得、これを実際の消臭
に供する。The above solvent was added at a ratio of approximately 20 m2 to 1 g of this powder, and after hot extraction at 60°C for 1 hour,
Perform a 24 hour room temperature extraction. After filtration, the same solvent is further added to the residue, followed by hot extraction at 60°C for 1 hour, followed by separate filtration, and the filtrate is combined with the previously separated extract and concentrated using a rotary evaporator or the like. After the concentrated solution is centrifuged to separate solids and dissolved components, only the dissolved components are diluted with water to a constant concentration in a volumetric flask to obtain a deodorizing solution. Further, this deodorizing liquid is dried under reduced pressure to obtain a solid deodorizing product, which is used for actual deodorizing.
〈作用〉
この固型物はそれ自身の臭気は極めて少ないため、従来
のマスキング剤の用に不快感をもたらすことがなく、か
つ種々の悪臭の除去に効果を有し、とくにアンモニア、
1−リメチルアミン、メチルメルカブタンに対してその
効果が優れている。また、この原料も安価にかつ容易に
入手可能であり、消臭成分を得る操作も簡単である。消
臭作用機構としては、植物抽出成分の多成分混成系中の
ポリフェノール類、アミノ酸類、クロロフィル等との中
和、分解、酸化還元、錯形成、包接作用等が複合的に行
われると推定されている。以下に実施例を挙げてさらに
詳しく本発明を説明する。<Effect> This solid substance itself has very little odor, so it does not cause discomfort when used with conventional masking agents, and is effective in removing various bad odors, especially ammonia,
Its effect is superior to 1-limethylamine and methylmercabutane. Moreover, this raw material is also easily available at low cost, and the operation for obtaining the deodorizing component is simple. It is estimated that the deodorizing mechanism is a complex combination of neutralization, decomposition, redox, complex formation, and clathration with polyphenols, amino acids, chlorophyll, etc. in a multi-component hybrid system of plant extract components. has been done. The present invention will be explained in more detail with reference to Examples below.
〈実施例1〉
アジサイの乾燥葉粉末6gと水:エタノールー1:4で
ある混合溶媒150威とを三角フラスコに入れ60゜C
で1時間湯浴ののち、室温にて15時間の抽出を行った
。吸引ろ過により抽出液を分離し、残渣には再び150
雁の同じ溶媒を加え60゜Cで1時間再抽出を行った。<Example 1> 6 g of dried hydrangea leaf powder and 150 g of a mixed solvent of water:ethanol-1:4 were placed in an Erlenmeyer flask and heated at 60°C.
After a 1-hour hot water bath, extraction was performed at room temperature for 15 hours. The extract was separated by suction filtration, and the residue was again
The same solvent as used for wild goose was added and re-extraction was carried out at 60°C for 1 hour.
吸引ろ過してろ液を先の抽出液と合わせて、ロータリー
エハボレーターを用いて濃縮ののち遠心分離器にかけて
固型物の分離を行い、液体分をメスフラスコにて、10
0mRに水で希釈し消臭液とした。このうち5 mlを
減圧下にて乾燥し固体消臭剤約58mgを得た。After suction filtration, the filtrate was combined with the previous extract, concentrated using a rotary evaporator, then centrifuged to separate the solids, and the liquid was collected in a volumetric flask for 10
It was diluted with water to 0 mR to obtain a deodorizing solution. 5 ml of this was dried under reduced pressure to obtain about 58 mg of solid deodorant.
く実施例2〉
アジサイの花びらの乾燥物の粉末2gを実施例1と同様
の操作を行い100成の消臭液を得た。このうち5成を
減圧下にて乾燥し固体消臭剤約37mgを得た。Example 2 2 g of dried hydrangea petal powder was treated in the same manner as in Example 1 to obtain a 100% deodorizing liquid. Of these, five components were dried under reduced pressure to obtain about 37 mg of solid deodorant.
〈実施例3〉
実施例1及び2で得た消臭液についてアンモニアの消臭
効果を測定した。<Example 3> The deodorizing effect of ammonia on the deodorant liquids obtained in Examples 1 and 2 was measured.
試験方法
消臭液5dを乾燥、固型化した消臭固型物と、アンモニ
アガス約2gを160mlの容量のガラスビンに入れて
密栓した。ブランクとして固型消臭剤を入れないサンプ
ルも用意した。これを20゜Cに設定した恒温槽内で保
存し、処理5時間後、各ビン中に残存するガス量をガス
クロマトグラフを用いて測定し、消臭剤を入れたビン中
のガスの減量(a)と、ブランクのビン中のガスの減量
、すなわちガラス器壁に吸着された量(b)とを求め、
a−bより消臭剤自身により消臭されたガスの量を算出
した。Test method A solid deodorizing product obtained by drying and solidifying 5d of deodorizing liquid and about 2 g of ammonia gas were placed in a 160 ml glass bottle and the bottle was tightly stoppered. A blank sample without solid deodorant was also prepared. This was stored in a thermostat set at 20°C, and after 5 hours of treatment, the amount of gas remaining in each bottle was measured using a gas chromatograph, and the amount of gas in the bottle containing the deodorant was measured ( Determine a) and the loss of gas in the blank bottle, i.e. the amount adsorbed on the glassware wall (b),
The amount of gas deodorized by the deodorant itself was calculated from a-b.
この計算結果から、乾燥物1gあたりに換算した消臭剤
のガス吸着量を求めて第1図に示した。ここでは比較の
ため同様の抽出方法により得た他の植物成分のガス吸着
量も載せた。From this calculation result, the amount of gas adsorption of the deodorant calculated per 1 g of dry matter was determined and shown in FIG. For comparison, the gas adsorption amounts of other plant components obtained using the same extraction method are also listed.
〈実施例4〉
実施例1及び2で得た消臭液についてトリメチルアミン
の消臭効果を測定した。<Example 4> The deodorizing effect of trimethylamine on the deodorant liquids obtained in Examples 1 and 2 was measured.
試験方法
トリメチルアミンガス約2gを用いて、実施例1と同様
の処理、測定を行った。結果も同様に計算し、乾燥物1
gあたりに換算した消臭剤のガス吸着量を第2図に示し
た。比較のため同様の抽出方法により得た他の植物成分
のガス吸着量も載せた。Test method The same treatments and measurements as in Example 1 were carried out using about 2 g of trimethylamine gas. Calculate the results in the same way, dry matter 1
Figure 2 shows the gas adsorption amount of the deodorant in terms of units per gram. For comparison, the gas adsorption amounts of other plant components obtained using the same extraction method are also listed.
〈実施例5〉
実施例2で得た消臭液についてメチルメルカブタンの消
臭効果を測定した。<Example 5> Regarding the deodorizing liquid obtained in Example 2, the deodorizing effect of methyl mercabutane was measured.
試験方法
メチルメルカプタンガス約2gを用いて実施例1と同様
の処理、測定を行った。結果も同様に計算し、乾燥物1
gあたりに換算した消臭剤のガス吸着量を第3図に示し
た。比較のため同様の抽出方法により得た他の植物成分
のガス吸着量も載せた。Test method The same treatment and measurement as in Example 1 were carried out using about 2 g of methyl mercaptan gas. Calculate the results in the same way, dry matter 1
Figure 3 shows the gas adsorption amount of the deodorant in terms of grams. For comparison, the gas adsorption amounts of other plant components obtained using the same extraction method are also listed.
〈発明の効果〉
以上のように、本発明により得られる消臭剤は原料の入
手が安価でかつ容易であり、製法も簡単なうえ、その効
果も大きい。消臭剤自身が極めて低臭であるため、不快
感を与えることなく様々な分野でその効果を発揮しうる
ちのである。また、これまで植物成分を利用した消臭剤
、例えばツバキ科、マツ科などの植物からの抽出物を利
用したものに関する発明があったが、それらの効果を上
まわることが図面のグラフ図よりわかり、極めて効果の
高い有効かつ実用的な消臭剤といえる。<Effects of the Invention> As described above, the deodorant obtained by the present invention has raw materials that are inexpensive and easy to obtain, a manufacturing method that is simple, and is highly effective. Since the deodorant itself has an extremely low odor, it can be effective in a variety of fields without causing discomfort. In addition, there have been inventions of deodorants that use plant ingredients, such as those that use extracts from plants such as Camellia and Pinaceae, but it is clear from the graphs in the drawings that their effects are superior to those of other deodorants. Understandably, it can be said to be an extremely effective and practical deodorant.
第1図から第3図までは、測定開始5時間後に、乾燥物
1gあたりに吸着された臭気ガスψ量を棒グラフで示す
グラフ図である。
特 許 出 願 人
凸版印刷株式会社
代表者 鈴木和夫1 to 3 are bar graphs showing the amount of odor gas ψ adsorbed per gram of dry matter 5 hours after the start of measurement. Patent application: Kazuo Suzuki, Representative of Toppan Printing Co., Ltd.
Claims (3)
は乾燥物を、極性溶媒を用いて抽出を行い、得られた抽
出物を有効成分とする消臭剤の製造方法。(1) A method for producing a deodorant using a polar solvent to extract living organisms or dried leaves or petals of a plant of the Saxifrage family, and using the obtained extract as an active ingredient.
(1)記載の消臭剤の製造方法。(2) The method for producing a deodorant according to claim (1), wherein the plant of the family Saxifrage is of the genus Hydrangea.
1:4である請求項(1)記載の消臭剤の製造方法。(3) The polar solvent is a mixture, water:ethanol=
The method for producing a deodorant according to claim (1), wherein the ratio is 1:4.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1061232A JPH0744949B2 (en) | 1989-03-14 | 1989-03-14 | Deodorants |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1061232A JPH0744949B2 (en) | 1989-03-14 | 1989-03-14 | Deodorants |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02239865A true JPH02239865A (en) | 1990-09-21 |
JPH0744949B2 JPH0744949B2 (en) | 1995-05-17 |
Family
ID=13165271
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1061232A Expired - Fee Related JPH0744949B2 (en) | 1989-03-14 | 1989-03-14 | Deodorants |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0744949B2 (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60174153A (en) * | 1984-02-20 | 1985-09-07 | 松下電工株式会社 | Deodorant |
JPS60261458A (en) * | 1984-06-08 | 1985-12-24 | 松下電工株式会社 | Production of deodorant |
JPS63309269A (en) * | 1987-06-12 | 1988-12-16 | Lion Corp | Deodorant |
-
1989
- 1989-03-14 JP JP1061232A patent/JPH0744949B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60174153A (en) * | 1984-02-20 | 1985-09-07 | 松下電工株式会社 | Deodorant |
JPS60261458A (en) * | 1984-06-08 | 1985-12-24 | 松下電工株式会社 | Production of deodorant |
JPS63309269A (en) * | 1987-06-12 | 1988-12-16 | Lion Corp | Deodorant |
Also Published As
Publication number | Publication date |
---|---|
JPH0744949B2 (en) | 1995-05-17 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |