JPS6068859A - Aromatic composition - Google Patents

Aromatic composition

Info

Publication number
JPS6068859A
JPS6068859A JP58176475A JP17647583A JPS6068859A JP S6068859 A JPS6068859 A JP S6068859A JP 58176475 A JP58176475 A JP 58176475A JP 17647583 A JP17647583 A JP 17647583A JP S6068859 A JPS6068859 A JP S6068859A
Authority
JP
Japan
Prior art keywords
fragrance
water
cmc
volatilization
thermally crosslinked
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP58176475A
Other languages
Japanese (ja)
Other versions
JPH0252508B2 (en
Inventor
兼松 哲夫
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.)
Daicel Corp
Original Assignee
Daicel Chemical Industries 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 Daicel Chemical Industries Ltd filed Critical Daicel Chemical Industries Ltd
Priority to JP58176475A priority Critical patent/JPS6068859A/en
Publication of JPS6068859A publication Critical patent/JPS6068859A/en
Publication of JPH0252508B2 publication Critical patent/JPH0252508B2/ja
Granted legal-status Critical Current

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  • Cosmetics (AREA)
  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
  • Fats And Perfumes (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は室内用芳香剤組成物に関するものである。詳し
くは、長期間にわたり均一な芳香を発散でき、かつ使用
終期に未揮散の香料を残存しないペースト状芳香剤に関
するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to room fragrance compositions. Specifically, the present invention relates to a paste-like fragrance that can emit a uniform fragrance over a long period of time and does not leave any unvolatilized fragrance at the end of use.

従来市販されている芳香剤は、大別すると固形タイプ、
溶液タイプおよびスプレータイプの3種がある。固形タ
イプの芳香剤は、パラクロルベンゾールなどの昇華性固
体を除くと、多くの場合カラギーナンや寒天などのゲル
化剤を用いて固形化されている(特開昭49−1204
6、特開昭5l−98337)。そして、このタイプの
芳香剤中の香料の揮散速度は、使用初期には太きいが、
ゲル強度が大きいため使用後期になると固形物がかなり
残存していても、香料がゲル内部に固(内包されている
ため、香料の揮散が非常に減少するか、もしくは全く揮
散しなくなり残存する欠点があった。
Traditionally, commercially available air fresheners can be roughly divided into solid types;
There are three types: solution type and spray type. Solid type fragrances, excluding sublimable solids such as parachlorobenzole, are often solidified using gelling agents such as carrageenan and agar (Japanese Patent Application Laid-Open No. 1204-1989).
6, Japanese Patent Publication No. 51-98337). The rate of volatilization of the fragrance in this type of fragrance is fast at the beginning of use, but
Due to the high gel strength, even if a considerable amount of solid matter remains in the later stages of use, the fragrance is solidified (encapsulated) inside the gel, so the volatilization of the fragrance is greatly reduced, or it does not volatilize at all and remains. was there.

一方、溶液タイプの芳香剤の場合には、低粘度の溶液で
あるため、使用中に液がこぼれるという欠点があり、こ
れを防ぐため香料の揮散口を非常に小さく調整したり、
多孔性の素材で栓をする形で香料蒸気のみを発散させる
などの工夫を必要とする。また、溶液タイプの芳香剤に
ザンサンガムなどの増粘剤を添加して、高粘度溶液とす
る工夫もなされているが、芳香の持続性を維持するため
にしばしば容器を振盪または芳香剤を攪拌する必要があ
り、実用上不便なものである(特公昭56−33104
)。
On the other hand, in the case of solution-type fragrances, since they are low-viscosity solutions, they have the disadvantage that the liquid spills during use.
It is necessary to devise measures such as capping with porous material to allow only the fragrance vapor to escape. In addition, attempts have been made to add thickeners such as xanthan gum to solution-type fragrances to create a highly viscous solution, but in order to maintain the persistence of the fragrance, the container is often shaken or the fragrance is stirred. It is necessary and practically inconvenient (Special Publication No. 56-33104)
).

また、スプレータイプの芳香剤は、特別な合冊と特別の
製造設備を必要とし、使用面からもその都度手をかけね
ばならないという大きな欠点を有していた。
In addition, spray-type air fresheners require a special set of books and special manufacturing equipment, and have a major disadvantage in that they must be handled each time they are used.

そこで本発明は、これらの各種タイプの室内用芳香剤の
欠点を解消し、香料本来の香りを変化させることなく、
香料の揮散速度を長期間にわたりi定なものとし、かつ
使用終期においては未揮散の香料を残存しない芳香剤を
得るべく検討した結果、本発明に到達したものである。
Therefore, the present invention eliminates the drawbacks of these various types of indoor air fresheners, and without changing the original scent of the fragrance.
The present invention was achieved as a result of studies aimed at obtaining a fragrance that maintains a constant volatilization rate over a long period of time and does not leave any unvolatilized fragrance at the end of use.

すなわち、本発明は、水と香料を主成分とする芳香剤に
、熱架橋カルボキシメチルセルロースアルカリ金属塩よ
りなる吸収性素材を添加することを特徴とするペースト
状の室内用芳香剤組成物である0本発明に使用する吸収
性素材の熱架橋カルボキシメチルセルロースアルカリ金
属塩(熱架橋CMC)はl特開昭56−28755、特
開昭58−104901に記載されたような公知の方法
で製造することができる0すなわち、遊離カルボン酸基
とカルボン酸アルカリ金属塩の共存する部分酸型カルボ
キシメチルセルロースを80〜200℃に加熱して架橋
させたものである。この熱架橋CMCの特徴は、高吸収
水性及び高保水性にあり、その能力は純水ならば自重の
数百倍、食塩などの塩を含む水でも数十倍の量を吸収し
、かつ加圧下においても保水できる吸収性累月である。
That is, the present invention is a paste-like indoor air freshener composition characterized in that an absorbent material made of a thermally crosslinked carboxymethyl cellulose alkali metal salt is added to an air freshener whose main components are water and fragrance. The thermally crosslinked carboxymethyl cellulose alkali metal salt (thermally crosslinked CMC) of the absorbent material used in the present invention can be produced by a known method as described in JP-A-56-28755 and JP-A-58-104901. In other words, partially acid type carboxymethylcellulose in which free carboxylic acid groups and alkali metal carboxylic acid salts coexist is heated to 80 to 200°C to crosslink it. The characteristics of this thermally crosslinked CMC are its high water absorption and high water retention properties, and its ability to absorb hundreds of times its own weight in pure water and tens of times its own weight in water containing salt such as table salt, and under pressure. It is an absorbent material that can retain water even in the middle of the day.

本発明に使用する熱架橋CMCの形状は、粉末状、頌粒
状、lPj、繊維状のいずれでもよく、その添加量は架
橋CMCの重合度および架橋度によって変化するが、芳
香剤中の0.3〜15重′I+IL%であり、好ましく
は1〜5%の範囲がよい。
The shape of the thermally crosslinked CMC used in the present invention may be powder, granule, lPj, or fibrous, and the amount added varies depending on the degree of polymerization and crosslinking of the crosslinked CMC, but the amount of the thermally crosslinked CMC used in the fragrance may vary depending on the degree of polymerization and crosslinking of the crosslinked CMC. The range is 3 to 15 F'I+IL%, preferably 1 to 5%.

本発明に使用する香料は特に限定されるものではなく、
居間用、台所用、会議室用、応接室用、食堂用、待合室
用、トイレ用など使用場所に応じて香水系、柑橘系、果
実系その他各種のものを使用することができる。また、
親油性の香料の場合、水中に均一に分散させるために必
要に応じて界面活性剤を添加してもよく、このほか必要
ならば、香料の溶解および分散剤としての低級アルコー
ルや着色剤、殺菌剤、凍結防止剤などを添加配合しても
よい。
The fragrance used in the present invention is not particularly limited,
Perfume-based, citrus-based, fruit-based, and other types of products can be used depending on the location of use, such as living room, kitchen, conference room, reception room, dining room, waiting room, and toilet. Also,
In the case of lipophilic fragrances, surfactants may be added as necessary to ensure uniform dispersion in water, and if necessary, lower alcohols, coloring agents, and sterilizers may be used as fragrance dissolving and dispersing agents. Agents, antifreeze agents, etc. may be added and blended.

本発明の特徴である熱架橋CMCの添加が、芳香剤に良
好な揮散特性を与える理由は次のように考えられる。す
なわち、部分酸型化されたカルボキシメチルセルロース
アルカリ金M塩(CMC)のJ 1%ftカルボン酸基
と近傍のCMC分子中の未反応水酸基が高温加熱処理に
よって脱水されて生成するエステ/l/型架橋部分は水
に不溶であるため、本発明のペースト状芳香剤itミク
ロ的に見ると水不溶性のエステル架橋結合で交差された
ゆるい網目構造を有していることになる。従って、この
芳香剤の使用初期および中期においてはCMCの強い親
水性および浸透圧効果による保水性によって水および香
料の揮散速度が適度に抑制され、更に使用後期において
は、他の水溶性高分子の場合と異なり、熱架橋CMCが
水不溶性の架橋結合からなるゆるい網目構造であるため
、多孔性の被膜構造を形成し、内部に残存する香料や水
の揮散を阻害しないため、 一定の揮散速度を示すもの
である。また、本発明の特徴の一つである香料本来の香
りが変化しない理由としては、熱架橋CMC自体が各種
香料と何ら特異な反応を起こさないこと>、bA末署力
−カロ執肋Lし■のみ11ネ、 リ −列士峡姶… シ
 1−イの第三物質を全く添加していないためである。
The reason why the addition of thermally crosslinked CMC, which is a feature of the present invention, gives the fragrance good volatilization properties is considered as follows. That is, the J1%ft carboxylic acid group of partially acidified carboxymethyl cellulose alkali gold M salt (CMC) and the unreacted hydroxyl group in the nearby CMC molecules are dehydrated by high temperature heat treatment to form an ester/l/type. Since the crosslinked portion is insoluble in water, microscopically, the pasty fragrance of the present invention has a loose network structure intersected by water-insoluble ester crosslinks. Therefore, in the early and middle stages of use of this fragrance, the volatilization rate of water and fragrance is moderately suppressed due to the strong hydrophilicity and water retention properties of CMC due to the osmotic pressure effect, and furthermore, in the later stages of use, the rate of volatilization of water and fragrance is moderately suppressed. Unlike other cases, thermally crosslinked CMC has a loose network structure consisting of water-insoluble crosslinks, so it forms a porous film structure and does not inhibit the volatilization of the fragrance and water remaining inside, so it maintains a constant volatilization rate. It shows. In addition, the reason why the original scent of the fragrance, which is one of the features of the present invention, does not change is that the thermally crosslinked CMC itself does not cause any peculiar reaction with various fragrances. This is because the third substance of (1) and (1) is not added at all.

以下実施例にて説明する。This will be explained below using examples.

実施例1〜3および比較例1 水100.li’に香料(香水系)iog、界面活性剤
0.31を加え、これに熱架橋CMCを1g(実施例1
)、3g(実施例2)、6.?(実施例a)加t”C1
各々をホモミキサーで攪拌した。
Examples 1 to 3 and Comparative Example 1 Water 100. Add fragrance (perfume type) iog and 0.31 surfactant to li', and add 1 g of thermally crosslinked CMC (Example 1).
), 3g (Example 2), 6. ? (Example a) Addition t"C1
Each was stirred with a homomixer.

その後各々を精秤した容器(開口面積32 cA )に
入れ再秤量したのち、約1カ月間開封したまま静置し、
香料および水分の揮故による重量変化を測定するととも
に5芳香の有無を確認した0熱架橋CMCを添加しない
ものについても同じ試験を比較のために行った。(比較
例1)これら芳香剤のM量変化(調合直後の芳香剤全重
量に対する5日間当りの揮散比率に))を下表に示した
After that, each was placed in a precisely weighed container (opening area: 32 cA), reweighed, and left unsealed for about a month.
For comparison purposes, the same test was conducted on samples without the addition of heat-crosslinked CMC, in which weight changes due to volatilization of fragrance and water were measured, and the presence or absence of 5 fragrances was confirmed. (Comparative Example 1) Changes in the amount of M (volatilization ratio per 5 days relative to the total weight of the fragrance immediately after preparation) of these fragrances are shown in the table below.

上表のごとく高吸収性熱架橋CMCの添加によって、香
料および水の揮散速度を大幅に抑制でき30〜40日間
有効な芳香を発することを確認した。なお、テスト後の
残留物の状況は実施例1〜3とも、容器す1(に密着し
たJi常に薄い被膜状の熱架橋CMCであり、香料は全
(残存していなかった0 比較例2および3゜ 比較のため、実施例2の処方で熱架橋CMCの代りにカ
ラギーナン(比較例2)、寒天(比較例3)を使い、加
熱溶解後冷却してつくったゲル状芳香剤について、同様
の揮散テストを行なった。
As shown in the table above, it was confirmed that by adding highly absorbent thermally crosslinked CMC, the volatilization rate of fragrance and water could be significantly suppressed, and an effective fragrance could be emitted for 30 to 40 days. In addition, the situation of the residue after the test was that in both Examples 1 to 3, there was always a thin film of thermally crosslinked CMC that adhered to the container (S1), and the fragrance was completely (no residue remained in Comparative Example 2 and 3゜For comparison, we used carrageenan (Comparative Example 2) and agar (Comparative Example 3) in place of thermally cross-linked CMC in the formulation of Example 2, and prepared gel-like fragrances by dissolving them by heating and then cooling them. I did a volatilization test.

その結果、40日後の残留量(重量%)が、カラギーナ
ンの場合で6%、寒天の場合でsXであり、これらの残
留物は共に香料を内包した硬い塊り状になっており、香
料の発散はほとんど感じられなかった。
As a result, the residual amount (wt%) after 40 days was 6% in the case of carrageenan and sX in the case of agar, and both of these residues were in the form of a hard lump containing the flavoring agent, and the amount of the remaining amount was 6% in the case of carrageenan and sX in the case of agar. I could hardly feel any divergence.

特許出願人 ダイセル化学工業株式会社patent applicant Daicel Chemical Industries, Ltd.

Claims (1)

【特許請求の範囲】[Claims] 水と香料を主成分とする芳香剤に熱架橋カルボキシメチ
ルセルロースアルカリ金属塩よりなる吸収性素材を添加
することを特徴とする芳香剤組成物。
A fragrance composition characterized by adding an absorbent material made of a thermally crosslinked carboxymethylcellulose alkali metal salt to a fragrance whose main components are water and fragrance.
JP58176475A 1983-09-26 1983-09-26 Aromatic composition Granted JPS6068859A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58176475A JPS6068859A (en) 1983-09-26 1983-09-26 Aromatic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58176475A JPS6068859A (en) 1983-09-26 1983-09-26 Aromatic composition

Publications (2)

Publication Number Publication Date
JPS6068859A true JPS6068859A (en) 1985-04-19
JPH0252508B2 JPH0252508B2 (en) 1990-11-13

Family

ID=16014317

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58176475A Granted JPS6068859A (en) 1983-09-26 1983-09-26 Aromatic composition

Country Status (1)

Country Link
JP (1) JPS6068859A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63109741A (en) * 1986-06-24 1988-05-14 Daicel Chem Ind Ltd Feed for raising fish

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5715901A (en) * 1980-05-14 1982-01-27 Yankuzatsuku Ierujii Saw device

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5715901A (en) * 1980-05-14 1982-01-27 Yankuzatsuku Ierujii Saw device

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63109741A (en) * 1986-06-24 1988-05-14 Daicel Chem Ind Ltd Feed for raising fish
JPH0685694B2 (en) * 1986-06-24 1994-11-02 ダイセル化学工業株式会社 Fish feed

Also Published As

Publication number Publication date
JPH0252508B2 (en) 1990-11-13

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