JP2007275343A - Aromatic substance - Google Patents

Aromatic substance Download PDF

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JP2007275343A
JP2007275343A JP2006106340A JP2006106340A JP2007275343A JP 2007275343 A JP2007275343 A JP 2007275343A JP 2006106340 A JP2006106340 A JP 2006106340A JP 2006106340 A JP2006106340 A JP 2006106340A JP 2007275343 A JP2007275343 A JP 2007275343A
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fragrance
shape
aqueous gel
hemispherical
present
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Shozo Endo
昭三 遠藤
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KAMIOKA SEIMITSU KAGAKU KK
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KAMIOKA SEIMITSU KAGAKU KK
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Abstract

<P>PROBLEM TO BE SOLVED: To provide an aromatic substance in an aqueous gel shape excellent in the sustained-release of a volatile substance such as perfume. <P>SOLUTION: The aromatic substance comprises aqueous gel containing gelatin, a cross linking agent and the perfume, and the aromatic substance is characterized in that the aqueous gel has a hemispherical or spherical shape, and the bloom strength of the aqueous gel is ≥15 when it has the hemispherical shape and is ≥13 when it has the spherical shape. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、新規の芳香剤、特に香料等の揮発物質の徐放性に優れた水性ゲル状の芳香剤に関する。   The present invention relates to a novel fragrance, particularly an aqueous gel fragrance excellent in sustained release of volatile substances such as fragrances.

香料や消臭成分、防虫成分等の揮発物質を含有する水性ゲルは、室内やトイレ等に使用される芳香剤や防虫剤として広く使用されている。
こうした水性ゲルからなる芳香剤や防虫剤は、ゲルが大気と直接接触するように配置すると、配合した香料等の揮発物質が大気中に揮散して芳香剤や防虫剤等としての機能を発揮し、また、視覚装飾としての機能も発揮する。
Aqueous gels containing volatile substances such as fragrances, deodorant ingredients and insect repellent ingredients are widely used as fragrances and insect repellents used in rooms and toilets.
When these fragrances and insect repellents composed of aqueous gels are placed so that the gel is in direct contact with the atmosphere, the volatile substances such as blended fragrances will volatilize into the atmosphere and function as a fragrance or insect repellent. In addition, it also functions as a visual decoration.

上記に示す従来の水性ゲルはアルギン酸等の多糖類をゲル基剤として用いたもの、あるいはゲルの透明性の観点からゼラチンをゲル基剤として用いたもの、さらに形状保持性を考慮してゼラチンにゲル化剤(架橋剤)を反応させてゼラチン水性架橋ゲルと為したものなど、様々なものが提案されている。
後者の例として、たとえば、エチレン性不飽和化合物−無水マレイン酸共重合体とゼラチンとの反応生成物からなる水性ゲル(特許文献1)、エチレン性不飽和化合物−無水マレイン酸共重合体のアンモニア反応物とゼラチンとの反応生成物からなる水性ゲル(特許文献2)などが提案されている。
特開平1−297484号 特開2000−192011号
The conventional aqueous gels shown above are those using polysaccharides such as alginic acid as a gel base, those using gelatin as a gel base from the viewpoint of gel transparency, and further considering shape retention. Various things, such as what made the gelatin aqueous | water-based crosslinked gel by making the gelatinizer (crosslinking agent) react, are proposed.
Examples of the latter include, for example, an aqueous gel comprising a reaction product of an ethylenically unsaturated compound-maleic anhydride copolymer and gelatin (Patent Document 1), and ammonia of an ethylenically unsaturated compound-maleic anhydride copolymer. An aqueous gel comprising a reaction product of a reaction product and gelatin has been proposed (Patent Document 2).
JP-A-1-297484 JP 2000-192011

ところで、上述の水性ゲルを用いた芳香剤は、一般に所定の容器にゲルを充填し、フィルム等にて密封して保存し、使用開始時にフィルムを剥がしてゲルが空気に直接接触できるように設置して使用する。このため、芳香剤に含まれる揮発物質の揮発面積が容器の口径に左右されることとなり、例えば1ヶ月使用後には揮散速度が大幅に低下するなど、満足できる揮散速度を得ることは難しかった。   By the way, the fragrance using the above-mentioned aqueous gel is generally placed in such a manner that a predetermined container is filled with the gel, sealed with a film or the like and stored, and the film is peeled off at the start of use so that the gel can be directly contacted with air. And use it. For this reason, the volatilization area of the volatile substance contained in the fragrance will depend on the diameter of the container, and it has been difficult to obtain a satisfactory volatilization rate, for example, the volatilization rate significantly decreases after one month of use.

本発明者らは、香料の徐放性に優れる新たな水性ゲル状の芳香剤を得るべく鋭意研究した結果、ゼラチン、架橋剤及び香料を含み、所定のブルーム強度を有する水性架橋ゲルを半球体若しくは球体形状に成形して芳香剤と為すことにより、含有する香料がほぼ全て揮散するまで揮散速度を一定に保つことができることを見出し、本発明を完成させた。   As a result of intensive research to obtain a new aqueous gel-like fragrance excellent in sustained release of a fragrance, the present inventors have found that an aqueous crosslinked gel containing gelatin, a crosslinking agent and a fragrance and having a predetermined bloom strength is a hemisphere. Alternatively, the present inventors have found that the volatilization rate can be kept constant until almost all of the fragrance contained therein is volatilized by forming it into a spherical shape and using it as a fragrance.

すなわち、本発明の芳香剤は、ゼラチン、架橋剤及び香料を含む水性ゲルからなる芳香剤であって、該水性ゲルが半球体または球体の形状を有し且つ該水性ゲルのブルーム強度が半球体形状の場合には15以上、球体形状の場合には13以上であることを特徴とする、芳香剤に関する。   That is, the fragrance of the present invention is a fragrance comprising an aqueous gel containing gelatin, a crosslinking agent and a fragrance, wherein the aqueous gel has a hemispherical shape or a spherical shape, and the bloom strength of the aqueous gel is hemispherical. The present invention relates to a fragrance characterized by being 15 or more in the case of a shape and 13 or more in the case of a sphere.

また前記水性ゲルが1cm乃至5cmの直径を有する半球体又は球体の形状有することを特徴とする、芳香剤に関する。   Further, the present invention relates to a fragrance, wherein the aqueous gel has a hemispherical shape or a spherical shape having a diameter of 1 cm to 5 cm.

本発明の芳香剤を容器に複数個入れて使用するとき、形状を半球体または球体と為したことによって、芳香剤同士が接触する面(接触面)の広さが六面体、八面体等の多面体形
状とした場合よりも小さくなり、結果、芳香剤が空気に触れる面(表面積)が六面体、八面体等の多面体形状とした場合より大きくなる。
また本発明の芳香剤にあっては、芳香剤同士の接触面が小さいことから、芳香剤同士の間に空隙がより広く存在することとなり、このより広い空隙を通って芳香剤中の香料が揮散することができる。
そして芳香剤が半球体形状の場合には使用直後の水性ゲルのブルーム強度を15以上、球体形状の場合には同13以上とすることによって、芳香剤が容器内で上下に重なり合った場合においても、その半球体又は球体形状を保つことができる。すなわち、上になった芳香剤の重さによって下になった芳香剤の形状が崩れ、芳香剤同士の接触面が大きくなることを防ぐことができる。
以上より、本発明の芳香剤は使用時の表面積(薬剤の揮発面積)を大きく保ち、且つ香料が揮散できる空隙をより広く形成することができ、これにより、香料の揮散速度を低下させず、香料が揮発してなくなるまで芳香剤を使用することが可能となる。
When the fragrance of the present invention is used in a plurality of containers, the shape of the fragrance is a hemisphere or a sphere, so that the surface (contact surface) where the fragrances contact each other is a polyhedron such as a hexahedron or an octahedron. As a result, the surface (surface area) on which the fragrance comes into contact with air becomes larger than that in the case of a polyhedral shape such as a hexahedron or an octahedron.
Further, in the fragrance of the present invention, since the contact surface between the fragrances is small, there is a wider gap between the fragrances, and the fragrance in the fragrance is passed through this wider gap. Can be stripped.
And when the fragrance is hemispherical, the bloom strength of the aqueous gel immediately after use is 15 or more, and when the fragrance is sphere, it is 13 or more so that the fragrance overlaps vertically in the container. The hemisphere or sphere shape can be maintained. That is, it is possible to prevent the shape of the fragrance underneath from being collapsed due to the weight of the fragrance above, and an increase in the contact surface between the fragrances.
From the above, the fragrance of the present invention can keep a large surface area (volatilization area of the drug) at the time of use, and can form a wider space through which the fragrance can be volatilized, thereby reducing the volatilization rate of the fragrance, The fragrance can be used until the fragrance is no longer volatilized.

本発明の芳香剤は、ゼラチン、架橋剤及び香料を含み、所望により界面活性剤、可溶化剤等のその他の成分を含む水性ゲルからなる芳香剤である。以下に本発明の各構成要素及びその機能に関してさらに説明する。
なお本発明において「芳香剤全質量基準」とは、ゼラチン、架橋剤、香料、及び、界面活性剤、可溶化剤又は揮散調整剤、水及びその他成分(消臭剤、色素、殺菌剤、保形剤、離形剤など)からなる芳香剤の全質量を基準とすることを意味するものである。
The fragrance of the present invention is a fragrance made of an aqueous gel containing gelatin, a crosslinking agent and a fragrance, and optionally containing other components such as a surfactant and a solubilizer. Hereinafter, each component of the present invention and its function will be further described.
In the present invention, “based on the total mass of the fragrance” means gelatin, a cross-linking agent, a fragrance, a surfactant, a solubilizer or a volatilizer, water and other components (deodorant, dye, bactericidal agent, preservative). It means to be based on the total mass of the fragrance comprising the form, release agent and the like.

<ゼラチン>
本発明の芳香剤に含まれるゼラチンとしては、例えばウシやブタなどの動物の骨、皮、靱帯又は腱などに含まれるコラーゲンを熱、酸、アルカリ又は酵素等のいずれの方法により変性して得られるものが使用される。
上記ゼラチンの配合量は、揮散速度や後述する所定のブルーム強度を有するゲルと為すことを考慮すると、半球体形状の芳香剤を為す場合には芳香剤全質量基準で好ましくは1.0質量%以上、より好ましくは同1.3質量%以上、球体形状の芳香剤を為す場合には好ましくは同0.8質量%以上、より好ましくは同1.3質量%であることが望ましい。また配合量の上限としては、本発明の目的の達成される限り特別の制限はないが、体積収縮による明確な終点を得るためには、芳香剤全質量基準で5質量%以下、好ましくは同2質量%以下が好ましい。
<Gelatin>
As the gelatin contained in the fragrance of the present invention, for example, collagen contained in bones, skins, ligaments or tendons of animals such as cattle and pigs can be denatured by any method such as heat, acid, alkali or enzyme. Is used.
The amount of gelatin is preferably 1.0% by mass based on the total mass of the fragrance when considering the volatilization rate and the gel having the predetermined bloom strength described below, when the hemispherical fragrance is formed. As described above, more preferably 1.3% by mass or more, and in the case of producing a fragrance having a spherical shape, it is preferably 0.8% by mass or more, more preferably 1.3% by mass. The upper limit of the blending amount is not particularly limited as long as the object of the present invention is achieved, but in order to obtain a clear end point due to volume shrinkage, it is 5% by mass or less based on the total mass of the fragrance, preferably the same. 2 mass% or less is preferable.

<架橋剤>
本発明の芳香剤に含まれる架橋剤としては、上記ゼラチンの官能基と反応して架橋できるものであればよいが、芳香剤を使用中に誤って倒したり、口にいれたりすることを考慮し、天然由来のものが好ましい。このような架橋剤として、多糖類、グアニール酸、セルロース、乳酸、ホウ酸等が挙げられ、これらを組み合わせて使用することが望ましい。
上記架橋剤の配合量は、前述のゼラチンとの架橋反応を円滑に進行させる上でゼラチン配合量をも考慮し、好ましくは芳香剤全質量基準で0.1乃至10質量%、より好ましくは同0.5乃至7.5質量%であることが望ましい。
<Crosslinking agent>
The cross-linking agent contained in the fragrance of the present invention is not particularly limited as long as it can cross-link by reacting with the functional group of the gelatin, but it is considered that the fragrance is mistakenly dropped or put into the mouth during use. However, those derived from nature are preferred. Examples of such a crosslinking agent include polysaccharides, guanearic acid, cellulose, lactic acid, boric acid, and the like, and it is desirable to use them in combination.
The blending amount of the crosslinking agent is preferably 0.1 to 10% by mass, more preferably the same based on the total mass of the fragrance, in consideration of the blending amount of gelatin in order to smoothly advance the crosslinking reaction with gelatin. The content is desirably 0.5 to 7.5% by mass.

<香料>
本発明の芳香剤に含まれる香料としては、当該技術分野において周知なものであればいずれも使用可能であり、例えば天然香料又は合成香料などを挙げることができる。これらは必要に応じて希釈又は乳化したものを本発明において使用することができる。
上記香料の配合量に特別な制限はないが、好ましくは芳香剤全質量基準で1乃至10質量%であることが望ましい。
<Fragrance>
As the fragrance contained in the fragrance of the present invention, any fragrance known in the art can be used, and examples thereof include natural fragrances and synthetic fragrances. Those which are diluted or emulsified as necessary can be used in the present invention.
Although there is no special restriction | limiting in the compounding quantity of the said fragrance | flavor, It is desirable that it is 1 to 10 mass% preferably based on the total mass of an aromatic.

<界面活性剤>
本発明の芳香剤には、香料の溶解分散性を高めるための界面活性剤を含むことができる。これら界面活性剤としては、例えば脂肪酸塩、アルキル硫酸エステル塩、アルキルベンゼンスルホン酸塩、ポリオキシエチレンアルキル又はアルキルアリール硫酸塩などの陰イオン性界面活性剤;ポリオキシエチレンアルキルエーテル又はポリオキシエチレンアルキルフェニルエーテルなどのポリオキシエチレンアルキルアリールエーテル類;ソルビタン脂肪酸エステル、ポリオキシエチレンソルビタン脂肪酸エステル、ポリオキシエチレンスルビトール脂肪酸エステル、ポリオキシエチレンヒマシ油又はポリオキシエチレン硬化ヒマシ油などの非イオン性界面活性剤等のうち1種以上を使用することができる。
上記界面活性剤の配合量は、本発明の芳香剤の透明性に悪影響を及ぼすことなどなく、その使用目的の達成される量であれば特別の制限はないが、好ましくは芳香剤全質量基準で1乃至15質量%とすることができる。
<Surfactant>
The fragrance of the present invention can contain a surfactant for enhancing the dispersibility of the fragrance. Examples of these surfactants include anionic surfactants such as fatty acid salts, alkyl sulfate esters, alkylbenzene sulfonates, polyoxyethylene alkyl or alkylaryl sulfates; polyoxyethylene alkyl ethers or polyoxyethylene alkylphenyls. Polyoxyethylene alkyl aryl ethers such as ethers; nonionic surfactants such as sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters, polyoxyethylene sulfitol fatty acid esters, polyoxyethylene castor oil or polyoxyethylene hydrogenated castor oil 1 or more types can be used.
The amount of the surfactant is not particularly limited as long as the purpose of use thereof is achieved without adversely affecting the transparency of the fragrance of the present invention, but preferably based on the total mass of the fragrance. 1 to 15% by mass.

<可溶化剤又は揮散調整剤>
本発明の芳香剤には、香料の可溶化助剤として機能する可溶化剤又は香料の揮発性を制御する揮散調整剤をさらに含むことができる。このような剤としては、メタノール、エタノール又はプロパノール等のアルコール類;エチレングリコール、プロピレングリコール又はグリセリン等の多価アルコール類;エチレングリコールアルキルエーテル、ジエチレングリコールアルキルエーテル又はプロピレングリコールアルキルエーテル等の多価アルコールアルキルエーテル類等の水溶性溶剤の1種、又はこれらの組合せを使用することができる。
上記可溶化剤又は揮散調整剤の配合量は、本発明の芳香剤の透明性に悪影響を及ぼすことなどなく、その使用目的の達成される量であれば特別の制限はないが、好ましくは芳香剤全質量基準で0乃至40質量%とすることができる。
<Solubilizer or volatilization regulator>
The fragrance of the present invention can further contain a solubilizer that functions as a solubilizing aid for the fragrance or a volatilization regulator that controls the volatility of the fragrance. Such agents include alcohols such as methanol, ethanol or propanol; polyhydric alcohols such as ethylene glycol, propylene glycol or glycerin; polyhydric alcohol alkyls such as ethylene glycol alkyl ether, diethylene glycol alkyl ether or propylene glycol alkyl ether. One of water-soluble solvents such as ethers, or a combination thereof can be used.
The blending amount of the solubilizer or volatilization modifier is not particularly limited as long as the purpose of use thereof is achieved without adversely affecting the transparency of the fragrance of the present invention. It can be 0 to 40% by mass based on the total mass of the agent.

<水>
水は、本発明の芳香剤の調整時に、上記ゼラチンの膨潤のために、又は上記香料の溶解に際して上述の可溶化剤との混合溶媒の形態で使用される。
この水には特別の制限はないが、香料の質や、芳香剤の保存安定性を考慮すると高純度のものが好ましく、例えば蒸留、イオン交換樹脂処理による精製水を好ましいものとして挙げることができる。
水の配合量は、好ましくは芳香剤全質量基準で50乃至90質量%とすることができる
<Water>
Water is used in the form of a mixed solvent with the above-described solubilizing agent in the preparation of the fragrance of the present invention, for swelling of the gelatin or upon dissolution of the fragrance.
Although there is no special restriction on this water, it is preferable to have high purity in consideration of the quality of the fragrance and the storage stability of the fragrance. For example, purified water by distillation or ion exchange resin treatment can be mentioned as a preferable one. .
The amount of water is preferably 50 to 90% by mass based on the total mass of the fragrance.

<その他の成分>
本発明の芳香剤には、上述の成分のほか、消臭剤、色素、殺菌剤、保形剤、離形剤等、芳香剤に使用され得る周知の成分を含むことができる。
<Other ingredients>
In addition to the above-described components, the fragrance of the present invention can contain well-known components that can be used in fragrances, such as deodorants, pigments, bactericides, shape-retaining agents, and release agents.

本発明の芳香剤は、例えば、使用する全ての上記原料を一挙に撹拌混合し、得られた混合物を半球体又は球体の成形型に入れ、架橋剤がゼラチンに作用する条件下に保持してゲル化させ、その後離型することで製造することができる。
上記のように製造される本発明の芳香剤は、水性ゲルのブルーム強度が半球体形状の場合には15以上、球体形状の場合には13以上であるように各成分の配合量を適宜調整する。なお、香料の揮散速度、半球体又は球体の形状保持能、ゼラチンの体積収縮等を考慮すると、上記ブルーム強度はいずれの形状においても25乃至32であることが最も望ましい。
また、本発明の芳香剤の大きさ(半球体又は球体の直径)は、その直径が1cm乃至5cmであることが望ましい。直径が上記範囲よりも大きい場合には表面積が大きいものとならず、また、上記範囲よりも小さい場合には水性ゲルの水吸収が速くなりすぎて、揮散速度が一週間程度で極端に遅くなる。
The fragrance of the present invention, for example, stirs and mixes all the above raw materials used at once, puts the obtained mixture into a hemisphere or a sphere mold, and maintains the conditions under which the crosslinking agent acts on gelatin. It can be manufactured by gelling and then releasing the mold.
In the fragrance of the present invention produced as described above, the blending amount of each component is appropriately adjusted so that the bloom strength of the aqueous gel is 15 or more when hemispherical, and 13 or more when spherical. To do. In view of the volatilization rate of the fragrance, hemisphere or sphere shape retention ability, volumetric shrinkage of gelatin, etc., the Bloom strength is most preferably 25 to 32 in any shape.
The size of the fragrance of the present invention (the diameter of a hemisphere or a sphere) is preferably 1 cm to 5 cm. When the diameter is larger than the above range, the surface area is not large, and when the diameter is smaller than the above range, water absorption of the aqueous gel becomes too fast, and the volatilization rate becomes extremely slow in about one week. .

以下、実施例を挙げて、本発明を更に詳しく説明するが、本発明は、これら実施例に限定されるものでない。   EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated in more detail, this invention is not limited to these Examples.

製造例
ゼラチン、架橋剤(多糖類、セルロース、ホウ酸)、香料、界面活性剤、可溶化剤を下記表1に記載の配合量に従って配合し、精製水で最終質量100gとした。
この配合物を320rpmで5分間撹拌して完全に混合させ、実施例1及び2並びに比較例1においては直径3cmの球体形状の成形型(複数個)に、比較例2においては6cm四方の直方体の成形型に注入し、室温で24時間放置し、ゲル化を進行させた。24時間経過後、各ゲルを成形型より離型し、実施例2及び比較例1においては球体形状を二分割して半球体形状とした。以上の手順により、実施例1(球体)、実施例2(半球体)、比較例1(半球体)及び比較例2(直方体)の芳香剤を製造した。
なお各芳香剤のブルーム強度をJIS K6503−1996に従い測定し、表1にあ
わせて示す。

Figure 2007275343
Production Example Gelatin, a crosslinking agent (polysaccharide, cellulose, boric acid), a fragrance, a surfactant, and a solubilizer were blended according to the blending amounts shown in Table 1 below, and the final mass was 100 g with purified water.
This blend was stirred at 320 rpm for 5 minutes to be thoroughly mixed, and in Examples 1 and 2 and Comparative Example 1, a 3 cm diameter spherical mold (multiple) was used, and in Comparative Example 2, a 6 cm rectangular parallelepiped. The mixture was poured into a mold and allowed to stand at room temperature for 24 hours to allow gelation to proceed. After the elapse of 24 hours, each gel was released from the mold, and in Example 2 and Comparative Example 1, the spherical shape was divided into two to form a hemispherical shape. The fragrance | flavor of Example 1 (sphere), Example 2 (hemisphere), Comparative example 1 (hemisphere), and Comparative example 2 (cuboid) was manufactured by the above procedure.
The bloom strength of each fragrance was measured according to JIS K6503-1996, and is shown together in Table 1.
Figure 2007275343

試験例1:形状保持性
製造した芳香剤のうち、球体形状及び半球体形状の芳香剤(実施例1及び2、比較例1)を6cm四方の透明な容器1に入れた。
このとき、図1乃至図3に示すように、実施例1(球体)及び実施例2(半球体)においては芳香剤2a及び2bは共に潰れることなくそのままの形状を保ったが、比較例1(半球体)においては芳香剤2cが潰れて半球体の形状を為していないことが目視にて確認された。
Test Example 1: Shape retention Among the manufactured fragrances, sphere-shaped and hemispherical-shaped fragrances (Examples 1 and 2 and Comparative Example 1) were placed in a 6 cm square transparent container 1.
At this time, as shown in FIGS. 1 to 3, in Examples 1 (sphere) and Example 2 (hemisphere), the fragrances 2 a and 2 b were both kept intact without being crushed. In (hemisphere), it was visually confirmed that the fragrance 2c was crushed and did not form a hemisphere.

試験例2:揮散速度
製造した芳香剤を6cm四方の透明な容器に入れ、これを25℃に調製された室内に設置し、その質量変化を60日経過後までほぼ5日毎に計量した。得られた結果を図4に示す。
Test Example 2: Volatilization rate The produced fragrance was placed in a 6 cm square transparent container, placed in a room prepared at 25 ° C., and its mass change was weighed approximately every 5 days until after 60 days. The obtained results are shown in FIG.

試験結果
上記試験例1が示すように、実施例1及び実施例2の芳香剤は、球体(又は半球体)形状の複数個のゲル状芳香剤を容器中に重ねて入れた場合においても、その形状が保たれた
。また試験例2においては、実施例1及び実施例2の芳香剤は、30日過ぎても揮散速度が低下せず、ほぼ60日まで揮散速度が保たれていたことが確認された。
一方、ブルーム強度が10である半球体の芳香剤である比較例1においては、容器中に重ねて入れるとその形状がかなり潰れて、空隙の少ない塊状のものとなった。そして比較例1及び比較例2においては、30日経過後までは実施例1及び実施例2と同様の揮散速度を有していたが、その後は急激に揮散速度が落ち、芳香剤が殆ど揮散していないことが確認された。
Test results As shown in Test Example 1 above, the fragrances of Example 1 and Example 2 were used even when a plurality of spherical (or hemispherical) gel fragrances were placed in a container. The shape was maintained. Further, in Test Example 2, it was confirmed that the fragrances of Examples 1 and 2 did not decrease the volatilization rate even after 30 days, and the volatilization rate was maintained until almost 60 days.
On the other hand, in Comparative Example 1, which is a hemispherical fragrance having a bloom strength of 10, the shape was considerably crushed when it was put in a container, resulting in a lump with few voids. And in the comparative example 1 and the comparative example 2, it had the same volatilization rate as Example 1 and Example 2 until after 30-day progress, but after that, the volatilization rate fell suddenly and the fragrance | flavor almost volatilized. Not confirmed.

図1は実施例1の球体形状の芳香剤2aを透明な容器1に入れた状態を容器正面からみた模式図である。FIG. 1 is a schematic view of a state in which the spherical fragrance 2a of Example 1 is placed in a transparent container 1 as seen from the front of the container. 図2は実施例2の半球体形状の芳香剤2bを透明な容器1に入れた状態を容器正面からみた模式図である。FIG. 2 is a schematic view of the state in which the hemispherical fragrance 2b of Example 2 is placed in a transparent container 1 as seen from the front of the container. 図3は比較例1の半球体形状の芳香剤2cを透明な容器1に入れた状態を容器正面からみた模式図である。FIG. 3 is a schematic view of the state in which the hemispherical fragrance 2c of Comparative Example 1 is placed in a transparent container 1 as seen from the front of the container. 図4は実施例1及び2、並びに比較例1及び2の芳香剤の質量減少率の経時変化を示す図である。FIG. 4 is a graph showing the change over time in the mass reduction rate of the fragrances of Examples 1 and 2 and Comparative Examples 1 and 2.

符号の説明Explanation of symbols

1・・・透明な容器
2・・・芳香剤
2a・・・球体形状の芳香剤(ブルーム強度25)
2b・・・半球体形状の芳香剤(ブルーム強度25)
2c・・・半球体形状の芳香剤(ブルーム強度10)
DESCRIPTION OF SYMBOLS 1 ... Transparent container 2 ... Air freshener 2a ... Spherical-shaped air freshener (Bloom strength 25)
2b ... hemispherical fragrance (bloom strength 25)
2c ... hemispherical fragrance (bloom strength 10)

Claims (2)

ゼラチン、架橋剤及び香料を含む水性ゲルからなる芳香剤であって、該水性ゲルが半球体または球体の形状を有し且つ該水性ゲルのブルーム強度が半球体形状の場合には15以上、球体形状の場合には13以上であることを特徴とする芳香剤。   A fragrance comprising an aqueous gel containing gelatin, a cross-linking agent and a fragrance, wherein the aqueous gel has a hemispherical shape or a spherical shape, and the bloom strength of the aqueous gel is a hemispherical shape, 15 or more. A fragrance characterized by being 13 or more in the case of shape. 前記水性ゲルが1cm乃至5cmの直径を有する半球体又は球体の形状を有することを特徴とする、請求項1記載の芳香剤。
The fragrance according to claim 1, wherein the aqueous gel has a hemispherical shape or a spherical shape having a diameter of 1 cm to 5 cm.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011050684A (en) * 2009-09-04 2011-03-17 Earth Chemical Co Ltd Medicine gel and method for diffusing medicine using the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011050684A (en) * 2009-09-04 2011-03-17 Earth Chemical Co Ltd Medicine gel and method for diffusing medicine using the same

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