JPH03173565A - Atomizer containing perfume - Google Patents
Atomizer containing perfumeInfo
- Publication number
- JPH03173565A JPH03173565A JP1313786A JP31378689A JPH03173565A JP H03173565 A JPH03173565 A JP H03173565A JP 1313786 A JP1313786 A JP 1313786A JP 31378689 A JP31378689 A JP 31378689A JP H03173565 A JPH03173565 A JP H03173565A
- Authority
- JP
- Japan
- Prior art keywords
- fragrance
- microcapsules
- perfumes
- capsules
- atomizer
- 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.)
- Pending
Links
- 239000002304 perfume Substances 0.000 title abstract description 8
- 239000003094 microcapsule Substances 0.000 claims abstract description 21
- 239000003205 fragrance Substances 0.000 claims description 35
- 239000006185 dispersion Substances 0.000 claims description 12
- 239000011230 binding agent Substances 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 7
- 238000013268 sustained release Methods 0.000 claims description 5
- 239000012730 sustained-release form Substances 0.000 claims description 5
- 239000003232 water-soluble binding agent Substances 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims 1
- 239000002775 capsule Substances 0.000 abstract description 8
- 150000002576 ketones Chemical class 0.000 abstract description 7
- 239000011162 core material Substances 0.000 abstract description 6
- 241000402754 Erythranthe moschata Species 0.000 abstract description 4
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- 150000002148 esters Chemical class 0.000 abstract description 4
- 230000002209 hydrophobic effect Effects 0.000 abstract description 4
- 229930195733 hydrocarbon Natural products 0.000 abstract description 3
- 150000002430 hydrocarbons Chemical class 0.000 abstract description 3
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 abstract description 2
- 150000001299 aldehydes Chemical class 0.000 abstract description 2
- 150000001408 amides Chemical class 0.000 abstract description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract description 2
- 229960002903 benzyl benzoate Drugs 0.000 abstract description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 abstract description 2
- 235000012343 cottonseed oil Nutrition 0.000 abstract description 2
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- 241000196324 Embryophyta Species 0.000 abstract 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 1
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- 239000000443 aerosol Substances 0.000 description 4
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- 239000001211 (E)-4-phenylbut-3-en-2-one Substances 0.000 description 1
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 description 1
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- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 1
- CRIGTVCBMUKRSL-FNORWQNLSA-N 1-(2,6,6-trimethylcyclohex-2-en-1-yl)but-2-enone Chemical compound C\C=C\C(=O)C1C(C)=CCCC1(C)C CRIGTVCBMUKRSL-FNORWQNLSA-N 0.000 description 1
- BGTBFNDXYDYBEY-UHFFFAOYSA-N 1-(2,6,6-trimethylcyclohexen-1-yl)but-2-en-1-one Chemical compound CC=CC(=O)C1=C(C)CCCC1(C)C BGTBFNDXYDYBEY-UHFFFAOYSA-N 0.000 description 1
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- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
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- 238000002156 mixing Methods 0.000 description 1
- 229940067137 musk ketone Drugs 0.000 description 1
- XMWRWTSZNLOZFN-UHFFFAOYSA-N musk xylene Chemical group CC1=C(N(=O)=O)C(C)=C(N(=O)=O)C(C(C)(C)C)=C1N(=O)=O XMWRWTSZNLOZFN-UHFFFAOYSA-N 0.000 description 1
- ALHUZKCOMYUFRB-UHFFFAOYSA-N muskone Natural products CC1CCCCCCCCCCCCC(=O)C1 ALHUZKCOMYUFRB-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- BWHOZHOGCMHOBV-BQYQJAHWSA-N trans-benzylideneacetone Chemical compound CC(=O)\C=C\C1=CC=CC=C1 BWHOZHOGCMHOBV-BQYQJAHWSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229930007850 β-damascenone Natural products 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Nozzles (AREA)
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、香料を内蔵した噴霧器に関し、特に快適な芳
香を楽しむことが出来る噴霧器に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an atomizer containing a fragrance, and particularly to an atomizer that allows the user to enjoy a pleasant fragrance.
従来、衣類や室内に芳香を持たせる方法の一つとして香
料或いは香料を含有する液を空気や噴射剤等の圧力を利
用して対象物に噴霧する方法がある。2. Description of the Related Art Conventionally, one of the methods for imparting a fragrance to clothes or a room is to spray a fragrance or a liquid containing a fragrance onto an object using the pressure of air, a propellant, or the like.
しかし、従来のこの方法の場合には、■噴霧の際に香料
が広範囲に飛散し易(、若番の対象である物思外にも強
い匂いが付き易い。■噴霧された直後は匂いが強すぎる
ため不快感を与える場合もある。■香料の揮散が速すぎ
て直ちに匂いが感じられなくなる等問題点を多く含んで
いる。However, in the case of this conventional method, ■ The fragrance tends to scatter over a wide area when spraying (it tends to have a surprisingly strong odor, which is the target of young people).■ The odor does not disappear immediately after being sprayed. It is too strong and may cause discomfort.■ It has many problems, such as the fragrance evaporating too quickly and the smell becoming impossible to perceive immediately.
本発明は、上記問題を有することがなく、快適な芳香を
楽しむことが出来る香料内蔵噴霧器を提供することを目
的とするものである。An object of the present invention is to provide a sprayer with a built-in fragrance that does not have the above-mentioned problems and allows the user to enjoy a pleasant fragrance.
香料を成分として内蔵する噴霧器において該香料がマイ
クロカプセルに内蔵されていることを特徴とする香料内
蔵噴霧器である。This is a fragrance-containing atomizer that contains a fragrance as a component, and is characterized in that the fragrance is contained in microcapsules.
本発明者は、研究の結果、噴霧器に使用する香料をマイ
クロカプセル化することによって、着香の対象となるも
の以外に香料が飛散してもそれが強(匂うことがなく、
又、噴霧直後の匂いの強さを快適な範囲にコントロール
出来ることを見出した。As a result of research, the present inventor found that by microcapsulating the fragrance used in the atomizer, even if the fragrance is scattered to other than the target object, it is strong (no smell),
We have also discovered that the intensity of the odor immediately after spraying can be controlled within a comfortable range.
本発明に使用できるマイクロカプセルとしては、摩擦等
の圧力を受けてカプセルが破壊された場合にのみ芯物質
である香料が放出される非除放性マイクロカプセルやカ
プセルが破壊されていない状態おいてもポーラスな壁膜
を通して香料が徐々に放出される除放性マイクロカプセ
ルが挙げられるが、匂いを楽しみたい時に於いてのみカ
プセルを破壊して香料を放出させることが出来、又、芳
香と無臭を交互に楽しむことが出来る等、同じ匂いを連
続して嗅ぐことによる不快感を生じることがない点で非
除放性マイクロカプセルの使用が好ましい。Microcapsules that can be used in the present invention include non-sustained release microcapsules that release the core fragrance only when the capsule is ruptured under pressure such as friction, and non-sustained release microcapsules that release the fragrance core material only when the capsule is ruptured under pressure such as friction. One example is sustained-release microcapsules, which release fragrance gradually through a porous wall membrane. It is preferable to use non-sustained release microcapsules because they can be enjoyed alternately and do not cause discomfort due to continuous sniffing of the same odor.
本発明に用いられるマイクロカプセルは、従来公知のコ
アセルベーション法(例えば米国特許第2800457
号、同2800458号等に示される方法)界面重合法
(例えば、特公昭38−19574号、特公昭4244
6号、特、公開42−771号、特公昭49−4513
3号等に開示されている方法) 1n−situ重合法
(例えば特公昭36−9158号、特公昭51−907
9号、特公昭53−84881号等に開示されている方
法)等の方法によって製造し得る。The microcapsules used in the present invention can be prepared by a conventionally known coacervation method (for example, U.S. Pat. No. 2,800,457).
Interfacial polymerization method (e.g., Japanese Patent Publication No. 38-19574, Japanese Patent Publication No. 4244)
No. 6, Special Publication No. 42-771, Special Publication No. 49-4513
3, etc.) 1n-situ polymerization method (for example, Japanese Patent Publication No. 36-9158, Japanese Patent Publication No. 51-907)
9, Japanese Patent Publication No. 53-84881, etc.).
本発明に用いられる香料としては、例えばケトン類、ア
ルデヒド類、エステル類、ラクトン類、エーテル類、合
成ムスク類、炭化水素類等が挙げられ、具体的には以下
のものが例示できる。Examples of the fragrance used in the present invention include ketones, aldehydes, esters, lactones, ethers, synthetic musks, hydrocarbons, and the like.
■脂肪族ケトン類:2−ヘプタン、3−オクタノン、2
−ウンデカノン等。■Aliphatic ketones: 2-heptane, 3-octanone, 2
- Undecanone et al.
■芳香族ケトン類: アニシルアセトン、ベンジリデン
アセトン、p−メチルアセトフェノン、p−メトキシア
セトフェノン等。■Aromatic ketones: anisyl acetone, benzylidene acetone, p-methylacetophenone, p-methoxyacetophenone, etc.
■脂環式ケトン類:α−イロン、β−イロン、T−イロ
ン、α−ダマスコン、β−ダマスコン、α−ダマセノン
、β−ダマセノン、テアスビロン等。■Alicyclic ketones: α-ylon, β-ylon, T-ylon, α-damascone, β-damascone, α-damascenone, β-damascenone, theasvirone, etc.
■テルペン系ケトン類:メントン、カルボン、プレボン
等。■Terpene ketones: menthone, carvone, prebon, etc.
■大環状ケトン類:ムスコン、アンプレットリド、シク
ロへキサデカリド等。■Macrocyclic ketones: muscone, ampletlide, cyclohexadecalide, etc.
■脂肪族アルデヒド類:ノナナール、トリデカナール、
テトラデカナール等。■Aliphatic aldehydes: nonanal, tridecanal,
Tetradecanal etc.
■芳香族アルデヒドR:シンナムアルデヒド、α−アル
ミシンアムアルデヒド、α−へキシルシンアムアルデヒ
ド、シクラメンアルデヒド等。■Aromatic aldehyde R: cinnamaldehyde, α-aluminamaldehyde, α-hexylcinamaldehyde, cyclamenaldehyde, etc.
■脂肪族酸エステル類:酢酸ゲラニル、酢酸リナリル、
酢酸シンナミル、プロピオン酸ベンジル等。■Aliphatic acid esters: geranyl acetate, linalyl acetate,
Cinnamyl acetate, benzyl propionate, etc.
■芳香族酸エステル類:安息香酸イソアミル、ケイ皮酸
エチル等。■Aromatic acid esters: isoamyl benzoate, ethyl cinnamate, etc.
■環状エーテル類二ローズオキサイド、1.8−シネオ
ール、オキサイドケトン等。O合成ムスク類:ムスクキ
シレン、ムスクケトン、ムスクアンブレッド等。■Cyclic ethers dirose oxide, 1,8-cineole, oxide ketone, etc. O Synthetic musks: musk xylene, musk ketone, musk unbread, etc.
■炭化水素類:リモネン、カンフエン、ピネン等。■Hydrocarbons: limonene, camphene, pinene, etc.
が挙げられる。又これらの香料は2種類以上を混合して
使用することも出来る。can be mentioned. Moreover, two or more types of these fragrances can also be used in combination.
カプセル化が容易に行う為に香料を他の疎水性媒体と混
合して芯物質とすることも可能である。For ease of encapsulation, it is also possible to mix the perfume with other hydrophobic media to form the core material.
かかる疎水性媒体としては、例えば安息香酸ベンジル、
フタル酸ジオクチル、アジピン酸ジオクチル、イソ吉草
酸イソアミル等のエステル類。アセトフェノン、メチル
シクロヘキサノン、ホロン等のケトン類。灯油、パラフ
ィン、ナフテン油等の鉱物油類。アルキル化ビフェニル
、アルキル化ナフタレン、ジフェニルアルカン等の芳香
族炭化水素類。N、N−ジメチルオクチルアミド等のア
ミド類。綿実油等の植物油類が挙げられ、更には、酸化
防止剤、紫外線吸収剤、有色染料等の各種助剤を添加し
てもよい。Such hydrophobic media include, for example, benzyl benzoate,
Esters such as dioctyl phthalate, dioctyl adipate, and isoamyl isovalerate. Ketones such as acetophenone, methylcyclohexanone, and holon. Mineral oils such as kerosene, paraffin, and naphthenic oil. Aromatic hydrocarbons such as alkylated biphenyls, alkylated naphthalenes, and diphenylalkanes. Amides such as N,N-dimethyloctylamide. Examples include vegetable oils such as cottonseed oil, and various auxiliary agents such as antioxidants, ultraviolet absorbers, and colored dyes may also be added.
香料内包マイクロカプセルは、通常水性系の分散液とし
て噴霧されるが、有機溶剤系の分散液として使用するこ
とも出来る。The perfume-containing microcapsules are usually sprayed as an aqueous dispersion, but they can also be used as an organic solvent dispersion.
本発明に使用される分散液は、マイクロカプセルと分散
媒のみからなる分散液でもかまわいないが、より好まし
いものとしては、若番対象物に強力に付着してマイクロ
カプセルが粉じんとして飛散する傾向を抑えたマイクロ
カプセルとバインダーを成分とする分散液が挙げられる
。The dispersion liquid used in the present invention may be a dispersion liquid consisting only of microcapsules and a dispersion medium, but it is more preferable that the dispersion liquid has a tendency to strongly adhere to a young object and cause the microcapsules to scatter as dust. Examples include dispersions containing suppressed microcapsules and a binder.
バインダーとしては、水溶性バインダー類、ラテックス
類、油溶性バインダー類が挙げられる。Examples of the binder include water-soluble binders, latexes, and oil-soluble binders.
水溶性バインダー類としては、例えば、ゼラチン、アル
ブミン、カゼイン、寒天、アラビアゴム、アルギン酸ゾ
ーダ、澱粉、酸化澱粉、エーテル化澱粉、エステル化澱
粉、カルボキシメチルセルロース、ヒドロキシエチルセ
ルロース、ポリビニルアルコール、ポリビニルピロリド
ン、ポリアクリル酸、ポリアクリルアミド、エチレン−
無水マレイン酸共重合体、スチレン−無水マレイン酸共
重合体、メチルビニルエーテル−無水マレイン酸共重合
体、イソブチレン−無水マレイン酸共重合体等が挙げら
れる。Examples of water-soluble binders include gelatin, albumin, casein, agar, gum arabic, alginate, starch, oxidized starch, etherified starch, esterified starch, carboxymethylcellulose, hydroxyethylcellulose, polyvinyl alcohol, polyvinylpyrrolidone, and polyacrylic. acid, polyacrylamide, ethylene-
Examples include maleic anhydride copolymer, styrene-maleic anhydride copolymer, methyl vinyl ether-maleic anhydride copolymer, isobutylene-maleic anhydride copolymer, and the like.
ラテックス類としては、例えば、スチレン−ブタジェン
ラテックス、アクリロニトリル−ブタジェンラテックス
、アクリル酸エステル系ラテックス、酢酸ビニル系ラテ
ックス、塩化ビニリデン系ラテックス、メチルメタクリ
レートーブタジエンラテックス及びこれらのカルボキシ
変性(例えばアクリル酸)ラテックス等が挙げられる。Examples of the latex include styrene-butadiene latex, acrylonitrile-butadiene latex, acrylic acid ester latex, vinyl acetate latex, vinylidene chloride latex, methyl methacrylate-butadiene latex, and carboxy-modified (for example, acrylic acid) thereof. Examples include latex.
油溶性バインダー類としては、例えば、ロジン、コバー
ル、ダマール、シェラツク、エチルセルロース、ヒドロ
キシプロピルセルロース、エチルヒドロキシエチルセル
ロース、アセチルセルロース、セルロースアセテートプ
ロピオネート、セルロースアセテートブチレート、ニト
ロセルロース、ポリビニルブチラール、ポリ塩化ビニル
、ポリ酢酸ビニル、塩化ビニル−酢酸ビニル共重合体、
エチレン−酢酸ビニル共重合体、ポリスチレン、塩素化
ポリプロピレンスチレン樹脂、アクリル樹脂、フェノー
ル樹脂、キシレン樹脂、尿素樹脂、メラミン樹脂、ケト
ン樹脂、クマロン・インデン樹脂、石油樹脂、テルペン
樹脂、環化ゴム、塩化ゴム、アルキド樹脂、ポリアミド
樹脂、エポキシ樹脂、ポリスレンタン等が挙げられる。Examples of oil-soluble binders include rosin, kovar, dammar, shellac, ethyl cellulose, hydroxypropyl cellulose, ethyl hydroxyethyl cellulose, acetyl cellulose, cellulose acetate propionate, cellulose acetate butyrate, nitrocellulose, polyvinyl butyral, and polyvinyl chloride. , polyvinyl acetate, vinyl chloride-vinyl acetate copolymer,
Ethylene-vinyl acetate copolymer, polystyrene, chlorinated polypropylene styrene resin, acrylic resin, phenol resin, xylene resin, urea resin, melamine resin, ketone resin, coumaron/indene resin, petroleum resin, terpene resin, cyclized rubber, chloride Examples include rubber, alkyd resin, polyamide resin, epoxy resin, and polystyrene.
中でも、使用後に洗濯等で極めて容易にその成分を除去
出来る点で水溶性バインダーを使用する系が特に好まし
い。Among these, systems using water-soluble binders are particularly preferred since the components can be removed extremely easily by washing or the like after use.
本発明の分散液には、必要に応じて更に酸化防止剤、紫
外線吸収剤、防腐剤、増粘剤、分散剤等の各種助剤を添
加することが出来る。Various auxiliary agents such as antioxidants, ultraviolet absorbers, preservatives, thickeners, and dispersants can be added to the dispersion of the present invention, if necessary.
本発明においては、マイクロカプセル化した香料以外に
、更ににカプセル化されていない香料やシクロデキスト
リン等の包接化合物に包含された形の香料を併用するこ
とも出来る。In the present invention, in addition to microencapsulated fragrances, non-encapsulated fragrances and fragrances included in clathrate compounds such as cyclodextrins can also be used in combination.
本発明に用いられるマイクロカプセルの粒子径は特に限
定されるものではないが、通常0.5〜50μmの平均
粒子径を有するものが使用される。Although the particle size of the microcapsules used in the present invention is not particularly limited, those having an average particle size of 0.5 to 50 μm are usually used.
本発明におけるマイクロカプセルと分散媒の比率は特に
限定されるものではないが、通常、分散媒100重量部
に対してカプセル1〜100重量部の範囲にある。又、
バインダーを使用する場合のその配合比率はカプセル1
00重量部に対してバインダー1〜10000重量部の
範囲である。The ratio of microcapsules to dispersion medium in the present invention is not particularly limited, but is usually in the range of 1 to 100 parts by weight of capsules to 100 parts by weight of dispersion medium. or,
If a binder is used, its blending ratio is 1 capsule.
The binder is in the range of 1 to 10,000 parts by weight per 1,000 parts by weight.
尚、本発明の分散液はバインダーの種類や配合量を適当
に選択することによって洗濯糊として使用することも出
来る。The dispersion of the present invention can also be used as a laundry paste by appropriately selecting the type and amount of the binder.
本発明の噴霧器としては空気を利用した霧吹、き器でも
よいが、最も好ましいものとしては噴射剤を利用したエ
アゾールタイプのものが挙げられる。The sprayer of the present invention may be a sprayer or a sprayer that uses air, but the most preferred one is an aerosol type that uses a propellant.
噴射剤としては、当業界公知の例えばフロンガス、LP
G、クロルメチルガス、ジメチルエーテル、炭酸ガス、
アルゴン等が使用される。Examples of propellants include those known in the art, such as fluorocarbon gas and LP.
G, chloromethyl gas, dimethyl ether, carbon dioxide gas,
Argon etc. are used.
本発明の噴霧器より放出された香料内包マイクロカプセ
ルは、服、下着、靴下、ハンカチ、ネクタイ、じゅうた
ん、畳等へ付着し、徐々に芳香を放ったり、或いは摩擦
等を受けて芳香を放つようになる。The fragrance-containing microcapsules released from the sprayer of the present invention adhere to clothes, underwear, socks, handkerchiefs, neckties, carpets, tatami mats, etc., and gradually emit a fragrance, or emit a fragrance when subjected to friction, etc. Become.
以下に実施例を挙げて本発明を説明するが、本発明がこ
れらのみに限定されるものではない。尚、部は重量部を
示す。The present invention will be explained below with reference to Examples, but the present invention is not limited to these examples. In addition, parts indicate parts by weight.
実施例1
酢酸ゲラニル100部に、キシリレンジイソシアネート
とトリメチロールプロパンの付加物(成田薬品工業■製
[商品名:タケネートD−110NJ)120部を溶解
して内相液(芯物質)を調製した。Example 1 An internal phase liquid (core material) was prepared by dissolving 120 parts of an adduct of xylylene diisocyanate and trimethylolpropane (manufactured by Narita Pharmaceutical Co., Ltd. [trade name: Takenate D-110NJ) in 100 parts of geranyl acetate. .
部分ケン化ポリビニルアルコール(クラレ(樽製「商品
名: PVA−217EEJ ’)の10%水溶fi1
80部に水220部を加え、平均粒子径2μmの乳化液
を得た。この乳化液を撹拌しながら60℃に昇温し、そ
のまま3時間反応させて酢酸ゲラニルを内包するマイク
ロカプセル分散液を得た。10% aqueous fi1 of partially saponified polyvinyl alcohol (Kuraray (Kurare product name: PVA-217EEJ'))
220 parts of water was added to 80 parts to obtain an emulsion having an average particle size of 2 μm. This emulsion was heated to 60° C. with stirring, and reacted for 3 hours to obtain a microcapsule dispersion containing geranyl acetate.
次いで、上記分散液と噴射剤であるLPGをエアゾール
容器に封入し、ハンカチに向けて噴射し着香した。噴射
の際の匂いは芳香と惑しるレベルの強さであり、又、得
られたハンカチも芳香と惑じるレベルの匂いの強さを示
した。又噴射後2時間経過したハンカチは全く無臭であ
ったが、これを手で揉むことによってカプセルが破壊さ
れ再び芳香を感じることが出来た。Next, the above dispersion liquid and LPG as a propellant were sealed in an aerosol container and sprayed toward a handkerchief to flavor it. The odor during spraying was so strong that it could be mistaken for a fragrance, and the obtained handkerchief also had an odor intensity so strong that it could be mistaken for a fragrance. Furthermore, the handkerchief that had been injected for two hours was completely odorless, but by rubbing it with your hands, the capsules were destroyed and you could feel the fragrance again.
実施例のカプセル分散液の代わりに酢酸ゲラニル100
部を用いた以外は実施例と同様にしてエアゾールを作成
し、ハンカチに向けて噴射し着香した。噴射の際の匂い
は強すぎて不快に惑しられ、又、得られたハンカチも同
様であった。又、噴射後2時間経過したハンカチは全く
無臭であり、更にこれを手で揉んでも匂いは全く感しら
れなかった。Geranyl acetate 100 instead of the capsule dispersion in Example
An aerosol was prepared in the same manner as in the example except that the sample was used, and the aerosol was sprayed onto a handkerchief to flavor it. The odor during spraying was so strong that it was unpleasant and distracting, and so was the resulting handkerchief. Furthermore, the handkerchief that had been sprayed for two hours was completely odorless, and even when it was rubbed with hands, no odor was detected at all.
Claims (1)
料がマイクロカプセルに内蔵されていることを特徴とす
る香料内蔵噴霧器 (2)マイクロカプセルが非除放性であることを特徴と
する請求項(1)記載の香料内蔵噴霧器(3)内蔵物が
香料内包マイクロカプセルとバインダーを成分とする分
散液である請求項(1)乃至(2)記載の香料内蔵噴霧
器 (4)バインダーが水溶性バインダーである請求項(3
)記載の香料内蔵噴霧器[Claims] (1) A sprayer containing a fragrance as a component, characterized in that the fragrance is contained in microcapsules (2) A sprayer with a built-in fragrance characterized in that the microcapsules are non-sustained release. A sprayer with a built-in fragrance (3) according to claim (1); A sprayer with a built-in fragrance (4) according to claims (1) to (2), wherein the built-in substance is a dispersion liquid containing a fragrance-containing microcapsule and a binder as components. Claim (3) wherein the binder is a water-soluble binder
) Atomizer with built-in fragrance
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1313786A JPH03173565A (en) | 1989-11-30 | 1989-11-30 | Atomizer containing perfume |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1313786A JPH03173565A (en) | 1989-11-30 | 1989-11-30 | Atomizer containing perfume |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03173565A true JPH03173565A (en) | 1991-07-26 |
Family
ID=18045514
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1313786A Pending JPH03173565A (en) | 1989-11-30 | 1989-11-30 | Atomizer containing perfume |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03173565A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5691303A (en) * | 1993-06-02 | 1997-11-25 | The Procter & Gamble Company | Perfume delivery system comprising zeolites |
WO2005025626A3 (en) * | 2003-09-11 | 2005-07-21 | Procter & Gamble | Compositions comprising a dispersant and microcapsules containing an active material and a stabilizer |
US20060258768A1 (en) * | 2002-04-18 | 2006-11-16 | Hirotaka Uchiyama | Compositions comprising a dispersant and microcapsules containing an active material |
JP2010509447A (en) * | 2006-11-22 | 2010-03-25 | ザ プロクター アンド ギャンブル カンパニー | Beneficial agent-containing delivery particles |
US20150037059A1 (en) * | 2012-02-23 | 2015-02-05 | Print-Rite Unicorn Image Products Co., Ltd. Of Zhuhai | Chip contact mechanism and developer cartridge |
JP2019524434A (en) * | 2016-07-27 | 2019-09-05 | フイルメニツヒ ソシエテ アノニムFirmenich Sa | Method for producing microcapsules |
CN114774216A (en) * | 2022-05-25 | 2022-07-22 | 浙江美生日化用品有限公司 | Fragrance retaining bead and production process thereof |
-
1989
- 1989-11-30 JP JP1313786A patent/JPH03173565A/en active Pending
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5691303A (en) * | 1993-06-02 | 1997-11-25 | The Procter & Gamble Company | Perfume delivery system comprising zeolites |
US20060258768A1 (en) * | 2002-04-18 | 2006-11-16 | Hirotaka Uchiyama | Compositions comprising a dispersant and microcapsules containing an active material |
US8329154B2 (en) * | 2002-04-18 | 2012-12-11 | The Procter & Gamble Company | Compositions comprising a dispersant and microcapsules containing an active material |
EP1495102B1 (en) | 2002-04-18 | 2016-08-24 | The Procter & Gamble Company | Compositions comprising a dispersant and microcapsules containing an active material |
EP1663323B1 (en) * | 2003-09-11 | 2018-08-22 | The Procter & Gamble Company | A method of spraying compositions comprising a dispersant and microcapsules containing an active material and a stabilizer |
WO2005025626A3 (en) * | 2003-09-11 | 2005-07-21 | Procter & Gamble | Compositions comprising a dispersant and microcapsules containing an active material and a stabilizer |
US7226607B2 (en) | 2003-09-11 | 2007-06-05 | The Procter & Gamble Company | Compositions comprising a dispersant and microcapsules containing an active material and a stabilizer |
JP2010509447A (en) * | 2006-11-22 | 2010-03-25 | ザ プロクター アンド ギャンブル カンパニー | Beneficial agent-containing delivery particles |
US20150037059A1 (en) * | 2012-02-23 | 2015-02-05 | Print-Rite Unicorn Image Products Co., Ltd. Of Zhuhai | Chip contact mechanism and developer cartridge |
JP2019524434A (en) * | 2016-07-27 | 2019-09-05 | フイルメニツヒ ソシエテ アノニムFirmenich Sa | Method for producing microcapsules |
US11471397B2 (en) | 2016-07-27 | 2022-10-18 | Firmenich Sa | Process for the preparation of microcapsules |
CN114774216A (en) * | 2022-05-25 | 2022-07-22 | 浙江美生日化用品有限公司 | Fragrance retaining bead and production process thereof |
CN114774216B (en) * | 2022-05-25 | 2023-08-08 | 浙江美生日化用品有限公司 | Fragrance-retaining bead and production process thereof |
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