JPH04332786A - Propellant composition for aerosol - Google Patents

Propellant composition for aerosol

Info

Publication number
JPH04332786A
JPH04332786A JP13191691A JP13191691A JPH04332786A JP H04332786 A JPH04332786 A JP H04332786A JP 13191691 A JP13191691 A JP 13191691A JP 13191691 A JP13191691 A JP 13191691A JP H04332786 A JPH04332786 A JP H04332786A
Authority
JP
Japan
Prior art keywords
aerosol
propellant composition
heptafluoropropane
hydrocarbons
ethers
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.)
Withdrawn
Application number
JP13191691A
Other languages
Japanese (ja)
Inventor
Tateo Kitamura
健郎 北村
Yoko Usami
宇佐見 陽子
Kazuo Oishi
大石 和男
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.)
AG Technology Co Ltd
Original Assignee
AG Technology Co 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 AG Technology Co Ltd filed Critical AG Technology Co Ltd
Priority to JP13191691A priority Critical patent/JPH04332786A/en
Publication of JPH04332786A publication Critical patent/JPH04332786A/en
Withdrawn legal-status Critical Current

Links

Abstract

PURPOSE:To provide a propellant composition for aerosol having an extremely small influence on destruction, etc., of ozonosphere with extremely remote danger of fire. CONSTITUTION:A propellant composition for aerosol consisting essentially of 1,1,1,2,2,3,3-heptafluoropropane. Furthermore, a propellant composition for the aerosol containing hydrocarbons such as LPG, ethers such as dimethyl ether, halogenated hydrocarbons such as dichlorotrifluoroethane or chlorodifluoroethane and the 1,1,1,2,2,3,3-heptafluoropropane is provided.

Description

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

【0001】0001

【産業上の利用分野】本発明はエアゾール用噴射剤組成
物に関するものである。
FIELD OF THE INVENTION This invention relates to propellant compositions for aerosols.

【0002】0002

【従来の技術】エアゾール用噴射剤に要求される特性と
して、適当な溶解力、適当な蒸気圧、無毒、化学的安定
性、容器等に対する腐蝕性のないこと、無臭、さらに不
燃であること等が挙げられる。従来、これらの要求を満
足するものとして、トリクロロモノフルオロメタン、ジ
クロロジフルオロメタン、トリクロロトリフルオロエタ
ン、ジクロロテトラフルオロエタン等のクロロフルオロ
カーボン系化合物(以下CFCという)があり、これら
のガスを単独又は混合して使用されてきた。
[Prior Art] Properties required for aerosol propellants include appropriate dissolving power, appropriate vapor pressure, non-toxicity, chemical stability, non-corrosion to containers, etc., odorless, and nonflammability. can be mentioned. Conventionally, there are chlorofluorocarbon compounds (hereinafter referred to as CFCs) such as trichloromonofluoromethane, dichlorodifluoromethane, trichlorotrifluoroethane, and dichlorotetrafluoroethane that satisfy these requirements, and these gases can be used alone or in combination. It has been used as

【0003】液化石油ガス(LPG)、DME(ジメチ
ルエーテル)等も用いられるが、可燃性ガスであるため
に、エアゾール製品の燃焼性が高く、使用、貯蔵時の火
災の危険性がある。
Liquefied petroleum gas (LPG), DME (dimethyl ether), etc. are also used, but since they are flammable gases, aerosol products are highly combustible and pose a risk of fire during use and storage.

【0004】0004

【発明が解決しようとする課題】前述のCFCは、噴射
剤として理想的な性状を有しているが、化学的に極めて
安定なため、対流圏内での寿命が長く、拡散して成層圏
に達し、ここで太陽光線により分解して発生する塩素ラ
ジカルがオゾンと連鎖反応を起こし、オゾン層を破壊す
るとのことから、その使用規制が実施されることとなっ
た。このため、従来のCFCに替わり、オゾン層を破壊
しにくい代替噴射剤の探索が活発に行なわれている。
[Problems to be Solved by the Invention] The above-mentioned CFC has ideal properties as a propellant, but because it is chemically extremely stable, it has a long life in the troposphere and diffuses into the stratosphere. The use of chlorine radicals, which are decomposed by sunlight and generated here, causes a chain reaction with ozone and destroys the ozone layer, so the use of chlorine radicals has been regulated. For this reason, in place of conventional CFCs, there is active search for alternative propellants that are less likely to destroy the ozone layer.

【0005】代替噴射剤として、前述のLPG、DME
の他に、クロロジフルオロメタン、クロロジフルオロエ
タン、ジクロロトリフルオロエタン等のハイドロクロロ
フルオロカーボン系化合物(以下HCFCという)等が
検討されているが、LPG,DMEは製品の燃焼性が高
く、事故の増加が予想され、特に人体へ直接使用するエ
アゾール製品に使用することは望ましくない。また、H
CFCは、CFCに比べれば水素を含有するので対流圏
での寿命が短く、オゾン層への影響は極めて小さいが零
ではなく、さらに環境への影響の少ない噴射剤の開発が
必要である。
[0005] As alternative propellants, the above-mentioned LPG, DME
In addition, hydrochlorofluorocarbon compounds (hereinafter referred to as HCFCs) such as chlorodifluoromethane, chlorodifluoroethane, and dichlorotrifluoroethane are being considered, but LPG and DME are highly flammable products and are likely to cause an increase in accidents. Therefore, it is not desirable to use it in aerosol products that are intended to be used directly on the human body. Also, H
Compared to CFC, CFC contains hydrogen, so it has a short life in the troposphere, and its impact on the ozone layer is extremely small, but not zero, and there is a need to develop propellants that have even less impact on the environment.

【0006】本発明は、従来のCFCが有している優れ
た特性を満足しながら環境への影響の極めて少ない代替
噴射剤として使用できる新規な噴射剤組成物を提供する
ことを目的とするものである。
The object of the present invention is to provide a novel propellant composition that can be used as an alternative propellant that has extremely little impact on the environment while satisfying the excellent properties of conventional CFC. It is.

【0007】[0007]

【課題を解決するための手段】本発明は、前述の問題点
を解決すべくなされたものであり、1,1,1,2,2
,3,3−ヘプタフルオロプロパン(以下R227cと
いう)を主成分とするエアゾール用噴射剤組成物および
炭化水素類、エーテル類およびハロゲン化炭化水素類か
ら選ばれる少なくとも1種とR227cを含むエアゾー
ル用噴射剤組成物を提供するものである。
[Means for Solving the Problems] The present invention has been made to solve the above-mentioned problems.
, 3,3-heptafluoropropane (hereinafter referred to as R227c) as a main component, and an aerosol propellant composition containing R227c and at least one selected from hydrocarbons, ethers, and halogenated hydrocarbons. The present invention provides a drug composition.

【0008】本発明において、炭化水素類としては、エ
タン、プロパン,n−ブタン、イソブタン、ブチレン、
シクロペンタン,n−ペンタン、イソペンタン等あるい
は液化プロパン(プロパン/プロピレン)、液化ブタン
(ブタン/ブチレン)等のLPGが挙げられ、好ましく
は炭素数2〜5の炭化水素類である。これらは単独でま
た2種以上の混合物として使用でき、好ましくはLPG
である。
In the present invention, hydrocarbons include ethane, propane, n-butane, isobutane, butylene,
Examples include LPG such as cyclopentane, n-pentane, isopentane, liquefied propane (propane/propylene), and liquefied butane (butane/butylene), and preferably hydrocarbons having 2 to 5 carbon atoms. These can be used alone or as a mixture of two or more, preferably LPG
It is.

【0009】また、エーテル類としては、ジメチルエー
テル、メチルエチルエーテル、メチルプロピルエーテル
、メチルブチルエーテル、ジエチルエーテル、エチルプ
ロピルエーテル等の炭素数2〜5のエーテル類が好まし
く、特に毒性が低いことからジメチルエーテルが好適で
ある。これらは、単独または2種以上の混合物として使
用できる。
[0009] As the ethers, ethers having 2 to 5 carbon atoms such as dimethyl ether, methyl ethyl ether, methyl propyl ether, methyl butyl ether, diethyl ether, and ethyl propyl ether are preferable, and dimethyl ether is particularly preferred because of its low toxicity. suitable. These can be used alone or as a mixture of two or more.

【0010】ハロゲン化炭化水素類としては、トリクロ
ロモノフルオロメタン、ジクロロジフルオロメタン、ク
ロロジフルオロメタン、トリクロロトリフルオロエタン
、ジクロロテトラフルオロエタン、ジクロロトリフルオ
ロエタン、クロロテトラフルオロエタン、テトラフルオ
ロエタン、ジクロロフルオロエタン、クロロジフルオロ
エタン、ジクロロペンタフルオロプロパン、クロロヘキ
サフルオロプロパン、オクタフルオロシクロブタン等R
227c以外のハロゲン化炭化水素であり、これらは単
独または2種以上の混合物として使用できる。
Examples of halogenated hydrocarbons include trichloromonofluoromethane, dichlorodifluoromethane, chlorodifluoromethane, trichlorotrifluoroethane, dichlorotetrafluoroethane, dichlorotrifluoroethane, chlorotetrafluoroethane, tetrafluoroethane, and dichlorofluoroethane. Ethane, chlorodifluoroethane, dichloropentafluoropropane, chlorohexafluoropropane, octafluorocyclobutane, etc. R
It is a halogenated hydrocarbon other than 227c, and these can be used alone or in a mixture of two or more.

【0011】さらにこれらの炭化水素類、エーテル類お
よびハロゲン化炭化水素類を2種以上混合して使用する
こともできる。
Furthermore, two or more of these hydrocarbons, ethers and halogenated hydrocarbons may be used in combination.

【0012】炭化水素類、エーテル類およびハロゲン化
炭化水素類から選ばれる少なくとも1種とR227cか
らなる混合物の混合割合は、R227cが50〜90w
t%、炭化水素類が0〜50wt%、好ましくは5〜5
0wt%、エーテル類が0〜50wt%、好ましくは5
〜50wt%、ハロゲン化炭化水素類が0〜50wt%
、好ましくは5〜50wt%である。
[0012] The mixing ratio of the mixture consisting of at least one selected from hydrocarbons, ethers and halogenated hydrocarbons and R227c is such that R227c is 50 to 90w.
t%, hydrocarbons from 0 to 50 wt%, preferably from 5 to 5
0 wt%, ethers 0 to 50 wt%, preferably 5
~50wt%, 0 to 50wt% of halogenated hydrocarbons
, preferably 5 to 50 wt%.

【0013】本発明の組成物には、皮膚薬、制汗剤、水
虫薬、消臭剤等の各種薬剤、エタノール、イソプロピル
アルコール等のアルコール系溶媒、タルク、カオリン、
セライト、ベンガラ等の疎水性粉末あるいはニトロメタ
ン、エピクロルヒドリン等の防蝕剤等を配合しエアゾー
ル組成物とすることができる。
The composition of the present invention includes various drugs such as skin medicines, antiperspirants, athlete's foot medicines, and deodorants, alcoholic solvents such as ethanol and isopropyl alcohol, talc, kaolin,
An aerosol composition can be prepared by blending hydrophobic powders such as celite and red iron or anticorrosive agents such as nitromethane and epichlorohydrin.

【0014】[0014]

【実施例】以下に本発明の実施例を示す。 [実施例1〜12]制汗剤として使用した例を表1に、
虫よけ剤として使用した例を表2に、ヘアスプレーとし
て使用した例を表3に示す。なお、数字の単位は重量部
である。また、2,2−ジクロロ−1,1,1− トリ
フルオロエタンはR123、1−クロロ−1,1−ジフ
ルオロエタンはR142bと称する。
[Examples] Examples of the present invention are shown below. [Examples 1 to 12] Examples of use as antiperspirants are shown in Table 1.
Examples of use as an insect repellent are shown in Table 2, and examples of use as a hair spray are shown in Table 3. Note that the units of numbers are parts by weight. Further, 2,2-dichloro-1,1,1-trifluoroethane is referred to as R123, and 1-chloro-1,1-difluoroethane is referred to as R142b.

【0015】[0015]

【表1】[Table 1]

【0016】[0016]

【表2】[Table 2]

【0017】[0017]

【表3】[Table 3]

【0018】[0018]

【発明の効果】本発明の1,1,1,2,2,3,3−
ヘプタフルオロプロパンは、水素原子を含むので対流圏
での寿命が短く、さらに塩素原子を含まないのでオゾン
層を全く破壊しない。さらに、1,1,1,2,2,3
,3−ヘプタフルオロプロパンは、不燃性であり火災の
危険性がない。したがって、本発明のエアゾール用噴射
剤は環境への影響が極めて小さく、かつ実施例に示した
ように火災の危険性が極めて少なく優れたものである。
Effect of the invention: 1,1,1,2,2,3,3- of the present invention
Since heptafluoropropane contains hydrogen atoms, it has a short lifetime in the troposphere, and since it does not contain chlorine atoms, it does not destroy the ozone layer at all. Furthermore, 1, 1, 1, 2, 2, 3
,3-heptafluoropropane is nonflammable and poses no fire hazard. Therefore, the aerosol propellant of the present invention has an extremely small impact on the environment, and as shown in the Examples, has an extremely low risk of fire and is therefore excellent.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】1,1,1,2,2,3,3−ヘプタフル
オロプロパンを主成分とするエアゾール用噴射剤組成物
Claims: 1. An aerosol propellant composition containing 1,1,1,2,2,3,3-heptafluoropropane as a main component.
【請求項2】炭化水素類、エーテル類およびハロゲン化
炭化水素類から選ばれる少なくとも1種と1,1,1,
2,2,3,3−ヘプタフルオロプロパンを含むエアゾ
ール用噴射剤組成物。
2. At least one selected from hydrocarbons, ethers and halogenated hydrocarbons and 1,1,1,
An aerosol propellant composition comprising 2,2,3,3-heptafluoropropane.
【請求項3】炭化水素類がLPGである請求項2のエア
ゾール用噴射剤組成物。
3. The aerosol propellant composition according to claim 2, wherein the hydrocarbon is LPG.
【請求項4】エーテル類がジメチルエーテルである請求
項2のエアゾール用噴射剤組成物。
4. The aerosol propellant composition according to claim 2, wherein the ether is dimethyl ether.
【請求項5】ハロゲン化炭化水素類がトリクロロモノフ
ルオロメタン、ジクロロジフルオロメタン、クロロジフ
ルオロメタン、トリクロロトリフルオロエタン、ジクロ
ロテトラフルオロエタン、ジクロロトリフルオロエタン
、クロロテトラフルオロエタン、テトラフルオロエタン
、ジクロロフルオロエタン、クロロジフルオロエタン、
ジクロロペンタフルオロプロパン、クロロヘキサフルオ
ロプロパン、およびオクタフルオロシクロブタンから選
ばれる少なくとも1種である請求項2のエアゾール用噴
射剤組成物。
5. The halogenated hydrocarbons are trichloromonofluoromethane, dichlorodifluoromethane, chlorodifluoromethane, trichlorotrifluoroethane, dichlorotetrafluoroethane, dichlorotrifluoroethane, chlorotetrafluoroethane, tetrafluoroethane, dichlorofluoro ethane, chlorodifluoroethane,
The propellant composition for aerosol according to claim 2, which is at least one selected from dichloropentafluoropropane, chlorohexafluoropropane, and octafluorocyclobutane.
JP13191691A 1991-05-08 1991-05-08 Propellant composition for aerosol Withdrawn JPH04332786A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13191691A JPH04332786A (en) 1991-05-08 1991-05-08 Propellant composition for aerosol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13191691A JPH04332786A (en) 1991-05-08 1991-05-08 Propellant composition for aerosol

Publications (1)

Publication Number Publication Date
JPH04332786A true JPH04332786A (en) 1992-11-19

Family

ID=15069191

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13191691A Withdrawn JPH04332786A (en) 1991-05-08 1991-05-08 Propellant composition for aerosol

Country Status (1)

Country Link
JP (1) JPH04332786A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996033913A1 (en) 1995-04-28 1996-10-31 Great Lakes Chemical Corporation Novel uses of heptafluoropropane
US5672293A (en) * 1994-03-11 1997-09-30 E. I. Du Pont De Nemours And Company Hydrofluorocarbon compositions
US5681501A (en) * 1995-10-11 1997-10-28 E. I. Du Pont De Nemours And Company Compositions including a hydrofluoropropane
US6531441B1 (en) 1994-03-11 2003-03-11 E. I. Du Pont De Nemours And Company Hydrofluorocarbon compositions

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5672293A (en) * 1994-03-11 1997-09-30 E. I. Du Pont De Nemours And Company Hydrofluorocarbon compositions
US5785883A (en) * 1994-03-11 1998-07-28 E. I. Du Pont De Nemours And Company Hydrofluorocarbon compositions with tetrafluoroethane and cyclopropane
US6531441B1 (en) 1994-03-11 2003-03-11 E. I. Du Pont De Nemours And Company Hydrofluorocarbon compositions
US6846792B2 (en) 1994-03-11 2005-01-25 E. I. Du Pont De Nemours And Company Hydrofluorocarbon compositions
WO1996033913A1 (en) 1995-04-28 1996-10-31 Great Lakes Chemical Corporation Novel uses of heptafluoropropane
US5681501A (en) * 1995-10-11 1997-10-28 E. I. Du Pont De Nemours And Company Compositions including a hydrofluoropropane

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Effective date: 19980806