JPH0827036A - Liquid solvent composition - Google Patents
Liquid solvent compositionInfo
- Publication number
- JPH0827036A JPH0827036A JP16020894A JP16020894A JPH0827036A JP H0827036 A JPH0827036 A JP H0827036A JP 16020894 A JP16020894 A JP 16020894A JP 16020894 A JP16020894 A JP 16020894A JP H0827036 A JPH0827036 A JP H0827036A
- Authority
- JP
- Japan
- Prior art keywords
- component
- solvent
- molecular weight
- composition
- agents
- 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
- 239000002904 solvent Substances 0.000 title claims abstract description 37
- 239000000203 mixture Substances 0.000 title claims abstract description 23
- 239000007788 liquid Substances 0.000 title claims abstract description 13
- 239000010702 perfluoropolyether Substances 0.000 claims abstract description 25
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims abstract description 9
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 9
- 239000000443 aerosol Substances 0.000 claims abstract description 7
- 150000002170 ethers Chemical class 0.000 claims abstract description 7
- 238000009835 boiling Methods 0.000 claims abstract description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 12
- 239000003380 propellant Substances 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 3
- 239000002216 antistatic agent Substances 0.000 claims description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 3
- 239000000314 lubricant Substances 0.000 claims description 3
- 230000003449 preventive effect Effects 0.000 claims description 3
- 239000003082 abrasive agent Substances 0.000 claims description 2
- 239000000853 adhesive Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 claims description 2
- 230000000844 anti-bacterial effect Effects 0.000 claims description 2
- 239000003899 bactericide agent Substances 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 238000004140 cleaning Methods 0.000 claims description 2
- 239000012459 cleaning agent Substances 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 239000002537 cosmetic Substances 0.000 claims description 2
- 238000001514 detection method Methods 0.000 claims description 2
- 239000003599 detergent Substances 0.000 claims description 2
- 239000002917 insecticide Substances 0.000 claims description 2
- 238000004078 waterproofing Methods 0.000 claims description 2
- 239000008199 coating composition Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 239000002932 luster Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract description 13
- 239000003960 organic solvent Substances 0.000 abstract description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract description 8
- 229930195733 hydrocarbon Natural products 0.000 abstract description 6
- 150000002430 hydrocarbons Chemical class 0.000 abstract description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 abstract description 6
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 4
- 239000001273 butane Substances 0.000 abstract description 4
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 abstract description 4
- 239000001294 propane Substances 0.000 abstract description 4
- 125000000217 alkyl group Chemical group 0.000 abstract description 3
- 238000005507 spraying Methods 0.000 abstract 1
- 238000002156 mixing Methods 0.000 description 9
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 7
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- 230000005484 gravity Effects 0.000 description 6
- 239000012046 mixed solvent Substances 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 3
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 2
- XNMQEEKYCVKGBD-UHFFFAOYSA-N 2-butyne Chemical compound CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 2
- PFEOZHBOMNWTJB-UHFFFAOYSA-N 3-methylpentane Chemical compound CCC(C)CC PFEOZHBOMNWTJB-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methylcyclopentane Chemical compound CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- -1 polysiloxane Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 description 2
- 239000012855 volatile organic compound Substances 0.000 description 2
- PMJHHCWVYXUKFD-PLNGDYQASA-N (3z)-penta-1,3-diene Chemical compound C\C=C/C=C PMJHHCWVYXUKFD-PLNGDYQASA-N 0.000 description 1
- FFJCNSLCJOQHKM-CLFAGFIQSA-N (z)-1-[(z)-octadec-9-enoxy]octadec-9-ene Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCCCCCCC\C=C/CCCCCCCC FFJCNSLCJOQHKM-CLFAGFIQSA-N 0.000 description 1
- QMMOXUPEWRXHJS-HYXAFXHYSA-N (z)-pent-2-ene Chemical compound CC\C=C/C QMMOXUPEWRXHJS-HYXAFXHYSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- PZHIWRCQKBBTOW-UHFFFAOYSA-N 1-ethoxybutane Chemical compound CCCCOCC PZHIWRCQKBBTOW-UHFFFAOYSA-N 0.000 description 1
- BPIUIOXAFBGMNB-UHFFFAOYSA-N 1-hexoxyhexane Chemical compound CCCCCCOCCCCCC BPIUIOXAFBGMNB-UHFFFAOYSA-N 0.000 description 1
- AOPDRZXCEAKHHW-UHFFFAOYSA-N 1-pentoxypentane Chemical compound CCCCCOCCCCC AOPDRZXCEAKHHW-UHFFFAOYSA-N 0.000 description 1
- HEWZVZIVELJPQZ-UHFFFAOYSA-N 2,2-dimethoxypropane Chemical compound COC(C)(C)OC HEWZVZIVELJPQZ-UHFFFAOYSA-N 0.000 description 1
- MHNNAWXXUZQSNM-UHFFFAOYSA-N 2-methylbut-1-ene Chemical compound CCC(C)=C MHNNAWXXUZQSNM-UHFFFAOYSA-N 0.000 description 1
- GXDHCNNESPLIKD-UHFFFAOYSA-N 2-methylhexane Natural products CCCCC(C)C GXDHCNNESPLIKD-UHFFFAOYSA-N 0.000 description 1
- AEXMKKGTQYQZCS-UHFFFAOYSA-N 3,3-dimethylpentane Chemical compound CCC(C)(C)CC AEXMKKGTQYQZCS-UHFFFAOYSA-N 0.000 description 1
- LAIUFBWHERIJIH-UHFFFAOYSA-N 3-Methylheptane Chemical compound CCCCC(C)CC LAIUFBWHERIJIH-UHFFFAOYSA-N 0.000 description 1
- JJDGTGGQXAAVQX-UHFFFAOYSA-N 6-methyl-1-(6-methylheptoxy)heptane Chemical compound CC(C)CCCCCOCCCCCC(C)C JJDGTGGQXAAVQX-UHFFFAOYSA-N 0.000 description 1
- DFVOXRAAHOJJBN-UHFFFAOYSA-N 6-methylhept-1-ene Chemical compound CC(C)CCCC=C DFVOXRAAHOJJBN-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- AQEFLFZSWDEAIP-UHFFFAOYSA-N di-tert-butyl ether Chemical compound CC(C)(C)OC(C)(C)C AQEFLFZSWDEAIP-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- ZUBZATZOEPUUQF-UHFFFAOYSA-N isononane Chemical compound CCCCCCC(C)C ZUBZATZOEPUUQF-UHFFFAOYSA-N 0.000 description 1
- 239000003915 liquefied petroleum gas Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- RVZRBWKZFJCCIB-UHFFFAOYSA-N perfluorotributylamine Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)N(C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F RVZRBWKZFJCCIB-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- FLTJDUOFAQWHDF-UHFFFAOYSA-N trimethyl pentane Natural products CCCCC(C)(C)C FLTJDUOFAQWHDF-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
Landscapes
- Medicinal Preparation (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Lubricants (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、溶剤組成物に係るもの
であって、不燃性のパーフルオロポリエーテルと、従来
混和することがないとされていた有機溶媒のうち、均一
混和可能なものを見出したものであって、火気に対する
災害危険が低減するため、家庭、工業、公共の産業分野
で、その利用範囲は極めて広いものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a solvent composition, which is a non-combustible perfluoropolyether and an organic solvent which has not been conventionally miscible, and which can be uniformly mixed. Since the risk of fire disaster is reduced, its application range is extremely wide in household, industrial, and public industrial fields.
【0002】[0002]
【従来の技術】低燃性の溶剤に関して、従来は、含塩素
有機溶剤ならびにフロン系溶剤をもって目的を達してい
た。エアゾールについても、フロン系噴射剤を用いた不
燃性が普通であった。然るに、オゾン層破壊の地球環境
問題からフロンおよび含塩素系溶剤の或種は規制対象と
なり、加えて発癌性物質さらにVOC(揮散性有機化合
物)の対象に挙げられ、それらの使用は殆んど出来ない
現状にある。即ち第4回モントリオール国際会議で、ト
リクロロエタンならびCFCは1996年をもって凍結
し、HCFCの数種は漸次縮小し2030年までに全廃
の方向に決定された。2. Description of the Related Art Conventionally, a low-flammability solvent has been achieved by using a chlorine-containing organic solvent and a fluorocarbon solvent. As for the aerosol, the non-flammability using the CFC propellant was common. However, due to global environmental problems such as ozone depletion, some of the CFCs and chlorine-containing solvents are subject to regulation, and in addition to carcinogenic substances and VOCs (volatile organic compounds), most of them are used. It is in a situation where it cannot be done. That is, at the 4th International Conference on Montreal, trichloroethane and CFC were frozen in 1996, and some HCFCs were gradually reduced, and by 2030 it was decided to abolish them.
【0003】これらの状況は環境問題からいえば当然で
あるとしても、他に代替溶剤を求めるとすれば、可燃性
溶剤を採用せざるを得ない故に、火炎の危険は免れず保
安上問題を生ずるケースがあり、早急に代替低燃性溶剤
の開発が嘱望されている現状にある。Even if these circumstances are natural from an environmental point of view, if alternative solvents are sought, flammable solvents have to be adopted, so that the danger of flames is inevitable and a safety problem arises. In some cases, there is an urgent need for the development of alternative low-flammability solvents.
【0004】[0004]
【発明が解決しようとする課題】低燃性溶剤の開発にあ
たり、まず燃性の少ない液体化合物を探索すると、パー
フルオロポリエーテル(以下PFPEとも記す。)が最
も有望である。本発明者の実験データでも、それ本体は
全く燃性を有せず、他物質の燃焼も阻止する能力も大で
ある。しかしPFPEの欠点は、己公知の文献によれ
ば、イ)フロン系溶剤を除き、有機溶剤・油脂・水に対
して全く不溶であること、ロ)使用目的上の有効成分を
溶解しないこと、ハ)比重が重すぎること、ニ)経済的
に価格が高いこと等」が挙げられている。In developing a low flammability solvent, when a liquid compound having low flammability is searched for, perfluoropolyether (hereinafter also referred to as PFPE) is most promising. According to the experimental data of the present inventor, the body itself has no flammability and has a great ability to prevent the burning of other substances. However, the disadvantages of PFPE are, according to self-known documents, a) that it is completely insoluble in organic solvents, fats and oils, except for freon-based solvents, and b) that it does not dissolve the active ingredient for its intended purpose. C) Too much specific gravity, d) Economically high prices, etc. ”
【0005】例えば、低燃性の塗料に対し、この塗料の
溶剤にPFPEを採用して燃性を抑制しようとした場
合、PFPEは塗料樹脂を全く溶解しないから、他の溶
剤を配合して修正しようとしても相溶せず分離してしま
う。微細コロイドにして分散する手段も、比重差が大き
過ぎて結局不適となるのである。本発明は上記の欠点を
克服し、不燃性のパーフルオロポリエーテルと有機溶媒
とが均一に相溶し、火気に対する災害危険が低減された
液体溶剤組成物を得ることを目的とする。For example, when it is attempted to suppress the flammability of a low-flammability paint by using PFPE as a solvent for this paint, PFPE does not dissolve the paint resin at all, and therefore other solvents are blended for correction. Even if you try, they will not be compatible and will separate. The means for dispersing in the form of fine colloid is also unsuitable because the difference in specific gravity is too large. It is an object of the present invention to overcome the above-mentioned drawbacks and to obtain a liquid solvent composition in which a non-flammable perfluoropolyether and an organic solvent are homogeneously compatible with each other and the risk of injury to fire is reduced.
【0006】[0006]
【課題を解決するための手段】本発明者は、上記の課題
を解決するため、フロン系溶剤以外で、PFPEと均一
に相溶する溶剤と、その範囲を探索し、「PFPEを4
〜96wt%と、分子量44〜129の脂肪族炭化水素
類及び/又は分子量46〜242のエーテル類を4〜9
6wt%の組成範囲」とすることにより、目的を達成し
た。この組成物を、洗浄剤・溶剤・化学反応用溶媒に用
いることが出来、また目的とする有効成分を溶解または
分散して、塗料、染料、被覆剤、艶光剤、潤滑剤、防錆
剤、接着剤、洗浄剤、研磨剤、防水剤、探傷剤、離型
剤、静電防止剤、殺虫剤、殺菌剤、化粧料または人体用
品等を製造することが出来、その内にはエアゾール製品
をも包含する。In order to solve the above-mentioned problems, the present inventor searched for a solvent other than a CFC-based solvent that is uniformly compatible with PFPE and its range, and found that "PFPE
.About.96 wt% and 4 to 9 of aliphatic hydrocarbons having a molecular weight of 44 to 129 and / or ethers having a molecular weight of 46 to 242.
The object was achieved by setting the composition range of 6 wt%. This composition can be used as a detergent / solvent / solvent for chemical reaction, and can dissolve or disperse a desired active ingredient to prepare a paint, dye, coating agent, brightening agent, lubricant, rust preventive agent. , Adhesives, cleaning agents, abrasives, waterproofing agents, flaw detection agents, mold release agents, antistatic agents, insecticides, bactericides, cosmetics or human products, among which aerosol products can be manufactured. Also includes.
【0007】さて、まずPFPEに各種溶剤を配合し、
均一に相溶するかを診た結果を表1に掲示するが、この
結果より、脂肪族炭化水素とエーテル類が均一に混和す
ることが伺える。この実験はPFPEと他の溶剤とを
1:1の割合で混合した結果であり、そのうち可能性の
ある上述の2類別した化合物系を詳細に調べた結果、表
2の如くであった。First, by mixing various solvents into PFPE,
The results of examining whether they are compatible with each other are shown in Table 1. From these results, it can be seen that the aliphatic hydrocarbons and ethers are uniformly mixed. This experiment was a result of mixing PFPE and another solvent in a ratio of 1: 1. As a result of detailed examination of the above-mentioned two categorized compound systems, it was as shown in Table 2.
【0008】表1、表2の結果をみると、従来、PFP
Eは「如何なる溶剤とも混合は困難で炭化水素とでも最
大4%である」とされていたが、本発明者は此の定説を
覆し、分子量44〜129の脂肪族炭化水素類と分子量
46〜242のエーテル類のみがPFPEと相溶するこ
とを見だしたのである。Looking at the results in Tables 1 and 2, it can be seen that the conventional PFP
E was said to be "it is difficult to mix with any solvent and the maximum is 4% with hydrocarbons", but the present inventor overturned this established theory, and aliphatic hydrocarbons having a molecular weight of 44 to 129 and molecular weights of 46 to It was found that only the 242 ethers were compatible with PFPE.
【0009】 分子量44〜129の脂肪族炭化水
素:プロパン、ブタンのような低分子量の物質にあって
は混合割合の全領域で均一に混和するが、C5 以上にな
ると分子量の増大に比例して均一混合の範囲は狭くな
り、C10以上は実用上無理があると認められる。ただ
し、側鎖型になると混和性は著しく増し、不飽和型も同
様に混和性は増す。シクロ型は混和性が劣るが使用でき
ないことはない。また工業的にはこれらの混合物、例え
ば石油エーテル、リグロイン、分解ナフサ、等も使用可
能である。Aliphatic hydrocarbons having a molecular weight of 44 to 129: For low molecular weight substances such as propane and butane, they are uniformly mixed in the entire mixing ratio region, but when C 5 or more, they are proportional to the increase in molecular weight. As a result, the range of uniform mixing becomes narrow, and it is recognized that C 10 or more is practically unreasonable. However, the miscibility of the side chain type increases remarkably, and the miscibility of the unsaturated type also increases. The cyclo type has poor miscibility but can be used. Further, industrially, mixtures of these, such as petroleum ether, ligroin, decomposed naphtha, etc., can also be used.
【0010】 分子量46〜242のエーテル:Oに
結合するアルキル基、R1 ,R2 において、C3 までは
混合割合の全領域で均一に混和する。分子量の増大と共
に混和範囲は狭くなり、C9 以上では実用性がない。炭
化水素と同様、側鎖型、不飽和型は混和性を著しく増
す。Ether having a molecular weight of 46 to 242: alkyl groups bonded to O, R 1 and R 2 , up to C 3 are uniformly mixed in the entire mixing ratio region. The mixing range becomes narrower as the molecular weight increases, and it is not practical for C 9 or more. Similar to hydrocarbons, the side-chain type and unsaturated type greatly increase the miscibility.
【0011】本発明の施用において、及び/又はか
ら選ばれた1種または2種以上を組み合わせるものであ
る。ここにおいて、プロパン、ブタン、ジメチルエーテ
ル等は常温ではガス体で、加圧下で液化ガスであるの
で、エアゾールの噴射剤としても用いるが、密閉容器内
では溶剤の作用をしている。In the application of the present invention, one kind or a combination of two or more kinds selected from and / or is selected. Here, propane, butane, dimethyl ether, and the like are gas bodies at room temperature and are liquefied gases under pressure, so they are also used as an aerosol propellant, but they act as a solvent in a closed container.
【0012】[0012]
【表1】 [Table 1]
【0013】[0013]
【表2】 [Table 2]
【0014】さて、本発明においていう、パーフルオロ
ポリエーテル(PFPE)とは、化学式〔I〕で示すフ
ッ化アルカンポリエーテルで、その重合数m,nによ
り、その物性は異なるが、何れも無色の比重の高い透明
液体で、化学的に極めて安定とされている。六フッ化プ
ロピレンを酸化重合して得られる。現在市販している商
品名とそのメーカー:i)“ガルデン”モンテカチーニ
社、ii) “フォンブリ”モンテフルオス社、iii)“フロ
リナート”スリーエム社があり、それらのカタログによ
れば、平均分子量380〜1550、沸点56〜252
℃、比重1.68〜2.03、粘度0.4〜73cSt
の広範囲にわたる間で、各々約10種類のバライティの
ある銘柄が挙げられている。In the present invention, the perfluoropolyether (PFPE) is a fluorinated alkane polyether represented by the chemical formula [I], the physical properties of which differ depending on the polymerization numbers m and n, but both are colorless. It is a transparent liquid with high specific gravity and is chemically extremely stable. It is obtained by oxidative polymerization of propylene hexafluoride. Trade names and their manufacturers currently on the market: i) "Garden" Montecatini, ii) "Fonburi" Montefluos, iii) "Florinato" 3M, and their catalogs show average molecular weights of 380 to 1550. Boiling point 56-252
C, specific gravity 1.68 to 2.03, viscosity 0.4 to 73 cSt
In each of a wide range of brands, about 10 types of varieties are listed.
【0015】[0015]
【化1】 Embedded image
【0016】次に、本発明においていう、分子量44〜
129の脂肪族炭化水素とは、概ね次掲のとおりである
が、異性体など多数あるのでそれら等は均等物として取
り扱う事とする。またこれらの混合物をメーカーから特
定商品として販売しているケースもある。Next, in the present invention, the molecular weight of 44 to
The 129 aliphatic hydrocarbons are generally as follows, but since there are many isomers and the like, they are treated as equivalents. There are also cases where these mixtures are sold as specific products by manufacturers.
【0017】i)飽和炭化水素;プロパン、ブタン、イ
ソブタン、ペンタン、イソペンタン、n−ヘキサン、2
−メチルペンタン、3−メチルペンタン、n−ヘプタ
ン、ジメチルペンタン、メチルヘキサン、n−オクタ
ン、トリメチルペンタン、ジメチルヘプタン、エチルメ
チルペンタン、等。I) saturated hydrocarbons: propane, butane, isobutane, pentane, isopentane, n-hexane, 2
-Methylpentane, 3-methylpentane, n-heptane, dimethylpentane, methylhexane, n-octane, trimethylpentane, dimethylheptane, ethylmethylpentane, etc.
【0018】ii) 不飽和炭化水素:イソプレン、イソブ
チレン、2−メチルプロペン、ブタジエン、2−メチル
−1,3−ブタジエン、1−ペンテン、cis−2−ペ
ンテン、2−メチル−1−ブテン、trans−2−ペ
ンテン、2−ブチン、cis−1,3−ペンタジェン、
ジイソブチレン、イソオクテン、等。Ii) Unsaturated hydrocarbons: isoprene, isobutylene, 2-methylpropene, butadiene, 2-methyl-1,3-butadiene, 1-pentene, cis-2-pentene, 2-methyl-1-butene, trans. -2-pentene, 2-butyne, cis-1,3-pentadiene,
Diisobutylene, isooctene, etc.
【0019】iii) 環状炭化水素:シクロペンタン、シ
クロヘキサン、シクロペンタジエン、シクロペンテン、
メチルシクロペンタン、等。 iv) 混合炭化水素商品:ベンジン、ガソリン、石油エー
テル(リグロイン)、吹付塗料シンナー、石油ナフサ、
水添ナフサ、ソルベントナフサ、n−パラフィン、キョ
ーワゾールC−600、等。Iii) Cyclic hydrocarbons: cyclopentane, cyclohexane, cyclopentadiene, cyclopentene,
Methylcyclopentane, etc. iv) Mixed hydrocarbon products: benzine, gasoline, petroleum ether (ligroin), spray paint thinner, petroleum naphtha,
Hydrogenated naphtha, solvent naphtha, n-paraffin, Kyowasol C-600, etc.
【0020】また次に、本発明においていう、分子量4
6〜242のエーテル類とは、具体的にRがC1 〜C8
のアルキル基をもつエーテル族であり、次掲のごとき化
合物である。ジメチルエーテル、エチルエーテル、イソ
プロピルエーテル、エチルブチルエーテル、ブチルエー
テル、tert−ブチルエーテル、アミルエーテル、ヘ
キシルエーテル、イソオクチルエーテル、エルチビニー
ルエーテル、2,2−ジメトキシプロパン、等。Further, in the present invention, the molecular weight of 4
The ethers of 6 to 242 specifically mean that R is C 1 to C 8
Is an ether group having an alkyl group of and is a compound as described below. Dimethyl ether, ethyl ether, isopropyl ether, ethyl butyl ether, butyl ether, tert-butyl ether, amyl ether, hexyl ether, isooctyl ether, eltivinyl ether, 2,2-dimethoxypropane, etc.
【0021】上記の脂肪族炭化水素およびエーテル類
で、分子量の小さいもの・側鎖型のものは、配合全領域
で相溶した混合溶剤となるが、分子量が大きくなるに従
って、その領域範囲は縮小する。相溶しない場合は、溶
質の偏斥が起きるし、比重差から可燃性溶剤が上層に浮
上し、炎を引火する故に、両成分は完全に均一な相とな
ることが必要条件である。その成分範囲は、両成分の各
個別の物質によっても異なり、また要求される燃焼性の
程度によっても制限が違うから一概に言えないが、4%
以下では溶剤の性質に際立った改質は認められなく、P
FPEにあっても然りであるので、本発明の液体溶剤組
成物を構成する各成分の組成範囲を4〜96wt%と設
定した。The above aliphatic hydrocarbons and ethers having a small molecular weight / side chain type are mixed solvents compatible with each other in the entire compounding region, but the range of the region decreases as the molecular weight increases. To do. When they are not compatible with each other, the solute is biased, the flammable solvent floats to the upper layer due to the difference in specific gravity, and the flame ignites. Therefore, it is necessary that both components be in a completely uniform phase. The range of its components varies depending on the individual substances of both components, and the limit varies depending on the degree of flammability required.
In the following, no remarkable modification of the properties of the solvent was observed.
Since this is true even for FPE, the composition range of each component constituting the liquid solvent composition of the present invention was set to 4 to 96 wt%.
【0022】[0022]
【作 用】不燃性溶剤の考え方として、溶媒の蒸気が燃
焼範囲外の構成となる組合わせとすることであり、PF
PEはその重合度によっても違うが25℃で165to
rのものがあり、これをもって可燃性溶剤の蒸気圧を押
さえる作用をする。[Operation] The idea of non-flammable solvents is to combine them so that the vapors of the solvents are out of the combustion range.
PE depends on the degree of polymerization, but at 165 to 25 ° C
There is one of r, which acts to suppress the vapor pressure of the flammable solvent.
【0023】図1は、PFPE<フロリナートPC−7
2>と、2−メチルペンタンまたはジイソプロピルエー
テルの各混合割合の引火点を求めた結果のグラフであ
る。この可燃有機溶剤は何れも第一種可燃物であるが、
PFPEの10%又は20%の配合によって、第二種可
燃物(引火点−7.6℃以上)となし得。そうすると消
防法規上の取扱いが異なってくる効果が見だせる。FIG. 1 shows PFPE <Fluorinert PC-7.
It is a graph of the result which calculated | required the flash point of each 2> and each mixing ratio of 2-methyl pentane or diisopropyl ether. All of these combustible organic solvents are Class I combustibles,
It can be made as a second class combustible substance (flash point -7.6 ° C or higher) by blending 10% or 20% of PFPE. If this is done, the effect that handling under the Fire Service Law will differ can be found.
【0024】また、他物質の溶解性は、混合組成の夫々
の性質をもつ。表3は、PFPE<ガルデンFTX>:
2−メチルペンタンまたはジイソプロピルエーテル=
1:1の混合溶媒が、他成分の溶解力を測定した結果を
纏めたものである。この実験では、混合溶媒が他成分を
大量に溶解すると二層に分離してしまう現象を示す場合
があり、この場合は二層分離しない迄の溶解度をSとし
て記した。この様に他物質を溶解する事実より、この混
合溶剤は各方面への応用が見だせる。Further, the solubility of other substances has respective properties of the mixed composition. Table 3 shows PFPE <Galden FTX>:
2-methylpentane or diisopropyl ether =
The 1: 1 mixed solvent is a collection of the results of measuring the dissolving power of other components. In this experiment, when the mixed solvent dissolves a large amount of other components, it may show a phenomenon of separating into two layers. In this case, the solubility until the two layers are not separated is described as S. Due to the fact that it dissolves other substances in this way, this mixed solvent finds application in various fields.
【0025】[0025]
【表3】 [Table 3]
【0026】[0026]
【実施例】以下実施例を挙げて本発明を具体的に説明す
るが、本発明はこれらに限定されるものではない。 実施例1 配合 PFPE<ガルデンFTX> 40wt% ジイソブチレン 30wt% ジブチルエーテル 30wt% 合 計 100wt% EXAMPLES The present invention will be described in detail with reference to the following examples, but the present invention is not limited thereto. Example 1 Formulation PFPE <Galden FTX> 40 wt% Diisobutylene 30 wt% Dibutyl ether 30 wt% Total 100 wt%
【0027】上記によって調合した混合物は、無色透
明、均一に相和した液体で、下記特性を有する。 比重 15/4 1.042 引火点 22℃ 粘度 cps 0.68 蒸発潜熱 Cal/kg 47.2The mixture prepared as described above is a colorless, transparent, and uniformly compatible liquid, and has the following characteristics. Specific gravity 15/4 1.042 Flash point 22 ° C Viscosity cps 0.68 Latent heat of vaporization Cal / kg 47.2
【0028】本品は洗浄液としての応用がある。例え
ば、ブレーキクリーナは自動車の定期点検に必須である
が、本品の使用実験では、汚染油・粉塵アスベストの洗
去がよく、適度の乾燥と作業性が優れているとの評価で
あった。なお現在使用のヘプタンに比べて、火気に対す
る危険性が極減するものである。This product has application as a cleaning liquid. For example, a brake cleaner is indispensable for periodical inspection of automobiles, but in the use experiment of this product, it was evaluated that contaminated oil and dust asbestos were washed off well, and that it was reasonably dry and excellent in workability. The risk of fire is much less than that of heptane currently used.
【0029】実施例2 処方 (1)原液 メチルポリシロキサン 4.0wt% パラフィン 6.0wt% ブチルエーテル 15.0wt% テトラエチレングリコールジメチルエーテル 5.0wt% PFPEガルデンHT100 70.0wt% 合 計 100wt%Example 2 Formulation (1) Stock solution Methyl polysiloxane 4.0 wt% Paraffin 6.0 wt% Butyl ether 15.0 wt% Tetraethylene glycol dimethyl ether 5.0 wt% PFPE Galden HT100 70.0 wt% Total 100 wt%
【0030】本品は建物・家具・自動車等の艶出剤、自
転車・サッシ等の金属製品の防錆剤、引き戸・蝶番等の
潤滑剤、に用いる。又、下記の様にエアゾールとしても
使用する。原液65重量部に対し、(2)噴射剤とし
て、3kg/cm2 G液化石油ガス35重量部の割合
で耐圧缶に充填し、常法により、エアゾールとする。火
炎長9.5cm。This product is used as a polish for buildings, furniture, automobiles, etc., a rust preventive for metal products such as bicycles, sashes, and a lubricant for sliding doors, hinges, etc. It is also used as an aerosol as described below. (2) 35 parts by weight of 3 kg / cm 2 G liquefied petroleum gas as a propellant with respect to 65 parts by weight of the stock solution is filled in a pressure-resistant can and made into an aerosol by a conventional method. Flame length 9.5 cm.
【0031】実施例3 処方 リン酸エステル化シリコーン 0.3wt% プロピレングリコール 0.3wt% ポリオキシエチレンオレイルエーテル 0.1wt% PFPEガルデンHT70 72.3wt% ジメチルエーテル 27.0wt% 合 計 100wt%Example 3 Formulation Phosphoesterified silicone 0.3 wt% Propylene glycol 0.3 wt% Polyoxyethylene oleyl ether 0.1 wt% PFPE Galden HT70 72.3 wt% Dimethyl ether 27.0 wt% Total 100 wt%
【0032】本品は、エアゾール製品であり、ガラスの
曇止め剤、静電防止剤、として用いられる。飛行機・戦
車などの軍事用、化学工場の監視用ブラウン管・ミラー
の磨き用に、引火の危険ある場所で使用するものであ
る。This product is an aerosol product and is used as an antifog agent for glass and an antistatic agent. It is used in places where there is a risk of ignition, such as for military purposes such as airplanes and tanks, and for polishing cathode ray tubes and mirrors for monitoring chemical plants.
【0033】[0033]
【発明の効果】本発明は、不燃性であるが他物質を全く
溶かさないPFPEと、他物質を溶かす能力はあるが可
燃性である有機溶剤を組合わせて、両方の特長を活かし
た混合溶剤を提供するにある。従来、PFPEはフロン
溶剤を除き他の有機溶剤と混合しないとされていたとこ
ろ、本発明者は詳細な探索を行い、2種類の相溶する有
機溶剤を見だして本発明を完成したものである。地球環
境問題から、フロン系・塩素系溶剤の特定物質規制によ
り、不燃溶剤はほとんど使用できなくなったが、場所・
場合により、必要となるケースがあり、本発明はその需
要に応えるものとして評価されるべきである。The present invention combines a non-flammable PFPE that does not dissolve other substances at all with an organic solvent that has the ability to dissolve other substances but is flammable, and is a mixed solvent that makes full use of the features of both. To provide. Conventionally, PFPE was considered not to be mixed with other organic solvents except for CFC solvents, but the present inventor conducted a detailed search and found two types of compatible organic solvents to complete the present invention. is there. Due to global environmental issues, non-flammable solvents have become almost unusable due to restrictions on CFC-based and chlorine-based solvents.
In some cases, this may be necessary and the present invention should be evaluated as meeting that need.
【図1】本発明の液体溶剤組成物の具体例において、P
FPEの混合割合による引火点の変化を調べた実験結果
を示すグラフである。FIG. 1 shows an example of the liquid solvent composition of the present invention, in which P
It is a graph which shows the experimental result which investigated the change of the flash point by the mixing ratio of FPE.
フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C07C 43/04 Z 7419−4H 43/12 7419−4H 43/275 C08L 71/02 LQE C09B 67/42 Z C09K 3/30 F R C10M 107/32 107/38 C11D 7/50 // C10N 40:36 Continuation of the front page (51) Int.Cl. 6 Identification number Reference number within the agency FI Technical indication location C07C 43/04 Z 7419-4H 43/12 7419-4H 43/275 C08L 71/02 LQE C09B 67/42 Z C09K 3/30 FR C10M 107/32 107/38 C11D 7/50 // C10N 40:36
Claims (4)
t%と、分子量44〜129の脂肪族炭化水素類及び/
又は分子量46〜242のエーテル類を4〜96wt%
の組成範囲にあって、均一に相溶してなる液体溶剤組成
物。1. Perfluoropolyether 4 to 96w
t% and aliphatic hydrocarbons having a molecular weight of 44 to 129 and /
Or 4-96 wt% of ethers having a molecular weight of 46-242
A liquid solvent composition having a uniform composition in the above composition range.
浄液、溶剤、または化学反応用溶媒。2. A cleaning liquid, a solvent, or a solvent for chemical reaction, which comprises the liquid composition according to claim 1.
的とする有効成分を溶解または分散してなる、塗料、染
料、被覆剤、艶光剤、潤滑剤、防錆剤、接着剤、洗浄
剤、溶洗剤、研磨剤、防水剤、探傷剤、離型剤、静電防
止剤、殺虫剤、殺菌剤、化粧料または人体用製剤。3. A coating composition, a dye, a coating, a luster, a lubricant, a rust preventive, an adhesive, which is obtained by dissolving or dispersing the liquid composition of claim 1 and the desired active ingredient. Cleaning agents, detergents, abrasives, waterproofing agents, flaw detection agents, release agents, antistatic agents, insecticides, bactericides, cosmetics or human body preparations.
沸点をもつ脂肪族炭化水素類及び/又はエーテル類を噴
射剤として用いることによりなるエアゾール製品。4. The aerosol product according to claim 1, which comprises using an aliphatic hydrocarbon and / or ether having a boiling point of −49 to + 20 ° C. as a propellant.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16020894A JPH0827036A (en) | 1994-07-12 | 1994-07-12 | Liquid solvent composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16020894A JPH0827036A (en) | 1994-07-12 | 1994-07-12 | Liquid solvent composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0827036A true JPH0827036A (en) | 1996-01-30 |
Family
ID=15710100
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16020894A Pending JPH0827036A (en) | 1994-07-12 | 1994-07-12 | Liquid solvent composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0827036A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1767091A3 (en) * | 2005-09-21 | 2007-08-22 | Clariant Produkte (Deutschland) GmbH | Biocidal compositions |
| JP2007314798A (en) * | 2000-10-27 | 2007-12-06 | Procter & Gamble Co | Method for treating or cleaning a domestic surface |
| US9705056B2 (en) | 2012-02-09 | 2017-07-11 | Dow Corning Corporation | Gradient polymer structures and methods |
-
1994
- 1994-07-12 JP JP16020894A patent/JPH0827036A/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007314798A (en) * | 2000-10-27 | 2007-12-06 | Procter & Gamble Co | Method for treating or cleaning a domestic surface |
| EP1767091A3 (en) * | 2005-09-21 | 2007-08-22 | Clariant Produkte (Deutschland) GmbH | Biocidal compositions |
| US9705056B2 (en) | 2012-02-09 | 2017-07-11 | Dow Corning Corporation | Gradient polymer structures and methods |
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