JPH01319581A - Solvent for removing adhesion moisture - Google Patents
Solvent for removing adhesion moistureInfo
- Publication number
- JPH01319581A JPH01319581A JP63152274A JP15227488A JPH01319581A JP H01319581 A JPH01319581 A JP H01319581A JP 63152274 A JP63152274 A JP 63152274A JP 15227488 A JP15227488 A JP 15227488A JP H01319581 A JPH01319581 A JP H01319581A
- Authority
- JP
- Japan
- Prior art keywords
- solvent
- dichloro
- tetrafluoropropane
- pentafluoropropane
- water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002904 solvent Substances 0.000 title claims abstract description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 6
- LYNCQSNLMRUIRI-UHFFFAOYSA-N 1,1,3-trichloro-1,2,2,3-tetrafluoropropane Chemical compound FC(Cl)C(F)(F)C(F)(Cl)Cl LYNCQSNLMRUIRI-UHFFFAOYSA-N 0.000 claims abstract 2
- WWNLOOSSVHRIFJ-UHFFFAOYSA-N 1,3,3-trichloro-1,1,2,2-tetrafluoropropane Chemical compound FC(F)(Cl)C(F)(F)C(Cl)Cl WWNLOOSSVHRIFJ-UHFFFAOYSA-N 0.000 claims abstract 2
- UJIGKESMIPTWJH-UHFFFAOYSA-N 1,3-dichloro-1,1,2,2,3-pentafluoropropane Chemical compound FC(Cl)C(F)(F)C(F)(F)Cl UJIGKESMIPTWJH-UHFFFAOYSA-N 0.000 claims abstract 2
- JMRCQLAMQGMJDF-UHFFFAOYSA-N 1,3-dichloro-1,1,2,2-tetrafluoropropane Chemical compound FC(F)(Cl)C(F)(F)CCl JMRCQLAMQGMJDF-UHFFFAOYSA-N 0.000 claims abstract 2
- FXSNEEBOGAOVIM-UHFFFAOYSA-N 1-chloro-1,2,2,3,3-pentafluoropropane Chemical compound FC(F)C(F)(F)C(F)Cl FXSNEEBOGAOVIM-UHFFFAOYSA-N 0.000 claims abstract 2
- COAUHYBSXMIJDK-UHFFFAOYSA-N 3,3-dichloro-1,1,1,2,2-pentafluoropropane Chemical compound FC(F)(F)C(F)(F)C(Cl)Cl COAUHYBSXMIJDK-UHFFFAOYSA-N 0.000 claims abstract 2
- WMCLYSGSAJGCJY-UHFFFAOYSA-N 3-chloro-1,1,2,2-tetrafluoropropane Chemical compound FC(F)C(F)(F)CCl WMCLYSGSAJGCJY-UHFFFAOYSA-N 0.000 claims abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 28
- 229930195733 hydrocarbon Natural products 0.000 claims description 9
- 150000002430 hydrocarbons Chemical class 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 5
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 150000002576 ketones Chemical class 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 2
- VOOXKKSIKFHMTJ-UHFFFAOYSA-N 1,1-dichloro-1,2,2-trifluoropropane Chemical compound CC(F)(F)C(F)(Cl)Cl VOOXKKSIKFHMTJ-UHFFFAOYSA-N 0.000 claims 1
- YZXSQDNPKVBDOG-UHFFFAOYSA-N 2,2-difluoropropane Chemical compound CC(C)(F)F YZXSQDNPKVBDOG-UHFFFAOYSA-N 0.000 claims 1
- 229920001971 elastomer Polymers 0.000 abstract description 4
- 239000000806 elastomer Substances 0.000 abstract description 4
- 239000002184 metal Substances 0.000 abstract description 4
- 229910052751 metal Inorganic materials 0.000 abstract description 4
- 229920003023 plastic Polymers 0.000 abstract description 4
- 239000004033 plastic Substances 0.000 abstract description 4
- 239000004973 liquid crystal related substance Substances 0.000 abstract description 3
- 150000002739 metals Chemical class 0.000 abstract description 3
- 150000005827 chlorofluoro hydrocarbons Chemical class 0.000 abstract 2
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- -1 inhexane Chemical compound 0.000 description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 8
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- 125000005907 alkyl ester group Chemical group 0.000 description 5
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 3
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N 1-nonene Chemical compound CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N 2,2-dimethylbutane Chemical compound CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 2
- OJVAMHKKJGICOG-UHFFFAOYSA-N 2,5-hexanedione Chemical compound CC(=O)CCC(C)=O OJVAMHKKJGICOG-UHFFFAOYSA-N 0.000 description 2
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 2
- ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 2
- MXLMTQWGSQIYOW-UHFFFAOYSA-N 3-methyl-2-butanol Chemical compound CC(C)C(C)O MXLMTQWGSQIYOW-UHFFFAOYSA-N 0.000 description 2
- HTSABYAWKQAHBT-UHFFFAOYSA-N 3-methylcyclohexanol Chemical compound CC1CCCC(O)C1 HTSABYAWKQAHBT-UHFFFAOYSA-N 0.000 description 2
- VLJXXKKOSFGPHI-UHFFFAOYSA-N 3-methylhexane Chemical compound CCCC(C)CC VLJXXKKOSFGPHI-UHFFFAOYSA-N 0.000 description 2
- HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 2
- MQWCXKGKQLNYQG-UHFFFAOYSA-N 4-methylcyclohexan-1-ol Chemical compound CC1CCC(O)CC1 MQWCXKGKQLNYQG-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- GOQYKNQRPGWPLP-UHFFFAOYSA-N heptadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- KPSSIOMAKSHJJG-UHFFFAOYSA-N neopentyl alcohol Chemical compound CC(C)(C)CO KPSSIOMAKSHJJG-UHFFFAOYSA-N 0.000 description 2
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 2
- SJWFXCIHNDVPSH-UHFFFAOYSA-N octan-2-ol Chemical compound CCCCCCC(C)O SJWFXCIHNDVPSH-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 125000006353 oxyethylene group Chemical group 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pentene-2 Natural products CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 description 2
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 229950011008 tetrachloroethylene Drugs 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 2
- NMRPBPVERJPACX-UHFFFAOYSA-N (3S)-octan-3-ol Natural products CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 1
- WUOACPNHFRMFPN-SECBINFHSA-N (S)-(-)-alpha-terpineol Chemical compound CC1=CC[C@@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-SECBINFHSA-N 0.000 description 1
- UKDOTCFNLHHKOF-FGRDZWBJSA-N (z)-1-chloroprop-1-ene;(z)-1,2-dichloroethene Chemical group C\C=C/Cl.Cl\C=C/Cl UKDOTCFNLHHKOF-FGRDZWBJSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- OZXIZRZFGJZWBF-UHFFFAOYSA-N 1,3,5-trimethyl-2-(2,4,6-trimethylphenoxy)benzene Chemical compound CC1=CC(C)=CC(C)=C1OC1=C(C)C=C(C)C=C1C OZXIZRZFGJZWBF-UHFFFAOYSA-N 0.000 description 1
- 239000005968 1-Decanol Substances 0.000 description 1
- VTBOTOBFGSVRMA-UHFFFAOYSA-N 1-Methylcyclohexanol Chemical compound CC1(O)CCCCC1 VTBOTOBFGSVRMA-UHFFFAOYSA-N 0.000 description 1
- HYFLWBNQFMXCPA-UHFFFAOYSA-N 1-ethyl-2-methylbenzene Chemical compound CCC1=CC=CC=C1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 1
- FDHDUXOBMHHFFJ-UHFFFAOYSA-N 1-pentylnaphthalene Chemical compound C1=CC=C2C(CCCCC)=CC=CC2=C1 FDHDUXOBMHHFFJ-UHFFFAOYSA-N 0.000 description 1
- WOFPPJOZXUTRAU-UHFFFAOYSA-N 2-Ethyl-1-hexanol Natural products CCCCC(O)CCC WOFPPJOZXUTRAU-UHFFFAOYSA-N 0.000 description 1
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 1
- TZYRSLHNPKPEFV-UHFFFAOYSA-N 2-ethyl-1-butanol Chemical compound CCC(CC)CO TZYRSLHNPKPEFV-UHFFFAOYSA-N 0.000 description 1
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- NDVWOBYBJYUSMF-UHFFFAOYSA-N 2-methylcyclohexan-1-ol Chemical compound CC1CCCCC1O NDVWOBYBJYUSMF-UHFFFAOYSA-N 0.000 description 1
- WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 description 1
- VSFMZSQMOLEVOM-UHFFFAOYSA-N 5-ethyl-5-methylcyclohexa-1,3-diene Chemical compound CCC1(C)CC=CC=C1 VSFMZSQMOLEVOM-UHFFFAOYSA-N 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 208000000453 Skin Neoplasms Diseases 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- OVKDFILSBMEKLT-UHFFFAOYSA-N alpha-Terpineol Natural products CC(=C)C1(O)CCC(C)=CC1 OVKDFILSBMEKLT-UHFFFAOYSA-N 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- 229940088601 alpha-terpineol Drugs 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- WVIIMZNLDWSIRH-UHFFFAOYSA-N cyclohexylcyclohexane Chemical compound C1CCCCC1C1CCCCC1 WVIIMZNLDWSIRH-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- SHOJXDKTYKFBRD-UHFFFAOYSA-N mesityl oxide Natural products CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- LQNPIBHEOATAEO-UHFFFAOYSA-N octanoate;octylazanium Chemical compound CCCCCCCCN.CCCCCCCC(O)=O LQNPIBHEOATAEO-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- BNIXVQGCZULYKV-UHFFFAOYSA-N pentachloroethane Chemical compound ClC(Cl)C(Cl)(Cl)Cl BNIXVQGCZULYKV-UHFFFAOYSA-N 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 210000002729 polyribosome Anatomy 0.000 description 1
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 description 1
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
- 201000000849 skin cancer Diseases 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Extraction Or Liquid Replacement (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明はレンズ、液晶表示装置部品、電子部品、精密機
械部品等の付着水除去用溶剤に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a solvent for removing water adhered to lenses, liquid crystal display device parts, electronic parts, precision mechanical parts, etc.
[従来の技術]
液晶表示装置部品、電子部品、精密機械部品等の水洗処
理後、水を付着したままでは製品とならない場合が多い
。従って、通常有機溶剤を用いて水の除去を行なってい
る。その有機溶剤として次に掲げるような種々の利点か
ら、1、L2−hリクロロー1.2.2−トリフルオロ
エタン(以下R113という)が広く使われている。[Prior Art] After washing parts of liquid crystal display devices, electronic parts, precision mechanical parts, etc., in many cases, products cannot be manufactured if water remains attached to them. Therefore, water is usually removed using an organic solvent. As the organic solvent, 1,L2-h-lichloro-1,2,2-trifluoroethane (hereinafter referred to as R113) is widely used because of the following various advantages.
R113は不燃性、非曝性で毒性が低く安定性も係れて
いる。しかも、金属、プラスチック、エラストマー等の
基材を侵さず何着水を除去することができる。一般に何
着水除去を行なう被処理物は金属、プラスチック、エラ
ストマー等からなる複合部品が多く、従ってこの点から
もR]、 13が有利であった。R113 is nonflammable, non-exposed, has low toxicity, and is stable. Furthermore, it is possible to remove water that has landed on the base material such as metal, plastic, or elastomer without damaging it. Generally, many of the objects to be treated are composite parts made of metals, plastics, elastomers, etc., and from this point of view as well, R], 13 was advantageous.
[発明が解決しようとする課題]
本発明は従来使用されていたR113が種々の利点を持
つにもかかわらず、成層圏のオゾンを破壊し、ひいては
皮膚ガンの発生をひき起す原因となる疑いがあることか
らそれに対応すべくR113と同様の水の除去が行なえ
る新規の付着水除去用溶剤を提供することを目的と1−
るものである。[Problems to be Solved by the Invention] The present invention solves the problem that although conventionally used R113 has various advantages, it is suspected that it destroys stratospheric ozone and causes skin cancer. Therefore, in order to cope with this problem, we aimed to provide a new solvent for removing adhered water that can remove water similar to R113.
It is something that
[課題を解決するだめの手段]
本発明は前述の目的を達成すべくなされたものであり、
炭素数が3である塩化弗化炭化水素を有効成分として含
有する44着水除去用溶剤を提供するものである。[Means for solving the problem] The present invention has been made to achieve the above-mentioned object,
The present invention provides a solvent for removing 44 water deposits containing a chlorofluorinated hydrocarbon having 3 carbon atoms as an active ingredient.
本発明の塩化弗化炭化水素としては1.]−ジクロ四−
2,2.3.3.3−ペンタフルオロプロパンfb、p
455°C)、1.3−シクロロー1.2,2.3.3
−ペンタフルオロプロパンい〕952°C) 、 1.
1.3−1−シクロロ−2,2,3,吐デトラフルオロ
ブロバン(b、p。The chlorinated fluorinated hydrocarbons of the present invention include 1. ]-Dichloro4-
2,2.3.3.3-pentafluoropropane fb,p
455°C), 1.3-cyclo1.2, 2.3.3
-Pentafluoropropane]952°C), 1.
1.3-1-cyclo-2,2,3,detrafluorobroban (b, p.
91.5°C) 、 1.3.3−1−シクロロー1.
2.2.3−テトラフルオロプロパン())、p、90
.5℃)、1−クロロ−1,,2,2,3,3−ペンタ
フルオロプロパン(11,p、 43.9”C)、1.
3−シフo v′I−2,2,3,3−テトラフルオロ
プロパン(b、 p、 68℃)、1−り四ロー2.2
.3.3−テトラフルオロプロパン(13,1)54°
C)、1.]−]ジクロロ−1,2,2−1−リフルオ
ロプロパン(1)、[]、 60.2”C)、1.3−
ジクロロ−2,2,−ジフルオロプロパン(1)、p、
9G、7°G1.1.X−シフOロー2,2.−ジフル
オロプロパン(b、p、79℃)及び1−り四ロー2.
2−シフルオロブロバン(b、 p、 55゜1°C)
等の水素含有塩化弗化炭化水素から選ばれる1種又(′
j2種以上の混合物が好ましい。91.5°C), 1.3.3-1-cyclo1.
2.2.3-Tetrafluoropropane ()), p, 90
.. 5°C), 1-chloro-1,,2,2,3,3-pentafluoropropane (11,p, 43.9”C), 1.
3-Schiffov'I-2,2,3,3-tetrafluoropropane (b, p, 68°C), 1-di-4-2.2
.. 3.3-tetrafluoropropane (13,1) 54°
C), 1. ]-]Dichloro-1,2,2-1-lifluoropropane (1), [], 60.2"C), 1.3-
Dichloro-2,2,-difluoropropane (1), p,
9G, 7°G1.1. X-Shiffo Low 2,2. -difluoropropane (b, p, 79°C) and 1-di-4-2.
2-cyfluoroblobane (b, p, 55°1°C)
One type selected from hydrogen-containing chlorinated fluorinated hydrocarbons such as
j A mixture of two or more types is preferred.
オ\発明の付着水除去用溶剤にも」、各種の目的に応し
てその他の各種成分を含有させることができる。例えば
、付着水除去効果を高めるために、炭化水素類、アルコ
ール類、ケトン類、又は、塩素化炭化水素類等の有機溶
剤あるい(」界面活性剤から選ばれる少なくとも1種を
含有させることができる。これらの有機溶剤の例着水除
去用溶剤中の含有割合は、0〜50重量%、好ましくは
10〜40重景%、置部に好ましくは20〜30重量%
である。本発明の塩化弗化炭化水素す〕と有機溶剤との
混合物に共沸組成が存在する場合には、その共沸組成で
の使用が好ましい。The solvent for removing adhered water of the invention can also contain various other components depending on various purposes. For example, in order to enhance the effect of removing attached water, at least one selected from organic solvents such as hydrocarbons, alcohols, ketones, or chlorinated hydrocarbons, or surfactants may be included. The content of these organic solvents in the solvent for removing deposited water is 0 to 50% by weight, preferably 10 to 40% by weight, and preferably 20 to 30% by weight.
It is. When the mixture of the chlorofluorinated hydrocarbon of the present invention and the organic solvent has an azeotropic composition, it is preferable to use the azeotropic composition.
界面活性剤の付着水除去用溶剤中の含有割合は、0〜1
0重量%、好ましくは0.1〜5重量%、さらに好まし
くは0.2〜1重量%である。The content ratio of surfactant in the solvent for removing adhered water is 0 to 1.
0% by weight, preferably 0.1-5% by weight, more preferably 0.2-1% by weight.
炭化水素類としては炭素数1〜15の直鎖又は環状の飽
和又は不飽和炭化水素類が好ましく、n−ペンタン、イ
ソペンタン、n−ヘキサン、インヘキサン、2−メチル
ペンタン、2.2−ジメチルブタン、2.3−ジメチル
ブタン、n−へブタン、イソへブタン、3−メチルヘキ
ザン、2.4−ジメチルペンクン、n−オフクン、2−
メチルへブタン、3−メチルヘブクン、4−メヂルヘブ
タン、2.2−シメヂルヘキ勺ン、2.5−ジメチルブ
タン、3.3−ジメチルブタン、2−メチル−3−エチ
ルベンクン、3−メチル−3−エチルベンクン、2、3
.3−1−リンチルベンクン、2,3.4−トリメチル
ベンクン、2.2.3−トリメチルペンクン、イソオフ
クン、ノナン、2.2.5− トリメチルヘキサン、デ
カン、ドデンカン、1−ペンテン、2−ペンテン、1−
ヘキサン、1−オクテン、1−ノネン、1−デセン、シ
クロベンクン、メチルシクロベンクン、シクロヘキサン
、メチルシクロヘキサン、エチルシクロヘキザン、ビシ
クロヘキサン、シクロヘキサン、α−ピネン、ジペンテ
ン、デカリン、テトラリン、アミクン、アミルナフタレ
ン等から選ばれるものである。より好ましくは、n−ベ
ンクン、n−ヘキサン、シクロヘキサン、n−へブタン
等である。The hydrocarbons are preferably linear or cyclic saturated or unsaturated hydrocarbons having 1 to 15 carbon atoms, such as n-pentane, isopentane, n-hexane, inhexane, 2-methylpentane, 2,2-dimethylbutane. , 2.3-dimethylbutane, n-hebutane, isohebutane, 3-methylhexane, 2.4-dimethylpenkune, n-ofukun, 2-
Methylhebutane, 3-methylhebutane, 4-methylhebutane, 2.2-dimethylbutane, 2.5-dimethylbutane, 3.3-dimethylbutane, 2-methyl-3-ethylbenzene, 3-methyl-3-ethylbenzene, 2, 3
.. 3-1-lyntylbencune, 2,3.4-trimethylbencune, 2.2.3-trimethylpencune, isofucune, nonane, 2.2.5-trimethylhexane, decane, dodencane, 1-pentene, 2 -Pentene, 1-
Hexane, 1-octene, 1-nonene, 1-decene, cyclobencune, methylcyclobencune, cyclohexane, methylcyclohexane, ethylcyclohexane, bicyclohexane, cyclohexane, α-pinene, dipentene, decalin, tetralin, amicun, amylnaphthalene, etc. It is selected from More preferred are n-benkune, n-hexane, cyclohexane, n-hebutane and the like.
アルコール類としては、炭素数1〜17の鎖状又は環状
の飽和又は不飽和アルコール類が好ましく、メタノール
、エタノール、n−プロピルアルコール、イソプロピル
アルコール、n−ブチルアルコール、5ec−ブチルア
ルコール、イソブチルアルコール、tert−ブチルア
ルコール、ペンデルアルコール、5ec−アミルアルコ
ール、1−エチル−1−プロパツール、2−メチル−1
−ブクノール、イソペンチルアルコール、tert−ペ
ンチルアルコール、3−メチル−2−ブタノール、ネオ
ペンチルアルコール、1−へギザノール、2−メチル−
1−ヘプタツール、4−メチル−2−ペンタノール、2
−エチル−1−ブタノール、1−ヘプタツール、2−へ
ノナノール、3−ヘプタツール、l−オクタノール、2
−オクタノール、2−エチル−1−ヘキサノール、1−
ノナノール、3.5.5−1−ジメチル−1−へギザノ
ール、1−デカノール、l−ウンデカノール、1−ドデ
カノール、アリルアルコール、プロパルギルアルコール
、ペンシルアルコール、シクロヘギザノール、1−メチ
ルシクロヘキサノール、2−メチルシクロへギザノール
、3−メチルシクロヘキサノール、4−メチルシクロヘ
キサノール、α−テルピネオール、アビエヂノール、2
.6−シメチルー4−ヘプタツール、トリメデルノニル
アルコール、テトラデシルアルコール、ヘプタデシルア
ルコール等がら選ばれるものである。より好ましくはメ
タノール、エタノール、イソプロピルアルコール等であ
る。The alcohols are preferably linear or cyclic saturated or unsaturated alcohols having 1 to 17 carbon atoms, such as methanol, ethanol, n-propyl alcohol, isopropyl alcohol, n-butyl alcohol, 5ec-butyl alcohol, isobutyl alcohol, tert-butyl alcohol, pendel alcohol, 5ec-amyl alcohol, 1-ethyl-1-propatol, 2-methyl-1
-Bukunol, isopentyl alcohol, tert-pentyl alcohol, 3-methyl-2-butanol, neopentyl alcohol, 1-hegizanol, 2-methyl-
1-heptatool, 4-methyl-2-pentanol, 2
-Ethyl-1-butanol, 1-heptatool, 2-henonanol, 3-heptatool, l-octanol, 2
-octanol, 2-ethyl-1-hexanol, 1-
Nonanol, 3.5.5-1-Dimethyl-1-hegizanol, 1-decanol, l-undecanol, 1-dodecanol, allyl alcohol, propargyl alcohol, pencil alcohol, cyclohegizanol, 1-methylcyclohexanol, 2 -Methylcyclohexanol, 3-methylcyclohexanol, 4-methylcyclohexanol, α-terpineol, abiedinol, 2
.. It is selected from 6-dimethyl-4-heptatool, trimedelnonyl alcohol, tetradecyl alcohol, heptadecyl alcohol and the like. More preferred are methanol, ethanol, isopropyl alcohol and the like.
、ロ
ケトン却としては、R−Co−R、R−CO,R−CO
−R’−炭素数]〜9の飽和又は不飽和炭化水素基)の
いずれかの−能代で示されるものが好ましく、アセトン
、メチルエチルケトン、2−ペンタノン、3−ペンタノ
ン、2−ヘキサノン、メチル−〇−ブグールケトン、メ
チルブヂルケトン、2−ヘプタノン、4−ヘプタノン、
ジイソブチルケトン、アセトニルアセトン、メシチルオ
キシド、ホロン、メチル−n−アミルケトン、エチルブ
ヂルケトン、メチルヘキシルケトン、シクロヘギザノン
、メチルシクロへギザノン、イソホロン、2.4−ペン
クンジオン、ジアセトンアルコール、アセトフェノン、
フェンチョン等から選ばれるものである。より好ましく
はアセトン、メチルエチルケトン等である。, as a rocketton, R-Co-R, R-CO, R-CO
-R'-carbon number] to 9 saturated or unsaturated hydrocarbon groups) represented by -Noshiro are preferred, such as acetone, methyl ethyl ketone, 2-pentanone, 3-pentanone, 2-hexanone, methyl-〇 -bugol ketone, methyl butyl ketone, 2-heptanone, 4-heptanone,
Diisobutyl ketone, acetonylacetone, mesityl oxide, holone, methyl-n-amyl ketone, ethyl butyl ketone, methylhexyl ketone, cyclohexanone, methylcyclohegizanone, isophorone, 2,4-penkendione, diacetone alcohol, acetophenone,
It is selected from Feng Chong et al. More preferred are acetone, methyl ethyl ketone and the like.
塩素化炭化水素類としては、炭素数1〜2の飽和又は不
飽和、塩素化炭化水素類が好ましく、塩化メチレン、四
塩化炭素、1,1−ジクロルエタン、1.2−ジクロロ
エタン、1.1.1−トリクロルエタン、1.1.2−
トリクロルエタン、1.1,1.2−テトラクロルエタ
ン、1.1.2.2−テトラクロルエタン、ペンタクロ
ルエタン、1.1−ジクロルエチレン、1,2−ジクロ
ルエチレン、トリクロルエタン、テトラクロルエチレン
等がら選ばれるものである。より好ましくは塩化メチレ
ン、]、、1.1〜トリクロルエタン、l・ジクロルエ
チレン、テトラクロルエチレン等である。The chlorinated hydrocarbons are preferably saturated or unsaturated chlorinated hydrocarbons having 1 to 2 carbon atoms, such as methylene chloride, carbon tetrachloride, 1,1-dichloroethane, 1.2-dichloroethane, 1.1. 1-Trichloroethane, 1.1.2-
Trichloroethane, 1.1,1.2-tetrachloroethane, 1.1.2.2-tetrachloroethane, pentachloroethane, 1.1-dichloroethylene, 1,2-dichloroethylene, trichloroethane, It is selected from tetrachlorethylene and the like. More preferred are methylene chloride, 1.1 to trichloroethane, l-dichloroethylene, tetrachlorethylene, and the like.
界面活性剤としては、付着水除去用として通常用いられ
る各種のものから選択可能であるが、好ましくは、ポリ
オキシエチレンアルキルエステル、ボリオキシエチレン
ポリオキシブロビレンアルキルエーテル、ポリオキシエ
チレンアルキルエステル、ボリオキシェヂレンボリオキ
シプロビレンアルキルエステル、ポリオギシエヂレンア
ルキルフェノール、ボリオギシエチレンボリブロピレン
アルキルフェノール、ポリオキシエチレンアルキルエス
テル、ボリオキシエヂレンボリオキシブロビレンソルビ
クンエステル、カプリル酸カプリルアミン、ポリオキシ
エチレンアルキルアミド等から選ばれるものある。より
好ましくはカプリル酸カプリルアミン、ポリオキシエチ
レンアルキルアミドである。The surfactant can be selected from various commonly used surfactants for removing adhered water, but preferably polyoxyethylene alkyl ester, polyoxyethylene polyoxybrobylene alkyl ether, polyoxyethylene alkyl ester, and polyoxyethylene alkyl ester are used. Oxyethylene polyoxypropylene alkyl ester, polyoxyethylene polyoxyethylene alkyl phenol, polyoxyethylene polyoxypropylene alkyl phenol, polyoxyethylene alkyl ester, polyoxyethylene polyoxypropylene sorbicune ester, caprylic acid caprylamine, poly Some are selected from oxyethylene alkylamides and the like. More preferred are caprylamine caprylate and polyoxyethylene alkylamide.
本発明の付着水除去用溶剤による付着水除去方法として
は、スプレーや、シャワーによる方法あるいは冷浴、温
浴、蒸気浴又は超音波浴による浸漬法あるいはこれらの
浴を組み合せる浸漬法を採用することができる。As a method for removing adhered water using the solvent for removing adhered water of the present invention, a method using a spray, a shower method, an immersion method using a cold bath, a hot bath, a steam bath, or an ultrasonic bath, or an immersion method using a combination of these baths may be adopted. I can do it.
[実施例]
実施例1〜16
下記第1表に示す付着水除去用溶剤を用いて付着水の除
去試験を行なった。[Example] Examples 1 to 16 A test for removing adhered water was conducted using the solvent for removing adhered water shown in Table 1 below.
30mmX 18mmX 5mm厚のガラス板を純水に
浸漬後、イ」着水除去用溶剤中に20秒間浸漬して水切
りを行ない、取り出したガラス板を無水メタノール中に
浸漬してその水分増加量から付着水の除去状況を調べた
。結果を第1表に示す。After immersing a 30 mm x 18 mm x 5 mm thick glass plate in pure water, immersing it in a solvent for removing water deposits for 20 seconds to drain the water, and then immersing the removed glass plate in anhydrous methanol to remove adhesion from the increased amount of water. The status of water removal was investigated. The results are shown in Table 1.
第1表
()内は混合比[重1%]
O良好に除去できる ○:はぼ良好△、微量残存
×:かなり残存[発明の効果]
本発明の付着水除去用溶剤は実施例から明らかなように
付着水の除去効果の優れたものである。Table 1 () shows the mixing ratio [1% by weight] O: Good removal ○: Very good △, trace amount remaining ×: Significant amount remaining [Effects of the invention] The solvent for removing adhered water of the present invention is clear from the examples. As shown, it has an excellent effect of removing attached water.
又、従来使用されていたR113と同様、金属、プラス
チック、エラストマー等を侵す作用が少ないことからこ
れらの複合部品の水切りに悪影響を与えることなく、付
着水な除去することができる。Also, like the conventionally used R113, it has little effect on attacking metals, plastics, elastomers, etc., so it is possible to remove adhering water without adversely affecting the drainage of these composite parts.
化111人(弁理士)平不1411イ111 people (patent attorneys) 1411 people
Claims (1)
して含有する付着水除去用溶剤。(2)塩化弗化炭化水
素が1,1−ジクロロ−2,2,3,3,3−ペンタフ
ルオロプロパン、1,3−ジクロロ−1,2,2,3,
3−ペンタフルオロプロパン、1,1,3−トリクロロ
−2,2,3,3−テトラフルオロプロパン、1,3,
3−トリクロロ−1,2,2,3−テトラフルオロプロ
パン、1−クロロ−1,2,2,3,3−ペンタフルオ
ロプロパン、1,3−ジクロロ−2,2,3,3−テト
ラフルオロプロパン、1−クロロ−2,2,3,3−テ
トラフルオロプロパン、1,1−ジクロロ−1,2,2
−トリフルオロプロパン、1,3−ジクロロ−2,2,
−ジフルオロプロパン、1,1−ジクロロ−2,2,−
ジフルオロプロパン、1−クロロ−2,2,−ジフルオ
ロプロパンである請求項1記載の付着水除去用溶剤。 (3)付着水除去用溶剤中には、炭化水素類、アルコー
ル類、ケトン類、塩素化炭化水素類又は界面活性剤から
選ばれる少なくとも1種が含まれている請求項1記載の
付着水除去用溶剤。[Scope of Claims] (1) A solvent for removing adhered water containing a chlorofluorinated hydrocarbon having 3 carbon atoms as an active ingredient. (2) Chlorinated fluorinated hydrocarbons include 1,1-dichloro-2,2,3,3,3-pentafluoropropane, 1,3-dichloro-1,2,2,3,
3-pentafluoropropane, 1,1,3-trichloro-2,2,3,3-tetrafluoropropane, 1,3,
3-Trichloro-1,2,2,3-tetrafluoropropane, 1-chloro-1,2,2,3,3-pentafluoropropane, 1,3-dichloro-2,2,3,3-tetrafluoro Propane, 1-chloro-2,2,3,3-tetrafluoropropane, 1,1-dichloro-1,2,2
-trifluoropropane, 1,3-dichloro-2,2,
-difluoropropane, 1,1-dichloro-2,2,-
The solvent for removing adhered water according to claim 1, which is difluoropropane or 1-chloro-2,2,-difluoropropane. (3) The adhered water removal method according to claim 1, wherein the adhered water removal solvent contains at least one selected from hydrocarbons, alcohols, ketones, chlorinated hydrocarbons, or surfactants. Solvent for use.
Priority Applications (23)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63152274A JPH0824805B2 (en) | 1988-06-22 | 1988-06-22 | Solvent for removing adhered water |
PCT/JP1989/000617 WO1989012674A1 (en) | 1988-06-22 | 1989-06-21 | Halogenated hydrocarbon solvents and use thereof |
CA000603532A CA1339150C (en) | 1988-06-22 | 1989-06-21 | Halogenated hydrocarbon solvents and use thereof |
SU894743271A RU1838449C (en) | 1988-06-22 | 1989-06-21 | Defatting agent, cleansing agent, agent for polishing composition removing, agent for flux removing, agent for residual water removing, agent for resist removing, and agent for resist development |
AU36685/89A AU615309B2 (en) | 1988-06-22 | 1989-06-21 | Halogenated hydrocarbon solvents and use thereof |
CS893732A CZ279988B6 (en) | 1988-06-22 | 1989-06-21 | Cleansing agent and use thereof |
KR1019900700377A KR950013923B1 (en) | 1988-06-22 | 1989-06-21 | Halogenated hydrocarbon solvents |
ES89111412T ES2083368T3 (en) | 1988-06-22 | 1989-06-22 | USE OF HALOGENATED HYDROCARBON SOLVENTS AS CLEANING AGENTS. |
AT89111412T ATE131863T1 (en) | 1988-06-22 | 1989-06-22 | USE OF HALOGENIC HYDROCARBON SOLVENT AS A CLEANING AGENT |
AT94112231T ATE187542T1 (en) | 1988-06-22 | 1989-06-22 | USE OF HALOGENIC HYDROCARBON SOLVENTS |
DE68925155T DE68925155T2 (en) | 1988-06-22 | 1989-06-22 | Use of halogenated hydrocarbon solvent as a cleaning agent |
EP94112231A EP0631190B1 (en) | 1988-06-22 | 1989-06-22 | Use of halogenated hydrocarbon solvents |
HU893192A HU207700B (en) | 1988-06-22 | 1989-06-22 | Halogenated hydrocarbon solvents and their application |
EP89111412A EP0347924B1 (en) | 1988-06-22 | 1989-06-22 | Use of halogenated hydrocarbon solvents as cleaning agents |
DE68929111T DE68929111T2 (en) | 1988-06-22 | 1989-06-22 | Use of halogenated hydrocarbon solvents |
ES94112231T ES2141183T3 (en) | 1988-06-22 | 1989-06-22 | USE OF HALOGENATED HYDROCARBON SOLVENTS. |
CN89104329A CN1035116C (en) | 1988-06-22 | 1989-06-22 | Hologenated hydsocarbon solvents and thereof |
NO900824A NO176443C (en) | 1988-06-22 | 1990-02-21 | Halogenated hydrocarbon solvents and their use |
US07/591,473 US5271775A (en) | 1988-06-22 | 1990-10-01 | Methods for treating substrates by applying a halogenated hydrocarbon thereto |
US07/602,041 US5116426A (en) | 1988-06-22 | 1990-10-25 | Method of cleaning a substrate using a dichloropentafluoropropane |
US07/984,241 US5302313A (en) | 1988-06-22 | 1992-12-01 | Halogenated hydrocarbon solvents |
GR960400761T GR3019361T3 (en) | 1988-06-22 | 1996-03-19 | Use of halogenated hydrocarbon solvents as cleaning agents |
GR20000400600T GR3032905T3 (en) | 1988-06-22 | 2000-03-08 | Use of halogenated hydrocarbon solvents. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63152274A JPH0824805B2 (en) | 1988-06-22 | 1988-06-22 | Solvent for removing adhered water |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01319581A true JPH01319581A (en) | 1989-12-25 |
JPH0824805B2 JPH0824805B2 (en) | 1996-03-13 |
Family
ID=15536924
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63152274A Expired - Fee Related JPH0824805B2 (en) | 1988-06-22 | 1988-06-22 | Solvent for removing adhered water |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0824805B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104294305A (en) * | 2014-09-30 | 2015-01-21 | 江苏中容铜业有限公司 | Quickly prepared copper material decontaminant |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01304195A (en) * | 1988-05-31 | 1989-12-07 | Daikin Ind Ltd | Azeotropic composition |
JPH01304194A (en) * | 1988-05-31 | 1989-12-07 | Daikin Ind Ltd | Azeotropic composition |
-
1988
- 1988-06-22 JP JP63152274A patent/JPH0824805B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01304195A (en) * | 1988-05-31 | 1989-12-07 | Daikin Ind Ltd | Azeotropic composition |
JPH01304194A (en) * | 1988-05-31 | 1989-12-07 | Daikin Ind Ltd | Azeotropic composition |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104294305A (en) * | 2014-09-30 | 2015-01-21 | 江苏中容铜业有限公司 | Quickly prepared copper material decontaminant |
Also Published As
Publication number | Publication date |
---|---|
JPH0824805B2 (en) | 1996-03-13 |
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