JPH01139104A - Solvent for removing adhered water - Google Patents
Solvent for removing adhered waterInfo
- Publication number
- JPH01139104A JPH01139104A JP29519187A JP29519187A JPH01139104A JP H01139104 A JPH01139104 A JP H01139104A JP 29519187 A JP29519187 A JP 29519187A JP 29519187 A JP29519187 A JP 29519187A JP H01139104 A JPH01139104 A JP H01139104A
- Authority
- JP
- Japan
- Prior art keywords
- solvent
- water
- dichloro
- removing adhered
- adhered 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.)
- Pending
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 39
- 239000002904 solvent Substances 0.000 title claims abstract description 23
- 239000004094 surface-active agent Substances 0.000 claims abstract description 6
- 150000001298 alcohols Chemical class 0.000 claims abstract description 5
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 claims abstract description 5
- 150000002576 ketones Chemical class 0.000 claims abstract description 5
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 4
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 4
- FRCHKSNAZZFGCA-UHFFFAOYSA-N 1,1-dichloro-1-fluoroethane Chemical compound CC(F)(Cl)Cl FRCHKSNAZZFGCA-UHFFFAOYSA-N 0.000 claims abstract 3
- SKDFWEPBABSFMG-UHFFFAOYSA-N 1,2-dichloro-1,1-difluoroethane Chemical compound FC(F)(Cl)CCl SKDFWEPBABSFMG-UHFFFAOYSA-N 0.000 claims abstract 3
- OHMHBGPWCHTMQE-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)C(Cl)Cl OHMHBGPWCHTMQE-UHFFFAOYSA-N 0.000 claims abstract 3
- 239000000203 mixture Substances 0.000 claims description 10
- 239000004480 active ingredient Substances 0.000 claims description 3
- 230000000694 effects Effects 0.000 abstract description 5
- 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
- 230000002411 adverse Effects 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract description 2
- -1 dodencane Chemical compound 0.000 description 19
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 9
- 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
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-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
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 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
- QPRQEDXDYOZYLA-UHFFFAOYSA-N 2-methylbutan-1-ol Chemical compound CCC(C)CO QPRQEDXDYOZYLA-UHFFFAOYSA-N 0.000 description 3
- GXDHCNNESPLIKD-UHFFFAOYSA-N 2-methylhexane Natural products CCCCC(C)C GXDHCNNESPLIKD-UHFFFAOYSA-N 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-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
- BZHMBWZPUJHVEE-UHFFFAOYSA-N 2,4-dimethylpentane Chemical compound CC(C)CC(C)C BZHMBWZPUJHVEE-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
- ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 2
- DUPUVYJQZSLSJB-UHFFFAOYSA-N 3-ethyl-2-methylpentane Chemical compound CCC(CC)C(C)C DUPUVYJQZSLSJB-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
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-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
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-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
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical group 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
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-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
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methylcyclopentane Chemical compound CC1CCCC1 GDOPTJXRTPNYNR-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
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 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
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 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
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 2
- WGECXQBGLLYSFP-UHFFFAOYSA-N (+-)-2,3-dimethyl-pentane Natural products CCC(C)C(C)C WGECXQBGLLYSFP-UHFFFAOYSA-N 0.000 description 1
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 1
- 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
- QVLAWKAXOMEXPM-UHFFFAOYSA-N 1,1,1,2-tetrachloroethane Chemical compound ClCC(Cl)(Cl)Cl QVLAWKAXOMEXPM-UHFFFAOYSA-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
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 1
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-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
- OKVWYBALHQFVFP-UHFFFAOYSA-N 2,3,3-trimethylpentane Chemical compound CCC(C)(C)C(C)C OKVWYBALHQFVFP-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
- AEXMKKGTQYQZCS-UHFFFAOYSA-N 3,3-dimethylpentane Chemical compound CCC(C)(C)CC AEXMKKGTQYQZCS-UHFFFAOYSA-N 0.000 description 1
- BODRLKRKPXBDBN-UHFFFAOYSA-N 3,5,5-Trimethyl-1-hexanol Chemical compound OCCC(C)CC(C)(C)C BODRLKRKPXBDBN-UHFFFAOYSA-N 0.000 description 1
- GIEZWIDCIFCQPS-UHFFFAOYSA-N 3-ethyl-3-methylpentane Chemical compound CCC(C)(CC)CC GIEZWIDCIFCQPS-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
- VGVHNLRUAMRIEW-UHFFFAOYSA-N 4-methylcyclohexan-1-one Chemical compound CC1CCC(=O)CC1 VGVHNLRUAMRIEW-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
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical group CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 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
- 229940088601 alpha-terpineol Drugs 0.000 description 1
- XTKDAFGWCDAMPY-UHFFFAOYSA-N azaperone Chemical compound C1=CC(F)=CC=C1C(=O)CCCN1CCN(C=2N=CC=CC=2)CC1 XTKDAFGWCDAMPY-UHFFFAOYSA-N 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- WVIIMZNLDWSIRH-UHFFFAOYSA-N cyclohexylcyclohexane Chemical compound C1CCCCC1C1CCCCC1 WVIIMZNLDWSIRH-UHFFFAOYSA-N 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- SHOJXDKTYKFBRD-UHFFFAOYSA-N mesityl oxide Natural products CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- LQNPIBHEOATAEO-UHFFFAOYSA-N octanoate;octylazanium Chemical compound CCCCCCCCN.CCCCCCCC(O)=O LQNPIBHEOATAEO-UHFFFAOYSA-N 0.000 description 1
- ACXGEQOZKSSXKV-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O.CCCCCCCC(O)=O ACXGEQOZKSSXKV-UHFFFAOYSA-N 0.000 description 1
- BNIXVQGCZULYKV-UHFFFAOYSA-N pentachloroethane Chemical compound ClC(Cl)C(Cl)(Cl)Cl BNIXVQGCZULYKV-UHFFFAOYSA-N 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000005437 stratosphere Substances 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 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
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、精密機械部品笠の水洗処
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(i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、1.1.2−1−リクロロー1.2.2− トリ
フルオロエタン(以ド旧13という)が広く使われてい
る。[Prior Art] After washing liquid crystal display device parts, electronic parts, and precision machinery parts caps with water, they often cannot be used as products if water remains attached to them. Therefore, water is usually removed using organic solvents.As the organic solvent, 1.1.2-1-lichloro1.2.2-trifluoroethane has various advantages as listed below. (hereinafter referred to as old 13) is widely used.
R113は不燃性、非曝性でJ性が低く安定性も優れて
いる。しかも、金属、プラスチック、エラストマー等の
基材を侵さず付着水を除去することができる。一般に付
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R113が有利であった。R113 is nonflammable, non-exposed, has low J properties, and has excellent stability. Moreover, adhering water can be removed without damaging base materials such as metals, plastics, and elastomers. In general, many of the objects to be treated from which attached water is removed are composite parts made of metal, plastic, elastomer, etc. Therefore, R113 was advantageous from this point as well.
[発明の解決しようとする問題点]
本発明は従来使用されていた旧13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
h’=1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
するものである。[Problems to be Solved by the Invention] Despite the conventionally used old 13 having various advantages, the present invention destroys ozone in the stratosphere and eventually causes the occurrence of skin h'=1 cancer. Since there is a suspicion that this may be a cause, the object of this invention is to provide a new solvent for removing adhered water that can remove water in the same way as R113.
[問題点を解決するための手段]
本発明は前述の目的を達成すべくなされたものであり、
1.1−ジクロロ−2,2,2−トリフルオロエタン(
以下R123という)又は1.2−ジクロロ−1,1−
ジフルオロエタン(以下RI32bという)の1種と1
.1−ジクロロ−1−フルオロエタン(以下R141b
という)との共沸組成物を有効成分として含有する付着
水除去用溶剤を提供するものである。[Means for solving the problems] The present invention has been made to achieve the above-mentioned objects,
1.1-dichloro-2,2,2-trifluoroethane (
(hereinafter referred to as R123) or 1,2-dichloro-1,1-
One type of difluoroethane (hereinafter referred to as RI32b) and one
.. 1-dichloro-1-fluoroethane (hereinafter referred to as R141b)
The purpose of the present invention is to provide a solvent for removing adhered water, which contains an azeotropic composition with (referred to as ) as an active ingredient.
本発明の付着水除去用溶剤の有効成分であるR123/
R141b=約67733の共沸組成物又はR132b
/R141b・約15.5/84.5の共沸組成物(共
沸側合は重量%)は、付着水除去を行なう被処理物を侵
さず付着水を除去できる等、従来のR113と同様な利
点を有する優れた溶剤である。これら2種の共沸組成物
はそれぞれ単独で又はこれらの混合物として用いること
ができる。R123/ which is the active ingredient of the solvent for removing adhered water of the present invention
R141b = azeotropic composition of about 67733 or R132b
The azeotropic composition of /R141b/approximately 15.5/84.5 (azeotropic side ratio by weight) is similar to conventional R113, such as being able to remove adhered water without attacking the object to be treated. It is an excellent solvent with many advantages. These two types of azeotropic compositions can be used individually or as a mixture thereof.
本発明の付着水除去用溶剤には、各種の目的に応じてそ
の他の各種成分を含有させることができる。例えば、付
r1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(7機溶
剤あるいは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。これらのイ1°機溶剤の付着水
除去用溶剤中の含有割合は、0〜50重量%、好ましく
は10〜40巾量%、さらに好ましくは20〜30市量
%である。本発明の共沸組成物と有機溶剤との混合物に
共沸組成がひ在する場合には、その共沸組成での使用が
好ましい。The solvent for removing adhered water of the present invention can contain various other components depending on various purposes. For example, in order to enhance the water removal effect, at least one solvent selected from hydrocarbons, alcohols, ketones, or chlorinated hydrocarbons or surfactants may be included. The content of these 1° mechanical solvents in the solvent for removing adhered water is 0 to 50% by weight, preferably 10 to 40% by width, and more preferably 20 to 30% by weight.The present invention When an azeotropic composition exists in the mixture of the azeotropic composition and the organic solvent, it is preferable to use the azeotropic composition.
界面活性剤の付着水除去用溶剤中の341割合は、0〜
l oia rit %、好マシ< t;tO,l 〜
5!1TfQ%、さらに好ましくは0.2〜) 市ri
1%である。The 341 ratio of the surfactant in the solvent for removing adhered water is 0 to 341.
l oia rit %, better <t; tO, l ~
5!1TfQ%, more preferably 0.2~) City ri
It is 1%.
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、イソヘキサン、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、イソヘプタン、3−メチルヘキ
サン、2,4−ジメチルペンタン、n−オクタン、2−
メチルへブタン、3−メチルへブタン、4−メチルへブ
タン、2.2−ジメチルヘキサン、2.5−ジメチルへ
キサ・ ン、3.3−ジメチルヘキサン、2−メチル−
3−エチルペンタン、3−メチル−3−エチルペンタン
。The hydrocarbons are preferably linear or cyclic saturated or unsaturated hydrocarbons having 1 to 15 carbon atoms, such as n-pentane, isopentane, n-hexane, isohexane, 2-methylpentane, 2,2-dimethylbutane, 2.3-dimethylbutane, n-hebutane, isoheptane, 3-methylhexane, 2,4-dimethylpentane, n-octane, 2-
Methylhebutane, 3-methylhebutane, 4-methylhebutane, 2.2-dimethylhexane, 2.5-dimethylhexane, 3.3-dimethylhexane, 2-methyl-
3-ethylpentane, 3-methyl-3-ethylpentane.
2、3.3− トリメチルペンタン、2.3.4− ト
リメチルペンタン、2.2.3− )ジメチルペンタン
、イソオクタン、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−ヘキセン、トオクテン、l−ノネン、l−デ
セン、シクロペンタン、メチルシクロペンタン、シクロ
ヘキサン、メチルシクロヘキサン。2,3.3-trimethylpentane, 2.3.4-trimethylpentane, 2.2.3-) dimethylpentane, isooctane, nonane, 2.2.5-trimethylhexane, decane, dodencane, 1-pentene, 2 -Pentene, 1-hexene, tooctene, l-nonene, l-decene, cyclopentane, methylcyclopentane, cyclohexane, methylcyclohexane.
エチルシクロヘキサン、ビシクロヘキサン、シクロヘキ
セン、a−ピネン、ジペンテン、デカリン、テトラリン
、アミジノ、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−ペンタン、n−ヘキサン、n
−ヘブターン等である。It is selected from ethylcyclohexane, bicyclohexane, cyclohexene, a-pinene, dipentene, decalin, tetralin, amidino, amylnaphthalene, and the like. More preferably n-pentane, n-hexane, n
- Hebtern et al.
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、sec〜ブチルア
ルコール、イソブチルアルコール、LcrL−ブチルア
ルコール、ペンチルアルコール、5QC−アミルアルコ
ール、1−エチル−1−プロパツール、2−メチル−1
−ブタノール、イソペンチルアルコール、LerL−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−ヘキサノール、2−ノナルー
1−ペンタノール、4−メチル−2−ペンタノール、2
−エチル−1−ブタノール、l−ヘプタツール、2−ヘ
プタツール、3−ヘプタツール、1−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−トリメチル−1−ヘキサノー
ル、1−デカノール、1−ウンデカノール、l−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、
ベンジルアルコール、シクロヘキサノール、1−メチル
シクロヘキサノール、2−メチルシクロヘキサノール、
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、アビニチノール、2.
6−シメチルー4−ヘプタツール、トリメチルノニルア
ルコール、テトラデシルアルコール、ヘプタデシルアル
コール等か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, sec-butyl alcohol, isobutyl alcohol, LcrL-butyl alcohol, pentyl alcohol, 5QC-amyl alcohol, 1-ethyl-1-propatol, 2-methyl-1
-Butanol, isopentyl alcohol, LerL-pentyl alcohol, 3-methyl-2-butanol, neopentyl alcohol, 1-hexanol, 2-nonal-1-pentanol, 4-methyl-2-pentanol, 2
-ethyl-1-butanol, l-heptatool, 2-heptatool, 3-heptatool, 1-octanol, 2
-octanol, 2-ethyl-1-hexanol, 1-
Nonanol, 3,5.5-trimethyl-1-hexanol, 1-decanol, 1-undecanol, l-dodecanol, allyl alcohol, propargyl alcohol,
Benzyl alcohol, cyclohexanol, 1-methylcyclohexanol, 2-methylcyclohexanol,
3-methylcyclohexanol, 4-methylcyclohexanol, α-terpineol, avinitinol, 2.
It is selected from 6-dimethyl-4-heptatool, trimethylnonyl alcohol, tetradecyl alcohol, heptadecyl alcohol, and the like. More preferred are methanol, ethanol, isopropyl alcohol and the like.
ケトン類としては、 R−CO−R’、R−CD、R−
GO−R’−rコ 7c1121
CD−R”、 R−CO−R″、 R−CO−R′(こ
こで、R,R’、R”は炭ふ数1〜9の飽和又は不飽和
炭化水素基)のいずれかの一般式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−ロープチ
ルケトン、メチルブチルケトン、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−〇−アミルケト
ン、エチルブチルケトン、メチルへキシルケトン、シク
ロヘキサノン、メチルシクロヘキサノン、イソホロン、
2.4−ペンタンジオン、ジアセトンアルコール、アセ
トフェノン、フェンチョン笠から選ばれるものである。Ketones include R-CO-R', R-CD, R-
GO-R'-rco 7c1121 CD-R'', R-CO-R'', R-CO-R' (where R, R', R'' are saturated or unsaturated carbonized carbon atoms of 1 to 9) Those represented by any of the general formulas (hydrogen group) are preferred, such as acetone, methyl ethyl ketone, 2-pentanone, 3-pentanone, 2-hexanone, methyl rope tyl ketone, methyl butyl ketone, 2-heptanone, 4-
Heptanone, diisobutyl ketone, acetonylacetone, mesityl oxide, holone, methyl-〇-amyl ketone, ethyl butyl ketone, methylhexyl ketone, cyclohexanone, methylcyclohexanone, isophorone,
It is selected from 2.4-pentanedione, diacetone alcohol, acetophenone, and Feng Chong Kasa.
より好ましくはアセトン、メチルエチルケトン笠である
。More preferred are acetone and methyl ethyl ketone.
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、l、 1.ll−ジクロルエタン、 1,1.
2−1−ジクロルエタン、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、トリクロルエチレン、ケトンクロル
エチレン等か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. i トリクロルエタン、トリク
ロルエチレン、ケトン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. ll-dichloroethane, 1,1.
2-1-dichloroethane, 1,1.1.2-tetrachloroethane, 1,1,2.2-tetrachloroethane, pentachloroethane, 1.1-dichloroethylene, 1.2-
It is selected from dichloroethylene, trichlorethylene, ketone chlorethylene, etc. More preferably methylene chloride, 1, 1. i Trichloroethane, trichlorethylene, ketone chlorethylene, etc.
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ーテル、ボリオキシエヂレン
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、ポリオキシエチレンポリオキ
シブロビレンアルキルエステル、ポリオキシエチレンア
ルキルフェノール、ボリオキシエヂレンボリブロビレン
アルキルフェノール、ポリオキシエチレンソルビタンエ
ステル、ボリオキシエチレンボリオキシブロビレンソル
ビタンエステル、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 ether, polyoxyethylene polyoxybrobylene alkyl ether, polyoxyethylene alkyl ester, Polyoxyethylene polyoxybrobylene alkyl ester, polyoxyethylene alkylphenol, polyoxyethylene polyoxybrobylene alkylphenol, polyoxyethylene sorbitan ester, polyoxyethylene polyoxybrobylene sorbitan ester, caprylic acid caprylic acid, polyoxyethylene alkylamide, etc. There are some to choose from. 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. Can be done.
[実施例]
実施例1〜7
下記第1表に示す付着水除去用溶剤を用いて付1′1水
の除去13f(験を1−1なった。[Examples] Examples 1 to 7 Removal of attached water 13f using the solvent for removing adhered water shown in Table 1 below (test result was 1-1).
30mmX 18mmX 5mm厚のガラス板を純水に
浸漬後、付71水除去用溶剤中に20秒間浸h°1シて
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jA ?s’(L/てその水分増加h1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, immerse it in a solvent for water removal (Appendix 71) for 20 seconds, drain the water, and remove the glass plate into anhydrous methanol. The removal status of adhering water was investigated from the increase in water content h1 by s'(L/).The results are shown in Table 1.
第1表
()内は混合比[重量%]
O:良好に除去できる △:少量残存
×:かなり一残存
[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 [wt%] O: Can be removed well △: A small amount remains ×: Quite a bit remains [Effects of the Invention] As is clear from the examples, the solvent for removing adhering water of the present invention does not remove adhering water. It has an excellent water removal effect.
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
着水を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.
Claims (2)
タン又は1,2−ジクロロ−1,1−ジフルオロエタン
の1種と1,1−ジクロロ−1−フルオロエタンとの共
沸組成物を有効成分として含有する付着水除去用溶剤。(1) Azeotropic composition of one type of 1,1-dichloro-2,2,2-trifluoroethane or 1,2-dichloro-1,1-difluoroethane and 1,1-dichloro-1-fluoroethane A solvent for removing adhered water containing as an active ingredient.
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種が含まれている特許請求の範囲
第1項記載の付着水除去用溶剤。(2) Claim 1, wherein the solvent for removing adhered water contains at least one selected from hydrocarbons, alcohols, ketones, chlorinated hydrocarbons, and surfactants. Solvent for removing adhered water.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29519187A JPH01139104A (en) | 1987-11-25 | 1987-11-25 | Solvent for removing adhered water |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29519187A JPH01139104A (en) | 1987-11-25 | 1987-11-25 | Solvent for removing adhered water |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01139104A true JPH01139104A (en) | 1989-05-31 |
Family
ID=17817381
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP29519187A Pending JPH01139104A (en) | 1987-11-25 | 1987-11-25 | Solvent for removing adhered water |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01139104A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4960535A (en) * | 1989-11-13 | 1990-10-02 | Allied-Signal Inc. | Azeotrope-like compositions of 1,1-dichloro-1-fluoroethane, dichlorotrifluoroethane and a mono- or di-chlorinated C2 or C3 alkane |
JPH02306927A (en) * | 1989-04-10 | 1990-12-20 | E I Du Pont De Nemours & Co | Azeotropic mixture of 1,1-dichloro-2,2,2- trifluoroethane and 1,1-dichloro-1-fluoro- ethane |
US4994201A (en) * | 1989-09-25 | 1991-02-19 | Allied-Signal Inc. | Azeotrope-like compositions of 1,1-dichloro-1-fluoroethane, dichlorotrifluoroethane, methanol and cyclopentane |
-
1987
- 1987-11-25 JP JP29519187A patent/JPH01139104A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02306927A (en) * | 1989-04-10 | 1990-12-20 | E I Du Pont De Nemours & Co | Azeotropic mixture of 1,1-dichloro-2,2,2- trifluoroethane and 1,1-dichloro-1-fluoro- ethane |
US4994201A (en) * | 1989-09-25 | 1991-02-19 | Allied-Signal Inc. | Azeotrope-like compositions of 1,1-dichloro-1-fluoroethane, dichlorotrifluoroethane, methanol and cyclopentane |
US4960535A (en) * | 1989-11-13 | 1990-10-02 | Allied-Signal Inc. | Azeotrope-like compositions of 1,1-dichloro-1-fluoroethane, dichlorotrifluoroethane and a mono- or di-chlorinated C2 or C3 alkane |
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