JPS6317312B2 - - Google Patents
Info
- Publication number
- JPS6317312B2 JPS6317312B2 JP57092931A JP9293182A JPS6317312B2 JP S6317312 B2 JPS6317312 B2 JP S6317312B2 JP 57092931 A JP57092931 A JP 57092931A JP 9293182 A JP9293182 A JP 9293182A JP S6317312 B2 JPS6317312 B2 JP S6317312B2
- Authority
- JP
- Japan
- Prior art keywords
- composition according
- sealant
- organosilane
- mixture
- refrigerant
- 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.)
- Expired
Links
- 239000000203 mixture Substances 0.000 claims description 95
- 239000003507 refrigerant Substances 0.000 claims description 57
- 239000000565 sealant Substances 0.000 claims description 46
- 150000001282 organosilanes Chemical class 0.000 claims description 35
- 238000004378 air conditioning Methods 0.000 claims description 23
- 238000005057 refrigeration Methods 0.000 claims description 23
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 22
- 239000012530 fluid Substances 0.000 claims description 22
- 150000001412 amines Chemical class 0.000 claims description 17
- TXDNPSYEJHXKMK-UHFFFAOYSA-N sulfanylsilane Chemical compound S[SiH3] TXDNPSYEJHXKMK-UHFFFAOYSA-N 0.000 claims description 17
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims description 16
- 238000007789 sealing Methods 0.000 claims description 11
- 229910021529 ammonia Inorganic materials 0.000 claims description 10
- 239000007788 liquid Substances 0.000 claims description 10
- 125000001424 substituent group Chemical group 0.000 claims description 10
- 125000004423 acyloxy group Chemical group 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 125000003282 alkyl amino group Chemical group 0.000 claims description 7
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 7
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 7
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 claims description 4
- 239000010687 lubricating oil Substances 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- VBYLGQXERITIBP-UHFFFAOYSA-N n-[dimethylamino(methyl)silyl]-n-methylmethanamine Chemical compound CN(C)[SiH](C)N(C)C VBYLGQXERITIBP-UHFFFAOYSA-N 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 3
- TVJPBVNWVPUZBM-UHFFFAOYSA-N [diacetyloxy(methyl)silyl] acetate Chemical group CC(=O)O[Si](C)(OC(C)=O)OC(C)=O TVJPBVNWVPUZBM-UHFFFAOYSA-N 0.000 claims description 3
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 claims description 3
- QULMGWCCKILBTO-UHFFFAOYSA-N n-[dimethylamino(dimethyl)silyl]-n-methylmethanamine Chemical compound CN(C)[Si](C)(C)N(C)C QULMGWCCKILBTO-UHFFFAOYSA-N 0.000 claims description 3
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 claims description 3
- UIUXUFNYAYAMOE-UHFFFAOYSA-N methylsilane Chemical compound [SiH3]C UIUXUFNYAYAMOE-UHFFFAOYSA-N 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 150000008065 acid anhydrides Chemical class 0.000 claims 1
- 239000000443 aerosol Substances 0.000 claims 1
- 238000002347 injection Methods 0.000 claims 1
- 239000007924 injection Substances 0.000 claims 1
- 230000002452 interceptive effect Effects 0.000 claims 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical group CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 claims 1
- VGIDQEAAXPEQBI-UHFFFAOYSA-N n-[dimethoxy(methyl)silyl]-n-methylmethanamine Chemical group CO[Si](C)(OC)N(C)C VGIDQEAAXPEQBI-UHFFFAOYSA-N 0.000 claims 1
- 239000010703 silicon Substances 0.000 claims 1
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 42
- 239000000178 monomer Substances 0.000 description 10
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- -1 organosilane compound Chemical class 0.000 description 8
- 229910000077 silane Inorganic materials 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 6
- 150000004756 silanes Chemical class 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- BTHCBXJLLCHNMS-UHFFFAOYSA-N acetyloxysilicon Chemical compound CC(=O)O[Si] BTHCBXJLLCHNMS-UHFFFAOYSA-N 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 230000007062 hydrolysis Effects 0.000 description 5
- 238000006460 hydrolysis reaction Methods 0.000 description 5
- 229920001296 polysiloxane Polymers 0.000 description 5
- 125000003368 amide group Chemical group 0.000 description 4
- 125000002344 aminooxy group Chemical group [H]N([H])O[*] 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229920005573 silicon-containing polymer Polymers 0.000 description 4
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000003205 fragrance Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- ARYZCSRUUPFYMY-UHFFFAOYSA-N methoxysilane Chemical compound CO[SiH3] ARYZCSRUUPFYMY-UHFFFAOYSA-N 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- SGVQWMHGPNLWSW-UHFFFAOYSA-N chloro(difluoro)methane;1-chloro-1,1,2,2,2-pentafluoroethane Chemical compound FC(F)Cl.FC(F)(F)C(F)(F)Cl SGVQWMHGPNLWSW-UHFFFAOYSA-N 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- AFYPFACVUDMOHA-UHFFFAOYSA-N chlorotrifluoromethane Chemical compound FC(F)(F)Cl AFYPFACVUDMOHA-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 2
- CWAFVXWRGIEBPL-UHFFFAOYSA-N ethoxysilane Chemical compound CCO[SiH3] CWAFVXWRGIEBPL-UHFFFAOYSA-N 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- CDGAMPJYYCQRJM-UHFFFAOYSA-N methyl-tris(methylsulfanyl)silane Chemical compound CS[Si](C)(SC)SC CDGAMPJYYCQRJM-UHFFFAOYSA-N 0.000 description 2
- DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 description 2
- 230000009972 noncorrosive effect Effects 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 1
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 description 1
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 1
- RFCAUADVODFSLZ-UHFFFAOYSA-N 1-Chloro-1,1,2,2,2-pentafluoroethane Chemical compound FC(F)(F)C(F)(F)Cl RFCAUADVODFSLZ-UHFFFAOYSA-N 0.000 description 1
- YQUSJXPLZZZDGP-UHFFFAOYSA-N 1-chlorosilyl-N,N-dimethylmethanamine Chemical compound Cl[SiH2]CN(C)C YQUSJXPLZZZDGP-UHFFFAOYSA-N 0.000 description 1
- WRFYAFFJEMOOMJ-UHFFFAOYSA-N 1-dichlorosilyl-N,N-dimethylmethanamine Chemical compound CN(C)C[SiH](Cl)Cl WRFYAFFJEMOOMJ-UHFFFAOYSA-N 0.000 description 1
- HYCLXVPTRJUJLW-UHFFFAOYSA-N 2-[phenyl-bis(2-sulfanylethyl)silyl]ethanethiol Chemical compound SCC[Si](CCS)(CCS)C1=CC=CC=C1 HYCLXVPTRJUJLW-UHFFFAOYSA-N 0.000 description 1
- GTHQSLVHSHAQMK-UHFFFAOYSA-N 3-[tris(dimethylamino)silyl]propanenitrile Chemical compound CN(C)[Si](N(C)C)(N(C)C)CCC#N GTHQSLVHSHAQMK-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- KWAQABZFJUOKRB-UHFFFAOYSA-N C1(CCCCC1)NC(NC1CCCCC1)[SiH3] Chemical compound C1(CCCCC1)NC(NC1CCCCC1)[SiH3] KWAQABZFJUOKRB-UHFFFAOYSA-N 0.000 description 1
- KZKAHJKIHVQEHQ-UHFFFAOYSA-N CO[SiH](C)N(C)C Chemical compound CO[SiH](C)N(C)C KZKAHJKIHVQEHQ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- XWCDCDSDNJVCLO-UHFFFAOYSA-N Chlorofluoromethane Chemical compound FCCl XWCDCDSDNJVCLO-UHFFFAOYSA-N 0.000 description 1
- 239000005046 Chlorosilane Substances 0.000 description 1
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 244000246386 Mentha pulegium Species 0.000 description 1
- 235000016257 Mentha pulegium Nutrition 0.000 description 1
- 235000004357 Mentha x piperita Nutrition 0.000 description 1
- BASWICOLKLXVRR-UHFFFAOYSA-N N,N'-di(propan-2-yl)-1-silylmethanediamine Chemical compound C(C)(C)NC(NC(C)C)[SiH3] BASWICOLKLXVRR-UHFFFAOYSA-N 0.000 description 1
- YGHFDTDSFZTYBW-UHFFFAOYSA-N O-silylhydroxylamine Chemical class NO[SiH3] YGHFDTDSFZTYBW-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- NOZAQBYNLKNDRT-UHFFFAOYSA-N [diacetyloxy(ethenyl)silyl] acetate Chemical compound CC(=O)O[Si](OC(C)=O)(OC(C)=O)C=C NOZAQBYNLKNDRT-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 125000004773 chlorofluoromethyl group Chemical group [H]C(F)(Cl)* 0.000 description 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- DFQPLGZDHXLIDJ-UHFFFAOYSA-N dichloro(difluoro)methane;1,1-difluoroethane Chemical compound CC(F)F.FC(F)(Cl)Cl DFQPLGZDHXLIDJ-UHFFFAOYSA-N 0.000 description 1
- FYWZMZSOODFYPG-UHFFFAOYSA-N dimethyl-bis(methylsulfanyl)silane Chemical compound CS[Si](C)(C)SC FYWZMZSOODFYPG-UHFFFAOYSA-N 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- ZZFVCUOAUFZRCN-UHFFFAOYSA-N methyl-bis(methylsulfanyl)silane Chemical compound C[SiH](SC)SC ZZFVCUOAUFZRCN-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- UMIDWCGJOJEULM-UHFFFAOYSA-N n-[bis(butylamino)-phenylsilyl]butan-1-amine Chemical compound CCCCN[Si](NCCCC)(NCCCC)C1=CC=CC=C1 UMIDWCGJOJEULM-UHFFFAOYSA-N 0.000 description 1
- ROXOSAWAZFQUNQ-UHFFFAOYSA-N n-[bis(dibutylamino)-pentylsilyl]-n-butylbutan-1-amine Chemical compound CCCCC[Si](N(CCCC)CCCC)(N(CCCC)CCCC)N(CCCC)CCCC ROXOSAWAZFQUNQ-UHFFFAOYSA-N 0.000 description 1
- AHKKZIUZTWZKDR-UHFFFAOYSA-N n-[bis(dimethylamino)-methylsilyl]-n-methylmethanamine Chemical compound CN(C)[Si](C)(N(C)C)N(C)C AHKKZIUZTWZKDR-UHFFFAOYSA-N 0.000 description 1
- CFZHOUYDAHXRLY-UHFFFAOYSA-N n-[chloro(dimethyl)silyl]-n-methylmethanamine Chemical compound CN(C)[Si](C)(C)Cl CFZHOUYDAHXRLY-UHFFFAOYSA-N 0.000 description 1
- UFIADHILIPVQSL-UHFFFAOYSA-N n-[fluoro(dimethyl)silyl]-n-methylmethanamine Chemical compound CN(C)[Si](C)(C)F UFIADHILIPVQSL-UHFFFAOYSA-N 0.000 description 1
- JACMPVXHEARCBO-UHFFFAOYSA-N n-pentylpentan-1-amine Chemical compound CCCCCNCCCCC JACMPVXHEARCBO-UHFFFAOYSA-N 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003139 primary aliphatic amines Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 150000005619 secondary aliphatic amines Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- UQMGAWUIVYDWBP-UHFFFAOYSA-N silyl acetate Chemical class CC(=O)O[SiH3] UQMGAWUIVYDWBP-UHFFFAOYSA-N 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- PJUMZJZRDZLDER-UHFFFAOYSA-N tris(methylsulfanyl)-pentylsilane Chemical compound CCCCC[Si](SC)(SC)SC PJUMZJZRDZLDER-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/12—Materials for stopping leaks, e.g. in radiators, in tanks
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
- C09K5/041—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
- C09K5/044—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Combustion & Propulsion (AREA)
- Thermal Sciences (AREA)
- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/397,191 US4442015A (en) | 1982-05-31 | 1982-07-12 | Self-sealing refrigerant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/269,969 US4379067A (en) | 1981-06-03 | 1981-06-03 | Self-sealing refrigerant |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57209982A JPS57209982A (en) | 1982-12-23 |
| JPS6317312B2 true JPS6317312B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1988-04-13 |
Family
ID=23029352
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57092931A Granted JPS57209982A (en) | 1981-06-03 | 1982-05-31 | Self-sealing coolant |
Country Status (3)
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4508631A (en) * | 1983-08-02 | 1985-04-02 | Joseph J. Packo | Dehydrating refrigerant |
| US5050388A (en) * | 1990-04-27 | 1991-09-24 | American Patent Group | Reclaiming of refrigerant fluids to make same suitable for reuse |
| US5417873A (en) * | 1994-02-02 | 1995-05-23 | American Patent Group, Inc. | Sealant containing partially hydrolized tetraalkoxy silone, for air conditioning and refrigeration circuits |
| KR19990007977A (ko) * | 1995-04-24 | 1999-01-25 | 버만 레니 | 시스템의 탈수, 표면 안정화 및 밀봉용 조성물 및 방법 |
| US5666812A (en) * | 1995-10-20 | 1997-09-16 | Ipg Corporation | Apparatus and process for renewing refrigerants |
| WO2002073102A1 (en) * | 2001-03-08 | 2002-09-19 | Ferris James E | Apparatus, method and compositions for placing for additive fluids into a refrigerant circuit |
| US20110167841A1 (en) | 2004-06-04 | 2011-07-14 | Brasscorp Limited | Compositions and methods for injection of sealants and/or drying agents into air conditioning and refrigeration systems |
| US7296423B2 (en) * | 2004-06-04 | 2007-11-20 | Brasscorp Limited | Composition and methods for injection of sealants into air conditioning and refrigeration systems |
| US8015998B2 (en) * | 2004-08-12 | 2011-09-13 | Harris Mud & Chemical, Inc. | Method for patching or sealing leaks in fluid systems |
| US7107781B2 (en) * | 2004-10-26 | 2006-09-19 | E.F. Products, Inc. | Pressure testing and refrigerant recharging hose assembly for automobiles |
| US7124598B2 (en) * | 2004-10-26 | 2006-10-24 | E.F. Products, Inc. | Pressure testing and refrigerant recharging conduit assembly for automobiles |
| US20090113901A1 (en) * | 2007-11-07 | 2009-05-07 | Interdynamics Inc. | Method and Apparatus for Servicing a Coolant System |
| US20110146801A1 (en) * | 2008-06-20 | 2011-06-23 | Bright Solutions International Llc | Injection additives into closed systems |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1529820A (fr) * | 1967-05-09 | 1968-06-21 | Rhone Poulenc Sa | Aminosilanes et compositions en contenant |
| BE754997A (fr) * | 1969-08-20 | 1971-02-19 | Packo Joseph J | Methode et compositions de colmatage des fuites |
| US3634560A (en) * | 1970-01-30 | 1972-01-11 | Packo Joseph J | Method for sealing leaks in vessels |
| US4046533A (en) * | 1972-12-21 | 1977-09-06 | Chevron Research Company | Refrigeration working fluid containing branched chain alkylbenzene lubricant |
| US4237172A (en) * | 1978-12-04 | 1980-12-02 | Joseph J. Packo | Sealing leaks by polymerization of volatilized aminosilane monomers |
| US4304805A (en) * | 1978-12-04 | 1981-12-08 | Joseph J. Packo | Sealing leaks by polymerization of volatilized aminosilane monomers |
-
1981
- 1981-06-03 US US06/269,969 patent/US4379067A/en not_active Expired - Lifetime
- 1981-07-30 CA CA000382857A patent/CA1174843A/en not_active Expired
-
1982
- 1982-05-31 JP JP57092931A patent/JPS57209982A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57209982A (en) | 1982-12-23 |
| US4379067A (en) | 1983-04-05 |
| CA1174843A (en) | 1984-09-25 |
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