KR100517105B1 - 염화이온 선택성 막 조성물 및 이를 이용한 염화이온 선택성 전극 - Google Patents
염화이온 선택성 막 조성물 및 이를 이용한 염화이온 선택성 전극 Download PDFInfo
- Publication number
- KR100517105B1 KR100517105B1 KR10-2002-0061556A KR20020061556A KR100517105B1 KR 100517105 B1 KR100517105 B1 KR 100517105B1 KR 20020061556 A KR20020061556 A KR 20020061556A KR 100517105 B1 KR100517105 B1 KR 100517105B1
- Authority
- KR
- South Korea
- Prior art keywords
- chloride
- selective membrane
- electrode
- chloride ion
- ion
- Prior art date
Links
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 title claims abstract description 212
- 239000012528 membrane Substances 0.000 title claims abstract description 140
- 239000000203 mixture Substances 0.000 title claims abstract description 81
- 239000003822 epoxy resin Substances 0.000 claims abstract description 51
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 51
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 50
- 150000001412 amines Chemical class 0.000 claims abstract description 48
- -1 halide ions Chemical class 0.000 claims abstract description 39
- 239000007790 solid phase Substances 0.000 claims abstract description 18
- 150000002500 ions Chemical class 0.000 claims description 56
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 22
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 14
- YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 claims description 11
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 10
- 239000003085 diluting agent Substances 0.000 claims description 10
- 229920000768 polyamine Polymers 0.000 claims description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 claims description 5
- 239000012088 reference solution Substances 0.000 claims description 5
- 150000003512 tertiary amines Chemical class 0.000 claims description 5
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 4
- ZRYCRPNCXLQHPN-UHFFFAOYSA-N 3-hydroxy-2-methylbenzaldehyde Chemical compound CC1=C(O)C=CC=C1C=O ZRYCRPNCXLQHPN-UHFFFAOYSA-N 0.000 claims description 3
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 3
- 150000008065 acid anhydrides Chemical class 0.000 claims description 3
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 claims description 3
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 claims description 3
- GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 claims description 3
- 229920001568 phenolic resin Polymers 0.000 claims description 3
- 150000003335 secondary amines Chemical class 0.000 claims description 3
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 3
- MCTWTZJPVLRJOU-UHFFFAOYSA-N 1-methyl-1H-imidazole Chemical compound CN1C=CN=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 claims description 2
- ZJRAAAWYHORFHN-UHFFFAOYSA-N 2-[[2,6-dibromo-4-[2-[3,5-dibromo-4-(oxiran-2-ylmethoxy)phenyl]propan-2-yl]phenoxy]methyl]oxirane Chemical compound C=1C(Br)=C(OCC2OC2)C(Br)=CC=1C(C)(C)C(C=C1Br)=CC(Br)=C1OCC1CO1 ZJRAAAWYHORFHN-UHFFFAOYSA-N 0.000 claims description 2
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 claims description 2
- XRBNDLYHPCVYGC-UHFFFAOYSA-N 4-phenylbenzene-1,2,3-triol Chemical group OC1=C(O)C(O)=CC=C1C1=CC=CC=C1 XRBNDLYHPCVYGC-UHFFFAOYSA-N 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 claims description 2
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 claims description 2
- JRPRCOLKIYRSNH-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC2OC2)C=1C(=O)OCC1CO1 JRPRCOLKIYRSNH-UHFFFAOYSA-N 0.000 claims description 2
- ZXOATMQSUNJNNG-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) benzene-1,3-dicarboxylate Chemical compound C=1C=CC(C(=O)OCC2OC2)=CC=1C(=O)OCC1CO1 ZXOATMQSUNJNNG-UHFFFAOYSA-N 0.000 claims description 2
- NEPKLUNSRVEBIX-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) benzene-1,4-dicarboxylate Chemical compound C=1C=C(C(=O)OCC2OC2)C=CC=1C(=O)OCC1CO1 NEPKLUNSRVEBIX-UHFFFAOYSA-N 0.000 claims description 2
- JDVIRCVIXCMTPU-UHFFFAOYSA-N ethanamine;trifluoroborane Chemical compound CCN.FB(F)F JDVIRCVIXCMTPU-UHFFFAOYSA-N 0.000 claims description 2
- FXTPGCJEKPTQLW-UHFFFAOYSA-N ethane;tetraphenylene Chemical compound CC.C1=CC=C2C3=CC=CC=C3C3=CC=CC=C3C3=CC=CC=C3C2=C1 FXTPGCJEKPTQLW-UHFFFAOYSA-N 0.000 claims description 2
- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 claims description 2
- ZETYUTMSJWMKNQ-UHFFFAOYSA-N n,n',n'-trimethylhexane-1,6-diamine Chemical compound CNCCCCCCN(C)C ZETYUTMSJWMKNQ-UHFFFAOYSA-N 0.000 claims description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- MCMFEZDRQOJKMN-UHFFFAOYSA-N 1-butylimidazole Chemical compound CCCCN1C=CN=C1 MCMFEZDRQOJKMN-UHFFFAOYSA-N 0.000 claims 1
- BBBUAWSVILPJLL-UHFFFAOYSA-N 2-(2-ethylhexoxymethyl)oxirane Chemical compound CCCCC(CC)COCC1CO1 BBBUAWSVILPJLL-UHFFFAOYSA-N 0.000 claims 1
- CAPWDGUUHUQHKM-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) 2,6-dichlorobenzene-1,4-dicarboxylate Chemical compound ClC=1C=C(C(=O)OCC2CO2)C=C(C=1C(=O)OCC1CO1)Cl CAPWDGUUHUQHKM-UHFFFAOYSA-N 0.000 claims 1
- HGXHJQLDZPXEOG-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) cyclohexane-1,4-dicarboxylate Chemical compound C1CC(C(=O)OCC2OC2)CCC1C(=O)OCC1CO1 HGXHJQLDZPXEOG-UHFFFAOYSA-N 0.000 claims 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 claims 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 claims 1
- 125000003916 ethylene diamine group Chemical group 0.000 claims 1
- YNOWBNNLZSSIHM-UHFFFAOYSA-N tris(oxiran-2-ylmethyl) benzene-1,2,4-tricarboxylate Chemical compound C=1C=C(C(=O)OCC2OC2)C(C(=O)OCC2OC2)=CC=1C(=O)OCC1CO1 YNOWBNNLZSSIHM-UHFFFAOYSA-N 0.000 claims 1
- 230000035945 sensitivity Effects 0.000 abstract description 45
- 229960001860 salicylate Drugs 0.000 abstract description 13
- 230000000694 effects Effects 0.000 abstract description 11
- 102000004169 proteins and genes Human genes 0.000 abstract description 9
- 108090000623 proteins and genes Proteins 0.000 abstract description 9
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract description 8
- 229910052794 bromium Inorganic materials 0.000 abstract description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract description 6
- 229920002521 macromolecule Polymers 0.000 abstract description 5
- 238000004519 manufacturing process Methods 0.000 abstract description 5
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract description 4
- 229910052740 iodine Inorganic materials 0.000 abstract description 4
- 239000011630 iodine Substances 0.000 abstract description 4
- 239000012472 biological sample Substances 0.000 abstract description 3
- 238000004445 quantitative analysis Methods 0.000 abstract description 3
- 230000007423 decrease Effects 0.000 abstract description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 230000004044 response Effects 0.000 description 57
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 26
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 24
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 23
- 229910021607 Silver chloride Inorganic materials 0.000 description 22
- 239000000243 solution Substances 0.000 description 22
- 239000012086 standard solution Substances 0.000 description 20
- 210000004369 blood Anatomy 0.000 description 18
- 239000008280 blood Substances 0.000 description 18
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 15
- 239000000523 sample Substances 0.000 description 14
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 229910052709 silver Inorganic materials 0.000 description 11
- 239000004332 silver Substances 0.000 description 11
- 239000004593 Epoxy Substances 0.000 description 10
- 239000007853 buffer solution Substances 0.000 description 10
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 9
- 210000002966 serum Anatomy 0.000 description 8
- 238000004458 analytical method Methods 0.000 description 7
- OWXMKDGYPWMGEB-UHFFFAOYSA-N HEPPS Chemical compound OCCN1CCN(CCCS(O)(=O)=O)CC1 OWXMKDGYPWMGEB-UHFFFAOYSA-N 0.000 description 6
- 230000002452 interceptive effect Effects 0.000 description 6
- 150000001450 anions Chemical class 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- GFGSZUNNBQXGMK-UHFFFAOYSA-N 2-chloro-4-nitrobenzamide Chemical compound NC(=O)C1=CC=C([N+]([O-])=O)C=C1Cl GFGSZUNNBQXGMK-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 238000006735 epoxidation reaction Methods 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 238000001179 sorption measurement Methods 0.000 description 4
- 239000000872 buffer Substances 0.000 description 3
- RCTYPNKXASFOBE-UHFFFAOYSA-M chloromercury Chemical compound [Hg]Cl RCTYPNKXASFOBE-UHFFFAOYSA-M 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
- 239000002555 ionophore Substances 0.000 description 3
- 230000000236 ionophoric effect Effects 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000011002 quantification Methods 0.000 description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 3
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 3
- 229960001124 trientine Drugs 0.000 description 3
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 2
- CXVOIIMJZFREMM-UHFFFAOYSA-N 1-(2-nitrophenoxy)octane Chemical compound CCCCCCCCOC1=CC=CC=C1[N+]([O-])=O CXVOIIMJZFREMM-UHFFFAOYSA-N 0.000 description 2
- IHPYMWDTONKSCO-UHFFFAOYSA-N 2,2'-piperazine-1,4-diylbisethanesulfonic acid Chemical compound OS(=O)(=O)CCN1CCN(CCS(O)(=O)=O)CC1 IHPYMWDTONKSCO-UHFFFAOYSA-N 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- SIXWIUJQBBANGK-UHFFFAOYSA-N 4-(4-fluorophenyl)-1h-pyrazol-5-amine Chemical compound N1N=CC(C=2C=CC(F)=CC=2)=C1N SIXWIUJQBBANGK-UHFFFAOYSA-N 0.000 description 2
- 206010070834 Sensitisation Diseases 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- UMYVIFNPTFWRLT-UHFFFAOYSA-L [3,4-dimethyl-2,5-dioctoxy-6-[(2,2,2-trifluoroacetyl)oxymercurio]phenyl]-(2,2,2-trifluoroacetyl)oxymercury Chemical compound CCCCCCCCOC1=C(C)C(C)=C(OCCCCCCCC)C([Hg]OC(=O)C(F)(F)F)=C1[Hg]OC(=O)C(F)(F)F UMYVIFNPTFWRLT-UHFFFAOYSA-L 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000012620 biological material Substances 0.000 description 2
- 238000011088 calibration curve Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
- RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- 230000008313 sensitization Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229920002379 silicone rubber Polymers 0.000 description 2
- 239000004945 silicone rubber Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- UDBAOKKMUMKEGZ-UHFFFAOYSA-K trichloromanganese Chemical compound [Cl-].[Cl-].[Cl-].[Mn+3] UDBAOKKMUMKEGZ-UHFFFAOYSA-K 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- GYTDJCTUFWFXBE-UHFFFAOYSA-M (2,2,2-trifluoroacetyl)oxymercury Chemical compound [Hg+].[O-]C(=O)C(F)(F)F GYTDJCTUFWFXBE-UHFFFAOYSA-M 0.000 description 1
- LTVUCOSIZFEASK-MPXCPUAZSA-N (3ar,4s,7r,7as)-3a-methyl-3a,4,7,7a-tetrahydro-4,7-methano-2-benzofuran-1,3-dione Chemical compound C([C@H]1C=C2)[C@H]2[C@H]2[C@]1(C)C(=O)OC2=O LTVUCOSIZFEASK-MPXCPUAZSA-N 0.000 description 1
- ITWBWJFEJCHKSN-UHFFFAOYSA-N 1,4,7-triazonane Chemical compound C1CNCCNCCN1 ITWBWJFEJCHKSN-UHFFFAOYSA-N 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical class C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 1
- AHDSRXYHVZECER-UHFFFAOYSA-N 2,4,6-tris[(dimethylamino)methyl]phenol Chemical compound CN(C)CC1=CC(CN(C)C)=C(O)C(CN(C)C)=C1 AHDSRXYHVZECER-UHFFFAOYSA-N 0.000 description 1
- FUIQBJHUESBZNU-UHFFFAOYSA-N 2-[(dimethylazaniumyl)methyl]phenolate Chemical compound CN(C)CC1=CC=CC=C1O FUIQBJHUESBZNU-UHFFFAOYSA-N 0.000 description 1
- HVOBSBRYQIYZNY-UHFFFAOYSA-N 2-[2-(2-aminoethylamino)ethylamino]ethanol Chemical compound NCCNCCNCCO HVOBSBRYQIYZNY-UHFFFAOYSA-N 0.000 description 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
- WXCVOOARLGLCOF-UHFFFAOYSA-N ClC=1C=C(C(=O)O)C=C(C1C(=O)O)Cl.C(C=1C(C(=O)OCC2CO2)=CC=CC1)(=O)OCC1CO1 Chemical compound ClC=1C=C(C(=O)O)C=C(C1C(=O)O)Cl.C(C=1C(C(=O)OCC2CO2)=CC=CC1)(=O)OCC1CO1 WXCVOOARLGLCOF-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 206010018852 Haematoma Diseases 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- JWCOLSMZTXUAIZ-UHFFFAOYSA-N [F].[F].[F].[Hg] Chemical compound [F].[F].[F].[Hg] JWCOLSMZTXUAIZ-UHFFFAOYSA-N 0.000 description 1
- AFEBJUVETRGQHK-UHFFFAOYSA-N [In].N1C(C=C2N=C(C=C3NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 Chemical compound [In].N1C(C=C2N=C(C=C3NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 AFEBJUVETRGQHK-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 210000000601 blood cell Anatomy 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229940006460 bromide ion Drugs 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000003869 coulometry Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229940061607 dibasic sodium phosphate Drugs 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000001516 effect on protein Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000003891 environmental analysis Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 210000003722 extracellular fluid Anatomy 0.000 description 1
- 238000001631 haemodialysis Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000000322 hemodialysis Effects 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229910001867 inorganic solvent Inorganic materials 0.000 description 1
- 239000003049 inorganic solvent Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 150000004658 ketimines Chemical class 0.000 description 1
- 150000002605 large molecules Chemical class 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 150000002731 mercury compounds Chemical class 0.000 description 1
- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 description 1
- 229910001510 metal chloride Inorganic materials 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920005597 polymer membrane Polymers 0.000 description 1
- 238000004313 potentiometry Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- FSJWWSXPIWGYKC-UHFFFAOYSA-M silver;silver;sulfanide Chemical compound [SH-].[Ag].[Ag+] FSJWWSXPIWGYKC-UHFFFAOYSA-M 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- RSPCKAHMRANGJZ-UHFFFAOYSA-N thiohydroxylamine Chemical compound SN RSPCKAHMRANGJZ-UHFFFAOYSA-N 0.000 description 1
- SBHRWOBHKASWGU-UHFFFAOYSA-M tridodecyl(methyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(CCCCCCCCCCCC)CCCCCCCCCCCC SBHRWOBHKASWGU-UHFFFAOYSA-M 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/46—Epoxy resins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/42—Electrodialysis; Electro-osmosis ; Electro-ultrafiltration; Membrane capacitive deionization
- B01D61/44—Ion-selective electrodialysis
- B01D61/46—Apparatus therefor
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/20—Manufacture of shaped structures of ion-exchange resins
- C08J5/22—Films, membranes or diaphragms
- C08J5/2206—Films, membranes or diaphragms based on organic and/or inorganic macromolecular compounds
- C08J5/2218—Synthetic macromolecular compounds
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/28—Electrolytic cell components
- G01N27/30—Electrodes, e.g. test electrodes; Half-cells
- G01N27/333—Ion-selective electrodes or membranes
- G01N27/3335—Ion-selective electrodes or membranes the membrane containing at least one organic component
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2313/00—Details relating to membrane modules or apparatus
- B01D2313/34—Energy carriers
- B01D2313/345—Electrodes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2323/00—Details relating to membrane preparation
- B01D2323/12—Specific ratios of components used
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2323/00—Details relating to membrane preparation
- B01D2323/15—Use of additives
- B01D2323/218—Additive materials
- B01D2323/2182—Organic additives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2323/00—Details relating to membrane preparation
- B01D2323/15—Use of additives
- B01D2323/218—Additive materials
- B01D2323/2182—Organic additives
- B01D2323/21834—Amines
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Water Supply & Treatment (AREA)
- Pathology (AREA)
- Inorganic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Analytical Chemistry (AREA)
- Physics & Mathematics (AREA)
- Urology & Nephrology (AREA)
- Electrochemistry (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Materials Engineering (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
- Epoxy Resins (AREA)
Abstract
Description
조성 1 | 조성 2 | 조성 3 | 조성 4 | 조성 5 | 조성 6 | 조성 7 | 조성 8 | |
에폭시 수지 | a50 | a40.5 | a40.1 | a30 | a50 | b50 | b40.5 | a50 |
경화제 | c50 | c40.5 | c40.1 | c30 | d50 | e50 | e40.5 | f50 |
DOAg | - | 19 | 18.6 | - | - | - | 19 | |
TDMAClh | - | - | 1.2 | - | - | - | - | |
희석제i | - | - | - | 40 | - | - | - | |
a: 비스페놀 A 디글리시딜에테르 > 60%,b: 비스페놀 A 프록실레이트디글리시딜에테르,c: 2,4,6-트리(다이메틸아미노메틸)페놀10-20%/멀캅토아민80-90%혼합물,d: 테트라에틸렌펜타아민, e: 메타-페닐렌 디아민, f: 메틸 나딕 무수물,g: 비스(2-에틸헥실)아디페이트, h: 트리도데실메틸암모늄 클로라이드i: 부틸 글리시딜 에테르 |
시료 유형 | 시료의 조성(또는 시약 구입시 첨부된 참고값) | 염화이온의 정량값 (mM) | ||
은/염화은(Ag/AgCl) 고체상 막을 사용한 전극 | 에폭시염화이온선택성 막을 사용한 전극 | 용매-고분자형 전극 (상업화된 분석기a) | ||
표준 용액 | Cl- 100mM | 100 | 100 | 99 |
Cl- 100mM + Br- 10mM | - | 102 | 124 | |
Cl- 100mM + Br- 20mM | - | 98 | - | |
a Blood analyzer (Nova Stat Profile Ultra M; Waltham, MA, USA). |
시료 유형 | 시료의 조성(또는 시약 구입시 첨부된 참고값) | 염화이온의 정량값 (mM) | ||
에폭시염화이온선택성 막을 사용한 전극 | 용매-고분자형 전극 (상용화된 이온선택성 물질a) | 용매-고분자형 전극 (상용화된 이온선택성 물질b) | ||
표준 용액 | Cl- 100mM | 100 | 100 | 100 |
Cl- 100mM + Sal- 1mM | 100 | - | 102 | |
Cl- 100mM + Sal- 2mM | 99 | - | 115 | |
Cl- 100mM + Sal- 3mM | 98 | - | 136 | |
a: Chloride Ionophore Ⅰ (5,10,15,20-테트라페닐-21H,23H-폴핀 망가네이즈(Ⅲ)클로라이드)b: Chloride Ionophore Ⅱ ([4,5-디메틸-3,6-디옥틸-1,2-페닐렌]-비스-(머큐리-트리플루오로아세테이트)) |
시료 유형 | 시료의 조성(또는 시약 구입시 첨부된 참고값) | 염화이온의 정량값 (mM) | ||
에폭시염화이온선택성 막을 사용하지 않은 전극 | 에폭시염화이온선택성 막을 사용한 전극 | 용매-고분자형 전극 (상업화된 분석기a) | ||
표준 용액b | Cl- 80 ±5 mM | 80.0 | 79.0 | 79.0 |
혈청c | Cl- 94.4 ±4 mM | 100.0 | 98.4 | 97.0 |
혈액d | Cl- 99 ±4 mM | 111.1 | 101.2 | 100 |
a: Blood analyzer (Nova Stat Profile Ultra M; Waltham, MA, USA).b: ALKO Diagnostic Corporation-Hollistonc: Nissui Pharmaceutical Co. (Tokyo, Japan)d: 혈액원에서 제공받음. |
Claims (9)
- 이온선택성 막과 내부기준전극 사이에 내부기준용액을 가지고 있는 재래식 염화이온 선택성 막전극과 난용성 금속염층과 이온선택성 막으로 구성되는 고체상 이온선택성 막전극에 구비되는 염화이온 선택성 막 조성물로서,에폭시 수지 및 아민성 경화제를 포함하고,상기 에폭시 수지는 글리시딜기(glycidyl groups)를 포함하는, 비스페놀 A 계; 비스페놀 A 브로미네이트계; 사이클로알리파틱계; 알리파틱 폴리글리시딜계; 글리시딜 아민계; 및 글리시딜 에스터(glycidyl esters)계 에폭지 수지로 이루어진 군에서 선택되고,상기 아민성 경화제는 지방족 폴리아민; 변성지방족 폴리아민; 제 2급 아민, 제 3급 아민으로 이루어진 군에서 선택되거나, 산무수물에 3급 아민과 이미다졸 그룹의 아민계 경화촉진제를 첨가한 혼합물로부터 선택되고,상기 에폭시 수지 및 아민성 경화제는 50∼94:6~50 중량%로 혼합되는,염화이온 선택성 막 조성물.
- 제 1항에 있어서, 상기 에폭시 수지가 비스페놀 A 디글리시딜 에테르; 테트라브로모 비스페놀 A 디글리시딜 에테르; 테트라페닐렌 에탄 테트라글리시딜 에테르, 트리히드록시바이페닐 트리글리시딜 에테르; 히드록시폴리페닐 폴리글리시딜 에테르, 페놀 포름알테히드 노블락 폴리글리시딜 에테르, o-크레졸포름알데히드 노블락 폴리글리시딜 에테르; 4,4-디아미노-디페닐메탄; 및 디글리시딜 아이소프탈레이트, 디글리시딜 테레프탈레이트, 디글리시딜 헥사히드로테레프탈레이트, 디글리시딜 프탈레이트, 디글리시딜 3,5 디클로로테레프탈레이트, 디글리시딜 디페노에이트, 트리글리시딜 트리메소에이트, 트리글리시딜 트리멜리테이트, 테트라글리시딜 피로멜리테이트로 이루어진 군에서 선택되는 글리시딜기(glycidyl groups)를 포함하는 에폭시 수지인 것을 특징으로 하는 염화이온 선택성 막조성물.
- 제 1항에 있어서, 상기 아민계 경화제가 에틸렌다이아민, 트리메틸헥사메틸렌다이아민, 다이에틸렌트리아민, 다이프로필렌트리아민, 트리에틸렌테트라아민, 테트라에틸렌펜타아민, 2-하이드록시에틸다이에틸렌트리아민, 다이에틸아미노프로필아민, N-아미노에틸렌파이퍼라진, m-자일렌다이아민, 벤질다이메틸아민, n-부틸이미다졸, 1-메틸이미다졸 및 보론 트리플루오라이드 모노에틸아민으로 이루어진 아민계열 그룹에서 선택된 것이거나;산무수물에 3급 아민과 이미다졸 그룹의 아민계 경화촉진제를 첨가한 혼합물인 것을 특징으로 하는 염화이온 선택성 막조성물.
- 제 1항에 있어서, 상기 에폭시 수지와 아민계 경화제가 50∼80:20∼50 중량%로 혼합되는 것을 특징으로 하는 염화이온 선택성 막조성물.
- 제 1항에 있어서, 추가로 희석제를 상기 막조성물 100 중량부에 대해 13∼65 중량부 포함하는 것을 특징으로 하는 염화이온 선택성 막조성물.
- 제 5항에 있어서, 상기 희석제가 테트라히드로퓨란, 아세톤, 메탄올, 사이클로헥산온, 디클로로메탄, 자일렌; 부틸 글리시딜 에테르, 페닐 글리시딜 에테르, 2-에틸헥실 글리시딜 에테르로 이루어진 군에서 선택되는 것을 특징으로 하는 염화이온 선택성 막조성물.
- 삭제
- 삭제
- 제 1항의 염화이온 선택성 막조성물로 이루어진 염화이온 선택성 막전극.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2002-0061556A KR100517105B1 (ko) | 2002-10-09 | 2002-10-09 | 염화이온 선택성 막 조성물 및 이를 이용한 염화이온 선택성 전극 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2002-0061556A KR100517105B1 (ko) | 2002-10-09 | 2002-10-09 | 염화이온 선택성 막 조성물 및 이를 이용한 염화이온 선택성 전극 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20040032429A KR20040032429A (ko) | 2004-04-17 |
KR100517105B1 true KR100517105B1 (ko) | 2005-09-27 |
Family
ID=37332326
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR10-2002-0061556A KR100517105B1 (ko) | 2002-10-09 | 2002-10-09 | 염화이온 선택성 막 조성물 및 이를 이용한 염화이온 선택성 전극 |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR100517105B1 (ko) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104374814B (zh) * | 2014-12-04 | 2017-05-10 | 上海惠中医疗科技有限公司 | 一种用于氯离子选择性电极感应膜及其生产方法 |
RU2017134295A (ru) * | 2015-05-18 | 2019-04-03 | Сименс Хелткэа Дайагностикс Инк. | Усовершенствованная хлорид-селективная мембрана |
GB202019249D0 (en) * | 2020-12-07 | 2021-01-20 | Univ Southampton | Reference electrode & ION selective membrane |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5858458A (ja) * | 1981-10-02 | 1983-04-07 | Saburo Yanagisawa | 被覆型塩素イオン選択性電極 |
JPS58174435A (ja) * | 1982-04-08 | 1983-10-13 | Sumitomo Bakelite Co Ltd | エポキシ樹脂系成形材料 |
JPH06138081A (ja) * | 1993-07-10 | 1994-05-20 | Horiba Ltd | 塩素イオン選択性電極用応答膜の製造方法 |
JPH0716434A (ja) * | 1993-06-30 | 1995-01-20 | Asahi Glass Co Ltd | 電気透析方法 |
US6340714B1 (en) * | 1999-09-13 | 2002-01-22 | F. Hoffmann-La Roche Ag | Chloride-sensitive electrode membrane |
-
2002
- 2002-10-09 KR KR10-2002-0061556A patent/KR100517105B1/ko active IP Right Grant
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5858458A (ja) * | 1981-10-02 | 1983-04-07 | Saburo Yanagisawa | 被覆型塩素イオン選択性電極 |
JPS58174435A (ja) * | 1982-04-08 | 1983-10-13 | Sumitomo Bakelite Co Ltd | エポキシ樹脂系成形材料 |
JPH0716434A (ja) * | 1993-06-30 | 1995-01-20 | Asahi Glass Co Ltd | 電気透析方法 |
JPH06138081A (ja) * | 1993-07-10 | 1994-05-20 | Horiba Ltd | 塩素イオン選択性電極用応答膜の製造方法 |
US6340714B1 (en) * | 1999-09-13 | 2002-01-22 | F. Hoffmann-La Roche Ag | Chloride-sensitive electrode membrane |
Also Published As
Publication number | Publication date |
---|---|
KR20040032429A (ko) | 2004-04-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0097960B1 (en) | Bis-crown-ether derivatives and their use | |
Liu et al. | Polymeric membrane salicylate-sensitive electrodes based on organotin (IV) carboxylates | |
US6663756B2 (en) | Microchip-type oxygen gas sensor based on differential potentiometry | |
Coll et al. | Ionic liquids promote selective responses towards the highly hydrophilic anion sulfate in PVC membrane ion-selective electrodes | |
EP0115346B1 (en) | Liquid film type, anion-selective electrode | |
US11747297B2 (en) | Enhanced chloride selective membrane | |
KR100517105B1 (ko) | 염화이온 선택성 막 조성물 및 이를 이용한 염화이온 선택성 전극 | |
KR100289469B1 (ko) | 친수성 폴리우레탄을 보호막으로 사용한 염화이온 선택성 전극 | |
Ganjali et al. | Highly selective liquid membrane sensor based on 1, 3, 5-Triphenylpyrylium perchlorate for quick monitoring of sulfate ions | |
Othman et al. | Potentiometric determination of dopamine in pharmaceutical preparations by crown ether-PVC membrane sensors | |
KR0185780B1 (ko) | 칼슘이온 센서의 전극에 구비되는 이온 선택성 막을 형성하기 위한 조성물 및 이것을 사용하여 이온 선택성 막을 형성하는 방법 | |
JP6634805B2 (ja) | 塩素イオン選択性電極 | |
JP5254123B2 (ja) | リチウムイオン選択性電極 | |
KR0185781B1 (ko) | 염화이온센서의 전극에 구비되는 이온 선택성 막을 형성하기 위한 조성물 및 이것을 사용하여 이온 선택성 막을 형성하는 방법 | |
KR100309223B1 (ko) | 평면형 고체상 전극 | |
KR100330739B1 (ko) | 폴리우레탄을 지지체로 사용한 칼슘이온선택성 막 조성물 | |
Kimura et al. | Application of macrocycles to ion-selective electrodes | |
KR100196111B1 (ko) | 음이온 선택성 막을 형성하기 위한 조성물 및 이것으로 형성된 막을 구비하는 음이온 센서 | |
Majdi et al. | Determination of Dexamethasone disodium phosphate using potentiometric sensors based on molecularly imprinted polymer in flow injection and batch systems | |
Nam et al. | Alternative polymer matrices for potentiometric chemical sensors | |
JP2729516B2 (ja) | 塩素イオン選択性電極 | |
JPH06138081A (ja) | 塩素イオン選択性電極用応答膜の製造方法 | |
Kimura et al. | Applications of crown compounds to analytical and separation chemistry: ion sensor and liquid chromatography | |
BAGHER et al. | Hydrogen ion selective poly (vinyl chloride) membrane electrode based on 2, 2'-N, N'-bis (salicylaldimino) azobenzene | |
JPH11337515A (ja) | 陰イオン選択性電極 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
FPAY | Annual fee payment |
Payment date: 20120827 Year of fee payment: 8 |
|
FPAY | Annual fee payment |
Payment date: 20130731 Year of fee payment: 9 |
|
FPAY | Annual fee payment |
Payment date: 20150805 Year of fee payment: 11 |
|
FPAY | Annual fee payment |
Payment date: 20160826 Year of fee payment: 12 |
|
FPAY | Annual fee payment |
Payment date: 20170811 Year of fee payment: 13 |
|
FPAY | Annual fee payment |
Payment date: 20180604 Year of fee payment: 14 |