JPS625928B2 - - Google Patents
Info
- Publication number
- JPS625928B2 JPS625928B2 JP53016457A JP1645778A JPS625928B2 JP S625928 B2 JPS625928 B2 JP S625928B2 JP 53016457 A JP53016457 A JP 53016457A JP 1645778 A JP1645778 A JP 1645778A JP S625928 B2 JPS625928 B2 JP S625928B2
- Authority
- JP
- Japan
- Prior art keywords
- vinylquinoline
- vinylpyridine
- exchange resin
- anion exchange
- copolymer
- 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
- 239000000178 monomer Substances 0.000 claims description 12
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 10
- 239000003957 anion exchange resin Substances 0.000 claims description 8
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims description 7
- XUGNJOCQALIQFG-UHFFFAOYSA-N 2-ethenylquinoline Chemical compound C1=CC=CC2=NC(C=C)=CC=C21 XUGNJOCQALIQFG-UHFFFAOYSA-N 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 230000000379 polymerizing effect Effects 0.000 claims description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- 238000000862 absorption spectrum Methods 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000010557 suspension polymerization reaction Methods 0.000 description 2
- QLLUAUADIMPKIH-UHFFFAOYSA-N 1,2-bis(ethenyl)naphthalene Chemical compound C1=CC=CC2=C(C=C)C(C=C)=CC=C21 QLLUAUADIMPKIH-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- DZGGGLJOCYPKHN-UHFFFAOYSA-N 4-ethenylquinoline Chemical compound C1=CC=C2C(C=C)=CC=NC2=C1 DZGGGLJOCYPKHN-UHFFFAOYSA-N 0.000 description 1
- LBFCGFOMLOEOBR-UHFFFAOYSA-N 6-ethenylquinoline Chemical compound N1=CC=CC2=CC(C=C)=CC=C21 LBFCGFOMLOEOBR-UHFFFAOYSA-N 0.000 description 1
- HITKJZPTWAZTDK-UHFFFAOYSA-N 7-ethenylquinoline Chemical compound C1=CC=NC2=CC(C=C)=CC=C21 HITKJZPTWAZTDK-UHFFFAOYSA-N 0.000 description 1
- WRTNGGDLQMFSJL-UHFFFAOYSA-N 8-ethenylquinoline Chemical compound C1=CN=C2C(C=C)=CC=CC2=C1 WRTNGGDLQMFSJL-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 230000000887 hydrating effect Effects 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- DBSDMAPJGHBWAL-UHFFFAOYSA-N penta-1,4-dien-3-ylbenzene Chemical compound C=CC(C=C)C1=CC=CC=C1 DBSDMAPJGHBWAL-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1645778A JPS54110186A (en) | 1978-02-17 | 1978-02-17 | Method of mamufacturing weak basic anion exchange resin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1645778A JPS54110186A (en) | 1978-02-17 | 1978-02-17 | Method of mamufacturing weak basic anion exchange resin |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS54110186A JPS54110186A (en) | 1979-08-29 |
JPS625928B2 true JPS625928B2 (es) | 1987-02-07 |
Family
ID=11916772
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1645778A Granted JPS54110186A (en) | 1978-02-17 | 1978-02-17 | Method of mamufacturing weak basic anion exchange resin |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS54110186A (es) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63130605A (ja) * | 1986-11-20 | 1988-06-02 | Tokuyama Soda Co Ltd | 陰イオン交換体の製造方法 |
AU666740B2 (en) * | 1992-07-08 | 1996-02-22 | Upjohn Company, The | 5'-indolinyl oxazolidinones useful against (mycobacterium tuberculosis) |
CA2769040A1 (en) * | 2009-07-28 | 2011-02-03 | Instraction Gmbh | Specific sorbent for binding proteins and peptides, and separation method using the same |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51144393A (en) * | 1975-06-09 | 1976-12-11 | Asahi Chem Ind Co Ltd | Process for producing porous anion exchange resin |
JPS51144394A (en) * | 1975-06-09 | 1976-12-11 | Asahi Chem Ind Co Ltd | Process for producing porous anion exchange resin |
JPS52140592A (en) * | 1976-05-18 | 1977-11-24 | Sumitomo Chem Co Ltd | Preparation of porous resins having nitrogen-containing heterocyclic structure |
JPS5310680A (en) * | 1976-07-16 | 1978-01-31 | Sumitomo Chem Co Ltd | Preparation of hig-molecular weight compound comprising vinyl pyridine |
-
1978
- 1978-02-17 JP JP1645778A patent/JPS54110186A/ja active Granted
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51144393A (en) * | 1975-06-09 | 1976-12-11 | Asahi Chem Ind Co Ltd | Process for producing porous anion exchange resin |
JPS51144394A (en) * | 1975-06-09 | 1976-12-11 | Asahi Chem Ind Co Ltd | Process for producing porous anion exchange resin |
JPS52140592A (en) * | 1976-05-18 | 1977-11-24 | Sumitomo Chem Co Ltd | Preparation of porous resins having nitrogen-containing heterocyclic structure |
JPS5310680A (en) * | 1976-07-16 | 1978-01-31 | Sumitomo Chem Co Ltd | Preparation of hig-molecular weight compound comprising vinyl pyridine |
Also Published As
Publication number | Publication date |
---|---|
JPS54110186A (en) | 1979-08-29 |
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