JPS625928B2 - - Google Patents

Info

Publication number: JPS625928B2
Authority: JP; Japan
Prior art keywords: vinylquinoline; vinylpyridine; exchange resin; anion exchange; copolymer
Prior art date: 1978-02-17
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

Application number

JP53016457A

Other languages

English (en)

Japanese (ja)

Other versions

JPS54110186A (en

Inventor

Hiroshi Kanbara

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Juki Corp

Original Assignee

Tokyo Juki Industrial Co Ltd

Priority date (The priority date 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 date listed.)

1978-02-17

Filing date

1978-02-17

Publication date

1987-02-07

1978-02-17 Application filed by Tokyo Juki Industrial Co Ltd filed Critical Tokyo Juki Industrial Co Ltd

1978-02-17 Priority to JP1645778A priority Critical patent/JPS54110186A/ja

1979-08-29 Publication of JPS54110186A publication Critical patent/JPS54110186A/ja

1987-02-07 Publication of JPS625928B2 publication Critical patent/JPS625928B2/ja

Status Granted legal-status Critical Current

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)

JP1645778A 1978-02-17 1978-02-17 Method of mamufacturing weak basic anion exchange resin Granted JPS54110186A (en)

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 (xx)	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 (xx)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Publication	Publication Date	Title
US5244926A (en)	1993-09-14	Preparation of ion exchange and adsorbent copolymers
DE3380847D1 (en)	1989-12-21	The manufacture of crosslinked copolymer beads, the copolymer beads themselves and their use as adsorbents or, on incorporation or addition of functional groups, as ion exchange resins
US3586646A (en)	1971-06-22	Cation exchanger with sponge structure
US5498678A (en)	1996-03-12	Suspension polymerization process for water-soluble monomers
US3941724A (en)	1976-03-02	Production of amphoteric resins in a reaction medium comprising formic acid
GB1492428A (en)	1977-11-16	Preparation of particulate cross-linked polymers
US3907720A (en)	1975-09-23	Insoluble porous polymeric iodine complexes useful as bactericides
JPH0524922B2 (xx)	1993-04-09
US4139499A (en)	1979-02-13	Thermally reversible amphoteric ion exchange resins of improved demineralization capacity
US3367889A (en)	1968-02-06	Process for the preparation of macroreticular-structured copolymers
US3716482A (en)	1973-02-13	Anion exchanger with sponge structure and process of using same
US6525156B1 (en)	2003-02-25	Styrene-containing popcorn polymers, method for producing same and utilisation
US4238569A (en)	1980-12-09	Preparation of hydrophilic material for gel chromatography
JPS6250486B2 (xx)	1987-10-26
JPS6151007A (ja)	1986-03-13	ポリビニルアミン架橋物の製造方法
JPS625928B2 (xx)	1987-02-07
US3870663A (en)	1975-03-11	Porous styrene polyfunctional methacrylate polymers
US4184020A (en)	1980-01-15	Preparation of hydrophilic material for gel chromatography
US4130512A (en)	1978-12-19	Ion exchange materials
EP0045824A1 (en)	1982-02-17	Ion exchange material, its preparation and use
DE19644227A1 (de)	1998-04-30	Verfahren zur Herstellung ausblutarmer Kationenaustauscher
US2768991A (en)	1956-10-30	Preparation of cation exchangers from co-polymerized carboxylic acid and cross-linking agent
JP2000007711A (ja)	2000-01-11	架橋球状ポリマ―の製造方法
USRE26934E (en)	1970-08-18	Chromatographic separation of substances of different molec- ular weight
SU464119A3 (ru)	1975-03-15	Способ получени ионообменных смол