NO117242B - - Google Patents
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- Publication number
- NO117242B NO117242B NO157266A NO15726665A NO117242B NO 117242 B NO117242 B NO 117242B NO 157266 A NO157266 A NO 157266A NO 15726665 A NO15726665 A NO 15726665A NO 117242 B NO117242 B NO 117242B
- Authority
- NO
- Norway
- Prior art keywords
- resin
- membranes
- membrane
- permselective
- polymers
- Prior art date
Links
- 239000012528 membrane Substances 0.000 claims description 48
- 229920000642 polymer Polymers 0.000 claims description 14
- 239000003957 anion exchange resin Substances 0.000 claims description 13
- 239000002245 particle Substances 0.000 claims description 13
- 125000000129 anionic group Chemical group 0.000 claims description 12
- 239000011159 matrix material Substances 0.000 claims description 10
- 239000002585 base Substances 0.000 claims description 8
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 claims description 7
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 5
- 238000005868 electrolysis reaction Methods 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 229920005992 thermoplastic resin Polymers 0.000 claims description 2
- 229910001508 alkali metal halide Inorganic materials 0.000 claims 1
- 150000008045 alkali metal halides Chemical class 0.000 claims 1
- 229910001507 metal halide Inorganic materials 0.000 claims 1
- 150000005309 metal halides Chemical class 0.000 claims 1
- 239000011347 resin Substances 0.000 description 25
- 229920005989 resin Polymers 0.000 description 25
- 238000000034 method Methods 0.000 description 12
- -1 polyethylene Polymers 0.000 description 11
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000004698 Polyethylene Substances 0.000 description 8
- 239000011230 binding agent Substances 0.000 description 8
- 229920000573 polyethylene Polymers 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000004811 fluoropolymer Substances 0.000 description 6
- 229920002313 fluoropolymer Polymers 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 150000001450 anions Chemical class 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 239000003456 ion exchange resin Substances 0.000 description 2
- 229920003303 ion-exchange polymer Polymers 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- 229920004459 Kel-F® PCTFE Polymers 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 150000003842 bromide salts Chemical class 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000002242 deionisation method Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 150000004694 iodide salts Chemical class 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/69—Benzenesulfonamido-pyrimidines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DESCH34826A DE1239690B (de) | 1964-03-19 | 1964-03-19 | Verfahren zur Herstellung von in 5-Stellung substituierten 2-Benzolsulfonamido-pyrimidinen |
DESCH34858A DE1283844B (de) | 1964-03-25 | 1964-03-25 | Verfahren zur Herstellung von 5-(ª‰-Hydroxyaethoxy)-pyrimidinderivaten |
DESC035070 | 1964-04-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
NO117242B true NO117242B (sv) | 1969-07-21 |
Family
ID=27212320
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO157266A NO117242B (sv) | 1964-03-19 | 1965-03-18 |
Country Status (12)
Country | Link |
---|---|
US (1) | US3431263A (sv) |
BE (1) | BE661386A (sv) |
CH (2) | CH461507A (sv) |
DK (5) | DK115263B (sv) |
ES (1) | ES310643A1 (sv) |
FI (1) | FI45448C (sv) |
FR (2) | FR1567854A (sv) |
GB (2) | GB1095217A (sv) |
IL (1) | IL23155A (sv) |
NL (1) | NL6503478A (sv) |
NO (1) | NO117242B (sv) |
SE (1) | SE327409B (sv) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2146986B (en) * | 1983-09-23 | 1987-06-17 | Lilly Co Eli | Process for preparing 5-substituted pyrimidines |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3288793A (en) * | 1961-10-12 | 1966-11-29 | Schering Ag | 2-tetrahydrofurfuryl-, 2-aliphatic-, and 2-aliphatic ether-sulfonamido-5-alkoxy-pyrimidines |
DE1545944A1 (de) * | 1964-06-19 | 1969-12-11 | Hoffmann La Roche | Verfahren zur Herstellung von neuen Sulfonamiden der Pyrimidinreihe |
-
1965
- 1965-03-15 IL IL23155A patent/IL23155A/en unknown
- 1965-03-16 ES ES0310643A patent/ES310643A1/es not_active Expired
- 1965-03-16 US US440312A patent/US3431263A/en not_active Expired - Lifetime
- 1965-03-18 SE SE03519/65A patent/SE327409B/xx unknown
- 1965-03-18 NO NO157266A patent/NO117242B/no unknown
- 1965-03-19 DK DK141265AA patent/DK115263B/da unknown
- 1965-03-19 GB GB11831/65A patent/GB1095217A/en not_active Expired
- 1965-03-19 FI FI650683A patent/FI45448C/sv active
- 1965-03-19 CH CH107368A patent/CH461507A/de unknown
- 1965-03-19 CH CH383665A patent/CH461504A/de unknown
- 1965-03-19 NL NL6503478A patent/NL6503478A/xx unknown
- 1965-03-19 BE BE661386A patent/BE661386A/xx unknown
- 1965-03-19 GB GB5404/67A patent/GB1095218A/en not_active Expired
- 1965-03-19 FR FR1567854D patent/FR1567854A/fr not_active Expired
- 1965-06-18 FR FR21361A patent/FR4448M/fr not_active Expired
-
1967
- 1967-01-30 DK DK52567AA patent/DK114979B/da unknown
- 1967-01-30 DK DK52867AA patent/DK116592B/da unknown
- 1967-01-30 DK DK52667AA patent/DK115117B/da unknown
- 1967-01-30 DK DK52767AA patent/DK115185B/da unknown
Also Published As
Publication number | Publication date |
---|---|
SE327409B (sv) | 1970-08-24 |
DK116592B (da) | 1970-01-26 |
DK114979B (da) | 1969-08-25 |
NL6503478A (sv) | 1965-09-20 |
FR1567854A (sv) | 1969-05-23 |
DK115117B (da) | 1969-09-08 |
CH461504A (de) | 1968-08-31 |
GB1095218A (en) | 1967-12-13 |
IL23155A (en) | 1968-10-24 |
ES310643A1 (es) | 1965-07-01 |
DK115185B (da) | 1969-09-15 |
DK115263B (da) | 1969-09-22 |
BE661386A (sv) | 1965-09-20 |
GB1095217A (en) | 1967-12-13 |
FI45448B (sv) | 1972-02-29 |
FI45448C (sv) | 1972-06-12 |
CH461507A (de) | 1968-08-31 |
US3431263A (en) | 1969-03-04 |
FR4448M (sv) | 1966-09-26 |
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