GB1141386A - Improvements in or relating to anion exchange resins - Google Patents
Improvements in or relating to anion exchange resinsInfo
- Publication number
- GB1141386A GB1141386A GB46085/66A GB4608566A GB1141386A GB 1141386 A GB1141386 A GB 1141386A GB 46085/66 A GB46085/66 A GB 46085/66A GB 4608566 A GB4608566 A GB 4608566A GB 1141386 A GB1141386 A GB 1141386A
- Authority
- GB
- United Kingdom
- Prior art keywords
- matrix
- diamine
- acrylonitrile
- reacting
- benzene
- 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
- 239000003957 anion exchange resin Substances 0.000 title abstract 2
- 239000011159 matrix material Substances 0.000 abstract 7
- 239000011347 resin Substances 0.000 abstract 5
- 229920005989 resin Polymers 0.000 abstract 5
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 abstract 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 abstract 2
- IRCKLQBEVKCOOS-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;prop-2-enenitrile Chemical compound C=CC#N.C=CC1=CC=CC=C1C=C IRCKLQBEVKCOOS-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- WVAFEFUPWRPQSY-UHFFFAOYSA-N 1,2,3-tris(ethenyl)benzene Chemical compound C=CC1=CC=CC(C=C)=C1C=C WVAFEFUPWRPQSY-UHFFFAOYSA-N 0.000 abstract 1
- JCYSHGJAXXCXEO-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;2-methylprop-2-enenitrile Chemical compound CC(=C)C#N.C=CC1=CC=CC=C1C=C JCYSHGJAXXCXEO-UHFFFAOYSA-N 0.000 abstract 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 abstract 1
- URFKATXMVVHHEY-UHFFFAOYSA-N 2-phenylbut-3-enenitrile Chemical compound C=CC(C#N)C1=CC=CC=C1 URFKATXMVVHHEY-UHFFFAOYSA-N 0.000 abstract 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 1
- JZRWCGZRTZMZEH-UHFFFAOYSA-N Thiamine Natural products CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 239000002585 base Substances 0.000 abstract 1
- MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000007334 copolymerization reaction Methods 0.000 abstract 1
- 150000004985 diamines Chemical class 0.000 abstract 1
- 229910003460 diamond Inorganic materials 0.000 abstract 1
- 239000010432 diamond Substances 0.000 abstract 1
- AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 abstract 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- 150000003949 imides Chemical class 0.000 abstract 1
- 239000003456 ion exchange resin Substances 0.000 abstract 1
- 229920003303 ion-exchange polymer Polymers 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- XTBLDMQMUSHDEN-UHFFFAOYSA-N naphthalene-2,3-diamine Chemical compound C1=CC=C2C=C(N)C(N)=CC2=C1 XTBLDMQMUSHDEN-UHFFFAOYSA-N 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 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 abstract 1
- 229920000768 polyamine Polymers 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 abstract 1
- 229960003495 thiamine Drugs 0.000 abstract 1
- 235000019157 thiamine Nutrition 0.000 abstract 1
- 239000011721 thiamine Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/42—Nitriles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/42—Nitriles
- C08F220/44—Acrylonitrile
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US49752865A | 1965-10-18 | 1965-10-18 | |
| US497527A US3389096A (en) | 1965-10-18 | 1965-10-18 | Weak-base anion exchange resins containing amide substituents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1141386A true GB1141386A (en) | 1969-01-29 |
Family
ID=27052533
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB46085/66A Expired GB1141386A (en) | 1965-10-18 | 1966-10-14 | Improvements in or relating to anion exchange resins |
Country Status (4)
| Country | Link |
|---|---|
| US (2) | US3389096A (OSRAM) |
| DE (1) | DE1595542A1 (OSRAM) |
| GB (1) | GB1141386A (OSRAM) |
| NL (1) | NL6614652A (OSRAM) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1579335A (en) * | 1976-07-03 | 1980-11-19 | Dia Prosim | Ion exchange resins |
| DE2803528C2 (de) * | 1977-03-09 | 1984-10-18 | Tabushi, Iwao, Kyoto | Schwermetallionen-Adsorbens und dessen Verwendung zum Adsorbieren von Schwermetallionen |
| GB8506361D0 (en) * | 1985-03-12 | 1985-04-11 | Courtaulds Plc | Cationic fibre |
| US4788223A (en) * | 1985-07-26 | 1988-11-29 | Rohm And Haas Company | Low-rinse, high-capacity, weakly basic acrylic ion exchange resin |
| GB2194752B (en) * | 1986-09-04 | 1990-01-10 | Mikhail Petrovich Zverev | Method for producing anion exchange fibres |
| CN114031715B (zh) * | 2021-10-18 | 2023-08-11 | 南开沧州渤海新区绿色化工研究有限公司 | 含硫代酰胺基树脂及其制备方法和用途 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2582194A (en) * | 1946-02-19 | 1952-01-08 | American Cyanamid Co | Anion exchange resins which are polyamine-polyacrylate reaction products |
| US2883349A (en) * | 1954-08-24 | 1959-04-21 | Asahi Chemical Ind | Anion exchange resins prepared in the presence of plasticizer and polymer |
| US3311572A (en) * | 1964-12-28 | 1967-03-28 | Rohm & Haas | Weakly basic anion exchange resins prepared from acrylonitrile-polyethylenically unsaturated compounds reacted with diamines and process for making same |
-
1965
- 1965-10-18 US US497527A patent/US3389096A/en not_active Expired - Lifetime
- 1965-10-18 US US497528A patent/US3423336A/en not_active Expired - Lifetime
-
1966
- 1966-10-14 GB GB46085/66A patent/GB1141386A/en not_active Expired
- 1966-10-18 DE DE19661595542 patent/DE1595542A1/de active Pending
- 1966-10-18 NL NL6614652A patent/NL6614652A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL6614652A (OSRAM) | 1967-04-19 |
| DE1595542A1 (de) | 1970-07-09 |
| US3423336A (en) | 1969-01-21 |
| US3389096A (en) | 1968-06-18 |
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