NL77406C - - Google Patents
Info
- Publication number
- NL77406C NL77406C NL77406DA NL77406C NL 77406 C NL77406 C NL 77406C NL 77406D A NL77406D A NL 77406DA NL 77406 C NL77406 C NL 77406C
- Authority
- NL
- Netherlands
- Prior art keywords
- membrane
- group
- compound
- replaced
- membranes
- Prior art date
Links
- 239000012528 membrane Substances 0.000 abstract 29
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 12
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 abstract 9
- 150000001875 compounds Chemical class 0.000 abstract 8
- 125000003010 ionic group Chemical group 0.000 abstract 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 8
- -1 methylol compound Chemical class 0.000 abstract 8
- 239000000126 substance Substances 0.000 abstract 8
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 abstract 6
- 239000000243 solution Substances 0.000 abstract 6
- 229920000856 Amylose Polymers 0.000 abstract 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract 4
- 239000007864 aqueous solution Substances 0.000 abstract 4
- 229910052801 chlorine Inorganic materials 0.000 abstract 4
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 150000002500 ions Chemical class 0.000 abstract 4
- 239000007788 liquid Substances 0.000 abstract 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 abstract 4
- 239000004627 regenerated cellulose Substances 0.000 abstract 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 4
- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 abstract 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- 238000000502 dialysis Methods 0.000 abstract 3
- 235000006408 oxalic acid Nutrition 0.000 abstract 3
- 239000001103 potassium chloride Substances 0.000 abstract 3
- 235000011164 potassium chloride Nutrition 0.000 abstract 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 abstract 2
- 239000004372 Polyvinyl alcohol Substances 0.000 abstract 2
- 239000004285 Potassium sulphite Substances 0.000 abstract 2
- 150000001408 amides Chemical class 0.000 abstract 2
- 239000012736 aqueous medium Substances 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000001913 cellulose Substances 0.000 abstract 2
- 229920002678 cellulose Polymers 0.000 abstract 2
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- 125000000962 organic group Chemical group 0.000 abstract 2
- 229920002451 polyvinyl alcohol Polymers 0.000 abstract 2
- 229910000027 potassium carbonate Inorganic materials 0.000 abstract 2
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 abstract 2
- 235000019252 potassium sulphite Nutrition 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 230000008961 swelling Effects 0.000 abstract 2
- 125000004954 trialkylamino group Chemical group 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- 238000011033 desalting Methods 0.000 abstract 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 abstract 1
- 235000019341 magnesium sulphate Nutrition 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- 238000005192 partition Methods 0.000 abstract 1
- 125000001453 quaternary ammonium group Chemical group 0.000 abstract 1
- 239000013535 sea water Substances 0.000 abstract 1
- 239000011780 sodium chloride Substances 0.000 abstract 1
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 1
- ZNCPFRVNHGOPAG-UHFFFAOYSA-L sodium oxalate Chemical compound [Na+].[Na+].[O-]C(=O)C([O-])=O ZNCPFRVNHGOPAG-UHFFFAOYSA-L 0.000 abstract 1
- 229940039790 sodium oxalate Drugs 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- B01D61/422—Electrodialysis
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0002—Organic membrane manufacture
- B01D67/0006—Organic membrane manufacture by chemical reactions
-
- 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
- B01D71/76—Macromolecular material not specifically provided for in a single one of groups B01D71/08 - B01D71/74
- B01D71/82—Macromolecular material not specifically provided for in a single one of groups B01D71/08 - B01D71/74 characterised by the presence of specified groups, e.g. introduced by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B11/00—Preparation of cellulose ethers
- C08B11/02—Alkyl or cycloalkyl ethers
- C08B11/04—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals
- C08B11/14—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals with nitrogen-containing groups
- C08B11/15—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals with nitrogen-containing groups with carbamoyl groups, i.e. -CO-NH2
-
- 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
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
-
- 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
- C08J5/2256—Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions other than those involving carbon-to-carbon bonds, e.g. obtained by polycondensation
-
- 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
- C08J5/2287—After-treatment
-
- 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
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/12—Chemical modification
-
- 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
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A20/00—Water conservation; Efficient water supply; Efficient water use
- Y02A20/124—Water desalination
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Water Supply & Treatment (AREA)
- Materials Engineering (AREA)
- Urology & Nephrology (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
Semi-permeable selective membranes are made of high molecular weight organic substances in which hydrogen atoms of reactive hydroxyl groups have been at least partly replaced by side chains of the formula <FORM:0733100/IV (a)/1> in which R represents an organic group containing at least one ionic group, i.e. an ionisable radical capable of dissociating in aqueous medium so that an electrically charged radical remains linked to the high molecular weight substance. A membrane of cellulose such as paper, transparent paper or regenerated cellulose, or of regenerated amylose, polyvinyl alcohol or similar high molecular weight substance with reactive hydroxyl groups may be reacted with a compound containing at least one N-methylol acid amide group with at least one ionic group or with a group which can readily be replaced by an ionic group in a second processing stage. A N-methylol compound of an acid amide wherein at least one hydrogen atom bound to a carbon atom has been replaced by halogen or by a trialkylamino, dialkylamino or sulphonic acid group may be used for introducing the desired groups into the substance of the membrane. For producing a positive membrane, the methylol compound of carbamidomethyl-trimethyl ammonium chloride or the methylol compound of chloro-acetamide may be used. For the production of a negative membrane from the compound thus obtained, the chlorine atom may be replaced by a sulphonic acid group, e.g. by the action of potassium sulphite. If the chlorine atom is replaced by dimethylamine, a positive membrane is obtained and the positive character may further be intensified by the action of methyl iodide. The membranes obtained preserve their selectivity in relatively strong salt concentrations in a liquid to be desalted and in the rinsing liquids. The selectivity of the membranes may be measured by determination of the concentration potential between solutions of potassium chloride of different concentrations separated by the membrane. A concentration potential of 55 mV, as compared with an ideal value of 58 mV, may be obtained when a membrane into which quaternary ammonium groups have been introduced is arranged as a partition between a 0.001 N KCl and a 0.01 N KCl solution. To reduce the swelling of the membranes in aqueous solutions, they may be reacted with compounds such as formaldehyde or the dimethylol compound of adipamide so as to form non-ionic bridge-bonds. Alternatively bridgebonds containing at least one ionic group may be formed, e.g. the cellulose or other membrane may be reacted with the methylol compound of a ,a 1-dibromoadipic diamide. In an example, a ,a 1 - bisdimethylamino - adipamide hydrochloride is dissolved in an aqueous solution of formaldehyde and then caustic soda is added. After one hour, oxalic acid is added and the precipitated sodium oxalate is filtered off. A regenerated cellulose membrane is soaked in the solution, dried, and then heated at 100 DEG C. In another example, a membrane of polyvinyl alcohol is impregnated with a solution obtained by heating a solution containing carbamido-methyl-trimethyl-ammonium chloride and adipamide with formaldehyde and potassium carbonate and subsequently acidifying with oxalic acid and hydrochloric acid to a pH of 2.0. The impregnated membrane is dried and then heated at 140 DEG C. for 10 minutes. The membranes have good ion-selective properties with respect to polyvalent ions and may be used for desalting brackish water containing magnesium sulphate. In an example, sea-water with a NaCl content of 30 gm./litre is placed in a three-chamber apparatus in which the anode compartment is separated from the dialysis compartment by a positive ion-selective membrane of regenerated cellulose which has been combined with the methylol compound of carbamidomethyl - trimethyl - ammonium chloride, and in which the cathode compartment is separated from the dialysis compartment by a negative ion-selective membrane of regenerated cellulose which has been combined with the methylol compound of a ,a 1-adipamide-disulphonic acid. The dialysis may be carried out at current densities of 2.5-25 m.Amp./sq. cm.ALSO:Semi-permeable selective membranes are made of high molecular weight organic substances in which hydrogen atoms of reactive hydroxyl groups have at least been partly replaced by side chains of the formula <FORM:0733100/IV (b)/1> in which R represents an organic group containing at least one ionic group, i.e. an ionizable radical capable of dissociating in aqueous medium so that an electrically charged radical remains linked to the high molecular weight substance. A membrane of regenerated amylose, or similar high molecular weight substance with reactive hydroxyl groups may be reacted with a compound containing at least one N-methylol acid amide group with at least one ionic group or with a group which can readily be replaced by an ionic group in a second processing stage. A N-methylol compound of an acid amide wherein at least one hydrogen atom bound to a carbon atom has been replaced by halogen or by a trialkylamino, dialkylamino, or sulphonic acid group may be used for introducing the desired groups into the substance of the membrane. For producing a positive membrane, the methylol compound of carbamidomethyl-trimethyl ammonium chloride or the methylol compound of chloro-acetamide may be used. For the production of a negative membrane from the compound thus obtained, the chlorine atom may be replaced by a sulphonic acid group, e.g. by the action of potassium sulphite. If the chlorine atom is replaced by dimethylamine, a positive membrane is obtained and the positive character may further be intensified by the action of methyl iodide. The membranes obtained preserve their selectivity in relatively strong salt concentrations in a liquid to be desalted and in the rinsing liquids. To reduce the swelling of the membranes in aqueous solutions, they may be reacted with compounds such as formaldehyde or the dimethylol compound of adipamide so as to form non-ionic bridge-bonds. Alternatively bridge-bonds containing at least one ionic group may be formed, e.g. the amylose membrane may be reacted with the methylol compound of a ,a -dibromoadipic diamide. In an example, a membrane of amylose is impregnated with a solution obtained by heating an aqueous solution containing carbamidomethyl-trimethyl-ammonium chloride, formaldehyde, and potassium carbonate and subsequently acidifying with oxalic acid to a pH of 2.0. The impregnated membrane is dried and then heated in air at 140 DEG C. for 10 minutes.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL733100X | 1952-02-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL77406C true NL77406C (en) |
Family
ID=19820332
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL77406D NL77406C (en) | 1952-02-11 |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE517435A (en) |
| GB (1) | GB733100A (en) |
| NL (1) | NL77406C (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4407976A (en) | 1980-06-16 | 1983-10-04 | Ciba-Geigy Corporation | Anionic adsorbent |
| US4577013A (en) * | 1983-12-22 | 1986-03-18 | Ciba-Geigy Corporation | Ionically modified cellulose material, its preparation and its use |
| AU571979B2 (en) * | 1984-07-06 | 1988-04-28 | Ciba-Geigy Ag | Ionically modified polysaccharides |
| CN113437341B (en) * | 2021-06-28 | 2022-04-12 | 泰山学院 | Amphoteric ion conduction membrane for flow battery and preparation method thereof |
-
0
- BE BE517435D patent/BE517435A/xx unknown
- NL NL77406D patent/NL77406C/xx active
-
1953
- 1953-02-11 GB GB3889/53A patent/GB733100A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB733100A (en) | 1955-07-06 |
| BE517435A (en) |
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