CA1107684A - Method and apparatus for installation of a membrane to an electrolytic cell - Google Patents
Method and apparatus for installation of a membrane to an electrolytic cellInfo
- Publication number
- CA1107684A CA1107684A CA318,503A CA318503A CA1107684A CA 1107684 A CA1107684 A CA 1107684A CA 318503 A CA318503 A CA 318503A CA 1107684 A CA1107684 A CA 1107684A
- Authority
- CA
- Canada
- Prior art keywords
- membrane
- cell
- securing means
- press plate
- fluorocarbon polymer
- 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
- 239000012528 membrane Substances 0.000 title claims abstract description 96
- 238000009434 installation Methods 0.000 title claims abstract description 37
- 238000000034 method Methods 0.000 title claims abstract description 29
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims abstract description 7
- 229910001514 alkali metal chloride Inorganic materials 0.000 claims abstract description 6
- 229920002313 fluoropolymer Polymers 0.000 claims description 17
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 10
- 229910045601 alloy Inorganic materials 0.000 claims description 10
- 239000000956 alloy Substances 0.000 claims description 10
- 229910052715 tantalum Inorganic materials 0.000 claims description 10
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 10
- 229910052719 titanium Inorganic materials 0.000 claims description 10
- 239000010936 titanium Substances 0.000 claims description 10
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 9
- 229910000856 hastalloy Inorganic materials 0.000 claims description 9
- 229910052726 zirconium Inorganic materials 0.000 claims description 9
- 238000005341 cation exchange Methods 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 150000002739 metals Chemical class 0.000 claims description 6
- -1 polypropylene Polymers 0.000 claims description 6
- 229920002430 Fibre-reinforced plastic Polymers 0.000 claims description 5
- 239000004743 Polypropylene Substances 0.000 claims description 5
- 229920001971 elastomer Polymers 0.000 claims description 5
- 239000011151 fibre-reinforced plastic Substances 0.000 claims description 5
- 239000011521 glass Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 229920001155 polypropylene Polymers 0.000 claims description 5
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 5
- 239000004800 polyvinyl chloride Substances 0.000 claims description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 238000005868 electrolysis reaction Methods 0.000 claims description 4
- 239000012982 microporous membrane Substances 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000010425 asbestos Substances 0.000 abstract description 13
- 229910052895 riebeckite Inorganic materials 0.000 abstract description 13
- 239000003014 ion exchange membrane Substances 0.000 abstract description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 45
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 16
- 238000012856 packing Methods 0.000 description 9
- 239000011780 sodium chloride Substances 0.000 description 8
- 239000004809 Teflon Substances 0.000 description 4
- 229920006362 Teflon® Polymers 0.000 description 4
- 238000007789 sealing Methods 0.000 description 4
- 229920000557 Nafion® Polymers 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- VSSLEOGOUUKTNN-UHFFFAOYSA-N tantalum titanium Chemical compound [Ti].[Ta] VSSLEOGOUUKTNN-UHFFFAOYSA-N 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910001362 Ta alloys Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 125000000565 sulfonamide group Chemical group 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B13/00—Diaphragms; Spacing elements
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B9/00—Cells or assemblies of cells; Constructional parts of cells; Assemblies of constructional parts, e.g. electrode-diaphragm assemblies; Process-related cell features
- C25B9/17—Cells comprising dimensionally-stable non-movable electrodes; Assemblies of constructional parts thereof
- C25B9/19—Cells comprising dimensionally-stable non-movable electrodes; Assemblies of constructional parts thereof with diaphragms
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16B—DEVICES FOR FASTENING OR SECURING CONSTRUCTIONAL ELEMENTS OR MACHINE PARTS TOGETHER, e.g. NAILS, BOLTS, CIRCLIPS, CLAMPS, CLIPS OR WEDGES; JOINTS OR JOINTING
- F16B5/00—Joining sheets or plates, e.g. panels, to one another or to strips or bars parallel to them
- F16B5/06—Joining sheets or plates, e.g. panels, to one another or to strips or bars parallel to them by means of clamps or clips
- F16B5/0607—Joining sheets or plates, e.g. panels, to one another or to strips or bars parallel to them by means of clamps or clips joining sheets or plates to each other
- F16B5/0621—Joining sheets or plates, e.g. panels, to one another or to strips or bars parallel to them by means of clamps or clips joining sheets or plates to each other in parallel relationship
- F16B5/0635—Joining sheets or plates, e.g. panels, to one another or to strips or bars parallel to them by means of clamps or clips joining sheets or plates to each other in parallel relationship fastened over the edges of the sheets or plates
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
Method and apparatus for installation of a membrane to a finger type electrolytic cell are provided. The method comprises covering the horizontal surfaces of a cathode of the cell, not opposing an anode with a membrane installation frame having a collar, positioning the membrane substantially parallel to the vertical surfaces of the cathode, and installing and securing the membrane to the collar by a mechanical securing means. Not only is efficiency of installation for the membrane to the electrolytic cell greatly improved, but also, in the case of an ion exchange membrane, an alkali metal hydroxide liquor containing hardly any alkali metal chloride is produced. According to the invention, a conventional asbestos diaphragm finger type electrolytic cell is advantageously converted to an ion exchange membrane electrolytic cell.
Method and apparatus for installation of a membrane to a finger type electrolytic cell are provided. The method comprises covering the horizontal surfaces of a cathode of the cell, not opposing an anode with a membrane installation frame having a collar, positioning the membrane substantially parallel to the vertical surfaces of the cathode, and installing and securing the membrane to the collar by a mechanical securing means. Not only is efficiency of installation for the membrane to the electrolytic cell greatly improved, but also, in the case of an ion exchange membrane, an alkali metal hydroxide liquor containing hardly any alkali metal chloride is produced. According to the invention, a conventional asbestos diaphragm finger type electrolytic cell is advantageously converted to an ion exchange membrane electrolytic cell.
Description
D76a~
DETAILED DESCRIPTION OF THE INVENTION
The present invention relates to a method and an apparatus for installation of membranes in an electrolytic cell7 more particularly, to a finger type electrolytic cell for electrolysis of an alkali metal chloride solution.
Sodium hydroxide has been commercially produced using asbestos or modified asbestos diaphragm cells. However, sodium hydro~ide prepared using these cells is poor in quality as about 0.9 to about 1.2% by weight of sodium chloride is usually contained in a 50% sodium hydroxide liquor. Sodium chloride contained in sodium hydroxide liquor produced in these cells may be removed by ammonia extraction, the use of hydrated sodium hydroxide or the like, but on an industrial scale, the sodium hydroxide liquor can only be purified, at best, to an extent ranging from about 500 to l,000 ppm, and still more significant, a relatively large expenditure is required`for puriEication. Sodium hydroxide used for the rayon industry can contain only 200 ppm or less of sodium chloride in a 50% sodium hydroxide liquor. Accordingly, it is rather difficult to produce sodium hydroxide for the rayon industry at a reasonable and moderate cost by thepurification of sodium hydroxide from the asbestos or modified asbestos diaphragm cells.
When asbestos or modified asbestos diaphragm cells are converted to the ~on exchange membrane cells according to the present invention, not only is the quality of the product improved, but also the operation of an electrolytic plant becomes feasible. That is, due to the fact that there is no precipitation of - salts in the evaporation system, washing of the slurry lines and the vessels and the like is not required, and the operation may be carried out automatically.
; Another advantage obtained by the conversion to the ion exchange membrane cell - method is ~hat a cell liquor containing hardly any NaCl is obtained. A further :
advantage is that sodium hydroxide which is to be used directly in the same plant or the like may be supplied for use without being concentrated by evaporation to :
' " ,~
~7~
45 to 50~, a low concentration being satisfactory. Asbestos or modified asbestos diaphragm cell liquor containing a large amount of sodium chloride, however, must be concentrated to from 45 to 50~ for use, even though used directly in the plant. By converting to the ion exchange membrane method, sodium hydroxide containing substantially no sodium chloride is obtained, and thus may be supplied for a variety of uses immediately by being cooled to the desired temperature, or may be mixed with a 50% sodium hydroxide to the desired concen-tration and then supplied for use.
However, it is very difEicult to install an ion exchange membrane to a finger type electrolytic cell comprising winding portions. The installation in a plain way of an ion exchange membrane onto the curved surfaces of a cathode always results in increased concentration of alkali metal chlorlde in the product alkali metal hydroxide liquor.
On the other hand, hydrodynamically permeable perforated membranes are known as microporous membranes. It is also difficult to locate these membranes in a finger type electrolytic cell which is typical and common as an asbestos -;
diaphragm cell, but these are not yet in use on an industrial scale because of this.
In order to solve the aforementioned problèms, the present inventors have studied a method and an apparatus which enable simple and easy installation of a substantially flat membrane in a finger type electrolytic cell.
Thus the present invention provides a feasible method and an apparatus for installing a membrane in a finger type electrolytic cell.
Secondly, the present invention provi.des a method and an apparatus for converting an asbestos or modified asbestos diaphragm cell to a cation exchange membrane cell, and preparing and alkali metal hydroxide liquor containing little alkali metal chloride or the like.
Thirdly, the present invention provides a method and an apparatus for
DETAILED DESCRIPTION OF THE INVENTION
The present invention relates to a method and an apparatus for installation of membranes in an electrolytic cell7 more particularly, to a finger type electrolytic cell for electrolysis of an alkali metal chloride solution.
Sodium hydroxide has been commercially produced using asbestos or modified asbestos diaphragm cells. However, sodium hydro~ide prepared using these cells is poor in quality as about 0.9 to about 1.2% by weight of sodium chloride is usually contained in a 50% sodium hydroxide liquor. Sodium chloride contained in sodium hydroxide liquor produced in these cells may be removed by ammonia extraction, the use of hydrated sodium hydroxide or the like, but on an industrial scale, the sodium hydroxide liquor can only be purified, at best, to an extent ranging from about 500 to l,000 ppm, and still more significant, a relatively large expenditure is required`for puriEication. Sodium hydroxide used for the rayon industry can contain only 200 ppm or less of sodium chloride in a 50% sodium hydroxide liquor. Accordingly, it is rather difficult to produce sodium hydroxide for the rayon industry at a reasonable and moderate cost by thepurification of sodium hydroxide from the asbestos or modified asbestos diaphragm cells.
When asbestos or modified asbestos diaphragm cells are converted to the ~on exchange membrane cells according to the present invention, not only is the quality of the product improved, but also the operation of an electrolytic plant becomes feasible. That is, due to the fact that there is no precipitation of - salts in the evaporation system, washing of the slurry lines and the vessels and the like is not required, and the operation may be carried out automatically.
; Another advantage obtained by the conversion to the ion exchange membrane cell - method is ~hat a cell liquor containing hardly any NaCl is obtained. A further :
advantage is that sodium hydroxide which is to be used directly in the same plant or the like may be supplied for use without being concentrated by evaporation to :
' " ,~
~7~
45 to 50~, a low concentration being satisfactory. Asbestos or modified asbestos diaphragm cell liquor containing a large amount of sodium chloride, however, must be concentrated to from 45 to 50~ for use, even though used directly in the plant. By converting to the ion exchange membrane method, sodium hydroxide containing substantially no sodium chloride is obtained, and thus may be supplied for a variety of uses immediately by being cooled to the desired temperature, or may be mixed with a 50% sodium hydroxide to the desired concen-tration and then supplied for use.
However, it is very difEicult to install an ion exchange membrane to a finger type electrolytic cell comprising winding portions. The installation in a plain way of an ion exchange membrane onto the curved surfaces of a cathode always results in increased concentration of alkali metal chlorlde in the product alkali metal hydroxide liquor.
On the other hand, hydrodynamically permeable perforated membranes are known as microporous membranes. It is also difficult to locate these membranes in a finger type electrolytic cell which is typical and common as an asbestos -;
diaphragm cell, but these are not yet in use on an industrial scale because of this.
In order to solve the aforementioned problèms, the present inventors have studied a method and an apparatus which enable simple and easy installation of a substantially flat membrane in a finger type electrolytic cell.
Thus the present invention provides a feasible method and an apparatus for installing a membrane in a finger type electrolytic cell.
Secondly, the present invention provi.des a method and an apparatus for converting an asbestos or modified asbestos diaphragm cell to a cation exchange membrane cell, and preparing and alkali metal hydroxide liquor containing little alkali metal chloride or the like.
Thirdly, the present invention provides a method and an apparatus for
- 2 -, .
, 7Ç~
producing an alkali metal hydroxide of high quality containing hardly any alkali metal chloride, by the use of a catlon exchange membrane installation frame.
Fourthly, the present invention provides a method and an apparatus which are free from danger to health and from environmental contamination due to asbestos.
Lastly, the present invention provides a method and an apparatus ~hich enable the production of an alkali metal hydroxide in an economically advantageous way.
According to the invention, the horizontal surfaces of a cathode not opposing an anode of the finger type electrolytic cell are covered with a membrane installation frame having a collar, the membrane is positioned substantially parallel to the vertical surfaces of the cathode, and the membrane is installed ; and secured to the collar by mechanlcal securing means.
As finger type electrolytic cells useful according to the present invention there are included not only a finger type construction cell such as that described at page 93, Chlorine Its Manufacture, Properties and Uses, edited by J. S. Scone, issued Reinhold Publishing Corporation, New York, 1962, but also a flattened tube type construction cell. Nowadays, the flattened tube type .
construction is also generally referred to as a finger type electrolytic cell.
As alkali metals herein, there are included sodium, potassium and the like.
An anode in a finger type electrolytic cell is commonly located and -~ embedded in an electroconductive bottom plate or side plate. According to the invention a membrane installation frame is positioned to cover the horizontal surfaces of a cathode not opposite an anode. That is, when the anode is embedded in the bottom plate, the installation frame is positioned to cover the horizontal surfaces of the cathode. When the membrane installation frame is electrically conductive, it is usually insulated from the cathode by insertion of packing, lining or by any other suitable means.
, 7Ç~
producing an alkali metal hydroxide of high quality containing hardly any alkali metal chloride, by the use of a catlon exchange membrane installation frame.
Fourthly, the present invention provides a method and an apparatus which are free from danger to health and from environmental contamination due to asbestos.
Lastly, the present invention provides a method and an apparatus ~hich enable the production of an alkali metal hydroxide in an economically advantageous way.
According to the invention, the horizontal surfaces of a cathode not opposing an anode of the finger type electrolytic cell are covered with a membrane installation frame having a collar, the membrane is positioned substantially parallel to the vertical surfaces of the cathode, and the membrane is installed ; and secured to the collar by mechanlcal securing means.
As finger type electrolytic cells useful according to the present invention there are included not only a finger type construction cell such as that described at page 93, Chlorine Its Manufacture, Properties and Uses, edited by J. S. Scone, issued Reinhold Publishing Corporation, New York, 1962, but also a flattened tube type construction cell. Nowadays, the flattened tube type .
construction is also generally referred to as a finger type electrolytic cell.
As alkali metals herein, there are included sodium, potassium and the like.
An anode in a finger type electrolytic cell is commonly located and -~ embedded in an electroconductive bottom plate or side plate. According to the invention a membrane installation frame is positioned to cover the horizontal surfaces of a cathode not opposite an anode. That is, when the anode is embedded in the bottom plate, the installation frame is positioned to cover the horizontal surfaces of the cathode. When the membrane installation frame is electrically conductive, it is usually insulated from the cathode by insertion of packing, lining or by any other suitable means.
- 3 -.~ I
37~
It is a feature of the present invention that installation of the substantia]ly flat membrane to the curved surfaces of the cathode can be facilitated by providing a collar with the installation frame. The collar is preferably located at an angle of about 90 degrees or less, more preferably from about 90 degrees to about 30 degrees, to the flat portion of the membrane installation frame. The most preferred angle is about 90 degrees since neither expansion nor contraction of the membrane is required. However, it is desirable to locate the collar close to the bottom plate or side plate in which the anode is embedded, at an angle of about 60 degrees to about 30 degrees, thereby facilitating assembly of the anode and the cathode to which the membrane has been positioned. In the case of an angle of less than 90 degrees, the membrane has to be flared to conform with the collar angle. The smaller the angle, the larger the flare of the membrane. While the flared membrane can be made from a polymer by heat-moulding without much difficulty, it is rather difficult to form a flared membrane from a flat membrane. Accordingly, the collar angle is decided upon in accordance with the degree of ease of processing the membrane and the operation efficiency. Therefore, the lower limit of an angle of 30 degrees i~ a matter of practice, not theory. Inversely, in the case of an angle of more than 90 degrees, the membrane must be contracted or folded to secure it to the collar. Care must be taken that the efficiency of assembly of the anode and the cathode is not disrupted, when the collar angle close to the bottom or side plate in which the anode is embedded, is more than 90 degrees.
The membrane is secured to the collar and the membrane installation frame by a mechanical securing ~eans. One such securing means is the use of ~ bolts. The use of a press plate and bolts provides better attachment. Nuts, ; washers, spring washers or ~he like may also be used, if desired. Another suitable securing means is clips. An effective seal is obtained by the combined use of a press plate and clips. Securing by clips is preferred because there
37~
It is a feature of the present invention that installation of the substantia]ly flat membrane to the curved surfaces of the cathode can be facilitated by providing a collar with the installation frame. The collar is preferably located at an angle of about 90 degrees or less, more preferably from about 90 degrees to about 30 degrees, to the flat portion of the membrane installation frame. The most preferred angle is about 90 degrees since neither expansion nor contraction of the membrane is required. However, it is desirable to locate the collar close to the bottom plate or side plate in which the anode is embedded, at an angle of about 60 degrees to about 30 degrees, thereby facilitating assembly of the anode and the cathode to which the membrane has been positioned. In the case of an angle of less than 90 degrees, the membrane has to be flared to conform with the collar angle. The smaller the angle, the larger the flare of the membrane. While the flared membrane can be made from a polymer by heat-moulding without much difficulty, it is rather difficult to form a flared membrane from a flat membrane. Accordingly, the collar angle is decided upon in accordance with the degree of ease of processing the membrane and the operation efficiency. Therefore, the lower limit of an angle of 30 degrees i~ a matter of practice, not theory. Inversely, in the case of an angle of more than 90 degrees, the membrane must be contracted or folded to secure it to the collar. Care must be taken that the efficiency of assembly of the anode and the cathode is not disrupted, when the collar angle close to the bottom or side plate in which the anode is embedded, is more than 90 degrees.
The membrane is secured to the collar and the membrane installation frame by a mechanical securing ~eans. One such securing means is the use of ~ bolts. The use of a press plate and bolts provides better attachment. Nuts, ; washers, spring washers or ~he like may also be used, if desired. Another suitable securing means is clips. An effective seal is obtained by the combined use of a press plate and clips. Securing by clips is preferred because there
- 4 -~J~
:
is no need to make holes in the membrane. The use of clips formed as part of the press plate increases efficiency of assembly. Combined use of bolts and clips is effective. For example, it is rather difficult ~o secure the membrane to the curved portion by clips alone or with the press plate, but this can be done with bolts alone or together with the press plate, while the membrane can be secured to the straight portion by clips singly or in combination with the press plate.
When press plates and bolts are used, it is preferred to use a press plate having a longitudinal edge flange or longitudinal edge flanges for strength considerations so that waving does not occur which can result in an imperfect seal. Without flanges on the press plate, more bolts are required to prevent the waving phenomenon from occurring. Obviously, a decrease in the number of bolts required increases efficiency of installation.
The membrane is secured to the collar even without using the press plate, but the press plate enables easier and more complete assembly. In cases where no press plate is employed, it is necessary that the secured portion of the membrane be hardened by thickening that portion during production of the ;- membrane or by folding the membrane twofold or threefold and heat-fusing. More effective securing is also obtained by applying bolts or clips at smaller ;~ 20 intervals than in the case where the press plate is used. When a microporous membrane is employed, insufficient securing is not necessarily problematical as compared with ion exchange membrane, since it is inherently hydrodynamically permeable.
The membrane installation frame, the press plate and the like have to be made from materials which are resistant for example to anolyte. Titanium, zirconium, tantalum or alloys thereof such as titanium-palladium, titanium-tantalum, Hastelloy* or the like are suitable. Organic materials other than the metallic materials as aforesaid, are suitable, as for example FRP ~glass *Trade Mar~ for nickel-base, corrosion resistant alloys ,. .. ..
..~
':
~76~4L
fibre-reinforced plastic), hea~-resistant polyvinyl chloride, polypropylene, fluorocarbon polymer, fluorocarbon polymer or rubber lined metals or the like.
Examples of fluorocarbon polymers are polymers of tetrafluoroethylene, hexafluoropropylene, perfluoroalkylvinylether, copolymers thereof, polytri-fluorochloroethylene, polyfluorovinylidene and the like.
I~hen the membrane installation frame is made of an electro-conductive ., ~' .,~
~ - 5a .~
material, insulating packing is interposed between the frame and the cathode, otherwise, a lining or coating is applied to at least the surface of the cathode.
When the membrane installation frame is of plastics, washers should be used.
The press plate is preferably made from metallic materials but a plastic press plate is desirably used with washers. As suitable materials for bolts, nuts, washers, clips and the clips formed as part of a press plate, metals such as titanium, tantalum, titanium-tantalum alloy and the like are preferred. Organic materials such as fluorocarbon polymer bolts may also be used.
In order to accomplish more complete securing and sealing, it is preferred to interpose a polyfluorocarbon packing, as for example, manufactured by E. I. Du Pont de Nemours & Company under the trade mark "Teflon", between thecollar and the membrane, and further between the membrane and the press plate, ~`! if necessary. As packing, "Teflon" thin film or the like may be suitably used which are known as a porous film or tape seal. A thin film of fluorocarbon polymer other than "Teflon", such as tetrafluoroethylene-hexafluoropropylene co-polymer, may also be used. Sealants such as "Teflon" paste, silicone grease and the like may be used with the packing to provide more perfect securing and sealing.
A membrane formed in a cylindrical shape is preferably used. The cylindrical membrane is obtained by extrusion moulding, heat-sealing, use of adhesives and the like.
` When a cation exchange membrane is employed, the cell liquor concentra-tion (sodium hydroxide concentration) can be increased over 30 to 40%. As cation exchange membranes, polyfluorocarbon membrane with sulfonic acid group, sulfonamide group, carboxylic acid group, as for example, "Nafion* #110", "#215", "#315", "#425" and the like which are produced and sold by E. I. Du Pont de Nemours & Company may be used.
In cases where the present invention is applied to a microporous * Trade Mark ~1 ' :.
3 ~ 6~
membrane, there are advantages that back flow of OH is reduced due to the amount of flux per unit area of membrane being increased, and the sodium hydroxide concentration in the cell liquor can be raised at the same oxygen concentration in chlorine. The operation costs can therefore be reduced on account of the decrease in cell voltage and the increase in the cell liquor concentration. Although it is difficult to apply an ion exchange membrane method -to an electrolysis plant where subterranean brine is used, if a microporous membrane method is carried out according to the method and apparatus of the present invention, operation costs can be reduced. As microporous membranes, "Nafion* #701", "#710" or the like which are manufactured and sold by E. I. ~u Pont de Nemours & Company are Stli table.
Figure 1 is a perspective vertical sectional view of a finger type electrolytic cell wherein the membrane installation frame for attachment of the membrane is located DO as to cover the surfaces of the cathode at right angles to an anode positioning direction between the cathodes.
` Figure 2 illustrates an enlarged partial sectional view of Figure 1.
Figure 3 is a sectional view illustrating attachment of the membrane to the installation frame.
Figures 4 and 8 illustrate perspective vertical sectional views of a finger type electrolytic cell to which the membrane is installed using clips according to the present invention.
Figures 5 and 9 are enlarged partial sectional views of Figures 4 and 8, respectively.
Figures 6 and 10 illustrate sectional views of the attachment of the membrane to the installati.on frame.
Figure 7 is a perspective view of a clip and Figure 11 is a perspective view of clips formed as part of a press plate.
Figure 12 is a perspective vertical sectional view of a finger type * Trade Mark .~
. . .
76~9l electrolytic cell wherein one collar close to the bottom plate provided with the anode is located at about ~5 degrees to, and the other collar is located at about 90 degrees to, the flat portion of the membrane installation frame, to which collars the membrane is attached.
Figure 13 is an enlarged partial sectional view of Figure 12 and Figure 1~ is a sectional view illustrating the membrane attachment to the lower collar (the collar close to the bottom plate embedding the anode).
The present invention will be illustrated in more detail by way of particular embodiments and examples, which are not, however, to be construed ` 10 in any manner as limiting to the invention. `
EXAMPI.E 1 . . .
As is shown in Figure 1, membranes 4, formed in a cylindrical shape are positioned adjacent to collars 7 located at about 90 degrees to the flat portion 7a of a membrane installation frame. The membranes are positioned substantially parallel to the vertical surfaces 11 of the cathodes and secured by means of bolts and nuts 3 to the collars using press plates 2, a packing 6 being interposed between the collar and the membrane (Figure 3). Thus, a cathode com-, . t:
partment 8 and an anode compartment 9 are completely isolated from each other tFigure 2). The membrane installation frames 1 are located in a manner that the surfaces 10 of the cathode at right angles to the anode 12 embedded in bottom plate 13 are covered with the flat portion 7a of the installation frame. The bottom plate 13 is insulated from the cathode box 5 by inserting an insulator 14 between the two. As the membrane, cation exchange membrane Nafion* #315 produced L
by E. I. Du Pont de Nemours & Company is employed.
To the anode compartment of such a cell was supplied`a hydrochloric ~-acid-containing sodium chloride solution, deionized water`was fed to the cathode compartment, and then 2,000A electric current supplied to the cell. The anode current density was 25A/dm . The brine supplied was 3N with respect to the Na~l L
*Trade Mark - 8 ~
~7~4 and the HCl was 0.2N in the brlne. After continuous operation for 7 daysJ the NaCl concentration was as low as 20 ppm in the catholyte and the NaOH concentration was 16~ in the catholyte.
:
As illustrated in Figure 4, cylindrical membrane 4 is positioned substantially parallel to the vertical surfaces of the cathode and secured by the use of the press plate 2 and clips 15 to the collars 7 located at about 90 degrees to the flat portion 7a of the membrane installation frame 1. At the curved portion securing is effected using bolts and nuts. Packing 6 is inserted between 10 the collar and the membrane (Figure 6). The cathode compartment and the anode compartment are thus iso]ated from each other (Figure 5). A suitable number of clips shown in Figure 7 are employed at desired intervals to accomplish securing and sealing. Operation efficiency is improved as compared with Example l.
A cylindrically formed membrane 4 is positioned, as is depicted in ; Figure 8 substantially parallel to the vertical surfaces of the cathodes and secured to the collars 7 which are located at about 90 degrees to the flat portion 7a of the membrane installation frame, using clips 16 which are part of a press plate. At the curved portion using a U-form press plate 2a is secured to the collars 7 with packing inserted therebetween, by bolts and nuts. The labor and time required for the installation of membranes to the electrolytic cell are markedly reduced. I
EXAMPLE 4 - i A cylindrical membrane 4 having one edge flared is positioned parallel to the surfaces of the cathode, then applied to the collars 7. While the upper part is located at about 90 degrees, the lower (close to the bottom plate in which the anode is embedded) is located at about 45 degrees to the flat portion 7a of the membrane installation frame l. The membrane is secured and sealed by means ~1 .
., ... : , ,:
: ,' ' : ' " ' ' 7~
of clips and the press plate to the collars. At .the curved portion, securing i5 achieved by screw bolts. Between the collar and the membrane a packing is inter-posed (Figure 14). The cathode compartment 8 is thus isolated from the anode compartment 9 (Figure 13). Assemblage of the membrane installed cathode box and the anode embedded bottom plate is effected by rotating the cathode box at an angle of 180 degrees. By locati.ng the collar 7 at 45 degrees to the flat portion 7a of the insta].lation frame, operation efficiency of assembly i~ greatly improved.
' :, ~
:
is no need to make holes in the membrane. The use of clips formed as part of the press plate increases efficiency of assembly. Combined use of bolts and clips is effective. For example, it is rather difficult ~o secure the membrane to the curved portion by clips alone or with the press plate, but this can be done with bolts alone or together with the press plate, while the membrane can be secured to the straight portion by clips singly or in combination with the press plate.
When press plates and bolts are used, it is preferred to use a press plate having a longitudinal edge flange or longitudinal edge flanges for strength considerations so that waving does not occur which can result in an imperfect seal. Without flanges on the press plate, more bolts are required to prevent the waving phenomenon from occurring. Obviously, a decrease in the number of bolts required increases efficiency of installation.
The membrane is secured to the collar even without using the press plate, but the press plate enables easier and more complete assembly. In cases where no press plate is employed, it is necessary that the secured portion of the membrane be hardened by thickening that portion during production of the ;- membrane or by folding the membrane twofold or threefold and heat-fusing. More effective securing is also obtained by applying bolts or clips at smaller ;~ 20 intervals than in the case where the press plate is used. When a microporous membrane is employed, insufficient securing is not necessarily problematical as compared with ion exchange membrane, since it is inherently hydrodynamically permeable.
The membrane installation frame, the press plate and the like have to be made from materials which are resistant for example to anolyte. Titanium, zirconium, tantalum or alloys thereof such as titanium-palladium, titanium-tantalum, Hastelloy* or the like are suitable. Organic materials other than the metallic materials as aforesaid, are suitable, as for example FRP ~glass *Trade Mar~ for nickel-base, corrosion resistant alloys ,. .. ..
..~
':
~76~4L
fibre-reinforced plastic), hea~-resistant polyvinyl chloride, polypropylene, fluorocarbon polymer, fluorocarbon polymer or rubber lined metals or the like.
Examples of fluorocarbon polymers are polymers of tetrafluoroethylene, hexafluoropropylene, perfluoroalkylvinylether, copolymers thereof, polytri-fluorochloroethylene, polyfluorovinylidene and the like.
I~hen the membrane installation frame is made of an electro-conductive ., ~' .,~
~ - 5a .~
material, insulating packing is interposed between the frame and the cathode, otherwise, a lining or coating is applied to at least the surface of the cathode.
When the membrane installation frame is of plastics, washers should be used.
The press plate is preferably made from metallic materials but a plastic press plate is desirably used with washers. As suitable materials for bolts, nuts, washers, clips and the clips formed as part of a press plate, metals such as titanium, tantalum, titanium-tantalum alloy and the like are preferred. Organic materials such as fluorocarbon polymer bolts may also be used.
In order to accomplish more complete securing and sealing, it is preferred to interpose a polyfluorocarbon packing, as for example, manufactured by E. I. Du Pont de Nemours & Company under the trade mark "Teflon", between thecollar and the membrane, and further between the membrane and the press plate, ~`! if necessary. As packing, "Teflon" thin film or the like may be suitably used which are known as a porous film or tape seal. A thin film of fluorocarbon polymer other than "Teflon", such as tetrafluoroethylene-hexafluoropropylene co-polymer, may also be used. Sealants such as "Teflon" paste, silicone grease and the like may be used with the packing to provide more perfect securing and sealing.
A membrane formed in a cylindrical shape is preferably used. The cylindrical membrane is obtained by extrusion moulding, heat-sealing, use of adhesives and the like.
` When a cation exchange membrane is employed, the cell liquor concentra-tion (sodium hydroxide concentration) can be increased over 30 to 40%. As cation exchange membranes, polyfluorocarbon membrane with sulfonic acid group, sulfonamide group, carboxylic acid group, as for example, "Nafion* #110", "#215", "#315", "#425" and the like which are produced and sold by E. I. Du Pont de Nemours & Company may be used.
In cases where the present invention is applied to a microporous * Trade Mark ~1 ' :.
3 ~ 6~
membrane, there are advantages that back flow of OH is reduced due to the amount of flux per unit area of membrane being increased, and the sodium hydroxide concentration in the cell liquor can be raised at the same oxygen concentration in chlorine. The operation costs can therefore be reduced on account of the decrease in cell voltage and the increase in the cell liquor concentration. Although it is difficult to apply an ion exchange membrane method -to an electrolysis plant where subterranean brine is used, if a microporous membrane method is carried out according to the method and apparatus of the present invention, operation costs can be reduced. As microporous membranes, "Nafion* #701", "#710" or the like which are manufactured and sold by E. I. ~u Pont de Nemours & Company are Stli table.
Figure 1 is a perspective vertical sectional view of a finger type electrolytic cell wherein the membrane installation frame for attachment of the membrane is located DO as to cover the surfaces of the cathode at right angles to an anode positioning direction between the cathodes.
` Figure 2 illustrates an enlarged partial sectional view of Figure 1.
Figure 3 is a sectional view illustrating attachment of the membrane to the installation frame.
Figures 4 and 8 illustrate perspective vertical sectional views of a finger type electrolytic cell to which the membrane is installed using clips according to the present invention.
Figures 5 and 9 are enlarged partial sectional views of Figures 4 and 8, respectively.
Figures 6 and 10 illustrate sectional views of the attachment of the membrane to the installati.on frame.
Figure 7 is a perspective view of a clip and Figure 11 is a perspective view of clips formed as part of a press plate.
Figure 12 is a perspective vertical sectional view of a finger type * Trade Mark .~
. . .
76~9l electrolytic cell wherein one collar close to the bottom plate provided with the anode is located at about ~5 degrees to, and the other collar is located at about 90 degrees to, the flat portion of the membrane installation frame, to which collars the membrane is attached.
Figure 13 is an enlarged partial sectional view of Figure 12 and Figure 1~ is a sectional view illustrating the membrane attachment to the lower collar (the collar close to the bottom plate embedding the anode).
The present invention will be illustrated in more detail by way of particular embodiments and examples, which are not, however, to be construed ` 10 in any manner as limiting to the invention. `
EXAMPI.E 1 . . .
As is shown in Figure 1, membranes 4, formed in a cylindrical shape are positioned adjacent to collars 7 located at about 90 degrees to the flat portion 7a of a membrane installation frame. The membranes are positioned substantially parallel to the vertical surfaces 11 of the cathodes and secured by means of bolts and nuts 3 to the collars using press plates 2, a packing 6 being interposed between the collar and the membrane (Figure 3). Thus, a cathode com-, . t:
partment 8 and an anode compartment 9 are completely isolated from each other tFigure 2). The membrane installation frames 1 are located in a manner that the surfaces 10 of the cathode at right angles to the anode 12 embedded in bottom plate 13 are covered with the flat portion 7a of the installation frame. The bottom plate 13 is insulated from the cathode box 5 by inserting an insulator 14 between the two. As the membrane, cation exchange membrane Nafion* #315 produced L
by E. I. Du Pont de Nemours & Company is employed.
To the anode compartment of such a cell was supplied`a hydrochloric ~-acid-containing sodium chloride solution, deionized water`was fed to the cathode compartment, and then 2,000A electric current supplied to the cell. The anode current density was 25A/dm . The brine supplied was 3N with respect to the Na~l L
*Trade Mark - 8 ~
~7~4 and the HCl was 0.2N in the brlne. After continuous operation for 7 daysJ the NaCl concentration was as low as 20 ppm in the catholyte and the NaOH concentration was 16~ in the catholyte.
:
As illustrated in Figure 4, cylindrical membrane 4 is positioned substantially parallel to the vertical surfaces of the cathode and secured by the use of the press plate 2 and clips 15 to the collars 7 located at about 90 degrees to the flat portion 7a of the membrane installation frame 1. At the curved portion securing is effected using bolts and nuts. Packing 6 is inserted between 10 the collar and the membrane (Figure 6). The cathode compartment and the anode compartment are thus iso]ated from each other (Figure 5). A suitable number of clips shown in Figure 7 are employed at desired intervals to accomplish securing and sealing. Operation efficiency is improved as compared with Example l.
A cylindrically formed membrane 4 is positioned, as is depicted in ; Figure 8 substantially parallel to the vertical surfaces of the cathodes and secured to the collars 7 which are located at about 90 degrees to the flat portion 7a of the membrane installation frame, using clips 16 which are part of a press plate. At the curved portion using a U-form press plate 2a is secured to the collars 7 with packing inserted therebetween, by bolts and nuts. The labor and time required for the installation of membranes to the electrolytic cell are markedly reduced. I
EXAMPLE 4 - i A cylindrical membrane 4 having one edge flared is positioned parallel to the surfaces of the cathode, then applied to the collars 7. While the upper part is located at about 90 degrees, the lower (close to the bottom plate in which the anode is embedded) is located at about 45 degrees to the flat portion 7a of the membrane installation frame l. The membrane is secured and sealed by means ~1 .
., ... : , ,:
: ,' ' : ' " ' ' 7~
of clips and the press plate to the collars. At .the curved portion, securing i5 achieved by screw bolts. Between the collar and the membrane a packing is inter-posed (Figure 14). The cathode compartment 8 is thus isolated from the anode compartment 9 (Figure 13). Assemblage of the membrane installed cathode box and the anode embedded bottom plate is effected by rotating the cathode box at an angle of 180 degrees. By locati.ng the collar 7 at 45 degrees to the flat portion 7a of the insta].lation frame, operation efficiency of assembly i~ greatly improved.
' :, ~
Claims (27)
1. Method of installation of a membrane to a finger type electrolytic cell for the production of chlorine, hydrogen and an alkali metal hydroxide by electrolysis of an aqueous alkali metal chloride solution which cell comprises a plurality of anodes and a cathode box providing a cathode between adjacent anodes, and a membrane between adjacent anodes and cathodes, which comprises covering the upper and lower horizontal surfaces of the cathode not opposing the anodes with upper and lower membrane installation frames having collars;
positioning cation exchange membranes in a cylindrical shape substantially parallel to the vertical surfaces of said cathodes, and installing and securing the membranes to the collars by mechanical securing means.
positioning cation exchange membranes in a cylindrical shape substantially parallel to the vertical surfaces of said cathodes, and installing and securing the membranes to the collars by mechanical securing means.
2. The method of claim 1, wherein the membrane is a cation exchange membrane and/or a microporous membrane.
3. The method of claim 1, wherein the angle of the collar is in the range of from about 90 degrees to about 30 degrees to the flat portion of the membrane installation frame.
4. The method of claim 1, wherein the mechanical securing means is bolts.
5. The method of claim 1, wherein the mechanical securing means is clips.
6. The method of claim 1, wherein the mechanical securing means comprises a press plate and bolts.
7. The method of claim 1, wherein the mechanical securing means comprises a press plate and clips.
8. The method of claim 1, wherein the mechanical securing means is clips formed with a press plate.
9. The method of claim 1, wherein the mechanical securing means is a press plate in combination with bolts and clips.
10. The method of claim 1, wherein the membrane installation frame is made of titanium, zirconium, tantalum or an alloy thereof, Hastelloy*; glass fibre-reinforced plastic, heat-resistant polyvinyl chloride, polypropylene, fluorocarbon polymer, or fluorocarbon polymer or rubber lined metals.
11. The method of claim 4, claim 6 or claim 9, wherein the bolts are made of titanium, zirconium, tantalum or an alloy thereof, Hastelloy* or fluorocarbon polymer.
12. The method of claim 5, claim 7 or claim 9, wherein the clips are made of titanium, zirconium, tantalum or an alloy thereof, Hastelloy* or fluorocarbon polymer.
13. The method of claim 7, claim 8 or claim 9, wherein the press plate is made of titanium, zirconium, tantalum or an alloy thereof, Hastelloy*, glass fibre-reinforced plastic, heat-resistant polyvinyl chloride, polypropylene, fluorocarbon polymer, or fluorocarbon polymer or rubber lined metals.
14. The method of claim 1 or claim 2, wherein the membrane is of cylindrical shape.
15. A finger type electrolytic cell for the production of chlorine, hydrogen and an alkali metal hydroxide by electrolysis of an aqueous alkali metal chloride solution which cell comprises a plurality of anodes and cathode box providing a cathode between adjacent anodes, and a membrane between adjacent anodes and cathodes, further comprising upper and lower membrane installation frames having collars positioned so as to cover the upper and lower horizontal surfaces of the cathodes not opposing the anodes, cation exchange membranes in a cylindrical shape located substantially parallel to the vertical surfaces of the cathodes, and mechanical securing means for installing and securing the membranes to the collars.
16. The cell of claim 15, wherein the collar is located at an angle of * Trade Mark about 90 degrees to about 30 degrees to the flat portion of the membrane installation frame,
17. The cell of claim 15, wherein a press plate is also used, and the membrane is interposed and secured between the press plate and the collar.
18. The cell of claim 15, wherein the mechanical securing means is bolts.
19. The cell of claim 15, wherein the mechanical securing means is clips .
20. The cell of claim 15, wherein the mechanical securing means is clips formed with a press plate.
21. The cell of claim 15, wherein the mechanical securing means is bolts and clips.
22. The cell of claim 15, wherein the membrane installation frame is made of titanium, zirconium, tantalum, or an alloy thereof, Hastelloy*, glass fibre-reinforced plastic,heat-resistant polyvinyl chloride, polypropylene, fluorocarbon polymer, or fluorocarbon polymer or rubber lined metals.
23. The cell of claim 15, wherein the bolts are made of titanium, zirconium, tantalum or an alloy thereof, Hastelloy* or fluorocarbon polymer.
24. The cell of claim 15, wherein the clips are made of titanium, zirconium, tantalum or an alloy thereof, Hastelloy* or fluorocarbon polymer.
25. The cell of claim 17, wherein the press plate is made of titanium, zirconium, tantalum or an alloy thereof, Hastelloy*, glass fibre-reinforced plastic, heat-resistant polyvinyl chloride, polypropylene, fluorocarbon polymer, or fluorocarbon polymer or rubber lined metals.
26. The cell of claim 17, wherein the securing means is bolts and the press plate has a longitudinal edge flange.
27. The cell of claim 17, wherein the securing means is bolts and the press plate has longitudinal edge flanges.
* Trade Mark
* Trade Mark
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP178714/1977 | 1977-12-26 | ||
JP1977178714U JPS5812836Y2 (en) | 1977-12-26 | 1977-12-26 | Membrane installation equipment for alkaline chloride electrolyzer |
JP1978107197U JPS5526015U (en) | 1978-08-03 | 1978-08-03 | |
JP107197/78 | 1978-08-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1107684A true CA1107684A (en) | 1981-08-25 |
Family
ID=26447246
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA318,503A Expired CA1107684A (en) | 1977-12-26 | 1978-12-22 | Method and apparatus for installation of a membrane to an electrolytic cell |
Country Status (4)
Country | Link |
---|---|
CA (1) | CA1107684A (en) |
DE (1) | DE2855837A1 (en) |
FR (1) | FR2412735A1 (en) |
GB (1) | GB2013242B (en) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5524963A (en) * | 1978-08-10 | 1980-02-22 | Kanegafuchi Chem Ind Co Ltd | Diaphragm fixing device |
US4229277A (en) * | 1979-08-30 | 1980-10-21 | Olin Corporation | Glove-like diaphragm structure for electrolytic cells |
US4283264A (en) * | 1979-09-14 | 1981-08-11 | Hooker Chemicals & Plastics Corp. | Electrolytic cell separator, tubular member component thereof and methods for manufacturing and using such separator and component |
JPS5719390A (en) * | 1980-07-11 | 1982-02-01 | Asahi Glass Co Ltd | Method for mounting ion exchange membrane to electrolytic cell |
JPS5723078A (en) * | 1980-07-17 | 1982-02-06 | Kanegafuchi Chem Ind Co Ltd | Diaphragm type electrolytic cell having bag-shaped diaphragm |
JPS5741386A (en) * | 1980-08-22 | 1982-03-08 | Chlorine Eng Corp Ltd | Electrolytic cell by ion exchange membrane method |
JPS5891179A (en) * | 1981-11-24 | 1983-05-31 | Chlorine Eng Corp Ltd | Electrolytic cell by ion exchange membrane method |
US4894128A (en) * | 1986-05-05 | 1990-01-16 | The Dow Chemical Company | Membrane unit for electrolytic cell |
DK501585A (en) * | 1984-11-05 | 1986-05-06 | Dow Chemical Co | MEMBRANE UNIT FOR AN ELECTROLYCLE CELL |
US4877499A (en) * | 1984-11-05 | 1989-10-31 | The Dow Chemical Company | Membrane unit for electrolytic cell |
US4915803A (en) * | 1988-09-26 | 1990-04-10 | The Dow Chemical Company | Combination seal and frame cover member for a filter press type electrolytic cell |
US4886586A (en) * | 1988-09-26 | 1989-12-12 | The Dow Chemical Company | Combination electrolysis cell seal member and membrane tentering means for a filter press type electrolytic cell |
US4898653A (en) * | 1988-09-26 | 1990-02-06 | The Dow Chemical Company | Combination electrolysis cell seal member and membrane tentering means |
US4892632A (en) * | 1988-09-26 | 1990-01-09 | The Dow Chemical Company | Combination seal member and membrane holder for an electrolytic cell |
US4940518A (en) * | 1988-09-26 | 1990-07-10 | The Dow Chemical Company | Combination seal member and membrane holder for a filter press type electrolytic cell |
JP3480988B2 (en) * | 1994-07-01 | 2003-12-22 | ジャパンゴアテックス株式会社 | Sealing and reinforcing membrane material for fluoropolymer solid electrolyte membrane, fluoropolymer solid electrolyte membrane using the same, and plating method thereof |
US5945192A (en) * | 1995-06-29 | 1999-08-31 | Japan Gore-Tex, Inc. | Sealing assembly for a solid polymer ion exchange membrane |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1797377A (en) * | 1928-09-29 | 1931-03-24 | Westinghouse Electric & Mfg Co | Electrolytic cell |
US3878082A (en) * | 1974-02-19 | 1975-04-15 | Basf Wyandotte Corp | Diaphragm cell including means for retaining a preformed sheet diaphragm against the cathode |
US3923630A (en) * | 1974-08-16 | 1975-12-02 | Basf Wyandotte Corp | Electrolytic cell including diaphragm and diaphragm-support structure |
US3980544A (en) * | 1975-07-14 | 1976-09-14 | Olin Corporation | Apparatus and method for securing a fabricated diaphragm to electrodes in an electrolytic cell |
-
1978
- 1978-12-21 GB GB7849589A patent/GB2013242B/en not_active Expired
- 1978-12-22 FR FR7836271A patent/FR2412735A1/en active Granted
- 1978-12-22 CA CA318,503A patent/CA1107684A/en not_active Expired
- 1978-12-22 DE DE19782855837 patent/DE2855837A1/en active Granted
Also Published As
Publication number | Publication date |
---|---|
GB2013242A (en) | 1979-08-08 |
FR2412735B1 (en) | 1985-03-15 |
GB2013242B (en) | 1982-06-16 |
FR2412735A1 (en) | 1979-07-20 |
DE2855837A1 (en) | 1979-07-12 |
DE2855837C2 (en) | 1987-08-13 |
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