USRE24989E - Peters - Google Patents
Peters Download PDFInfo
- Publication number
- USRE24989E USRE24989E US24989DE USRE24989E US RE24989 E USRE24989 E US RE24989E US 24989D E US24989D E US 24989DE US RE24989 E USRE24989 E US RE24989E
- Authority
- US
- United States
- Prior art keywords
- electrodes
- sintered
- porous
- electrolyte
- accumulator
- 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
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Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/34—Gastight accumulators
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
- H01M10/52—Removing gases inside the secondary cell, e.g. by absorption
-
- 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
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Definitions
- This invention relates to electric accumulators and more especially to the permanently sealed type of accumulators operating with alakaline electrolytes.
- This invention also involves the technical improvement of rendering it possible to dispense with all special actions to guarantee, during the sealing of the accumulator, a higher charging capacity of the negative electrode as compared with the positive electrode. It is obvious that this ⁇ leads to -a saving of material and space.
- FIG. 1 is a vertical section of an accumulator according to this invention.
- Fig. 2 is an elevation of a sintered electrode plate.
- This accumulator comprises two electrodes 2 and 3 of any type suitable for an alkaline accumulator which are enclosed in a suitable jar 4, and have lead elements 5, 5 extending through insulators 6, 6 into the circumambient air, thereby forming a gas-tight and hermetically sealed arrangement.
- the electrolyte is held by capillary action entirely within a porous separator l1 which holds apart the respective facing surfaces of bot-h electrodes.
- the electrodes have a porous skeleton structure of sintered nickel.
- the electrode structure is shown in Fig. 2.
- Here 7 represents the porous nickel skeleton with which is intermixed the active mass of the electrode, held in the skeleton as a carrier.
- the active mass has been at least partly removed, so as to expose a large area of sintered nickel.
- This surface 8 is preferably the surface which is free to absorb the gas, i.e. the sur-face not in contact with the separator 1.
- Fig. 1 is an elevation of a sintered electrode plate
- Fig. 2 a vertical
- Fig. 3 a horizontal section, on the lline A-B in Fig. 2, of an accumulator according to this invention.
- An accumulator of the hermetically sealed alkaline type having two composite electrodes comprising a porous skeleton structure of sintered nickel and active mass, said skeleton of sintered nickel having one surface uncovered by the active mass, a porous separator closely bound between the respective electrodes, and an electrolyte substantially completely absorbed within said separator, whereby oxygen freed by electrolysis is substantially completely absorbed by said uncovered surface] 2.
- An accumulator of the hermetically sealed alkaline type comprising, in combination, two composite electrodes, each including a porous skeleton structure of sintered nickel and active mass, and having inner faces being spaced from and facing each other and outer faces, said porous skeleton structure of sintered nickel of at least one of said electrodes having at least a surface portion of its outer face uncovered by the active mass; a porous .separator arranged between said inner faces of said electrodes in contact therewith and at least substantially covering the same; and an electrolyte substantially completely absorbed within said porous separator, whereby oxygen freed by electrolysis is substantially completely taken up by said uncovered surface portion.
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Secondary Cells (AREA)
- Cell Electrode Carriers And Collectors (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Electrodes For Compound Or Non-Metal Manufacture (AREA)
- Hybrid Cells (AREA)
Description
F. PETERS May 23, v1961 OXIDIZABLE ELECTRODE FOR SEALED ALKALINE STORAGE CELLS Original Filed Ilarch 23. 1953 lllli:
@Warm/sys United States Patent (XDIZABLE' ELECTRODE FOR SEALED 'ALKALINE STORAGE CELIS Freimnt Peters, Hagen, Westphalia, Germany, assignor to A n-Fabrik Aktiengesellschaft, Hagen, Westphalia, Germany, a joint-stock company of Germany No. 2,798,110, dated July 2, 1957, Ser. No. 344,210, Mar. 23, 1953. Application for reissue July 1, 1959, Ser. No. 824,444
Claims priority, application Germany Mar. 28, 1952 1 Claim. (Cl. 136-6) Matter enclosed in heavy brackets appears in the original patent but forms no of this reissue specilication; matter printed in indicates the additions made by reissue.
This invention relates to electric accumulators and more especially to the permanently sealed type of accumulators operating with alakaline electrolytes.
It is an object of this invention to provide new means for absorbing the gases developed in these cells.
It has already been suggested to cope with the gases developed -in such accumulators by altogether fixing the electrolyte in a porous separator and thereby bringing the electrolyte as well as the gases developed therein by capillary action into contact with the electrodes for the purpose of `getting the -gases absorbed. In accumulators of this type the capacities of the two electrodes had to be brought to a predetermined ratio by using a larger negative electrode and taking care to create predetermined charging conditions when gastightly sealing the container. The negative electrode was required to have a higher capacity for accumulating a charging current than the positive electrode, in order to avoid as far as possible the development of hydrogen. The reason for this was that, in contrast to the oxygen which during charging is freed yat the positive electrode, it was not possible outright to obtain an yabsorption of the hydrogen.
It has also been suggested to bring about the absorption of the `gases by using skeleton structures consisting of a sintered metal, for instance sintered nickel, to induce the oxygen and the hydrogen to enter anew into reaction with each other. In the operating of this process it appeared to be particularly advantageous to altogether immerse the electrodes in the electrolyte, but it was found that with `accumulators of this kind the effects desired could not be obtained.
I have now found to my surprise that sintered metals, and quite especially sintered nickel, if used as the carriers of the active mass, have the faculty of absorbing the gases provided the electrolyte is stored by capillary action in a porous separator. If this is done, a combined action takes place insofar as I was in a position of showing by tests that after a short period of time a state of equilibrium is reached in which no hydrogen is developed any more. I have found that the negative electrode oxidized to such an extent that during charging of t-he accumulator the potential of hydrogen development is not reached any more.
This invention also involves the technical improvement of rendering it possible to dispense with all special actions to guarantee, during the sealing of the accumulator, a higher charging capacity of the negative electrode as compared with the positive electrode. It is obvious that this `leads to -a saving of material and space.
In the drawing illustrating diagrammatically by way of example an embodiment of the invention:
Re. 24,989 Reissued May 23, 1961 Fig. 1 is a vertical section of an accumulator according to this invention; and
Fig. 2 is an elevation of a sintered electrode plate.
This accumulator comprises two electrodes 2 and 3 of any type suitable for an alkaline accumulator which are enclosed in a suitable jar 4, and have lead elements 5, 5 extending through insulators 6, 6 into the circumambient air, thereby forming a gas-tight and hermetically sealed arrangement. The electrolyte is held by capillary action entirely within a porous separator l1 which holds apart the respective facing surfaces of bot-h electrodes. The electrodes have a porous skeleton structure of sintered nickel. Y
The electrode structure is shown in Fig. 2. Here 7 represents the porous nickel skeleton with which is intermixed the active mass of the electrode, held in the skeleton as a carrier. At the surface 8 the active mass has been at least partly removed, so as to expose a large area of sintered nickel. This surface 8 is preferably the surface which is free to absorb the gas, i.e. the sur-face not in contact with the separator 1.
The advantages offered by this combination increase by providing, apart from the oxidizable sintered metal skelet0n [l] 7, also a highly porous sinter cake portion of the skeleton [l] 7 which is capable of forming or holding the active mass and being in an electric yand preferably a mechanical connection with the frame or main body of one or both of the two electrodes [3 and 4] 2 and 3. 'I'his combination greatly increases the influence of the sintered metal on the absorption of the gases by increasing the freely accessible oxidation surface of the sintered porous metal structure as compared with a structure altogether covered or embedded in the active mass.
[In the drawing illustrating diagrammatically by way of example an embodiment of the invention.
Fig. 1 is an elevation of a sintered electrode plate,
Fig. 2 a vertical, and
Fig. 3 a horizontal section, on the lline A-B in Fig. 2, of an accumulator according to this invention.
In the drawing 1 is is a positive and 2, 2 are two negative electrodes. Between them is Iarranged the porous separator 3 which retains by capillary action the entire electrolyte. A gas-and-liquid tightly closed container 4 surrounds these parts. The terminals 5 and 6 are fixed in the container wall and isolated therefrom. Owing to the fixing of the electrolyte within the separator the gas (oxygen) developed in the container lls the empty cavities 7 within this cell and in contact with the large-surface sintered negative electrodes so far depolarizes these electrodes that on the accumulator being char-ged no hydrogen is developed] Various changes may be made in the composition and arrangement of the various components of accumulators according to this invention without departing from it or sacriiicing the advantages thereof.
I claim:
[1. An accumulator of the hermetically sealed alkaline type having two composite electrodes comprising a porous skeleton structure of sintered nickel and active mass, said skeleton of sintered nickel having one surface uncovered by the active mass, a porous separator closely bound between the respective electrodes, and an electrolyte substantially completely absorbed within said separator, whereby oxygen freed by electrolysis is substantially completely absorbed by said uncovered surface] 2. An accumulator of the hermetically sealed alkaline type comprising, in combination, two composite electrodes, each including a porous skeleton structure of sintered nickel and active mass, and having inner faces being spaced from and facing each other and outer faces, said porous skeleton structure of sintered nickel of at least one of said electrodes having at least a surface portion of its outer face uncovered by the active mass; a porous .separator arranged between said inner faces of said electrodes in contact therewith and at least substantially covering the same; and an electrolyte substantially completely absorbed within said porous separator, whereby oxygen freed by electrolysis is substantially completely taken up by said uncovered surface portion.
References Cited in t he le of this patent or the original patent UNITED STATES PATENTS Dassler Jan. 11, 1938 Lange etal. Sept. 27, 1938 Neumann Sept. 8, 1953 Hagspihl et al Nov. 22, 1955 FOREIGN PATENTS Great Britain Miay 9, 1951
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2798110X | 1952-03-28 | ||
DE322027X | 1952-12-01 | ||
DEA20396A DE1037536B (en) | 1952-03-28 | 1954-05-24 | Permanently gas- and liquid-tight sealed accumulator with alkaline electrolyte |
DEA24117A DE1013341B (en) | 1952-03-28 | 1956-01-11 | Permanently gas- and liquid-tight sealed alkaline accumulator |
DEA15453A DE1011022B (en) | 1952-03-28 | 1956-01-11 | Permanently gas-tight sealed alkaline accumulator with porous electrodes made of sintered metals |
Publications (1)
Publication Number | Publication Date |
---|---|
USRE24989E true USRE24989E (en) | 1961-05-23 |
Family
ID=32330088
Family Applications (5)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US24989D Expired USRE24989E (en) | 1952-03-28 | Peters | |
US344210A Expired - Lifetime US2798110A (en) | 1952-03-28 | 1953-03-23 | Oxidizable electrode for sealed alkaline storage cells |
US395265A Expired - Lifetime US2997516A (en) | 1952-03-28 | 1953-11-30 | Gastight enclosed alkaline accumulator |
US633425A Expired - Lifetime US3003014A (en) | 1952-03-28 | 1957-01-10 | Gas-tight sealed alkaline accumulators |
US742912A Expired - Lifetime US3031517A (en) | 1952-03-28 | 1958-06-18 | Permanently sealed gas-tight accumulator |
Family Applications After (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US344210A Expired - Lifetime US2798110A (en) | 1952-03-28 | 1953-03-23 | Oxidizable electrode for sealed alkaline storage cells |
US395265A Expired - Lifetime US2997516A (en) | 1952-03-28 | 1953-11-30 | Gastight enclosed alkaline accumulator |
US633425A Expired - Lifetime US3003014A (en) | 1952-03-28 | 1957-01-10 | Gas-tight sealed alkaline accumulators |
US742912A Expired - Lifetime US3031517A (en) | 1952-03-28 | 1958-06-18 | Permanently sealed gas-tight accumulator |
Country Status (7)
Country | Link |
---|---|
US (5) | US2798110A (en) |
BE (4) | BE554100A (en) |
CH (4) | CH324312A (en) |
DE (3) | DE1037536B (en) |
FR (4) | FR1073058A (en) |
GB (2) | GB772594A (en) |
NL (1) | NL92024C (en) |
Families Citing this family (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1015874B (en) * | 1951-07-26 | 1957-09-19 | Accumulatoren Fabrik Ag | Permanently tightly sealed alkaline accumulator with a hydrogen-absorbing additional electrode |
BE524571A (en) * | 1952-03-28 | |||
US2988585A (en) * | 1952-06-23 | 1961-06-13 | Accumulatoren Fabrik Ag | Hermetically sealed alkaline storage battery |
NL112050C (en) * | 1956-04-06 | |||
LU35728A1 (en) * | 1957-01-28 | |||
US2951106A (en) * | 1957-02-19 | 1960-08-30 | Electric Storage Battery Co | Storage battery construction |
US3005943A (en) * | 1957-04-10 | 1961-10-24 | Electric Storage Battery Co | Sealed storage cell using liquid electrolyte |
US2951802A (en) * | 1957-06-05 | 1960-09-06 | Joseph C White | Electrolytic oxygen generator |
US2984607A (en) * | 1957-06-05 | 1961-05-16 | Joseph C White | Method of producing oxygen and hydrogen by electrolysis |
DE1135535B (en) * | 1958-01-11 | 1962-08-30 | Willi Krebs | Gas and liquid-tight accumulator |
NL235404A (en) * | 1958-01-25 | |||
US3023258A (en) * | 1958-03-28 | 1962-02-27 | Accumulatoren Fabrik Ag | Hermetically sealed galvanic smoothing or stabilization cell |
US2980745A (en) * | 1958-05-02 | 1961-04-18 | Accumulatoren Fabrik Ag | Counterelectromotive-force cell |
JPS3514315B1 (en) * | 1958-10-10 | 1960-09-29 | Union Carbide Corp | Rechargeable dry cell |
US2976341A (en) * | 1958-11-21 | 1961-03-21 | Union Carbide Corp | Elimination of formation of alkaline secondary cells |
DE1181292B (en) * | 1958-12-31 | 1964-11-12 | Varta Ag | Arrangement to prevent electrolyte leakage at the joints between housing parts made of metal and those made of plastic |
US3057943A (en) * | 1959-05-04 | 1962-10-09 | Electric Storage Battery Co | Gas permeable negative electrode |
US2941022A (en) * | 1959-05-05 | 1960-06-14 | Hyman J Mandel | Hermetically sealed nickel-cadmium storage battery |
US2980747A (en) * | 1959-08-10 | 1961-04-18 | Union Carbide Corp | Sealed nickel cadmium cell |
DE1194017B (en) * | 1960-08-17 | 1965-06-03 | Tesla Np | Permanently gas- and liquid-tight sealed alkaline accumulator |
US3223556A (en) * | 1961-04-13 | 1965-12-14 | Engelhard Ind Inc | Fuel cell |
FR82314E (en) * | 1961-07-05 | 1964-01-24 | Accumulateurs Fixes | Improvements made to electrolytic cells and more particularly to sealed accumulators operating without gas release |
US3170819A (en) * | 1961-09-05 | 1965-02-23 | Electric Storage Battery Co | Electric battery |
FR1398713A (en) * | 1961-12-07 | 1965-05-14 | Accumulateurs Fixes | Method of constructing electric accumulators and sealed electrolytic cells and articles obtained |
DE1271799B (en) * | 1962-12-21 | 1968-07-04 | Hans Vogt Dr H C | Process for forming alkaline accumulators to be operated in a gastight manner |
GB1066339A (en) * | 1962-12-21 | 1967-04-26 | Vogt Hans | Method of forming alkaline accumulators |
GB1080992A (en) * | 1963-05-22 | 1967-08-31 | Alkaline Batteries Ltd | Improvements relating to electric storage batteries |
US3304204A (en) * | 1963-10-02 | 1967-02-14 | Gould National Batteries Inc | Chemical formation of positive nickel electrodes |
ES304428A1 (en) * | 1963-10-09 | 1965-02-01 | Ab Tudor | Electrolytic element device hermetically closed, especially accumulator elements. (Machine-translation by Google Translate, not legally binding) |
US3347707A (en) * | 1966-06-23 | 1967-10-17 | Union Carbide Corp | Charged secondary cell |
US3427205A (en) * | 1966-09-01 | 1969-02-11 | Nasa | Spacecraft battery seals |
US3507699A (en) * | 1968-02-02 | 1970-04-21 | Yardney International Corp | Process for making a nickel electrode |
US3711331A (en) * | 1970-04-27 | 1973-01-16 | Gen Electric | Method of making an improved electrode for dischargeable cell |
US3804671A (en) * | 1972-09-18 | 1974-04-16 | Power Conversion Inc | Non-aqueous battery construction and method of sealing same by cold welding |
DE2826780C2 (en) * | 1978-06-19 | 1986-12-11 | Varta Batterie Ag, 3000 Hannover | Galvanic element |
SE454828B (en) * | 1984-05-07 | 1988-05-30 | Erik Sundberg | END BLYACKUMULATOR WITH ELECTROLYTE RESERVE |
SE8403704L (en) * | 1984-07-13 | 1986-01-14 | Tudor Ab | END OF LEAD BATTERY FOR OXYGEN RECOVERY |
FR2766972A1 (en) * | 1997-07-31 | 1999-01-29 | Cit Alcatel | WATERPROOF ELECTROCHEMICAL GENERATOR WITH RECOMBINATION DEVICE |
DE19754361A1 (en) * | 1997-12-08 | 1999-06-17 | Voit Willy Gmbh & Co | Method for producing a motor housing of an electric motor and motor housing of an electric motor |
JP4370027B2 (en) * | 1999-10-08 | 2009-11-25 | パナソニック株式会社 | Assembled battery |
US8338025B2 (en) * | 2010-08-09 | 2012-12-25 | Siemens Aktiengesellschaft | Self-sealed metal electrode for rechargeable oxide-ion battery cells |
US11611115B2 (en) | 2017-12-29 | 2023-03-21 | Form Energy, Inc. | Long life sealed alkaline secondary batteries |
US11552290B2 (en) | 2018-07-27 | 2023-01-10 | Form Energy, Inc. | Negative electrodes for electrochemical cells |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1468259A (en) * | 1917-09-08 | 1923-09-18 | Us Light & Heat Corp | Storage-battery practice |
GB383201A (en) * | 1932-05-14 | 1932-11-10 | Chloride Electrical Storage Co | Improvements relating to electric accumulators |
DE602702C (en) * | 1933-05-18 | 1934-09-14 | Accumulatoren Fabrik Ag | Galvanic element, in particular an electric accumulator |
NL39005C (en) * | 1933-05-18 | |||
DE674829C (en) * | 1933-11-18 | 1939-04-26 | Accumulatoren Fabrik Akt Ges | Electric collector |
US2361533A (en) * | 1943-10-11 | 1944-10-31 | Willard Storge Battery Company | Storage battery and grid therefor |
BE480966A (en) * | 1947-03-14 | |||
US2487499A (en) * | 1947-11-05 | 1949-11-08 | Chrysler Corp | Spirally wound storage cell |
BE492340A (en) * | 1947-12-15 | |||
US2571927A (en) * | 1947-12-20 | 1951-10-16 | Tech Gautrat S A R L Bureau | Electrolytic cell and in particular, alkaline cell |
BE486928A (en) * | 1948-02-04 | |||
GB677770A (en) * | 1948-02-04 | 1952-08-20 | Tech Gautrat Bureau | Electric storage battery cell |
US2634303A (en) * | 1949-02-02 | 1953-04-07 | Edison Inc Thomas A | Storage battery |
BE498790A (en) * | 1949-11-05 | |||
BE499395A (en) * | 1949-11-22 | |||
FR1000836A (en) * | 1949-11-23 | 1952-02-18 | Improvements to alkaline accumulator plates | |
US2614138A (en) * | 1950-01-26 | 1952-10-14 | Pierre A C Jacquier | Sealable storage battery construction |
US2642469A (en) * | 1950-10-30 | 1953-06-16 | Jr Wright W Gary | Alkaline battery |
LU31125A1 (en) * | 1950-12-09 | |||
US2653179A (en) * | 1951-07-26 | 1953-09-22 | John H Baldwin | Primary battery and method of making the same |
BE510102A (en) * | 1951-11-09 | |||
BE524571A (en) * | 1952-03-28 | |||
NL100375C (en) * | 1953-03-06 | |||
NL92641C (en) * | 1953-11-26 | 1900-01-01 | ||
US2842607A (en) * | 1954-03-29 | 1958-07-08 | Accumulatoren Fabrik Ag Fa | Hermetically-sealed storage battery |
-
0
- BE BE524571D patent/BE524571A/xx unknown
- BE BE518800D patent/BE518800A/xx unknown
- NL NL92024D patent/NL92024C/xx active
- BE BE537926D patent/BE537926A/xx unknown
- US US24989D patent/USRE24989E/en not_active Expired
- BE BE554100D patent/BE554100A/xx unknown
-
1953
- 1953-03-09 CH CH324312D patent/CH324312A/en unknown
- 1953-03-17 GB GB7418/53A patent/GB772594A/en not_active Expired
- 1953-03-18 FR FR1073058D patent/FR1073058A/en not_active Expired
- 1953-03-23 US US344210A patent/US2798110A/en not_active Expired - Lifetime
- 1953-11-16 CH CH322027D patent/CH322027A/en unknown
- 1953-11-19 GB GB32136/53A patent/GB741345A/en not_active Expired
- 1953-11-30 FR FR1088498D patent/FR1088498A/en not_active Expired
- 1953-11-30 US US395265A patent/US2997516A/en not_active Expired - Lifetime
-
1954
- 1954-05-24 DE DEA20396A patent/DE1037536B/en active Pending
-
1955
- 1955-04-23 CH CH345928D patent/CH345928A/en unknown
- 1955-04-29 FR FR67803D patent/FR67803E/en not_active Expired
-
1956
- 1956-01-11 DE DEA24117A patent/DE1013341B/en active Pending
- 1956-01-11 DE DEA15453A patent/DE1011022B/en active Pending
-
1957
- 1957-01-03 CH CH4122957A patent/CH382243A/en unknown
- 1957-01-10 US US633425A patent/US3003014A/en not_active Expired - Lifetime
- 1957-01-11 FR FR72015D patent/FR72015E/en not_active Expired
-
1958
- 1958-06-18 US US742912A patent/US3031517A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
BE524571A (en) | |
FR1073058A (en) | 1954-09-20 |
FR67803E (en) | 1958-03-24 |
CH322027A (en) | 1957-05-31 |
DE1011022B (en) | 1957-06-27 |
BE537926A (en) | |
NL92024C (en) | |
DE1037536B (en) | 1958-08-28 |
CH324312A (en) | 1957-09-15 |
US3003014A (en) | 1961-10-03 |
DE1013341B (en) | 1957-08-08 |
FR72015E (en) | 1960-03-21 |
US3031517A (en) | 1962-04-24 |
US2997516A (en) | 1961-08-22 |
FR1088498A (en) | 1955-03-08 |
BE554100A (en) | |
BE518800A (en) | |
GB741345A (en) | 1955-11-30 |
US2798110A (en) | 1957-07-02 |
CH382243A (en) | 1964-09-30 |
GB772594A (en) | 1957-04-17 |
CH345928A (en) | 1960-04-30 |
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