US3658400A - Method of making a multialkali photocathode with improved sensitivity to infrared light and a photocathode made thereby - Google Patents
Method of making a multialkali photocathode with improved sensitivity to infrared light and a photocathode made thereby Download PDFInfo
- Publication number
- US3658400A US3658400A US15742A US3658400DA US3658400A US 3658400 A US3658400 A US 3658400A US 15742 A US15742 A US 15742A US 3658400D A US3658400D A US 3658400DA US 3658400 A US3658400 A US 3658400A
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- US
- United States
- Prior art keywords
- sensitivity
- photocathode
- maximum
- until
- evaporating
- Prior art date
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- Expired - Lifetime
Links
- 230000035945 sensitivity Effects 0.000 title claims description 57
- 238000004519 manufacturing process Methods 0.000 title description 4
- 238000001704 evaporation Methods 0.000 claims abstract description 35
- 238000000034 method Methods 0.000 claims abstract description 33
- 229910052787 antimony Inorganic materials 0.000 claims abstract description 19
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims abstract description 19
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229910052700 potassium Inorganic materials 0.000 claims abstract description 16
- 239000011591 potassium Substances 0.000 claims abstract description 16
- 239000000758 substrate Substances 0.000 claims description 14
- 230000007423 decrease Effects 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 6
- 230000005540 biological transmission Effects 0.000 claims description 5
- 229910052792 caesium Inorganic materials 0.000 claims description 5
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 3
- 230000001235 sensitizing effect Effects 0.000 claims description 3
- 238000004140 cleaning Methods 0.000 claims description 2
- 238000007872 degassing Methods 0.000 claims description 2
- 230000008020 evaporation Effects 0.000 abstract description 15
- 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 abstract description 8
- 229910052708 sodium Inorganic materials 0.000 abstract description 8
- 239000011734 sodium Substances 0.000 abstract description 8
- 238000012545 processing Methods 0.000 description 7
- 108091006146 Channels Proteins 0.000 description 6
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 5
- 229910052721 tungsten Inorganic materials 0.000 description 5
- 239000010937 tungsten Substances 0.000 description 5
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000012544 monitoring process Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 102000004257 Potassium Channel Human genes 0.000 description 2
- 108010052164 Sodium Channels Proteins 0.000 description 2
- 102000018674 Sodium Channels Human genes 0.000 description 2
- 239000013256 coordination polymer Substances 0.000 description 2
- 108020001213 potassium channel Proteins 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- QLOKJRIVRGCVIM-UHFFFAOYSA-N 1-[(4-methylsulfanylphenyl)methyl]piperazine Chemical compound C1=CC(SC)=CC=C1CN1CCNCC1 QLOKJRIVRGCVIM-UHFFFAOYSA-N 0.000 description 1
- 229910001245 Sb alloy Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 239000002140 antimony alloy Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- BROHICCPQMHYFY-UHFFFAOYSA-N caesium chromate Chemical compound [Cs+].[Cs+].[O-][Cr]([O-])(=O)=O BROHICCPQMHYFY-UHFFFAOYSA-N 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
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000001883 metal evaporation Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- PXLIDIMHPNPGMH-UHFFFAOYSA-N sodium chromate Chemical compound [Na+].[Na+].[O-][Cr]([O-])(=O)=O PXLIDIMHPNPGMH-UHFFFAOYSA-N 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J9/00—Apparatus or processes specially adapted for the manufacture, installation, removal, maintenance of electric discharge tubes, discharge lamps, or parts thereof; Recovery of material from discharge tubes or lamps
- H01J9/02—Manufacture of electrodes or electrode systems
- H01J9/12—Manufacture of electrodes or electrode systems of photo-emissive cathodes; of secondary-emission electrodes
Definitions
- a method for making a muliialkali photocathode includes simultaneous evaporation of sodium and antmony alternately with simultaneous evaporation of potassium and antimony.
- the disclosure includes a photocathode made by the method 8 Claims, 3 Drawing Figures PATNTEDAPRZS 1912 Y 3,658,400 SHEET 10F 2 7447' MAX/MIM,- 7*//5/14 INVENTOR IBI/m19.
- FIG. l is a flow chart of steps 1-18 used for practicing a preferred embodiment of the novel method.
- a phototube 26 shown in FIG. 2 is provided with a photocathode surface 28 having improved sensitivity to infrared light.
- the tube 26 has a tubular glass wall section 30 about inches long, 2 inches outside diameter and one-sixteenth inch thickness.
- One end of the wall section 30 is closed by a glass faceplate 32, which is flat on the outside and concave on the inside with a radius of curvature of about l.9 inches.
- the other end ofthe wall section 30 is closed by a stem 34 having a number of electrical lead-in pins 35.
- a stem 34 having a number of electrical lead-in pins 35.
- dynodes 36 Along the interior of the tube are spaced a series of dynodes 36. Near the dynodes 36 are spaced three channels 38,40, 42 of tantalum foil containing, respectively, substances for evaporating potassium, sodium, and cesium.
- the potassium channel 38 contains potassium chromate, aluminum, and tungsten.
- the sodium channel 40 contains sodium chromate, aluminum, and tungsten.
- the cesium channel 42 contains cesium chromate, zirconium and tungsten.
- a resistance filament situated near the faceplate has two antimony alloy beads 44 attached to it for evaporating antimony.l
- the channels 38, 40, 42 and the filament 44 are suitably connected by internal leads to electrical current sources through the pins 35 so that they can be activated separately by electrical resistance heating.
- Light transmission through the faceplate 32 is monitored by directing light from an incandescent tungsten filament at an angle through the faceplate 32 and Wall 30 to a light sensing tube.
- Photoemissive sensitivity of the interior faceplate surface is monitored by collecting the emitted electrons with one or more of the internal electrodes, such as the electrode 46.
- the electrode 46 is impressed with a voltage of between 50 and 150 volts positive with respect to the photocathode 28 through a lead 48 going from a lead-in pin 35 to ari aluminum coating on the wall 30 and in contact with the photocathode 28 and lead 50 also from a lead-in pin 35 to the electrode 46.
- the sensitivity is expressed in terms of microamperes of emitted electron current per lumen of light incident on the photocathode 28.
- the tube is continuously evacuated through exhausted tubulation 47 in the stem.
- the tubulation is of about l inch inside diameter and about 2 inches long. It
- the tube 26 is placed in an-oven which has been preheated to about 190 C.
- the channels 38, 40, 42 are preheated to clean and degas them. Then the potassium channel 38 current is set so that the channel will release potassium vapor when the faceplate 32 temperature reaches about 180 C.
- Potassium is evaporated on the antimony layer until maximum sensitivity is reached. The maximum is generally about l.5 l-5) microamperes per lumen.
- the oven temperature is increased to about 220 (215- 230) C and the sodium channel 40 current adjusted so that sodium vapor willbe released when the faceplate 32 reaches about 210 (205220) C.
- Sodium is evaporated until a maximum sensitivity is reached.
- the maximum is generally about 20 (l5-80) microamperes per lumen.
- Steps 7 through 10 are repeated at least several times until the maximum sensitivity in step l0 is about 30 percent (2S-35 percent) of the highest maximum sensitivity reached in any of the previous steps 5 through 10.
- the photocathode will take on a light blue hue when the proper sensitivity for this step is reached.
- the tube 26 is cooled gradually to about 160 (155 -l65) C over a period of about 5 (5-10) minutes.
- the tube 26 is baked at 160 (l55-l65) C until a new maximum sensitivity is reached.
- Antimony is evaporated until the sensitivity decreases to about IO percent (5-15 percent) of the maximum reached in step 14).
- the tube is baked at (l55-l65) C until a new maximum sensitivity is reached.
- Steps 15) and 16) are repeated until the maximum sensitivity of step 16) stabilizes and the infrared sensitivity is between 0.5 and I6 microamperes per lumen.
- the tube 26 is slowly cooled to room temperature at a rate of about l0 C per minute and removed from the oven. After the exhaust tubulation 47 is sealed 0H, the tube 26 is operative.
- Sensitivity of the evaporated layers is measured separately for visible light and infrared light. lt is desirable to be able to measure both visible and infrared sensitivity almost simultaneously so that the photocathode may be processed to give a favorable relative value of both sensitivities.
- two separate incandescent tungsten light sources are used, each about 0.1 lumen in output. The sources are spaced apart a short distance from the faceplate. Interposed between one source and the faceplate is a glass light filter passing infrared light but no visible light. For instance, a filter passing less than 0.025 percent at 750 nanometers wavelength, percent at 900 nanometers and about 90 percent at about 1,250 nanometers is suitable.
- the sensitivity of the photocathode to both visible and infrared light may be measured separately and almost simultaneously by manual switching from one light source to the other.
- the rates of evaporation of the evaporated elements are limited by the speed and accuracy at which the sensitivity can be monitored. A relatively slow evaporation rate makes the monitoring less critical.
- the novel method can be used to form photocathodes having improved red response in tubes, such as image tubes for which internal processing may not be as useful as external processing because of possible contamination of electrodes.
- the novel method results in high reproducibility of photocathodes and is thus particularly well suited for automated fabrication of photocathodes. With present methods, complete automation is not feasible because of a relatively low degree of reproducibility in the absence of a highly skilled operator. Furthermore, by the novel method it takes considerably less time, as much as 50 percent less, to make a multialkali photocathode than by present methods.
- present multialkali photocathodes have a thickness on the order of 30 nanometers, whereas photocathodes made by the novel method may have a thickness on the order of
- the greater thickness accounts in part for an increase in the sensitivity of the photocathode to red light, as shown in FIG. 3.
- the curve 52 in FIG. 3 represents the approximate response characteristic of a commonly used multialkali photocathode made by present methods. The response is seen to be quite low in the 700 nanometer wavelength region.
- the curve 54 represents the approximate response characteristic of a photocathode made by the novel method.
- the photocathode made by the novel method has a more nearly constant and higher sensitivity throughout the visual spectrum than present multialkali photocathodes.
- novel photocathode is made by a series of evaporations, it is presently not possible to define precisely the actual finished structure, since there is an alloying of the evaporated substances.
- the chemical compositions of the various thickness portions of the photocathode are not known. Therefore, the novel photocathode can presently be best described as the product of the novel method.
- the novel photocathode may be used as a photoemitter on an opaque substrate or as a secondary electron emitting surface.
- step a of forming said base layer includes:
- sensitizing includes:
- step 1 cooling said substrate from the temperature at which said evaporating of potassium is carried out to a temperature sitivity of step 1 stabilizes to a value of at least 0.1 microampere per lumen for infrared light. 5.
- An electron emissive photocathode made by the method defined in claim l.
- An electron emissive photocathode made by the method defined in claim 2.
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Common Detailed Techniques For Electron Tubes Or Discharge Tubes (AREA)
- Formation Of Various Coating Films On Cathode Ray Tubes And Lamps (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1574270A | 1970-03-02 | 1970-03-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3658400A true US3658400A (en) | 1972-04-25 |
Family
ID=21773337
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US15742A Expired - Lifetime US3658400A (en) | 1970-03-02 | 1970-03-02 | Method of making a multialkali photocathode with improved sensitivity to infrared light and a photocathode made thereby |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3658400A (enExample) |
| JP (1) | JPS5032194B1 (enExample) |
| CA (1) | CA930256A (enExample) |
| DE (1) | DE2109903C2 (enExample) |
| FR (1) | FR2083948A5 (enExample) |
| GB (1) | GB1345778A (enExample) |
| NL (1) | NL174098C (enExample) |
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3838304A (en) * | 1973-07-12 | 1974-09-24 | Rca Corp | Method of making a bialkali photocathode with improved sensitivity and high temperature operating characteristics |
| US3858955A (en) * | 1973-01-15 | 1975-01-07 | Rca Corp | Method of making a iii-v compound electron-emissive cathode |
| US3884539A (en) * | 1972-12-11 | 1975-05-20 | Rca Corp | Method of making a multialkali electron emissive layer |
| US3992071A (en) * | 1975-04-01 | 1976-11-16 | The United States Of America As Represented By The Secretary Of The Army | Processes for activating S-1 cathode |
| US4002735A (en) * | 1975-06-04 | 1977-01-11 | Rca Corporation | Method of sensitizing electron emissive surfaces of antimony base layers with alkali metal vapors |
| US4198106A (en) * | 1978-02-21 | 1980-04-15 | Varo, Inc. | Method of manufacturing a photocathode for an image intensifier tube |
| US4305972A (en) * | 1980-06-30 | 1981-12-15 | Rca Corporation | Method for expeditiously processing a sodium-potassium-cesium-antimony photocathode |
| US4306188A (en) * | 1979-10-30 | 1981-12-15 | Rca Corporation | Photomultiplier tube having a photocurrent collector |
| US4333031A (en) * | 1979-03-30 | 1982-06-01 | Rca Corporation | Photomultiplier tube having directional alkali metal vapor evaporation means |
| US4357368A (en) * | 1978-12-26 | 1982-11-02 | Rca Corporation | Method of making a photosensitive electrode and a photosensitive electrode made thereby |
| US4370585A (en) * | 1980-08-29 | 1983-01-25 | Rca Corporation | Evaporator support assembly for a photomultiplier tube |
| US4407857A (en) * | 1981-06-30 | 1983-10-04 | Rca Corporation | Method for processing a lithium-sodium-antimony photocathode |
| US4568567A (en) * | 1984-10-09 | 1986-02-04 | Rca Corporation | Method of removing trace quantities of alkali metal impurities from a bialkali-antimonide photoemissive cathode |
| US4585935A (en) * | 1984-02-10 | 1986-04-29 | Rca Corporation | Electron discharge device having a substantially spherical electrostatic field lens |
| US4671778A (en) * | 1986-03-19 | 1987-06-09 | Rca Corporation | Imaging device having an improved photoemissive cathode appendage processing assembly |
| US4682021A (en) * | 1986-01-29 | 1987-07-21 | Rca Corporation | Header assembly for an intensified charge coupled image sensor |
| CN1052811C (zh) * | 1996-11-06 | 2000-05-24 | 南京理工大学 | 多碱光电阴极的制造方法 |
| CN115125491A (zh) * | 2022-06-15 | 2022-09-30 | 北方夜视技术股份有限公司 | 一种多碱光电阴极制备用碱源的蒸发特性测量的方法 |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2431401A (en) * | 1940-06-25 | 1947-11-25 | Rca Corp | Method of manufacturing photoelectric tubes |
| US2770561A (en) * | 1954-03-08 | 1956-11-13 | Rca Corp | Photoelectric cathode and method of producing same |
| US2914690A (en) * | 1955-12-05 | 1959-11-24 | Rca Corp | Electron-emitting surfaces and methods of making them |
| US3179835A (en) * | 1960-11-22 | 1965-04-20 | Rca Corp | Pickup tube having a cesiated photocathode and a substantially leakagefree target, and method of making the same |
| US3372967A (en) * | 1966-07-06 | 1968-03-12 | Rca Corp | Method of making a multi-alkali cathode |
| US3498834A (en) * | 1967-02-03 | 1970-03-03 | Weston Instruments Inc | Photoelectric surfaces and methods for their production |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB892504A (en) * | 1957-06-26 | 1962-03-28 | Emi Ltd | Improvements in or relating to a method of forming a photoemissive surface |
| US3434876A (en) * | 1965-11-23 | 1969-03-25 | Rca Corp | Photosensitive cathodes |
-
1970
- 1970-03-02 US US15742A patent/US3658400A/en not_active Expired - Lifetime
-
1971
- 1971-01-15 CA CA102900A patent/CA930256A/en not_active Expired
- 1971-02-24 FR FR7106244A patent/FR2083948A5/fr not_active Expired
- 1971-02-26 JP JP46009915A patent/JPS5032194B1/ja active Pending
- 1971-03-01 NL NLAANVRAGE7102696,A patent/NL174098C/xx not_active IP Right Cessation
- 1971-03-02 DE DE2109903A patent/DE2109903C2/de not_active Expired
- 1971-04-19 GB GB2288071A patent/GB1345778A/en not_active Expired
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2431401A (en) * | 1940-06-25 | 1947-11-25 | Rca Corp | Method of manufacturing photoelectric tubes |
| US2770561A (en) * | 1954-03-08 | 1956-11-13 | Rca Corp | Photoelectric cathode and method of producing same |
| US2914690A (en) * | 1955-12-05 | 1959-11-24 | Rca Corp | Electron-emitting surfaces and methods of making them |
| US3179835A (en) * | 1960-11-22 | 1965-04-20 | Rca Corp | Pickup tube having a cesiated photocathode and a substantially leakagefree target, and method of making the same |
| US3372967A (en) * | 1966-07-06 | 1968-03-12 | Rca Corp | Method of making a multi-alkali cathode |
| US3498834A (en) * | 1967-02-03 | 1970-03-03 | Weston Instruments Inc | Photoelectric surfaces and methods for their production |
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3884539A (en) * | 1972-12-11 | 1975-05-20 | Rca Corp | Method of making a multialkali electron emissive layer |
| US3858955A (en) * | 1973-01-15 | 1975-01-07 | Rca Corp | Method of making a iii-v compound electron-emissive cathode |
| US3838304A (en) * | 1973-07-12 | 1974-09-24 | Rca Corp | Method of making a bialkali photocathode with improved sensitivity and high temperature operating characteristics |
| US3992071A (en) * | 1975-04-01 | 1976-11-16 | The United States Of America As Represented By The Secretary Of The Army | Processes for activating S-1 cathode |
| US4002735A (en) * | 1975-06-04 | 1977-01-11 | Rca Corporation | Method of sensitizing electron emissive surfaces of antimony base layers with alkali metal vapors |
| US4198106A (en) * | 1978-02-21 | 1980-04-15 | Varo, Inc. | Method of manufacturing a photocathode for an image intensifier tube |
| US4357368A (en) * | 1978-12-26 | 1982-11-02 | Rca Corporation | Method of making a photosensitive electrode and a photosensitive electrode made thereby |
| US4333031A (en) * | 1979-03-30 | 1982-06-01 | Rca Corporation | Photomultiplier tube having directional alkali metal vapor evaporation means |
| US4306188A (en) * | 1979-10-30 | 1981-12-15 | Rca Corporation | Photomultiplier tube having a photocurrent collector |
| US4305972A (en) * | 1980-06-30 | 1981-12-15 | Rca Corporation | Method for expeditiously processing a sodium-potassium-cesium-antimony photocathode |
| US4370585A (en) * | 1980-08-29 | 1983-01-25 | Rca Corporation | Evaporator support assembly for a photomultiplier tube |
| US4407857A (en) * | 1981-06-30 | 1983-10-04 | Rca Corporation | Method for processing a lithium-sodium-antimony photocathode |
| US4585935A (en) * | 1984-02-10 | 1986-04-29 | Rca Corporation | Electron discharge device having a substantially spherical electrostatic field lens |
| US4568567A (en) * | 1984-10-09 | 1986-02-04 | Rca Corporation | Method of removing trace quantities of alkali metal impurities from a bialkali-antimonide photoemissive cathode |
| US4682021A (en) * | 1986-01-29 | 1987-07-21 | Rca Corporation | Header assembly for an intensified charge coupled image sensor |
| US4671778A (en) * | 1986-03-19 | 1987-06-09 | Rca Corporation | Imaging device having an improved photoemissive cathode appendage processing assembly |
| CN1052811C (zh) * | 1996-11-06 | 2000-05-24 | 南京理工大学 | 多碱光电阴极的制造方法 |
| CN115125491A (zh) * | 2022-06-15 | 2022-09-30 | 北方夜视技术股份有限公司 | 一种多碱光电阴极制备用碱源的蒸发特性测量的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2109903A1 (de) | 1971-09-30 |
| GB1345778A (en) | 1974-02-06 |
| NL7102696A (enExample) | 1971-09-06 |
| DE2109903C2 (de) | 1986-03-27 |
| CA930256A (en) | 1973-07-17 |
| FR2083948A5 (enExample) | 1971-12-17 |
| NL174098B (nl) | 1983-11-16 |
| JPS5032194B1 (enExample) | 1975-10-18 |
| NL174098C (nl) | 1984-04-16 |
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