US3472691A - Stable resistance films of ni-cr - Google Patents
Stable resistance films of ni-cr Download PDFInfo
- Publication number
- US3472691A US3472691A US623924A US3472691DA US3472691A US 3472691 A US3472691 A US 3472691A US 623924 A US623924 A US 623924A US 3472691D A US3472691D A US 3472691DA US 3472691 A US3472691 A US 3472691A
- Authority
- US
- United States
- Prior art keywords
- resistance
- nickel
- chromium
- oxygen
- resistivity
- 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 - Lifetime
Links
- 239000010408 film Substances 0.000 description 22
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 18
- 239000001301 oxygen Substances 0.000 description 18
- 229910052760 oxygen Inorganic materials 0.000 description 18
- VNNRSPGTAMTISX-UHFFFAOYSA-N chromium nickel Chemical compound [Cr].[Ni] VNNRSPGTAMTISX-UHFFFAOYSA-N 0.000 description 16
- 229910018487 Ni—Cr Inorganic materials 0.000 description 15
- 238000000151 deposition Methods 0.000 description 15
- 238000000034 method Methods 0.000 description 12
- 238000001704 evaporation Methods 0.000 description 8
- 230000008020 evaporation Effects 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 6
- 230000006641 stabilisation Effects 0.000 description 5
- 230000008021 deposition Effects 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000010409 thin film Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910000623 nickel–chromium alloy Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000007669 thermal treatment Methods 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/0021—Reactive sputtering or evaporation
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01C—RESISTORS
- H01C17/00—Apparatus or processes specially adapted for manufacturing resistors
- H01C17/06—Apparatus or processes specially adapted for manufacturing resistors adapted for coating resistive material on a base
- H01C17/075—Apparatus or processes specially adapted for manufacturing resistors adapted for coating resistive material on a base by thin film techniques
- H01C17/08—Apparatus or processes specially adapted for manufacturing resistors adapted for coating resistive material on a base by thin film techniques by vapour deposition
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01C—RESISTORS
- H01C7/00—Non-adjustable resistors formed as one or more layers or coatings; Non-adjustable resistors made from powdered conducting material or powdered semi-conducting material with or without insulating material
Definitions
- Such resistors may be used in minature circuits. When used for this purpose, it is desirable that the resistors should have a lo-W temperature coefficient and a high stability even if the ambient temperature is comparatively high. Further it is desirable that, if subsequent to the application of the resistance material to the carrier, variations in resistivity of unreversible nature occur, for example, during a thermal threatment for thermal stabilisation, this variation is reproducible.
- Nickel-chromium resistors are generally manufactured by evaporating a nickel-chromium alloy (80-20) in a vacuum having a residual gas pressure of 10P5 mm. Hg and depositing the vapour evolved onto a carrier which has a temperature of approximately 300 C. After a certain resistivity is reached, the evaporation-deposition is stopped. The films thus obtained are generally found to have still an inadequate thermal stability. Consequently, in practice, such resistance films are also heated for a short time in air, for example, at approximately 300 C. During this heating treatment oxidation and recrystallization processes presumably take place in the resistance film, resulting in a permanent variation in resistivity which progressively decreases, so that a desired stability is ultimately obtained.
- resistivity upon stabilisation it applies in general that the higher the film resistance, that is to say the thinner the resistance film, the greater is the variation in resitivity upon stabilisation by heating. In practice, this has been found to happen in a manner which is poorly reproducible and hence not well predictable.
- An object of the invention is to manufacture resistors of the type consisting of a thin film of nickel-chromium on a carrier by evaporation-deposition in vacuo, the resistivity of which resistors varies to a comparatively small extent upon thermal treatment in air for stabilisation.
- This object is attained in a process in which in a first step a film of nickel-chromium is evaporation-deposited on a carrier in an atmosphere of oxygen at a pressure of the order of 10-5 mm. Hg until the desired resistance of the film is obtained, whereafter in a second step oxygen is admitted up to a pressure of the order of 10-4 mm. Hg
- the atmosphere of oxygen at a pressure ofthe order of 10F5 mm. Hg may be obtained, for example, by reducing the residual gas pressure in the space in which the resistance films are provided to a pressure of the order of l0-6 mm. Hg or less and then admitting oxygen to the space until a pressure of the order of 10-5 mm. Hg is reached.
- a pressure of the order of 10-5 mm. Hg is reached.
- a substantially constant content of oxygen for the resistance film is thus ensured.
- more oxygen is admitted to an extent such that, with continued deposition of nickelchromium, variation in the resistivity of the film deposited at a pressure of oxygen in the order of 10-5 mm. Hg does not occur any more.
- this pressure is found to be of the order of 10-4 mm. Hg. It appears to be preferable also in the second step to maintain the pressure constant, by steadily admitting oxygen to the evaporation space.
- Nickel-chromium is deposited by evaporation on a plurality of glass plates in a vacuum recipient containing a holder for the Said plates, a source of evaporation consisting of a foil of nickel-chromium alloy (-20) which may be heated by the passage of electric current, an aperture through which the space may be exhausted and an inlet for the oxygen to -be supplier, and means for heating the substrates to be deposited on.
- a source of evaporation consisting of a foil of nickel-chromium alloy (-20) which may be heated by the passage of electric current, an aperture through which the space may be exhausted and an inlet for the oxygen to -be supplier, and means for heating the substrates to be deposited on.
- One glass plate has previously been provided with metal contacts, included in an electric circuit so that the resistivity of the film can be observed during the depositing process. After reaching a pressure of 10-6 mm. Hg, oxygen is admitted to the vacuum space up to a pressure of 1 to 2.105 mm. Hg
- the glass plates are heated to a temperature of approximately 300 C. by radiation heating and nickel-chromium is evaporation-deposited until the desired resistivity is reached. Subsequently, more oxygen is admitted, without interrupting the depositing process, until the pressure is, for example, from 0.6 to 0.7 l04 mm. Hg. This pressure has to be such that the resistivity of the film does not vary any more with continued deposition of the nickel-chromium.
- the depositing process is stopped after some time, in this example after 2 minutes.
- the table following hereinafter shows several representative values of variations in resistance if the resistance films are heated at 200 C., for example for 24 hours.
- the first column shows the resistivities per square of the resistance films, the next column shows whether an oxidic covering layer as described has been applied, and the last column shows the variation in resistance after heating at 200 C. in air for 24 hours.
- Oxidie layer 1n an' provided From literature it is known that, upon thermal treatment of resistance lms having resistivities of 10052 to 1500 per square, variations in resistivity between and may occur upon thermal after-treatment. Said resistivities were obtained by evaporationdeposition at a residual gas pressure lower than 10-4 mm. Hg.
- the temperature coefficient of the resistors according to the invention is low and usually of the order of -50 ppm. per C.
- a substrate 1 for example of glass, is covered with a first nickel-chromium layer 2 of a low content of oxygen and the desired resistivity and with a second nickel-chromium layer 3 which is rich in a oxygen.
- the last-mentioned layer, which has no electric conductivity, is of a composition which is not known but possibly consists of a mixture of oxides of nickel and chromium.
- a method of manufacturing a thin film resistor comprising the steps depositing on a carrier, in an oxygen atmosphere of about 10-5 mm. Hg, a first evaporation layer of chromium-nickel until a desired resistivity is achieved and then time stabilizing the resistivity of said layer by depositing thereon, in an oxygen atmosphere of about 10-4 mm. Hg, a second evaporation layer of chromium-nickel having a thickness at which the resistivity of the composite layer is no longer substantially effected by time.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacturing & Machinery (AREA)
- Apparatuses And Processes For Manufacturing Resistors (AREA)
- Non-Adjustable Resistors (AREA)
Description
Oct. 14, 1969 c. KooY E'rAL STABLE RESISTANCE FILM OF Ni-GR Filed March 1'?, 196'? m W` W m w m M W M w w W.
GEN
United Statesv Patent O 3,472,691 STABLE RESISTANCE FILMS F Ni-Cr Cornelis Kooy, Enno 'Coert Munk, and Piet Hein Rem, Emmasingel, Eindhoven, Netherlands, assignors, by mesne assignments, to U.S. Philips Company Inc., New York, N.Y., a corporation of Delaware Filed Mar. 17, 1967, Ser. No. 623,924 Claims priority, application Netherlands, Mar. 23, 1966, 6603768 Int. Cl. H01b 1/02; C23c 13/02 U.S. Cl. 117-217 2 Claims ABSTRACT 0F THE DISCLOSURE Produce nickel-chromium thin film resistors by deposition in oxygen atmosphere of 5 mm. Hg and then in oxygen atmosphere of 110-4 mm. Hg.
This invention relates to methods of manufacturing resistors consisting of thin films of nickel-chromium, by evaporation-deposition in vacuo.
Such resistors may be used in minature circuits. When used for this purpose, it is desirable that the resistors should have a lo-W temperature coefficient and a high stability even if the ambient temperature is comparatively high. Further it is desirable that, if subsequent to the application of the resistance material to the carrier, variations in resistivity of unreversible nature occur, for example, during a thermal threatment for thermal stabilisation, this variation is reproducible.
Nickel-chromium resistors are generally manufactured by evaporating a nickel-chromium alloy (80-20) in a vacuum having a residual gas pressure of 10P5 mm. Hg and depositing the vapour evolved onto a carrier which has a temperature of approximately 300 C. After a certain resistivity is reached, the evaporation-deposition is stopped. The films thus obtained are generally found to have still an inadequate thermal stability. Consequently, in practice, such resistance films are also heated for a short time in air, for example, at approximately 300 C. During this heating treatment oxidation and recrystallization processes presumably take place in the resistance film, resulting in a permanent variation in resistivity which progressively decreases, so that a desired stability is ultimately obtained. For this variation is resistivity upon stabilisation it applies in general that the higher the film resistance, that is to say the thinner the resistance film, the greater is the variation in resitivity upon stabilisation by heating. In practice, this has been found to happen in a manner which is poorly reproducible and hence not well predictable.
It is thus difficult on a large scale to obtain miniature circuits in which the resistances satisfy comparatively narrow tolerances such as, for example, between :t3% of the desired value.
The variation in the resistance of the film upon thermal stabilisation in air, in practice also sets a limit to the value of this resistance. From literature it appears, for example, that for this reason also the resistance is chosen to be not higher than 2000 to 3000 per square.
An object of the invention is to manufacture resistors of the type consisting of a thin film of nickel-chromium on a carrier by evaporation-deposition in vacuo, the resistivity of which resistors varies to a comparatively small extent upon thermal treatment in air for stabilisation.
This object is attained in a process in which in a first step a film of nickel-chromium is evaporation-deposited on a carrier in an atmosphere of oxygen at a pressure of the order of 10-5 mm. Hg until the desired resistance of the film is obtained, whereafter in a second step oxygen is admitted up to a pressure of the order of 10-4 mm. Hg
"ice
and the deposition of nickel-chromium is continued for some further time, whereby the resistivity of the deposited film does not vary.
The atmosphere of oxygen at a pressure ofthe order of 10F5 mm. Hg may be obtained, for example, by reducing the residual gas pressure in the space in which the resistance films are provided to a pressure of the order of l0-6 mm. Hg or less and then admitting oxygen to the space until a pressure of the order of 10-5 mm. Hg is reached. During the evaporation-deposition of the nickelchromium, a certain oxidation already takes place. It is therefore preferable during this process to admit oxygen steadily in order to maintain the pressure of the order of 10-5 mm. Hg. A substantially constant content of oxygen for the resistance film is thus ensured. After the desired resistance is reached, more oxygen is admitted to an extent such that, with continued deposition of nickelchromium, variation in the resistivity of the film deposited at a pressure of oxygen in the order of 10-5 mm. Hg does not occur any more.
In practice, this pressure is found to be of the order of 10-4 mm. Hg. It appears to be preferable also in the second step to maintain the pressure constant, by steadily admitting oxygen to the evaporation space.
The thickness of the oxidic covering layer on the resistance film depends upon the extent of protection and thermal stability which it is desired to obtain and upon the possibility of contacting and etching.
The total time needed for evaporation-deposition of the resistance film and the covering layer depends upon a number of geometrical factors, such as the distance between source of evaporation and substrate to be deposited on; this distance may be determined in a simple manner in each individual case.
In order that the invention may be readily carried into effect, one embodiment of the method according thereto will now be explained in detail, with reference to the example following hereinafter and the accompanying drawing, the sole figure of which shows dagrammatically the structure of a resistor according to the invention.
EXAMPLE Nickel-chromium is deposited by evaporation on a plurality of glass plates in a vacuum recipient containing a holder for the Said plates, a source of evaporation consisting of a foil of nickel-chromium alloy (-20) which may be heated by the passage of electric current, an aperture through which the space may be exhausted and an inlet for the oxygen to -be supplier, and means for heating the substrates to be deposited on. `One glass plate has previously been provided with metal contacts, included in an electric circuit so that the resistivity of the film can be observed during the depositing process. After reaching a pressure of 10-6 mm. Hg, oxygen is admitted to the vacuum space up to a pressure of 1 to 2.105 mm. Hg. The glass plates are heated to a temperature of approximately 300 C. by radiation heating and nickel-chromium is evaporation-deposited until the desired resistivity is reached. Subsequently, more oxygen is admitted, without interrupting the depositing process, until the pressure is, for example, from 0.6 to 0.7 l04 mm. Hg. This pressure has to be such that the resistivity of the film does not vary any more with continued deposition of the nickel-chromium.
The depositing process is stopped after some time, in this example after 2 minutes.
As a measure of the increased stability of such resistance film according to the invention, the table following hereinafter shows several representative values of variations in resistance if the resistance films are heated at 200 C., for example for 24 hours.
The first column shows the resistivities per square of the resistance films, the next column shows whether an oxidic covering layer as described has been applied, and the last column shows the variation in resistance after heating at 200 C. in air for 24 hours.
R/R in percent after 24 hours heating at 200 C.
Oxidie layer 1n an' provided From literature it is known that, upon thermal treatment of resistance lms having resistivities of 10052 to 1500 per square, variations in resistivity between and may occur upon thermal after-treatment. Said resistivities were obtained by evaporationdeposition at a residual gas pressure lower than 10-4 mm. Hg.
From the table it may be seen that a considerable improvement in this respect is obtained by combination of the two steps.
The temperature coefficient of the resistors according to the invention is low and usually of the order of -50 ppm. per C.
It is also known to protect nickel-chromium resistors from atmospheric inuences by covering the resistance film by evaporation with a layer of SiO2 or MgF2. The effect thus envisaged is obtained in a considerably simpler manner by using the method in accordance with the invention.
The first step of the method according to the invention has more particularly for its purpose to obtain higher 3 resistivities at comparatively thicker layers in a reproducible manner.
The sole figure in the drawing shows, on an enlarged scale, the structure of a resistor obtained in accordance with the invention. A substrate 1, for example of glass, is covered with a first nickel-chromium layer 2 of a low content of oxygen and the desired resistivity and with a second nickel-chromium layer 3 which is rich in a oxygen. The last-mentioned layer, which has no electric conductivity, is of a composition which is not known but possibly consists of a mixture of oxides of nickel and chromium.
What is claimed is:
1. A method of manufacturing a thin film resistor, said method comprising the steps depositing on a carrier, in an oxygen atmosphere of about 10-5 mm. Hg, a first evaporation layer of chromium-nickel until a desired resistivity is achieved and then time stabilizing the resistivity of said layer by depositing thereon, in an oxygen atmosphere of about 10-4 mm. Hg, a second evaporation layer of chromium-nickel having a thickness at which the resistivity of the composite layer is no longer substantially effected by time.
2. A resistor produced by the method of claim 1.
References Cited UNITED STATES PATENTS 2,586,752 2/1952 Weber et al. 1l7-107 X 2,882,377 4/1959 Rinehart 117-107 X 2,962,393 ll/1960 Ruckelshaus 117-212 2,981,611 4/1961 Ashworth 117-107 X 3,059,197 10/1962 Ruckelshaus 117-107 X ANDREW G. GOLIAN, Primary Examiner U.S. Cl. X.R. 117--107, 229
'1' UNITED STATES PATENT OFFICE Pfl-10s f/w) p CERTIFICATE OF CORRECTION Patent No. 3.4721691 Dated October 14, 1969 Inventor(s) CORNELIS KOOY ET AL It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
|-' 1 Column l, line 5, "Company" should read Corporation Column l, line 46, "is" should read in Column 2, line 50, supplier" should read supplied Signed and sealed this 28th day of July 1970.
...v-Www asm) new HMH-BMI*- mw xfsunm. m.
omission of hun.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL6603768A NL6603768A (en) | 1966-03-23 | 1966-03-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3472691A true US3472691A (en) | 1969-10-14 |
Family
ID=19796062
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US623924A Expired - Lifetime US3472691A (en) | 1966-03-23 | 1967-03-17 | Stable resistance films of ni-cr |
Country Status (8)
Country | Link |
---|---|
US (1) | US3472691A (en) |
AT (1) | AT274966B (en) |
CH (1) | CH464644A (en) |
DE (1) | DE1665236A1 (en) |
FR (1) | FR1515479A (en) |
GB (1) | GB1133402A (en) |
NL (1) | NL6603768A (en) |
SE (1) | SE305994B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3607384A (en) * | 1968-07-11 | 1971-09-21 | Western Electric Co | Thin-film resistors having positive resistivity profiles |
US3637421A (en) * | 1969-08-27 | 1972-01-25 | Joseph Paul Gimigliano | Vacuum vapor coating with metals of high vapor pressure |
US3833410A (en) * | 1971-12-30 | 1974-09-03 | Trw Inc | High stability thin film alloy resistors |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2902244C2 (en) * | 1979-01-20 | 1982-11-11 | W.C. Heraeus Gmbh, 6450 Hanau | Stretch marks with a metal alloy measuring grid applied in a vacuum to an adhesive plastic carrier |
DE3429607A1 (en) * | 1984-08-09 | 1986-02-20 | Klaus 1000 Berlin Oppermann | MEASURING VALUE FOR ELECTRICAL MEASUREMENT OF FORCES, PRESSURES AND TENSIONS |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2586752A (en) * | 1946-09-26 | 1952-02-19 | Polytechnic Inst Brooklyn | Alloy resistance element and method for manufacturing same |
US2882377A (en) * | 1951-10-24 | 1959-04-14 | Pittsburgh Plate Glass Co | Electrical resistor metal coatings on refractory materials |
US2962393A (en) * | 1953-04-21 | 1960-11-29 | John G Ruckelshaus | Method of preparing electrical resistors |
US2981611A (en) * | 1956-03-14 | 1961-04-25 | Metropolitanvickers Electrical | Manufacture of printed electrical circuits or components |
US3059197A (en) * | 1952-06-07 | 1962-10-16 | John G Ruckelshaus | Potentiometer |
-
1966
- 1966-03-23 NL NL6603768A patent/NL6603768A/xx unknown
-
1967
- 1967-03-17 US US623924A patent/US3472691A/en not_active Expired - Lifetime
- 1967-03-20 CH CH398367A patent/CH464644A/en unknown
- 1967-03-20 AT AT263967A patent/AT274966B/en active
- 1967-03-20 SE SE3839/67A patent/SE305994B/xx unknown
- 1967-03-20 GB GB12864/67A patent/GB1133402A/en not_active Expired
- 1967-03-20 DE DE19671665236 patent/DE1665236A1/en active Pending
- 1967-03-22 FR FR99791A patent/FR1515479A/en not_active Expired
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2586752A (en) * | 1946-09-26 | 1952-02-19 | Polytechnic Inst Brooklyn | Alloy resistance element and method for manufacturing same |
US2882377A (en) * | 1951-10-24 | 1959-04-14 | Pittsburgh Plate Glass Co | Electrical resistor metal coatings on refractory materials |
US3059197A (en) * | 1952-06-07 | 1962-10-16 | John G Ruckelshaus | Potentiometer |
US2962393A (en) * | 1953-04-21 | 1960-11-29 | John G Ruckelshaus | Method of preparing electrical resistors |
US2981611A (en) * | 1956-03-14 | 1961-04-25 | Metropolitanvickers Electrical | Manufacture of printed electrical circuits or components |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3607384A (en) * | 1968-07-11 | 1971-09-21 | Western Electric Co | Thin-film resistors having positive resistivity profiles |
US3637421A (en) * | 1969-08-27 | 1972-01-25 | Joseph Paul Gimigliano | Vacuum vapor coating with metals of high vapor pressure |
US3833410A (en) * | 1971-12-30 | 1974-09-03 | Trw Inc | High stability thin film alloy resistors |
Also Published As
Publication number | Publication date |
---|---|
GB1133402A (en) | 1968-11-13 |
CH464644A (en) | 1968-10-31 |
DE1665236A1 (en) | 1971-01-21 |
SE305994B (en) | 1968-11-11 |
FR1515479A (en) | 1968-03-01 |
NL6603768A (en) | 1967-09-25 |
AT274966B (en) | 1969-10-10 |
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