US3842495A - Control of rate of change of resistance as a function of temperature in manufacture of resistance elements - Google Patents
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- US3842495A US3842495A US00326430A US32643073A US3842495A US 3842495 A US3842495 A US 3842495A US 00326430 A US00326430 A US 00326430A US 32643073 A US32643073 A US 32643073A US 3842495 A US3842495 A US 3842495A
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- 238000004519 manufacturing process Methods 0.000 title description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 39
- 238000000034 method Methods 0.000 claims abstract description 27
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 19
- 238000010438 heat treatment Methods 0.000 claims abstract description 16
- 230000005855 radiation Effects 0.000 claims abstract description 3
- 229910000510 noble metal Inorganic materials 0.000 claims description 8
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 150000004706 metal oxides Chemical class 0.000 claims description 5
- 229910052707 ruthenium Inorganic materials 0.000 claims description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 3
- 150000002739 metals Chemical class 0.000 claims description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 2
- 239000008246 gaseous mixture Substances 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- 229910052709 silver Inorganic materials 0.000 claims description 2
- 239000004332 silver Substances 0.000 claims description 2
- 229910044991 metal oxide Inorganic materials 0.000 claims 1
- 239000000463 material Substances 0.000 description 6
- 239000000919 ceramic Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 3
- 238000004377 microelectronic Methods 0.000 description 3
- 238000012216 screening Methods 0.000 description 3
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 2
- 229910002113 barium titanate Inorganic materials 0.000 description 2
- 238000005538 encapsulation Methods 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229910001925 ruthenium oxide Inorganic materials 0.000 description 2
- WOCIAKWEIIZHES-UHFFFAOYSA-N ruthenium(iv) oxide Chemical compound O=[Ru]=O WOCIAKWEIIZHES-UHFFFAOYSA-N 0.000 description 2
- 238000009966 trimming Methods 0.000 description 2
- PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical compound [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 description 1
- JMGVPAUIBBRNCO-UHFFFAOYSA-N [Ru].[Ag] Chemical compound [Ru].[Ag] JMGVPAUIBBRNCO-UHFFFAOYSA-N 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 239000005388 borosilicate glass Substances 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 239000011195 cermet Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- JUWSSMXCCAMYGX-UHFFFAOYSA-N gold platinum Chemical compound [Pt].[Au] JUWSSMXCCAMYGX-UHFFFAOYSA-N 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910001120 nichrome Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- SWELZOZIOHGSPA-UHFFFAOYSA-N palladium silver Chemical compound [Pd].[Ag] SWELZOZIOHGSPA-UHFFFAOYSA-N 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01C—RESISTORS
- H01C17/00—Apparatus or processes specially adapted for manufacturing resistors
- H01C17/22—Apparatus or processes specially adapted for manufacturing resistors adapted for trimming
- H01C17/26—Apparatus or processes specially adapted for manufacturing resistors adapted for trimming by converting resistive material
- H01C17/265—Apparatus or processes specially adapted for manufacturing resistors adapted for trimming by converting resistive material by chemical or thermal treatment, e.g. oxydation, reduction, annealing
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/49082—Resistor making
- Y10T29/49085—Thermally variable
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/49082—Resistor making
- Y10T29/49099—Coating resistive material on a base
Definitions
- These glaze resistor materials typically consist of mixtures of particular oxides of noble metals and glass frit, disbursed in a suitable resin base.
- the resistors are commonly formed by silk screening a paste or paint form of the resistor material onto a ceramic substrate (for example barium titanate), and thereafter baking the film material on the ceramic chip at a temperature between 400 and 800C.
- wire-wound resistors While the completed resistors compare favorably with so-called wire-wound resistors in certain respects, they do not exhibit the very low temperature stability found with wire-wound resistors. The latter, of course, are not generally suited to micro-electronics applications due to their undesirably large size.
- Such film materials typically consist of a noble metal oxide in glassy state.
- the method of the invention involves heating the film form resistance element at relatively high temperature and while exposed to a gaseous environment containing nitrogen in greater percentage concentration than is found in air, and continuing such heating for a time interval to significantly reduce the rate of change of resistance of theelement as a function of temperature change.
- the gas which may consist of a mixture of air and nitrogen, is maintained at a temperature of between 650C and 750C and in contact with the resistor film during the heating interval.
- the percentage of nitrogen in the mixture may be selected to produce a parts per million change in resistance per degree Centigrade change in temperature of about 10, as will be seen.
- Additional objects include the encapsulation and laser trimming of the treated resistance element, in the manner to be described, so as to provide the container with an extremely accurate resistor exhibiting a high degree of temperature stability, for use in microelectronic circuitry.
- FIG. 1 is a flow chart
- FIG. 2 is a plan view of a resistor element
- FIG. 3 is a section on lines 3--.-3 of FIG. 2;
- FIG. 4 is an elevation showing heating of the resistance film, in a nitrogen environment
- FIG. 5 is an elevation showing laser trimming of the FIG. 2 resistance element after encapsulation
- FIG. 6 is a graph
- FIG. 7 is a graph.
- Temperature stability of resistors generally expressed as the number of parts per million change in resistance per degree Centigrade change in temperature, can be mathematically expressed as follows:
- the temperature stability of glaze film resistors exhibited rather wide tolerance levels, as for example is represented in FIG. 6.
- the material DP 1131 exhibits a PPM slope of:
- such resistors are produced by mixing between 20 and 60 weight parts of noble metal oxide particulate with between 4 and 20 weight parts of glass frit, adding between 50 and 60 weight parts of a liquid resin (as for example acryloid) and silk screening the mixture onto a ceramic substrate or chip.
- Suitable noble metals and oxides include Ruthenium, Ruthenium silver, and Palladium silver paste of a particle size 0.3m the glass frit may consist of lead borosilicate glass of a particle size 5p.; and the chip may consist of barium titanate ceramic material.
- Commercial pastes and inks of this variety include Du Pont Berox," Sel- Rex Resonate, and Electro-Materials Corp. of America Firon.
- FIGS. 2 and 3 show the film 19 on the ceramic substrate 20, with end terminals 21 fused in position.
- Dp 1131 consists of a glazed film of noble metal oxide (50 percent Ruthenium, 25 percent Ruthenium oxide and 25 percent lead borosilicate frit) having a thickness of about 1 mil after firing, and DP 1161 consists of a glassy filmof noble metal oxide (35 percent Ruthenium, 40 percent Ruthenium oxide and 25 percent lead borosilicate frit) having the same thickness. These may be considered as Cermet" type resistors.
- Reference to FIG. 6 shows that DP 1131 exhibitsa 1.4 percent change in, electrical resistance over the temperature range 0 to 100 C, which corresponds to the 1 40RPM previously referred to, and which. is. considered as lacking in desired temperature stability.
- the glazed film is heated at a relatively high temperature and while exposed to a gaseous. environment containing nitrogen in greater percentage consentration than found in air, such heating being continued for a time interval characterized in that the rate of change of resistance as a function of temperature change is significantly reduced; for example, the parts per million change in electrical resistance of the film per degree Centigrade change in temperature is substantially reduced.
- the nitrogen containing gaseous environment should be at a temperature of between 650C and 750C (and preferably about 700C) and in contact with the resistor element during the heating interval, the gas being at about atmospheric pressure; and the heating interval should be less than 1 minute, and preferably between 20 and 40 seconds (about 30 seconds for optimum results).
- Steps 15, 16 and 16 a in FIG. 1 respectively indicate initial PPM testing of the resistance film, nitrogen treatment, and subsequent PPM testing of the resistance film.
- the graph in FIG. 7 contains three curves 30, 31 and 32.
- Positive slope curve 30 corresponds to the 140 PPM curve for DP 1131 in FIG. 6;
- negative slope curve 31 shows that -100 PPM is obtained for DP 1131 upon heat treatment at 700C for 30 seconds in a 100 percent nitrogen environment 25 in FIG. 4;
- curve 32 shows that -14 PPM is obtained for DP 1131 (for temperature changes in the range about about 25C) upon heat treatment at about 700C for 30 seconds.
- a gaseous environment consisting of 80 percentair and 20 percent nitrogen Accordingly, the nitrogen concentration in the gaseous environment 25 should be above that of air, but less than 100 percent nitrogen, for minimizing the PPM results. If that environment consists of 86 percent air and 14 percent nitrogen, a PPM level of about is obtained, for DP 1131 fired at about 700C for 30 seconds.
- FIG. 5 shows the use of a laser beam 130 emanating from source or generator 131 and directed to impinge on the resistance element 19, thereby to effect a change in the electrical resistance of the precision resistor to a desired value at a temperature or temperatures within the range of interest.
- the beam may be caused to impinge on successively different portions of each of several resistors supported and displaced on a belt 132.
- the beam may be controlled, as by control means 33 connected with the generator, to interrupt the beam when the measured resistance of the resistor 19 arrives at the precise desired value, and for that purpose a source of voltage 34 and a precision ohmmeter 35 may be temporarilyconnected in series with the leads 21 projecting form the opposite ends of the film 19.
- beam impingement on the relatively moving resistance element is continued for a time interval of between 0.10 and 60 seconds, depending on the amount of resistance increase desired, and the intensity of the beam.
- the laser beam may "b'f lo vv frequency with wave length the order of one thousandth of a millimeter or longer. It is found that the resistance element can be tuned, in this manner, over a relatively wide range, i.e., up to around three times its original resistance value, and to a resolution or tolerance of 0.01 percent of a given or desired resistance value, at a selected temperature. As an example, a raw, randomly selected resistor exhibiting a resistance of 21,850 ohms, after nitrogen treatment as described above, may be tuned in this manner to a value of 62,000 i 6 ohms.
- the invention is also applicable to film type resistors where the resistance film is applied to a substrate by sputtering techniques, the metal of the element consisting for example of chronium, and alloys therewith, an example being Nichrome.
- the method of claim 1 including the step of directing a laser beam to impinge on said element and thereby effect a change in the electrical resistance of said element to a desired value.
- the method of claim 9 including the step of effecting relative movement of the beam and element to impinge the beam on different portions of the element.
- the element including a temperature range.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Apparatuses And Processes For Manufacturing Resistors (AREA)
Abstract
The method of improving the properties of a film type electrical resistance element having a characteristic rate of change of resistance as a function of temperature change, within a selected temperature range, the steps that include A. HEATING SAID ELEMENT WHILE EXPOSED TO A GASEOUS MEDIUM CONTAINING NITROGEN IN SUFFICIENT CONCENTRATION TO REDUCE SAID RATE, AND B. THEREAFTER IMPINGING LASER RADIATION ON THE RESISTANCE ELEMENT TO CONTROLLABLY ALTER THE RESISTANCE LEVEL THEREOF, AT TEMPERATURES WITHIN SAID SELECTED TEMPERATURE RANGE.
Description
United States Patent 1191 Bennett et al.
[ l Oct. 22, 1974 LII CONTROL OF RATE OF CHANGE OF RESISTANCE AS A FUNCTION OF TEMPERATURE IN MANUFACTURE OF RESISTANCE ELEMENTS Inventors: Kenneth R. Bennett, San Diego; Joseph W. Crownover, La Jolla, both of Calif.
Assignee: GT1 Corporation, Pittsburgh, Pa.
Filed: Jan. 24, 1973 Appl. No.: 326,430
us. 01 29/620, 29/612, 117/201, 219/121 LM lm. c1 H016 7/00, HOlC 17/00 Field of Search 29/620, 621, 613, 612; 117/201; 219/121 L, 121 LM References Cited UNITED STATES PATENTS 3/l967 Bullard et al. 29/620 7/1969 Ireland et al 8/l969 Phillips l0/l970 Falanga et al. 29/621 X 3,607,386 9/1971 cinder-.11. ..29/62OX OTHER PUBLICATIONS Laser-Induced Resistivity Changes in Film Resistors" Presented by Lins et al. representing Sperry Rand at Wescon, Aug. 23-26, 1966.
Primary ExaminerCharles W. Lanham Assistant ExaminerVictor A. DiPalma Attorney, Agent, or FirmSmyth, Roston & Pavitt a. heating said element while exposed to a gaseous medium containing nitrogen in sufficient concentration to reduce said rate, and
b. thereafter impinging laser radiation. on the resistance element to controllably alter the resistance level thereof, at temperatures within said selected temperature range.
12 Claims, 7 Drawing Figures TEIQM/NIQL HPPL /c A 77 ON 20:52 7 rem/Mme PEODUC T 16 CONTROL OF RATE OF CHANGE OF RESISTANCE AS A FUNCTIONOF TEMPERATURE IN MANUFACTURE OF RESISTANCE ELEMENTS BACKGROUND OF THE INVENTION This invention relates generally to controlling the temperature stability of resistance elements, and more particularly concerns reducing the parts per million change in resistance per degeree Centigrade change in temperature of film glaze resistor elements.
Recently, so called film glaze resistance elements have been developed for use in micro-electronics applications. These glaze resistor materials typically consist of mixtures of particular oxides of noble metals and glass frit, disbursed in a suitable resin base. The resistors are commonly formed by silk screening a paste or paint form of the resistor material onto a ceramic substrate (for example barium titanate), and thereafter baking the film material on the ceramic chip at a temperature between 400 and 800C.
While the completed resistors compare favorably with so-called wire-wound resistors in certain respects, they do not exhibit the very low temperature stability found with wire-wound resistors. The latter, of course, are not generally suited to micro-electronics applications due to their undesirably large size.
SUMMARY OF THE INVENTION It is a major object of the invention to control the temperature stability of glaze film resistor elements so as to achieve stabilities comparing favorably with those of wire-wound resistors. Such film materials typically consist of a noble metal oxide in glassy state.
Basically, the method of the invention involves heating the film form resistance element at relatively high temperature and while exposed to a gaseous environment containing nitrogen in greater percentage concentration than is found in air, and continuing such heating for a time interval to significantly reduce the rate of change of resistance of theelement as a function of temperature change. Typically, the gas, which may consist of a mixture of air and nitrogen, is maintained at a temperature of between 650C and 750C and in contact with the resistor film during the heating interval. The percentage of nitrogen in the mixture may be selected to produce a parts per million change in resistance per degree Centigrade change in temperature of about 10, as will be seen.
Additional objects include the encapsulation and laser trimming of the treated resistance element, in the manner to be described, so as to provide the container with an extremely accurate resistor exhibiting a high degree of temperature stability, for use in microelectronic circuitry.
These and other objects and advantages of the invention, as well as the details of an illustrative embodiment, will be more fully understood from the following description and drawings, in which:
DRAWING DESCRIPTION FIG. 1 is a flow chart;
FIG. 2 is a plan view of a resistor element;
FIG. 3 is a section on lines 3--.-3 of FIG. 2;
FIG. 4 is an elevation showing heating of the resistance film, in a nitrogen environment;
FIG. 5 is an elevation showing laser trimming of the FIG. 2 resistance element after encapsulation;
FIG. 6 is a graph; and
FIG. 7 is a graph.
DETAILED DESCRIPTION Temperature stability of resistors, generally expressed as the number of parts per million change in resistance per degree Centigrade change in temperature, can be mathematically expressed as follows:
PPM AR X IO /RAC where:
R resistance AR change in resistance AC change in temperature expressed in degrees Centigrade.
Heretofore, the temperature stability of glaze film resistors exhibited rather wide tolerance levels, as for example is represented in FIG. 6. Thus, the material DP 1131 exhibits a PPM slope of:
Characteristically, such resistors are produced by mixing between 20 and 60 weight parts of noble metal oxide particulate with between 4 and 20 weight parts of glass frit, adding between 50 and 60 weight parts of a liquid resin (as for example acryloid) and silk screening the mixture onto a ceramic substrate or chip. Suitable noble metals and oxides include Ruthenium, Ruthenium silver, and Palladium silver paste of a particle size 0.3m the glass frit may consist of lead borosilicate glass of a particle size 5p.; and the chip may consist of barium titanate ceramic material. Commercial pastes and inks of this variety include Du Pont Berox," Sel- Rex Resonate, and Electro-Materials Corp. of America Firon.
After mixing, silk screening and drying as appear at 10-12 in FIG. 1, metal terminals (for example platinum gold) are applied to the opposite ends of the film (as represented by step 13 in FIG. 1) and the assembly is baked in air at betewen 400 and 800C for approximately /2 hour, (as represented by step 14 in FIG. 1). The resultant dry film is glassy or glazed, and has a thickness between 0.5 and 1.5 mil, after firing. FIGS. 2 and 3 show the film 19 on the ceramic substrate 20, with end terminals 21 fused in position.
In accordance with the invention, the glazed film is heated at a relatively high temperature and while exposed to a gaseous. environment containing nitrogen in greater percentage consentration than found in air, such heating being continued for a time interval characterized in that the rate of change of resistance as a function of temperature change is significantly reduced; for example, the parts per million change in electrical resistance of the film per degree Centigrade change in temperature is substantially reduced. For best results, the nitrogen containing gaseous environment should be at a temperature of between 650C and 750C (and preferably about 700C) and in contact with the resistor element during the heating interval, the gas being at about atmospheric pressure; and the heating interval should be less than 1 minute, and preferably between 20 and 40 seconds (about 30 seconds for optimum results). FIG. 4 shows the resistance element 19 in a nitrogen gas environment 25 within a container 26, a heater 27 being operated to maintain the gas at the described temperature or temperatures. A door for the container appears at 26a. Steps 15, 16 and 16 a in FIG. 1 respectively indicate initial PPM testing of the resistance film, nitrogen treatment, and subsequent PPM testing of the resistance film.
The graph in FIG. 7 contains three curves 30, 31 and 32. Positive slope curve 30 corresponds to the 140 PPM curve for DP 1131 in FIG. 6; negative slope curve 31 shows that -100 PPM is obtained for DP 1131 upon heat treatment at 700C for 30 seconds in a 100 percent nitrogen environment 25 in FIG. 4; and curve 32 shows that -14 PPM is obtained for DP 1131 (for temperature changes in the range about about 25C) upon heat treatment at about 700C for 30 seconds. in a gaseous environment consisting of 80 percentair and 20 percent nitrogen. Accordingly, the nitrogen concentration in the gaseous environment 25 should be above that of air, but less than 100 percent nitrogen, for minimizing the PPM results. If that environment consists of 86 percent air and 14 percent nitrogen, a PPM level of about is obtained, for DP 1131 fired at about 700C for 30 seconds.
Turning to FIG. 5, it shows the use of a laser beam 130 emanating from source or generator 131 and directed to impinge on the resistance element 19, thereby to effect a change in the electrical resistance of the precision resistor to a desired value at a temperature or temperatures within the range of interest. For this purpose, the beam may be caused to impinge on successively different portions of each of several resistors supported and displaced on a belt 132. Also, the beam may be controlled, as by control means 33 connected with the generator, to interrupt the beam when the measured resistance of the resistor 19 arrives at the precise desired value, and for that purpose a source of voltage 34 and a precision ohmmeter 35 may be temporarilyconnected in series with the leads 21 projecting form the opposite ends of the film 19. Typically, beam impingement on the relatively moving resistance element is continued for a time interval of between 0.10 and 60 seconds, depending on the amount of resistance increase desired, and the intensity of the beam.
W The laser beam may "b'f lo vv frequency with wave length the order of one thousandth of a millimeter or longer. It is found that the resistance element can be tuned, in this manner, over a relatively wide range, i.e., up to around three times its original resistance value, and to a resolution or tolerance of 0.01 percent of a given or desired resistance value, at a selected temperature. As an example, a raw, randomly selected resistor exhibiting a resistance of 21,850 ohms, after nitrogen treatment as described above, may be tuned in this manner to a value of 62,000 i 6 ohms.
The invention is also applicable to film type resistors where the resistance film is applied to a substrate by sputtering techniques, the metal of the element consisting for example of chronium, and alloys therewith, an example being Nichrome.
We claim:
1. The method of improving the temperature stability of an electrical resistance element in film form and which has been fired at relatively high temperature in air, the element including a component selected from the group consisting of noble metals and oxides thereof, that includes:
a. heating said element at relatively high temperature between about 650C and 750C and while the element is exposed to a gaseous environment containing nitrogen in greater percentage than found in air, and
b. continuing said heating for a time interval characterized in that the rate of change of resistance of the element as a function of temperature change is substantially reduced.
2. The method of claim 1 wherein said metals include ruthenium, palladium and silver.
3. The method of claim 1 wherein said gas is at a temperature of about 700C and in contact with the resistor element during said interval.
4. The method of claim 1 wherein said time interval is less than 1 minute.
5. The method of claim 3 wherein said time interval is between about 20 and 40 seconds.
6. The method of claim 1 wherein the resistance element film is in glassy state.
7. The method of claim 5 wherein the resistance element film is in glassy state.
8. The method of claim 7 wherein the percentage of nitrogen, by weight, in the gaseous mixture is selected to produce a parts per million change in resistance per C change in temperature of about 10.
9. The method of claim 1 including the step of directing a laser beam to impinge on said element and thereby effect a change in the electrical resistance of said element to a desired value.
10. The method of claim 9 wherein the laser beam exhibits a wave length of at least about one thousandth of a millimeter.
11. The method of claim 9 including the step of effecting relative movement of the beam and element to impinge the beam on different portions of the element.
12. The method of improving the properties of a film type electrical resistance element having a characteristic rate of change of resistance as a function of temperature change, within a selected temperature range be;
tween xout 0C to C, the element including a temperature range.
Claims (12)
1. THE METHOD OF IMPROVING THE TEMPERATURE STABILITY OF AN ELECTRICAL RESISTANCE ELEMENT IN FILM FORM AND WHICH HAS BEEN FIRED AT RELATIVELY HIGH TEMPERATURE IN AIR, THE ELEMENT SELECTED FROM THE GROUP CONSISTING OF NOBLE METALS AND OXIDES THEREOF, THAT INCLUDES: A. HEATING SAID ELEMENT AT RELATIVELY HIGH TEMPERATURE BETWEEN ABOUT 650*C AND 750*C AND WHILE THE ELEMENT IS EXPOSED TO A GASEOUS ENVIRONMENT CONTAINING NITROGEN IN GREATER PERCENTAGE THAN FOUND IN AIR, AND B. CONTINUING SAID HEATING FOR A TIME INTERVAL CHARACTERIZED IN THAT THE RATE OF CHANGE OF RESISTANCE OF THE ELEMENT AS
2. The method of claim 1 wherein said metals include ruthenium, palladium and silver.
3. The method of claim 1 wherein said gas is at a temperature of about 700*C and in contact with the resistor element during said interval.
4. The method of claim 1 wherein said time interval is less than 1 minute.
5. The method of claim 3 wherein said time interval is between about 20 and 40 seconds.
6. The method of claim 1 wherein the resistance element film is in glassy state.
7. The method of claim 5 wherein the resistance element film is in glassy state.
8. The method of claim 7 wherein the percentage of nitrogen, by weight, in the gaseous mixture is selected to produce a parts per million change in resistance per *C change in temperature of about 10.
9. The method of claim 1 including the step of directing a laser beam to impinge on said element and thereby effect a change in the electrical resistance of said element to a desired value.
10. The method of claim 9 wherein the laser beam exhibits a wave length of at least about one thousandth of a millimeter.
11. The method of claim 9 including the step of effecting relative movement of the beam and element to impinge the beam on different portions of the element.
12. The method of improving the properties of a film type electrical resistance element having a characteristic rate of change of resistance as a function of temperature change, within a selected temperature range between about 0*C to 100*C, the element selected from the group consisting of metals and metal oxides, the steps that include a. heating said element while exposed to a gaseous medium containing nitrogen in greater percentage than found in air to reduce said rate, and b. thereafter impinging laser radiation on the resistance element to controllably alter the resistance level thereof, at temperature within said selected temperature range.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US00326430A US3842495A (en) | 1973-01-24 | 1973-01-24 | Control of rate of change of resistance as a function of temperature in manufacture of resistance elements |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US00326430A US3842495A (en) | 1973-01-24 | 1973-01-24 | Control of rate of change of resistance as a function of temperature in manufacture of resistance elements |
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|---|---|
| US3842495A true US3842495A (en) | 1974-10-22 |
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| US00326430A Expired - Lifetime US3842495A (en) | 1973-01-24 | 1973-01-24 | Control of rate of change of resistance as a function of temperature in manufacture of resistance elements |
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Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4176445A (en) * | 1977-06-03 | 1979-12-04 | Angstrohm Precision, Inc. | Metal foil resistor |
| US4183136A (en) * | 1977-08-03 | 1980-01-15 | Johnson Controls, Inc. | Temperature sensing resistance device |
| JPS55143001A (en) * | 1979-03-05 | 1980-11-08 | Trw Inc | Electric resistor and method of fabricating same |
| US4284872A (en) * | 1978-01-13 | 1981-08-18 | Burr-Brown Research Corporation | Method for thermal testing and compensation of integrated circuits |
| US4826328A (en) * | 1983-04-29 | 1989-05-02 | Robert Bosch Gmbh | Apparatus for measuring the mass of a flowing medium and method for producing an apparatus for measuring the mass of a flowing medium |
| US4962294A (en) * | 1989-03-14 | 1990-10-09 | International Business Machines Corporation | Method and apparatus for causing an open circuit in a conductive line |
| US20040085181A1 (en) * | 2000-10-20 | 2004-05-06 | Ballantine Arne W. | Changing an electrical resistance of a resistor |
| WO2013082080A1 (en) * | 2011-11-29 | 2013-06-06 | Kla-Tencor Corporation | Compact high-voltage electron gun |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3308528A (en) * | 1963-11-06 | 1967-03-14 | Ibm | Fabrication of cermet film resistors to close tolerances |
| US3457636A (en) * | 1964-11-12 | 1969-07-29 | Bunker Ramo | Thin-film resistor adjustment |
| US3462723A (en) * | 1966-03-23 | 1969-08-19 | Mallory & Co Inc P R | Metal-alloy film resistor and method of making same |
| US3535778A (en) * | 1968-03-27 | 1970-10-27 | Western Electric Co | Optical trimming of coated film resistors |
| US3607386A (en) * | 1968-06-04 | 1971-09-21 | Robert T Galla | Method of preparing resistive films |
-
1973
- 1973-01-24 US US00326430A patent/US3842495A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3308528A (en) * | 1963-11-06 | 1967-03-14 | Ibm | Fabrication of cermet film resistors to close tolerances |
| US3457636A (en) * | 1964-11-12 | 1969-07-29 | Bunker Ramo | Thin-film resistor adjustment |
| US3462723A (en) * | 1966-03-23 | 1969-08-19 | Mallory & Co Inc P R | Metal-alloy film resistor and method of making same |
| US3535778A (en) * | 1968-03-27 | 1970-10-27 | Western Electric Co | Optical trimming of coated film resistors |
| US3607386A (en) * | 1968-06-04 | 1971-09-21 | Robert T Galla | Method of preparing resistive films |
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| Title |
|---|
| Laser-Induced Resistivity Changes in Film Resistors Presented by Lins et al. representing Sperry Rand at Wescon, Aug. 23 26, 1966. * |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4176445A (en) * | 1977-06-03 | 1979-12-04 | Angstrohm Precision, Inc. | Metal foil resistor |
| US4183136A (en) * | 1977-08-03 | 1980-01-15 | Johnson Controls, Inc. | Temperature sensing resistance device |
| US4284872A (en) * | 1978-01-13 | 1981-08-18 | Burr-Brown Research Corporation | Method for thermal testing and compensation of integrated circuits |
| JPS55143001A (en) * | 1979-03-05 | 1980-11-08 | Trw Inc | Electric resistor and method of fabricating same |
| US4826328A (en) * | 1983-04-29 | 1989-05-02 | Robert Bosch Gmbh | Apparatus for measuring the mass of a flowing medium and method for producing an apparatus for measuring the mass of a flowing medium |
| US4962294A (en) * | 1989-03-14 | 1990-10-09 | International Business Machines Corporation | Method and apparatus for causing an open circuit in a conductive line |
| US20040085181A1 (en) * | 2000-10-20 | 2004-05-06 | Ballantine Arne W. | Changing an electrical resistance of a resistor |
| US7271699B2 (en) * | 2000-10-20 | 2007-09-18 | International Business Machines Corporation | Changing an electrical resistance of a resistor |
| US20070229212A1 (en) * | 2000-10-20 | 2007-10-04 | Ballantine Arne W | Changing an electrical resistance of a resistor |
| US7804391B2 (en) * | 2000-10-20 | 2010-09-28 | International Business Machines Corporation | Changing an electrical resistance of a resistor |
| WO2013082080A1 (en) * | 2011-11-29 | 2013-06-06 | Kla-Tencor Corporation | Compact high-voltage electron gun |
| US8957394B2 (en) | 2011-11-29 | 2015-02-17 | Kla-Tencor Corporation | Compact high-voltage electron gun |
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