US3231522A - Thermistor - Google Patents
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- US3231522A US3231522A US311686A US31168663A US3231522A US 3231522 A US3231522 A US 3231522A US 311686 A US311686 A US 311686A US 31168663 A US31168663 A US 31168663A US 3231522 A US3231522 A US 3231522A
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/46—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates
- C04B35/462—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates
- C04B35/465—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates based on alkaline earth metal titanates
- C04B35/468—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates based on alkaline earth metal titanates based on barium titanates
- C04B35/4682—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates based on alkaline earth metal titanates based on barium titanates based on BaTiO3 perovskite phase
- C04B35/4684—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates based on alkaline earth metal titanates based on barium titanates based on BaTiO3 perovskite phase containing lead compounds
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/46—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates
- C04B35/462—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates
- C04B35/465—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates based on alkaline earth metal titanates
- C04B35/468—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates based on alkaline earth metal titanates based on barium titanates
- C04B35/4682—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates based on alkaline earth metal titanates based on barium titanates based on BaTiO3 perovskite phase
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- 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
- H01C7/02—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 having positive temperature coefficient
-
- 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
- H01C7/02—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 having positive temperature coefficient
- H01C7/022—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 having positive temperature coefficient mainly consisting of non-metallic substances
- H01C7/023—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 having positive temperature coefficient mainly consisting of non-metallic substances containing oxides or oxidic compounds, e.g. ferrites
- H01C7/025—Perovskites, e.g. titanates
Definitions
- This invention relates to thermistors having a positive temperature coeflicient of electrical resistance and to processes for making such thermistors.
- the derivation of the Word thermistor arises out of the contraction of the expression thermally sensitive resistor.
- Thermistors of this type iind widespread applications. They may be used for highly sensitive thermostats an-d for automatic controls. Because of their high tempera ture coefficient in the temperature range of 110 to 120 degrees C. they can provide a fail safe protection cir cuit for electric motors by placing a thermistor in series with a relay. When the temperature exceeds the safe limit, the relay will open thereby cutting the power to the motor.
- a transistor of the present type in series with a light bulb, or an alarm, and a voltage source pro vides an excellent level indicator.
- PTC positive temperature coeflicient thermistor
- a PTC can do double duty as a control element and as a heating element.
- a PTC and a negative temperature coefficient resistor in series with a light bulb and a voltage source form a thermic oscillator. Further, since current in a PTC resistor will reach a maximum value, or even decrease with increasing voltage, it can be used for current stabilization or current limiting applications.
- the 'main object of this invention is to provide novel thermistors in which a greater degree of control can be exerted over the shape of the temperature ⁇ versus resistance curve.
- Another object of this invention is to provide new sintered barium titanate-based thermistors containing certain rare earth metal oxides as dopants.
- An additional object of this invention is to provide sintered doped barium titanate-based thermistor compositions which have switch points at 60, 80, 120 and 1 80 degrees centigrade.
- a still further object of this invention is to provide a process for preparing a barium titanate-based body which will exhibit the switch points noted in the preceding object.
- FIGURE l is an elevational view of a thermistor in accord with the invention:
- FIGURES 2 to 5 are graphs of the temperature versus the resistance for various compositions of the invention.
- the thermistors of the present invention consist of ceramic-materials composed essentially of, in rnole per cents, ⁇ 0.4 to 0.998 of barium oxide; 0.997 to 1.003 of titanium oxide, O to ⁇ 0.300 of strontium oxide; 0 to 0.150 of lead oxide, 0005 to 0.020 of tin oxide and from 0.001 to 0.006 of an oxide of a rare earth metal selected from the group consisting of praseodymium, neodymium, samarium and a mixture of rare earth metal oxides made up of cerium, lanthanum, neodymium, praseodyrnilrm,
- samarium, gadolinium, and yttrium are intimately mixed in rubber lined balls mills with some distilled water, and then dried, calcined, reground, remilled, formed into pellets and fired.
- mzmbers having a diameter of 9.52 mm. and 2.17 mm. in thickness.
- Barium Vor strontium is provided in the form of carbonates in SL or reagent grades.
- Tin is provided in the tin oxide form, the reagent grade being preferred.
- Lead oxide may be introduced in that form, the analytical grade being preferred.
- the rare earth metal oxides are provided in that form while the mixture thereof is added in the form of a product sold commercially under the name REO mixture.
- the desired proportions of the constituents are weighed to the nearest 0.001 gm. and placed in rubber-lined balls mills with 1250 gm. of Burundum balls which previously are rinsed out with distilled water. Two mole equivalents of material and 500 ce. of distilled water are used per mill. Milling for about S hours at r.p.m. gives a suitably homogeneous mixture which is oven dried at degrees C.
- the dried powder next is placed in a refractory Crucible, such as one of zirconia, and calcined at 1090" C.
- the sintered material plus 250 cc.
- the sintered bodies are then provided with electrical contacts. These contacts are applied ultrasonically using pure indium, indium-silver or lead-tin solders. Number l2 solder composed of 90% lead, 5% indium and 5% silver gives the best bond and the lowest yohnlic resistance. Suitable Wire leads suitably made of copper can then be soldered to the contacts.
- FIGURE l sh-ows a thermistor 2 in accordance with the invention and comprising a body prepared from the compositions herein disclosed.
- An upper metal contact 1t is secured in ohmic contact with the body and a suitable electric lead 6 is welded or otherwise secured thereto.
- a lower contact S and its lead l0 are similarly provided on the bottom of the thermistor member.
- Epoxy encapsulating material was used on thermistors designed for a maximum operating temperature of C. and silicone on thermistors with a maximum operating temperature of 250 C.
- D.C. resistance was measured on an impedance-type bridge, with the thermistors in an oil bath which was stirred at a constant rate of speed as the bath temperature was increased by an electric hot plate.
- compositions of the invention were heated according to the following conditions.
- thermoistors were prepared from the following compositions:
- composition 9 The resistance versus temperature curves for the above compositions are shown in FIGURE 3.
- maximum temperature coefficient of resistance was
- the addition tin improved substantially the steepness of the curve.
- composition No. 14 where 0.020 mole tin were added the curve has been shifted downward somewhat and still maintained a steep curve.
- This type of thermistor has applications for controlling hot Water.
- Example 3 Thermistors were prepared by the method of the invention using the following compositions:
- Example 2 ThermistorsY were prepared by the method of the invention using the following compositions:
- Composition.. 13 14 Barium 0. 995 0. 995 Tin 0.005 0.020 Titanium 0. 998 0. Q83 Rare earth oxide (REO) 0.005 0.005
- Thermistors were prepared by the method of the in- Rar earthoxide umm" vention using the following compositions:
- compositions have a switch point of apprOXi- Barium 0. S98 0.897 0. 995 0. 79s 0.797 0.795 mately 120 C.
- the optimum properties are summarized gg (1)- 1)- inthe following table: 40 Samarium 0. 002 0. 003 01005 0.002 02003 01005 Maximum Rare earth Mole pereent Lowest initial temp. coelll- Composltlon 23 24 25 dopant resistance cient; of
- the resistance versus temperature curves for the above compositions are shown in FIGURE 5.
- the effect of strontium additions is to shift the switch point from 120 C. to C. for composition 191.100 Sr) to 60 C. for composition 22 (.200 Sr)'to 30 C. for composition 24 (.300 Sr).
- a thermistor composition consisting essentially of a fired body formed from a mixture of 0.998 mole percent of barium oxide, 1.003 mole percent of titanium dioxide and 0.002 mole percent of praseodymium oxide.
- a thermistor composition consisting essentially of Ya fired body formedfrom a mixture of 0.998 mole percent ofbarium oxide, 1.003 mole percent of titanium dioxide and 0.002 molerpercent of neodymium oxide.
- a thermistor composition consisting essentiallyrof a tired body formed from a mixture of 0.997 mole percent of barium oxide, 1.003 mole percent 'of titanium dioxide and 0.003 mole percent of samarium oxide.
- a thermistor composition consisting essentially of a tired body formed from a mixture of 0.898'mole per- 3,231,522 5 6 cent of barium oxide, 0.100 mole percent of strontium FOREIGN PATENTS oxide, 1.003 mole percent of titanium dioxide and 0.002 714 965 9 /1954 Great Britain mole percent of samarium oxide.
Description
Jan 25, 1966 w. E. BLoDGET-r ETAL 3,231,522
THERMISTOR 4 Sheets-Sheet 1 Filed Sept. 26, 1963 oo P EEQQEE.
O v- Om- ON- O: OO- Om Om Oh Ow Om 0.? Om ON O O N no moo.; mmm um moo Em, m v \|\l|-||||.|||| m Il' Il 'IN WM |l|l m moo.. mmm. moo. \w\\`\\\\\ IIIII lfAll. E. om J2 no 32:. mmm um moo 0mm N n M w h m \/lmo 30:... mmm om moo i N v m m w\ m ATTORNEY THERMISTOR 4 Sheets-Sheet 2 Filed Sept. 26, 1963 o EEQQEPP ONO.
mmm.
UINKDIDQ'M N OOO son get? Std mo .u N NRE R WM ml. m il T JWP NW Y B sumo aoumsgsag Jan. 25, 1966 THERMISTOR Filed Sept. 26, 1963 W. E. BLODGETT ETAL 4 Sheets-Sheet 5 Temperature C IOOOOO sumo aaumsgsag Fig. 4.
INVENTORS Jqhg M. Robertson wnlhum E. B lodgeH 3y Paul l. Keehng ATTORN EY Jan. 25, 1966 Filed Sept. 26, 1963 W. E. BLODGETT THERMISTOR ETAL 3,231,522
4 Sheets-Sheet 4 Temperature 6 .695 Sr.30o Tim03 03 REO Q05 Ba locuooo9 noooo sumo eoumsgssg INVENTORS John M. oBbertson Wllhum aodgeft BY Paul I. Keelmg ATTORNEY United States Patent 3,231,522 THERMISTQR William E. lilodgett, Paul I. Keeling, and John M. Robertson, Louisville, Ky., assignors to American Radiator &
Standard Sanitary Corporation, New York, N.Y., a
corporation of Delaware Filed Sept. 26, 1963, Ser. No. 311,686 4 Claims. (Cl. 252-521) This invention relates to thermistors having a positive temperature coeflicient of electrical resistance and to processes for making such thermistors. The derivation of the Word thermistor arises out of the contraction of the expression thermally sensitive resistor.
Thermistors of this type iind widespread applications. They may be used for highly sensitive thermostats an-d for automatic controls. Because of their high tempera ture coefficient in the temperature range of 110 to 120 degrees C. they can provide a fail safe protection cir cuit for electric motors by placing a thermistor in series with a relay. When the temperature exceeds the safe limit, the relay will open thereby cutting the power to the motor. A transistor of the present type in series with a light bulb, or an alarm, and a voltage source pro vides an excellent level indicator. When submerged the positive temperature coeflicient thermistor, hereinafter called PTC, cannot develop suflicient heat to cause a `noticeable change in resistance but when the liquid level drops, exposing the PTC, it will heat up and extinguish the light or set off the alarm. In very small thermostats, a PTC can do double duty as a control element and as a heating element. A PTC and a negative temperature coefficient resistor in series with a light bulb and a voltage source form a thermic oscillator. Further, since current in a PTC resistor will reach a maximum value, or even decrease with increasing voltage, it can be used for current stabilization or current limiting applications.
With a view to obtaining new positive temperature coefficient thermistors having improved properties, the 'main object of this invention is to provide novel thermistors in which a greater degree of control can be exerted over the shape of the temperature `versus resistance curve.
Another object of this invention is to provide new sintered barium titanate-based thermistors containing certain rare earth metal oxides as dopants.
An additional object of this invention is to provide sintered doped barium titanate-based thermistor compositions which have switch points at 60, 80, 120 and 1 80 degrees centigrade.
A still further object of this invention is to provide a process for preparing a barium titanate-based body which will exhibit the switch points noted in the preceding object.
These and other related objects, features and advantages of the present invention will be more readily under- Vstood as the description thereof proceeds, particularly When taken together with the accompanying drawing wherein:
FIGURE l is an elevational view of a thermistor in accord with the invention:
FIGURES 2 to 5 are graphs of the temperature versus the resistance for various compositions of the invention.
The thermistors of the present invention consist of ceramic-materials composed essentially of, in rnole per cents, `0.4 to 0.998 of barium oxide; 0.997 to 1.003 of titanium oxide, O to `0.300 of strontium oxide; 0 to 0.150 of lead oxide, 0005 to 0.020 of tin oxide and from 0.001 to 0.006 of an oxide of a rare earth metal selected from the group consisting of praseodymium, neodymium, samarium and a mixture of rare earth metal oxides made up of cerium, lanthanum, neodymium, praseodyrnilrm,
ICC
samarium, gadolinium, and yttrium. These components are intimately mixed in rubber lined balls mills with some distilled water, and then dried, calcined, reground, remilled, formed into pellets and fired. In accordance with the invention there are provide mzmbers having a diameter of 9.52 mm. and 2.17 mm. in thickness. In the practice of this invention, titanium is provided in the =form of titanium dioxide in electronic grade. Barium Vor strontium is provided in the form of carbonates in SL or reagent grades. Tin is provided in the tin oxide form, the reagent grade being preferred. Lead oxide may be introduced in that form, the analytical grade being preferred. The rare earth metal oxides are provided in that form while the mixture thereof is added in the form of a product sold commercially under the name REO mixture. The desired proportions of the constituents are weighed to the nearest 0.001 gm. and placed in rubber-lined balls mills with 1250 gm. of Burundum balls which previously are rinsed out with distilled water. Two mole equivalents of material and 500 ce. of distilled water are used per mill. Milling for about S hours at r.p.m. gives a suitably homogeneous mixture which is oven dried at degrees C. The dried powder next is placed in a refractory Crucible, such as one of zirconia, and calcined at 1090" C. The sintered material plus 250 cc. of distilled water are placed in the mill and reground for 7 hours. One percent of a l0 percent of polyvinyl alcohol is added and milling is continued for about an hour. The mixture is then dried at 70 C. and screened through a minus 20 mesh screen. Pellets are formed at a pressure of about 10,000-20,000 p.s.i. and fired in an electric tube furnace, preferably in air, to either 1260 C., l315 C. at 150 C. rise per hour.
vThe formed pellets are soaked for one to four hours and cooled to room temperature. Previous patents have suggested elabrate tiring techniques using argon. This is not only costly but produces PTC thermistors of inferior quality and lower temperature coefficients of resistance than those of the claimed compositions.
The sintered bodies are then provided with electrical contacts. These contacts are applied ultrasonically using pure indium, indium-silver or lead-tin solders. Number l2 solder composed of 90% lead, 5% indium and 5% silver gives the best bond and the lowest yohnlic resistance. Suitable Wire leads suitably made of copper can then be soldered to the contacts.
Referring to the drawing now, FIGURE l sh-ows a thermistor 2 in accordance with the invention and comprising a body prepared from the compositions herein disclosed. An upper metal contact 1tis secured in ohmic contact with the body and a suitable electric lead 6 is welded or otherwise secured thereto. A lower contact S and its lead l0 are similarly provided on the bottom of the thermistor member. Epoxy encapsulating material was used on thermistors designed for a maximum operating temperature of C. and silicone on thermistors with a maximum operating temperature of 250 C.
ln evaluating the various thermistor compositions of this invention, D.C. resistance was measured on an impedance-type bridge, with the thermistors in an oil bath which was stirred at a constant rate of speed as the bath temperature was increased by an electric hot plate.
Various sintering schedules were employed in the preparation of the thermistors of the invention. The results obtained indicate that tiring in argon lowers the PTC and the initial resistance and as more air is introduced into the tiring cycle, the initial resistance increases as does the PTC effect. As a general rule, optimum properties are `obtained by using still air conditions. However, the PTC effect can be increased by the introduction of very small amounts of circulating air at the expense of increasing the resistance at a given temperature.
The compositions of the invention were heated according to the following conditions.
Condition No. 1.Room temperature to 1260 C., 150 C./hour rise, 1 hour soak, ired in still air, cooled to room temperature in hours.
Condition No. 2,-Room temperature to 13l5 C., 150 C./hour rise, 1 hour soak, fired in still air, cooled t-o room temperature inv 10 hours.
Condition No. 3.-Room temperature to 1370 C., 150 C./hour rise, 1 hour soak, red in still air, cooled to room temperature in 10 hours.
Condition No. 4.-Same as above except top temperature held two hours.
The following examples serve to illustrate but do not limit the invention:
Example 1 Following the above described method, thermistors were prepared from the following compositions:
Example 3 Thermistors were prepared by the method of the invention using the following compositions:
Composition.; 15 16 Barium 0. 895 0. 845 0.100 0.150 1. 003 1. 003
Rare earth oxide (REO) 0.005 0.005
The resistance versus temperature curves for the above compositions are shownin FIGURE 2. Maximum temperature coefiicient is achieved with praseodymium as Vlow initial resistances neodymium and REOblend is ideal. The dopant used not only has an effect on slope of the curve but also in the initial resistance.
Example 2 ThermistorsY were prepared by the method of the invention using the following compositions:
Composition.. 13 14 Barium 0. 995 0. 995 Tin 0.005 0.020 Titanium 0. 998 0. Q83 Rare earth oxide (REO) 0.005 0.005
Cerium, 45.6%; lanthanum 22.8%; neodymum, 16.2%; praseodymium 4.7%; samarium, 2.8%; gadolinium, 1.9%; yttrium. 0.2%.
gr Thermistors were prepared by the method of the in- Rar earthoxide umm" vention using the following compositions:
. 35 Cerium 45.67; lanthanum, 22.8%; neodymium, 16.207; raseodym- Y ium, 4.7%? samaiium, 2.8%; gadolinium, 1.9%; yttrinm, 0.2 o. Composltwn 17 18 19 20 21 22 These compositions have a switch point of apprOXi- Barium 0. S98 0.897 0. 995 0. 79s 0.797 0.795 mately 120 C. The optimum properties are summarized gg (1)- 1)- inthe following table: 40 Samarium 0. 002 0. 003 01005 0.002 02003 01005 Maximum Rare earth Mole pereent Lowest initial temp. coelll- Composltlon 23 24 25 dopant resistance cient; of
051991193 Barium- 0. 69s 0. 095 0. 090 Y 45 tlontium.-
0.300 0.300 1. 003 1 003 Praseodymlum 0.005 l2 ohms +257/ C. 1 amum Neodymumm 0. 005 6 ohms 17% o C, Rare earth oxide (REO)- 0.002 0.005 0.010 amariyiun-.-" L 0.005 ,50 ohms |25%/2 C.
REQ, blend-H 0'003 7 Ohms +17%/ Cerium, 4.5.6%;1anthanum, 22.8%; neodymium, 16.2%; praseodymium,
Y Y 4.7%; samarmm, 2.8%; gadolinium, 1.9%; yttrium, 0.2%.
The resistance versus temperature curves for the above compositions are shown in FIGURE 5. The effect of strontium additions is to shift the switch point from 120 C. to C. for composition 191.100 Sr) to 60 C. for composition 22 (.200 Sr)'to 30 C. for composition 24 (.300 Sr). l
Obviously many modifications and variations of the present invention are possible in the light of the above teachings. It is, therefore, to be understood that within the scope of the appended claims the invention may be practiced otherwise than as specifically described.
What is claimed is: j 1
1. A thermistor composition consisting essentially of a fired body formed from a mixture of 0.998 mole percent of barium oxide, 1.003 mole percent of titanium dioxide and 0.002 mole percent of praseodymium oxide.
2. A thermistor composition consisting essentially of Ya fired body formedfrom a mixture of 0.998 mole percent ofbarium oxide, 1.003 mole percent of titanium dioxide and 0.002 molerpercent of neodymium oxide.
3. A thermistor composition consisting essentiallyrof a tired body formed from a mixture of 0.997 mole percent of barium oxide, 1.003 mole percent 'of titanium dioxide and 0.003 mole percent of samarium oxide.
4. A thermistor composition consisting essentially of a tired body formed from a mixture of 0.898'mole per- 3,231,522 5 6 cent of barium oxide, 0.100 mole percent of strontium FOREIGN PATENTS oxide, 1.003 mole percent of titanium dioxide and 0.002 714 965 9 /1954 Great Britain mole percent of samarium oxide.
series, June 15, 1957, pp. 1358-9.
References Cited by the Examiner UNITED STATES PATENTS 2,976,505 3/ 1961 Ichikawa 252-520 XR 2,981,699 4/1961 Ichikawa 252 520 JULIUS GREENWALD, Prlmary Examzner. 3,023,390 2/ 1962 Morats et al 252-520 J. D. WELSH, Assistant Examiner.
Claims (1)
1. A THERMISTOR COMPOSITION CONSISTING ESSENTIALLY OF A FIRED BODY FORMED FROM A MIXTURE OF 0.998 MOLE PERCENT OF BARIUM OXIDE, 1.003 MOLE PERCENT OF TITANIUM DIOXIDE AND 0.002 MOLE PERCENT OF PRASEODYMIUM OXIDE.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US311686A US3231522A (en) | 1963-09-26 | 1963-09-26 | Thermistor |
DE19641465109 DE1465109A1 (en) | 1963-09-26 | 1964-09-18 | Thermistor |
FR989043A FR1434144A (en) | 1963-09-26 | 1964-09-23 | Thermistor with positive temperature coefficient of resistance |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US311686A US3231522A (en) | 1963-09-26 | 1963-09-26 | Thermistor |
Publications (1)
Publication Number | Publication Date |
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US3231522A true US3231522A (en) | 1966-01-25 |
Family
ID=23207999
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US311686A Expired - Lifetime US3231522A (en) | 1963-09-26 | 1963-09-26 | Thermistor |
Country Status (3)
Country | Link |
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US (1) | US3231522A (en) |
DE (1) | DE1465109A1 (en) |
FR (1) | FR1434144A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3375774A (en) * | 1967-01-05 | 1968-04-02 | Matsushita Electric Ind Co Ltd | Fully automatic electric coffee pot |
US3416957A (en) * | 1965-05-10 | 1968-12-17 | Sprague Electric Co | Resistance element utilizing group iii or v-b metal |
US3500634A (en) * | 1968-01-02 | 1970-03-17 | Texas Instruments Inc | Control system and actuator used therein |
US3637531A (en) * | 1970-05-01 | 1972-01-25 | Texas Instruments Inc | Method for making ceramic titanate elements and materials therefor |
US3766511A (en) * | 1972-12-26 | 1973-10-16 | Gen Electric | Thermistors |
US3948438A (en) * | 1974-07-17 | 1976-04-06 | Lennox Industries Inc. | Thermostat system |
US4053864A (en) * | 1976-12-20 | 1977-10-11 | Sprague Electric Company | Thermistor with leads and method of making |
US4275508A (en) * | 1980-01-09 | 1981-06-30 | Eaton Corporation | Clothes dryer temperature control system |
US6346496B2 (en) * | 1998-07-24 | 2002-02-12 | Murata Manufacturing Co., Ltd. | Composite material for positive temperature coefficient thermistor, ceramic for positive temperature coefficient thermistor and method for manufacturing ceramics for positive temperature coefficient thermistor |
WO2017151965A1 (en) * | 2016-03-02 | 2017-09-08 | Watlow Electric Manufacturint Company | Heater element having targeted decreasing temperature resistance characteristics |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB714965A (en) * | 1951-05-23 | 1954-09-08 | Philips Electrical Ind Ltd | Improvements in or relating to semi-conductive material |
US2976505A (en) * | 1958-02-24 | 1961-03-21 | Westinghouse Electric Corp | Thermistors |
US2981699A (en) * | 1959-12-28 | 1961-04-25 | Westinghouse Electric Corp | Positive temperature coefficient thermistor materials |
US3023390A (en) * | 1960-03-17 | 1962-02-27 | Westinghouse Electric Corp | Applying electrodes to ceramic members |
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1963
- 1963-09-26 US US311686A patent/US3231522A/en not_active Expired - Lifetime
-
1964
- 1964-09-18 DE DE19641465109 patent/DE1465109A1/en active Pending
- 1964-09-23 FR FR989043A patent/FR1434144A/en not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB714965A (en) * | 1951-05-23 | 1954-09-08 | Philips Electrical Ind Ltd | Improvements in or relating to semi-conductive material |
US2976505A (en) * | 1958-02-24 | 1961-03-21 | Westinghouse Electric Corp | Thermistors |
US2981699A (en) * | 1959-12-28 | 1961-04-25 | Westinghouse Electric Corp | Positive temperature coefficient thermistor materials |
US3023390A (en) * | 1960-03-17 | 1962-02-27 | Westinghouse Electric Corp | Applying electrodes to ceramic members |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3416957A (en) * | 1965-05-10 | 1968-12-17 | Sprague Electric Co | Resistance element utilizing group iii or v-b metal |
US3375774A (en) * | 1967-01-05 | 1968-04-02 | Matsushita Electric Ind Co Ltd | Fully automatic electric coffee pot |
US3500634A (en) * | 1968-01-02 | 1970-03-17 | Texas Instruments Inc | Control system and actuator used therein |
US3637531A (en) * | 1970-05-01 | 1972-01-25 | Texas Instruments Inc | Method for making ceramic titanate elements and materials therefor |
US3766511A (en) * | 1972-12-26 | 1973-10-16 | Gen Electric | Thermistors |
US3948438A (en) * | 1974-07-17 | 1976-04-06 | Lennox Industries Inc. | Thermostat system |
US4053864A (en) * | 1976-12-20 | 1977-10-11 | Sprague Electric Company | Thermistor with leads and method of making |
US4275508A (en) * | 1980-01-09 | 1981-06-30 | Eaton Corporation | Clothes dryer temperature control system |
US6346496B2 (en) * | 1998-07-24 | 2002-02-12 | Murata Manufacturing Co., Ltd. | Composite material for positive temperature coefficient thermistor, ceramic for positive temperature coefficient thermistor and method for manufacturing ceramics for positive temperature coefficient thermistor |
WO2017151965A1 (en) * | 2016-03-02 | 2017-09-08 | Watlow Electric Manufacturint Company | Heater element having targeted decreasing temperature resistance characteristics |
US10544722B2 (en) | 2016-03-02 | 2020-01-28 | Watlow Electric Manufacturing Company | Virtual sensing system |
US10648390B2 (en) | 2016-03-02 | 2020-05-12 | Watlow Electric Manufacturing Company | System and method for axial zoning of heating power |
US10724417B2 (en) | 2016-03-02 | 2020-07-28 | Watlow Electric Manufacturing Company | Dual-purpose heater and fluid flow measurement system |
US10760465B2 (en) | 2016-03-02 | 2020-09-01 | Watlow Electric Manufacturing Company | Heater element having targeted decreasing temperature resistance characteristics |
US10934921B2 (en) | 2016-03-02 | 2021-03-02 | Watlow Electric Manufacturing Company | Heater element as sensor for temperature control in transient systems |
EP4047193A1 (en) * | 2016-03-02 | 2022-08-24 | Watlow Electric Manufacturing Company | Heater element having targeted decreasing temperature resistance characteristics |
Also Published As
Publication number | Publication date |
---|---|
DE1465109A1 (en) | 1969-01-16 |
FR1434144A (en) | 1966-04-08 |
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