|Publication number||US3801839 A|
|Publication date||Apr 2, 1974|
|Filing date||Dec 1, 1972|
|Priority date||Dec 3, 1971|
|Also published as||DE2259368A1, DE2259368B2, DE2259368C3|
|Publication number||US 3801839 A, US 3801839A, US-A-3801839, US3801839 A, US3801839A|
|Original Assignee||Rion Co|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (1), Referenced by (28), Classifications (28)|
|External Links: USPTO, USPTO Assignment, Espacenet|
BlO BOQ X5 398Ol83 v'yv'z fir, e P 6 m Umted Stat 16 1 X 1 an 1111] 3 801 839 4 I a 9 r f 1 i Y0 K i? 1 .1 1451 -Apr.2, 1974 MECHANICAL TO ELECTRICAL  References Cited TRANSDUCER DEVICE UNITED STATES PATENTS  Inventor: Kiyotoshi Yo, Tokyo, Japan 2,231,159 2/1941 Gerlach 310/8 A :R' Kbh'k'KhTk  sslgnee :32 8 us I I ms 0 Primary ExaminerGerald Goldberg Assistant Examiner-Mark O. Budd  Filed 9 Attorney, Agent, or FirmWenderoth, Lind & Ponack  Appl. No.: 311,433
I  ABSTRACT  Foreign Application Priority Data A transducer element is disclosed herein made of, for example, a vulcanized chloroprene eiastomer mixed DEC. 3, Japan channel black to electrostrictive proper ties and biased with a DC voltage to convert a me- 310/8 fiis sl 'g chanical impact or vibration to corresponding electri-  Field of Search 310/8, 9.5; 252/629 cal energy 4 Claims, 3 Drawing Figures l 2 7/ \k ./1 4 A 1 6 ,1 11 K I' ll Q 1 0 I PATENTED 2 I974 FIG.
RECORDER DISPLAY AUXILIARY DEVICE A TRANSDUCER MECHANICAL TO ELECTRICAL TRANSDUCER DEVICE BACKGROUND OF THE INVENTION This invention relates to a mechanical-to-electrical transducer device utilizing an electrostrictive material consisting essentially of an elastomer, and more particularly to such a device for converting a mechanical force, for example, a sound or a mechanical vibration to electrical energy and vice versa.
In addition to single crystal Rochelle salt, quartz, lead zirconate-titanate porcelains etc., there have been previously discovered synthetic high molecular compounds specially processed as piezoelectric materials. These synthetic high molecular compounds have been utilized in the form of film, such as polyvinylidene fluorides, polyvinyl chlorides, polycarbonates, ll-nylon etc. It is well known that films of such high molecular compounds can be rendered considerably high in piezoelectric properties by elongating the film maintained at a temperature adjacent to the'softening point thereof, applying a DC voltage across the film in the direction of thickness thereof and raising the temperature of the film while the DC voltage continues to be applied thereacross. Then the film is allowed to be cooled to room temperature after which the voltage is removed from the film. It is said that this improvement in the piezoelectric properties of the high molecular .films attributes to both spontaneous polarization caused from the rearrangement of dipoles therein due to the effect of polarization and the electrostriction of the films.
On the other hand, the spontaneous polarization has been heretofore difficult to effect in rubber-like materials or elastomers although the electrostriction is a longestablished phenomenon occurring in such elastomers. This is because such materials include bridged bonds formed of high molecular components and effect the micro-brownian motion. Therefore it is considered presently difficult to impart piezoelectric properties to such elastomers.
SUMMARY OF THE INVENTION It is an object of the present invention to provide a new and improved transducer device utilizing an electrostrictive material consisting essentially of an elastomer for converting mechanical energy to an electrical energy with a high efficiency.
It is another object of the present invention to provide a new mechanical to electrical transducer device having a high flexibility in both shape and size depending upon the desired performance.
The present invention accomplishes these objects by the provision of a mechanical to electrical transducer device including a transducer element for converting mechanical energy to electrical energy, characterized in that the transducer element is formed ofa vulcanized elastomer having mixed therewith a predetermined amount of a filler of electrically conductive material and has a DC biasing voltage applied thereacross.
The elastomers may be preferably selected from the group consisting of chloroprene rubbers, nitrile rubbers, isoprene rubbers, chlorosulfonated polyethylene elastomers, and fluoro-elastomers including polar substituents in the side chains thereof. Alternatively, it
may be a butadiene elastomer not including no polar substituents inthe side chains thereof.
The electrically conductive material of the filler may be advantageously selected from the group consisting of carbon black and graphite.
BRIEF DESCRIPTION OF THE DRAWING The present invention will become more readily apparent from the following detailed description taken in conjunction with the accompanying drawing in which:
FIG. I is a sectional view of a mechanical-toelectrical transducer device with an electric circuit embodying the principles of the present invention;
FIG. 2 is a view similar to FIG. 1 but illustrating a modificationof the invention; and
FIG. 3 is a block diagram illustrating one application of the invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTS volved, and the mixing and kneading process.
It has been found that the filler formed of a suitable electrically conductive material such as carbon black much enhances the electrostrictive properties of the vulcanized elastomers. Particularly, after elastomers including polar substituents in the side chains thereof, for example, chloroprene rubbers, chlorosulfonated polyethylene elastomer, polyisoprene rubbers, and fluoro-elastomers etc. have been suitably mixed with channel black and vulcanized, the elastomers thus processed can have electrostrictive constants amounting to a value to 10' c.g.s. in e.s.u. When put in a DC electric field having, for example, a strength of 300 volts per each centimeter of the thickness of the material, the vulcanized elastomers exhibit piezoelectric properties. For example, their piezoelectric constants d have been measured to be in the order of 10 c.g.s. in e.s.u. This figure is substantially identical to the value of the piezoelectric constant of lead zirconate porcelains. Also a 14" constant (41rd /e representing a voltage sensitivity is in the order of 0.5 volt per gramscentimeter. That is, a force of one dyne per square centimeter is'converted to an electric output of 0.5 X 10*" volt. This means that microphones formed of the elastomers materials as above described to receive directly a sound pressure has a sensitivity of 66 dB. sufficient for practical purposes.
It has been also found that the present invention is effective for imparting high electrostrictive and piezoelectric properties to some elastomers not including polar substituents in the side chains thereof as will be described hereinafter.
EXAMPLE I parts of a chloroprene rubber of the W type, 4 parts of magnesia(MgO), 1 part of stearic acid and 35 parts of channel black were thoroughly mixed with one another and then vulcanized at a temperature of C for 30 minutes. The vulcanized elastomer had a dielectric constant and an electrostrictive constant measured at 90 and 10' c.g.s. in e.s.u. respectively.
For comparison purposes, the same starting materials were used in the same amounts as above described except for channel black being omitted and the process as above described was repeated. The resulting dielectric constant and electrostrictive constant had measured values of 11 and 10" c.g.s. in e.s.u. respectively.
EXAMPLE I1 100 parts of a nitrile rubber including 30 percent of nitrile and commercially available under l-lycar DN 302 (trade mark), 5 parts of zinc oxide(ZnO), 1 part of stearic acid, 1.5 parts of dibenzothiazol disulfide, and 40 parts of furnace black were intimately mixed with one another and vulcanized at 150C for 20 minutes. The results of various measurements indicated a dielectric constant of 52 and an electrostrictive constant of c.g.s. in e.s.u. With furnace black omitted, the process as above described was repeated to yield a dielectric constant of 8 and a electrostrictive constant of 10 c.g.s. in e.s.u.
Nitrile rubbers are inherently inferior in electrostriction to chloroprene rubbers but the substitution of furnace black for channel black improves the electrostriction. For example, the same results as above described were given with 20 parts by weight of channel black.
EXAMPLE 111 100 parts of an isoprene elastomer, 5 parts of zinc oxide(ZnO), 3 parts of stearic acid, 2.5 parts of sulfur, l
' part of dibenzothiazolyl disulfide, 0.2 part of tetramethylthiuram disulfide and 20 parts of channel black were fully mixed with one another and vulcanized at 160C for minutes. The product was measured to have a dielectric constant of 80 and an electrostrictive constant of 2.3 X 10" c.g.s. in e.s.u.
As in Example I, the same materials were used in the same amount as described above with the channel black omitted and the above process was repeated. The results of measurements indicated that the dielectric constant and electrostrictive constant had respective values of 2.8 and 2.6 X 10' c.g.s. in e.s.u.
EXAMPLE IV The process as above described was repeated with the same materials but the channel black omitted to provide a dielectric constant of 9.5 and an electrostrictive modulus of 5 X 10' c.g.s. in e.s.u.
EXAMPLE V 100 parts of a chlorosulfonated polyethylene elastomer; 10 parts of magnesia(MgO), 2 parts of dipentamethylenethiuram tetrasulfide, 10 parts of dioctyl phthalate and 15 parts of channel black were formed into an intimate mixture. Then the mixture was vulcanized at 150C for 30 minutes.
The results of measurements indicated a dielectric constant of and an electrostrictive constant of 10 c.g.s. in e.s.u. The product could be continuously used at C and exhibited a chemical resistance.
The process as above described was repeated with the channel black and dioctyl phthalate omitted to provide a dielectric constant of- 5.6 and an electrostrictive constant of 6 X 10 c.g.s. in e.s.u.
EXAMPLE VI 100 parts of a butadiene rubber of high transtype (which does not include polar substituents in the side chains thereof), 5 parts of zinc oxide(ZnO), 2 parts of stearic acid, 3 parts of tetra-methylthiuram disulfide and 20 parts of channel black was used. The vulcanization was effected at C for 15 minutes. The dielectric constant and electrostrictive constant had measured values of 54 and 5 X 10 c.g.s. in e.s.u. respectively.
With the channel black omitted, a dielectric constant and an electrostrictive constant were measured at 14 and 1.2 X 10 c.g.s. in e.s.u. respectively.
In the above Examples, the dielectric constant and electrostrictive constant were measured in an electric field having a strength of 300 volts per centimeter.
Examples of elastomers for use in practicing the present invention involve chloroprene rubbers, nitrile rubbers, isoprene rubbers, fluoro-elastomers, chlorosulfonated polyethylene elastomers, butadiene rubbers. Preferable examples of those elastomers may be chloroprene rubbers and nitrile rubbers high in content of nitrile. Among the fluoro-elastomers, a copolymer of propylene hexafluoride and vinylidene fluioride is ad vantageously used and the butadien rubbers are preferably of high trans-type.
The amount of carbon black added depends upon both the type thereof and the type of the elastomer. It has been found that the maximum amount of the carbon black should not exceed a magnitude above which the associated elastomer after having been vulcanized become conductive, that is, has a resistivity of 10 megohms-centimeter or less. In other words, the carbon black can be added to the associated elastomer in an amount of ranging from 5 to 40 part relative to, 100 parts of the weight of the elastomer. As above described in conjunction with Example ll, channel black is superior to furnace black. That is, channel black may be used in amounts less than that of furnace black and still give similar results.
Also it has been found that the DC voltage applied across the electrostrictive element has preferably a value sufficient to establish an electric field whose strength ranges from 10 to 10 X 10 volts per centimeter of the thickness of the element.
Referring now to FIG. 1 of the drawing, there is illustrated a mechanical-to-electrical transducer device constructed in accordance with the principles of the present invention whereby an impulsive motion, for example, an impact or a mechanical strain is converted to corresponding electrical energy. The arrangement illustrated comprises a disc-shaped transducer element 10 formed of an electrostrictive elastomer such as above described in conjunction with the Examples of the present invention, a hot electrode 14 of any suitable metallic material such as brass coextensive with and disposed on one of the opposite faces of the disc, and an electrically insulating block 14 encircling in contact relationship both the lateral surface of the interconnected element and electrode and 12, respectively and the exposed surface of the electrode 12 to leave only the central exposed portion of the electrode surface with an output electrode 16 disposed on that exposed surface portion. Then the assembly thusproduced has the entire surface covered with a metallic shield 18 except for the exposed surface portion and a damper element 20 is formed, for example, ofa foamed urethane attached to the other face of the transducer element 10 through the metallic shield 18. Then the output electrode 16 and the metallic shield 18 are connected to a pair of output terminals 22.
In order to bias the transducer element 10 with a DC voltage, a source 24 of DC voltage is connected across the output electrode 16 and the metallic shield 20 through a resistor 26.
Under these circumstances, an impact can be applied to the damper element 20 in the direction of the arrow A shown in FIG. 1. This results in the generation of a corresponding AC output at the output terminals 22. With the transducer element 10 formed into a thickness of 2 millimeters of the electrostrictive elastomer of Example V and having a bias voltage of 18 volts applied thereacross, the transducer device as shown in FIG. 1 could generate an output of 50 millivolts in response to an iron ball(not shown) with a weight of 12 grams falling upon the damper element 20 thereof. Thus it will be appreciated that the present invention provides a durable impact meter having a high sensitivity. This is because the elastomer involved is soft enough to decrease its mechanical impedance to an extremely small value and still the elastomer itself serving as a sensor element which is very tough to motions of mechanical systems, for example, impacts. I
FIG. 2 shows a modification of the present invention applied to a vibration pick-up device. As shown, a twopart housing has a disc-shaped transducer element 32 formed of an electrostrictive material prepared in accordance with the present invention and suitably fixed on one of two opposite faces thereof to the inner surface of the wall of the housing 30 through a thin metallic electrode 34 and a weight 36 coextensive with and disposed on the other face of the element 32 through another thin metallic electrode 38. Then both electrodes 34 and 38 are connected to a pair of output terminals 40 through leads and across a bias source 42 of DC voltage.
In operation, any vibration is applied to the device in direction of the arrow B shown in FIG. 2. This results in the generation of a corresponding AC output across the output terminals 40.
FIG. 3 illustrates a transducer device 44 suc as shown in FIG. 1 connected through any suitableA/ti xiliary device 46 to both an display device 48 and a recorder 50. The auxiliary device 46 may be arfamplifier for suitably amplifying the output from the transducer device 44 or a translator for changing the output from the transducer device 44 to another electric quantity through electrical computations. Then the output from the device 44 is displayed on the display device 48 and recorded by the recorder device 50.
The present invention is very superior in utility to the prior art type of piezo-electric single crystals and porcelains because the-elastomer involved is extremely small in mechanical impedance and formed in any desired shape and size. Further the invention can readily and economically provide mechanical-to-electrical transducer devices having any desired performance by properly combining various types of elastomers with one another.
While the present invention has been described in conjunction with a few preferred embodiments thereof it is to be understood that various changes and modifications may be resorted to without departing from the spirit and scope of the invention. For example, the present invention is equally applicable to electrical-tomechanical transducer devices.
What is claimed is:
l. A mechanical-to-electrical transducer device comprising a transducer element for converting mechanical energy to electrical energy, formed of a vulcanized elastomer having mixed therewith 5 to 40 parts, based on the weight of the elastomer, of an electrically conductive material selected from the group consisting of channel black and furnace black and means for applying a DC biasing voltage across said transducer element.
2. A mechanical-to-electrical transducer device as claimed in claim 1, wherein said elastomer is selected from the group consisting of chloroprene rubbers, nitrile rubbers, isoprene rubbers, chlorosulfonated polyethylene elastomers and fluoro-elastomers including polar substituents in the side chains thereof.
3. A mechanical-to-electrical transducer device as claimed in claim 1, wherein said elastomer is selected from butadiene elastomers not including polar substituents in the side chains thereof.
4. A mechanical-to-electrical transducer device as claimed in claim 1, wherein said DC voltage across said transducer element has a value sufficient to establish an electric field whose strength ranges from 10 to l() X l() volts per centimeter of the thickness of the transducer element.
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|U.S. Classification||310/357, 310/329, 310/800, 310/319, 252/62.90R, 310/328, 310/326|
|International Classification||G01D5/14, G01D5/16, B06B1/06, H04R17/00, H04R17/08, H01L41/113, H01L41/193, G01H11/08, G01L1/16, G01L1/00, H01L41/18|
|Cooperative Classification||Y10S310/80, H01L41/193, H01L41/113, G01L1/005, H04R17/08, B06B1/0662|
|European Classification||H01L41/113, G01L1/00B, B06B1/06E6, H01L41/193|