US2731573A - Ultrasonic coupling means for piezoelectric crystals - Google Patents
Ultrasonic coupling means for piezoelectric crystals Download PDFInfo
- Publication number
- US2731573A US2731573A US325602A US32560252A US2731573A US 2731573 A US2731573 A US 2731573A US 325602 A US325602 A US 325602A US 32560252 A US32560252 A US 32560252A US 2731573 A US2731573 A US 2731573A
- Authority
- US
- United States
- Prior art keywords
- crystal
- coupling means
- bond
- acoustical
- piezoelectric crystals
- 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
- 239000013078 crystal Substances 0.000 title description 22
- 230000008878 coupling Effects 0.000 title description 5
- 238000010168 coupling process Methods 0.000 title description 5
- 238000005859 coupling reaction Methods 0.000 title description 5
- 239000000463 material Substances 0.000 claims description 17
- 239000000126 substance Substances 0.000 description 17
- 238000002844 melting Methods 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 4
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 4
- 150000001491 aromatic compounds Chemical class 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 229960000969 phenyl salicylate Drugs 0.000 description 2
- 238000004781 supercooling Methods 0.000 description 2
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 2
- 238000006664 bond formation reaction Methods 0.000 description 1
- 239000007767 bonding agent Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- PSBAIJVSCTZDDB-UHFFFAOYSA-N phenyl acetylsalicylate Chemical compound CC(=O)OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 PSBAIJVSCTZDDB-UHFFFAOYSA-N 0.000 description 1
- 229950009058 phenyl acetylsalicylate Drugs 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B06—GENERATING OR TRANSMITTING MECHANICAL VIBRATIONS IN GENERAL
- B06B—METHODS OR APPARATUS FOR GENERATING OR TRANSMITTING MECHANICAL VIBRATIONS OF INFRASONIC, SONIC, OR ULTRASONIC FREQUENCY, e.g. FOR PERFORMING MECHANICAL WORK IN GENERAL
- B06B1/00—Methods or apparatus for generating mechanical vibrations of infrasonic, sonic, or ultrasonic frequency
- B06B1/02—Methods or apparatus for generating mechanical vibrations of infrasonic, sonic, or ultrasonic frequency making use of electrical energy
- B06B1/06—Methods or apparatus for generating mechanical vibrations of infrasonic, sonic, or ultrasonic frequency making use of electrical energy operating with piezoelectric effect or with electrostriction
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/01—Manufacture or treatment
- H10N30/07—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base
- H10N30/072—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base by laminating or bonding of piezoelectric or electrostrictive bodies
- H10N30/073—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base by laminating or bonding of piezoelectric or electrostrictive bodies by fusion of metals or by adhesives
Definitions
- This invention relates to ultrasonic coupling means for piezoelectric crystals as used, for example, in radar delay lines.
- phenyl salicylate In addition to the materials above mentioned, it has been proposed to use phenyl salicylate, acetyl phenyl salicylate and triphenylmethane as bonding agents for piezoelectric crystals.
- the chief defects of these substances lies in the low melting point of the phenyl salicylate, the lack of chemical stability in both salicylates, and the lack of physical stability in the triphenylmethane, the bond being weak, or becoming so, with time.
- the objects of the invention are included in the provision of a bond which has strong physical adherence to the surface of piezoelectric crystals and the supporting base throughout the temperature range of use; which has a satisfactory chemical stability through the heat range of use; which possesses a sharp melting point above the maximum temperature of use but sufiiciently low to permit easy application; which exhibits the phenomenon known as super-cooling to permit easy application; which has an impedance sufiiciently high to provide a close acoustical match to the crystal; which is capable of providing an acoustical band-width of adequate dimensions; which is capable of withstanding vibration at an amplitude and frequency yielding 10 G stress per vibration for a total of at least ten million vibrations without deterioration; and which is electrically non-conducting.
- the piezoelectric crystal may take the form of the plate 5.
- the bond or coupling means for obtaining an adequate physical integration with the supporting acoustical transmission material 6, 7 is indicated by numerals 8, 9.
- the bond substances are preferably one of the aromatic compounds benzil (CsHsCOCOCsI-Is) or paramethoxybiphenyl (CsHCsH4OCH3), these chemicals meeting satisfactorily the necessary requirements for bonds subjected to ultrasonic vibrations.
- Both of these subice stances have melting points between 90 C. and 100 C. so that temperatures up to may be reached in the crystal unit without harm to the bond.
- Both chemicals are physically and chemically stable and the chemical stability is not destroyed by short exposures to temperatures as high as 130 C.
- Both of these chemicals develop an acoustical band-width which measures between one-eighth and one-half of the center frequency.
- Both chemicals are electrically non-conducting. Both chemicals effect a strong bond which is permanent and which, when subjected to vibration at a frequency and amplitude to give 10 G stress, is maintained for at least ten million total vibrations, where G is the gravitational constant.
- the adjoining crystal and base surfaces should be flat and preferably roughened as by lapping with size 600 grit. These surfaces may be plated if desired. After cleaning the surfaces, they are heated in air to a point somewhat above 100 C., and a small amount of the chemical placed on one of the surfaces to be united. The surfaces then are joined, subjected to a small pressure as for example, ten pounds, and allowed to cool to room temperature.
- the bond junction may be easily made, particularly since the melting points of the chemicals are below 100 C. and no special ambient gas conditions are required. Also, maintenance of the acoustical bond up to 85 is entirely adequate, this being five degrees below the lowest melting point of for para-methoxybiphenyl. In certain respects, para-methoxybiphenyl is preferred since it has good super-cooling properties making bond formation relatively easy. Also this compound has better mechanical strength and band width.
- An additional advantage of both chemicals lies in their non-conductance of electricity so that the electrodes are not shorted and the bonding material may thus be used in excess, if desired. Also, the bond, as described, readily transmits either compressional or transverse vibrations, and has noteworthy life in use.
- a coupled piezo-electric unit for high frequency vibrations comprising a piezoelectric crystal, an acoustical transmitting material, and a bond connecting said crystal and material selected from the group consisting of paramethoxybiphenyl and benzil.
- a coupled piezo-electric unit for high frequency vibrations comprising a piezoelectric crystal, an acoustical transmitting material, and a bond connecting said crystal and material consisting of para-methoxybiphenyl.
- a coupled piezo-electric unit for high frequency vibrations comprising a piezoelectric crystal, an acoustical transmitting material, and a bond connecting said crystal and material consisting of benzil.
- a coupled piezo-electric unit for high frequency vibration comprising a piezoelectric crystal, an acoustical transmitting material, and a permanent bond connecting said crystal and material consisting of an aromatic compound having a melting point between 90 C. and C., a chemical stability not destroyed by short exposures to temperatures in excess of 100 C. and not over C., an acoustical band width measuring between one-eighth and one-half of the center frequency, and insulating resistance to flow of electric current.
- a coupled piezo-electric unit for high frequency vibrations comprising a piezoelectric crystal, an acoustical transmitting material, and a permanent bond connecting said crystal and material consisting of a fused mass of an 7.
- the coupled piezo-electric unit for high frequency aromatic compound having a melting point between 90 vibrations as defined in claim 3 with said benzil being in C. and 100 C., a chemical stability not destroyed by the form of afused mass.
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- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
S RCHJ RQUM Jan- 17, J. R, ET AL ULTRASONIC COUPLING MEANS FOR PIEZOELECTRIC CRYSTALS Filed Oct. 17, 1952 zmwcnfom J RICHARD HA NSF/V GERHARD SPREWGL lNG' United States Patent ULTRASONIC COUPLING MEANS FOR PIEZO- ELECTRIC CRYSTALS J. Richard Hansen, Pittsburgh, and Gerhard Sprengling, Verona, Pa., assignors to the United States of America as represented by the Secretary of the Navy Application October 17, 1952, Serial No. 325,602
7 Claims. (Cl. 310-848) This invention relates to ultrasonic coupling means for piezoelectric crystals as used, for example, in radar delay lines.
Where it is desired to couple a piezoelectric crystal to a solid support for transmission of high frequency or, more particularly, ultrasonic vibrations, the nature of the bonding material becomes of considerable importance. Many commonly used bonds are found to be unsatisfactory for this type of transmission. In the case of metals employed as solders, considerable difliculty is involved in finding a metal having the proper purity and flow characteristics, and in devising a technique of application suitable for the high temperatures and inert or reducing atmospheres required. In the case of plastics a lack of match in acoustical impedances is the outstanding difiiculty.
In addition to the materials above mentioned, it has been proposed to use phenyl salicylate, acetyl phenyl salicylate and triphenylmethane as bonding agents for piezoelectric crystals. The chief defects of these substances lies in the low melting point of the phenyl salicylate, the lack of chemical stability in both salicylates, and the lack of physical stability in the triphenylmethane, the bond being weak, or becoming so, with time.
The bonds as hereinafter described overcome satisfactorily the difficulties of prior art bonds for use with ultrasonic vibrations.
The objects of the invention are included in the provision of a bond which has strong physical adherence to the surface of piezoelectric crystals and the supporting base throughout the temperature range of use; which has a satisfactory chemical stability through the heat range of use; which possesses a sharp melting point above the maximum temperature of use but sufiiciently low to permit easy application; which exhibits the phenomenon known as super-cooling to permit easy application; which has an impedance sufiiciently high to provide a close acoustical match to the crystal; which is capable of providing an acoustical band-width of adequate dimensions; which is capable of withstanding vibration at an amplitude and frequency yielding 10 G stress per vibration for a total of at least ten million vibrations without deterioration; and which is electrically non-conducting.
Other objects and features will become apparent on consideration of the following description taken in conjunction with the single figure of drawing disclosing the relationship of crystal to the base substance.
As appears from the drawing, the piezoelectric crystal may take the form of the plate 5. The bond or coupling means for obtaining an adequate physical integration with the supporting acoustical transmission material 6, 7 is indicated by numerals 8, 9.
The bond substances are preferably one of the aromatic compounds benzil (CsHsCOCOCsI-Is) or paramethoxybiphenyl (CsHCsH4OCH3), these chemicals meeting satisfactorily the necessary requirements for bonds subjected to ultrasonic vibrations. Both of these subice stances have melting points between 90 C. and 100 C. so that temperatures up to may be reached in the crystal unit without harm to the bond. Both chemicals are physically and chemically stable and the chemical stability is not destroyed by short exposures to temperatures as high as 130 C. Both of these chemicals develop an acoustical band-width which measures between one-eighth and one-half of the center frequency. Both chemicals are electrically non-conducting. Both chemicals effect a strong bond which is permanent and which, when subjected to vibration at a frequency and amplitude to give 10 G stress, is maintained for at least ten million total vibrations, where G is the gravitational constant.
In applying this substance to the base material, the adjoining crystal and base surfaces should be flat and preferably roughened as by lapping with size 600 grit. These surfaces may be plated if desired. After cleaning the surfaces, they are heated in air to a point somewhat above 100 C., and a small amount of the chemical placed on one of the surfaces to be united. The surfaces then are joined, subjected to a small pressure as for example, ten pounds, and allowed to cool to room temperature.
It is apparent from the above description that the bond junction may be easily made, particularly since the melting points of the chemicals are below 100 C. and no special ambient gas conditions are required. Also, maintenance of the acoustical bond up to 85 is entirely adequate, this being five degrees below the lowest melting point of for para-methoxybiphenyl. In certain respects, para-methoxybiphenyl is preferred since it has good super-cooling properties making bond formation relatively easy. Also this compound has better mechanical strength and band width. An additional advantage of both chemicals lies in their non-conductance of electricity so that the electrodes are not shorted and the bonding material may thus be used in excess, if desired. Also, the bond, as described, readily transmits either compressional or transverse vibrations, and has noteworthy life in use.
Variations may, of course, be made in the precise disclosure as hereinabove set forth, and hence no limitation is implied other than may be required by the following claims.
What is claimed is:
1. A coupled piezo-electric unit for high frequency vibrations comprising a piezoelectric crystal, an acoustical transmitting material, and a bond connecting said crystal and material selected from the group consisting of paramethoxybiphenyl and benzil.
2. A coupled piezo-electric unit for high frequency vibrations comprising a piezoelectric crystal, an acoustical transmitting material, and a bond connecting said crystal and material consisting of para-methoxybiphenyl.
3. A coupled piezo-electric unit for high frequency vibrations comprising a piezoelectric crystal, an acoustical transmitting material, and a bond connecting said crystal and material consisting of benzil.
4. A coupled piezo-electric unit for high frequency vibration comprising a piezoelectric crystal, an acoustical transmitting material, and a permanent bond connecting said crystal and material consisting of an aromatic compound having a melting point between 90 C. and C., a chemical stability not destroyed by short exposures to temperatures in excess of 100 C. and not over C., an acoustical band width measuring between one-eighth and one-half of the center frequency, and insulating resistance to flow of electric current.
5. A coupled piezo-electric unit for high frequency vibrations comprising a piezoelectric crystal, an acoustical transmitting material, and a permanent bond connecting said crystal and material consisting of a fused mass of an 7. The coupled piezo-electric unit for high frequency aromatic compound having a melting point between 90 vibrations as defined in claim 3 with said benzil being in C. and 100 C., a chemical stability not destroyed by the form of afused mass.
short exposures to temperatures in excess of 100 C. and
not over 130 C., an acoustical band width measuring 5 References Cited inthe file of this patent between one-eighth and one-half of the center frequency, UNITED STATES PATENTS and Insulating reslstance to flow of electric current. 2,420,864 Chflowsky y 20, 1947 6. The coupled piezo-electric unit for high frequency vibrations as defined in claim 2 with said para-methoxybiphenyl being in the form of a fused mass. 10
Claims (1)
1. A COUPLED PIEZO-ELECTRIC UNIT FOR HIGH FREQUENCY VIBRATIONS COMPRISING A PIEZOELECTRIC CRYSTAL, AN ACOUSTICAL TRANSMITTING MATERIAL, AND A BOND CONNECTING SAID CRYSTAL AND MATERIAL SELECTED FROM THE GROUP CONSISTING OF PARAMETHOXYBIPHENYL AND BENZIL.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US325602A US2731573A (en) | 1952-10-17 | 1952-10-17 | Ultrasonic coupling means for piezoelectric crystals |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US325602A US2731573A (en) | 1952-10-17 | 1952-10-17 | Ultrasonic coupling means for piezoelectric crystals |
Publications (1)
Publication Number | Publication Date |
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US2731573A true US2731573A (en) | 1956-01-17 |
Family
ID=23268571
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US325602A Expired - Lifetime US2731573A (en) | 1952-10-17 | 1952-10-17 | Ultrasonic coupling means for piezoelectric crystals |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3042550A (en) * | 1958-05-23 | 1962-07-03 | Corning Glass Works | Solid delay line improvements |
US3350582A (en) * | 1965-01-13 | 1967-10-31 | Union Special Machine Co | Vibratory apparatus |
US3378705A (en) * | 1966-01-26 | 1968-04-16 | Budd Co | Ultrasonic transducers and method of manufacture thereof |
US3480492A (en) * | 1967-02-20 | 1969-11-25 | Branson Instr | Method of bonding using exothermic adhesive activated by ultrasonic energy |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2420864A (en) * | 1943-04-17 | 1947-05-20 | Chilowsky Constantin | Piezoelectric plastic material and method of making same |
-
1952
- 1952-10-17 US US325602A patent/US2731573A/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2420864A (en) * | 1943-04-17 | 1947-05-20 | Chilowsky Constantin | Piezoelectric plastic material and method of making same |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3042550A (en) * | 1958-05-23 | 1962-07-03 | Corning Glass Works | Solid delay line improvements |
US3350582A (en) * | 1965-01-13 | 1967-10-31 | Union Special Machine Co | Vibratory apparatus |
US3378705A (en) * | 1966-01-26 | 1968-04-16 | Budd Co | Ultrasonic transducers and method of manufacture thereof |
US3480492A (en) * | 1967-02-20 | 1969-11-25 | Branson Instr | Method of bonding using exothermic adhesive activated by ultrasonic energy |
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