ULTRASONIC TRANSDUCER USING AEROGEL AS FILLER MATERIAL

Abstract

Disclosed is an ultrasonic transducer and a manufacturing method thereof. The transducer comprises a piezoelectric composite array having an array of rigid posts made of a piezoelectric material, with kerf spaces between the posts filled with a low density aerogel material.

Claims

1. An ultrasonic transducer comprising: a layer of ultrasonic composite having an emitting face and a non-emitting face, the layer of ultrasonic composite further comprising: an array of posts made of a piezoelectric material, each of the posts having two endings, one ending being a post connection surface and the other ending partially forming the emitting face, and, each of the posts being surrounded at least partially by neighboring posts separated by kerf spaces; and, a filler material filling the kerf spaces between the posts, wherein the filler material is an aerogel material; a layer of connection circuit having a first face with an array of conductive contacts, each conductive contact making electrical contact with a corresponding post connection surface; and a backing layer attached to a second face of the layer of connection circuit, the backing layer substantially preventing acoustic emission from the non-emitting face.

2. The transducer of claim 1 wherein each of the posts has a post height and a post width, and the kerf spaces have a kerf spacing.

3. The transducer of claim 2 wherein the post height is between 300 and 1000 microns, the post width is between 30 and 400 microns and the kerf spacing is between 15 and 250 microns.

4. The transducer of claim 1 wherein the aerogel material is a silica aerogel.

5. The transducer of claim 1 wherein the aerogel material is a carbon aerogel.

6. The transducer of claim 1 wherein the aerogel material is a metal oxide aerogel.

7. The transducer of claim 1 wherein the aerogel material is a metal aerogel.

8. The transducer of claim 1 wherein the aerogel material is a nanotube aerogel.

9. The transducer of claim 1 wherein the aerogel material is a metal chalcogenide aerogel.

10. The transducer of claim 1 wherein the aerogel material is a biofoam material.

11. The transducer of claim 1 wherein the aerogel material has a density between 0.001 and 0.35 g/cm.sup.3.

12. The transducer of claim 1 wherein the aerogel material has a degradation temperature greater than 1000? C.

13. A method of manufacturing an ultrasonic transducer comprising the steps of: providing a layer of ultrasonic composite having an emitting face and a non-emitting face, which further comprises the steps of, forming an upper block section of a piezoelectric ceramic block to form an array of posts, leaving an unworked lower block section, wherein neighboring posts are separated by kerf spaces, the posts having top post surfaces and lower connections to the lower block section; filling the kerf spaces with a filler material comprising an aerogel precursor material, the filler material having a top filler surface after the filling; drying the filler material to form an aerogel filler material; removing the lower block section, thereby exposing bottom post surfaces and a bottom filler surface; providing a layer of connection circuit having a first face with an array of conductive contacts, each conductive contact making electrical contact with a corresponding post connection surface; and, providing a backing layer attached to a second face of the layer of connection circuit, the backing layer substantially preventing acoustic emission from the non-emitting face.

14. The method of claim 13 comprising the additional steps of: applying a top metal to cover the top post surfaces and the top filler surface with a top metallization; applying a bottom metal to cover the bottom post surfaces and the bottom filler surface with a bottom metallization; polarizing the upper block section by applying a voltage between the top metallization and the bottom metallization; patterning the top metallization to remove the top metal from the top filler surface; and, patterning the bottom metallization to remove the bottom metal from the bottom filler surface.

15. The method of claim 13 comprising the additional step of attaching a matching layer to the bottom post surfaces and the bottom filler surface, the matching layer configured to maximize an acoustic transmission from the bottom post surfaces into a test object.

16. The method of claim 13 further comprising a step of allowing the aerogel precursor material to set after the step of filling and before the step of drying.

17. The method of claim 13 further comprising a step of applying chemicals to cause the aerogel precursor material to set after the step of filling and before the step of drying.

18. The method of claim 13 wherein the step of drying the filler material comprises evaporative drying.

19. The method of claim 13 wherein the step of drying the filler material comprises supercritical drying.

20. The method of claim 13 wherein the step of drying the filler material comprises freeze drying.

21. The method of claim 13 wherein the filler material is a liquid.

22. The method of claim 13 wherein the filler material is a gel.

23. The method of claim 13 wherein the aerogel filler material comprises a dendritic structure.

24. The method of claim 23 wherein the posts are supported by the dendritic structure after completion of the step of removing the lower block section.

25. An ultrasonic composite array comprising: an array of posts made of a piezoelectric material, each of the posts being surrounded at least partially by neighboring posts separated by kerf spaces; and, a filler material filling the kerf spaces between the posts, wherein the filler material is an aerogel material.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0021] FIG. 1A is a schematic diagram of a piezoelectric ceramic which has been diced.

[0022] FIG. 1B is a schematic diagram of a piezoelectric ceramic in which the kerf spaces have been filled by a filler material.

[0023] FIG. 1C is a schematic diagram of a ceramic composite in which the base of the piezoelectric ceramic has been ground away.

[0024] FIG. 1D shows the components of an ultrasonic transducer.

[0025] FIG. 2 is a phase of diagram illustrating different methods of drying.

[0026] FIG. 3 is a micrograph showing the dendritic structure of a graphitic aerogel.

[0027] FIG. 4A is a flow diagram of a manufacturing method in existing practice.

[0028] FIG. 4B is a flow diagram of a manufacturing method according to the present disclosure.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENT

[0029] FIGS. 1A, 1B and 1C schematically illustrate an existing typical transducer manufacturing process. FIG. 1A shows a solid piezoelectric ceramic block 2, comprising a diced upper block section 2a and a lower block section 2b, which is not diced. Upper block section 2a is diced into a grid, thereby forming an array of posts having top post surfaces 3a, the posts being mechanically supported by the material of lower block section 2b at lower connections 7. Note that there may be thousands of posts, and in current practice typical dimensions of each individual post may range from 30-400 microns wide by 300 to 1000 microns tall, with kerf spacing between these individual posts ranging from 15 to 250 microns.

[0030] In FIG. 1B, the kerf spaces of the grid have been filled by a filler material 4 having a top filler surface 5a. The purpose of filler material 4 is to mechanically support and acoustically isolate each post. In existing practice, filler material 4 is a rigid epoxy material which is slow cured to reduce contraction of the epoxy, which could damage the posts by deforming or fracturing them. In FIG. 1C, the base of piezoelectric ceramic 2 is ground away, exposing bottom post surfaces 3b (not shown) and a bottom filler surface 5b (not shown). The remaining structure after grinding is a piezoelectric composite array 8 which comprises an array of piezoelectric posts supported by the epoxy matrix.

[0031] FIG. 1D is a schematic illustration of an ultrasonic transducer 16. Ultrasonic transducer 16 comprises piezoelectric composite array 8, a connection circuit 10, a backing layer 12 and a matching layer 14. Connection circuit 10, connected to the non-emitting side of piezoelectric composite array 8, comprises a circuit board or flexible ribbon having a metallization pattern configured to make electrical contacts with top post surfaces 3a, and to interface the electrical contacts to a multi-conductor cable (not shown). Backing layer 12 is attached to connection circuit 10, and comprises a material configured to damp the ultrasonic vibrations thereby preventing emission from that side of piezoelectric composite array 8. Matching layer 14 is configured to match the acoustic impedance of piezoelectric composite array 8, thereby maximizing transmission and minimizing reflections of acoustic energy from the emitting side of piezoelectric composite array 8.

[0032] In a piezoelectric composite array according to the present disclosure, the rigid epoxy filler material of existing practice is replaced by an aerogel material. An aerogel is a synthetic porous ultralight material (density less than 10 mg/cm.sup.3) which is derived from a gel in which the liquid component of the gel has been replaced with a gas. Aerogels created from silica, carbon and metal oxide are known in the art.

[0033] Silica aerogels are typically synthesized using a sol-gel process or homogenous solution, in which a colloidal suspension of solid particles (sol) is hydrolyzed to form a gel having a jellylike consistency. The gel has a liquid component which contains a network of solid bridge material linking the colloidal particles. Finally, during the drying process of the aerogel, the liquid surrounding the network is carefully removed and replaced with air, while keeping the aerogel intact. The resulting aerogel filler material may comprise greater than 96% air. However the remaining micro-dendritic structure within the filler provides stabilization of the micron-sized posts of piezoelectric ceramic.

[0034] An aerogel may be dried either using evaporative (sub-critical) drying or using the technology of supercritical drying. Supercritical drying is used in cases where evaporative or subcritical drying would cause the aerogel structure to collapse on itself due to internal stresses caused by surface tension of the liquid-gas interface. Supercritical drying allows creation of lower density (higher porosity) aerogels, but usually requires high pressure and multiple solvents. Subcritical or evaporative drying is typically used for higher compressive strength aerogels or aerogels that need enhanced hydrophobicity. Subcritical or evaporative drying requires multiple solvents and specialized preparations and may create slightly higher density aerogels than supercritical drying. However, aerogels having porosity as high as 95% may be produced.

[0035] Supercritical drying, also known as critical point drying, may be used to achieve aerogels with high porosity and low density. In supercritical drying, the liquid in the aerogel is replaced by a carrier fluid which is forced into a supercritical fluid state by increasing the temperature and pressure. By subsequently dropping the pressure, the carrier fluid is instantly gasified and thereby removed from the aerogel.

[0036] FIG. 2 is a phase diagram illustrating various drying methods. In FIG. 2, a line 22 represents the transition between solid and gas, a line 24 represents the transition between solid and liquid, and a line 26 represents the transition between liquid and gas. Conventional evaporative drying is represented by an arrow 32, which crosses the liquid/gas boundary. However, the surface tension forces in evaporative drying may cause damage to the micro-dendritic aerogel structures. An arrow 34 represents freeze drying, which may also damage delicate micro-structures at the solid/gas boundary. Supercritical drying is represented by an arrow 36. In this case, the drying occurs at high temperature and pressure such that the material passes through a supercritical region delineated by a critical point 28, which is the condition of temperature and pressure at which the liquid and gas densities are equal. Thus the critical point drying process avoids phase transitions which may result in damaging forces. Since the critical point of water occurs at inconveniently high temperature and pressure (347? C. and 3,212 psi), the water content may be replaced by carbon dioxide (critical point at 31? C. and 1,072 psi) as a carrier fluid for the purpose of supercritical drying.

[0037] FIG. 3 is a micrograph of the dendritic structure of an exemplary aerogel filler material after the drying process has been completed. The example shown in FIG. 3 is of a carbon-based aerogel made from carbon microtubes and having a density of less than 0.00018 g/cm.sup.3.

[0038] FIG. 4A is a flowchart of a method in existing practice of manufacturing a piezoelectric composite transducer. In step 42, piezoelectric ceramic block 2 is scribed to form diced upper block 2a as illustrated in FIG. 1A, thereby forming a multiplicity of ceramic posts. In step 44, the kerf spaces between the posts are filled with epoxy filler material 4 as illustrated in FIG. 1B, and in step 46 the epoxy is allowed to set. In step 48 the base material of the ceramic is ground away as illustrated in FIG. 1C. In step 50, the top and bottom surfaces of the composite are metallized to allow polarization of the piezoelectric material in step 52. Polarization step 52, depending on the type of piezoelectric material, may comprise application of suitable voltage between the top and bottom surfaces of the composite. In step 54, the metallization is patterned by etching or other means, so that each individual ceramic post is metallized, and in step 56 signal wires and ground wires are attached to each ceramic post.

[0039] FIG. 4B is a flowchart of a method according to the present disclosure of manufacturing a piezoelectric composite transducer having aerogel filler material. Note that the manufacturing steps of FIG. 4B may be performed using any piezoelectric material, including, but not limited to, lead titanate, barium titanate and lithium niobate. Step 42, scribing the piezoelectric material, is the same as in existing practice. In step 62, filler material 4 comprising an aerogel precursor, such as a colloidal mixture or sol-gel of an aerogel material having the desired final properties, is prepared. In step 64, the kerf spaces between the posts in the composite structure are filled with the aerogel precursor. The precursor is designed to have low enough viscosity to allow the precursor to flow into the kerf spaces. After allowing or causing the precursor to set or gel in step 66, the mixture is dried in step 68, either by sub-critical or by supercritical drying, depending on the aerogel formulation. After drying, the resultant aerogel dendritic structure is sufficiently strong to support micron-sized posts and therefore the remaining manufacturing steps may be the same as in existing practice, namely grinding step 48, metallizing step 50, polarizing step 52, patterning step 54 and attaching signal wires step 56.

[0040] Aerogels which may be suitable for the above manufacturing process include, but are not limited to the following: [0041] a. Silica aerogels, such as those available from Aerogel Technologies Inc. [0042] b. Carbon aerogels, such as Aerographite or Aerographene. See, for example, Mecklenburg et al, Aerographite: Ultra Lightweight, Flexible Nanowall, Carbon Microtube Material with Outstanding Mechanical Performance, Advanced Materials. 24, 3486-3490, (2012) [0043] c. Metal oxide aerogels, including aluminum oxide, nickel-aluminum oxide, iron oxide, chromium oxide and zirconium oxide. [0044] d. Metal Aerogels. [0045] e. Nanotube Aerogels. See, for example, B. Zheng, Y. Li, J. Liu, CVD synthesis and purification of single-walled carbon nanotubes on aerogel-supported catalyst, Applied Physics A, 74, 345-348 (2002). [0046] f. Metal Chalcogenide Aerogels. See, for example, Jaya L. Mohanan et al, Porous Metal Chalcogenide Aerogels, Science 307, 397-400 (2005). [0047] g. Biofoam. See, for example, U.S. Pat. Nos. 5,382,285 and 5,360,828

TABLE-US-00001 TABLE 1 Material EPO-TEK 301 Epoxy Silica Aerogel Density ~1.2 g/cm.sup.3 .sup..001 to 0.35 g/cm.sup.3 Sound Speed ~2.6 mm/?sec <=0.07 to 1.3 mm/?sec Dielectric Constant ~4.0 1.008 to 2.3 Continuous Operating ~55 to 200 C. Up to 1000 C. Temperature Degradation Temp 430? C. >1200? C.

[0048] Table 1 compares the properties of a commonly used filler epoxy in current practice (Epo-Tek 301) with the range of properties exhibited by silica aerogels. Of particular note is the low density of the aerogel, the low sound velocity and the high continuous operating temperature and degradation temperature. The aerogel properties shown in Table 1 are particularly desirable for use as a filler material.

[0049] Although the present invention has been described in relation to particular embodiments thereof, it can be appreciated that various designs can be conceived based on the teachings of the present disclosure, and all are within the scope of the present disclosure.