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Title:
SOFT ACTUATORS AND ARTIFICIAL MUSCLES
Document Type and Number:
WIPO Patent Application WO/1997/026039
Kind Code:
A1
Abstract:
A chemical (coating and reduction)/mechanical/electrical treatment of ion-exchange materials (preferably ion-exchange membranes) to convert them to artificial muscles. The figure is a perspective view of an actuator of the invention showing the treated membrane actuator (A) with electrodes (25 and 26) placed at one end of the membrane, the electrodes being further attached to a power source (35). Artificial muscles created by the inventive method are capable of undergoing electrically-controllable large deformations resembling the behavior of biological muscles. A typical flap muscle of 0.2 - 0.4 mm thickness, 2 - 5 mm width and 20 mm length manufactured by the inventive process can achieve a completely reversible maximum deflection of 12 - 15 mm under a maximum voltage of 2.0 - 2.5 volts.

Inventors:
SHAHINPOOR MOHSEN (US)
MOJARRAD MEHRAN (US)
Application Number:
PCT/US1996/017870
Publication Date:
July 24, 1997
Filing Date:
November 06, 1996
Export Citation:
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Assignee:
UNIV NEW MEXICO (US)
SHAHINPOOR MOHSEN (US)
MOJARRAD MEHRAN (US)
International Classes:
A61F2/08; B25J9/10; B25J15/02; B25J18/06; B64C9/00; B64C13/50; B64C27/72; F03G7/00; A61F2/50; (IPC1-7): A61M25/09; A61F2/08; B05D3/02; B05D3/04; B05D3/10; B25J11/00; B25J15/00; B64C33/00; B64C33/02; B66C3/00; G05B15/02; G05B19/00; G05B19/04
Foreign References:
US4364803A1982-12-21
US5268082A1993-12-07
US4959132A1990-09-25
US4748737A1988-06-07
US4328086A1982-05-04
US4449599A1984-05-22
US4565487A1986-01-21
US4578045A1986-03-25
US4818353A1989-04-04
US5038821A1991-08-13
US5279559A1994-01-18
US5531664A1996-07-02
US5556700A1996-09-17
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Claims:
CLAIMS
1. What is claimed is: A method of preparing an actuator comprising the steps of: (a) rinsing an ionexchange material; (b) coating the ionexchange material with a substance which undergoes chemical reduction in the presence of a reducing agent; and (c) reducing the coating on the ionexchange material by exposing the ionexchange material to a reducing agent.
2. The method of claim 1 wherein the ionexchange material comprises a material selected from the group consisting of ionexchange membranes, ionomer membranes, ion exchange resins, gels, beads, powders, filaments, and fibers.
3. The method of claim 2 wherein the ionexchange material is an ionexchange membrane.
4. The method of claim 3 wherein the ionexchange material is a polymer ionexchange membrane.
5. The method of claim 4 wherein the ionexchange material is a perfluorinated sulfonic acid ionexchange polymer membrane.
6. The method of claim 1 wherein the rinsing step is performed in water.
7. The method of claim 1 wherein the ionexchange material has at least two surfaces and the rinsing step comprises roughening the surfaces of the ionexchange material.
8. The method of claim 7 wherein the roughening step is performed prior to rinsing in the rinsing step.
9. The method of claim 7 wherein the roughening step is performed by sandblasting.
10. The method of claim 9 wherein the roughening step is performed by sandblasting with fine glass bead sandblast.
11. The method of claim 1 wherein the rinsing step comprises cleaning the ionexchange material.
12. The method of claim 11 wherein the cleaning step is performed prior to rinsing in the rinsing step.
13. The method of claim 11 wherein the cleaning step is performed in an ultrasonic water bath cleaner.
14. The method of claim 11 wherein the cleaning step comprises heating the ion exchange material.
15. The method of claim 14 wherein the heating step is conducted in solution.
16. The method of claim 15 wherein the heating step is performed by boiling the ion exchange material in the solution.
17. The method of claim 14 wherein the heating step is conducted in an acidic solution.
18. The method of claim 17 wherein the heating step is conducted in a solution containing HCl.
19. The method of claim 1 wherein the ionexchange material has at least two surfaces and the rinsing step comprises the steps of: (a) roughening the surfaces of the ionexchange material; (b) cleaning the ionexchange material; (c) rinsing the ionexchange material in water; and (d) boiling the ionexchange material in an aqueous solution.
20. The method of claim 19 wherein the boiling step is conducted in an acidic solution.
21. The method of claim 20 wherein the boiling step is conducted in a solution containing HCl.
22. The method of claim 19 wherein the steps are performed in the order (a) through (d).
23. The method of claim 1 wherein the rinsing step comprises at least two steps of rinsing and boiling the ionexchange material in solution.
24. The method of claim 23 wherein the second rinsing and boiling step comprises rinsing and boiling the ionexchange material in water.
25. The method of claim 23 wherein the second rinsing and boiling step comprises boiling the ionexchange material for a sufficient time to completely swell the ionexchange material.
26. The method of claim 1 wherein the coating step comprises coating with at least one member selected from the group consisting of metals.
27. The method of claim 26 wherein the coating step comprises coating with at least one member selected from the group consisting of noble metals.
28. The method of claim 27 wherein the coating step comprises coating with platinum.
29. The method of claim 1 wherein the coating step is performed for a time sufficient to cover the ionexchange material with a coating of approximately 3.75 mg/cm2 of the coating substance.
30. The method of claim 1 wherein the coating step comprises the steps of: (a) immersing the ionexchange material; and (b) stirring.
31. The method of claim 30 wherein the immersing step comprises immersing the ion exchange material into a solution.
32. The method of claim 31 wherein the immersing step comprises immersing the ion exchange material into a solution containing a salt of a metal selected from the group consisting of noble metals, palladium, and nickel.
33. The method of claim 32 wherein the immersing step comprises immersing the ion exchange material into a solution containing a platinum salt.
34. The method of claim 33 wherein the immersing step comprises immersing the ion exchange material into a solution containing a platinumamine complex.
35. The method of claim 34 wherein the immersing step comprises immersing the ion exchange material into a solution containing Pt(NH3)4CI2.
36. The method of claim 1 wherein the reducing step comprises exposing the ion exchange material to NaBH4.
37. The method of claim 1 wherein the reducing step is conducted in solution.
38. The method of claim 37 wherein the reducing step is conducted in a solution comprising water.
39. The method of claim 37 wherein the reducing step is conducted in a solution comprising a reducing enhancer.
40. The method of claim 39 wherein the reducing step is conducted in a solution comprising NH4OH.
41. The method of claim 37 wherein the reducing step comprises continuously raising the temperature of the solution to a predetermined temperature.
42. The method of claim 1 wherein the reducing step is conducted at an elevated temperature.
43. The method of claim 1 wherein the reducing step is conducted in solution in a water bath at an elevated temperature and comprises the step of simultaneously stirring the solution in the water bath.
44. The method of claim 1 wherein the reducing step comprises the steps of simultaneously stirring the solution while adding the reducing agent.
45. The method of claim 44 wherein the stirring step is performed at low speed.
46. The method of claim 1 wherein the reducing step comprises the steps of simultaneously: (a) continuously raising the temperature of the solution to a predetermined temperature; and (b) adding supplementary reducing agent at intervals.
47. The method of claim 46 further comprising the steps of maintaining the temperature at the predetermined temperature and simultaneously adding a final amount of supplementary reducing agent when the predetermined temperature is reached.
48. The method of claim 47 further comprising the step of continuously stirring the solution after the step of adding the final amount of supplementary reducing agent is performed.
49. The method of claim 48 further comprising the step of rinsing the ionexchange material and the step of storing the ionexchange material.
50. The method of claim 49 wherein the rinsing step is conducted in water.
51. The method of claim 49 wherein the storing step is conducted in solution.
52. The method of claim 49 wherein the storing step is conducted in an HCl solution.
53. The method of claim 1 wherein the reducing step comprises at least one reducing step comprising the steps of: (a) rinsing the ionexchange material; (b) immersing the ionexchange material in a solution containing a reducing agent; (c) rinsing the ionexchange material; and (d) storing the ionexchange material.
54. The method of claim 53 wherein the steps are performed in the order (a) through (d).
55. The method of claim 53 wherein immersing the ionexchange material comprises immersing in a solution containing a salt of a metal selected from the group consisting of noble metals, palladium, and nickel.
56. The method of claim 55 wherein immersing the ionexchange material comprises immersing in a solution containing a platinum salt.
57. The method of claim 56 wherein immersing the ionexchange material comprises immersing in a solution containing a platinumamine complex.
58. The method of claim 57 wherein immersing the ionexchange material comprises immersing in a solution containing Pt(NH3)4CI2.
59. The method of claim 53 wherein immersing the ionexchange material comprises immersing in a solution containing a reducing enhancer.
60. The method of claim 59 wherein immersing the ionexchange material comprises immersing in a solution containing NH4OH.
61. The method of claim 53 wherein immersing the ionexchange material comprises immersing in a solution containing H2NOH«HCI.
62. The method of claim 53 wherein immersing the ionexchange material comprises immersing in a solution containing H2NNH2»H20.
63. The method of claim 53 wherein immersing the ionexchange material comprises immersing in a solution containing water.
64. The method of claim 53 wherein the reducing step comprises the steps of simultaneously: (a) continuously raising a temperature of the solution to a predetermined temperature; and (b) adding supplementary reducing agent at regular intervals for a time sufficient to substantially complete reduction.
65. The method of claim 64 additionally comprising the step of testing the solution for completion of reduction.
66. The method of claim 65 wherein the testing step comprises monitoring a color change produced by reduction.
67. The method of claim 53 wherein rinsing step (c) comprises at least two rinsing steps.
68. The method of claim 67 wherein the first rinsing step of the at least two rinsing steps comprises rinsing in water.
69. The method of claim 67 wherein the first rinsing step of the at least two rinsing steps comprises rinsing in an acidic solution.
70. The method of claim 69 wherein the first rinsing step of the at least two rinsing steps comprises rinsing in an HCl solution.
71. The method of claim 67 wherein the first rinsing step of the at least two rinsing steps comprises rinsing in water followed by rinsing in an acidic solution.
72. The method of claim 71 wherein the first rinsing step of the at least two rinsing steps comprises rinsing in water followed by rinsing in an HCl solution.
73. The method of claim 67 wherein the first rinsing step of the at least two rinsing steps is performed for a time sufficient to exchange cations in the ionexchange material for H+ cations outside the ionexchange material.
74. The method of claim 67 wherein the second rinsing step of the at least two rinsing steps comprises rinsing in water.
75. The method of claim 67 wherein the second rinsing step of the at least two rinsing steps comprises rinsing in a basic solution.
76. The method of claim 75 wherein the second rinsing step of the at least two rinsing steps comprises rinsing in an NaOH solution.
77. The method of claim 67 wherein the second rinsing step of the at least two rinsing steps comprises rinsing in water followed by rinsing in a basic solution.
78. The method of claim 77 wherein the second rinsing step of the at least two rinsing steps comprises rinsing in water followed by rinsing in an NaOH solution.
79. The method of claim 67 wherein the second rinsing step of the at least two rinsing steps is performed for a time sufficient to exchange cations in the ionexchange material.
80. The method of claim 79 wherein H* cations in the ionexchange material are exchanged for alkali metal cations outside the ionexchange material.
81. The method of claim 80 wherein H* cations in the ionexchange material are exchanged for Na* cations outside the ionexchange material.
82. The method of claim 67 further comprising the step of repeating a second of the at least one reducing steps and the rinsing step (c).
83. The method of claim 82 further comprising a final rinsing step after the repeating step.
84. The method of claim 83 wherein the final rinsing step is performed in water.
85. The method of claim 67 further comprising the step of cleaning the ionexchange material after the at least two rinsing steps.
86. The method of claim 85 wherein the cleaning step is conducted in an ultrasonic cleaner.
87. The method of claim 53 wherein the storing step (d) is performed in water.
88. A method of preparing an actuator comprising: (a) at least one cleaning step; (b) at least one step of rinsing an ionexchange material; (c) at least one step of coating the ionexchange material with a substance which undergoes chemical reduction in the presence of a reducing agent; (d) at least one step of reducing the coating on the ionexchange material by exposing the ionexchange material to a reducing agent; (e) testing the solution for the completion of reduction; and (0 at least one step of storing the treated ionexchange material.
89. The method of claim 88 wherein the ionexchange material comprises a material selected from the group consisting of ionexchange membranes, ionomer membranes, ion exchange resins, gels, beads, powders, filaments, and fibers.
90. The method of claim 89 wherein the ionexchange material is an ionexchange membrane.
91. The method of claim 90 wherein the ionexchange material is a polymer ion exchange membrane.
92. The method of claim 91 wherein the ionexchange material is a perfluorinated sulfonic acid ionexchange polymer membrane.
93. The method of claim 88 wherein the at least one rinsing step is performed in water.
94. The method of claim 88 wherein the at least one rinsing step is performed in solution.
95. The method of claim 94 wherein the at least one rinsing step is performed in an acidic solution.
96. The method of claim 95 wherein the at least one rinsing step is performed in an HCl solution.
97. The method of claim 94 wherein the at least one rinsing step is performed in a basic solution.
98. The method of claim 97 wherein the at least one rinsing step is performed in an NaOH solution.
99. The method of claim 94 wherein the at least one rinsing step comprises heating the ionexchange material.
100. The method of claim 99 wherein the heating step is performed by boiling the ion exchange material in the solution.
101. The method of claim 88 wherein at least two rinsing steps are performed before the coating step.
102. The method of claim 88 wherein the coating substance of the at least one coating step comprises at least one member selected from the group consisting of metals.
103. The method of claim 102 wherein the coating substance of the at least one coating step comprises at least one member selected from the group consisting of noble metals, palladium, and nickel.
104. The method of claim 103 wherein the coating substance of the at least one coating step comprises platinum.
105. The method of claim 88 wherein at least one of the at least one rinsing step is performed before each of the at least one reducing step.
106. The method of claim 88 wherein at least one of the at least one rinsing step is performed after each of the at least one reducing step.
107. The method of claim 88 wherein at least one of the at least one reducing step is performed in a presence of a reducing enhancer.
108. The method of claim 107 wherein at least one of the at least one reducing step is performed in a presence of NH4OH.
109. The method of claim 88 wherein the exposing step comprises exposing to a reducing agent comprising NaBH4.
110. The method of claim 88 wherein the exposing step comprises exposing to a reducing agent comprising H2NOHHCI.
111. The method of claim 88 wherein the exposing step comprises exposing to a reducing agent comprising H2NNH2«H20.
112. The method of claim 88 wherein the exposing step for a first of the at least one reducing step comprises exposing to NaBH4, and for a second of the at least one reducing step comprises exposing to at least one member selected from the group consisting of H2NOH«HCI and H2NNH2«H20.
113. The method of claim 88 wherein the at least one reducing step is conducted in solution and the at least one reducing step further comprises the steps of: (a) heating the reducing solution; (b) continuously stirring the ionexchange material in the coating solution at low speed; and (c) simultaneously raising the temperature of the solution while adding supplementary reducing agent.
114. The method of claim 88 wherein the testing step comprises the steps of: (a) mixing a test solution comprising a portion of the reducing solution; (b) boiling the test solution; and (c) detecting a color change in the testing solution during boiling.
115. The method of claim 114 wherein the portion of reducing solution is about 2 ml and the testing step comprises: (a) adding NaBH4 to the test solution during the boiling step; and (b) adding supplemental reducing agent to the reducing solution in which the ionexchange material is immersed if a coloration is detected in the test solution during boiling.
116. The method of claim 115 wherein the testing step comprises terminating the at least one reducing step if no coloration is detected in the test solution during the boiling step.
117. The method of claim 88 wherein the at least one storing step is conducted in solution.
118. The method of claim 117 wherein the solution comprises water.
119. The method of claim 117 wherein the solution is acidic.
120. The method of claim 119 wherein the solution comprises HCl.
121. A method of preparing an actuator from an ionexchange material comprising: (a) a step of roughening the ionexchange material; (b) a first step of cleaning the roughened ionexchange material; (c) a first step of rinsing the ionexchange material; (d) a first step of boiling the ionexchange material; (e) a second step of rinsing the ionexchange material; (f) a second step of boiling the ionexchange material wherein boiling is performed for a sufficient time to completely swell the ionexchange material; (g) a step of coating the ionexchange material with a substance comprising platinum; (h) a third step of rinsing the ionexchange material; (i) a first step of reducing the coating on the ionexchange material by immersing the coated ionexchange material in a solution comprising a reducing agent whereby the coating undergoes chemical reduction in the presence of the solution comprising the reducing agent; (j) simultaneously heating and stirring the ionexchange material in the reducing agent; (k) a fourth step of rinsing the ionexchange material; (I) a first step of storing the ionexchange material; (m) a fifth step of rinsing the ionexchange material; (n) a second step of reducing the coating on the ionexchange material by immersing the coated ionexchange material in a solution comprising a reducing agent whereby the coating undergoes chemical reduction in the presence of the solution comprising the reducing agent; (o) simultaneously heating and stirring the ionexchange material in the reducing agent; (p) at least one step of sequentially rinsing the ionexchange material; (q) a second step of cleaning the ionexchange material; and (r) a second step of storing the ionexchange material.
122. The method of claim 121 wherein the steps are performed in the order (a) through (r).
123. The method of claim 121 wherein the steps (n), (o), (p), and (q) are repeated and further comprising a final rinsing step prior to the second storing step.
124. An actuator produced by the method of claim 121 , comprising a treated ion exchange material capable of a completely reversible deflection and means operably connected to said ionexchange material for electrically driving the deflection of said ionexchange material.
125. An actuator for use in a gripper mechanism comprising: at least two actuators produced by the method of claim 1 , said at least two actuators being positioned opposite to each other and being capable of bending in equal and opposing directions, and each of said actuators having a first end; means for providing power to said actuators to drive the mechanical bending of said actuators in opposing directions; means, operably attached to said first end of each of said actuators, for conducting electrical impulses across said actuators; and wiring means, operably attached to said conducting means and to said means for providing power, for electrically connecting said actuators to said power source.
126. An actuator for providing threedimensional movement, comprising: three actuators produced by the method of claim 1 , comprising a hollow triangular tube having a longitudinal axis and a first end wherein each of said actuators of said tube comprises a face of said tube; means, operably attached to said first end of each of said actuators, for conducting a signal across each of said faces of said tube, thereby stimulating each face of said tube at a phase angle apart from each adjacent face to produce a motion around said longitudinal axis of said tube; and means for providing power to said signal conducting means; and means, attached to said signal conducting means, for operably connecting said tube to said power providing means.
127. The actuator of claim 126 wherein said signal comprises a low amplitude alternating signal.
128. An actuator for use as a wing flap, comprising: at least two actuators produced by the method of claim 1 sandwiched in series in a stack configuration, each of said actuators formed in a planar layer and capable of acting as a series resistor element and said stack having first and second ends, a top surface and a bottom surface; means, operably attached to said stack at said first end and said top and bottom surfaces, for conducting power across said stack; means for supplying power to said stack; and means for connecting said power supplying means to said power conducting means.
129. The actuator of claim 128 additionally comprising adhesive means between said at least two actuators.
130. The actuator of claim 129 wherein said adhesive means is conductive.
131. The actuator of claim 129 wherein said adhesive means is noncontmuously applied.
132. An actuator for use as a robotic swimming structure, comprising: at least two actuators produced by the method of claim 1 , formed in an ion exchange material having a first end, said ionexchange material comprising a plurality of polymer gel fibers imprinted with means for conducting power through said ionexchange material; means, operably attached to said ionexchange material at said first end, for conducting an alternating low voltage across said ionexchange material; means for providing power to said conducting means; means for modulating speed of bending of said ionexchange material varying the frequencies of the applied voltage; and means for operably connecting said conducting means to said power providing means.
133. The actuator of claim 129 further comprising means for varying the buoyancy of the swimming structure and a sealed housing, operably attached to said ionexchange material at said first end, said housing comprising means for generating signals and means for generating power.
134. The actuator of claim 130 wherein said signal generating means comprises an erasable programmable chip and said power generating means comprises a battery.
135. The actuator of claim 129 wherein said ionexchange material is elastic The actuator of claim 129 wherein said ionexchange material is rigid .
136. An actuator for use as a resonant flying machine, comprising: at least one ionexchange material actuator prepared by the method of claim 1 in the form of a planar layer having first and second ends, a top surface and a bottom surface; means for conducting power across said ionexchange material actuator, operably attached to said top and bottom surfaces of said ionexchange material and along a central axis of said ionexchange material equidistant from said first and second ends, whereby said ionexchange material actuator is capable of reversibly bending in a flapping motion upon receiving power; means for providing power to said conducting means; and means for connecting said conducting means to said power providing means.
137. An actuator for use as a guide wire in medical applications, comprising: at least one ionexchange material actuator prepared by the method of claim 1 and formed in a small strip; means for providing power to said strip; and means for connecting said strip to said power supply.
Description:
SOFT ACTUATORS AND ARTIFICIAL MUSCLES

CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit of the filing of Provisional Application Serial No. 60/013,617, entitled Method of Manufacturing and Applications of Electrically Controllable

Artificial Muscles from Polymeric Ion-Exchange Membranes, filed on January 18, 1996.

GOVERNMENT RIGHTS The Government has rights in this invention pursuant to Contract No. AE-4721-94 between the Department of Energy and the University of New Mexico and Contract No. DAAH04-93-0220 between the Department of Defense and the University of New Mexico.

BACKGROUND OF THE INVENTION Field of the Invention The present invention relates to a novel method of manufacturing actuators, e.g., artificial muscles, and novel applications of the actuators manufactured according to the novel method. More particularly, the invention relates to a novel chemical / mechanical / electrical treatment of membranes, e.g. ion-exchange membranes, to convert them to artificial muscles capable of undergoing electrically-controllable large deformations resembling the behavior of biological muscles. The invention further relates to a number of novel techniques for packaging and application of the said artificial muscles.

Background Art:

The creation of controllable actuators, or synthetic muscles, is known. Artificial muscles or actuators made from ion-exchange membranes are relatively new but also known.

U.S. Patent No. 4,522,698, to Maget, discloses a prime mover that uses pressure increases and decreases induced by converting molecules of electrochemically active material to ions, transporting ions through an electrolytic membrane and reconverting the ions to molecules. The prime mover includes gas-tight compartments filled with an electrochemically active material and separated by an electrolytic membrane, such as an ion-exchange membrane, that incorporates electrodes so that a voltage gradient can be established across the membrane to induce current flow through the membrane. When the current flows through the membrane, molecules travel through the membrane and are reconverted to molecules in the opposite compartment causing a pressure increase in the receiving compartment and a pressure decrease in the other compartment. The pressure changes are converted to mechanical motion which can be used as a driver for a mechanical load. The disadvantages of this technique are that the resulting motion is small and the pressure increase may rupture the membrane.

U.S. Patent No. 5,100,933, to Tanaka, et al., discloses the use of ionized cross-linked polyacrylamide gels as engines or artificial muscles; the gels can contain a metal ion and are capable of discontinuous volume changes induced by infinitesimal changes in environment. The gel is made by dissolving acrylamide monomers and bisacrylamide monomers in water, adding a polymerization initiator (in particular, ammonium persulfate and TEMED, or tetramethyl-ethylene- diamine) to the solution, soaking the gel sample in water to wash away all residual monomers and initiators, immersing the gel in a basic solution of TEMED for up to 60 days, then immersing the gel in a solvent (in particular, acetone, acetone in water, ethanol and water, or methanol and water). The primary disadvantages of these actuators are generally that the response time of the gel is much longer than that of other known actuator components and that the gel must be contained in the solvent bath. The gels are also mechanically brittle and easily broken.

U.S. Patent No. 5,250,167, to Adolf, er al., discloses actuators or synthetic muscles, using polymeric gels contained in compliant containers with their solvents; these actuators undergo substantial expansion and contraction when subjected to changing environments. The actuators may be rigid or flexible and may be computer-controlled. The driver may also be electrolytic, where application of a voltage across the polymer gel causes a pH gradient to evolve between

the electrodes. For example, filling the polymer fibers with platinum by alternatively treating them with solutions of platinic chloride and sodium borohydride obtains a reversible expansion and contraction of the fiber with the application of an electric field. The actuating gel itself is the only moving part required and the electric field may be only on the order of a few volts per centimeter. The disadvantage is that actuator performance is dictated by the parameters of the polymeric gel used. Furthermore, liquid containment is required to make the actuators stronger and not so easily broken.

U.S. Patent No. 5,389,222, to Shahinpoor, discloses electrically controllable polymeric gel actuators or synthetic muscles, using gels made of polyvinyl alcohol, polyacrylic acid, polyacrylonitrile, or polyacrylamide contained in an electrolytic solvent bath. These actuators operate by reacting to changes in the ionization of a surrounding electrolyte by expanding or contracting, and can be spring-loaded and/or mechanically biased for specific applications. Polymeric gel configurations such as sheets, solid shapes or fiber aggregates are contemplated, as are the use of a salt water solution for the electrolyte, and a platinum catalyst in the actuator housing to recombine the hydrogen and oxygen produced as a result of electrolysis during ionization of the electrolyte. Again, liquid containment is required to maintain strength and electric controllability, and not enough deformation or displacement is generated.

Thus, there is an existing need for a soft actuator that performs activation noiselessly and efficiently (as do biological muscles) with a low ratio of mass to power or a high ratio of power or force to mass.

SUMMARY OF THE INVENTION (DISCLOSURE OF THE INVENTION) In view of the above-described needs, it is a primary object of this invention to provide a soft activation means resembling biological muscles.

The limitations associated with existing actuators and the methods for their manufacture are overcome by the present invention which provides a method of preparing actuators (synthetic muscles) comprising the steps of: rinsing an ion-exchange material; coating the ion-exchange

material with a substance which undergoes chemical reduction in the presence of a reducing agent; and reducing the coating on the ion-exchange material by exposing the ion-exchange material to a reducing agent. In the preferred embodiment, the ion-exchange material comprises a material selected from the group consisting of ion-exchange membranes, ionomer membranes, ion-exchange resins, gels, beads, powders, filaments, and fibers, preferably an ion-exchange membrane, more preferably a polymer ion-exchange membrane, and most preferably a perfluorinated sulfonic acid ion-exchange polymer membrane. Rinsing is best performed in water. The ion-exchange material preferably has at least two surfaces and rinsing is preceded by roughening the surfaces of the ion-exchange material, such as by sandblasting with fine glass bead sandblast. Rinsing is also preferably preceded by cleaning the ion-exchange material in an ultrasonic water bath cleaner. The cleaning includes heating (preferably boiling) the ion- exchange material in solution (preferably acidic, most preferably HCl). Most preferably, the ion- exchange material has at least two surfaces and rinsing comprises (in order): roughening the surfaces of the ion-exchange material; cleaning the ion-exchange material; rinsing the ion- exchange material in water; and boiling the ion-exchange material in an aqueous solution

(preferably acidic, such as an HCl solution). Rinsing preferably comprises at least two steps of rinsing and boiling the ion-exchange material in solution (in water, for a sufficient time to completely swell the ion-exchange material). Coating is preferably done with a metal, more preferably a noble metal, and most preferably with platinum, and is performed for a time sufficient to cover the ion-exchange material with a coating of approximately 3.75 mg/cm 2 of the coating substance. Coating best comprises: immersing the ion-exchange material; and stirring. Immersing is preferably done into a solution containing a salt of a metal, such as a noble metal, palladium, or nickel, preferably a platinum salt, more preferably a platinum-amine complex, and most preferably Pt(NH 3 ) 4 CI 2 . The reducing step best comprises exposing the ion-exchange material to NaBH 4 . Reducing is preferably done in solution (e.g., aqueous) containing a reducing enhancer such as NH„OH, and involves continuously raising the temperature of the solution to a predetermined temperature. Reducing is best done at an elevated temperature in solution in a water bath at an elevated temperature and includes simultaneously stirring the solution in the water bath, and preferably simultaneously stirring the solution (at low speed) while adding the reducing agent. Most preferably, reducing comprises simultaneously: continuously raising the

temperature of the solution to a predetermined temperature; and adding supplementary reducing agent at intervals. This preferably includes maintaining the temperature at the predetermined temperature and simultaneously adding a final amount of supplementary reducing agent when the predetermined temperature is reached, continuously stirring the solution after adding the final amount of supplementary reducing agent, rinsing the ion-exchange material (in water or HCl solution), and storing the ion-exchange material. Preferably, the reducing step comprises at least one reducing step comprising (in order): rinsing the ion-exchange material; immersing the ion- exchange material in a solution containing a reducing agent; rinsing the ion-exchange material; and storing the ion-exchange material. Preferably, the immersing is in a solution (aqueous) containing a salt of a metal such as a noble metal, palladium, or nickel, preferably a platinum salt, more preferably a platinum-amine complex, and most preferably Pt(NH 3 ) 4 CI 2 , as well as a reducing enhancer such as NH 4 OH, as well as a reducing agent such as H 2 NOH«HCI or H 2 NNH 2 »H 2 0. Reducing preferably comprises simultaneously: continuously raising the temperature of the solution to a predetermined temperature; and adding supplementary reducing agent at regular intervals for a time sufficient to substantially complete reduction, as well as testing the solution for completion of reduction such as by monitoring a color change produced by reduction. Rinsing preferably involves at least two rinsing steps, the first in water or an acidic (HCl) solution, or both in sequence, and is performed for a time sufficient to exchange cations in the ion-exchange material for H+ cations outside the ion-exchange material. The second is in water or a basic (NaOH) solution, or both in sequence, and is performed for a time sufficient to exchange cations in the ion-exchange material, such as H+ cations in the ion-exchange material are exchanged for alkali metal (Na+) cations outside the ion-exchange material. Preferably, a second of the at least one reducing and the rinsing are repeated, followed by a final rinsing step in water. After the two preferred rinsing steps, the ion-exchange material is preferably cleaned ultrasonically. Storing is preferably done in water.

The invention is also of a method of preparing an actuator comprising: at least one cleaning step; at least one step of rinsing an ion-exchange material; at least one step of coating the ion- exchange material with a substance which undergoes chemical reduction in the presence of a reducing agent; at least one step of reducing the coating on the ion-exchange material by

exposing the ion-exchange material to a reducing agent; testing the solution for the completion of reduction; and at least one step of storing the treated ion-exchange material. In the preferred embodiment, the ion-exchange material is an ion-exchange membrane, an ionomer membrane, an ion-exchange resin, a gel, beads, a powder, filaments, or fibers, preferably an ion-exchange membrane, more preferably a polymer ion-exchange membrane, and most preferably a perfluorinated sulfonic acid ion-exchange polymer membrane. Rinsing is preferably done in water or solution (acidic, such as HCl, or basic, such as NaOH), and involves heating (boiling in solution) the ion-exchange material. At least two rinsings are best performed before coating. Coating is preferably done with a metal, preferably a noble metal, palladium, or nickel, and most preferably platinum. Preferably, at least one rinsing occurs before and after each reducing, and the reducing is done in the presence of a reducing enhancer (NH 4 OH). Exposing is best done to a reducing agent (NaBH 4 , H 2 NOH«HCI, or H 2 NNH 2 «H 2 0), preferably first to NaBH 4 , and later to H 2 NOH«HCI or H 2 NNH 2 *H 2 0. Preferably, reducing is done in solution and includes: heating the reducing solution; continuously stirring the ion-exchange material in the coating solution at low speed; and simultaneously raising the temperature of the solution while adding supplementary reducing agent. Testing preferably includes: mixing a test solution comprising a portion of the reducing solution; boiling the test solution; and detecting a color change in the testing solution during boiling. The portion is preferably about 2 ml and testing includes: adding NaBH 4 to the test solution during boiling; and adding supplemental reducing agent to the reducing solution in which the ion-exchange material is immersed if a coloration is detected in the test solution during boiling, and terminating reducing otherwise. Storing is best done in water or in solution (acidic, such as HCl).

The invention is additionally of a method of preparing an actuator from an ion-exchange material comprising: roughening the ion-exchange material; a first step of cleaning the roughened ion-exchange material; a first step of rinsing the ion-exchange material; a first step of boiling the ion-exchange material; a second step of rinsing the ion-exchange material; a second step of boiling the ion-exchange material wherein boiling is performed for a sufficient time to completely swell the ion-exchange material; a step of coating the ion-exchange material with a substance comprising platinum; a third step of rinsing the ion-exchange material; a first step of

reducing the coating on the ion-exchange material by immersing the coated ion-exchange material in a solution comprising a reducing agent whereby the coating undergoes chemical reduction in the presence of the solution comprising the reducing agent; simultaneously heating and stirring the ion-exchange material in the reducing agent; a fourth step of rinsing the ion- exchange material; a first step of storing the ion-exchange material; a fifth step of rinsing the ion- exchange material; a second step of reducing the coating on the ion-exchange material by immersing the coated ion-exchange material in a solution comprising a reducing agent whereby the coating undergoes chemical reduction in the presence of the solution comprising the reducing agent; simultaneously heating and stirring the ion-exchange material in the reducing agent; at least one step of sequentially rinsing the ion-exchange material; a second step of cleaning the ion-exchange material; and a second step of storing the ion-exchange material. The steps are preferably performed in the above order, and the last four repeated and including a final rinsing step prior to the second storing step.

The present invention is also of an actuator, produced by any of the above summary methods, comprising a treated ion-exchange material capable of a completely reversible deflection and means operably connected to the ion-exchange material for electrically driving the deflection of the ion-exchange material.

The invention is further of an actuator for use in a gripper mechanism comprising: at least two actuators, produced by any of the above methods, positioned opposite to each other and being capable of bending in equal and opposing directions; a power supply to the actuators to drive the mechanical bending of the actuators in opposing directions; electrical impulse conductors operably attached to the first end of each of the actuators for conducting electrical impulses across the actuators; and wiring, operably attached to the conductors and to the power supply, for electrically connecting the actuators to the power supply.

The invention is additionally of an actuator for providing three-dimensional movement, comprising: three actuators produced by any of the above methods, comprising a hollow triangular tube having a longitudinal axis wherein each of the actuators of the tube comprises a

face of the tube, signal conductors, operably attached to the first end of each of the actuators, for conducting a signal across each of the faces of the tube, thereby stimulating each face of the tube at a phase angle apart from each adjacent face to produce a motion around the longitudinal axis of the tube, and a power supply for providing power to the signal conducting means; and a power conductor, attached to the signal conductors, for operably connecting the tube to the power supply. The signal is preferably a low amplitude alternating signal

The present invention is still further of an actuator for use as a wing flap, comprising at least two actuators, produced by any of the above methods, sandwiched in series in a stack configuration, each of the actuators formed in a planar layer and capable of acting as a series resistor element, power conductors, operably attached to the stack at the first end and the top and bottom surfaces, for conducting power across the stack; a power supply for supplying power to the stack; and connectors for connecting the power supplying means to the power conducting means. In the preferred embodiment, adhesive is placed between the actuators, preferably conductive and non-continuously applied

The invention is also of an actuator for use as a robotic swimming structure, comprising at least two actuators produced by any of the above methods, formed in an ion-exchange material having a first end, the ion-exchange material comprising a plurality of polymer gel fibers imprinted with means for conducting power through the ion-exchange material, conductors, operably attached to the ion-exchange material at the first end, for conducting an alternating low voltage across the ion-exchange material, a power supply for providing power to the conductors, a modulator for modulating speed of bending of the ion-exchange material varying the frequencies of the applied voltage, and a connector for operably connecting the conducting means to the power providing means In the preferred embodiment, the actuator includes a buoyancy vaπer for varying the buoyancy of the swimming structure and a sealed housing, operably attached to the ion-exchange material at the first end, the housing comprising a signal generator (erasable programmable chip) and a power generator (a battery) The ion exchange material may be elastic or ngid.

The invention is yet further of an actuator for use as a resonant flying machine, comprising at least one ion-exchange material actuator, prepared by any of the above methods, in the form of a planar layer having first and second ends, a top surface and a bottom surface, power conductors for conducting power across the ion-exchange material actuator, operably attached to the top and bottom surfaces of the ion-exchange matenal and along a central axis of the ion- exchange material equidistant from the first and second ends, whereby the ion-exchange matenal actuator is capable of reversibly bending in a flapping motion upon receiving power, a power supply for providing power to the conductors, and connectors for connecting the conductors to the power supply

The invention is also of an actuator for use as a guide wire or a micro-catheter in intra-cavity medical applications, comprising at least one ion-exchange material actuator prepared by any of the above methods, and formed in a small strip, a power supply for providing power to the strip, and connectors for connecting the strip to the power supply

The invention is also of a sphincter-type or a squeeze-type actuator used in medical applications for incontinence and cardiac-assist devices

Additional objects, advantages and novel features, and further scope of applicability of the present invention will be set forth in part in the detailed description to follow, taken in conjunction with the accompanying Figures, and in part will become apparent to those skilled in the art upon examination of the following detailed description, or may be learned by practice of the invention The objects and advantages of the invention may be realized and attained by means of the instrumentalities and combinations particularly pointed out in the appended claims

BRIEF DESCRIPTION OF THE DRAWINGS The accompanying Figures, which are incorporated into and form a part of the specification illustrate several embodiments of the present invention and, together with the description, serve to explain the principles of the invention However, these Figures, as well as the following

detailed description and the examples, are only for the purpose of illustrating a preferred embodiment of the invention and are not to be construed as limiting the invention. In the drawings:

FIGURE 1 is a perspective view of the actuator of the invention showing the treated membrane actuator with electrodes placed at one end of the membrane and terminals connected to a power source at the other end.

FIGURE 2 is a perspective view of the actuator of the invention showing use of the treated membrane actuator as an electrically controlled tweezer with terminals connected to a power source at one end.

FIGURE 3 is a perspective view of the actuator of the invention showing the treated membrane actuator packaged in three dimensional form for use with a three-phase generator box. Terminals are disposed at the end of the actuator positioned nearest the generator box.

FIGURE 4 is a perspective view of the actuator of the invention showing multiple, stacked treated membrane actuators in a composite structure with terminals connected to a power source at one end to be used as a composite wing-flap.

FIGURE 5 is a schematic view in elevation of the actuator of the invention showing the treated membrane actuator in elastic form with imprinted electrodes for use as a robotic swimming structure. The membrane is connected to an electronic guidance and control system at one end.

FIGURE 6 is a plan view from the top of the actuator of the invention showing the treated membrane actuator imprinted with multiple electrodes spaced throughout and formed in a single rigid structure with the power source at one end. The actuator packaged in this form is suitable for use as a robotic fish.

FIGURE 7 is a perspective view of the actuator of the invention showing the treated membrane actuator with terminals extending through a central axis of the membrane and connected to a power source. The membrane is packaged in this form for application as a resonant flying machine.

DESCRIPTION OF THE PREFERRED EMBODIMENTS (BEST MODES FOR CARRYING OUT THE INVENTION)

The invention involves methods of manufacturing, packaging and use of ion-exchange membrane actuators made from ion-exchange membranes (or any ionomer membrane, ion- exchange resin, gel, beads, powder, filaments, or fiber) by chemically, mechanically and electrically treating them with at least one noble metal such as platinum.

A method of the invention of preparing an actuator comprises rinsing a membrane, coating the membrane with a substance which undergoes chemical reduction in the presence of a reducing agent, reducing the coating on the membrane by exposing the membrane to a reducing agent. The proposed manufacturing technique produces a typical flap muscle of 0.2 - 0.4 mm thickness, 2 - 5 mm width and 20 mm length which can achieve a completely reversible maximum deflection of 12 - 15 mm under a maximum voltage of 2.0 - 2.5 volts. More particularly, in the method for manufacturing actuators according to the subject invention, electrically controllable artificial muscles are produced from polymeric ion-exchange membranes by a method comprising a first cleaning step, at least one step (preferably two steps) of rinsing a membrane, at least one step of coating the membrane with a substance which undergoes chemical reduction in the presence of a reducing agent, at least one step (preferably two steps) of reducing the coating on the membrane by exposing the membrane to a reducing agent, a second cleaning step, and at least one step (preferably two steps) of storing the treated membrane. Several of these steps, in particular the reducing steps, may be repeated as needed to obtain a desired result.

The invention also includes a number of novel applications, devices and actuators made from this specially treated material. Preferred uses of the treated membrane of the invention

include any application requiring noiseless propulsion in water Further applications include its use as a gripper (tweezers), an three dimensional actuator for use with a generator, a composite wing flap, an autonomous robotic swimming structure, a resonant flying machine, a snake-like robot, a wobble motor, and a multi-fingered robotic hand

The present invention having been generally described, the following preferred specific embodiments are provided to illustrate some of the properties and demonstrate the practical advantages thereof, and to allow one skilled in the art to utilize the present invention to its fullest extent These examples included are to be construed as merely illustrative, and not limitative of the remainder of the disclosure or the claims in any way whatsoever

The manufacturing method of the present invention was performed using ion-exchange membranes (or any ionomer membrane) such as a perflounnated sulfonic acid polymer or ionomer such as Nafion™ (Dupont deNemours & Company trademark) which is a perfluoπnated sulfonic acid ion-exchange polymer membrane are used for separation processes, production of caustic sodas and fuel cell application in the industry Ion-exchange membranes are hydrophilic ionic polymers and swell up to 16% in water at room temperature

The following lists the step-by-step preparation of an exemplary actuator from a 2 by 2 square inch Nafion™ 117 membrane (0 007 inch thick)

1 Both surfaces of the membrane are roughened using a smooth sandpaper (such as Norton 600A) Alternatively, roughening can be accomplished with short bursts of fine glass bead sandblast (2 sec/cm 2 )

2 The membrane is then cleaned in an ultrasonic water bath cleaner for about 10 minutes

3 The membrane is rinsed with pure (deionized) water and boiled in a 2 4N aqueous solution of HCl for about 30 minutes

4. The membrane is again rinsed with pure water and boiled in pure water for about 30 minutes to completely swell the membrane.

5. The membrane is then immersed in a solution of 0.2% platinum-amine complex (Pt(NH 3 ) 4 Cl 2 ) (tetra-amine platinum chloride hydrate, 98%) for 8 hours at room temperature while slowly stirring the solution. The final amount of platinum deposited on the membrane must be about 3.75 mg/sq cm for each face of the membrane surface. This produces a pair of porous dendritic electrodes on the surface of the membrane.

6. The membrane is then rinsed again with pure water and immersed in a reducing solution consisting of 180 ml H 2 0, 0.5 ml NH 4 OH 30%, and 2 ml NaBH 4 5% in a water bath at 40°C while stirring at low speed (150 RPM). Additions of 2 ml NaBH 4 5% are made every 30 minutes for about 3 and a half hours while gradually raising the temperature to 60°C, at which point 20 ml NaBH 4 5% is added, and the mixture is stirred for an additional one and a half hours. Then the membrane is rinsed with pure water and stored in a 0.5% solution of HCl for 8 hours.

7. Following its removal from storage, the membrane is again rinsed with pure water and immersed in a solution containing 300 ml H 2 0, 0.2 grams Pt(NH 3 ) 4 CI 2 , 3 ml H 2 NOH«HCI 5% (hydroxylamine hydrochloride, 99%), 1.5 ml H 2 NNH 2 «H 2 0 20% (hydrazine monohydrate, 98%), and 0.5 ml NH 4 OH 30% at 40°C while stirring at low speed (approximately 60 RPM). Reducing agents consisting of 3 ml H 2 NOH«HCI 5% and 1.5 ml H 2 NNH 2 «H 2 0 20% were then added every 30 minutes for 4 hours while gradually increasing the temperature to 60°C. After the process is over, the solution containing the membrane was tested for any residual Pt by boiling 2 ml of the solution with 2 ml NaBH 4 5%. If the color of the mixture turns black, the addition of reducing agents must continue for longer time. If no color change is visually detected, the process is complete. Step 7 is part of the developing process to deposit more platinum in the polymer matrix.

8. When reduction is complete, the membrane is rinsed with pure water and then with 0.1 N HCl solution to remove any other cations in the membrane. Steps 7 and 8 are necessary to insure high level of activity in the final actuator.

9. The membrane is rinsed again with pure water and then with 0.1 N NaOH solution to replace H+ cations in the membrane with Na+ cations.

10. The membrane is then cleaned in an ultrasonic cleaner for 5 seconds and removed.

11. Steps 7, 8, and 9 are repeated and followed by rinsing with pure water. The membrane is then stored in pure water at room temperature. Step 10 repeats the developing process to increase the amount of platinum deposited. If one starts out with a higher concentration of platinum salt in step 7, it is possible to deposit sufficient platinum on the membrane on the first pass, thereby eliminating the need for step 11. However, this will increase the risk of oxidation as well as crowding phenomena on surfaces of the membrane in a short time period.

A flap muscle with dimensions of 0.2 - 0.4 mm thickness, 5 mm width and 40 mm length is typically cut from sheets of 100 mm x 150 mm membrane muscles produced by the performance of the above-described steps. This muscle can achieve a completely reversible maximum deflection of 22 - 25 mm under a maximum voltage of 2.0 - 2.5 volts and provides noticeable power to weight ratio at low voltages to perform useful work. A major advantage is that one can cut any shape and size muscle from the sheet. In particular, micro-muscles in down to approximately 200 microns in length and 40 microns in width may be cut from such sheets.

Figure 1 depicts such an actuator made by chemically and mechanically treating Nafion™ membranes with platinum according to the method of the invention. Figure 1 is a perspective view of a treated membrane actuator A in planar form comprising a top surface 10, bottom surface 11 (not shown), sides 12 (shown) and 13 (not shown), a first end 14 (not shown) and a second end 15. As shown, electrodes 20 extend through sides 12 and end 15. Preferably, electrodes 20 are platinum. At end 14, terminals 25 and 26 are attached at their first ends 25a

and 26a, respectively, to top surface 10 and bottom surface 11 of actuator A. Terminals 25 and 26 at their second ends 25b and 26b, respectively are connected by wires 31 and 32, respectively, to a power source 35.

Membrane actuators can be manufactured and packaged for specific applications. These actuators produce a bending motion when placed in a low voltage electric field. The membrane always bends toward the anode and then back to cathode and null position when a low voltage is applied and removed sequentially. The bandwidth of the membrane depends on its size and geometry; forthe typical actuator, the bandwidth is about 40 Hz. Also, forthe typical actuator produced by the method above, the current across the membrane is about 100 mA sq cm, and the applied voltage necessary for actuation is about 1.5 - 2.5 volts. The most important aspect here is to chemically deposit (or coat) porous (perforated) platinum electrodes on the membrane surface with some penetration inside the membrane across its thickness. For purposes of the specification and claims, "coating" is defined as depositing a layer (porous or non-porous), when used as a verb, and as a deposit (porous or non-porous), when used as a noun.

The actuators of the invention are hydrophilic and operate in moist environments. Therefore, for application in open-air systems, they are preferably encapsulated in an elastic membrane such as latex.

Industrial Applicability:

The invention is further illustrated by the following non-limiting examples.

The following examples are additional embodiments of the present invention and illustrate novel applications of the artificial muscles and actuators resulting from experiments using the method of manufacturing of the subject invention.

Example 1 Membrane Grippers The membrane can be fabricated to act as a micro- or macro- gripper, e.g., tweezers, for gripping action when two membranes are wired and sandwiched in a way so that they bend in opposing direction. Figure 2 is a perspective view of an embodiment of the invention showing two treated membrane actuators 40 and 50 packaged as an electrically controlled gripper B. Actuators 40 and 50 each comprise respectively top surfaces 41 and 51, bottom surfaces 42 and 52 (not shown), sides 43 and 53 (shown), sides 44 and 54 (not shown), first ends 45 and 55 (shown) and second ends 46 and 56 (not shown). Actuators 40 and 50 are disposed opposite to each other with bottom surface 42 of actuator 40 facing top surface 51 of actuator 50. The first ends 60a and 61a of terminals 60 and 61 are attached to the top surface 41 and the bottom surface 42, respectively, at the second end 46 of actuator 40, and the first ends 62a and 63a of terminals 62 and 63 are attached to the top surface 51 and the bottom surface 52, respectively, at the second end 56 of actuator 50. Terminals 60 and 63 are connected to each other and to one pole of the power supply 70 by electrical wire 71 attached to their ends 60b and 63b, respectively. Terminals 61 and 62 are connected to each other by electrical wire 72 attached to their ends 61b and 62b, and to the other pole of the power supply 70 by electrical wire 73, respectively. The length of wire 72 depends on the required gap between the two actuators 40 and 50 depending on application.

Example 2 Three-dimensional Membrane Actuator Figure 3 is a perspective view of a three-dimensional membrane actuator C packaged in three-dimensional form for use with a three-phase generator box M. Actuator C comprises a hollow triangular tube configuration consisting of three independent membrane actuators 77

(shown), 78 (shown) and 79 (partially shown) attached and electrically insulated along the long edges with three external faces 80 (shown), 81 (shown) and 82 (not shown), respectively and a first end 83 (free) and second end 84 which is fixed to the generator box M. External terminals 90 (shown), 91 (shown), and 92 (not shown) are disposed at the second end 84 of actuator C for connection to electrodes 95a (shown), 95b (shown), 95c (shown), respectively

incorporated in generator box M. Internal faces of the actuators 85 (not shown), 86 (not shown), and 87 (shown) are connected via internal terminals 97 (partially shown), 98 (partially shown) and 99 (not shown) to electrodes 96a (shown), 96b (shown) and 96c (shown) of the generator box M, respectively. Membrane actuator C is fabricated to produce a 3-dimensional movement by positioning each of actuators 77, 78, and 79 to be stimulated at a phase angle apart from the adjacent actuator by a low amplitude alternating signal, therefore inducing wobble-like motion around the long imaginary axis of the combined actuator tube in null position.

In Fig. 3, the three actuators 77, 78, and 79 are joined together by a flexible adhesive (such as LOCTITE SUPERFLEX™) at the edges (seams). Each actuator has its own terminal connections to each phase of a typical 3-phase power generator (M) or a multi-phase power supply (programmable function generators / power supplies exist that have phase-separated outputs). Each of these actuators has its external and internal faces similar to the top and bottom faces of the tweezer shown in Fig. 2. The final actuator, then, looks like a triangular hollow tube fixed at one end to a platform and free at the other end to wobble or rotate around an imaginary vertical axis. Each output pair of the 3-phase generator is connected to an input terminal pair of each actuator. Each actuator has a pair of terminals (one on the inside and one on the outside of the actuator). Fig. 3 illustrates this arrangement.

Example 3

Composite Wing-Flap Figure 4 is a perspective view showing multiple, treated membrane actuators in a stacked (sandwiched), configuration D which is designed to accommodate more power for specific actuations. Actuators 10a, 10b, 10c, 10d, and 10e are each independent planar actuators of different lengths (to provide different stiffness, and therefore resonant frequency, of the composite wing) manufactured according to the process of the invention and formed in a stacked configuration D which as a whole comprises a top surface 100 (shown), a bottom surface 101 (not shown), a first end 102 and a second end 103. Terminals 110 and 111 are connected to top surface 100 and bottom surface 101 , respectively, at first end 102 of actuator D. Terminals 110 (shown) and 111 (not shown) are also connected by electrical wires 114 and 116, respectively, to

a power source 120. Electrical wire 116 contains an on-off switch 121. Several of these membrane actuators 10 can be assembled in series and multiple amounts of voltage applied to increase power in the composite actuator. Actuators 10a-e act as series resistor elements especially at higher frequencies.

The actuator of Fig. 4 is a resistive element by nature. Therefore, as one stacks several of the actuators, in effect one increases the overall resistance of the combined system. This in turn can allow for higher input voltages. The variation in length of each actuator is due to the desired stiffness of the wing as a whole. Since each actuator has conductivity through its thickness, there is no need to connect wires to faces. By just stacking them one can produce a thicker and more powerful actuator that can handle higher loads. The only necessary terminal connections are on the top face 100 of the top layer 10a and the bottom face 101 of the bottom layer 10e to an alternating (oscillating) source of voltage.

Example 4

Robotic Swimming Structure Figure 5 shows one embodiment of a robotic swimming structure made by cutting and packaging strips of treated ion-exchange membranes 130 to desired size and shape and consequently placing an alternating low voltage (1.5 - 2.5 V-peak per strip) across the muscle assembly E as shown. In this Figure, muscle assembly E is formed of said polymer gel strips 130 which may be encapsulated into an elastic membrane 135 with electrodes 140 (not shown) imprinted on each strip therein and with a first end 136 (free) and a second end 137 (fixed). Second end 137 is attached to an appropriate electronics and wiring structure 141 for providing guidance and control to actuate the muscle assembly E. Structure 141 as shown comprises a sealed housing module 142 containing therein a means for generating a signal 143 and a means for generating power 144. The tail assembly consists of electrically actuated artificial muscles such as ion-exchange membranes cut in tiny fibers or strips. The tail is then encapsulated in an elastic membrane. The ends of fibers closer to the head assembly 142 are wired to a miniature printed circuit board (PCB) or like assembly to a signal generator assembly

consisting of an oscillator circuit and batteries or other power source. The head assembly is preferably sealed to protect the circuitry and electronics from the elements.

By varying the frequency of the applied voltage to the membrane muscle, the speed of muscle-bending oscillation of muscle assembly E, and therefore propulsion of the swimming structure, can be modulated. In this manner, robotic swimming fishes and submarine structures containing a sealed signal and power-generating module (preferably in the head assembly) can be made to swim at various depths by varying the buoyancy of the structure by conventional means. Remote commands via radio signals can then be sent to modulate propulsion speed and buoyancy by radio controls.

Example 5

Robotic Fish

Figure 6 is a plan view of the actuator of the invention showing another embodiment of the treated membrane actuator in a elastic construction with imprinted electrodes for use as a robotic swimming structure, more specifically a robotic fish. Figure 6 shows a robotic swimming structure made by cutting and packaging strips of treated ion-exchange membranes 150 in two rows of desired size and shape and imprinted with electrodes 160 spaced throughout and in a single structure. In this Figure, muscle assembly structure F is formed of said polymer gel strips 150 that may be encapsulated into an elastic membrane 155 with multiple electrodes 160 imprinted therein and with a first end 156 (tail) and a second end 157 (head). Head assembly 157 contains appropriate electronics and wiring structure 161 for providing power, guidance and controls to the muscle assembly F. Structure 161 is contained in a sealed housing module 162, containing therein a means for generating a signal 163 and a means for generating power 164. The power source 164 at end 157 places an alternating low voltage (1.5-2.5 V-peak per strip) across the muscle assembly F as shown. Power source 164 includes an erasable, programmable (EPROM) chip 165 and batteries 166. Note the two rows of small actuators in parallel. Each has two terminals that are connected individually to the multi-phase signal generator 163 located in the head assembly 157. There are also batteries (or other power source) housed in this section for required voltage input. By energizing one pair (across) of actuators at a time and then the

consequent pairs downstream, one can produce a propagating or traveling wave downstream on each side of the fish. This will produce a sting-ray type of motion which propels the swimming structure forward. The middle terminals or spines act as conductors that connect the signal generator outputs in the head assembly to each actuator in the tail or wing assembly.

By varying the frequency of the applied voltage, the speed of muscle-bending oscillation of the membranes 150, and therefore propulsion of the swimming structure F, can be modulated. In this manner, robotic swimming fishes and submarine structures containing a sealed signal and power-generating module (preferably in the head assembly) can be made to swim at various depth by varying the buoyancy of the structure by conventional means. Remote commands via radio signals can then be sent to modulate propulsion speed and buoyancy by radio controls.

Example 6 Resonant Flvinα Machine Figure 7 is a perspective view of the actuator of the invention showing a flying machine G constructed from treated membrane actuator 170 formed in a single sheet having a top surface 171 (shown), a bottom surface 172 (not shown), a first end 173, a second end 174 (not shown) and a central axis 175. Terminal 180, attached to top surface 171, extends along the central axis 175 of the membrane 170 equidistant from first end 173 and second end 174, and diametrically opposed terminal 181 (not shown), attached to bottom surface 172, extends along the central axis 175 of the membrane 170 equidistant from first end 173 and second end 174. Terminals 180 and 181 are connected at their ends 180a and 181a to a power supply 190 by electric wires 191 and 192 respectively. As shown, wire 191 connecting terminal 180 to power supply 190, includes an on-off switch 195.

The membrane is packaged in this form for application as a resonant flying machine. In this configuration, the treated membranes ("muscles") can flap like a pair of wings and create a flying machine. "Resonant" means excitation at the resonant frequency of the membrane, which causes the most violent vibration of the membrane. Each body of mass has a resonant frequency at which it will attain its maximum displacement when shaken by some input force or

power. To obtain large displacements of the actuator, one should apply oscillating signals at a frequency close to its body resonant frequency.

In Fig. 7 one sees a large actuator strip with a pair of electrodes (terminals) in the middle fixed to the actuator surfaces of top and bottom. By connecting the circuit to an AC-power source (alternating current signal generator), one can produce oscillating motion of the membrane actuator similar to a hummingbird's or insect's wing-flap motion. Furthermore, if one applies the input voltage signal at or near the resonant frequency of the wing structure, large deformations can be obtained which will vibrate the wing structure in a resonant mode. The wing assembly is preferably encapsulated in a thin elastic membrane to prevent dehydration of the actuator.

Example 7 Surgical Tool The actuator can also be used as a guide wire or a micro-catheter in biomedical applications for intra-cavity endoscopic surgery and diagnostics. Small internal cavities in the body can be navigated by using these membrane actuators when used in small strips.

Example 8 Metering Valves

Metering valves may be manufactured from the membrane of the invention, the size of an inside dimension plus required tolerances, for any tube that will permit control of aqueous fluid flow by varying the degree of bending displacement of the membrane and applying a calibrated amount of direct current.

Example 9 Bellows Pumos Bellows pumps can be made by attaching two planar sections of slightly different sizes of membrane sections and properly placing electrodes on the resulting cavity. This gives rise to

modulating the volume trapped between the membranes when the applied voltage amplitude and frequency is set properly in order to control the flow and volume of fluid being pumped.

Example 10 Peristaltic Pumps

Peristaltic pumps can be made from tubular sections of the membrane of the invention and placement of the electrodes in appropriate locations. Modulating the volume trapped in the tube is possible by applying appropriate input voltage at the proper frequency.

Example 11

Microelectromechanical Systems A variety of microelectromechanical systems (MEMS) can be made by packaging and fabricating the membranes of the present invention in small, miniature, and micro sizes. Some examples include biomedical applications such as active microsurgical tools as well as biomimetics such as micro-propulsion engines for material transport in liquid media. Other applications will involve micro-pumps, micro-valves, and micro-actuators. Flagella and cilia type actuators fall under this category.

Example 12 Electromechanical Relay Switches

Non-magnetic, self-contained, electromechanical relay switches can be made from the membranes of the present invention by incorporating their bending characteristics in small applied voltages to close a circuit because they are also good conductors. In this manner, several of these actuators can be arranged to make a multipole-multithrow relay switch.

Example 13 Artificial Smooth Muscle Actuators Artificial smooth muscle actuators similar to biological smooth muscles can be made by attaching several segments of tubular sections from membranes of the present invention and employing a simple control scheme to sequentially activate each segment to produce a traveling

wave of volume change in the combined tube sections. This motion can be used to transport material or liquid contained in tube volume. The activation of each segment is similar to the peristaltic pump, above. Artificial veins, arteries, intestines made with the membrane of the present invention can be fabricated and packaged in variety of sizes depending on the application.

Example 14

Artificial Sphincter and Ocular Muscles Artificial sphincter and ocular muscles can also be made from the membrane of the present invention by incorporating thin strips of the actuators in a bundle form similar to the parallel actuator configuration. A typical application is in treatment of incontinence.

Example 15 Artificial Ventricular or Cardiac-Assist Muscles Artificial ventricular assist type muscles can also be made for heart patients with heart abnormalities associated with cardiac muscle functions.

Example 16 Continuous Variable Aperture Mirrors and Antenna Dishes Continuous variable aperture mirrors and antenna dishes can be made by cutting circular sections of the membrane of the present invention and placing electrodes at strategic locations. The focal point of the resulting parabolic dish can be varied by strategic placement of the electrodes and varying the amplitude of the applied voltage.

Example 17

Linear Actuators Linear actuators can be made to produce a variety of robotic manipulators including platform type or parallel platform actuators.

Example 18 Slithering Device Snake-like locomotion can be accomplished by arranging proper segments of the membrane of the invention in series and controlling each segment's bending by applying sequential input power to each segment in a cascade mode.

Example 19 Parts Orientation / Feeding Soft parts orientors or feeders for delicate handling of parts in a manufacturing assembly line can be made from flaps made out of the membrane of the invention.

Example 20 Incontinence Assist Devices Various configurations of the muscles of the invention may be used in medical applications involving incontinence. In these systems, a patient can activate the muscles by means of a push-button switch, or the like, to prevent leakage and control discharge by pressing the switch, which is preferably battery operated.

Although the invention has been described in detail with particular reference to these preferred embodiments, other embodiments can achieve the same results. Variations and modifications of the present invention will be obvious to those skilled in the art, and it is intended to cover in the appended claims all such modifications and equivalents. The entire disclosures of all references, applications, patents, and publications cited above, are hereby incorporated by reference.