Many pressure producing elements use a moving part to create a pressure increase. The use of a moving part may produce drawbacks, especially in difficult operating conditions. Recently there has been considerable interest in the development of materials to convert electrical energy directly to mechanical energy and a number of new actuating materials are being developed to this end. These include electrochemically responsive conducting polymers, capacitance-driven carbon nanotube actuators, pH responsive hydrogels, ionic polymer metal composites, electric field responsive elastomers, and field electrostrictive polymers. An impetus behind this development is the desire to create more efficient transduction which can be scaled to size or weight demands that cannot be fulfilled by conventional electric motors, pumps, and switches. These constraints are particulary relevant to the emerging fields of microfluidics, microelectromechanical systems (MEMS), and robotics. While many of the new materials under investigation exhibit useful specific properties, e.g., large stresses, sizable strains, or fast cycling time, they commonly suffer from inherent limitations that severely restrict their general applicability.
According to the present system, an electrically operable cell, one without moving parts, is disclosed. This device uses electrolytic phase transformation. This system may use electrochemically generated gas for the reversible and controllable application of pressure and/or motion as used for actuation. In an embodiment, the device uses high surface area electrodes for rapid electrochemical response, and the separation of the electrochemical half reactions, as in, for example, a fuel cell, for full control of the volume and pressure change processes. In an embodiment, the cell is constructed in a flexible housing, as in a membrane, for direct application of pressure/volume. Another embodiment uses a rigid housing for the external direction of the pressure/volume changes by fluid flow in or out of the cell via tubing.
These and other aspects will now be described in detail with reference to the accompanying drawings, wherein:
The present system describes a fuel cell configured for electrolytic generation of gas from a liquid. The generation of gas from the liquid may produce volume/pressure changes. According to the present system, the volume may change-theoretically by large factors. In addition, the process is reversible, that is the gas can be recombined into a liquid, and occurs at a controlled rate.
Rapid recombination of gases is facilitated by electrodes having large effective catalyst surface area. Control of the recombination is achieved by physically separating the half reactions. Both conditions are present in fuel cells, that are well-known in the art. A common fuel cell configuration seperates the two half-reactions by an ionically conducting membrane.
The present application operates by repeatedly running a cell, e.g. a electrochemically-reacting cell such as a fuel cell, “in reverse, that is to generate the necessary gases electrolytically, for the forward or generating portion of the cycle. This occurs in a 3:2 stoichiometric ratio of gas to liquid.
Specifically, for a hydrogen-oxygen electrochemical reaction:
2H2O(l)O2(g)+4H+(aq)+4e− (1)
4H(aq)+4e−2H2(g) (2)
Net: 2H2O(l)O2(g)+2H2(g) (3)
The fuel cell may then be operated in the conventional way to consume the gas, and return the system to its initial state. In this part of the operation, some energy may be recouped.
A reversible actuator, according to an embodiment, is shown in
The compartments 130, 131 are filled with an aqueous electrolyte solution that may be comprised of 1 molar sulphuric acid or a phosphate buffer. The cell assembly is sealed either by an epoxy seal 122 or by a rubber gasket.
The device embodiment with a rigid housing 299 is shown with its control system in
The generation of gas increases the pressure and/or volume in the cell. In the
The consumption of gas continues until the device has returned to its initial condition.
Since an actuator device based on these reactions is powered by the gas it generates, its response will be governed approximately by the ideal gas law:
PV=nRT (4)
The relationship provides two limiting scenarios:
(A) Expansion under isobaric conditions: This represents the maximum fractional change in length ΔL/L, or strain, that can be achieved in the form of linear displacement of a piston as the volume of the system grows. The charge passed during electrolysis and the reaction stoichiometry determine the volume of gas produced. The maximum strain that can be achieved with a piston driven by this process is a function of the volume of gas produced (equation 5) and the volume of water consumed (equation 6).
At constant pressure,
Vgas=(3/2)n
Vliquid=n
Where M
(B) Pressurization at constant volume: The buildup of pressure within the system by electrolysis represents the maximum force per cross-sectional area, or stress, that can be generated and applied through a piston. In the absence of piston motion (and flex in the system components), the maximum stress is reached when the gas is confined to the small volume made available by the water consumed (see equation 6):
The performance of the device has been demonstrated under these two limiting conditions. In both cases, it was shown that the device behaves in accordance with the predicted response indicated above within experimental error. Representative results are presented in
Although only a few embodiments have been disclosed in detail above, other modifications are possible. All such modifications are intended to be encompassed within the following claims.
This application claims benefit of U.S. Provisional Application No. 60/282,951, filed Apr. 13, 2001.
| Number | Date | Country | |
|---|---|---|---|
| 60282951 | Apr 2001 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10121030 | Apr 2002 | US |
| Child | 11455886 | Jun 2006 | US |