Person:

Clarke, David

Focus tunable, adaptive lenses provide several advantages over traditional lens assemblies in terms of compactness, cost, efficiency, and flexibility. To further improve the simplicity and compact nature of adaptive lenses, we present an elastomer-liquid lens system which makes use of an inline, transparent electroactive polymer actuator. The lens requires only a minimal number of components: a frame, a passive membrane, a dielectric elastomer actuator membrane, and a clear liquid. The focal length variation was recorded to be greater than 100% with this system, responding in less than one second. Through the analysis of membrane deformation within geometrical constraints, it is shown that by selecting appropriate lens dimensions, even larger focusing dynamic ranges can be achieved.

Electrically tunable adaptive lenses provide several advantages over traditional lens assemblies in terms of compactness, speed, efficiency, and flexibility. We present an elastomer-liquid lens system which makes use of an in-line, transparent electroactive polymer actuator. The lens has two liquid-filled cavities enclosed within two frames, with two passive outer elastomer membranes and an internal transparent electroactive membrane. Advantages of the lens design over existing systems include large apertures, flexibility in choosing the starting lens curvature, and electrode encapsulation with a dielectric liquid. A lens power change up to 40 diopters, corresponding to focal length variation up to 300%, was recorded during actuation, with a response time on the order of tens of milliseconds.

In this review, we describe the creation of a large database of thermoelectric materials prepared by abstracting information from over 100 publications. The database has over 18,000 data points from multiple classes of compounds, whose relevant properties have been measured at several temperatures. Appropriate visualization of the data immediately allows certain insights to be gained with regard to the property space of plausible thermoelectric materials. Of particular note is that any candidate material needs to display an electrical resistivity value that is close to 1 mΩcm at 300 K, i.e., samples should be significantly more conductive than the Mott minimum metallic conductivity. The Herfindahl-Hirschman index, a commonly accepted measure of market concentration, has been calculated from geological data (known elemental reserves) and geopolitical data (elemental production) for much of the periodic table. The visualization strategy employed here allows rapid sorting of thermoelectric compositions with respect to important issues of elemental scarcity and supply risk.

Far greater voltage-actuated deformation is achievable for a dielectric elastomer under equal-biaxial dead load than under rigid constraint usually employed. Areal strains of 488% are demonstrated. The dead load suppresses electric breakdown, enabling the elastomer to survive the snap-through electromechanical instability. The breakdown voltage is found to increase with the voltage ramp rate. A nonlinear model for viscoelastic dielectric elastomers is developed and shown to be consistent with the experimental observations.

A membrane of a dielectric elastomer deforms when a voltage is applied through its thickness. The achievable voltage-induced deformation is strongly affected by how mechanical loads are applied. Large voltage-induced deformation has been demonstrated for a membrane under equal-biaxial forces, but only small voltage-induced deformation has been observed for a membrane under a uniaxial force. This difference is interpreted here theoretically. The theory also predicts that, when the deformation of a membrane is constrained in one direction, a voltage applied through the thickness of the membrane can cause it to deform substantially in the other direction. Experiments are performed on membranes under equal-biaxial forces and uniaxial forces, as well as on fiber-constrained membranes of two types: a dielectric elastomer membrane with carbon fibers on both faces, and two dielectric elastomer membranes sandwiching nylon fibers. The experimental observations are compared with the theory.

Predictive understanding of cell signaling network operation based on general prior knowledge but consistent with empirical data in a specific environmental context is a current challenge in computational biology. Recent work has demonstrated that Boolean logic can be used to create context-specific network models by training proteomic pathway maps to dedicated biochemical data; however, the Boolean formalism is restricted to characterizing protein species as either fully active or inactive. To advance beyond this limitation, we propose a novel form of fuzzy logic sufficiently flexible to model quantitative data but also sufficiently simple to efficiently construct models by training pathway maps on dedicated experimental measurements. Our new approach, termed constrained fuzzy logic (cFL), converts a prior knowledge network (obtained from literature or interactome databases) into a computable model that describes graded values of protein activation across multiple pathways. We train a cFL-converted network to experimental data describing hepatocytic protein activation by inflammatory cytokines and demonstrate the application of the resultant trained models for three important purposes: (a) generating experimentally testable biological hypotheses concerning pathway crosstalk, (b) establishing capability for quantitative prediction of protein activity, and (c) prediction and understanding of the cytokine release phenotypic response. Our methodology systematically and quantitatively trains a protein pathway map summarizing curated literature to context-specific biochemical data. This process generates a computable model yielding successful prediction of new test data and offering biological insight into complex datasets that are difficult to fully analyze by intuition alone.

The thermal conductivity of yttria-stabilized zirconia (YSZ) thermal barrier coatings increases with high-temperature aging. This common observation has been attributed to the densification of the coatings as porosity sinters out and pores and cracks spheroidize to minimize their surface energy. We show that the thermalconductivity of fully-dense 3 mol. % Y({2})O({3}) stabilized zirconia (3YSZ) also increases with high-temperature aging, indicating that densification and pore shape changes alone are not responsible for all the observed increase in thermalconductivity of coatings. Instead, there are also increases due to a combination of phase separation and grain growth. The increase in thermal conductivity can be described by a Larson–Miller parameter. It is also found that the increase in thermal conductivity with aging is greatest when measured at room temperature and decreases with increasing measurement temperature. Measured at 1000 °C, the thermal conductivity of zirconia is almost temperature independent and the changes in thermal conductivity with aging are less than 15%, even after aging for 50 h at 1400 °C.

Three dimensional curls (“hemi-helices”) consisting of multiple, periodic and alternating helical sections of opposite chiralities, separated by perversions, are one of a variety of complex shapes that can be produced by a simple generic process consisting of pre-straining one elastomeric strip, joining it side-by-side to another and then releasing the bi-strip. The initial wavelength of the hemi-helix and the number of perversions are determined by the strip cross-section, the constitutive behavior of the elastomer and the value of the pre-strain. The hemi-helix has no net twist. Topologically, the perversions separate regions of the hemi-helix deforming principally by bending from those where twisting dominates.

Cylindrical actuators are made with dielectric elastomer sheets stiffened with fibers in the hoop direction. When a voltage is applied through the thickness of the sheets, large actuation strains are achievable in the axial direction, with or without pre-straining and mechanical loading. For example, actuation strains of 35.8% for a cylinder with a prestrain of 40%, and 28.6% for a cylinder without pre-strain have been achieved without any optimization. Furthermore, the actuation strain is independent of the aspect ratio of the cylinder, so that both large strains and large displacements are readily actuated by using long cylinders.

Dielectric elastomer generators (DEGs) are attractive candidates for harvesting electrical energy from mechanical work since they comprise relatively few moving parts and large elastomer sheets can be mass produced. Successfully demonstrations of the DEG prototypes have been reported from a diverse of energy sources, including ocean waves, wind, flowing water and human movement. The energy densities achieved, however, are still small compared with theoretical predictions. We show that significant improvements in energy density (550 J/kg with an efficiency of 22.1%), can be achieved using an equi-biaxial mechanical loading configuration, one that produces uniform deformation and maximizes the capacitance changes. Analysis of the energy dissipations indicates that mechanical losses, which are caused by the viscous losses both within the acrylic elastomer and within the thread materials used for the load transfer assembly, limits the energy conversion efficiency of the DEG. Addressing these losses is suggested to increase the energy conversion efficiency of the DEG. © (2013) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.