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1. Planar Compliance Realization With Two 3-Joint Serial Mechanisms

   https://doi.org/10.1115/1.4053284  

   Huang, Shuguang; Schimmels, Joseph M. (October 2022, Journal of Mechanisms and Robotics)

   Abstract In this paper, the realization of any specified planar compliance with two 3R serial elastic mechanisms is addressed. Using the concept of dual elastic mechanisms, it is shown that the realization of a compliant behavior with two serial mechanisms connected in parallel is equivalent to its realization with a 6-spring fully parallel mechanism. Since the spring axes of a 6-spring parallel mechanism indicate the geometry of a dual 3R serial mechanism, a new synthesis procedure for the realization of a stiffness matrix with a 6-spring parallel mechanism is first developed. Then, this result is extended to a geometric construction-based synthesis procedure for two 3-joint serial mechanisms. 

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2. Developing elastic mechanisms: ultrafast motion and cavitation emerge at the millimeter scale in juvenile snapping shrimp

   https://doi.org/10.1242/jeb.244645  

   Harrison, Jacob S.; Patek, S. N. (February 2023, Journal of Experimental Biology)

   ABSTRACT Organisms such as jumping froghopper insects and punching mantis shrimp use spring-based propulsion to achieve fast motion. Studies of elastic mechanisms have primarily focused on fully developed and functional mechanisms in adult organisms. However, the ontogeny and development of these mechanisms can provide important insights into the lower size limits of spring-based propulsion, the ecological or behavioral relevance of ultrafast movement, and the scaling of ultrafast movement. Here, we examined the development of the spring-latch mechanism in the bigclaw snapping shrimp, Alpheus heterochaelis (Alpheidae). Adult snapping shrimp use an enlarged claw to produce high-speed strikes that generate cavitation bubbles. However, until now, it was unclear when the elastic mechanism emerges during development and whether juvenile snapping shrimp can generate cavitation at this size. We reared A. heterochaelis from eggs, through their larval and postlarval stages. Starting 1 month after hatching, the snapping shrimp snapping claw gradually developed a spring-actuated mechanism and began snapping. We used high-speed videography (300,000 frames s−1) to measure juvenile snaps. We discovered that juvenile snapping shrimp generate the highest recorded accelerations (5.8×105±3.3×105 m s−2) for repeated-use, underwater motion and are capable of producing cavitation at the millimeter scale. The angular velocity of snaps did not change as juveniles grew; however, juvenile snapping shrimp with larger claws produced faster linear speeds and generated larger, longer-lasting cavitation bubbles. These findings establish the development of the elastic mechanism and cavitation in snapping shrimp and provide insights into early life-history transitions in spring-actuated mechanisms. 

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3. Model Reveals Joint Properties for Which Co-contracting Antagonist Muscles Increases Joint Stiffness.

   Kudyba, Isabella M.; Szczecinski, Nicholas S. (August 2023, Biomimetic and Biohybrid Systems. Living Machines 2023.)

   Meder, F.; Hunt, A.; Margheri, L.; Mura, A.; Mazzolai, B. (Ed.)

   A challenge in robotics is to control interactions with the environment by modulating the stiffness of a manipulator’s joints. Smart servos are controlled with proportional feedback gain that is analogous to torsional stiffness of an animal’s joint. In animals, antagonistic muscle groups can be temporarily coactivated to stiffen the joint to provide greater opposition to external forces. However, the joint properties for which coactivation increases the stiffness of the joint remain unknown. In this study, we explore possible mechanisms by building a mathematical model of the stick insect tibia actuated by two muscles, the extensor and flexor tibiae. Muscle geometry, passive properties, and active properties are extracted from the literature. Joint stiffness is calculated by tonically activating the antagonists, perturbing the joint from its equilibrium angle, and calculating the restoring moment generated by the muscles. No reflexes are modeled. We estimate how joint stiffness depends on parallel elastic element stiffness, the shape of the muscle activation curve, and properties of the force-length curve. We find that co-contracting antagonist muscles only stiffens the joint when the peak of the force-length curve occurs at a muscle length longer than that when the joint is at equilibrium and the muscle force versus activation curve is concave-up. We discuss how this information could be applied to the control of a smart servo actuator in a robot leg. 

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4. Model Reveals Joint Properties for Which Co-contracting Antagonist Muscles Increases Joint Stiffness

   https://doi.org/10.1007/978-3-031-39504-8_1  

   Kudyba, Isabella; Szczecinski, Nicholas S (August 2023, Springer, Cham.)

   A challenge in robotics is to control interactions with the environment by modulating the stiffness of a manipulator’s joints. Smart servos are controlled with proportional feedback gain that is analogous to torsional stiffness of an animal’s joint. In animals, antagonistic muscle groups can be temporarily coactivated to stiffen the joint to provide greater opposition to external forces. However, the joint properties for which coactivation increases the stiffness of the joint remain unknown. In this study, we explore possible mechanisms by building a mathematical model of the stick insect tibia actuated by two muscles, the extensor and flexor tibiae. Muscle geometry, passive properties, and active properties are extracted from the literature. Joint stiffness is calculated by tonically activating the antagonists, perturbing the joint from its equilibrium angle, and calculating the restoring moment generated by the muscles. No reflexes are modeled. We estimate how joint stiffness depends on parallel elastic element stiffness, the shape of the muscle activation curve, and properties of the force-length curve. We find that co-contracting antagonist muscles only stiffens the joint when the peak of the force-length curve occurs at a muscle length longer than that when the joint is at equilibrium and the muscle force versus activation curve is concave-up. We discuss how this information could be applied to the control of a smart servo actuator in a robot leg. 

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5. Convex Optimization for Spring Design of Parallel Elastic Actuators

   Guo, S.; Gregg, R.; Bolivar-Nieto, E. (January 2022, Proceedings of the American Control Conference)

   Elastic actuation can improve human-robot interaction and energy efficiency for wearable robots. Previous work showed that the energy consumption of series elastic actuators can be a convex function of the series spring compliance. This function is useful to optimally select the series spring compliance that reduces the motor energy consumption. However, series springs have limited influence on the motor torque, which is a major source of the energy losses due to the associated Joule heating. Springs in parallel to the motor can significantly modify the motor torque and therefore reduce Joule heating, but it is unknown how to design springs that globally minimize energy consumption for a given motion of the load. In this work, we introduce the stiffness design of linear and nonlinear parallel elastic actuators via convex optimization. We show that the energy consumption of parallel elastic actuators is a convex function of the spring stiffness and compare the energy savings with that of optimal series elastic actuators. We analyze robustness of the solution in simulation by adding uncertainty of 20% of the RMS load kinematics and kinetics for the ankle, knee, and hip movements for level-ground human walking. When the winding Joule heating losses are dominant with respect to the viscous losses, our optimal PEA designs outperform SEA designs by further reducing the motor energy consumption up to 63%. Comparing to the linear PEA designs, our nonlinear PEA designs further reduced the motor energy consumption up to 31%. From our convex formulation, our global optimal nonlinear parallel elastic actuator designs give two different elongation-torque curves for positive and negative elongation, suggesting a clutching mechanism for the final implementation. In addition, the different torque-elongation profiles for positive and negative elongation for nonlinear parallel elastic actuators can cause sensitivity of the energy consumption to changes in the nominal load trajectory. 

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