合作式连续机器人的动态操纵和刚度调节:理论与实验

Amir Jalali, Farrokh Janabi-Sharifi
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摘要

协同连续机器人(CCR)由多个耦合连续臂组成,可协同执行操纵任务。它们可以通过提供额外的刚度来大大提高单个连续臂的性能,从而提高机器人的精度、有效载荷能力和动态稳定性。本研究旨在研究肌腱驱动的支撑型 CCR(S-CCR)的刚度分析。为此,首先提出了一个用于 S-CCR 动态数学表述和数值求解的通用框架,获得了其对复杂场景的动态响应,并对模型的准确性进行了实验评估。然后,研究了 S-CCR 的刚度调节能力。肌腱驱动的 S-CCR 具有随结构配置改变刚度的潜在能力,可在设计层面提供主动刚度控制。因此,在本研究中,研究了支撑臂与操作臂的连接点位置/角度以及支撑臂施加的肌腱限制对机器人刚度的影响,进而对动态有效载荷操纵的影响,并提出了实用的解决方案,以开发一种简单而有效的刚度控制机制。研究结果表明,仅通过模块化连接器设计,典型的 S-CCR 就能在操纵过程中将刚度提高 84%,为 CCR 的刚度调节带来了新的机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dynamic Manipulation and Stiffness Modulation of Cooperative Continuum Robots: Theory and Experiment
Cooperative continuum robots (CCRs) are composed of multiple coupled continuum arms to cooperatively conduct manipulation tasks. They can highly enhance the performance of individual continuum arms by providing extra stiffness, leading to increased accuracy, payload capacity, and dynamic stability of the robot. This study aimed to investigate the stiffness analysis of tendon-driven supportive-type CCRs (S-CCRs). For this purpose, first, a generalized framework for the dynamic mathematical formulation and numerical solution of S-CCRs was proposed and their dynamic response to complex scenarios was obtained and the accuracy of the model was experimentally evaluated. Then, the capability of stiffness modulation of S-CCRs was studied. Tendon-driven S-CCRs are potentially capable of changing the stiffness with structural configuration, providing active stiffness control at the design level. Hence, in this study, the effects of the connection point location/angle of the supportive arms to the operative arm, as well as the imposed tendon limitations of the supportive arm on the stiffness of the robot, and consequently on the dynamic payload manipulation were studied and practical solutions were proposed to develop a simple but effective stiffness control mechanism. It showed that a typical S-CCR can increase its stiffness, just by a modular connector design up to 84% during manipulation, bringing a novel opportunity for stiffness modulation of CCRs.
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