Raben Jaime S, Hariharan Prasanna, Robinson Ronald, Malinauskas Richard, Vlachos Pavlos P
School of Biomedical Engineering and Sciences, Virginia Tech, Blacksburg, VA, USA.
Food and Drug Administration, Silver Spring, MD, USA.
Cardiovasc Eng Technol. 2016 Mar;7(1):7-22. doi: 10.1007/s13239-015-0251-9. Epub 2015 Dec 1.
We present advanced particle image velocimetry (PIV) processing, post-processing, and uncertainty estimation techniques to support the validation of computational fluid dynamics analyses of medical devices. This work is an extension of a previous FDA-sponsored multi-laboratory study, which used a medical device mimicking geometry referred to as the FDA benchmark nozzle model. Experimental measurements were performed using time-resolved PIV at five overlapping regions of the model for Reynolds numbers in the nozzle throat of 500, 2000, 5000, and 8000. Images included a twofold increase in spatial resolution in comparison to the previous study. Data was processed using ensemble correlation, dynamic range enhancement, and phase correlations to increase signal-to-noise ratios and measurement accuracy, and to resolve flow regions with large velocity ranges and gradients, which is typical of many blood-contacting medical devices. Parameters relevant to device safety, including shear stress at the wall and in bulk flow, were computed using radial basis functions. In addition, in-field spatially resolved pressure distributions, Reynolds stresses, and energy dissipation rates were computed from PIV measurements. Velocity measurement uncertainty was estimated directly from the PIV correlation plane, and uncertainty analysis for wall shear stress at each measurement location was performed using a Monte Carlo model. Local velocity uncertainty varied greatly and depended largely on local conditions such as particle seeding, velocity gradients, and particle displacements. Uncertainty in low velocity regions in the sudden expansion section of the nozzle was greatly reduced by over an order of magnitude when dynamic range enhancement was applied. Wall shear stress uncertainty was dominated by uncertainty contributions from velocity estimations, which were shown to account for 90-99% of the total uncertainty. This study provides advancements in the PIV processing methodologies over the previous work through increased PIV image resolution, use of robust image processing algorithms for near-wall velocity measurements and wall shear stress calculations, and uncertainty analyses for both velocity and wall shear stress measurements. The velocity and shear stress analysis, with spatially distributed uncertainty estimates, highlights the challenges of flow quantification in medical devices and provides potential methods to overcome such challenges.
我们展示了先进的粒子图像测速(PIV)处理、后处理和不确定性估计技术,以支持医疗器械计算流体动力学分析的验证。这项工作是之前由美国食品药品监督管理局(FDA)赞助的多实验室研究的扩展,该研究使用了一种被称为FDA基准喷嘴模型的模拟医疗器械几何形状。在模型的五个重叠区域,针对喷嘴喉部雷诺数为500、2000、5000和8000的情况,使用时间分辨PIV进行了实验测量。与之前的研究相比,图像的空间分辨率提高了两倍。使用总体相关性、动态范围增强和相位相关性对数据进行处理,以提高信噪比和测量精度,并解析具有大速度范围和梯度的流动区域,这在许多与血液接触的医疗器械中很常见。使用径向基函数计算与设备安全相关的参数,包括壁面和整体流动中的剪应力。此外,根据PIV测量计算了场内空间分辨的压力分布、雷诺应力和能量耗散率。速度测量不确定性直接从PIV相关平面估计,并且使用蒙特卡罗模型对每个测量位置的壁面剪应力进行不确定性分析。局部速度不确定性变化很大,并且在很大程度上取决于局部条件,如粒子播种、速度梯度和粒子位移。当应用动态范围增强时,喷嘴突然扩张段低速区域的不确定性大幅降低了一个数量级以上。壁面剪应力不确定性主要由速度估计的不确定性贡献主导,结果表明其占总不确定性的90 - 99%。本研究通过提高PIV图像分辨率、使用稳健的图像处理算法进行近壁速度测量和壁面剪应力计算以及对速度和壁面剪应力测量进行不确定性分析,在PIV处理方法上比之前的工作有所进步。具有空间分布不确定性估计的速度和剪应力分析突出了医疗器械中流动量化的挑战,并提供了克服此类挑战的潜在方法。