RESUMEN
To measure the 3D microdisplacement of a self-oscillating polymer gel driven by the Belousov-Zhabotinsky reaction, we propose, to the best of our knowledge, a new particle detection and tracking method based on a phase image/volume template matching using digital holographic microscopy. We demonstrate the precision of the proposed method and compare it with conventional approaches. The method is applied to 3D measurement of the motions of particles attached to the surface of an oscillating gel. Measurement results show that the local area of the gel oscillates periodically, and the motion propagates throughout the gel. Our method can measure rapid and complex 3D microdisplacement change.
RESUMEN
[Purpose] The aims of this study were to evaluate the type and extent of error in the measurement of range of motion and to evaluate the effect of evaluators' proficiency level on measurement error. [Subjects and Methods] The participants were 45 university students, in different years of their physical therapy education, and 21 physical therapists, with up to three years of clinical experience in a general hospital. Range of motion of right knee flexion was measured using a universal goniometer. An electrogoniometer attached to the right knee and hidden from the view of the participants was used as the criterion to evaluate error in measurement using the universal goniometer. The type and magnitude of error were evaluated using the Bland-Altman method. [Results] Measurements with the universal goniometer were not influenced by systematic bias. The extent of random error in measurement decreased as the level of proficiency and clinical experience increased. [Conclusion] Measurements of range of motion obtained using a universal goniometer are influenced by random errors, with the extent of error being a factor of proficiency. Therefore, increasing the amount of practice would be an effective strategy for improving the accuracy of range of motion measurements.
RESUMEN
Fluoride-shuttle batteries (FSBs), which are based on fluoride-ion transfer, have attracted attention because of their high theoretical energy densities. The fluorination and defluorination reactions at the electrodes are the possible rate-determining steps in FSBs, and understanding the mechanism is important to achieve smooth charge/discharge. In this study, we discuss the thermodynamically favored pathways for the fluorination and defluorination reactions and compare the reactions through the solid-solution and two-phase-coexistent states by density functional theory (DFT) calculations. The free energies of the solid-solution and two-phase states approximate the energies calculated by DFT, and their accuracy was validated by comparison with experimental formation enthalpies and free energies. The relative formation enthalpies of typical, transition, and relativistic metal (Tl, Pb, and Bi) fluorides are well reproduced by DFT calculations within 0.1, 0.2, and 0.4 eV, respectively. We also show that the reaction pathway can be determined by comparing the formation enthalpies of the metal fluoride H, a fluorine vacancy HV, and an interstitial fluorine defect HI from the simple selection rule. The enthalpy relation of HI > H > -HV observed in all the calculations strongly suggests that fluorination and defluorination in FSB electrodes occur by a two-phase reaction. This fluorination and defluorination mechanism will be useful to clarify the rate-determining step in FSBs.