Physics‐based model of lithium‐ion batteries running on a circuit simulator

The authors developed a physics‐based equivalent circuit model of a lithium‐ion battery (LIB) whose parameters are continually updated, reflecting the theoretical calculation results of the Butler‐Volmer equation, diffusion equations of the lithium‐ion and lithium, and Nernst equations of the liquid and solid phases. The developed model was applied to the charge/discharge simulations of an LIB, and the experimental and simulated results of constant current discharges and pulsed‐charge/discharge were found to be in excellent agreement. In particular, using the developed model, analyzing transient responses of the LIB derived from the transition of the electric double layer charging to the electrode reaction is possible. These results demonstrate that the electrochemical performance of an LIB can be calculated on a circuit simulator using the developed model.     

Coordinate-Based Evaluation of Two Dimensional Artefact Calibration Value as the Reference Standards for Coordinate Measuring Machines

Two dimensional standards are important materials which are used in the calibration and the verification of coordinate measuring machines. In several countries, the national metrology institutes or accredit laboratories provide the calibration services of the two dimensional standards such as ball plates, hole plates and grid plates. The metrological equivalence of the measurement standards among the calibration providers is validated through the key comparison program. In the previous key comparison for a ball plate and a hole plate, the equivalences among the participants’ calibration results were verified on the distances between the No. 1 ball/hole (i.e., the origins of the workpiece coordinates) and other balls/holes on the plates respectively. The essential measurands of the two dimensional standards are the coordinates of the feature points, however, the measurement equivalences on them have not been verified. In this study, the authors propose the coordinates-based evaluation of the reference values and their uncertainty in two dimensional standard calibration comparison.     

Determination of atomistic deformation of tricalcium silicate paste with high-volume fly ash

We examined the effect of incorporating high-volume fly ash on the atomic arrangement and interatomic deformation behavior of calcium silicate hydrates in tricalcium silicate paste upon exposure to external forces. The interatomic structural changes and strains under compressive load were assessed using synchrotron in situ high-energy X-ray scattering-based atomic pair distribution function analysis. Three different types of strains, which were (a) macroscopic strains from gauges on the surfaces of specimen, (b) strains in a reciprocal space (Bragg peak shift), and (c) strains in real space (PDF peak shift), were compared to each other. All monitored and calculated strains for tricalcium silicate-fly ash (50 wt% fly ash) paste were compared with the counterparts of the pure tricalcium silicate paste. Pair distribution function analysis in the range of r < 10 Å indicated that the atomic arrangement of tricalcium silicate-fly ash was similar to that of synthetic calcium silicate hydrates followed by that of pure tricalcium silicate paste. Moreover, the pair distribution function refinement results revealed that the calcium silicate hydrate structure in tricalcium silicate-fly ash paste was similar to tobermorite 11 Å, unlike that in pure tricalcium silicate paste. The interatomic strain of tricalcium silicate-fly ash in the real space (r < 20 Å) was smaller than that of tricalcium silicate under compression, which suggested that the incompressibility of calcium silicate hydrates at atomistic scale was enhanced by the incorporation of fly ash into it. This was likely to be caused by the increased silicate polymerization of calcium silicate hydrates, which was attributed to the increase in the amount of silicate in their structure via the addition of fly ash.     

Carbon radicals generated by solid polymers: Electron spin resonance spectroscopy for detection of species in water

Radicals generated in plastic medical devices (solid phase) by γ-rays or electron-beam irradiation during sterilization are known to cause oxidation of protein drugs, resulting in a loss or reduction in drug efficacy. The generation of radical species in water by the radical species in solid polymers has not been proved. Using electron spin resonance (ESR) spectroscopy, we confirm the generation of new radicals in water by γ-ray irradiated cyclic olefin polymers (COP). ESR measurements are obtained using 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPOL) as a spin probe and 5-(2,2-dimethyl-1,3-propoxycyclophosphoryl)-5-methyl-1-pyrroline N-oxide (CYPMPO) as a spin trap, in which the irradiated COP was immersed. The ESR signals indicate the TEMPOL radicals decline over time, suggesting the generation of new radicals. Conversely, the characteristic ESR signals of the adduct formed by the reaction between CYPMPO and the hydroxyl radical are observed. Thus, hydroxyl radicals are generated because of the migration of the radicals from COP to water. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48604.     

Deoxidation of Ti Melt by Newly Developed Two-Step Plasma Arc Melting Process Using Hydrogen

Metallurgical and Materials Transactions B - A two-step plasma arc melting process, comprising a first step under Ar-30&nbsp;pct H2 gas flow and the second step under Ar gas flow, has been...     

Properties evaluation and fabrication of green clay reformulated from water sludge

Water sludge from Sungai Dua Penang fresh water processing plant has been successfully converted into functional pottery clay with improved physicochemical behavior and properties. Water sludge was generally made of kaolinite mineral that consisted of silica and alumina. At 7 h of milling duration, water sludge demonstrated a narrow particle size distribution at the size range of 107–150 µm. Water sludge owned a specific surface area of 27 m²/g with 8.8 nm (diameter) pore size and 0.05 cm³/g pore volume. Plasticity of clay body increased when clay formulation involved fine particles, e.g. water sludge or bentonite, which promote water adsorption ability. Fine particles with large surface area and better compaction also explained the enhanced hardness of pottery clay. The incorporation of clay minerals such as bentonite and sodium silicate into the formulation has facilitated metals immobilization within the clay body. Final clay product has a terra cotta color and performed a uniform shrinkage without obvious fracture. The fabrication of pottery wares from water sludge with minimized metals leakage has not only higher reutilize value but also a cost effective green method for handling waste and environmental issues.