Coated particle fuel to improve safety, design, economics in water-cooled and gas-cooled reactors

In the context of Inert Matrix Fuels (IMF), coated particles (CP)s may play an important role to reduce the problems connected to the plutonium (Pu) and minor actinides stockpiles. In addition, the coatings of the fuel kernels made of different low and high-density ceramic layers allow a safe containment of fission products in operational, accidental and disposal conditions. Pu-based CPs embedded in a ceramic matrix (e.g. graphite, like in HTR fuel elements) can be judged as a special cercer type. There is a wide variety of different coatings and kernel compositions that has not yet been explored beyond the HTR development. Thus it can be expected that the CP technology can be applied to other reactor systems, too. For getting full benefit of the fission product retention capability of the CPs, not only the particle design but also the core geometry as well as power densities etc. have to be adopted to each specific requirement.     

A scalable model for trilayer conjugated polymer actuators and its experimental validation

Conjugated polymers are promising actuation materials for bio/micromanipulation systems, biomimetic robots, and biomedical devices. For these applications, it is highly desirable to have predictive models available for feasibility study and design optimization. In this paper a scalable model is presented for trilayer conjugated polymer actuators based on J. Madden's diffusive-elastic-metal model. The proposed model characterizes actuation behaviors in terms of intrinsic material parameters and actuator dimensions. Experiments are conducted on polypyrrole actuators of different dimensions to validate the developed scaling laws for quasi-static force and displacement output, electrical admittance, and dynamic displacement response.     

Effects of moisture content on formaldehyde emission and mechanical properties of plywood

Wood is a hygroscopic material and has ability to exchange its moisture content with air. Many mechanical properties are affected by changes in moisture content below the fiber saturation point of wood. This study evaluates the formaldehyde emission and some mechanical properties of poplar and spruce plywood panels manufactured from rotary cut veneers having different moisture content by using urea–formaldehyde (UF) and modified urea formaldehyde by melamine (M+UF). Rotary cut veneers obtained from poplar and spruce logs were classified into three groups and veneers in each group were then conditioned in a climate chamber to either 4–6%, 10–12% or 16–18% moisture content. Plywood panels with three plies and in 6 mm thickness were manufactured for each group. Formaldehyde emission, shear strength, bending strength and modulus of elasticity values of plywood panels were determined. Best bonding results were obtained in plywood panels with veneers having 4–6% moisture content. Lowest mechanical properties were found for plywood panels manufactured from veneers conditioned to 16–18% moisture content. Formaldehyde emission values of poplar and spruce plywood panels decreased with increasing veneer moisture content for both glue types. Formaldehyde emission content of panels decreased with melamine addition into the urea formaldehyde glue mixture.     

A cellular neural network methodology for deformable object simulation.

This paper presents a new methodology to simulate soft object deformation by drawing an analogy between a cellular neural network (CNN) and elastic deformation. The potential energy stored in an elastic body as a result of a deformation caused by an external force is propagated among mass points by a nonlinear CNN. The novelty of the methodology is that: 1) CNN techniques are established to describe the potential energy distribution of the deformation for extrapolating internal forces and 2) nonlinear materials are modeled with nonlinear CNNs rather than geometric nonlinearity. Integration with a haptic device has been achieved for deformable object simulation with force feedback. The proposed methodology not only predicts the typical behaviors of living tissues, but it also accommodates isotropic, anisotropic, and inhomogeneous materials, as well as local and large-range deformation.     

Investigation of mechanical and creep properties of polypyrrole by depth-sensing indentation

In this study, we used depth-sensing indentation (DSI) technique to investigate some mechanical properties (reduced elastic modulus, indentation hardness, and creep) of polypyrrole (PPy) conducting polymer obtained with different support electrolyte concentration. The influence of support electrolyte concentration on these parameters was also determined. The order of doping degree of the samples was determined by cyclic voltammetry. The indentation load–displacement curves of the samples were obtained under different peak load levels with a 70 s holding time at maximum load. Reduced elastic modulus and hardness values were determined by analysis of these curves using the Feng–Ngan (F–N) and Tang–Ngan (T–N) methods, respectively. Both reduced elastic modulus (E _r) and indentation hardness (H) exhibited significant peak load dependence, i.e., indentation size effect (ISE). It was found that both E _r and H values decreased as the support electrolyte concentration was increased. This was explained by an increase in the free volume as the doping degree was raised. The creep behavior of the samples was monitored from the load holding segment of the load–unload curves. It was found that creep increases with the increasing support electrolyte concentration.     

All‐carbon hybrids for high performance supercapacitors

A hybrid nanostructure with partially reduced graphene oxide (rGO) and carbon nanofibers (CNFs) was fabricated and used as supercapacitor electrodes. A straightforward, environmentally friendly, and low‐cost microwave‐assisted reduction process was developed for the synthesis of rGO/CNF hybrid structures. The fabricated supercapacitor devices showed a specific capacitance of 95.3 F g^?1 and a superior long‐term cycling stability. A capacitance retention of more than 97% after 11 000 galvanostatic charge discharge cycles was obtained. These and other results reported in this paper indicate that high‐rate, all‐carbon, rGO/CNF hybrid nanostructures are highly promising supercapacitor electrode materials.     

Preparation and characterization of sepiolite‐poly(ethyl methacrylate) and poly(2‐hydroxyethyl methacrylate) nanocomposites

Poly(ethyl methacrylate) (PEMA) and poly(2‐hydroxyethyl methacrylate) (PHEMA) nanocomposites with sepiolite in pristine and silylated form were prepared using the solution intercalation method and characterized by the measurements of XRD, TEM, FTIR‐ATR, TG/DTG, and DSC. The TEM analysis indicated that the volume fraction of fibers in sepiolite decreased and the fiber bundles dispersed in PEMA and PHEMA at a nanometer scale. These results regarding TEM micrographs were in agreement with the data obtained by XRD. The increase in thermal stability of nanocomposites of PEMA is higher than that of PHEMA according to the data obtained from TG curves. The DTG analysis revealed that sepiolite/modified sepiolite caused some changes, as confirmed by FTIR in the thermal degradation mechanism of the polymers. T_g temperatures of PEMA and PHEMA usually increased upon the addition of sepiolite/modified sepiolite. In addition, modification of sepiolite with 3‐APTS had a slight influence on thermal properties of the nanocomposites. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Poly(styrene‐co‐maleic anhydride)‐graft‐fatty acids as novel solid–solid PCMs for thermal energy storage

A solid–solid phase change material (S‐SPCM) can store and release a specific amount of latent heat during its phase transition. In this regard, poly(styrene‐co‐maleic anhydride) (SMA)‐graft‐fatty acids (FA) copolymers were synthesized as novel S‐SPCMs for thermal energy storage (TES). The chemical structures of the SMA‐g‐FA copolymers were characterized by proton nuclear magnetic resonance (¹H NMR) and Fourier transform infrared (FT‐IR) spectroscopy techniques. The phase transformations of the copolymers form crystalline phase to amorphous phase were monitored using polarized optical microscopy (POM). The latent heat TES (LHTES) properties, thermal cycling reliability, and thermal stability of the S‐SPCMs were investigated by differential scanning calorimetry and thermogravimetric analysis methods. The SMA‐g‐FA copolymers produced as S‐SPCMs showed solid–solid phase transitions at about 40°C–60 °C range and had latent heat storage and release ability between 84 and 127 J/g, respectively. The S‐SPCMs had stable chemical structures and reliable LHTES characteristics even after 5,000 thermal cycling. They had reasonable thermal conductivity value changed in the range of 0.15–0.19 W/mK. Furthermore, it was concluded that the SMA‐g‐FA copolymers can be considered as promising S‐SPCMs for TES utilizations. POLYM. ENG. SCI., 59:E337–E347, 2019. © 2019 Society of Plastics Engineers