Validation of MAAP model enhancement for Fukushima Dai-ichi accident analysis with Phenomena Identification and Ranking Table (PIRT)

The Modular Accident Analysis Program (MAAP) model enhancement items to improve the simulation capability for molten corium behavior in the accidents at the Fukushima Dai-ichi nuclear power plants were validated with the Phenomena Identification and Ranking Table (PIRT). The importance ranks of the identified phenomena were evaluated for each time phase through brainstorming and discussion with the experts in the Atomic Energy Society of Japan and the members of the MAAP model enhancement project. When the current MAAP evaluation models were reviewed with the PIRT, it is found that 95 of the 386 high-ranked phenomena were not considered in MAAP 5.0.1. While 62 of these phenomena will have been addressed in the MAAP enhancement project and 25 others are not suitable to be analyzed by MAAP, 8 important phenomena should be considered in post-MAAP enhancement project with additional experiments or fundamental studies.     

Specifying and proving properties of timed I/O automata using Tempo

Timed I/O automata (TIOA) is a mathematical framework for modeling and verification of distributed systems that involve discrete and continuous dynamics. TIOA can be used for example, to model a real-time software component controlling a physical process. The TIOA model is sufficiently general to subsume other models in use for timed systems. The Tempo Toolset, currently under development, is aimed at supporting system development based on TIOA specifications. The Tempo Toolset is an extension of the IOA toolkit, which provides a specification simulator, a code generator, and both model checking and theorem proving support for analyzing specifications. This paper focuses on the modeling of timed systems and their properties with TIOA and on the use of TAME4TIOA, the TAME (Timed Automata Modeling Environment) based theorem proving support provided in Tempo, for proving system properties, including timing properties. Several examples are provided by way of illustration.     

Enzymatic properties and transglycosylation of α-galactosidase from Penicillium oxalicum SO

Penicillium oxalicum SO α-galactosidase demonstrated weak hydrolysing activity but a high rate of transglycosylation in the reaction with melibiose, where the major product was 6-α-galactosyl melibiose. The transfer ratio was 83.6% and was maintained over a long reaction time of 80 h. The molecular weight was estimated to be 124,000 by SDS–PAGE. The optimal pH was ∼3 and a stable pH, with a range of 2.4–9.5, was found. The optimal temperature was ∼60 °C and the activity was stable below 60 °C. With respect to acceptor specificity, mono-alcohols, sugar alcohols and sugars were poor acceptors, but the di-alcohol ethylene glycol and the tri-alcohol glycerin were good acceptors. The percentage of transglycosylation to glycerin increased up to 41.7%, as that to melibiose decreased, with the initial glycerin concentration of 40%. The production of α-d-galactosylglycerol was 293 mg for each gram of melibiose used by the enzymatic reaction.     

Sintering Metal–Organic Framework Gels for Application as Structural Adhesives

Metal–organic frameworks (MOFs)/coordination polymers are promising materials for gas separation, fuel storage, catalysis, and biopharmaceuticals. However, most applied research on MOFs is limited to these functional materials thus far. This study focuses on the potential of MOFs as structural adhesives. A sintering technique is applied to a zeolitic imidazolate framework-67 (ZIF-67) gel that enables the joining of Cu substrates, resulting in a shear strength of over 30 MPa, which is comparable to that of conventional structural adhesives. Additionally, systematic experiments are performed to evaluate the effects of temperature and pressure on adhesion, indicating that the removal of excess 2-methylimidazole and the by-product (acetic acid) from the sintered material by vaporization results in a microstructure composed of large spherical ZIF-67 crystals that are densely aggregated, which is essential for achieving a high shear strength.     

Studies on bulk diffusion and local diffusion of polystyrene in melt

Results of bulk viscosity (η) and local viscosity (ξ) of various molecular weights of polystyrene (PS) have been reported. In this paper the relationship between η and bulk diffusion coefficient (D_B), and that between ξ and local diffusion coeffizient (D_L) are presented. Data obtained lead to several conclusions. From the results of unperturbed dimensions and a universal constant (Φ), it was found that F. Bueche's equation D_B · η = const. is valid for polystyrenes with molecular weights over 600. Temperature and component concentration dependence of bulk diffusion coefficient for the two-component blend system may be interpreted in terms of the free volume theory. At an iso-free volume state, molecular weight dependences of bulk diffusion coefficients for both PS of narrow distribution of molecular weight and blend PS can be composed to a single curve, which is composed of two straight lines in a double logarithmic presentation with intersection at M_w = 1.78 × 10⁴ g/mol. The slopes of these two lines were ? 1.0 and ? 3.3, respectively. The product D_L · ξ was determined to be 1.10 × 10^?7 (c.g.s) for n-paraffines from the data of self-diffusion coefficient and ξ. This made it possible to determine D_L from ξ. For higher molecular weights of PS, log D_B is a linear function of log M_w while log D_L stays almost constant.     

Calculating process control parameters from steady state operating data

The tutorial paper will show that chemical process control parameters can be obtained from steady state operating data in combination with simple algebraic equations. The parameters include steady state process gain, feedforward control factor and approximate process time constant. Here, we treat ‘self-regulating’ processes first. Integrating processes and unstable processes are treated separately, unlike the standard method of setting up linear differential equations followed by Laplace transformations. With the standard method, a steady state portion of dynamic response, if there is any, appears as a part of equations of a complex variable. Many control engineers in the chemical industries who might have studied the method, do not use it because of mathematical difficulties. Instead, they may resort to plant tests that are often time consuming and costly. The parameters obtained by this paper's method will aid improvement of control systems. We will address the relation of this method with that of commercial software, which implement advanced process controls based on plant tests.     

Tough and Self‐Recoverable Thin Hydrogel Membranes for Biological Applications

Tough and self‐recoverable hydrogel membranes with micrometer‐scale thickness are promising for biomedical applications, which, however, rarely be realized due to the intrinsic brittleness of hydrogels. In this work, for the first time, by combing noncovalent DN strategy and spin‐coating method, we successfully fabricated thin (thickness: 5–100 µm), yet tough (work of extension at fracture: 10⁵–10⁷ J m^?3) and 100% self‐recoverable hydrogel membranes with high water content (62–97 wt%) in large size (≈100 cm²). Amphiphilic triblock copolymers, which form physical gels by self‐assembly, were used for the first network. Linear polymers that physically associate with the hydrophilic midblocks of the first network, were chosen for the second network. The inter‐network associations serve as reversible sacrificial bonds that impart toughness and self‐recovery properties on the hydrogel membranes. The excellent mechanical properties of these obtained tough and thin gel membranes are comparable, or even superior to many biological membranes. The in vitro and in vivo tests show that these hydrogel membranes are biocompatible, and postoperative nonadhesive to neighboring organs. The excellent mechanical and biocompatible properties make these thin hydrogel membranes potentially suitable for use as biological or postoperative antiadhesive membranes.     

Relationship between degree of polymerization and optical and thermal properties of fluorene in polycarbonate polymers

The influences of average degree of polymerization (D_p) and terminal group on thermal and optical properties of high refractive indexed transparent polymers were investigated. In this study, 9,9‐bis[4–(2‐hydroxyethoxy) phenyl] fluorene (BPEF) homo polymer was selected because it has been used as a representative monomer in high refractive index polymers as well as its unique property. BPEF has stable amorphous phase and reacts like a polymer. Its unique reaction allows continuous investigation from monomer to polymer. For hydroxyl‐terminated polymer, the refractive index (n_d) decreased with increasing D_p. On the other hand, for a phenolic‐terminated group, n_d increased with increasing D_p, and both converged to same value in high D_p region. As for glass transition temperatures (T_g), both terminal group series were increased as D_p increased. Though T_g of hydroxyl‐terminated polymer was higher than that of phenolic‐terminated polymer in the low D_p region, both converged to the same value and the inverse number of T_g had linear correlation against the weight percentage of carbonyl groups (CO), which was calculated by D_p. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45042.     

Elastomeric Fibrous Hybrid Scaffold Supports In Vitro and In Vivo Tissue Formation

Biomimetic materials with biomechanical properties resembling those of native tissues while providing an environment for cell growth and tissue formation, are vital for tissue engineering (TE). Mechanical anisotropy is an important property of native cardiovascular tissues and directly influences tissue function. This study reports fabrication of anisotropic cell‐seeded constructs while retaining control over the construct's architecture and distribution of cells. Newly synthesized poly‐4‐hydroxybutyrate (P4HB) is fabricated with a dry spinning technique to create anelastomeric fibrous scaffold that allows control of fiber diameter, porosity, and rate ofdegradation. To allow cell and tissue ingrowth, hybrid scaffolds with mesenchymalstem cells (MSCs) encapsulated in a photocrosslinkable hydrogel were developed. Culturing the cellularized scaffolds in a cyclic stretch/flexure bioreactor resulted in tissue formation and confirmed the scaffold's performance under mechanical stimulation. In vivo experiments showed that the hybrid scaffold is capable of withstanding physiological pressures when implanted as a patch in the pulmonary artery. Aligned tissue formation occurred on the scaffold luminal surface without macroscopic thrombus formation. This combination of a novel, anisotropic fibrous scaffold and a tunable native‐like hydrogel for cellular encapsulation promoted formation of 3D tissue and provides a biologically functional composite scaffold for soft‐tissue engineering applications.     

Photo-induced valence tautomerism in Co complexes

A number of photofunctional molecular compounds have been developed recently. Typical examples of these are phototunable valence tautomeric compounds, which are now attracting great attention. When the charge-transfer bands of some Co valence tautomeric compounds are excited at low temperature, metastable redox isomers can be created after irradiation. The lifetimes of the metastable states can be more than several hours. These transformations can involve changes in the magnetic properties of the compounds, as well as their color. Hence, these compounds can be regarded as novel photomagnetic materials. The photoresponsive behaviors of these valence tautomeric compounds are similar to those of spin-crossover complexes (light-induced excited spin-state trapping effects).