Liquid crystalline epoxy resin with improved thermal conductivity by intermolecular dipole–dipole interactions

To address tremendous needs for developing efficiently heat dissipating materials with lightweights, a series of liquid crystalline epoxy resins (LCEs) are designed and synthesized as thermally conductive matrix. All prepared LCEs possess epoxies at the molecular side positions and cyanobiphenyl mesogenic end groups. Based on several experimental results such as differential scanning calorimetry, polarized optical microscopy, and X‐ray diffraction, it is found that the LCEs exhibited liquid crystalline mesophases. When LCE is cured with a diamine crosslinker, the cured LCE maintains the oriented LC domain formed in the uncured state, ascribing to a presence of dipole–diploe and π–π interactions between cyanobiphenyl mesogenic end groups. Due to the anisotropic molecular orientation, the cured LCE exhibits a high thermal conductivity of 0.46 W m^?1 K^?1, which is higher than those of commercially available crystalline or amorphous epoxy resins. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 708–715     

Efficient preparation of UCl3 by ZnCl2 mediated chlorination

Journal of Radioanalytical and Nuclear Chemistry - U chlorination is demonstrated using electrochemical and chemical reactions with ZnCl2 in LiCl–KCl molten salts. Voltammetric studies...     

Design and Sensing Properties of a Self‐Assembled Supramolecular Oligomer

Supramolecular polymers are a class of macromolecules stabilized by weak non‐covalent interactions. These self‐assembled aggregates typically undergo stimuli‐induced reversible assembly and disassembly. They thus hold great promise as so‐called functional materials. In this work, we present the design, synthesis, and responsive behavior of a short supramolecular oligomeric system based on two hetero‐complementary subunits. These “monomers” consist of a tetrathiafulvalene‐functionalized calix[4]pyrrole (TTF‐C[4]P) and a glycol diester‐linked bis‐2,5,7‐trinitrodicyanomethylenefluorene‐4‐carboxylate (TNDCF), respectively. We show that when mixed in organic solvents, such as CHCl₃, CH₂ClCH₂Cl, and methylcyclohexane, supramolecular aggregation takes place to produce short oligomers stabilized by hydrogen bonding and donor–acceptor charge‐transfer (CT) interactions. The self‐associated materials were characterized by ¹H NMR and UV/Vis/NIR absorption spectroscopy, as well as by concentration‐ and temperature‐dependent absorption spectroscopy and dynamic light scattering (DLS) analyses of both the monomeric and oligomerized species. The self‐associated system produced from TTF‐C[4]P and TNDCF exhibits a concentration‐dependent aggregation behavior typical of supramolecular polymers. Further support for the proposed self‐assembly came from theoretical calculations. The fluorescence emitting properties of TNDCF are quenched under conditions that promote the formation of supramolecular aggregates containing TTF‐C[4]P and TNDCF. This quenching effect has been utilized as a probe for the detection of substrates in the form of anions (i.e., chloride) and nitroaromatic explosives (i.e., 1,3,5‐trinitrobenzene). Specifically, the addition of these substrates to mixtures of TTF‐C[4]P and TNDCF produced a fluorescence “turn‐on” response.     

Accuracy analysis on concentration determination of molecular iodine in gamma irradiated solutions

Journal of Radioanalytical and Nuclear Chemistry - The gamma irradiated aqueous samples containing I2 and I? were measured by two different analysis methods using an UV–VIS...     

Operation and preventive maintenance scheduling for containerships: Mathematical model and solution algorithm

This paper considers the problem of determining operation and maintenance schedules for a containership equipped with various subsystems during its sailing according to a pre-determined navigation schedule. The operation schedule, which specifies working time of each subsystem, determines the due-date of each maintenance activity and the maintenance schedule specifies the actual start time of each maintenance activity. The main constraints are subsystem requirements, workforce availability, working time limitation, and inter-maintenance time. To represent the problem mathematically, a mixed integer programming model is developed. Then, due to the complexity of the problem, we suggest a heuristic algorithm that minimizes the sum of earliness and tardiness between the due-date and the actual start time for each maintenance activity. Computational experiments were done on various test instances and the results are reported. In particular, a case study was done on a real instance and a significant amount of improvement is reported over the experience based conventional method.     

INVESTIGATION OF A QUASI-STEADY LIQUID CRYSTAL TECHNIQUE FOR FILM COOLING HEAT TRANSFER MEASUREMENTS

A quasi-steady technique to simultaneously measure the local heat transfer coefficient and cooling effectiveness on surfaces involving film cooling situations is investigated. The method employs a composite slab consisting of a very thin laminate layer of low-thermal-conductivity material superposed upon a highly conductive metal substrate. The resulting heat transfer in the thin laminate is described by one-dimensional conduction. A very thin coating of thermochromic liquid crystals sprayed onto the surface of the laminate is used in conjunction with a computer image processing procedure to provide local surface temperature data. This information, combined with the substrate and mainstream gas temperatures, provides highly detailed (90 video pixels/cm²) local convection heat transfer distributions. The method is used to conduct flat-plate film cooling experiments consisting of a single row of discrete holes inclined at 35 to the mainstream flow. The local surface temperature is influenced by the combination of two interacting fluid streams at different temperatures. A numerical analysis was performed to assess the assumptions underlying the data reduction procedure. The experimental uncertainty of 7% in the heat transfer coefficient is comparable to prior studies. Furthermore, the uncertainty of 5% in the film cooling effectiveness, coupled with the negligible lateral conduction errors, indicates the present technique offers a unique capability for accurate measurement of the local film cooling effectiveness.     

Characterization of Oil-Wax Gel with Higher Velocity Gradient

The properties of solid surface on oil-wax gel are one of the most important factors which decide the quality of products such as cosmetics. The thixotropic property of solid surface depends on the velocity gradient and it is increased with higher velocity gradient as controlling the morphology on solid surface of oil-wax gel. The morphological change of oil-wax gel in compliance with surface properties of wax matrix can cause different rheological behaviors. Rheological behavior of oil-wax gel regarding the surface transition range in accordance with shear strain was observed to characterize surface properties. In an earlier article, the morphological mechanism of causing surface transition range and the factors of influencing surface transition range were examined by studying the rheological behaviors of a solid-state emulsion. Here, we investigated, in the lattice structure terms, the morphological change of oil-wax gel by measuring surface transition range depending on velocity gradient, which could influence the hardness and sweating phenomenon. We confirmed that the morphological change of oil-wax gel was accompanied by crystal size, crystal conformation, the degree of crystallinity. Surface transition range depending on velocity gradient was shown in large and regular lattice structure of oil-wax gel better than small and irregular one.