Influence of covalent and non-covalent modification of graphene on the mechanical,thermal and electrical properties of epoxy/graphene nanocomposites: a review

Abstract

Graphene is emerged as a highly sought after reinforcing filler for epoxy matrix in view of its superior electrical, mechanical and thermal properties. Dispersion of low concentration of graphene can significantly enhance the epoxy/graphene nanocomposites properties. Dispersion of graphene in epoxy matrix depends on processing protocols used, and interfacial interaction between epoxy matrix and graphene. Interfacial interaction between epoxy matrix and graphene can be achieved by covalent and non-covalent modification of graphene. This paper comprehensively review the influence of different processing protocols adopted for the processing of epoxy/graphene nanocomposites, and its effect on mechanical, thermal and electrical properties. In addition, covalent and non-covalent strategies adopted for modification of graphene, and its influence on mechanical, thermal and electrical properties of epoxy/graphene nanocomposites are extensively discussed. The future challenges associated with graphene reinforced epoxy nanocomposites processing have been discussed.     

New band systems of NiBr molecule in visible region

Thermal emission spectrum of NiBr molecule excited by vacuum graphite tube furnace revealed the existence of ten new band sub-systems in the region λλ 5540-4720 Å which were attributed toA→X,B→X,C→X andD→X transitions. Vibrational analysis was carried out for each of the systems mentioned above.A ² Δ has been suggested as the ground state of NiBr molecule with an electronic interval of about 533 cm^?1. Transitions responsible for NiBr spectrum appear to be of the type²π–²Δ and²Δ–²Δ.     

On the low-temperature thermal conductivity of Ni-doped Al2O3

An attempt is made to explain the lower resonance anomaly in the thermal conductivity of Ni-doped Al₂O₃ by using τ_r ～ ω^-4s(ω² ? ω²_r)². An agreement between theory and experiment needs s = 0.71, and this is interpreted to mean that the frequency dependence of impurity-phonon coupling is approximately described by ω^0.71 for phonons having frequencies in close neighbourhood of ω_r.     

Physicochemical characterization of an Indian traditional medicine, Jasada Bhasma: detection of nanoparticles containing non-stoichiometric zinc oxide

Herbs and minerals are the integral parts of traditional systems of medicine in many countries. Herbo-Mineral medicinal preparations called Bhasma are unique to the Ayurvedic and Siddha systems of Indian Traditional Medicine. These preparations have been used since long and are claimed to be the very effective and potent dosage form. However, there is dearth of scientific analytical studies carried out on these products, and even the existing ones suffer from incomplete analysis. Jasada Bhasma is a unique preparation of zinc belonging to this class. This particular preparation has been successfully used by traditional practitioners for the treatment of diabetes and age-related eye diseases. This work presents a first comprehensive physicochemical characterization of Jasada Bhasma using modern state-of-the-art techniques such as X-ray photoelectron spectroscopy (XPS), inductively coupled plasma (ICP), elemental analysis with energy dispersive X-ray analysis (EDAX), dynamic light scattering (DLS), and transmission electron microscopy (TEM). Our analysis shows that the Jasada Bhasma particles are in oxygen deficient state and a clearly identifiable fraction of particles are in the nanometer size range. These properties like oxygen deficiency and nanosize particles in Jasada Bhasma might impart the therapeutic property of this particular type of medicine. A. C. Joshi: Private Practitioner (Vaidya).     

N = 4 Supersymmetric (Dyonic) Hypermultiplets in String Theory

In four-dimensional N = 4 supersymmetric gauge theory, we obtain an exact metric on the moduli space of quantum vacua and analyze the spectra of BPS states in weak as well as in strong coupling regions. Identifying the hypermultiplet of the dyonic state as a string stretched between D₃-brane probe and a 7-brane, we demonstrate that the two hypermultiplets, which become massless at two singularities in supersymmetric theory, correspond to open strings beginning on the D₃-brane and ending on the respective 7-brane.     

Asymptotic Behavior of the Fourth Painlevé Transcendents in the Space of Initial Values

We study the asymptotic behavior of solutions of the fourth Painlevé equation as the independent variable goes to infinity in its space of (complex) initial values, which is a generalization of phase space described by Okamoto. We show that the limit set of each solution is compact and connected and, moreover, that any solution that is not rational has an infinite number of poles and infinite number of zeros.     

Ply-by-Ply Failure Analysis of Laminates Under Dynamic Loading

Ply-by-ply failure analysis of symmetric and anti-symmetric laminates under uniform sinusoidal transverse dynamic loading is performed for a specified duration. The study investigates the first ply failure load, followed by the detection of successive ply failures along with their failure modes using various failure theories. Some of the well-established failure theories, mostly used by the researchers, are considered for the failure prediction in laminates. The finite element computational model based on higher order shear deformation displacement field is used for the failure analysis and the complete methodology is computer coded using FORTRAN. The ply-discount stiffness reduction scheme is employed to modify the material properties of the failed lamina. The failure theories used in the analysis are compared according to their ability to predict failure load, failed ply, failure mode and progression of failure. The failure analysis is performed for both the cross-ply and angle-ply laminates with all edges simply supported and clamped. The significance of fibre orientation and stacking sequence in terms of the strength of a laminate and failure progression is also highlighted.     

First direct kinetic measurement of i-C4H5 (CH2CHCCH2) + O2 reaction: Toward quantitative understanding of aromatic ring formation chemistry

The kinetics of the i-C₄H₅ (buta-1,3-dien-2-yl) radical reaction with molecular oxygen has been measured over a wide temperature range (275–852 K) at low pressures (0.8–3 Torr) in direct, time-resolved experiments. The measurements were performed using a laminar flow reactor coupled to photoionization mass spectrometer (PIMS), and laser photolysis of either chloroprene (2-chlorobuta-1,3-diene) or isoprene was used to produce the resonantly stabilized i-C₄H₅ radical. Under the experimental conditions, the measured bimolecular rate coefficient of i-C₄H₅ + O₂ reaction is independent of bath gas density and exhibits weak, negative temperature dependency, and can be described by the expression k₃ = (1.45 ± 0.05) × 10^?12 × (T/298 K)^{?(0.13±0.05)} cm³ s^?1. The measured bimolecular rate coefficient is surprisingly fast for a resonantly stabilized radical. Under combustion conditions, the reactions of i-C₄H₅ radical with ethylene and acetylene are believed to play an important role in forming the first aromatic ring. However, the current measurements show that i-C₄H₅ + O₂ reaction is significantly faster under combustion conditions than previous estimations suggest and, consequently, inhibits the soot forming propensity of i-C₄H₅ radicals. The bimolecular rate coefficient estimates used for the i-C₄H₅ + O₂ reaction in recent combustion simulations show significant variation and are up to two orders of magnitude slower than the current, measured value. All estimates, in contrast to our measurements, predict a positive temperature dependency. The observed products for the i-C₄H₅ + O₂ reaction were formaldehyde and ketene. This is in agreement with the one theoretical study available for i-C₄H₅ + O₂ reaction, which predicts the main bimolecular product channels to be H₂CO + C₂H₃ + CO and H₂CCO + CH₂CHO.     

Optimum oxide thickness for dye-sensitized solar cells—effect of porosity and porous size. A numerical approach

The microstructure of the metal semiconductor oxide which forms the heart of a dye-sensitized solar cell (DSSC) has proved to play a key role in the enhancement of photoelectric conversion efficiency of the cell. In this work, a numerical simulation of the system TiO₂ photo-sensitive dye of a TiO₂ DSSC focuses on the effect that the oxide porosity and the size of the pores have on the cell's performance. The steady-state numerical model used is based on the continuity and transport equations for charge species involved in the system, in connection to Poisson's equation. Light absorption coefficient is set dependent on both porosity and the size of pores in TiO₂. At a first approximation, electron mobility is considered dependent upon porosity following an iteration procedure dependent also upon local field in the oxide. An effective dielectric constant dependent upon the porosity of TiO₂, as well, is used in the model. Electron lifetime in the bulk is set dependent upon electron distribution following the iteration procedure with electron lifetime at the surface taking into consideration surface recombination. Results for different values of TiO₂ porosity and pores' size in connection to the oxide thickness are discussed and found in accordance with results reported in the literature.