An investigation of dynamic mechanical, thermal, and electrical properties of housing materials for outdoor polymeric insulators

The present paper reports the results about a study of mechanical, thermal, dynamic mechanical and electrical properties of housing (weather shed) materials for outdoor polymeric insulators. Silicone rubber, ethylene-propylene-diene monomer (EPDM) and alloys of silicon-EPDM are known polymers for use as housing in high voltage insulators. The result of dynamical mechanical measurement shows that the storage modulus of blends enhances with increase EPDM in formulation. It can be seen from the result of TGA measurement that initial thermal degradation of silicone rubber improves by the effect of EPDM in blends. The blends of silicone-EPDM show good breakdown voltage strength compared to silicone rubber. Surface and volume resistance of silicone rubber improve by EPDM content. The mechanical properties of EPDM such as strength, modulus and elongation at break improve by silicone.     

Influence of ionic liquid counterions on activity and selectivity of ethylene trimerization using chromium-based catalysts in biphasic media

In recent years ionic liquids (ILs) have attracted much interest because of their widespread use in various fields. Several trimerization and oligomerization catalysts have been evaluated in ILs with different organic–inorganic hybrid structures. High catalytic activity and selectivity, easy product separation, and recycling of the catalyst are the advantages of a biphasic catalyst system compared to the homogeneous catalysts. In this study, the influence of IL counter-anions on activity and selectivity of the ethylene trimerization catalysts based on Cr-SNS-R was investigated. All synthesized materials were characterized using Fourier-transform infrared spectroscopy, ¹H NMR, ¹³C NMR, UV–Vis. spectroscopy, thin-layer chromatography, and elemental analysis (CHNS). In ethylene trimerization reaction, the dodecyl substituent in the SNS ligand exhibited better activity and selectivity than the butyl substituent. The results revealed that the presence of BF₄⁻ as a counter-anion in the IL led to an increase in activity and selectivity compared to Br⁻ and I⁻ counter-anions. It was found that the BF₄⁻ counter-anion plays a conclusive role in the development of 1-hexene activity and selectivity to a maximum amount of 71,132 g_1-C6/(g_Cr × h) and more than 99%, respectively. Finally, the catalyst was reused thrice without losing its 1-hexene selectivity.     

Guaranteed cost nonlinear sampled-data control: applications to a class of chaotic systems

Nonlinear Dynamics - This paper addresses the guaranteed cost sampled-data controller synthesis and analysis problems with application to nonlinear chaotic systems. A linear parameter-varying (LPV)...     

Acid-induced gelation behavior of sonicated casein solutions

Casein gels were made from solutions sonicated by 24 and 130 kHz ultrasounds for 0, 60 and 120 min, followed by acidification with glucono-δ-lactone at 30 °C. The dynamics of gel formation were studied using rheological methods and microstructure of gels was monitored using scanning electron microscopy. Sonication postponed the gelation point to a lower pH value and increased the elasticity of freshly formed gels. It also resulted in gels with a more interconnected structure and smaller non-distinguishable particulates. This structure was especially dominant for the gel made from the solution already sonicated for 120 min.     

A heterogeneous and reusable nanopolymer-supported palladium catalyst for the copper- and phosphine-free Sonogashira coupling reaction under aerobic conditions in water

We report here the synthesis of a nanopolymer-supported palladium(II) complex catalyst, [PS-tet-Pd(II)] using a simple protocol. The catalyst was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), FT-IR, and energy dispersive X-ray spectroscopy (EDS). PS-tet-Pd(II) proves to be a useful heterogeneous catalyst in the copper- and phosphine-free Sonogashira coupling reaction in water. The catalyst can be recovered from the reaction mixture by simple filtration and reused several times without any significant loss of catalytic activity.     

An Extended-FEM Model for CO2 Leakage Through a Naturally Fractured Cap-Rock During Carbon Dioxide Sequestration

In this paper, a numerical model is developed for the assessment of carbon dioxide transport through naturally fractured cap-rocks during CO₂ sequestration in underground aquifers. The cap-rock contains two types of fracture with different length scales: micro-cracks (fissures) and macro-cracks (faults). The effect of micro-cracks is incorporated implicitly by modifying the intrinsic permeability tensor of porous matrix, while the macro-cracks are modeled explicitly using the extended finite element method (X-FEM). The fractured porous medium is decomposed into the porous matrix and fracture domain, which are occupied with two immiscible fluid phases, water and CO₂. The flow inside the matrix domain is governed by the Darcy law, while the flow within the fracture is modeled using the Poiseuille flow. The mass conservation law is fulfilled for each fluid phase at both porous matrix and fracture domain; moreover, the mass exchange between the matrix and fracture is guaranteed through the integral formulation of mass conservation law. Applying the X-FEM technique, the explicit representation of macro-cracks is modeled by enriching the standard finite element approximation space with an enrichment function. Finally, several numerical examples of CO₂ injection into a brine aquifer below a naturally fractured cap-rock are modeled in order to investigate the effects of cracks’ aperture and orientation as well as the temperature of aquifer and the depth of injection on the leakage pattern of the carbon dioxide through the cap-rock.

     

A study on sol–gel synthesis and characterization of SiC nano powder

Nano sized β-SiC particles were synthesized from sol–gel process. Mono dispersed β-SiC nano particles with semi spherical morphology were obtained by employing APC as a dispersant agent and adjusting pH in the range of 2.5–4. Phenolic resin and TEOS were employed as precursors and heat treatment was conducted up to 1500 °C. Different techniques such as XRD, DTA, FTIR, PSA, SEM and TEM were used to characterize the formation of β-SiC. The (Si–O-C) bonds were formed by hydrolysis and condensation reactions in the gel while the nucleation of crystalline β-SiC was found to be initiated at 1400 °C. The primary particles in the sol were found to be (< 10 nm) while the size distribution in the final product was recorded in the range of 30–50 nm.     

Orientations of graphs avoiding given lists on out-degrees

Let $G$ be a graph and $F:V\left(G\right)\to 2^{\mathbb{N}}$ be a mapping. The graph $G$ is said to be $F$- avoiding if there exists an orientation $O$ of $G$ such that $d_O^{+}\left(v\right)\notin F\left(v\right)$ for every $v\in V\left(G\right)$, where $d_O^{+}\left(v\right)$ denotes the out-degree of $v$ in the directed graph $G$ with respect to $O$. In this paper it is shown that if $G$ is bipartite and $\mid F\left(v\right)\mid \le d_G\left(v\right)/2$ for every $v\in V\left(G\right)$, then $G$ is $F$-avoiding. The bound $\mid F\left(v\right)\mid \le d_G\left(v\right)/2$ is best possible. For every graph $G$, we conjecture that if $\mid F\left(v\right)\mid \le \frac{1}{2}\left(d_G\left(v\right)-1\right)$ for every $v\in V\left(G\right)$, then $G$ is $F$-avoiding. We also argue about this conjecture for the best possibility of the conditions and also show some partial solutions.     

Electrocatalytic Oxidation of Ethanol on the Surface of Graphene Based Nanocomposites: An Introduction and Review to it in Recent Studies

This review gives an overview of the electrochemical investigations about the properties of various types of graphene composites in the ethanol oxidation. Various routes to provide appropriate graphene‐based materials required electrochemical techniques for investigation of different types of the materials as well as their performance and efficacy in ethanol oxidation are discussed in detail. Furthermore, it is demonstrated that the incorporation of suitable materials, e. g. noble metals (graphene‐supported binary and ternary metal nanoparticles), metal oxides, conductive polymer, etc, with graphene results in excellent electrocatalytic activity, superb durability and selectivity in ethanol oxidation. Immobilization of electrocatalytically active NPs on graphene supports using physical approaches is considered as an effective route to prepare direct ethanol fuel cell (DEFC) anode catalysts.