Interacting Entropy-Corrected Holographic Chaplygin Gas Model

Holographic dark energy (HDE), presents a dynamical view of dark energy which is consistent with the observational data and has a solid theoretical background. Its definition follows from the entropy-area relation S(A), where S and A are entropy and area respectively. In the framework of loop quantum gravity, a modified definition of HDE called “entropy-corrected holographic dark energy” (ECHDE) has been proposed recently to explain dark energy with the help of quantum corrections to the entropy-area relation. Using this new definition, we establish a correspondence between modified variable Chaplygin gas, new modified Chaplygin gas and the viscous generalized Chaplygin gas with the entropy corrected holographic dark energy and reconstruct the corresponding scalar potentials which describe the dynamics of the scalar field.     

ESR spectra of the OD radical in the 2Π32, J = 32 state, v = 0–5 levels

The paramagnetic resonance absorption spectrum of the OD radical in the excited vibrational levels up to v = 5 of the ground ${}^2\text{Π}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}$, $\text{J =}\text{3}\text{2}$ state has been observed at X-band frequencies. The theory of the Zeeman effect of a paramagnetic ²Π state of a light diatomic molecule has been applied to analyze the spectrum. The Λ-doubling frequencies, the molecular g factors, coefficients of the second order Zeeman effect, and the hyperfine interaction constants were determined for each of the vibrational levels. The experimental results agree reasonably well with the values calculated from (a) optical data and (b) ab initio data. The experimental determinations are still much better than theoretical calculations.     

Ethyl Acetate—Propionic Acid as Green Mobile Phase System for Selective Densitometric Identification of Maltose with Preliminary Separation on Silica High-Performance Thin-Layer Chromatographic Plates

JPC – Journal of Planar Chromatography – Modern TLC - A mobile phase system comprising of ethyl acetate and propionic acid in 1:1 (v/v) ratio was identified as the most suitable green...     

Nephroprotective Effects of Alhagi camelorum against Cisplatin-Induced Nephrotoxicity in Albino Wistar Rats

Alhagi camelorum (AC) is an old plant with a significant therapeutic value throughout Africa, Asia, and Latin America. The overuse of cisplatin (Cis > 50 mg/m²) is associated with observed nephrotoxicity, ototoxicity, gastrotoxicity, myelosuppression, and allergic reactions. Remedial measures are needed for the protection of nephrotoxicity against cisplatin. Thus, we investigated the nephroprotective effects of AC plant extract to prevent cisplatin-induced nephrotoxicity in albino Wistar rats. The presence of polyphenols, phenolic compounds, tannins, and saponins was revealed during phytochemical investigation, and a significantly intense antioxidant activity was recorded. There were no toxicological symptoms in the treated rats, and no anatomical, physiological, or histological abnormalities were found compared to the control rats. The results of correcting cisplatin-induced nephrotoxicity revealed that the extract has a significant ability to treat kidney damage, with most parameters returning to normal after only three weeks of therapy. It is concluded that co-administration of cisplatin with AC extract showed exceptional nephroprotective effects at a dose of 600 mg/kg for Cis-induced nephrotoxicity.     

Liquid-Repellent Metal Oxide Photocatalysts

Metal oxide photocatalysts (MOPCs) decompose organic molecules under illumination. However, the application of MOPCs in industry and research is currently limited by their intrinsic hydrophilicity because MOPCs can be wetted by most liquids. To achieve liquid repellency, the surface needs to possess a low surface energy, but most organic molecules with low surface energy are degraded by photocatalytic activity. Herein, current methods to achieve liquid repellency on MOPCs, while preventing degradation of hydrophobic coatings, are reviewed. Classically, composite materials containing MOPCs and hydrophobic organic compounds possess good liquid repellency. However, composites normally form irregular coatings and are hard to prepare on surfaces such as those that are mesoporous or nanostructured. In addition, the adhesion of composites to substrates is often weak, resulting in delamination. Recent studies have shown that the direct grafting reaction of polydimethylsiloxane (PDMS) from silicone oil (methyl-terminated PDMS) under illumination results in a stable polymer brush. This easy and simple grafting method allows us to create stable liquid-repellent surfaces on MOPCs of various types, structures, and sizes. In particular, super-liquid-repellent drops with an underlying air layer can be created on PDMS-grafted nano-/microstructured MOPCs. Potential applications of surfaces combining liquid repellency and photocatalytic activity are also discussed; thus offering new ways of using MOPCs in a wider range of applications.     

Conceptualization and Synthesis of the First Inosito-Inositol (Decahydroxydecalin,DHD): In silico Binding to β-Amyloid Protein

Previously unknown entities in the form of 1,2,3,4,5,6,7,8,9,10-decahydroxydecalins (DHDs) have been conceptualized and the first member of this class, an inosito-inositol, has been synthesized from aromatic hydrocarbon naphthalene following a flexible strategy that is amenable to diversity creation. The DHD accessed here has been subjected to preliminary in silico evaluation with Aβ and may hold some promise in Alzheimer's disease therapeutics.     

On electromagnetic properties of rotating nuclei in crpa

An analysis of quasiparticle correlations with special emphasis on transition matrix elements have been done for a self-consistent cranking model. It is pointed out that a second order of the boson representation of a transition operator leads to a signature dependence of transition probabilities between excited one-phonon states in even-even nuclei. Moreover, it brings about the new contribution to an expectation value of electromagnetic moments in the yrast line states of deformed nuclei.     

Dissolution of Cellulose and Lignin with Biobased Ionic Liquids

Journal of Solution Chemistry - Choline-based ionic liquids, involving various alkyl chains lengths and carboxylates derived from biobased acids, have been synthetized with high yields through a...     

Study of allelopathic effects of Eucalyptus erythrocorys L. crude extracts against germination and seedling growth of weeds and wheat

Allelopathic materials inside a tree can produce positive or negative change in the survival, growth, reproduction and behaviour of other organisms if they escape into the environment. To assess these effects, this work was carried out to evaluate the allelopathic impact of Eucalyptus erythrocorys L. on seed germination and seedling growth of two weeds: Sinapis arvensis L. and Phalaris canariensis L.; on one cultivated crop: Triticum durum L. Aqueous; and on ethanolic leaf extracts of E. erythrocorys L. The study was effected using four concentrations (10, 20, 25 and 30 μL/mL) while distilled water was used as a control. The results showed that the E. erythrocorys L. crude extracts had an inhibitory effect on seed germination and seedling growth of both studied weeds and wheat. The inhibition rate was increased by the increase in extract concentration. Only ethanolic extracts of E. erythrocorys L. induced a significant inhibition of seed germination of durum wheat. The effect of E. erythrocorys L. crude extracts was more severe on weeds than on durum wheat. These results indicate that the seedling growth, especially radicle elongation, was the more sensitive indicator to evaluate the effects of extracts than was the seed germination.     

Synthesis and characterization of some Schiff-base-containing polyimides

The diamine, 4-aminophenyloxy-N-4-[(4-amiophenyloxy)benzylidene]aniline, was prepared via the nucleophilic substitution reaction and was polymerized with different dianhydrides either by one-step solution polymerization reaction or two-step procedure. The latter includes ring-opening polyaddition to give poly(amic acid), followed by cyclodehydration to polyimides. The inherent viscosity ranges from 0.61–0.79 dl/g. Some of the polymers were soluble in most of the organic solvents such as DMSO, DMF, DMAc, NMP, and m-cresol even at room temperature. The degradation temperature of the resultant polymers falls in the ranges from 240–500 °C in nitrogen with only 10% weight loss. Specific heat capacity at 200 °C ranges from 1.0929–2.6275 J g⁻¹ k⁻¹. The temperature at which the maximum degradation of the polymer occurs ranges from 600–630 °C. The glass transition temperature (Tg) values of the polyimides ranged from 185 to 272 °C. The activation energy and enthalpy of the polyimides ranged from 47.5–55.0 kJ/mole and 45.7–53.0 kJ/mole and the moisture absorption in the range of 0.23–0.72%.