Observation of Quantum Beats of Two-Photon-Excited States of Xe upon Photoionization

Optics and Spectroscopy - Ionization of coherently two-photon-excited superposition of 4f states of Xe in a supersonic atomic beam is studied by means of femtosecond pump–probe spectroscopy....     

Mesomorphism of Dichotomous Compounds; X-Ray Diffraction Analysis of 4-Chlorophenyl Hexadecyl Ether

Crystallography Reports - The crystal and molecular structures of Cl–C6H4–O–C16H33 (I) have been studied, and its differential scanning calorimetry (DSC) study is performed....     

Model of Dynamics of the IBR-2M Pulsed Reactor with Temperature and Power Fast Feedback Effects

Physics of Atomic Nuclei - A model of dynamics with separate temperature feedback formed by average temperatures of the fuel and the coolant is constructed for the IBR-2M pulsed reactor of periodic...     

Effect of monomer hydrophilicity on ARGET–ATRP kinetics in aqueous mini-emulsion polymerization

Activators regenerated by electron transfer (ARGET) atom transfer radical polymerization (ATRP)-based aqueous miniemulsion polymerization where the polymerization takes place in the stabilized monomer droplets is described. In this work, we compared styrene, n-butyl methacrylate (nBMA) and tert-butyl methacrylate (tBMA) and investigated the influence of their hydrophobicity on dispersity, molecular weight and particle stability based their partition coefficients (logP) (2.67, 2.23, and 1.86, respectively). Tetrabutylammonium bromide (TBAB) was used as a phase transfer agent for the controlled delivery of Cu²⁺-Br/tris(2-pyridylmethyl)amine (TPMA), a hydrophilic catalyst, into monomer droplets of varying hydrophobicity. The resulting dispersity and particle stability of each polymer is a function of its logP value, with the most hydrophobic monomer (styrene) displaying the narrowest dispersity and most control (Đ < 1.3), and the most hydrophilic polymer poly(tert-butyl methacrylate) (PtBMA) having reduced emulsion stability, determined by the observation of aggregate formation. Selected polymerization parameters, including effects of total ascorbic acid feed concentration and the monomer concentration and their effects on dispersity are reported. The controlled polymerizations of hydrophilic monomers using ARGET-ATRP in miniemulsion conditions and understanding the effect of monomer hydrophilicity on the emulsion stability will broaden the use of ARGET-ATRP in emulsion polymerization for the synthesis of polymer-grafted nanoparticles with hydrophilic corona.     

Controlling thermomechanical behavior of semicrystalline hydrogenated polynorbornene through the cis- to trans-cyclopentylene ratio

Though polynorbornene synthesized by ring-opening metathesis polymerization has an intrinsically all-cis configuration of the cyclopentylene backbone rings, a fraction of these rings can be epimerized to the trans configuration during hydrogenation over suitable catalysts. By varying the method of hydrogenation, semicrystalline hydrogenated polynorbornenes (hPNs) with trans levels between 0 and 36% were obtained. With increasing trans content, the glass transition temperature, melting point, and enthalpy of melting decrease modestly. By contrast, the temperature at which the hPN crystal transitions into a rotationally disordered polymorph varies strongly with trans content, ranging from 126 °C (all-cis) to 71 °C at 27% trans; at trans contents of 34% and above, no rotationally-ordered phase is observed at any temperature. The room-temperature Young's modulus shows no dependence on trans content, while the yield stress drops by 20% at 1% trans content and slowly decreases further with additional epimerization. The temperature dependence of the Young's modulus differs for trans-containing versus all-cis polymers, while the temperature dependence of the yield stress is set by the polymorph type (rotationally ordered vs. disordered).     

Reply to comment on “Limitation of uranium and thorium traces in charnockite matrix‐PIXE analyses at 3 MeV with Si (Li) detector”

Journal of Radioanalytical and Nuclear Chemistry -     

Secondary Metabolites of Litchi chinensis

Chemistry of Natural Compounds -     

Nanoporous NiO@SiO2 photo-catalyst prepared by ion-exchange method for fast elimination of reactive dyes from wastewater

Photo-catalytic elimination of organic contaminants plays a significant role in wastewater treatment. Developing a highly efficient photo-catalyst is one of the leading research topic. Herein, we reported the fabrication of a novel nanoporous NiO@SiO₂ photo-catalyst by a simple ion-exchange method to eliminate the reactive dyes. The synthesized NiO@SiO₂ catalyst exhibited fast photo-degradation and excellent adsorption capability and could efficiently remove Red FN-3GL dye from wastewater, due to a high loading of NiO and a large specific surface area, abundant electron-withdrawing groups, as well as narrow bandgap energy. In addition, the NiO@SiO₂ photo-catalyst also displayed a high capability to remove reactive dyes over a wide range of pH values (pH 3–9). The prominent adsorption and photo-degradation of dyes were strongly dependent on the surface charge of the catalyst and the generation of hydroxyl radicals (OH^?) by the catalyst, respectively. Furthermore, the NiO@SiO₂ photo-catalyst also exhibited excellent recyclability, thus demonstrating the feasibility of practical applications in industries. The strategy of covering the metal oxide to nanoporous silica is a promising method for developing active photo-catalysts and applying them in the wastewater treatments.     

Completely discrete schemes for 2D Sobolev equations with Burgers’ type nonlinearity

Numerical Algorithms - Inthis paper, we discuss two first-order completely discrete schemes based on Backward Euler and its linearized variant methods for the 2D Sobolev equations with...     

Viscoelastic-mapping of cellulose nanofibrils using low-total-force contact resonance force microscopy (LTF-CRFM)

Cellulose - Low-total-force contact resonance force microscopy (LTF-CRFM), an atomic force microscopy method, is introduced as a non-destructive means to quantify the local viscoelastic loss...