Depositing nanoparticles inside millimeter-size hollow tubing

The inner and the outer walls of hollow tubing with an inner diameter of 0.4-0.9 cm and an outer diameter of 0.6-1.3 cm were coated with silver nanoparticles (NPs) by a one-step process using ultrasound irradiation. The structure and morphology of the nanoparticles (NPs) inside the hollow tubing and on the outer surface were characterized using methods such as XRD, TEM, HR-TEM, and HRSEM. The inner surface of the tubing was found to be coated with more silver than the outer surface. The coating was done on tubing made of rubber, PVC, Teflon and polyethylene. Sonochemistry is demonstrated as a method for depositing nanoparticles on the inner wall of a tube.     

An efficient synthesis of new polyfunctional hexahydro pyrido[1,2-a]pyrazin-1-ones

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Solvability of Integral Equations with Endogenous Delays

This paper performs a systematic study of some nonlinear integral equations with unknown lower limits of integration, which arise in economics, operations research, population biology and environmental sciences. A general investigation technique is developed for systems of such equations and several theorems about the existence and uniqueness of a solution are proven. The links to other functional equations with state-dependent delays are discussed. Applied interpretation of the obtained results is provided.     

Thermodynamic Limit for Directed Polymers and Stationary Solutions of the Burgers Equation

The first goal of this paper is to prove multiple asymptotic results for a time-discrete and space-continuous polymer model of a random walk in a random potential. These results include: existence of deterministic free energy density in the infinite-volume limit for every fixed asymptotic slope, concentration inequalities for free energy implying a bound on its fluctuation exponent, and straightness estimates implying a bound on the transversal fluctuation exponent. The culmination of this program is almost sure existence and uniqueness of polymer measures on one-sided infinite paths with given endpoint and slope, and interpretation of these infinite-volume Gibbs measures as thermodynamic limits. Moreover, we prove that marginals of polymer measures with the same slope and different endpoints are asymptotic to each other. The second goal of the paper is to develop ergodic theory of the Burgers equation with positive viscosity and random kick forcing on the real line without any compactness assumptions. Namely, we prove a one force–one solution principle, using the infinite-volume polymer measures to construct a family of stationary global solutions for this system, and proving that each of those solutions is a one-point pullback attractor on the initial conditions with the same spatial average. This provides a natural extension of the same program realized for the inviscid Burgers equation with the help of action minimizers that can be viewed as zero temperature limits of polymer measures. © 2018 Wiley Periodicals, Inc.     

Controlled ring‐opening homo‐ and copolymerization of ɛ‐caprolactone and d,l‐lactide by iminophenolate aluminum complexes: An efficient approach toward well‐defined macromonomers

The aluminum complexes containing two iminophenolate ligands of the type (p‐XC₆H₄NCHC₆H₄O‐o)₂AlR' (R′=Me ( 3, 4 ) or R′=O(CH₂)₄OCH=CH₂ ( 5, 6 ), X=H ( 3, 5 ), F( 4, 6 )) were synthesized and characterized by ¹H, ¹³C NMR spectroscopy, and X‐ray crystallography. The reaction of AlMe₃ with two equivalents of substituted iminophenols gave five‐coordinated {ONR}₂AlMe ( 3, 4 ) complexes. Subsequent reaction of these methyl complexes with unsaturated alcohol, HO(CH₂)₄OCH=CH₂, resulted in target compounds 5 and 6 in a good yield. It was shown that the complexes ( 3 ‐ 6 ) are monomeric in solution (NMR) and in solid state (X‐ray analysis). The catalytic activity of the complexes 5 and 6 towards ring‐opening polymerization (ROP) of ?‐caprolactone and d,l ‐lactide was assessed. Complex 5 showed higher activity as compared with 6 , while both of these catalysts induced controlled homo‐ and copolymerization to afford the macromonomers with high content of vinyl ether end groups (F_n > 80%) in a broad range of molecular weights (M_n = 4000–30,000 g mol^?1) with relatively narrow MWD (M_w/M_n = 1.1–1.5). © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1237–1250     

Rate constants of the reactions of O(3P) atoms with Br2 and NO2 over the temperature range 220-950 K

The kinetics of the reactions of Br₂ and NO₂ with ground state oxygen atoms have been studied over a wide temperature range, T = 220-950 K, using a low-pressure flow tube reactor coupled with a quadrupole mass spectrometer: O + NO₂ → NO + O₂ (1) and O + Br₂ → Br + BrO (2). The rate constant of reaction (1) was determined under pseudo–first-order conditions, either monitoring the kinetics of O-atom or NO₂ consumption in excess of NO₂ or of the oxygen atoms, respectively: k₁ = (6.1 ± 0.4) × 10⁻¹² exp((155 ± 18)/T) cm³ molecule⁻¹ s⁻¹ (where the uncertainties represent precision at the 2σ level, the estimated total uncertainty on k₁ being 15% at all temperatures). The temperature dependence of k₁, found to be in excellent agreement with multiple previous low-temperature data, was extended to 950 K. The rate constant of reaction (2) determined under pseudo–first-order conditions, monitoring the kinetics of Br₂ consumption in excess of O-atoms, showed upward curvature at low and high temperatures of the study and was fitted with the following three-parameter expression: k₂ = 9.85 × 10⁻¹⁶ T^1.41 exp(543/T) cm³ molecule⁻¹ s⁻¹ at T = (220-950) K, which is recommended from the present study with an independent of temperature conservative uncertainty of 15% on k₂.     

New nanomolar negative modulators of AMPA receptors

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