Nickel catalyst supported on mesoporous MgAl2O4 nanopowders synthesized via a homogenous precipitation method for dry reforming reaction

Research on Chemical Intermediates - Mesoporous MgAl2O4 nanopowders were synthesized via the homogenous precipitation method and employed as a support for Ni catalysts in the dry reforming...     

The suppression of selected acoustic frequencies in MRI

A study is made of certain dominant frequencies in the acoustic noise spectrum of the magnetic resonance imaging system. Motivated by both spring and string ideas, we investigate whether the contributions to the sound from certain frequencies can be canceled by the appropriate gradient pulse sequence design. From both simulations and experiments, vibrations resulting from an impulsive force associated with a ramping up of a gradient pulse are shown to be cancelled immediately upon the application of another impulsive force coming from the subsequent appropriately timed ramping down of that pulse. A general approach to suppression of multiple-frequency contributions involving a series of gradient pulses with variable timings is given for the cancellations between pairs of impulsive forces. Various examples are confirmed through string simulations, MRI experiments, and linear response theory. This also provides a foundation to explain some results in previous papers on this subject. The method suggests that a variety of pulse profiles and timing combinations can be used to attenuate important contributions to the acoustic spectrum.     

Carbon Ceramic Electrodes Modified with Laccase from Trametes hirsuta: Fabrication,Characterization and Their Use for Phenolic Compounds Detection

Fungal laccase (Lc) from the basidiomycete Trametes hirsuta was immobilized on top of a carbon ceramic electrode using physical absorption. Direct, unmediated heterogeneous electron transfer between Lc and the carbon ceramic electrode (CCE) under aerobic conditions was shown. The bioelectrocatalytic reduction of oxygen on Lc‐CCE started at about 430 mV vs. Ag|AgCl|KCl_sat at pH 3.5 and moved with about 57 mV in the cathodic region per pH unit. The Lc‐modified CCE was then used as a biosensing detection element in a single line flow injection system for the amperometric determination of a variety of phenolic substrates of the enzyme. The experimental conditions were studied and optimized for catechol serving as a model compound. Statistical aspects were applied and the sensor characteristics and Michaelis‐Menten constants of the investigated phenolic compounds were calculated and compared with those obtained for solid graphite electrodes modified with Trametes hirsuta laccase. The results showed that the CCE based biosensor in comparison with the solid graphite based biosensor offers a lower detection limit, a wider linear dynamic range, and excellent operational stability with no sensor passivation, indicating that the sol–gel lattice improves the electrochemical behavior of the biosensor.     

The Effect of Morphological and Topological Characteristics on Effective Diffusivity and Permeability of Dual-Structural-Scale Synthetic Porous Medium

Transport in Porous Media - Image-based simulations at pore scale provide direct insight into the impact of the microstructure on flow and transport processes in porous media. Diffusion is an...     

{[K.18-Crown-6]Br3}n:保护胺和醇的三溴化催化剂（英文）

{[K.18-Crown-6]Br3}n , a unique tribromide-type catalyst, was utilized for the N-boc protection of amines and trimethylsilylation (TMS) and tetrahydropyranylation (THP) of alcohols. The method is general for the preparation of N-boc derivatives of aliphatic (acyclic and cyclic) and aromatic, and primary and secondary amines and also various TMS-ethers and THP-ethers. The simple separation of the catalyst from the product is one of the many advantages of this method.     

Fabrication of durable superhydrophobic nanofibrous filters for oil‐water separation using three novel modified nanoparticles (ZnO‐NSPO,AlOO‐NSPO,and TiO2‐NSPO)

Three reusable and durable superhydrophobic nanofibrous filters were prepared by dip coating the nanofibrous fabric in the three different dispersed solutions of the newly modified nanoparticles (ZnO‐NSPO, AlOO‐NSPO, and titanium dioxide [TiO₂]‐NSPO). The contact angle results proved that the TiO₂‐NSPO coated nanofibrous polyacrylonitrile (PAN) filter was hydrophobic with the water contact angle (WCA) of 141° while the ZnO‐NSPO and AlOO‐NSPO coated nanofibrous PAN filters were superhydrophobic with the WCA of 168° and 152°, respectively. The as‐prepared filters can be utilized as an effective martial for oil‐water separation with separation efficiency of over 98%.     

A simple graphical approach to predict local residue conformation using NMR chemical shifts and density functional theory

The dependency of amino acid chemical shifts on φ and ψ torsion angle is, independently, studied using a five‐residue fragment of ubiquitin and ONIOM(DFT:HF) approach. The variation of absolute deviation of ¹³C^α chemical shifts relative to φ dihedral angle is specifically dependent on secondary structure of protein not on amino acid type and fragment sequence. This dependency is observed neither on any of ¹³C^β, and ¹H^α chemical shifts nor on the variation of absolute deviation of ¹³C^α chemical shifts relative to ψ dihedral angle. The ¹³C^α absolute deviation chemical shifts (ADCC) plots are found as a suitable and simple tool to predict secondary structure of protein with no requirement of highly accurate calculations, priori knowledge of protein structure and structural refinement. Comparison of Full‐DFT and ONIOM(DFT:HF) approaches illustrates that the trend of ¹³C^α ADCC plots are independent of computational method but not of basis set valence shell type. © 2016 Wiley Periodicals, Inc.     

New orthopalladated complexes of phosphorus ylides: Crystal structure of [Pd{CH{P(C7H6)(p-tolyl)2}COCH3}Cl{P(p-tolyl)3}]

This work reports on the preparation of the complexes [PdCl₂(Y¹)₂], [PdCl₂(Y²)₂] (Y¹ = (p-tolyl)₃PCHCOCH₃ (1a); Y² = Ph₃PCHCO₂CH₂Ph (1b)), [Pd{CHP(C₇H₆)(p-tolyl)₂COCH₃}(μ-Cl)]₂ (2a), [Pd{CHP(C₆H₄)Ph₂CO₂CH₂Ph}(μ-Cl)]₂ (2b), [Pd{CH{P(C₇H₆)(p-tolyl)₂}COCH₃}Cl(L)] (L = PPh₃ (3a), P(p-tolyl)₃ (4a)) and [Pd{CH{P(C₆H₄)Ph₂}CO₂CH₂Ph}Cl(L)] (L = PPh₃ (3b), P(p-tolyl)₃ (4b)). Orthometallation and ylide C-coordination in complexes 2a–4b are demonstrated by an X-ray diffraction study of 4a.