Novel mixed ligand complexes of Co(II), Ni(II), Cu(II), and Zn(II) with 1,10-phenanthroline and acesulfame. Synthesis,structural analysis and hydrogen adsorption study

Four novel metal organic framework (MOF) structures containing acesulfame (ace) and 1,10-phenanthroline (phen) ligands of Co²⁺, Ni²⁺, Cu²⁺ and Zn²⁺ metal cations were synthesized. The crystal structure analysis of three compounds (1, 2, and 3) was also performed. The structural formula for complex 4 is proposed based on spectroscopic and thermal analysis data. It has been determined that structures 1, 2, and 4 are in a distorted octahedral geometry. It has been suggested that the charge balance of the coordination sphere with 2+ is provided by two monoanionic ace ligands located outside the coordination sphere as counter-ion. In structure 3, there are two Cu^II metal cations, two phen ligands coordinated as bidentate to each metal cation and ace ligand that provides monoanionic-monodentate coordination. The Cu²⁺ cation has distorted bipyramidal geometry. The maximum hydrogen gas adsorption has been found 1.4575 mL/g (0.046 wt%) for the Ni complex.     

Remote cutting of Li-ion battery electrodes with infrared and green ns-pulsed fibre lasers

Thin sheet anode and cathode materials made in composite structures constitute some of the most important components of a Li-ion battery. These materials are currently cut by punching technology, which shows degrading behaviour as the tool wears out. A viable option for Li-ion battery electrode manufacturing is the use of remote laser cutting. However, the operation requires fulfilling both productivity and quality aspects to substitute the conventional production method. One of the most critical aspects in quality is the clearance width, which is defined as the extent of the exposed middle layer of the sandwich at the laser cut kerf. This work investigates the quality aspects of laser cutting of Li-ion electrodes when a green fibre laser source (λ?=?532 nm, τ?=?1 ns) is used rather than the more traditional infrared (IR) fibre laser source (λ?=?1,064 nm, τ?=?250 ns). The processing conditions were investigated to reveal the technological feasibility zones. Clearance width was studied within the technological feasibility zones for all the material-laser combinations. Results showed that high productivity criterion is met by the IR system, since cutting speed could reach 30 m/min with 54 W average laser power on both anode and cathode. On the other hand, the green laser provided clearance width below 20 μm. In the best case, the clearance on anode could be eliminated with the green laser system. Although the maximum cutting speed was 4.5 m/min, upscaling of green laser power can provide required productivity.     

Hydrogen liberation from the dehydrocoupling of dimethylamine–borane at room temperature by using novel and highly monodispersed RuPtNi nanocatalysts decorated with graphene oxide

Addressed herein, we reported the fabrication of the graphene oxide (GO) supported monodispersed ruthenium–platinum–nickel (RuPtNi) nanomaterials (3.40 ± 0.32 nm) to be utilized as a catalyst in the process of dimethylamine borane (DMAB) dehydrogenation. The nanoparticles were fabricated through the ultrasonication method by co-reducing the Ru³⁺, Pt²⁺ and Ni²⁺ cations and then the nanomaterials were characterized by X-ray diffraction (XRD), Raman spectroscopy, transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), electron energy loss spectroscopy (EELS), inductively coupled plasma optical emission spectrometry (ICP-OES), and X-ray photoelectron spectroscopy (XPS). The fabricated nanomaterials showed outstanding efficiency and remarkable reusability in addition to their record catalytic activity at low temperatures and with extreme low concentrations. They had a significantly high turnover frequency (TOF) (727 h^?1) and low activation energy (E_a) (49.43 ± 2 kJ mol^?1) for DMAB dehydrocoupling. To the best of our knowledge, RuPtNi@GO NPs become a very promising candidate as the best catalyst ever.     

On-Chip-Integrated Nanowire Device Platform With Controllable Nanogap for Manipulation, Capturing, and Electrical Characterization of Nanoparticles

We propose and demonstrate nanowire (NW) device platforms on-chip integrated using electric-field-assisted self-assembly. This platform integrates from nanoprobes to microprobes, and conveniently allows for on-chip manipulation, capturing, and electrical characterization of nanoparticles (NPs). Synthesizing segmented (Au-Ag-Au) NWs and aligning them across predefined microelectrode arrays under ac electric field, we controllably form nanogaps between the self-aligned end (Au) segments by selectively removing the middle (Ag) segments. We precisely control and tune the size of this middle section for nanogap formation in the synthesis process. Using electric field across nanogaps between these nanoprobes, we capture NPs to electrically address and probe them at the nanoscale. This approach holds great promise for the construction of single NP devices with electrical nanoprobe contacts.     

Degradation kinetics of PVC plasticized with different plasticizers under isothermal conditions

The aim of the present work is to elucidate the degradation kinetics of polyvinyl chloride (PVC) plasticized with some phthalate and nonphthalate plasticizers. A PVC thermomat instrument was utilized to maintain the isothermal degradation conditions at 140 and 160°C, and to suppress the oxidative degradation by means of nitrogen flow. The conductivity measurements were performed to follow hydrogen chloride (HCl) gas which is released upon PVC degradation and trapped in water. Dehydrochlorination of plasticized PVC films occurred with activation energies of about 23–160 and 26–117 kJ mol^?1 and the isokinetic temperatures, at which the dehydrochlorination rate constants of all p‐PVC films would have the same value, were found to be 171 and 128°C for initial and linear regions of dehydrochlorination curve, respectively. Plasticizer incorporation contributes to the stability of the films particularly after the consumption of stabilizer due to the dehydrochlorination. Influence of temperature rise by 20°C on the degradation rate constant is the lowest for DINCH having p‐PVC films as 0.36 and 0.42% increment at the initial region and linear region, respectively. On the other hand, DOTP reveals greater stability than the others do since the compensation ratio of the PVC film having DOTP is greater than the other films. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41579.     

Functionalized Hybrid Coatings on ABS Surfaces by PLD and Dip Coatings

It is important to give water-repellent and antibacterial properties to the acrylonitrile butadiene styrene (ABS) surfaces of the hearing aids. In this study, the sol–gel Si and sol–gel Ti solutions were prepared from the reactions of silicon ethoxide, titanium butoxide and methacrylic acid. The catalyst and Dynasylan F8815 were added to the sol–gel solutions to give hydrophobic properties onto the ABS surfaces. Additionally, silver nanoparticles were synthesized by nanosecond laser and added to the coating solutions to give extra antibacterial properties. The surfaces of the ABS targets were coated using the sol–gel dip coating and pulsed laser deposition techniques. The coatings with good adhesion between film and substrate and good water-repellent properties were achieved. The average contact angles for the coated ABS surfaces were measured in the range between 120 and 125 degrees. The obtained sol–gel materials and produced thin films onto the ABS surfaces were also analyzed in terms of the antibacterial properties. The highly antibacterial properties were observed in the sol–gel solutions and the thin films.     

Utilization of Electrospun Polystyrene Membranes as a Preliminary Step for Rapid Diagnosis

Recent advances in clinical practice drive deoxyribonucleic acid (DNA) as an important class of biomarker. Monitoring the change in their concentration suggests the initiation and/or progression of various disorders. However, low quantity of DNA biomarkers in body fluids requires a delicate isolation methodology that provides efficient separation and easy handling. This study describes a newer‐generation separation technology relying on electrospun fibers of sub‐micrometer diameter of a commodity polymer for DNA biomarkers in simulative serum. Fibrous polystyrene membranes are prepared by electrospinning and they are subjected to post‐modification with Au. The composite membranes may provide a convenient environment for the removal of bovine serum albumin (BSA) from BSA and DNA mixtures. The eluent can be used as an efficient tool for detection of DNA biomarkers associated with diagnosis of numerous life‐threatening diseases.

     

AC susceptibility and FC-ZFC magnetic properties of SrTb_xFe_(12-x)O_(19) and SrTm_xFe_(12-x)O_(19) hexaferrites:a comparative study

In this comparative study,Tb and Tm substituted Sr-hexafe rrites(HFs) with the chemical compositions of SrTb_xFe_(12-x)O_(19) and SrTm_xFe_(12-x)O_(19)(x=0.00,0.02 and 0.04) were fabricated via citrate sol-gel approach.The AC susceptibility and FC-ZFC magnetization were investigated.The product structure and morphologies were also investigated via XRD,TEM and SEM along with EDX.Measurements of temperature dependence of magnetization M-T and AC magnetic susceptibility versus temperature were carried out.The various synthesized HFs displayed ferrimagnetic behavior within 10-325 K.At lower temperatures,super-spin glass-like behavior was noticed.Neel-Arrhenius and Vogel-Fulcher models were employed to explore the experimental data of AC susceptibility.