Optical properties of multi-stacked BaTiO3/SrTiO3 thin films synthesized via chemical method

In this work, the BaTiO₃ and SrTiO₃ thin films as well as BaTiO₃/SrTiO₃ lamellar composites are synthesized via sol-gel spin-coating method. The formation of corresponding phases from their sols is investigated by virtue of X-ray diffraction on their powders, which confirms the formation of tetragonal structure for BaTiO₃, but cubic structure for SrTiO₃. The field emission scanning electron microscopy images show that crack-free films with different morphologies are formed in each sample. Likewise, by changing periodicity of the samples, the morphology of the composite samples is changed. As the number of layers increases from 1 to 20, the band gap reduces from 4.38 eV to 4.10 eV for BaTiO₃ samples and from 4.13 eV to 3.80 eV for SrTiO₃ samples confirmed by UV–Vis spectra. The band gap of periodicity = 1 sample is higher than that of BaTiO₃, while band gaps of periodicity = 2 and 5 composites mount between those of BaTiO₃ and SrTiO₃. In addition, the refractive indices of multi-stacked composites are about 0.2 lesser than refractive indices of BaTiO₃ sample in high wavelengths. The periodicity dependence of optical frequency dielectric constant, dielectric loss, impedance, Urbach tail, extinction coefficient, and electric modulus of multi-stacked composites are also studied.     

A Silicon on Nothing LDMOS with Two Air Pillars in Gate Insulator for Power Applications

Silicon - This paper proposes a new silicon on nothing lateral double-diffused metal-oxide-semiconductor with two air gaps in the gate insulator (SON-APG LDMOS). Utilizing air for the buried layer...     

Effect of waste serpentine on the properties of basic insulating refractories

Basic insulating refractories were fabricated by the pressing route using dead-burned magnesia, pure calcined alumina, expanded perlite, and calcined waste serpentine as starting raw materials in four compositions from F1 to F4. Periclase and forsterite were major phases in F1 and F2 compositions, while spinel was also detected in the XRD patterns of F3 and F4 samples. Quantitative phase analysis showed that F4 sample sintered at 1450?°C has the highest forsterite content among all other samples. On the other hand, it has lower thermal conductivity compared to F1 to F3, and even lower than aluminosilicate IFBs with the same bulk density. It is concluded that forsterite is a highly insulating material, compared to periclase, corundum, periclase-spinel, aluminosilicates, such as mullite, etc.     

Temperature/pH/magnetic triple‐sensitive nanogel–hydrogel nanocomposite for release of anticancer drug

Hydrogels, nanogels and nanocomposites show increasing potential for application in drug delivery systems due to their good chemical and physical properties. Therefore, we were encouraged to combine them to produce a new compound with unique properties for a long‐term drug release system. In this regard, the design and application of a nanocomposite hydrogel containing entrapped nanogel for drug delivery are demonstrated. To this aim, we first prepared an iron oxide nanocomposite nanogel based on poly(N‐isopropylacrylamide)‐co‐((2‐dimethylaminoethyl) methacrylate) (PNIPAM‐co‐PDMA) grafted onto sodium alginate (NaAlg) as a biocompatible polymer and iron oxide nanoparticles (ION) as nanometric base (PND/ION‐NG). This was then added into a solution of PDMA grafted onto NaAlg. Through dropwise addition of mixed aqueous solution of iron salts into the prepared polymeric solution, a novel hydrogel nanocomposite with excellent pH, thermal and magnetic responsivity was fabricated. The synthesized samples were fully characterized using Fourier transform infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy with energy‐dispersive X‐ray analysis, vibrating sample magnetometry and atomic force microscopy. A mechanism for the formation of PNIPAM‐co‐PDMA/NaAlg‐ION nanogel–PDMA/NaAlg‐ION hydrogel and PND/ION nanogel is suggested. Swelling capacity was measured at various temperatures (25 to 45 °C), pH values (from 2 to 11) and magnetic field and under load (0.3 psi) and the dependence of swelling properties of the nanogel–hydrogel nanocomposite on these factors was well demonstrated. The release rate of doxorubicin hydrochloride (DOX) as an anticancer drug was studied at different pH values and temperatures in the presence and absence of a magnetic field. The results showed that these factors have a high impact on drug release from this nanocomposite. The result showed that DOX release could be sustained for up to 12.5 days from these nanocomposite hydrogels, significantly longer than that achievable using the constituent hydrogel or nanogel alone (<1 day). The results indicated that the nanogel–hydrogel nanocomposite can serve as a novel nanocarrier for anticancer drug delivery. © 2019 Society of Chemical Industry     

In situ emulsion polymerization and characterization of PVAc nanocomposites including colloidal silica nanoparticles for wood specimens bonding

Polyvinyl acetate (PVAc) nanocomposites for wood adhesives containing different amounts of colloidal silica nanoparticles (CSNs) were synthesized via in situ one-step emulsion polymerization. The adhesion strength of wood specimens bonded by PVAc nanocomposites was investigated by the tensile test. Thermal properties of PVAc nanocomposites were also characterized by differential scanning calorimetry and thermogravimetric analysis. Rheological and morphological properties of the PVAc nanocomposites were investigated using rheometric mechanical spectrometry and field emission scanning electron microscopy (FESEM), respectively. The obtaining results showed that the shear strength of PVAc nanocomposite including 1 wt. % CSNs has the highest shear and tensile strength about 4.7 and 3.2 MPa, respectively. A small increment of T_g (~3 °C) and considerable increment of the ash content proved the enhancement of PVAc thermal characterization in the presence of CSNs. FESEM results showed uniform dispersion of nanoparticles throughout the PVAc matrix due to using the in situ emulsion polymerization process. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48570.     

Reinforcement of maleated polyethylene/ground tire rubber thermoplastic elastomers using talc and wood flour

Maleated polyethylene (MAPE)/Ground tire rubber (GTR) thermoplastic elastomer with 50 vol % GTR was reinforced by incorporation of talc powder and wood flour. Scanning electron microscopy (SEM) reveals that maleated polyethylene (MAPE) has good compatibility with wood flour, but the adhesion with talc particles is weak. Tensile moduli of MAPE/GTR increase more significantly after inclusion of talc particles compared to wood flour. Prediction of the tensile modulus of hybrid MAPE/GTR/particle composites is successfully performed using a combination of Kerner and Halpin‐Tsai models. Elastic moduli are shown to depend strongly on both aspect ratio and level of particle dispersion in the matrix. Measurement of compression sets shows that elastic recovery of the compounds decreases after addition of solid particles. Samples having better particles/matrix compatibility show higher elastic recovery. Thermogravimetric analysis shows that inclusion of wood flour decreases thermal stability of compounds. Density and hardness of MAPE/GTR are also shown to increase after inclusion of particulate reinforcements. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40195.     

Merger of Energetic Affinity and Optimal Geometry Provides New Class of Boron Nitride Based Sorbents with Unprecedented Hydrogen Storage Capacity

Hydrogen is an ideal synthetic fuel because it is lightweight, abundant and its oxidation product (water) is environmentally benign. However, its utilization is impeded by the lack of an efficient storage device. A new building block approach is proposed for an exhaustive search of optimal hydrogen uptakes in a series of low density boron nitride (BN) nanoarchitectures via extensive 3868 ab initio‐based multiscale simulations. By probing various geometries, temperatures, pressures, and doping ratios, these results demonstrate a maximum uptake of 8.65 wt% at 300 K, the highest hydrogen uptake on sorbents at room temperature without doping. Li⁺ doping of the nanoarchitectures offers a set of optimal combinations of gravimetric and volumetric uptakes, surpassing the US Department of Energy targets. These findings suggest that the merger of energetic affinity and optimal geometry in BN building blocks overcomes the intrinsic limitations of sorbent materials, putting hybrid BN nanoarchitectures on equal footing with hydrides while demonstrating a superior capacity‐kinetics–thermodynamics relationship.     

Piperazine and methyldiethanolamine interrelationships in CO2 absorption by aqueous amine mixtures. Part II—Saturation rates of mixed reagent solutions

This work is a companion to a previous article, Part I, published in The Canadian Journal of Chemical Engineering, dealing with CO₂ absorption in aqueous solutions containing a single aminic reagent (specifically methyldiethanolamine (MDEA) or piperazine (PZ)). In this second part, different PZ/MDEA mixtures are experimentally studied and their performances are compared with that of the single reagents. It is indeed well known that small quantities of PZ added to MDEA aqueous solutions are sufficient to obtain a significant improvement in the kinetics of the process. PZ is considered an activator or promoter for MDEA, but the mechanism of this synergy has still not been clearly demonstrated. The aim of this study is an attempt to understand how PZ and MDEA can interact by experimentally analyzing this beneficial mutual effect and by explaining it with the help of a suitable yet not complex model. We believe that the involved chemistry is not more complex than that reported in Part I for the single reagents. According to our findings, it is MDEA that enhances the action of PZ, as opposed to what many authors claim. Moreover, our results seem to rule out the existence of any PZ shuttle effect.