Structure, Properties and Behavior of Kyanite： Use in Refractory Monolithics

1 Introduction Kyanite is an important naturally occurring in-dustrial mineral and is used in the manufacture of avariety of industrial ceramic products; notable exam-ples include refractories and porcelains. It is a high-pressure polymorph of the aluminosilicates of the ne-sosilicate group, which includes kyanite, sillimanite,and andalusite. These three aluminous or alumina-rich minerals are chemically identical with the compo-sition, Al_2SiO_5, but have different crystal structuresand physical properties. It is, however, their alumina     

The use of RO to remove emerging micropollutants following CAS/UF or MBR treatment of municipal wastewater

The removal of various organic micropollutants (OMPs), including six antibiotics (ERY, ROX, CLA, SMX, SMZ, and TMP), three pharmaceuticals (ibuprofen, salicylic acid, and diclofenac), one industrial product (BPA), and one hormone (cholesterol), was investigated in two pilot plants treating the same raw sewage of the Tel-Aviv WWTP. The effluent production by CAS-UF was 45 m³/h while that of MBR was 40 L/h. Each system's effluent constituted the feed for its RO, which comprised three RO steps after the CAS/UF and a semi-batch RO system after the MBR. Despite significant molecular differences between the selected OMPs, high removal rates were achieved after the RO stage (> 99% for macrolides, pharmaceuticals, cholesterol, and BPA, 95% for diclofenac, and > 93% removal of sulfonamides). However, low antibiotics concentrations and 28–223 ng/L residuals of ibuprofen, diclofenac, salicylic acid, cholesterol, and BPA in the MBR/RO and CAS-UF/RO permeates showed that although RO is an efficient removal solution, it cannot serve as an absolute barrier to OMPs. Therefore, additional treatment techniques should be considered to be incorporated aside the RO to ensure complete removal of such substances.     

Effect of temperature and thermodynamic quality of solvent over unperturbed chain dimensions of nylon 6

A nylon 6 sample having average molecular mass 4.825 × 10⁵ g mol^?1 was fractionated into five different fractions with respect to molecular mass, which ranged from 3691 to 999,000 g mol^?1. The light scattering and intrinsic viscosity measurements were made in m‐cresol and its mixture with 1,4‐dioxane. The second virial coefficient, radius of gyration and Mark Houwink's constant and unperturbed chain dimensions were determined by light scattering and viscosity measurement. It has been observed that all these parameters are composition of solvent and temperature dependent. The solvent having composition of 97% m‐cresol and 3% dioxane, was best and it deteriorated with the increase/decrease in percentage of 1,4‐dioxane in m‐cresol. However, its thermodynamic quality was enhanced with the temperature. Such variation in quality of solvent was reflected in all the estimated parameters and showed maxima at this composition of solvent. The unperturbed dimensions obtained by different methods though, differed in values but showed same trend and NA‐MKB method gave close results to the one obtained through [η_o]. A new expression has also been proposed relating k_o to solvent quality and temperature and the data obtained by us for nylon‐6 and the one obtained from the literature for dextran obeyed this expression up to large extent irrespective of the solvent composition and temperature. The proposed equations have also been applied to dextran/methoxy ethylene and dextran/ethylene glycol systems and worked well. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.     

A generalized equation for the prediction of melting temperatures of homopolymers and copolymers

A generalized equation was derived to calculate the melting temperatures of homopolymers and copolymers. The Gibbs‐Thomson equation for homopolymers and a modified application to copolymers were derived using the proposed equation. The melting temperature T_m⁰ in the Flory equation corresponds to the melting temperature T_m^C,∞ of copolymer crystals with stems of infinite length. Also, T_m^C,n*, the melting temperature for copolymer crystals with stems containing the maximum possible number of structural units, n*, should be used instead of T_m⁰ as the basis of supercooling in crystallization. The proposed equation shows good agreement with experimental data for α‐alkene‐ethylene homogeneous copolymers.     

Phenolic profiles of Turkish olives and olive oils

Phenolic compound distribution of Turkish olive cultivars and their matching olive oils together with the influence of growing region were investigated. One hundred and one samples of olives from 18 cultivars were collected during two crop years from west, south and south‐east regions of Turkey. The olives were processed to oils and both olive and olive oil samples were evaluated for their phenolic compound distribution. The results have shown that main phenolics of Turkish olives were tyrosol, oleuropein, p‐coumaric acid, verbascoside, luteolin 7‐O‐glucoside, rutin, trans cinnamic acid, luteolin, apigenin, cyanidin 3‐O‐glucoside and cyanidin 3‐O‐rutinoside. Oleuropein and trans cinnamic acid were present in higher amounts among all phenolics. Principal component analyses showed that the growing region did not have drastic effect on phenolic profile of olives. The major phenolic compounds of olive oils were tyrosol, syringic acid, p‐coumaric acid, luteolin‐7‐O‐glucoside, trans cinnamic acid, luteolin and apigenin. Luteolin is a predominant phenolic compound in almost all oil samples. Total phenol concentrations of Southeast Anatolian oils were found to be lower than those of the other regions.     

Properties of PET/clay nanocomposite films

Polyethylene terephthalate (PET) nanocomposite films were prepared by cast extrusion followed by uniaxial stretching, using chill rolls. Transmission electron microscopy (TEM) and wide angle X‐ray diffraction (WAXD) showed that the clay layers were aligned in the machine direction (MD) in the PET/clay nanocomposite (PCN) films. Differential scanning calorimetry (DSC) showed that PCN films have higher crystallinity than the neat PET films, possibly due to the nucleating role of the silicate layers. The PCN films became hazier as the clay content increased, but the film transparency remained in the acceptable range. Oxygen permeability of the PCN films decreased by 23% compared to the neat PET film. This is comparable with predictions of models proposed in the literature. Silicate incorporation brought about 20% increase in the tensile modulus, while the puncture and tear propagation resistance were reduced, due to brittleness of the PCN films. The measured modulus (1.7 GPa) was somewhat smaller than the values predicted using the Pseudoinclusion model (2.1 GPa). POLYM. ENG. SCI., 2012. © 2011 Society of Plastics Engineers     

Quantum chemical studies on corrosion inhibition for series of thio compounds on mild steel in hydrochloric acid

Quantum chemical calculations were performed on ten thio compounds using semi-empirical method PM3 within program package of Material Studio 5.5. The effect of molecular structure on the corrosion inhibition efficiency was investigated using the quantum chemical calculations. The electronic properties such as highest occupied molecular orbital (HOMO), lowest unoccupied molecular orbital (LUMO) energy levels, (LUMO–HOMO) energy gap, dipole moment (λ) and fraction of electron transfer (ΔN) were calculated and discussed. A relationship between the corrosion inhibition efficiency and several quantum parameters was established with coefficient correlation (R²) of 0.8894.     

Design of High Sensitive Temperature Sensor Based on Two-Dimensional Photonic Crystal

In this effort, a two-dimensional photonic crystal ring resonator (2DPCRR) is simulated. This device is developed for temperature detection in harsh enviro     

The Effect of Spray-Freeze Drying of Montmorillonite on the Morphology,Dispersion, and Crystallization in Polypropylene Nanocomposites

The spray-freeze drying (SFD) technique was applied to sonicated aqueous suspensions of spray-dried montmorillonite clay (MMT) to produce highly porous agglomerates (SFD-MMT). Both MMT (used as a reference) and SFD-MMT were subsequently incorporated in polypropylene (PP) via melt compounding to produce 2 wt % nanocomposites with and without maleic anhydride grafted polypropylene (PP-g-MA). Polypropylene nanocomposites containing SFD-MMT exhibited thinner silicate flake layers compared to large agglomerates in PP/MMT nanocomposites. SFD-MMT particles became even more finer in the presence of PP-g-MA (i.e., in PP/PP-g-MA /SFD-MMT) where it hindered PP crystallization instead of serving as nucleation sites for the PP crystallization during rapid cooling. SFD-MMT improved the thermal stability of PP/PP-g-MA by 30°C compared to only 5–8°C for MMT/nanocomposites. MMT acts as a heterogeneous nucleating agent in the nucleation-controlled PP nanocomposites, but the hindrance effect was observed for the PP/PP-g-MA with SFD-MMT. PP/PP-g-MA/SFD-MMT exhibited twice the edge surface energy as compared to PP/PP-g-MA/MMT. The incorporation of both types of MMT raised the tensile moduli of PP and PP/PP-g-MA, with no improvement in their tensile strength and a decrease in the elongation at break. The PP/PP-g-MA/SFD-MMT showed brittle failure. POLYM. ENG. SCI., 60:168–179, 2020. © 2019 Society of Plastics Engineers     

Poly(azomethine-imide)s containing siloxane moities: Optical,thermal, mechanical,and morphological properties

A new series of poly(azomethine-imide)s having siloxane moities in backbone was prepared using different dianhydrides.Thermal, optical, and morphological properties of these polymers were clarified. Also, bulky  CO and  CF₃ group effects and meta or para-substituted aldeyhde effects on the mentioned properties were evaluated. The structural characterization of poly(azomethine-imide)s was carried out using a FT-IR spectroscopy. The optical properties of the polymers were performed via an UV–Vis spectrophotometer. Optical band gap of the poly(imide)s containing azomethine was calculated between 2.20 and 2.33 eV. Thermal behavior of poly(azomethine-imide)s was also studied using TG-DTA, DSC, and DMA techniques. The onset degradation temperature and percentage char values of the polyimides were found in the range from 429 to 545 °C and 22 to 35%, respectively. Thermal stability results demonstrated that benzophenone bearing poly(azomethine-imide)s have higher onset temperature, percentage char, and the glass transition temperature than poly(azomethine-imide)s derived from hexafluoroisopropylidene. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48364.