Template‐Based Synthesis of Aluminum Nitride Hollow Nanofibers Via Plasma‐Enhanced Atomic Layer Deposition

Aluminum nitride (AlN) hollow nanofibers were synthesized via plasma‐enhanced atomic layer deposition using sacrificial electrospun polymeric nanofiber templates having different average fiber diameters (~70, ~330, and ~740 nm). Depositions were carried out at 200°C using trimethylaluminum and ammonia precursors. AlN‐coated nanofibers were calcined subsequently at 500°C for 2 h to remove the sacrificial polymeric nanofiber template. SEM studies have shown that there is a critical wall thickness value depending on the template's average fiber diameter for AlN hollow nanofibers to preserve their shapes after the template has been removed by calcination. Best morphologies were observed for AlN hollow nanofibers prepared by depositing 800 cycles (corresponding to ~69 nm) on nanofiber templates having ~330 nm average fiber diameter. TEM images indicated uniform wall thicknesses of ~65 nm along the fiber axes for samples prepared using templates having ~70 and ~330 nm average fiber diameters. Synthesized AlN hollow nanofibers were polycrystalline with a hexagonal crystal structure as determined by high‐resolution TEM and selected area electron diffraction. Chemical compositions of coated and calcined samples were studied using X‐ray photoelectron spectroscopy (XPS). High‐resolution XPS spectra confirmed the presence of AlN.     

Effects of Surfactants on the Properties of Styrene/Methacrylate–Type Superplasticizer in Cement Paste

Copolymer emulsion lattices based on styrene (St) with methacrylate monomers, were synthesized with composition ratio (5/5) in the presence of a co-surfactants that consists of dodecyl benzene sodium sulfonate with polyvinyl alcohol (DBSS/PVA) and DBBS with polyoxyethylene glycol monomethyl ether (DBBS/POE). The obtained latices were characterized by ¹H NMR, rheological and morphological techniques. The effect of latices on the physicomechanical properties of ordinary Portland cement (OPC) pastes was investigated. The results showed that the addition of water mixed to the cement with copolymer improves most of the specific characteristics of OPC.     

Some Semiconductor Properties of Carboxymethyl Cellulose-Copper Complexes

Metal chelates of three grades of carboxymethyl cellulose (CMC) (LI-L3) with Cu(II) ions, either originating from CuCl₂ or CuSO₄, were prepared and characterized by elemental analysis, infrared spectra, and electrical conductivity studies. The results showed that the degree of substitution of CMCs and the origin of the Cu(II) ion have a profound effect on the amount of metal included in the polymer complexes and the structure and the electrical conductivity of the prepared complexes. CMC acts as a uninegatively charged bidentate ligand when it is chelated with Cu(II) of CuCl₂ via the carboxymethyl group and exhibits the formula Cu(L)₂, whereas it acts as a binegatively charged bitentate ligand when it is chelated with CuSO₄ via the carboxymethyl and secondary hydroxyl groups and exhibits the formula CuL.2H₂O. The investigation revealed that the electrical conductivity depends on the temperature and has two maximum peaks. The values of the activation energy for the conductivity of CMC and their complexes indicated that the samples changed from a low-semiconductor to a high-semiconductor property with heating. It is found that CMC-Cu(II) complexes formed from CuSO₄ exhibit a high-semiconductor property compared to complexes derived from CuCl₂.     

Acetanilide-loaded injectable hydrogels with enhanced bioactivity and biocompatibility for potential treatment of periodontitis

Chronic periodontitis poses long-term challenges in dentistry, requiring the development of innovative dental composites with biocompatibility, bone regeneration, and antibacterial properties. This study focuses on synthesis of novel injectable thermoresponsive hydrogels composed of chitosan, sodium bicarbonate, bioactive glass (20 and 40% w/w), and acetanilide drug (0.3 and 0.6% w/w). These hydrogels exhibit a sol–gel transition at 37°C, addressing periodontal challenges with reduced gelation time. The smooth flow characteristic was evaluated through 17-22 gauge syringe needles at low temperature. Rheological studies demonstrated pseudoplastic behavior, with viscosity decreasing as shear rate increases. Fourier transform infrared and x-ray diffraction analysis confirmed the bioactivity of hydrogels, forming a bone-like apatite layer in simulated body fluid. The drug-loaded hydrogels demonstrated promising in vitro antibacterial properties against dental pathogens, specifically Staphylococcus aureus and Pseudomonas aeruginosa. Drug dissolution analysis revealed relatively high release rate at 37°C, highlighting its role in rapidly eliminating bacterial colonies at the target site, while the subsequent sustained release contributes to the prevention of infection recurrence. Finally, biocompatibility was assessed with fibroblast, where the cells were observed anchoring into the polymeric chains of hydrogel through extended filopodia.     

Smoldering combustion of rice husk dusts on a hot surface

An accumulated combustible dust layer on some hot process equipment, such as grinders, dryers, hot bearings, etc., can be ignited and lead to fires if the hot surface temperature is sufficiently high. Experimental tests are used to determine the minimum hot surface temperature for dust ignition, the ignition temperature of dust itself, and the ignition times in this study. Egyptian rice husk dust is sieved into different sizes (particle diameters) to be used in this investigation. The effects of the dust particle size and the sample size (depth of the dust layer) on ignition parameters are tested. The boundary between the ignition and non-ignition conditions is investigated precisely through a large number of tests. The results show that the minimum hot plate temperature for ignition of dusts decreases as the dust layer depth increases.     

Substituted Thiadiazole, Oxadiazole, Triazole and Triazinone as Antimicrobial and Surface Activity Compounds

Stearic acid ( 1 ) was utilized as a new cheap starting material in the manufacture of important biologically active heterocycles as thiadiazole, oxadiazole, triazole and triazinone derivatives ( 2 – 11 ) by treating with different nucleophiles. These heterocycles bears active hydrogen atom (SH, NH and NH₂) which could be propoxylated by different moles of propylene oxide (5, 10, 15 mol) to produce nonionic compounds ( 12 – 21 ) a – c having functions as surface and antimicrobial activities. The structural elucidation of these compounds is based on IR, ¹H NMR, ¹³C NMR and elemental analysis. The surface properties (surface and interfacial tension, cloud point, witting time, foaming properties and emulsion stability) and the biodegradability were screened beside these compounds have been tested for their antimicrobial activity.     

A Systematic Study of Mixed Surfactant Solutions of a Cationic Ester-Bonded Dimeric Surfactant with Cationic, Anionic and Nonionic Monomeric Surfactants in Aqueous Media

A novel cationic biodegradable dimeric (gemini) surfactant, ethane-1,2-diyl bis(N,N-dimethyl-N-hexadecylammoniumacetoxy) dichloride (16-E2-16), containing an ester-linked spacer was synthesized. Its pure and mixed micellization properties with monomeric surfactants cetyl trimethyl ammonium chloride, cetyl pyridinium chloride, sodium dodecyl sulfate, sodium dodecyl benzene sulfonate, cetyl alcohol ethoxylate (20EO) and tert-octylphenol ethoxylate (9.5EO) were investigated by surface tension measurements at 30 °C. The critical micelle concentration (CMC) of 16-E2-16 is well below that of cetyl trimethyl ammonium chloride containing the same number of carbon atoms in the hydrophobic tail per polar head. At different mole fractions of the gemini surfactant, the CMCs of the gemini-conventional binary mixtures were determined and were found to be less than the ideal CMC values in all the cases indicating synergistic interactions. Aggregation number and Stern–Volmer constant, obtained by the fluorescence quenching technique, also support the synergistic behavior of the surfactant systems.     

A Chemometric Approach to Assess the Frying Stability of Cottonseed Oil Blends During Deep-Frying Process: I. Polar and Polymeric Compound Analyses

The main goal of the present study was (i) to determine the formation of degradation products in cottonseed oil (CSO) blends during deep frying process by adsorption and high performance size exclusion chromatography techniques and (ii) to evaluate the impacts of food additives on total polar (TPC) and polymeric compound (PTAG) formation using a chemometric approach. In order to prepare the frying CSO blends; ascorbic palmitate, mixed tocopherols, dimethylpolysiloxane, lecithin and sesame oils were used as additives. To determine the real impacts of additives, a quarter-fraction factorial experimental design with two levels and five factors was used. The changes in TPC and PTAG data were carefully evaluated during 10 h of frying at 170 ± 5 °C with normal distribution (ND) graphs and analyzed using a one-way analysis of variance (ANOVA), followed by Tukey’s Post-hoc test (α = 0.05). The results indicated that the increasing values for TPC and PTAG during the frying processes for all blends, TPC and PTAG contents reached maximum levels of 16.37 and 6.01 % respectively, which are below the limit values stated by official authorities for the quality assessment of frying oils. The ANOVA test results were in good agreement with ND graphs and data indicated that the impact of mixed tocopherols was significant for TPC formation, meanwhile the impact of lecithin and ascorbic palmitate × dimethylpolysiloxane were significant for PTAG formation. Thus, the present study should be considered to be a very useful guide for developing new frying oil formulations based on CSO by using food additives.     

Preparation and characterization of crednerite glass–ceramics in the MnO·CuO·SiO2 system

Nanoscale crednerite (CuMnO₂) was prepared in the system MnO·CuO·SiO₂, using glass–ceramics technique for the first time. Based on obtained data from differential thermal analysis (DTA), the prepared samples were heat-treated at 700 and 800 °C for 2 h. The presence of crystalline phases after and before heat treatment was investigated by X-ray diffraction analysis. Crystallization of crednerite (CuMnO₂), manganese silicate (Mn₂SiO₄) and traces of cuprite (Cu₂O) and cristobalite (SiO₂) phases were recognized. Transmission electron microscopy showed nanoscale crystals in the range 5–10 nm. The prepared glass–ceramics showed ferrimagnetic properties with wide range coercivity from 53 to 2217 Hci and magnetization saturation from 0.21708 to 1.2 emu/g. From IR reflection data; the reflection intensity of the light is high in the range of orange–red color and violet–blue colors and low in the range of green color.     

Microwave Dehydration of Borax: Characterization,Dehydration Kinetics,and Modelling

Glass Physics and Chemistry - In the present study, borax (Na2B4O7·10H2O) was dehydrated using microwave radiation and the dehydration rate curves were calculated. The kinetic parameters and...