Boost the Crystal Installation and Magnetic Features of Cobalt Ferrite/M-Type Strontium Ferrite Nanocomposites Double Substituted by La3+ and Sm3+ Ions (2CoFe2O4/SrFe12-2xSmxLaxO19).

Spinel cobalt ferrite/hexagonal strontium hexaferrite (2CoFe2O4/SrFe12-2xSmxLaxO19; x = 0.2, 0.5, 1.0, 1.5) nanocomposites were fabricated using the tartaric acid precursor pathway, and the effects of La3+-Sm3+ double substitution on the formation, structure, and magnetic properties of CoFe2O4/SrFe12-2xSmxLaxO19 nanocomposite at different annealing temperatures were assayed through X-ray diffraction, scanning electron microscopy, and vibrating sample magnetometry. A pure 2CoFe2O4/SrFe12O19 nanocomposite was obtained from the tartrate precursor complex annealed at 1100 °C for 2 h. The substitution of Fe3+ ion by Sm3-+La3+ions promoted the formation of pure 2CoFe2O4/SrFe12O19 nanocomposite at 1100 °C. The positions and intensities of the strongest peaks of hexagonal ferrite changed after Sm3+-La3+ substitution at ≤1100 °C. In addition, samples with an Sm3+-La3+ ratio of ≥1.0 annealed at 1200 °C for 2 h showed diffraction peaks for lanthanum cobalt oxide (La3Co3O8; dominant phase) and samarium ferrite (SmFeO3). The crystallite size range at all constituent phases was in the nanocrystalline range, from 39.4 nm to 122.4 nm. The average crystallite size of SrFe12O19 phase increased with the number of Sm3+-La3+ substitutions, whereas that of CoFe2O4 phase decreased with an x of up to 0.5. La-Sm co-doped ion substitution increased the saturation magnetization (Ms) value and the subrogated ratio to 0.2, and the Ms value decreased with the increasing number of double substitutions. A high saturation magnetization value (Ms = 69.6 emu/g) was obtained using a La3+-Sm3+ co-doped ratio of 0.2 at 1200 for 2 h, and a high coercive force value (Hc = 1192.0 Oe) was acquired using the same ratio at 1000 °C.

Mesopores silica nanotubes-based sensors for the highly selective and rapid detection of Fe2+ ions in wastewater, boiler system units and biological samples.

Mesopores silica nanotubes (MSNTs)-based chemical sensors for the rapid detection and of highly selective Fe2+ ions have been prepared. The novel nanosensors were prepared via immobilization of 1,10-phenanthroline-5-amine (PA) and bathophenanthroline (BP) onto the MSNTs. The resultant PA and BP sensors display high sensitivity for detection the Fe2+ ions in tap water, river water, sea water, two units in simple cycle power station, and biological samples. More interestingly, upon meeting ultra-trace amount of Fe2+ ions, a red complex appears at once. Color changes can be seen from the naked eye and tracked with a smartphone or spectrophotometric techniques. The response time that is necessary to achieve a stable signal was less than 15 s. The Univariate (Univar) calibration technique had been utilized for the determination of figures of merits. The detection limit obtained from the digital image analysis was 19 ppb (7.04 × 10-7 M) for Fe2+ ions, while the obtained from the spectrophotometric method was 6.7 ppb (2.48 × 10-7 M). Therefore, the two sensors had been successfully used in the determination of Fe2+ in several real samples with high sensitivity and selectivity. In addition, they can be used as a simple, rapid, and portable method to detect and quantify the pre rust in any cooler system.

Development of New Thiazole Complexes as Powerful Catalysts for Synthesis of Pyrazole-4-Carbonitrile Derivatives under Ultrasonic Irradiation Condition Supported by DFT Studies.

In this study, we are interested in preparing Fe(III), Pd(II), and Cu(II) complexes from new thiazole derivatives. All syntheses were elaborately elucidated to estimate their molecular and structural formulae, which agreed with those of mononuclear complexes. The square-planer geometry of Pd(II) complex (MATYPd) was the starting point for its use as a heterocatalyst in preparing pyrazole-4-carbonitrile derivatives 4a-o using ultrasonic irradiation through a facile one-pot reaction. The simple operation, short-time reaction (20 min), and high efficiency (97%) were the special advantages of this protocol. Furthermore, this green synthesis strategy was advanced by examination of the reusability of the catalyst in four consecutive cycles without significant loss of catalytic activity. The new synthesis strategy presented remarkable advantages in terms of safety, simplicity, stability, mild conditions, short reaction time, excellent yields, and use of a H2O solvent. This catalytic protocol was confirmed by the density functional theory (DFT) study, which reflected the specific characteristics of such a complex. Logical mechanisms have been suggested for the successfully exerted essential physical parameters that confirmed the superiority of the Pd(II) complex in the catalytic role. Optical band gap, electrophilicity, and electronegativity features, which are essential parameters for the catalytic behavior of the Pd(II) complex, are based mainly on the unsaturated valence shell of Pd(II).

Developed Process Circuit Flowsheet of Al Amar Ore for Production of Nanocrystalline Ferrite and Improving Gold Recovery.

Al Amar gold ore is rich in sulfides of base metals and is commercially applied for the production of copper concentrate via floatation and gold bullion by cyanidation of tailing. The current process flowsheet suffers from low gold recovery (∼60%) and loss of metals in the hazardous stockpiled residue. This work addresses these drawbacks by a newly experimental redesign of the process circuit. The innovative flowsheet comprises a sequence of operations, including acid leaching of the roasted ore, gold recovery from the leach residue, and preparation of a valuable zinc-copper-lead ferrite from the filtrate by coprecipitation followed by heat treatment. The ore is roasted at 650 °C and then leached in 20% HCl, where most of Zn, Cu, Pb, and Fe contents are dissolved, while pristine gold remains in the residue. Most of the gold (∼93%) can be recovered by cyanidation of the acid leach residue. Stoichiometric ratios of dissolved Zn, Cu, Pb, and Fe in the acid leach solution can be kept at 0.6:0.3:0.1:2.0, respectively, only by adding a small amount of ferric chloride. These metals are coprecipitated at varying pH values from 8 to 10, and the produced powders are annealed at temperatures from 600 to 1100 °C. X-ray diffraction (XRD) charts reveal sharp peaks of the targeted Zn0.6Cu0.3Pb0.1Fe2O4 phase at 600 °C, while a highly crystalline single phase is obtained at 1100 °C, independently of precipitation pH. The crystalline size of the produced powders increases with annealing temperatures (from 18-27 nm at 600 °C to 85-105 nm at 1100 °C). The finest size is found at pH 12. Scanning electron microscopy (SEM) investigation shows uniform cubic microstructures of samples annealed at 1100 °C. The produced ferrite powders exhibit soft magnetic characteristics. Saturation magnetization, M s, substantially increases with pH. Coercivity, H c, increases with increasing annealing temperatures, from 600 to 800 °C, and decreases above 800 °C. Preliminary cost-benefit analysis revealed that the profit margin of the proposed process flowsheet is promising. The wastewater is almost free of heavy metals. Our advances in high gold recovery and preparation of valuable magnetic nanocrystalline ferrite provide exciting opportunities to enhance and maximize Al Amar ore production for practical applications.

Synthesis of Carbon Nanotube-Nanotubular Titania Composites by Catalyst-Free CVD Process: Insights into the Formation Mechanism and Photocatalytic Properties.

This work presents the synthesis of carbon nanotubes (CNTs) inside titania nanotube (TNTs) templates by a catalyst-free chemical vapor deposition (CVD) approach as composite platforms for photocatalytic applications. The nanotubular structure of TNTs prepared by electrochemical anodization provides a unique platform to grow CNTs with precisely controlled geometric features. The formation mechanism of carbon nanotubes inside nanotubular titania without using metal catalysts is explored and explained. The structural features, crystalline structures, and chemical composition of the resulting CNTs-TNTs composites were systematically characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. The deposition time during CVD process was used to determine the formation mechanism of CNTs inside TNTs template. The photocatalytic properties of CNTs-TNTs composites were evaluated via the degradation of rhodamine B, an organic model molecule, in aqueous solution under mercury-xenon Hg (Xe) lamp irradiation monitored by UV-visible spectroscopy. The obtained results reveal that CNTs induces a synergestic effect on the photocatalytic activity of TNTs for rhodamine B degradation, opening new opportunities to develop advanced photocatalysts for environmental and energy applications.

Photoswitchable membranes based on peptide-modified nanoporous anodic alumina: toward smart membranes for on-demand molecular transport.

A smart and reversibly photoswitchable membrane based on an azobenzene photo-switch containing peptides attached inside the pores of nanoporous anodic alumina membranes (NAAMs) is presented. The transport of molecules of interest across the photoswitchable peptide (PSP) functionalized NAAMs can be effectively controlled and manipulated as a function of the photostationary state of the azobenzene group in a PSP.

Localized drug delivery of selenium (Se) using nanoporous anodic aluminium oxide for bone implants.

Electrochemically engineered nanoporous anodized aluminium oxide (AAO) prepared on aluminium (Al) foil by anodization process was employed as a platform for loading different forms of selenium (Se) in order to investigate their release behaviour and potential application for localized drug delivery targeting bone cancer. Several forms of Se including inorganic Se (H2SeO3), organic Se ((C6H5)2Se2), metallic Se, their chitosan composites, electrodeposited (ED) and chemical vapour deposited (CVD) Se were explored and combined with another model drug (indomethacin). Structural, drug-loading and in vitro drug-releasing characteristics of prepared Se-based drug delivery carriers were characterized by scanning electron microscopy (SEM), thermogravimetric analysis (TGA) and UV-visible spectroscopy (UV-Vis), respectively. Sustained and controlled release of Se was demonstrated through chitosan-composites of inorganic, organic or metallic forms of Se loaded into nanoporous AAO carriers. Cell viability studies showed decreasing toxicity to cancer cells in the order: inorganic Se > ED Se > CVD Se > metallic Se > organic Se. The study suggests new alternatives for localized drug treatment based on low-cost nano-engineered carriers loaded with Se having anti-cancer properties.