Anchoring of Copper(II)-Schiff Base Complex in SBA-15 Matrix as Efficient Oxidation and Biomimetic Catalyst.

A new mononuclear Cu(II) complex [Cu(L2)(H2O)2], where L is the Schiff base 2-[2-(3-bromopropoxy)benzylideneamino] benzoic acid, was synthesized and covalently anchored onto an amino-functionalized SBA-15 mesoporous silica in order to obtain an efficient heterogeneous catalyst. The elemental, structural, textural and morphological characterization confirmed the coordination of the central Cu(II) ion with two ligands and two H2O molecules in the synthesized complex and its successful immobilization into the inner pore surface of the NH2-functionalized support without the loss of the mesoporous structure. The catalytic activity of the free or immobilized Cu(II) complex was tested in the oxidation of cyclohexene with H2O2 under an air atmosphere and the dismutation reaction of the superoxide radical anions with very good results. In addition, catalyst reuse tests claim its suitability in alkene oxidation processes or as a biomimetic catalyst.

Fe-Ce/Layered Double Hydroxide Heterostructures and Their Derived Oxides: Electrochemical Characterization and Light-Driven Catalysis for the Degradation of Phenol from Water.

Fe-Ce/layered double hydroxides (LDHs) were synthesized via a facile route by exploiting the "structural memory" of the LDH when the calcined MgAlLDH and ZnAlLDH were reconstructed in the aqueous solutions of FeSO4/Ce(SO4)2. XRD analysis shows the formation of heterostructured catalysts that entangle the structural characteristics of the LDHs with those of Fe2O3 and CeO2. Furthermore, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, TG/DTG, SEM/EDX and TEM results reveal a complex morphology defined by the large nano/microplates of the reconstructed LDHs that are tightly covered with nanoparticles of Fe2O3 and CeO2. Calcination at 850 °C promoted the formation of highly crystallized mixed oxides of Fe2O3/CeO2/ZnO and spinels. The photo-electrochemical behavior of Fe-Ce/LDHs and their derived oxides was studied in a three-electrode photo-electrochemical cell, using linear sweep voltammetry (LSV), Mott-Schottky (M-S) analysis and photo-electrochemical impedance spectroscopy (PEIS) measurements, in dark or under illumination. When tested as novel catalysts for the degradation of phenol from aqueous solutions, the light-driven catalytic heterojunctions of Fe-Ce/LDH and their derived oxides reveal their capabilities to efficiently remove phenol from water, under both UV and solar irradiation.

Characterization of Titanium Alloy Obtained by Powder Metallurgy.

Ti-based alloys are an important class of materials suitable especially for medical applications, but they are also used in the industrial sector. Due to their low tribological properties it is necessary to find optimal technologies and alloying elements in order to develop new alloys with improved properties. In this paper, a study on the influence of sintering treatments on the final properties of a titanium alloy is presented. The alloy of interest was obtained using the powders in following weight ratio: 80% wt Ti, 8% wt Mn, 3% wt Sn, 6% wt Aluminix123, 2% wt Zr and 1% wt graphite. Two sintering methods were used, namely two-step sintering (TSS) and multiple-step sintering (MSS), as alternatives to conventional sintering which uses a single sintering dwell time. Evolution of sample morphology, composition and crystalline structure with sintering method was evidenced. The lower values for the friction coefficient and for the wear rate was attained in the case of the sample obtained by TSS.

Bioactive Co(II), Ni(II), and Cu(II) Complexes Containing a Tridentate Sulfathiazole-Based (ONN) Schiff Base.

New Co(II), Ni(II), and Cu(II) complexes were synthesized with the Schiff base ligand obtained by the condensation of sulfathiazole with salicylaldehyde. Their characterization was performed by elemental analysis, molar conductance, spectroscopic techniques (IR, diffuse reflectance and UV-Vis-NIR), magnetic moments, thermal analysis, and calorimetry (thermogravimetry/derivative thermogravimetry/differential scanning calorimetry), while their morphological and crystal systems were explained on the basis of powder X-ray diffraction results. The IR data indicated that the Schiff base ligand is tridentate coordinated to the metallic ion with two N atoms from azomethine group and thiazole ring and one O atom from phenolic group. The composition of the complexes was found to be of the [ML2]∙nH2O (M = Co, n = 1.5 (1); M = Ni, n = 1 (2); M = Cu, n = 4.5 (3)) type, having an octahedral geometry for the Co(II) and Ni(II) complexes and a tetragonally distorted octahedral geometry for the Cu(II) complex. The presence of lattice water molecules was confirmed by thermal analysis. XRD analysis evidenced the polycrystalline nature of the powders, with a monoclinic structure. The unit cell volume of the complexes was found to increase in the order of (2) < (1) < (3). SEM evidenced hard agglomerates with micrometric-range sizes for all the investigated samples (ligand and complexes). EDS analysis showed that the N:S and N:M atomic ratios were close to the theoretical ones (1.5 and 6.0, respectively). The geometric and electronic structures of the Schiff base ligand 4-((2-hydroxybenzylidene) amino)-N-(thiazol-2-yl) benzenesulfonamide (HL) was computationally investigated by the density functional theory (DFT) method. The predictive molecular properties of the chemical reactivity of the HL and Cu(II) complex were determined by a DFT calculation. The Schiff base and its metal complexes were tested against some bacterial strains (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Bacillus subtilis). The results indicated that the antibacterial activity of all metal complexes is better than that of the Schiff base.

A microscopic insight of the morphological changes induced by dental zirconia prosthetic structures.

As zirconia is today probably the dental material with the largest increase in the frequency of use in dental prosthetics, the reason for this study was based on a series of clinical observations made following its use in clinical prosthetics. Thus, we were interested in two aspects: the histological evaluation of the response of the oral soft tissues to the presence of the prosthetic structures in zirconia, and the microscopic evaluation of the abrasion lesions that appeared in the hard dental tissues of the zirconia prostheses antagonists. For the first part, samples from three zirconia-based dental prosthetics commercial products were implanted submucosal in the oral cavity of male Wistar rats. After six weeks, the oral soft tissue reaction was clinically and then histologically investigated. For the second part, we made two study groups to investigate the influence of the zirconia-glazed surface vs. polished surface to the wear pattern of the antagonist enamel, using a tribological equipment and a dedicated software. Our study showed a good clinical response of the oral soft tissues surrounding the inserted zirconia samples, with subclinical, only histological revealed, signs of inflammation, of a foreign body reaction, while polished zirconia samples determined abrasion surfaces, with a different pattern and significantly smaller dimensions, compared to zirconia glazed samples, at the level of the hard dental tissues of the antagonist teeth. Despite the generally good response of the biological structures to the presence of zirconia prosthetic structures in the oral environment, more scientifically proved information is needed to obtain the desired biological responses in all clinical situations.

Mesoporous silica functionalized with 1-furoyl thiourea urea for Hg(II) adsorption from aqueous media.

New organic-inorganic hybrid materials were prepared by covalently anchoring 1-furoyl thiourea on mesoporous silica (SBA-15). By means of various characterization techniques (X-ray diffraction, nitrogen adsorption-desorption, thermogravimetric analysis, and FTIR spectroscopy) it has been established that the organic groups were successfully anchored on the SBA-15 surfaces and the ordering of the inorganic support was preserved during the chemical modifications. The hybrid sorbents exhibited good ability to remove Hg(II) from aqueous solution. Thus, at pH 6, the adsorption capacity of mercury ions reached 0.61 mmol g(-1).