Hazardous metal geochemistry of sedimentary phosphate rock used for fertilizer (Maz?dag, SE Anatolia, Turkey)

Composition of phosphate rocks mostly depend on their type and origin. Sedimentary rocks contain high concentration of heavy metals. Phosphate rocks are mainly used for the manufacturing of phosphate fertilizers. The contents of heavy metals Cd, Co, Cu, Fe, Mn, Ni, Pb and Zn, as well as rare earth elements Ce, La, and Th were determined in sedimentary phosphate rock used for production of fertilizer in Turkey. The Kasrik-Semikan, Mazidag (Mardin, SE Anatolia, Turkey) high-grade phosphate rock used in this study is situated near the border with Syria and was deposited during the Turonian and Senonian (Cretaceous) ages. Total phosphorus (P) concentration in the rock is 18.5% on the average. Microwave acid digestion (MW-AD) followed by ?nductively Coupled Plasma-Optical Emission Spectrophotometry (ICP-OES) was carried out for the determination of all the elements of interest in phosphate rock. The results revealed that hazardous metal content of the phosphate rock was lower in Mazidag phosphate than that in samples imported from other countries and were within the safety limits.     

Amplitude and phase of light scattered by micro-scale aggregates of dielectric spheres: Comparison between theory and microwave analogy experiments

Light scattering is a useful diagnostic tool for characterization of particles. Direct scattering measurements for arbitrarily shaped micro-scale particles is difficult due to small-scale limitations. Microwave analogy is a convenient approach to realize such measurements as it enables realization of analogous experiments with larger model particles in a spectral domain where wavelengths are on centimeter scale. In the present study a test model analogous to light scattering by a micro-scale aggregate of dielectric spheres was constructed and experimentally characterized in the microwave regime. Measured amplitude and phase of the scattered field were compared with theoretical predictions obtained from quasi-exact multiple-scattering T-matrix method and discrete dipole approximation (DDA). Excellent agreement demonstrates the validities of both the experiment and the models.     

Equation structure and the meaning of the equal sign: The impact of task selection in eliciting elementary students’ understandings

This paper reports results from a written assessment given to 290 third-, fourth-, and fifth-grade students prior to any instructional intervention. We share and discuss students’ responses to items addressing their understanding of equation structure and the meaning of the equal sign. We found that many students held an operational conception of the equal sign and had difficulty recognizing underlying structure in arithmetic equations. Some students, however, were able to recognize underlying structure on particular tasks. Our findings can inform early algebra efforts by highlighting the prevalence of the operational view and by identifying tasks that have the potential to help students begin to think about equations in a structural way at the very beginning of their early algebra experiences.     

Synthesis and characterization of two oxo-bridged oxo(arylimido) [tris(3,5-dimethylpyrazolyl)borato]molybdenum(V) complexes and crystal structure of [MoTp*(O)Cl](μ-O)[MoTp*(Cl)(≡NC6H4OMe)]

Reaction of the oxo-molybdenum(V) compound, [MoTp*(O)Cl₂], [Tp*=hydrotris(3,5-dimethylpyrazol-1-yl)borate] with p-methoxy and p-nitroaniline in the presence of Et₃N under N₂, afforded the oxo-bridged oxo(arylimido) molybdenum(V) complexes, [MoTp*(O)Cl](-O)[MoTp*(Cl)(NC₆H₄R)] (1, R=OMe; 2, R=NO₂). The new compounds were characterized by elemental analysis, i.r., mass, and ¹H-n.m.r. spectra. The single crystal X-ray crystallographic determination of [MoTp*(O)Cl](-O)[MoTp*(Cl)(NC₆H₄OMe)] was carried out to confirm that there is a Mo—O—Mo bridge and a near linear arylimido group in the structure.     

Synthesis and antifungal evaluation of 1-aryl-2-dimethyl- aminomethyl-2-propen-1-one hydrochlorides

The development of resistance to current antifungal therapeutics drives the search for new effective agents. The fact that several acetophenone-derived Mannich bases had shown remarkable antifungal activities in our previous studies led us to design and synthesize some acetophenone-derived Mannich bases, 1-8 and 2-acetylthiophene-derived Mannich base 9, 1-aryl-2-dimethylaminomethyl-2-propen-1-one hydrochloride, to evaluate their antifungal activities. The designed chemical structures have α,β-unsaturated ketone moieties, which are responsible for the bioactivities of the Mannich bases. The aryl part was C?H?(1); 4-CH?C?H? (2); 4-CH?OC?H? (3); 4-ClC?H? (4); 4-FC?H? (5); 4-BrC?H? (6); 4-HOC?H? (7); 4-NO?C?H? (8); and C?H?S(2-yl) (9). In this study the designed compounds were synthesized by the conventional heating method and also by the microwave irradiation method to compare these methods in terms of reaction times and yields to find an optimum synthetic method, which can be applied for the synthesis of Mannich bases in further studies. Since there are limited number of studies reporting the synthesis of Mannich bases by microwave irradiation, this study may also contribute to the general literature on Mannich bases. Compound 7 was reported for the first time. Antifungal activities of all compounds and synthesis of the compounds by microwave irradiation were also reported for the first time by this study. Fungi (15 species) were used for antifungal activity test. Amphotericin B was tested as an antifungal reference compound. In conclusion, compounds 1-6, and 9, which had more potent (2-16 times) antifungal activity than the reference compound amphotericin B against some fungi, can be model compounds for further studies to develop new antifungal agents. In addition, microwave irradiation can be considered to reduce reaction period, while the conventional method can still be considered to obtain compounds with higher reaction yields in the synthesis of new Mannich bases.     

Glucocorticoid-loaded core-cross-linked polymeric micelles with tailorable release kinetics for targeted therapy of rheumatoid arthritis

Polymerizable and hydrolytically cleavable dexamethasone (DEX, red dot in picture) derivatives were covalently entrapped in core-cross-linked polymeric micelles that were prepared from a thermosensitive block copolymer (yellow and gray building block). By varying the oxidation degree of the thioether in the drug linker, the release rate of DEX could be controlled. The DEX-loaded micelles were used for efficient treatment of inflammatory arthritis in two animal models.     

Synthesis and characterization of [Ir(1,5-cyclooctadiene)(μ-H)]4: a tetrametallic Ir4H4-core, coordinatively unsaturated cluster

Reported herein is the synthesis of the previously unknown [Ir(1,5-COD)(μ-H)](4) (where 1,5-COD = 1,5-cyclooctadiene), from commercially available [Ir(1,5-COD)Cl](2) and LiBEt(3)H in the presence of excess 1,5-COD in 78% initial, and 55% recrystallized, yield plus its unequivocal characterization via single-crystal X-ray diffraction (XRD), X-ray absorption fine structure (XAFS) spectroscopy, electrospray/atmospheric pressure chemical ionization mass spectrometry (ESI-MS), and UV-vis, IR, and nuclear magnetic resonance (NMR) spectroscopies. The resultant product parallels--but the successful synthesis is different from, vide infra--that of the known and valuable Rh congener precatalyst and synthon, [Rh(1,5-COD)(μ-H)](4). Extensive characterization reveals that a black crystal of [Ir(1,5-COD)(μ-H)](4) is composed of a distorted tetrahedral, D(2d) symmetry Ir(4) core with two long [2.90728(17) and 2.91138(17) ?] and four short Ir-Ir [2.78680 (12)-2.78798(12) ?] bond distances. One 1,5-COD and two edge-bridging hydrides are bound to each Ir atom; the Ir-H-Ir span the shorter Ir-Ir bond distances. XAFS provides excellent agreement with the XRD-obtained Ir(4)-core structure, results which provide both considerable confidence in the XAFS methodology and set the stage for future XAFS in applications employing this Ir(4)H(4) and related tetranuclear clusters. The [Ir(1,5-COD)(μ-H)](4) complex is of interest for at least five reasons, as detailed in the Conclusions section.     

A shift scheduling model for employees with different seniority levels and an application in healthcare

This paper addresses the problem of scheduling medical residents that arises in different clinical settings of a hospital. The residents are grouped according to different seniority levels that are specified by the number of years spent in residency training. It is required from the residents to participate in the delivery of patient care services directly by working weekday and weekend day shifts in addition to their regular daytime work. A monthly shift schedule is prepared to determine the shift duties of each resident considering shift coverage requirements, seniority-based workload rules, and resident work preferences. Due to the large number of constraints often conflicting, a multi-objective programming model has been proposed to automate the schedule generation process. The model is implemented on a real case in the pulmonary unit of a local hospital for a 6-month period using sequential and weighted methods. The results indicate that high quality solutions can be obtained within a few seconds compared to the manually prepared schedules expending considerable effort and time. It is also shown that the employed weighting procedure based on seniority levels performs much better compared to the preemptive method in terms of computational burden.     

Synthesis,antioxidant activity and SAR study of novel spiro-isatin-based Schiff bases

Molecular Diversity - A new series of 21 Schiff bases of spiro-isatin was synthesized, and their DPPH, CUPRAC and ABTS cation radical scavenging abilities were investigated for antioxidant...