Reservoir recultivation versus forms of heavy metals in sediments: the case of the Kielce City Lake

The Kielce Lake is a water reservoir located in the Kielce city zone. Areas around the reservoir are used for recreational, residential and industrial purposes. Additionally, the nearby state road to the city of Łódź, is a source of transportation pollution, including heavy metals. The reservoir is fed by a watercourse which receives municipal wastewater from the town of Masłów near Kielce. The amount and diversity of organic and inorganic compounds which flow into the reservoir causes heavy pollution of the Lake waters. To reduce the degree of reservoir pollution, a pulverizing aerator was installed in the middle of the Kielce Lake in May 2008. Sediment samples were collected at a depth of 0–20 cm between July 2008 and May 2010 at five sites in the littoral zone of the recultivation area. These environmental samples underwent a five-stage sequential extraction procedure, assisted by microwave radiation. The concentrations of trace metals Zn, Cu, Ni, Cr, Pb, Mn, Fe and Cd in various extracts were determined by means of F-AAS and GF-AAS. The results have shown a high concentration of analytes in reservoir sediments.     

Complexation of [2.2]paracyclophane with β- and γ-cyclodextrins studied by HPLC and NMR

The NMR spectra of [2.2]paracyclophane with β- or γ-cyclodextrin in DMF-d₇ at room temperature do not show significant complexation, while HPLC of the complexes in mixed H₂O:alcohol solvents demonstrate complexation with different stoichiometries. At 243 K in DMF solution the H3 and H5 NMR signals of γ-cyclodextrin (but not β) exhibit complexation-induced chemical shifts denoting complex formation. According to HPLC, at room temperature the [2.2]paracyclophane complex with β-cyclodextrin in 20% H₂O:EtOH exhibits 1:2 stoichiometry with K ₁ = 1×10² ± 2, K ₂ = 9.0×10⁴ ± 2×10³ (K = 9×10⁶) while that with γ-cyclodextrin in 50% H₂O:MeOH exhibits 1:1 stoichiometry with K ₁ = 4×10³ ± 150 M⁻¹. Thermodynamic parameters for both complexes have been estimated from the retention time temperature dependence. For the β-cyclodextrin complexation at 25°C ΔG ⁰ _CD is −39.7 kJ mol⁻¹ while ΔH ⁰ _CD and ΔS ⁰ _CD are −88.2 kJ mol⁻¹ and −0.16 kJ mol⁻¹ K⁻¹. For γ-cyclodextrin, the corresponding values are ΔG ⁰ _CD = −20.5 kJ mol⁻¹, ΔH ⁰ _CD = −33.5 kJ mol⁻¹ and ΔS ⁰ _CD = −0.04 kJ mol⁻¹ K⁻¹.      

Activity of Cuban propolis extracts on Leishmania amazonensis and Trichomonas vaginalis

In this paper we analyzed the antiprotozoal effects of eighteen Cuban propolis extracts (brown, red and yellow type) collected in different geographic areas, using Leishmania amazonensis (as a model of intracellular protozoa) and Trichomonas vaginalis (as a model of extracellular protozoa). All evaluated propolis extracts caused inhibitory effect on intracellular amastigotes of L. amazonensis. However, cytotoxicity on peritoneal macrophages from BALB/c mice was observed. Only five samples decreased the viability of T. vaginalis trophozoites at concentrations lower than 10 microg/mL. No correlation between the type of propolis and antiprotozoal activity was found. Cuban propolis extracts demonstrated activity against both intracellular and extracellular protozoa model, as well as the potentialities of propolis as a natural source to obtain new antiprotozoal agents.     

A unified quantum <Emphasis Type="Italic">SO</Emphasis>(3) invariant for rational homology 3-spheres

Given a rational homology 3-sphere M with |H ₁(M,ℤ)|=b and a link L inside M, colored by odd numbers, we construct a unified invariant I _M,L belonging to a modification of the Habiro ring where b is inverted. Our unified invariant dominates the whole set of the SO(3) Witten–Reshetikhin–Turaev invariants of the pair (M,L). If b=1 and L=∅, I _M coincides with Habiro’s invariant of integral homology 3-spheres. For b>1, the unified invariant defined by the third author is determined by I _M . Important applications are the new Ohtsuki series (perturbative expansions of I _M ) dominating quantum SO(3) invariants at roots of unity whose order is not a power of a prime. These series are not known to be determined by the LMO invariant.     

History-dependent subdifferential inclusions and hemivariational inequalities in contact mechanics

We consider a class of subdifferential inclusions involving a history-dependent term for which we provide an existence and uniqueness result. The proof is based on arguments on pseudomonotone operators and fixed point. Then we specialize this result in the study of a class of history-dependent hemivariational inequalities. Such kind of problems arises in a large number of mathematical models which describe quasistatic processes of contact between a deformable body and an obstacle, the so-called foundation. To provide an example we consider a viscoelastic problem in which the frictional contact is modeled with subdifferential boundary conditions. We prove that this problem leads to a history-dependent hemivariational inequality in which the unknown is the velocity field. Then we apply our abstract result in order to prove the unique weak solvability of the corresponding contact problem.     

Degradation modeling of 2 fatigue‐crack growth characteristics based on inverse Gaussian processes: A case study

Most modern products that are highly reliable are complex in their inner and outer structures. This situation indicates quality characterization by the interaction of multiple performance characteristics, which motivates the utilization of robust reliability models to obtain robust estimates. It is paramount to obtaining substantial information about a product's life cycle; therefore, when multiple performance characteristics are dependent, it is important to find models that address the joint distribution of performance degradation of such. In this paper, a reliability model for products with 2 fatigue‐crack growth characteristics related to 2 degradation processes is developed. The proposed model considers the dependence among degradation processes by using copula functions considering the marginal degradation processes as inverse Gaussian processes. The statistical inference is performed by using a Bayesian approach to estimate the parameters of the joint bivariate model. A time‐scale transformation is considered to assure monotone paths of the degradation trajectories. The comparison results of the reliability analysis, under both dependent and independent assumptions, are reported with the implementation of the proposed modeling in a case study, which consists of the crack propagation data of 2 terminals of an electronic device.     

Enzyme mediated incorporation of zirconium-89 or copper-64 into a fragment antibody for same day imaging of epidermal growth factor receptor

Identification of tumors which over-express Epidermal Growth Factor Receptor (EGFR) is important in selecting patients for anti-EGFR therapies. Enzymatic bioconjugation was used to introduce positron-emitting radionuclides (⁸⁹Zr, ⁶⁴Cu) into an anti-EGFR antibody fragment for Positron Emission Tomography (PET) imaging the same day as injection. A monovalent antibody fragment with high affinity for EGFR was engineered to include a sequence that is recognized by the transpeptidase sortase A. Two different metal chelators, one for ⁸⁹Zr^IV and one for ⁶⁴Cu^II, were modified with a N-terminal glycine to enable them to act as substrates in sortase A mediated bioconjugation to the antibody fragment. Both fragments provided high-quality PET images of EGFR positive tumors in a mouse model at 3 hours post-injection, a significant advantage when compared to radiolabeled full antibodies that require several days between injection of the tracer and imaging. The use of enzymatic bioconjugation gives reproducible homogeneous products with the metal complexes selectively installed on the C-terminus of the antibody potentially simplifying regulatory approval.

Enzymatic bioconjugation to introduce positron-emitting radionuclides (⁸⁹Zr, ⁶⁴Cu) into an anti-EGFR antibody fragment allows same day imaging with positron emission tomography.     

Some Novel Cobalt Diphenylphosphine Complexes: Synthesis,Characterization, and Behavior in the Polymerization of 1,3-Butadiene

Some novel cobalt diphenylphosphine complexes were synthesized by reacting cobalt(II) chloride with (2-methoxyethyl)diphenylphosphine, (2-methoxyphenyl)diphenylphosphine, and 2-(1,1-dimethylpropyl)-6-(diphenylphosphino)pyridine. Single crystals suitable for X-ray diffraction studies were obtained for the first two complexes, and their crystal structure was determined. The novel compounds were then used in association with methylaluminoxane (MAO) for the polymerization of 1,3-butadiene, and their behavior was compared with that exhibited in the polymerization of the same monomer by the systems CoCl₂(PⁿPrPh₂)₂/MAO and CoCl₂(PPh₃)₂/MAO. Some significant differences were observed depending on the MAO/Co ratio used, and a plausible interpretation for such a different behavior is proposed.