Molecular weight characteristics of humic substances from different environments as determined by size exclusion chromatography and their statistical evaluation

Recorded molecular weights (MWs) for humic substances (HS) range from a few hundred to millions of daltons. For purposes of defining HS as a specific class of chemical compounds, it is of particular importance to ascertain if this broad range of MWs can be attributed to actual variability in molecular properties or is simply an artifact of the analytical techniques used to characterize HS. The main objectives of this study were (1)to establish if a preferential range of MWs exists for HS and (2) to determine any consistent MW properties of HS. To reach the goal, we have undertaken an approach to measure under standardized conditions the MW characteristics of a large set of HS from different natural environments. Seventy-seven humic materials were isolated from freshwater, soil, peat, and coal, such that each possessed a different fractional composition: humic acid (HA), fulvic acid (FA), and a nonfractionated mixture of HA and FA (HF). Size exclusion chromatography (SEC) was used as the analytical technique to determine molecular weight characteristics. The MW distributions were characterized by number (Mn) and weight (Mw) average MW, and by polydispersity. The complete range of Mw values varied within 4.7-30.4 kDa. The maximum Mw values were observed for peat HF and soil HA, whereas the smallest weights were measured for river water HF. Maximum values of polydispersity (3.5-4.4) were seen for peat HF and soil HA, while much lower values (1.6-3.1) were found for all preparations isolated with XAD-resins. Statistical evaluation showed consistent Mw and Mn variations with the HS source, while polydispersity was mostly a function of the isolation procedure used. A conclusion was made that HS have a preferential range of MW values that could characterize them as a specific class of chemical compounds.     

Enhancement of magnetic losses in hybrid polymer composites with MnZn-ferrite and conductive fillers

Polymer composites (PCs) with a polyurethane (PU) matrix filled with magnetic filler (MnZn ferrite) and hybrid polymer composites (HPCs) consisting of this magnetic filler and various types of conductive fillers (carbon black, carbon fibers, aluminum powder, polypyrrole) are prepared. The matrix structure of a HPC is formed (i) by a polymer filled with conductive filler, which forms the skeleton of an infinite cluster, and (ii) by ferrite particles that are larger than conductive particles. Thus, an HPC represents an ensemble of ferrite particles each of which is surrounded by a conductive medium and can be considered as a “core–shell” structure. The development of a core–shell structure is evidenced by the lower electric percolation threshold in an HPC compared with that in PU filled with conductive filler. Magnetic and dielectric spectra of PCs and HPCs are studied in the frequency range from 1 MHz to 10 GHz. Hybrid systems exhibit a considerable enhancement of magnetic losses compared with PCs. The enhancement of magnetic losses in HPCs is due to the conduction currents that are induced in the conductive shell by a microwave magnetic field.     

Low complexity adaptive power and subcarrier allocation for OFDMA

The problem of low complexity sub-optimal power and subcarrier allocation for OFDMA systems is addressed in the paper. We propose a heuristic non-iterative method that is an extension of the ordered subcarrier selection algorithm recently proposed for a single user case to the OFDMA systems. The suggested method improves the average BER-performance of the system and it also provides fairness between the users in terms of the bit rates. Both the theoretical analysis and simulation results confirm efficiency of the proposed technique. Based on the proven lemma about inversion of power gains, we strengthen the suggested method by low complexity power loading that consists in equalization of the received signal-to-noise ratios of each user     

Effect of temperature on hot-air drying rate and on retention of antioxidant capacity in apple leathers

Fruit leathers are pectic gels, eaten as snack or dessert, obtained by dehydrating fruit purees. In this work, apple leathers were prepared by a hot-air drying process which allows the formation of a gel, following the “saccharide–acid–high methoxyl pectin” gelation mechanism. Leathers were produced at 50, 60 and 70 °C, from two formulations: control and added with potassium metabisulphite (KM) as antioxidant. The drying process was studied applying a diffusive model, while antioxidant capacity (AC) losses were represented by a first-order model. Activation energy for drying (20.6 kJ/mol) was lower than those estimated for AC losses in control (31.5 kJ/mol) and KM-added (37.9 kJ/mol) leathers. Therefore, the drying time reduction achieved by increasing air temperature is not sufficient to decrease AC losses in the range covered. AC retention decreased in both formulations at increasing air temperature. KM-added samples showed higher AC retention than the controls, except for those dried at 70 °C. Kinetic constants were lower for KM-added samples, suggesting a protective effect of the additive, especially at moderate air temperatures. In the most favorable situation, AC retention was of only 16%. Therefore, the functional character of these products may not be preserved if dried with hot air and the research on economically viable, less-severe drying technologies should be intensified.     

Polarizability,Susceptibility, and Dielectric Constant of Nanometer‐Scale Molecular Films: A Microscopic View

The size‐dependence of the polarizability, susceptibility, and dielectric constant of nanometer‐scale molecular layers is explored theoretically. First‐principles calculations based on density functional theory are compared to phenomenological modeling based on polarizable dipolar arrays for a model system of organized monolayers composed of oligophenyl chains. Size trends for all three quantities are primarily governed by a competition between out‐of‐plane polarization enhancement and in‐plane polarization suppression. Molecular packing density is the single most important factor controlling this competition and it strongly affects the bulk limit of the dielectric constant as well as the rate at which it is approached. Finally, the polarization does not reach its “bulk” limit, as determined from the Clausius–Mossotti model, but the susceptibility and dielectric constant do converge to the correct bulk limit. However, whereas the Clausius–Mossotti model describes the dielectric constant well at low lateral densities, finite size effects of the monomer units cause it to be increasingly inaccurate at high lateral densities.     

Effect of metal purity and testing procedure on surface tension measurements of liquid tin

The surface tension of liquid tin of three different grades of purity (99.85, 99.96, and 99.999%) was measured by the classical sessile drop method over the temperature range 523–1023 K, in heating and cooling regimes. The results obtained show that the metal purity affects the values of surface tension and its temperature dependence. The highest values of surface tension and smooth linear temperature dependence were obtained in cooling regime for tin of the highest purity. With increasing content of impurities, both surface tension and its temperature coefficient decrease while the scatter of the data increases. The surface tension values measured on heating regime show higher scatter, compared to those obtained in cooling regime, and the temperature dependence of the surface tension is curvilinear rather than linear.     

The Influence of Strontium on Bone Tissue Metabolism and Its Application in Osteoporosis Treatment

Osteoporosis is a chronic disease characterized by low bone mass caused by increased bone turnover and impaired bone microarchitecture. In treatment, we use antiresorptive or anabolic drugs, which usually have a unidirectional effect, i.e., they inhibit the activity of osteoclasts or stimulate the effect of osteoblasts. Strontium ranelate is an anti-osteoporosis drug with a unique mechanism of action (used primarily in postmenopausal women). Unlike other medicines, it has a multidirectional effect on bone tissue, intensifying osteoblastogenesis while inhibiting osteoclastogenesis. It turns out that this effect is demonstrated by strontium ions, an element showing physical and chemical similarity to calcium, the basic element that builds the mineral fraction of bone. As a result, strontium acts through the calcium-sensing receptor (CaSR) receptor in bone tissue cells. In recent years, there has been a significant increase in interest in the introduction of strontium ions in place of calcium ions in ceramics used as bone replacement materials for the treatment of bone fractures and defects caused by osteoporosis. The aim of this study was to summarize current knowledge about the role of strontium in the treatment of osteoporosis, its effects (in various forms), and the ways in which it is administered.     

Structure and phase behavior of a disk-necklace polymer: Cyclolinear polymethylsiloxane

The structure and phase transitions of cyclolinear polyorganosiloxane copolymer containing 12-member polysiloxane rings have been studied using synchrotron WAXS, DSC, TEM, variable-temperature AFM and polarized optical microscopy. The primary structure of this polymer can be viewed as a necklace of disk-shaped entities (cyclic groups) connected via flexible linkers.In the mesomorphic state, the presence of two different LC phases has been derived from the analysis of WAXS fiber diffractograms. The morphology of one of the phases shows a conventional hexagonal packing of LC chains where the chain axes are perpendicular to the plane of the 2D hexagonal lattice. The other one, so-called R-phase, has a vertically oriented rectangular 2D lattice formed by inter-chain correlations between the bulky polysiloxane cycles (disks). To our knowledge, such a disk-necklace mesophase in which the LC lattice is parallel to the backbone direction has not been reported in the literature so far.