Dissolved organic carbon in the southern Baltic Sea: Quantification of factors affecting its distribution

During a cruise of r/v ‘Oceania’ in May 2006, seven vertical dissolved organic carbon (DOC) concentration profiles were produced against a background of CTD, chlorophyll a (chl a) and phaeopigment concentration profiles. The results indicate distinct vertical and spatial DOC fluctuations, ranging from 248 ± 7 μmol C dm⁻³ at 70 m depth at the westernmost station G/06 to 398 ± 5 μmol C dm⁻³ at 5 m depth at station A/06 in the western Gulf of Gdańsk. DOC concentrations were the highest at 10 m depth, where phytoplankton activity was relatively intensive, as reflected by the active chl a concentration distribution. DOC concentrations decreased towards the sea bottom.     

Tides and Arp's hypothesis about distribution of Hii regions

We discuss Arp's hypothesis that the HII regions are more numerous and more conspicuous on the side of a galaxy facing its companion. Arp's hypothesis seems not to be true if we add to Hodge's sets of galaxies only the most probably tidally-interacting cases.     

The asymmetry of the velocity distribution in the rotating ring in U Gem stars

It is shown that the non-keplerian character of the rotation of the ring of gas particles in a close binary system gives too large an amplitude of the radial velocity curve if this amplitude is determined from the positions of the emission lines of the ring.     

CO 2 emission trading model with trading prices

In this paper we consider the buying/selling prices of carbon dioxide (CO₂) emission permits in trading models with uncertainty. Permission prices, although usually omitted from standard models, may significantly influence the trading market. We thus undertook to construct a more realistic trade model and to compare it with the standard one. To do this, we introduced several important changes to the standard model, namely, (1) a new optimized quality function; and (2) transactions with price negotiations between regions. We also enhanced the model using methods described in the literature to allow it to deal with reported emissions uncertainty. Additionally, we used an original method of simulating this kind of market based on a specialized evolutionary algorithm (EA).     

Application of electron paramagnetic resonance spectroscopy to examination of carbonized coal blends

Paramagnetic centers in two- and three-component coal blends carbonized at 1000 °C were studied by X-band (9.3 GHz) electron paramagnetic resonance (EPR) technique. The blends were prepared from three different Polish coals with carbon contents [wt.%]: 88.66, 86.21, and 82.67, respectively. The aim of this work was to compare EPR parameters and concentrations of paramagnetic centers in the initial and carbonized coal samples. Furthermore the spin–spin and spin–lattice interactions were characterized.EPR spectra were measured with magnetic modulation 100 kHz and microwave power 0.7 mW. Amplitudes and linewidths of EPR spectra were obtained. g-Factors were calculated from resonance condition. Concentrations of paramagnetic centers in the samples were determined. Influence of microwave power in the range 0.7–70 mW on EPR spectra was analyzed.All the studied samples revealed paramagnetism. Unpaired electrons are localized in the same atoms, because similar g-values in the range 2.0035–2.0038 were obtained for all the original samples. The EPR parameters of coal blends were additive in comparison with the parent coals. EPR spectra strongly changed after carbonization of the coal samples. Narrower EPR lines were measured for the original coal samples than for carbonized ones. We detected lower concentrations of paramagnetic centers in carbonized three-component coal blends than in two-component carbonized blends. EPR lines of the studied carbonized blends were not saturated at the microwave power used, which suggests fast spin–lattice relaxation processes in the samples. EPR examination proved chemical interactions between coal constituents during carbonization of coal blends.     

Binary gas sorption/desorption experiments on a bituminous coal: Simultaneous measurements on sorption kinetics,volumetric strain and acoustic emission

There is still no clear understanding of the specific interactions between coal and gas molecules. In this context sorption–desorption studies of methane and carbon dioxide, both in a single gas environment and gas mixtures, are of fundamental interest. This paper presents the results of unique simultaneous measurements of sorption kinetics, volumetric strain and acoustic emission (AE) on three tetragonal coal samples subjected to sorption of carbon dioxide and methane mixtures. The coal was a high volatile bituminous C coal taken from the Budryk mine in the Upper Silesia Basin, Poland. Three different gas mixtures were used in the sorption tests, with dominant CO₂, with dominant CH₄ and a 50/50 mixture.The experimental set-up was designed specially for this study. It consisted of three individual units working together: (i) a unit for gas sorption experiments using a volumetric method, (ii) an AE apparatus for detecting, recording and analysing AE, and (iii) a strain meter for measuring strains induced in the coal sample by gas sorption/desorption. All measurements were computer aided.The experiments indicated that the coal tested showed preferential sorption of CH₄ at 2.6 MPa pressure and exhibited comparable affinities for CH₄ and CO₂ at higher pressures (4.0 MPa). The results of chromatographic analysis of the gas released on desorption suggested that the desorption of methane from the coal was favoured. The relationship between the volumetric strain and the amount of sorbed gas was found to be non-linear. These results were contrary to common opinions on the coal behaviour. Furthermore, it appeared that the swelling/shrinkage of coal was clearly influenced by the network of fractures. Besides, the AE and strain characteristics suggested common sources of sorption induced AE and strain.The present results may have implications for the sequestration of carbon dioxide in coal seams and enhanced coalbed methane recovery (ECBM).