Structure of the cokes obtained from the group components separated from coking coal vitrites by selective thermosolvolysis

The examination of the structure of cokes obtained from extracts separated from preheated vitrites of coking coals by progressive and continuous extraction with chloroform was carried out. The structural ordering (interplanar spacing and crystallite dimensions) of the cokes depends on the rank of the parent vitrites but it does not depend on the degree of extraction. The occurrence of optical anisotropy in cokes from the extracts is connected with both the rank of the parent vitrite and the degree of extraction. In the formation of the optical anisotropic structure during the carbonization of coking coal vitrites, the part of the extract which is of small size, which partially undergoes decomposition, is an important factor.     

Isolation and amino acid sequence of a serine proteinase inhibitor from common flax (Linum usitatissimum) seeds

LUTI (Linum usitatissimum trypsin inhibitor), a member of the potato inhibitor I family, has been isolated from seeds of flax by ethanol fractionation, ion exchange chromatography on CM-Sephadex C-25, affinity purification on immobilized methylchymotrypsin (alpha-chymotrypsin in which His57 has been converted to 3-methylhistidine) in the presence of 5M NaCl, and finally by reversed-phase HPLC. The 7655 Da inhibitor consists of a single polypeptide chain of 69 residues with one disulfide bridge. The molecule is acetylated at the N terminus. Its primary structure has been determined after limited proteolysis of the native molecule with trypsin at the reactive site, cleavage with cyanogen bromide or arginyl endopeptidase (Arg-gingipain), and alcoholytic deacetylation of the N-terminally blocked serine. The association constants (K(a)) of LUTI with bovine beta-trypsin and alpha-chymotrypsin are 3.58x10(10) M(-1) and 5.02x10(5) M(-1), respectively. High NaCl concentration (3M) increased the association constant of LUTI with alpha-chymotrypsin to 6.64x10(7) M(-1). To our knowledge, LUTI is the first serine-proteinase-type inhibitor isolated from a plant of the Linaceae family.     

Fly ash as a sorbent for boron removal from aqueous solutions: Equilibrium and thermodynamic studies

ABSTRACT

This study presents the application of fly ash from brown coal and biomass burning power plant as a sorbent for the removal of boron ions from an aqueous solution. The adsorption process efficiency depended on the parameters, such as adsorbent dosage, pH, temperature, agitation time and initial boron concentration. The experimental data fitted well with the Freundlich isotherm model and the maximum capacity was found to be 16.14 mg g^?1. The adsorption kinetics followed the pseudo-second-order model. Also, the intra-particle diffusion model parameters were calculated. Thermodynamic parameters such as change in free energy (ΔG°), enthalpy (ΔH°), entropy (ΔS°) revealed on exothermic nature of boron adsorption onto the fly ash.     

Selective separation of yttrium from rare earth elements by ion interaction chromatography. Analytical and larger scale applications

ABSTRACT

New ion interaction chromatographic (IIC) method employing Kromasil 100 C₁₈ column and tetra-n-butylammonium hydroxide (TBAOH) as an ion interaction reagent (IIR) is able to separate yttrium from Rare Earth Elements (REE) as anionic complexes with nitrilotriacetic acid (NTA). New method for the chromatographic determination of Y in REE mixture was devised and validated by the analysis of the certified reference material (CRM). Potential possibilities of the new chromatographic system for larger scale applications including macro-micro events were demonstrated.     

Iris-based human identity recognition with machine learning methods and discrete fast Fourier transform

Innovations in Systems and Software Engineering - One of the most important modules of computer systems is the one that is responsible for user safety. It was proven that simple passwords and...     

Charge trapping in bilayers of conducting polymers under open circuit conditions: a protection of conducting polymer films from spontaneous charging/discharging

Spontaneous charging/discharging processes of polymers: polypyrrole and poly(N-methylpyrrole), doped with perchlorate (anion exchanging PPy and PMPy, respectively) and poly(4-styrenesulphonate) ions (cation exchanging PPy(PSS) and PMPy(PSS)) occurring in aqueous electrolyte solutions were studied using different electrochemical techniques. These reactions (oxidation of the polymer by dissolved oxygen and discharge of the polymer redox capacitance) are usually undesired processes leading to alteration of the charge accumulated in the polymer films. This paper points out that these processes can be significantly limited in polymer bilayers due to effect of charge trapping.     

Defect structure and chemical diffusion in nickel sulfide β-Ni3S2

The chemical composition, defect structure, and diffusion in nickel sulfide -Ni₃S₂ have been investigated in H₂S-H₂ mixtures containing between 1 and 65% H₂S between 560 and 700°C. Gravimetric, density, and X-ray studies were carried out. In the thermodynamically stable compound the ratio of Ni/S varied between 1.3 and 1.75. The X-ray examination showed a step change in the lattice parameter at the Ni/S ratio 1.4. A linear dependence of the density values (between 5.5 and 6.2 g/cm³) on the composition was observed. On the basis of the chemical composition and density measurements the number of nickel and sulfur atoms in 1 cm³ were determined. It has been shown that the Ni₃S₂ phase is defected in both anion and cation sublattices and that its chemical formula may be described as follows: Ni_3±yS_2x, where y 2x. It has been found that in the mixture containing 10% H₂S the process of defect formation is determined by their diffusion in the sulfide. The temperature dependence of the diffusion coefficient is described by the equation D = 13.15 exp(-30,000/RT) cm²/sec. No dependence of D on the sulfur partial pressure was observed, but this may be due to the relatively large uncertainties in the measurement of the diffusion coefficients.     

Kinetics of copper sulfidation at temperatures 570–1123 K

The kinetics of copper sulfidation have been studied as a function of temperature (570–1120 K) by the use of the modified Wagner's pellet method. It has been found that sulfidation follows a parabolic rate law with different activation energies in the low- and high-temperature ranges: $$k_{p}^{'} = 10.2 exp - (70 \pm 4)[kJ/mole]/RT (570 - 780 K)$$ and $$k_{p}^{'} = 1.69 \times 10^{ - 3} exp - (13 \pm 1.0)[kJ/mole]/RT (780 - 1120 K)$$ Using thermodynamic data as well as interfacial chemical potentials and ionic conductivity, the parabolic rate constants of sulfidation of copper have been calculated with good agreement with experimental results. Parabolic rate constants of sulfidation have been used to calculate average self-diffusion coefficients of copper in Cu₂S, the temperature dependence of which is as follows: $$\bar D_{Cu} = 8.76 \times 10^{ - 4} exp - (22.4 \pm 1)[kJ/mole]/RT$$      

A two‐level detector of short‐term unique changes in time series based on a similarity method

In the paper, a novel two‐level algorithm of time‐series change detection is presented. In the first level, to identify non‐stationary sequences in a processed signal, preliminary detection of events is performed with a short‐term prediction comparison. In the second stage, to confirm the changes detected in the first level, a similarity method aimed at identification of unique changes is employed. The detection of changes in a non‐stationary time series is discussed, implemented algorithms are described and the results produced on a sample four financial time series are shown. General conditions for implementing the proposed algorithm as an immune‐like event detector are discussed.