A study on the crystallization of amorphous arsenic

The results of DTA analysis of amorphous arsenic in combination with electron microscopical study of the samples through the whole temperature range reveal that no changes of the initial state of the sample occur on heating up to crystallization temperature. Close above this temperature the spontaneous crystallization starts. It differs markedly from the case of glassy materials, like As₂Te₃, in which case at temperatures as low as the transition region T_g the crystallization nuclei of geometrically defined shapes appear and grow into crystalline grains on further heating.     

Assessment of the mean-value of 17-hydroxypregnenolone in the umbilical blood of newborns by the exploratory analysis of biochemical data

The main aim of data analysis in biochemical metrology is the extraction of relevant information from biochemical data measurements. A system of extended exploratory data analysis (EDA) based on the concept of graphical tools for sample data summarization and exploration is proposed and the original EDA algorithm in S-Plus is available on the Internet at http://www.trilobyte.cz/EDA. To check basic assumptions about biochemical and medical data is to examine the independence of sample elements, sample normality and homogeneity. The exact assessment of the mean-value and the variance of steroid levels in controls is necessary for the correct assessment of the samples from patients. Data examination procedures are illustrated by a determination of the mean-value of 17-hydroxypregnenolone in the umbilical blood of newborns. For an asymmetric, strongly skewed sample distribution corrupted with outliers the best estimate of location seems to be the median. The Box–Cox transformation improves a sample symmetry. The proposed procedure gives reliable estimates of a mean-value for an asymmetric distribution of 17-hydroxypregnenolone when the arithmetic mean can not be used.     

Biodegradability of ethylenediamine-based complexing agents

Biological degradability of ethylenediamine derivatives depends on the type and number of substituents. The susceptibility to biodegradation decreases in the sequence of substituents -COCH3, -CH3, -C2H5, -CH2CH2OH, -CH2COOH and with polysubstitution. The biodegradability depends also on the kind and number of nitrogen atoms. Complexing agents with a single-nitrogen atom in the molecule (e.g. NTA) succumb relatively readily to biodegradation whereas, compounds with two or more tertiary amino groups are biologically highly stable and do not undergo biodegradation even in experiments with activated sludge adapted at an age of up to 30 days (EDTA, DTPA, PDTA, HEDTA). A lowering of the degree of substitution brings about an increased susceptibility to biodegradation. This holds, e.g., for replacement of tertiary amino groups with secondary ones; thus the symmetrically disubstituted ethylenediamine-N,N'-diacetic acid (EDDA) possesses still sufficient complexing ability while belonging already to the group of potentially degradable substances.     

Ternary Copper(II) Complexes in Solution Formed With 8-Aza Derivatives of the Antiviral Nucleotide Analogue 9-[2-(Phosphonomethoxy)Ethyl]Adenine (PMEA)

The stability constants of the mixed-ligand complexes formed between Cu(Arm)(2+), where Arm= 2,2'-bipyridine (Bpy) or 1,10-phenanthroline (Phen), and the dianions of 9-[2-(phosphonomethoxy)ethyl]-8-azaadenine (9,8aPMEA) and 8-[2-(phosphonomethoxy)ethyl]-8-azaadenine (8,8aPMEA) (both also abbreviated as PA(2-)) were determined by potentiometric pH titrations in aqueous solution (25 ( degrees )C; I = 0.1 M, NaNO(3)). All four ternary Cu(Arm)(PA) complexes are considerably more stable than corresponding Cu(Arm)(R-PO(3)) species, where R-PO(3) (2-) represents a phosph(on)ate ligand with a group R that is unable to participate in any kind of interaction within the complexes. The increased stability is attributed to intramolecular stack formation in the Cu(Arm)(PA) complexes and also to the formation of 5-membered chelates involving the ether oxygen present in the -CH(2)-O-CH(2)-PO(3) (2-) residue of the azaPMEAs. A quantitative analysis of the intramolecular equilibria involving three structurally different Cu(Arm)(PA) species is carried out. For example, about 5% of the Cu(Bpy)(8,8aPMEA) system exist with the metal ion solely coordinated to the phosphonate group, 14% as a 5-membered chelate involving the -CH(2)-O-CH(2)-PO(3) (2-)residue, and 81% with an intramolecular stack between the 8-azapurine moiety and the aromatic rings of Bpy. The results for the other systems are similar though with Phen a formation degree of about 90% for the intramolecular stack is reached. The existence of the stacked species is also proven by spectrophotometric measurements. In addition, the Cu(Arm)(PA) complexes may be protonated, leading to Cu(Arm)(H;PA)(+) species for which it is concluded that the proton is located at the phosphonate group and that the complexes are mainly formed by a stacking adduct between Cu(Arm)(2+) and H(PA)(-). Conclusions regarding the biological properties of these azaPMEAs are shortly indicated.     

NICE h : a higher-order explicit numerical scheme for integration of constitutive models in plasticity

The article introduces, as a result of further development of the first-order scheme NICE, a simple and efficient higher-order explicit numerical scheme for the integration of a system of ordinary differential equations which is constrained by an algebraic condition (DAE). The scheme is based on the truncated Taylor expansion of the constraint equation with order h of the scheme being determined by the highest exponent in the truncated Taylor series. The integration scheme thus conceived will be named NICE ^h , considering both principal premises of its construction. In conjunction with a direct solution technique used to solve the boundary value problem, the NICE ^h scheme is very convenient for integrating constitutive models in plasticity. The plasticity models are defined mostly by a system of algebraic and differential equations in which the yield criterion represents the constraint condition. To study the properties of the new integration scheme, which, like the forward-Euler scheme, is characterised by its implementation simplicity due to the explicitness of its formulations, a damage constitutive model (Gurson–Tvergaard–Needleman model) is considered. The general opinion that the implicit backward-Euler scheme is much more accurate than the thus-far known explicit schemes is challenged by the introduction of the NICE ^h scheme. The accuracy of the higher-order explicit scheme in the studied cases is significantly higher than the accuracy of the classical backward-Euler scheme, if we compare them under the condition of a similar CPU time consumption.     

New system theory and its impact on control theory

Real systems can include two types of state variables – dynamic and static. While dynamic state variables are a common part of each system, static variables are not and their presence in a system may cause some problems if standard system theories are used. In this paper, it is shown that, due to a new system theory (NST), it is possible to work correctly with systems and subsystems which include not only dynamic state variables, but also static state variables. If standard system theories are used, static variables in the real system cause not only problems in describing systems but also some challenges in control theory. These challenges involve, for example, some questions of controllability, reachability, or observability of a plant that includes static variables or the optimal control design of a plant that includes statical state variables. Some of the challenges mentioned are addressed in this paper after a brief introduction of the NST.     

A new method for computing fuzzy functional dependencies in relational database systems

In this paper, we present a new method for computing fuzzy functional dependencies between attributes in fuzzy relational database systems. The method is based on the use of fuzzy implications. A literature analysis has shown that there is no algorithm that would enable the identification of attribute relationships in fuzzy relational schemas. This fact was the motive for development a new methodology in the analysis of fuzzy functional dependencies over a given set of attributes. Solving this, not so new problem, is not only research challenge having theoretical importance, but it also has practical significance. Possible applications of the proposed methodology include GIS, data mining, information retrieval, reducing data redundancy in fuzzy relations through implementation of logical database model, estimation of missing values etc.     

Stabilization of nonlinear delay systems using approximate predictors and high-gain observers

We provide a solution to the heretofore open problem of stabilization of systems with arbitrarily long delays at the input and output of a nonlinear system using output feedback only. The solution is global, employs the predictor approach over the period that combines the input and output delays, addresses nonlinear systems with sampled measurements and with control applied using a zero-order hold, and requires that the sampling/holding periods be sufficiently short, though not necessarily constant. Our approach considers a class of globally Lipschitz strict-feedback systems with disturbances and employs an appropriately constructed successive approximation of the predictor map, a high-gain sampled-data observer, and a linear stabilizing feedback for the delay-free system. The obtained results guarantee robustness to perturbations of the sampling schedule and different sampling and holding periods are considered. The approach is specialized to linear systems, where the predictor is available explicitly.     

DRYING RESEARCH AND DEVELOPMENT IN CZECHOSLOVAKIA

This paper provides general information on drying R 6D activities in Czechoslovakia. This survey report lists the main topics in drying according to individual industrial sectors in which drying plays an important role. Drying R 6D carried out in Czechoslovak Universities is also cited. The paper includes an extensive list of references, mainly proceedings of national drying conferences, symposia, and meetings     

Tetrapyrazinoporphyrazines with different number of peripheral pyridyl rings: Synthesis,photophysical and photochemical properties

Zinc tetrapyrazinoporphyrazines comprising different numbers of pyridin-2-yl and tert-butylsulfanyl substituents were prepared by the statistical condensation of two precursors – 5,6-bis(tert-butylsulfanyl)pyrazine-2,3-dicarbonitrile (A) and 5,6-dipyridin-2-yl-pyrazine-2,3-dicarbonitrile (B). The ensuing zinc tetrapyrazinoporphyrazines were chromatographically separated on silica column and characterized. Adjacent (AABB) and opposite (ABAB) isomers were not separated. The prepared zinc tetrapyrazinoporphyrazines did not differ in their Q-band position but the B-band position was shifted hypsochromically for compounds bearing more pyridyl units; in addition, a weak band at 450–520 nm decreased with increasing number of pyridyl substituents. Singlet oxygen quantum yields (Φ_Δ in the range 0.69–0.53) decreased with increasing number of pyridyl units on the macrocyclic core, while fluorescence quantum yields showed the reverse tendency (Φ_F in the range 0.22–0.26).