Further study on the one-pot synthesis of (E)-2-nonenal from castor oil

A one-step procedure is described for the synthesis of (E)-2-nonenal from commercial castor oil by ozonolysis in methanol, followed by reduction of the ozonide products with dimethyl sulfide and exposure of the resulting intermediate product to dilute sulfuric acid. The developed process allows the production of the aldehyde with a yield of 80% at a purity of 95%. The method has advantages over all those reported earlier, because of inexpensive raw material and reducing agent, recycling of the solvent and its unusual simplicity.     

Detecting Fixed Patterns in Chordal Graphs in Polynomial Time

The Contractibility problem takes as input two graphs G and H, and the task is to decide whether H can be obtained from G by a sequence of edge contractions. The Induced Minor and Induced Topological Minor problems are similar, but the first allows both edge contractions and vertex deletions, whereas the latter allows only vertex deletions and vertex dissolutions. All three problems are NP-complete, even for certain fixed graphs H. We show that these problems can be solved in polynomial time for every fixed H when the input graph G is chordal. Our results can be considered tight, since these problems are known to be W[1]-hard on chordal graphs when parameterized by the size of H. To solve Contractibility and Induced Minor, we define and use a generalization of the classic Disjoint Paths problem, where we require the vertices of each of the k paths to be chosen from a specified set. We prove that this variant is NP-complete even when k=2, but that it is polynomial-time solvable on chordal graphs for every fixed k. Our algorithm for Induced Topological Minor is based on another generalization of Disjoint Paths called Induced Disjoint Paths, where the vertices from different paths may no longer be adjacent. We show that this problem, which is known to be NP-complete when k=2, can be solved in polynomial time on chordal graphs even when k is part of the input. Our results fit into the general framework of graph containment problems, where the aim is to decide whether a graph can be modified into another graph by a sequence of specified graph operations. Allowing combinations of the four well-known operations edge deletion, edge contraction, vertex deletion, and vertex dissolution results in the following ten containment relations: (induced) minor, (induced) topological minor, (induced) subgraph, (induced) spanning subgraph, dissolution, and contraction. Our results, combined with existing results, settle the complexity of each of the ten corresponding containment problems on chordal graphs.     

Dyes based on the 2(1H)‐quinolone skeleton as potential colorimetric and fluorescent sensors for cyanide anions

The sensing properties of dyes based on 2(1H) quinolones containing dicyanoethylene groups towards selected anions such as CN^?, F^?, I^?, Cl^?, SCN^?, CH₃COO^?, and were evaluated. The spectroscopic responses of these compounds were investigated in a solution of acetonitrile/water (1:9, v/v) and phosphate buffer at a pH of 7.4. These dyes were found to act as efficient colorimetric and high turn–off fluorescent sensors to cyanide anions. The fluorescence intensity was linearly related to the concentration of CN^? from 1 to 10 µmol/L, and the detection limits reached a micromolar level of 6.7, 11.1, 3.8 and 7.2 µmol/L for 1‐4 , respectively. The cytotoxic effect of the dyes against human neuroblastoma cells (SH‐SY5Y) was also determined by MTT assay. The examined compounds exhibited slight cytotoxicity against cells under experimental conditions.     

Upgrading a Granular Computing Based Data Mining Framework to a Relational Case

One of the popular methods to develop an algorithm for mining data stored in a relational structure is to upgrade an existing attribute‐value algorithm to a relational case. Current approaches to this problem have some shortcomings such as (1) a dependence on the upgrading process of the algorithm to be extended, (2) complicated redefinitions of crucial notions (e.g., pattern generality, pattern refinement), and (3) a tolerant limitation of the search space for pattern discovery. In this paper, we propose and evaluate a general methodology for upgrading a data mining framework to a relational case. This methodology is defined in a granular computing environment. Thanks to our relational extension of a granular computing based data mining framework, the three above problems can be overcome.     

Unsteady radiative heat transfer within a suspension of ZnO particles undergoing thermal dissociation

An emitting, absorbing, and anisotropically scattering plain medium containing a suspension of ZnO particles is considered, in which the particles are directly exposed to high-flux irradiation and undergo shrinkage during their endothermic dissociation into Zn(g) and O₂ at above 2100 K. The unsteady energy equation that links the rate of radiative heat transfer to the rate of the chemical reaction is formulated and solved numerically by the finite volume technique and the explicit Euler time-integration scheme. The path-length Monte Carlo method is applied for modeling the radiative transfer within the suspension using the absorption/scattering coefficients and the scattering phase function obtained from the Mie theory. It is found that the particle suspension can be heated rapidly from its initial 300 K to over 1800 K in less than 0.1 s, resulting in a more uniform temperature profile as the reaction progresses, particles shrink, and the suspension becomes optically thinner. The chemical conversion increases with decreasing initial particle diameter and volume fraction due to the efficient radiative absorption.     

New method for the on-line signature verification based on horizontal partitioning

Verification of identity based on the analysis of dynamic signatures is an important problem of biometrics. The effectiveness of the verification significantly increases when the dynamic characteristics of signature (e.g. velocity of the pen) are considered. These characteristics are individual for each user and difficult to imitate. The effectiveness of the verification can be further improved by using partitioning. In this paper we propose a new method which uses partitioning. In our method partitions represent areas of high and low speed of signature and high and low pen?s pressure. All selected partitions are used by our algorithm, but more important in the classification process are these partitions, in which the signatures of the user acquired during training phase are more stable. Moreover, final classification is interpretable. In this paper we present the simulation results of the proposed method for the two databases: SVC2004 and BioSecure Database.     

Ionic liquids as electrolytes

Salts having a low melting point are liquid at room temperature, or even below, and form a new class of liquids usually called room temperature ionic liquids (RTIL). Information about RTILs can be found in the literature with such key words as: room temperature molten salt, low-temperature molten salt, ambient-temperature molten salt, liquid organic salt or simply ionic liquid. Their physicochemical properties are the same as high temperature ionic liquids, but the practical aspects of their maintenance or handling are different enough to merit a distinction. The class of ionic liquids, based on tetraalkylammonium cation and chloroaluminate anion, has been extensively studied since late 1970s of the XX century, following the works of Osteryoung. Systematic research on the application of chloroaluminate ionic liquids as solvents was performed in 1980s. However, ionic liquids based on aluminium halides are moisture sensitive. During the last decade an increasing number of new ionic liquids have been prepared and used as solvents. The general aim of this paper was to review the physical and chemical properties of RTILs from the point of view of their possible application as electrolytes in electrochemical processes and devices. The following points are discussed: melting and freezing, conductivity, viscosity, temperature dependence of conductivity, transport and transference numbers, electrochemical stability, possible application in aluminium electroplating, lithium batteries and in electrochemical capacitors.     

Synergistic effect in gamma-irradiated poly(vinyl chloride) hard foils stabilized by plasticizer–stabilizer systems

Changes in transparency and color as well as G_HCl values of hard PVC foils exposed to gamma radiation were investigated while using different amounts of the stabilizers ethylene glycol bis-β-aminocrotonate (I), calcium/zinc laurate + epoxy compounds (II), and magnesium/zinc stearate + sorbitol + epoxy compounds (III), and plasticizers dioctyl phthalate (DOP) (IV), dioctyl sebacate (V), propylene glycol polyadipate + octyl alcohol composition (VI), and diisotridecyl phthalate (VII). A strong synergistic effect was observed in systems containing both plasticizer and stabilizer. Best results were obtained for the I + II + IV, I + II + V, and I + III + V systems.     

Morphology and thermal properties of two polymethacrylates modified by a polymer liquid crystal

We have studied blends of a polymer liquid crystal (PLC) with poly(cyclohexylethyl methacrylate) (PCHEMA) or poly(cyclohexylpropyl methacrylate) (PCHPMA). The PLC is PET/0.6PHB where PET = poly(ethylene terephthalate), PHB = p-hydroxybenzoic acid and 0.6 is the mole fraction of the latter in the copolymer. The microstructure was studied by scanning electron microscopy (SEM). PCHEMA + PLC (20 wt% of the latter, blend E) has a fine texture with LC islands evenly distributed in the matrix and good adhesion between the phases resulting from their partial miscibility. The PCHPMA + PLC (20 wt% of the latter, blend P) shows only limited compatibility. The SEM results are confirmed by values of the glass transition temperatures T_g determined via thermal mechanical analysis. The T_g value of the blend E is shifted towards the T_g of PLC; T_g of blend P is practically equal to that of PCHPMA. The linear isobaric expansivity α_L values for both blends are lower than the respective values for pure PCHPMA and PCHEMA. Thermal stabilities of the blends determined by thermogravimetry are also better than those of pure polymethacrylates. The temperature of 50% weight degradation for blend E is higher than that for pure PCHEMA by more than 60 K Copyright © 2004 Society of Chemical Industry