Raman spectra of high‐density,low‐density,and linear low‐density polyethylene pellets and prediction of their physical properties by multivariate data analysis

Raman spectra have been measured for pellets of five samples of high‐density polyethylene (HDPE), seven samples of low‐density polyethylene (LDPE), and six samples of linear low‐density polyethylene (LLDPE). The obtained Raman spectra have been compared to find out characteristic Raman bands of HDPE, LDPE, and LLDPE. Principal component analysis (PCA) was applied to the Raman spectra in the 1600–650 cm^?1 region after multiplicative scatter correction (MSC) to discriminate the Raman spectra of the three different PE species. They are classified into three groups by a score plot of PCA factor 1 vs. 2. HDPE with high density and high crystallinity gives high scores on the factor 1 axis, while LDPE with low density and low crystallinity yields negative scores on the same axis. It seems that factor 1 reflects the density or crystallinity. A PC weight loadings plot for factor 1 shows six upward peaks corresponding to the bands arising from the crystalline parts or all‐trans ? (CH₂)_n? groups and seven downward peaks ascribed to the bands of the amorphous or anisotropic regions and those arising from the short branches. Partial least‐squares (PLS‐1) regression was applied to the Raman spectra after MSC to propose calibration models that predict the density, crystallinity, and melting points of the polyethylenes. The correlation coefficient was calculated to be 0.9941, 0.9800, and 0.9709 for the density, crystallinity, and melting point, respectively, and their root‐mean‐square error of cross validation (RMSECV) was found to be 0.0015, 3.3707, and 2.3745, respectively. The loadings plot of factor 2 for the prediction of melting point is largely different from those for the prediction of density and crystallinity. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 443–448, 2002     

A Mathematical Model for the Calculation of the Adhesion of a Flame Sprayed Coating of Aluminum on S 235 JR Steel

In this work the method of response surfaces was used for the purpose of drawing up a mathematical model for the calculation (forecasting) of the adhesion of a flame sprayed coating of powdered aluminum on S 235 JR steel. Experimental work was conducted according to a fractional central-composite design at three levels. The adhesion of the coatings made with combinations of input parameters of the procedure according to the experiment plan mentioned is measured in line with the EN 582 standard. A mathematical model was derived describing the dependence of the experimentally obtained adhesion values on the input parameters of the procedure. The possibility of analyzing the influence of the parameters on the adhesion for a certain combination of input parameters has been presented with the use of perturbation plots.     

Synthesis and characterization of interpenetrating polymer networks with hyperbranched polymers through thermal-UV dual curing

The aim of this study was to investigate the possibility of using acrylated hyperbranched polyesters (HBP) as UV curable component in dual curing automotive applications. Dual curing is one of possible ways to obtain fast curing, scratch resistant coatings for use in OEM and car refinish applications. Dual curing systems, upon hardening, can give interpenetrating networks (IPNs).     

Lipids and Antiplatelet Therapy: Important Considerations and Future Perspectives

Lipids play an essential role in platelet functions. It is known that polyunsaturated fatty acids play a role in increasing platelet reactivity and that the prothrombotic phenotype plays a crucial role in the occurrence of major adverse cardiovascular events. The ongoing increase in cardiovascular diseases’ incidence emphasizes the importance of research linking lipids and platelet function. In particular, the rebound phenomenon that accompanies discontinuation of clopidogrel in patients receiving dual antiplatelet therapy has been associated with changes in the lipid profile. Our many years of research underline the importance of reduced HDL values for the risk of such a rebound effect and the occurrence of thromboembolic events. Lipids are otherwise a heterogeneous group of molecules, and their signaling molecules are not deposited but formed “on-demand” in the cell. On the other hand, exosomes transmit lipid signals between cells, and the profile of such changes can be monitored by lipidomics. Changes in the lipid profile are organ-specific and may indicate new drug action targets.     

Influence of surface activation on the hydrogen permeation properties of PdAg cathode membrane

The influence of surface oxidation and hydrogen upload into the Pd_0.79Ag_0.21 membrane on hydrogen permeation was examined by measuring the permeation of: 1) gas-phase H₂ sent from the electrode back-side and 2) electrolytic H₂ produced on electrolyte side. It was verified that hydrogen upload into PdAg lattice has positive effect i.e. increases hydrogen permeation, while surface oxides formed during and after electrolysis cycles are the main factors acting on decrease of hydrogen permeation. Particularly, silver oxides are identified as permeation-blocking species. Consequently, several treatments were proposed aiming to reduce electrode deactivation; beside wet chemistry treatments applicable after electrolysis, the in situ electrode reactivation by ultrasonic pulses was presented.     

Adaptive nonuniform polar quantization application to high quality speech compression

The logarithmic companding technique has shown to be extremely useful in speech quantization with rate of 8 bits/sample. However, for lower bit rates it is not the ideal solution for high quality speech coding. Because of that, in this paper we establish source coding scheme which enables better spectrum efficiency for input that has a large dynamic range. Since our wish is also to improve signal quality in comparison with quality defined with standards G.711 and G.712, we opt for adaptive technique application to the speech coding. Our research shows that proper design of forward gain-adaptive polar quantization can enable compression of about 1 bit/sample as well as significantly better quality than in case of using coder designed according to standard G.711. Furthermore, performances can be sustained over the whole speech dynamic range. Also, if the requisite speech quality is not supposed to be lower than G.712 standard quality, the achieved compression can be almost 1.5 bits/sample. Besides, we propose knew simple encoding rule which can additionally reduce bit rate for 0.1 bit/sample.     

Phase-synchroniser based on gm-C all-pass filter chain with sliding mode control

Phase-synchronisers have many applications in VLSI circuit designs. They are used in CMOS RF circuits including phase (de)modulators, phase recovery circuits, multiphase synthesis, etc. In this article, a phase-synchroniser based on g_m-C all-pass filter chain with sliding mode control is presented. The filter chain provides good controllable delay characteristics over the full range of phase and frequency regulation, without deterioration of input signal amplitude and waveform, while the sliding mode control enables us to achieve fast and predetermined finite locking time. IHP 0.25 µm SiGe BiCMOS technology has been used in design and verification processes. The circuit operates in the frequency range from 33 MHz up to 150 MHz. Simulation results indicate that it is possible to achieve very fast synchronisation time period, which is approximately four time intervals of the input signal during normal operation, and 20 time intervals during power-on.     

A study of the photocatalytic degradation of metamitron in ZnO water suspensions

The photocatalytic degradation of the herbicide metamitron in water using ZnO under Osram ULTRA-VITALUX® lamp light was studied. The effect of the operational parameters such as initial concentration of catalyst, initial metamitron concentration, initial salt concentration (NaCl, Na₂CO₃ and Na₂SO₄) and pH was studied. The optimal concentration of catalyst was found to be 2.0 g/l. First-order rate constants were calculated for the uncatalysed reactions. On the base of the Langmuir-Hinshelwood mechanism, a pseudo first-order kinetic model was illustrated and the adsorption equilibrium constant and the rate constant of the surface reaction were calculated (0.119 l mg^− 1 and 0.836 mg l^− 1 min^− 1, respectively). The photodegradation rate was higher in acidic than in alkaline conditions. When salt effect was studied, it was found that sodium carbonate was the most powerful inhibitor used, while sodium chloride was the weakest one. A negligible inhibition was observed when the concentration of sodium chloride was 20 mM.The rate of photodecomposition of metamitron was measured using UV spectroscopy and HPLC, while its mineralization was followed using ion chromatography (IC), as well as total organic carbon (TOC) and total nitrogen (TN) analysis.Under the employed conditions, almost complete disappearance of 9 mg/ml of herbicide, 56% TOC and 34% TN removal, occurred within 4 h. The ion chromatography results showed that the mineralization led to ammonium, nitrite and nitrate ions during the process.     

Kinetics and mechanism of deposition of zinc from zincate in concentrated alkali hydroxide solutions

Galvanostatic investigation has been carried out of the kinetics of the reaction on zinc amalgam hanging mercury drop immersed in alkaline zincate solutions at KOH concentrations ranging from 1 to 14 normal. Three kinds of data have been extracted: (i) the pseudo-capacitance as a function of overpotential from the portion of the charging curves prior to plateaux, (ii) the Tafel plots from quasi-steady state values at the plateaux and (iii) the Sand's products as function of current density from transition times. In (i), the pseudo-capacitance was found to increase with overpotential, in (ii), two slopes (60 mV dec^?1 and 120 mV dec^?1) have been found in the cathodic direction and a limiting current in the anodic one; in (iii), the Sand's product was found to decrease with increasing (i). On the basis of the above findings the reaction mechanism has been suggested to be of the cece type, with the chemical dissociation of the intermediate univalent zinc complex in between the two elctrochemical steps as rate-determining. A modification of the method of evaluating the reaction orders was introduced to account for a simultaneous change of more than one activity of reactants in concentrated solutions. Using this, reaction order was found to be 2 with respect to both OH^? ions and water, suggesting that the electroactive species is not only reduced in the number of ligands but also dehydrated with respect to the prevailing species. The anodic limiting current appears to be due to the accumulation of Zn(OH) species to cover all the surface free of adsorbed Zn(OH)₂. Exchange cd and rate constants of all the four steps of the reaction have been estimated.