Stretching and deformation vibrations of CH2, C(CH3) and O(CH3) groups of poly(methyl methacrylate)

Infrared and Raman spectra of atactic PMMA and infrared spectra of stereoregular PMMA and of its four deuterated derivatives

, were measured. They were used to assign the bands of stretching and deformation vibrations of CH₂, CCH₃ and OCH₃ groups in the infrared and Raman spectra and to discuss the effect of stereoregularity on these bands in the infrared spectra.     

Corrosion protection of aluminium in acidic chloride solutions with nontoxic inhibitors

Corrosion kinetics of 99.6% aluminium covered by a thin spontaneously formed oxide film in hydrochloric acid solution with and without the presence of substituted N-aryl pyrroles was studied using electrochemical impedance spectroscopy and quasi steady-state polarization. Measurements were performed on a rotating disc electrode in an argon-deaerated solution in the temperature range 20 to 50°C. The addition of inhibitor considerably increases overvoltage of the cathodic process (HER) and shifts Ecorr to negative potential values. The activation energy of the hydrogen evolution reaction was Ea=50±5kJmol–1 and was not affected by the presence of inhibitor. The inhibitory action occurs by -bonding between the adsorbed inhibitor molecules and the electrode surface. The electrode coverage follows the Langmuir adsorption isotherm with an adsorption equilibrium constant K=1.1–2.64×105dm3mol–1. The adsorption of organic compound prevents the adsorption of chloride ions and slow down the rate of corrosion.     

The potentiometric behaviour of copolymers of methacrylic acid in water-ethanol solutions

Summary The synthesis is reported of copolymers of styrene with methacrylic acid and of methyl methacrylate with methacrylic acid by radical copolymerization, of copolymers of methyl methacrylate with methacrylic acid by partial alkaline hydrolysis of poly(methyl methacrylate), and of block copolymers of styrene with methacrylic acid. Modified titration curves of all these copolymers were recorded in water and water-ethanol solutions. In a solution containing 50 mass.% ethanol, only small differences could be observed between the potentiometric behaviour of the individual copolymers and polymethacrylic acid. Also, there were no essential differences in any of the solvents used between the potentiometric behaviour of block copolymers of styrene with methacrylic acid, on the one hand, and polymethacrylic acid, on the other. On the contrary, maxima and minima were always observed on the modified titration curves of statistical copolymers with a higher content of the hydrophobic comonomer in solutions with a high water content. Thus, using the modified titration curves, it is possible to decide whether a given copolymer is of the block or statistical type.     

Contribution to the hydration of expansive cement on the basis of metakaolinite

The study of hydration of expansive cement prepared from 64% portland cement clinker, 23% metakaolinite and 13% CaSO₄.2H₂O is described. It was found that in the course of a 10-day hydration period, all the gypsum entered the reaction with the formation of ettringite. In 7–10 days, after the termination of the expansion processes, typical stalk-like crystals were transformed into leaf-shaped or other formations. Ettringite was identified even after 4 months of hydration. Monosulphate (3CaO.Al₂O₃.CaSO₄.12H₂O) was found in none of the investigated high-expansion cement paste samples.     

The correlation between electrical properties and structure of substituted polyacetylenes

Summary The electrical conductivity of polyphenylacetylenes and polyhalophenylacetylenes was measured in dependence on the temperature and on the type of catalyst used for polymerization. The electrical conductivity increased with increasing temperature. The energy gap was calculated from the temperature dependence on the electrical conductivity; it decreased with increasing number of conjugated double bonds in the polymer chain and with the regularity of structure of the polymer. The number of double bonds, cyclization and configurations were determined by ¹H and ¹³C-NMR. In polyphenylacetylenes only aliphatic carbons deriving from cyclohexadiene units were found but no such units were found in polyhalophenylacetylenes. By UV-vis measurement the number of conjugated double bonds in segments was estimated. The synthesized polymers were amorphous. Their molecular weight was between 2000 and 74.000.     

Microstructure and physical properties of transparent thoria-yttria ceramics

The investigation of microstructure, some electrical and optical parameters of transparent ThO₂-15 mol % yo_1.5 ceramics has shown: (a) a very low porosity, close to zero; (b) a higher electrical conductivity than is usual for ThO₂ ceramics of the same composition, with the activation energy 1.12 eV; (c) a relative permittivity _r 33 under the given conditions; (d) confirmation of a single-phase fluorite-type cubic structure by means of Raman and infrared spectra.     

Design of Lu2O3-reinforced Cf/SiC-ZrB2-ZrC ultra-high temperature ceramic matrix composites: Wetting and interfacial reactivity by ZrSi2 based alloys

The wettability and infiltration of molten ZrSi₂ and ZrSi₂-Lu₂O₃ alloys into C_f/SiC and B₄C-infiltrated C_f/SiC composites were investigated to understand the interfacial interactions that occur during the development of C_f/SiC-ZrC and C_f/SiC-ZrB₂-ZrC-Lu₂O₃ materials. A significant evaporation of Si from the liquid affected the wetting behaviour of the alloy when tested in a vacuum at 1670 °C. The better wetting and spreading of the alloy over the surface was observed for the composites with lower overall porosity (12 %). On the other hand, the formation of an outer dense layer, followed up by the uniform infiltrated region up to ～ 1 mm was observed for the C_f/SiC with higher porosity (21 %). The infiltrated alloy reacted with SiC matrix to form ZrC or with B₄C-infiltrated SiC matrix to form ZrB₂-ZrC-SiC. The Lu₂O₃ particles were not wetted by the melt, and were pushed away of the reaction zone by the solidification front.