Publications by authors named "Ilona Pyszka"

Billions of patients struggle with dental diseases every year. These mainly comprise caries and related diseases. This results in an extremely high demand for innovative, polymer composite filling materials that meet a number of dental requirements.

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In this work, photoinitiation systems based on dibenzo[a,c]phenazine sensitivity to visible light were designed for their potential application in dentistry. Modification of the structure of dibenzo[a,c]phenazine consisted of introducing electron-donating and electron-withdrawing substituents and heavy atoms into position 11. The synthesized compounds are able to absorb radiation emitted by dental lamps during photoinitiation of the polymerization process.

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Advances in electronics and medical diagnostics have made organic dyes extremely popular as key functional materials. From a practical viewpoint, it is necessary to assess the spectroscopic and physicochemical properties of newly designed dyes. In this context, the condensation of 1,3-dimethylbarbituric acid with electron-rich alkylaminobenzaldehyde derivatives has been described, resulting in a series of merocyanine-type dyes.

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Dyes based on quinoline and quinoxaline skeletons were designed for application as visible light photoinitiators. The obtained compounds absorb electromagnetic radiation on the border between ultraviolet and visible light, which allows the use of dental lamps as light sources during the initiation of the photopolymerization reaction. Their another desirable feature is the ability to create a long-lived excited state, which enables the chain reaction to proceed through the mechanism of intermolecular electron transfer.

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A polymeric inclusion membrane (PIM) consisting of matrix CTA (cellulose triacetate), ONPPE (o-nitrophenyl pentyl ether) and phosphonium salts (Cyphos 101, Cyphos 104) was used for separation of Cu(II), Zn(II) and Ni(II) ions. Optimum conditions for metal separation were determined, i.e.

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Modern dentistry places great demands on the dental composites used for filling tooth cavities or treating cavitated tooth decay. The aim of the work was to modify the properties of composites by changing the initiators and co-initiators. This was achieved by using initiators based on a quinoxaline skeleton and co-initiators that are derivatives of acetic acid, which is an advantage of these photoinitiating systems due to the elimination of aromatic amines from the photocurable composition.

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A series of dyes based on the acenaphthoquinoxaline skeleton was synthesized. Their structure was modified by introducing electron-withdrawing and electron-donating groups, increasing the number of conjugated double bonds and the number and position of nitrogen atoms, as well as the arrangement of aromatic rings (linear or angular). The dyes were investigated as a component in the photoinitiating systems of radical polymerization for a potential application in dentistry.

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This study indicates that a new amine derivative of β-diketone (EDAB-acac) can be successfully used in an acidic medium (HCl) to separate a mixture containing Au(III), Pd(II), and Pt(IV) ions using solvent extraction. The study was conducted in single and ternary model solutions. The impact of acid concentration and the type of solvent (toluene, chloroform, methylene chloride, 2-ethylhexanol) on separation efficiency was discussed.

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A series of dyes based on the phenazine skeleton were synthesized. They differed in the number of conjugated double bonds, the arrangement of aromatic rings (linear and/or angular system), as well as the number and position of nitrogen atoms in the molecule. These compounds were investigated as potential singlet oxygen sensitizers and visible light absorbers in dye photoinitiating systems for radical polymerization.

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The new polymer inclusion membrane (PIM) with a 1-alkyltriazole matrix was used to separate palladium(II) ions from aqueous chloride solutions containing a mixture of Zn-Pd-Ni ions. The effective conditions for transport studies by PIMs were determined based on solvent extraction (SX) studies. Furthermore, the values of the stability constants and partition coefficients of M(II)-alkyltriazole complexes were determined.

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The new polymer inclusion membrane (PIM) with ethylenediamine-bis-acetylacetone (EDAB-acac) matrix was used for the separation of Zn(II) solutions containing non-ferrous metal ions (Co(II), Ni(II) Cu(II), Cd(II)). The effective conditions for carrying out transport studies by PIMs were determined on the basis of solvent extraction studies. The values of the stability constants and partition coefficients of M(II)-EDAB-acac complexes were determined from the extraction studies.

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New materials, such as polymer inclusion membranes, can be used for water and wastewater treatment. In this paper, the selective transport of silver(I) and zinc(II) ions from nitrate solutions through the polymer inclusion membranes (PIMs), which consist of cellulose triacetate as a polymeric support, -nitrophenyl pentyl ether as a plasticizer, and either 1-hexylimidazole () or 1-hexyl-2-methylimidazole () as an ion carrier, is studied. Both Zn(II) and Ag(I) model solutions (C = 0.

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Polymer inclusion membranes (PIMs) doped with ethylenodiamino-bis-acetylacetone as fixed carrier was applied for the investigation of the facilitated transport of Zn(II), Cr(III), and Ni(II) ions from an aqueous nitrate feed phase (c = 0.001 mol/dm). The optimal membrane composition (amount of carrier and -NPPE-plasticizer) was determined.

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New bis(imidazo)pyridine dye has been synthesized and tested as a potential photoinitaitor for free-radical polymerization induced with the visible emission of an argon ion laser. The X-ray analysis based on data collected at 170 and 130 K, as well as density functional theory (DFT) calculations, revealed the presence of two different forms of imidazopyridine rings within the same molecule. These two forms of the same moiety had not only different geometries but different electronic structures as well.

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2-Oxo-2,3-dihydro-1H-imidazo[1,2-a]pyridinium bromide and its C3-substituted derivatives have been synthesized and structurally characterized by X-ray crystallography and quantum chemical calculations. Their potential as photoinitiators for free-radical polymerization has been investigated experimentally and compared with theoretical results. It has been established that the course of the reaction that introduces the substituted benzylidene group to the imidazole ring is different in the protic and dipolar aprotic solvents, and also depends on the character of the substituent, as the energy change in the reaction favours either R1R2C=CHR3 or R1R2CH-CH(OCH3)R3 formation.

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