Roofing foils are known for several years as building material for roof hydro insulation but their life service is not yet fully known. This thesis is focused on problematics of life service of roofing foils. In theoretical part there is discribed structure of foils and impacts which assist degradation processes. Practical part modifies the methodology artificial aging which is simulated in QUV tester and Q-SUN XE3 tester lumber-rooms. The thesis is trying reach with the results to natural aging as close as possible. The testing captures attributes which are more prone to degradation.

This diploma thesis deals with the study of isothermal crystallization of nanocomposite materials based on isotactic polypropylene (iPP) and nanosilica, depending on the volume fraction (0, 2, 4 and 6 %) and type of silica and the crystallization temperature. Fumed silica and four types of silica with different surface treatment were used as filler. The crystallization performed at temperatures 136, 138, 140 and 142 °C has been studied in-situ using polarized optical microscope and the crystallization rate was evaluated from the growing radius of spherulites. It can be stated that particles of silica have been inbuilt into the spherulites due to the linear growth of spherulites of all composite materials. The most significant increase of the crystallization rate of iPP was caused by fumed silica, the most significant decrease was caused by silica TS-720 at volume fraction 4 %. The crystallization rate (G) has been slightly increased with the increasing volume fraction of filler at 136 °C, the G slightly decreased at 138 °C and there was no trend of G for two higher temperatures. Also, it was not possible to exactly evaluate the influence of the surface treatments. The reason is the most probably uneven (non-homogenous) distribution of nanosilica as revealed thermogravimetric analysis. The crystallization kinetics was evaluated according to the Lauritzen-Hoffmann theory. The morphological part of the study showed that iPP was in ? and ß-structure and spherulites of ? phase were of the type I, II and mixed.

Charles University Faculty of Pharmacy in Hradec Králové Department of Pharmaceutical Technology Consultant: doc. RNDr. Milan Dittrich, CSc. Student: Andrea Balciarová Title of Thesis: Formulation and testing of rifampicin-loaded branched polyesters nanoparticles In presented thesis, the main attention in theoretical part is focused on nanoparticles for targeted drug delivery, their types, structure and carriers used for their preparation. Moreover, in this part there is an overview of physicochemical characteristics and preparation methods of polymeric nanoparticles applicable in formulation of pharmaceutical products. The experimental part is concerned on studying the influence of the concentration of biodegradable polymers, the presence of cationic surfactants and rifampicin as model drug substance on nanoparticles΄ size and zeta-potential. The main attention is given to nanoparticles decoration with anionic biopolymers, hyaluronic acid and xanthan gum. The simple method of preparation which is usable in nanosystems formulation that influence biological functions purposefully was tried and tested in different contexts.

This diploma thesis deals with 1) the preparation of biodegradable polymer films based on polyhydroxyalkanoates (PHA) and 2) their modification by lignin as an active additive. The motivation for this work was to prepare active packaging material for food packaging. Polymer films were prepared by blending of neat crystalline poly(3hydroxybutyrate) (P3HB) and amorphous polyhydroxyalkanoate (PHA). The lignin was isolated from grape seeds derived from grape pomace. The solubility of lignin in chloroform was improved by acetylation. The properties of the isolated lignin were determined by elemental analysis, ash content, and infrared spectroscopy (FTIR). Lignin was used as an active additive for the modification of polymeric films prepared by solution casting of P3HB or P3HB blended with amorphous polyhydroxyalkanoate. The effect of different concentrations of lignin in the range of 1 to 10 % was tested. The lignin type and concentration had a different influence on the final thermal and mechanical behaviour of polymeric films. Lignin increased the values of the Young modulus and tensile strength of the prepared films. Differential scanning calorimetry data confirmed that lignin positively modified crystallization kinetics of P3HB. Thermogravimetry was used to analyse the thermal stability of PHA films. Lignin markedly increased the thermal stability of PHA films. However, acetylated lignin harms the mechanical properties of films. Moreover, this work showed that lignin isolated from grape seeds and added into PHA films proved its high antioxidant capacity. PHA films with lignin displayed much better gas barrier properties compared with PHA films without lignin. The prepared bioactive PHA films fulfil the requirements for sustainable food packaging with high antioxidant capacity and excellent gas barrier properties.

This thesis is focused on synthesis and polymerization of caprolactone and its derivatives by living ring opening polymerization (LROP), Self-assembly in aqueous solutions produced nanoaggregates comprised of amphiphilic block copolymers or telechelic polymers with incorporated boron compounds (phenyl boronic acids and boron clusters). Incorporation of boron compounds was facilitated either by covalent or non-covalent bonding. Obtained complex nanoparticle structures manifested stimuli-responsive behaviour and were investigated under varying conditions by combination of light scattering, fluorescence spectroscopy and electron microscopy. The obtained results on solution behaviour of polymers in combination with added value of boron compounds, yield general aspects of nano aggregate morphology, responsive character tuning and practical aspects of synthesis and self-assembly overcame in the preparation process. The publications wrote during this thesis are therefore adding valuable information to researchers engaged in biomedical utilization of such nano assemblies.

The Thesis describe my studies based on self-assembly and co-assembly of block copolymer micelles that I conducted at the Department of Physical and Macro- molecular Chemistry at the Charles University, Prague in the research group of my supervisor, Prof. Dr. Karel Procházka, DrSc. The Thesis based on my publications and consists of four parts. Here I studied the formation of polymeric nanoparticles in aqueous solutions formed by polyelectrolytes with hydrophobic backbones by a combination of several experimental methods. The achieved results enabled me to explain the structure and properties of studied self- and co-assembled nanoparticles and to outline the decisive trends of their behavior. The spontaneous formation, sol- ubility and stability of complex nanoparticles depend not only on the electrostatic attractive forces but also on the hydrophobic effects. As the enthalpy-to-entropy interplay is very complex, a number of external factors such as temperature, pH, salinity and concentration affect the assembling process and structure of formed nanoparticles. 1

The purpose of this diploma thesis is to describe the influence of input parameters (rolling speed, load, temperature, dynamic viscosity and pressure coefficient of the lubricant) on film thickness in point and elliptical contacts using optical interferometry. Regression based film thickness formula has been obtained using universal form of non-dimensional parameters of entrainment speed U, load W and material G. Equations were also complemented by the function of ellipticity k. New regression formulas for central and minimum film thickness have been compared with existing EHL thickness equations. These film thickness measurement and new regression formulas have applicability to our understanding of the performance and more effective design of lubricated gears from polymeric materials.

Title: Multicomponent plasma polymers with spatially controlled properties Author: MSc. Pavel Pleskunov Department / Institute: Department of Macromolecular Physics/Charles University Supervisor of the doctoral thesis: Prof. Ing. Andrey Shukurov, PhD, Department of Macromolecular Physics / Charles University Abstract: Mixing of two (or more) polymers often leads to phase separation and to the formation of nanoscale architecture, which can be highly attractive in various applications including controllable drug delivery, fabrication of separation and solid electrolyte membranes, gas storage, etc. Different wet-chemistry techniques already exist to produce nanophase-separated polymers; however, capturing the resultant polymeric structure in a predictable manner remains a challenging task. In this thesis, a low-temperature plasma-based strategy is investigated for the production of multicomponent thin films of plasma polymers with spatially discriminated nanoscale domains. Gas aggregation cluster source is used for the fabrication of nanoparticles of plasma polymerized acrylic acid, whereas Plasma-Assisted Vapor Phase Deposition is used for the deposition of thin films of poly(ethylene oxide) plasma polymer. Embedding of nanoparticles into matrices of thermodynamically incompatible plasma polymer as well as...

4 ABSTRACT The synthesis has been described yielding a new type of rigid conjugated polymer networks which possess a high content of permanent micropores and macropores and exhibit high surface areas up to 1469 m2/g. The networks have been prepared via chain-growth coordination polymerization catalysed with insertion catalysts based on Rh complexes. This polymerization has been newly applied to bifunctional acetylenic monomers of diethynylarene type (1,4-diethynylbenzene, 1,3-diethynylbenzene and 4,4'-diethynylbiphenyl). The covalent structure of the networks consists of the polyacetylene main chains densely connected by arylene struts. The W and Mo metathesis catalysts have been revealed as inefficient for the synthesis of these networks. The increase in the polymerization temperature and time has been shown to affect positively the content and the diameter (up to 22 nm) of the mesopores in the networks. A mechanism has been proposed that explains the mesopores formation as a result of mutual knitting of small particles of the microporous polymer. The application of emulsion polymerization technique allowed to prepare texturally hierarchical polyacetylene networks possessing interconnected open macropores (diameter up to 4,8 μm) the walls of which exhibited micro/mesoporous texture. It was demonstrated...