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Blends of PLA with thermoplastics
Petruš, Josef ; Petrůj, Jaroslav (referee) ; Kučera, František (advisor)
Diploma thesis deals with preparation of polymer blend of polymer A and polymer B. Knowledge of polymer blends forming, thermodynamics and function of compatibilizer is contained in the theoretical part. Polymer blend A/B of weight ratios 75/25, 50/50 and 25/75 wt% were prepared by physical compatibilization. Concentration of compatibilizer was 5 wt%, in the case of A/B 50/50 wt% concentration of compatibilizer was 10 and 30 wt%, respectively. Blending was achieved with twin-screw extruder at 230 °C and 100 rpm. Second method used for A/B blending was based on reactive compatibilization which was achieved with Brabender kneader at 230 °C, 50 rpm and reaction time 10 minutes. Concentration ratios of A/B were 75/25, 50/50 and 25/75 wt%. Itaconic acid anhydride and maleic anhydride 0.5 and 5 wt% were used as monomer. 2,5-dimethyl-2,5-bis(tert-buthylperoxy)hexan was (Luperox 101) used as an initiator. Difference between compatibilized and noncompatibilized blends was characterized by scanning electron microscopy, tensile test, differential scanning calorimetry, melt flow index measuring, acid-base titration and FT-IR spectroscopy.
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The Study of Lactides Syntheses from Esters of Lactic Acide
Tomala, Libor ; Chamradová, Ivana (referee) ; Petrůj, Jaroslav (advisor)
This master thesis deals with the synthesis of lactide from lactic acid esters. The theoretical part focuses on the current understanding of technology of lactic acid, its alkyl esters and the cyclic lactic acid dimer - lactide, which is mainly used as a precursor for the synthesis of high moleculat weight biodegradable polylactide (PLA) and other copolymers. Experimental part is then focused on the synthesis of lactide from lactic acid alkyl esters, especially ethyl lactate. Examines the design of a suitable apparatus for this synthesis and the application of the most appropriate reaction conditions (temperature, pressure, catalysis) to optimize the preparation of the desired product. In the end, parameters of prepared lactide are characterized by using of various analytical techniques.
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The Influence of Nanoparticles on The Properties of Hard Polyurethane Foams
Eliáš, Filip ; Kotlík, Josef (referee) ; Petrůj, Jaroslav (advisor)
The theoretical part of the thesis focuses on general principles of polyurethane chemistry. Nanotechnologies are also discussed, in particular using nanoparticles in the production of polyurethane foams. There are also mentioned selected preparation methods of silver and titanium dioxide nanoparticles. The experimental part describes mainly a novel method for synthesis of the concentrated solution of titanium dioxide nanoparticles in glycerol and their analysis by using confocal microscopy, scanning electron microscopy, dynamic light scattering and UV-VIS spectroscopy. Finally, there are suggested particular steps for further investigation of prepared nanoparticles for the production of rigid polyurethane foams, and also for other applications.
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The study of using lactic acid esters for preparing lactides and PLA
Vida, Mikuláš ; Figalla, Silvestr (referee) ; Petrůj, Jaroslav (advisor)
This diploma thesis deals with use of lactic acid esters for preparation of lactides and PLA. In the theoretical part, it has been processed literature review focus on manufacturing technologies and properties of lactic acid and its esters (especially ethyl ester and lactides). In the experimental part, it has been designed and realized functional laboratory apparatus for preparation of cyclic dimer of lactic acid – lactides. On this apparatus, there were carried out principal laboratory experiments leading to optimization of lactides yields using various catalysts.
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Thermal Dilatation Measurement of Elastomeric Plastic Sheets
Mahel, Jindřich ; Kučera, Jaroslav (referee) ; Petrůj, Jaroslav (advisor)
The aim of the thesis was to design and build an apparatus for measuring linear thermal expansion of plastic waterproofing sheets. In the theoretical part of the thesis the methods used for measuring linear thermal expansion of solids were compared and the principle of thermoelectric cooling was described . For the measuring the Abbe comparator has been chosen , which has been equipped with a tempered chamber with a cascade of thermoelectric Peltier elements for cooling and heating of specimen. The experimental part of the thesis deals with the construction of the device and the actual measuring in the specified temperature range.
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Study of optimizing thermoinsulation properties of rigid polyurethane foams
Eliáš, Filip ; Vojtová, Lucy (referee) ; Petrůj, Jaroslav (advisor)
The thesis deals with the processes that occur in the course of the manufacturing of rigid polyurethane-polyisocyanurate (PU-PIR) foams, their properties and technology. It deals above all with principles of foam nucleation and stability. The purpose of understanding these principles is their possible use for improving thermo-insulating properties of the material. The experimental part of the thesis studies the influence of additives and ultrasound on the PU-PIR foam properties. It has been found that low molecular weight compounds with perfluorinated chain leads to decreasing foam cell size and its lower thermal conductivity. The additives mentioned act probably on the surfactants principle by facilitating nucleation and stabilizing growing centres of bubbles. They probably form also part of blowing agents mixture inside the foam cells which cause lowering of thermal conductivity as well. Compounds with similar chemical structure have unique influence on the properties of rigid PU-PIR foams. Further research ought to be focused on cheaper modes of producing perfluorinated compounds.
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PLA Synthesis in Solution
Svítil, Jan ; Zdeněk, Přikryl (referee) ; Petrůj, Jaroslav (advisor)
This thesis is studying PLA syntheses using polymerization of lactides in solution. Theoretical part deals with properties and production of lactic acid, lactides and polylactides. In the experimental part, possibilities of lactides polymerization in solution has been summerised and verified. Syntheses were performed via “solvothermal” method using 7 solvents (toluene, chloroforme, 1,2-chlorobenzene, acetone, tetrahydrofurane, cyclohexane and hexane). Using hexane as solvent, at concentration ratio catalyzer/lactide 1 : 1 000, polymerization temperature 160 °C and reaction time 20 h, polylactide of viscosity average molecular weight 179 000 gmol–1 was synthetized from the lactide.
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New Processes of Lactid Acid Polymers Preparation
Figalla, Silvestr ; Svěrák, Tomáš (referee) ; Herink,, Tomáš (referee) ; Petrůj, Jaroslav (advisor)
The work focuses on new processes for the preparation of lactic acid derivatives. The main objective was to verify the feasibility of preparing high molecular weight polylactide using ethyl lactate as a precursor of lactide synthesis. Part of the work is devoted to the new ethyl lactate synthesis method. The experimental part of the thesis is divided into partial key steps on the way from the lactic acid to the high molecular polylactide. The preparation of anhydrous ethyl ester of lactic acid (EtLA) was solved in an innovative way using alcoholysis of the oligomeric lactic acid. A kinetic model for isothermal alcoholysis and equimolar reactants ratio was derived from this method. The ethyl lactate was oligomerized by transesterification into the low and high molecular weight oligomer with the help of newly found catalysts suitable for the reaction medium. Stannous lactate was used as catalyst for oligomerization of the low molecular weight polymer suitable for the preparation of lactide (Mn 1000 g.mol-1). Experimental polymerization of ethyl lactate into high molecular weight product in tens of kDa has been investigated with newly synthesized tetraethyllactoyl titanate, Ti(EtLA)4. The laboratory method was derived for the depolymerization of the oligomer into lactide. Optimal conditions found for lactidation are as follow: temperature 225 ° C, pressure 2 kPa, catalysis 0,05 mol% of stannous lactate (with respect to oligomer lactate units). The prepared lactide was refined to polymer grade purity by distillation and subsequent recrystallization from ethyl acetate and toluene. The method for the preparation of high molecular weight PLA through ROP polymerization of lactide has been optimized. By optimization, suitable catalyst concentration was found in combination with the polymerization temperature and the polymerization length. An equimolar mixture of Tin 2-ethylhexanoate and 1-decanol was used as the catalytic system. The optimal ROP conditions for achieving the maximum molecular weight and suppressed polymer coloration (yellowing) are: catalyst concentration 0,01 mol%, temperature 160 °C, and polymerization length 4 hours. PLA with molecular weight Mw= 447 ± 7,8 kg.mol-1 was prepared at these conditions and good repeatability of the result was achieved. The effect of naturally occurring lactide contaminants and their influence on the course and ROP result was experimentally verified on the optimized polymerization system. The purpose was to explore the effect of lactide contamination with water and ethanol as natural lactide contaminants. The results clearly confirm the orderly lower sensitivity of the polymerization system for the presence of ethanol as compared to water contamination. In the case of the presence of water, the course and the result of the polymerization in terms of both the conversion and achieved molecular weights are negatively affected, even when the water content is in the order of 0,001%. Conversely, the presence of ethanol has a positive effect on lactide conversion and polymer polydispersity. Lactides with an alcohol content of about one-tenth of a percent are suitable to reach molecular weights of PLA similar to commercially available products. This difference shoves a significant advantage in the proposed technology of preparing PLA from ethyl lactate, especially for easier purification of crude lactide into polymer grade purity.
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Modification of Polyethylene by Reactive Compounding
Horkel, Ondřej ; Kučera, Jaroslav (referee) ; Petrůj, Jaroslav (advisor)
This Master’s thesis deals with the problematics of radically initiated compounding of polyethylene by 1-vinyladamantane. Theoretical part focuses on the theory of grafting processes and how they are influenced by chosen process parameters, as well as the properties of used monomer. In experimental part, two sets of experiments were designed, in both cases the chemicals used were polyethylene LITEN MB 87, (2,5-dimethyl-2,5-bis(tert-butylperoxy) hexane), also called Trigonox 101, as the initiator, and chemicals called Ionol and Irgafos 168 as stabilizers. The experiments were carried out in a Brabender batch mixer, the temperature was 180 – 185 °C, the reaction time was 5 minutes. The analytic methods used to evaluate the prepared samples’ properties were the tensile testing, the Charpy notch test, measuring of the melt flow index, analyzing the torque during kneading and the analysis of infrared spectra of the samples. By carrying out of these experiments it was found that excessive crosslinking was present with mass fraction of initiator being as low as 2 %. It was also concluded that under these conditions the modification does not improve tensile properties of the material, but it does improve the impact strength, albeit slightly. The influence of the modification on flow properties needs to be investigated further. A presence of vinyl groups was observed in infrared spectra, suggesting the presence of ungrafted vinyladamantane.
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Chemical modifications of polypropylene surfaces
Pospíšek, Marek ; Petrůj, Jaroslav (referee) ; Kučera, František (advisor)
Diploma thesis is focused on modification and characterization of polypropylene (PP) products surfaces by the chemical way. In theoretical part of thesis are summarized the current knowledge of this topic including characterization methods. Polypropylene surfaces were modified by acrylic monomers (acrylic acid, acrylic acid with 20 mol% content of sodium acrylate and acryl amide). Modified surfaces were characterized by infrared spectroscopy with ATR technique. The comparative parameter was carbonyl index determined from absorption peaks of functional methyl groups (2950 cm-1 ) and functional carbonyl groups (1700-1750 cm-1) of FTIR-ATR spectra. Determination of effect of initiator concentration on the modification process was done for acetophenone and benzophenone. There were determined the time dependence of carbonyl index for time from 0 to 600 s of mentioned monomers. In the same condition were modified test specimens designed for preparation of adhesive joints. Joints were bonded by cyanoacrylate adhesive that provide reaction with surface of polyacrylic acid. There were founded conditions of modification that provided strength of adhesive joints higher than strength of original PP. There were identified changes of surface roughness by using of confocal microscopy.
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