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Novel nonterminal liquid crystalline epoxy resin has been synthesized, and its structure and nature have been determined via nuclear magnetic resonance (NMR) and polarized optical microscopy (POM). Then, it was cured with the use of 4,4'-diaminodiphenylmethane (4,4'-DDM). The curing process has been investigated via differential scanning calorimetry (DSC) and infrared spectroscopy (FTIR) methods. Polymerization has been conducted with (1.2 T) and without the presence of a strong magnetic field. The properties of the obtained polymers have been described using DSC, thermogravimetric analysis (TGA), scanning electron microscopy (SEM), dielectric spectroscopy (DS) and X-ray scattering studies (WAXS/SAXS). It has been proved that the magnetic field induces molecular ordering and increases the glass transition temperature (Tg) by over 20 °C. The obtained ordered polymers are thermally stable up to over 300 °C, undergo vitrification at slightly elevated temperature (37.5 °C), and their electrical conductivity rises significantly at the transition to an elastic state, which, among other possibilities, makes them a proper candidate for a smart, lightweight polymers with tuneable properties by a subtle temperature rise and possibility of tailoring its structure by a magnetic field. [ABSTRACT FROM AUTHOR]

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Poly(3-hydroxybutyrate) is a biopolymer which is used to production of implants in the human body. On the other hand, the physical and mechanical properties of poly(3-hydroxybutyrate) are compared to the properties of isotactic polypropylene what makes poly(3-hydroxybutyrate) possible substitute for polypropylene. Unfortunately, the melting point of poly(3-hydroxybutyrate) is almost equal to its degradation temperature what gives very narrow window of its processing conditions. Therefore, numerous attempts are being made to improve the poly(3-hydroxybutyrate) properties. In the present work, hybrid nanobiocomposites based on poly(3-hydroxybutyrate) as a matrix with the use of organic nanoclay - Cloisite 30B and linear polyurethane as a second filler have been manufactured. The linear polyurethane was based on diphenylmethane 4,4'-diisocyanate and diol with imidazoquinazoline rings. The obtained nanobiocomposites were characterized by X-ray diffraction, scanning and transmission electron microscopies, thermogravimetry, differential scanning calorimetry and their selected mechanical properties were tested. The resulting hybrid nanobiocomposites have intercalated/exfoliated structure. The nanobiocomposites characterize a higher thermal stability and a wider range of processing temperatures compared to the unfilled matrix. The plasticizing influence of nanofillers was also observed. In addition, the mechanical properties of the discussed nanobiocomposites were examined and compared with those ones of the unfilled poly(3-hydroxybutyrate). The new-obtained nanobiocomposites based on poly(3-hydroxybutyrate) containing 1% Cloisite 30B and 5% by mass of the linear of polyurethane characterized the highest improvement of processing conditions. They have the biggest difference between the temperature of degradation and the onset melting temperature, about 100°C. [ABSTRACT FROM AUTHOR]

In this work, research concerning the synthesis and properties of linear polyurethanes (PUs) with the imidazoquinazoline rings was represented. Reaction conditions of 2,6-bis(2-hydroxyethyl)-1-phenylimida-zo[1,5-c]quinazoline-3,5-dione (BHPIQ) with 1,6-hexamethylene diisocyanate were determined and optimized. These conditions are adapted to reaction of BHPIQ with 4,4′-diphenylmethane diisocyanate and 2,4-toluene diisocyanate. New PUs with imidazoquinazoline rings were characterized by spectral methods (1H-NMR and IR spectroscopies), which confirm their structures. Their molar masses and dispersity index were measured by size exclusion chromatography method. The wide-angle X-ray scattering and differential scanning calorimetry (DSC) studies have shown that all PUs based on BHPIQ are amorphous. Moreover, thermal properties of PUs were investigated by thermogravimetry analysis, standard DSC, and temperature-modulated DSC methods. During thermogravimetric measurements, the exhaust gases were analyzed by FTIR method. Incorporation of imidazoquinazoline ring into the PU chains escalates their glass transition temperature; thus, their heat resistance was enhanced. Furthermore, their degradation rate and the amount of released degradation products were reduced. The investigated properties of the obtained PUs with imidazoquinazoline rings were compared with those ones of suitable PUs based on 1,4-butanediol. Linear polyurethanes were obtained in reaction of 1-phenyl-2,6-bis(2-hydroxyethylimidazo[1,5-c]quinazoline-3,5-dione with hexamethylene 1,6-diisocyanate, 4,4′-diphenylmethane diisocyanate and toluene 2,4-diisocyanate. Their composition and structure were confirmed. The phase contents and thermal properties were investigated [ABSTRACT FROM AUTHOR]

TG-DSC thermal analysis involved two new BioCo foundry binders in the form of a composition with poly(acrylic acid) and modified polysaccharides (dextrin, sodium salt of carboxymethyl starch). Thermal analysis was conducted to determine the effect of the thermal decomposition conditions and polymer structure on the progress of degradation in terms of processes occurring in the foundry sands, when they contact with liquid metal. Thermal analysis of the composition allowed for determining the temperature range where they do not undergo degradation, by which they do not lose their binding properties. It was evidenced that the course of thermal decomposition is complex (mixed degradation mechanism). With temperature increase, physical and chemical changes occur, related to evaporation of solvent water (20-100 °C) and next release of constitution water, while finally intermolecular dehydration (100-220 °C). In this temperature range, mainly reversible processes take place. Within the temperature range of 220-300 °C, polymer chains decompose, including decomposition of side chains and glycosidic bonds. Within the temperature range of 300-500 °C, polymer compositions decompose, and gas products of destruction are generated. A part of the compound that did not decompose at the temperature of approx 550 °C can contain carbonised coal. It was evidenced that if the composition includes sodium atoms, inorganic compounds are formed which decompose at the temperature of approx 800 °C. [ABSTRACT FROM AUTHOR]

The reactivity of a system comprising commercial epoxy resin Epidian 6 (E6) and triethylenetetramine (Z-1) hardener was studied. The system was modified with two low-molecular siloxane modifiers: 1,3-bis(glycidyloxypropyl)-1,1,3,3-tetramethyldisiloxane (DS1) and 1,3-bis(aminopropyl)-1,1,3,3-tetramethyldisiloxane (DS2). The modifiers replaced 10 mass% of E6 or Z-1, respectively. The systems E6/DS2 and DS1/Z-1 were also studied. Enthalpy of curing was determined for all systems in isothermal conditions and dynamically, i.e., in the range of 0-250 °C with linearly increasing temperature at the rate of 2, 5, 10, and 20 °C min. The activation energy of curing was determined using isoconversional methods by Friedman and Kissinger-Akahira-Sunose. The epoxy systems containing siloxane modifiers had generally lower activation energies than the reference E6/Z-1 system. The time to gelation measurements were taken using the temperature-modulated differential scanning calorimetry. [ABSTRACT FROM AUTHOR]