Michał Strankowski

Polyurethane Nanocomposites Containing Reduced Graphene Oxide, FTIR, Raman, and XRD Studies

Recently, graphene and other graphene-based materials have become an essential part of composite science and technology. Their unique properties are not only restricted to graphene but also shared with derivative compounds like graphene oxide, reduced graphene oxide, functionalized graphene, and so forth. One of the most structurally important materials, graphene oxide (GO), is prepared by the oxidation of graphite. Though removal of the oxide groups can create vacancies and structural defects, reduced graphene oxide (rGO) is used in composites as effective filler similar to GO. Authors developed a new polyurethane nanocomposite using a derivative of grapheme, thermally reduced graphene oxide (rGO), to modify the matrix of polyurethane elastomers, by rGO.

Morphology and the physical and thermal properties of thermoplastic polyurethane reinforced with thermally reduced graphene oxide

Abstract In this study, thermally reduced graphene oxide (TRG)-containing polyurethane nanocomposites were obtained by the extrusion method. The content of TRG incorporated into polyurethane elastomer systems equaled 0.5, 1.0, 2.0 and 3.0 wt%. The morphology, static and dynamic mechanical properties, and thermal stability of the modified materials were investigated. The application of TRG resulted in a visible increase in material stiffness as confirmed by the measurements of complex compression modulus (E′) and glass transition temperature (Tg). The Tg increased with increasing content of nanofiller in the thermoplastic system. The addition of thermally reduced graphene oxide had a slight effect on thermal stability of the obtained materials. The incorporation of 0.5, 1.0, 2.0 and 3.0 wt% of TRG into a system resulted in increased char residues compared to unmodified PU elastomer. Also, this study demonstrated that after exceeding a specific amount of TRG, the physicomechanical properties of modified materials start to deteriorate.

Evaluation of the photoprotective effect of β-cyclodextrin on the emission of volatile degradation products of ranitidine.

The process of the photo-excitation of ranitidine hydrochloride (RAN) in a solid state makes visible changes to its colour and generates an unpleasant odour. The purpose of the present study was to observe the protective effects of β-cyclodextrin (CD) complexation as well as the effect of the mixture of two stoichiometries 1:1 and 1:2 (RAN:CD, IC) on the photostability of samples in a solid state. Samples of inclusion complexes (IC) and physical mixtures (PM) were prepared and irradiated for 48h in a Suntest CPS+ chamber. Irradiated samples were analyzed using nuclear magnetic resonance ((1)H NMR), infrared spectroscopy (FT-IR), the differential scanning calorimetry method (DSC) and thermogravimetry analysis (TGA). Volatiles were monitored with the use of headspace-solid phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS). The protective effect of CD was noticed with respect to IC, and also PM. Achieved photostabilization of complexed RAN against photodegradation could be explained due to either the inclusion of the furan part of RAN into the CD cavity as shown by the (1)H NMR ROESY (rotation frame nuclear Overhauser effect spectroscopy) spectrum or the screening effect of CD. FT-IR spectra, DSC curves and microscope images of irradiated samples of protected RAN did not indicate any physical changes, such as phase transfer.

Morphology, Mechanical and Thermal Properties of Thermoplastic Polyurethane Containing Reduced Graphene Oxide and Graphene Nanoplatelets

Polyurethane/graphene nanocomposites were synthesized using commercial thermoplastic polyurethane (TPU, Apilon 52DE55), and two types of graphene derivatives: graphene nanoplatelets (GNP) and reduced graphene oxide (RGO). Fourier Transformation Infrared Spectroscopy Fourier Transformation Infrared Spectroscopy (FTIR) spectroscopy, TEM, and SEM microscopy and XRD techniques were used to chemically and structurally characterize GNP and RGO nanofillers. The properties of the new TPU nanocomposite materials were studied using thermal analysis techniques (Dynamical Mechanical Analysis (DMA), Differential Scanning Calorimetry (DSC), Thermogravimetric Analysis (TG)) to describe the influence of graphene nanofillers on polyurethane matrix. Our investigation describes the comparison of two types of graphene derivatives, commercial one (GNP) and synthesized (RGO) on thermoplastic polyurethanes. These nanofillers provides opportunities to achieve compatibility with the TPU matrix. The property enhancements are attributed commonly to high aspect ratio of graphene nanoplatelets and filler–polymer interactions at the interface. The obtained nanocomposites exhibit higher thermal and mechanical properties due to the good dispersion of both nanofillers into TPU matrix. It was found that the addition of 2 wt % of the nanofiller could lead to a significant reinforcement effect on the TPU matrix. Also, with high content of nanofiller (GNP and RGO), the Payne effect was observed.

Polyurethane/ground tire rubber composite foams based on polyglycerol: Processing, mechanical and thermal properties

During the synthesis of rigid polyurethane foams, petrochemical polyol was substituted with polyglycerol, the product of thermo-catalytic polycondensation of waste glycerol, resulting from biodiesel production. Two types of ground tire rubbers, untreated and thermo-mechanically reclaimed, were used to obtain “green” polyurethane-polyglycerol composite foams. Samples were prepared by a single-step method for the ratio of NCO/OH groups equal to 2. Foams containing different types of fillers showed noticeably various appearances, which suggested significant differences in the matrix–filler interactions between materials modified with untreated and reclaimed ground tire rubber. Addition of rubber particles shortened the processing time by more than 20 s and reduced the temperature during synthesis. Incorporation of ground tire rubber increased the size of the cells in comparison to unmodified foam. Modifications of rigid polyurethane foams resulted in the increase of apparent density and compressive strength even by 40% compared to neat foam. Enhancement was stronger for samples containing thermo-mechanically reclaimed ground tire rubber as a result of better developed surface of filler particles and their interfacial interactions with polyurethane matrix. Prepared polyurethane foams filled with untreated rubber particles also showed slightly enhanced thermal stability compared to neat foam.

Thermal and Mechanical Properties of Microporous Polyurethanes Modified with Reduced Graphene Oxide

Microporous polyurethanes (MPU) were modified by adding 0.25%–1.25 wt% of reduced graphene oxide (RGO). The materials were prepared without solvent via in situ polymerization. From a technological point of view, it is very important to obtain functional materials by using reacting compounds only. The thermal characteristics of obtained MPU were investigated using TGA, DSC, and DMA techniques. In comparison to nonmodified microporous polyurethane, the thermal stability and mechanical properties of the modified systems have significantly improved. The temperature corresponding to the maximum degradation rate () for nanocomposites containing 1% and 1.25 wt% of RGO was 51°C higher than that observed for pure microporous PU system. The increase of tensile strength was also observed for matrix with the addition of 0.5 wt% RGO nanofiller.

Rigid polyurethane foams modified with ground tire rubber - mechanical, morphological and thermal studies

Rigid polyurethane foams, prepared by a single step method, were modified with the two types of ground tire rubber particles, i.e. untreated and thermo-mechanically reclaimed using a co-rotating twin screw extruder. The foaming process as well as the structure and the physical, mechanical and thermal properties of the resulting foams were investigated. The presence of ground tire rubber decreased the rate of polymerization. The incorporation of ground tire rubber decreased the total crosslink density of the produced material, as confirmed by a decrease in glass transition temperature measured by dynamic mechanical analysis and differential scanning calorimetry. The temperatures associated with a 10% and 50% mass loss of foam, determined by thermogravimetric analysis, increased due to the addition of ground tire rubber particles.

Mechanical, Structural and Diffusion Studies of Hydrogel Polyurethane Nanocomposites Containing Modified Montmorillonite

Polyurethane hydrogels nanocomposites belong to a new class of hybrid biomaterials with unique swelling properties in comparison to unmodified hydrogels. These materials combine the typical properties of gels (elasticity and permeability) with the reinforcing properties of clay nanoparticles. Therefore, nanohydrogels might be applied in pharmacy for the controlled release and delivery of drugs and other biologically active agents, as well as in cosmetology as strong absorbents. We synthesized nanohydrogel polyurethanes with Cloisite® 30B organically modified clay nanoparticles of montmorillonite to obtain hybrid materials possessing great swelling properties. These materials were studied by XRD, DMA, and water absorption capacity measurements. The synthesis procedure yielded stable and homogeneous hydrogel materials. Addition of clay nanoparticles causes an increase in the absorptivity of water molecules in the polyurethane matrix.

Nonlinear Viscoelasticity in Three Dimensional Filler Reinforced Rubber Composites and Nanocomposites

This chapter describes the influence of three-dimensional nanofillers used in elastomers on the nonlinear viscoelastic properties. In particular, this part focuses and investigates the most important three-dimensional nanoparticles, which are used to produce rubber nanocomposites. The rheological and the dynamic mechanical properties of elastomeric polymers, reinforced with spherical nanoparticles, like POSS, titanium dioxide and nanosilica, were described. These (3D) nanofillers in are used polymeric matrices, to create new, improved rubber nanocomposites, and these affect many of the system’s parameters (mechanical, chemical, physical) in comparison with conventional composites. The distribution of the nanosized fillers and interaction between nanofiller-nanofiller and nanofiller-matrix, in nanocomposite systems, is crucial for understanding their behavior under dynamic-mechanical conditions.

Polymer-Dependent Layer Structures in Montmorillonite Nanocomposites

We have studied structural differences among tetrahedral and octahedral sodium Montmorillonite layer arrangements in naturally occurring and synthetic montmorillonite clay minerals, as well as their poly(ethylene oxide) and poly(e-coprolatone) polymer nanocomposites.