Crown Ether-Modified Clays and their Polystyrene Nanocomposites

Crown ether-modified clays were obtained by the combination of sodium and potassium clays with crown ethers and cryptands. Polystyrene nanocomposites were prepared by bulk polymerization in the presence of these clays. The structures of nanocomposites were characterized by X-ray diffraction and transmission electron microscopy. Their thermal stability and flame retardancy were measured by thermogravimetric analysis and cone calorimetry, respectively. Nanocomposites can be formed only from the potassium clays; apparently the sodium clays are not sufficiently organophilic to enable nanocomposite formation. The onset temperature of the degradation is higher for the nanocomposites compared to virgin polystyrene, and the peak heat release rate is decreased by 25% to 30%

Novel Polymerically-Modified Clays Permit the Preparation of Intercalated and Exfoliated Nanocomposites of Styrene and its Copolymers by Melt Blending

Two new organically-modified clays have been made and used to produce nanocomposites of polystyrene, high impact polystyrene and acrylonitrile–butadiene–styrene terploymer. At a minimum, intercalated nanocomposites of all of these polymers have been produced by melt blending in a Brabender mixer and, in some cases, exfoliated nanocomposites have been obtained. The systems have all been characterized by X-ray diffraction, transmission electron microscopy, thermogravimetric analysis, cone calorimetry and the measurement of mechanical properties. These novel new clays open new opportunities for melt blending of polymers with clays to obtain nanocomposites with important properties

Study on the thermal stability of Polystyryl surfactants and its modified clay nanocomposites

Five oligomeric styrene surfactants, N,N,N-trimethylpolystyrylammonium, N,N-dimethyl-N-benzylpolystyrylammonium, N,N-dimethyl-N-hexadecylpolystyrylammonium, 1,2-dimethyl-3-polystyrylimidazolium, and triphenylpolystyrylphosphonium chlorides were synthesized and used to prepare organically modified clays. Both styrene and methyl methacrylate nanocomposites were prepared by melt blending and the type of nanocomposite was evaluated by X-ray diffraction and transmission electron microscopy. The thermal stability of the organically modified clays and the nanocomposites were studied by thermogravimetric analysis; these systems do give clays which have good thermal stability and may be useful for melt blending with polymers that must be processed at higher temperatures

Correlation between chemical and mineralogical characteristics and permeability of phyllite clays using multivariate statistical analysis

Phyllite clays are applied as a layer on a surface to be waterproofed and subsequently compacted. For this purpose, phyllite clays deposits can be grouped by their chemical and mineralogical characteristics, and these characteristics can be connected with their properties, mainly permeability, in order to select those deposits with the lowest permeability values. Several deposits of phyllite clays in the provinces of Almería and Granada (SE Spain) have been studied. The results of applying a multivariate statistical analysis (MVA) to the chemical data analysed from 52 samples determined by XRF, mineralogical analysis by XRD and permeability are reported. Permeability, a characteristic physical property of phyllite clays, was calculated using the results for experimental nitrogen gas adsorption and nitrogen adsorption-desorption permeability dependence. According to the results, permeability values differentiated two groups, i.e. group 1 and group 2, with two subgroups in the latter. The influence of chemical as well as mineralogical characteristics on the permeability values of this set of phyllite clays was demonstrated using a multiple linear regression model. Two regression equations were deduced to describe the relationship between adsorption and desorption permeability values, which support this correlation. This was an indication of the statistical significance of each chemical and mineralogical variable, as it was added to the model. The statistical tests of the residuals suggested that there was no serious autocorrelation in the residuals.Peer ReviewedPostprint (author's final draft

Polystyrene Nanocomposites based on Carbazole-Containing Surfactants

New organically-modified clays containing a carbazole unit were prepared and the number of long alkyl chains on the surfactant was varied. The clay was used to prepare polystyrene nanocomposites by both bulk polymerization and melt blending. The dispersion of these clays in the polymer matrix was evaluated using X-ray diffraction (XRD) and transmission electron microscopy (TEM). The thermal stability of the clays and the nanocomposites were analyzed by thermogravimetric analysis (TGA) while the fire properties were evaluated by cone calorimetry. If more than two alkyl chains were present, the gallery spacing is apparently overcrowded, leading to poor dispersion. Bulk polymerization gave nanocomposites with better dispersion and reduced flammability when compared to the melt blending process

Poly(Methyl Methacrylate), Polypropylene and Polyethylene Nanocomposite Formation by Melt Blending using Novel Polymerically-Modified Clays

Two new organically-modified clays that contain an oligomeric styrene or methacrylate have been prepared and used to produce nanocomposites of poly(methyl methacryate), polypropylene and polyethylene. Intercalated nanocomposites and, in some cases, exfoliated or mixed intercalated/exfoliated nanocomposites of all of these polymers have been produced by melt blending in a Brabender mixer. The use of the styrene-containing clay permits the direct blending of the clay with polypropylene, without the usual need for maleation, to produce the nanocomposites. The systems have all been characterized by X-ray diffraction, transmission electron microscopy, thermogravimetric analysis, cone calorimetry and the measurement of mechanical properties. These novel new clays open new opportunities for melt blending of polymers with clays to obtain nanocomposites with important propertie

Modelling the thermo-mechanical volume change behaviour of compacted expansive clays

Compacted expansive clays are often considered as a possible buffer material in high-level deep radioactive waste disposals. After the installation of waste canisters, the engineered clay barriers are subjected to thermo-hydro-mechanical actions in the form of water infiltration from the geological barrier, heat dissipation from the radioactive waste canisters, and stresses generated by clay swelling under almost confined conditions. The aim of the present work is to develop a constitutive model that is able to describe the behaviour of compacted expansive clays under these coupled thermo-hydro-mechanical actions. The proposed model is based on two existing models: one for the hydro-mechanical behaviour of compacted expansive clays and another for the thermo-mechanical behaviour of saturated clays. The elaborated model has been validated using the thermo-hydro-mechanical test results on the compacted MX80 bentonite. Comparison between the model prediction and the experimental data show that this model is able to reproduce the main features of volume changes: heating at constant suction and pressure induces either expansion or contraction; the mean yield stress changes with variations of suction or temperature

Mixed-metal pillared layer clays and their pillaring precursors

Mixed-metal pillared layer clays (Fe,Al-PILCs and Cr,Al-PILCs) of various compositions and the pillaring precursors have been prepared and characterised with a combination of chemical and instrumental methods. Chemical analysis data, IR, (57)Mossbauer and Al-27 NMR spectroscopic measurements on the precipitated pillaring precursors and comparison of redox behaviour [temperature-programmed reduction (TPR) results and Fe-57 Mossbauer measurements on the heat-treated and the reduced samples] of the ion-exchanged and Al-pillared and mixed-metal pillared clays revealed that isomorphous substitution of Al for Fe or Cr did not occur in either the tetrahedral or the octahedral positions. Heat treatment, however, resulted in mixed-metal pillared clays which were active in both acid- catalysed and redox transformations