ABSTRACT
Regularly arranged chains strongly affect the electrical conductivity of conductive polymers (e.g., polypyrrole). One of the easiest ways to achieve this arrangement is the insertion of the polymer into the interlayer space of solid inorganic layered matrix, i.e., the intercalation process. Among various kinds of layered materials, the clay minerals, especially the smectite group, deserves particular attention. Negative charge of smectite layers helps the intercalation process resulting in higher conductivity of the polymer in clay/polymer intercalates. Characterization of stevensite-rich Moroccan clay and intercalation of electrically conductive polypyrrole into stevensite-rich Moroccan clay in order to obtain material with higher conductivity in comparison with pure polypyrrole were two main purposes of this work. Two forms of stevensite/polypyrrole nanocomposites were studied: powder and pressed tablets. X-ray fluorescence spectroscopy, X-ray diffraction analysis, atomic force microscopy, thermogravimetry, infrared spectroscopy, Raman microspectroscopy, and scanning electron microscopy in conjunction with energy dispersive X-ray spectroscopy were used to study the composition and structure of the nanocomposites. Measurement of electrical conductivity of polypyrrole in stevensite/polypyrrole nanocomposites revealed enhanced conductivity for all samples and also anisotropy in the conductivity of the samples pressed in the tablets.
ABSTRACT
Photoactive and non-hazardous kaolinite/ZnO nanocomposite with 50 wt.% of ZnO nanoparticles was prepared using simple and cheap hydrothermal method. The resulting solid phase was separated by decantation, and dried at 105 °C. Calcination of the nanocomposites at 600 °C led to the kaolinite-metakaolinite phase transformation, to further growth of ZnO crystallites, and to significant increase in photodegradation activity. Whereas, for the several applications, e.g., in brake industry, the larger amount of composites is needed, thus, the evaluation of the reproducibility of preparation process is one of the crucial parameter. Prepared nanocomposites were deeply characterized by using X-ray fluorescence spectroscopy, X-ray powder diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, and Rietveld quantitative phase analysis. Photodegradation activity was evaluated by the discoloration of Acid Orange 7 aqueous solution under UV irradiation. All used analytical techniques and methods confirm the reproducibility of the preparation process and as well that ZnO nanoparticles are anchored tightly on the clay surface which prevents the release to the environment.
ABSTRACT
Wear debris from automotive brake systems represents a major source of non-exhaust emissions from road traffic and its production increases with number of cars worldwide. However, impact of brake wear debris on the environment and organisms is still not clear. One of the most possible ways by which these particles may affect living organisms is oxidative stress. Production of reactive oxidative species may cause damage of basic cell components, lipids, proteins, etc. Aim of this study is to perform characterization of airborne and nonairborne fractions of brake wear debris generated during standard dynamometer tests and evaluation of its potential to induce oxidative stress via lipid peroxidation and carbonylation of proteins in non-cellular system. Elemental and phase composition were determined by scanning electron microscopy, Raman microspectroscopy, and X-ray powder diffraction analysis. Carbon in amorphous form and graphite, copper, and iron in form of oxides were identified as major components in both studied fractions. Characteristic size of studied wear particles was evaluated by dynamic light scattering. Both airborne and nonairborne samples showed ability to induce oxidative stress which results from determination of carbonylated proteins.
