A simple, low-cost, and reproducible method for creating materials with even silver nanoparticles (AgNP) dispersion was established. Chitosan nanofibers with silica phase (CS/silica) were synthesized by an electrospinning technique to obtain highly porous 3D nanofiber scaffolds. Silver nanoparticles in the form of a well-dispersed metallic phase were synthesized in an external preparation step and embedded in the CS/silica nanofibers by deposition for obtaining chitosan nanofibers with silica phase decorated by silver nanoparticles (Ag/CS/silica). The antibacterial activity of investigated materials was tested using Gram-positive and Gram-negative bacteria. The results were compared with the properties of the nanocomposite without silver nanoparticles and a colloidal solution of AgNP. The minimum inhibitory concentration (MIC) of obtained AgNP against Staphylococcus aureus (S. aureus) ATCC25923 and Escherichia coli (E. coli) ATCC25922 was determined. The physicochemical characterization of Ag/CS/silica nanofibers using various analytical techniques, as well as the applicability of these techniques in the characterization of this type of nanocomposite, is presented. The resulting Ag/CS/silica nanocomposites (Ag/CS/silica nanofibers) were characterized by small angle X-ray scattering (SAXS), X-ray diffraction (XRD), and atomic force microscopy (AFM). The morphology of the AgNP in solution, both initial and extracted from composite, the properties of composites, the size, and crystallinity of the nanoparticles, and the characteristics of the chitosan fibers were determined by electron microscopy (SEM and TEM).
Agricultural waste materials (strawberry seeds and pistachio shells) were used for preparation of activated carbons by two various methods. Chemical activation using acetic acid and physical activation with gaseous agents (carbon dioxide and water vapor) were chosen as mild and environmentally friendly methods. The effect of type of raw material, temperature, and activation agent on the porous structure characteristics of the materials was discussed applying various methods of analysis. The best obtained activated carbons were characterized by high values of specific surface area (555–685 m2/g). The Guinier analysis of small-angle X-ray scattering (SAXS) curves showed that a time of activation affects pore size. The samples activated using carbon dioxide were characterized mostly by the spherical morphology of pores. Adsorbents were utilized for removal of the model organic pollutants from the single- and multicomponent systems. The adsorption capacities for the 4-chloro-2-methyphenoxyacetic acid (MCPA) removal were equal to 1.43–1.56 mmol/g; however, for adsorbent from strawberry seeds it was much lower. Slight effect of crystal violet presence on the MCPA adsorption and inversely was noticed as a result of adsorption in different types of pores. For similar herbicides strong competition in capacity and adsorption rate was observed. For analysis of kinetic data various equations were used.
Current reports in the field of nanotechnology indicate that the properties of metal nanoparticles are determined by their features such as size, shape, composition as well as a degree of crystallinity and stability. These, in turn, may depend heavily on their preparation way, treatment during and after synthesis and finally on properties of the supports and matrices. The goal of presented work was to determine the shape, size, and distribution of silver nanoparticles depending on preparation conditions. In particular, the issues of the formation of silver nanostructures (AgNP) with various shapes and sizes depending on functionalized silica surface as well as on the conditions of the impregnation step by noble metal ions (especially pH) were considered. In particular, the comprehensive approach to determine the impact of pH conditions on the properties of metallic nanoparticles is laid down in this work. Three types of fumed silica materials were selected as the supports of silver nanostructures (Aerosil 150, Aerosil 300 and Silochrom C-120). Silica materials were chemically functionalized by thiol and amine groups and treated with diamminesilver(I) ions [Ag(NH 3 ) 2 ] + . As a result of their reduction silicas adorned with silver nanostructures were obtained. In this work, the AgNP in the form of very small nanoparticles, longitudinal and spherical forms and greater structures with nondescript shape were successfully received and characterized through changing the form of functional groups on the solid surface by adjusting the pH conditions. It turns out that protonation and deprotonation of thiol, amino, and hydroxyl groups can be responsible for possible interactions between noble metal ions and functional groups in the form of both attractive and repulsive electrostatic interactions. The Ag nanoparticle/silica nanocomposites were investigated by X-ray diffraction, atomic force microscopy, potentiometric titration and X-ray photoelectron spectroscopy.
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