ABSTRACT
Agro-industrial wastes such as wheat husk (WH) are renewable sources of organic and inorganic substances, including cellulose, lignin, and aluminosilicates, which can be transformed into advanced materials with high added value. The use of geopolymers is a strategy to take advantage of the inorganic substances by obtaining inorganic polymers, which have been used as additives, e.g., for cement and refractory brick products or ceramic precursors. In this research, the WH native to northern Mexico was used as a source to produce wheat husk ash (WHA) following its calcination at 1050 °C. In addition, geopolymers were synthesized from the WHA by varying the concentrations of the alkaline activator (NaOH) from 16 M to 30 M, namely Geo 16M, Geo 20M, Geo 25M, and Geo 30M. At the same time, a commercial microwave radiation process was employed as the curing source. Furthermore, the geopolymers synthesized with 16 M and 30 M of NaOH were studied for their thermal conductivity as a function of temperature, in particular at 25, 35, 60, and 90 °C. The chemical composition of the WHA, determined by ICP, revealed a SiO2 content close to 81%, which is similar to rice husk. The geopolymers were characterized using various techniques to determine their structure, mechanical properties, and thermal conductivity. The findings showed that the synthesized geopolymers with 16M and 30M of NaOH had significant mechanical properties and thermal conductivity, respectively, compared to the other synthesized materials. Finally, the thermal conductivity regarding the temperature revealed that Geo 30M presented significant performance, especially at 60 °C.
ABSTRACT
The structural modification of biopolymers is a current strategy to develop materials with biomedical applications. Silk fibroin is a natural fiber derived from a protein produced by the silkworm (Bombyx mori) with biocompatible characteristics and excellent mechanical properties. This research reports the structural modification of silk fibroin by incorporating polyaniline chain grafts through a one-pot process (esterification reaction/oxidative polymerization). The structural characterization was achieved by 1H-NMR and FT-IR. The morphology was studied by scanning electron microscopy and complemented with thermogravimetric analysis to understand the effect of the thermal stability at each step of the modification. Different fibroin silk (Fib): polyaniline (PAni) mass ratios were evaluated. From this evaluation, it was found that a Fib to PAni ratio of at least 1 to 0.5 is required to produce electroactive polyaniline, as observed by UV-vis and CV. Notably, all the fibroin-g-PAni systems present low cytotoxicity, making them promising systems for developing biocompatible electrochemical sensors.
ABSTRACT
In this work, the chromatic behavior of a poly(10,12-pentacosadiinoic acid)/titanium dioxide (TiO2) nanocomposite was studied. Infrared spectroscopy showed that above 55 °C the peak of the carboxyl groups undergoes a shift from 1690 cm-1 (25-55° C) to 1710 cm-1 (≥60 °C), which is reversible after cooling regardless of whether the sample was in the blue or red phase prior to heating. This indicates that the thermochromic behavior and the hydrogen bond shifting are not completely related, since the signal of the hydrogen bond is influenced by temperature, but is reversible; however, the color change is not. Importantly, TiO2 does favor thermochromic reversibility, unlike that indicated in previous reports. Computational chemistry showed that the effect of temperature on a polydiacetylene oligomer with three repeating units produces torsion, which directly impacts the strength of the hydrogen bonds between the carboxyl groups, coinciding with the experimental work.
ABSTRACT
In this study, carbon black/polystyrene electrically conductive composites were obtained by suspension polymerization technique. The composite was characterized using transmission electron microscopy, which indicated two outstanding features concerning to the carbon black; first, that the carbon particles were adsorbed onto the surface of the polystyrene particles, similarly as in the Pickering emulsion phenomenon and second, that the primary aggregate structure of the carbon black was significantly affected by the dispersion process. On the other hand, the composite resistivity was in the order of 200 Ωcm, which was attributed to the direct contact of primary carbon black particles (percolation) and not to the tunneling effect. The obtained composite was evaluated as the electrically conductive element in SBR matrix.
