Different SBA-15 (SBA, Santa Barbara Amorphous) materials were synthetized at different temperature and time during of the hydrothermal treatment. The obtained SBA-15 were characterized by N2 adsorption isotherms, scanning electron microscopy (SEM), X-ray diffraction (DRX), and density in order to establish the influence of these variables on their properties. Mixtures of the obtained catalysts with 3R4F tobacco were prepared and smoked under the ISO 3308 conditions. Temperature of the hydrothermal treatment slightly affects the tars that evolved in the smoking process of the corresponding catalyst tobacco mixtures. Contrarily, the time of the hydrothermal treatment has a marked effect on the reductions of toxic compounds in the smoke. Developed porosity has a positive correlation with the observed tar reduction, whereas the apparent density has a negative correlation with the reduction in toxicity. Moreover, the removal of the supernatant liquors during the hydrothermal treatment does not strongly modify the properties of the materials and may represent an interesting simplification of the process.
SBA-15 has been employed as a tobacco additive with the objective of reducing the toxic and carcinogenic components in tobacco smoke. The effect of the synthesis conditions (temperature, time, and stirring rate) on this application was studied in this paper. The SBA-15 was characterized (RDX, N2 adsorption isotherms, SEM and apparent density), mixed with the 3R4F reference tobacco, and smoked under standard conditions. The composition of the gas and condensed fractions also was analyzed. The morphology of the material plays an important role on this application and is highly influenced by the three variables studied. Long fibers show improved efficiency compared to short fibers. The tar reduction effect was improved when increasing the time of synthesis. Nevertheless, a maximum was observed with temperature (40 °C) and stirring rate (700 rpm). The optimal synthesis conditions obtained were 24 h, 40 °C and 700 rpm, yielding reductions as high as 68% for tar, 67% for nicotine, and 31% for CO. The scaling-up process has only been reported in terms of grams but never in a preindustrial scale (around 4 kg), and thus the results of this analysis show a promising material with properties and behavior similar with respect to the sample synthesized at laboratory scale.
Nowadays, the use of tobacco biomass as an energy source is being valued. Therefore, it is important to know the processes that take place during combustion and pyrolysis, as well as the substances that are formed. In this work, we study the compounds obtained during the decomposition of NNN as a function of temperature under inert and oxidant atmospheres. Moreover, the effect of the addition of SBA-15 and MCM-41 is analyzed. Two different techniques, i.e., TG/FTIR (low heating rates) and EGA Py/GC/MS (high heating rates), are used. At low temperatures NNN is almost unaltered, but it is volatilized and dragged by the carrier gas. When increasing the temperature, decomposition takes place, with pyridines being one of the most abundant compounds observed. The main compound obtained during the pyrolysis are 3- pyridinecarbonitrile, myosmine and nornicotine, which are precursors of NNN. When NNN is mixed with SBA-15, the decomposition of the NNN nitrosamine is favored at low temperatures where the yield in pyridine compounds increases. The catalysts modify the temperature and intensity of the processes, especially under an oxidative atmosphere where the residue is oxidized, showing a third loss of weight. These materials modify the compositions of gases, mainly under an O2 atmosphere (3-pyridinecarbonitrile and myosmine showed the major effect). SBA-15 with fibrous morphology obtains the best reductions at pyrolysis conditions.
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