ABSTRACT
Regenerated cellulose (RC) produced from waste pineapple leaves was used to develop a colorimetric sensor as a Cu-PAN sheet (RCS). Microcrystalline cellulose derived from dried pineapple leaves was combined with Cu-PAN, dissolved in NaOH and urea, and made into an RC sheet using Na2SO4 as a coagulant. The RCS was used as an H2S indicator at various H2S concentrations (0-50 ppm) and temperatures (5-25 °C). The RCS color changed from purple to New York pink when exposed to H2S. A colorimeter method was used to develop prediction curves with values of R2 > 0.95 for H2S concentrations at 5-25 °C. The physicochemical properties of fresh and spent RCS were characterized using various techniques (Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy/energy-dispersive X-ray spectroscopy, and thermogravimetric analysis). In addition, when stored at 5 and 25 °C for 90 days, the RCS had outstanding stability. The developed RCS could be applied to food packaging as an intelligent indicator of meat spoilage.
ABSTRACT
The oxidative coupling of methane (OCM) converts CH4 to value-added chemicals (C2+), such as olefins and paraffin. For a series of MnTiO3-Na2WO4 (MnTiO3-NW) and MnOx-TiO2-Na2WO4 (Mn-Ti-NW), the effect of loading of MnTiO3 or MnOx-TiO2, respectively, on two different supports (sol-gel SiO2 (SG) and commercial fumed SiO2 (CS)) was examined. The catalyst with the highest C2+ yield (21.6% with 60.8% C2+ selectivity and 35.6% CH4 conversion) was 10 wt% MnTiO3-NW/SG with an olefins/paraffin ratio of 2.2. The catalyst surfaces with low oxygen-binding energies were associated with high CH4 conversion. Stability tests conducted for over 24 h revealed that SG-supported catalysts were more durable than those on CS because the active phase (especially Na2WO4) was more stable in SG than in CS. With the use of SG, the activity of MnTiO3-NW was not substantially different from that of Mn-Ti-NW, especially at high metal loading.
ABSTRACT
Oxidative coupling of methane (OCM) is a reaction to directly convert methane into high value-added hydrocarbons (C2+) such as ethylene and ethane using molecular oxygen and a catalyst. This work investigated lanthanum oxide catalysts for OCM, which were promoted with alkaline-earth metal oxides (Mg, Ca, Sr, and Ba) and prepared by the solution-mixing method. The synthesized catalysts were characterized using X-ray powder diffraction, CO2-programmed desorption, and X-ray photoelectron spectroscopy. The comparative performance of each promoter showed that promising lanthanum-loaded alkaline-earth metal oxide catalysts were La-Sr and La-Ba. In contrast, the combination of La with Ca or Mg did not lead to a clear improvement of C2+ yield. The most promising LaSr50 catalyst exhibited the highest C2+ yield of 17.2%, with a 56.0% C2+ selectivity and a 30.9% CH4 conversion. Catalyst characterization indicated that their activity was strongly associated with moderate basic sites and surface-adsorbed oxygen species of O2 -. Moreover, the catalyst was stable over 25 h at a reactor temperature of 700 °C.
ABSTRACT
Na2WO4-TiO2-MnO x /SiO2 (SM) catalysts with alkali (Li, K, Rb, Cs) or alkali earth (Mg, Ca, Sr, Ba) oxide additives, which were prepared using incipient wetness impregnation, were investigated for oxidative coupling of methane (OCM) to value-added hydrocarbons (C2+). A screening test that was performed on the catalysts revealed that SM with Sr (SM-Sr) had the highest yield of C2+. X-ray photoelectron spectroscopy analyses indicated that the catalysts with a relatively low binding energy of W 4f7/2 facilitated a high CH4 conversion. A combination of crystalline MnTiO3, Mn2O3, α-cristobalite, Na2WO4, and TiO2 phases was identified as an essential component for a remarkable improvement in the activity of the catalysts in the OCM reaction. In attempts to optimize the C2+ yield, 0.25 wt % Sr onto SM-Sr achieved the highest C2+ yield at 22.9% with a 62.5% C2+ selectivity and a 36.6% CH4 conversion. A stability test of the optimal catalyst showed that after 24 h of testing, its activity decreased by 18.7%.
ABSTRACT
Direct gas phase epoxidation of propylene to propylene oxide (PO) using O2 is a challenging problem in catalysis research. Silica-supported ruthenium-copper-based catalysts have been recently reported to be promising for propylene epoxidation. In this work, mesoporous silica supports modified with RuO2, CuO, and TeO2 with and without TiO2 were investigated for propylene epoxidation to PO. The prepared catalysts were divided into two groups. The first group consisted of mesoporous silica supports modified with RuO2, CuO, and TeO2, and the second group consisted of the same components as the first group but adding TiO2. The prepared supports and catalysts were characterized using BET surface area analysis and other advanced instrument techniques. It was found that the catalyst made with RuO2 and TeO2 impregnated onto porous silica modified with CuO and TiO2 (denoted as RuTe/CuTiSi) exhibited an excellent PO formation of 344 gPO h-1 kg-1cat, which was superior to that of the other prepared catalysts. Moreover, the addition of TiO2 into the catalyst greatly improved the PO formation rate and the arrangement of active components in the catalyst and strongly influenced catalytic performance.
