The elemental uptake and distribution, in various parts of the admired herbal plant, Hypoxis hemerocallidea, the 'African potato' and its ability to accumulate elements in response to the growth soil quality are investigated. The total and exchangeable concentrations of twelve elements in the growth soils and their distribution in the roots, potato bulb and leaves of the plants grown under four different settings were compared. The typical concentrations of the twelve selected elements, in the bulb and leaves of the plant grown in a nursery pot (site 2) were (in microg g(-1)dry weight) Ca (8430 and 27075), Mg (2113 and 1566), Fe (66 and 150), Al (10 and 368), Zn (105 and 6.1), Mn (42 and 51), Cu (7.2 and 20.8), Ba (0.23 and 4.44), Co (0.20 and 0.42), As (2.05 and 24.56), Hg (0.92 and 1.82) and Cr (0.13 and 0.33). Except for Ca, Mg, Zn and Mn, the exchangeable cation concentrations in all the growth soils were low. Ca, Mg, Mn, Zn and As had bioaccumulation factors >1. Fe, Al and Co concentrations were high in the roots with little in the rest of the plant. High concentration of arsenic (approximately 13 microg g(-1) dry weight) with bioaccumulation factors of 7 and 20 were observed in the roots and leaves of the plant respectively (site 2), but the concentration of mercury in bulb was very low (0.92 microg g(-1) dry weight).
Non-coking stable alkaline earth metal (M = Mg, Sr, and Ba) modified Ga-NaY catalysts were prepared by ionic-exchange and tested in oxidative dehydrogenation (ODH) of n-octane using air as the source of oxygen. The role of the alkaline earth metals in NaY was to poison the acid sites while enhancing the basic sites responsible for ODH. The exception was the calcium modified NaY, which was more acidic than the parent NaY, coking and unstable under the ODH conditions used in this study. The role of gallium was to enhance the dehydrogenation pathway and improve the stability of NaY. The sequence of increasing selectivity to octenes followed the order: CaGa-NaY < Ga-NaY< MgGa-NaY < SrGa-NaY < BaGa-NaY. The highest octene selectivity obtained was 37% at iso-conversion of 6 ± 1% when BaGa-NaY was used at a temperature of 450 °C. The activity of the catalysts was directly proportional to the reducibility of the catalysts, which is in agreement with expectations.
The effect of the thermal treatment of some zeolitic materials was studied on oxidative dehydrogenation (ODH) of n-octane. Gallium containing faujasite catalysts were synthesized using isomorphic substitution, specifically, a galosilicalite (Ga-BaY(Sil)) and an aluminosilicalite substituted with gallium (Ga-BaY(IS)), with constant Si/M ratio. The catalysts were thermally treated at different temperatures (250, 550, and 750 °C) before catalytic testing. The quantification of total and strength of acid sites by FT-IR (O-H region), pyridine-IR, and NH3-temperature-programmed desorption (TPD) confirmed a decrease in the number of Brønsted acid sites and an increase in the number of Lewis acid sites upon increasing the calcination temperature. Isothermal n-octane conversion also decreased with the catalysts’ calcination temperature, whereas octene selectivity showed the opposite trend (also at iso-conversion). The COx selectivity showed a decrease over the catalysts calcined from 250 to 550 °C and then an increase over the 750 °C calcined catalysts, which was due to the strong adsorption of products to strong Lewis acid sites on the catalysts leading to the deep oxidation of the products. Only olefinic-cracked products were observed over the 750 °C calcined catalysts. This suggested that the thermal treatment increases Lewis acid sites, which activate n-octane using a bimolecular mechanism, instead of a monomolecular mechanism.
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