946 research outputs found

    Bioelectrohydrogenesis and inhibition of methanogenic activity in microbial electrolysis cells - A review

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    Microbial electrolysis cells (MECs) are a promising technology for biological hydrogen production. Compared to abiotic water electrolysis, a much lower electrical voltage (~0.2V) is required for hydrogen production in MECs. It is also an attractive waste treatment technology as a variety of biodegradable substances can be used as the process feedstock. Underpinning this technology is a recently discovered bioelectrochemical pathway known as bioelectrohydrogenesis . However, little is known about the mechanism of this pathway, and numerous hurdles are yet to be addressed to maximize hydrogen yield and purity. Here, we review various aspects including reactor configurations, microorganisms, substrates, electrode materials, and inhibitors of methanogenesis in order to improve hydrogen generation in MECs

    Bioelectrohydrogenesis and inhibition of methanogenic activity in microbial electrolysis cells - A review

    Get PDF
    Microbial electrolysis cells (MECs) are a promising technology for biological hydrogen production. Compared to abiotic water electrolysis, a much lower electrical voltage (~0.2V) is required for hydrogen production in MECs. It is also an attractive waste treatment technology as a variety of biodegradable substances can be used as the process feedstock. Underpinning this technology is a recently discovered bioelectrochemical pathway known as bioelectrohydrogenesis . However, little is known about the mechanism of this pathway, and numerous hurdles are yet to be addressed to maximize hydrogen yield and purity. Here, we review various aspects including reactor configurations, microorganisms, substrates, electrode materials, and inhibitors of methanogenesis in order to improve hydrogen generation in MECs

    The Schrodinger equation with Hulthen potential plus ring-shaped potential

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    We present the solutions of the Schro¨\ddot{o}dinger equation with the Hultheˊ\acute{e}n potential plus ring-shape potential for 0\ell\neq 0 states within the framework of an exponential approximation of the centrifugal potential.Solutions to the corresponding angular and radial equations are obtained in terms of special functions using the conventional Nikiforov-Uvarov method. The normalization constant for the Hultheˊ\acute{e}n potential is also computed.Comment: Typed with LateX,12 Pages, Typos correcte

    Understorey plant community and light availability in conifer plantations and natural hardwood forests in Taiwan

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    Questions: What are the effects of replacing mixed species natural forests with Cryptomeria japonica plantations on understorey plant functional and species diversity? What is the role of the understorey light environment in determining understorey diversity and community in the two types of forest? Location: Subtropical northeast Taiwan. Methods: We examined light environments using hemispherical photography, and diversity and composition of understorey plants of a 35‐yr C. japonica plantation and an adjacent natural hardwood forest. Results: Understorey plant species richness was similar in the two forests, but the communities were different; only 18 of the 91 recorded understorey plant species occurred in both forests. Relative abundance of plants among different functional groups differed between the two forests. Relative numbers of shade‐tolerant and shade‐intolerant seedling individuals were also different between the two forest types with only one shade‐intolerant seedling in the plantation compared to 23 seedlings belonging to two species in the natural forest. In the natural forest 11 species of tree seedling were found, while in the plantation only five were found, and the seedling density was only one third of that in the natural forest. Across plots in both forests, understorey plant richness and diversity were negatively correlated with direct sunlight but not indirect sunlight, possibly because direct light plays a more important role in understorey plant growth. Conclusions: We report lower species and functional diversity and higher light availability in a natural hardwood forest than an adjacent 30‐yr C. japonica plantation, possibly due to the increased dominance of shade‐intolerant species associated with higher light availability. To maintain plant diversity, management efforts must be made to prevent localized losses of shade‐adapted understorey plants

    Cratoxylum glaucum and cratoxylum arborescens (Guttiferae)-two potential source of antioxidant agents.

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    Our detailed chemical studies on Cratoxylum glaucum and C. arborescens have revealed the presence of 5-demethoxycadensin G (1), fuscaxanthone C (2), b-mangostin (3), 3-geranyloxy-6-methyl-1,8-dihydroxyanthraquinone (4), vismiaquinone (5), 1,8-dihydroxy-3-methoxy-6-methylanthraquinone (6), stigmasterol (7) and friedelin (8). Structural elucidations of these compounds were achieved by using 1D and 2D NMR spectroscopic experiments. Antioxidant tests conducted on these two plant species gave promising results with both species indicating good antioxidant inhibiting properties. This is a first report on 5-demethoxycadensin G (1) and b-mangostin (3) from Cratoxylum glaucum as well as the antioxidant properties of these two species

    Oseltamivir- and Amantadine-Resistant Influenza Viruses A (H1N1)

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    Surveillance of amantadine and oseltamivir resistance among influenza viruses was begun in Hong Kong in 2006. In 2008, while both A/Brisbane/59/2007-like and A/Hong Kong/2652/2006-like viruses (H1N1) were cocirculating, we detected amantadine and oseltamivir resistance among A/Hong Kong/2652/2006-like viruses (H1N1), caused by genetic reassortment or spontaneous mutation
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