Study of the kinetic behaviour of biomass and coal during oxyfuel co-combustion

In this study, the thermogravimetric analysis(TGA) method has been used to evaluate the kinetic behavior of biomass, coal and its blends during oxyfuel co-combustion. The thermogravimetric results have been evaluated by the Coats–Redfern method and validated by Criado's method. TG and DTG curves indicate that as the oxygen concentration increases the ignition and burn out temperatures approach a lower temperature region. The combustion characteristic index shows that biomass to coal blends of 28% and 40% respectively can achieve enhanced combustion up to 60% oxygen enrichment. In the devolatilization region, the activation energies for coal and blends reduce while in the char oxidation region, they increase with rise in oxygen concentration. Biomass, however, indicates slightly different combustion characteristic of being degraded in a single step and its activation energies increase with rise in oxygen concentration. It is demonstrated in this work that oxygen enrichment has more positive combustion effect on coal than biomass. At 20% oxygen enrichment, 28% and 40% blends indicate activation energy of 132.8 and 125.5 kJ·mol~(-1) respectively which are lower than coal at 148.1 kJ·mol~(-1) but higher than biomass at 81.5 kJ·mol~(-1) demonstrating synergistic effect of fuel blending. Also, at char combustion step, an increase in activation energy for 28% blend is found to be 0.36 kJ·mol~(-1) per rise in oxygen concentration which is higher than in 40% blend at 0.28 kJ·mol~(-1).     

Activation of trehalase during growth induction by nitrogen sources in the yeast Saccharomyces cerevisiae depends on the free catalytic subunits of camp-dependent protein kinase,but not on functional ras proteins

Addition of a nitrogen-source to glucose-repressed, nitrogen-starved G0 cells of the yeast Saccharomyces cerevisiae in the presence of a fermentable carbon source induces growth and causes within a few minutes a five-fold, protein-synthesis-independent increase in the activity of trehalase. Nitrogen-activated trehalase could be deactivated in vitro by alkaline phosphatase treatment, supporting the idea that the activation is triggered by phosphorylation. Yeast strains containing only one of the three TPK genes (which encode the catalytic subunit of cAMP-dependent protein kinase) showed different degrees of nitrogen-induced trehalase activation. The order of effectiveness was different from that previously reported for glucose-induced activation of trehalase in glucose-derepressed yeast cells. Further reduction of TPK-encoded catalytic subunit activity by partially inactivating point mutations in the remaining TPK gene further diminished nitrogen-induced trehalase activation, while deletion of the BCY1 gene (which encodes the regulatory subunit) in the same strains resulted in an increase in the extent of activation. Deletion of the RAS genes in such a tpk^w1 bcy1 strain had no effect. These results are consistent with mediation of nitrogen-induced trehalase activation by the free catalytic subunits alone. They support our previous conclusion that cAMP does not act as second messenger in this nitrogen-induced activation process and our suggestion that a novel nitrogen-induced signaling pathway integrates with the cAMP pathway at the level of the free catalytic subunits of protein kinase A. Western blot experiments showed that the differences in the extent of trehalase activation were not due to differences in trehalase expression. On the other hand, we cannot completely exclude that protein kinase A influences the nitrogen-induced activation mechanism itself rather than acting directly on trehalase. However, any such alternative explanation requires the existence of an additional, yet unknown, mechanism for activation of trehalase besides the well-established regulation by protein kinase A.     

Morphology of the radial head: a reverse engineering based evaluation using three-dimensional anatomical data of radial bone

The proximal part of the radius has a complex shape and dimension that cannot be precisely determined by standard roentgenogram for real three-dimensional anatomical shape which is important for prosthesis design. This study presents a method by which computer tomography (CT) images are combined with the reverse engineering technique to obtain and analyse the three-dimensional inner and outer geometry of the proximal radius. The three-dimensional models were reconstructed from CT images obtained from 40 radial bones and approximated with two- and three-dimensional fitting algorithms based on reverse engineering methods. The mean total length of the radius was 240.0 mm [standard deviation (SD) = 17.3]. The radial head in this study is more likely to be circular with an average diameter of 20.5 mm (SD = 1.9). The outer diameter of the radial neck averages 14.7 mm (SD = 1.0). The thickness of the radial head averages 12.9 mm (SD = 1.4). The intramedullary canal diameter of the radial neck averages 7.4 mm (SD = 1.4). The depth of the fossa at the articular surface averages 1.5 mm (SD = 0.4).     

Lake-specific responses in sedimentary sulphur, after additions of copper sulphate to lakes in Michigan, USA

Copper sulphate (CuSO₄) is commonly added to lakes and reservoirs to manage nuisance and exotic species. Several studies have previously reported that CuSO₄ is very useful for this purpose, and that the copper is ultimately stored in lake sediments. In contrast, there has been little study on the fate of the sulphate from CuSO₄ additions. The purpose of this study was to elucidate the effects of CuSO₄ additions on sedimentary sulphur. Concentrations, isotopes, and fluxes of total and reduced sulphur in sediment cores from four Michigan lakes were compared, including two reference lakes that have never received CuSO₄ additions, and two treatment lakes that have received CuSO₄ additions by lake managers totalling 1–3 kg sulphate ha^?1 year^?1 since 1940. The results of this study confirm that sediments do not consistently provide records of sulphate loading across lakes. Isotopic evidence indicates this inconsistency is caused, in part, by lakes with well‐mixed sediments, in which sulphate is reduced to sulphide, but then subsequently reoxidized to sulphate and remobilized to the overlying water column. One of the treatment lakes, however, exhibited a clear correlation between CuSO₄ additions and an increased sulphur flux to the sediment. During any given year, however, the sulphate added from CuSO₄ additions amounted to no more than 10% of the sulphate added from wet deposition. Based on this seemingly insignificant quantity of sulphate, ascribing any effect of CuSO₄ additions on sedimentary sulphur is tenuous at best. One possibility is that the addition of CuSO₄ at rates that do not overwhelm the natural sulphur cycle of a lake or reservoir is a reasonable management tool for nuisance and exotic species.     

Synthesis and in vitro and in vivo Antifungal Activity of the Hydroxy Metabolites of Saperconazole

Herein we describe the scalable diastereoselective and enantioselective syntheses of eight enantiomers of hydroxy metabolites of saperconazole. The in vitro antifungal activity of the eight stereoisomers (compounds 1 – 8 ) was compared against a broad panel of Candida spp. (n=93), Aspergillus spp. (n=10), Cryptococcus spp. (n=19), and dermatophytes (n=27). The four 2S isomers 1 – 4 of the new agent were generally slightly more active than the four 2R isomers 5 – 8 . All eight isomers were tested in a model of experimental A. fumigatus infection in guinea pigs by intravenous inoculation of the fungal conidia. Treatment doses were 1.25 mg kg^?1 and 2.5 mg kg^?1 per day. Infection severity was measured in terms of mean survival time (MST) after infection and mean tissue burdens in brain, liver, spleen, and kidney at postmortem examination. Among the eight isomers, the 2S diastereomers 1 – 4 showed a generally higher level of activity than the 2R diastereomers 5 – 8 , revealing compounds 1 and 4 as the most potent overall in eradicating tissue burden and MST. Compared with reference compounds itraconazole and saperconazole, the hydroxy isomers 1 – 8 are less potent inhibitors of the growth of A. fumigatus in vitro and of ergosterol biosynthesis in both A. fumigatus and C. albicans.     

Deposition and cycling of sulfur controls mercury accumulation in Isle Royale fish

Mercury contamination of fish is a global problem. Consumption of contaminated fish is the primary route of methylmercury exposure in humans and is detrimental to health. Newly mandated reductions in anthropogenic mercury emissions aim to reduce atmospheric mercury deposition and thus mercury concentrations in fish. However, factors other than mercury deposition are important for mercury bioaccumulation in fish. In the lakes of Isle Royale, U.S.A., reduced rates of sulfate deposition since the Clean Air Act of 1970 have caused mercury concentrations in fish to decline to levels that are safe for human consumption, even without a discernible decrease in mercury deposition. Therefore, reductions in anthropogenic sulfur emissions may provide a synergistic solution to the mercury problem in sulfate-limited freshwaters.