Velocity fluctuation near the detonation limits

In this study, the velocity fluctuation near the detonation limits is investigated experimentally. Five explosive mixtures in five different diameter tubes were used and the choice of the mixtures included those considered as “stable” with regular cellular pattern and “unstable” with highly irregular cellular pattern. Photodiodes spaced at regular intervals along the tube were used to measure the detonation velocity. Piezoelectric transducers were also used to record the pressure profiles. Smoked foils were used to register the cellular detonation structure. Away from the limits, the detonation is found to propagate at a steady velocity throughout the length of the tube and the fluctuations of the local velocity are generally small. For stable mixtures with high argon dilution, the onset of the detonation limits is indicated by an abrupt drop in the detonation velocity to about 0.4V_CJ after a short distance of travel. The detonation may continue to propagate at this low velocity before decaying eventually to a deflagration wave. For deflagrations the optical detector sometimes failed to register a signal due to low luminosity of the front. In unstable mixtures, galloping detonations are observed only in small diameter tubes (e.g., D = 12.7, 3.2 and 1.5 mm). A large number of fairly reproducible cycles of galloping detonations can be observed in very small diameter tubes. In large diameter tubes (e.g., D = 31.7 and 50.8 mm), no galloping detonations are observed in all stable and unstable mixtures. For stable mixtures, no galloping detonations are observed even in small diameter tubes of D = 3.2 and 1.5 mm. Smoked foils records show that the cellular detonation structure changes from multi-headed to single-headed spin as the limit is approached. In a galloping detonation cycle, a decay from multi-headed to single-headed detonation is observed. However, the cellular structure vanishes for further decay of the galloping detonation to the low velocity phase of the galloping cycle. Although galloping detonations could be considered to define the boundary for detonation limits, this definition lacks generality since galloping detonations are not always observed in all mixtures and in all tube diameters. Thus the onset of single-headed spin is perhaps the most appropriate criterion of the detonation limits in tubes.     

Comparison performances of membrane bioreactor and conventional activated sludge prcesses on sludge reduction induced by Oligochaete

Pilot-scale experiments were carried out to compare sludge reduction induced by Oligochaete in a submerged membrane bioreactor (MBR) and a conventional activated sludge (CAS) reactor for 345 d. Worm growth in the CAS reactor was much better than in the MBR. The average worm density of the aeration tank in the CAS reactor was 71 total worms/mg of volatile suspended solids (VSS), much higher than that in the MBR (10 total worms/mg of VSS). Worms did not naturally produce in the MBR, and the dominant worm type in the MBR depended on sludge inoculation from the CAS reactor. Only two types of worms were found in the MBR, Aeolosoma hemprichicii and Nais elinguis. Worm presence and disappearance in the MBR alternated. Worms in the CAS reactor occurred nearly throughout the operating period and were continuously maintained at over 30 total worms/mg of VSS in the aeration tank for 172 d. Three types of worm were found in the CAS reactor, A. hemprichicii, Pristina aequiseta, and N. elinguis, but P. aequiseta was present only occasionally. The alternating dominance of worm types in both reactors changed between Aeolosoma and Nais, and the time of Aeolosoma dominance was longer than that of Nais dominance. Worm growth in the MBR contributed to neither sludge reduction nor improvement of sludge settling characteristics because of low density. But worm presence and bloom in the CAS reactor greatly decreased sludge yield and improved sludge settling characteristics at high density. Both the average sludge yield (0.17 kg of suspended solids (SS)/kg of chemical oxygen demand removed (CODremoved)) and sludge volume index (60 mL/g) in the CAS reactor were much lower than those in the MBR (0.40 kg of SS/kg of CODremoved and 133 mL/g). Nais had more potential for sludge reduction than Aeolosoma. Worm growth had little impact on effluent quality in the MBR but affected effluent quality very much in the CAS reactor.     

Highly unsaturated fatty acid synthesis in marine fish: Cloning, functional characterization, and nutritional regulation of fatty acyl Δ6 desaturase of Atlantic cod (Gadus morhua L.)

This study reports the cloning, functional characterization, tissue expression, and nutritional regulation of a Δ6 fatty acyl desaturase of Atlantic cod (Gadus morhua). PCR primers were designed based on the sequences of conserved motifs in available fish desaturases and used to isolate a cDNA fragment from cod liver, with full-length cDNA obtained by rapid amplification of cDNA ends. The cDNA for the putative desaturase was shown to comprise 1980 bp, including a 261-bp 5′-UTR, a 375-bp 3′-UTR, and an ORF of 1344 bp that specified a protein of 447 amino acids. The protein sequence included three histidine boxes, two transmembrane regions, and an N-terminal cytochrome b₅ domain containing the heme-binding motif HPGG, all characteristic of microsomal fatty acyl desaturases. The cDNA displayed Δ6 desaturase activity in a yeast expression system. Quantitative real-time PCR assay of gene expression in cod showed that the Δ6 desaturase gene was expressed highly in brain, to a slightly lesser extent in liver, kidney, intestine, red muscle, and gill, and at much lower levels in white muscle, spleen, and heart. The expression of the Δ6 desaturase gene did not appear to be under significant nutritional regulation, with levels in liver and intestine being barely altered in fish fed a vegetable oil blend, in comparison with levels in fish fed fish oil. This was reflected in enzyme activity, as hepatocytes or enterocytes showed very little highly unsaturated FA biosynthesis activity irrespective of diet. Further studies are required to determine why the Δ6 desaturase appears to be barely functional in cod under the conditions tested.     

Position-controlled interconnected InAs nanowire networks

We demonstrate here a method for controlled production of complex self-assembled three-dimensional networks of InAs nanowires on a substrate, based on sequentially seeded epitaxial nanowire structures, or "nanotrees". A position-controlled array of trunk nanowires is first produced using lithographically defined Au particles as seeds. With these wires positioned along the proper crystallographic directions with respect to each other, nanotree branches grow toward neighboring trunks, connecting them together. Finally, we investigate the crystal structure of the interconnected nanotrees, demonstrating that branch growth after the contact with the second trunk has an epitaxial relationship to that trunk.     

Ultrafast gas chromatography on single-wall carbon nanotube stationary phases in microfabricated channels

The key to rapid temperature programmed separations with gas chromatography are a fast, low-volume injection and a short microbore separation column with fast resistive heating. One of the major problems with the reduction of column dimensions for micro gas chromatography is the availability of a stationary phase that provides good separation performance. In this report, we present the first integration of single-wall carbon nanotubes (SWNTs) as a stationary phase into 100 mum x 100 mum square and 50-cm-long microfabricated channels. The small size of this column with integrated resistive heater and the robustness of the SWNT phase allow for fast temperature programming of up to 60 degrees C/s. A combination of the fast temperature programming and the narrow peak width of small-volume injections that can be obtained from a high-speed, dual-valve injection system allows for rapid separations of gas mixtures. We demonstrate highly reproducible separations of four-compound test mixtures on these columns in less than 1 s using fast temperature programming.     

Occurrence of sapogenins in leaves and seeds of quinoa (Chenopodium quinoa Willd)

Seeds of the Andean seed crop quinoa usually contain saponins in the seed coat. Saponins give a bitter taste sensation and are a serious antinutritional factor. Therefore selection of sweet genotypes with a very low saponin content in the seeds is a main breeding goal. However, selection for sweet genotypes is retarded by cross‐pollination. Early identification of sweet and bitter quinoa genotypes before anthesis would speed up breeding considerably. The ability to distinguish sweet and bitter genotypes was investigated in a glasshouse and in a field experiment. In the glasshouse experiment the content of sapogenins was determined in leaves of sweet and bitter quinoa genotypes at successive stages of plant development and finally in the seeds. Detectable amounts of sapogenins were found earliest 82 days after sowing in leaves of both sweet and bitter quinoa genotypes. The total sapogenin content in leaves of sweet and bitter genotypes increased during plant development but remained lower than the content found in the seeds. The sapogenin content in seeds of sweet genotypes varied from 0.2 to 0.4 g kg⁻¹ dry matter and in seeds of bitter genotypes from 4.7 to 11.3 g kg⁻¹ dry matter. The difference in sapogenin content between leaves and seeds was much higher in bitter genotypes than in sweet genotypes. Hederagenin was the major sapogenin found in leaves, and oleanolic acid in seeds. In the field experiment it was found that the content of sapogenins in the leaves of F2 plants of crosses between both quinoa types did not differ between sweet and bitter genotypes. The obtained results demonstrated that sweet genotypes could not be selected before anthesis on the basis of the sapogenin content in the leaves. © 2000 Society of Chemical Industry     

Computationally Supported Inversion of Ketoreductase Stereoselectivity

Whereas directed evolution and rational design by structural inspection are established tools for enzyme redesign, computational methods are less mature but have the potential to predict small sets of mutants with desired properties without laboratory screening of large libraries. We have explored the use of computational enzyme redesign to change the enantioselectivity of a highly thermostable alcohol dehydrogenase from Thermus thermophilus in the asymmetric reduction of ketones. The enzyme reduces acetophenone to (S)-1-phenylethanol. To invert the enantioselectivity, we used an adapted CASCO workflow which included Rosetta for enzyme design and molecular dynamics simulations for ranking. To correct for unrealistic binding modes, we used Boltzmann weighing of binding energies computed by a linear interaction energy approach. This computationally cheap method predicted four variants with inverted enantioselectivity, each with 6–8 mutations around the substrate-binding site, causing only modest reduction (2- to 7-fold) of k_cat/K_M values. Laboratory testing showed that three variants indeed had inverted enantioselectivity, producing (R)-alcohols with up to 99 % enantiomeric excess. The broad substrate range allowed reduction of acetophenone derivatives with full conversion to highly enantioenriched alcohols. The results demonstrate the use of computational methods to control ketoreductase stereoselectivity in asymmetric transformations with minimal experimental screening.