Linear codes for the sum mod-2 multiple-access channel withrestricted access

Transmission of information through a multiple-access-modulo-2 adder channel is addressed for the situation that out of a fixed family of N potential users at most some m, m相似文献   

Magnetron sputtered tungsten oxide films activated by dip-coated platinum for ppm-level hydrogen detection

Platinum-activated tungsten oxide (Pt-WO₃) films are prepared for hydrogen (H₂) sensing applications. In this study, WO₃ films were fabricated by reactive magnetron sputtering and Pt clusters were deposited on them by dip-coating. The microstructure, chemical composition and phase structure of Pt-WO₃ films were characterized by scanning electron microscopy, X-ray photoelectron spectroscopy and X-ray diffraction, respectively. It was observed that a reconditioning period is required after a rest period of the sensor for obtaining a stable signal. A thermal treatment at 450 °C for 24 h is proposed to solve this problem.     

Evidence for multiple open and inactivated states of the hKv1.5 delayed rectifier

We previously found in human blood a fraction of low-density lipoprotein (LDL) that is characterized by a reduced content of sialic acid. Desialylated LDL also has a low neutral carbohydrate level, decreased content of major lipids, small size, high density, increased electronegative charge and altered tertiary apolipoprotein B structure. Unlike native LDL, this fraction of desialylated (multiple-modified) LDL induces the accumulation of lipids in smooth muscle cells cultured from unaffected human aortic intima, i.e. it exhibits atherogenic properties. In this study, we attempted to elucidate the mechanism of desialylation and other changes in the multiple-modified LDL by investigating the possibility of LDL modification by different cells and the blood plasma. A 24-h incubation at 37 degrees C of lipoprotein with intact endotheliocytes, hepatocytes, macrophages and smooth muscle cells or cell homogenates did not cause alterations either in the physical properties or in the chemical composition of native LDL. On the other hand, a significant fall in the lipoprotein sialic acid level was observed already after a 1-h incubation of native LDL with an autologous plasma-derived serum. While LDL sialic acid level continuously decreased, LDL became capable of inducing the accumulation of total cholesterol in the smooth muscle cells cultured from unaffected human aortic intima after 3 h of incubation. Starting from the sixth hour of LDL incubation with serum, a steady decrease in the lipoprotein lipid content was observed as well as the related reduction of LDL size. Following 36 h of incubation, an increase in the negative charge of lipoprotein particles was also seen. Prolonged incubation of LDL with plasma-derived serum (48 and 72 h) leads to the loss of alpha-tocopherol by the LDL as well as to an increase in LDL susceptibility to copper oxidation and to accumulation of cholesterol covalently bound to apolipoprotein B, a marker of lipoperoxidation. Degradation of apolipoprotein B starts within the same period of time. Hence, desialylation of LDL particles represents one of the first or the primary act of modification which is, apparently, a sufficient prerequisite for the development of atherogenic properties. Subsequent modifications just enhance the atherogenic potential of LDL. The loss of sialic acid by LDL occurred at neutral pH and was not inhibited by the sialidase inhibitor 2,3-dehydro-2-deoxy-N-acetylneuraminic acid. The [3H]sialic acid removed from LDL was not found in free form, but in the plasma fraction precipitated by trichloroacetic acid. These data along with the fact that cytidine-5'-triphosphate inhibited LDL desialylation suggest that enzymes close to sialyltransferases play a role in this process. Thus, this study demonstrated that the LDL modification processes imparting atherogenic properties to this lipoprotein can take place in human blood plasma. Multiple modification of LDL is a cascade of successive changes in the lipoprotein particle: desialylation, loss of lipids, reduction in particle size, increase of its electronegative charge and peroxidation of lipids.     

Composition–constitution–morphology relationship of Al2O3 thin films deposited by plasma assisted chemical vapor deposition

We have studied the correlation between the chemical composition, constitution and morphology of Al₂O₃ using experimental and theoretical means. Combining scanning electron microscopy, transmission electron microscopy, electron dispersive X-ray analysis and ab initio calculations, we have investigated the formation of pores. Desorption measurements show chlorine release from γ- and α-alumina films. Based on ab initio calculations, we have established that Cl can be incorporated in both γ- and α-alumina. Furthermore, two Cl atoms are likely to agglomerate since the total energy is reduced, compared to an unagglomerated configuration. We propose that Cl agglomeration is the first step towards Cl₂ formation and subsequent precipitation and bubble formation. It can be learned that the Cl incorporation has to be minimized during growth of dense alumina coatings.     

Towards the understanding of plasma polymer film behaviour in ethanol: A multi-technique investigation

Plasma polymer films (PPFs) of allylamine are prepared varying the mean power injected in the plasma (P_mean). The PPF behaviour in ethanol is studied through the analysis of the PPF physico-chemistry and the composition of the resulting ethanol solutions. By Visible light Spectroscopic Ellipsometry (VISSE), it is observed that the well-known decrease of the PPF thickness (Δd) upon immersion decreases as a function of P_mean. This behaviour is attributed to an increase of the PPF cross-linking density (χ). By means of time-of-flight secondary ion mass spectrometry (ToF-SIMS) and further statistical processing of the data by principal component analysis (PCA), we propose a method to discriminate the samples according to χ. A significant increase in the PPF oxygen content is also observed after immersion which is ascribed to reaction between ethanol molecules and trapped radicals of the PPF network. On the other hand, taking into account the specificities of the gas chromatography–mass spectrometry (GC–MS) method, the resulting ethanol solutions are demonstrated to be free of chemical species containing a number of carbon atoms ranging from 7 to 40. However, Δd (accounting for PPF restructuring) might come with the dissolution of PPF materials having less than 7 carbon atoms.     

A review of triticale uses and the effect of growth environment on grain quality

Triticale (× Triticosecale sp. Wittmack ex A. Camus 1927) is an anthropogenic cereal designed to incorporate the functionality and high yield of wheat (Triticum spp. Linnaeus 1753) and durability of rye (Secale cereale Linnaeus 1753). The potential of triticale has remained largely unrealised, and in the 135 years since A. Stephen Wilson first crossed wheat and rye, triticale has mostly been used as animal feed. Growing demand for food resources has led to an increased interest in triticale development. Efforts to breed cultivars appropriate for baking have met with difficulty, although relatively new approaches to triticale end-use propose greater applicability for human consumption. Further, environmental awareness has generated interest in the use of triticale within biofuel production. We review environmental and genetic effects on triticale yield with a view towards increased demand on a hardy and useful cereal crop. We find triticale could satisfy many of the hopes originally placed upon it, and may be useful in foodstuffs and fuel, but only when growth environment is carefully considered.     

Molecular determinants of stereoselective bupivacaine block of hKv1.5 channels

Enantiomers of local anesthetics are useful probes of ion channel structure that can reveal three-dimensional relations for drug binding in the channel pore and may have important clinical consequences. Bupivacaine block of open hKv1.5 channels is stereoselective, with the R(+)-enantiomer being 7-fold more potent than the S(-)-enantiomer (Kd = 4.1 mumol/L versus 27.3 mumol/L). Using whole-cell voltage clamp of hKv1.5 channels and site-directed mutants stably expressed in Ltk- cells, we have identified a set of amino acids that determine the stereoselectivity of bupivacaine block. Replacement of threonine 505 by hydrophobic amino acids (isoleucine, valine, or alanine) abolished stereoselective block, whereas a serine substitution preserved it [Kd = 60 mumol/L and 7.4 mumol/L for S(-)- and R(+)-bupivacaine, respectively]. A similar substitution at the internal tetraethylammonium binding site (T477S) reduced the affinity for both enantiomers similarly, thus preserving the stereoselectivity [Kd = 45.5 mumol/L and 7.8 mumol/L for S(-)- and R(+)-bupivacaine, respectively]. Replacement of L508 or V512 by a methionine (L508M and V512M) abolished stereoselective block, whereas substitution of V512 by an alanine (V512A) preserved it. Block of Kv2.1 channels, which carry valine, leucine, and isoleucine residues at T505, L508, and V512 equivalent sites, respectively, was not stereoselective [Kd = 8.3 mumol/L and 13 mumol/L for S(-)- and R(+)-bupivacaine, respectively]. These results suggest that (1) the bupivacaine binding site is located in the inner mouth of the pore, (2) stereoselective block displays subfamily selectivity, and (3) a polar interaction with T505 combined with hydrophobic interactions with L508 and V512 are required for stereoselective block.     

The physical reason for the apparently low deposition rate during high-power pulsed magnetron sputtering

In high-power pulsed magnetron sputtering, a large power density is applied giving rise to a high degree of ionization. From an application point of view, the major drawback of this technology is the considerably lower deposition rate as compared to DC magnetron sputtering. Using transport-of-ions-in-matter simulations, we show that the apparently low deposition rate can be understood based on the non-linear energy dependence of the sputtering yields. Our calculations are consistent with deposition-rate measurements on Cu films as well as with published deposition-rate data for Ti [Konstantinidis S, Dauchot JP, Ganciu M, Ricard A, Hecq M. J Appl Phys 2006;99:013307].     

Controlling the Formation of Nanocavities in Kirkendall Nanoobjects through Sequential Thermal Ex Situ Oxidation and In Situ Reduction Reactions

Controlling the porosity, the shape, and the morphology of Kirkendall hollow nanostructures is the key factor to tune the properties of these tailor‐made nanomaterials which allow in turn broadening their applications. It is shown that by applying a continuous oxidation to copper nanowires following a temperature ramp protocol, one can synthesize cuprous oxide nanotubes containing periodic copper nanoparticles. A further oxidation of such nanoobjects allows obtaining cupric oxide nanotubes with a bamboo‐like structure. On the other hand, by applying a sequential oxidation and reduction reactions to copper nanowires, one can synthesize hollow nanoobjects with complex shapes and morphologies that cannot be obtained using the Kirkendall effect alone, such as necklace‐like cuprous oxide nanotubes, periodic solid copper nanoparticles or hollow cuprous oxide nanospheres interconnected with single crystal cuprous oxide nanorods, and aligned and periodic hollow nanospheres embedded in a cuprous oxide nanotube. The strategy demonstrated in this study opens new avenues for the engineering of hollow nanostructures with potential applications in gas sensing, catalysis, and energy storage.