Heat Transfer and Exergy Analysis of a Spiral Heat Exchanger

The heat transfer effectiveness of a countercurrent spiral heat exchanger is expressed as a function of number of transfer units, ratio of flow capacity rates, number of spiral turns, and dimensionless start-point angle of spiral (dimensionless angular angle of the start point of a spiral curve constituting the solid wall of the heat exchanger). The heat transfer effectiveness is weakly dependent on the dimensionless start-point angle of spiral, but moderately increases with the number of spiral turns. As the number of spiral turns is larger than 20, the heat transfer effectiveness of the spiral heat exchanger approaches that of a counterflow heat exchanger. The heat transfer effectiveness of the spiral heat exchanger has a maximum. The optimum number of transfer units at the maximum heat transfer effectiveness increases with the number of spiral turns, whereas it increases with a decrease of the ratio of flow capacity rates. In the second-law analysis, an optimum hot flow-to-cold flow capacity-rate ratio is found. For obtaining a large net recovered exergy rate, the spiral heat exchanger needs to possess a large number of transfer units (greater than 2.0) and operate at a near balanced-flow condition. In addition, a small consumed mechanical power is demanded.     

A real time procedure for affinely dependent parametric model order reduction using interpolation on Grassmann manifolds

Model order reduction helps to reduce the computational time in dealing with large dynamical systems, for example, during simulation, control, optimization. In many cases, the considered model depends on parameters; Model order reduction techniques are, therefore, preferred to symbolically preserve this dependence or to be adaptive to the change of the model caused by the variation in the values of the parameters. In this paper, we first present the application of the interpolation technique on Grassmann manifolds to this problem. We then improve the method for the models whose system matrices depend affinely on parameters by considerably reducing the computational complexity on the basis of analyzing the structure of sums of singular value decompositions and decomposing the whole procedure into offline and online stages. A numerical example is shown to illustrate the method as well as to prove its effectiveness. Copyright © 2012 John Wiley & Sons, Ltd.     

Synthesis and properties of light weight magnesium–cenosphere composite

Significantly light weight magnesium composite foams are synthesised by addition of fly ash cenosphere particles (waste from coal-fired power plants) in biocompatible pure magnesium using solidification-based disintegrated melt deposition technique. The density of the composite foams synthesised in this study approaches that of plastics- and polymer-based composites. Microstructure development of Mg/cenosphere composite foams was favourable as they exhibited better dimensional stability (reduced coefficient of thermal expansion) and remarkable improvements in tensile strengths, compressive strengths, compressive total strain and microhardness. The present study highlights the processing, microstructure and mechanical properties of Mg/cenosphere composite foams which hold great potential as light weight metal-based green materials for diverse weight critical applications spanning from engineering to biomedical sector.     

Characterization of synthetic and activated sludge and conditioning with cationic polyelectrolytes

This study investigates the effect of cationic polyelectrolytes on the final properties of synthetic and activated sludge. Synthetic sludge was prepared according to established procedures. Activated sludge was produced in a labscale, continuous-flow reactor which was fed with live activated sludge from a waste-water treatment plant. Capillary suction time (CST) was used to evaluate the sludge dewatering behaviour. The results from experiments indicated that the cationic polyelectrolytes had a critical effect on sludge dewatering, and made an improvement in the final properties of sludge. The two types of sludge have very similar dewatering characteristics after cationic polymer conditioning. The development of synthetic sludge is suggested also to be a possible surrogate for studying the final properties of activated sludge.     

Influence of cobalt ions on the anodic oxidation of a lead alloy under conditions typical of copper electrowinning

The influence of cobalt ions in the solution on the anodic oxidation of a commercial Pb–Ca–Sn alloy under conditions typical of copper electrowinning was studied using cyclic voltammograms and potential decay transients. The cobalt ions changed the structure, morphology and chemical composition of the surface film from a loose porous film to a thin dense film. This change of surface film is the cause for the decreased rate of oxidation for the lead anode in the presence of cobalt ions. The steady state potential of the alloy during anodic oxidation decreased with (i) increasing cobalt ion concentration, (ii) increasing rotation speed, (iii) increasing temperature, (iv) decreasing acid concentration and (v) decreasing current density. The steady state potentials were lower in the presence of cobalt ions. This decrease in the steady state potential may indicate that oxygen evolution is more rapid on the more compact film formed in the presence of cobalt ions. Alternatively, an additional pathway of oxidation may be provided by the cobalt ions.     

Review of the textile coloration industry in Vietnam

This review discusses the recent development and current state of the textile coloration industry in Vietnam. With an overview of the textile and garment industry, focus is also on the garments and raw materials that are available for import/export. In addition, the main problems facing the coloration industry are covered, along with measures to improve the competitive advantage of the industry. Finally, environmental concerns and challenges for the future are reviewed.     

Sequential interval motif search: unrestricted database surveys of global MS/MS data sets for detection of putative post-translational modifications

Tandem mass spectrometry is the prevailing approach for large-scale peptide sequencing in high-throughput proteomic profiling studies. Effective database search engines have been developed to identify peptide sequences from MS/MS fragmentation spectra. Since proteins are polymorphic and subject to post-translational modifications (PTM), however, computational methods for detecting unanticipated variants are also needed to achieve true proteome-wide coverage. Different from existing "unrestrictive" search tools, we present a novel algorithm, termed SIMS (for Sequential Motif Interval Search), that interprets pairs of product ion peaks, representing potential amino acid residues or "intervals", as a means of mapping PTMs or substitutions in a blind database search mode. An effective heuristic software program was likewise developed to evaluate, rank, and filter optimal combinations of relevant intervals to identify candidate sequences, and any associated PTM or polymorphism, from large collections of MS/MS spectra. The prediction performance of SIMS was benchmarked extensively against annotated reference spectral data sets and compared favorably with, and was complementary to, current state-of-the-art methods. An exhaustive discovery screen using SIMS also revealed thousands of previously overlooked putative PTMs in a compendium of yeast protein complexes and in a proteome-wide map of adult mouse cardiomyocytes. We demonstrate that SIMS, freely accessible for academic research use, addresses gaps in current proteomic data interpretation pipelines, improving overall detection coverage, and facilitating comprehensive investigations of the fundamental multiplicity of the expressed proteome.     

Analysis of major protein-protein and protein-metal complexes of erythrocytes directly from cell lysate utilizing capillary electrophoresis mass spectrometry

The separation and detection of the major protein-protein and protein-metal complexes of erythrocytes directly from cell lysate under native conditions has been accomplished for the first time using capillary electrophoresis electrospray ionization-mass spectrometry (CE/ESI-MS). All three major protein-protein and protein-metal complexes in human red blood cells (RBCs) with a concentration dynamic range of approximately 3 orders of magnitude were successfully detected. Intact complexes detected in lysed RBCs included carbonic anhydrase II (CAII-Zn at approximately 0.8 amol/cell) complexed with its zinc cofactor, carbonic anhydrase I (CAI-Zn at approximately 7 amol/cell) complexed with its zinc cofactor, and hemoglobin A (Hb-tetramer at approximately 450 amol/cell)a tetramer formed by two alpha-beta-subunits and four heme groups. The average molecular weights measured for these complexes were consistent with their theoretical values within 0.01% mass accuracy. The use of Polybrene as a self-coating reagent in conjunction with ammonium acetate at pH approximately 7.4, narrow capillary for high separation efficiency, and forward polarity CE to avoid acid production at the tip of the capillary were overriding experimental factors for successful analysis of protein complexes. Diluting the lysed blood sample in ammonium acetate for a minimum of 6 h before injecting the sample into the CE was essential for obtaining the mass accuracy consistent with their theoretical average molecular weights. At physiological pH, the mass spectrum of the electrophoretic peak of Hb-tetramer included a small amount of the monomers and Hb-dimer. The migration time and peak profile of these species were almost identical to that of the tetramer, indicating that they are formed from decomposition of the Hb-tetramer during the ESI process. A separate electrophoretic peak for the Hb-dimer was only detected when the pH of the BGE was lowered from 7.4 to approximately 6.6. Running CE in forward polarity mode was essential for detection of the intact Hb-tetramer as well as CAI-Zn and CAII-Zn complexes. Under forward polarity mode, CE outlet/ESI shared electrode acts as the cathode of the CE circuit and the anode (positive voltage for positive ions) of the ESI circuit, thereby maintaining approximately neutral pH at the CE outlet/ESI electrode. In addition, under forward polarity mode, CAII-Zn and CAI-Zn migrated ahead of Hb-tetramer, avoiding being masked by 562x and 64x, respectively, molar excess of Hb-tetramer.     

New Raman spectrometer using a digital micromirror device and a photomultiplier tube detector for rapid on-line industrial analysis. Part I: description of the prototype and preliminary results

In this paper, a prototype of a new generation of Raman spectrometers, based on the use of a monochromator, a digital micromirror device as light modulator, and a photomultiplier tube as detector of the Raman light, is described. This spectrometer, containing no moving parts, is inexpensive, robust, and very precise. New in concept, this spectrometer makes it possible to record, in addition to classical Raman spectra, the intensity at several selected points of the spectrum and/or the total intensity in several selected intervals at the same time with great accuracy, thus giving new possibilities for analytical applications. Also, the work presented demonstrates the possibilities of this very simple prototype for rapid on-line industrial analysis, with an example of quantitative analysis of binary and ternary mixtures of xylene isomers. The precision obtained is satisfactory (errors of prediction approximately 3% in 5-6 seconds per sample).