Multistep temperature prediction for proactive thermal management on chip multiprocessors

The Journal of Supercomputing - In chip multiprocessors, the thermal hot spot prediction is vital to take proactive thermal management decisions for mitigating its impact on the performance of the...     

Performance of an activated carbon made from waste palm shell in simultaneous adsorption of SO<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript> and NO<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript> of flue gas at low temperature

This study examined the individual and simultaneous adsorption of SO{in{itx}} (SO{in{it2}}) and NO{in{itx}} (NO-NO{in{it2}}) on activated carbon prepared from waste palm shell. The adsorption process was examined in a fixed bed reactor at low temperatures (100\2-300\dgC). For individual adsorption without any catalytic activation, SO{in{itx}} showed good adsorption whereas NO{in{itx}} was very much poor. In the simultaneous adsorption of SO{in{itx}} and NO{in{itx}}, SO{in{itx}} showed greater adsorption affinity than NO{itx}. For palm shell activated carbon (PSAC) impregnated with metal catalyst (Ni and Ce) the concentration adsorbed profile showed that the amount of SO{in{itx}} adsorbed decreased regularly, while the amount of the adsorbed NO{in{itx}} increased irregularly. The properties of the pure and impregnated PSAC were analyzed by BET, SEM and EDX. These investigations indicated that PSAC impregnated with metal catalyst is the determining factor in the adsorption of SO{in{itx}} and NO{in{itx}} simultaneously. Supported financially by Yayasan FELDA, Malaysia (Grant No. 6050075)     

Estimation of sharma constant and thermoacoustic properties of fatty acids

From the volume expansivity α, a number of thermoacoustic parameters, including the Sharma constant,S ₀, are estimated for four fatty acids as a function of temperature. The Sharma constant, which was established to be a constant with the characteristic value 1.11 ± 0.01 over a number of systems investigated by earlier investigators, is also found to be a constant with the same value for all fatty acids under investigation. Further, the Sharma constant,S ₀, is independent of temperature and dependent only on α. All other parameters estimated are discussed and compared with the values reported in the literature by earlier workers for different systems.     

CO2 methanation over Ni and Rh based catalysts: Process optimization at moderate temperature

H₂ was produced from aluminum/water reaction and reacted with CO₂ over Ni and Rh based catalysts to optimize the process conditions for CO₂ methanation at moderate temperature. Monometallic catalysts were prepared by incorporating Ni and Rh using nickel nitrate hexahydrate (Ni(NO₃)₂·6H₂O) and rhodium(III) chloride trihydrate (RhCl₃·3H₂O)as a precursor chemical. The preliminary study of the catalysts revealed higher activity and CH₄ selectivity for Rh based catalyst compared to that of Ni based catalyst. Further, Rh based catalyst was investigated using response surface methodology (RSM) involving central composite design. The quadratic model was employed to correlate the effects of variable parameters including methanation temperature, %humidity, and catalyst weight with the %CO₂ conversion, %CH₄ selectivity, and CH₄ production capacity. Analysis of variance revealed that methanation temperature and humidity play an important role in CO₂ methanation. Higher response values of CO₂ conversion (54.4%), CH₄ selectivity (73.5%) and CH₄ production capacity (8.4 μmol g^?1 min^?1) were noted at optimum conditions of 206.7°C of methanation temperature, 12.5% humidity and 100 mg of the catalyst. The results demonstrated the ability of Rh catalyst supported on palm shell activated carbon (PSAC) for CO₂ methanation at low temperature and atmospheric pressure.     

Development of a food frequency questionnaire for Sri Lankan adults

ABSTRACT: BACKGROUND: Food Frequency Questionnaires (FFQs) are commonly used in epidemiologic studies to assess long-term nutritional exposure. Because of wide variations in dietary habits in different countries, a FFQ must be developed to suit the specific population. Sri Lanka is undergoing nutritional transition and diet-related chronic diseases are emerging as an important health problem. Currently, no FFQ has been developed for Sri Lankan adults. In this study, we developed a FFQ to assess the regular dietary intake of Sri Lankan adults. METHODS: A nationally representative sample of 600 adults was selected by a multi-stage random cluster sampling technique and dietary intake was assessed by random 24-h dietary recall. Nutrient analysis of the FFQ required the selection of foods, development of recipes and application of these to cooked foods to develop a nutrient database. We constructed a comprehensive food list with the units of measurement. A stepwise regression method was used to identify foods contributing to a cumulative 90% of variance to total energy and macronutrients. In addition, a series of photographs were included. RESULTS: We obtained dietary data from 482 participants and 312 different food items were recorded. Nutritionists grouped similar food items which resulted in a total of 178 items. After performing step-wise multiple regression, 93 foods explained 90% of the variance for total energy intake, carbohydrates, protein, total fat and dietary fibre. Finally, 90 food items and 12 photographs were selected. CONCLUSION: We developed a FFQ and the related nutrient composition database for Sri Lankan adults. Culturally specific dietary tools are central to capturing the role of diet in risk for chronic disease in Sri Lanka. The next step will involve the verification of FFQ reproducibility and validity.     

Role of SiC substrate polarity on the growth and properties of bulk AlN single crystals

Two symmetrically nonequivalent silicon carbide (SiC) substrate orientations, (0001) Si-terminated and \((000\overline{1} )\) C-terminated, were used in the physical vapour transport growth of bulk aluminium nitride (AlN) single crystals. The crystals grown on Si-faces always exhibit an Al-polar growth surface. AlN growth on \((000\overline{1} )\) C-terminated surfaces of the SiC substrates was performed to obtain N-polar growth surfaces. An abrupt interface was observed between the AlN crystal and the C-face substrate which is in contrast to the growth on Si-faces where hexagonally shaped SiC hillocks are formed. The growth on C-faces is usually dominated by multi-site nucleation. Applying similar supersaturation conditions that led to step-flow growth on Si-faces to the C-faces resulted in a spiral growth mode, even on highly off-oriented substrates. The obtained broad X-ray diffraction rocking curves of such samples (full-width at half-maximum ≈380 arcsec) indicate the presence of more misfit dislocations and significant misfit stress. In addition, polarity inversion is observed in C-face grown crystals. Though the structural properties of the crystals grown on C-face are inferior to that of the crystals grown on Si-face, the incorporation of unintentional Si impurity was found to be lower (<2 wt%).     

Copper-doped flower-like molybdenum disulfide/bismuth sulfide photocatalysts for enhanced solar water splitting

A facile synthesis approach to fabricate Cu-doped MoS₂/Bi₂S₃ (Cu-MoS₂/Bi₂S₃) photocatalysts is reported. The photocatalyst samples with varying amounts of Cu are applied in the photocatalytic splitting of water to produce H₂ under the irradiation of simulated solar light. The Cu-MoS₂/Bi₂S₃ photocatalysts with an optimum Cu loading of 20 mol% exhibited high photocatalytic performance, achieving a total H₂ yield of 32.4 μmol/h after 6 h of reaction. The photoactivity of the Cu-doped sample was shown to have risen more than 40% than that of pure MoS₂/Bi₂S₃. The improved performance is attributed to the impurity states generated within Cu-doped MoS₂, which serve as trapping sites for photogenerated electrons. The effective charge transfer mechanism achieved was evidenced by photoelectrochemical measurements. Based on the experimental results obtained, a plausible mechanism for the photocatalytic process associated with Cu-MoS₂/Bi₂S₃ was proposed.     

Seamless vertical handoff using modified weed optimization algorithm for heterogeneous wireless networks

In the global scenario, a variety of wireless access networks are available. Different types of applications such as real time, nonreal time, and high bandwidth availability are used for heterogeneous wireless networks. Therefore, it is necessary for a service provider to make an appropriate connection support. For better performance, connections are to be exchanged among the different networks using seamless vertical handoff (VHO). The proposed algorithm shows the effect of optimization technique, which involves handoff decision process using vertical handoff triggering and selection of the network. The handoff triggering is initiated by using the received signal strength (RSS). In traditional method, handoff triggering is initiated by using RSS only. This method, modified weed optimization (M-WO) algorithm, reduces the unnecessary handoff by considering both RSS and velocity of the mobile node in handoff triggering. The parameters such as battery lifetime, handoff call dropping rate, load, dynamic weights adaptation and so on are to be considered individually or combined to make an effective network selection process. This paper highlights a novel effect ofM-WOalgorithm for decision making during the VHO. Our effort is to essentially optimize the system load, so that it reduces the handoff call dropping rate and the battery power consumption of the mobile node (MN). Weight of each QoS metrics is adjusted along with the networks changing conditions to trace the M-WO. Therefore, the novel VHO decision-making algorithm is superior to the existing SSF and OPTG methods. The simulation results show that the performance ofM-WOalgorithm is far better than SSF andOPTGmethods in terms of load, handoff call dropping rate and battery lifetime of MN.     

Effects of solvent, pH, salts and resin fatty acids on the dechlorination of pentachlorophenol using magnesium-silver and magnesium-palladium bimetallic systems

The effects of pH, organic co-solvent, salts such as sodium chloride, sodium sulfate, and co-pollutants, resin and fatty acids (RFAs) on the dechlorination of pentachlorophenol (PCP) by magnesium/silver (Mg/Ag) and magnesium/palladium (Mg/Pd) systems were examined in the present investigations. Such studies provide relevant information about the applicability of bimetallic systems for remediation of raw wastewaters (such as pulp bleaching effluents) or groundwater. Removal efficiencies of 10 mg L(-1) PCP by Mg/Pd and Mg/Ag systems at the end of 1 h reaction were 93% and 78%, respectively, in the presence of acetone (1% v/v). On the other hand, the removal efficiencies were 86% and 70% for reactions conducted in alcoholic solvents (1% v/v) using Mg/Pd and Mg/Ag systems, respectively. The efficiencies of PCP removal by the two bimetallic systems could be correlated to the dipole moments of co-solvents used. The second order reaction rate constant for PCP removal by Mg/Ag system was highest (0.03 L mg(-1) min(-1)) in the absence of any pH-control mechanism. Optimum pH for the dechlorination of PCP by Mg/Pd system was found to be approximately 5.5 and >92% of the compound was removed within 15 min of reaction. Presence of chlorinated and non-chlorinated resin fatty acids (RFAs) resulted in substantial reduction in the rate and extent of PCP removal by Mg/Ag system whereas dechlorination by Mg/Pd remained unaffected. Presence of sodium sulfate or sodium chloride in the reaction phase reduced the rate and extent of PCP removal by Mg/Ag system. PCP dechlorination by Mg/Pd system was adversely impacted by the addition of sodium chloride and unaffected by the presence of sodium sulfate.     

Dechlorination of chlorophenols using magnesium-palladium bimetallic system

Ninety-four percent removal of 10 mg L(-1) of pentachlorophenol (PCP) was achieved by treatment with 154.5mM Mg(0) and 0.063 mM K(2)PdCl(6) in the presence of 175 mM acetic acid in 1h reaction time. Dechlorination of PCP was found to be sequential and phenol was identified as the end product along with accumulation of trace concentrations of tetra- and trichlorophenols. Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX) revealed that palladium in its metallic form (Pd(0)) produced by reduction of Pd4+, was spatially separated from magnesium granules when acid was included in the reaction. These colloidal palladium particles generated active reductive species of hydrogen and dechlorinated chlorophenols. In the absence of acid, the efficiency of dechlorination of PCP by Pd/Mg(0) system was very low and chief mechanism of removal of the compound was through sorption onto solid surfaces. Thus, it was important to include acid in the system to: (a) facilitate corrosion of Mg(0) and reduction of Pd4+ to Pd(0), (b) provision of protons to produce H2, (c) retard formation of insoluble oxides and hydroxides that may deposit on the magnesium granules and sorb PCP and its partially dechlorinated products and. Application of 154.5 mM Mg(0)/0.063 mM K(2)PdCl(6) on PCP, 2,4,5-trichlorophenol (TCP) and 2-chlorophenol (MCP) with organic chloride equivalence showed that the rate and extent of removal increased with decrease in number of chlorine atoms on phenol.