SERC Reliability Corporation

About: SERC Reliability Corporation is a based out in . It is known for research contribution in the topics: Turbulence & Reynolds number. The organization has 520 authors who have published 604 publications receiving 14793 citations.

Global estimates of mortality associated with long-term exposure to outdoor fine particulate matter

Abstract: Exposure to ambient fine particulate matter (PM2.5) is a major global health concern. Quantitative estimates of attributable mortality are based on disease-specific hazard ratio models that incorporate risk information from multiple PM2.5 sources (outdoor and indoor air pollution from use of solid fuels and secondhand and active smoking), requiring assumptions about equivalent exposure and toxicity. We relax these contentious assumptions by constructing a PM2.5-mortality hazard ratio function based only on cohort studies of outdoor air pollution that covers the global exposure range. We modeled the shape of the association between PM2.5 and nonaccidental mortality using data from 41 cohorts from 16 countries-the Global Exposure Mortality Model (GEMM). We then constructed GEMMs for five specific causes of death examined by the global burden of disease (GBD). The GEMM predicts 8.9 million [95% confidence interval (CI): 7.5-10.3] deaths in 2015, a figure 30% larger than that predicted by the sum of deaths among the five specific causes (6.9; 95% CI: 4.9-8.5) and 120% larger than the risk function used in the GBD (4.0; 95% CI: 3.3-4.8). Differences between the GEMM and GBD risk functions are larger for a 20% reduction in concentrations, with the GEMM predicting 220% higher excess deaths. These results suggest that PM2.5 exposure may be related to additional causes of death than the five considered by the GBD and that incorporation of risk information from other, nonoutdoor, particle sources leads to underestimation of disease burden, especially at higher concentrations.

Epidemiology of primary liver cancer.

Abstract: Liver cancer (LC) ranks fifth in frequency in the world with an estimated number of 437,000 new cases in 1990. In developing countries, incidence rates are two- to three-fold higher than in developed countries. The geographic areas at highest risk are located in Eastern Asia, with age-adjusted incidence rates (AAIRs) ranking from 27.6 to 36.6 per 100,000 in men; Middle Africa, with AAIRs ranking from 20.8 to 38.1 per 100,000 in men; and some countries of Western Africa, with AAIRs ranking from 30 to 48 per 100,000 in men. The geographic areas at lowest LC risk are Northern Europe, Australia, New Zealand, and the Caucasian populations in North and Latin America, with AAIRs below 5.0 per 100,000 in men. Excess of LC incidence among men compared to women is universal, with sex ratios between 1.5 and 3.0. Significant variations in LC incidence among different ethnic groups living in the same geographical area and among migrants of the same ethnic groups living in different areas have been extensively described. The variability of LC incidence rates between countries and within countries, strongly suggests differences in exposure to risk factors. The role of chronic infection with the Hepatitis B and hepatitis C viruses (HBV and HCV) in the etiology of LC is well established. The attributable risk estimates for LC for each of these hepatotropic viruses vary among countries but the combined effects of persistent HBV or HCV infections account for well over 80% of LC cases worldwide. Other documented risk factors such as aflatoxin exposure in diets, cigarette smoking, alcohol consumption, and oral contraceptives may explain the residual variation between and within countries. Interactions between some risk factors have been postulated, and are subject of active research. New laboratory techniques and biological markers such as polymerase chain reaction detection of HBV DNA and HCV RNA, as well as specific mutations related to aflatoxin exposure may help to provide quantitative estimates of the risk related to each these factors.

The 2p absorption spectra of 3d transition metal compounds in tetrahedral and octahedral symmetry

Abstract: The authors present the 2p (L2,3) absorption spectra of first-row transition metal ions in tetrahedral and octahedral crystal field symmetry. These have been calculated using a localized description for the 3dn to 2p53dn+1 excitation including electrostatic and spin-orbit interactions. The spectra are significantly different from those already presented where the 3d spin-orbit interaction was neglected. The spectral shape provides a valence- and symmetry-selective probe. Whereas it changes gradually with the crystal field, abrupt changes in the spectra are indicative of high-spin to low-spin transitions. These spin transitions are accompanied by a strong decrease in the 2p branching ratio. The calculated spectra provide a basis for the use of L2,3 absorption spectroscopy in materials science and biological science. The limitations of these calculations and the use of configuration interaction are discussed.

The energy and elastic dipole tensor of defects in ionic crystals calculated by the supercell method

Abstract: The energy, the elastic dipole tensor and the entropy of point defects in ionic crystals are usually calculated by the Mott-Littleton approach, which treats a single defect in an infinite crystal. The authors suggest that there may be advantages, particularly for the dipole tensor and the entropy, in performing the calculations in periodically repeating geometry. They examine how this 'supercell' method can be used for the energy and the dipole tensor, paying attention to the problem that for charged defects the repeating unit carries a net charge, so that the Coulomb energy is divergent. They test the supercell method on a number of both charged and uncharged defects, and show that the results for the energy and dipole tensor are in close agreement with those obtained by the conventional approach.

A review on encapsulation techniques for inorganic phase change materials and the influence on their thermophysical properties

Abstract: Phase change materials (PCM) are characterized for storing a large amount of thermal energy while changing from one phase to another (generally solid-liquid states) at a specific temperature and presenting a high specific heat of phase change process. PCMs can be classified as organic, inorganic and eutectic. Such materials present some limitations, including subcooling, phase segregation, flammability, low thermal conductivity and thermal instability, among others. In order to overcome these problems, encapsulation of PCMs is being successfully developed, providing decreased subcooling, large heat transfer area, and controlling the volume change of the storage materials when the phase transition occurs. A considerable amount of studies has been published in the field of encapsulation methods for organic PCMs. Nevertheless, the information available on inorganic PCMs is scattered. Furthermore, the influence of the encapsulation techniques on thermophysical properties of PCMs is not reported in these reviews most of the time. Hence, the aim of this review is to summarize the encapsulation and characterization techniques for inorganic PCMs and to provide the analysis about the influence of synthesis parameters on thermophysical properties of encapsulated PCMs. Two principal types of encapsulated inorganic PCMs were found: core-shell PCMs (core-shell EPCMs) and shape stabilized PCMs (SS-PCMs). Classification of encapsulation methods of core-shell EPCMs and SS-PCMs are reported in this work. Among all the microencapsulation methods, inverse Pickering emulsion, electroplating, solvent evaporation–precipitation method and mechanical packaging are the most common methods described in the literature for the production of core-shell EPCM. On the other hand, for SS-PCMs, mainly sol-gel process, infiltration and impregnation encapsulation methods were found. Scientific works report a reduction in the heat of phase change for core-shell EPCMs. This is mostly because of the low content of salt in the final material. Moreover, an improvement of thermal conductivity was procured for SS-PCMs. Finally, PCM percentage, particle size, stirring rate, type of crosslinking agent and solvent properties were established as principal factors influencing the final properties of the encapsulated materials. For the best of our knowledge, this is the first profound review of encapsulation techniques for inorganic PCM.