Design optimization of a large scale rooftop photovoltaic system

This paper presents the optimization process of a grid connected photovoltaic (PV) system, which is intended to replace a large-scale thermal solar system on the rooftop of a Federal office building. A PV energy conversion model is described. Based on this model, array surface tilt angle and array size are optimized. The optimization method is based on maximizing the utilization of the array output energy, and, at the same time, minimizing the electricity power sold to grid. An effectiveness factor is introduced that takes into account both of these parameters. The array configuration and the output parameters are determined by comparing several PV modules. A 43.2 kW PV system is designed and operational problems such as harmonic effects and anti-islanding are discussed. Finally, the system performance is simulated and through economic analysis it has shown that the cost of PV system can be recouped in 13 years under the current renewable energy incentive program by the state of Illinois.     

Optimum tilt of solar collector for maximum natural flow

A theoretical treatment to determine the natural flow rate through a flat plate collector having heat losses is made. The governing equations have been expressed in terms of Grashof and Prandtl numbers and a dimensionless heat loss parameter. The method predicts the optimum tilt of the flat plate collector for the maximum draught for a given latitude and insolation. The experimental verification of the theoretical results shows a fair agreement.

A method to calibrate the hot wire anemometer at the desired temperature is evolved for the range of velocities encountered in practice for the flat plate solar collector.     

Dielectric and electro-optical study of ZnO nano rods doped ferroelectric liquid crystals

Addition of Nano rods results change in the dielectric and electro-optical properties of pure Ferroelectric Liquid Crystal (FLC) considerably. The present study is devoted to characterize the dielectric and electro-optical parameters of the FLC nano rods composite system. The size of nano rods is usually much bigger than that of FLC molecules, therefore, when they are doped in different concentrations, in pure FLC, their volume fraction plays considerable role in deciding the molecular dynamics of the resultant composite system. For the lesser concentrations, the nano rods offer mechanical strength to system geometry while at higher concentration of nano rods, they offer additional constraints on the system. In present report both of these aspects have been analyzed and explained.     

Design and validation of a novel multiplex real-time PCR assay for Vibrio pathogen detection

Three species--Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus--account for the majority of vibrio infections in humans. Rapid and accurate identification of Vibrio species has been problematic because phenotypic characteristics are variable within species. Additionally, biochemical identification and confirmation require 2 or more days to complete. Rapid and sensitive molecular techniques for the detection of vibrio pathogens would be useful for the surveillance and management of outbreaks. To facilitate the identification of human-pathogenic species, we designed and validated a highly sensitive, specific, and robust multiplex real-time PCR assay to identify V. cholerae, V. parahaemolyticus, and V. vulnificus using a four-dye configuration in a convenient lyophilized format. Multiple Vibrio strains were sequenced to verify candidate target TaqMan sites. Several individual assays within the multiplex contain multiple primers or probes to ensure detection of polymorphic variants. V. cholerae, V. parahaemolyticus, and V. vulnificus were detected either individually or in mixtures at ≤30 genomic copies. V. cholerae was specifically detected in the presence or absence of Vibrio mimicus. The Vibrio multiplex assay showed 100% specificity to all targets analyzed and no detection of nearest neighbor strains. Each assay exhibited 100% ± 10% efficiency. Multiplex real-time PCR can simplify pathogen detection and reduce costs per test since three species can be analyzed in a single reaction tube. Rapid and accurate detection of pathogenic vibrios in shellfish or seawater samples will improve the microbiological safety of seafood for consumers.     

Turnover of inositol polyphosphate pyrophosphates in pancreatoma cells

There is little information concerning the intracellular function of inositol 1,3,4,5,6-pentakis- and hexakisphosphate, despite their being the most abundant inositol polyphosphates. Current opinions that they play passive roles as antioxidants (Graf, E., Mahoney, J. R., Bryant, R. G., and Eaton, J. W. (1987) J. Biol. Chem. 259, 3620-3624) or "housekeeping" molecules (Berridge, M. J., and Irvine, R. F. (1989) Nature 341, 197-205) arises from belief in their metabolic lethargy. However, we have discovered that cell homogenates, incubated with 5 mM fluoride and 5 mM ATP, converted both inositol hexakisphosphate (Km = 2 +/- 0.5 microM, Vmax = 9 +/- 2 pmol/mg of protein/min) and inositol 1,3,4,5,6-pentakisphosphate (Km = 13 +/- 4 microM, Vmax = 11 +/- 5 pmol/mg of protein/min) to more polar products. These reactions were also observed in intact cells treated with 0.5-20 mM fluoride, and the precursor/product relationships were confirmed by comparing the effects of fluoride on cells differentially labeled with [3H]inositol in either short-term or pulse-chase protocols. The novel products were determined to be inositol pyrophosphates because of their relatively specific hydrolysis by tobacco pyrophosphatase and alkaline phosphatase. The pyrophosphates were metabolized rapidly by cell homogenates back to their pentakisphosphate and hexakisphosphate precursors. This endogenous pyrophosphatase activity was inhibited by up to 99% by 5 mM fluoride in vitro. In intact cells incubated with 10 mM fluoride, about 20% of the inositol 1,3,4,5,6-pentakisphosphate pool, and 50% of the inositol hexakisphosphate pool were each converted to pyrophosphate derivatives within 1 h.     

Scrapie infection of transgenic mice leads to network and intrinsic dysfunction of cortical and hippocampal neurones

The human prion encephalopathy Creutzfeldt-Jakob disease often is manifest as rapidly progressing dementia with myoclonus and synchronous, periodic discharges. To investigate the electrophysiology of prion disease we used intra- and extra-cellular recordings from brain slices from Tg(SHaPrP+/+) 81 mice, which express Syrian hamster prion protein and which are susceptible to hamster-passaged scrapie isolates. Forty days after intracerebral inoculation with scrapie isolate Sc237, we recorded prolonged, epileptiform discharges in cortex and hippocampus. Neurological signs were subtle and histopathology was minimal. Central nervous system (CNS) dysfunction progressed; by 57 days the mice were ataxic, had spongiform histopathology and they died in <63 days. During the terminal phase, intrinsic neuronal properties changed dramatically and action potentials broadened from <4 to 20-100 ms in 30% of cortical cells. We conclude that brain dysfunction in experimental scrapie precedes clinical signs and spongiform histopathology, and is preserved in slices maintained in vitro, making it accessible to electrophysiological analysis.