Experimental analysis of heat transfer through multiple reflecting bodies in a reactor-based cooling vault

In a nuclear reactor power plant, massive amount of heat generated in the reactor core causes the Reactor vault (RV) temperature to rise, which should be maintained at a permissible temperature range of 65°C–80°C. In order to address this issue we propose to incorporate thermal insulation, which consists of thin stainless steel (SS) sheets of 0.1?mm-thick stacked with uniform gap between them, introduced between the core and RV. The SS sheets (emissivity?=?0.05) are of highly polished, reflective type (mirror finish conforming to No. 8 as per ASTM A480/480M), which are made in the form of panels of suitable size and shape covering the entire outer contour. These types of insulations work on the principle of thermal radiation shielding Heat radiations from the reactor core falling on these reflective plates are reflected back thereby restricting the heat flux into the RV concrete. In order to estimate the effectiveness, 10 such plates are arranged over a length of 150?mm inside a casing made of an insulating material. A plate heater attached at the one end produces the desired heat transfer to analyse the thermal behaviour of the reflective plates. Thermocouples are attached to each plate to understand the temperature distribution in the system. Solidworks simulation and numerical calculations will be carried out.     

Modeling,control and simulation of a chain link STATCOM in EMTP-RV

This paper describes an alternative STATic synchronous COMpensator (STATCOM), by connecting a number of gate turn off (GTO) thyristor converters in series on the ac side of the system. Each GTO converter forms one ‘link’ of a 1-phase, full-bridge voltage–source-converter (VSC) and is referred to as a ‘Chain Link Converter’ (CLC). Each GTO of a chain link STATCOM (CLS), is switched ‘ON/OFF’ only once per cycle of the fundamental frequency by using a sinusoidal pulse width modulation (SPWM) technique. Approximate models of a 3-phase CLS using dq-transformation are derived to design two controllers for controlling reactive current and ac voltage to stabilize the system voltage at the point of common coupling (PCC). A novel technique, called the rotated gate signal pattern (RGSP), is used for balancing the voltages of the link dc capacitors. The performance investigation of the CLS system when used in a radial line is carried out under steady- and transient-state operating conditions by means of the simulation package; EMTP-RV and the results are presented.     

Development of highly sensitive non-enzymatic sensor for the selective determination of glucose and fabrication of a working model

Copper oxide (CuO)/copper oxalate (CuOx) modified non-enzymatic electrochemical sensor for the detection of glucose in alkaline medium was fabricated by electrochemical anodisation of copper electrodes in potassium oxalate solution. Morphology of the modified copper electrode was studied by Scanning Electron Microscopy (SEM) and its electrochemical behaviour by Cyclic Voltammetry (CV) and Electrochemical Impedance Spectroscopy (EIS). The formation of CuOx on the copper electrode was confirmed by the Infra-red Reflection Absorption Spectrum (IRRAS). The modified electrodes were found to be microporous and rough. Linear Sweep Voltammetry (LSV) and amperometry were adopted to investigate the direct electrocatalytic oxidation of glucose on CuO/CuOx modified electrode in alkaline medium which showed excellent catalytic activity. The best performance of the sensor was obtained at 0.7 V and in 0.1 M sodium hydroxide (NaOH). At this optimum potential, the sensor was highly selective to glucose in the presence of ascorbic acid (AA) and uric acid (UA) which are common interfering species in biological fluids. The sensitivity was found to be very high (1890 μA mM⁻¹ cm⁻²) with excellent linearity (R = 0.9999) up to 15 mM having a low detection limit of 0.05 μM (S/N = 3). The modified electrode was tested for glucose level in blood serum. Based on the optimised conditions, a working model of the sensor was made and successfully tested for glucose.     

Fabrication and mechanisms of densification of ZrB2-based ultra high temperature ceramics by reactive hot pressing

Dense ZrB₂–SiC (25–30 vol%) composites have been produced by reactive hot pressing using stoichiometric Zr, B₄C, C and Si powder mixtures with and without Ni addition at 40 MPa, 1600 °C for 60 min. Nickel, a common additive to promote densification, is shown not to be essential; the presence of an ultra-fine microstructure containing a transient plastic ZrC phase is suggested to play a key role at low temperatures, while a transient liquid phase may be responsible at temperatures above 1350 °C. Hot Pressing of non-stoichiometric mixture of Zr, B₄C and Si at 40 MPa, 1600 °C for 30 min resulted in ZrB₂–ZrC_x–SiC (15 vol%) composites of 98% RD.     

Characterizing Indoor and Outdoor 15 Minute Average PM 2.5 Concentrations in Urban Neighborhoods

While a number of studies have looked at the relationship between outdoor and indoor particulate levels based on daily (24 h) average concentrations, little is known about the within-day variability of indoor and outdoor PM levels. It has been hypothesized that brief airborne particle excursions on a time scale of a few minutes to several hours might be of health significance. This article reports variability in measurements of daily (24 h) average PM 2.5 concentrations and short-term (15 min average) PM 2.5 concentrations in outdoor and indoor microenvironments. Daily average PM 2.5 concentrations were measured using gravimetry, while measurements of 15 min average PM 2.5 mass concentrations were made using a light scattering photometer whose readings were normalized using the gravimetric measurements. The measurements were made in 3 urban residential neighborhoods in the Minneapolis-St. Paul metropolitan area over 3 seasons: spring, summer, and fall of 1999. Outdoor measurements were made at a central monitoring site in each of the 3 communities, and indoor measurements were made in 9-10 residences (with nonsmoking occupants) in each community. Residential participants completed a baseline questionnaire to determine smoking status, sociodemographics, and housing characteristics. Outdoor PM 2.5 concentrations across the Minneapolis-St. Paul metropolitan area appear to be spatially homogeneous on a 24 h time scale as well as on a 15 min time scale. Short-term average outdoor PM 2.5 concentrations can vary by as much as an order of magnitude within a day. The frequency distribution of outdoor 15 min averages can be described by a trimodal lognormal distribution, with the 3 modes having geometric means of 1.1 w g/m 3 (GSD = 2.1), 6.7 w g/m 3 (GSD = 1.6), and 20.8 w g/m 3 (GSD = 1.3). There is much greater variability in the within-day 15 min indoor concentrations than outdoor concentrations (as much as ～40-fold). This is most likely due to the influence of indoor sources and activities that cause high short-term peaks in concentrations. The indoor 15 min averages have a bimodal lognormal frequency distribution, with the 2 modes having geometric means of 8.3 w g/m 3 (GSD = 1.66) and 35.9 w g/m 3 (GSD = 1.8), respectively. The correlation between the matched outdoor and indoor 15 min average PM 2.5 concentrations showed a strong seasonal effect, with higher values observed in the spring and summer ( R 2 adj = 0.49 - 0.33) and lower values in the fall ( R 2 adj = 0.13 - 0.13).     

Spectroscopic studies of large sheets of graphene oxide and reduced graphene oxide monolayers prepared by Langmuir-Blodgett technique

Graphene oxide (GO) sheets prepared by chemical exfoliation were spread at the air-water interface and transferred to silicon substrates by Langmuir-Blodgett technique as closely spaced monolayers of 20-40 μm size. Hydrazine exposure followed by annealing in vacuum and argon ambient results in the formation of reduced graphene oxide (RGO) monolayers, without significantly affecting the overall morphology of the sheets. The monolayer character of both GO and RGO sheets was ascertained by atomic force microscopy. X-ray photoelectron spectroscopy supported by Fourier transform infrared spectroscopy revealed that the reduction process results in a significant decrease in oxygen functionalities, accompanied by a substantial decrease in the ratio of non-graphitic to graphitic (sp² bonded) carbon in the monolayers from 1.2 to 0.35. Raman spectra of GO and RGO monolayers have shown that during the reduction process, the G-band shifts by 8-12 cm^− 1 and the ratio of the intensities of D-band to G-band, I(D)/I(G) decreases from 1.3 ± 0.3 to 0.8 ± 0.2, which is in tune with the smaller non-graphitic carbon content of RGO monolayers. The significant decrease in I(D)/I(G) has been explained by assuming that substantial order is present in precursor GO monolayers as well as RGO monolayers obtained by solid state reduction.