High temperature creep of polyvinyl chloride

The creep behaviour of polyvinyl chloride (PVC) has been studied in the temperature range 280 to 340° F under constant stress varying from 3.4 to 22.7 p.s.i. It is shown that the steady-state creep rate is an exponential function of stress as suggested by Norton but the exponent decreases with temperature. The activation energy for creep is determined using an activated-state rate process and it is found to be a decreasing function of stress with a higher value at temperatures 320° F and above. It is shown that the time dependent strain can be represented by $$\gamma = \gamma _0 + \dot \gamma _s t + \gamma _T \left[ {1 - \exp \left( { - K\dot \gamma _s t} \right)} \right]$$ where γ ₀ is the instantaneous strain on stressing, \(\dot \gamma _s\) the secondary creep rate, γ _T transient strain, and K is a constant. Scanning electron micrograph studies of the fracture surface and the change in activation energy apparently support the probability of two different deformation mechanisms i.e., domain flow and chain segmental or molecular flow at temperatures below and above 320° F, respectively.     

Conversion of monolithic gels to glasses in a multicomponent silicate glass system

Multicomponent silicate glasses of composition (wt%) 66SiO₂-18B₂O₃-7Al₂O₃-6Na₂O-3BaO were prepared by three sol-gel processes which differed primarily in the extent of hydrolysis of the metal alkoxide precursors. Gels which were prepared from solutions in which a stoichiometric excess of water was added, causing extensive replacement of OR groups (R (C _x H(_2x+1))^s–1 by hydroxyl groups, were converted to fully dense, organic-free, monolithic glasses at temperatures near the glass transition temperature. Gels containing large numbers of OR groups showed enhanced densification at lower temperatures due to condensation reactions, but these gels could not be converted to fully dense, organic-free glasses. This investigation has shown that at least three possible densification mechanisms might be operative during the gel to glass conversion: volume relaxation, condensation reactions and viscous sintering.A US Department of Energy Facility.     

Temporal scale effect of loading data on instream nitrate-nitrogen load computation

The temporal scale effect of loading data on nitrate-nitrogen load computation was examined using outputs of watershed modeling tool Hydrologic Simulation Program-FORTRAN (HSPF) for the Amite River in Louisiana, USA. The daily nitrate-nitrogen concentrations simulated using the HSPF were employed first to obtain daily, weekly, bi-weekly, and monthly average data and then to develop load duration curves for the data with four different temporal scales. The duration curves exhibited high variability in the load estimated using daily data as compared with those based on bi-weekly and monthly data. According to daily data, the nitrate-nitrogen load in the winter was found to be 2,780 kg. The nitrate-nitrogen load decreased with increasing temporal (daily, weekly, bi-weekly, and monthly) scale (commonly used in water quality monitoring) of the data. The coefficient of variation, used to quantify the effect of temporal scale on the load, was found to be linearly and inversely correlated with the logarithm of the time scale. Based on the finding, empirical equations were proposed to extrapolate near real-time data for flow and nitrate-nitrogen, greatly simplifying nutrient monitoring and reducing the cost involved in water quality monitoring.     

Modeling mineral phase change chemistry of groundwater in a rural-urban fringe

This research paper aims to determine the genetic origin of the chemical elements in groundwater. It deals with the results of physicochemical parameters, to evaluate the hydro-geochemistry of groundwater in rural-urban fringe of district Bareilly, India. Pre- and post-monsoon sampling has been carried out, which reveals inter-seasonal variability effect on the hydro-geochemical processes. Geochemical modeling especially computation of saturation index was undertaken using the WATEQ4F model. Majority of samples fall in the category of undersaturation, which further suggests that groundwater still has potential to dissolve more minerals. Chemical categorizations of groundwater samples were performed with the help of the Aquachem model. Grouping of groundwater on the Piper diagram reveals a common composition and origin. In most of the area, water facies is of Ca(2+)-HCO(3)(-) type in both the seasons. It also indicates that in pre-monsoon, ion exchange is the dominant process, whereas in post-monsoon, both ion exchanges as well as reverse ion exchanges are reported in the groundwater of the study area.     

Delineation of Groundwater Potential Zones in Arid Region of India—A Remote Sensing and GIS Approach

The present research is an attempt to find out the groundwater potential zones within an arid region of India supported by the scientific investigation of lithology, geomorphology, geohydrological characterization of geological formations and their interrelationship. Thematic layers of drainage, lithology, geomorphology, lineaments, slope, soil, digital elevation model, rainfall, landuse/land cover and well inventory have been generated by using ancillary data, digital satellite image, water level data of 90 observation wells for last 11?years (2000?C2010), litholog data along with ground truthing. The groundwater potential zones have been classified into five categories like very poor, poor, moderate, good and excellent. The potential zones were obtained by weighted overlay combination using the spatial analyst tool in ArcGIS 9.2. During weighted overlay analysis, the ranking was given for each individual parameter of each thematic map and weights were assigned according to their influence such as lithology (20?%), geomorphology (15?%), lineament density (15?%), drainage density (15?%), soil (10?%), slope (10?%), rainfall (5?%), land use and land cover (5?%) and digital elevation model (DEM) (5?%) and it was found that the potential zones in terms of very poor, poor, moderate, good and excellent zones covered 13.7?%, 42.8?%, 27.3?%, 10.8% and 5.4% respectively of the total area. The result also has been validated by yield data collected from existing sources and it confirms that the higher yield categories are falling within excellent groundwater potential zones where yield ranges from 23 to 40.3?l/s and lower values ranging from 8.1 to 10.6?l/s are falling within poor groundwater potential zones.     

Porous Titania Thin Films Grown by Anodic Oxidation for Hydrogen Sensors

Porous titanium dioxide (Titania) thin films were grown by anodic oxidation using high purity (99.7%) titanium foil in a dilute sulphuric acid (1 M) medium. The anodization process was carried out for 30 minutes with 20 mA/cm² and 50 mA/cm² current densities. The samples were characterized by XRD, SEM, and AFM techniques. It was found that the grown porous titania films were less sensitive to 500 ppm hydrogen in air ambient below 300°C; however, the sensitivity and response behavior of the film at 300°C are very much dependent on the growth conditions. Particularly, the films grown at current density 50 mA/cm² and 1 M acid concentration exhibited the lowest response time of 151 sec at 300°C.     

Towards the Development of a New Iron Age

Steel in its various forms is the most widely utilized metallic alloy and comprises over 80 % by weight of all metallic alloys in industrial use.^[1] The development of steel microstructures is based on manipulation of a very specific solid/solid state transformation called an eutectoid transformation (i.e. γ_austenite → α_ferrite+ Fe₃C_cementite). The control of this transformation is the primary factor resulting in wide variety of microstructures and resulting properties found in commercial steel alloys. However, the full benefit of its main constituent, iron has never been realized. Based on the metallic bonding in iron, the theoretical tensile strength has been calculated to be 13.2 GPa but ultra high strength steels, even today, only achieve maximum tensile strength levels from 1 to 1.5 GPa. Thus, our modern technological society has been established utilizing approximately only ～ 10 % strength level of iron. Here we demonstrate that a high level of strength (6.2 GPa) and strength to weight ratio of 8.3 × 10⁴/m³ may be obtained in iron‐based alloys by their solidification into metallic glasses, as well as, by employing another solid state transformation called glass devitrification.     

一种可编程ExpressCard解决方案

ExpressCard模块是由PCMCIA推出的一种更薄、更快、更轻的抽屉式插卡,用以取代现有的PC卡和CardBus模块,主要用于笔记本计算机后继市场中的功能性升级和扩展.同样,ExpressCard模块最初旨在服务于笔记本计算机后继市场(图1a).     

Catalytic oxidation of carbon monoxide over radiolytically prepared Pt nanoparticles supported on glass

Platinum nanoparticles have been prepared by radiolytic and chemical methods in the presence of stabilizer gelatin and SiO₂ nanoparticles. The formation of Pt nanoparticles was confirmed using UV-vis absorption spectroscopy and transmission electron microscopy (TEM). The prepared particles were coated on the inner walls of the tubular pyrex reactor and tested for their catalytic activity for oxidation of CO. It was observed that Pt nanoparticles prepared in the presence of a stabilizer (gelatin) showed a higher tendency to adhere to the inner walls of the pyrex reactor as compared to that prepared in the presence of silica nanoparticles. The catalyst was found to be active at ≥150 °C giving CO₂. Chemically reduced Pt nanoparticles stabilized on silica nanoparticles gave ∼7% CO conversion per hour. However, radiolytically prepared Pt nanoparticles stabilized by gelatin gave ∼10% conversion per hour. Catalytic activity of radiolytically prepared platinum catalyst, coated on the inner walls of the reactor, was evaluated as a function of CO concentration and reaction temperature. The rate of reaction increased with increase in reaction temperature and the activation energy for the reaction was found to be ∼108.8 kJ mol⁻¹. The rate of CO₂ formation was almost constant (∼1.5 × 10⁻⁴ mol dm⁻³ h⁻¹) at constant O₂ concentration (6.5 × 10⁻³ mol dm⁻³) with increase in CO concentration from 2 × 10⁻⁴ mol dm⁻³ to 3.25 × 10⁻³ mol dm⁻³. The data indicate that catalytic oxidation of CO takes place by Eley-Rideal mechanism.