Synthesis and thermal studies of block copolymers from NR and MDI‐based polyurethanes

Five series of block copolymers based on natural rubber and polyurethane were prepared from hydroxyl terminated liquid natural rubber (HTNR) and polyurethane (PU) formed by the reaction of diphenyl methane—4,4′—diisocyanate (MDI) with a chain extender diol, viz., ethylene glycol (EG)/propylene glycol (PG)/1,4‐butane diol (1,4‐BDO)/1,3‐butane diol (1,3‐BDO)/bisphenol A (BPA), by solution polymerization. Structural characterization of the block copolymers was done by infrared (IR) analysis. Thermal studies and kinetic analysis on thermal degradation of the block copolymers were undertaken with the view of characterizing them. Energy of activation and entropy change for the degradation were determined and a probable mechanism for the solid state degradation was suggested which corresponds to a three dimensional diffusion mechanism. DSC analysis has been used for the study of microphase separation in the block copolymers. Thermal transition of the hard segment significantly varies with the extender diol which highlights the effect of extender diol structure on the chain stiffening mechanism. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Methane Hydrate Formation and Dissociation in the presence of Bentonite Clay Suspension

The present work reports the effect of bentonite clay on methane hydrate formation and dissociation in synthetic seawater of salinity 3.55 % of total dissolved salts. Extensive observations of pressure‐temperature equilibrium during formation and decomposition of methane hydrate under different conditions have been made. It is observed that phase equilibrium conditions of hydrate are affected on changing the concentration of bentonite clay in synthetic seawater. Induction time for hydrate nucleation has been measured under different concentrations of clay and subcooling conditions. The presence of bentonite clay in synthetic seawater reduces the induction time of hydrate formation. Enthalpy of hydrate dissociation is calculated by Clausius‐Clapeyron equation using measured phase equilibrium data. The amount of gas consumed during hydrate formation has been calculated using real gas equation. It is found that a larger amount of gas is consumed upon addition of bentonite clay in synthetic seawater.     

Thermodynamics and kinetics of methane hydrate formation and dissociation in presence of calcium carbonate

Huge amount of gas hydrate deposits are identified in deep marine sediments, which may be considered as a future source of energy. Since carbonate is one of the major components of marine sediments, in the present study attention has been given to characterize methane hydrate formation and dissociation in presence of calcium carbonate. Experiments were performed with 0%, 2%, 4%, 6% and 10% by weight of calcium carbonate in distilled water. Extensive investigations have been done on pressure-temperature equilibrium behavior of hydrate formation and dissociation at varying concentrations of calcium carbonate. Hydrate formation rate was found to vary with concentration of calcium carbonate as the solubility of calcium carbonate in water is controlled by the presence of simultaneous chemical equilibria involving a high number of species like Ca²⁺, CO₃^2?, HCO₃^?, CO₂, etc. Induction time for hydrate formation has also been measured at different concentrations of carbonate. Nucleation point for the hydrate formation was observed to be slightly higher at higher concentration of calcium carbonate due to increased heat absorption. Dissociation enthalpy of hydrates was calculated by using Clausius-Clapeyron at different measured conditions. Moles consumption of methane gas during hydrate formation at different concentrations of carbonate was measured using real gas equation and found to be minimum at 10?wt%.     

Detection of mosaic virus disease in cassava plants by sunlight-induced fluorescence imaging: a pilot study for proximal sensing

Cassava mosaic disease (CMD) is a prominent virus infection that causes considerable crop damage and yield reduction. Early detection of crop damage by remote sensing could be a useful tool for initiating remedial measures to reduce further crop damage. This article presents a non-destructive method for detection and classification of CMD infection, based on the red:far-red chlorophyll (chl) fluorescence image ratio. This pilot study was carried out in 14 varieties of potted cassava plants (Manihot esculenta Crantz) with a multispectral imaging system (MSIS) consisting of an electron multiplying charge coupled device (EMCCD) camera. Sunlight-induced chl fluorescence (SICF) images of plant leaves were recorded using the MSIS at the Fraunhofer lines of O₂-B at 687 nm and O₂-A at 759.5 nm and their off-lines at 684 and 757.5 nm. The recorded images were analysed using the Fraunhofer line discrimination (FLD) technique to extract the SICF from the solar reflectance in the recorded images. The chl fluorescence image ratio (red:far-red, F₆₈₇:F₇₆₀) was computed and correlated with the laser-induced chl fluorescence (LICF) ratio (F₆₈₅:F₇₃₅) determined by point monitoring, chl content variation, and the net photosynthetic rate (P_n). The scatter plot of the F₆₈₇:F₇₆₀ image ratio showed good discrimination between different levels of CMD infection as evidenced by the high sensitivity and specificity values. It is observed that the fluorescence image ratio (F₆₈₇:F₇₆₀) has a good correlation with P_n (coefficient of determination (R²) = 0.85), chl content (R² = 0.82), and the LICF ratio (F₆₈₅:F₇₃₅) (R² = 0.80), thereby highlighting the potential of the SICF image ratio in the discrimination of CMD infection. The results clearly indicate that changes in the red:far-red fluorescence image ratio due to CMD stress can easily be detected at an early stage and the technique has great potential for monitoring the health of crops and vegetation from proximal sensing platforms.     

Kinetics and mechanism of the thermal decomposition of potassium persulphate ions in aqueous solutions at 50°C in the presence of nitrogen gas and methacrylonitrile monomer

The initial rate of persulphate (I) decomposition at 50°C in the presence of nitrogen and methacrylonitrile (MAN) in an unbuffered aqueous solution (pH 4–7) may be written as: in the concentration ranges of persulphate (I) (0.25–2.50) × 10^?2 (m/dm³) and of (MAN) 0.18–0.36 (m/dm³). During the reaction, a white substance (polymethacrylonitrile) separates out in the colloidal state or in the precipitate form from the medium depending on the ionic strength of the medium. The pH of the medium was found to decrease rapidly and continuously with time in the absence of methacrylonitrile, but it decreased slowly and continuously with time in the presence of the monomer, MAN. If an additional quantity of MAN is injected late in a run, the rate of persulphate decomposition is further accelerated in a given run. However, the rate of persulphate decomposition is found to decrease continuously in the presence of MAN with time, i.e., as the monomer is converted to polymer. It is suggested that MAN accelerates the decomposition of persulphate ions, due to the following reactions in the aqueous phase: and where (M_j^˙)w is a-water soluble oligomeric or polymeric (j = 1–10) free radical. The estimated values of k₅ and k₁₀ are 1.05 × 10^?5 and 1.14 × 10³ (in dm³/m/s), respectively.     

Wide-Range Precision Speed Measurement with Adaptive Optimization Using a Microcomputer

A new speed measurement method using a microcomputer is presented. In the initial part of the measurement, a definite small fraction of time for one revolution is counted using a software technique. A definite bit-size of the count is maintained by continuing counting over an optimum multiple of the initially measured time interval in case the bit-size of the initial count is less than a preset value. The multiple of the initial time period is measured with the help of an external counter, without any break in the continuity of counting. The speed is computed from the time count and displayed. For this measurement, only a standard digital speed transducer, a counter, and a microcomputer kit are required. The method has a small data acquisition and processing time, and gives a high accuracy that is programmable over a wide range of speed. The method is also quite economical.