Pervaporation separation of IPA‐water mixtures through 4A zeolite‐filled sodium alginate membranes

Incorporation of zeolites into natural polymers has been shown experimentally to enhance both the flux and selectivity in pervaporative dehydration separation of organic compounds. Pervaporation is a promising membrane technique for separation of volatile organic compounds (VOCs)/water mixtures. In this study, hydrophilic sodium alginate (SA) mixed membranes were prepared using solution casting technique by incorporating zeolites into the polymer matrix. The prepared membranes were characterized by ATR‐Fourier transform infrared spectroscopy (FTIR), X‐ray diffraction (XRD), scanning electron microscopy (SEM), Thermal Gravimetric Analysis (TGA), and differential scanning calorimetry (DSC) were tested in a laboratory scale pervaporation experimental set‐up. The effect of experimental parameters such as the type and composition of zeolites on permeation flux and selectivity was investigated. When tested on IPA‐water mixtures, the zeolite‐filled membrane was found to give much higher selectivity. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Miscibility studies of sodium carboxymethylcellulose/poly(vinyl alcohol) blend membranes for pervaporation dehydration of isopropyl alcohol

Miscibility studies of sodium carboxymethylcellulose/poly(vinyl alcohol) (NaCMC/PVA) blends of different compositions (100/0, 80 : 20, 60 : 40, 50 : 50, 40 : 60, 20 : 80, and 0 : 100) were investigated using viscometric method. NaCMC, PVA, and their blend membranes were prepared by solution‐casting technique and were then crosslinked with glutaraldehyde (GA). The effect of blend composition on mechanical, swelling, and pervaporation results (flux and selectivity) was also investigated in this study. Attenuated total reflectance–Fourier transform infrared spectroscopy (ATR–FTIR) results showed that the blends are miscible over the entire studied composition range and further confirmed the crosslinking reaction with GA. FTIR studies reveal that the blends containing 50 : 50 (NaCMC/PVA) are an optimum miscible blend. Thermogravimetric analysis confirms that the thermal stability increased with increase in NaCMC content in NaCMC/PVA blend membrane. XRD and DSC showed a corresponding decrease in crystallinity and increase in melting point with increase in NACMC content, respectively. NaCMC/PVA blends of all the composition under study were used for dehydration of isopropyl alcohol at different compositions of IPA/water mixture (90 : 10, 87.5 : 12.5, 85 : 15, and 82.5 : 17.5) at 35°C. Swelling studies and PV results reveal that increase in NaCMC content in the blend leads to an increase in flux of water, whereas selectivity decreases. The optimum flux and selectivity were observed for the blend containing 50 : 50 NaCMC/PVA content at a feed ratio of 87.5 : 12.5 IPA/water. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Effect of pro‐oxidants on biodegradation of polyethylene (LDPE) by indigenous fungal isolate,Aspergillus oryzae

Proxidant additives represent a promising solution to the problem of the environment contamination with polyethylene film litter. Pro‐oxidants accelerate photo‐ and thermo‐oxidation and consequent polymer chain cleavage rendering the product apparently more susceptible to biodegradation. In the present study, fungal strain, Aspergillus oryzae isolated from HDPE film (buried in soil for 3 months) utilized abiotically treated polyethylene (LDPE) as a sole carbon source and degraded it. Treatment with pro‐oxidant, manganese stearate followed by UV irradiation and incubation with A. oryzae resulted in maximum decrease in percentage of elongation and tensile strength by 62 and 51%, respectively, compared with other pro‐oxidant treated LDPE films which showed 45% (titanium stearate), 40% (iron stearate), and 39% (cobalt stearate) decrease in tensile strength. Fourier transform infrared (FTIR) analysis of proxidant treated LDPE films revealed generation of more number of carbonyl and carboxylic groups (1630–1840 cm⁻¹ and 1220–1340 cm⁻¹) compared with UV treated film. When these films were incubated with A. oryzae for 3 months complete degradation of carbonyl and carboxylic groups was achieved. Scanning electron microscopy of untreated and treated LDPE films also revealed that polymer has undergone degradation after abiotic and biotic treatments. This concludes proxidant treatment before UV irradiation accelerated photo‐oxidation of LDPE, caused functional groups to be generated in the polyethylene film and this resulted in biodegradation due to the consumption of carbonyl and carboxylic groups by A. oryzae which was evident by reduction in carbonyl peaks. Among the pro‐oxidants, manganese stearate treatment caused maximum degradation of polyethylene. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Review: Investigation of Partially Pre-mixed Charge Ignitions (PPCI) Engine Mode

This paper embraces the key points of unpolluted internally combusted engine emissions. Core objective is focused on the recent effort to improve compression ignition(CI) and spark ignition(SI) engine to have fuel-efficient and minimized pollutant emissions. There are many advanced internal combustion engines to overcome the challenges of conventional compression ignition engines of the high level of particulate matter(PM) and oxides of nitrogen emission. One of the latest options on which many ...     

A Fast-Response DC Motor Speed Control System

This paper describes the design, construction, and testing of a thyristorized speed control unit for a separately excited dc motor. The motor is fed from a three-phase six-pulse fully controlled thyristor bridge. A speed loop with a proportional plus integral controller maintains the desired speed irrespective of the load variations on the motor. An inner current control loop protects the thyristors from overcurrents. This loop also provides fast response overcoming the effect of disturbances such as variations in supply voltage. The design aspects of the control loops are discussed, and experimental results are given.     

Molecular Sensing Using Hyperpolarized Xenon NMR Spectroscopy

Molecular imaging is the determination of the spatial location and concentration of specific molecules in a sample of interest. Sophisticated modern magnetic resonance imaging machines can collect NMR spectra from small-volume elements within a sample, enabling local chemical analysis. However, abundant water and fat signals limit detection of metabolites to near mM concentrations. Alternatively, targeted relaxation contrast agents enhance the relaxation of the strong water signal where they bind. A comparison of images with and without a contrast agent shows the target distribution, but high µM concentrations are needed. We have developed an approach that exploits the strong signals of hyperpolarized ¹²⁹Xe (an inert reporter introduced for imaging). The imaging contrast agents are composed of a biological recognition motif to localize the agent (antibodies or aptamers) and covalently tethered cryptophane cages. Xenon binds to the cryptophane and though chemical exchange saturation transfer creates contrast in a xenon image. Imaging agents can deliver many cages per target, giving detection limits in the pM concentration range. The evolution and principles of this approach are described herein.     

Photo-Chemically-Deposited and Industrial Cu/ZnO/Al2O3 Catalyst Material Surface Structures During CO2 Hydrogenation to Methanol: EXAFS,XANES and XPS Analyses of Phases After Oxidation,Reduction, and Reaction

Catalysis Letters - Industrial Cu/ZnO/Al2O3 or novel rate catalysts, prepared with a photochemical deposition method, were studied under functional CH3OH synthesis conditions at the set temperature...     

Biosorption of chromium onto Erythrina Variegata Orientalis leaf powder

The biosorption of chromium from an aqueous solution onto Erythrina Variegata Orientalis leaf powder was investigated in batch operations. The equilibrium agitation time was 180 min. The extent of chromium biosorption increased from 74.2% to 86.4% with decrease in biosorbent size from 150 to 45 μm for a dosage of 30 g/L. The biosorption decreased from 99.1 (0.45 mg/g) to 45.5% (1.64 mg/g) with an increase in chromium initial concentration (C _o ) from 22.5 to 180 mg/L. The extent of biosorption was maximum at pH=3. The experimental data were well explained by Langmuir and Redlich-Peterson isotherm models. The biosorption data followed second-order kinetics with a rate constant of 0.078 g/mg-min for 50 g/L of 45 μm size biosorbent. The biosorption was exothermic and feasible. The biosorption was tending towards irreversibility with increasing temperature.     

A new fluoride mediated synthesis of mesoporous silica and their usefulness in controlled delivery of duloxetine hydrochloride a serotonin re-uptake inhibitor

A new type of mesoporous silica nanoparticle (MSN) was synthesized in fluoride media via sol–gel technique using TritonX 100 and Tween-20. The surface area and pore volume of the MSN particles were modified by varying the concentration of Tween-20. The prepared MSN nanoparticles with large surface area and pore volume (T-2, T-3) were selected to accommodate the model drug duloxetine hydrochloride (DX) for evaluation of their drug-loading and release abilities. Calcined and DX loaded nanoparticles were characterized by Brunauer–Emmett–Teller technique (BET), powder X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric (TG) analysis and UV-diffuse reflectance (UV-DRS). In vitro release studies proved that the particle displays an initial burst release followed by sustained release for up to 140 h. From the studies it is evident that the synthesized particle may be useful as a carrier for sustained release of active pharmaceutical ingredients (APIs).