Preparation and physicochemical study of jute and glass composites of epoxy resin of (2E, 6E)-bis(4-hydroxybenzylidene)cyclohexanone

Polymer Bulletin - Jute and glass composites of epoxy resin of (2E, 6E)-bis(4-hydroxybenzylidene)cyclohexanone (EBHBC) were prepared by compressing molding technique using three different hardeners...     

Solvothermal synthesis of greigite (Fe3S4)– Conducting polypyrrole nanocomposite and its application towards arsenic removal

In the present investigation, Greigite-conducting polypyrrole nanocomposite (GPPy nanocomposite) was prepared, characterized and used to remove arsenite and arsenate from aqueous solution. Fe₃S₄ was synthesized using solvothermal synthetic method and it was grafted to conducting polypyrrole matrix. The nanocomposite was characterized using FE-SEM, EDX, XRD, FTIR, TGA/DSC and BET surface area. Kinetic studies revealed that the removal process followed first order kinetics. Batch isotherm studies were performed to determine the binding capacity. Thermodynamic parameters were also computed and it indicated the spontaneous nature of the process. Electrophoretic studies were carried out to determine the point of zero charge.     

Effect of a Hydrophilic PEO–PPO–PEO Copolymer on Cetyltrimethyl Ammonium Tosylate Solutions in Water

Cetyltrimethyl ammonium tosylate (CTAT) in water forms long flexible wormlike micelles at concentrations above 10 mM, leading to highly viscous solutions and viscoelastic stiff gels above 100 mM. In the presence of a nonmicellar hydrophilic PEO–PPO–PEO triblock copolymer F87 (TBC-F87, Total mol.wt. = 7,700, EO = 70%) these wormlike micelles RE transformed into smaller structures, as evident from a sharp decrease in viscosity and increase in specific conductance. These results are quantified by small angle neutron scattering (SANS) measurements. The PPO middle block of TBC-F87 gets inserted in the CTAT micelle, the size and total aggregation number of CTAT/TBC-F87 mixed micelles decreased but the number of TBC-F87 molecules in the mixed micelles increased with an increase in [TBC-F87]. Two break points in the typical specific conductance versus CTAT concentration plot at various [TBC-F87] amounts represent interactions between CTAT and TBC-F87. The penetration of PPO of TBC-F87 inside CTAT micelles decreases hydrophobicity of the core while the presence of PEO end blocks enhances hydrophilicity each favoring smaller micelles.     

INTRODUCTION TO INCONEL ALLOY 740: AN ALLOY DESIGNED FOR SUPERHEATER TUBING IN COAL-FIRED ULTRA SUPERCRITICAL BOILERS

1. IntroductionW hile w orldw ide environm entalrestrictionsare requiring pow ercom paniesto reduce SO x,N O x andCO 2 em issions, econom ic pressuresare sim ultaneously necessitating im provem entsin the therm aleffi-ciency ofallcoal-fired plants. A ddin…     

Synthesis and characterization of poly(ether sulfone) grafted poly(styrene sulfonic acid) for proton conducting membranes

Two-step synthesis of proton-conducting poly(ether sulfone) (PES) graft copolymer electrolyte membrane is proposed. Fridel Craft alkylation reaction was used to introduce chloromethyl pendant group onto the PES polymer backbone. Later on, atom transfer radical polymerization (ATRP) was applied to synthesize a series of poly(ether sulfone) grafted poly(styrene sulfonic acid) (PES-g-PSSA). Successful chloromethyl substitution and grafting of the pendant group was characterized by the ¹H-NMR and elemental analysis. Electrochemical properties such as ion exchange capacity (IEC), water uptake and proton conductivity increased with increasing PSSA contents. Thermal gravimetric analysis (TGA) showed the thermal stability of membranes up to 270 °C. Proton conductivity for maximum amount of grafting was 0.00297 S/cm.     

Preparation and characterization of proton conducting polysulfone grafted poly(styrene sulfonic acid) polyelectrolyte membranes

The syntheses of series of proton conducting comb copolymer membrane involving polysulfone back bone as main chain and poly(styrene sulfonic acid) (PSSA) being side chain, i.e. polysulfone grafted poly(styrene sulfonic acid) (PSU-g-PSSA) are presented. Chloromethylation of the polysulfone backbone was done by Fridel Craft alkylation reaction. Atom transfer radical polymerization was used for control grafting from the chloromethylated positions. The successful substitution of the chloromethyl group and its grafting with PSSA was characterized by elemental analysis and proton nuclear magnetic resonance. Water uptake, electrochemical properties like ion exchange capacity (IEC) and proton conductivities increase with increase in PSSA contents. Thermal gravimetric analysis (TGA) showed the thermal stability of membranes up to 250 °C. Proton conductivity for maximum amount of grafting is 0.02 S/cm.     

Experimental study of chemical treatment of coal fly ash to reduce the mobility of priority trace elements

Coal fired electric power plants produce large volumes of fly ash and other coal combustion by-products (CCBs) every year. Although almost 50% of the fly ash produced in the US is recycled for beneficial use, most of the ash material is disposed in dry landfills and ash lagoon impoundments. Fly ash may contain hazardous leachable trace elements such as As, B, Cr, Mo, Ni, Se, Sr and V which have a negative impact on the environment due to potential leaching by acid rain and groundwater with time. Many of the older CCB disposal facilities are unlined and unmonitored and as a result the EPA is currently developing national standards for monitoring CCB disposal sites. The cost to the US electric power industry could exceed one billion dollars if existing and closed CCB disposal facilities come under regulation. Thus simple, low-cost and effective in situ chemical treatment techniques are needed to stabilize hazardous leachable trace elements in the coal combustion by-product (CCB) materials. This paper reports the results of experiments designed to chemically treat fly ash with ferrous sulfate solutions to immobilize hazardous leachable trace elements after disposal.The current study is focused on three acidic and one alkaline fly ash samples collected from electric power plants located in the southeastern United States that were treated with two ferrous sulfate treatment solutions. The first treatment solution contained ferrous sulfate (FS) to give 322 mg/L of dissolved iron, while the second treatment solution contained the same concentration of ferrous sulfate along with excess calcium carbonate (FS + CC) to buffer the pH. Fly ash treatment experiments were carried out at solid:liquid (S:L) ratios of 1:3 and 1:30. The effectiveness of the treatment methods was evaluated by sequentially leaching the treated and the untreated fly ash samples using a synthetic acid rain (SAR) solution (US EPA Method 1312B SPLP fluid) as the leachate. The best overall treatment result was shown by the unbuffered ferrous sulfate solution at the 1:30 S:L ratio, which substantially reduced the mobility of the oxyanion trace elements. The overall mobility reduction achieved for As was 23-72%, B mobility was reduced by 43-80%, Cr by 45-77%, Mo by 21-90%, Se by 41-85% and V by 41-53% The unbuffered ferrous sulfate treatment was not effective for immobilization of the cationic trace elements Ni and Sr.