Radiation grafting: A voyage from bio-waste corn husk to an efficient thermostable adsorbent.

The initiator free environmentally benign gamma radiation is employed to graft poly-acrylic acid (PAA) onto the widely produced bio-waste corn husk to develop promising, cheap, efficient and reusable adsorbent (AAc-g-husk) having specific adsorption capacity of 1682.7mgg-1 of methylene blue (MB) at pH 9.0 and 320K. The most suitable grafting yield is found by optimizing absorbed dose, dose rate and concentrations of monomer, Mohr's salt and inorganic acid. The inter-planar hydrogen bonding among (002) planes of cellulose in the husk decreases after diversifying grafting of PAA on ad-axial, ribs and micro-fibrils surfaces of the corn husks. The chemically and structurally modified AAc-g-husk shows superior thermal stability. The mechanism of MB dye adsorption by AAc-g-husk has been discussed through six two-parameters adsorption isotherm and ten three-parameters adsorption isotherm models at three different temperatures (300, 310 and 320K), seven kinetic models at room temperature, FT-IR and desorption studies in different solvent compositions.

Mineralization and biodegradability enhancement of Methyl Orange dye by an effective advanced oxidation process.

An effective process for the oxidation of Methyl Orange dye (MO) was determined by comparing the mineralization efficiency between two advanced oxidation processes (AOPs) viz., ozonolysis and gamma radiolysis in presence and absence of an added inorganic salt potassium persulfate (K2S2O8). The effects of various operating parameters such as ozone flow rate and reaction temperature were optimized to achieve the best possible mineralization extent of MO by ozonolysis. The mineralization efficiency of MO was significantly enhanced during gamma radiolysis in presence of K2S2O8 (γ+K2S2O8) compared to in absence of K2S2O8. The presence of methyl group at the amine of phenyl ring assisted the mineralization of dye during γ+K2S2O8. The oxygen-equivalent chemical-oxidation capacities (OCC) of ozonolysis and γ+K2S2O8 for 75% mineralization of the dye solution were calculated as 7.008 and 0.0336kg equiv. O2 m-3, respectively which signifies that γ+K2S2O8 can be explored as an effective AOP. The non-biodegradable MO dye solution became biodegradable even after the dose of 0.5 kGy during γ+K2S2O8 compared to 1 kGy in absence of K2S2O8. The study concludes that a lower dose γ+K2S2O8 could be one of the efficient pretreatment steps before undergoing biological degradation of dye solution.

Efficient degradation of butylparaben by gamma radiolysis.

Gamma radiolysis and ozonolysis are two competitive advanced oxidation processes for degradation of organic pollutants present in the ground water. In this paper, the gamma radiolytic degradation of an emerging organic pollutant Butylparaben (BP) in aqueous solution has been investigated for the first time at different absorbed doses. The effect of the absorbed dose rate in the degradation and mineralization of BP has been investigated. About 65% mineralization of BP was observed at absorbed dose of 70kGy and dose rate of 0.7kGyh-1. Interestingly, turbidity appeared in the solution during radiolysis at doses higher than 2kGy, which disappeared again at very higher dose (~90kGy) making the solution again transparent. At lower dose rate of 0.175kGyh-1 the turbidity was appeared at much lower dose about 1kGy. However, the dose rate showed no effect in the dose of the disappearance of the turbidity. The hydrophobic fragments insoluble in water were generated during the initial stage of gamma radiolysis and those were completely mineralized to CO2 and H2O by direct absorption of gamma radiation. About 90kGy dose was required to achieve ~90% mineralization of BP. On the contrary, maximum 50% mineralization was achieved after 5h of ozonation at the O3 flow rate of 0.5Lmin-1 at pH 7.5 and it remained even constant upon prolonged ozonation. The oxygen-equivalent-chemical-oxidation-capacity (OCC) was used as the parameter to compare the % mineralization efficiencies of the two oxidative processes studied here and the gamma radiolysis was found to be more efficient between those processes. The phytotoxicity of the treated BP solution to agricultural seeds showed that the radiolytically generated fragments were less toxic compared to ozonolytically generated fragments. Thus gamma radiolysis is effective for reducing the organic burden and the toxicity of water polluted with emerging pollutants like BP.

Melt-compounded composites of ethylene vinyl acetate with magnesium sulfate as flexible EPR dosimeters: Mechanical properties, manufacturing process feasibility and dosimetric characteristics.

Novel polymeric composites for radiation dosimetry were developed. The composites were prepared by solvent-free melt compounding of ethylene vinyl acetate (EVA) (40% vinyl) and magnesium sulfate (MgSO4). Mechanical properties, melt flow characteristics and dosimetric properties were investigated. The composites with up to 50% (wt) of MgSO4 were flexible and capable of flow. The dose response of the EPR signal of the composites was studied in the dose range 3Gy-4kGy and found to be linear between 18Gy and 4kGy. The reproducibility of dose measurements was good. The signal fading rate and the energy dependence of the dose response were found to be acceptable.

Synthesis of a flexible poly(chloroprene)/methyl red film dosimeter using an environment-benign shear compounding method.

The paper reports synthesis of a new film dosimeter based on a solvent-free route. Methyl red (MR) dye was introduced into poly(chloroprene) (PC) in various concentrations. The films were intensely red with λmax ~515nm. The absorbance decreased linearly with absorbed radiation dose up to 30kGy without a significant change in λmax. Color coordinates of the films were also analyzed. Optical micrographs of the films showed no signs of inhomogeneous distribution of MR in the PC matrix, which was attributed to the polarity of PC. Radiation sensitivity, dose response linearity, effects of irradiation temperature and humidity, as well as the rate of fading, were also investigated.

Development of adsorbent from Teflon waste by radiation induced grafting: equilibrium and kinetic adsorption of dyes.

Mutual radiation grafting technique was employed to graft polyacrylic acid (PAA) onto Polytetrafluoroethylene (Teflon) scrap using high energy gamma radiation. Polyacrylic acid-g-Teflon (PAA-g-Teflon) adsorbent was characterized by grafting extent measurement, FTIR spectroscopy, SEM and wet ability & surface energy analysis. The PAA-g-Teflon adsorbent was studied for dye adsorption from aqueous solution of basic dyes, namely, Basic red 29 (BR29) and Basic yellow 11 (BY11). The equilibrium adsorption data were analyzed by Langmuir and Freundlich adsorption isotherm models, whereas, adsorption kinetics was analyzed using pseudo-first order, pseudo-second order and intra-particle diffusion kinetic models. Equilibrium adsorption of BR29 was better explained by Langmuir adsorption model, while that of BY11 by Freundlich adsorption model. The adsorption capacity for BY11 was more than for BR29. Separation factor (R(L)) was found to be in the range 0 < R(L) < 1, indicating favorable adsorption of dyes. Higher coefficient of determination (r(2) > 0.99) and better agreement between the q(e,cal) and q(e,exp) values suggested that pseudo-second order kinetic model better represents the kinetic adsorption data. The non-linearity obtained for intra-particle diffusion plot indicated, more than one process is involved in the adsorption of basic dyes. The desorption studies showed that ~95% of the adsorbed dye could be eluted in suitable eluent.

Swelling response of radiation synthesized 2-hydroxyethylmethacrylate-co-[2-(methacryloyloxy)ethyl] trimethylammonium chloride hydrogels under various in vitro conditions.

High-energy (60)Co gamma radiation has been used to synthesize 2-hydroxyethylmethacrylate-co-[2-(methacryloyloxy)ethyl]trimethylammonium chloride (HEMA-co-MAETC) polyelectrolyte hydrogels. HEMA-co-MAETC co-polymer gels were characterized and investigated for swelling behaviour in different swelling conditions. Fourier transformed infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM) techniques were used to characterize the co-polymer gels. Swelling extent of the gels was found to be a linear function of MAETC content in the gels. The effect of ionic strength, temperature, pH, some solutes of biological importance like glucose, urea, and surfactants such as Triton-X and deoxycholic acid on swelling behavior have been reported. The swelling of gels at higher temperature enhanced the swelling rates but not the swelling extent. HEMA-co-MAETC hydrogel exhibited an excellent responsive characteristic to the ionic strength of the swelling medium. It was found that the swelling of the co-polymer gel at 60 degrees C reduced the swelling-deswelling cycle time by approx. 30% without altering the swelling extent. The gels were also investigated for their swelling in aqueous solutions of anionic dyes, acid blue 25 (AB25), acid blue (AB74) and acid yellow 99 (AY99), and were found to be suitable for dye uptake applications.

Electron beam irradiation: a novel technology for the development of transdermal system of isosorbide dinitrate.

The development of a transdermal delivery system for isosorbide dinitrate (ISDN) using electron beam irradiation was studied. The solid state stability of the drug to irradiation was assessed. The drug was dissolved in 2-ethylhexylacrylate (EHA)-acrylic acid (AA) system and this solution was directly irradiated on a backing membrane (Scotchpak1006) at different doses to get transdermal patches. The developed systems were evaluated for residual monomer content, equilibrium weight swelling ratios (EWSR), differential scanning calorimetry (DSC), weight uniformity, thickness uniformity, drug content and content uniformity, peel strength, in vitro release, skin permeation kinetics and skin irritation potential. The developed system possessed excellent adhesive properties. Increase in the irradiation doses did not have a significant effect on the peel strength values. The systems exhibited promising skin permeation kinetics and no skin irritating potential, both of which are important properties for transdermal drug delivery. The ISDN-EHA-AA system developed at an irradiation dose of 50 kGy showed a higher skin permeation profile as compared to an internationally marketed transdermal matrix system of ISDN.