Sodium ion conducting gel polymer electrolytes based on polyacrylonitrile (PAN) with ethylene carbonate and dimethyl formamide as plasticizing solvents are prepared by the solution cast technique. These electrolyte films are free standing, transparent and dimensionally stable. Na ? ions are derived from NaI. The structural properties of pure and complex formations have been examined by X-ray diffraction, Fourier transform infrared spectroscopic studies and differential scanning calorimetric studies. The variation of the conductivity with salt concentration ranging from 10 to 40 wt% is studied. The sample containing 30 wt% of NaI exhibits the highest conductivity of 2.35 9 10 -4 S cm -1 at room temperature (303 K) and 1 9 10 -3 S cm -1 at 373 K. The conductivity-temperature dependence of polymer electrolyte films obeys Arrhenius behavior with activation energy in the range of 0.25-0.46 eV. The transport numbers both electronic (t e ) and ionic (t i ) are evaluated using Wagner's polarization technique. It is revealed that the conducting species are predominantly due to ions. The ionic transport number of highest conducting film is found to be 0.991. Solid-state battery with configuration Na/(PAN ? NaI)/(I 2 ? C ? electrolyte) is developed using the highest conducting gel polymer electrolyte system and the discharge characteristics of the cell are evaluated over the load of 100 KX.

ZnFe2O4 is one of the most important technological material having applications in radio engineering, radio technology, semiconductors, bio-medical applications etc. ZnFe2O4 when in bulk form shows paramagnetic behavior at room temperature. When ZnFe2O4 is synthesized by some techniques it was possible to see the ferromagnetic behavior. Also, ZnFe2O4 in nanocrystalline form exhibit different magnetic properties. Therefore in the present work we intend to present the properties of particle size behavior of ZnFe2O4 nanoparticles. ZnFe2O4 nanoparticles were synthesized by oxalic acid based precursor method. The obtained ZnFe2O4 nano powders were thermally annealed from 300 to 600 °C. The structural and magnetic characterization were measured using X-ray diffraction (XRD), scanning electron microscope (SEM), IR measurements and vibrating sample magnetometer (VSM). XRD patterns clearly showed the formation of zinc ferrite. The particle size was observed to increase from 19 to 35 nm with increasing annealing temperature. The lattice constants were observed to decrease with increasing particle size. The nanoparticles size were confirmed using SEM measurements. IR measurements were carried to confirm the phase formation of ZnFe2O4 nanoparticles. The Infrared spectra showed the characteristic features of vibrational bands corresponding to spinel ferrite. Room temperature ferromagnetic properties were observed for zinc ferrite having particle sizes 19 and 21 nm. For the particle size 29 and 35 nm it showed paramagnetic nature. The magnetic properties of zinc ferrite nanoparticles were observed to be dependent on the particle size.

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Purpose: The authors report comprehensive commissioning and quality assurance (QA) procedures for Intrabeam, Intra-Operative radiotherapy (IORT) unit. The Intrabeam system miniature X-ray source is a 50 kV and 40 µA unit. Methods: The authors' tests include measurements of output, beam deflection, isotropy, kVp and mAs measurements, quality index, isodose, reproducibility, linearity, depth dose verification, and 3D dose distribution. IC ionization chamber and the UNIDOSE dosimeter were used for the output commissioning. Probe adjuster/ionization chamber holder (PAICH) was used to check the mechanical straightness of the probe. For radiation tests, NACP parallel plate chamber, Standard Imaging electrometer, 30 × 30 × 30 cm 3 IAEA water phantom, solid water slabs, EDR-2 Films with RIT software, and ionization based survey meters were used. Unfors Xi platinum edition kVp meter was used to measure the kVp and mAs. Results: In mechanical QA test, X-Beam position (-0.09 mm), Y-Beam position (0.01 mm), and radial position (0.11 mm) errors were within the tolerance level. Isotropy test with PDA, survey meter, ion chamber, and film measurements also produced results within the specifications. Output measurements with PAICH and external chamber measurements were matched. Beam quality, linearity, and reproducibility values were ascertained at 50KV and 40 µA and found to be within limits. Isodose, 3D dose distribution, transverse, and horizontal profiles showed the good isotropy of the source. Conclusion: The authors' methodology provides comprehensive commissioning and calibration procedures for the Intrabeam system.