Perturbative effects on ultra-short soliton self-switching

A numerical study of ultra-short self-soliton switching along with the corresponding analysis of coupler parameters is carried out for a Kerr coupler with intermodal dispersion. The influence of perturbations like third-order dispersion, self-steepening and intrapulse Raman scattering, on switching characteristics is also studied.      

Synthesis of new 1,2-dideoxy C-linked carbo-β-amino acids and α/β-peptides with 11/9-helix,helix-turn and helix-turn-helix structures

The present study describes the synthesis of new C-linked carbo-β-amino acids [β-Caa_(1,2-ddx)], with a 1,2-dideoxy D-xylo furanoside side chain (a tetrahydro furan derivative). The stereochemistry at the newly created amine centers was determined by modified Mosher method. The (S)-β-Caa_(1,2-ddx) prepared from d-mannose diacetonide were utilized for the synthesis of 1:1 α/β-peptides with L-Ala. The conformational analysis (NMR, MD and CD) revealed the presence of 11/9-helix, helix induced helix-turn (HT) and helix-turn-helix (HTH) in these peptides. These side chains with tetrahydrofuran ring facilitated the formation of robust helix, unlike some other side chains from earlier studies.     

Synchrotron μ‐XRF study on compositional uniformity of uranium–thorium oxide pellets prepared by different processes

A μ‐XRF study to assess the distribution of uranium and thorium in (U,Th)O₂ pellets covering the composition of advanced heavy water reactor (AHWR) fuel pellets prepared by powder metallurgical compaction (PMC) and coated agglomerate pelletization (CAP) routes was made using micro‐focus beam line (BL‐16) of Indus‐2 synchrotron radiation facility. The methodology thus developed was successfully applied to these pellets. The study reveals that the uranium distribution in pellets prepared by PMC route is uniform, whereas the pellets prepared through CAP route have a wide range of compositional variation. In addition, the uniformity in CAP route‐prepared pellets improves with increase in the relative amount of uranium in the pellets. The sample preparation in present methodology is very simple compared with scanning electron microscopy. The study reveals the utility of synchrotron‐based μ‐XRF for fuel pellet characterization of AHWR reactors. Alhough CAP route of fuel pellet preparation requires less exposure of personnel to high radiation dose, the non‐uniformity in the fuel pellet must be considered when using these pellets in reactors. Copyright © 2014 John Wiley & Sons, Ltd.     

A comparative study on determination of uranium and thorium in their mixed oxides by EDXRF using tube and radioisotope X‐ray sources

Studies on the matrix effects of uranium and thorium on the determinations of each other in their mixed oxides using energy dispersive X‐ray fluorescence (EDXRF) spectrometry with tube and radioisotope excitations of U Lα and Th Lα are reported. An internal standard method for the determination of uranium and thorium in these mixed oxides is found suitable. Comparison of the analytical results of EDXRF determinations of uranium and thorium using tube and radioisotope excitation sources has been made. The analytical methodology involves preparation of mixed oxide calibration/sample mixtures of uranium and thorium oxides, mixing of internal standard yttrium in these mixtures, pelletizing the mixtures after thorough mixing and grinding using boric acid binder and measuring EDXRF spectra of the specimens thus prepared using Rh X‐ray tube as well as ¹⁰⁹Cd radioisotope source. The samples were analyzed for uranium and thorium on the basis of the calibration plots obtained by plotting the intensity ratios of the analyte and internal standard characteristic X‐ray lines and their corresponding amount ratios. An average precision of 1.2% (1 s RSD) was observed for the determination of U and Th and the results deviated from the corresponding expected values by 3% on average. Due to the refractory nature of thorium oxide, comparatively more grinding time was required for thorium determinations. Copyright © 2011 John Wiley & Sons, Ltd.     

Experimental investigation of the effect of initial fuel particle shape, size and bed temperature on devolatilization of single wood particle in a hot fluidized bed

Considerable amount of investigation on the subject of devolatilization of wood is found in the open literature. However, a systematic study of the effect of initial particle size and shape, and bed temperature on devolatilization time and char yield of wood in a hot fluidized bed is still missing. This paper attempts to fill this gap through a systematic experimental investigation to determine the devolatilization time and char yield of a typical woody biomass, “Casuarina equisetifolia” particles of different initial sizes and shapes at various fluidized bed temperatures. Experiments are conducted using 10, 15, 20, and 25 mm Casuarina wood particles of three shapes, namely, cube, cylinder, and sphere at bed temperatures of 1023, 1123, and 1223 K.It is found that the initial wood particle size has the strongest influence on devolatilization time followed by the shape of initial wood particle and the bed temperature. Correlation for devolatilization time (τ_d) as a function of initial wood particle size (d_eq), sphericity (?), and bed temperature (T_b), is developed using 573 experimental data points exhibiting a correlation coefficient of 0.96 and predictions falling well within a deviation band of ±20%. The predictions of the present correlation are compared with the predictions of the existing correlations in literature for conditions also out of the present study and the deviation is found to be ±30%.Char yield, defined as the ratio of the residual mass at the end of devolatilization process to the initial mass of the wood particle is found to be in the range of 9-14% for all sizes, shapes, and bed temperatures. Char yield does not depict any definite trend with the variation of initial particle size, shape and bed temperature.