Phase knife-edge laser Schlieren diffraction interferometry with boundary diffraction wave theory

Within the framework of boundary diffraction wave theory it has been shown that the first bright fringe on either side of the central dark fringe of the phase knife-edge Fresnel diffraction pattern could be broadened to cover the whole field of view. Broadening of the first diffraction fringe, instead of conventionally modifying the spatial frequency spectrum, enhances the sensitivity of the Schlieren system. The use of phase knife-edge as viewing diaphragm in Schlieren diffraction interferometry not only enhances the fringe contrast but also avoids the loss in phase information as it lets through light from all parts of the test object and its thin interfacing makes the method suitable even for studying weak disturbances.      

Small angle neutron scattering study of U(VI) third phase formation in HNO<Subscript>3</Subscript>/DHDECMP-<Emphasis Type="Italic">n</Emphasis>-dodecane system

Small angle neutron scattering studies (SANS) were carried out to understand the formation of third phase in DHDECMP-dodecane-UO₂(NO₃)₂/HNO₃ system. It was observed that third phase formation takes place due to the formation of UO₂(NO₃)₂.DHDECMP reverse micelles in the dodecane phase. SANS data obtained were interpreted with particle interaction model using Baxter sticky spheres model.      

Longitudinal double-spin asymmetry for inclusive jet production in p[over -->] + p[over -->] collisions at sqrt[s]=200 GeV

We report a new STAR measurement of the longitudinal double-spin asymmetry A(LL) for inclusive jet production at midrapidity in polarized p + p collisions at a center-of-mass energy of sqrt[s]=200 GeV. The data, which cover jet transverse momenta 5相似文献   

Suppression of high-p{T} neutral pion production in central Pb+Pb collisions at sqrt[S{NN}]=17.3 GeV relative to p+C and p+Pb collisions

Neutral pion transverse momentum spectra were measured in p+C and p+Pb collisions at sqrt[S{NN}]=17.4 GeV at midrapidity (2.3 less than or approximately equal eta{lab} less than or approximately equal 3.0) over the range 0.7 less than or approximately equal p{T} less than or approximately equal 3.5 GeV/c. The spectra are compared to pi{0} spectra measured in Pb+Pb collisions at sqrt[S{NN}]=17.3 GeV in the same experiment. For a wide range of Pb+Pb centralities (N{part} less than or approximately equal 300), the yield of pi{0}'s with p{T} greater than or approximately equal 2 GeV/c is larger than or consistent with the p+C or p+Pb yields scaled with the number of nucleon-nucleon collisions (N{coll}), while for central Pb+Pb collisions with N{part}greater than or approximately equal 350, the pi{0} yield is suppressed.     

Divergent,Stereospecific Mono‐ and Difluoromethylation of Boronic Esters

There is considerable interest in incorporating fluorine into agrochemicals and pharmaceuticals to improve their biological properties. Whilst a number of methods have been reported for installing CH₂F and CHF₂ groups, they are mainly limited to radical reactions, which are invariably racemic. Herein, we report the divergent, stereospecific reaction of fluoroiodomethyllithium with boronic esters to give α‐fluoro‐boronic esters. These unique intermediates can be readily transformed into the corresponding mono‐ or difluoromethylated compounds through proto‐ or fluorodeboronation, respectively. The use of the highly unstable fluoroiodomethyllithium was key to allowing rapid 1,2‐migration over competing decomposition of the carbanion. DFT calculations informed and supported the experimental findings.     

Ring-Opening Lithiation–Borylation of 2-Trifluoromethyl Oxirane: A Route to Versatile Tertiary Trifluoromethyl Boronic Esters

Stereogenic trifluoromethyl-substituted carbon centers are highly sought-after moieties in pharmaceutical and agrochemical discovery. Here, we show that lithiation–borylation reactions of 2-trifluoromethyl oxirane give densely functionalized and highly versatile trifluoromethyl-substituted α-tertiary boronic esters. The intermediate boronate complexes undergo the desired 1,2-rearrangement of the carbon-based group with complete retentive stereospecificity, a process that was only observed in non-polar solvents in the presence of TESOTf. Although the trifluoromethyl group adversely affects subsequent transformations of the α-boryl group, Zweifel olefinations provide trifluoromethyl-bearing quaternary stereocenters substituted with alkenes, alkynes and ketones.     

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.     

Octave spanning supercontinuum in an As₂S₃ taper using ultralow pump pulse energy

An octave spanning spectrum is generated in an As?S? taper via 77 pJ pulses from an ultrafast fiber laser. Using a previously developed tapering method, we construct a 1.3 μm taper that has a zero-dispersion wavelength around 1.4 μm. The low two-photon absorption of sulfide-based chalcogenide fiber allows for higher input powers than previous efforts in selenium-based chalcogenide tapered fibers. This higher power handling capability combined with input pulse chirp compensation allows an octave spanning spectrum to be generated directly from the taper using the unamplified laser output.     

Asymmetric synthesis of tertiary and quaternary allyl- and crotylsilanes via the borylation of lithiated carbamates

Tertiary allyl- or crotylsilanes have been prepared in high er and dr via the lithiation-borylation reaction of alkyl carbamates with silaboronates. Using a related strategy, quaternary allylsilanes could be accessed in similarly high er.