Controlled Transverse Emittance Blow-up in the CERN SPS

For several years, a large variety of beams have been prepared in the LHC injectors, such as single-bunch and multi-bunch beams, with 25 ns, 50 ns and 75 ns bunch spacings, nominal and intermediate intensities per bunch. As compared to the nominal LHC beam (i.e. with nominal bunch intensity and 25 ns spacing) the other beams can be produced with lower transverse emittances. Beams of low transverse emittances are of interest during the commissioning phase for aperture considerations and because of the reduced long-range beam-beam effects. On the other hand machine protection considerations might lead to prefer nominal transverse emittances for safe machine operations. The purpose of this paper is to present the results of controlled transverse emittance blow-ups using the transverse feedback and octupoles. The procedures tested in the SPS in 2008 allow to tune the transverse emittances up to nominal values at SPS extraction

Physical Modelling of the Flow Field in an Undular Tidal Bore

A tidal bore may form in a converging channel with a funnel shape when the tidal range exceeds 6-9 m. The advancing surge has a major impact on the estuarine ecosystem. Physical modelling of an undular bore has been conducted based upon a quasi-steady flow analogy. The experimental data highlight rapid flow redistributions between successive wave troughs and crests as well as large bottom shear stress variations. The results suggest a sediment transport process combining scour beneath wave troughs associated with upward matter dispersion between a trough and the following wave crest. The process is repeated at each trough and significant sediment transport takes place with deposition in upstream intertidal zones. The conceptual model is supported by field observations showing murky waters after the bore passage and long-lasting chaotic waves

First Results for the Beam Commissioning of the CERN Multi-Turn Extraction

The Multi-Turn Extraction (MTE), a new type of extraction based on beam trapping inside stable islands in horizontal phase space, has been commissioned during the 2008 run of the CERN Proton Synchrotron. Both singleand multi-bunch beams with a total intensity up to 1.4 1013 protons have been extracted with efficiencies up to 98%. Furthermore, injection tests in the CERN Super Proton Synchrotron were performed, with the beam then accelerated and extracted to produce neutrinos for the CERN Neutrino-to-Gran Sasso experiments. The results of the extensive measurement campaign are presented and discussed in detail

Energy dispersive detector for white beam synchrotron x-ray fluorescence imaging

A novel, "single-shot" fluorescence imaging technique has been demonstrated on the B16 beamline at the Diamond Light Source synchrotron using the HEXITEC energy dispersive imaging detector. A custom made furnace with 200μm thick metal alloy samples was positioned in a white X-ray beam with a hole made in the furnace walls to allow the transmitted beam to be imaged with a conventional X-ray imaging camera consisting of a 500 μm thick single crystal LYSO scintillator, mirror and lens coupled to an AVT Manta G125B CCD sensor. The samples were positioned 45° to the incident beam to enable simultaneous transmission and fluorescence imaging. The HEXITEC detector was positioned at 90° to the sample with a 50 μm pinhole 13cm from the sample and the detector positioned 2.3m from pinhole. The geometric magnification provided a field of view of 1.1×1.1mm2 with one of the 80×80 pixels imaging an area equivalent to 13μm2. Al-Cu alloys doped with Zr, Ag and Mo were imaged in transmission and fluorescence mode. The fluorescence images showed that the dopant metals could be simultaneously imaged with sufficient counts on all 80x80 pixels within 60s, with the X-ray flux limiting the fluorescence imaging rate. This technique demonstrated that it is possible to simultaneously image and identify multiple elements on a spatial resolution scale ~10μm or higher without the time consuming need to scan monochromatic energies or raster scan a focused beam of X-rays. Moving to high flux beamlines and using an array of detectors could improve the imaging speed of the technique with element specific imaging estimated to be on a 1s timescale

Mapping of multi-elements during melting and solidification using synchrotron X-rays and pixel-based spectroscopy.

A new synchrotron-based technique for elemental imaging that combines radiography and fluorescence spectroscopy has been developed and applied to study the spatial distribution of Ag, Zr and Mo in an Al alloy during heating and melting to 700, and then re-soldification. For the first time, multi-element distributions have been mapped independently and simultaneously, showing the dissolution of Ag- and Zr-rich particles during melting and the inter-dendritic segregation of Ag during re-solidification. The new technique is shown to have wide potential for metallurgical and materials science applications where the dynamics of elemental re-distribution and segregation in complex alloys is of importance

Characterization of a submicro-X-ray fluorescence setup on the B16 beamline at Diamond Light Source

An X-ray fluorescence setup has been tested on the B16 beamline at the Diamond Light Source synchrotron with two different excitation energies (12.7 and 17 keV). This setup allows the scanning of thin samples (thicknesses up to several micrometers) with a sub-micrometer resolution (beam size of 500 nm × 600 nm determined with a 50 µm Au wire). Sensitivities and detection limits reaching values of 249 counts s−1 fg−1 and 4 ag in 1000 s, respectively (for As Kα excited with 17 keV), are presented in order to demonstrate the capabilities of this setup. Sample measurements of a human bone and a single cell performed at B16 are presented in order to illustrate the suitability of the setup in biological applications.</jats:p

Unlocking full and fast conversion in photocatalytic carbon dioxide reduction for applications in radio-carbonylation

Harvesting sunlight to drive carbon dioxide (CO2) valorisation represents an ideal concept to support a sustainable and carbon-neutral economy. While the photochemical reduction of CO2 to carbon monoxide (CO) has emerged as a hot research topic, the full CO2-to-CO conversion remains an often-overlooked criterion that prevents a productive and direct valorisation of CO into high-value-added chemicals. Herein, we report a photocatalytic process that unlocks full and fast CO2-to-CO conversion (&lt;10 min) and its straightforward valorisation into human health related field of radiochemistry with carbon isotopes. Guided by reaction-model-based kinetic simulations to rationalize reaction optimisations, this manifold opens new opportunities for the direct access to 11C- and 14C-labeled pharmaceuticals from their primary isotopic sources [11C]CO2 and [14C]CO2