The new Batch Mode Ion Source for stand-alone operation at the Facility for Rare Isotope Beams (FRIB)

Gas stoppers have been used for a long-standing successful science program at Michigan State University with stopped and rare-isotope beams produced by projectile fragmentation. The National Superconducting Cyclotron Laboratory’s Coupled Cyclotron Facility has recently transitioned into the Facility for Rare Isotope Beams (FRIB) laboratory to provide rare isotopes using a high-power superconducting linear accelerator and new production facilities. To allow the science program with stopped and reaccelerated beams to continue during the transition period, a stand-alone capability was added. The Batch Mode Ion Source (BMIS) was built and has been providing beams of long-lived and stable isotopes of a variety of elements for successful user experiments. The BMIS system is described and results from the production of various beams are presented

Effective coupling of phenol adsorption and photodegradation at the surface of micro-and mesoporous TiO2-activated carbon materials

International audienceNovel titania supported activated carbon catalysts were prepared by a straightforward titania coating route of a microporous activated carbon (AC) derived from shea nut shells, and investigated in phenol photocatalytic degradation. The proposed coating method enables a fixation of the preformed titania anatase nanoparticles (TiO2 NPs) in the external porosity thus allowing their accessibility towards UV irradiation, without causing any reduction of the AC specific area. Interestingly, the coating treatment reshapes the porous texture of the as-prepared TiO2–AC composite materials resulting in an improvement of the adsorption capacity and the formation of an additional mesoporosity on the TiO2-AC surface. Photocatalytic experiments carried out in a batch reactor led to 97% elimination rate of phenol in an aqueous solution with the AC catalysts containing TiO2 NPs in the range from 11 to 34 wt%. The photodegradation performance of the TiO2–AC catalysts was maintained over several successive cycles, without the need of any regeneration treatment. Considering both the textural and microstructural features of the composite materials and their associated phenol removal kinetics, in this paper, we provide new insights into phenol photodegradation pathway involving an effective coupling of adsorption and photodegradation functionalities, resulting in a photo-assisted regeneration mechanism of the catalyst