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- MIGRATE: mobile device virtualisation through state transferPublication . Santa, José; Ortiz, Jordi; Fernandez, Pedro J.; Luís, Miguel; Gomes, Christian; Oliveira, Jorge; Gomes, Diogo; Sanchez-Iborra, Ramon; Sargento, Susana; Skarmeta, Antonio F.Delegation of processing tasks to the network has moved from cloud-based schemes to edge computing solutions where nearby servers process requests in a timely manner. Virtualisation technologies have recently given data cloud and network providers the required flexibility to offer such on-demand resources. However, the maintenance of close computing resources presents a challenge when the served devices are on the move. In this case, if processing continuity is desired, a transference of processing resources and task state should be committed to maintain the service to end devices. The solution here presented, MIGRATE, proposes the concept of virtual mobile devices (vMDs) implemented as Virtual Functions (VxF) and acting as virtual representatives of physical processing devices. vMDs are instantiated at the edge of the access network, following a Multi-Access Edge Computing (MEC) approach, and move across different virtualisation domains. MIGRATE provides seamless and efficient transference of these software entities to follow the real location of mobile devices and continue supporting their physical counterparts. Software Defined Networks and Management and Operation functions are exploited to "migrate" vMDs to new virtualisation domains by forwarding data flows to the former domain until the new one is prepared, while a distributed data base avoids the transference of data. The solution has been deployed in a reference vehicular scenario at the Institute of Telecommunications Aveiro premises within the 5GINFIRE European project. In particular, the system has been evaluated under different virtualisation domains to study the operation of the migration approach in a vehicular monitoring scenario. The results validate the system from the application viewpoint with a Web monitoring tool, and the migration of the digital twin provided as VxF is analysed attending to the modification of data flows, indicating a seamless transition between virtualisation domains in a timely manner.
- Enhancement of CO2/N2 selectivity and CO2 uptake by tuning concentration and chemical structure of imidazolium-based ILs immobilized in mesoporous silicaPublication . Duczinski, Rafael; Polesso, Barbara B.; Bernard, Franciele L.; Ferrari, Henrique Z.; Almeida, Pedro L.; Corvo, Marta C.; Cabrita, Eurico J; Menezes, Sónia; Einloft, SandraImidazolium-based ionic liquids (ILs) with different cation alkyl chain ([i-C5mim] or [C4mim]) and inorganic anions ([Cl−], [Tf2N−], [PF6−] and [DCA−]) were synthesized and immobilized in commercial mesoporous silica. The synthesized supported ILs (SILs) were characterized using NMR, FTIR, TGA, BET, SEM and TEM. CO2 sorption capacity, reusability and CO2/N2 selectivity were assessed by the pressure-decay technique. The effects of IL concentration, cation and anion chemical structure in CO2 sorption capacity and CO2/N2 separation performance wereevaluated. Tests evidencedthatthe presenceofbranching on thecation alkylsidechainincreases CO2/N2 selectivity. The immobilization of the IL [i-C5TPIm][Cl] on mesoporous silica in different concentrations (50, 20, 10 and 5 %) revealed that lower IL concentration results in higher CO2 sorption capacity. Immobilization of ILs containing fluorinated anions at low concentrations in the mesoporous silica support may promote the improvement of the CO2/N2 selectivity without interfering on CO2 sorption capacity of the original support. CO2 sorption capacity value shown by sample SIL-5 % - [i-C5TPIm][Tf2N] (79.50 ± 0.70mg CO2 g-1) was close to the value obtained for the pristine mesoporous silica (81.70 ± 2.20mg CO2g-1) and the selectivity (4.30 ± 0.70) was more than twice of the one obtained for the support alone (2.32 ± 0.4). Recycle tests demonstrated that the ILs immobilized in mesoporous silica samples are stable, providing a new option to be used in CO2 capture processes.