Search results for: Tomaso Trombetti

Authors: Vittoria Laghi, Giada Gasparini, Tomaso Trombetti

Abstract:

The digitalization of the construction sector could potentially produce more efficient structures, reduce material waste and increase work safety. Current strategies for the realization of automated steel constructions see the application of metal Additive Manufacturing processes (and in particular Wire-and-Arc Additive Manufacturing, WAAM) as an opportunity to build a new generation of efficient steel structures with reduced material use. This, though, requires advanced multidisciplinary knowledge in manufacturing, metallurgy, structural engineering and computational design. Recent efforts have been made in order to combine computational design with current digital fabrication procedures to realize resource-efficient steel structures for the future. The present work aims to provide an integrated design approach to develop resource-efficient structural elements combining computational design algorithms with considerations on the WAAM fabrication process, structural considerations and verifications. The idea comes from the preliminary results achieved in terms of new structural optimization theories, fabrication of large-scale elements with WAAM and structural verification of first prototypes. The approach is applied to two classes of structural elements (beam and column). The results aim to increase the application of metal Additive Manufacturing in construction through the development of a new generation of resource-efficient structural members.

Keywords: additive manufacturing, wire-and-arc, steel structures, structural optimization

Procedia PDF Downloads 0

Authors: Olena Mayboroda, Angel Gonzalez Benito, Jonathan Sabate Del Rio, Marketa Svobodova, Sandra Julich, Herbert Tomaso, Ciara K. O'Sullivan, Ioanis Katakis

Abstract:

DNA amplification is required for most molecular diagnostic applications but conventional PCR has disadvantages for field testing. Isothermal amplification techniques are being developed to respond to this problem. One of them is the Recombinase Polymerase Amplification (RPA) that operates at isothermal conditions without sacrificing specificity and sensitivity in easy-to-use formats. In this work RPA was used for the optical detection of solid-phase amplification of the potential biowarfare agent Yersinia pestis. Thiolated forward primers were immobilized on the surface of maleimide-activated microtitre plates for the quantitative detection of synthetic and genomic DNA, with elongation occurring only in the presence of the specific template DNA and solution phase reverse primers. Quantitative detection was achieved via the use of biotinylated reverse primers and post-amplification addition of streptavidin-HRP conjugate. The overall time of amplification and detection was less than 1 hour at a constant temperature of 37oC. Single-stranded and double-stranded DNA sequences were detected achieving detection limits of 4.04*10-13 M and 3.14*10-16 M, respectively. The system demonstrated high specificity with negligible responses to non-specific targets.

Keywords: recombinase polymerase amplification, Yersinia pestis, solid-phase detection, ELONA

Procedia PDF Downloads 307

Authors: Samuel B. Dulay, Sandra Julich, Herbert Tomaso, Ciara K. O'Sullivan

Abstract:

An early, rapid and definite detection for the presence of biowarfare agents, pathogens, viruses and toxins is required in different situations which include civil rescue and security units, homeland security, military operations, public transportation securities such as airports, metro and railway stations due to its harmful effect on the human population. In this work, an electrochemical genosensor array that allows simultaneous detection of different biowarfare agents within an integrated microsystem that provides an easy handling of the technology which combines a microfluidics setup with a multiplexing genosensor array has been developed and optimised for the following targets: Bacillus anthracis, Brucella abortis and melitensis, Bacteriophage lambda, Francisella tularensis, Burkholderia mallei and pseudomallei, Coxiella burnetii, Yersinia pestis, and Bacillus thuringiensis. The electrode array was modified via co-immobilisation of a 1:100 (mol/mol) mixture of a thiolated probe and an oligoethyleneglycol-terminated monopodal thiol. PCR products from these relevant biowarfare agents were detected reproducibly through a sandwich assay format with the target hybridised between a surface immobilised probe into the electrode and a horseradish peroxidase-labelled secondary reporter probe, which provided an enzyme based electrochemical signal. The potential of the designed microsystem for multiplexed genosensor detection and cross-reactivity studies over potential interfering DNA sequences has demonstrated high selectivity using the developed platform producing high-throughput.

Keywords: biowarfare agents, genosensors, multipled detection, microsystem

Procedia PDF Downloads 276