0000000000353128

AUTHOR

Giuseppe Portale

showing 11 related works from this author

Why laparoscopists may opt for three-dimensional view: a summary of the full HTA report on 3D versus 2D laparoscopy by S.I.C.E. (Società Italiana di …

2018

Background Three-dimensional view in laparoscopic general, gynaecologic and urologic surgery is an efficient, safe and sustainable innovation. The present paper is an extract taken from a full health technology assessment report on three-dimensional vision technology compared with standard two-dimensional laparoscopic systems. Methods A health technology assessment approach was implemented in order to investigate all the economic, social, ethical and organisational implications related to the adoption of the innovative three-dimensional view. With the support of a multi-disciplinary team, composed of eight experts working in Italian hospitals and Universities, qualitative and quantitative d…

Three Dimensional Vision . Laparoscopy. Surgery- Health Technology assessment. Systemic ReviewTechnology Assessment BiomedicalHealth technology assessment Laparoscopy; Surgery Systematic review Three-dimensional visionOperative TimeSustainable innovationEndoscopic surgeryThree-dimensional vision03 medical and health sciencesImaging Three-DimensionalPostoperative Complications0302 clinical medicineEconomicaHumansUrologic surgeryMedicineHealth technology assessmentLaparoscopyDepth PerceptionMedical educationmedicine.diagnostic_testbusiness.industryHealth technologyMultiple-criteria decision analysisNew TechnologyHealth technology assessment; Laparoscopy; Surgery; Systematic review; Three-dimensional vision; SurgeryItaly030220 oncology & carcinogenesisCosts and Cost AnalysisSystematic review030211 gastroenterology & hepatologyHealth technology assessment; Laparoscopy; Surgery; Systematic review; Three-dimensional vision;LaparoscopySurgeryPatient SafetybusinessHealthcare providersPsychomotor PerformanceSystematic search
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Structural and electrochemical investigation on re-cast Nafion membranes for polymer electrolyte fuel cells (PEFCs) application

2006

Abstract Starting from a 5 wt% ion power Nafion® solution and dissolving the dry residue in a suitable solvent (10 wt% solution in dimethylacetammide), re-cast Nafion films were developed for polymer electrolyte fuel cells (PEFCs) application. The used Doctor-Blade casting technique allowed to prepare scaled-up membranes comparable to the commercial Nafion ones with good mechanical resistance, thickness homogeneity and an excellent reproducibility. The differences between the re-cast membrane nanostructure and that of the commercial Nafion were investigated by synchrotron small-angle X-ray scattering. The obtained re-cast membrane shows at ambient conditions a semi-crystalline structure wit…

PERFLUORINATED IONOMER MEMBRANESNanostructureMaterials sciencedoctor-blade casting method; pefcs; re-cast nafion membrane; re-cast nation membrane; saxsSmall-angle X-ray scatteringSMALL-ANGLE SCATTERINGFiltration and SeparationSAXSElectrochemistryBiochemistrychemistry.chemical_compoundMembranechemistryChemical engineeringNafionX-RAYIonic conductivityMEDIUM-TEMPERATUREGeneral Materials SciencePhysical and Theoretical ChemistryIonomerDissolutionRe-cast Nafion membrane; PEFCs; Doctor-Blade casting method; SAXSJournal of Membrane Science
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Formation and growth of palladium nanoparticles inside porous poly(4-vinyl-pyridine) monitored by operando techniques: The role of different reducing…

2017

In this work we followed the formation of palladium nanoparticles, starting from palladium (II) acetate precursor, inside a poly(4-vinylpyridine-co-divinylbenzene) polymer in presence of different reducing agents. The formation and growth of palladium nanoparticles in presence of H-2 was followed as a function of temperature by simultaneous XANES-SAXS techniques, coupled with DRIFT spectroscopy in operando conditions. It was found that the pyridyl functional groups in the polymer plays a fundamental role in the stabilization of the palladium (II) acetate precursor, as well as in the stabilization of the palladium nanoparticles. The effect of a thermal treatment in alcohol (ethanol and 2-pro…

inorganic chemicalsReducing agentInfrared spectroscopychemistry.chemical_element02 engineering and technologyThermal treatment010402 general chemistryPhotochemistry01 natural sciencesAEROBIC ALCOHOL OXIDATIONCatalysisCatalysiCatalysisP4VPRUTHENIUM NANOPARTICLESMoleculeOrganic chemistryOperandoCATALYTIC-ACTIVITYchemistry.chemical_classificationPD NANOPARTICLESDRIFT; Operando; P4VP; Palladium nanoparticles; SAXS; XANESChemistryIN-SITUChemistry (all)SAXSGeneral ChemistryPolymerPalladium nanoparticleSELECTIVE OXIDATION021001 nanoscience & nanotechnologyPalladium nanoparticlesXANESX-RAY-SCATTERINGPARTICLE-SIZE0104 chemical sciencesDRIFTColloidal goldGOLD NANOPARTICLESVIBRATIONAL PROPERTIESDRIFT; Operando; P4VP; Palladium nanoparticles; SAXS; XANES; Catalysis; Chemistry (all)0210 nano-technologyPalladiumCatalysis Today
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Induced Chirality in Confined Space on Halogen Gold Complexes

2015

The solubilization of HAuCl4 in toluene within optically active reverse micelles and lamellar structures formed by (1R,2S)-Dodecyl(2-hydroxy-1-methyl-2-phenylethyl)- dimethylammonium bromide (DMEB) has allowed us to evidence the complex phenomenology accompanying the confinement of Au salt within these nanostructures. Together with a chloride/bromide exchange process occurring in the first coordination sphere of an Au ion, UV−vis and electronic circular dichroism (ECD) spectra reveal the appearance of an induced dichroic signal attributable to Au complexes entrapped in the hydrophilic domain of the DMEB chiral nanostructures. Interestingly, change of the effective oxidation state and coordi…

Circular dichroismSupramolecular chiralityCoordination spherechirality confined space DMEBPhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergychemistryBromideRAY-ABSORPTION SPECTROSCOPY; BODY DISTRIBUTION-FUNCTIONS; NEAR-EDGE STRUCTURE; STABILIZED MICROEMULSIONS; SUPRAMOLECULAR CHIRALITY; CINCHONIDINE ADSORPTION; ELECTRONIC-STRUCTURES; CHIROPTICAL ACTIVITY; UNDECAGOLD CLUSTERS; CONDENSED MATTERPhysical and Theoretical ChemistryAbsorption (chemistry)SpectroscopyChirality (chemistry)Settore CHIM/02 - Chimica FisicaCoordination geometryThe Journal of Physical Chemistry C
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The Pyridyl Functional Groups Guide the Formation of Pd Nanoparticles Inside A Porous Poly(4-Vinyl-Pyridine)

2015

The reactivity of palladium acetate inside a poly(4-vinylpyridine-co-divinylbenzene) polymer is strongly influenced by the establishment of interaction between the Pd precursor and the pyridyl functional group in the polymer. Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and simultaneous X-ray absorption near edge structure (XANES) and small angle X-ray scattering (SAXS) techniques have been applied to monitor the reactivity of palladium acetate in the presence of H-2 and CO as a function of temperature. H-2 reduces palladium acetate to Pd nanoparticles and acetic acid. The pyridyl groups in the polymer play a vital role both in stabilizing the formed acetic acid, thu…

INFRARED-SPECTRADiffuse reflectance infrared fourier transformpolymersmall angle X-ray scatteringInfrared spectroscopychemistry.chemical_elementPALLADIUM(II) ACETATEIR spectroscopy; nanoparticles; palladium; polymers; small angle X-ray scattering; X-ray absorption spectroscopyPhotochemistryCatalysisCatalysisInorganic ChemistryAcetic acidchemistry.chemical_compoundRUTHENIUM NANOPARTICLESPARTICLE FORMATIONENVIRONMENTALLY BENIGNReactivity (chemistry)Physical and Theoretical ChemistryCARBON-MONOXIDEpolymerschemistry.chemical_classificationPOLYMERIC SUPPORTSnanoparticleIN-SITUOrganic ChemistryIR spectroscopy; nanoparticles; palladium; polymers; small angle X-ray scattering; X-ray absorption spectroscopy; Inorganic Chemistry; Organic Chemistry; Physical and Theoretical Chemistry; CatalysisX-ray absorption spectroscopyPolymerpalladiumchemistryIR spectroscopynanoparticlesPalladium(II) acetateTRANSITION-METAL COORDINATIONRESOLVED SAXS ANALYSISPalladium
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Morphology and local organization of water-containing (1R,2S)-Dodecyl(2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium bromide reverse micelles disp…

2014

The structure of (1R,2S)-dodecyl(2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium bromide (DMEB) reverse micelles, at various water-to-surfactant molar ratio (R-w, R-w = [water]/[DMEB]) and DMEB concentrations, has been investigated by small angle X-ray scattering (SAXS) and extended X-ray absorption fine structure spectroscopy (EXAFS). SAXS data of dry reverse micelles are consistent with a model of spherical hydrophilic core surrounded by DMEB alkyl chains whose polydispersity decreases significantly with surfactant concentration. By adding water, a sphere to cylinder transition occurs leading to a one-dimensional growth of reverse micellar cores with R-w and surfactant concentration. Th…

chemistry.chemical_classificationChiral EXAFS SAXS liquid crystalSmall-angle X-ray scatteringAnalytical chemistryGeneral Physics and AstronomyMicellechemistry.chemical_compoundCrystallographychemistryPulmonary surfactantBromideLamellar structurePhysical and Theoretical ChemistryCounterionAbsorption (chemistry)Alkyl
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Formation and Growth of Pd Nanoparticles Inside a Highly Cross-Linked Polystyrene Support: Role of the Reducing Agent

2014

Simultaneous time-resolved SAXS and XANES techniques were employed to follow in situ the formation of Pd nanoparticles in a porous polystyrene support, using palladium acetate as a precursor and gaseous H2 or CO as reducing agents. These results, in conjunction with data obtained by diffuse reflectance UV–vis and DRIFT spectroscopy and TEM measurements, allowed unraveling of the different roles played by gaseous H2 and CO in the formation of the Pd nanoparticles. In particular, it was found that the reducing agent affects (i) the reduction rate (which is faster in the presence of CO) and (ii) the properties of the hosted nanoparticles, in terms of size (bigger with CO), morphology (spherica…

Materials scienceExtended X-ray absorption fine structureReducing agentSmall-angle X-ray scatteringchemistry.chemical_elementNanoparticlePd nanoparticles; SAXS; EXAFSSAXSXANESSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistry.chemical_compoundEXAFSGeneral EnergyPd nanoparticleschemistryChemical engineeringPalladium nanoparticles time-resolved X-ray Absorption Spectroscopy Small Angle X-ray Spectroscopy Transmission Electron MicroscopyDiffuse reflectionPolystyrenePhysical and Theoretical ChemistryPalladium
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Influence of metal–support interaction on the surface structure of gold nanoclusters deposited on native SiOx/Si substrates

2014

The structure of small gold nanoclusters (R ~ 2.5 nm) deposited on different silica on silicon substrates is investigated using several characterization techniques (AFM, XRD, EXAFS and GISAXS). The grain morphology and the surface roughness of the deposited gold clusters are determined by AFM. The in-plane GISAXS intensity is modelled in order to obtain information about the cluster size and the characteristic length scale of the surface roughness. AFM and GISAXS results are in excellent agreement and show that the surface morphology of the deposited clusters depends on whether defect-rich (native) or defect-free (thermal) silica is used as a substrate. Gold clusters show a strong tendency …

Gold clusterMaterials scienceExtended X-ray absorption fine structureGeneral Physics and AstronomyNanoparticleNanotechnologySubstrate (electronics)Thermal treatmentgoldNanoclustersEXAFSsurfaces nanoparticles GISAXS AFMChemical engineeringSurface roughnessGrazing-incidence small-angle scatteringPhysical and Theoretical ChemistryGISAXSmetal-support interactionPhysical Chemistry Chemical Physics
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Combined small-angle x-ray scattering/extended x-ray absorption fine structure study of coated Co nanoclusters in bis(2-ethylhexyl)sulfosuccinate

2009

Chemically stable cobalt nanostructures have been prepared with Co(II) reduction in the confined space of cobalt bis(2-ethylhexyl)sulfosuccinate, Co(AOT)2, reverse micelles dispersed in n-heptane. The reaction was carried out by adding a solution of sodium borohydride in ethanol (1% weight) to a 0.2M micellar solution of Co(AOT)2 in n-heptane at a reductant to Co(II) molar ratio of 4. This procedure involves the rapid formation of surfactant-coated Co nanoparticles followed by their slow separation as nanostructures embedded in a sodium bis(2-ethylhexyl)sulfosuccinate matrix. The resulting composites, characterized by extended x-ray absorption fine structure and small-angle x-ray scattering…

Materials scienceExtended X-ray absorption fine structureSmall-angle X-ray scatteringInorganic chemistryGeneral Physics and Astronomychemistry.chemical_elementNanoparticleMicelleNanoclustersSodium borohydridechemistry.chemical_compoundchemistrySAXS EXAFS micelle cobalt nanoparticleAbsorption (chemistry)CobaltNuclear chemistry
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Pd nanoparticles formation inside porous polymeric scaffolds followed by in situ XANES/SAXS

2015

International audience; Simultaneous time-resolved SAXS and XANES techniques were employed to follow in situ the formation of Pd nanoparticles from palladium acetate precursor in two porous polymeric supports: polystyrene (PS) and poly(4-vinyl-pyridine) (P4VP). In this study we have investigated the effect of the use of different reducing agents (H-2 and CO) from the gas phase. These results, in conjunction with data obtained by diffuse reflectance IR (DRIFT) spectroscopy and TEM measurements, allowed us to unravel the different roles played by gaseous H-2 and CO in the formation of the Pd nanoparticles for both PS and P4VP hosting scaffolds

HistoryMaterials scienceAbsorption spectroscopyNanoparticlechemistry.chemical_elementreduction02 engineering and technologypolystyrene010402 general chemistry01 natural sciencesEducationP4VPchemistry.chemical_compoundPdPd nanoparticles formation inside porous polymeric scaffoldspaladumchemistry.chemical_classification[PHYS]Physics [physics]Small-angle X-ray scatteringnanoparticlein situSAXS XANES Pd paladum nanoparticle polystyrene P4VP DRIFT TEM reduction in situSAXSPolymer021001 nanoscience & nanotechnologyXANESXANES0104 chemical sciencesComputer Science ApplicationsCrystallographyDRIFTchemistryChemical engineeringTEMPolystyreneDiffuse reflection0210 nano-technologyPalladium
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Structural Characterization of Surfactant-Coated Bimetallic Cobalt/Nickel Nanoclusters by XPS, EXAFS, WAXS, and SAXS

2011

Cobalt nickel bimetallic nanoparticles were synthesized by changing the sequence of the chemical reduction of Co(II) and Ni(II) ions confined in the core of bis(2-ethylhexyl)phosphate (2)., and Ni(DEHP)(2). The reduction was carried out by mixing, sequentially or contemporaneously, fixed amounts of n-heptane solution of Co(DEHP)2 and Ni(DEHP)2 micelles with a solution of sodium borohydride in ethanol at a fixed (reductant)/(total metal) molar ratio. This procedure involves the rapid formation of surfactant-coated nanoparticles, indicated as Co/Ni (Co after Ni), Ni/Co (Ni after Co), and Co + Ni (simultaneous), followed by their slow separation as nanostructures embedded in a sodium bis(2-eth…

inorganic chemicalsendocrine systemMaterials sciencechemistry.chemical_elementNanoparticleNanoclustersMetalSodium borohydridechemistry.chemical_compoundX-ray photoelectron spectroscopyNANOPARTICLESPARTICLESBimetallic Cobalt/Nickel Nanoclusters. XPS. EXAFS. WAXS. SAXS.GOLDPhysical and Theoretical ChemistryBimetallic stripMICELLESSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyNickelGeneral Energychemistryvisual_artNANOPARTICLES; PARTICLES; GOLD; MICELLESvisual_art.visual_art_mediumCobaltNuclear chemistry
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