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    Optical properties of incipient soot

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    The exact knowledge of the optical properties of soot nanoparticles is fundamental for several aspects including the correct determination of the soot concentration in combustion environments using optical diagnostics and the correct estimation of the environmental impact of the emitted particles. Although extensive researches over the years have led to a substantial agreement on the optical properties of mature soot particles, the optical properties of the incipient soot nanoparticles are still uncertain. From the particle inception point to the formation of large and more mature soot particles, the evolution of the optical properties must account for variations due to the size and the physicochemical transformation of the investigated particles. This work aims to determine the refractive index and optical properties of inception particles formed in lightly sooting flames. A previous determination based on in-situ light absorption and scattering measurements is revisited taking advantage of particle size measurements by differential mobility analysis. The spectral dependencies of the optical properties are derived by the Kramers-Krӧnig analysis of the ex-situ VUV-NIR light absorption measurements. Results confirm the strong decrease in the absorptivity in the vis-NIR region of inception particles with unimodal size distribution and d63∼3 nm, and confirm a strong size dependency of soot optical properties. The thermal-optical analysis of the sampled particles shows that the particle mass absorption coefficient also correlates with organic carbon content

    Particle inception in a Laminar premixed flame of benzene

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    Spectral optical techniques, including light extinction and laser induce fluorescence and incandescence measurements, are combined to characterize large-molecule soot precursors and soot in a slightly sooting flame of benzene at atmospheric pressure. Light absorption coupled to in-situ light scattering measurements and ex-situ Atomic Force Microscopy also allowed the evaluation of particle sizes. In the benzene flame high molecular mass structures with typical sizes of 3-4nm are formed in the main oxidation region of the flame. The radical-rich flame environment in which these compounds are formed promotes their dehydrogenation increasing the level of their aromaticity. As a result, nanoparticles with typical sizes of about 5nm, absorbing and fluorescing in the visible are formed. These compounds reach a maximum concentration just before the appearance of incandescent soot particles

    Nano Organic Carbon and Soot in Turbulent non-Premixed Ethylene Flames

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    Spectral optical techniques are combined to characterise the distribution of large-molecule soot precursors, nanoparticles of organic carbon, and soot in two turbulent non-premixed ethylene flames with differing residence times. Laser-induced fluorescence, laser-induced incandescence and light scattering are used to define distributions across the particle size distribution. From the scattering and laser-induced emission measurements it appears that two classes of particles are formed. The first ones are preferentially formed in the fuel-rich region of the flame closer to the nozzle, have sizes of the order of few nanometers but are not fully solid particles, because the constituent molecules still maintain their individual identity exhibiting strong broadband fluorescence in the UV. The second class of particles constituted by solid particles, with sizes of the order of tens of nanometers are able to absorb a sufficient number of photons to be heated to incandescent temperatures. These larger particles are formed at larger residence times in the flame since they are the result of slow growth processes such as coagulation or carbonization. The flames are also modeled in order to produce mixture fraction maps. A new discovery is that nanoparticles of organic carbon concentration, unlike soot, does correlate well with mixture fraction, independent of position in the flame. This is likely to be a significant benefit to future modelling of soot inception processes in turbulent nonpremixed flames

    Thermophoretic sensors for combustion formed nanoparticles

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    It is well established that ultrafine carbonaceous particles represent the major source of carbon aerosols in the atmosphere, and their formation has been intensively investigated over the last decades due to their negative effects on human health and environment. Moreover, combustion-formed nanoparticles represent a broad class of compounds since they can be highly variable in terms of size, chemical composition, morphology and optical properties. In the light of the above, the development of highly sensitive, costly effective combustion aerosols sensors, capable to give both qualitative and quantitative information is needed. In this work, thermocouple particle densitometry (TPD) technique, which is based on the thermophoretic sampling principle, has been carried out to detect nanoparticles produce in a slightly sooting laminar premixed flame at different height above the burner (HAB). With this technique, the particle emissivity and the total particulate volume fraction have been obtained and results are compared with the ones determined by on-line measurements using a Scanning Mobility Particle Sizer system (SMPS). The good agreement between results obtained with the two independent measurements demonstrates that transient-thermocouple measurement is a powerful technique to detect the total particulate volume fraction, together with particle emissivity. In addition, thermophoretic sampling has been adopted for the collection and electrical characterization of combustion nanoparticles with different graphitization degree. This work demonstrates that the feasibility of such an approach can be useful for the development of conductometric combustion aerosol sensors

    Particle Inception in a Laminar Premixed Benzene Flame

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    Spectral optical techniques, including light extinction and laser induce fluorescence and incandescence measurements, are combined to characterize large-molecule soot precursors and soot in a slightly sooting flame of benzene at atmospheric pressure. Light absorption coupled to in-situ light scattering measurements and ex-situ Atomic Force Microscopy also allowed the evaluation of particle sizes. In the benzene flame high molecular mass structures with typical sizes of 3–4nm are formed in the main oxidation region of the flame. The radical-rich flame environment in which these compounds are formed promotes their dehydrogenation increasing the level of their aromaticity. As a result, nanoparticles with typical sizes of about 5 nm, absorbing and fluorescing in the visible are formed. These compounds reach a maximum concentration just before the appearance of incandescent soot particles

    Flame-formed carbon nanoparticles: Morphology, interaction forces, and hamaker constant from AFM

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    Interaction forces acting between combustion-generated carbon particles were studied by using atomic force microscopy (AFM). To this aim, carbon nanoparticles were produced in fuel-rich ethylene/air laminar premixed flames with different equivalent ratios Φ, and analyzed at a fixed residence time in the flame. Particles were collected on mica substrates by means of a thermophoretic sampling system and then analyzed by AFM. A characterization of particle dimension and morphology were performed operating AFM in semicontact mode, showing that the shape of the particles collected on a sampling plate is never spherical. Increasing the flame-equivalent ratio, particle shape moves from an almost atomically thick object to thicker compounds, indicating the transformation from particles made of small, defective graphene-like sheets to particles containing stacked aromatic layers. Attractive and adhesive forces between a titanium nitride probe and sampled particles were calculated from force-distance curves acquired in AFM force spectroscopy mode. Assuming that van der Walls forces are the main contribution to attractive forces, the measurement of attractive forces allowed the evaluation of the Hamaker constant for the carbon particles as a function of the flame-equivalent ratio. The comparison of the measured Hamaker constants with the values for benzene and HOPG, suggests a continuous increase of the aromatic domains and the three-dimensional order within the particles when the flame-equivalent ratio increases

    Editorial: Experimental and modelling approaches for clean combustion technologies

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    The aim of this research topic was to present new results, findings, and developments in various disciplines associated with combustion science and pollutant formation and destruction

    Carbon-Ti02 nanostructures: Flame synthesis and characterization

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    The synthesis of pure titania and carbon-titania nano-powders in a premixed atmospheric fuel-rich flame was studied. The variation of the flame C/O ratio allows to produce both pure titania and carbon-TiO2 nanoparticles. Raman Spectroscopy, X-ray Diffraction, Atomic Force Microscopy, Electrical Low Pressure Impactor and Scanning Electron Microscopy were used to characterize the synthesized nano-powders, in terms of crystallinity, phase content, size and morphology. Produced nano-powders with a dimension of 25-40 nm are composed by both rutile and anatase phases, with rutile being the predominant one. Reactive Oxygen Species analysis performed on the synthesized nano-powders showed that the inclusion of carbon in the nano- powders results in a reduced adverse health effect, in terms of ROS production
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