Mobility size distributions of soot particles produced from a fuel-rich, laminar premixed ethylene flat flame were obtained by in situ probe sampling and online analysis using a nano scanning mobility particle sizer. The emphasis of the work was the development of an in situ sampling technique to follow the evolution of nanoparticles formed in flames. Particle size distribution functions were obtained along the centerline of the flame in a spatially resolved manner. Considerable efforts were made to eliminate particle losses in the sample probe. To this end, the effect of dilution on particle losses in the sample probe was systematically studied. It is demonstrated that particle losses due to coagulation and diffusive wall deposition were negligible using a dilution ratio greater than ∼10 4 . The sampling technique is shown to be capable of closely following the evolution of particle size distribution from the nucleation mode to mass growth mode dominated by particle coagulation and gas-surface reactions. Beyond the particle nucleation region of the flame, the size spectra were found to be distinctively bimodal, indicating sustained particle nucleation throughout the flame studied.
The application of microscopic Fourier transform infrared (micro-FT-IR) spectroscopy combined with complementary methods of particle analysis is demonstrated here for investigations of phase transitions and hygroscopic growth of micron-sized particles. The approach utilizes the exposure of substrate-deposited, isolated particles to humidified nitrogen inside a sample cell followed by micro-FT-IR spectroscopy over a selected sample area. Phase transitions of NaCl, sea salt, NaNO3, and (NH4)2SO4 particles are monitored with this technique to evaluate its utility and applicability for particle hydration studies. The results are found in excellent agreement with literature data in terms of (a) reliable and reproducible detection of deliquescence and efflorescence phase transitions, (b) quantitative measurements of water-to-solute ratios in particles as a function of relative humidity, and (c) changes in the IR spectra resulting from phase transitions and changing relative humidity. Additional methods of particle analysis are employed to complement and assist in the interpretation of particle hygroscopicity data obtained from micro-FT-IR measurements. The analytical approach and the experimental setup presented here are relatively simple, inexpensive, readily available and therefore may be practical for hydration studies of environmental particles collected in both laboratory and field studies.
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