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Original Articles

A Comparative Study of Different Methods for the Sampling of High Temperature Combustion Aerosols

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Pages 811-821 | Received 14 May 2004, Accepted 27 Jun 2005, Published online: 23 Feb 2007

Figures & data

FIG. 1 Schematic view of the thermophoretic probe tip.

FIG. 1 Schematic view of the thermophoretic probe tip.

FIG. 2 Schematic view of the aerodynamic-quenching particle sampling (AQPS) probe.

FIG. 2 Schematic view of the aerodynamic-quenching particle sampling (AQPS) probe.

FIG. 3 Partial view of the dilution probe used in this work.

FIG. 3 Partial view of the dilution probe used in this work.

FIG. 4 Elemental mass composition of the fine particles emitted in orujillo combustion in a previous EFR experiment (at 1300°C and 5% O2 in excess).

FIG. 4 Elemental mass composition of the fine particles emitted in orujillo combustion in a previous EFR experiment (at 1300°C and 5% O2 in excess).

FIG. 5 TEM-XEDS analyses of samples collected with the AQPS probe at 900°C, 560°C, and 360°C burning orujillo. α and β refer to the Kα and Kβ lines of the potassium spectrum, respectively. Curves have been normalized by the height of the potassium (Kα) peak.

FIG. 5 TEM-XEDS analyses of samples collected with the AQPS probe at 900°C, 560°C, and 360°C burning orujillo. α and β refer to the Kα and Kβ lines of the potassium spectrum, respectively. Curves have been normalized by the height of the potassium (Kα) peak.

FIG. 6 TEM image of the particles collected with the AQPS probe at 1300°C.

FIG. 6 TEM image of the particles collected with the AQPS probe at 1300°C.

FIG. 13 TEM-XEDS group analysis of the particles collected at the outlet of the dilution probe when sampling at 1300, 900, and 560°C.

FIG. 13 TEM-XEDS group analysis of the particles collected at the outlet of the dilution probe when sampling at 1300, 900, and 560°C.

FIG. 8 Macroscopic (∼20 × 20 μm2) analysis of the samples collected, near the probe and 3.7 s after it at 1300°C.

FIG. 8 Macroscopic (∼20 × 20 μm2) analysis of the samples collected, near the probe and 3.7 s after it at 1300°C.

FIG. 7 TEM-XEDS analysis of the ultrafine particles collected at 1300°C and 900°C. The energies associated to chlorine and sulphur (Kα lines) are indicated for reference.

FIG. 7 TEM-XEDS analysis of the ultrafine particles collected at 1300°C and 900°C. The energies associated to chlorine and sulphur (Kα lines) are indicated for reference.

FIG. 9 TEM image of a sample collected with the AQPS at 900°C and after a delay of 0.02 s from sampling to impaction on the TEM grid.

FIG. 9 TEM image of a sample collected with the AQPS at 900°C and after a delay of 0.02 s from sampling to impaction on the TEM grid.

FIG. 10 Elemental atomic composition vs. size of the particles collected with the dilution probe at 900°C (a) and 560°C (b), determined with the BLPI and SEM analysis.

FIG. 10 Elemental atomic composition vs. size of the particles collected with the dilution probe at 900°C (a) and 560°C (b), determined with the BLPI and SEM analysis.

FIG. 11 Approximate KCl, K2SO4 mass distribution vs. particle size for samples collected with the dilution probe at 900°C (a) and 560°C (b), derived from the data of and the particle size distributions measured with the BLPI.

FIG. 11 Approximate KCl, K2SO4 mass distribution vs. particle size for samples collected with the dilution probe at 900°C (a) and 560°C (b), derived from the data of Figure 10 and the particle size distributions measured with the BLPI.

FIG. 12 TEM image of the particles sampled with the dilution probe at 1300°C.

FIG. 12 TEM image of the particles sampled with the dilution probe at 1300°C.

FIG. 14 Typical particles observed on the carbon grid film after collection by thermophoresis at 900°C.

FIG. 14 Typical particles observed on the carbon grid film after collection by thermophoresis at 900°C.

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