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Original Articles

An Improved Method for Charging Submicron and Nano Particles with Uniform Charging Performance

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Pages 259-265 | Received 24 Apr 2006, Accepted 01 Dec 2006, Published online: 17 Jan 2007

Figures & data

FIG. 1 Experimental setup for measuring (a) the size distribution of classified and evaporated particles and condensed droplets by SMPS spectrometer and Aerosizer (b) and measuring the total charge, number concentration and electrical mobility distribution of highly-charged particles by aerosol electrometer, CPC and SMPS spectrometer.

FIG. 1 Experimental setup for measuring (a) the size distribution of classified and evaporated particles and condensed droplets by SMPS spectrometer and Aerosizer (b) and measuring the total charge, number concentration and electrical mobility distribution of highly-charged particles by aerosol electrometer, CPC and SMPS spectrometer.

FIG. 2 Schematic diagram of the condenser.

FIG. 2 Schematic diagram of the condenser.

FIG. 3 Schematic diagram of the indirect corona charger.

FIG. 3 Schematic diagram of the indirect corona charger.

FIG. 4 (a) The aerodynamic mean diameter (b) and GSD of the condensed droplets, as a function of the diameter of classified particles.

FIG. 4 (a) The aerodynamic mean diameter (b) and GSD of the condensed droplets, as a function of the diameter of classified particles.

FIG. 5 The geometric mean diameter and GSD of evaporated particles with the temperature of the evaporator, when the temperature of the saturator was 45° C, 50° C, and 55° C.

FIG. 5 The geometric mean diameter and GSD of evaporated particles with the temperature of the evaporator, when the temperature of the saturator was 45° C, 50° C, and 55° C.

FIG. 6 (a) Comparison of the geometric mean diameter (b) and GSD of evaporated particles with that of classified particles and (c) the error when the temperature of the saturator was 45° C, 50° C, and 55° C.

FIG. 6 (a) Comparison of the geometric mean diameter (b) and GSD of evaporated particles with that of classified particles and (c) the error when the temperature of the saturator was 45° C, 50° C, and 55° C.

FIG. 7 The average charge of particles with corona voltage and external voltage, which was calculated by dividing the total charge by the number concentration (which were measured by using aerosol electrometer and CPC), when the diameter of the classified particle was 22.4 nm and the temperature of the saturator was 55° C.

FIG. 7 The average charge of particles with corona voltage and external voltage, which was calculated by dividing the total charge by the number concentration (which were measured by using aerosol electrometer and CPC), when the diameter of the classified particle was 22.4 nm and the temperature of the saturator was 55° C.

FIG. 8 The average charge, which was calculated by dividing the total charge by the number concentration (which were measured by aerosol electrometer and CPC) of the evaporated particles, when the temperature of the saturator was 45° C, 50° C and 55° C.

FIG. 8 The average charge, which was calculated by dividing the total charge by the number concentration (which were measured by aerosol electrometer and CPC) of the evaporated particles, when the temperature of the saturator was 45° C, 50° C and 55° C.

FIG. 9 Comparison of the average charges, which was calculated in two ways, SMSP and aerosol electrometer(AE)/CPC, for several charging conditions when the diameter of the particles was 16.9 nm, 23.7 nm, 33.4 nm, and 51.4 nm, when the corona voltage and external voltage were +4 kV and −1 kV, respectively and the temperature of the saturator was 55° C.

FIG. 9 Comparison of the average charges, which was calculated in two ways, SMSP and aerosol electrometer(AE)/CPC, for several charging conditions when the diameter of the particles was 16.9 nm, 23.7 nm, 33.4 nm, and 51.4 nm, when the corona voltage and external voltage were +4 kV and −1 kV, respectively and the temperature of the saturator was 55° C.

FIG. 10 The shift of the electrical mobility distribution of highly-charged particles compared with evaporated particles with a charge of +1 when the diameter of the evaporated particles was (a) 56.4 nm (b) and 16.9 nm when the corona voltage and external voltage were +4 kV and −1 kV, respectively, and the temperature of the saturator was 55° C.

FIG. 10 The shift of the electrical mobility distribution of highly-charged particles compared with evaporated particles with a charge of +1 when the diameter of the evaporated particles was (a) 56.4 nm (b) and 16.9 nm when the corona voltage and external voltage were +4 kV and −1 kV, respectively, and the temperature of the saturator was 55° C.

FIG. 11 The charge distribution of evaporated particles when the corona voltage and external voltage were +4 kV and −1 kV, respectively, and the temperature of the saturator was 55° C.

FIG. 11 The charge distribution of evaporated particles when the corona voltage and external voltage were +4 kV and −1 kV, respectively, and the temperature of the saturator was 55° C.

FIG. 12 Comparison of the average charge of the condensed droplets and evaporated particles that of previous researches. The average charges of the evaporated particles were measured by two methods; SMPS and CPC/AE.

FIG. 12 Comparison of the average charge of the condensed droplets and evaporated particles that of previous researches. The average charges of the evaporated particles were measured by two methods; SMPS and CPC/AE.

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