The AC3 was designed at NASA Langley inspired by a previous Straub and Collett (2004) version. The probe samples in-situ cloud water by separating droplets from the main airflow. This is accomplished by imparting swirl on an axial flow following an in-line stator, and collecting droplets that have impacted on the probes outer walls. Cloud-water is then transferred into the aircraft cabin using teflon tubing and manually collected into vials. Cloud-water can then be analyzed by a number of laboratory analytical techniques including ion-chromatography, pH electrodes, or total organic content. The probe utilizes a shutter to inhibit sample contamination by aerosols.
Ion Chromatography
As part of the measurement team on the NASA DC-8 we operate two related installations: a mist chamber/ion chromatograph (MC/IC) sampling/analysis system providing near real time results for selected species, and a bulk aerosol system that collects particulates onto filters for subsequent analysis. We use ion chromatography on aqueous extracts of the bulk aerosol samples collected on Teflon filters to quantify soluble ions (Cl-, Br-, NO3-, SO42-, C2O42-, Na+, NH4+, K+, Ca+, and Mg+). Filters are exposed on all level flight legs. Below 3 km exposure times are 5 minutes or less, increasing at higher altitudes to a maximum sample time of 15 minutes. Aerosols participate in heterogeneous chemistry, impact radiative transfer, and can be detected from space. Our measurements help to validate and extend retrievals of aerosol distributions and properties by MODIS, MISR and CALIPSO. In addition, several of the particle-associated ions are tracers of sources of gas and aerosol pollutants (e.g., SO42- from industrial emissions of SO2, enhancements of C2O42-, K+, and NH4+ indicate encounters with biomass burning plumes, Na+, and Cl- are tracers of seasalt, Mg2+ and Ca2+ are tracers of dust). Our system has two inlets, allowing collection of paired samples simultaneously.
The Particle Into Liquid Sampler (PILS) was developed for rapid automated on-line and continuous measurement of ambient aerosol bulk composition. The general approach is based on earlier devices in which ambient particles are mixed with saturated water vapor to produce droplets easily collected by inertial techniques. The resulting liquid stream is analyzed with an ion chromatograph to quantitatively measure the bulk aerosol ionic components. In this instrument, a modified version of a particle size magnifier is employed to activate and grow particles comprising the fine aerosol mass. A single jet inertial impactor is used to collect the droplets onto a vertical glass plate that is continually washed with a constant water diluent flow of nominally 0.10 ml min-1. The flow is divided and then analyzed by a dual channel ion chromatograph. In its current form, 4.3 min integrated samples were measured every 7 min. The instrument provides bulk composition measurements with a detection limit of approximately 0.1 µg m-3 for chloride, nitrate, sulfate, sodium, ammonium, calcium, and potassium.