NASA - National Aeronautics and Space Administration

The NCAR NOxyO3 instrument is a 4-channel chemiluminescence instrument for the measurement of NO, NO2, NOy, and O3. NOx (NO and NO2) is critical to fast chemical processes controlling radical chemistry and O3 production. Total reactive nitrogen (NOy = NO + NO2 + HNO3 + PANs + other organic nitrates + HO2NO2 + HONO + NO3 + 2*N2O5 + particulate NO3- + …) is a useful tracer for characterizing air masses since it has a tendency to be conserved during airmass aging, as NOx is oxidized to other NOy species.

NOx (NO and NO2), NOy (total reactive nitrogen), and O3 are measured using the NCAR 4-channel chemiluminescence instrument, previously flown on the NASA WB-57F and the NCAR C130. NO is measured via addition of reagent O3 to the sample flow to generate the chemiluminescent reaction producing excited NO2, which is detected by photon counting with a dry-ice cooled photomultiplier tube. NO2 is measured as NO following photolytic conversion of NO2, with a time response of about 3 sec due to the residence time in the photolysis cell. NO is measured with an identical time response due to use of a matching volume. NOy is measured via Au-catalyzed conversion of reactive nitrogen species to NO, in the presence of CO, with a time response of slightly better than 1 sec. O3 is measured using the same chemiluminescent reaction but with the addition of reagent NO to the sample flow. Time response for the ozone measurement is slightly better than 1 s.

An inlet collects ambient air from the free air stream and adds reagents, including O2 or N2 dilutents, and NO and SO2 reagent gases. This method, called "oxygen dilution modulation" leads to nearly 100% measurement of HO2 and RO2 in the O2 dilution/low reagent concentration mode, whereas RO2 is measured with less than 10% efficiency in the N2 dilution/higher reagent concentration mode. This is because the chemistry converts peroxy radicals to H2SO4 efficiently in the O2 mode, but RO2 radicals are converted to RONO in the N2 mode. The H2SO4 thus produced is ionized by reaction with NO3- ions. The reagent and product ions are detected by mass spectrometry using quadrupole mass filtering and counting by a channel electron multiplier operating in the negative ion mode.

The Center has been developing a wideband radar altimeter that operates over the frequency range from 13 to 17 GHz. The primary purpose of this radar is high precision surface elevation measurements over polar ice sheets. The data collected with this radar can be analyzed in conjunction with laser-altimeter data to determine thickness of snow over sea ice. The radar has been flown on a NASA DC-8 aircraft, and the NSF provided a Twin Otter aircraft.

Langley Aerosol Research Group Experiment (LARGE).  The "classic" suite of instrumenation measures in-situ aerosol micrphysical and optical properties. The package can be tailored for specific science objectives and to operate on a variety of aircraft. Depending on the aircraft, measurments are made from either a shrouded single-diffuser "Clarke" inlet, from a BMI (Brechtel Manufacturing Inc.) isokinetic inlet, or from a HIML inlet. Primary measurements include:

1.) total and non-volatile particle concentrations (3nm and 10nm nominal size cuts),
2.) dry size distributions from 3nm to 5µm diameter using a combination of mobilty-optical-aerodynamic sizing techniques,
3.) dry and humidified scattering coefficients (at 450, 550, and 700nm wavelength), and
4.) dry absorption coefficients (470, 532, and 670nm wavelength). 

LARGE derived products include particle size statistics (integrated number, surface area, and volume concentrations for ultrafine, accumulation, and coarse modes), dry and ambient aerosol extinction coefficients, single scattering albedo, angstrom exponent coefficients, and scattering hygroscopicity parameter f(RH).

Wideband Integrated Bioaerosol Sensor (WIBS-4A) - Droplet Measurement Technologies.  Dectection of Fluorescent Biological Aerosol Particle (FBAP) number concentrations.  Single particle analysis using dual wavelength (280nm and 370nm by xenon lamps) excitation on two parallel broadband visible-wavelength detectors (310-400nm and 420-650nm). Particles are classified by a combination of fluorescence excitation and emission characteristics, as well as their optical size measured by forward-scattering using a 635nm continuous-wave diode laser.    

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.

Droplet Measurement Technologies (DMT) Single Particle Soot Photometer (SP2). Signle particle measurement of accumulation-mode refractory black carbon (rBC) mass concentrations based on laser-induced incancescence.   

The Whole Air Sampler (WAS) collects samples from airborne platforms for detailed analysis of a wide range of trace gases. The compounds that are typically measured from the WAS includes trace gases with sources from industrial midlatitude emissions, from biomass burning, and from the marine boundary layer, with certain compounds (e.g. organic nitrates) that have a unique source in the equatorial surface ocean. The use of a broad suite of tracers with different sources and lifetimes provides powerful diagnostic information on air mass history and chemical processing that currently is only available from measurements from whole air samples. Previous deployments of the whole air sampler have shown that the sampling and analytical procedures employed by our group are capable of accessing the wide range of mixing ratios at sufficient precision to be used for tracer studies. Thus, routine measurement of species, such as methyl iodide, at <= 0.1 x 10-12 mole fraction, or NMHC at levels of a few x 10-12 mole fraction are possible. In addition to the tracer aspects of the whole air sampler measurements, we measure a full suite of halocarbon species that provide information on the role of short-lived halocarbons in the tropical UT/LS region, on halogen budgets in the UT/LS region, and on continuing increasing temporal trends of HFCs (such as 134a), HCFCs (such as HCFC 141b), PFCs (such as C2F6), as well as declining levels of some of the major CFCs and halogenated solvents. The measurements of those species that are changing rapidly in the troposphere also give direct indications of the age and origin of air entering the stratosphere.