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In Situ Airborne Formaldehyde

The NASA GSFC In Situ Airborne Formaldehyde (ISAF) instrument measures formaldehyde (CH2O) on both pressurized and unpressurized (high-altitude) aircraft. Using laser induced fluorescence (LIF), ISAF possesses the high sensitivity, fast time response, and dynamic range needed to observe CH2O throughout the troposphere and lower stratosphere, where concentrations can range from 10 pptv to hundreds of ppbv.

Formaldehyde is produced via the oxidation of hydrocarbons, notably methane (a ubiquitous greenhouse gas) and isoprene (the primary hydrocarbon emitted by vegetation). Observations of CH2O can thus provide information on many atmospheric processes, including:
 - Convective transport of air from the surface to the upper troposphere
 - Emissions of reactive hydrocarbons from cities, forests, and fires
 - Atmospheric oxidizing capacity, which relates to formation of ozone and destruction of methane
In situ observations of CH2O are also crucial for validating retrievals from satellite instruments, such as OMI, TROPOMI, and TEMPO.

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Trace Organic Gas Analyzer

TOGA measures volatile organic compounds (VOCs). TOGA was deployed with an Agilent quadrupole mass spectrometer from 2006 through 2018. Since 2019, the TOGA has been equipped with a TOFWERK high-resolution time-of-flight (HR-TOF) mass spectrometer detector (TOGA-TOF). Specific data will be obtained for radical precursors, tracers of anthropogenic and biogenic activities, tracers of urban and biomass combustion emissions, tracers of ocean emissions, products of oxidative processing, precursors to aerosol formation, and compounds important for aerosol modification and transformation. TOGA measures a wide range of VOCs with high sensitivity (low to sub-ppt), frequency (2 minutes or better), accuracy (20% or better), and precision (<3%). Over 100 species are routinely measured throughout the troposphere and lower stratosphere from the surface to 16 km or higher. See table for list of VOCs that have been quantified using TOGA and TOGA-TOF. The TOGA-TOF is contained in a dual extended HIAPER rack, weighs approximately 225 kg and consumes ~1 kW of power. The major components of the instrument are the inlet, cryogenic preconcentrator, gas chromatograph, time-of-flight mass spectrometer detector, zero air/calibration system, and the control/data acquisition system. All processes and data acquisition are computer controlled.

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DC-8 - AFRC, Gulfstream V - NSF, C-130 - NSF
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Proton-Transfer-Reaction Mass Spectrometer

PTR-MS is a chemical ionization mass spectrometry technique that allows for fast measurements of organic trace gases. In combination with the CHARON inlet, it measures the organic composition of submicrometer aerosol particles.

 

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NCAR NOxyO3

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.

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CU Aircraft High-Resolution Time-of-Flight Aerosol Mass Spectrometer

Principle: The CU aircraft version of the Aerodyne High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS) detects non-refractory submicron aerosol composition by impaction on a vaporizer at 600°C, followed by electron ionization and time-of-flight mass spectral analysis. Size-resolved composition can be quantified by measuring the arrival times of the aerosol at the vaporizer.

Aircraft Operation: (1 min cycles, can be adjusted to meet mission goals):
46 s total concentration measurements (1 s resolution, can be increased to up to 10 Hz upon request)
5 s speciated size distribution measurements (with improved S/N detection due to ePToF acquisition)
9 s Background + Overhead
Higher accuracy due to flight day calibrations using built-in system
Custom pressure controlled inlet with confirmed performance up to 45 kft

Real Time Data Products: 
PM1 Aerosol Mass Concentrations:
Organic aerosol (OA) , SO4, NO3, NH4, Chloride 
OA Chemical Markers: f44 (Secondary OA), f57 (hydrocarbon-like OA), f60 (biomass burning OA), f82 (isoprene epoxide-SOA), other fx upon request

More Advanced Products:
- PM1 Seasalt, ClO4, total I, total Br, MSA concentrations
- O/C, H/C, OA/OC, OSc
- Particle organic nitrates (pRONO2)
- Ammonium Balance, estimated pH
- OA components by positive matrix factorization (PMF)
- Particle eddy covariance fluxes of all species
- Speciated Aerosol size distributions

Detection Limits (1s, ng sm-3), (1 min, ng sm-3) from start of the flight (due to custom cryopump):
Sulfate: 40, 15
Nitrate: 15, 6
Ammonium: 3, 1
Chloride: 30, 12
OA: 200, 80
For detailed OA analysis, longer averaging (3-30 s, depending on OA concentration) is needed. A 1 min product is hence provided as well.

 

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Langley Aerosol Research Group Experiment

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).

Aircraft: 
DC-8 - AFRC, C-130H - WFF, P-3 Orion - WFF, HU-25 Falcon - LaRC, King Air B-200 - LaRC, Twin Otter - CIRPAS - NPS
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Soluble Acidic Gases and Aerosols

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.

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Chemical Ionization Mass Spectrometer

The CIMS instrument consists of a low pressure ion molecule reactor (IMR) coupled to a quadrupole mass filter by an actively pumped collisional dissociation chamber (CDC) and an octopole ion guide. The vacuum system is a 100 mm outer diameter stainless steel chamber evacuated with two small turbo pumps (70 l s-1). The mass filter is a set of 9.5 mm diameter quadrupole rods housed in the main vacuum chamber. The CDC is a short 80 mm diameter chamber that houses an octopole ion guide and is evacuated with a hybrid molecular drag pump. The IMR is evacuated with a scroll pump (300 l min-1) that also serves as the backing pump for the mass spectrometer.

Click here for the Collaborative Ground and Airborne Observations description page.

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DC-8 - AFRC, Gulfstream V - NSF
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Whole Air Sampler

The UC-Irvine research group collected whole air samples aboard the NASA DC-8 aircraft during the summer 2019 NASA Fire Influence on Regional to Global Environments Experiment - Air Quality (FIREX-AQ) field mission. More than 70 trace gases were identified and quantified at our Irvine laboratory, including C2-C10 NMHCs, C1-C2 halocarbons, C1-C5 alkyl nitrates, and selected sulfur compounds using our established technique of airborne whole air sampling followed by laboratory analysis using gas chromatography (GC) with flame ionization detection (FID), electron capture detection (ECD), and mass spectrometric detection (MSD). Our experimental procedures build on those that have been successfully employed for numerous prior NASA field missions, for example PEM Tropics A and B, TRACE-P, INTEX-A and B, ARCTAS, DC-3, SEAC4RS, ATom, KORUS-AQ, FIREX-AQ, and SARP.

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Meteorological Measurement System

The Meteorological Measurement System (MMS) is a state-of-the-art instrument for measuring accurate, high resolution in situ airborne state parameters (pressure, temperature, turbulence index, and the 3-dimensional wind vector). These key measurements enable our understanding of atmospheric dynamics, chemistry and microphysical processes. The MMS is used to investigate atmospheric mesoscale (gravity and mountain lee waves) and microscale (turbulence) phenomena. An accurate characterization of the turbulence phenomenon is important for the understanding of dynamic processes in the atmosphere, such as the behavior of buoyant plumes within cirrus clouds, diffusions of chemical species within wake vortices generated by jet aircraft, and microphysical processes in breaking gravity waves. Accurate temperature and pressure data are needed to evaluate chemical reaction rates as well as to determine accurate mixing ratios. Accurate wind field data establish a detailed relationship with the various constituents and the measured wind also verifies numerical models used to evaluate air mass origin. Since the MMS provides quality information on atmospheric state variables, MMS data have been extensively used by many investigators to process and interpret the in situ experiments aboard the same aircraft.

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