NASA - National Aeronautics and Space Administration

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.

The SAFS instruments determine wavelength dependent actinic flux from 280-420 nm. The actinic flux in combination with the absorption cross section and quantum yield molecular data will be used to calculate the photolysis frequencies of multiple photochemically important molecular processes, including O3, NO2, HONO, CH2O, H2O2, CH3OOH, HNO3, PAN, CH3NO3, CH3CH2NO3, and CH3COCH3.

The SAFS measurement is based on a 2p steradian hemisphere hemispherical quartz light collector, a double monochromator, and a low dark current photomultiplier. The monochromator employs dual 2400 G/mm gratings which produce a 1 nm FWHM spectral resolution and very low straylight. The instrument package on the aircraft includes two independent, but time synchronized (IRIG-B) spectroradiometer systems to measure the up- and down-welling fluxes in a 10 second scan time. Summing these produces the spherically integrated actinic flux.

POS AV is a hardware and software system specifically designed for direct georeferencing of airborne sensor data. By integrating precision GNSS with inertial technology, POS AV enables geospatial projects to be completed more efficiently, effectively, and economically. POS AV is engineered for aerial cameras, scanning lasers, imaging sensors, synthetic aperture radar, and LIDAR technology.

Provides information on aircraft position, orientation and meteorological variables.

The Ames PANAK instrument is a computerized 3- channel Capillary Gas Chromatographic system designed for the collection and analysis of low ppt (10-12 v/v) levels of peroxyacyl nitrates (PANs), alkyl nitrates, and tertrachloroethene in Channels 1 and 2; and C2-C3 aldehydes, C1-C2 alcohols, C3-C4 ketones, and C1-C2 nitriles in channel 3. Channels 1 and 2 use ECD detectors and have a sampling frequency of 2.5 minutes. Channel 3 uses a Photo Ionization detector placed in series with a Reduction Gas detector and has a sampling frequency of 5 minutes. The main manifold draws 5 SL/min of ambient air through a heated Teflon lined probe from which each of the three instrument channels draws a 200 ml aliquot of sample air. This aliquot is dried by passing it through a –35 °C cold trap, cooled to -140 °C for constituent pre concentration, and then heat desorbed into the gas chromatographic columns. All calibrations are performed in-flight by using an installed dilution system and in a manner that mimics ambient air sampling. Primary standards are generally referred to a series of permeation tubes. In addition high concentration standards are also carried on board. Sensitivities under typical conditions are: 1-3 ppt PANs, 1-5 ppt alkyl nitrates, 5-20 ppt OVOC, and 20-30 ppt nitriles.

The PAN-CIGAR chemical ionization mass spectrometer which measures up to 7 PAN species simultaneously and semi-continuously with a time resolution of ~2 seconds. The method is based on the detection of the acylperoxy radicals formed from thermal decomposition of the PAN species at the inlet by reacting them with iodide ions, which are formed by passing methyl iodide diluted in nitrogen through an α–particle source. The reaction of the peroxy acyl radicals with I- forms IO and the acyl ion, which is detected using a quadrupole mass spectrometer (Extrel) at a mass to charge ratio of 59 in the case of PAN. The method is very specific for PAN type compounds and the limit of detection is ~1 pptv/s or better for most PAN species. The instrument employs a realtime continuous calibration using isotopically labeled PAN produced in-situ by a photolytic calibration source.

A modified LI-COR model 6252 infrared gas analyzer forms the basis of a CO2 sampling system. The LI-COR is small (13 x 24 x 34 cm) and composed of dual 12 cm3 volume sample/reference cells; a feedback stabilized infrared source; 500 Hz chopper; thermoelectrically-cooled solid state PbSe detector; and a narrow band (150 nm) interference filter centered on the 4.26 μm CO2 absorption band. Using synchronous signal detection techniques, it operates by sensing the difference in light absorption between the continuously flowing sample and reference gases occupying each side of the dual absorption cell. Thus, by selecting a reference gas of approximately the same concentration as background air (~ 378 ppmv), very minute fluctuations in atmospheric concentration can be quantified with high precision (≤ 0.07 ppmv). The system is operated at constant pressure (250 torr) and has a 0.1 second electronic time response.

During ambient sampling, air is continuously drawn through a Rosemount inlet probe, a permeable membrane dryer to remove H2O(v), the LI-COR, and then exchanged through a diaphragm pump that vents overboard. In-flight calibrations are performed every 15 minutes using standards traceable to the primary standards maintained by the WMO Central CO2 Laboratory. By interpolating between these calibrations, slow drifts in instrument response are effectively suppressed, yielding high precision values. Temperature control of the instrument minimizes thermal drift thus maximizing ambient sampling time by decreasing calibration frequency. The CO2 measurement accuracy is closely tied to the accuracy of the standards obtained from NOAA/CMDL, Boulder, CO prior to the mission.

1) Time of Flight Aerosol Mass Spectrometer (ToF-AMS)

Total and single particle characterization of volatile aerosol ionic and organic components (50-700nm). Uncertainty depends on species and concentration.

2) Single Particle Soot Photometer (SP2)

Single particle measure of BC (soot) mass in particles and determination of mixed particle size and non-BC coating using laser scattering and incandescence. 70-700nm. Single particle counting up to 10,000 per sec.

3) A size-resolved thermo-optic aerosol discriminator (30 s avg.):

Aerosol size distribution from 0.12 up to 7.0 μm, often where most aerosol mass, surface area and optical effects are dominant. Uses a modified Laser Optical Particle Counter (OPC) and computer controlled thermal conditioning system is used upstream (airstream dilution dried). Characterizes aerosol components volatile at 150, 300 and 400C and refractory aerosol at 400C (sea salt, dust and soot/flyash). (Clarke, 1991, Clarke et al., 2004). Uncertianty about 15%

4) Condensation Nuclei - heated and unheated (available at 1Hz)

Two butanol based condensation nuclei (CN) counter (TSI 3010) count all particles between 0.01-3.0 um. Total CN, refractory CN (those remaining at 300C after sulfate is removed) and volatile CN (by difference) are obtained as a continuous readout as a fundamental air mass indicator (Clarke et al. 1996). Uncertainty ~ 5%.

5) Aerodynamic Particle Sizer – (APS-TSI3320) – (<5min/scan)

To further characterize larger “dry” particles, including dust, an APS is operated which sizes particles aerodynamically from 0.8 to 20 μm into 50 channels. Uncertainty~10%.

6) Differential Mobility Analyzer with thermal conditioning – (<3 min/scan)

Volatility tandem thermal differential mobility analyzer (VTTDMA) with thermal analysis that provides size information (mass, surface area, number distributions) and their state of mixing over the 0.01 to 0.3μm size range (Clarke et al., 1998, 2007) for sampling times of about 1-3 minutes. Uncertainty ~10%

7) Nephelometer (10-7 m-1 detection for 60s avg., recorded every 1 sec.)

A 3 wavelength nephelometer (450, 550, 700nm) is used for total scattering and submicrometer scattering values using a Radiance Research single wavelength nephelometer (and thereby coarse dust scattering by difference).

8) Two Particle Soot Absorption Photometers (PSAP-Radiance Research; detection <0.1μg m-3 for 5 min. avg. )

The PSAP is used to quantify the spectral light absorption coefficient of the total and submicron aerosol (eg. soot, BC) at three wavelengths (450, 550, 660nm).

9) Humidity Dependent Light-Scattering (10-6 m-1 detection for 60s avg.; recorded every 1 s)

Two additional Radiance Research single-wavelength nephelometers are operated at two humidities (high/low) to establish the humidity dependence of light scattering, f(RH).

The DLH has been successfully flown during many previous field campaigns on several aircraft, most recently ACTIVATE (Falcon); FIREX-AQ, ATom, KORUS-AQ, and SEAC4RS (DC-8); POSIDON (WB-57); CARAFE (Sherpa); CAMP2Ex and DISCOVER-AQ (P-3); and ATTREX (Global Hawk). This sensor measures water vapor (H2O(v)) via absorption by one of three strong, isolated spectral lines near 1.4 μm and is comprised of a compact laser transceiver and a sheet of high grade retroflecting road sign material to form the optical path. Optical sampling geometry is aircraft-dependent, as each DLH instrument is custom-built to conform to aircraft geometric constraints. Using differential absorption detection techniques, H2O(v) is sensed along the external path negating any potential wall or inlet effects inherent in extractive sampling techniques. A laser power normalization scheme enables the sensor to accurately measure water vapor even when flying through clouds. An algorithm calculates H2O(v) concentration based on the differential absorption signal magnitude, ambient pressure, and temperature, and spectroscopic parameters found in the literature and/or measured in the laboratory. Preliminary water vapor mixing ratio and derived relative humidities are provided in real-time to investigators.

The in‐situ diode laser spectrometer system, referred to by its historical name DACOM, includes three tunable diode lasers providing 4.7, 4.5, and 3.3 μm radiation for accessing CO, N2O, and CH4 absorption lines, respectively. The three laser beams are combined by the use of dichroic filters and are then directed through a small volume (0.3 liter) Herriott cell enclosing a 36 meter optical path. As the three coincident laser beams exit the absorption cell, they are spectrally isolated using dichroic filters and are then directed to individual detectors, one for each laser wavelength. Wavelength reference cells containing CO, CH4, and N2O are used to wavelength lock the operation of the three lasers to the appropriate absorption lines. Ambient air is continuously drawn through a Rosemount inlet probe and a permeable membrane dryer which removes water vapor before entering the Herriott cell and subsequently being exhausted via a vacuum pump to the aircraft cabin. To minimize potential spectral overlap from other atmospheric species, the Herriott cell is maintained at a reduced pressure of ~90 Torr. At 5 SLPM mass flow rate, the absorption cell volume is exchanged nominally twice per second. Frequent but short calibrations with well documented and stable reference gases are critical to achieving both high precision and accuracy. Calibration for all species is accomplished by periodically (~4 minutes) flowing calibration gas through this instrument. Measurement accuracy is closely tied to the accuracy of the reference gases obtained from NOAA/ESRL, Boulder, CO. Both CO and CH4 mixing ratios are provided in real-time to investigators aboard the DC‐8.