Quantifying functional group compositions of household fuel-burning emissions.

Globally, billions of people burn fuels indoors for cooking and heating, which contributes to millions of chronic illnesses and premature deaths annually. Additionally, residential burning contributes significantly to black carbon emissions, which have the highest global warming impacts after carbon dioxide and methane. In this study, we use Fourier transform infrared spectroscopy (FTIR) to analyze fine-particulate emissions collected on Teflon membrane filters from 15 cookstove types and 5 fuel types. Emissions from three fuel types (charcoal, kerosene, and red oak wood) were found to have enough FTIR spectral response for functional group (FG) analysis. We present distinct spectral profiles for particulate emissions of these three fuel types. We highlight the influential FGs constituting organic carbon (OC) using a multivariate statistical method and show that OC estimates by collocated FTIR and thermal-optical transmittance (TOT) are highly correlated, with a coefficient determination of 82.5 %. As FTIR analysis is fast and non-destructive and provides complementary FG information, the analysis method demonstrated herein can substantially reduce the need for thermal-optical measurements for source emissions.

Water Activity from Equilibrium Molecular Dynamics Simulations and Kirkwood-Buff Theory.

Water activity and related thermodynamic properties are calculated for several aqueous solutions using equilibrium molecular dynamics in conjunction with the recent extension of the Kirkwood-Buff (KB) theory for closed systems. The general applicability of this method is evaluated on aqueous mixtures of ethanol, glyoxal, malonic acid, and NaCl, which represent different types of condensed-phase interactions. Solution microstructures are analyzed using KB integrals and cluster analysis to identify molecular associations due to hydrophobic interactions, hydrate formation, hydrogen bonding, or electrostatic forces affecting solution nonideality in the different systems. Activity estimation by this implementation-subvolume-KB molecular dynamics, or SKBMD, simulation-agrees well with experimental measurements and UNIFAC calculations over a wide range of nonideality, with the exception of the malonic acid/water system. Systematic deviations for this system are attributed to the deficiency of the standard OPLS force field, and are partially remediated with a Non-Bonded FIX (NBFIX) correction to reduce its extensive hydrogen-bonded clustering. Comparison of water and solute excess chemical potentials against other molecular simulation techniques for NaCl/water mixtures shows the SKBMD method to be competitive in performance with those requiring additional external constraints or computational complexity. Equilibrium molecular dynamics and KB theory can therefore be suitable for estimation of solution properties and testing the suitability of force fields, though strongly associating components leading to large and long-lived molecular clusters (either in reality or as a result of a bias in atom-atom potentials) can lead to inefficient sampling and higher estimation errors.

Electrospray Film Deposition for Solvent-Elimination Infrared Spectroscopy.

The application of electrospray (ES) for quantitative transfer of analytes from solution to an internal reflection element for analysis by attenuated total reflection Fourier transform infrared (ATR FT-IR) spectroscopy has been developed in this work. The ES ATR FT-IR method is evaluated with non-volatile and semi-volatile organic and inorganic compounds dissolved in pure organic solvents or organics in a mixture with water. The technique demonstrates the capability for rapid solvent evaporation from dilute solutions, facilitating the creation of thin films that allow ATR FT-IR to generate transmission-mode-like spectra. Electrospray ATR FT-IR with multiple reflections displays a linear response ( R2 = 0.95-0.99) in absorbance with the deposited mass and instrumental detection limit < 100 ng, which demonstrates potential for quantitative applications. The method is applicable when crystalline substances are present, even though the formation of particles restricts the upper limit of mass loadings relative to substances forming homogeneous films. In addition to the solvent, semi-volatile compounds can evaporate during the ES process; the magnitude of losses will depend on solution composition and temperature.

Long-Term Strategy for Assessing Carbonaceous Particulate Matter Concentrations from Multiple Fourier Transform Infrared (FT-IR) Instruments: Influence of Spectral Dissimilarities on Multivariate Calibration Performance.

Matching the spectral response between multiple spectrometers is a mandatory procedure when developing robust calibrations whose prediction is independent of instrument-related signal variations. A viable alternative to complex calibration transfer methods consists of matching the instrument spectral response by controlling a set of key instrumental and environmental parameters. This paper discusses the applicability of such an approach to three Fourier transform infrared (FT-IR) spectrometers used for the routine assessment of carbonaceous particulate matter concentrations in the Interagency Monitoring of PROtected Visual Environments (IMPROVE) speciation network. The effectiveness of the proposed matching procedure is evaluated by comparing the spectral response for each individual instrument in order to characterize the extent, and nature, of the remaining inter-instrument spectral dissimilarities. Instrument-related contributions to the signal were determined to be small compared with the spectral variability induced by the filter type used for sample collection. The impact of spectral differences on prediction was addressed through the comparison of model performance derived from multiple calibration scenarios. A hybrid model yielding accurate and homogeneous prediction regardless of the instrument was proposed for organic carbon (OC) and elemental carbon (EC), two major constituents of atmospheric particulate matter. Coefficients of determination of 0.98 (OC) and 0.90 (EC) with median biases not exceeding 0.20 µg (OC) and 0.07 µg (EC) are reported. The long-term stability, assessed from weekly measurements of reference samples, shows a deviation in predicted concentrations of less than ±5% over a 2.5-year period for most of the data collected. Extending OC and EC hybrid models to the prediction of ambient samples collected during the two subsequent years provides satisfactory performance. The proposed instrument matching procedure coupled with the relative simplicity of the hybrid model is an alternative to computationally advanced calibration transfer methodologies for the characterization of carbonaceous particulate matter using multiple FT-IR instruments.

Regional Similarities and NOx-related Increases in Biogenic Secondary Organic Aerosol in Summertime Southeastern U.S.

During the 2013 Southern Oxidant and Aerosol Study, Fourier Transform Infrared Spectroscopy (FTIR) and Aerosol Mass Spectrometer (AMS) measurements of submicron mass were collected at Look Rock (LRK), Tennessee, and Centreville (CTR), Alabama. Carbon monoxide and submicron sulfate and organic mass concentrations were 15-60% higher at CTR than at LRK but their time series had moderate correlations (r~0.5). However, NOx had no correlation (r=0.08) between the two sites with nighttime-to-early-morning peaks 3~10 times higher at CTR than at LRK. Organic mass (OM) sources identified by FTIR Positive Matrix Factorization (PMF) had three very similar factors at both sites: Fossil Fuel Combustion (FFC) related organic aerosols, Mixed Organic Aerosols (MOA), and Biogenic Organic Aerosols (BOA). The BOA spectrum from FTIR is similar (cosine similarity > 0.6) to that of lab-generated particle mass from the photochemical oxidation of both isoprene and monoterpenes under high NOx conditions from chamber experiments. The BOA mass fraction was highest during the night at CTR but in the afternoon at LRK. AMS PMF resulted in two similar pairs of factors at both sites and a third nighttime NOx-related factor (33% of OM) at CTR but a daytime nitrate-related factor (28% of OM) at LRK. NOx was correlated with BOA and LO-OOA for NOx concentrations higher than 1 ppb at both sites, producing 0.5 ± 0.1 µg m-3 for CTR-LO-OOA and 1.0 ± 0.3 µg m-3 for CTR-BOA above 1 ppb additional biogenic OM for each 1 ppb increase of NOx.

Aerosol Health Effects from Molecular to Global Scales.

Poor air quality is globally the largest environmental health risk. Epidemiological studies have uncovered clear relationships of gaseous pollutants and particulate matter (PM) with adverse health outcomes, including mortality by cardiovascular and respiratory diseases. Studies of health impacts by aerosols are highly multidisciplinary with a broad range of scales in space and time. We assess recent advances and future challenges regarding aerosol effects on health from molecular to global scales through epidemiological studies, field measurements, health-related properties of PM, and multiphase interactions of oxidants and PM upon respiratory deposition. Global modeling combined with epidemiological exposure-response functions indicates that ambient air pollution causes more than four million premature deaths per year. Epidemiological studies usually refer to PM mass concentrations, but some health effects may relate to specific constituents such as bioaerosols, polycyclic aromatic compounds, and transition metals. Various analytical techniques and cellular and molecular assays are applied to assess the redox activity of PM and the formation of reactive oxygen species. Multiphase chemical interactions of lung antioxidants with atmospheric pollutants are crucial to the mechanistic and molecular understanding of oxidative stress upon respiratory deposition. The role of distinct PM components in health impacts and mortality needs to be clarified by integrated research on various spatiotemporal scales for better evaluation and mitigation of aerosol effects on public health in the Anthropocene.

Molecular Structure Inhibiting Synergism in Charged Surfactant Mixtures: An Atomistic Molecular Dynamics Simulation Study.

Synergistic and nonsynergistic surfactant-water mixtures of sodium dodecyl sulfate (SDS), lauryl betaine (C12B), and cocoamidopropyl betaine (CAPB) systems are studied using molecular simulation to understand the role of interactions among headgroups, tailgroups, and water on structural and thermodynamic properties at the air-water interface. SDS is an anionic surfactant, while C12B and CAPB are zwitterionic; CAPB differs from C12B by an amide group in the tail. While the lowest surface tensions at high surface concentrations in the SDS-C12B synergistic system could not be reproduced by simulation, estimated partitioning between surface and bulk shows trends consistent with synergism. Structural analysis shows the influence of the SDS headgroup pulling C12B to the surface, resulting in closely packed structures compared to their respective homomolecular-surfactant systems. The SDS-CAPB system, on the other hand, is nonsynergistic when the surfactants are mixed on account of the tilted structure of the CAPB tail. The translational excess entropy due to the tailgroup interactions discriminates between the synergistic and nonsynergistic systems. The implications of such interactions on surfactant effects in complex, multicomponent atmospheric aerosols are discussed.

Carbon Density Is an Indicator of Mass Accommodation Coefficient of Water on Organic-Coated Water Surface.

The condensational growth of a water droplet follows water vapor accommodation and is described by the mass accommodation coefficient, α. To determine α for droplets coated by straight chain and branched alcohols, we perform molecular dynamics simulations with umbrella sampling and direct impinging. The free energy profiles of water from gas phase to bulk water coated by organic are estimated by the former method. These free energy profiles exhibit a barrier to accommodation in the monolayers containing alcohols with zero and one-level of branching. However, the barrier is not observed for monolayers containing alcohols with two-levels of branching. These profiles and friction coefficients estimated from simulation are used to calculate α from the transition state and Grote-Hynes theory. Results are compared with sticking probabilities estimated from direct impinging simulations, and their differences are interpreted through processes included in each theory. At a low surface coverage of these surface active molecules, the underlying bulk solution is exposed and the resistance to vapor accommodation is reduced. We estimate the carbon density in water surfaces coated by straight-chain alcohols, branched alcohols, and straight-chain fatty acids used in study by Takahama and Russell,1 and show that this quantity is related monotonically to the mass accommodation coefficient.

Efflorescence transitions of ammonium sulfate particles coated with secondary organic aerosol.

Ammonium sulfate particles were generated by atomization and introduced into a smog chamber where they were coated with secondary organic aerosol from ozonolysis of limonene or alpha-pinene. These mixed particles were then sampled with a humidified Tandem-DMA system where a monodisperse aerosol population was selected, humidified, and dried to observe the relative humidity (RH) at which the particles returned to the original dry diameter. The volume fraction of secondary organic aerosol (SOA) in the mixed particles ranged from 0.59 to 0.94 for limonene SOA and 0.54 to 0.72 for alpha-pinene SOA. Efflorescence RHs for our mixed aerosols were in the range of 28-34%, similar to our observation of 32% ERH for pure ammonium sulfate nanoparticles. These findings indicate that the effect of SOA on the ERH of inorganic salts in the atmosphere may be negligible.