Partitioning of NH3-NH4+ in the Southeastern U.S.

The formation of inorganic fine particulate matter (i.e., iPM2.5) is controlled by the thermodynamic equilibrium partitioning of NH3-NH4+. To develop effective control strategies of PM2.5, we aim to understand the impacts of changes in different precursor gases on iPM2.5 concentrations and partitioning of NH3-NH4+. To understand partitioning of NH3-NH4+ in the southeastern U.S., responses of iPM2.5 to precursor gases in four seasons were investigated using field measurements of iPM2.5, precursor gases, and meteorological conditions. The ISORROPIA II model was used to examine the effects of changes in total ammonia (gas + aerosol), total sulfuric acid (aerosol), and total nitric acid (gas + aerosol) on iPM2.5 concentrations and partitioning of NH3-NH4+. The results indicate that reduction in total H2SO4 is more effective than reduction in total HNO3 and total NH3 to reduce iPM2.5 especially under NH3-rich condition. The reduction in total H2SO4 may change partitioning of NH3-NH4+ towards gas-phase and may also lead to an increase in NO3− under NH3-rich conditions, which does not necessarily lead to full neutralization of acidic gases (pH < 7). Thus, future reduction in iPM2.5 may necessitate the coordinated reduction in both H2SO4 and HNO3 in the southeastern U.S. It is also found that the response of iPM2.5 to the change in total H2SO4 is more sensitive in summer than winter due to the dominance of SO42− salts in iPM2.5 and the high temperature in summer. The NH3 emissions from Animal Feeding Operations (AFOs) at an agricultural rural site (YRK) had great impacts on partitioning of NH3-NH4+. The Multiple Linear Regression (MLR) model revealed a strong positive correlation between cation-NH4+ and anions-SO42− and NO3−. This research provides an insight into iPM2.5 formation mechanism for the advancement of PM2.5 control and regulation in the southeastern U.S.

Capture of Acidic Gases from Flue Gas by Deep Eutectic Solvents

Up to now, many kinds of deep eutectic solvents (DESs) were investigated for the capture of acidic gases from flue gases. In this review, non-functionalized and functionalized DESs, including binary and ternary DESs, for SO2, CO2 and NO capture, are summarized based on the mechanism of absorption, physical interaction or chemical reaction. New strategies for improving the absorption capacity are introduced in this review. For example, a third component can be introduced to form a ternary DES to suppress the increase in viscosity and improve the CO2 absorption capacity. DESs, synthesized with halogen salt hydrogen bond acceptors (HBAs) and functionalized hydrogen bond donors (HBDs), can be used for the absorption of SO2 and NO with high absorption capacities and low viscosities after absorption, due to physicochemical interaction between gases and DESs. Emphasis is given to introducing the absorption capacities of acidic gases in these DESs, the mechanism of the absorption, and the ways to enhance the absorption capacity.

Honeycomb wet scrubber for acidic gas control: modeling and long-term test results

A laboratory scale, 1.0 CMM (m3 min− 1) wet scrubber packed with water-absorbing honeycomb material (HWS) with a very large geometric surface area of 480 m2 m− 3 and a low pressure drop developed in our previous study was shown to achieve a very high removal efficiency for acidic gases but there were no long-term test data. In this study, the HWS scaled up to operate at a 100 CMM flow rate was tested for removing mixed acidic gases at a semiconductor fab for a very long period of 3.5 yr. Results showed that the removal efficiency for the mixed gases emitted from the fab always maintained as high as > 95% for HF, CH3COOH, HCl, HNO3, HNO2, and H2SO4 with the inlet concentrations ranging from supper-ppmv to sub-ppmv, during a 3.5-yr period. With water jet cleaning of the honeycomb modules once per year, the pressure drop of the HWS remained to be low at 0.5–0.8 cm H2O, indicating minimal scaling in the HWS. Additionally, the predicted height and removal efficiencies of the HWS were very close to the experimental data. The excellent long-term performance of the HWS warrants its potential applications in many areas in which liquid absorption is the preferred treatment method and the theoretical equations can facilitate the design of the HWS.

The importance of size ranges in aerosol instrument intercomparisons: a case study for the Atmospheric Tomography Mission

Aerosol intercomparisons are inherently complex as they convolve instrument-dependent detection efficiencies vs. size (which often change with pressure, temperature, or humidity) and variations in the sampled aerosol population, in addition to differences in chemical detection principles (e.g., inorganic-only nitrate vs. inorganic plus organic nitrate for two instruments). The NASA Atmospheric Tomography Mission (ATom) spanned four separate aircraft deployments which sampled the remote marine troposphere from 86∘ S to 82∘ N over different seasons with a wide range of aerosol concentrations and compositions. Aerosols were quantified with a set of carefully characterized and calibrated instruments, some based on particle sizing and some on composition measurements. This study aims to provide a critical evaluation of inlet transmissions impacting aerosol intercomparisons, and of aerosol quantification during ATom, with a focus on the aerosol mass spectrometer (AMS). The volume determined from physical sizing instruments (aerosol microphysical properties, AMP, 2.7 nm to 4.8 µm optical diameter) is compared in detail with that derived from the chemical measurements of the AMS and the single particle soot photometer (SP2). Special attention was paid to characterize the upper end of the AMS size-dependent transmission with in-field calibrations, which we show to be critical for accurate comparisons across instruments with inevitably different size cuts. Observed differences between campaigns emphasize the importance of characterizing AMS transmission for each instrument and field study for meaningful interpretation of instrument comparisons. Good agreement (regression slope =0.949 and 1.083 for ATom-1 and ATom-2, respectively; SD =0.003) was found between the composition-based volume (including AMS-quantified sea salt) and that derived from AMP after applying the AMS inlet transmission. The AMS captured, on average, 95±15 % of the standard PM1 volume (referred to as the URG Corp. standard cut 1 µm cyclone operated at its nominal efficiency). These results support the absence of significant unknown biases and the appropriateness of the accuracy estimates for AMS total mass and volume for the mostly aged air masses encountered in ATom. The particle size ranges (and their altitude dependence) that are sampled by the AMS and complementary composition instruments (such as soluble acidic gases and aerosol, SAGA, and particle analysis by laser mass spectrometry, PALMS) are investigated to inform their use in future studies.

Soluble Salts Quantitative Characterization and Thermodynamic Modeling on Roman Bricks to Assess the Origin of Their Formation

The environmental weathering and the formation of efflorescences on the brick walls are studied at the “Casa di Diana” Mithraeum at Ostia Antica archaeological site. Previous studies on subsoil, bedrock, hydrological systems and environmental conditions, and new ion chromatography analysis combined with ECOS-RUNSALT and Medusa-Hydra thermodynamic modelling software, had allowed us to identify the subsoil contamination related to soluble salts. The atmospheric acidic gases, CO2 and SO2, are determined as the main salt weathering species. A dry deposition after a subsequent hydration action from the shallow freshwater aquifer that reaches up to 1 m on the walls is identified as the mechanism of salt formation. An evaluation of potential sources such as the nearby Fiumicino airport, CO2-rich gases inputs from fumaroles and CO2 inputs was also debated. The risk level of contamination the surfaces of the materials should be considered mildly/very polluted with a medium/high risk of hygroscopic moisture due to the high concentration of sulphates.

Life cycle impact assessment of metal production industries in Australia

Metal production industries are associated with positive economic benefits, however their activities are significantly resource and energy intensive, contributing to emission of pollutants and greenhouse gases to the environment. The balance between the economic inputs and environmental footprint of the metal production industries determines their contribution to sustainability. This work provides environmental impact assessment of the production of aluminium, copper, gold, iron and steel, lead, nickel and zinc, and considers their contribution to the economy. The emissions of selected representative industries in Australia were sourced from public national emission inventories and used as input parameters in the openLCA software. ReCiPe midpoint and endpoint hierarchist impact assessment methods were used to investigate the environmental impacts of the selected industries. The results indicate that lead, followed by aluminium and nickel production had the largest environmental impacts. The work further revealed the specific emissions for better control for each industry taking into consideration their relative environmental and economic impacts. For instance, adoption of renewable energy sources would significantly decrease the greenhouse gas emissions and the associated environmental impacts of the copper, zinc, gold, and iron and steel production industries. Improvement of sustainability of the production of lead would require further control of trace metal emissions, while for aluminium and nickel production, improved control of emissions of particles and the acidic gases SO2 and NOx.

Failure Mechanisms of the Wellbore Mechanical Barrier Systems: Implications for Well Integrity

Energy sustainability is the main motive behind the evolution of the concept of well integrity in the oil and gas industry. The concept of well integrity adopts technical, operational, environmental, organizational, and safety measurements to secure the energy supply throughout the life of the well. Technically, a high quality well performance can be maintained by establishing robust barrier systems that are responsible for preventing, controlling, and mitigating potential risks that could arise during the well life cycle. A barrier system is conventionally nested from one or multiple elements that act individually or collectively to scaffold the well integrity. The protection layers in a wellbore can be lost if the integrity of the barrier system is compromised according to the failure of one or all of its elements. Failure can be triggered by technical or non-technical factors. In this study, technical aspects that drive barrier failure mechanisms have given more emphasis. The failure mechanisms of the key mechanical barrier systems, such as casing strings, cement, diverters, blowout preventers (BOPs), production stream valves, and seal assemblies, have been thoroughly investigated. In this study, a comprehensive review of barriers failure mechanisms has been conducted to identify the roots of failures and to outline some of the essential safety measures adopted to avoid the loss of well control. The major findings of this paper revealed that well barrier systems are highly susceptible to failure in unconventional reservoirs, deep and ultra-deep offshore wells, and geothermal wells. The predominant failures identified are casing collapse resulting from cyclic loads, cement percolation by gas migration, cement carking by hoop stress, BOPs wear and tear promoted by frequent tests, and elastomeric materials disintegration caused by acidic gases. Considering these failure mechanisms while designing a wellbore can help the engineers improve the construction quality. In addition, it can assist the operation and maintenance crews in optimizing safe operation boundaries.

Association Between Preeclampsia Risk and Fine Air Pollutants and Acidic Gases: A Cohort Analysis in Taiwan

Background: Fine air pollutant particles have been reported to be associated with risk of preeclampsia. The association between air pollutant exposure and preeclampsia risk in heavily air polluted Taiwan warrants investigation.Methods: We combined data from Taiwan National Health Insurance (NHI) Research Database (NHIRD) and Taiwan Air Quality Monitoring Database. Women aged 16–55 years were followed from January 1, 2000, until appearance of ICD-9 coding of preeclampsia withdrawal from the NHI program, or December 31, 2013. Daily concentration of NOx, NO, NO2, and CO was calculated by Kriging method. The Cox proportional hazard regression model was used for risk assessment.Results: For NOx, Relative to Quartile [Q] 1 concentrations, the Q2 (adjusted hazard ratio adjusted = 2.20, 95% CI = 1.50–3.22), Q3 (aHR = 7.28, 95% CI = 4.78–11.0), and Q4 (aHR = 23.7, 95% CI = 13.7–41.1) concentrations were associated with a significantly higher preeclampsia or eclampsia risk. Similarly, for NO, relative to Q1 concentrations, the Q2 (aHR = 1.82, 95% CI = 1.26–2.63), Q3 (aHR = 7.53, 95% CI = 5.12–11.0), and Q4 (aHR = 11.1, 95% CI = 6.72–18.3) concentrations were correlated with significantly higher preeclampsia or eclampsia risk. Furthermore, for NO2, relative to Q1 concentration, the Q2 (aHR = 1.99, 95% CI = 1.37–2.90), Q3 (aHR = 6.15, 95% CI = 3.95–9.57), and Q4 (aHR = 32.7, 95% CI = 19.7–54.3) concentrations also associated with a significantly higher preeclampsia or eclampsia risk.Conclusion: Women exposed to higher NOX, NO, NO2, and CO concentrations demonstrated higher preeclampsia incidence.

Recent Progress in Synthesis and Application of Nanosized and Hierarchical Mordenite—A Short Review

Zeolites with their unique properties find applications in various fields, including medicine, agronomy, ecology, production of detergents and drying agents, and in a number of industrial processes. Among zeolites, mordenite is particularly widespread because of its high silica/alumina ratio, which allows it to resist exposure to high temperatures and to acidic gases and liquids. Mordenite is commercially available as a natural mineral and as a synthesized material. This zeolite is mostly used in its synthetic form as an acid catalyst in the petrochemical industry for the isomerization of alkanes and aromatics. In this review, we consider the scientific literature on the structure, synthesis, and two main types of modifications that solve the diffusion difficulties during catalytic processes. The first type of modifications is related to a reduction of the size of the mordenite crystals obtained to submicron or nanometric range, whereas the second ones aim to obtain hierarchical mordenite samples by appropriate post-synthetic treatments. Both types of modifications find many other applications besides solving diffusion constraints in catalytic processes. Attempts to fine-tune and control the particle size in the first type of modifications or the pore size in the second ones by adjusting various parameters during the synthesis are described.