Hydrocarbon Production and Photochemical Ozone Formation in Forest Burn Plumes

The purpose of this paper is to describe ozone production in forest slash burn plumes. Plumes from controlled fires in the state of Washington were monitored using an instrumented aircraft. Ozone, oxides of nitrogen, condensation nuclei, and visual range (nephelometer) were measured continuously on board the plane. Airborne grab samples were collected for detailed hydrocarbon analysis.

The slash burn plumes were found to contain significant quantities of ozone. A buildup of 40–50 ppb above the ambient background ozone concentrations was not unusual. Hydrocarbon analyses revealed the presence of many photochemically reactive olefins in the plume. Hydrocarbon/NO _x ratios were favorable for photochemical oxidant production.     

Formaldehyde Concentrations Inside Private Residences: A Mail-Out Approach to Indoor Air Monitoring

Abstract

The main objective of this study was to monitor the volatile organic compounds (VOCs) in the stack gas released from organic chemical industrial plants to determine emission factors. Samples from 52 stacks, with or without air pollution control devices (APCDs), from seven industrial processes were taken and VOCs measured using U.S. Environmental Protection Agency (EPA) Method 18. These 7 processes, including 26 plants, were the manufacturers of acrylonitrile–butadiene–styrene (ABS), polyvinyl chloride (PVC), polystyrene (PS), acrylic resin (ACR), vinyl chloride (VC), para–terephthalic acid (PTA), and synthetic fiber (SYF). The results clearly indicate significant variations of emission factors among the various industrial processes, particularly emission factors for those without APCDs. As expected, those with APCDs yield much less emission factors. Regardless of those with or without APCDs, the order of manufacturing processes with regard to VOC emission factors is SYF > ABS > PS > ACR > PTA > PVC > VC. The emission factors for some processes also differ from those in EPA–42 data file. The VOC profiles further indicate that some VOCs are not listed in the U.S. VOC/Particulate Matter Speciation Data System (SPECIATE). The potential O₃ formation is determined from the total amount of VOC emitted for each of seven processes. The resultant O₃ yield varied from 0.22 (ACR) to 2.33 g O₃ g^–1 VOC (PTA). The significance of this O₃ yield is discussed.     

Evaluation of wireless sensor networks (WSNs) for remote wetland monitoring: design and initial results

Here, we describe and evaluate two low-power wireless sensor networks (WSNs) designed to remotely monitor wetland hydrochemical dynamics over time scales ranging from minutes to decades. Each WSN (one student-built and one commercial) has multiple nodes to monitor water level, precipitation, evapotranspiration, temperature, and major solutes at user-defined time intervals. Both WSNs can be configured to report data in near real time via the internet. Based on deployments in two isolated wetlands, we report highly resolved water budgets, transient reversals of flow path, rates of transpiration from peatlands and the dynamics of chromophoric-dissolved organic matter and bulk ionic solutes (specific conductivity)—all on daily or subdaily time scales. Initial results indicate that direct precipitation and evapotranspiration dominate the hydrologic budget of both study wetlands, despite their relatively flat geomorphology and proximity to elevated uplands. Rates of transpiration from peatland sites were typically greater than evaporation from open waters but were more challenging to integrate spatially. Due to the high specific yield of peat, the hydrologic gradient between peatland and open water varied with precipitation events and intervening periods of dry out. The resultant flow path reversals implied that the flux of solutes across the riparian boundary varied over daily time scales. We conclude that WSNs can be deployed in remote wetland-dominated ecosystems at relatively low cost to assess the hydrochemical impacts of weather, climate, and other perturbations.     

Does Riparian Fencing Protect Stream Water Quality in Cattle-Grazed Lands?

Environmental Management - Cattle degrade streams by increasing sediment, nutrient, and fecal bacteria levels. Riparian fencing is one best management practice that may protect water quality within...     

Elimination of 10 polybrominated diphenyl ether (PBDE) congeners and selected polychlorinated biphenyls (PCBs) from the freshwater mussel, Elliptio complanata

Mussel biomonitors are widely used as screening tools for polybrominated diphenyl ethers (PBDEs) in marine and aquatic environments. This study determined elimination rate coefficients (k(tot)) for eight PBDE and five PCB congeners in the freshwater mussel, Elliptio complanata, over a 120d depuration period. Elimination of BDE 15, 28, 47, 75 and 100 was similar to PCBs of equivalent hydrophobicity and negatively related to chemical K(OW). Rapid elimination of BDE 190 and an inferred rapid elimination of BDE 183 indicate mussels are capable of biotransformation of certain highly brominated PBDEs. Time to 90% steady state ranged from 48 to 66d for di- and tribromoDE congeners and from 91 to >250d for tetra- to hexabromoDE congeners. Given the long time periods required for steady state, mussel accumulated PBDE residues should be interpreted in the context of calibrated bioaccumulation models.     

Evaluation of the STP model: comparison of modelled and experimental results for ten polycyclic aromatic hydrocarbons (PAHs)

Screening level risk assessment models are used by many countries to assess the treatability of organic chemicals during the sewage treatment process, especially those that are new to commerce. The performance of one such model, the sewage treatment plant model, is evaluated in the current study by comparing model predictions with actual measurement data collected at various stages of a typical full-scale activated sludge type sewage treatment plant. A suite of ten polycyclic aromatic hydrocarbons (PAHs) with widely varying physico–chemical properties were monitored for the comparison. Model predicted removal efficiencies were in very good agreement with those measured for all ten PAHs. Observed chemical concentrations and their trends at various stages of the sewage treatment process were also well simulated by the model. Results also suggest that a reasonable first approximation estimate of a range for the biodegradation half-life needed for the model may be obtained by dividing reported aqueous biodegradation half-life by scaling factors of 50 and 150.     

Quantifying the availability and the stability of trace cationic elements in fly ash

For adsorption-desorption controlled leaching processes, the total leachable mass and the adsorption constant are parameters representing the availability and the stability of trace elements in solid media. With these parameters, one can predict the leaching behavior of trace elements from solids under various pH and solid-to-liquid ratio conditions. An approach was developed in this paper to determine these parameters for model elements Cu(II), Cd(II), and Ni(II) in fly ash. This approach consists of a batch equilibrium titration, a batch equilibrium leaching with and without target element addition, and mathematical modeling. Results indicated that the adsorption constant of a trace element can be determined by modeling the adsorption ratio of the added element to the system as a function of pH. Results also indicated that the trace element originally present in fly ash had similar adsorption-desorption behavior as that added externally. By modeling the batch leaching data with and without external element addition, the total leachable mass and adsorption constant of the target element can be determined simultaneously. The total leachable mass is in agreement with experimental data from 50mM EDTA extraction.     

Reaction hazards of triethylaluminum under closed conditions

We evaluate the reaction hazards of triethylaluminum (TEA) under closed conditions for safe treatment of aluminum alkyls. The explosive reactions of TEA are difficult to be estimated using thermal analysis because the estimate reactions are too slow under these conditions. The results of our closed vessel tests and chemical equilibrium calculations show that the TEA and water system mixture in closed conditions decomposes into lower-molecular-weight compounds than the products by using well-known hydrolysis of TEA. The present work also demonstrates that large temperature and pressure increases could occur because of the existence of TEA and aluminum hydroxide. Since aluminum hydroxide contains water as alumina hydrates, aluminum hydroxide could have been the source of water at high temperatures and could have contributed to the mixed reaction between TEA and water.