ASsessment Of Alcohol Ethoxylate Surfactants And Fatty Alcohols Mixtures In River Sediments And Prospective Risk Assessment

A feasible and relatively readily available analytical method was adapted for the assessment of alcohol ethoxylates (AE) and fatty alcohols (FA) in sediments. This study illustrates the simultaneous measurement of 38 of 114 possible alcohol ethoxylate ethoxymers (AE) and fatty alcohols (FA) found in commercially important AE products. We predicted toxicity for all identified fractions, as well as the total mixture toxicity, relative to three exposure scenarios via sewage treatment plants (STP) for these widely used chemicals in consumer products and hence generate a preliminary environmental risk screening for AE and FA in sediments. The method is based on derivatization of solvent or solid-phase extracts with 2-fluoro-N-methylpyridinium p-toluenesulfonate (Pyr+). The derivatized extracts were analyzed with liquid chromatography/mass spectrometry (LC/MS) operating in the positive ion electrospray mode. The extraction efficiency of AE and FA in three different sediments of varying composition was evaluated with spike-recovery studies, ranging from 64% to 80%. The detection limits for individual ethoxymers typically ranged from 1 to 5ngg⁻¹on a dry weight basis. The mean limit of detection (LOD) was 6ngg⁻¹and the median LOD was 3ngg⁻¹. AE and FA in sediments were found to be stable for two weeks if preserved with 3% (v/v) formalin and stored at 4–6^∘C. Based on equilibrium partitioning, background concentrations of AE and FA were predicted to be below concentrations known to elicit chronically toxic effects. Total worst case mixture toxicities for all AE ethoxymers combined with FA were predicted to result in a risk quotient less than 0.6. Activated sludge treatment (STP) significantly reduced the release of total AE and FA by four-fold, suggesting that the total mixture risk quotient would be < 0.15 for sediment dependent organisms.     

Effect of diffusion limitation and substrate inhibition on steady states of a biofilm reactor treating a single pollutant

The occurrence of multiple steady states in a toluene biodegrading, diffusion-limited biofilm under aerobic conditions was investigated by computer models: one steady-state, and one nonsteady-state. Two stable and one unstable intermediate steady-state were identified in a narrow set of combinations of parameters values. The nonsteady-state model predicts conditions that evolve to a steady state that is within 0.02–1% of the solution of the steady-state model, depending on the number of grid points used, confirming the algorithms are valid. Multiple steady states occur if, (1) a biofilm is exposed to a constant gas-phase pollution concentration, which exceeds or undershoots a certain threshold, (2) in a narrow range of parameter values and (3) provided that the pollutant degradation follows Haldane kinetics. Such a biofilm displays half-saturation (i.e., Michaelis-Menten)-like apparent (“falsified”) kinetics from a concentration range starting at zero up to the occurrence of a second steady state. Multiple steady states and falsified kinetics can negatively affect a biofilter and the experimental determination of kinetic parameters, respectively.

Implications: The occurrence of multiple steady states in a VOC treating biofilm, shows the significant impact of degradation kinetics and diffusion limitation on the biofilm behavior. Moreover, the implied possible sudden drop of removal efficiency of a biofilter, based on the occurrence of multiple steady states lead to possible bottle-necks in biofilter application and operation.     

Fume Control in Rubber Processing By Direct-Flame Incineration

The application of direct-flame incineration to successfully eliminate a smoke-oil-mist and odor problem in the manufacture of rubber-base rug underlay, is presented. The investigation of various air pollution control processes leading to the development and adoption of the direct-flame incineration system, is covered. The rug-underlay curing process incorporating the direct-flame incineration system with primary heat recovery is described. Results and discussion of a source test to determine the effectiveness of direct-flame incineration in this application are included.     

Evaluation of Canisters for Measuring Emissions of Volatile Organic Air Pollutants from Hazardous Waste Incineration

Regulation to control air emissions of toxic organic compounds require the collection and analysis of effluent gas from low level sources such as hazardous waste incinerators. The standard SW- 846 Method specifies the use of Tenax and Tenax/charcoal adsorbent traps for collection of volatile organics from incinerators. This study evaluates passivated stainless steel canisters as an alternative to adsorbent traps to eliminate some of the problems associated with adsorbent sampling. Initially the stability of 18 nonpolar, volatile organic compounds was determined in Summa-treated stainless steel canisters with greater than 100 ppmv HCI and saturated with water vapor. All 18 components were stable for a twoweek period; however, an Interference caused a 10-fold increase In the FID response of trlchloroethylene, toluene, and chlorobenzene. No Interference of the ECD response was found for any of the 11 compounds detected with the ECD including trlchloroethylene. A pilot scale incinerator was sampled using canisters, and the destruction efficiency of 1,1,1-trichloroethane was determined at a concentration of less than 0.5 ppbv while determining 1,1-dichloroethylene, the major product of Incomplete combustion, at a concentration of 8000 ppbv from the same sample.     

Evaluating the impact of interdisciplinary networking in environmental geochemistry and health: reviewing SEGH conferences and workshops

The Society for Environmental Geochemistry and Health (SEGH) is a forum for multidisciplinary interaction relating the geochemical environment to health. With national funding, SEGH identified collaborative opportunities through the MULTITUDE series of workshops (2007–2011). We reviewed the meetings by electronic questionnaire (39?% response). Smaller meetings saw most returning delegates, suggesting networking and personal interaction is a key positive feature of SEGH; 31?% of practitioners and 25?% of academics participated in more than one meeting. Collaboration between SEGH participants resulted in joint funding (13 academics, 4 practitioners, 1 other) and joint papers (19, 5, 3). Evidence of behavioural change was seen in comments in five themes regarding the impacts of the conferences: support for current direction; impact on education practice (academics); new approaches; networking; multidisciplinary work. Multidisciplinary meetings and resulting networking were seen as having real value by many respondents, who encouraged further active pursuit of these activities. SEGH is eager to continue these activities which transform research, education and practice, resulting in a better understanding of the structure and processes comprising the broad geochemical environment on health. Comments showed the value and strength of small, well-organised conferences, bringing together a mixed group of disciplines, both research and applied, in a relaxed atmosphere. The absence of serious negative critique along with clear, positive comments suggests that there is a substantial level of support for, and even pleasure in, SEGH multidisciplinary conferences and workshops over the past years. It is encouraging that annual European conferences are viewed as such a positive achievement.