Effects of long exposure to low temperatures on nitrifying biofilm and biomass in wastewater treatment

Attached growth biological treatment systems are a promising solution to ammonia removal in cold-temperature climates. Environmental scanning electron microscopy (ESEM) and confocal laser scanning microscopy in combination with fluorescent in situ hybridization (FISH) was used to investigate the effects of 4 months of exposure to 4 degrees C on nitrifying biofilm and biomass. These molecular and microscopic methods were modified to minimize loss of mass and distortion of in situ perspectives. Environmental scanning electron microscopy revealed that nitrifying biofilm did not exhibit significant changes in volume with exposure to 4 degrees C. Confocal laser scanning microscopy in combination with FISH showed that the number of ammonia-oxidizing bacteria (AOB) cells present in the biofilm was statistically consistent during exposure to 4 degrees C. The RNA content of AOB cells remained sufficient for FISH enumeration. The number of nitrite-oxidizing bacteria cells remained steady during exposure to 4 degrees C; however, the RNA content of the cells appeared to decrease with exposure to 4 degrees C, thereby preventing their enumeration using FISH.     

2,5,6,9,10-Pentabromocyclododecanols (PBCDOHs): a new class of HBCD transformation products

Pentabromocyclododecanols (PBCDOHs) are potential environmental transformation products of hexabromocyclododecanes (HBCDs). They are also potential stage one metabolites of biological HBCD transformations. Herein, we present analytical evidence that PBCDOHs are also constituents of technical HBCDs and flame-proofed polystyrenes (FP-PSs). PBCDOHs are possibly formed during the synthesis of technical HBCD, presumably during the bromination of cyclododecatrienes in aqueous isobutanol together with isobutoxypentabromocyclododecanes (iBPBCDs), which have been identified in these materials recently. Of the 64 stereoisomers possible, eight pairs of enantiomers, named α-, β-, γ-, δ-, ε-, ζ-, η-, and θ-PBCDOHs were separated with a combination of normal-, reversed- and chiral-phase LC. Crystal structure analysis revealed the stereochemistry of the α-PBCDOH pair of enantiomers, which was assigned to (1S,2S,5R,6S,9S,10R)-2,5,6,9,10-pentabromocyclododecanol and its enantiomer. Mass spectrometric data are in accordance with the expected isotope patterns. On a C₁₈-RP-column, the polar PBCDOHs eluted before the HBCD and iBPBCD classes of compounds. PBCDOHs were also found in FP-PS materials. The stereoisomer patterns varied considerably in these materials like those of HBCDs and iBPBCDs. Expanded polystyrenes were rich in late-eluting stereoisomers, similar to technical HBCD mixtures. Extruded polystyrenes contained more of the polar, faster-eluting isomers. The presented chromatographic and analytical methods allow a stereoisomer-specific search for PBCDOHs in biota samples, which might have experienced metabolic HBCD transformation reactions. Besides this potential source, it has to be recognized that PBCDOHs are by-products in technical HBCDs and in flame-proofed polystyrenes. Therefore, it is likely that PBCDOHs and iBPBCDs are released to the environment together with HBCD-containing plastic materials.     

The toxicity of phthalocyanines to the aquatic plant Lemna minor (duckweed) - testing of 31 compounds

Phthalocyanines are prospective chemicals that have applications in industry, medicine and biology due especially to their architectural flexibility and production of reactive oxygen species. Although they are used in so many areas of human activities nowadays, there is still little knowledge of their ecotoxicity. Here we present the first observation of their toxic effects on representatives of the aquatic plants Lemna minor. The tested phthalocyanines possess a wide spectrum of phytotoxicity ranging from seldom (>50 mg L⁻¹) to highly toxic 0.11 mg L⁻¹. Moreover, the potential of phthalocyanines to be used as selective cyanocides or herbicides is discussed as well.     

Combined MODFLOW‐FRACTRAN Application to Assess Chlorinated Solvent Transport and Remediation in Fractured Sedimentary Rock

Detailed field investigations and numerical modeling were conducted to evaluate transport and fate of chlorinated solvent contamination in a fractured sedimentary bedrock aquifer (sandstone/siltstone/mudstone) at a Superfund site in central New Jersey. Field investigations provided information on the fractured rock system hydrogeology, including hydraulic gradients, bulk hydraulic conductivity, fracture network, and rock matrix, and on depth discrete contaminant distribution in fractures (via groundwater sampling) and matrix (via detailed subsampling of continuous cores). The numerical modeling endeavor involved application of both an equivalent porous media (EPM) model for flow and a discrete fracture network (DFN) model for transport. This combination of complementary models, informed by appropriate field data, allowed a quantitative representation of the conceptual site model (CSM) to assess relative importance of various processes, and to examine efficacy of remedial alternatives. Modeling progressed in two stages: first a large‐scale (20 km x 25 km domain) 3‐D EPM flow model (MODFLOW) was used to evaluate the bulk groundwater flow system and contaminant transport pathways under historic and current aquifer stress conditions and current stresses. Then, results of the flow model informed a 2‐D DFN transport model (FRACTRAN) to evaluate transport along a 1,000‐m flowpath from the source represented as a 2‐D vertical cross‐section. The combined model results were used to interpret and estimate the current and potential future extent of rock matrix and aqueous‐phase contaminant conditions and evaluate remedial strategies. Results of this study show strong effects of matrix diffusion and other processes on attenuating the plume such that future impacts on downgradient well fields under the hydraulic stresses modeled should be negligible. Results also showed futility of source remediation efforts in the fractured rock, and supported a technical impracticability (TI) waiver for the site. © 2013 Wiley Periodicals, Inc.     

Gas-Particle Distribution Factors for Organic and Other Pollutants in the Los Angeles Atmosphere

The distribution of organic pollutants between the gas and particu-late phases was measured for 6 days Including one with the highest ozone level observed in Pasadena In 1973 (7/25). Gas phase pollutants were monitored continuously while particulates were sampled over a one hour interval by filtration. The filters were extracted using a polar and a non-polar solvent; particulate organic carbon was determined using a carbon analyzer, and chemical analysis carried out by fractionation, gas chromatography, infrared, and CHON analysis.

The organic carbon fraction (OCF) was always large, up to 43% of the total particulates (TP). Most of the organics were oxygenated compounds of photochemical origin. There was a linear relation between O₃, OCF, and the infrared carbonyl band intensities of the extracts. Hourly variations of OCF and TP are discussed with respect to the gas phase pollutants and conversion processes.

Although secondary pollutant concentrations were found in the order: organics > nitrates > sulfates, nitrates were more efficient than organics in visibility degradation, based on a statistical evaluation of the data. The secondary aerosol contribution varied with O₃, accounting for up to 95% of TP when the O₃ peaked. The unusual nitrate peak observed for 7/25 is discussed with the atmospheric chemistry of other nitrogen compounds.

We define an organic carbon distribution factor: f_c = particulate organic carbon (POC, μg/m³C)/[POC + gas phase reactive hydrocarbons (μg/m³C)]. The gas-particle distribution factors for organics (f_c), nitrates (f_N) and sulfates (f_s) are in inverse order of their aerosol concentrations: f_c < f_N < f_s . The measured f_c are low: average 2–3%, highest value 6% for 7/25, and correspond to a conversion rate ≤2% hour^?1. Ambient f_c are much lower than f_c measured for certain specific hydrocarbon precursors.     

Inhibition of the antioxidant activity of catalase and superoxide dismutase from Fusarium verticillioides exposed to a Jacquinia macrocarpa antifungal fraction

The aim of this study was to investigate the in vitro effect of an antifungal fraction obtained from Jacquinia macrocarpa plant (JmAF) in the generation of reactive oxygen species (ROS) and the activity of the catalase (CAT) and superoxide dismutase (SOD) enzymes from Fusarium verticillioides, as well as their influence in the viability of the fungus spores. The compounds present in the JmAF were determined by gas chromatography/quadrupole time-of-flight mass spectrometry (GC/QTOF-MS). The effect of the exposition to JmAF on the generation of ROS, as well as in the CAT and SOD activities in F. verticillioides, was determined. The main compounds detected were γ-sitosterol, stephamiersine, betulinol and oleic acid. JmAF showed very high ability in inhibiting the spore viability of F. verticillioides, and their capacity to cause oxidative stress by induction of ROS production. JmAF induced the highest ROS concentration and also inhibited CAT and SOD activities. The results obtained in this study indicate that JmAF is worthy of being considered for the fight against phytopathogenic fungi.     

An Equilibrium Analysis of Some Chlorinated Hydrocarbons in Stoichiometric to Fuel-rich Post-flame Combustion Environments

The equilibrium composition of product gases from the combustion of chlorinated hydrocarbons (CHC) has been studied for varying ratios of C, H, Cl, and O under stoichiometric to fuel-rich conditions. An interactive, PC-compatible FORTRAN program, STANJAN, was utilized in conjunction with thermochemical data sources to calculate equilibrium compositions of gas mixtures as a function of temperature. The predicted results, when judiciously Interpreted, assist in the understanding of the potential for formation of residual organic substance emissions (ROSEs) in post-flame environments of an incinerator.

Arguments are presented for the potential formation of chlorinated species, which are stable at ambient temperature, if locally fuel-rich mixtures penetrate into the lower temperature zones of an incinerator. ROSEs that have been observed in field tests of incinerators burning chlorinated compounds are predicted to form under the fuel-rich condition. Furthermore, when the equivalence ratio is greater than unity by even a slight amount, the degree of chlorination of product gases increases markedly when the Cl/H ratio also exceeds unity. In that case, time, temperature, turbulence and an overall fuel-lean stoichiometry may not be sufficient to guarantee elimination of measurable levels of chlorinated products. Possible implications of the equilibrium calculations are discussed. Further systematic studies with additional CHCs, nitrogen?, sulfur?, and heavy metal-bearing compounds are recommended as well as continued efforts to carry out kinetic studies.     

Detection Limits for Hazardous and Radioactive Elements in Airborne Aerosols Using Inductively Coupled Air Plasma – Atomic Emission Spectrometry

Abstract

This research presents investigations into the use of inductively coupled air plasma – atomic emission spectrometry (air-plasma ICPAES) to determine the presence of inorganic contaminants in airborne aerosols. Limits of detection (LOD) in the ppm to ppb range for 19 hazardous metals and radionuclides were determined for aerosols of solutions nebulized into the air plasma. For many elements, the determined LOD surpass the threshold limit values established by the American Conference of Governmental Industrial Hygienists by one to three orders of magnitude. The potential of air-plasma ICPAES for continuous on-line monitoring of airborne contaminants is discussed.     

Nutrient Limitation in a Compost Biofilter Degrading Hexane

Abstract

A laboratory-scale compost-based biofilter was operated over a six-month period to study the requirements for removal of n-hexane from air. Hexane is a relatively short chain aliphatic hydrocarbon with a high Henry's coefficient and a low water solubility. Acclimation of the biofilter was slow, but removal efficiencies around 80% were achieved after one month of operation. However, performance decreased during the next two months of operation to 50% removal efficiency. Nutrient limitation was proposed as a reason for the decrease in reactor performance. After the addition of a concentrated nitrogen solution, reactor performance increased almost immediately to >99%. Removal efficiency remained above 99% for the following two months of operation at inlet concentrations of 0.7 g/m3 (200 ppmv), at superficial bed velocities approaching 50 m/h, and empty bed residence times of about one minute. Thus, nutrient availability may well limit biofilter performance even in compost- based units. It was shown that nutrients can be added effectively in a soluble form if compost quality is poor and a method is proposed for the evaluation of compost quality.     

Aerobic Treatment of a Nitrogen-Limited Chemical Process Waste water

Abstract

Nitrogen transformations and their effect on aerobic suspended growth treatment of an industrial wastewater were studied in three parallel bench-scale reactors operated at 5 "C at mean cell residence times (MCRT) of 15, 30, and 60 days. In normal process wastewater, the bulk of influent nitrogen was in organic form, and the fraction transformed was almost totally incorporated into synthesized biomass. Assimilative control by heterotrophs maintained ammonianitrogen levels below permitted effluent levels, and nitrification was not significant. Although volatile suspended solids had a nitrogen content of only 5% to 8%, effective organics removal was maintained, and total organic carbon and filtered daily average five-day biochemical oxygen demand (BODS) were below permitted effluent levels. A marked improvement in settleability and lower effluent total suspended solids was achieved by adding ammonia-nitrogen to the wastewater in excess of stoichiometric growth requirements.

During a batch production cycle of a cationic chemical, the ratio of nitrogen to chemical oxygen demand and the fraction of the total influent nitrogen in soluble form increased in the wastewater. Reactor effluent ammonia levels increased to above permit levels at all three MCRTs during treatment of wastewater containing cationic production effluents. The magnitude of ammonia increase was greater for longer MCRTs, suggesting that synthesis of cell mass was not capable of assimilating the increased ammonia supply under these non-steady conditions. The experimental results suggest several potential strategies for operating the aerobic process at the treatment facility, including adding nitrogen to improve settleability and discontinuing these additions when wastewater contains a high ratio of nitrogen to chemical oxygen demand and an elevated soluble nitrogen fraction