Evaluation of the potential methane yield of industrial wastewaters used in bioreactor landfills

To increase the moisture content of waste disposed in a bioreactor landfill, it is critical to secure the moisture source. In this study, industrial wastewater was evaluated as a potential moisture source for a bioreactor landfill with respect to the impact on methane generation. Industrial wastewater samples were collected from fishery, brewery and dairy industries. These samples were tested for basic water chemistry parameters, heavy metals, and methane generation using the regular and modified biochemical methane potential (BMP) assays. Despite high sodium and total phosphate concentrations in the fishery wastewater, a significant methane yield was observed (0.313?m³ CH₄/kg COD). However, a relatively large amount of fishery wastewater added at the phase of methane generation acceleration adversely affected microbial activity. Samples from the brewery and dairy wastewater did not indicate significant inhibitory effects on methane generation in either the regular or the modified BMP assay. This study demonstrates the utility of wastewater as an alternative to traditional moisture sources when used to enhance methane production in a bioreactor landfill.     

Standard purity and response factors of perfluorinated compounds

It has been reported that the relative response factors of isotopically labeled standards and unlabeled standards of the same perfluorinated compounds could be different. Individual (100 ng mL^?1) solutions of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) were analyzed using high-performance liquid chromatography tandem mass-spectrometry under negative-ion electrospray to detect any impurities present down to 0.5%–0.1% relative to the major component. Purity of the standards ranged from approximately 86% to ≥ 97%. Standard solutions of unlabeled and isotopically labeled materials were analyzed to compare the response factors of isotopically labeled analytes versus their nonlabeled counterparts in three different matrices at equivalent concentrations: organic solvent (methanol), serum extract, and water present individually and concurrently. Not all labeled analytes have the same response factor as their nonlabeled complement, and in at least one case the matrix in which the standard is present may cause significant suppression of response. Standard solutions of electrochemical fluorination produced PFOA and PFOS were quantified under multiple reaction monitoring mode, using calibration curves prepared from standards consisting primarily of linear standards only. The use of linear only standards may cause under-prediction of concentrations, and that the working range of these standards may be limited.     

Effect of acute whole-body proton irradiation on hematological and intestinal variables in mice

Female C57BL/6 mice were exposed to a single dose of protons or ⁶⁰Co gamma rays at 20 mGy and 2 Gy, which represent the recommended limit for annual occupational exposure and the daily fractional dose for patients undergoing radiotherapy, respectively. A control group was not exposed to radiation. The number of peripheral blood, bone marrow, and spleen cells was assessed 24 h after radiation to investigate the marrow suppression. The number of lymphocytes and neutrophils in peripheral blood was significantly lower in mice exposed to the higher dose of radiation than in the nonirradiated mice. However, at a low dose of radiation, there were no discernable hematological effects. The frequency of micronuclei in bone marrow cells was increased only after the high dose of gamma radiation. Radiation-induced intestinal apoptosis was measured using terminal deoxynucleotide transferase labeling assay. The magnitude of damage was greater after gamma irradiation than after proton irradiation at the same dose. Among the systemic biological end point to predict whole body radiation effect, the apoptosis of intestinal crypts may be the most sensitive parameter to provide information even at low dose of radiation.     

The effect of preparation conditions of Pt/Al2O3 on its catalytic performance for the H2-SCR in the presence of oxygen

Selective catalytic reduction of NO _x by H₂ in the presence of oxygen has been investigated over Pt/ Al₂O₃ catalysts pre-treated under different conditions. Catalyst preparation conditions exert significant influence on the catalytic performance, and the catalyst pre-treated by H₂ or H₂ then followed by O₂ is much more active than that pre-treated by air. The higher surface area and the presence of metallic Pt over Pt/Al₂O₃ pre-treated by H₂ or pretreated by H₂ then followed by O₂ can contribute to the formation of NO₂, which then promotes the reaction to proceed at low temperatures.     

A New Flood Index for Use in Evaluation of Local Flood Severity: A Case Study of Small Ungauged Catchments in Korea1

Ahn, Jae Hyun and Hyun Il Choi, 2013. A New Flood Index for Use in Evaluation of Local Flood Severity: A Case Study of Small Ungauged Catchments in Korea. Journal of the American Water Resources Association (JAWRA) 49(1): 1‐14. DOI: 10.1111/jawr.12025 Abstract: The aim of this article is to develop a new index measuring the severity of floods in small ungauged catchments for initial local flood information by the regression analysis between the new flooding index and rainfall patterns. Although a rapid local flood caused by heavy storm in a short period of time is now one of common natural disasters worldwide, such a sudden and violent hydrologic event is difficult to forecast. As local flooding rises rapidly with little or no advance warning, the key to local flood forecasting is to quickly identify when and where local flooding above a threshold is likely to occur. The new flooding index to characterize local floods is measured by the three normalized relative severity factors for the flood magnitude ratio, the rising curve gradient, and the flooding duration time, quantifying characteristics of flood runoff hydrographs. The new flooding index implemented for the two selected small ungauged catchments in the Korean Peninsula shows a very high correlation with logarithm of the 2‐h maximum rainfall depth. This study proposes 30 mm of rainfall in a 2‐h period as a basin‐specific guidance of precaution for the incipient local flooding in the two study catchments. It is expected that the best‐fit regression equation between the new flooding index and a certain rainfall rate can provide preliminary observations, the flood threshold, and severity information, for use in a local flood alert system in small ungauged catchments. Editor's note: This paper is part of a featured series on Korean Hydrology. The series addresses the need for a new paradigm of river and watershed management for Korea due to climate and land use changes.     

Removal of trichloroethylene from soil using the hydration of calcium oxide

Quicklime addition to soil at a remediation site was observed to sufficiently reduce TCE levels, but the cause of the removal could not be confirmed with the field data collected. Potential mechanisms for CaO treatment of trichloroethylene (TCE) in soil include degradation and volatilization. Since earlier studies found TCE degradation to occur during the hydration of CaO under conditions where volatilization was limited, research was conducted on mechanisms of TCE removal from soil by CaO application under conditions where volatilization was allowed to occur. TCE volatilization in soil treated with 0%, 5%, 10%, and 20% CaO doses was measured in experiments where the degree of volatilization could be tracked. The total TCE removal from soil spiked with TCE at CaO doses from 5% to 20% ranged from 97% to 99% of the initial TCE mass. Volatilization accounted for 64.4-92.5% of the TCE removal, with unrecovered TCE and TCE degradation accounting for the remaining fraction. The greater heat encountered with higher CaO doses helped minimize obstacles to TCE volatilization, such as high soil organic and clay content. Treatment with a 20% CaO dose, however, led to the formation of byproducts such as dichloroacetylene. TCE degradation to dichloroacetylene at the 20% CaO dose ranged from 2.7% to 6.4% of the initial TCE. Volatilization was concluded to be the dominant process for TCE removal from soil during CaO treatment.     

Properties of alkali-activated systems with stone powder sludge

This article investigates the effects of stone powder sludge on the microstructure and strength development of alkali-activated fly ash and blast furnace slag mixes. Stone powder sludge produced from a crushed aggregate factory was used to replace fly ash and granulated blast furnace slag at replacement ratios of 0%, 10%, 20%, and 30% by mass. The unit weight and compressive strength of the samples were measured, and scanning electron microscopy/energy dispersive spectroscopy and X-ray diffraction (XRD) analyses were performed. The test results indicated that the compressive strength of alkali-activated blast furnace slag mixes using stone powder sludge was higher than that of the alkali-activated blast furnace slag control mix, but the compressive strength of alkali-activated fly ash mixes decreased with increasing replacement ratio of stone powder sludge. Microscopy results indicated that for alkaliactivated blast furnace slag samples, broken surfaces were more evident than for the alkali-activated fly ash samples. For all XRD diagrams, broad and diffuse peaks were observed around 2θ = 35° (d = 2.96–3.03 Å), implying amorphous or short-ordering structure phases.     

Emission factors for high-emitting vehicles based on on-road measurements of individual vehicle exhaust with a mobile measurement platform

Fuel-based emission factors for 143 light-duty gasoline vehicles (LDGVs) and 93 heavy-duty diesel trucks (HDDTs) were measured in Wilmington, CA using a zero-emission mobile measurement platform (MMP). The frequency distributions of emission factors of carbon monoxide (CO), nitrogen oxides (NO(x)), and particle mass with aerodynamic diameter below 2.5 microm (PM2.5) varied widely, whereas the average of the individual vehicle emission factors were comparable to those reported in previous tunnel and remote sensing studies as well as the predictions by Emission Factors (EMFAC) 2007 mobile source emission model for Los Angeles County. Variation in emissions due to different driving modes (idle, low- and high-speed acceleration, low- and high-speed cruise) was found to be relatively small in comparison to intervehicle variability and did not appear to interfere with the identification of high emitters, defined as the vehicles whose emissions were more than 5 times the fleet-average values. Using this definition, approximately 5% of the LDGVs and HDDTs measured were high emitters. Among the 143 LDGVs, the average emission factors of NO(x), black carbon (BC), PM2.5, and ultrafine particle (UFP) would be reduced by 34%, 39%, 44%, and 31%, respectively, by removing the highest 5% of emitting vehicles, whereas CO emission factor would be reduced by 50%. The emission distributions of the 93 HDDTs measured were even more skewed: approximately half of the NO(x) and CO fleet-average emission factors and more than 60% of PM2.5, UFP, and BC fleet-average emission factors would be reduced by eliminating the highest-emitting 5% HDDTs. Furthermore, high emissions of BC, PM2.5, and NO(x) tended to cluster among the same vehicles.     

Ozone Artifacts and Carbonyl Measurements Using Tenax GR,Tenax TA,Carbopack B,and Carbopack X Adsorbents

Abstract

Four popular thermally desorbable adsorbents used for air sampling (Tenax TA, Tenax GR, Carbopack B, and Carbopack X) are examined for the potential to form artifacts with ozone (O₃) at environmental concentrations. The performance of these adsorbents for the ketone and alde-hyde species identified as O₃-adsorbent artifacts was also characterized, including recovery, linearity, and method detection limits (MDLs). Using gas chromatography/mass spectrometry, 13 different artifacts were identified and confirmed for both Tenax TA and Tenax GR, 9 for Carbopack B, but none for Carbopack X. Several O₃ artifacts not reported previously were identified, including: pentanal, 3-hexanone, 2-hexanone, hexanal, 3-heptanone, and heptanal with Tenax TA; pentanal, 3-hexanone, 2-hexanone, hexanal, and 3-heptanone on Tenax GR; and 1-octene and 1-nonene with Carbopack B. Levels of straight-chain aldehyde artifacts rapidly diminished after a few cycles of adsorbent conditioning/O₃ exposure, and concentrations could be predicted using a first-order model. Phenyl-substituted carbonyl artifacts (benzalde-hyde and acetophenone) persisted on Tenax TA and GR even after 10 O₃ exposure-conditioning cycles. O₃ breakthrough through the adsorbent bed was most rapid in adsorbents that yielded the highest levels of artifacts. Overall, artifact composition and concentration are shown to depend on O₃ concentration and dose, conditioning method, and adsorbent type and age. Calibrations showed good linearity, and most compounds had reasonable recoveries, for example, 90 ±15% for Tenax TA, 97 ±23% for Tenax GR, 101 ±24% for Carbopack B, and 79 ±25% (91 ±9% for n-aldehydes) for Carbopack X. Benzeneacetaldehyde recovery was notably poorer (22–63% across the four adsorbents). MDLs for several compounds were relatively high, up to 5 ng. By accounting for both artifact formation and method performance, this work helps to identify which carbonyl compounds can be measured using thermally desorbable adsorbents and which may be prone to bias because of the formation of O_3- adsorbent artifacts.