Sorption of radiolabelled glyphosate on biochar aged in contrasting soils

Glyphosate mobility from terrestrial to aquatic environments has raised concerns about it. Utilizing soil’s inherent properties along with sorption properties of aged biochar, we hypothesized that selective application of biochar would be more effective in economic terms for glyphosate sorption on contrasting soils. To test this hypothesis, batch experiments and liquid scintillation counting for ¹⁴ Okada, E.; Costa, J. L.; Bedmar, F. Adsorption and mobility of glyphosate in different soils under no-till and conventional tillage. Geoderma 2016, 263, 78–85.[Crossref], [Web of Science ®] , [Google Scholar]C labeled glyphosate were used. The sorption behavior of glyphosate was examined in four contrasting Australian soil types (Oxisol, Vertisol, Entisol, and Inceptisol) amended with aged biochar to determine glyphosate concentrations by measuring ¹⁴ Okada, E.; Costa, J. L.; Bedmar, F. Adsorption and mobility of glyphosate in different soils under no-till and conventional tillage. Geoderma 2016, 263, 78–85.[Crossref], [Web of Science ®] , [Google Scholar]C activity using liquid scintillation counting. Freundlich parameters were calculated for soil-soil/biochar combinations. The pattern of glyphosate sorption was Oxisol?>?Vertisol?>?Entisol?>?Inceptisol. Oxisol adsorbed approximately five times more glyphosate compared with Inceptisol. Oxisol soil system adsorbed maximum amount of glyphosate principally due to the presence of iron-aluminum oxides exhibiting variable charges which got increased due to the presence of aged biochar. Considering all the soil/soil-biochar systems, Inceptisol soil system showed the least adsorption of glyphosate. A significant contribution of char was observed only in the Entisol soil system and the finding is valuable as char can be applied in Entisol soil systems to control glyphosate mobility.     

The influence of hydroxyl volatile organic compounds on the oxidation of aqueous sulfur dioxide by oxygen

Although the effect of volatile organic compounds (VOCs) on the oxidation of dissolved sulfur dioxide by oxygen has been the subject of many investigations, this is the first study which examines the effect of a large number of precisely 16 hydroxy compounds. The kinetics both in the absence and the presence of VOCs was defined by rate laws (A and B): A $$ \hbox{-} \mathrm{d}\left[\mathrm{S}\left(\mathrm{IV}\right)\right]/\mathrm{dt}={R}_o={k}_o\left[\mathrm{S}\left(\mathrm{IV}\right)\right] $$ B $$ \hbox{-} \mathrm{d}\left[\mathrm{S}\left(\mathrm{IV}\right)\right]/\mathrm{dt}={R}_i={k}_i\left[\mathrm{S}\left(\mathrm{IV}\right)\right] $$ where R _o and k _o are the initial rate and first-order rate constant, respectively, in the absence of VOCs, R _i , and k _i are the initial rate and the first-order rate constant, respectively, in the presence of VOCs, and [S(IV)] is the concentration of dissolved sulfur dioxide, sulfur(IV). The nature of the dependence of k _i on the concentration of inhibitor, [Inh], was defined by Eq. (C). C $$ {k}_i={k}_0/\left(1+B\left[\mathrm{Inh}\right]\right) $$ where B is an empirical inhibition parameter. The values of B have been determined from the plots of 1/k _i versus [Inh]. Among aliphatic and aromatic hydroxy compounds studied, t-butyl alcohol and pinacol were without any inhibition effect due to the absence of secondary or tertiary hydrogen. The values of inhibition parameter, B, were related to k _inh , the rate constant for the reaction of SO₄ ^? radical with the inhibitor, by Eq. (D). D $$ B=\left(9\pm 2\right)\times 1{0}^{-4}\times {k}_{inh} $$ Equation (D) may be used to calculate the values of either of B or k _inh provided that the other is known. The extent of inhibition depends on the value of the composite term, B[Inh]. However, in accordance with Eq. (C), the extent of inhibition would be sizeable and measurable when B[Inh]?>?0.1 and oxidation of S(IV) would be almost completely stopped when B[Inh]?≥?10. B[Inh] value can be used as a guide whether the reaction step: SO₄ ^??+?organics? \( \overset{k_{inh}}{\to } \) ?SO₄ ^2??+?non-chain products: should be included in the multiphase models or not.     

A new approach to characterize emission contributions from area sources during optical remote sensing technique testing

In the method termed “Other Test Method-10,” the U.S. Environmental Protection Agency has proposed a method to quantify emissions from nonpoint sources by the use of vertical radial plume mapping (VRPM) technique. The surface area of the emitting source and the degree to which the different zones of the emitting source are contributing to the VRPM computed emissions are often unknown. The objective of this study was to investigate and present an approach to quantify the unknown emitting surface area that is contributing to VRPM measured emissions. Currently a preexisting model known as the “multiple linear regression model,” which is described in Thoma et al. (2009 Thoma, E.R., Green, R., Hater, G., Goldsmith, C., Swan, N., Chase, M. and Hashmonay, R. 2010. Development of EPA OTM-10 for landfill applications. J. Environ. Eng., 136: 769–776. [Crossref], [Web of Science ®] , [Google Scholar]), is used for quantifying the unknown surface area.

The method investigated and presented in this paper utilized tracer tests to collect data and develop a model much like that described in Thoma et al. (2009 Thoma, E.R., Green, R., Hater, G., Goldsmith, C., Swan, N., Chase, M. and Hashmonay, R. 2010. Development of EPA OTM-10 for landfill applications. J. Environ. Eng., 136: 769–776. [Crossref], [Web of Science ®] , [Google Scholar]). However, unlike the study used for development of the multiple linear regression model, this study is considered a very limited study due to the low number of pollutant releases performed (seven total releases). It was found through this limited study that the location of an emitting source impacts VRPM computed emissions exponentially, rather than linearly (i.e., the impact that an emitting source has on VRPM measurements decreases exponentially with increasing distances between the emitting source and the VRPM plane). The data from the field tracer tests were used to suggest a multiple exponential regression model. The findings of this study, however, are based on a very small number of tracer tests. More tracer tests performed during all types of climatic conditions, terrain conditions, and different emissions geometries are still needed to better understand the variation of capture efficiency with emitting source location. This study provides a step toward such an objective.

Implications The findings of this study will aid in the advancement of the VRPM technique. In particular, the contribution of this study is to propose a slight improvement in how the area contributing to flux is determined during VRPM campaigns. This will reduce some of the technique's inherent uncertainties when it is employed to estimate emissions from an area source under nonideal conditions.     

A field trial of nutrient stimulation of methanotrophs to reduce greenhouse gas emissions from landfill cover soils

Landfills are among the major sources of anthropogenic methane (CH₄) estimated to reach 40?×?10⁹kg per year worldwide by 2015 (IPCC, 2007 IPCC. 2007. Intergovernmental Panel on Climate Change, Synthesis Report on Contributions of Work Groups 1, 2, and 3 to the Fourth Assessment Report Core Writing Team, Edited by: Pauchar, R.K. and Reisinger, A. Geneva, Switzerland: IPCC.  [Google Scholar]). A 2½-year field experiment was conducted at a closed landfill in western Michigan where methanotrophs, methane-consuming bacteria, were stimulated by nutrient addition to the soil without significantly increasing biogenic nitrous oxide (N₂O) production. The effects of the nitrogen amendments (KNO₃ and NH₄Cl), phenylacetylene (a selective inhibitor of nitrifying bacteria that contribute to N₂O production), and a canopy (to reduce direct water infiltration) on the vertical soil gas profiles of CH₄, CO₂, and O₂ were measured in the top meter of the soil. Methane and nitrous oxide fluxes were calculated from the corresponding soil gas concentration gradients with respect to depth and a Millington–Quirk diffusivity coefficient in soil derived empirically from soil porosity, water content, and diffusivity coefficients in air from the literature. Methane flux estimates were as high as 218.4 g m^?2 day^?1 in the fall and 12.8 g/m^?2 day^?1 in the summer. During the spring and summer, CH₄ fluxes were reduced by more than half by adding KNO₃ and NH₄Cl into the soil as compared to control plots, while N₂O fluxes increased substantially. The concurrent addition of phenylacetylene to the amendment decreased peak N₂O production by half and the rate of peak methane oxidation by about one-third. The seasonal average methane and N₂O flux data were extrapolated to estimate the reduction of CH₄ and N₂O fluxes into the atmosphere by nitrogen and inhibitor addition to the cover soils. The results suggest that such additions coupled with soil moisture management may provide a potential strategy to significantly reduce greenhouse gas emissions from landfills.

Implications The results of a 2½-year study of effects of nutrient stimulation on methane oxidation in landfill cover soils demonstrates that nutrient addition does decrease methane emissions. The work further underscores the control which soil moisture exerts on methane oxidation. Water management is critical to the success of methane oxidation strategies.     

Experimental investigation of performance and emissions of a VCR diesel engine fuelled with <Emphasis Type="Italic">n</Emphasis>-butanol diesel blends under varying engine parameters

The continuous rise in the cost of fossil fuels as well as in environmental pollution has attracted research in the area of clean alternative fuels for improving the performance and emissions of internal combustion (IC) engines. In the present work, n-butanol is treated as a bio-fuel and investigations have been made to evaluate the feasibility of replacing diesel with a suitable n-butanol-diesel blend. In the current research, an experimental investigation was carried out on a variable compression ratio CI engine with n-butanol-diesel blends (10–25% by volume) to determine the optimum blending ratio and optimum operating parameters of the engine for reduced emissions. The best results of performance and emissions were observed for 20% n-butanol-diesel blend (B20) at a higher compression ratio as compared to diesel while keeping the other parameters unchanged. The observed deterioration in engine performance was within tolerable limits. The reductions in smoke, nitrogen oxides (NO _x ), and carbon monoxide (CO) were observed up to 56.52, 17.19, and 30.43%, respectively, for B20 in comparison to diesel at rated power. However, carbon dioxide (CO₂) and hydrocarbons (HC) were found to be higher by 17.58 and 15.78%, respectively, for B20. It is concluded that n-butanol-diesel blend would be a potential fuel to control emissions from diesel engines.

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Graphical abstract ?

     

Fine Particle Removal Performance of a Two-Stage Wet Electrostatic Precipitator Using a Nonmetallic Pre-Charger

ABSTRACT

A novel two-stage wet electrostatic precipitator (ESP) has been developed using a carbon brush pre-charger and collection plates with a thin water film. The electrical and particle collection performance was evaluated for submicrometer particles smaller than 0.01～0.5 μm in diameter by varying the voltages applied to the pre-charger and collection plates as well as the polarity of the voltage. The collection efficiency was compared with that calculated by the theoretical models. The long-term performances of the ESP with and without water films were also compared in tests using Japanese Industrial Standards dust. The experimental results show that the carbon brush pre-charger of the two-stage wet ESP had approximately 10% particle capture, while producing ozone concentrations of less than 30 ppb. The produced amounts of ozone are significantly lower than the current limits set by international agencies. The ESP also achieved a high collection rate performance, averaging 90% for ultrafine particles, as based on the particle number concentration at an average velocity of 1 m/sec corresponding to a residence time of 0.17 sec. Higher particle collection efficiency for the ESP can be achieved by increasing the voltages applied to the pre-charger and the collection plates. The decreased collection efficiency that occurred during dust loading without water films was completely avoided by forming a thin water film on the collection plates at a water flow rate of 6.5 L/min/m2 Zukeran, A., Ikeda, Y., Ehara, Y., Matsuyama, M., Ito, T., Takahashi, T., Kawakami, H. and Takamatsu, T. 1999. Two-Stage-Type Electrostatic Precipitator Re-entrainment Phenomena under Diesel Flue Gases. IEEE. Trans. Ind. Appl, 35: 346–351. [Crossref], [Web of Science ®] , [Google Scholar].

IMPLICATIONS Current two-stage electrostatic precipitators (ESPs) have several technical problems such as a drop in collection efficiencies by small-particle re-entrainment during rapping and corrosion of metallic electrodes of the ESPs by corrosive gases. This paper evaluates a novel two-stage ESP that uses a nonmetallic pre-charger and water film collection plates to avoid the above mentioned problems of other ESPs. This ESP can be used not only for industrial applications but also for residential purposes because it has a high removal performance for fine particles with low ozone generation and maintains its efficiency due to the continuous cleaning of the collection plates with water film.     

Triclocarban: UV photolysis,wastewater disinfection,and ecotoxicity assessment using molecular biomarkers

Triclocarban (TCC) is an antibacterial agent found in pharmaceuticals and personal care products (PPCP). It is potentially bioaccumulative and an endocrine disruptor, being classified as a contaminant of emerging concern (CEC). In normal uses, approximately 96% of the used TCC can be washed down the drain going into the sewer system and eventually enter in the aquatic environment. UV photolysis can be used to photodegrade TCC and ecotoxicity assays could indicate the photodegradation efficiency, since the enormous structural diversity of photoproducts and their low concentrations do not always allow to identify and quantify them. In this work, the TCC was efficiently degraded by UVC direct photolysis and the ecotoxicity of the UV-treated mixtures was investigated. Bioassays indicates that Daphnia similis (48 h EC₅₀ = 0.044 μM) was more sensitive to TCC than Pseudokirchneriella subcapitata (72 h IC₅₀ = 1.01 μM). TCC and its photoproducts caused significant effects on Eisenia andrei biochemical responses (catalase and glutathione-S-transferase); 48 h was a critical exposure time, since GST reached the highest activity values. UVC reduced the TCC toxic effect after 120 min. Furthermore, TCC was photodegraded in domestic wastewater which was simultaneously disinfected for total coliform bacterial (TCB) (360 min) and Escherichia coli (60 min).

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Graphical abstract TCC degradation and ecotoxicological assessment