Estimation of the intrinsic maximum substrate utilization rate using batch reactors with denitrifying biofilm: a proposed methodology.

A method for estimation of the maximum substrate utilization rate (q(max)) using batch reactors with denitrification biofilm was introduced and compared with the traditional method of using batch reactors with suspended growth for q(max) estimation. The values of q(max) obtained from the suspended-growth reactors (0.69 to 0.71 g N/g volatile suspended solids [VSS] x d) and from the attached-biomass reactors (0.74 to 0.85 g N/g VSS x d) are similar and within the range of the values reported in the literature (0.23 to 2.88 g N/g VSS x d). Therefore, the intrinsic kinetic parameter, q(max), can be obtained using attached-growth batch reactors, if the effectiveness factor, eta, is approximately equal to 1 and the bulk concentration of the rate-limiting substrate, C, is much higher than the half-velocity constant, K(S). The attached-growth batch reactor method is unique, because the biomass used in the batch tests is the same as that present in the parent reactor under investigation.     

Suspended particulate matter determines physical speciation of Fe,Mn, and trace metals in surface waters of Loire watershed

This study investigates the spatiotemporal variability of major and trace elements, dissolved organic carbon (DOC), total dissolved solids (TDS), and suspended particulate matter (SPM) in surface waters of several hydrosystems of the Loire River watershed in France. In particular, this study aims to delineate the impact of the abovementioned water physicochemical parameters on natural iron and manganese physical speciation (homoaggregation/heteroaggregation) among fine colloidal and dissolved (<?10 nm), colloidal (10–450 nm) and particulate (>?450 nm) phases in Loire River watershed. Results show that the chemistry of the Loire River watershed is controlled by two end members: magmatic and metamorphic petrographic context on the upper part of the watershed; and sedimentary rocks for the middle and low part of the Loire. The percentage of particulate Fe and Mn increased downstream concurrent with the increase in SPM and major cations concentration, whereas the percentage of colloidal Fe and Mn decreased downstream. Transmission electron microscopy analyses of the colloidal and particulate fractions (from the non-filtered water sample) revealed that heteroaggregation of Fe and Mn rich natural nanoparticles and natural organic matter to the particulate phase is the dominant mechanism. The heteroaggregation controls the partitioning of Fe and Mn in the different fractions, potentially due to the increase in the ionic strength, and divalent cations concentration downstream, and SPM concentration. These findings imply that SPM concentration plays an important role in controlling the fate and behavior of Fe and Mn in various sized fractions.

Physical speciation by heteroaggregation of (Fe-Mn) compounds: high [SPM]?→?[Fe-Mn] particulate faction; low {SPM]?→?[Fe-Mn] colloid-dissolved fraction.

     

Competitive role of nitrogen functionalities of N doped GO and sensitizing effect of Bi2O3 QDs on TiO2 for water remediation

The promising solar irradiated photocatalyst by pairing of bismuth oxide quantum dots (BQDs) doped TiO₂ with nitrogen doped graphene oxide (NGO) nanocomposite (NGO/BQDs-TiO₂) was fabricated. It was used for degradation of organic pollutants like 2,4-dichlorophenol (2,4-DCP) and stable dyes, i.e. Rhodamine B and Congo Red. X-ray diffraction (XRD) profile of NGO showed reduction in oxygenic functional groups and restoring of graphitic crystal structure. The characteristic diffraction peaks of TiO₂ and its composites showed crystalline anatase TiO₂. Morphological images represent spherical shaped TiO₂ evenly covered with BQDs spread on NGO sheet. The surface linkages of $\text{NO}?\mathrm{O}?\text{Ti}$, $\mathrm{C}?\mathrm{O}?\text{Ti}$, $\mathrm{B}\mathrm{i}?\mathrm{O}?\text{Ti}$ and vibrational modes are observed by Fourier transform infrared spectroscopy (FTIR) and Raman studies. BQDs and NGO modified TiO₂ results into red shifting in visible region as studied in diffused reflectance spectroscopy (DRS). NGO and BQDs in TiO₂ are linked with defect centers which reduced the recombination of free charge carriers by quenching of photoluminescence (PL) intensities. X-ray photoelectron spectroscopy (XPS) shows that no peak related to $\mathrm{C}?\mathrm{O}$ in NGO/BQDs-TiO₂ is observed. This indicated that doping of nitrogen into GO has reduced some oxygen functional groups. Nitrogen functionalities in NGO and photosensitizing effect of BQDs in ternary composite have improved photocatalytic activity against organic pollutants. Intermediate byproducts during photo degradation process of 2,4-DCP were studied through high performance liquid chromatography (HPLC). Study of radical scavengers indicated that ${\mathrm{O}}_2^{·?}$ has significant role for degradation of 2,4-DCP. Our investigations propose that fabricated nanohybrid architecture has potential for degradation of environmental pollutions.     

Groundwater-dependent irrigation costs and benefits for adaptation to global change

The effects of a 1.5 °C global change on irrigation costs and carbon emissions in a groundwater-dependent irrigation system were assessed in the northwestern region of Bangladesh and examined at the global scale to determine possible global impacts and propose necessary adaptation measures. Downscaled climate projections were obtained from an ensemble of eight general circulation models (GCMs) for three representative concentration pathways (RCPs), RCP2.6, RCP4.5, and RCP8.5 and were used to generate the 1.5 °C warming scenarios. A water balance model was used to estimate irrigation demand, a support vector machine (SVM) model was used to simulate groundwater levels, an energy-use model was used to estimate carbon emissions from the irrigation pump, and a multiple linear regression (MLR) model was used to simulate the irrigation costs. The results showed that groundwater levels would likely drop by only 0.03 to 0.4 m under a 1.5 °C temperature increase, which would result in an increase in irrigation costs and carbon emissions ranging from 11.14 to 148.4 Bangladesh taka (BDT) and 0.3 to 4% CO₂ emissions/ha, respectively, in northwestern Bangladesh. The results indicate that the impacts of climate change on irrigation costs for groundwater-dependent irrigation would be negligible if warming is limited to 1.5 °C; however, increased emissions, up to 4%, from irrigation pumps can have a significant impact on the total emissions from agriculture. This study revealed that similar impacts from irrigation pumps worldwide would result in an increase in carbon emissions by 4.65 to 65.06 thousand tons, based only on emissions from groundwater-dependent rice fields. Restricting groundwater-based irrigation in regions where the groundwater is already vulnerable, improving irrigation efficiency by educating farmers and enhancing pump efficiency by following optimum pumping guidelines can mitigate the impacts of climate change on groundwater resources, increase farmers’ profits, and reduce carbon emissions in regions with groundwater-dependent irrigation.     

Long-term (≥20 years) application of fertilizers and straw return enhances soil carbon storage: a meta-analysis

Increasing soil carbon (C) storage is crucial to addressing climate change and ensuring food security. The C sequestration potential of the world’s cropland soil is 0.4–0.8 Pg soil C year^?1, which may be achieved through the adoption of recommended management practices (RMPs), including fertilizer management. This study aimed to quantitatively evaluate the influence of long-term application of different fertilizers and straw retention on soil organic carbon (SOC) storage, to compare the calculated response ratios with Intergovernmental Panel on Climate Change (IPCC)-recommended default relative stock change factors, and to propose recommendations for enhancing SOC sequestration. The meta-analysis indicated that the long-term application of chemical fertilizers (CF), organic fertilizers (OF), combined chemical and organic fertilizers (CFOF), and straw return (SR) significantly enhanced the SOC storage. Response ratios varied significantly (p < 0.05) across different fertilization measures and climatic zones, and was sensitive to the initial SOC content. The mean response ratio was 0.94 for no fertilizer (NF), 1.08 for CF, 1.48 for OF, 1.38 for CFOF, and 1.28 for SR. When IPCC default values for response ratios were applied, SOC storage with OF and CFOF treatments in warm temperate regions with a dry climate was underestimated by 26%, and in the cool temperate region with a moist climate was overestimated by 25% (p < 0.05). Analysis showed that sustained application of organic fertilizers and straw return could be a beneficial measures to mitigate climate change and ensure food security in China. Our findings highlight the importance of deriving SOC stock change factors for a detailed classification of cropland by fertilizer management, climate, and soil types in order to more accurately reflect the effects of policy measures.     

Effect of water chemistry on the aggregation and photoluminescence behavior of carbon dots

Carbon dots are rapidly emerging carbon-based nanomaterials that, due to their growing applications, will inevitable find their way to natural waters; however, their environmental fate is mostly unknown. Carbon dots with different surface functionality were fabricated and characterized by TEM and FT-IR. Their surface charge, given by the zeta potential, and their hydrodynamic diameter in suspension were investigated under a variety of environmentally relevant conditions. The effect of ionic strength was studied in the presence of monovalent (NaCl) and divalent (CaCl₂) cations, for pH levels from 3 to 11; humic acid was used as a model for dissolved natural organic matter. Total potential energies of interactions were modeled by classical DLVO theory. The experimental results showed that water chemistry altered the surface charge of the nanomaterials, but their hydrodynamic size could not be correlated to those changes. Evidence of specific interactions was found for the amino functionalized particles in most cases, as well as the plain carbon dots in the presence of Ca^2 + and humic acid. Nanoparticles remained largely stable in suspension, with some exception at the highest ionic strength considered. DLVO theory did not adequately capture the aggregation behavior of the system. Moreover, cation and/or humic acid adsorption negatively affected the emission intensity of the particles, suggesting limitations to their use in natural water sensing applications. The particular stability shown by the carbon dots results in exposure to organisms in the water column and the possibility of contamination transported to significant distances from their source.     

Removal of basic dye from waste-water using silica as adsorbent

The kinetics of removal of Basic Blue 3 from a textile effluent was studied using silica as an adsorbent. The adsorption was found to follow a first-order process. The influences on the rate of adsorption of various factors, such as temperature, concentration of dye solution, pH of the system and the amount of adsorbent have been investigated. On the basis of the isotherm studies, the various thermodynamical parameters have been calculated. The effect of electrolytes and surfactants has also been seen on the removal of the dye from the waste-water.