Denitrification (DNF) and dissimilatory nitrate reduction to ammonium (DNRA) are two competing nitrate reduction pathways that remove or recycle nitrogen, respectively. However, factors controlling the partitioning between these two pathways are manifold and our understanding of these factors is critical for the management of N loads in constructed wetlands. An important factor that controls DNRA in an aquatic ecosystem is the electron donor, commonly organic carbon (OC) or alternatively ferrous iron and sulfide. In this study, we investigated the role of natural organic carbon (NOC) and acetate at different OC/NO ratios and ferrous iron on the partitioning between DNF and DNRA using the N-tracer method in slurries from four constructed stormwater urban wetlands in Melbourne, Australia. The carbon and nitrate experiments revealed that DNF dominated at all OC/NO ratios. The higher DNF and DNRA rates observed after the addition of NOC indicates that nitrate reduction was enhanced more by NOC than acetate. Moreover, addition of NOC in slurries stimulated DNRA more than DNF. Interestingly, slurries amended with Fe showed that Fe had significant control on the balance between DNF and DNRA. From two out of four wetlands, a significant increase in DNRA rates (p < .05) at the cost of DNF in the presence of available Fe suggests DNRA is coupled to Fe oxidation. Rates of DNRA increased 1.5-3.5 times in the Fe treatment compared to the control. Overall, our study provides direct evidence that DNRA is linked to Fe oxidation in some wetland sediments and highlights the role of Fe in controlling the partitioning between removal (DNF) and recycling (DNRA) of bioavailable N in stormwater urban constructed wetlands. In our study we also measured anammox and found that it was always <0.05% of total nitrate reduction in these sediments.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.scitotenv.2019.02.225 | DOI Listing |
Angew Chem Int Ed Engl
December 2024
Institut Chimie radicalaire ICR-UMR 7273, Facult� de Saint jerome, avenue Escadrille-Normandie-Niemen, service 562, 13397, Marseille, FRANCE.
Efforts to understand radical stability have led to considerable progress in radical chemistry. In this article, we investigated a novel approach to enhancing the radical stability of carbon-centered radicals through space electron delocalization within [2,2]-paracyclophanes. Alkoxyamines possessing a paracyclophane scaffold exploit face-to-face π-π-interactions between the aromatic rings to effectively lower bond dissociation energy (BDE) for NO-C bond homolysis.
View Article and Find Full Text PDFOrg Lett
December 2024
Yunnan Key Laboratory of Modern Separation Analysis and Substance Transformation, College of Chemistry and Chemical Engineering, Yunnan Normal University, Kunming 650500, China.
A copper-catalyzed [2,3]-sigmatropic rearrangement of azide-ynamides via selenium ylides is disclosed, which leads to the practical and divergent synthesis of a variety of tricyclic heterocycles bearing a quaternary carbon stereocenter in generally moderate to excellent yields. Significantly, this method represents the first [2,3]-sigmatropic rearrangement of the selenium ylide based on alkynes and an unprecedented [2,3]-sigmatropic rearrangement via α-imino copper carbenes.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
South China University of Technology, School of Chemistry and Chemical Engineering, Wushan St., 510640, Guangzhou, CHINA.
Electroreduction of CO2 to CO represents a highly promising way for artificial carbon cycling, but obtaining high selectivity over a wide potential window remains a challenge due to the sluggish CO generation and diffusion kinetics. Here we report an integration of long-range P modified asymmetrical bismuth atomic site on an ordered macroporous carbon skeleton with mesoporous "wall" (MW-BiN3-POMC) for efficient electroreduction of CO2. In-depth in-situ investigations with theoretical computations reveal that the incorporation of long-range P atom is able to strengthen the orbital interaction between the C 2p of CO2 and Bi 6p, thereby establishing an electronic transport bridge for the activation of CO2 molecule.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Wuhan University, Department of Chemistry, Luojia Hill, 430072, Wuhan, CHINA.
The heterojunction photocatalysts composed of organic dyes and polymeric carbon nitride (PCN) have great potential for photocatalytic hydrogen evolution (PHE). However, serious charge recombination exists at the dye/PCN interface for the large gaps in time scales and the poor driving force of charge transfer process. Herein, both the excited triplet states of organic dyes with long lifetimes and strong internal electric fields (IEF) as charge transfer driving forces are achieved by the construction of high dipole moments with aromatic-core engineering, and modulation of dye aggregates by alkyl modification.
View Article and Find Full Text PDFChem Commun (Camb)
December 2024
Instrumentation Center, National Taiwan University, Taipei, 106, Taiwan.
A visible light photocatalytic cascade reaction was developed, involving sequential self-[2+2] photodimerization of benzoylacetones, De Mayo reaction, acetalization, and alkoxylation, yielding tetrahydrofurans with high stereoselectivity, three stereogenic centers, and two quaternary carbons, under mild conditions with a cycloaddition-rearrangement strategy. Given the significance of photoreaction and rearrangement in organic chemistry, this method provides a valuable approach for the synthesis of tetrahydrofurans.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!