There are good prospects for phosphorus recovery from excess sludge by vivianite crystallization while a large number of extracellular polymeric substances in sludge will have impact on vivianite precipitation. In this study, as a representative of extracellular polymeric substance, the effect of sodium alginate (SA) on phosphorus recovery by vivianite precipitation under different initial SA concentrations (0-800 mg/L), pH values (6.5-9.0) and Fe/P molar ratios (11-2.41) was investigated using synthetic wastewater. The results showed that SA in low concentrations (≤400 mg/L) had little inhibitory effect on the phosphorus recovery rate. However, when the concentration of SA was larger than 400 mg/L, the phosphorus recovery rate decreased significantly with increasing SA concentrations. The inhibition rate of 800 mg/L SA was about 3 times as large as that of 400 mg/L SA. It was worth noting that the inhibitory effect of SA on vivianite precipitation decreased with increasing initial pH and Fe/P molar ratios. Additionally, SA has no obvious influence on the composition of products, but the morphology of harvested crystals was transformed from branches to plates or rods in uneven sizes.Certain plants have demonstrated the capability to take up and accumulate metals, thus offering the potential to remediate metal-contaminated water and sediment. Several aquatic species have further been identified which can take up metal and metal oxide engineered nanoparticles (ENPs). It is important to evaluate if aquatic plants exhibiting potential for metal phytoremediation can be applied to remediation of metallic ENPs. Understanding the interactions between ENPs and aquatic plants, and evaluating possible influences on metal uptake and phytoremediation processes is therefore essential. This review article will address the feasibility of green plants for treatment of ENP-affected aquatic ecosystems. Discussion will include common types of ENPs in current use; transformations of ENPs in aquatic systems; the importance of microorganisms in supporting plant growth; ENP entry into the plant; the influence of microorganisms in promoting plant uptake; and recent findings in phytoremediation of ENP-affected water, including applications to constructed wetlands.Aquatic contamination of diclofenac (DCF), an emergent non-steroidal anti-inflammatory drug (NSAIDs), can result in adverse effects to many ecosystems through biomagnification. Hence, introducing effective remediation techniques to sequester the pharmaceutical wastes is highly fundamental to prevent their accumulation in the environment. Generally, adsorption has been presented as a green and efficient approach. Herein, we report the characterization and application of the novel magnetic nanocomposite (GO@CoFe2O4) derived from cobalt-based ferrite (CoFe2O4) and graphene oxide (GO) for DCF adsorption. For the optimization procedure, the response surface methodology (RSM) was adopted to investigate the impacts of DCF concentration (1.6-18.4 mg/L), DCF dosage (0.08-0.92 g/L), and solution pH (2.6-9.4) to find the optimum conditions for DCF removal, at 10.5 mg/L, 0.74 g/L, and pH 4, respectively. For the adsorption experiments, the kinetic, isotherm, thermodynamic, and intraparticle diffusion models were systematically studied. Moreover, we have elucidated the role of functional groups on the surface of GO@CoFe2O4 in enhancing the adsorption of DCF drug. With good removal efficiency (up to 86.1%), high maximum adsorption capacity (32.4 mg/g), GO@CoFe2O4 can be a potential candidate to eliminate DCF drug from water.Ground-level ozone (O3) has become a critical pollutant impeding air quality improvement in Yangtze River Delta region of China. In this study, we present O3 pollution characteristics based on one-year online measurements during 2016 at an urban site in Nanjing, Jiangsu Province. Then, the sensitivity of O3 to its precursors during 2 O3 pollution episodes in August was analyzed using a box model based on observation (OBM). The relative incremental reactivity (RIR) of hydrocarbons was larger than other precursors, suggesting that hydrocarbons played the dominant role in O3 formation. The RIR values for NOX ranged from -0.41%/% to 0.19%/%. The O3 sensitivity was also analyzed based on relationship of simulated O3 production rates with reductions of VOC and NOX derived from scenario analyses. Simulation results illustrate that O3 formation was between VOCs-limited and transition regime. Xylenes and light alkenes were found to be key species in O3 formation according to RIR values, and their sources were determined using the Positive Matrix Factorization (PMF) model. Paints and solvent use was the largest contributor to xylenes (54%), while petrochemical industry was the most important source to propene (82%). Discussions on VOCs and NOX reduction schemes suggest that the 5% O3 control goal can be achieved by reducing VOCs by 20%. To obtain 10% O3 control goal, VOCs need to be reduced by 30% with VOCs/NOX larger than 31.Chlorine dioxide (ClO2), an alternative disinfectant to chlorine, has a superior ability to inactivate microorganisms, in which protein damage has been considered as the main inactivation mechanism. However, the reactivity of ClO2 with amino acid residues in oligopeptides and proteins remains poorly investigated. AG-14361 order In this research, we studied the reaction rate constants of ClO2 with tryptophan residues in five heptapeptides and four proteins using stopped-flow or competition kinetic method. Each heptapeptide and protein contain only one tryptophan residue and the reactivity of tryptophan residue with ClO2 was lower than that of free tryptophan (3.88 × 104 (mol/L)-1sec-1 at pH 7.0). The neighboring amino acid residues affected the reaction rates through promoting inter-peptide aggregation, changing electron density, shifting pKa values or inducing electron transfer via redox reactions. A single amino acid residue difference in oligopeptides can make the reaction rate constants differ by over 60% (e.g. 3.01 × 104 (mol/L)-1sec-1 for DDDWNDD and 1.85 × 104 (mol/L)-1sec-1 for DDDWDDD at pH 7.0 (D aspartic acid, W tryptophan, N asparagine)). The reaction rates of tryptophan-containing oligopeptides were also highly pH-dependent with higher reactivity for deprotonated tryptophan than the neutral specie. Tryptophan residues in proteins spanned a 4-fold range reactivity toward ClO2 (i.e. 0.84 × 104 (mol/L)-1sec-1 for ribonuclease T1 and 3.21 × 104 (mol/L)-1sec-1 for melittin at pH 7.0) with accessibility to the oxidant as the determinating factor. The local environment surrounding the tryptophan residue in proteins can also accelerate the reaction rates by increasing the electron density of the indole ring of tryptophan or inhibit the reaction rates by inducing electron transfer reactions. The results are of significance in advancing understanding of ClO2 oxidative reactions with proteins and microbial inactivation mechanisms.