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0-33.5% increase in PERI for SSC-amended FGS) or high (a 140% increase in PERI for SSC-amended APMS). NSC 649890 clinical trial Ni, Cd and Cu were identified as the three main HMs responsible for increasing the ecological risk in soil which was mainly composed of fine-grained particles, whereas Cd and As were key ecological risks HMs in soil that was mainly composed of coarse-grained particles. The problem of sulfate pollution is becoming increasingly serious in freshwater and wetlands. Since paddy fields are the largest constructed wetland in Earth's surface, the increased sulfate input may have great effect on dissolved organic matter (DOM) in paddy soils. To understand these effects, a 24-day anaerobic incubation experiment was conducted with four Chinese paddy soils amended with high concentrations (0, 10, 25, 50, and 100 mmol L-1) of Na2SO4. Dissolved organic carbon (DOC) and chlorophyll a (Chl a) concentrations were determined after incubation. Parallel factor analysis (PARAFAC) of the excitation-emission matrix (EEM) spectra was used to analyze the DOM composition. In all four soils, DOC concentrations generally increased with increasing sulfate concentration, while the Chl a concentrations decreased. The EEM spectra of DOM were resolved into four components by PARAFAC. With increasing sulfate concentration, the proportion of the ultraviolet C humic acid-like compound decreased and the tyrosine-like compound increased in two algae-rich soils (Sichuan and Tianjin). No obvious variation was observed in the humification index (HIX) or the ratio of peak β to peak α (βα) in any soils with added sulfate. Specific ultra-violet absorbance at 254 nm (SUVA254) decreased with increasing sulfate concentration in Jilin, Tianjin, and Ningxia soils, and the fluorescence index (FI) decreased in two algae-rich soils. In conclusion, although sulfate addition increased the DOC concentration, the DOM composition depended more strongly on soil type and physicochemical properties than sulfate. Sulfate addition only affected soil DOM origin and composition by inhibiting algal growth in algae-rich paddy soils. Spent potlining (SPL) as a hazardous solid waste has a high content of inorganic fluorine. This study aimed at characterizing its transformation, retention and leaching behaviors with(out) the addition of red mud (RM) during the SPL incineration. The RM addition positively affected its retention and leaching rates. Its Ca-containing compounds caused Na3AlF6 and NaF to turn into more CaF2. 30% RM converted water-soluble NaF into more stable CaF2 than did SPL at 850 °C, thus reducing the leaching rate by 45.15%. 30% RM captured HF through its Ca content and enhanced its retention rate by 66.96%. 66.01% of the total fluorine was stably retained in the bottom ash, and thus, significantly reduced the toxicity of the SPL incineration products. SiO2 and Al2O3 exerted a thermally positive effect on NaF turning into CaF2. The fluoride retention of the bottom ash was mainly dominated by CaF2 and NaF with(out) RM. Smaller, coarser and more loose structures of the co-incinerated solid particles pointed to a synergistic interaction between SPL and RM. The heavy metals (HMs) soils contamination is a growing concern since HMs are not biodegradable and can accumulate in all living organisms causing a threat to plants and animals, including humans. Phytoremediation is a cost-efficient technology that uses plants to remove, transform or detoxify contaminants. In recent years, phytoremediation is entering the stage of large-scale modelling via various mathematical models. Such models can be useful tools to further our understanding and predicting of the processes that influence the efficiency of phytoremediation and to precisely plan such actions on a large-scale. When dealing with extremely complicated and challenging variables like the interactions between the climate, soil and plants, modelling before starting an operation can significantly reduce the time and cost of such process by granting us an accurate prediction of possible outcomes. Research on the applicability of different modelling approaches is ongoing and presented work compares and discusses available models in order to point out their specific strengths and weaknesses in given scenarios. The main aim of this paper is to critically evaluate the main advantages and limitations of available models for large-scale phytoremediation including, among others, the Decision Support System (DSS), Response Surface Methodology (RSM), BALANS, PLANTIX and various regression models. link2 Study compares their applicability and highlight existing gaps in current knowledge with a special reference to improving the efficiency of large-scale phytoremediation of sites contaminated with heavy-metals. The presented work can serve as a useful tool when choosing the most suitable model for the phytoremediation of contaminated sites. Environmental pollution and energy scarcity is a major issue of the current scenario which forbear the progress of developing world. To overcome these problems towards a sustainable future, the utilization of sunlight by means of photocatalysis can be regarded as a best and suitable pathway. To validate this purpose, design and development of efficient heterogeneous photocatalyst for harvesting solar energy should be the major research concern for scientific community. In this regard herein, we have prepared a series of stable and efficient CoTiO3/UiO-66-NH2 p-n junction mediated heterogeneous photocatalyst by hydrothermal method. The functionalised linker of UiO-66-NH2 provided an intimate interfacial contact with CoTiO3 by Co/TiON ionic interaction, as proved by HRTEM and XPS analysis. Moreover the inverted V-shaped Mott-Schottky plot confirmed the junction formation in the optimised CoTiO3/UiO-66-NH2 material. link3 In addition, EIS and PL analysis also provides sufficient evidence about the hindrance of active species recombination in composite as a result of p-n hetero junction. LC-MS characterization technique traces the assorted intermediate species produced in the course of photodegradation of Norfloxacin and confirms its complete degradation to corresponding CO2, H2O and NH4+ by the optimised CoTiO3/UiO-66-NH2. The highest photo-catalytic activity obtained towards Norfloxacin degradation is 90.13% and H2 production is 530.87 µmol in 1 h. The enhanced photo-catalytic reaction follows Type-II p-n hetero junction charge transfer mechanism and thus, paves a new way to design MOF based heterojunction photocatalyst for diverse photo catalytic performance. Development of high-performance ammonia (NH3) sensor is imperative for monitoring NH3 in the living environment. In this work, to obtain a high performance NH3 gas sensor, structurally well-defined WO3@SnO2 core shell nanosheets with a controllable thickness of SnO2 shell layer have been employed as sensing materials. The prepared core shell nanosheets were used to obtain a miniaturized gas sensor based on micro-electro-mechanical system (MEMS). By tuning the thickness of SnO2 layer via atomic layer deposition, a series of WO3@SnO2 core-shell nanosheets with tunable sensing properties were realized. Particularly, the sensor base on the fabricated WO3@SnO2 nanosheets with 20-nm SnO2 shell layer demonstrated superior gas sensing performance with the highest response (1.55) and selectivity toward 15 ppm NH3 at 200 °C. This remarkable enhancement of NH3 sensing ability could be ascribed to the formation of unique WO3-SnO2 core-shell heterojunction structure. The detailed mechanism was elucidated by the heterojunction-depletion model with the help of specific band alignment. Framework crystallization is an unresolved challenge in the chemistry of covalent organic frameworks (COFs) due to the poorly controlled simultaneous polymerization and crystallization processes. Here, we report the first morphogenesis of COF mesocrystals with two-dimensional hexagonal p6m symmetry through the combination of alkyl amine as a dynamic modulator and 2,4,6- triformylresorcinol imine as an asymmetrical building block. The amine modulator depresses the lateral growth of 2D sheets, and the slow kinetics combined with the asymmetrical conformation of 2,4,6-triformylresorcinol imine lead to the formation of transient imine macrocycles, which further undergo mesoscale self-assembly into nanotubular structures. The nanotubular structures tend to join together into rod-like bundles with ordered hexagonal rods, which finally grow into uniform hexagonal COF mesocrystals. The present strategy opens a nonclassical nucleation and crystal growth approach to create COFs with unexplored mesocrystal structures, which further extends the scope of crystalline framework materials and provides a new strategy for crystal morphogenesis. HYPOTHESIS Surfactants are commonly used as corrosion inhibitors for oil-and-gas pipelines. The alkyl chain of surfactants and their overall conformation contributes to the adsorption, flotation, and foam separation in the inhibition process. We hypothesize that the conformation of shorter alkyl chains and chemical nature of surfactants has an effect on the ordering of water molecules at the air-water interface which is not yet well understood. EXPERIMENTS Alkyl (C4, C6, C8, C10, and C12) dimethylbenzylammonium bromides (Quats) were synthesized. Aqueous solutions at 0% and with different salt concentrations were studied at the air-liquid interface using sum frequency generation spectroscopy. Surface tension and pH measurement were also conducted for comparison. FINDINGS Surfactant solutions at 0%, 1%, and 10% salt showed a zigzag trend for the number of gauche defects. At 0% salt, an increasing trend of OH band intensity at 3182 cm-1 was observed from C6 to C12 SFG spectra. Yet, C4 showed a more prominent SFG signal from strongly hydrogen-bonded water molecules compared to C6. The headgroup's chemical nature was found to play a role in the ordering of water molecules for a C4 alkyl chain length. The OH band intensity decreases with increasing ionic strength. HYPOTHESIS Interfacially active magnetic Janus nanoparticles (M-Janus NPs) of asymmetric surface wettability are more interfacially active than biwettable nanoparticles (M-CMC-EC NPs) of uniform surface wettability as such that they could anchor more securely at an oil-water interface to separate emulsified oil droplets from oily wastewaters more effectively by magnetic separation. EXPERIMENTS Interfacial tension and interfacial pressure-area isotherms of M-Janus NPs at oil-water interface were measured and the results were correlated to coalescence time of oil droplets determined in various types of aqueous phase (wastewaters) and to the performance of oil removal or recovery from corresponding oily wastewaters by M-Janus NPs and M-CMC-EC NPs of uniform surface wettability by an external magnetic field. FINDINGS Despite the presence of natural/synthetic surfactants in the oily wastewaters, M-Janus NPs exhibited stronger interfacial activities and anchored more firmly at oil-water interfaces than M-CMC-EC NPs of uniform surface wettability. The application of M-Janus NPs could remove/recover >91.5% oil from oily wastewaters by an external magnetic field as compared with >84.3% achieved by M-CMC-EC NPs of uniform surface wettability for treating different oily wastewaters. The M-Janus NPs could be facilely recycled and efficiently reused in the subsequent applications to oil removal/recovery without complex regeneration.