Maxwellrocha0223

On-road measurement results indicated that fuel consumption under the low-speed phase of the CLTC-P increased by 12% due to the STT off, although only a 4% increase on average over the entire cycle. More fuel consumption increases (52%) were attributed to air conditioning usage and full passenger capacity. Strong correlations (R2 > 0.9) between relative fuel consumption and average speed were also identified. Under traffic congestion (average speed below 25 km/hr), fuel consumption was highly sensitive to changes in vehicle speed. Thus, we suggest that real-world driving conditions cannot be ignored when evaluating the fuel economy and GHGs reduction of LDGVs.Herein, a one-step co-pyrolysis protocol was adopted for the first time to prepare a novel pyrogenic carbon-Cu0/Fe3O4 heteroatoms (FCBC) in CO2 ambiance to discern the roles of each component in PDS activation. During co-pyrolysis, CO2 catalyzed formation of reducing gases by biomass which facilitated reductive transformation of Fe3+ and Cu2+ to Cu0 and Fe3O4, respectively. According to the analysis, the resulting metal (oxide) catalyzed graphitization of biocharand decomposition of volatile substances resulting in an unprecedented surface area (1240 m2/g). The resulting FCBC showed greater structural defects and less electrical impedance. Batch experiments indicated that Rhodamine B (RhB) degradation by FCBC (100%) was superior to Fe3O4 (50%) and Cu0/Fe3O4 (76.4%) in persulfate (PDS) system, which maintained reasonable efficiency (75.6%-63.6%) within three cycles. The reactive oxygen species (ROS) associated with RhB degradation was identified by an electron paramagnetic resonance and confirmed by scavenging experiments. RhB degradation invoked both (sulfate and dominantly hydroxyl) radical and non-radical (singlet oxygen, 1O2) pathways. Regarding FCBC, Cu0 can continuously react with Fe3+ in Fe3O4 to generate larger quantities of Fe2+, and both Cu0 and Fe2+ activated PDS to yield sulfate radicals which was quickly converted to hydroxyl radical. Besides, Cu0/Cu2+ could complex with PDS to form a metastable complex, which particularly contributed to 1O2 generation. These cascade reactions by FCBC were reinforced by carbonyl group of biochar and favorable electron transfer ability. This work highlighted a new approach to prepare a magnetic and environment-benign heterogonous catalyst to remove organic pollutants in water.Glyphosate, the most extensively used herbicide globally, has raised ecotoxicological concerns because it can be transported into the aquatic environment and cause adverse effects on the aquatic system. However, the functional mechanism of glyphosate on cyanobacteria are not completely disentangled. In this study, we selected six common cyanobacteria to evaluate glyphosate effects on cyanobacterial growth in monoculture experiment. Results showed that the growth of five tested cyanobacterial species were promoted under different degrees, and only Pseudanabaena was inhibited by glyphosate. In the phylogenetic tree based on gene sequences of 5-enol-pyruvylshikimate-3-phosphate synthase (EPSPS), a target for glyphosate, we found that the position of Pseudanabaena is the closest to plant, which was sensitive to glyphosate, thereby explaining the inhibitory effect of Pseudanabaena following glyphosate exposure. The primary degraded metabolites or analogs did not induce cyanobacterial growth, laterally demonstrating that glyphosate was used as a source of phosphorus to accelerate cyanobacterial growth because phosphorus levels increased in the medium of glyphosate treatment. Overall, this study provides a better understanding of the influence of glyphosate on the composition of aquatic microbiota and explains the mechanism of cyanobacterial response to glyphosate.High-efficiency photocatalysts are of great significance for the application of photocatalytic technology in water treatment. In this study, N/Cu co-doped ZnS nanosphere photocatalyst (N/Cu-ZnS) is synthesized by a hydrothermal method for the first time. After doping, the texture of nanosphere becomes loose, the nanometer diameter is reduced, making the specific surface area of catalyst increased from 34.73 to 101.59 m2/g. The characterization results show that more ZnS (111) crystal planes are exposed by N/Cu co-doping; the calculations of density functional theory show that N/Cu co-doping can increase the catalytic activity of the ZnS (111) crystal plane, enhance the adsorption capacity of (111) crystal plane to O2, and promote the generation of •O2-. The energy levels of the introduced impurities can be hybridized with the energy levels of S and Zn at the top of valence band and the bottom of conduction band, which makes the band gap narrower, thus enhancing the absorption of visible light. Compared with pure ZnS, the degradation rates of 2,4-dichlorophenol (2,4-DCP) and tetracycline (TC) by N/Cu-ZnS under visible light (>420 nm) are increased by 83.7 and 51 times, respectively. In this research, a promising photocatalyst for photocatalytic degradation of organic pollutants in wastewater is provided.Heterogeneous agglomeration (HA) is a very potential technology for coal-fired flue gas treatment. In this paper, the distribution and migration mechanisms of trace elements (TEs) such as Se, As and Pb in CFPPs were studied on a 30,000 m3/hr pilot-scale experimental platform. The influences of HA on the removal efficiency of gaseous and particulate TEs were well analyzed. The results showed that Se, As and Pb were enriched in fly ash, and their sensitivity to particle size is quite different. The content of Se was the highest in PM1, reaching 193.04 mg/kg at the electrostatic precipitator (ESP) outlet. The average particle size of the total dust before ESP increased significantly from 21.686 to 62.612 µm after injecting the heterogeneous agglomeration adsorbent, conducive to its further removal by ESP. In addition, the concentrations of gaseous Se, As and Pb in the flue gas decreased after adsorbent spray, and accordingly, their contents in the hierarchical particles increased, indicating that the adsorbent could effectively promote the adsorption of gaseous trace elements in fly ash and reduce the possibility of their escape to the atmosphere. Total concentrations of Se, As and Pb emitted by wet flue gas desulfurization (WFGD) are 0.223, 0.668 and 0.076 µg/m3, which decreased by 59.98%, 47.69% and 90.71%, respectively. Finally, a possible HA mechanism model was proposed, where chemical adsorption, physical condensation and collision agglomeration of gaseous TEs and fine particles with adsorbent droplets occurred to form larger agglomerates.Citrate (Ct) was chosen as a typical chelator used in the Fe2+-peroxydisulfate (PDS) process to improve sludge dewaterability. The PDS-Fe2+-Ct process exhibited better performance in sludge dewatering than PDS-Fe2+. Specifically, with a PDS dosage of 1.2 mmol/g VS, the molar ratio of PDS/Fe2+ and Ct/Fe2+ were 45 and 14, respectively, the capillary suction time decreased from 155.8 to 24.8sec, and the sludge cake water content decreased from 82.62% to 64.11% (-0.06MPa). The oxidation led to a reduced negative charge and a decrease in particle size. The enhanced sludge dewaterability and changes of sludge properties were attributed to the decomposition of extracellular polymeric substances, and it was explored by protein, polysaccharide, 3D-EEMs, and FT-IR. Additionally, the quenching experiments of radical species demonstrated that SO4-• played a more important role than •OH, and its productivity was improved with the addition of Ct. read more Moreover, the reasons for the improved productivity of radicals with the addition of Ct were discussed. The results of this study could serve as a basis for improving sludge dewatering using the PDS-Fe2+-Ct process and suggest that the addition of Ct may improve the productivity of SO4-• in the activation of PDS via Fe2+.Vacuum ultraviolet (VUV) photolysis is recognized as an environmental-friendly treatment process. Nitrate (NO3-) and natural organic matter (NOM) are widely present in water source. We investigated trichloronitromethane (TCNM) formation during chlorination after VUV photolysis, because TCNM is an unregulated highly toxic disinfection byproduct. In this study (1) we found reactive nitrogen species that is generated under VUV photolysis of NO3- react with organic matter to form nitrogen-containing compounds and subsequently form TCNM during chlorination; (2) we found the mere presence of 0.1 mmol/L NO3- can result in the formation of up to 63.96 µg/L TCNM; (3) we found the changes in pH (6.0-8.0), chloride (1-4 mmol/L), and bicarbonate (1-4 mmol/L) cannot effectively diminish TCNM formation; and, (4) we established the quantitative structure-activity relationship (QSAR) model, which indicated a linear relationship between TCNM formation and the Hammett constant (σ) of model compounds; and, (5) we characterized TCNM precursors in water matrix after VUV photolysis and found 1161 much more nitrogen-containing compounds with higher aromaticity were generated. Overall, this study indicates more attention should be paid to reducing the formation risk of TCNM when applying VUV photolysis process at scale.Little information is available on influences of the conversion of dissolved organic phosphorus (DOP) to inorganic phosphorus (IP) on algal growth and subsequent behaviors of arsenate (As(V)) in Microcystis aeruginosa (M. aeruginosa). In this study, the influences factors on the conversion of three typical DOP types including adenosine-5-triphosphate disodium salt (ATP), β-glycerophosphate sodium (βP) and D-glucose-6-phosphate disodium salt (GP) were investigated under different extracellular polymeric secretions (EPS) ratios from M. aeruginosa, and As(V) levels. Thus, algal growth, As(V) biotransformation and microcystins (MCs) release of M. aeruginosa were explored in the different converted DOP conditions compared with IP. Results showed that the three DOP to IP without EPS addition became in favor of algal growth during their conversion. Compared with IP, M. aeruginosa growth was thus facilitated in the three converted DOP conditions, subsequently resulting in potential algal bloom particularly at arsenic (As) contaminated water environment. Additionally, DOP after conversion could inhibit As accumulation in M. aeruginosa, thus intracellular As accumulation was lower in the converted DOP conditions than that in IP condition. As(V) biotransformation and MCs release in M. aeruginosa was impacted by different converted DOP with their different types. Specifically, DMA concentrations in media and As(III) ratios in algal cells were promoted in converted βP condition, indicating that the observed dissolved organic compositions from βP conversion could enhance As(V) reduction in M. aeruginosa and then accelerate DMA release. The obtained findings can provide better understanding of cyanobacteria blooms and As biotransformation in different DOP as the main phosphorus source.Sb(III) is often detected in contaminated soil and groundwater. Hence, high-efficiency technology is needed. In this study, bimetallic organic frameworks were used for the first time to immobilize Sb(III) from contaminated soil and groundwater. The materials were synthesized by the hydrothermal method. Both ends of the prepared material were hexagonal tip rods, and the length became shorter as the ratio of Fe/Mg decreased. The bimetallic organic framework with a Fe/Mg feeding ratio of 0.5 was the optimum material for Sb(III) removal, which could effectively immobilize Sb(III). The adsorption isotherm was fitted well with the Freundlich model, and the optimal adsorption capacity can reach 106.97 mg/g. The adsorption capacity of 84% can be completed in 10 min, which conformed to the pseudo-second-order kinetics. The Fe3+ could enhance the stability of the material, and the Mg2+ was conducive to freeing up adsorption sites for binding Sb(III) and forming stable chemical adsorption. Ion exchange is the predominant mechanism to remove Sb(III).