ABSTRACT
In previous work, a methodology was developed to discuss the influence of meteorological factors, policies, and surrounding cities on PM2.5 concentrations in a city. Two models were constructed using Zibo City, Shandong Province, as the target city. Initially, we improved the established PM2.5-Meteorological-Policy (PMP) model and applied it to six other target cities in Shandong Province. Concurrently, a novel model named the PM2.5-Interregional (PI) model was further developed in each city to directly express the influence of surrounding cities on the target cities. The model construction period was from January 2014 to August 2022, with the extended prediction period until November 2022. The results confirmed that disparities in the spatial distribution in seasons became smaller after the implementation of environmental policies. Moreover, two models in each city revealed good interpretation with high adjusted R2 values (>0.7) and lower MAPE and RMSE values (the lowest was 5.53% and 2.57), suggesting reasonable short-term prediction. Additionally, meteorological factors and the combined implementation of different policy types played crucial roles in reducing PM2.5 concentrations in all cities. Specifically, the temperature and wind speed were negatively correlated with PM2.5 concentrations in all models, with temperature having a stronger influence. The Law of the People's Republic of China on the Prevention and Control of Atmospheric Pollution (LAPAP), implemented in 2016, had a clear influence on reducing PM2.5 concentrations, with the highest absolute fitted coefficient in most cities (-0.166 to -0.344). On the contrary, the influence of temperature seemed to be more significant compared to policies, due to the larger standardized coefficient in each city (-0.606 to -0.864).
ABSTRACT
Antibiotics are used extensively throughout the world and their presence in the environment has caused serious pollution. This review summarizes natural methods and enhanced technologies that have been developed for antibiotic degradation. In the natural environment, antibiotics can be degraded by photolysis, hydrolysis, and biodegradation, but the rate and extent of degradation are limited. Recently, developed enhanced techniques utilize biological, chemical, or physicochemical principles for antibiotic removal. These techniques include traditional biological methods, adsorption methods, membrane treatment, advanced oxidation processes (AOPs), constructed wetlands (CWs), microalgae treatment, and microbial electrochemical systems (such as microbial fuel cells, MFCs). These techniques have both advantages and disadvantages and, to overcome disadvantages associated with individual techniques, hybrid techniques have been developed and have shown significant potential for antibiotic removal. Hybrids include combinations of the electrochemical method with AOPs, CWs with MFCs, microalgal treatment with activated sludge, and AOPs with MFCs. Considering the complexity of antibiotic pollution and the characteristics of currently used removal technologies, it is apparent that hybrid methods are better choices for dealing with antibiotic contaminants.
Subject(s)
Microalgae , Water Pollutants, Chemical , Anti-Bacterial Agents/therapeutic use , Sewage , Waste Disposal, Fluid/methods , Wastewater/analysis , Water Pollutants, Chemical/analysis , WetlandsABSTRACT
The quantitative evaluation of azelaic acid is becoming critical in the development of new medicinal products and in environment. A feasible method for the determination of azelaic acid in cosmetics by gas chromatographic-mass spectrometer detector (GC-MS) with derivation was developed and optimized. The derivative effect was good, when azelaic acid was derivatized through ethanol at room temperature for 10 min with 800 µL of sulfuric acid as a catalyst. A good linear relationship of azelaic acid derivative was present from 10 to 1000 mg L-1 (R 2 = 0.9997). Detection limit and quantitative limit of GC was 15 and 50 mg kg-1, respectively. The recovery rate was in the range from 87.7% to 101% with all relative standard deviation (RSD) values less than 4%, denoting the method meeting the requirement of the analysis. Therefore, this method has the advantages of strong anti-interference ability and accurate results. Among the eight samples nominally azelaic acid, only three were detected. The respective content was 78â¯133, 16â¯710, and 2431 mg kg-1. The results showed that the actual addition of the azelaic acid in the market was quite different with label identification, being worthy of further attention. Further, it also provided a favorable experience for the monitoring of azelaic acid in the environment.
ABSTRACT
A hybrid system of flocculation-photocatalysis (HSFP) was applied to evaluate the color removal from simulative dye wastewater. The decolorization performance of HSFP was investigated considering four key factors: flocculant dosage, pH, turbidity, and ionic strength. Compared with flocculation alone, HSFP showed better decolorization effectiveness for simulative Crystal Violet-Reactive Red X-3B dye wastewater (CV-RR) and simulative Crystal Violet-Acid Orange II dye wastewater (CV-AO). The dosage of flocculant was determined by the molecular structure of target dyes. A higher dosage was required for the color removal of dyes with a lower molecular weight and less sulfonic acid groups. The dominant decolorization mechanism was different with different initial pH values of simulative dye wastewater, which influenced the decolorization efficiency of flocculation and photocatalysis. For dyes with a lower molecular weight and less sulfonic acid groups, better decolorization performance was achieved under neutral conditions, mainly depending on strong charge neutralization and adsorption bridging capacity. For dyes with a higher molecular weight and more sulfonic acid groups, decolorization efficiency was improved with an increase in pH, due to stronger deprotonation. An increase of turbidity reduced the dye removal efficiency of flocculation alone and HSFP. The presence of NaCl, CuCl2, and CrCl3 led to a different decrease in the flocculation efficiency and photodegradation efficiency.
ABSTRACT
The effect of extracellular polymeric substances (EPS), vital organic matters and nutrient elements in the natural environment, on the behavior and toxicology of silver nanoparticles (AgNPs) and ions remains ambiguous. In this study, the role of EPS on the toxicity of AgNPs and dissolved silver ions (from AgNO3) to a green algae Chlorella vulgaris was investigated. After the removal of EPS, algae accumulated more silver, about 7.41- and 1.25-fold of those in the algae with EPS for AgNPs and AgNO3 treatments, respectively. The large amount of accumulated silver was bound to the algal cell surface for AgNPs treatment and was internalized in the algae for AgNO3 treatment, irrespective of the presence of EPS in algae. After exposure to AgNPs, the ruffles in the surfaces of algal cells were filled by AgNPs, and almost invisible. FTIR showed that for both AgNPs and AgNO3, the aldehyde groups on the cell surface were oxidized to carboxyl groups by silver ions, irrespective of the presence of EPS in algal cells, indicating that silver ions were released from the oxidization of AgNPs and reacted with algal cells. The content of chlorophyll showed that AgNPs depressed algal growth more remarkably than did AgNO3, independent of the presence of EPS in algae, suggesting that AgNPs had greater toxic effects on algae than did silver ions. The findings suggest that the barrier effect of EPS gave nanoparticles an extraordinary edge over ions, but EPS had no discerning effect on the interaction of algal cells with the silver ions released from AgNPs and AgNO3, and also on the effect of AgNPs and AgNO3 on algal growth.
Subject(s)
Chlorella vulgaris/drug effects , Extracellular Polymeric Substance Matrix/chemistry , Metal Nanoparticles/toxicity , Silver/toxicity , Chlorella vulgaris/growth & development , Chlorella vulgaris/metabolism , Chlorophyll/metabolism , Chlorophyll A/metabolism , Environmental Pollutants/toxicity , Ions/toxicity , Metal Nanoparticles/chemistry , Oxidation-Reduction , Silver/chemistry , Silver/metabolism , Spectroscopy, Fourier Transform InfraredABSTRACT
To systematically study CO2 adsorption performance, semicoke from the low-rank lignite was further activated and functionalized for CO2 capture from flue gases. The effect of the activation conditions, such as the activation temperature, activation time and HCl washing, and the tetraethylenepentamine (TEPA)-functionalization on CO2 adsorption were investigated; the pore structure and surface morphology of the semicoke under different activation conditions were characterized. Both the surface structure and adsorption performance of the activated semicoke could be improved under appropriate activation and acid-treatment conditions. The optimal breakthrough and equilibrium adsorption capacity for the TEPA-functionalized HCl-washed activated semicoke were separately 2.68 and 3.70 mmol g-1 at 60 °C for the simulated flue gas of 15 vol% CO2 and 85 vol% N2. After ten adsorption-desorption cycles, the equilibrium adsorption capacity was still 3.43 mmol g-1, and the semicoke-based sorbent showed good regenerability.
ABSTRACT
The adsorption and photocatalytic degradation of gaseous benzene were investigated considering the operating variables and kinetic mechanism using nano-titania agglomerates in an annular fluidized bed photocatalytic reactor (AFBPR) designed. The special adsorption equilibrium constant, adsorption active sites, and apparent reaction rate coefficient of benzene were determined by linear regression analysis at various gas velocities and relative humidities (RH). Based on a series of photocatalytic degradation kinetic equations, the influences of operating variables on degradation efficiency, apparent reaction rate coefficient and half-life were explored. The findings indicated that the operating variables have obviously influenced the adsorption/photocatalytic degradation and corresponding kinetic parameters. In the photocatalytic degradation process, the relationship between photocatalytic degradation efficiency and RH indicated that water molecules have a dual-function which was related to the structure characteristics of benzene. The optimal operating conditions for photocatalytic degradation of gaseous benzene in AFBPR were determined as the fluidization number at 1.9 and RH required related to benzene concentration. This investigation highlights the importance of controlling RH and benzene concentration in order to obtain the desired synergy effect in photocatalytic degradation processes.
Subject(s)
Benzene/chemistry , Photolysis , Adsorption , Humidity , ThermodynamicsABSTRACT
OBJECTIVE: To investigate the photocatalytic degradation of gaseous ammonia in static state by using nano-TiO2 as photocatalyst supported on latex paint film under UV-irradiation. METHODS: Experiments were conducted to study the relationship between the initial concentration of ammonia and the degradation products competing to be adsorbed on catalyst surface. Degradation of ammonia and its products were detected by spectrophotometry and catalytic kinetic spectrophotometry, respectively. RESULTS: On the one hand, TiO2 catalyst was excellent for degradation of ammonia, and the crystal phase of TiO2, anatase or rutile, had little effect on degradation of ammonia, but the conversion of ammonia grew with the increase of catalyst content. On the other hand, apparent rate constant and conversion of ammonia decreased with the increase of initial concentration of ammonia, and the photocatalytic degradation reaction followed a pseudo-first-order expression due to the evidence of linear correlation between -lnC/C0 vs. irradiation time t, but the relationship between initial concentration and the degradation products was not linear in low initial concentration. CONCLUSION: Whether the photocatalytic degradation of ammonia in static state follows a first-order reaction depends on the initial ammonia concentration due to competition in adsorption between reactant and the degradation products.