Biomimetic Mineralization of Ca-Mg Carbonates: Relevance to Microbial Cells and Extracellular Polymeric Substances.

Research on Ca-Mg carbonate crystallization and phase transition regulated by microbial cells and extracellular polymeric substances (EPS) is significant for carbon sequestration, remediation of polluted soil and water, and synthesis of functional biomaterials. This study focused on the mineralogical transformation from amorphism to crystal, and interaction among cells, EPS, and minerals. By tracing the law of mineral growth and morphological evolution, the influences of cells and EPS on mineral formation were investigated. The results revealed that calcification and the template of rod-shaped cells of strain HJ-1 were the basis for the formation of dumbbell-shaped particles, and directional aggregation and differential growth were the keys to the development and stability of dumbbells. Cell participation had a noticeable impact on mineral prototypes, instead of determining the polymorphism. EPS contributed to aragonite formation and stability. The acidic amino acids or proteins in EPS were likely to cause an increase in MgCO3 content in Mg-calcite. EPS promoted aggregation of particles and induced spherical formation. Exopolysaccharides and proteins were the main components of EPS that can affect carbonate mineralization. EPS could influence the morphology and polymorphism by providing nucleation sites, interacting with Mg2+, adsorbing or incorporating mineral lattices, and inducing particle aggregation.

Spatiotemporal dynamics of near-surface ozone concentration and potential source areas in northern China during 2015-2020.

Near-surface ozone (O3) pollution has become one of the main factors hampering urban air quality in northern China. However, on a spatiotemporal scale, dynamic transport paths and potential source areas of O3 in northern China are ambiguous. In addition, we suspect that the contribution of transportation activities to urban O3 concentrations developed in northern China may be underestimated. In this study, the HYSPLIT, PSCF, CWT and GTWR model were used to study the transmission paths, potential source areas and driving factors of urban O3 concentration on a spatiotemporal scale. The average annual concentration of surface O3 (the 90th percentile of MDA8) was 172 ± 29 µg/m3 in northern China from 2015 to 2020. In terms of inter-annual variation, the urban O3 concentration increased from 2015 to 2018, and decreased after 2018. On the spatial scale, the areas with high O3 concentration were mainly clustered in industrial cities (Tangshan, Baoding, Shijiazhuang, Xingtai and Handan). During the study period, the area with high O3 concentration in northern China shifted from northwest to southeast. From 2015 to 2020, the influence of long-distance air mass trajectories from Xinjiang and Siberi on airflow transport in Beijing city dominates (78.60%) The average percentage of short-distance transport trajectories from Shandong Peninsula region is about 21.40%. The core potential source areas of O3 pollution shifted from northwest to southeast, but the contribution to O3 pollution in Beijing gradually weakened during the same period. Temperature and relative humidity were the main meteorological driving factors affecting O3 concentration in the study area, while population density, the proportion of secondary industry in GDP, industrial smoke (dust) emissions, and passenger traffic were the main non-meteorological factors. During the period study, the influence of industrial and traffic emissions had a more significant impact on O3 concentration in northern China, which will require that more attention be paid to emission mitigation in the regional industrial and passenger transportation sector, as well as the joint prevention and control of O3 pollution in northern China in the future.

Urban Surface Ozone Concentration in Mainland China during 2015-2020: Spatial Clustering and Temporal Dynamics.

Urban ozone (O3) pollution in the atmosphere has become increasingly prominent on a national scale in mainland China, although the atmospheric particulate matter pollution has been significantly reduced in recent years. The clustering and dynamic variation characteristics of the O3 concentrations in cities across the country, however, have not been accurately explored at relevant spatiotemporal scales. In this study, a standard deviational ellipse analysis and multiscale geographically weighted regression models were applied to explore the migration process and influencing factors of O3 pollution based on measured data from urban monitoring sites in mainland China. The results suggested that the urban O3 concentration in mainland China reached its peak in 2018, and the annual O3 concentration reached 157 ± 27 µg/m3 from 2015 to 2020. On the scale of the whole Chinese mainland, the distribution of O3 exhibited spatial dependence and aggregation. On the regional scale, the areas of high O3 concentrations were mainly concentrated in Beijing-Tianjin-Hebei, Shandong, Jiangsu, Henan, and other regions. In addition, the standard deviation ellipse of the urban O3 concentration covered the entire eastern part of mainland China. Overall, the geographic center of ozone pollution has a tendency to move to the south with the time variation. The interaction between sunshine hours and other factors (precipitation, NO2, DEM, SO2, PM2.5) significantly affected the variation of urban O3 concentration. In Southwest China, Northwest China, and Central China, the suppression effect of vegetation on local O3 was more obvious than that in other regions. Therefore, this study clarified for the first time the migration path of the gravity center of the urban O3 pollution and identified the key areas for the prevention and control of O3 pollution in mainland China.

Transmission paths and source areas of near-surface ozone pollution in the Yangtze River delta region, China from 2015 to 2021.

Near-ground ozone in the Yangtze River Delta (YRD) region has become one of the main air pollutants that threaten the health of residents. However, to date, the transport behavior and source areas of ozone in the YRD region have not been systematically analyzed. In this study, by combining the ozone observational record with a HYSPLIT (hybrid single-particle Lagrangian integrated trajectory) model, we tried to reveal the spatiotemporal regularity of the airflow transport trajectory of ozone. Spatially, high ozone concentrations mainly clustered in industrial cities and resource-based cities. Temporally, the center of the ozone pollution shifted westward of Nanjing from 2015 to 2021. With the passage of time, the influence of meteorological elements on the ozone concentration in the YRD region gradually weakened. Marine atmosphere had the most significant impact on the transmission path of ozone in Shanghai, of which the trajectory frequency in 2021 accounted for 64.21% of the total frequency. The transmission trajectory of ozone in summer was different from that in other seasons, and its transmission trajectory was mainly composed of four medium-distance transmission paths: North China-Bohai Sea, East China Sea-West Pacific Ocean, Philippine Sea, and South China Sea-South China. The contribution source areas mainly shifted to the southeast, and the emission of pollutants from the Shandong Peninsula, the Korean Peninsula-Japan, and the Philippine Sea-Taiwan area increased the impact of ozone pollution in the Shanghai area from 2019 to 2021. This study identified the regional transport path of ozone in the YRD region and provided a scientific reference for the joint prevention and control of ozone pollution in this area.

Preparation of nano-ferrous sulfide modified with phytate for efficient Cr(VI) removal in aqueous solutions.

Phytate-modified nano-ferrous sulfide (IP6-nano-FeS) was successfully prepared to overcome the low efficiency of heavy metal removal by nano-ferrous sulfide (nano-FeS) due to the agglomeration and easy oxidization of this reducing agent. The results showed that IP6-nano-FeS improved the dispersion of nano-FeS particles, and the maximum Cr(VI) removal reached 436.94 ± 25.40 mg/g. A more novel contribution of this study is that Cr(VI) removal by IP6-nano-FeS was enhanced in the presence of Mg2+, Ca2+, and O2. The removal efficiency increased by ∼10% and ∼8.5% in the presence of conventional cations (Mg2+ and Ca2+: 2-10 g/L) and O2, respectively. The application potential of IP6-nano-FeS for the rapid removal of Cr(VI)-contamination in the presence of aerobic and coexisting cations was confirmed in this study.

Spatiotemporal Distribution and Evolution of Digestive Tract Cancer Cases in Lujiang County, China since 2012.

This study aims to analyze the spatiotemporal distribution and evolution of digestive tract cancer (DTC) in Lujiang County, China by using the geographic information system technology. Results of this study are expected to provide a scientific basis for effective prevention and control of DTC. The data on DTC cases in Lujiang County, China, were downloaded from the Data Center of the Center for Disease Control and Prevention in Hefei, Anhui Province, China, while the demographic data were sourced from the demographic department in China. Systematic statistical analyses, including the spatial empirical Bayes smoothing, spatial autocorrelation, hotspot statistics, and Kulldorff's retrospective space-time scan, were used to identify the spatial and spatiotemporal clusters of DTC. GM(1,1) and standard deviation ellipses were then applied to predict the future evolution of the spatial pattern of the DTC cases in Lujiang County. The results showed that DTC in Lujiang County had obvious spatiotemporal clustering. The spatial distribution of DTC cases increases gradually from east to west in the county in a stepwise pattern. The peak of DTC cases occurred in 2012-2013, and the high-case spatial clusters were located mainly in the northwest of Lujiang County. At the 99% confidence interval, two spatiotemporal clusters were identified. From 2012 to 2017, the cases of DTC in Lujiang County gradually shifted to the high-incidence area in the northwest, and the spatial distribution range experienced a process of "dispersion-clustering". The cases of DTC in Lujiang County will continue to move to the northwest from 2018 to 2025, and the predicted spatial clustering tends to be more obvious.

Efficient removal of organic compounds in eutrophic water via a synergy of cyanobacterial extracellular polymeric substances and permanganate.

This study provides a new thinking for the efficient utilization of permanganate (Mn (VII)) in eutrophic water treatment. Eutrophic water contained a large amount of extracellular polymeric substances (EPS) with reduction and chelation; this study used phenol as typical organic matter and cyanobacteria EPS as a representative EPS to explore the mechanism by which EPS influences the oxidation of phenol by Mn(VII) at pH 5.0-9.0. The results showed that under the condition of pH 5.0-7.0, adding 0.2-10 mg/L EPS to the Mn(VII) system could effectively improve the oxidation efficiency of Mn(VII) for phenol. EPS promoted the continuous formation and stability of in situ EPS-MnO2 colloids and significantly enhanced the oxidation of Mn(VII). EPS also combined with phenol and increased the electron cloud density to promote the oxidation of phenol by Mn(VII).

Large alpine deep lake as a source of greenhouse gases: A case study on Lake Fuxian in Southwestern China.

Freshwater lakes are recognized as potential sources of greenhouse gases (GHGs) that contribute to global warming. However, the spatiotemporal patterns of GHG emissions have not been adequately quantified in large deep lakes, resulting in substantial uncertainties in the estimated GHG budgets in global lakes. In this study, the spatial and seasonal variability of diffusive GHG (CO2, CH4, and N2O) emissions from Lake Fuxian located on a plateau in Southwestern China were quantified. The results showed that the surface lake water was oversaturated with dissolved GHG concentrations, and the average concentrations were 24.25 µM CO2, 0.044 µM CH4, and 14.28 nM N2O, with diffusive emission rates of 8.82 mmol CO2 m-2 d-1, 31.94 µmol CH4 m-2 d-1, and 4.94 µmol N2O m-2 d-1, respectively. Diffusive CH4 flux exhibited high temporal and spatial variability similar to that in most lakes. In contrast, diffusive CO2 and N2O flux showed distinct seasonal variability and similar spatial patterns, emphasizing the necessity for increasing the temporal resolution in GHG flux measurements for integrated assessments. Water temperature and/or oxygen concentrations were crucial in regulating seasonal variability in GHG emissions. However, no limnological parameter was found to govern the spatial GHG patterns. The frequent advection mixing caused by wind-driven currents might be the reason for the low spatial heterogeneity in GHGs, in which the inconspicuous mechanism requires further research. It was recommended that at least 11 locations were needed for representative whole lake flux estimates at each sampling campaign. In addition, the maximum peak of CH4 in the oxycline from Lake Fuxian indicated that low CH4 oxidation occurred in oxic waters. Overall, this study suggests that, compared to other tropical and temperate lakes, this alpine deep lake is a minor CO2 and CH4 source, but a moderate N2O source, which are horizontally uniform.

Inactivation Mechanism of Algal Chlorophyll by Allelochemical Quercetin.

Cyanobacteria harmful algal blooms (CyanoHABs) are a global concern. Application of allelochemicals is a promising solution for cyanobacteria control, due to its high efficiency, low cost and ecological safety. Flavonoids (natural polyphenols produced by aquatic plants) are reported capable of effectively inhibiting the growth of algae; however, the molecular mechanism of algae chlorophyll inactivation is still unclear. In this study, quercetin was used as a typical flavonoid, to investigate the inactivation effect of allelochemical on Microcystis aeruginosa chlorophyll a. The absorption and fluorescence spectra showed that chlorophyll reacted with quercetin to form pheophytin, and the formation rate of pheophytin increased with increasing quercetin concentration (1 × 10-5-1 × 10-2 M). FTIR spectra and DFT calculation showed that Mg2+ complexed with the 3-OH and 4-C = O groups in the quercetin ring C so that chlorophyll was inactivated due to the loss of Mg2+ ions. Overall, this study revealed that quercetin inactivated chlorophyll a of cyanobacteria by capturing Mg2+ ions, providing insights into the molecular mechanisms of algal bloom control by allelochemicals.

Removal kinetics and mechanisms of tetrabromobisphenol A (TBBPA) by HA-n-FeS colloids in the absence and presence of oxygen.

The colloid of ferrous sulfide modified by humic acid (HA-n-FeS) shows good reduction and immobilization efficiency for variable-valence heavy metals in wastewater. The removal efficiency of HA-n-FeS for halogenated organic pollutants, however, remains unclear, especially in the absence and presence of oxygen. This study addressed this issue by exploring the effect and mechanism of dissolved oxygen on the degradation of tetrabromobisphenol A (TBBPA) by the HA-n-FeS colloid in water. The results showed that the removal efficiency of different concentrations of TBBPA (5,10, and 20 µm) by the HA-n-FeS colloid was 33.16%, 20.48%, and 22.37% in the absence of oxygen, respectively. When TBBPA reacted with the HA-n-FeS colloid, the concentration of Fe(II) and S(-II) remained stable. The adsorption of HA-n-FeS was the main mechanism of removing TBBPA in the absence of oxygen. In the presence of oxygen, the removal efficiency of TBBPA by the HA-n-FeS colloid was 82.37%, 56.80%, and 43.78% (for the above-mentioned TBBPA concentrations), respectively. In addition, the removal capacity of TBBPA by HA-n-FeS was 39.63, 52.21, and 89.75 mg/g, respectively. The concentration of Fe(II) and S(-II) decreased rapidly in time. Among them, the HA-n-FeS colloid removed part of the TBBPA through chemical adsorption. The main way of chemical adsorption was pore adsorption and functional group (olefin CC, phenolic hydroxyl group O-H, alcohol group C-O) combination. Besides, the HA-n-FeS colloid degraded part of the TBBPA into BPA through reduction, in which 17.72% of TBBPA was removed by the reduction of HA-n-FeS colloid. Fe(II) was the main contributor to the reductive degradation of TBBPA. Furthermore, active species (1O2 and •O2-) played a minor role in the removal of TBBPA by the HA-n-FeS colloids with oxygen, where 13% of TBBPA was removed by 1O2 and •O2-. Therefore, in practical applications, the aeration method can be used to significantly improve the removal efficiency of TBBPA by HA-n-FeS colloids in water.

Methyl silicate promotes the oxidative degradation of bisphenol A by permanganate: Efficiency enhancement mechanism and solid-liquid separation characteristics.

Permanganate (Mn (VII)) is an environmentally-friendly mild oxidant in the field of advanced oxidation treatment, however, manganese colloids are produced as byproducts, which is difficult to separate from water, resulting in secondary pollution. This study used potassium methyl silicates (PMS) as surface modifiers to improve the aggregation of colloidal particles by increasing the hydrophobicity of the colloidal surface, and then explored the oxidation of bisphenol A (BPA) by Mn (VII) under the influence of potassium methyl silicate and the solid-liquid separation performance of the reaction system. The results showed that PMS and sodium silicate (SS) substantially enhanced the degradation of BPA by Mn (VII), and the promotion effect of potassium methyl silicate was greater than that of sodium silicate. PMS provided not only enough adsorption sites for MnO2 colloidal particles formed in the reaction process, but also reaction space for Mn (VII) to catalyze the oxidation of BPA. PMS combined with the hydroxyl group of MnO2 through hydrogen bonds and forms hydrophobic PMS-MnO2 complexes which accelerated sedimentation by polycondensation. The strong adsorption ability of in situ formed MnO2 colloids also accelerated the deposition of PMS-MnO2 complex. This study solved the low efficiency problem of Mn (VII) oxidation degradation of organic pollutants and difficult separation of manganese containing colloids and provided a new strategy for the efficient utilization of Mn (VII).

Visible light promoted the removal of tetrabromobisphenol A from water by humic acid-FeS colloid.

Ferrous sulfide (FeS) and humic acid (HA) are typical black substances in black bloom water. Based on the strong reduction ability of FeS and the photosensitivity of HA, the transformation of toxic organic pollutants by the combination of FeS and HA (HA-FeS) is not clear. In order to explore this issue, the stability of HA-FeS was analyzed by measuring the hydrodynamic diameter and zeta potential of HA-FeS, and then the removal mechanism and possible degradation pathway of tetrabromobisphenol A (TBBPA) by HA-FeS under continuous illumination were discussed. The results showed that the hydrodynamic diameter of FeS was reduced and the stability of FeS was improved, and it was easily suspended after FeS combined with the HA in the water. The combination of HA and FeS promoted the removal of TBBPA in water, no matter it was in the presence or absence of light. Besides, compared with the absence of light, the removal efficiency of TBBPA was improved by HA-FeS with continuous light. There were two reasons for the increase in the removal efficiency of TBBPA by HA-FeS. On the one hand, Fe2+ and S2- of HA-FeS had more stable chemical valence and obtained better reducibility under continuous light than that in the dark. On the other hand, light induced the release of active species (O2-, 1O2, and OH) in the HA-FeS composite colloid and further promoted the degradation of organic pollutants. Therefore, the black substances (FeS) of black blooms may play a beneficial role in the removal of pollutants under sunlight.

Distribution Characteristics and Relevance of Heavy Metals in Soils and Colloids Around a Mining Area in Nanjing, China.

Heavy metal pollution in agricultural soils poses a direct threat to food safety and human health. It has been shown that the colloids is the carrier of heavy metal transport in the polluted soil by heavy metals, but the sources of heavy metals in the soil and colloids and their interrelations are not transparent at present. This study aims to investigate the distribution characteristics of heavy metals in agricultural soils near mining areas, and reveal the relevance of heavy metal content in colloids with total content in soils and their chemical species in soils. Results showed that the concentrations of Mn, Zn, and Pb in agricultural soils and colloids were higher than those of other heavy metals. The content of heavy metals in colloids was positively correlated with the total content of heavy metals in soil. Heavy metals in soil could be easily combined by humus-like substances and tryptophan-like protein in the colloids. The primary source of heavy metals in soil and colloids was mining activities. This study provides theoretical support for revealing the pollution characteristics and migration of heavy metals in agricultural soils and colloids around mining areas.

Cool Roof and Green Roof Adoption in a Metropolitan Area: Climate Impacts during Summer and Winter.

This study, for the first time, estimates the climate impacts of adopting green roofs and cool roofs on the seasonal urban climate of 16 cities that comprise the Yangtze River Delta metropolitan. We use a suite of regional climate simulation to compare the local climate impacts of the implementation of different roof strategies in summer and winter. The results indicate that in summer, the 2 m surface temperature reduced significantly when these two roof strategies are adopted, with peak reductions of 0.74 and 1.19 K for green roofs and cool roofs, respectively. The cooling impact of cool roofs is more effective than that of green roofs under the scenarios assumed in this study. Besides, rooted in the different mechanisms influencing urban heat flux, significant indirect effects were also observed: adopting cool roofs leads to a decreased precipitation in summer and an apparent reduction in wintertime temperatures in the urban area. Although cool roofs can be an effective way to reduce high temperatures during the summer, green roofs have fewer adverse impacts on other climate conditions. These results underline the need for comprehensive climate change policies that incorporate place-based solutions and extend beyond the nearly exclusive focus on summertime cooling.

A novel colloid composited with polyacrylate and nano ferrous sulfide and its efficiency and mechanism of removal of Cr(VI) from Water.

Nano ferrous sulfide (n-FeS) colloids show an excellent performance in the application of remediation in situ soil and groundwater. However, due to the interfacial effect and high reactivity of the nano sized FeS, n-FeS easy to agglomerate, which reduces their remediation efficiency. In this study, a novel composite colloid was synthesized using polyacrylic acid salt (PAA) and n-FeS. The PAA-n-FeS colloid was used to remove Cr(VI) in water remediation, and its removal mechanism and efficiency were explored. The results showed that the hydrodynamic diameter of PAA-n-FeS ranged from 65.04-90.09 nm and the zeta potential was from -27 to -54 mV at pH varying from 4.5-9.0. PAA was coated on the surface of n-FeS, which improved the dispersibility and stability of n-FeS by increasing the steric hindrance and electrostatic repulsion between n-FeS particles. Moreover, the Cr(VI) maximum removal amount PAA-n-FeS was 432.79 mg/g, which was significantly higher than that of n-FeS (218.29 mg/g) and PAA (12.32 mg/g). The mechanism of PAA-n-FeS removal of Cr(VI) was mainly derived from its own reducibility. The reaction products were mainly Cr(OH)3, Cr(III)-Fe(III), Cr2O3, and Cr2S3. This research not only finds a new stabilizer for preventing n-FeS agglomeration, but also provides a novel n-FeS composited colloid for promoting the practical application to Cr(VI) removal from water.

Highly efficient degradation of iohexol on a heterostructured graphene-analogue boron nitride coupled Bi2MoO6 photocatalyst under simulated sunlight.

Iohexol (IOH), as a typical iodinated X-ray contrast media (ICMs) with potential threat to human health, is difficult to be removed with the conventional wastewater treatment methods. In this work, new boron nitride coupled Bi2MoO6 layered microspheres (BN/Bi2MoO6) composites were applied to remove IOH from water via photocatalytic degradation. The degradation constant kapp of IOH over 3.5 wt% BN/Bi2MoO6 was 0.016 min-1, which was 3.2 times that of Bi2MoO6 (0.005 min-1). The degradation rate of IOH on 3.5 wt% BN/Bi2MoO6 reached 92% in 150 min. The enhanced photocatalytic activity of BN/Bi2MoO6 can be attributed to the heterojunction between BN and Bi2MoO6. The matched type-I band alignment heterojunction of two semiconductors prominently improved the charge separation. Based on the trapping experiments, holes and superoxide radicals were proved to be the main active species for photocatalytic IOH degradation. Besides, the degradation products of IOH were analyzed by LC-HRMS and the possible degradation mechanism of IOH was also proposed in this work.

Transport of arsenic loaded by ferric humate colloid in saturated porous media.

The transport behavior of arsenic (As(V)) loaded by ferric humate (HA-Fe) colloid, denoted as HA-Fe/As(V), moving in a saturated quartz sand column, was tested in the laboratory under varying pH values, ionic strengths, and HA and Fe(III) content. The time-fractional advection-dispersion equation (fADE) model was then employed to analyze the observed migration of HA-Fe/As(V). Results showed that the stability of the HA-Fe colloid exhibited an upward trend with an increasing pH and HA content. An increasing HA content led to a decrease in the particle size of the HA-Fe colloid. However, the effect of Fe(III) concentration on colloidal particle size exhibited the opposite phenomenon. The ability of the HA-Fe colloid to load As(V) gradually increased with the increase of the Fe(III) concentration. During the co-transport of the HA-Fe/As(V) colloid, transport of As(V) was promoted with increasing pH, increasing HA and Fe(III) content, and decreasing ionic strength in the saturated porous medium. The transport behavior of As(V) can be well fitted by the fADE model. The model analysis revealed that sub-diffusion of As(V) was weakened in the HA-Fe/As(V) colloid with high HA content. Sub-diffusion of As(V) in the low pH colloid was stronger than that of the high-pH colloid, and the molecular diffusion and mechanical dispersion were more weakened in the high-pH colloid than that of the low-pH colloid. When observing varying ionic strengths, As(V) exhibited stronger sub-diffusion in the HA-Fe/As(V) colloid with a higher ionic strength. As for the Fe(III) content, transport of As(V) was mainly affected by sub-diffusion in the HA-Fe/As(V) colloid with a low Fe(III) content. These findings provided direct and necessary insights into the effects of the HA-Fe colloid on the migration of As(V) throughout saturated porous media under different hydrochemical conditions found in natural environments.

Distribution characteristics and influencing factors of heavy metals in scalp hair of Huainan urban residents.

In order to explore the level of heavy metal pollution in human hair of residents in Huainan City and provide theoretical guidance for prevention and control of heavy metal pollution, human hair samples from 174 residents in Huainan City were collected so that heavy metal (Cr, Cu, Pb, Zn, As, and Fe) concentrations in scalp hair could be tested, and meanwhile their relationship with sex, age, and spatial distribution characteristics could be explored as well. According to the final analysis, the average concentration of Cr, Pb, Cu, Fe, Zn, and As in human hair amounted to 1.56, 6.41, 14.96, 31.13, 166.54, and 1.07 mg/kg. The highest average of Cr and Pb contents in human hair occurred in the area of Xiejiaji District; Fe, Zn, and Hg were in Datong District; and Cu and As were in Panji District respectively. Overall, the lowest risk of heavy metal exposure existed in Tianjia'an District. Heavy metal content in hair varied across sexes and ages. Pb concentration in hair would decrease as age increased. The highest Pb concentration appeared in children between ages 0 and 10, the amount of which was significantly different from that in other age groups; hence, children appear to be more susceptible to Pb pollution than other ages. Contents of Cr, Fe, Zn, and As in hair would also increase with age; Fe content in hair was particularly correlated with age. The contents of Cr, Pb, Fe, and As in men's hair were higher than those in women's, whereas the case of Cu and Zn was just the opposite. There were significant differences between sexes concerning the contents of Cr, Cu, and As, and a highly significant difference about Zn between sexes as well. These results indicated that the contents of heavy metal in residents' hair would be closely related to the features of the local environment and population.

Properties of particulate matter and gaseous pollutants in Shandong, China: Daily fluctuation, influencing factors, and spatiotemporal distribution.

Characteristics of the spatial and temporal distribution of air pollutants may reveal the cause of air pollution, especially for large regions where the anthropogenic pollutant emission is concentrated. This study addresses this issue by focusing on Shandong province, which has the highest air pollutant emissions in China. First, the spatial and temporal variation characteristics of the observed concentrations of conventional pollutants are analyzed in detail. The most prominent indicator of the problem (PM2.5), was selected as the key analytical object. On the spatial scale, the Multivariate Moran model was used to identify factors affecting the spatial distribution of PM2.5. On the time scale, wavelet analysis was used to explore the fluctuation characteristics of PM2.5 at different time periods. Results show that there are significant regional differences in pollutant concentration within Shandong province. The concentration of particulate matter and gaseous pollutants in western and northern Shandong is significantly higher than eastern Shandong. The average concentrations of PM2.5, PM10, SO2 and NO2 were highest in winter and lowest in summer, whereas concentration of O3 peaked in summer. For PM2.5, the annual mean concentration has a significant spatial correlation with SO2 emission, GDP per capita, population density and energy consumption per unit of GDP; in addition, the correlation between different regions and various indices is different. On the time scale, the fluctuation energy of PM2.5 concentrated in Dezhou and Liaocheng is the strongest on December 18 and 19, 2015. The inversion temperature has a strong influence on the daily variation of PM2.5 concentration. The formation and evolution of atmospheric pollution, therefore, can be explored by combining the temporal and spatial distribution of pollutants, providing a comprehensive analytical method for atmospheric pollution in different regions.

Efficient removal of sulfamerazine (SMR) by ozonation in acetic acid solution after enrichment SMR from water using granular activated carbon.

Sulfamerazine (SMR) as a persistent organic pollutant in waste streams is of growing environmental concern. This study explores the extraction SMR from water into an acetic acid (AA) solution using granular activated carbon (GAC), and removal of SMR by ozonation in AA solution. Systematic experiments have shown that GAC can be used as an adsorbent to transfer sulfamerazine from water to AA solution. SMR removal efficiency is 99.5% in 10% AA aqueous solution, which is better than in water. The removal rate of SMR in the AA solution decreased as the initial molar ratio of SMR and O3 increased. The removal rate of SMR decreased with Fe3+ present in the reactive system. The removal of SMR is dominated by indirect ozonation in water, while the SMR removal is an effect of both direct and indirect ozonation in AA solution. It is a very efficient process for the degradation of SMR in micro polluted water when using combined GAC adsorption-desorption in AA solution and ozonation of the resulting solution.