Markedly boosted peroxymonosulfate- and periodate-based Fenton-like activities of iron clusters on sulfur/nitrogen codoped carbon: Key roles of a sulfur dopant and compared activation mechanisms.

Highly dispersed iron nanoclusters on carbon (FeNC@C) hold great promise for wastewater purification in Fenton-like reactions. The microenvironment engineering of central Fe atom is promising to boost the activation capacity of FeNC@C, which is however remains a challenge. This study developed a self-sacrificed templating strategy to S, N-codoped carbon supported Fe nanoclusters (FeNC@SNC) activator and find the key role of sulfur heteroatoms in regulating the electron structure of Fe sites and final activation property. Investigations revealed that the FeNC@SNC composite exhibited unusual bifunctional activity in both peroxymonosulfate (PMS)- and periodate (PI)-based Fenton-like reactions. We also offered insights into the differences between the degradation of organics by the FeNC@SNC/PMS and FeNC@SNC/PI systems. Specifically, under identical conditions, the FeNC@SNC/PMS system delivered a higher oxidation capability and stronger resistance to nontarget matrix constituents, but showed more severe Fe leaching than the FeNC@SNC/PI system. Furthermore, while mediated electron-transfer process was identified as the major route for pollutant decomposition in both systems, the high-valent Fe-oxo species [Fe (IV)] was the auxiliary reactive species found only in the FeNC@SNC/PMS system. Based on these findings, our results provide profound insights into the design of active and durable Fe-based activators toward highly efficient Fenton-like reactions.

Tribological Behavior of Reduced Graphene Oxide-Al2O3 Nanofluid: Interaction among Testing Force, Rotational Speed and Nanoparticle Concentration.

The tribological properties of nanofluids are influenced by multiple factors, and the interrelationships among the factors are deserving of further attention. In this paper, response surface methodology (RSM) was used to study the tribological behavior of reduced graphene oxide-Al2O3 (rGO-Al2O3) nanofluid. The interaction effects of testing force, rotational speed and nanoparticle concentration on the friction coefficient (µ), wear rate (Wr) and surface roughness (Ra) of steel disks were investigated via the analysis of variance. It was confirmed that all the three input variables were significant for µ and Wr values, while testing force, nanoparticle concentration and its interaction with testing force and rotational speed were identified as significant parameters for Ra value. According to regression quadratic models, the optimized response values were 0.088, 2.35 × 10-7 mm3·N-1·m-1 and 0.832 µm for µ, Wr and Ra, which were in good agreement with the actual validation experiment values. The tribological results show that 0.20% was the optimum mass concentration which exhibited excellent lubrication performance. Compared to the base fluid, µ, Wr and Ra values had a reduction of approximately 45.6%, 90.3% and 56.0%. Tribochemical reactions occurred during the friction process, and a tribofilm with a thickness of approximately 20 nm was generated on the worn surface, consisting of nanoparticle fragments (rGO and Al2O3) and metal oxides (Fe2O3 and FeO) with self-lubrication properties.

Pitting Corrosion Behavior and Surface Microstructure of Copper Strips When Rolled with Oil-in-Water Emulsions.

Copper strips experience severe corrosion when rolled with an oil-in-water (O/W) emulsions lubricant. The effects of rolling reduction on the pitting corrosion behavior and surface microstructure of Cu strips were studied in detail using electrochemical measurements and electron back scattered diffraction (EBSD) analysis. It was found that the corrosion current densities of the rolled Cu strips increased with accumulated reduction, which also lowered the pitting potentials and weakened their corrosion resistances. Therefore, the corrosive tendency of Cu strips under different rolling reductions (ε) followed the order of ε0% < ε20.7% < ε50.6% < ε77.3%. The Cu surface easily reacted with chlorine, sulfur, and carbon components from O/W emulsions to generate pitting corrosion. Under the interactive effect of pitting corrosion and stress corrosion, pits expanded along the rolling direction. The aggregation of anions in surface defects, such as dislocations, metastable pits, and microcracks, further accelerated the pitting corrosion of the surface.

Coumarin as a green inhibitor of chloride-induced aluminum corrosion: theoretical calculation and experimental exploration.

In the present work, the adsorption mechanism and corrosion inhibition effect of coumarin as a green inhibitor was characterized. Quantum chemical calculation and molecular dynamics simulation of the coumarin molecule were performed to get insight into the adsorption model by assessing the frontier orbital parameters and adsorption configuration. The theoretical calculation disclosed that coumarin exhibited a higher adsorption reactivity in the water phase than that in the gas phase, and the C[double bond, length as m-dash]O structure in coumarin was the most favorable site for adsorption occurring. Coumarin could adsorb spontaneously on an aluminum surface in a parallel manner, where electron donation occurred from the aluminum surface to the inhibitor. Additionally, the experimental investigation determined that coumarin decreased the aluminum dissolution by suppressing both the anodic and cathodic reactions. The optimal coumarin concentration of 0.5 wt% resulted in a maximum inhibition efficiency (89.6%), but coumarin at a higher concentration would lead to the competitive and unstable adsorption of inhibitor molecules, thus decreasing the inhibition effect. Moreover, surface chemical characterization confirmed the formation of Al-coumarin complexes, which was in accordance with the theoretical calculation.

Electrochemical and adsorption behaviors of thiadiazole derivatives on the aluminum surface.

The electrochemical and adsorption behaviors of BODTA were studied in a 3.0 wt% NaCl solution via different electrochemical methods. Different concentrations of 2,5-bis(octyldithio)-1,3,4-thiadiazole (BODTA) were dissolved in rolling oil, and then aluminum electrodes coated with rolling oil were applied as the working electrode. The morphology and the elements of the electrode surface were studied via SEM, EDS and XPS. Results showed that BODTA had a slight inhibition efficiency of 10.75% when its concentration was 0.1 wt%; however, with the changes in the BODTA concentration from 0.3 wt%, 0.5 wt% to 0.7 wt%, BODTA had an antagonistic effect on the aluminum surface and accelerated the corrosion. The corresponding inhibition efficiencies became negative, which were -21.53%, -30.34%, and -18.82%. The analysis of elements and chemical states on the surface indicated that Al-N and Al-S bonds were formed between aluminum and BODTA. Furthermore, quantum chemical calculations were also performed, which manifested that N and S atoms were the main reactive sites. S atoms on side chains had a stronger reactivity than those in the thiadiazole ring. Finally, the present study was helpful to understand the electrochemical and adsorption behaviors of BODTA on aluminum, and made contributions to the application of BODTA in rolling oil.

Application of graphene derivatives and their nanocomposites in tribology and lubrication: a review.

Reducing friction and increasing lubrication are the goals that every tribologist pursues. Accordingly, layered graphene materials have attracted great research interest in tribology due to their anti-friction, anti-wear and excellent self-lubricating properties. However, recent studies have found that other forms of graphene derivatives not only perform better in tribological and lubricating applications, but also solve the problem of graphene being prone to agglomeration. Based on a large number of reports, herein, we review the research progress on graphene derivatives and their nanocomposites in tribology and lubrication. In the introduction, the topic of the article is introduced by highlighting the hazards and economic losses caused by frictional wear and the excellent performance of graphene materials in the field of lubrication. Then, by studying the classification of graphene materials, the research status of their applications in tribology and lubrication is introduced. The second chapter introduces the application of graphene derivatives in improving tribological properties. The main types of graphene are graphene oxide (GO), doped graphene (doped elements such as nitrogen, boron, phosphorus, and fluorine), graphene-based films, and graphene-based fibers. The third chapter summarizes the application of graphene-based nanocomposites in improving friction and anti-wear and lubrication properties. According to the different functional modifiers, they can be divided into three categories: graphene-inorganic nanocomposites (sulfides, metal oxides, nitrides, metal nanoparticles, and carbon-containing inorganic nanoparticles), graphene-organic nanocomposites (alkylation, amine functionalization, ionic liquids, and surface modifiers), and graphene-polymer nanocomposites (carbon chain polymers and heterochain polymers). Graphene not only exhibits an excellent performance in traditional processing and lubrication applications, but the fourth chapter proves that it has a good application prospect in the field of ultra-low friction and superlubricity. In the application part of the fifth chapter, the lubrication mechanism proposed by graphene as a nano-lubricant is introduced first; then, the main application research status is summarized, including micro-tribology applications, bio-tribology applications, and liquid lubrication additive applications. The last part is based on the following contents. Firstly, the advantages of graphene-based nanocomposites as lubricants and their current shortcomings are summarized. The challenges and prospects of the commercial applications of graphene-based nanocomposites in tribology and lubrication are further described.

The Role of Nano-TiO2 Lubricating Fluid on the Hot Rolled Surface and Metallographic Structure of SS41 Steel.

In this paper, nano-TiO2lubricating fluid was chosen as an advanced rolling lubricant to investigate its effect on the hot rolled surface and metallographic structure of SS41 steel strips. The tribological performances of nano-TiO2 lubricating fluid were measured by a four-ball tribotester. The hot rolling experiments under different lubrication conditions were carried out by a four-high rolling mill. The surface morphology, oxide scales and metallographic structure after hot rolling were observed using a confocal laser scanning microscope and scanning electron microscope (SEM), respectively. The composition of surface attachments was analyzed with X-ray photoelectron spectroscopy (XPS). The results indicate that the nano-TiO2 lubricating fluid has a better tribological performance. The surface defects on the hot rolled surface could be decreased. The phase composition of the surface still appears as a mixture of ferrite and pearlite. The surface of steel strips is not micro-alloyed with titanium as predicted. Additionally, the grain size of rolled steel strips which were lubricated with the nano-TiO2lubricating fluid decreased by nearly 50%, compared with traditional lubricating fluid. Furthermore, it was found that the thickness of the oxide layers on the surface reduced, whilst the Rockwell hardness of the oxide layers was enhanced as nano-TiO2 lubricating fluid was applied.

Experimental insight into the chemical corrosion mechanism of copper with an oil-in-water emulsion solution.

Chemical corrosion mechanism of copper in an oil-in-water (O/W) emulsion is worthy of study since it would contribute to emulsion-lubrication in a metal-working process and for copper storage. The immersion experiments were carried out and the corrosion rates were measured using the weight-loss method. Surface morphology of the copper specimen was observed using a scanning electron microscope (SEM). The compositions of the corrosive residues were analyzed using an energy dispersive spectrometer (EDS) and an X-ray photoelectron spectrometer (XPS). It was found that the corrosion rate of copper in an emulsion linearly increases and the kinetics relationship could be deduced as D 1 = 2.66 × 10-3 t 11.68 at room temperature (25 °C). After 1488 h of immersion time, the corrosion products on the copper surface were determined to be Cu2O, CuO, Cu(OH)2, CuCO3 and Cu2(OH)2CuCO3, which also changed the appearance of the emulsion. During adsorption, copper is more likely to coordinate with hydroxide, carboxylate or ester anions to generate copper compounds. The surfactants were consumed and the efficiency of emulsification characteristics was lost and finally, the O/W emulsion separated into two layers, which might hint the significance of introducing an inhibitor to protect the copper surfaces.

[Pollution of Halogenated Polycyclic Aromatic Hydrocarbons in Atmospheric Particulate Matters of Shenzhen].

Concentrations of halogenated polycyclic aromatic hydrocarbons ( HPAHs) in atmospheric PM10 and PM2.5 samples collected from Shenzhen were determined using GC-MS. Total concentrations of nine HPAHs in atmospheric PM10 and PM2.5 samples ranged from 118 to 1,476 pg · m(-3) and 89 to 407 pg · m(-3), respectively. In PM10 and PM(2.5) samples, the concentration of 9-BrAnt was the highest, followed by 7-BrBaA and 9, 10-Br2Ant. Seasonal levels of total HPAHs in atmospheric PM10 and PM2.5 samples in Shenzhen decreased in the following order: winter > autumn > spring > summer, whereas concentrations of individual HPAHs showed different seasonal levels. Meteorological conditions, including temperature, precipitation, and relative humidity, might be important factors affecting the seasonal levels of HPAHs in atmospheric PM10 and PM2.5 In addition, there were significant correlations between concentrations of HPAHs and parent PAHs. Finally, the toxic equivalency quotients (TEQs) of HPAHs were estimated. The TEQs of HPAHs in atmospheric PM10 and PM2.5 samples ranged from 17.6 to 86.2 pg · m(-3) and 14.6 to 70.4 pg · m(-3), respectively. Among individual HPAHs, 7-BrBaA contributed greatly to the total TEQs of HPAHs. Our results indicated that the total TEQs of HPAHs were lower than parent PAHs in atmospheric PM10 and PM2.5 samples in Shenzhen.

Plant uptake, translocation, and return of polycyclic aromatic hydrocarbons via fine root branch orders in a subtropical forest ecosystem.

Fine roots of woody plants are a heterogeneous system differing markedly in structure and function. Nevertheless, knowledge about the plant uptake of organic pollutants via fine roots is scarce to date. In the present study, plant uptake, translocation, and return of polycyclic aromatic hydrocarbons (PAHs) via fine roots in a subtropical forest ecosystem were investigated. Levels of Σ15PAHs in different fine root branch orders of Michelia macclurei, Cryptocarya concinna, Cryptocarya chinensis, and Canthium dicoccums varied from 5072±1419 ng g(-1) to 6080±1656 ng g(-1), 4037±410 ng g(-1) to 6101±972 ng g(-1), 3308±1191 ng g(-1) to 4283±237 ng g(-1), and 3737±800 ng g(-1) to 4895±1216 ng g(-1), respectively. Overall, concentrations of low-molecular-weight PAHs with 2-3 aromatic rings were higher than high-molecular-weight PAHs with 4-6 aromatic rings in all fine root branch orders. There were obvious translocations of PAHs between adjacent branch orders and a net accumulation of PAHs may occur in the fourth- and fifth-order roots. The storage of PAHs in the fine root system showed an obvious increasing trend along the branch orders ascending for all tree species. The return flux of PAHs via fine roots mortality showed an obvious decreasing trend with the branch orders ascending across the four tree species. Lower order roots contributed greatly to the total PAHs return flux. Our results indicated that fine roots turnover is an effective pathway for perennial tree species to remove environmental toxicants absorbed into them.

Parent and halogenated polycyclic aromatic hydrocarbons in farmed cockroaches and implications for human exposure.

Medicinal insects have been widely used to cure human diseases for ages. Nevertheless, knowledge about the toxic chemicals accumulated in medicinal insects and their effects on human health was insufficient. In the present study, sixteen priority polycyclic aromatic hydrocarbons (PAHs) and nine halogenated PAHs (HPAHs) were determined in farmed medicinal cockroaches to address this issue. Total concentrations of PAHs in young nymphs, old nymphs, and adults ranged from 162 to 1025, 252 to 967, and 267 to 1168 ng/g, respectively. Levels of the sum of HPAHs varied from 0.84 to 9.17, 1.86 to 5.21, and 1.01 to 8.60 ng/g for young nymphs, old nymphs, and adults, respectively. The daily intake and excess cancer risk of PAHs and HPAHs were calculated for people who take cockroach-related drugs. Our results indicated that females and children have slightly higher exposure levels from the perspectives of gender and age, respectively. The estimated excess cancer risk of PAHs and HPAHs were both lower than the priority risk level (10(-4)), indicating a low potential carcinogenic risk with the medicinal cockroach consumption.

Cumulative health risk assessment of halogenated and parent polycyclic aromatic hydrocarbons associated with particulate matters in urban air.

Halogenated polycyclic aromatic hydrocarbons (HPAHs) have been reported to occur widely in urban air. Nevertheless, knowledge about the human health risk associated with inhalation exposure to HPAHs is scarce so far. In the present study, nine HPAHs and 16 PAHs were determined in atmospheric particulate matter (PM) collected from Shenzhen, China to address this issue. Concentrations of Σ9HPAHs varied from 0.1 to 1.5 ng/m(3) and from 0.09 to 0.4 ng/m(3) in PM10 and PM2.5 samples, respectively. As for individuals, 9-bromoanthracene, 7-bromobenz(a)anthracene, and 9,10-dibromoanthracene were the dominant congeners. Levels of Σ16PAHs in PM10 and PM2.5 samples ranged from 3.2 to 81 ng/m(3) and from 2.8 to 85 ng/m(3), respectively. Among individual PAHs, chrysene, benzo[b]fluoranthene, and indeno[1,2,3-c,d]pyrene were the main congeners. According to the season, concentrations of HPAHs and PAHs in atmospheric PM10/PM2.5 samples show a similar decreasing trend with an order: winter>autumn>spring>summer. The daily intake (DI) of PM10/PM2.5-bound HPAHs and PAHs were estimated. Our results indicated that children have the highest DI levels via inhalation exposure. The incremental lifetime cancer risk (ILCR) induced by PM10/PM2.5-bound HPAHs and PAHs were calculated. The ILCR values showed a similar decreasing trend with an order: adults>children>seniors>adolescent. Overall, the ILCR values induced by HPAHs and PAHs were far below the priority risk level (10(-4)), indicating no obvious cancer risk. To our knowledge, this is the first study to investigate the human health risk associated with inhalation exposure to PM10/PM2.5-bound HPAHs.

[Occurrence and spatial differentiation of polycyclic aromatic hydrocarbons in surface soils from Shenzhen, China].

188 surface soil samples were collected in Shenzhen of China to determine the occurrence and spatial differentiation of polycyclic aromatic hydrocarbons (PAHs), based on which we studied the correlation between PAHs concentrations and urbanization levels, as well as the PAHs ecological risk. The total concentrations of 28 PAHs (sigma28 PAHs), 16 EPA PAHs (sigma 16 PAHs) and 7 carcinogenic PAHs (sigma7 CarPAHs) ranged from 5 to 7939 ng x g(-1), 2 to 6745 ng x g(-1) and not detected to 3786 ng x g(-1), respectively. 8 kinds of land use types according to sigma16 PAHs average levels in descending order were: transportation lands, commercial lands, industrial lands, agricultural lands, residential lands, urban green space, orchards and woodland. And sigma16 PAHs of construction and non-construction lands samples were mainly derived from combustion of various fossil fuels with contribution of 75.1% and 68.2%, respectively. Significant positive correlation was also found between PAHs concentrations of high molecular weight and urbanization levels. And PAHs pollution in the top soils of Shenzhen was at a low-end level of the world.

Polycyclic aromatic hydrocarbons in soils from the Tibetan Plateau, China: distribution and influence of environmental factors.

Thirty four sampling sites along an elevation transect in the Tibetan Plateau region were chosen. Soil cores were divided into several layers and a total of 175 horizon soil samples were collected from July to September 2011, for determination of polycyclic aromatic hydrocarbons (PAHs). The measured PAHs concentration in surface soils was 56.26 ± 45.84 ng g(-1), and the low molecular weight PAHs (2-3 rings) predominated, accounting for 48% and 35%. We analyzed the spatial (altitudinal and vertical) distribution of PAHs in soil, and explored the influence of related environmental factors. Total organic carbon (TOC) showed a controlling influence on the distribution of PAHs. PAH concentrations declined with soil depth, and the composition patterns of PAHs along soil depth indicated that the heavy PAHs tended to remain in the upper layers (0-10 cm), while the light fractions were transported downward more easily. PAHs inventories (8.77-57.92 mg m(-2)) for soil cores increased with mean annual precipitation, while the topsoil concentrations decreased with it. This implies that an increase in precipitation could transfer more PAHs from the atmosphere to the soil and further transport PAHs from the topsoil to deeper layers.

PBDEs as indicator chemicals of urbanization along an urban/rural gradient in South China.

Fourteen polybrominated diphenyl ethers (PBDEs) were measured in surface sediments collected from an urban watershed in a rapidly urbanizing region, Shenzhen, China. BDE209 was the predominant congener of PBDEs detected in surface sediments, which was consistent with the fact that technical deca-BDE mixtures are the dominant PBDE formulation used in China, especially the Pearl River Delta. A positive association between sediment PBDEs and catchment degree of urbanization suggested that the rapid urbanization process may be affecting the PBDEs levels in surface sediments. Similar to the "urban heat island effect", an "urban pollution island effect" was observed in the present study. These results indicated that PBDEs can be used as potential indicator chemicals of catchment's urbanization process in the present region.

Halogenated polycyclic aromatic hydrocarbons in the environment.

Halogenated polycyclic aromatic hydrocarbons (HPAHs) have been reported to occur in air, sediment, fly ash, and biota samples. This review summarized current existing data on the environmental occurrence, behavior, physicochemical properties, emission sources, and toxic equivalents of HPAHs. Firstly, the physicochemical properties of HPAHs were summarized. Then, an overview of environmental occurrence of HPAHs in ambient matrices including biological samples was reviewed. Meanwhile, the emission sources and possible formation mechanisms of HPAHs were discussed. Apart from that, the aryl hydrocarbon receptor (AhR)-mediated activities were summarized, which indicated that the position and number of halogen atoms on the parent PAHs molecule were important determinant factors affecting the AhR-mediated activity of individual HPAHs congeners. Finally, some research recommendations on HPAHs were given.

[Halogenated polycyclic aromatic hydrocarbons in surface sediments of Maozhou River, Shenzhen].

Surface sediments collected from the Maozhou River watershed in Shenzhen were analyzed for the concentration levels and spatial distribution characteristics of halogenated polycyclic aromatic hydrocarbons (HPAHs) using GC-MS. Total concentrations of three chlorinated polycyclic aromatic hydrocarbons (ClPAHs) and six brominated polycyclic aromatic hydrocarbons (BrPAHs) of concern ranged from 3.00 to 301 ng x g(-1) and 7.52 to 285 ng x g(-1), respectively. Source appointments indicated that the HPAHs in these surface sediments were mainly derived from waste incineration, fossil fuel combustion, vehicle emission, and burning of crop straw, accounting for 40%, 20.5% 11.9%, and 11.7% of the total loading, respectively. Additionally, the toxic equivalency quotients (TEQ) of total ClPAHs and BrPAHs ranged from 7.95 to 38.1 pg x g(-1) and 38.1 to 105 pg x g(-1) respectively. Finally, the relationships between the HPAHs levels and different land use types were examined. Results indicated that the levels of HPAHs in surface sediments showed a decreasing trend after the first increase to the peak with the density of industrial land, but inversely proportional to the density of agricultural land.

Sedimentary record of polycyclic aromatic hydrocarbons in a sediment core from a maar lake, Northeast China: evidence in historical atmospheric deposition.

A maar lake is an excellent ecosystem to study the atmospheric deposition of pollutants, as its contaminants are primarily by atmospheric deposition. In this study, a sediment core from Sihailongwan Maar Lake, Northeast China, was collected and the historical atmospherically deposited polycyclic aromatic hydrocarbons (PAHs) were analyzed. The concentrations of TPAHs (the sum of the US EPA proposed 16 priority PAHs, excluding naphthalene and pyrene) ranged from 473.9 to 2289 ng g(-1) with a slow increasing stage in the deeper sediments and a sharp increasing stage in the upper sediments. The input rate of TPAHs, especially that of PAH(9) (the sum of fluoranthene, benzo(a)anthracene, chrysene, benzo(b)fluoranthene, benzo(k)fluoranthene, benzo(a)pyrene, indeno(1,2,3-cd)pyrene, dibenzo(ah)anthrathene, and benzo(ghi)perylene), correlated well to the Chinese historical socioeconomic data. This indicates that sediment PAHs were mainly derived from human activities and PAH(9) can be regarded as a better indicator of the local socioeconomic development. Source identification suggested that PAHs were originated primarily from mixed sources (e.g., coal and biomass burning and petroleum combustion), except for perylene which was mostly of diagenetic origin. In addition, the down-core PAHs profile clearly illustrated that PAHs sources in Northeast China experienced a transformation from low- and moderate temperature to high-temperature combustion processes, especially after the late 1980s. Additionally, an ecological risk assessment using two redefined biological thresholds (TEQ(ERL) and TEQ(ERM)) indicated that most of the PAHs measured in the present sediment core would not cause an immediate toxic effect; only FLU and PHEN are a potential source of concern for biological impairment.

Ecological risk assessment of parent and halogenated polycyclic aromatic hydrocarbons in surface sediments from an urban river in south China.

In the present study, 16 priority polycyclic aromatic hydrocarbons (Σ(16) PAHs), including seven carcinogenic PAHs (Σ(7) PAHs) designated by the U.S. Environmental Protection Agency, in surface sediment from an urban river (Shenzhen, south China) were measured. The concentrations of Σ(16) PAHs and Σ(7) PAHs ranged from 27.92 to 7409 ng/g and 0.53 to 2326 ng/g, respectively. Source appointments indicated that the PAHs in surface sediments were mainly derived from coal combustion (36.6%), oil spills (22.2%), vehicle emission (19.5%), and waste incineration (12.1%). The ecological risks posed by PAHs and several halogenated PAHs in these sediment samples were assessed using two redefined guidelines incorporating the toxic equivalency quotients (TEQs) of individual PAH congeners: (1) TEQs effect range-low, and (2) TEQs effect range-median. The authors' results suggested that the PAHs they measured in most of the sediments in this urban river would not cause acute biological effects. On the contrary, the ecological risk posed by some halogenated PAHs was much higher than that of their corresponding parent PAHs. Finally, the relationships between PAH levels and catchment urbanization processes were examined. The results indicated that rapid urbanization has led to an obvious increase in PAH contamination in surface sediments.