Search

Petrochemical industries are widely distributed in China. As a negative consequence, heavy metals in petrochemical area can result in soil contamination. However, the relevant research of heavy metals contamination in petrochemical area was few. In this study, a total of 103 topsoil samples (20 cm) and 25 profile soil samples were collected and examined in a retired petrochemical industrial area, South China. The results showed the mean contents of Hg, Cd, As, Pb, Ni and Cu were 0.18, 0.69, 16.22, 47.24, 31.62 and 93.06 mg kg

Quantitative evaluation of different contaminated soil remediation technologies in multiple dimensions is beneficial for the optimization and comparative selection of technology. Ex situ thermal desorption is widely used in remediation of organic contaminated soil due to its excellent removal effect and short engineering period. In this study, a comprehensive evaluation method of soil remediation technology, covering 20 indicators in five dimensions, was developed. It includes the steps of constructing an indicator system, accounting for the indicator, normalization, determining weights by analytic hierarchy process, and comprehensive evaluation. Three ex situ thermal desorption technology—direct thermal desorption, indirect thermal desorption, and indirect thermal heap—in China were selected for the model validation. The results showed that the direct thermal desorption had the highest economic and social indicator scores of 0.068 and 0.028, respectively. The indirect thermal desorption had the highest technical and environmental indicator scores of 0.118 and 0.427, respectively. The indirect thermal heap had the highest resource indicator score of 0.175. With balanced performance in five dimensions, the indirect thermal desorption had the highest comprehensive score of 0.707, which is 1.6 and 1.4 times higher than the direct thermal desorption and indirect thermal heap, respectively. The comprehensive evaluation method analyzed and compared the characteristics of the ex situ thermal desorption technology from different perspectives, such as specific indicators, multiple dimensions, and single comprehensive values. It provided a novel evaluation approach for the sustainable development and application of soil remediation technology.

Thermal desorption (TD) is generally considered to be an effective but unsustainable technology. Decontamination performance, charring behaviors and physicochemical properties during TD of dibenzofuran-contaminated soil (DCS) are explored. After treatment at 300 °C for 20 min, the dibenzofuran concentration decreases from 3969.37 mg/kg to 17.29 mg/kg, lower than Chinese risk screening value. More than 99% of dibenzofuran in soil are removed at low temperature of 300 °C, meanwhile the organic carbon is partially retained in soil. Removal mechanism of DCS at 300 °C is proposed, including desorption, cracking, and charring. Char material of low H:C ratio is produced by the generation, polymerization and dehydrogenation of aromatic intermediates, and then increases carbon stocks and reduces the carbon footprint of contaminated soil. Meanwhile, due to the char generated, pH, cation exchange capacity and specific surface area of DCS heated at 300 °C are higher than those of raw DCS, promoting ecological restoration and enhancing carbon sink in soil ecosystems. The aforesaid saving energy, reducing carbon footprint and enhancing carbon sink are exactly the main innovative technologies for achieving carbon neutrality. Hence, it may be a contribution to climate change mitigation, in addition to a robust and sustainable remediation of organic contaminated soil.

The effects of temperature and CaO introduction on polycyclic aromatic hydrocarbons (PAHs) contents, distribution patterns and toxicity of the products from hydrothermal carbonization (HTC) of swine manure (SM) were investigated in this study for the first time. The results indicated that increasing temperature decreased total PAHs content of the hydrochar, while the PAHs toxicity firstly decreased and then increased during HTC of SM. For the aqueous product, the total PAHs content and toxicity gradually decreased with increasing temperature. CaO introduction during HTC of SM significantly suppressed the PAHs formation and promoted the transformation from higher molecular weight PAHs into lower molecular weight PAHs in HTC products, resulting in the remarkably decreased content and toxicity of PAHs. The lowest total PAHs content (1428.57 μg/kg) and TEQ value (21.33 μg/kg) of the hydrochar were obtained by 15% CaO introduction at 200 °C and 180 °C, respectively, and compared to SM, they were decreased by 73.73% and 79.51%, respectively. Moreover, 3-ring PAHs were the predominant PAHs in HTC products regardless of CaO introduction. The present study demonstrated that CaO assisted HTC at temperature lower than 220 °C was effective to reduce the total content and toxicity of PAHs in SM, and the prepared hydrochar was a promising soil amendment in view of the elimination of PAHs toxicity.

The hydrochars derived from swine manure were prepared by CaO assisted hydrothermal carbonization (HTC), and their properties were investigated for the first time. The results showed that the pH and yield of the hydrochar were largely increased by CaO addition. HTC of swine manure increased the phosphorus (P) content in the hydrochar, and appropriately 100% of P as apatite-P was enriched in the hydrochar by CaO assisted HTC. Additionally, the CaO addition during HTC improved the porosity of the hydrochar. The FTIR analysis revealed that substantial functional groups were present on the surface of the hydrochar, indicating the facilitated exchange between the hydrochar and hydrophilic soil when the hydrochar was used for soil amendment. This study demonstrated that CaO assisted HTC was a novel strategy to quickly convert swine manure to the promising soil amendment especially for acidic soils.

Disposal of organic-contaminated soil through ceramsite production can not only generate ceramsite with acceptable properties but also completely remediate the organic-contaminated soil owing to high treatment temperature. However, the removal mechanism of organic pollutants and the gas-solid phase distribution of the pollutants remain unclear. In this study, coking contaminated soils with high concentrations of polycyclic aromatic hydrocarbons (PAHs) and petroleum hydrocarbon (PHC) were used to prepare ceramsite at 1160 °C. The quality of ceramsite met the required product standard when the disposal ratio of contaminated soil was up to 60%. The concentration of PAHs and PHC in the soil was 57.7 mg kg

Formation and emission of dioxins is a great concern during thermal desorption remediation of organic contaminated soil. The differential formation of dioxins from chlorine organic contaminated soil (COCS) and non-chlorine organic contaminated soil (NCOCS) is still unclear and the control technique for the dioxins generated is an urgent need. In this study, the formation and distribution characteristics of dioxins were investigated in the thermal desorption unit combined with flue gas purification system during COCS and NCOCS treatments. Although organic contaminates were well desorbed, de-novo formation of dioxins was observed for both COCS and NCOCS, as well as synthesis from precursors for NCOCS. The gas-phase dioxin in the flue gas purification system continuously decreased during NCOCS thermal desorption, while the dioxin concentration in the quench tower sharply increased from 0.46 to 2.13 ng/Nm

Soil polycyclic aromatic hydrocarbons (PAHs) contamination caused by factory relocations is a serious environmental issue across the world. Electrical resistance heating (ERH) and chemical oxidation are two promising in-situ methods for treating volatile and semi-volatile organic pollutants in contaminated soil. Coupling of ERH and chemical oxidation technologies to improve the remediation efficiency for PAH-contaminated soil was estimated in this study. PAH removal ratio in contaminated soils using ERH treatment were significantly negatively correlated with the boiling point of the pollutants (P = 0.002), and 21.63% (DBA high boiling point) to 71.53% (Nap low boiling point) of PAHs in the contaminated soil were removed in 120 min. With oxidant Na

The hydrological and pollution processes are an important science problem for aquatic ecosystem. In this study, the samples of river water, reservoir water, shallow groundwater, deep groundwater, and precipitation in mining area are collected and analyzed. δD and δ18O are used to identify hydrological process. δ15N-NO3- and δ18O-NO3- are used to identify the sources and pollution process of NO3−. The results show that the various water bodies in Fenhe River Basin are slightly alkaline water. The ions in the water mainly come from rock weathering. The concentration of SO42- is high due to the impact of coal mining activity. Deep groundwater is significantly less affected by evaporation and human activity, which is recharged by archaic groundwater. There are recharge and discharge between reservoir water, river water, soil water, and shallow groundwater. NO3− is the main N species in the study area, and forty-six percent of NO3−-N concentrations exceed the drinking water standard of China (NO3−-N ≤ 10 mg/L content). Nitrification is the main forming process of NO3−. Denitrification is also found in river water of some river branches. The sources of NO3− are mainly controlled by land use type along the riverbank. NO3− of river water in the upper reaches are come from nitrogen in precipitation and soil organic N. River water in the lower reaches is polluted by a mixture of soil organic N and fertilizers.

Thermal desorption is widely adopted for the remediation of organic compounds, yet is generally considered a non-green-sustainable manner owing to its energy-intensive nature and potential to deteriorate soil reuse. Here, lube oil-contaminated soils were remediated at 200–500 °C in nitrogen atmosphere, upon which removal behaviors of lube oil and physicochemical properties of soils were explored. Illumina 16S ribosomal RNA (rRNA) and 18S rRNA amplicon sequencing were employed to determine the relative abundances and diversities of bacteria and fungi in soils, respectively. The results indicated that, after heating at 350 °C for 60 min, 93% of the lube oil was reduced, with the residual lube oil concentration lower than the Chinese risk intervention values (GB 36600–2018). The weakly-alkaline, multi-phosphorus and char-rich soils after indirect thermal desorption could provide a nutrient source and favorable habitat space for living organisms, and the decomposition of minerals in soils is more conducive to the survival of organisms. Microbial species in soils after heating at 350 °C became extinct, however, microbial species after 3 days of recolonization were enough to carry out DNA extraction when these soils were exposed to natural grass land. Though the microbial richness and diversity in heated soils after 3 days of recolonization were still little lower than those in contaminated soils, Firmicutes (29.41%) and Basidiomycota (9.33%) became dominant at phyla level, while Planomicrobium (16.37%), Massilia (10.09%), Jeotgalibaca (7.91%) and Psychrobacter (6.84%) were dominant at general level, whose ecological function was more conducive to nutrient cycling and ecological resiliency. Overall, this innovative research provides a new perspective: low temperature indirect thermal desorption may also achieve a sustainable remediation, due to its energy-saving (low temperature), favorable physicochemical properties and the rapid recolonization capacity of microbial communities in heated soils.

Electrical resistance heating (ERH) is a promising thermal remediation method for treating volatile soil pollutants. However, the remediation of soil contaminated by polycyclic aromatic hydrocarbons (PAHs) based on lab-scale ERH devices must be extensively studied to determine the factors affecting the remediation. Therefore, this study used a lab-scale ERH equipment to investigate the influence factors of ERH, PAH removal efficiency, and changes in soil properties through the treatment process. The results suggested that moisture and salinity were basic factors affecting electric conductive capability; heating 15 g of soil to the target temperature required at least 4 g solution of 0.1% salt. Meanwhile, higher electric strength can ensure heating efficiency and maximum temperature. The removal efficiency of PAHs, which is highly related to boiling point, was significantly affected by its benzene rings and bond structure; during 90 min ERH treatment, more than 40% of the pollutants were removed synchronously with the evaporation of water. Hence, co-boiling with water was confirmed to be the primary mechanism of ERH. The influence of the treatment on soil properties (organic matter, particle size, fertility, enzymatic activity) was limited, suggesting that soil functionality can be retained by ERH.

Coexistence of antibiotics/heavy metals and the overexpression of resistance genes in the vermicompost has become an emerging environmental issue. Little is known about the interaction and correlation between chemical pollutants and biological macromolecular compounds. In this study, three typical vermicompost samples were selected from the Yangtze River Delta region in China to investigate the antibiotic, heavy metal and corresponding antibiotic resistance genes (ARGs) and heavy metal resistance genes (HRGs). The results indicated the prevalence of tetracycline (TC), copper (Cu), zinc (Zn), cadmium (Cd), corresponding TC-resistance genes (tetA, tetC, tetW, tetM, tetO, and tetS) and HRGs (copA, pcoA, cusA, czcA, czcB, and czcR) in the three vermicompost samples. In addition, the ARG level was positively associated with the water-soluble TC fraction in the vermicompost, and it was same between the HRG abundance and exchangeable heavy metal content (p

High abundances of antibiotic-resistant pathogenic bacteria (ARPB) and antibiotic resistance genes (ARGs) in agricultural soil-plant systems have become serious threats to human health and environmental safety. Therefore, it is crucial to develop targeted technology to control existing antibiotic resistance (AR) contamination and potential dissemination in soil-plant systems. In this work, polyvalent bacteriophage (phage) therapy and biochar amendment were applied separately and in combination to stimulate ARPB/ARG dissipation in a soil-lettuce system. With combined application of biochar and polyvalent phage, the abundance of Escherichia coli K-12 (tetR) and Pseudomonas aeruginosa PAO1 (ampR + fosR) and their corresponding ARGs (tetM, tetQ, tetW, ampC, and fosA) significantly decreased in the soil after 63 days' incubation (p

The emerging mixed contamination of antibiotics and microplastics in greenhouse soil has made the control of antibiotic resistant gene (ARG) transmission a novel challenge. In this work, surfactant sophorolipid was applied to enhance the dissipation of tetracycline (TC) and tet genes in the presence of microplastics in greenhouse soil. During 49days of incubation, soil bacteria and phages were both found to be the crucial reservoirs of ARGs. Meanwhile, microplastic's presence significantly inhibited the dissipation of TC and ARGs in the soil. However, sophorolipid application was proved to outweigh the negative impact caused by microplastic existence, and lead to the highest dissipation of soil TC and ARGs. Significant positive correlation was detected between the dissipation rate of water-soluble and exchangeable TC content and bacteria/phage co-mediated ARG levels. This also held true between the two fractions of soil TC and the ratio of ARG level in the bacteria to that in the phages (BARGs/PARGs). The opposite impacts of microplastic presence and sophorolipid amendment on the TC/ARG dissipation found in this work provides new information for understanding ARG transmission between bacteria and phages in the mixed contaminated greenhouse soil.

Accumulation and potential health risk of cadmium (Cd), lead (Pb), copper (Cu), and zinc (Zn) in a plot-scale vegetable production peri-urban area near Nanjing city, China was investigated through element balance method, model simulation and dietary risk assessment. The heavy metals accumulated in the surface soils were due to long-term and heavy application of organic fertilizers, among which the accumulation of Cu and Zn were greater than those of Cd and Pb. The result of a mass balance model simulation indicated that intensive vegetable production would result in accumulation of Cd, Pb, Cu and Zn in soils exceeding the target values in 55, 36, 34 and 71 years, respectively. The estimated dietary intakes of Cd, Pb, Cu, and Zn were far below the tolerable limits and the hazard quotient values were below one for both children and adults. Although there is no imminent health risk from heavy metals through vegetable consumption, more attention should be paid to the long-term accumulation and risk, especially for children.

Application of phosphate fertilizer can be a significant contributor of potentially hazardous trace elements such as arsenic, cadmium, and lead in croplands. These trace elements have the potential to accumulate in soils and be transferred through the food chain. We articulated the environmental risks of trace elements associated with long-term phosphate fertilizer applications by combining data from the literature and results from model simulations. Results illustrate that under normal cropping practice, the impact of phosphate fertilizers applications on trace element accumulation in receiving soils has been limited and localized. Their plant uptake varied greatly depending on the fertilizer application rates, soil and plant characteristics. This has led to a great deal of uncertainty in characterizing soil distribution coefficients, Kd, and plant uptake factors, PUF, two of the most used parameters in assessing the risks of accumulations. Therefore, the risks may be more appropriately assessed based on the probabilistic distributions of Kd and PUF.

We studied the source, concentration, spatial distribution and health risk of 16 polycyclic aromatic hydrocarbons (PAHs) in urban soils of Beijing. The total mass concentration of 16 PAHs ranged from 93 to 13,141 μg kg(-1) with a mean of 1228 μg kg(-1). The contour map of soil PAH concentrations showed that the industrial zone, the historical Hutong district and the university district of Beijing have significantly higher concentrations than those in remainder of the city. The results of sources identification suggested that the primary sources of PAHs were vehicle exhaust and coal combustion and the secondary source was the atmospheric deposition of long-range transported PAHs. The incremental lifetime cancer risks (ILCRs) of exposing to PAHs in the urban soils of Beijing for adult were 1.77 × 10(-6) and 2.48 × 10(-5), respectively under normal and extreme conditions. For child, they were 8.87 × 10(-7) and 6.72 × 10(-6), respectively under normal and extreme conditions.

Spatial variability and temporal trends in concentrations of the organochlorine pesticides (OCPs), hexachlorocyclohexane (HCH) and dichlorodiphenyltrichloroethane (DDT), in surface soils around Beijing Guanting Reservoir (GTR) were studied in 2003 and 2007. Concentrations of the two OCPs in soils around GTR were generally less than reference values set by the Chinese government for the protection of agricultural production and human health. Among the OCPs, β-HCH and p, p'-DDE were the two predominant compounds. This result indicates that the HCH and DDT residues in soils were primarily from historical use. Based on kriging, a spatial distribution of HCH and DDT around the GTR was observed. Spatial variability indicated how HCH and DDT had been applied and been distributed in the past. Between 2003 and 2007, concentrations of HCH and DDT decreased more rapidly in orchard soils than those in fallow soils.

The factors that influence the dynamics of hexachlorocyclohexane (HCH) and dichlorodiphenyltrichloroethane (DDT) in soils around the watersheds of Beijing reservoirs were examined. Compared with other studies on HCH and DDT in soils and established reference values, the concentrations of HCH and DDT in soils around our study area were relatively low. The relationships between HCH and DDT concentrations and land use, soil texture, and soil properties were discussed. HCH and DDT concentrations were higher in arable soils than those in uncultivated fallow soils. Although land use was the most important factor affecting HCH and DDT residues, additional factors such as soil texture and soil total organic carbon were also involved in pesticide retention in soils. The results indicated that the historical agricultural applications of HCH and DDT were the major source of their residues. Atmospheric deposition, as well as long-distance transportation and inputs from surrounding weathered agricultural soils may also serve as important sources of HCH and DDT residues in the watersheds.

Topsoil samples (n = 105) were collected to Study the distribution of dichlorodiphenyltrichloroethane (DDT) and hexachlorocyclohexane (HCH) residues in the vicinity of chemical industrial parks in Tianjin, China. The occurrence and distribution of target organochlorine pesticides (OCPs) were mapped to identify, the spatial variation using Geographical Information System (GIS). In general, the concentrations of OCPs were higher in soils near the industrial parks, even some hotspots showed very high OCP contaminations which could cause ecological risk. The relationships between contaminant concentrations and other factors (land use and soil properties) were discussed. Significant correlations (P

Concentrations of organochlorine pesticides (OCPs; dichlorodiphenyltrichloroethanes (DDTs), hexachlorocyclohexanes (HCHs), hexachlorobenzene (HCB)) were investigated in 105 soil samples collected in vicinity of the chemical industrial parks in Tianjin, China. OCP concentrations significantly varied in the study area, high HCH and DDT levels were found close to the chemical industrial parks. The intensity of agricultural activity and distance from the potential OCP emitters have important influences on the OCP residue distributions. Principal component analysis indicates that HCH pollution is a mix of historical technical HCH and current lindane pollution and DDT pollution input is only due to technical DDT sources. The significant correlations of OCP compounds reveal that HCHs, DDTs and HCB could have some similar sources of origin.

Fates and transport of 9 commonly found PPCPs of the reclaimed water were simulated based on the HYDRUS-1D software that was validated with data generated from field experiments. Under the default scenario in which the model parameters and input data represented the typical conditions of turf grass irrigation in southern California, the adsorption, degradation, and volatilization of clofibric acid, ibuprofen, 4-tert-octylphenol, 4-n-nonylphenol, naproxen, triclosan, diclofenac sodium, bisphenol A and estrone in the receiving soils were tracked for 10 years. At the end, their accumulations in the 90 cm soil profile varied from less than 1 ng g(-1) to about 140 ng g(-1), and their concentrations in the drainage water in the 90 cm soil depth varied from nil to jig L-1 levels. The adsorption and microbial degradation processes interacted to contain the PPCPs entirely within surface 40 cm of the soil profiles. Leaching and volatilization were not significant processes governing the PPCPs in the soils. The extent of accumulations in the soils did not appear to produce undue ecological risks to the soil biota. PPCPs did not represent any potential environmental harm in reclaimed water irrigation. (C) 2013 Elsevier Ltd. All rights reserved.

Safety of agricultural irrigation with reclaimed water is of great concern as some potential hazardous compounds like heavy metals may be accumulated in soils over time. Impacts of long-term reclaimed water on soil Cd pollution were evaluated based on the field investigation in two main crop areas in Beijing with long irrigation history and on simulation results of STEM-profile model. Under long-term reclaimed water, Cd content in the top 20 cm soil layer was greatly elevated and was more than 2 times higher than that in the deep soil layer. There was very small differences between the field measured and model simulated Cd content in the plow layer (top 20 cm) and entire soil layer. Long-term model prediction showed that reclaimed water irrigation had a low environmental risk of soil Cd pollution, but the risk would be aggravated when there were high metal loading from other sources. The risk is also depending on the soil and plant properties.

Polycyclic aromatic hydrocarbons (PAHs) and their health risks in surface soils (n = 31) collected from coastal and estuarine areas of the northern Bohai and Yellow Seas (CEANBYS), China, were investigated. Total concentrations of PAHs ranged from 6.6 × 10(1) to 9.2 × 10(2) ng g(-1) dry weight, with an average of 3.1 × 10(2) ng g(-1) dw. The locations where greater concentrations of PAHs were observed were all near factories emitting black smoke or on the edge of the urban areas. These observations are consistent with concentrations of PAHs in soils being influenced by human activities, especially industrialization and urbanization. Concentrations of PAHs were significantly correlated with concentrations of organic carbon in soils. The patterns of relative concentrations and types of PAHs observed as well as knowledge of the potential sources were consistent with the primary sources of PAHs in soils of the CEANBYS being derived from the pyrolytic processes such as combustion of fossil fuel. The incremental lifetime cancer risks of exposing to PAHs for child, youth, and adult were 1.6 × 10(-6), 1.2 × 10(-6), and 1.9 × 10(-6).

Concentrations of As and selected metals were determined in surface soils of the Miyun Reservoir watershed of Beijing, China. The degree to which concentrations of As and metals exceeded the corresponding background concentration of soils was: Cr>Cu>Zn>As>Ni with no apparent anthropogenic contamination with Cd and Pb. Based on the results of a combination of multivariate statistics and geostatistical analysis, greater concentrations of Cr and Ni in soils were determined to be primarily from iron ore mining near where the Chaohe River enters the northeast portion of the reservoir. Agricultural activities were responsible for the observed elevated concentrations of Cu and Zn in soils. Relatively great concentrations of As were found in soils near the upstream regions of the Baihe River in Chicheng County where small gold mining activities have taken place. The greatest potential for adverse effects of Cr and Cu occurred along the eastern shore of Miyun Reservoir.

The concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) were determined by gas chromatography equipped with a mass spectrometry detector in 105 topsoil samples from an industrial area around Bohai Bay, Tianjin in the North of China. Results demonstrated that concentrations of PAHs in 104 soil samples from this area ranged from 68.7 to 5,590 ng g (-aEuro parts per thousand 1) dry weight with a mean of a16PAHs 814 +/- 813 ng g (-aEuro parts per thousand 1), which suggests that there exists mid to high levels of PAH contamination. The concentration of a16PAHs in one soil sample from Tianjin Port was exceptionally high (48,700 ng g (-aEuro parts per thousand 1)). Ninety-three of the 105 soil samples were considered to be contaminated with PAHs (> 200 ng g (-aEuro parts per thousand 1)), and 25 were heavily polluted (> 1,000 ng g (-aEuro parts per thousand 1)). The sites with high PAHs concentration are mainly distributed around chemical industry parks and near highways. Two low molecular weight PAHs, naphthalene and phenanthrene, were the dominant components in the soil samples, which accounted for 22.1% and 10.7% of the a16PAHs concentration, respectively. According to the observed molecular indices, house heating in winter, straw stalk combustion in open areas after harvest, and petroleum input were common sources of PAHs in this area, while factory discharge and vehicle exhaust were the major sources around chemical industrial parks and near highways. Biological processes were probably another main source of low molecular weight PAHs.