Polycyclic aromatic hydrocarbons (PAHs) are a class of organic compounds commonly found as soil contaminants. Fungal degradation is considered as an environmentally friendly and cost-effective approach to remove PAHs from soil. Acenaphthylene (Ace) and Benzo[a]anthracene (BaA) are two PAHs that can coexist in soils; however, the influence of the presence of each other on their biodegradation has not been studied. The biodegradation of Ace and BaA, alone and in mixtures, by the white rot fungus Pleurotus ostreatus was studied in a sandy soil.
Materials and methods
Experimental microcosms containing soil spiked with different concentrations of Ace and BaA were inoculated with P. ostreatus. Initial (t0) and final (after 15 days of incubation) soil concentrations of Ace and BaA were determined after extraction of the PAHs.
Results and discussion
P. ostreatus was able to degrade 57.7% of the Ace in soil spiked at 30 mg kg?1 dry soil and 65.8% of Ace in soil spiked at 60 mg kg?1 dry soil. The degradation efficiency of BaA by P. ostreatus was 86.7 and 77.4% in soil spiked with Ace at 30 and 60 mg kg?1 dry soil, respectively. After 15 days of incubation, there were no significant differences in Ace concentration between soil spiked with Ace and soil spiked with Ace + BaA, irrespective of the initial soil concentration of both PAHs. There were also no differences in BaA concentration between soil spiked with BaA and soil spiked with BaA + Ace.
Conclusions
The results indicate that the fungal degradation of Ace and BaA was not influenced by the presence of each other’s PAH in sandy soil. Bioremediation of soils contaminated with Ace and BaA using P. ostreatus is a promising approach to eliminate these PAHs from the environment. 相似文献
Sugarcane waste products (boiler ash, filter cake, and vinasse) from an ethanol production plant were used as soil amendments by adding 3 % (w/w) in single and/or in combination, with a research focus towards stabilization of cadmium (Cd) and zinc (Zn) in contaminated soils. The objective of this laboratory study was to evaluate the effects of adding these sugarcane waste products on bioavailability of Cd and Zn over time (aging) in Cd- and Zn-contaminated agricultural soils of Thailand.
Materials and methods
Two agricultural contaminated soils of low (<3 mg kg?1) and high (10–15 mg kg?1) Cd concentrations were collected from Tak Province, Northwest Thailand. Fourteen treatments were sampled at 2-week intervals for 84 days for metal bioavailability using BCR extraction procedures (proposed by The Standards, Measurements and Testing Programme of the European Union, SM&T) that determined exchangeable (BCR1), reducible (BCR2), oxidizable (BCR3), and residual (BCR4) fractions, and total concentration was determined using aqua regia digestion and microwave digestion.
Results and discussion
Cd was potentially bioavailable, predominantly in exchangeable (BCR1) and reducible (BCR2) fractions, while the higher contribution of Zn was more prevalent in refractory fractions (BCR2 and BCR4). Aging had an influence on fractionation of Cd and Zn, most notably in the first two fractions (BCR1 and BCR2) of BCR sequential extraction, which resulted in reduction of exchangeable Cd during the first few weeks of incubation (T?=?0 to 28 days). At the end of pot experiment, the exchangeable Cd fraction in the low Cd (LCdS) soil was reduced from 2.3 to 4.7 % and 9.4 to 39.9 % in low and high Cd (HCdS)-contaminated soils, respectively, as compared to nonamended soils.
Conclusions
The observed reduction in exchangeable Cd (BCR1) in the amended soils at the 3 % (w/w) application rate, the low total metal concentrations, and the significant amount of essential plant nutrients (N, P, and K) within these waste products highlight the benefits of amending metal-rich soils with them. 相似文献
Many amendments have been applied to immobilize heavy metals in soil. However, little information is available on the changes of immobilization efficiencies of heavy metals in contaminated soils over time. This work investigated the immobilization efficiencies of copper (Cu) and cadmium (Cd) in contaminated soils in situ remediated with one-time application of three amendments for 1 year and 4 years.
Materials and methods
Apatite, lime, and charcoal were mixed with the topsoil of each plot with the amounts of 22.3, 4.45, and 66.8 t/ha, respectively. Soil chemical properties and fractions of Cu and Cd were examined after in situ remediation for 1 year and 4 years. Soil sorption and retention capacities and desorption proportions for Cu and Cd were investigated by batch experiments.
Results and discussion
The addition of amendments significantly increased soil pH, but decreased exchange acid and aluminum (Al). The amendments significantly decreased the CaCl2 extractable Cu and Cd and transformed them from active to inactive fractions. After the application of amendments for 1 year, the maximum sorption capacities ranged from 35.6 to 38.8 mmol/kg for Cu and from 14.4 to 17.0 mmol/kg for Cd, which were markedly higher than those of the application of amendments for 4 years (Cu, 29.6–34.7 mmol/kg; Cd, 10.9–16.4 mmol/kg). Desorption proportions (D) of Cu and Cd using three extractants followed the order of \( {D}_{{\mathrm{NaNO}}_3}<{D}_{{\mathrm{CaCI}}_2}<{D}_{{\mathrm{MgCI}}_2} \). Moreover, the retention capacities (R) of Cu and Cd both increased and followed the order of Rapatite?>?Rlime?>?Rcharcoal, resulting in higher Cu and Cd in the amended soils than the untreated soil.
Conclusions
Apatite, lime, and charcoal increased the soil sorption and retention capacities of Cu and Cd and resulted in higher immobilization efficiencies in the amended soils than the untreated soil. However, the immobilization efficiencies of Cu and Cd decreased with the decrease of sorption capacities after 4 years. It was concluded that apatite had the best effect on the long-term stability of immobilized Cu and Cd and can be applied to immobilize heavy metals in contaminated soils. 相似文献
The purpose of this study was to determine the natural atrazine degradation activity and the genetic potential in a soil profile spanning down to the groundwater zone, collected in Finland at a site where past use of atrazine has contaminated the groundwater, and in Indian agricultural topsoils having different histories of atrazine use.
Materials and methods
Atrazine degradation potential was assessed by quantifying the atrazine degradation genes atzA, trzN, and atzB by quantitative PCR reaction. Atrazine mineralization was studied by radiorespirometry in order to find out if these genes were expressed.
Results and discussion
Indian soils contained a large number up to 104–105 copies (g?1 dry weight (dw) soil) of atrazine degradation genes after the first treatment with atrazine. These genes were also expressed, as up to 55 % of atrazine mineralized. Some unspecific binding of primers required thorough investigation and confirmation by sequencing of the qPCR products in the agricultural soil samples. The degradation capability of the nonagricultural boreal soil profile was much lower: atrazine degradation genes were present at detection limit (102 copies g?1 soil), but mineralization studies indicated that these genes were not transcribed, since no or very little atrazine mineralization was observed.
Conclusions
Our results indicate that when atrazine was applied in agricultural practice, the soil atrazine degradation capacity was high. The organisms responsible for the degradation were effectively degrading atrazine already 3 months after the first treatment with atrazine. However, in boreal soil, decades after atrazine use had been discontinued, residual atrazine was not degraded even though a small number of degradation genes could still be detected in soil. There is a need for more specific primers for qPCR in tropical soils. 相似文献
Previous investigations—field samplings and laboratory experiments—support the hypothesis that the degradation of s-triazines is enhanced in previously exposed as compared to pristine soils in terrestrial environments. Despite this, bottlenecks of soil sampling and various soil modification practices in microcosm studies have made it difficult to guarantee that previous contamination history enhances contaminant degradation regardless of soil origin in terrestrial ecosystems. We test the hypothesis that the degradation of simazine (2-chloro-4,6-bis(ethylamino)-s-triazine) is enhanced in previously exposed soils as compared to pristine soils in 10 l buckets at the mesocosm scale.
Materials and methods
We collected soil at three separate sites consisting of a previously exposed and a pristine field. At every field, soil was collected at three separate plots and simazine degradation (days 0 and 65) and the response to atzB degrader gene primers (days 0 and 110) were followed. We analyzed the results using analysis of covariance (ANCOVA). Previous exposure and field site were assessed as fixed factors and initial simazine concentration and abiotic soil conditions as covariates.
Results and discussion
After the 65-day exposure, remaining simazine concentrations depended on previous exposure but not on collection site. The response to atzB gene primers was positive in all mesocosms where simazine degradation had been rapid. Soil moisture, pH, and organic matter content were insignificant. If soil moisture was not included in the ANCOVA model, previous exposure did not appear as a significant factor.
Conclusions
The results support the hypothesis that simazine is degraded more rapidly in previously exposed soils as compared to pristine environments, provided that degradation genes are available. Previously exposed soil might be used to enhance the degradation of simazine in recently contaminated terrestrial soils, supposing that the central requirements for microbial growth are adequate. 相似文献
Middle-European floodplain soils are often contaminated with mercury (Hg) and periodically flooded. In this study, the influence of a flooding event and subsequent dewatering on the volatilization of elemental Hg and methylated species was investigated in a laboratory experiment.
Material and methods
Undisturbed soil cores were taken from a topsoil (12.1?±?0.75 mg kg?1 Hg) at the Elbe River in Lower Saxony, Germany. Soil columns were incubated at 20 °C with varying soil moisture (water-saturated for 2 weeks, 95 and 90 % water content for 1 week each), and the redox potential (EH) was recorded. The gaseous Hg that accumulated in the headspace of the flux chamber of the columns was pumped over cooled traps filled with adsorber material and analyzed by gas chromatography/inductively coupled plasma mass spectrometry for the various Hg species.
Results and discussion
The watering of the soil resulted in a rapid decrease in the EH and the achievement of strongly reducing conditions (EH??1 Hg at the beginning to 5.78 μg L?1 Hg at the end of the experiment. Species analyses revealed that exclusively elemental Hg volatilized. The volatilization rate was between 1.73 and 824 ng m?2 h?1 Hg, which is consistent with other studies at the Elbe River.
Conclusions
Even when flooded for a longer period of time, floodplain soils should show neither emission of methylated Hg nor exceptionally high volatilization of elemental Hg. 相似文献
The objective of the present study was to explore the effect of initial pH on the decomposition rate of plant residues and the effect of residue type on soil pH change in three different paddy soils.
Materials and methods
Two variable charge paddy soils (Psammaquent soil and Plinthudult soil) and one constant charge paddy soil (Paleudalfs soil) were used to be incubated at 45 % of field capacity for 105 days at 25 °C in the dark after three plant residues (Chinese milk vetch, wheat straw, and rice straw) were separately added at a level of 12 g?kg?1 soil. Soil pH, CO2 escaped, DOC, DON, MBC, MBN, NH4+, and NO3? during the incubation period were dynamically determined.
Results and discussion
Addition of the residues increased soil pH by 0.1–0.8 U, and pH reached a maximum in the Psammaquent and Plinthudult soils with low initial pH at day 105 but at day 3 in the Paleudalfs soil with high initial pH. Incorporation of Chinese milk vetch which had higher concentration of alkalinity (excess cations) and nitrogen increased soil pH more as compared with incorporation of rice and wheat straws. Microbial activity was the highest in Chinese milk vetch treatment, which resulted in the highest increase of soil pH as compared with addition of rice and wheat straws. However, nitrification seemed to be inhibited in the variable charge soils of Psammaquent and Plinthudult but not in the constant charge soil of Paleudalfs.
Conclusions
The effectiveness of increasing soil pH after incorporation of the plant materials would be longer in low initial pH soils of Psammaquent and Plinthudult than in high initial pH soil of Paleudalfs. In order to achieve the same degree of pH improvement, higher amounts of plant residues should be applied in constant charge soils than in variable charge soils. 相似文献
This work examines the rates of bioremediation during a landfarming process. A field study was performed using three types of soil, which were contaminated with two different hydrocarbon concentrations: 20,000 and 50,000 ppm of total petroleum hydrocarbons (TPH). They were subjected to landfarming under the action of different treatments, based on the provision of irrigation, aeration by rototilling, fertilizer, and surfactant. The biodegradation of TPH, considering concentration and families of hydrocarbon compounds (including polycyclic aromatic hydrocarbons, PAHs), was precisely measured for a period of 486 days. The results show how biodegradation rates depend on soil texture, initial contamination level, and type of amendment. Thus, the combination of fertilizer, irrigation, and aeration was the best treatment for treating the soil contaminated with 20,000 ppm of TPH (TPH final concentrations were reduced to a range of 49 to 62% depending on the soil texture). In the case of parcels contaminated with 50,000 ppm of TPH, the most effective treatment combined the supply of fertilizer, surfactant, irrigation, and aeration (TPH final concentrations were reduced to a range of 47 to 63%, depending on the soil texture). The best biodegradation results are obtained for soils with coarser textures and using the treatment with fertilizer, irrigation, and aeration. In addition, the application of surfactant did not imply a significant improvement in the level of biodegradation of hydrocarbons in soil contaminated with 20,000 ppm of TPH, whereas in soils contaminated with 50,000 ppm of TPH, it played a leading role.
Biochar can be used to reduce the bioavailability and leachability of heavy metals, as well as organic pollutants in soils through adsorption and other physicochemical reactions. The objective of the study was to determine the response of microbial communities to biochar amendment and its influence on heavy metal mobility and PCBs (PCB52, 44, 101, 149, 118, 153, 138, 180, 170, and 194) concentration in application of biochar as soil amendment.
Materials and methods
A pot (macrocosm) incubation experiment was carried out with different biochar amendment (0, 3, and 6 % w/w) for 112 days. The CaCl2-extractable concentration of metals, microbial activities, and bacterial community were evaluated during the incubation period.
Results and discussion
The concentrations of 0.01 M CaCl2-extractable metals decreased (p?>?0.05) by 12.7 and 20.5 % for Cu, 5.0 and 15.6 % for Zn, 0.2 and 0.5 % for Pb, and 1.1 and 8.9 % for Cd, in the presence of 3 and 6 % of biochar, respectively, following 1 day of incubation. Meanwhile, the total PCB concentrations decreased from 1.23 mg kg?1 at 1 day to 0.24 mg kg?1 at 112 days after 6 % biochar addition, representing a more than 60 % decrease relative to untreated soil. It was also found out that biochar addition increased the biological activities of catalase, phosphatase, and urease activity as compared with the controls at the same time point. Importantly, the Shannon diversity index of bacteria in control soils was 3.41, whereas it was 3.69 and 3.88 in soils treated with 3 and 6 % biochar soil. In particular, an increase in the number of populations with the putative ability to absorb PCB was noted in the biochar-amended soils.
Conclusions
The application of biochar to contaminated soils decreased the concentrations of heavy metals and PCBs. Application of biochar stimulated Proteobacteria and Bacteroides, which may function to absorb soil PCB and alleviate their toxicity.
Effects of phytoextraction by Sedum alfredii H., a native cadmium hyperaccumulator, on metal removal from and microbial property improvement of a multiple heavy metals contaminated soil were studied under greenhouse conditions.
Materials and methods
A rhizobox experiment with an ancient silver-mining ecotype of S. alfredii natively growing in Zhejiang Province, China, was conducted for remediation of a multiple heavy metals contaminated soil. The rhizobox was designed combining the root-shaking method for the separation of rhizospheric vs near-rhizospheric soils and prestratifying method for separation of sublayers rhizospheric soils (0–10 mm from the root) and bulk soil (>10 mm from the root). Soil and plant samplings were carried out after 3 and 6 months of plant growth.
Results and discussion
Cadmium (Cd), zinc (Zn), and lead (Pb) concentrations in shoots were 440.6, 11,893, and 91.2 mg kg?1 after 6 months growth, and Cd, Zn, and Pb removed in the shoots were 0.862, 25.20, and 0.117 mg/plant. Microbial biomass C, basal respiration, urease, acid phosphatase, and invertase activities of the rhizospheric soils were significantly higher than that of unplanted soils after 6 months growth. Microbial biomass carbon (MBC) of 0–2 mm and basal respiration (BR) rate of 0–8 mm sublayer rhizospheric soils were significantly higher than that of bulk soil after 6 months growth. So were the three enzyme activities of 0–4 mm sublayer rhizospheric soils. BR rate and urease were significantly negatively correlated with soluble Cd, so were MBC, acid phosphatase, and intervase activities with soluble Zn, MBC, BR rate, and three enzyme activities with soluble Pb.
Conclusions
Harvesting shoots of S. alfredii could remove remarkable amounts of Cd, Zn, Pb, and lower water-soluble Cd, Zn, and Pb concentrations in the rhizospheric soils. MBC, BR rate, and enzyme activities of the metal polluted soil, especially the rhizospheric soils increased with phytoextraction process, which is attributed to the stimulation of soil microbes by planting as well as the decrease in soil-soluble metal concentration. 相似文献
The concentration of human activities in urban systems generally leads to urban environmental contamination. Beijing is one of ancient and biggest cities on the world. However, information is limited on Beijing’s soil contamination, especially for roadside and campus soils. Thus, the aims of this study were to investigate the contents and chemical forms of toxic heavy metals Cd, Cr, Cu, Ni, Pb, and Zn in the road-surface dust, roadside soils, and school campus soils of Beijing. In addition, enrichment and spatial variation of these toxic heavy metals in the soils and dust were assessed.
Materials and methods
Topsoil samples were collected from the schools and roadside adjacent to main ring roads, and dust samples were collected from the surface of the main ring roads of Beijing. These samples were analyzed for total contents and chemical forms of Cd, Cr, Cu, Ni, Pb, Sc, Zn, Al, and Fe. Enrichment factors (EFs, relative to the background content) were calculated to evaluate the effect of human activities on the toxic heavy metals in soils.
Results and discussion
Heavy metal contents in the road dust ranged from 0.16 to 0.80, 52.2 to 180.7, 18.4 to 182.8, 11.9 to 47.4, 23.0 to 268.3, and 85.7 to 980.9 mg kg?1 for Cd, Cr, Cu, Ni, Pb, and Zn, respectively. In the roadside soil and school soil, Cd, Cr, Cu, Ni, Pb, and Zn contents ranged from 0.13 to 0.42, 46.1 to 82.4, 22.7 to 71.6, 20.7 to 29.2, 23.2 to 180.7, and 64.5 to 217.3 mg kg?1, respectively. The average EF values of these metals were significantly higher in the dust than in the soils. In addition, the average EF values of Cd, Cu, Pb, and Zn in the soils near second ring road were significantly higher than those near third, fourth, and fifth ring roads. Anthropogenic Cd, Pb, and Zn were mainly bound to the carbonates and soil organic matter, while anthropogenic Cu was mainly bound to oxides. The mobility and bioavailability of these metals in the urban soils of Beijing generally decreased in the following order: Cd?>?Zn?>?Pb?>?Cu?>?Ni?>?Cr; while in the dust, they decreased in the following order: Zn, Cu, and Cd?>?Pb?>?Ni?>?Cr.
Conclusions
Both EF and chemical forms documented that Cr and Ni in the soils and dust mainly originated from native sources, while Cd, Cu, Pb, and Zn partially originated from anthropogenic sources. In overall, Beijing’s road dust was significantly contaminated by Cd and Cu and moderately contaminated by Cr, Pb, and Zn, while Beijing’s roadside soil and school soil were moderately contaminated by Cd and Pb. However, the maximal hazard quotients (HQs) for individual Cd, Cr, Cu, Ni, Pb, and Zn and comprehensive hazard index (HI) of these metals in the dust and soil were less than 1, indicating that the heavy metals in the dust and soil generally do not pose potential health effects to children, sensitive population. 相似文献
Few studies have examined the effects of biochar on nitrification of ammonium-based fertilizer in acidic arable soils, which contributes to NO3? leaching and soil acidification.
Materials and methods
We conducted a 42-day aerobic incubation and a 119-day weekly leaching experiment to investigate nitrification, N leaching, and soil acidification in two subtropical soils to which 300 mg N kg?1 ammonium sulfate or urea and 1 or 5 wt% rice straw biochar were applied.
Results and discussion
During aerobic incubation, NO3? accumulation was enhanced by applying biochar in increasing amounts from 1 to 5 wt%. As a result, pH decreased in the two soils from the original levels. Under leaching conditions, biochar did not increase NO3?, but 5 wt% biochar addition did reduce N leaching compared to that in soils treated with only N. Consistently, lower amounts of added N were recovered from the incubation (KCl-extractable N) and leaching (leaching plus KCl-extractable N) experiments following 5 wt% biochar application compared to soils treated with only N.
Conclusions
Incorporating biochar into acidic arable soils accelerates nitrification and thus weakens the liming effects of biochar. The enhanced nitrification does not necessarily increase NO3? leaching. Rather, biochar reduces overall N leaching due to both improved N adsorption and increased unaccounted-for N (immobilization and possible gaseous losses). Further studies are necessary to assess the effects of biochar (when used as an addition to soil) on N. 相似文献
Diethyl phthalate (DEP) is one of the most commonly used plasticizers as well as a soil contaminant. Using biochar to remediate soils contaminated with DEP can potentially reduce the bioavailability of DEP and improve soil properties. Therefore, a laboratory study was conducted to evaluate the effect of biochar on soil adsorption and desorption of DEP.
Materials and methods
Two surface soils (0–20 cm) with contrasting organic carbon (OC) contents were collected from a vegetable garden. Biochars were derived from bamboo (BB) and rice straw (SB) that were pyrolyzed at 350 and 650 °C. Biochars were added to two types of soil at rates of 0.1 and 0.5 % (w/w). A batch equilibration method was used to measure DEP adsorption-desorption in biochar treated and untreated soils at 25 °C. The adsorption and desorption isotherms of DEP in the soils with or without biochar were evaluated using the Freundlich model.
Results and discussion
The biochar treatments significantly enhanced the soil adsorption of DEP. Compared to the untreated low organic matter soil, the soils treated with 0.5 % 650BB increased the adsorption by more than 19,000 times. For the straw biochar treated soils, the increase of DEP adsorption followed the order 350SB?>?650SB. However, for the bamboo biochars, the order was 650BB?>?350BB. Bamboo biochars were more effective than the straw biochars in improving soils’ adsorption capacity and reducing the desorption ability of DEP.
Conclusions
Adding biochar to soil can significantly enhance soil’s adsorption capacity on DEP. The 650BB amended soil showed the highest adsorption capacity for DEP. The native soil OC contents had significant effects on the soils’ sorption capacity treated with 650BB, whereas they had negligible effects on the other biochar treatments. The sorption capacity was affected by many factors such as the feedstock materials and pyrolysis temperature of biochars, the pH value of biochar, and the soil organic carbon levels. 相似文献
The purpose of the present study was to investigate the distribution of antimony (Sb) and its species in soil fractions in order to understand better the real risk associated with Sb in the environment.
Materials and methods
Nine surface soil samples contaminated from lead/zinc and iron smelting operations and coal fired power plants were examined using: (1) four-step sequential extraction procedure (BCR); (2) two-step sequential extraction including ethylenediaminetetraacetic acid (EDTA), sodium hydroxide (NaOH) and NH4F; and (3) single extraction with EDTA and NaOH. Liquid phase extraction was used for redox speciation of Sb. The distribution of Sb between soil fulvic and humic acids was determined after their chemical separation. The concentrations of Sb were measured by electrothermal atomic absorption spectrometry.
Results and discussion
The main part of total Sb (2.5–105 mg?kg?1) was associated with the residual fraction in all soils. The exchangeable/carbonate-bound concentrations were 0.83–4.7 % of total Sb. Up to 6.8 % was in the reducible and up to 1.4 % was in the oxidizable fraction. EDTA removed 7.2–11.4 % of total content. Sb(V) was the predominant form in acetic acid and EDTA extracts. Single extraction with 0.1 mol?l?1 NaOH released up to 13.7 % of soil antimony. The main part of Sb was complexed to the higher molecular weight fraction of soil-derived humic substances.
Conclusions
For highly contaminated soils, 4 % solubility in acetic acid could represent risk of contamination of ground water under specific conditions. Also, the relatively high phytoavailable Sb (7–11 %) can represent a significant proportion in highly polluted soils. Pentavalent antimony was the main antimony species extracted from soils. The main part of the organically antimony was found to be present as complexes with higher molecular weight humic acids fraction. 相似文献
Diesel fuel represents a permanent source of soil pollution, and its removal is a key factor for human health. To address the limitations of conventional remediation techniques, microwave (MW) heating could be employed due to its great potentiality. This work presents the lab-scale experiments performed to study the potential of MW processing for diesel-polluted soils treatment and related modeling for the optimization of MW systems operating conditions.
Materials and methods
A sandy soil was artificially contaminated with diesel fuel, moisturized with different amounts of water content, and thermally treated by MW radiation using a lab-scale apparatus to investigate the effect of soil moisture on soil temperature profiles and contaminant removal kinetics. An operating power, ranging from 100 to 1,000 W, and treatment times of 5, 10, 18, 30, and 60 min were investigated. Contaminant residual concentration values were fitted using the first order kinetic model, and desorption parameters were calculated for each soil at different operating powers.
Results and discussion
Main results show that the operating power applied significantly influences the contaminant removal kinetics, and the moisture content in soil has a major effect on the final temperature reachable during MW heating. Minimal contaminant concentrations were achievable by applying powers higher than 600 W for a treatment time longer than 60 min. For remediation times shorter than 10 min, which result in a soil temperature of about 100 °C, the effect of the distillation process increases the contaminant removal, whereas for longer times, soil temperature is the main key factor in the remedial treatment.
Conclusions
MW thermal desorption of diesel-polluted soil was shown to be governed by pseudo-first-order kinetics, and it could be a better choice for remediation of diesel-polluted soils, compared to several biological, chemical–physical, or conventional thermal treatments, due to its excellent removal efficiency. The results obtained are of scientific and practical interest and represent a suitable tool to optimize the treatment operating conditions and to guide the design and the scale-up of MW treatments for full-scale remediation activities of diesel-polluted soils. 相似文献
The present work evaluates the influence of different soil properties and constituents on As solubility in laboratory-contaminated soils, with the aim of assessing the toxicity of this element from the use of bioassays to evaluate the soil leachate toxicity and thereby propose soil guideline values for studies of environmental risk assessment in soil contamination.
Materials and methods
Seven soils with contrasting properties were artificially contaminated in laboratory with increasing concentrations of As. Samples were incubated for 4 weeks, and afterwards, soil solution (1:1) was obtained after shaking for 24 h. The soil leachate toxicity was assessed with two commonly used bioassays (seed germination test with Lactuca sativa and Microtox ® test with Vibrio fischeri).
Results and discussion
The relationship between soluble As and soil properties indicated that iron oxides and organic matter content were the variables most closely related to the reduction of the As solubility, while pH and CaCO3 increased As solubility in the soil solutions. Toxicity bioassays showed significant differences between soils depending on their properties, with a reduction of the toxicity in the iron-rich soil (no observed effect concentration (NOEC)?=?150 mg kg?1) and a significant increase in the highly carbonate samples (NOEC between 15 and 25 mg kg?1).
Conclusions
Soil guideline values for regulatory purposes usually set a single value for large areas (regions or countries) which can produce over- or underestimation of efforts in soil remediation actions. These values should consider different levels according to the main soil properties controlling arsenic mobility and the soil leachate toxicity. 相似文献
The choice and timing of microorganisms added to soils for bioremediation is affected by the dominant bioavailable contaminants in the soil. However, changes to the concentration of bioavailable PAHs in soil are not clear, especially when several PAHs coexist. This study investigated the effects of PAH concentration and chemical properties on desorption in meadow brown soil after a 1-year aging period, which could reflect changes of PAH bioavailability during bioremediation.
Materials and methods
Based on the percentage of different molecular weights in a field investigation, high-level contaminated soil (HCS) and low-level contaminated soil (LCS) were prepared by adding phenanthrene (PHE), pyrene (PYR) and benzo(a)pyrene (BaP) to uncontaminated meadow brown soil. The concentrations of HCS and LCS were 250 mg?kg?1 (PHE, PYR, and BaP: 100, 100, and 50 mg?kg?1) and 50 mg?kg?1 (PHE, PYR, and BaP: 20, 20, and 10 mg?kg?1) respectively. The soils were aged for 1 year, after which desorption was induced by means of a XAD-2 adsorption technique over a 96-h period.
Results and discussion
The range of the rapidly desorbing fraction (Frap) for PHE, PYR, and BaP in HCS and LCS was from 1.9 to 27.8 %. In HCS, desorption of PYR was most difficult, and the rate constant of very slow desorption (Kvs) of PYR was 8 orders of magnitude lower than that of BaP, which had similar very slow desorbing fractions (49.8 and 50.5 %, respectively). However, in LCS, desorption of PYR was the easiest; the Kvs of PYR was 8–10 orders of magnitude higher than those of PHE and BaP. In HCS, the time scale for release of 50 % of the PAHs was ranked as BaP?>?PYR?>?PHE, while in LCS this was BaP?>?PHE?>?PYR.
Conclusions
The combined effect of PAH concentrations and properties should be taken into account during desorption. The desorption of PAH did not always decrease with increasing molecular weight, and the desorption of four-ring PAHs might be special. These results are useful for screening biodegrading microbes and determining when they should be added to soils based on the dominant contaminants present during different periods, thus improving the efficiency of soil bioremediation. 相似文献
The nitrification inhibitor dicyandiamide (DCD) has been shown to be highly effective in reducing nitrate (NO3?) leaching and nitrous oxide (N2O) emissions when used to treat grazed pasture soils. However, there have been few studies on the possible effects of long-term DCD use on other soil enzyme activities or the abundance of the general soil microbial communities. The objective of this study was to determine possible effects of long-term DCD use on key soil enzyme activities involved in the nitrogen (N) cycle and the abundance of bacteria and archaea in grazed pasture soils.
Materials and methods
Three field sites used for this study had been treated with DCD for 7 years in field plot experiments. The three pasture soils from three different regions across New Zealand were Pukemutu silt loam in Southland in the southern South Island, Horotiu silt loam in the Waikato in the central North Island and Templeton silt loam in Canterbury in the central South Island. Control and DCD-treated plots were sampled to analyse soil pH, microbial biomass C and N, protease and deaminase activity, and the abundance of bacteria and archaea.
Results and discussion
The three soils varied significantly in the microbial biomass C (858 to 542 μg C g?1 soil) and biomass N (63 to 28 μg N g?1), protease (361 to 694 μg tyrosine g?1 soil h?1) and deaminase (4.3 to 5.6 μg NH4+ g?1 soil h?1) activity, and bacteria (bacterial 16S rRNA gene copy number: 1.64?×?109 to 2.77?×?109 g?1 soil) and archaea (archaeal 16S rRNA gene copy number: 2.67?×?107 to 3.01?×?108 g?1 soil) abundance. However, 7 years of DCD use did not significantly affect these microbial population abundance and enzymatic activities. Soil pH values were also not significantly affected by the long-term DCD use.
Conclusions
These results support the hypothesis that DCD is a specific enzyme inhibitor for ammonia oxidation and does not affect other non-target microbial and enzyme activities. The DCD nitrification inhibitor technology, therefore, appears to be an effective mitigation technology for nitrate leaching and nitrous oxide emissions in grazed pasture soils with no adverse impacts on the abundance of bacteria and archaea and key enzyme activities. 相似文献
Currently, there are large areas of soils contaminated with hexachlorocyclohexane (HCH) isomers which are included in the group of persistent organic pollutants. For the bioremediation of such soils, a new HCH-degrading Rhodococcus wratislaviensis strain Ch628 was isolated from long-term organochlorine contaminated soils. The strain Ch628 was able to degrade 32.3% γ-hexachlorocyclohexane (γ-HCH/lindane), 25.2% hexachlorobenzene, and 100% chlorobenzene in resting cell conditions. The strain Ch628 was bioaugmented in chronically HCH-contaminated soil. The results showed that the bioaugmentation of contaminated soil with the strain Ch628 led to HCH degradation. In the bioaugmented system, the efficiency of HCH removal at the initial concentration of about 238.7 ± 4.9 mg kg?1 soil was 44.8%, while the system with indigenous microflora (without R. wratislaviensis strain Ch628) and the system with abiotic control removed 33.3 and 16.4% of this compound during the same period, respectively. Strain Ch628 could effectively degrade α-, β-, and γ-isomers of HCH (77.1, 100, and 100%, respectively) and heptachlorocyclohexane (69.9%) in the model soil systems. Moreover, the bioaugmentation with the strain Ch628 led to degradation of tri-, tetra-, and penta-chlorobenzenes, which are of HCH degradation metabolites. For the first time, it was found that the bioaugmentation with the bacterial strain Rhodococcus wratislaviensis Сh628 led to a significant reduction of the toxicity of the HCH-contaminated soil for the test organisms, such as Chlorella vulgaris Beijer and Daphnia magna Straus. 相似文献
Using reactive industrial by-products (IBPs) to reduce phosphorus (P) losses associated with diffuse water pollution is a potentially cost-effective mitigation strategy. However, IBPs must be screened to assess their effectiveness and optimum application rates. This requires accurate estimates of parameters such as the maximum P sorption capacity. Traditionally, these parameters have been derived from the Langmuir model applied to data from batch sorption experiments following a 24-h equilibration period. In this paper, we examined (i) how equilibration time can influence estimates of the maximum P sorption capacity for IBPs and (ii) the relative P sorption characteristics of a range of IBPs available in the UK.
Materials and methods
Four IBPs containing different reactive components including ochre, aluminium (Al)-based water treatment residual (WTR), iron (Fe)-based WTR and Fe-lime (CaO)-based WTR were selected for this study. The maximum P sorption capacities of these IBPs were determined using a linearized Langmuir model applied to batch sorption data collected at different equilibration times of 24 h, 5 days and 10 days.
Results and discussion
The maximum P sorption capacity of ochre, Al-based WTR, Fe-based WTR and Fe-CaO-based WTR estimated from the linearized Langmuir model following a 24-h equilibration period was 10.1, 13.7, 2.4 and 9.3 mg P g?1, respectively. However, extending the equilibration time from 24 h to 5 days increased the estimated maximum P sorption capacity for these IBPs by factors of 2.2, 2.1, 6.8 and 2.3, respectively. No significant increase was found in estimates of the maximum P sorption capacity when further extending the equilibration time to 10 days.
Conclusions
A minimum equilibration period of 5 days is recommended to avoid underestimating the maximum P sorption capacity of the IBPs examined in this paper. Each of the IBPs we evaluated was able to sorb P from solution, although with variable capacity (maximum sorption capacity after 5 days of equilibration ranged from 16.3–28.5 mg P g?1). These findings emphasise the importance of accurate quantification of the P sorption capacity of IBPs before application. 相似文献
