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1.
Feasibility of electrokinetic (EK) process combined with Fenton-like reaction was investigated for the removal of phenanthrene in a two-dimensional cell. Sandy soil and bentonite were selected as a model soil and a filling material to inhibit the leak of electrolyte solution within the electrode reservoirs into the soil by hydraulic pressure difference, respectively. The effects of parameters including current, electroosmotic flow (EOF), electrolyte pH, and moisture content on the removal efficiency were examined under constant voltage.

At the end of operation for 21 days, the concentration of phenanthrene near the anode was lower than the other positions of soil specimen and increased gradually towards the cathode because hydrogen peroxide solution was supplied from anode to cathode region following the direction of EOF. The concentration of phenanthrene at the bottom soil was lower than that at the top soil. Because capillary attraction in the sandy soil with high porosity was too low to maintain appropriate moisture at the top of the cell, EOF moved through the bottom soil with higher moisture content. Overall removal efficiency at 140 V was 81.6%, which was higher than 68.9% at 100 V because total EOF increased by a factor of 1.5 upon increase of the voltage from 100 to 140 V. In addition, power consumptions at 100 and 140 V were 7.2 and 19.4 kWh, respectively.  相似文献   


2.
《Applied Geochemistry》2001,16(11-12):1419-1428
The effect of nonionic surfactants on the solubility and biodegradation of polycyclic aromatic hydrocarbons (PAHs) in the aqueous phase and in the soil slurry phase, as well as the fate of these surfactants, were investigated. The PAH solubility was linearly proportional to the surfactant concentration when above the critical micelle concentration (CMC), and increased as the hydrophile–lipophile balance (HLB) value decreased. Substantial amounts of the sorbed phenanthrene in the soil particles were desorbed by non-ionic surfactants into the liquid phase when the ratio of soil to water was 1:10 (g/ml). Brij 30 was the most biodegradable surfactant tested, showed no substrate inhibition up to a concentration of 1.5 g/l, and was definitely used as a C source by the bacteria. Naphthalene and phenanthrene were completely degraded by phenanthrene-acclimatised cultures within 60 h, but a substantial amount of naphthalene was lost due to volatilization. The limiting step in the soil slurry bioremediation was bioavailability by the micro-organisms for the sand slurry and mass transfer from a solid to aqueous phase in the clay slurry.  相似文献   

3.
One large group of persistent and toxic contaminants is the hydrophobic organic contaminants. Among them, perchloroethylene (PCE) has been recognized as a representative group of these pollutants with low solubility. This study reports on the effects of electrokinetic remediation with non-ionic surfactant on PCE-contaminated soil. The performance of electrokinetic process was investigated in the treatment of clay soil that artificially contaminated with two levels: 10,000 and 30,000 mg/kg PCE and 0.33 g/kg Triton X-100. A DC power supply with electric voltage (1 V/cm) was used for 8–16 days. A negatively charged soil surface resulted in a more negative zeta potential and greater electroosmotic flow toward the cathode. The PCE was measured after extraction using n-hexane and analyzed by Fourier transform infrared spectroscopy instrument. The water content of soil was kept 25 % (w/w). Results were shown that PCE removal efficiency achieved was 74 and 89 % for 10,000 and 30,000 mg/kg PCE, respectively, for 16 days. Therefore, in this study, the integration of electrokinetic with non-ionic surfactant as a hybrid method was most effective for the remediation of PCE-contaminated soils.  相似文献   

4.
Surfactant-enhanced remediation of contaminated soil: a review   总被引：48，自引：0，他引：48  
Extracting aqueous solutions with or without additives are employed to solubilize contaminants in soil. Since water solubility is the controlling removing mechanism, additives are used to enhance efficiencies. These additives can reduce the time to treat a site compared to the use of water alone. Additives must be of low toxicity and biodegradable. The research in this area has focussed mainly on halogenated volatile organic compounds (VOCs) and is still quite limited for metal removal. Additives include surfactants, organic and inorganic acids, sodium hydroxide, which can dissolve organic soil matter, water-soluble solvents such as methanol, displacement of cations with nontoxic ones, complexing agents such as EDTA, acids in combination with complexing agents or oxidizing/reducing agents. Cationic, anionic and nonionic surfactants are particularly used for soil washing or flushing. They contain both hydrophobic and hydrophilic portions, making them ideal for solubilization of hydrophobic compounds. Numerous studies have indicated that surfactants enhance recoveries of non-aqueous phase liquids (NAPLs). There have also been indications that pretreatment of soil with surfactant washing to solubilize hydrophobic compounds such as PAHs enhances biodegradation of these contaminants. A few in situ field studies have been performed with surfactants. Large-scale treatment has been done mostly for organic removal. Soil pH, soil type, cation exchange capacity (CEC), particle size, permeabilities and contaminants all affect removal efficiencies. High clay and organic matter contents are particularly detrimental. Understanding the chemistry of the binding of the contaminant and the hydrogeology of the site are very important. Once the water is pumped from the soil, it must be extracted and then treated to remove the hydrocarbons and metals. Several technologies exist such as sodium hydroxide or sodium sulfide precipitation, ion exchange, activated carbon adsorption, ultrafiltration, reverse osmosis, electrodialysis and biological processes. Recycling of the surfactants is desired to decrease treatment costs.

This paper will provide an overview of the laboratory research, field demonstration and full-scale application of surfactants for the remediation of contaminated soil. The majority of pilot scale in situ flushing tests, particularly in the United States, have involved the use of surfactants and co-solvents. There are only a few full-scale projects however. Recent laboratory scale efforts by the authors concerning the use of biosurfactants, biologically produced surfactants, to enhance the removal of copper, cadmium and zinc from contaminated soils and sediments are discussed. Three types of biosurfactants were evaluated for their effectiveness. They included a lipopeptide called surfactin from Bacillus subtilis, a rhamnolipid from Pseudomonas aeruginosa and a sophorolipid from Torulopsis bombicola. The results indicated the feasibility of removing the metals with the anionic biosurfactants even though the exchangeable fractions were not significant.  相似文献   


5.
The aim of this study was to select the appropriate surfactant for the remediation of dichlorodiphenyltrichloroethane-contaminated soil using an in situ foam-flushing technique. The research investigated the performance of the nonionic surfactants polyethylene glycol octyl phenyl ether, polysorbate, and polyoxyethylene lauryl ether, as well as the anionic surfactant sodium dodecyl sulfate, in foam static characteristics, solubility enhancement of dichlorodiphenyltrichloroethane, adsorption loss onto soil, and dichlorodiphenyltrichloroethane desorption from contaminated soil using a foam-flushing approach. Considering the above four criteria, the overall performance suggested polyethylene glycol octyl phenyl ether should be selected for the remediation of dichlorodiphenyltrichloroethane-contaminated soil due to its better foamability and stability, relatively high solubilization ability for dichlorodiphenyltrichloroethane, and greatest contaminant desorption efficiency from soil via foam flushing. Results of the dichlorodiphenyltrichloroethane desorption experiments showed that desorption efficiency of dichlorodiphenyltrichloroethane by different surfactants was largely influenced by foam static characteristics and solubility enhancement of dichlorodiphenyltrichloroethane rather than adsorption loss onto soil, which indicated that foam static characteristics and solubilization ability of surfactants were two key criteria for selection of high-performance foam surfactant.  相似文献   

6.
Electrokinetic remediation of metal contaminated glacial tills   总被引：2，自引：0，他引：2  
This paper presents the results of an experimental investigation which studied the feasibility of using the electrokinetic process to remediate contaminated clays of glacial origin, otherwise known as glacial tills. An overview of the electrokinetic phenomena, as well as previously performed laboratory and field investigations, is first presented. The methodology of the electrokinetic experiments which were conducted to investigate the removal of metals from a glacial till is then described. A total of 16 experiments were conducted using glacial till samples obtained from a project site near Chicago. Sodium and calcium were used as the surrogate cationic metallic contaminants. These experiments demonstrated that ion transport during the electrokinetic process occurs due to both electro-osmosis and electromigration, but that due to electromigration is significantly higher than that due to electro-osmosis. Unlike other clays such as kaolinite, the glacial till used for this investigation possessed high buffering capacity because of its high carbonate content which prevented the acid front migration from the anode to the cathode during the electrokinetic process. The ion removal efficiency of the electrokinetic process was found to increase when: (1) the voltage gradient applied to the soil was increased, (2) the initial concentration of the contaminants was increased, and (3) the duration of the treatment process was increased. The ion removal efficiency was also greater for smaller ions which possess less ionic charge and when the ions existed independently in the soil as compared to when they coexisted. This investigation suggests that the electrokinetic process has significant potential for remediating glacial tills contaminated with metals. However, the properties of Na and Ca are not representative of contaminants, such as heavy metals, so further investigations are needed.  相似文献   

7.
应用表面活性剂的协合效果研制高效润滑剂   总被引：1，自引：0，他引：1  
黄振国 《铀矿地质》1992,8(2):118-122
  相似文献   

8.
One of the environmental concerns in recent decades is the prevalence of different pollutants in soil. Hence, the importance of remediation has led to the development of various methods to remediate polluted soil. Among these methods, soil washing has gained significant attention to treat polluted soils. In this paper, the response surface methodology was applied in order to determine the optimal conditions for total petroleum hydrocarbon remediation using nonionic surfactant Brij35 in soil environment. The effect of different factors in soil washing process including surfactant solution concentration and volume, washing time, age of pollution and frequency of washing are evaluated. The predicted values for total petroleum hydrocarbon remediation efficiency by the response functions are in a very close agreement with experimental data (R-2= 98.75 %). The second order model was developed as experimented response and optimal conditions were obtained by analyzing the contour and surface plots and also by solving the regression equation using LINGO 9.0 software. The optimal concentrations (8 g/L), volume of surfactant solution (500 mL), washing time (75 min), age of pollution (29 days) and frequency of washing (three times) are determined. In this optimal condition, the removal efficiency has been observed to be 93.54 % which conforms to the results of process optimization using response surface methodology. Based on the results, it can be concluded that the response surface methodology is a suitable approach to determine the optimal conditions of soil washing to remediate organic hydrophobic pollutants using the nonionic surfactant Brij35 from the soil.  相似文献   

9.
A crude contaminated soil, arising from an oil production zone in Tabasco, Mexico was studied. A sample of about 40 kg was dried and screened through meshes 10–100. Total petroleum hydrocarbons and 6 metals (Cd, Cu, Cr, Ni, V and Zn) were determined to the different portions. For soil which passed mesh 10, six non-ionic, three anionic and one zwitterionic surfactant solutions (0.5%) were employed to wash the soil. Additional tests using surfactant salt mixtures and surfactants mixtures were carried out. Once the best soil washing conditions were identified, these experimental conditions were applied for washing the rest of the soil portions obtained (meshes 4, 6, 20, 40, 60, 80, 100). Total petroleum hydrocarbons values were in the range of 51, 550 to 192, 130 mg/kg. Cd was not found in any of the soils portions, and the rest of the metals were found at different concentrations, for every soil mesh. Treatability tests applied to the soils indicated that it is possible to get removals between 9.1 to 20.5%. For the case of a sodium dodecyl sulphate 1% solution, total petroleum hydrocarbons removal was as high as 35.4%. Combinations of sodium docecyl sulphate and salts, gave removal rates up to 49.5%. Total petroleum hydrocarbons concentrations for the whole soil were about 150,600 mg/kg. The higher the particle size, the lower the washing removal rate. The combined effect of particle size and total petroleum hydrocarbons concentration, determines the total petroleum hydrocarbons removal efficiencies. These facts are very important for designing an appropriate soil washing remediation process.  相似文献   

10.
Feasibility of electrolyte conditioning with strong alkaline solution on electrokinetic remediation of fluorine-contaminated field soil was investigated in the laboratory. The initial concentration of fluorine, pH and organic matter content in the soil were 1,058 mg kg−1, 8.17 and 20.51 g kg−1, respectively. Electrokinetic experiments were conducted under two different concentrations of alkaline solution and three different voltage gradients. The removal of fluorine increased with the concentration of the alkaline solution and applied voltage and fluorine removed up to 73% within 10 days. Anolyte enhanced electrokinetic process could promote effectively the migration of fluoride in soil. The electromigration was the main transport mechanism and the electroosmotic flow had an effect on the migration of fluoride in soil. Appropriate anolyte enhanced electrokinetic method could be applied to remediate fluorine from contaminated field soil and has significant potential for removing other anionic pollutants such as arsenate and chromate from soil.  相似文献   

11.
Electrokinetic and ultrasonic remediation technologies were studied for the removal of heavy metal and polycyclic aromatic hydrocarbon (PAH) in contaminated soils. The study emphasized the coupled effects of electrokinetic and ultrasonic techniques on migration as well as clean-up of contaminants in soils. The laboratory soil flushing tests combined electrokinetic and ultrasonic technique were conducted using specially designed and fabricated devices to determine the effect of both techniques. The electrokinetic technique was applied to remove mainly the heavy metal and the ultrasonic technique was applied to remove mainly organic substance in contaminated soil. A series of laboratory experiments involving electrokinetic and electrokinetic and ultrasonic flushing tests were carried out. Natural clay was used as a test specimen and Pb and phenanthrene were used as contaminants. An increase in out flow, permeability and contaminant removal rate was observed in electrokinetic and ultrasonic tests. Some practical implications of these results are discussed in terms of technical feasibility of in situ implementation of electrokinetic ultrasonic remediation technique.  相似文献   

12.
Triton X-100 (TX100) and Brij 35 (B35) were used to investigate the elevated critical micelle concentration (CMC) induced by surfactant sorption and its influence on PAH removal in soil washing systems. The surface tension technique was applied to determine the CMC and the apparent CMC (CMCsoil) in soil–water systems. Surfactant sorption experiments were conducted by the batch equilibration technique. Surfactants sorbed on the soil at concentrations below the CMCsoil were quantified with data from the surface tension experiments for both an aqueous system and a soil–water system. Due to sorption, the CMCsoil values of the two surfactants are 2.75 and 6.31 times their corresponding CMC values in aqueous solutions, respectively. At concentrations below CMCsoil, the loss of B35 (92–99.7 %) was greater than that of TX100 (63–92 %). The PAH removal efficiencies are greatly dependent on the CMCsoil value. At surfactant concentrations below CMCsoil, the PAH removal is very low and remains almost invariable. Whereas, at concentrations above CMCsoil, the PAH removal increases greatly. B35 inhibited PAH desorption at concentrations below its CMCsoil. For TX100, some degree of PAH desorption enhancement was observed at concentrations below its CMCsoil. CMCsoil is a key parameter while selecting a surfactant for a specific soil washing system, only surfactant concentrations above their CMCsoil should be evaluated.  相似文献   

13.
王艳  傅俊醒  唐强  胡安详  刘佳鑫 《岩土力学》2016,37(Z1):329-333
表面活性剂随着工业、农业、日常生活等各种活动进入到土体及地下水中,不仅会带来环境污染的风险,还会改变土体的结构等从而影响土体的工程性质。为了合理评估表面活性剂污染土体的工程适宜性,采用阴离子表面活性剂十二烷基苯磺酸钠(SDBS)和阳离子表面活性剂三甲基十六烷基溴化铵(CTAB)对粉土进行改性,通过直剪试验研究其对粉土强度特性的影响。结果表明,表面活性剂改性后的粉土内摩擦角减小,随着表面活性剂浓度的增大,内摩擦角减小的幅值越大,当表面活性剂浓度达2%时,粉土内摩擦角减小23.9%;SDBS改性后的粉土黏聚力大大减小,SDBS浓度为2%时,黏聚力减小91.8%,CTAB改性后粉土黏聚力增大,最大增幅达41.8%;改性粉土中加入不同pH的表面活性剂时,内摩擦角变化很小,表明表面活性剂的酸碱程度对土样内摩擦角影响较小,随着表面活性剂溶液pH的增大,改性粉土的黏聚力呈现出下降的趋势,pH改变了土壤的电荷的分配,改变了土粒间的静电作用,从而引起土体黏聚力的变化。  相似文献   

14.
Wanshan mercury mine is the largest cinnabar deposit in Guizhou, China. Few effective methods had been achieved to remedy Hg heavily contaminated field soils. In this paper, a modified EK method with approaching cathodes (AC-EK) and an I−/I2 lixiviant was described to remedy mercury-contaminated field soils near Wanshan mercury mine. Paddy Soil I and Paddy Soil II were sampled and contained 576.73 ± 45.50 and 491.35 ± 4.73 mg/kg Hg, respectively. Although they contained 6.9 and 9.4% organic matter respectively, more than 92 and 89% Hg were removed by AC-EK within 5 days. Removal ratio increased by 0.21 and 0.68 times using EK process with ACs over that with one single cathode (SC-EK). AC-EK method saved nearly 26.4–28.1% electric power as compared to SC-EK method. As an I−/I2 lixiviant solution was used to solubilize HgS(HgO) during EK process, the bonding of Hg to organic functional S groups should be less important than the binding to inner sites of organic matter in soil. The relationship between EK remediation effect and soil organic matter content was fitted to a linear model. It turned out that when soil OM increased by 1.0%, EK removal ratio (%) of Hg would decrease by 2.63%.  相似文献   

15.
A laboratory study was executed to investigate the effect of surfactants to enhance sorption of polycyclic aromatic hydrocarbon (PAH) contaminants in loess soil. Phenanthrene and naphthalene were chosen as organic contaminant indicators in loess soil modified by the cation surfactant hexadecyltrimethylammonium (HDTMA) bromide. The kinetic behavior of sorption during transport in natural and modified loess soil was studied. The results indicated that sorption rate in the cation surfactant modified loess soils was at least 3 times faster than that of the natural soil. A first-order kinetics model fitted the sorption data well for both soils. The sorption rates of the two organic compounds were related to their primary residual quantity on the soils. The experiments showed that sorption amounts approached constant values approximately within 30 and 90 min for naphthalene and phenanthrene at 298–318 K, respectively. The rate constants, however, displayed negative correlation with increasing temperature. With changing temperature, the activation energy was calculated at –6.196–1.172 kJ/mol for naphthalene and –28.86–15.70 kJ/mol for phenanthrene at 298–318 K. The results can be used to predict the sorption kinetics of phenanthrene and naphthalene in loess soils, and in a wider perspective, be used to better understand the transport of petroleum contaminants in the soil environment.  相似文献   

16.
A series of laboratory experiments were carried out in this study to investigate the remediation of phenanthrene contaminated soil using ultrasound and soil washing. The results indicated that ultrasound and soil washing could significantly enhance the remediation efficiency of each other. The performance of the combined ultrasonic and soil washing process was then investigated, and the impacts of four experimental variables including the initial concentration of phenanthrene in soil, sonication time, pH of washing solution, and washing flow rate were examined using an orthogonal experimental design method. The analysis of variance (ANOVA) of experimental results revealed that the initial phenanthrene concentration, sonication time and soil washing flow rate showed significant effects (P ≤ 0.05) on the remediation efficiency. A pseudo-first-order kinetics model was developed for describing the remediation process, and a maximum remediation efficiency of 69.5% was observed in the study after 20 min of treatment under the experimental conditions. Therefore, the results indicate that the combined ultrasonic and soil washing process could represent a promising technology for the effective remediation of phenanthrene contaminated soil.  相似文献   

17.
Chlorophenols are persistent toxins in the natural environment. In this investigation, 2,4-dichlorophenol (2,4-DCP) and pentachlorophenol (PCP) in aqueous media were degraded using an electrokinetic process (EK) and an electro-Fenton process (EF) using stainless steel and graphite as the anode and cathode, respectively. Chlorophenols were degraded via direct electrolysis at the surface of the electrode in the EK process. However, in the EF process, the degradation mechanism includes direct electrolysis and oxidation by hydroxyl radicals. The optimal conditions were a current density of 0.75 mA/cm2 and an air flow of 0.7 l/min at pH 4. Under the optimal conditions, the 2,4-DCP and PCP removal rates in the EF process were 80.18 and 64.03 %, respectively. The mineralization efficiencies of 2,4-DCP and PCP were 78.23 and 75.77 %, respectively. The results of dechlorination reveal that almost all of the chlorines were released, but some were retained in the intermediates. The dechlorination efficiency revealed that the EF and EK4 processes two chlorines from 2,4-DCP. They released four or five chlorines and four chlorines from PCP, respectively. The kinetic results provide evidence of pseudo-first degradation. The rate constant (k cp) declined as pHi was increased from 4 to 10. The k cp values reveal that the pH is an important factor that affects the degradation efficiency in the electrochemical process.  相似文献   

18.
Remediation with surfactant foam of PCP-contaminated soil   总被引：5，自引：0，他引：5  
An investigation was made into evaluating the capability of surfactants in the form of foam for removing the contaminant pentachlorophenol (PCP), a highly toxic, wood preservative, from soil. Several surfactants were investigated for their ability to make foam. Two of them, Triton X-100 and JBR425 (a rhamnolipid biosurfactant), generated foam with higher quality (99%) and higher stability than other surfactants. Triton X-100 and JBR425 were then used to investigate the removal efficiency in soils contaminated with pentachlorophenol (PCP). Triton X-100 showed better results in terms of final removal efficiency. Triton X-100 (1%) removed 85% and 84% of PCP from fine sand soil and sandy-silt, respectively, contaminated with 1000 mg/kg PCP. These values were 60% and 61% for JBR425 (1%). Of this, 66% and 57% of the PCP was removed by volatilization by Triton X-100 and 36% and 44% by JBR425. Further experiments with Triton X-100 indicated that 1% Triton X-100 removed more than 0.5% and that PCP removal was approximately the same for 1% Triton X-100 for a higher contaminant level (3000 mg/kg) but more pore volumes of foam were required for fine sand (23 pore volumes compared to 12). For the sandy-silt soil, PCP removal was higher for the higher contaminant level, 84% compared to 76%. More pore volumes were required (35 compared to 21). Comparison of liquid and foam injection of 1% Triton X-100 indicated that the foam removed more than twice as much PCP in all cases than the liquid surfactant solution. The results of this study on a sandy and sandy-silt media, thus, found that the foam can be used as a fluid to enhance soil remediation under low pressures compared to other fluids such as liquid surfactant solutions.  相似文献   

19.
Montmorillonites (MMT) was modified with nonionic surfactant Trion X-100 (OP-10) and anionic surfactants sodium stearate (SSTA) and sodium dodecyl benzene sulfonate (SDBS) respectively. In this study, the effects of anionic surfactant types and MMT types on modification montmorillonite were investigated. XRD analysis results showed that SSTA/OP-10/MMT and SDBS/OP-10/MMT were successfully obtained. The basal spacing of SSTA/OP-10/MMT reached 5.07nm and the SSTA intercalation reaction was relatively stable. Different types of MMT (Xinjiang natural sodium montmorillonite(MMT-1), Jianping sodium montmorillonite (MMT-2) and artificial sodium montmorillonite(MMT-3)) were modified with SSTA/OP-10. XRD test results showed that MMT-1, MMT-2 and MMT-3 can be modified by SSTA/OP-10. Anion-nonionic organic montmorillonite (SSTA/OP-10/MMT-1, SSTA/OP-10/MMT-2 and SSTA/OP-10/MMT-3 were successfully obtained respectively. The higher expansion capacity was found to be beneficial to organic modification.  相似文献   

20.
通过对取自MBR膜生物反应器中的活性污泥加入菲进行富集培养、驯化,分离、纯化出一株能以菲为唯一碳源和能源的短杆状革兰氏阴性菌J-1,细菌长2～5μm,宽1～3μm;研究了初始底物浓度、温度、pH对菌株J-1降解菲的影响,探讨了菌株J-1胞内酶对菲降解的底物抑制动力学。试验表明:菌株J-1在48h内能将不同浓度菲的水溶液中的菲完全降解;菲浓度增加,达到完全降解的时间延长。温度对细菌的降解能力影响较大,菌株J-1对菲降解的最佳温度为28℃。1.15mg·L-1的菲,28℃时48h内能完全降解,而相同时间内10℃时的降解率仅为36.65%。菌株J-1对pH的波动具有一定的适应性,pH在一定范围内(6.0～8.4)变化对菲降解的影响不大,降解反应的最佳pH为7.2。菌株J-1对菲的降解符合一级动力学反应方程。较高的底物浓度对酶促降解反应具有抑制作用,酶促反应的最大速率常数vm=1.17mg·L-1·h-1,米氏常数Km=61.70mg·L-1;底物抑制常数kS=49.60mg·L-1;最佳底物浓度[S]opt=55.32mg·L-1。  相似文献   

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