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Qian YAO Hua ZHANG Jun WU Liming SHAO Pinjing HE 《Frontiers of Environmental Science & Engineering》2010,4(3):286-294
Batch biosorption experiments were conducted to remove Cr(III) from aqueous solutions using activated sludge from a sewage treatment plant. An investigation was conducted on the effects of the initial pH, contact time, temperature, and initial Cr(III) concentration in the biosorption process. The results revealed that the activated sludge exhibited the highest Cr(III) uptake capacity (120 mg·g−1) at 45°C, initial pH of 4, and initial Cr(III) concentration of 100 mg·L−1. The biosorption results obtained at various temperatures showed that the biosorption pattern accurately followed the Langmuir model. The calculated thermodynamic parameters, ΔGo (−0.8– −4.58 kJ·mol−1), ΔHo (15.6–44.4 kJ·mol−1), and ΔSo (0.06–0.15 kJ·mol−1·K−1) clearly indicated that the biosorption process was feasible, spontaneous, endothermic, and physical. The pseudo first-order and second-order kinetic models were adopted to describe the experimental data, which revealed that the Cr(III) biosorption process conformed to the second-order rate expression and the biosorption rate constants decreased with increasing Cr(III) concentration. The analysis of the values of biosorption activation energy (Ea = −7 kJ·mol−1) and the intra-particle diffusion model demonstrated that Cr(III) biosorption was film-diffusion-controlled. 相似文献
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Zhi-Long Ye Yujun Deng Yaoyin Lou Xin Ye Shaohua Chen 《Frontiers of Environmental Science & Engineering》2018,12(3):7
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Endocrine disrupting compounds (EDCs), pharmaceuticals and personal care products (PPCPs) have attracted much attention due to widespread contamination in aquatic environment. In this study, we determined 13 EDCs and PPCPs in fish blood, bile and muscle by using gas chromatography-mass spectrometry (GC-MS). The limits of quantitation (LOQ) were in the ranges of 0.23–2.54, 0.22–2.36 ng·mL−1, and 0.24–2.57 ng·g−1 dry weight (dw) for fish blood, bile and muscle, respectively. Recoveries of target compounds spiked into sample matrices and passed through the entire analytical procedure ranged from 65% to 95%, from 60% to 92% and from 62% to 91% for blood, bile and muscle, respectively. The methods were applied to the analysis of fish from a lake in California. Target compounds were relatively low in bile, and only bisphenol A (BPA) and diclofenac were measurable near the LOQ. Seven of 13 compounds were detected in blood, with total concentrations up to 39 ng·mL−1. Only BPA was frequently found in muscle, with mean concentration of 7.26 ng·g−1 dw. The estimated daily intake of BPA through fish consumption for U.S. resident was significantly lower than the tolerable daily intake recommended by the European Food Safety Authority. This study showed that the exposure to the bisphenol A from fish diet is unlikely to pose a health risk. 相似文献
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Qingyun CHANG Jingwen ZHANG Xin DU Jingjun MA Jingci LI 《Frontiers of Environmental Science & Engineering》2010,4(2):187-195
A simple and efficient liquid-phase microextraction (LPME) technique was developed using ultrasound-assisted emulsification solidified floating organic drop microextraction (USAE-SFODME) combined with flame atomic absorption spectrometry, for the extraction and determination of trace copper in water samples. 1-(2-Pyridylazo)-2-naphthol (PAN) was used as chelating agent. Microextraction efficiency factors (including extraction solvent type, extraction volume, time, temperature, and pH), the amount of the chelating agent, and salt effect were investigated and optimized. Under the optimum extraction conditions, figures of merit of the proposed method were evaluated. The calibration graph was linear in the range of 20–600 mg·L−1 with a detection limit of 0.76 mg·L−1. The relative standard deviation (R.S.D) for ten replicate measurements of 20 and 400 mg·L−1 of copper was 3.83% and 2.65%, respectively. Finally, the proposed method was applied to tap water, river water, and sea water, and accuracy was assessed through the analysis of certified reference water or recovery experiments. 相似文献
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Mingxing GAO Yingying LI Hong YANG Yucheng GU 《Frontiers of Environmental Science & Engineering》2016,10(1):1-10
Pymetrozine is a selective insecticide with a unique chemical structure and mode to control hemipteran and homopteran. While pymetrozine has brought great benefits to crop production by killing insects, its residues in soil may have a detrimental effect on environment. Therefore, it is of great importance to investigate its behaviors in soil. In this study, the sorption and desorption of pymetrozine on six Chinese soils were investigated using a batch equilibrium approach to understand its mobile behavior in the soils. Both sorption and desorption isotherms of pymetrozine were in good agreement with the Freundlich model. The sorption coefficient KF varied between 3.37 and 58.32 mL∙g−1 and the sorption isotherms were nonlinear, with 1/n ranging from 0.57 to 0.91. A regression equation was proposed to predict the sorption of pymetrozine on six different soil samples: log KF = 4.3708 − 4.5709 × log (pH in 0.01mol·L−1 CaCl2) + 0.4700 × log OC% + 0.0057 × sand (%) + 0.0022 × CEC(clay), with R2 = 0.9982. The organic carbon content of soil positively affected the sorption of pymetrozine, but soil pH had a negative effect on the sorption. Additionally, effects of CaCl2 concentration, soil to solution ratio and pesticide form were investigated. The sorption was promoted with an increase in soil to solution ratio and a decrease in CaCl2 concentration. The possible variation of the five formulated products of pymetrozine was also investigated. 相似文献
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Siyu Chen Lee Blaney Ping Chen Shanshan Deng Mamatha Hopanna Yixiang Bao Gang Yu 《Frontiers of Environmental Science & Engineering》2019,13(4):59
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Pan Gao Yuan Song Shaoning Wang Claude Descorme Shaoxia Yang 《Frontiers of Environmental Science & Engineering》2018,12(1):8
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北京地区3种污灌土壤镉最大吸附容量的推求 总被引:2,自引:0,他引:2
土壤对重金属的吸附容量是土壤重金属污染风险评价的一项重要指标,研究土壤对重金属的最大吸附容量对加强土壤环境的科学管理具有重要意义.采用阳离子交换量、平衡吸附方程和实验实测法推求了北京地区3种污灌土壤对重金属镉的最大吸附容量.由阳离子交换量(CEC)推求的北野厂、衙门口和永乐店3种污灌土壤对镉的最大吸附容量分别为:4822、4148和4721mg·kg-1;由单表面Langmuir方程推求的3种污灌土壤对镉的最大吸附容量均为5000mg·kg-1,由传统双表面Langmuir方程推求的3种土壤对镉的最大吸附容量分别为7040、6950和6994mg·kg-1,由双表面Langmuir方程的Sposito方法推求的3种污灌土壤对镉的最大吸附容量均为6200mg·kg-1;恒温25℃条件下,上述3种污灌土壤对镉的单分子层最大吸附容量实测值分别为5700、5600和5600mg·kg-1,多分子层最大吸附容量实测值分别为9000、8000和8120mg·kg-1.比较而言,双表面Langmuir方程是目前推求污灌土壤对镉最大吸附容量的较好方法. 相似文献
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Robert D. ARTHUR Jagadish TORLAPATI Kyung-Hee SHIN Daniel K. CHA Yeomin YOON Ahjeong SON 《Frontiers of Environmental Science & Engineering》2014,8(3):386-393
Process control parameters influencing microbial perchlorate reduction via a flow-through zero-valent iron (ZVI) column reactor were investigated in order to optimize perchlorate removal from water. Mixed perchlorate reducers were obtained from a wastewater treatment plant and inoculated into the reactor without further acclimation. Examined parameters included hydraulic residence time (HRT), pH, nutrients requirement, and perchlorate reduction kinetics. The minimum HRT for the system was concluded to be 8 hr. The removal efficiency of 10 mg. L-1 influent perchlorate concentration was reduced by 20%-80% without control to the neutral pH (HRT = 8 hr). Therefore pH was determined to be an important parameter for microbial perchlorate reduction. Furthermore, a viable alternative to pH buffer was discussed. The microbial perchlorate reduction followed the first order kinetics, with a rate constant (K) of 0.761 hr-1. The results from this study will contribute to the implementation of a safe, cost effective, and efficient system for perchlorate reduction to below regulated levels. 相似文献
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Shuai Wang Tong Li Chen Chen Baicang Liu John C. Crittenden 《Frontiers of Environmental Science & Engineering》2018,12(2):3
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Chen Zhou Ermias Gebrekrstos Tesfamariam Youneng Tang Ang Li 《Frontiers of Environmental Science & Engineering》2023,17(9):107
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Lijing DONG Zhiliang ZHU Yanling QIU Jianfu ZHAO 《Frontiers of Environmental Science & Engineering》2016,10(1):28-36
A novel composite adsorbent, hydroxyapatite/manganese dioxide (HAp/MnO2), has been developed for the purpose of removing lead ions from aqueous solutions. The combination of HAp with MnO2 is meant to increase its adsorption capacity. Various factors that may affect the adsorption efficiency, including solution pH, coexistent substances such as humic acid and competing cations (Ca2+, Mg2+), initial solute concentration, and the duration of the reaction, have been investigated. Using this composite adsorbent, solution pH and coexistent calcium or magnesium cations were found to have no significant influence on the removal of lead ions under the experimental conditions. The adsorption equilibrium was described well by the Langmuir isotherm model, and the calculated maximum adsorption capacity was 769 mg·g−1. The sorption processes obeyed the pseudo-second-order kinetics model. The experimental results indicate that HAp/MnO2 composite may be an effective adsorbent for the removal of lead ions from aqueous solutions. 相似文献
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Wei WANG Yan MA Qing ZHOU Chendong SHUANG Mancheng ZHANG Aimin LI 《Frontiers of Environmental Science & Engineering》2015,9(1):96
A rapid and effective method based on a novel permanent magnetic hypercrosslinked resin W150 was proposed for the removal of organic micropollutants in drinking water. W150 was prepared by suspension and post-crosslinking reaction and found to possess a high specific surface area of 1149.7 m2·g-1, a small particle size of 50 μm to 100 μm, and a saturation magnetization as high as 8 emu·g-1. W150 was used to eliminate nitrofurazone (NFZ) and oxytetracycline (OTC) from drinking water compared with commercial adsorbents XAD-4 and F400D. The adsorption kinetics of NFZ and OTC onto the three adsorbents well fitted the pseudo-second-order equation (r>0.972), and the adsorption isotherms were all well described by the Freundlich equation (r>0.851). Results showed that the reduction in adsorbent size and the enlargement in sorbent pores both accelerated adsorption. Moreover, the effect of particle size on adsorption was more significant than that of pore width. Given that the smallest particle size and the highest specific surface area were possessed by W150, it had the fastest adsorption kinetics and largest adsorption capacity for NFZ (180 mg·g-1) and OTC (200 mg·g-1). For the adsorbents with dominant micropores, the sorption of large-sized adsorbates decreased because of the inaccessible micropores. The solution pH and ionic strength also influenced adsorption. 相似文献
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不同部位梧桐生物质炭对水溶液中镉吸附的机理 总被引:1,自引:0,他引:1
为了探究梧桐不同部位废弃物所制备的生物质炭(皮、枝、叶)对Cd2+的吸附效率和稳定修复的机理,以此为园林废弃物炭化利用在重金属污染修复方面的应用提供科学依据.利用实验室模拟法,通过高温煅烧法制备梧桐不同部位生物质炭,采用元素分析仪、比表面积及孔隙分析(BET)、X射线衍射仪(XRD)、扫描电镜/能谱(SEM/EDS)及衰减全反射红外光谱(ATR-IR)等技术研究不同反应时间、重金属浓度和溶液初始pH条件下生物质炭对Cd2+吸附效果的影响,并运用四步萃取法和脱附实验分析生物质炭上Cd2+的吸附形态和稳定性.3种生物质炭都在8 h左右达到吸附平衡,最终吸附量依次为树皮炭>枝条炭>叶片炭;溶液初始浓度为0.5—2 g·L-1时Cd2+的吸附量呈增长趋势,在2.5—3g·L-1时逐渐平缓;生物质炭Cd2+吸附量均随着pH的升高而升高,但在pH值为5—8时,吸附的趋势逐渐平稳;树皮炭的酸溶态和非生物利用态的稳定Cd形态要高于枝条炭和叶片炭;比表面积不是影响梧桐生物质炭吸附Cd2+的主要影响因素,吸附动力学,ATR,XRD和重金属形态萃取均证实Cd碳酸盐类矿物生成是主导吸附机理;3种生物质炭的脱附量在4 h后逐渐趋于平衡,其中脱附量最大为叶片炭,最小为树皮炭.梧桐不同部位的初始性质对生物质炭吸附Cd2+具有明显的影响,其中梧桐皮具备更高的吸附量和重金属稳定形态,并且相比其他种类生物质炭有明显优势.因此,从吸附效果和生产成本的角度,本研究建议以梧桐皮为主,枝条和叶片为辅的生物质炭对重金属Cd进行修复治理. 相似文献
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Junguo HE Guangming ZHANG Haifeng LU 《Frontiers of Environmental Science & Engineering》2010,4(3):334-339
The conventional treatment method of soybean wastewater is expensive and generates waste sludge that requires further handling. Purple nonsulfur bacteria (PNSB) wastewater treatment is a clean technology and can generate single cell protein while degrading pollutants. A wild strain of PNSB, Rhodobacter sphaeroides Z08, was isolated from local soil and was used to treat soybean wastewater. To develop a cost-effective process, the work was performed under natural conditions without artificial light, aeration, nutrients addition, or pH and temperature adjustment. The results showed that the wild strain Rhodobacter sphaeroides Z08 could grow well under natural conditions. The growth curve showed two quick-growth periods and a turning point. The Z08 treatment of soybean wastewater was zero order reaction and COD reduction was 96% after 10 d. The major byproducts of the process were C2-C5 organic acids, predominantly butyric acid. No alcohol was found in the effluent. The initial COD/bacterial-mass ratio (F/M) had a significant effect on soybean wastewater treatment efficiency. When the initial F/M was lower than 10 mg-COD/mg-bacteria, a sufficient amount of time to achieve 90% of COD reduction was only three days. The Z08 biomass yield was 0.28g·g−1, and the bacterial protein content was 52%. 相似文献
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Fangfang CHANG Jiuhui QU Xu ZHAO Wenjun LIU Kun WU 《Frontiers of Environmental Science & Engineering》2011,5(4):512-518
Fe-Mn binary oxide incorporated into porous diatomite (FMBO-diatomite) was prepared in situ and regenerated in a fixed-bed column for arsenite [As(III)] and arsenate [As(V)] removal. Four consecutive adsorption cycles were operated under the following conditions: Initial arsenic concentration of 0.1 mg·L-1, empty bed contact time of 5 min, and pH 7.0. About 3000, 3300, 3800, and 4500 bed volumes of eligible effluent (arsenic concentration≤0.01 mg·L-1) were obtained in four As(III) adsorption cycles; while about 2000, 2300, 2500, and 3100 bed volumes of eligible effluent were obtained in four As(V) adsorption cycles. The dissection results of FMBO-diatomite fixed-bed exhibited that small amounts of manganese and iron were transferred from the top of the fixed-bed to the bottom of the fixed-bed during As(III) removal process. Compared to the extremely low concentration of iron (<0.01 mg·L-1), the fluctuation concentration of Mn2+ in effluent of the As(III) removal column was in a range of 0.01–0.08 mg·L-1. The release of manganese suggested that manganese oxides played an important role in As(III) oxidation. Determined with the US EPA toxicity characteristic leaching procedure (TCLP), the leaching risk of As(III) on exhausted FMBO-diatomite was lower than that of As(V). 相似文献
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The objective of this experiment was to study the effects of malic, tartaric, oxalic, and citric acid on the adsorption and desorption characteristics of Cd by two typical anthropic soils (lou soil and irrigation-silted soil) in North-west China. Cadmium adsorption and desorption were studied under a range of temperatures (25°C, 30°C, 35°C, 40°C), organic acid concentrations (0.5–5.0 mmol·L-1), and pH values (2–8). The results showed that the Cd adsorption capacity of the lou soil was significantly greater than that of the irrigation-silted soil. Generally, Cd adsorption increased as the temperature increased. In the presence of NaNO3, the adsorption of Cd was endothermic with ΔH values of 31.365 kJ·mol-1 for lou soil and 28.278?kJ·mol-1 for irrigation-silted soil. The endothermic reaction indicated that H bonds were the main driving force for Cd adsorption in both soils. However, different concentrations of organic acids showed various influences on the two soils. In the presence of citric acid, chemical adsorption and van der Waals interactions were the main driving forces for Cd adsorption rather than H bonds. Although the types of organic acids and soil properties were different, the effects of the organic acids on the adsorption and desorption of Cd were similar in the two soils. The adsorption percentage of Cd generally decreased as organic acid concentrations increased. In contrast, the adsorption percentage increased as the pH of the initial solution increased. The exception was that adsorption percentage of Cd increased slightly as oxalic acid concentrations increased. In contrast, the desorption percentage of Cd increased with increasing concentrations of organic acids but decreased as the initial solution pH increased. 相似文献