Coupled production and transport of selenium vapor in unsaturated soil: evaluation by experiments and numerical simulation

Volatilization of selenium (Se) from soil to the atmosphere involves several sequential chemical reactions that form volatile Se species, followed by transport of the gaseous Se through the soil. This paper describes a numerical model that simulates the chemical and physical processes governing the production and transport of Se vapor in unsaturated soil. The model couples the four Se species involved in the production of Se vapor through chemical reactions, and allows each to migrate through the soil by advection, liquid or vapor diffusion depending on its affinity for the dissolved or vapor phase. The coupled transformations and transport of the four Se species, i.e., selenate, selenite, elemental and organic Se, and Se vapor, were calculated based on the Crank-Nicolson finite difference method. The model was used to analyze fluxes of Se vapor measured from a soil amended with inorganic Se in the form of selenate and covered with unamended clean soil of various thicknesses. Evolution of Se vapor from the soil was very fast, with measurable amounts of Se detected within 24 h. The peak of Se volatilization, detected at the 6th day, reached 3.31 Se microgram/day for the uncovered soil, but was reduced to near the detection limit (0.05 microgram/day) in the presence of a 8- or 16-cm clean soil cover. With two reaction rate coefficients fitted to the data, the model described Se volatilization very well. The estimated rate coefficient of Se methylation was unexpectedly high, with a value of 0.167/day. The net volatilization of Se, however, was severely inhibited by the fast demethylation, i.e., the reverse reaction which converted volatile Se species back into nonvolatile forms. As a result, Se vapor only penetrated a few centimeters in the soil. The demethylation rate coefficient, assessed by independent transport experiments using dimethyl selenide, was estimated as 186.8/day, corresponding to a half-life of only 5.3 min for Se vapor. Results of this study indicated that rapid demethylation of Se vapor during its diffusive transport through a soil is probably an important limiting factor in the volatilization of Se under natural conditions.     

排污收费对企业污染控制技术创新激励作用的研究

运用模型方法研究了排污收费和行政手段对企业污染控制技术创新的激励作用,为环境管理政策应用提供了理论依据。结果表明,无论对创新企业还是模拟企业,在“技术创新－创新扩散－最优啮合反应”的技术创新过程中,排污收费更能刺激企业的污染控制技术创新行为。     

酸雨对污染环境中重金属化学行为的影响

综述了酸雨对污染环境中重金属化学行为的影响。在酸雨作用下 ,不同环境介质中重金属活性明显增强 ,化学形态转化明显 ,迁移能力和生态危害能力亦明显加强。探讨了控制酸雨发生、重金属污染环境修复技术以及开展复合污染环境化学风险评价的必要性     

盘式曝气器的结构优化设计

盘式曝气器是目前城市污水处理厂主要采用的曝气设备之一.但目前盘式曝气器存在充氧能力低、阻力损失大、使用寿命短等技术问题,增加了城市污水处理厂运行成本,降低了运行效能.针对这些问题,对盘式曝气器进行了结构优化设计.通过结构优化,既改善了曝气器的抗撕裂性和自闭性,同时又提高了充氧能力,降低了曝气阻力损失.     

可张孔曝气器曝气能耗试验研究

通过试验研究,总结出可张孔曝气阻力损失的影响因素,以优化产品的结构设计参数,降低产品在工程应用中的能耗,获取更好的经济效益。     

An alternative supercritical fluid extraction system for aqueous matrices and its application in pesticides residue analysis

Supercritical fluid extraction (SFE) is a rapid and convenient method for the isolation of organic compounds from environmental samples. This paper describes a supercritical carbon dioxide (CO2) extraction system that uses a newly designed extraction cell to recover organic compounds from an aqueous matrix. Analysis of the extracts by gas chromatography-electron capture detector (GC-ECD) indicated that the herbicide trifluralin (2,6-dinitro-N,N-dipropyl-4-trifluoromethylaniline) could be quantitatively extracted by using the SFE system proposed with small amounts of sample. The percentage of recovery obtained with the SFE system described was twice as high as the result obtained using a conventional solid-phase extraction technique. Extraction by SFE was completed in a short period of time using a simple and low-cost home-made system that did not require the use of organic solvents.     

Solventless sample preparation for pesticides analysis in environmental water samples using solid-phase microextraction-high resolution gas chromatography/mass spectrometry (SPME-HRGC/MS)

Solid-phase micro-extraction (SPME) coupled on line with high resolution gas chromatography and mass spectrometric detection is described for the analysis of pesticides in environmental water samples. Experiments were performed in order to optimize the SPME extraction conditions for selected pesticides including tiomethon, trichorfon, dimethoate, diazinon, malathion, dicofol, methidathion, ethion, bromopropylate and pyrazophos from spiked water solutions. To enhance the SPME efficiency, experimental conditions including the fiber composition, stirring rate, temperature, adsorption time, desorption time and salt concentration were optimized. After validation, the SPME-GC/MS methodology was applied to real-world environmental water samples.     

Comparison of the effects of aluminum and iron(Ⅲ) salts on ultrafiltration membrane biofouling in drinking water treatment

Coagulation plays an important role in alleviating membrane fouling, and a noticeable problem is the development of microorganisms after long-time operation, which gradually secrete extracellular polymeric substances(EPS). To date, few studies have paid attention to the behavior of microorganisms in drinking water treatment with ultrafiltration(UF)membranes. Herein, the membrane biofouling was investigated with different aluminum and iron salts. We found that Al_2(SO_4)_3·18 H_2O performed better in reducing membrane fouling due to the slower growth rate of microorganisms. In comparison to Al_2(SO_4)_3·18H_2O,more EPS were induced with Fe_2(SO_4)_3·x18H_2O, both in the membrane tank and the sludge on the cake layer. We also found that bacteria were the major microorganisms, of which the concentration was much higher than those of fungi and archaea. Further analyses showed that Proteobacteria was dominant in bacterial communities, which caused severe membrane fouling by forming a biofilm, especially for Fe_2(SO_4)_3·x18H_2O. Additionally, the abundances of Bacteroidetes and Verrucomicrobia were relatively higher in the presence of Al_2(SO_4)_3·18 H_2O,resulting in less severe biofouling by effectively degrading the protein and polysaccharide in EPS. As a result, in terms of microorganism behaviors, Al-based salts should be given preference as coagulants during actual operations.     

Investigation on mechanism of phosphate removal on carbonized sludge adsorbent

For the removal of phosphate (PO₄^3 -) from water, an adsorbent was prepared via carbonization of sewage sludge from a wastewater treatment plant: carbonized sludge adsorbent (CSA). The mechanism of phosphate removal was determined after studying the structure and chemical properties of the CSA and its influence on phosphate removal. The results demonstrate that phosphate adsorption by the CSA can be fitted with the pseudo second-order kinetics and Langmuir isotherm models, indicating that the adsorption is single molecular layer adsorption dominated by chemical reaction. The active sites binding phosphate on the surface are composed of mineral particles containing Si/Ca/Al/Fe. The mineral containing Ca, calcite, is the main factor responsible for phosphate removal. The phosphate removal mechanism is a complex process including crystallization via the interaction between Ca^2 + and PO₄^3 -; formation of precipitates of Ca^2 +, Al^3 +, and PO₄^3 -; and adsorption of PO₄^3 - on some recalcitrant oxides composed of Si/Al/Fe.     

高校学生公寓应急疏散模拟与优化

运用应急疏散软件Pathfinder对某高校学生公寓的人员疏散进行了模拟,结果表明,休息时间段内公寓发生的突发事件更容易造成人员疏散运动时间的延长;同等条件下女生比男生所需要的人员疏散运动时间更长。通过合理规划疏散路线,对原有模型进行了优化,并使用人员疏散运动时间和单位有效疏散宽度使用率两个指标,来定量对比优化前后人员疏散的均衡度和疏散效果,给高校学生公寓的应急和安全管理工作提供参考。