Solvent extraction for heavy crude oil removal from contaminated soils

A new strategy of heavy crude oil removal from contaminated soils was studied. The hexane-acetone solvent mixture was used to investigate the ability of solvent extraction technique for cleaning up soils under various extraction conditions. The mixtures of hexane and acetone (25 vol%) were demonstrated to be the most effective in removing petroleum hydrocarbons from contaminated soils and approx 90% of saturates, naphthene aromatics, polar aromatics, and 60% of nC₇-asphaltenes were removed. Kinetic experiments demonstrated that the equilibrium was reached in 5 min and the majority of the oil pollutants were removed within 0.5 min. The effect of the ratio between solvent and soil on the extraction efficiency was also studied and results showed that the efficiency would increase following the higher solvent soil ratio. Then the multistage continuous extraction was considered to enhance the removal efficiency of oil pollutants. Three stages crosscurrent and countercurrent solvent extraction with the solvent soil ratio 6:1 removed 97% oil contaminants from soil. Clearly the results showed that the mixed-solvent of hexane and acetone (25 vol%) with character of low-toxic, acceptable cost and high efficiency was promising in solvent extraction to remove heavy oil fractions as well as petroleum hydrocarbons from contaminated soils.     

污水湿地处理工程水力停留时间的测定

利用ＵＡＰ对一个湿地处理工程的实际水力停留时间进行了测定,进而对相关问题进行了探讨。     

长株潭区域一次重度污染过程气象成因

利用PM_2.5质量浓度、地面气象要素、NCEP、ERSST＿V3、GBL等资料,研究了2021年12月7—11日长株潭地区一次重度空气污染过程的特征及成因。结果表明,高空平直环流、无明显槽脊影响,地面弱冷空气活跃是本次重度空气污染过程的主要环流形势特征;地面均压场、小风和升温增湿是此次重度空气污染过程的主要气象要素特征。污染物浓度变化与主导风向和污染通道密切相关,本地风速对混合层的高度、污染物水平扩散影响较大,600～700 hPa逆温层有利于污染物在主导风作用下近距离传输及在低层交换积累。我国中东部污染物积聚是长株潭区域重要的污染来源,长株潭地区存在区域性同步污染现象。低层流入长株潭区域气流轨迹差异及地理条件是长株潭污染物空间分布差异的重要因素。     

Identification and ecotoxicity assessment of intermediates generated during the degradation of clofibric acid by advanced oxidation processes

The aim of this study was to identify the intermediates in clofibric acid degradation under various advanced oxidation processes, namely ultraviolet (UV), UV/H₂O₂, vacuum ultraviolet (VUV), VUV/H₂O₂, and solar/TiO₂ processes, as well as to assess the toxicity of these intermediates. Eleven intermediates have been detected by gas chromatography-mass spectrometer, most of which were reported for the first time to our best knowledge. Combining the evolution of the dissolved organic carbon, Cl^- and specific ultraviolet absorption at 254 nm, it could be deduced that cleavage of aromatic ring followed by dechlorination was the mechanism in solar/TiO₂ process, while dechlorination happened first and accumulation of aromatic intermediates occurred in the other processes. Different transformation pathways were proposed for UV-, VUV-assisted and solar/TiO₂ processes, respectively. The acute toxicity was evaluated by means of Photobacterium phosphoreum T₃ spp. bioassay. It was believed that aromatic intermediates increased the toxicity and the ring-opening pathway in solar/TiO₂ process could relieve the toxicity.     

全氟化合物污染现状及风险评估的研究进展

全氟化合物(polyfluorinated compounds,PFCs)是近年来受到广泛关注的一类新型持久性有机污染物。PFCs因具有优良的化学稳定性、耐热性以及高表面活性,而被广泛应用于生活消费和工业生产等领域。PFCs具有难降解、生物富集和长距离迁移等特点,已在大气、土壤和水体等环境介质及生物体中检出。在生态环境中,PFCs能够通过食物链不断传递放大,其具有的多种毒性效应已对生态系统和人类造成了一定的威胁。本文主要综述了PFCs在各类环境介质的污染现状、生物的毒性效应、人类摄入健康风险评估以及PFCs的降解研究,以期为未来PFCs的研究提供参考。     

异菌脲在土壤中的降解和移动性研究

为明确异菌脲在土壤中的迁移和归趋特征,采用室内模拟方法研究异菌脲在4种不同类型土壤中的降解和移动性以及不同因素对异菌脲降解的影响。结果表明,异菌脲在不同类型土壤中的降解顺序为东北黑土青海草甸土南京黄棕壤江西红壤,降解半衰期分别为7.2、8.6、12.7和16.9 d,异菌脲在4种土壤中均属于易降解农药。土壤湿度越大,异菌脲降解越快,渍水条件下降解速率加快,说明厌氧微生物对异菌脲降解起重要作用。微生物和有机质对异菌脲在土壤降解过程中有一定的促进作用,在微生物、有机质存在的条件下异菌脲降解速率分别提高1.8倍、3.7倍。薄层层析试验表明,异菌脲在南京黄棕壤、东北黑土、江西红壤和青海草甸土的比移值(R_f)分别为0.19、0.17、0.29和0.17,异菌脲在4种土壤中均属于不易移动,土柱淋溶试验结果表明,异菌脲在4种土壤中均属于难淋溶,不易通过淋溶作用造成地下水污染。     

Removal of pharmaceutical and personal care products by sequential ultraviolet and ozonation process in a full-scale wastewater treatment plant

The application of appropriate advanced treat- ment process in the municipal wastewater treatment plants （WWTPs） has become an important issue considering the elimination of emerging contaminants, such as pharma- ceutical and personal care products （PPCPs）. In the present study, the removal of 13 PPCPs belonging to different therapeutic classes by the sequential ultraviolet （UV） and ozonation process in a full-scale WWTP in Beijing was investigated over the course of ten months. Most of the target PPCPs were effectively removed, and the median removal efficiencies of individual PPCPs, ranging from -13% to 89%, were dependent on their reaction rate constants with molecular ozone. Noticeable fluctuation in the removal efficiencies of the same PPCPs was observed in different sampling campaigns. Nevertheless, the sequential UV and ozonation process still made a significant contribution to the total elimination of most PPCPs in the full-scale WWTP, by compensating for the poor or fluctuant removal performance of PPCPs by biologic treatment process.     

臭氧污染胁迫下植物的抗氧化系统调节机制

工业和农业的快速发展导致近地层O3浓度不断提高,这对陆地生态系统的动物、植物、微生物和人类健康造成伤害。O3对植物的影响尤其是对农作物的影响将关系到世界粮食的安全生产。O3污染胁迫可诱导植物产生活性氧物质,破坏植物的膜系统,影响植物的光合作用等正常生理功能。植物在自然适应过程中,可形成一套抗氧化机制来缓解O3胁迫伤害。综述了国内外近年来有关O3胁迫下植物抗氧化系统调节机制的研究进展,包括植物通过调节体内的抗氧化酶活性和非酶类物质含量来缓解O3对植物伤害的机制。O3污染胁迫下植物可调节其叶片超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)、抗坏血酸过氧化物酶(APX)、脱氢抗坏血酸还原酶(DHAR)和单脱氢抗坏血酸还原酶(MDAR)等抗氧化酶的活性。抗坏血酸(AsA)、类胡萝卜素(Car)和谷胱甘肽(GSH)等非酶类物质在清除O3胁迫产生活性氧方面具有重要的作用。另外,根据目前的研究进展,提出了一些需要继续深入探讨的问题。     

O3浓度升高对麦田土壤碳、氮含量和酶活性的影响

近地层O₃作为全球最重要的大气污染物之一,其对作物的生长发育、土壤酶活性、土壤碳、氮的影响机制已成为人们关注的重要问题。采用开顶式气室(OTCs)法模拟研究O₃浓度升高对冬小麦土壤碳、氮含量和酶活性的影响。结果表明,O₃浓度升高导致麦田0~10 cm和10~20 cm土层的全碳(TC)和全氮(TN)含量呈现出下降的趋势。O₃浓度升高对土壤酶活性也有影响。在冬小麦灌浆期,O₃胁迫可促进土壤脱氢酶活性提高。当O₃浓度为120 nL·L^-1时,0~10 cm、10~20 cm和20~40 cm土层的脱氢酶活性分别比对照处理提高59.4%、51.5%和22.2%。O₃胁迫对土壤转化酶活性的影响随着冬小麦生长期和土壤采样深度的不同而发生变化。在冬小麦拔节期,O₃处理对不同土层脲酶活性的影响没有达到显著差异水平,但是在灌浆期,20~40 cm土层的脲酶活性随着O₃浓度的增加而提高,在120 nL·L^-1浓度O₃处理下脲酶活性比对照处理提高24.6%。在O₃胁迫条件下土壤转化酶活性与土壤全碳含量、土壤脲酶活性与土壤全氮含量均呈现出显著的正相关关系。     

Review on research and application of mesoporous transitional metal oxides in water treatment

This paper reviews the application of meso- porous transitional metal oxides in water treatment on basis of the catalysis and adsorption. Mesoporous transitional metal oxides are characterized by their intrinsic features, such as a high surface area, a highly ordered array of unidimensional pores with a very narrow pore size distribution, and highly dispersed active sites. Finally, the suggestions of further study on application are proposed.