疏水性有机污染物在草甸土中的吸附和解吸行为

研究5种有机污染物在草甸土中的吸附和解吸行为.结果表明,污染物在土壤中的吸附主要受疏水性作用的影响,吸附数据基本符合传统的线性模型.解吸行为则表现出明显的滞后现象,解吸实验结果与"双元平衡解吸(DED)模型"的预测值相吻合.DED模型能够更加准确地定量描述疏水性有机污染物的解吸行为.     

环境介质中有机污染物运移的数值模型

在综合考虑有机污染物在土壤-水环境体系中扩散、吸附解吸、分配以及土壤-水界面微生物降解条件下，建立了环境介质中有机污染物迁移转化的非平衡动力学模型，并编制相应的有限元程序，利用该程序对落地原油在土壤中迁移转化非平衡模式与平衡模式进行对比模拟分析，探讨了模型参数kd、λ、λ^*的变化对有机污染物迁移的影响，为定量研究土壤中有机污染物在土壤-水环境中分配与归宿提供了可靠的理论依据，同时为土壤环境质量评价及污染预测、预报与污染防治提供科学的根据与途径．图4表1参11     

土壤中反应性溶质保持模拟模型概述

水溶性污染物和有机污染物在非饱和带的运动规律是当前土壤物理学研究的前沿领域．模拟反应性溶质的运移模型，必须包含溶质和土壤基质之间的保持和释放反应．本文简要综述土壤对溶质保持反应的平衡模型、动力学模型和多反应模型的主要特点．     

酸性土壤中Cd2+的吸附与运移特性

采用平衡吸附和室内土柱淋溶实验研究Cd2 在酸性土壤中的吸附和运移规律.结果表明:红壤和砖红壤中Cd2 的吸附,在其低浓度范围内符合线性等温方程,Cd2 在砖红壤上的分配系数是红壤上的8倍,能较好地用一级动力学方程的两点和一点模型拟合Cd2 的吸附.红壤快反应的比例约为50%-60%,砖红壤快反应的比例约为90%-95%.采用两点位非平衡模型,红壤β值范围为0.50-0.70,f值的范围是0.40-0.60,仅有40%-60%的吸附点位是瞬间完成,还有一部分吸附点位受速率限制,用非平衡两点模型比用平衡模型能更好地描述Cd2 的运移规律;而砖红壤β值在0.93-0.99,f＞0.92,有大于 90%的吸附点位是瞬间完成,不到10%受速率限制,很容易达到局部平衡,运用平衡模型可能更适合,这与动力学方程的结果基本一致.     

生物炭的制备温度及酸处理对卡马西平的吸附动力学影响

本研究考察了卡马西平(CBZ)在9种不同条件(裂解温度200、300、500℃,无酸,HCI和HCI-HF)处理的生物炭上的吸附动力学,分别应用拟一级、拟二级和双室一级3种动力学模型对实验数据进行拟合.研究结果表明,双室一级动力学模型对吸附动力学提供了更精确的描述.裂解温度和酸处理对CBZ的吸附动力学有显著影响,具体表现为不同酸洗导致矿物含量发生显著变化,矿物对生物炭吸附CBZ的快室吸附单元起主要作用,生物炭内部的芳香环随生物炭的升高而更加致密,生物炭内部的芳香环结构主要贡献于慢室吸附单元.生物炭的矿物组分一方面屏蔽了有机质上的一些吸附点位,另一方面矿物自身可以有效地吸附污染物,酸洗去矿物对生物炭吸附污染物的表观影响可能取决于两个方面的平衡.     

蚯蚓活动对重金属在土柱中淋溶行为的影响

采用土柱淋溶方法,以溴离子为示踪离子,研究了蚯蚓活动形成的土壤大孔隙对铜和锌离子在土柱中迁移行为的影响.运用平衡和非平衡对流-弥散模型对溴离子和铜、锌离子在不同土柱中的穿透曲线进行拟合.结果表明,蚯蚓活动形成的蚯蚓孔能够产生明显的优势流现象,这种优势流极大地加快了重金属离子在土柱中垂直向下迁移的速度.非平衡对流-弥散模型能很好地预测溴离子和铜、锌离子在蚯蚓孔土柱中的流出趋势,而平衡对流-弥散模型适合于预测溶质在对照（匀质）土柱中的流出趋势.     

土壤胶体对重金属运移行为的影响

累积在表层土壤中的重金属,在一定条件下可以向地下迁移,进而影响地下水水质.由于现有污染物运移预测模型对重金属等污染物在土壤中运移的预测与实际监测结果偏差巨大,土壤胶体对土壤重金属运移的影响越来越受到人们的重视.土壤胶体组成丰富,在土壤环境中广泛存在.土壤胶体能够与重金属等污染物质相结合,对重金属等污染物质的运移产生重要影响.土壤胶体运移和土壤胶体与重金属的相互作用受到水动力、pH、离子强度、胶体粒径、土壤含水率等多种物理化学条件的影响.本文综述了土壤胶体对土壤重金属运移影响的诸多因素,介绍了胶体作用下重金属等污染物在多孔介质中的运移模型,提出了当前研究中存在的问题,并对今后需要展开的工作提出了建议.     

江河有机污染物迁移转化过程的实验室模拟

本文研究了第二松花江10种有机污染物的迁移转化规律,得到挥发、微生物降解、光解、沉积物吸附与解吸过程均遵守一级动力学.计算了动力学参数,并用箱式模型和所取得的参数预测了有机污染物的迁移转化规律,预测结果与实测值符合较好.     

针铁矿/蒙脱石与黑炭复合物对泰乐菌素的吸附

黑炭作为大气PM2.5的核心组分,可以通过大气的干湿沉降进入到土壤,从而对土壤中有机污染物的迁移转化产生一定的影响.而土壤中普遍存在的矿物会与黑炭发生一定的界面作用.因此,明确这种作用对污染物迁移转化的影响,会为科学合理评价污染物的生态环境风险提供理论依据.本文以针铁矿和蒙脱石为矿物代表,以泰乐菌素(TYL)为有机污染物的代表,系统研究了针铁矿/蒙脱石与黑炭复合物对TYL的吸附特性.吸附动力学、吸附等温线、以及pH和离子强度的实验表明,黑炭与针铁矿/蒙脱石复合后其对TYL的吸附能力明显高于单独的针铁矿和蒙脱石;黑炭与针铁矿复合物(Fe OOH-BC)和黑炭与蒙脱石复合物(MT-BC)对TYL的吸附动力学可以用拉格朗日二级动力学模型较好地拟合;吸附等温线用线性模型和Freundlich模型拟合的效果相对较好;pH和离子强度的实验表明,溶液pH和离子强度可以明显地影响Fe OOH-BC和MT-BC对TYL的吸附;Fe OOH-BC对TYL的吸附主要是氢键作用、范德华力和表面络合作用,而MT-BC对TYL吸附机理则主要是静电作用和离子交换.     

土壤和地下水中污染物迁移模型研究进展

国内外学者已建立了多种模型来描述污染物在土壤和地下水中的环境行为。要选择一个合适的模型在实际中成功地应用,或建立一个新的模型,必须掌握和了解污染物迁移模型的研究现状。文章评述了现有的模型,并对模型的结构作了一定的阐述。     

不同含水量细砂介质中挥发苯的有效扩散系数研究

挥发性有机污染物在土壤多孔介质中的有效扩散系数是土壤气相抽提(soil vapor extraction,SVE)传质过程中的一个重要参数.笔者以苯为研究对象,采用土柱扩散试验,对不同含水量条件下挥发苯在细砂介质中的有效扩散系数和扩散规律进行研究.结果表明,对于吸附型矿物含量少的细砂介质,含水量大小在一定程度上影响了挥发苯的扩散过程.含水量在50 g·kg-1时,扩散最快;低于50 g·kg-1时,随含水量增大扩散能力增强;高于50 g·kg-1时,扩散能力则随含水量增大而减弱.同一扩散柱中,随着扩散距离增加,挥发苯的有效扩散系数增大,这可能与其蒸汽分压降低有关.     

大气挥发性有机化合物环境基准研究进展与展望

挥发性有机化合物(VOCs)中的许多物种对人体具有危害性,同时,VOCs对大气环境产生着重要的影响。目前我国部分区域大气VOCs污染已经十分严重,控制大气VOCs污染对于改善环境空气质量,保护人体健康具有重要意义。国际上许多国家或国际组织制定了大气VOCs环境基准或者发布了大气VOCs环境基准指导值,这对于加强VOCs污染控制及环境管理可以起到重要作用。我国尚未制定大气VOCs环境基准,亟待开展系统的研究工作。在综述国际大气VOCs环境基准研究进展,介绍当前我国大气VOCs环境基准研究情况的基础上,分析了我国大气VOCs环境基准的研究需求,并对今后的系统研究提出了建议。     

VOCs走航监测:技术方法与案例应用

挥发性有机物(VOCs)来源广泛、组成复杂,是臭氧(O3)和二次有机气溶胶(SOA)的重要前体物,且其中一些组分对人体健康存在潜在威胁。VOCs的主要排放方式包括点源、面源和无组织源排放,排放过程具有瞬时性,难以控制和监测。与传统的离线监测和在线监测相比,走航监测技术具有监测范围大、响应快速、机动性强的特点,但中国VOCs的走航监测研究还鲜有报道。该研究通过使用装载了单质谱分析仪与便携式气相色谱-质谱联用仪(GC-MS)的走航车对珠三角沿海城市某工业集聚区进行VOCs走航监测,走航过程中对环境空气中的TVOCs进行快速监测并对TVOCs质量浓度高值点进行采样及VOCs组分的成分和浓度分析。该次走航共监测到32种优控污染因子和CW加油(加气)站、JH加油站、G空调电器生产企业的两器车间及南门货场等多个TVOCs质量浓度高值点,并通过分析进一步判断VOCs排放源。结合监测结果和实地调研推断:加油站的VOCs高值主要来源于油气挥发及机动车尾气排放;G空调企业的VOCs高值则主要来源于两器车间的喷涂、烘干、洗网工序及厂区内的机动车尾气排放。尽管VOCs走航监测技术目前还存在一定不足,该方法的应用能够为掌握区域VOCs污染现状及分布特征提供新的技术手段,为实现VOCs精细化管控提供新的思路。     

香港大气中有毒挥发性有机物研究

用吸附／热脱除－ＧＣ＝／ＭＳ方法研究了香港不同功能区大气中挥发笥有机物的组成。分析结果表明，香港大气中存在６０多种ＶＯＣＳ，其主要成分是苯系物，烷烃和卤代烃。在检出物中有１７种是有毒挥发性有机物，其主要成分是苯系物和氯代烃。其中氯仿，苯，甲苯，四氯乙烯，三氯乙烯和１，２－二氯乙烷是含量最高的组分。     

A review on application of dielectric barrier discharge plasma technology on the abatement of volatile organic compounds

• Applications of non-thermal plasma reactors for reduction of VOCs were reviewed. • Dielectric barrier discharge (DBD) plasma was considered. • Effect of process parameters was studied. • Effect of catalysts and inhibitors were evaluated. Volatile organic compounds (VOCs) released from the waste treatment facilities have become a significant issue because they are not only causing odor nuisance but may also hazard to human health. Non-thermal plasma (NTP) technologies are newly developed methods and became a research trend in recent years regarding the removal of VOCs from the air environment. Due to its unique characteristics, such as bulk homogenized volume, plasma with high reaction efficiency dielectric barrier discharge (DBD) technology is considered one of the most promising techniques of NTP. This paper reviews recent progress of DBD plasma technology for abatement of VOCs. The principle of plasma generation in DBD and its configurations (electrode, discharge gap, dielectric barrier material, etc.) are discussed in details. Based on previously published literature, attention has been paid on the effect of DBD configuration on the removal of VOCs. The removal efficiency of VOCs in DBD reactors is presented too, considering various process parameters such as initial concentration, gas feeding rate, oxygen content and input power. Moreover, using DBD technology, the role of catalysis and inhibitors in VOCs removal are discussed. Finally, a modified configuration of the DBD reactor, i.e. double dielectric barrier discharge (DDBD) for the abatement of VOCs is discussed in details. It was suggested that the DDBD plasma reactor could be used for higher conversion efficiency as well as for avoiding solid residue deposition on the electrode. These depositions can interfere with the performance of the reactor.     

Source apportionment and ozone formation potential of volatile organic compounds in Lagos (Nigeria)

Concentrations of volatile organic compounds (VOCs) of the city air in Oba Akran road, Lagos were investigated. The chlorinated VOCs and xylene in Oba Akran were high. The average benzene/toluene ratio in Oba Akran was 1.7 suggesting that vehicular emission was a possible VOC source in most areas of Oba Akran. The toluene/(m+p-xylene) ratio also suggests a common source of toluene and xylene at these sites, presumably organic solvent used by industries located at Oba Akran. Our results showed that 7.10 tons of CO ₂ equivalents of VOCs are being emitted per year from Oba Akran. Xylenes were found to be the largest contributor to the ozone formation followed by trichloroethylene. A multivariate statistical analysis (Factor analysis extracted with Principal Component Analysis) has been applied to a set of data, and it was found that the main principal components, extracted from the air VOC pollution data, were related to gasoline and oil combustion/industrial activities.     

易挥发有机化合物在Pt/Al_2O_3-Si纤维催化剂上的低温氧化

本文合成了一种新型的Pt负载在Al_2O_3涂膜强力富硅纤维载体的催化剂,研究低温下催化易挥发有机化合物的行为.用四种有机化合物检验实验参数对催化剂分解有机化合物分解率的影响.讨论了流速、浓度、有机物的本性、预热温度、反应热等参数的影响,并给出了催化剂对苯、甲苯在特定实验条件下的活化能、反应级数和指前因子的数值.     

土壤原位修复技术研究与应用进展

土壤原位修复技术是指不经挖掘,直接在污染场地就地修复污染土壤的土壤修复技术,具有投资低,对周边环境影响小的特点,是土壤修复的研究热点。土壤原位修复技术主要有淋洗,气相抽提（SVE）,多相抽提（MPVE）,气相喷射（IAS）,生物降解,原位化学氧化（ISCO）,原位化学还原,污染物固定,植物修复等。淋洗法主要用于治理高渗透性土壤中的重金属和难挥发降解的有机物。土壤气相抽提和喷射技术适用于处理土壤中的易挥发污染物,并有常与加热技术,生物处理技术等联用,可以起到促进污染物挥发,增氧促分解的作用。多相抽提法主要用于治理存在大量非水相流体的污染场地,可将土壤中有机相污染物直接抽出。生物降解有生物好氧降解、生物厌氧降解、生物还原降解多种,降解方式由污染物种类和地质条件决定。化学方法可将污染物氧化或还原为低毒无毒物质,周期一般较短。固定污染物可以直接加入药剂反应生成沉淀,也可制造合适条件使微生物生成可沉淀重金属的离子。植物修复主要用于富集重金属,成本低廉,但富集了重金属的植物体的有效利用尚待进一步研究。土壤原位修复需要因地制宜,灵活结合工期、污染情况、地质条件、地面设施等,得出最经济实用的修复方法,并在辅助提高技术上展开更多研究,使原位修复技术更经济有效。     

Volatile organic compounds of Acacia longifolia and their effects on germination and early growth of species from invaded habitats

Acacia longifolia, a highly invasive species that invades coastal ecosystems in Mediterranean areas, produces significant impacts at different scales. Abundant foliage and thick canopies create a dense atmosphere that led us to hypothesise that the release of volatile organic compounds (VOCs) could play a role in the reduction of biodiversity observed in invaded areas. Therefore, we suggested that VOCs emitted by A. longifolia could exert inhibitory effects on physiological and biochemical parameters of native species. Using glass chamber bioassays, we evaluated the effect of aerial contact between VOCs from different plant parts of A. longifolia material and some native species. Volatile chemical composition was further analysed using GC-MS. Our results indicated that VOCs produced a notably reduction of seed germination. Furthermore, volatiles from leaves and flowers significantly decreased root length, shoot length and biomass for all species. Proline and malondialdehyde content did not significantly increase after contact with VOCs. Finally, chemical profile of VOCs from flowers, leaves and litter was significantly different, both qualitatively and quantitatively. As far as we know, our results constitute the first evidence of phytotoxicity induced by VOCs from A. longifolia, suggesting that flowers and leaves could influence its surrounding environment through VOCs release.     

Trends of chemical speciation profiles of anthropogenic volatile organic compounds emissions in China, 2005–2020

This study estimates the detailed chemical profiles of China＇s anthropogenic volatile organic com- pounds （VOCs） emissions for the period of 2005-2020. The chemical profiles of VOCs for seven activity sectors are calculated, based on which the Photochemical Ozone Creation Potential （POCP） of VOCs for these sectors is evaluated. At the national level, the VOCs species emitted in 2005 include alkanes, alkenes and alkynes, aromatic compounds, alcohols, ketones, aldehydes, esters, ethers and halocarbons, accounting for 26.4wt.%, 29.2wt.%, 21.3 wt.%, 4.7 wt.%, 5.4 wt.%, 1.7 wt.%, 2.1 wt.%, 0.7 wt. % and 2.2wt.% of total emissions, respectively. And during 2005-2020, their mass proportions would respec- tively grow or decrease by - 34.7%, -48.6%, 108.5%, 6.9%, -32.7%, 7.3%, 65.3%, 100.5%, and 55.4%. This change would bring about a 13% reduction of POCP for national VOCs emissions in the future. Thus, although the national VOCs emissions are expected to increase by 33% over the whole period, its ozone formation potential is estimated to rise only by 14%. Large discrepancies are found in VOCs speciation emissions among provinces. Compared to western provinces, the eastern provinces with a more developed economy would emit unsaturated hydrocarbons and benzene with lower mix ratios, and aromatic compounds except benzene, oxidized hydrocar- bons and halocarbons with higher mix ratios. Such differences lead to lower POCP of VOCs emitted in eastern provinces, and higher POCP of VOCs emitted in western provinces. However, due to the large VOCs emissions from Chinese eastern region, the ozone forma- tion potential of VOCs emission in eastern provinces would be much higher than those in western provinces by about 156%-235%.