焦化废水中多环芳烃的成分谱及污染特征

液-液萃取-高效液相色谱法分析了焦化废水中EPA优先控制的16种多环芳烃含量,总结出其成分谱及污染特征。结果表明:16种多环芳烃在焦化废水中浓度差异较大,主要以在水中溶解度较大的萘、苊、芴、菲、荧蒽、芘为主。其中萘对多环芳烃总量的贡献最大,占总量的36.70%~86.78%。焦化企业排放废水中6种多环芳烃的总量无超标现象,苯并[a]芘单体超标较普遍。     

用含油污泥制备油田调剖剂

采用油田含油污泥研制了油田调剖剂（含油污泥调剖剂）,对其性能进行了评价,并进行了现场应用。综合考虑性能成本等因素,含油污泥调剖剂的最佳配方为（w）：聚丙烯酰胺0.20%,交联剂A 0.30%,稳定剂B 0.15%,含油污泥10%~20%。含油污泥调剖剂对岩心的封堵率比常规调剖剂高3.5%,且二者对岩心的封堵率均大于90%。含油污泥调剖剂现场应用5井次,累计处理含油污泥1 880 t,注水压力平均上升2 MPa,累计增油160 t,减水6 500 m3,经济创效583 000元,投入产出比为1∶1.5。     

平流层臭氧深度侵入对典型城区的影响过程分析

中纬度平流层臭氧深度侵入是造成对流层至近地面臭氧浓度突增的原因之一。筛选春夏季臭氧浓度升高时段的高分辨率大气再分析数据ERA5,以位涡值的下沉趋势分析了对流层顶折叠位置及变化过程;以AIRS数据反演了臭氧浓度、一氧化碳浓度和相对湿度的垂直廓线,并估计了其分布及相关性;以近地表污染物浓度变化、HYSPLIT模型后向轨迹分析结果证实了臭氧侵入气团的运移轨迹和局地效应;通过激光雷达监测结果观测臭氧垂直浓度分布,确定了臭氧浓度最大值所处高度,判定了受影响近地点的浓度升高时刻;以边界层高度变化、气象条件分析结果及当地与周边城市地面监测数据的逐小时变化情况等综合信息,进行了区域确认和近地面影响判定。通过以上数值综合分析,对城市地区受平流层臭氧深度侵入影响的过程和具体时间进行了详细再现,可为排除非人为排放因素导致的近地表臭氧浓度增加提供回溯分析,为臭氧污染防控决策提供依据。     

Vertical distribution and environmental significance of sulfur and oxygen heterocyclic aromatic hydrocarbons in soil samples collected from Beijing, China

Vertical distribution of the concentration and composition of some sulfur and oxygen heterocyclic aromatic hydrocarbons (SOHAHs), such as, fluorene, dibenzofuran, dibenzothiophene and their alkyl homologues in 10 soil profiles in Beijing have been investigated. The results showed that the concentrations and composition of SOHAHs in topsoil (0-30cm) from different profiles are different. The concentrations of SOHAHs in topsoils are much higher than that in bottom soils where the concentrations are relatively constant. The fingerprints of SOHAHs from same profile are similar in topsoil samples, which are obviously different at the deep part, which suggested that the sources of these compounds are consistent in topsoil and are discriminating between surface and bottom soils. The main sources of SOHAHs in surface soil were fossil fuel combustion, petroleum and wastewater irrigation, while those at deep part were likely derived from the degradation products of soil organic matters.     

休耕对抚仙湖周边农田土壤剖面和浅层地下水中氮累积的影响

减少外源氮投入能有效降低农田土壤氮累积和地下水氮污染,休耕是减少外源氮投入的重要措施之一.为探讨农田休耕对土壤剖面和浅层地下水中氮累积的影响,以抚仙湖周边农田土壤剖面和浅层地下水为研究对象,分析了休耕前（2017年12月）和休耕后（2020年8月和2021年4月）农田0~100 cm土壤剖面氮累积和浅层地下水中氮浓度的变化及其两者的关系.结果表明:休耕显著降低了土壤剖面氮含量和储量,休耕后0~30、30~60和60~100 cm土壤剖面TN、ON、DTN、NO₃ ^--N和NH₄ ⁺-N含量分别降低18.4 %~36.5 %、16.1 %~26.8 %、54.0 %~130.2 %、59.5 %~90.8 %和60.1 %~110.6 %.休耕前0~100 cm土壤TN、ON、DTN、 NO₃ ^--N和NH₄ ⁺-N储量分别为（17.20 ±0.97）t·hm^-2、（15.50 ±1.23）t·hm^-2、（0.68 ±0.06）t·hm^-2、（266.8 ±31.17）kg·hm^-2和（18.7 ±3.04）kg·hm^-2,休耕后各形态氮储量分别下降了25.5 %、23.3 %、44.7 %、80.1 %和59.9 %.休耕也改变了浅层地下水中氮浓度和形态构成,休耕后地下水中TN、ON、NO₃ ^--N和NH₄ ⁺-N浓度分别下降了88.4 %、82.7 %、92.1 %、65.8 %,ON/TN和NH₄ ⁺-N/TN从休耕前的26 %和6 %升高至休耕后的39 %和17 %,而NO₃ ^--N/TN从休耕前的61 %降至休耕后的41 %.地下水氮浓度和形态变化与休耕前后土壤中DTN、NH₄ ⁺-N、NO₃ ^--N和地下水中pH、ORP、DO等因素密切相关.可见,休耕有效降低了农田土壤剖面氮累积,缓解了浅层地下水氮污染,有利于防止高原湖泊的水质恶化.     

Initial Adjustments Within a New River Channel: Interactions Between Fluvial Processes, Colonizing Vegetation, and Bank Profile Development

A conceptual model of the morphological development of the riparian margins of newly cut river channels is presented, suggesting early feedbacks between vegetation growth and bank form. To test the model, observations of long and cross profiles, bank sediment and seed deposition, and bank vegetation development were collected over the first 2 years of river flows through a reach of the River Cole, West Midlands, UK. The newly created channel had a sinuous planform and varying asymmetric trapezoidal cross section in sympathy with the planform. No imposed bedforms or bank reseeding were included in the design. Over the 2 years, development of bedforms was rapid, with bed sediment sorting and bank profile adjustment occurring more steadily and progressively. Six classes of bank profile were identified by the end of the study period, illustrating close associations with sediment aggradation, vegetation colonization, and growth patterns. Vegetation colonization of the banks was seeded predominantly from local sources during the summer and from hydrochory (transport by the river) during the winter. Colonizing vegetation on the riverbanks appeared to act as a significant propagule source by the second summer and as an increasingly important roughness element, trapping both propagules and sediment, within the second year and providing early feedback into bank evolution. As a result, the time required for riparian margin development in the conceptual model was found to be considerably longer than observed in the study river. In addition, the role of surface wash/bank failure in modifying the bank profile and transporting seeds onto the upper bank face during the first year of bank development was found to be important in initiating rapid bank vegetation colonization and surface stabilization. This set of processes had not been incorporated in the initial conceptual model. In relation to channel restoration, this research illustrates that in small temperate rivers of modest energy the provision of an initial, sinuous corridor is sufficient to induce rapid development of fluvial features and vegetation cover without the need to construct bed forms or to seed the banks.     

室内多环芳烃污染源的化学组成特征研究

运用环境舱模拟源排放的方法采集了烹调油烟与环境烟草烟雾的样本,对18种PAHs进行了定量分析.比较了不同食用油与不同品牌香烟产生PAHs组成特征的差异,初步建立了2类室内PAHs来源的化学成分谱.结果表明:烹调油烟中3环以下的PAHs为主体,Fluo,Pyr和Flu相对含量较为稳定;香烟烟雾以3～4环组分为主体,Flu,Phe,InP和BaA较为稳定,Cor含量较烹调油烟而言显著增加.2类源的ρ(BaA)/ρ(Chy),ρ(BeP)/ρ(BaP)与ρ(InP)/ρ(BghiP)稳定且存在显著差异,可以用来解析室内PAHs以及PAHs暴露的来源.运用等效毒理学因子估算了其危害程度,结果表明:每100 g食用油在烹调过程(60 min)中释放产生PAHs的毒理学效应仅为吸烟过程中每g烟草所产生PAHs毒理效应的一半.      

黄土高原沟壑区小流域不同地形下土壤性质分布特征

地形条件是影响黄土高原地区土壤性质分布的主要因素,研究不同地形条件下土壤性质的分布是合理评价黄土区土壤质量状况的重要前提。论文研究了黄土高原沟壑区小流域地形条件对土壤性质剖面分布的影响,结果表明土壤硝态氮、速效磷、碱性磷酸酶和蔗糖酶为高度变异的土壤性质;pH值和过氧化氢酶为小变异土壤性质。塬面和沟道土壤pH值和过氧化氢酶活性较低,阳离子交换量较高。土壤有机质、全氮、全磷、速效磷、碱性磷酸酶和蔗糖酶活性在土壤剖面随土层深度的增加逐渐降低,且均表现为塬面>梯田>坡地>沟道的趋势。不同地形条件下土壤pH值的变化由地形条件引起的土壤过程及硝态氮在土壤中的累积引起;阳离子交换量的变化由成土过程、pH值和有机质的差异引起;土壤有机质及氮、磷养分的差异由与地形条件对应的土地利用方式引起;土壤酶活性的差异则是有机质的差异引起的。     

A performance comparison between nonlinear similarity functions in bulk parameterization for very stable conditions

Three sets of nonlinear similarity functions for strong stability are selected to compare their performance in bulk parameterization. To uncover their advantages and disadvantages, theoretical and measurement analyses are made with four profile metrics and the Deacon number technique. Main disadvantages include the negligence of the different transfer efficiency between momentum and heat, the flux cutoff due to the upper limit in gradient Richardson number (Ri) and the ignorance of limited stability range where the dimensionless gradient functions ( and ) approach constants. Accordingly, three suggestions are made for future improvement. First, the functions for wind velocity and potential temperature should have the same function form, but with different coefficients. Second, and should approach constants only within a certain stability range. Third, the limit value in Ri should be avoided to widen their applicability in flux modeling. Furthermore, quantitative comparisons in transfer coefficients for moment and sensible heat (C _D and C _H) are made among the similarity functions in the bulk Richardson number (Ri _B) range 0 < Ri _B < 1. Generally, significant discrepancy is found, which may approach a factor of two and three at large Ri _B in C _D and C _H, respectively. Finally, a new recommendation is made to one of the three sets, mainly because of its ability to predict C _D and C _H that decrease rather slowly in very stable conditions.     

Source profiles of particulate organic matters emitted from cereal straw burnings

Cereal straw is one of the most abundant biomass burned in China but its contribution to fine particulates is not adequately understood. In this study, three main kinds of cereal straws were collected from five grain producing areas in China. Fine particulate matters （PMzs） from the cereal straws subjected to control burnings, both under smoldering and flaming status, were sampled by using a custom made dilution chamber and sampling system in the laboratory. Element carbon （EC） and organic carbon （OC） was analyzed. 141 compounds of organic matters were measured by gas chromatography-mass spectrum （GC-MS）. Source profiles of particulate organic matters emitted from cereal straw burnings were obtained. The results indicated that organic matters contribute a large fraction in fine particulate matters. Levoglucosan had the highest contributions with averagely 4.5% in mass of fine particulates and can be considered as the tracer of biomass burnings. Methyloxylated phenols from lignin degradation also had high concentrations in PM2.5, and contained approximately equal amounts of guaiacyl and syringyl compounds. 13-Sitostrol also made up relatively a large fraction of PMz5 compared with the other sterols （0.18%-0.63% of the total fine particle mass）. Normal alkanes, PAHs, fatty acids, as well as normal alkanols had relatively lower concentrations compared with the compounds mentioned above. Carbon preference index （CPI） of normal alkanes and alkanoic acids showed characteristics of biogenic fuel burnings. Burning status significantly influenced the formations of EC and PAHs. The differences between the emission profiles of straw and wood combustions were displayed by the fingerprint compounds, which may be used to identify the contributions between wood and straw burnings in source apportionment researches.