Seasonal variation of polycyclic aromatic hydrocarbons in soil and air of Dalian areas, China: an assessment of soil-air exchange

The seasonal variations of concentrations of PAHs in the soil and the air were measured in urban and rural region of Dalian, China in 2007. In soil, mean concentrations of all PAHs in summer were larger than those in winter, whereas the concentrations of heavier weight PAHs in winter were larger than those in summer. Winter/summer concentration ratios for individual PAHs (R(W/S)) increased with the increase of molecular weight of PAHs in soil, indicating that PAHs with high molecular weight were more easily deposited to soil in winter than summer. In air, mean concentrations of all PAHs in winter were larger than those in summer. In comparison with the R(W/S) in soil, all the values of R(W/S) in air were larger than one indicating that the entire individual PAH concentrations in winter were larger than those in summer. The average concentration composition for each PAH compound in soil and air samples was determined and the seasonal change of PAH profile was very small. It was suggested that PAHs in soils and air had the same or similar sources both in winter and summer. The approach to the soil-air equilibrium was assessed by calculating fugacity quotients between soil and air using the soil and air concentrations. The calculated soil-air fugacity quotients indicated that soil acted as a secondary source to the atmosphere for all lighter weight PAHs (two-three rings) and it will continue to be a sink for heavier weight PAHs (five-six rings) in the Dalian environment, both in winter and summer. Medium weight PAHs (four-five rings) were close to the soil-air equilibrium and the tendency shifted between soil and air when season or function region changed. The fugacity quotients of PAHs in summer (mean temperature 298 K) were larger than those in winter (mean temperature 273 K), indicating a higher tendency in summer than winter for PAHs to move from soil to air. The variation of ambient conditions such as temperature, rainfall, etc. can influence the movement of PAHs between soil and air. Most of the fugacity quotients of PAHs for the urban sites were larger than that for the rural site both in winter and summer. This phenomenon may be related with that the temperatures in urban sites were higher than those in the rural site because of the urban heat island effect.     

广州市白云山降水的化学特征及源解析

以2006年广州市白云山降水监测资料为基础,对其降水样品的化学特征进行了分析。结果表明,白云山降水样品pH值分布为3.04—6.41,雨量加权pH平均值为4.26,酸雨频率为70.2％,降水中的主要阳离子是Ca^2＋和NH^＋4分别占阳离子总量的46.4％和17.5％;主要阴离子为SO^2-4和NO^-3,分别占阴离子总量的59.0％和19.9％。相对酸度（FA）和中和因子（NF）计算结果表明,约有84.7％的降水酸度被碱性成分Ca^2＋和NH^＋4中和。利用富集系数方法,计算结果表明SO^2-4和NO^-3主要来源于人类活动,而Ca^2＋和K^＋主要来源于岩石／土壤风化。     

Column studies on transport of deicing additive benzotriazole in a sandy aquifer and a zerovalent iron barrier

Benzotriazole (BTA), a chemical with wide industrial applications, is a typical additive in deicer/anti-icer used at airport. To achieve a better understanding of the transport behaviour and environmental fate of BTA, laboratory column studies have been performed on subsoil samples from Oslo Airport, Gardermoen. To explore possibilities for aquifer remediation, BTA behaviour was also studied in a column of granular zerovalent iron (Fe(0)). The subsoil column study demonstrates a very limited retardation of BTA. Consecutive loadings of BTA of the subsoil column showed no change of the break-through curve (BTC) and complete desorption was observed. The sorption behaviour of BTA to metallic iron (Fe(0)) was rather complex. Considerable retardation was observed in the Fe(0) column and repeated BTA loading resulted in an earlier break-through. Between 20% and 50% of the input concentration was retained permanently in the iron (Fe(0)) column. The BTA sorption to metallic iron was found to be enhanced by chloride which lowered the break-through concentration (i.e the C/C(0) plateau). The fraction of BTA remaining in the iron column was found to vary with the flow rate, indicating a time dependant multilayer sorption mechanism. The steady increase in the amount of adsorbed BTA to the iron column during loading corresponds to a rather strong bonding of 4-15 BTA layers to the iron surface. A very slow desorption of BTA was observed; even after flushing with 753 pore volumes of BTA free water, 7.5% of the BTA remained in the column. A geochemical model was developed based on PHREEQC-2 to simulate the sorption and transport of BTA in the tested materials. The BTA sorption was modelled with Freundlich sorption isotherms, as earlier determined in batch experiments. A slight adjustment of the Freundlich parameters was required to fit the observed column break-through. However, our model was not able to simulate the long-term retainment of BTA in the granular iron columns. The simulations confirm the high mobility of BTA in groundwater aquifers and suggest that zerovalent iron could be used to retain a BTA plume, although oxidation of the sorbent might reduce the long-term performance of such a remediation scheme and slow desorption has been observed.     

A biomimetic absorbent for removal of trace level persistent organic pollutants from water

A novel biomimetic absorbent containing the lipid triolein was developed for removing persistent organic pollutants (POPs) from water. The structural characteristics of the absorbent were obtained by SEM and a photoluminescence method. Under optimum preparation conditions, triolein was perfectly embedded in the cellulose acetate (CA) spheres, the absorbent was stable and no triolein leaked into the water. Dieldrin, endrin, aldrin and heptachlor epoxide were effectively removed by the CA--triolein absorbent in laboratory batch experiments. This suggests that CA-triolein absorbent may serve as a good absorbent for those selected POPs. Triolein in the absorbent significantly increased the absorption capacity, and lower residual concentrations of POPs were achieved when compared to the use of cellulose acetate absorbent. The absorption rate for lipophilic pollutants was very fast and exhibited some relationship with the octanol--water partition coefficient of the analyte. The absorption mechanism is discussed in detail.     

江苏省危险化学品生产状况调查分析及监管对策

根据《危险化学品名录》,分析江苏省取得危险化学品安全生产许可证的1774家企业的化学品种类、数量、生产企业类型分布情况.结果表明,江苏省危险化学品生产企业在地域分布上苏南多于苏北;化工、建材行业的危险化学品生产企业所占比例较高;危险化学品涉及除爆炸品外的6大类,达3 790种,以生产易燃液体的企业数目为最多;有31家企业生产10种以上危险化学品.笔者建议,通过评估摸清企业安全生产状况,严格控制危险化学品企业安全生产许可证发放,实现危险化学品运输企业的动态管理,建立安全监测预警技术平台.     

低温试验能力验证中的不确定度分析评估

本文简述电气领域如何评定测量不确定度过程,并结合CNAS T0346低温试验能力验证计划,识别和具体分析低温试验中各测量不确定度的来源,对各种影响因素进行评价,论述人、机、料、法、环、测各环节对测量结果的影响,给出了低温试验测量结果不确定度的评估过程。     

建设项目竣工环境保护验收监测应注意的问题

针对建设项目竣工环境保护验收监测中存在的问题,阐述了工况控制、总量监测、环境相容性等环节的技术要求和注意事项,并就与之相关的公众参与、监测人员的素质等问题展开了讨论。     

中国水旱灾害危险性的时空格局研究

水灾与旱灾之间,不论在形成的原因上或是在治理措施上,都存在着相当密切的关系。受季风气候影响,中国的洪水和干旱灾害同时并存,近年来我国遭受极端水旱灾害事件的次数比以往增加很多。基于县域统计单元的水旱灾害信息,以总时段（1949—2005年）、分时段（1956—1965年,1996—2005年）、分季度和分月份4种时间尺度来划分,选取2359个县域单元上的灾害频数作为衡量水旱灾害危险性的指标,主要从危险性整体转移、高危险区转移、转移的形成因素以及高危险区的防灾减灾对策几个角度,探讨了中国水灾、旱灾以及水旱综合灾害的危险性时空分异规律。研究表明：近57年来,中国水旱灾害危险性的整体格局呈现东西分异,东部远远高于西部,这是气候一地貌一人类活动相互作用的产物。1956—1965年,我国水旱灾害危险性格局的东西分异明显;1996—2005年,水旱灾害危险性格局不变,高值区域明显增大,向东北、西北、南方扩展。水旱灾害危险性格局的季节变化显著,整体呈现夏季水旱灾害危险性高,春季次之,秋冬季危险性低的状况;月际变化与降水带的推移和承灾体的月际变化相似,7月水旱灾害危险性达到峰值。上述研究结果可为水旱灾害风险区划以及水旱灾害高危险区的减灾战略规划提供科学依据。     

面向作物病害识别的高光谱波谱库设计与开发

自20世纪70年代以来,国内外波谱数据库发展迅速,但都存在着针对性不强的缺陷,不能满足我国现阶段遥感应用的需要。该文通过以小麦条锈病为案例的高光谱波谱库的设计与开发,实现了波谱查询、影像管理、用户管理、数据管理、反演模型等功能,可供其它面向病害识别的高光谱波谱库的建立参考。     

人类抗灾体适能理论架构的研究

介绍了河北省教育科学“十一五”规划课题——体育培养大学生抗灾体适能的实践研究的阶段性研究成果。基于生物学、心理学和社会学的理论研究,通过文献资料法、访谈法和开放式调查法,提出了抗灾体适能的概念,分析了抗灾体适能的内涵和外延,并就将抗灾体适能结构划分为三个维度进行了研究,探讨了人类抗灾体适能理论模型的研究框架,提出了通过体育途径培养抗灾体适能的初步设想。