绿色食品产地土壤中PAHs测定方法研究

对绿色食品产地土壤中多环芳烃的气相色谱质谱联用分析法进行了研究。样品经索氏提取后硅胶氧化铝复合柱净化,最后用GC/MS内标法进行定性定量分析。方法相关系数除苯并(a,h)蒽的相关系数R2=0.9970外,其余目标化合物的相关系数R2均大于0.9991,各化合物线性关系良好。方法加标回收率大多在70%至90%间,各目标化合物的方法检测限为2.2～40ng/kg。     

驯化菌株降解油制气废水能力的比较

从3种污泥中驯化筛选出10种菌株,研究了各菌株对油制气废水不同污染指标的处理能力差别,以及各菌株对废水中芳烃化合物的降解能力.结果表明,各菌株可在初始阶段提高废水的BOD值,在高低废水浓度条件的降解能力基本一致;酚的去除率可达93.9%,但对废水中氨氮的去除率小于27.3%;实验采用的3种菌株对废水中的芳烃化合物都能降解,但其对芳环数≤3的芳烃化合物的降解能力强于对芳环数为4~6的芳烃化合物的降解能力.图4表2参10     

取代芳烃对绿藻、斜生栅列藻急性毒性的自相关拓扑指数

本文提出新的原子生物活性值 (ai) ,由其建构自相关拓扑指数 ( mL) . 1 6种氯代芳烃对绿藻的急性毒性 ( -lgEC50 )与其0 L ,1L的回归方程为 :-lgEC50 =0 6 1 99+2 6 1 6 3× 1 0 - 6　1L2 5+ 0 0 0 92 0 L ,r=0 936 3. 1 8种苯酚、苯胺类化合物对斜生栅列藻的急性毒性 ( -lgEC50 )可以表示为 :-lgEC50 =1 1 374 + 0 1 4 4 71L0 6+ 0 0 0 2 70 L,r=0 95 35 .用Jackknife法检验 ,以上模型具有总体稳健性 .     

Survey of polycyclic aromatic hydrocarbons (PAHs) in arterial street air of Hangzhou

ＩｎｔｒｏｄｕｃｔｉｏｎＰｏｌｙｃｙｃｌｉｃａｒｏｍａｔｉｃｈｙｄｒｏｃａｒｂｏｎｓ (ＰＡＨｓ)ａｒｅｗｉｄｅｓｐｒｅａｄｅｎｖｉｒｏｎｍｅｎｔａｌｐｏｌｌｕｔａｎｔｓｉｎｔｈｅａｔｍｏｓｐｈｅｒｅ.Ｔｈｅｙａｒｅｇｅｎｅｒａｔｅｄｉｎｔｈｅｃｏｍｂｕｓｔｉｏｎ .Ｔｈｅｍａｊｏｒｓｏｕｒｃｅｓｉｄｅｎｔｉｆｉｅｄｉｎｃｌｕｄｅｆｏｓｓｉｌｆｕｅｌｓ,ｖｅｈｉｃｕｌａｒｔｒａｆｆｉｃ,ｉｎｄｕｓｔｒｉａｌｐｒｏｃｅｓｓｅｓ,ｓｍｏｋｉｎｇａｎｄｄｏｍｅｓｔｉｃｈｅａｔｉｎｇ (Ｐｅｌｔｏｎｅｎ ,1995) .Ｔ…     

Partition of polycyclic aromatic hydrocarbons on organobentonites from water

ＩｎｔｒｏｄｕｃｔｉｏｎＴｈｅａｌｕｍｉｎｏｓｉｌｉｃａｔｅｓｈｅｅｔｓｏｆｂｅｎｔｏｎｉｔｅｐｏｓｓｅｓｓａｎｅｔｎｅｇａｔｉｖｅｅｌｅｃｔｒｉｃａｌｃｈａｒｇｅｃｏｍｐｅｎｓａｔｅｄｆｏｒｂｙｉｎｏｒｇａｎｉｃｅｘｃｈａｎｇｅａｂｌｅｃａｔｉｏｎｓ(ｅ.ｇ.,Ｎａ+ａｎｄＣａ2+),ｗｈｉｃｈｓｔｒｏｎｇｌｙｈｙｄｒａｔｅｄｉｎｔｈｅｐｒｅｓｅｎｃｅｏｆｗａｔｅｒ.Ｓｕｒｆａｃｅｐｒｏｐｅｒｔｉｅｓｏｆｎａｔｕｒａｌｂｅｎｔｏｎｉｔｅｃａｎｂｅｍｏｄｉｆｉｅｄｂｙｓｉｍｐｌｅｉｏｎｅｘｃｈａｎｇｅｗｉ…     

Detection of polycyclic aromatic hydrocarbons using a high performance-single particle aerosol mass spectrometer

The real-time detection of the mixing states of polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs in ambient particles is of great significance for analyzing the source, aging process, and health effects of PAHs and nitro-PAHs; yet there is still few effective technology to achieve this type of detection. In this study, 11 types of PAH and nitro-PAH standard samples were analyzed using a high performance-single particle aerosol mass spectrometer (HP-SPAMS) in lab studies. The identification principles ‘parent ions’ and ‘mass-to-charge (m/z) = 77’ of each compound were obtained in this study. It was found that different laser energies did not affect the identification of the parent ions. The comparative experiments of ambient atmospheric particles, cooking and biomass burning emitted particles with and without the addition of PAHs were conducted and ruled out the interferences from primary and secondary organics on the identification of PAHs. Besides, the reliability of the characteristic ions extraction method was evaluated through the comparative study of similarity algorithm and deep learning algorithm. In addition, the real PAH-containing particles from vehicle exhaust emissions and ambient particles were also analyzed. This study improves the ability of single particle mass spectrometry technology to detect PAHs and nitro-PAHs, and HP-SPAMS was superior to SPAMS for detecting single particles containing PAHs and nitro-PAHs. This study provides support for subsequent ambient observations to identify the characteristic spectrum of single particles containing PAHs and nitro-PAHs.     

Uptake and accumulation of phenanthrene and pyrene in spiked soils by Ryegrass(Lolium perenne L.)

Phytoremediation has long been recognized as a cost-effective method for the removal of polycyclic aromatic hydrocarbons （PAHs） from soil. A study was conducted to investigate the uptake and accumulation of PAHs in root and shoot of Lolium perenne L. Pot experiments were conducted with series of concentrations of 3.31-378.37 mg/kg for phenanthrene and those of 4.22-365.38 mg/kg for pyrene in a greenhouse. The results showed that both ryegrass roots and shoots did take up PAHs from spiked soils, and generally increased with increasing concentrations of PAH in soil. Bioconcentration factors（BCFs） of phenanthrene by shoots and roots were 0.24- 4.25 and 0.17-2.12 for the same treatment. BCFs of pyrene by shoots were 0.20-1.5, except for 4.06 in 4.32 mg/kg treatment, much lower than BCFs of pyrene by roots （0.58-2.28）. BCFs of phenanthrene and pyrene tended to decrease with increasing concentrations of phenanthrene and pyrene in soil. Direct uptake and accumulation of these compounds by Lolium perenne L. was very low compared with the other loss pathways, which meant that plant-promoted microbial biodegradation might be the main contribution to plant-enhanced removal of phenanthrene and pyrene in soil. However, the presence of Lolium perenne L. significantly enhanced the removal of phenanthrene and pyrene in spiked soil. At the end of 60 d experiment, the extractable concentrations of phenanthrene and pyrene were lower in planted soil than in non-planted soil, about 83.24%-91.98% of phenanthrene and 68.53%-84.10% of pyrene were removed from soils, respectively. The results indicated that the removal of PAHs in contaminated soils was a feasible approach by using Lolium perenne L.     

Development of a continuously stirred flow cell for investigating sorption mass transfer

This paper introduces a new reversible-flow design for a continuously stirred reactor used to study sorption mass transfer in soil and solvent systems. The stirred reactor has potential advantages over conventional packed column or batch reactors because it isolates intraparticle sorption rate limitations from advective-dispersive transport, yet allows changes to flux through the reactor for analysis of sorption kinetics under dynamic conditions. Previously, stirred reactors have often failed due to clogging of sediment on the effluent frit. The reverse-flow backwashing design allows longer life and higher confidence in maintaining mixed conditions than previous designs. Mass transfer 'rate coefficients estimated from stirred and column experiments are compared; both techniques produced results consistent with a published correlation. The data also show that fitted sorption mass transfer coefficients can be strongly dependent on the choice of equilibrium partition coefficient (i.e. batch or first-moment derived values), and that the conventional two-site sorption kinetics model fails to accurately predict sorption mass transfer in the presence of changing solvent velocity through the reactor.     

人工湿地处理系统中多环芳烃的行为

采用Oasis HLB柱固相萃取的前处理技术,以气相色谱质谱联用仪(GC/MS)的分析方法,对我国北方永定河上游黑土洼人工湿地中多环芳烃污染的特征以及分布规律进行了研究.结果表明,该湿地系统以低环数多环芳烃污染为主,其中浓度最高的是菲和蒽,未检出高环数(5环、6环)多环芳烃.通过比较进水和出水的浓度,湿地系统总体上不能有效去除进水中的多环芳烃.但是比较不同工艺单元进出水浓度,复氧、植物根系及微生物等均影响到多环芳烃的去除效果,去除率在28%～65%之间.     

人工湿地处理系统中多环芳烃的行为

采用Oasis HLB柱固相萃取的前处理技术,以气相色谱质谱联用仪（GC/MS）的分析方法,对我国北方永定河上游黑土洼人工湿地中多环芳烃污染的特征以及分布规律进行了研究.结果表明,该湿地系统以低环数多环芳烃污染为主,其中浓度最高的是菲和蒽,未检出高环数（5环、6环）多环芳烃.通过比较进水和出水的浓度,湿地系统总体上不能有效去除进水中的多环芳烃.但是比较不同工艺单元进出水浓度,复氧、植物根系及微生物等均影响到多环芳烃的去除效果,去除率在28%～65%之间.