微生物对土壤与沉积物吸附多环芳烃的影响

以枯草芽孢杆菌为接种微生物,研究微生物对沉积物和湿地土壤吸附多环芳烃（PAHs）菲、苯并［a］芘过程的影响.结果表明,枯草芽孢杆菌对菲与苯并［a］芘都可进行吸附或生物降解,48h液相PAHs浓度达到平衡时,微生物对菲消除了98％,对苯并［a］芘消除85％;接种的样品48h吸附等温线均呈线形,能较好地符合线性方程;在接种微生物情况下,沉积物与土壤对菲和苯并［a］芘吸附特征均发生较大变化,对菲的吸附量增大约35倍,而对苯并［a］芘的吸附量却降低了2/3左右;未接种微生物的土壤和沉积物对菲解吸率为20％,接种的样品组为2.9％,而对苯并［a］芘的解吸结果与菲相反,未接种的对照组为4％,接种的样品组为13％.微生物在土壤与沉积物吸附PAHs的过程中起主导作用.     

土壤中多环芳烃的SPMD辅助解吸行为研究

为了开发一种表征土壤中憎水性有机污染物解吸及生物有效性的新方法,建立了半透膜被动采样装置（SPMD）研究土壤中有机污染物解吸行为的方法,利用SPMD分析了多环芳烃菲、芘和苯并［a］芘在3种不同性质土壤中的辅助解吸行为.结果表明,SPMD是一种很好地表征土壤中憎水性有机污染物解吸及生物有效性的手段. SPMD辅助解吸多环芳烃的效率与土壤有机质及多环芳烃性质有关.随着土壤有机质含量的降低,土壤中菲和芘的SPMD解吸率逐渐升高,对于10 mg/kg染毒水平,当土壤有机质含量由18.68%降低到0.3%时,2种化合物的解吸率分别由56.45%和48.28%上升到接近100%;但是对于苯并［a］芘,粘土表现出明显的滞留能力,在有机质含量（0.3%）很低、粘土含量（39.05%）较高的3号土壤中,苯并［a］芘的解吸率仅有66.97%.不同多环芳烃SPMD辅助解吸率差别很大,随着土壤有机质含量的降低,以及污染物浓度的提高,菲和芘的解吸差异逐渐缩小,而苯并［a］芘与上述2种多环芳烃的差异很大,主要是由于苯并［a］芘具有高度亲脂性,并且分子较大,造成其容易滞留在粘土的微孔及有机质的致密结构中.     

TiO2 nanotubes as solid-phase extraction adsorbent for the determination of polycyclic aromatic hydrocarbons in environmental water samples

An analytical method based on TiO2 nanotubes solid-phase extraction (SPE) combined with gas chromatography (GC) was established for the analysis of seven polycyclic aromatic hydrocarbons (PAHs): acenaphtylene, acenaphthene, anthracene, fluorene, phenanthrene, fluoranthene and pyrene. Factors a ecting the extraction e ciency including the eluent type and its volume, adsorbent amount, sample volume, sample pH and sample flow rate were optimized. The characteristic data of analytical performance were determined to investigate the sensitivity and precision of the method. Under the optimized extraction conditions, the method showed good linearity in the range of 0.01–0.8 g/mL, repeatability of the extraction (RSD were between 6.7% and 13.5%, n = 5) and satisfactory detection limits (0.017–0.059 ng/mL). The developed method was successfully applied to the analysis of surface water (tap, river and dam) samples. The recoveries of PAHs spiked in environmental water samples ranged from 90% to 100%. All the results indicated the potential application of titanate nanotubes as solid-phase extraction adsorbents to pre-treat water samples.     

Sedimentary record of polycyclic aromatic hydrocarbons in Lake Erhai, Southwest China

The temporal distribution of polycyclic aromatic hydrocarbons (PAHs) was investigated in a sediment core from Lake Erhal in Southwest China using gas-chromatography/mass spectrometry (GC/MS) method.The total organic carbon (TOC) normalized total PAHs concentrations (sum of US Environmental Protection Agency proposed 16 priority PAHs) ranged from 31.9 to 269 μg/g dry weight (dw),and were characterized by a slowly increasing stage in the deeper sediments and a sharp increasing stage in the upper sediments.The PAHs in the sediments were dominated by low molecular weight (LMW) PAHs,suggesting that the primary source of PAHs was low- and moderate temperature combustion processes.However,both the significant increase in high molecular weight (HMW) PAHs in the upper sediments and the vertical profile of diagnostic ratios pointed out a change in the sources of PAHs from low-temperature combustion to high-temperature combustion.The ecotoxicological assessment based on consensus-based sediment quality guidelines implied that potential adverse biological impacts were possible for benzo(ghi)perylenelene and most LMW PAHs.In addition,the total BaP equivalent quotient of seven carcinogenic polycyclic aromatic hydrocarbons (BaA,CHr,BbF,BkF,BaP,DBA and INP) was 106.1 ng/g,according to the toxic equivalency factors.Although there was no great biological impact associated with the HMW PAlls,great attention should be paid to these PAH components based on their rapid increase in the upper sediments.     

武汉市长江北岸耕地中多环芳烃垂向与纵向分布特征

文章对武汉市长江北岸农用耕地中多环芳烃的含量进行了调查。结果表明除紧靠马路边一个点位的荧蒽浓度高于荷兰制定的土壤修复标准之外,其余各点各类多环芳烃均在此标准值之内;随着点位距污染源越远多环芳烃的含量越来越低;并且多环芳烃在垂直方向上的迁移存在色谱效应。通过分析不同采样点土壤中的多环芳烃含量,分析得出结论汽车尾气所排放的...     

《环境科学与技术》总目次

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稀土磁盘水处理方案技术经济比较

文章针对日照钢铁集团公司2150热轧水处理工程浊环水处理方案选择,对传统沉淀过滤法和先进的稀土磁盘法进行了对比和分析,稀土磁盘法在效果、占地、投资和运行维护费用上有较多优势,最终选用该工艺。     

Removal of polycyclic aromatic hydrocarbons from aqueous solution by raw and modified plant residue materials as biosorbents

Removal of polycyclic aromatic hydrocarbons （PAHs）, e.g., naphthalene, acenaphthene, phenanthrene and pyrene, from aqueous solution by raw and modified plant residues was investigated to develop low cost biosorbents for organic pollutant abatement. Bamboo wood, pine wood, pine needles and pine bark were selected as plant residues, and acid hydrolysis was used as an easily modification method. The raw and modified biosorbents were characterized by elemental analysis, Fourier transform infrared spectroscopy and scanning electron microscopy. The sorption isotherms of PAHs to raw biosorbents were apparently linear, and were dominated by a partitioning process. In comparison, the isotherms of the hydrolyzed biosorbents displayed nonlinearity, which was controlled by partitioning and the specific interaction mechanism. The sorpfion kinetic curves of PAHs to the raw and modified plant residues fit well with the pseudo second-order kinetics model. The sorption rates were faster for the raw biosorbents than the corresponding hydrolyzed biosorbents, which was attributed to the latter having more condensed domains （i.e., exposed aromatic core）. By the consumption of the amorphous cellulose component under acid hydrolysis, the sorption capability of the hydrolyzed biosorbents was notably enhanced, i.e., 6-18 fold for phenanthrene, 6-8 fold for naphthalene and pyrene and 5-8 fold for acenaphthene. The sorpfion coefficients （Kd） were negatively correlated with the polarity index [（O＋N）/C], and positively correlated with the aromaticity of the biosorbents. For a given biosorbent, a positive linear correlation between logKoc and logKow for different PAHs was observed. Interestingly, the linear plots of logKoc-logKow were parallel for different biosorbents. These observations suggest that the raw and modified plant residues have great potential as biosorbents to remove PAHs from wastewater.     

土壤剖面部分多环芳烃源识别参数的纵向变化及成因

通过对北京和天津地区18条土壤剖面样品中PAHs的分析检测及PAHs的土柱淋滤实验模拟研究,得出了部分反映PAHs污染源的分子标志物参数在土壤剖面(或淋滤土柱)上的纵向变化特征,分析了PAHs化合物的纵向迁移作用对这些参数的影响,讨论了部分用于识别土壤中PAHs污染源的分子标志物参数的有效性。结果表明:在土壤剖面0~50 cm范围内,An/Ph,MPI1,MP/P值均有随深度增加而逐渐降低的趋势,在深层(>50 cm)不同剖面之间这些参数值差别不大;Fl/Py随深度增大呈现一定的波动性,但总体波动范围较小,且在0~40 cm变化不大;C0/(C0+C1)P/A和C0/(C0+C1)F/P值变化较为复杂。土柱淋滤实验表明,在0~50 cm范围内,部分PAHs污染源识别参数(An/178、MPI1、MP/P、C0/(C0+C1)F/P和C0/(C0+C1)P/A等)随深度的变化趋势与自然土壤剖面中的变化趋势基本一致,在深层50~100 cm范围内,这些参数值的大小逐渐与原土中的接近。表明淋滤作用(迁移过程)对表层土及土壤剖面浅部(50 cm范围内)部分PAHs污染源参数值的大小有不同程度的影响,运用PAHs污染源识别参数时,这些参数的有效性应引起足够的注意;而剖面深部(>50 cm)PAHs参数值受表层污染物组成的影响较小,其大小主要反映原土中化合物组成及成因。不同剖面受淋滤作用影响的范围存在一定的差别,这主要取决于土壤中TOC的分布特征。     

合肥市大气颗粒物PM_(10)和PM_(2.5)中PAHs的污染特征及健康风险评估

以夏、秋、冬三个季节合肥大气颗粒物PM10和PM2.5中PAHs为研究对象,通过采样、测定与分析,得出如下结论:合肥市大气PM10和PM2.5中PAHs的浓度季节变化特征明显,冬季秋季夏季。夏季PM10中不同环数PAHs的分布规律与该季PM2.5不同,而秋冬季则相同,分布规律都是5~6环4环2~3环。通过采用BaP毒性当量法对PAHs进行健康风险评估,发现合肥大气PM10和PM2.5中PAHs的BEQ值除了夏季低于国家标准限值外,秋、冬季节均高于国家标准限值和国际标准限值。