大气粉尘中常见多环芳烃类化合物的提取及含量测定

采用便携式PM2.5采样器和玻璃纤维滤膜对大气粉尘进行采样,以加压液体萃取、超声波辅助提取和微波辅助提取3种方法对多环芳烃类化合物进行提取,以超高效液相色谱和质谱联用方法进行测定。共检测出16种多环芳烃类化合物,分别为:萘、苊、苊烯、芴、菲、蒽、荧蒽、芘、苯并[a]蒽、■、苯并[b]荧蒽、苯并[k]荧蒽、苯并[a]芘、二苯并[a,h]蒽、茚并[1,2,3-c,d]芘和苯并[g,h,i]苝。3种提取方法均可有效提取大气粉尘中的多环芳烃类化合物,加压液体萃取法的提取效率最高、超声波辅助提取法次之、微波辅助提取法最低。超高效液相色谱和质谱连用方法可有效地分析大气粉尘中的多环芳烃类化合物,线性方程的相关系数不低于0.998 3,测定值的相对标准偏差不超过0.80%,检出限不高于0.27 ng/g。     

某在役炼化场地特征污染物识别与分析

以多水期污染监测数据为基础，采用内梅罗污染指数(Pn)法对某在役炼化场地的特征污染物进行识别，并对识别结果进行分析。研究表明：该炼化场地土壤中优先控制的特征污染物有砷、钴、苯、苯并[a]芘、乙苯和石油烃(C₁₀～C₄₀)，一般特征污染物有铊、铍、铅、钒、镍、间/对-二甲苯和二苯并[a,h]蒽等；地下水中优先控制的特征污染物有钒、铊、钼、苯乙烯、苯并[a]芘、石油烃(C₁₀～C₄₀)、苯、硫化物、氨氮、耗氧量、硫酸盐、挥发酚和氯化物，一般特征污染物有钴、砷、镍、铍、铅、甲苯、1,2-二氯丙烷、乙苯、间/对-二甲苯、二苯并[a,h]蒽、氟化物、亚硝酸盐和硝酸盐；本工作构建的特定场地特征污染物识别方法简捷有效、科学合理。     

萘降解菌的筛选及其对多环芳烃的降解

从柴油污染土壤中筛选分离出一株萘降解菌N-3,进行了菌种鉴定及萘双加氧酶基因(nah)验证,并考察了该菌对不同种类多环芳烃(PAHs)的降解能力及降解过程中脱氢酶活性的变化。实验结果表明:该菌为铜绿假单胞菌(Pseudomonas aeruginosa),含有nah基因;当分别对液体培养基中质量浓度为50 mg/L的萘、菲、蒽、芘、芴降解84 h时,菌株N-3对萘、菲、蒽、芘、芴的降解率分别为28.81%,34.83%,36.65%,27.50%,23.47%。菌株N-3的脱氢酶活性与其对不同PAHs的降解率呈一定的正相关性。该菌不仅能有效降解萘,且对其他种类PAHs也有一定降解作用。     

沥青纺丝工段的环境检测

沥青碳纤维以其廉价和独特的性能而受到注目。在沥青碳纤维的制作和使用中必须重视环境与劳动保护。本文提出了以高效液相色谱(HPLC)分离、紫外、荧光联用的方法检测沥青纺丝工段空气中苯并(a)芘(Bap)、萤蒽、甲基胆蒽等稠环芳烃的浓度,掌握空气污染情况。 1.实验部分 (1)仪器、试剂岛津LC-3A高速液相色谱仪,配有RF-510荧光多波长检测器,UVD-2紫外检测器。色谱柱直径为5.6毫米     

助剂作用下超声浸取电解锰渣

用8-羟基喹啉、黄原酸钾、十六烷基三甲基溴化铵、磷酸三丁酯、柠檬酸5种物质作浸取助剂,考察了助剂作用下超声辅助浸取法从电解锰渣中提取锰的工艺条件。实验结果表明：用1%（质量分数）柠檬酸作浸取助剂,在固液比（g/mL）为1∶4、酸矿比（mL/g）为0.3∶1、浸取温度为70℃的条件下,超声浸取15min,锰浸出率平均可达57.28%,是加热酸浸法锰浸出率的2.72倍,是无助剂超声辅助浸取法锰浸出率的1.52倍。     

废SCR催化剂中钒和钨的有机酸浸出

在对废SCR催化剂组成进行分析的基础上,采用草酸和酒石酸两种有机酸浸取废SCR催化剂中的V和W。实验结果表明：草酸对V、W的浸出率均大于酒石酸;在草酸浓度为1.00 mol/L、浸取温度为80 ℃、液固比为10 mL/g、浸取时间为180 min时,V和W的浸出率分别为63.50%和13.12%;在酒石酸浓度为0.5 mol/L、浸取温度为100 ℃、液固比为10 mL/g、浸取时间为180 min时,V和W的浸出率分别为44.00%和9.00%。酸性浸出未改变SCR催化剂中TiO₂的晶型,剩余残渣中依然保留着TiO₂骨架,可继续作为催化剂载体使用。     

烟道气中苯并(α)芘的测定方法

煤、石油及各种燃料,在燃烧过程中,由于一部分不完全燃烧,经过裂解、环化、聚合产生相当复杂的多环芳烃,多数经烟道向大气中排放。苯并(α)芘(Bap)一类的多环芳烃化合物具有极强的致癌物,危害人体健康。因此,本文采用滤膜阻留,冰水冷凝,聚氨蟋泡沫塑料(PUF)吸附。索氏提     

从废感光胶片中回收银

研究了以Fe3 -乙二胺四乙酸二钠-N a2S2O3体系为浸取剂从废感光胶片中回收银的方法,考察了浸出银的最佳工艺条件。实验表明,当浸取剂中FeC l3.6H2O质量浓度为35g/L、N a2S2O3.5H2O质量浓度为150g/L、pH为7、固液质量比为3∶10时,浸取剂可重复使用6次,胶片上银的浸出率可达99%以上;浸取液中的银采用硼氢化钠还原回收,粗银粉配以熔剂高温熔炼可得到纯度达99.78%的银,银回收率达96.88%,回收银后的浸取液可循环使用。     

化工污泥中苯并(a)芘的降低及对农作物的影响

石油化工污泥含有650—4500微克/公斤苯并(a)芘,经过消化、曝气或者堆沤处理,一般能降低苯并(a)芘50％左右。施用处理过的污泥5000斤/亩以下,一般增产小麦、玉米一成以上,在小麦、玉米、辣椒、茄子的可食部分及小麦的茎、叶、穗部,未见苯并(a)芘的明显积累;在土壤中有少量残留,残留期约为一个生长季。因此,在控制污泥的施用量及进行适当预处理的情况下,可以避免污泥中苯并(a)芘进入食物链。     

焦化项目大气污染特征及环境影响评价

以甘肃省酒泉市阿克塞哈萨克族自治县某焦化项目为案例，在分析其工艺流程和排污环节的基础上，利用AERMOD模型定量预测评价该焦化项目对区域大气环境质量的影响程度。预测结果表明：SO2，NO2，NH3，H2S的区域最大地面小时质量浓度占标率分别为15.8%，29.6%，16.8%，24.8%;SO2、NO2、苯并[a]芘、固体悬浮物（TSP）的区域最大日均质量浓度占标率分别为7.5%，11.4%，7.2%，95.8%;TSP最大日均质量浓度坐标点为（500，0），位于厂界内部，高浓度是由焦化厂低矮面源造成的，且浓度随距离消减得较快。     

Ethanol washing of PAH-contaminated soil and Fenton oxidation of washing solution

As a means to remediate soil contaminated by polycyclic aromatic hydrocarbons, we investigated a combined process involving ethanol washing followed by a Fenton oxidation reaction. Artificial loamy soil was contaminated with various representative polycyclic aromatic hydrocarbons (i.e., fluorene, anthracene, pyrene, benzo(b)fluoranthene, or benzo(a)pyrene) at concentrations ten times higher than regulatory soil standards of The Netherlands or Canada, and then washed four times in ethanol, which reduced the concentration of polycyclic aromatic hydrocarbon contamination to below the regulatory standard. Fenton oxidation of ethanol solutions containing anthracene, benzo(a)pyrene, pyrene, acenaphthylene, acenaphthene, benz(a)anthracene, benzo(j)fluoranthene, or indeno(1,2,3-cd)pyrene showed a removal efficiency of 73.3%–99.0%; by contrast, solutions containing naphthalene, fluorene, fluoranthene, phenanthrene, or benzo(b)fluoranthene showed a removal efficiency of 9.6%–27.6%. Since each of the nonremediated polycyclic aromatic hydrocarbons, excluding benzo(b)fluoranthene, are easily biodegradable, these results indicate that the proposed treatment can be successfully applied to polycyclic aromatic hydrocarbon-contaminated soil that does not contain high concentrations of benzo(b)fluoranthene. The main reaction products resulting from Fenton oxidation of ethanol solutions containing anthracene or benz(a)anthracene were anthraquinon or benz(a)anthracene-7,12-dione, respectively; while 1,8-naphthalic anhydride was produced by solutions of acenaphthylene and acenaphthene, and 9-fluorenone by a fluorene solution. Received: June 9, 1998 / Accepted: March 24, 1999     

Permanganate oxidation of sorbed polycyclic aromatic hydrocarbons

The polycyclic aromatic hydrocarbons (PAH) that contaminate soils at many industrial and government sites are resistant to natural biotic and abiotic degradation processes. The recalcitrant nature of these compounds may require aggressive chemical treatment to effectively remediate these sites. This study was conducted to assess the viability of permanganate oxidative treatment as a method to reduce PAH concentration in contaminated soils. Study results demonstrated a reduction in soil sorbed concentration for a mixture of six PAHs that included anthracene, benzo(a)pyrene, chrysene, fluoranthene, phenanthrene, and pyrene by potassium permanganate (KMnO4) oxidative treatment. The greatest reduction in soil concentration was observed for benzo(a)pyrene, pyrene, phenanthrene, and anthracene at 72.1, 64.2, 56.2, and 53.8%, respectively, in 30 min at a KMnO4 concentration of 160 mM. Minimal reductions in fluoranthene and chrysene concentration were observed at 13.4 and 7.8%, respectively, under the same conditions. A relative chemical reactivity order of benzo(a)pyrene>pyrene>phenanthrene>anthracene>fluoranthene>chrysene towards permanganate ion was observed. Aromatic sextet theory was applied to the degradation results to explain the highly variable and compound-specific chemical reactivity order.     

Solvent extraction and soil washing treatment of contaminated soils from wood preserving sites: Bench‐scale studies

Bench‐scale solvent extraction and soil washing studies were performed on soil samples obtained from three abandoned wood preserving sites included in the National Priority List. The soil samples from these sites were contaminated with high levels of polyaromatic hydrocarbons (PAHs), pentachlorophenol (PCP), dioxins, and heavy metals. The effectiveness of the solvent extraction process was assessed using liquefied propane or dimethyl ether as solvents over a range of operating conditions. These studies have demonstrated that a two‐stage solvent extraction process using dimethyl ether as a solvent at a ratio of 1.61 per kg of soil could decrease dioxin levels in the soil by 93.0 to 98.9 percent, and PCP levels by 95.1 percent. Reduction percentages for benzo(a)pyrene (BaP) potency estimate and total detected PAHs were 82.4 and 98.6 percent, respectively. Metals concentrations were not reduced by the solvent extraction treatment. These removal levels could be significantly improved using a multistage extraction system. Commercial scale solvent extraction using liquefied gases costs about $220 per ton of contaminated soil. However, field application of this technology at the United Creosote site, Conroe, Texas, failed to perform to the level observed at bench scale due to the excessive foaming and air emission problem. Soil washing using surfactant solution and wet screening treatability studies were also performed on the soil samples in order to assess remediation strategies for sites. Although aqueous phase solubility of contaminants seemed to be the most important factor affecting removal of contaminants from soil, surfactant solutions (3 percent by weight) having nonionic surfactants with hydrophile‐lipophile balance (HLB) of about 14 (Makon‐12 and Igepal CA 720) reduced the PAH levels by an average of 71 percent, compared to no measurable change when pure deionized water was used. Large fractioza of clay and silt (<0.06mm), high le!ezielsof orgaizic contami‐ nants and hzimic acid can makesoil washing less applicable.     

The Effect of Interaction Between White-rot Fungi and Indigenous Microorganisms on Degradation of Polycyclic Aromatic Hydrocarbons in Soil

White-rot fungi applied for soil bioremediation have to compete with indigenous soil microorganisms. The effect of competition on both indigenous soil microflora and white-rot fungi was evaluated with regard to degradation of polycyclic aromatic hydrocarbons (PAH) with different persistence in soil. Sterile and non-sterile soil was artificially contaminated with ¹⁴C-labeled PAH consisting of three (anthracene), four (pyrene, benz[a]anthracene) and five fused aromatic rings (benzo[a]pyrene, dibenz[a,h]anthracene). The two fungi tested,Dichomitus squalens and Pleurotus ostreatus, produced similar amounts of ligninolytic enzymes in soil, but PAH mineralization by P. ostreatus was significantly higher. Compared to the indigenous soil microflora, P.ostreatus mineralized 5-ring PAH to a larger extent, while the indigenous microflora was superior in mineralizing 3-ring and 4-ring PAH. In coculture the special capabilities of both soil microflora and P. ostreatus were partly restricted due to antagonistic interactions, but essentially preserved. Thus, soil inoculation with P. ostreatus significantly increased the mineralization of high-molecular-weight PAH, and at the same time reduced the mineralization of anthracene and pyrene. Regarding the mineralization of low-molecular-weight PAH, the stimulation of indigenous soil microorganisms by straw amendment was more efficient than application of white-rot fungi.     

Use of fungal technology in soil remediation: A Case Study

Two white rot fungi Irpex lacteus and Pleurotus ostreatus and a PAH-degrading bacterial strain of Pseudomonas putida were used as inoculum for bioremediation of petroleum hydrocarbon-contaminated soil from a manufactured-gas-plant-area. Also two cocultures comprising a fungus with Pseudomonas putida were applied. After 10-week treatment out of 12 different PAHs, concentration of phenanthrene, anthracene, fluoranthene and pyrene decreased up to 66%. The ecotoxicity of the soil after bioremediation did not reveal any effect on the survival of Daphnia magna, a crustacian. However, the toxic effect on seed germination of plant Brassica alba and oxidoreductase activity of bacterium Bacillus cereus decreased after 5 and 10 weeks of treatment.     

Occurence and Distribution of Polycyclic Aromatic Hydrocarbons in Ankara Precipitation

Urban atmospheric environment contains many trace organic pollutants that are related to the incomplete fuel combustion in domestic heating, industrial plants and automobile traffic. Removal of these pollutants from the atmosphere takes place through wet and dry deposition as well as chemical transformations. In this study, concentrations of polycyclic aromatic hydrocarbons (PAHs) in wet deposition samples were determined at an urban site of Turkey. Wet and dry deposition samples were collected using Andersen Rain Sampler. The sampler was modified accordingly for the collection of organic pollutants. Collected samples were preconcentrated by using solid phase extraction (SPE) disks and consecutively analyzed by Gas Chromatography-Mass Spectrometry (GC-MS). Among the 13 compounds quantified in this study, anthracene, fluoranthene, and pyrene were found more frequently and at elevated concentrations (202, 271 and 260 ng L^-1 mean concentrations, respectively).Concentrations of PAHs were found to be high in winter period.     

Slurry phase bioremediation of PAHs in industrial landfill samples at laboratory scale

The effect of Tween 80 and selected bacteria additions on the bioremediation of PAH contaminated landfill soil (70.38mgkg(-1)) was evaluated in a slurry phase bioreactor. A phenanthrene-degrading consortium was selected by enrichment cultures and used as autochthonous inoculum. The Tween 80 addition increased the aqueous concentration of both high and low molecular weight PAHs. In the experiment with Tween 80 and inoculum addition, added microorganisms improved (>90%) the biodegradation of two- and three-ring PAHs as well as of the four-ring PAHs pyrene and fluoranthene. Biodegradation of the higher molecular weight PAHs was about 30% in experiments with Tween 80 addition, with and without inoculum addition.     

Toxicity and source assignment of polycyclic aromatic hydrocarbons in road dust from urban residential and industrial areas in a typical industrial city in Korea

This study analyzed the toxicity and sources of polycyclic aromatic hydrocarbons (PAHs) in road dust from six representative areas (three urban residential areas and three industrial areas) from a typical industrial city in Korea. The concentrations and the toxicity equivalent concentrations (TEQs) in road dust varied by area, depending on the type of traffic and industrial activities and the PAHs identified. High correlations between the total concentration and the TEQ of PAHs in road dust were found in road dust from both the urban and industrial areas. To identify the sources of PAHs, this study utilized a factor loading method in a principal component analysis, the ratio of PAHs from combustion sources to total PAHs (ΣCOMB to ΣPAH), and bivariate plots of phenanthrene/anthracene (PA/Ant) versus fluoranthene/pyrene (FL/Pyr), and ΣCOMB/ΣPAH versus FL/Pyr in road dust. The identified origin of the PAHs was fuel combustion, including gasoline, diesel, oil, and coal, used in urban and industrial areas.