加速溶剂萃取-固相萃取净化-高效液相色谱法测定玉米作物中多环芳烃含量

建立了加速溶剂萃取-固相萃取净化-高效液相色谱测定玉米作物中15种多环芳烃的方法,优化了试验条件.方法线性关系良好,15种多环芳烃的检出限在0.003 8～0.079μg/kg之间,空白加标试验的相对标准偏差在3.9%～11.7%之间,基质加标回收率在69.3%～115.3%之间.实际样品的测定结果表明,该方法分离效果...     

云南曲靖某煤化工基地及周边土壤中多环芳烃的检测研究

采用快速溶剂提取处理土壤样品,利用气相色谱质谱内标法测定土壤中多环芳烃,其检出限范围为2.01~3.68μg/kg,相对标准偏差为2.6%~14.7%,加标回收率为67.1%~119%。结果表明,此方法具有良好的灵敏度、准确度和精密度。本研究对11个不同采样点土壤进行了检测分析,并考察了土壤中多环芳烃的污染水平。     

Characteristics of microorganisms isolated from technogenic soils of the Kama region

Microorganisms capable of degrading monocyclic and polycyclic aromatic hydrocarbons and several chlorinated aromatic compounds were isolated from soils polluted with industrial waste from chemical plants. They were identified as representatives of the genera Pseudomonas, Flavobacterium, Alcaligenes, Rhodococcus, Microbacterium, Cellulomonas, Arthrobacter, and Brevibacterium. Among them, bacteria capable of utilizing xenobiotics in a wide range of ambient temperatures and pH and in the presence of high sodium chloride concentrations were revealed.     

Contaminants in Muscle of Plaice and Halibut Collected From the St. Lawrence Estuary and Northwest Atlantic

Levels of aromatic hydrocarbons in muscle or plaice and halibut were determined by fluorescence, using the chrysene standard, as recommended by the International Oceanographic Commision, for the analysis of PAH in environmental extracts. Concentrations were highest in muscle of halibut collected at the most contaminated, nearshore site, in the Saguenay Fjord of the St. Lawrence Estuary, compared to other locations further from shore. Although concentrations of fluorescing compounds were not statistically different in plaice, the saturated hydrocarbons displayed unquestionably more biodegradation, with a decrease of n-alkanes and increase of branched aliphatics, at the less contaminated site. Synchronous fluorescence indicated the presence of benzenoid and biphenyl hydrocarbons in the extracted mixtures, while GC-MS-TIC analysis tentatively identified the presence of a series of benzenoid (alkyl benzenes), chlorinated (PCB and DDE), N (trialkylamines) and O (phenols) hydrocarbons. These anthropogenic compounds could derive from petroleum products, surfactants and common products used in industry and households. This study emphasizes the importance of a multispectroscopic approach when investigating complex environmental mixtures.     

Electrocatalytic oxidation of gaseous toluene in an all-solid cell using a foam Ti/Sb-SnO2/β-PbO2 anode

Mineralization of benzene, toluene, and xylene (BTX) with high efficiency at room temperature is still a challenge for the purification of indoor air. In this work, a foam Ti/Sb-SnO₂/β-PbO₂ anode catalyst was prepared for electrocatalytically oxidizing gaseous toluene in an all-solid cell at ambient temperature. The complex Ti/Sb-SnO₂/β-PbO₂ anode, which was prepared by sequentially deposing Sb-SnO₂ and β-PbO₂ on a foam Ti substrate, shows high electrocatalytic oxidation efficiency of toluene (80%) at 7 hr of reaction and high CO₂ selectivity (94.9%) under an optimized condition, i.e., a cell voltage of 2.0 V, relative humidity of 60% and a flow rate of 100 mL/min. The better catalytic performance can be ascribed to the high production rate of ⋅OH radicals from discharging adsorbed water and the inhibition of oxygen evolution on the surface of foam Ti/Sb-SnO₂/β-PbO₂ anode when compared with the foam Ti/Sb-SnO₂ anode. Our results demonstrate that prepared complex electrodes can be potentially used for electrocatalytic removal of gaseous toluene at room temperature with a good performance.     

The potential of algae blooms to produce renewable gaseous fuel

Ulva lactuca (commonly known as sea letuce) is a green sea weed which dominates Green Tides or algae blooms. Green Tides are caused by excess nitrogen from agriculture and sewage outfalls resulting in eutrophication in shallow estuaries. Samples of U. lactuca were taken from the Argideen estuary in West Cork on two consecutive years. In year 1 a combination of three different processes/pretreatments were carried out on the Ulva. These include washing, wilting and drying. Biomethane potential (BMP) assays were carried out on the samples. Fresh Ulva has a biomethane yield of 183 L CH₄/kg VS. For dried, washed and macerated Ulva a BMP of 250 L CH₄/kg VS was achieved. The resource from the estuary in West Cork was shown to be sufficient to provide fuel to 264 cars on a year round basis. Mono-digestion of Ulva may be problematic; the C:N ratio is low and the sulphur content is high. In year 2 co-digestion trials with dairy slurry were carried out. These indicate a potential increase in biomethane output by 17% as compared to mono-digestion of Ulva and slurry.     

北京市昌平区大气环境PM10中多环芳烃的含量及变化趋势

通过采集了2004～2006年北京市昌平区四个季节中大气PM10样品,采用超声抽提方法,使用GC/MS分析了该区PAHs含量和组成.结果显示,三年中四个季度的18种PAHs总量范围分别为21.64～656.39ng/m3、31.94～164.33ng/m3和7.294～209.3ng/m3,其中致癌性极强的苯并[a]芘含量范围为2.69～36.95 ng/m3、1.44～6.6ng/m3和0.256～8.625ng/m1,其变化趋势与PAHs总量有较好的相关性.PAHs的浓度是冬季＞秋季＞夏季＞春季,这与夏季时雨水冲刷和阳光照射强度大导致PAHs光解,冬季时燃煤排放大等影响因素有关.文章还使用多种方法判断昌平区大气PM10中的PAHs主要来源于燃煤和汽车尾气,其它污染源贡献较小.     

红枫湖地表水中多环芳烃的分布及来源

将固相微萃取与气相色谱联用,对贵阳红枫湖水样中16种美国环境保护署优控的多环芳烃进行分析。结果表明：红枫湖水中16种多环芳烃总量为0167 1~0336 4 μg/L,与国内其它水系相比,湖中存在多环芳烃轻度污染。7种（萘、荧蒽、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、茚并(1,2,3-cd)芘和苯并(ghi)苝）多环芳烃的总量未超出中国城市供水行业对多环芳烃规定的限值,但作为饮用水源,红枫湖水中的苯并(a)芘含量已超出我国标准GB3838-2002中生活饮用水地表水源地的苯并(a)芘限值,并且苯并(a)蒽、〖JX-*9〗〖SX（B-25x〗〖HT7,5”〗艹〖〗〖HT6”,5”〗屈〖HT5”〗〖SX）〗〖JX*9〗、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、茚并(1,2,3-cd)芘的含量也超过了美国环境保护署地表水水质标准限值。通过多环芳烃特征参数的比值,分析了红枫湖水中多环芳烃的污染来源。污染源分析表明,湖中多环芳烃的主要来源为燃烧源,包括木材、煤以及化石燃料的燃烧,同时也有一部分多环芳烃是来源石油类物质的输入.     

大气中芳香胺及吡啶类化合物的离子色谱法测定

采用GDX-501富集大气中芳香胺及吡啶类化合物,经沸水解吸后解吸液直接注入离子色谱仪,用紫外/可见光检测器进行测定。方法灵敏、简便,可同时测定吡啶、2-甲基吡啶、3-甲基吡啶、苯胺、邻-甲苯胺、间-甲苯胺等。当采样体积为30L时,方法的最低检出浓度范围为0.05～0.10mg/m3(吡啶～间甲苯胺),测定的回收率为84.7%～95.9%,相对标准偏差为4.0%～6.6%。