杭州市主要交通干线大气中非甲烷总烃的分布规律

通过对杭州市主要交通干线大气中非甲烷总烃（ＮＭＨＣ）的测定，得出了杭州市主要交通干线大气中非甲烷总烃的行为规律。结果表明，杭州市主要交通干线大气中ＮＭＨＣ的浓度日变化存在明显的双峰规律，上午８：００左右，下午１６：００左右各出现一次峰值浓度；夏季浓度略高于冬季；各交通干线大气中非甲烷烃浓度稍有差异。     

大气中非甲烷烃的色谱测定法

非甲烷烃是光化学烟雾的重要监测项目之一,国外多采用色谱法测定,并有专用仪器生产,其流程大同小异,基本上是先通过一个空柱测定总烃,再经过一分离柱只测定甲烷,两者之差即非甲烷烃,以ppm CH_4表示结果。分离的方法有冷冻、反吹、吸附,选择燃烧和柱分离。实际上它测定的并不全是烃,而是包括了大气中所有能在氢火焰上给出响应的有机物。目前,关于非甲烷烃,国内尚未统一测定方法和制定控制指标。鉴于近几年来,国     

糖脂类生物表面活性剂去除污染含水层中石油烃的研究

研究了糖脂类生物表面活性剂对石油烃的增溶,并将其用于污染含水层中石油烃的去除。结果表明:石油烃溶解度随着糖脂类生物表面活性剂浓度的增大而增大,糖脂类生物表面活性剂质量浓度为1 200mg/L时,石油烃溶解度达10 077.7mg/L;界面张力随着糖脂类生物表面活性剂浓度的增加而减小,糖脂类生物表面活性剂质量浓度为1mg/L时,界面张力为34.3mN/m,糖脂类生物表面活性剂质量浓度为800mg/L时,界面张力为5.2 mN/m。采用糖脂类生物表面活性剂对污染含水层进行清洗处理,在固液比(质量体积比)为1g∶2mL的体系中,糖脂类生物表面活性剂质量浓度为3 000mg/L,120r/min、10℃下振荡12h,石油烃去除率达70.82%。污染含水层柱冲洗结果表明,糖脂类生物表面活性剂质量浓度分别为1 200、3 000mg/L时,10倍孔隙体积的表面活性剂冲洗后,分别从污染砂样中去除41.81%和63.30%的石油烃。     

土壤气相抽提去除土壤中汽油烃污染物柱试验研究

原位处理土壤石油污染对于土壤和地下水的有机污染控制具有极其重要的现实意义.通过砂土柱试验研究了原位物理通风的主要工艺形式及运行参数,并初步分析了汽油烃在砂土柱中的迁移和通风去除机制.结果表明,顶部真空抽提与底部注气两种通风方式相比,顶部真空抽提效果较好,砂土柱汽油烃初始质量浓度为2.937 mg/g时,经过104.5 h通风,砂土柱中汽油烃去除率达80.49%.土壤汽油烃初始浓度影响其在土壤中的迁移和去除,土壤汽油烃初始浓度越大,相同通风条件下,物理通风方法去除土壤中挥发性有机物的效率越低.通风及通风方式对砂土中的汽油烃的去除影响很大,连续通风可在砂土柱中形成稳定的负压环境,在汽油烃初始质量浓度为35.730 mg/g时,连续真空抽提264 h,砂土柱中的汽油烃平均去除率达89.29%;间歇通风在砂土柱中形成的负压环境不稳定,但也可以去除砂土柱中的汽油烃.初步分析认为,汽油烃存在负压作用下的向上挥发和重力作用下的向下迁移两个过程,其综合作用的结果导致汽油烃在砂土柱中的分布状况.     

石油烃对海洋浮游植物生长的影响研究进展

石油烃是主要的海洋污染物之一,而浮游植物是石油烃进人海洋食物链的起点.从种群生长和群落结构、代谢活动等几个方面,综述了石油烃对海洋浮游植物的生物学及生态学效应研究进展,并讨论了影响石油烃毒性效应的主要影响因素,最后对相关研究的未来发展方向进行了展望.     

厌氧菌群JAC1降解石油烃能力及其群落结构的解析

利用苯酚诱导获得厌氧菌群JAC1强化去除土壤中的石油烃，对其在厌氧条件下的石油烃降解条件进行了优化，得到最适降解条件为：pH 7.5～8.5,土壤总石油烃(TPH)质量浓度50 mg/kg, NaCl质量分数0.3%,JAC1接菌量0.15 mL/g。厌氧菌群JAC1对石油烃的降解符合一级动力学模型。通过气相色谱质谱联用仪分析，芳香烃较直链烷烃更难降解，推测部分长链烷烃在降解过程中会分解为短链烷烃后再进行降解。基于土壤宏基因组测序分析可知，土壤微生物群落多样性与TPH浓度呈负相关，投加JAC1后土壤中与石油烃降解有关的功能菌群相对丰度呈现出不同程度增高，说明JAC1有助于建立一个高效的微生物降解体系来强化石油烃降解。     

土壤石油烃污染的植物毒性及植物-微生物联合降解

通过盆栽实验研究了土壤石油烃污染对玉米和水稻根伸长的影响，并在土壤中接种经过筛选得到的石油烃降解菌，研究石油烃降解菌对石油烃毒性的影响以及对土壤中石油烃的降解。研究结果表明，石油烃浓度低于1 000 mg/kg时对玉米的根系生长有一定的刺激生长作用，随着石油烃浓度的增加，刺激根长生长的作用逐渐降低，研究结果表明，水稻根长受石油烃影响较小。通过对不同处理土壤中石油烃降解的研究结果表明，土壤中种植水稻对石油烃有一定的降解作用，但是不同处理下土壤中的石油烃降解率不同，其中水稻微生物联合处理下土壤中石油烃的降解速率最快，培养期内的降解效率达到53.3%。     

石油烃降解菌的细胞表面疏水性的研究进展

细胞表面疏水性是影响微生物吸收和降解疏水性石油烃的主要因素。结合国内外的研究现状,综述了细胞表面疏水性的测定方法,探讨了培养基成分、培养时间、温度、pH等环境因素对细胞表面疏水性的影响,总结了石油烃降解菌的细胞表面疏水性与石油烃微生物降解的关系、表面活性剂对细胞表面疏水性及生物降解的影响,最后对细胞表面疏水性研究方向进行了展望。     

不同处理条件对石油污染土壤植物修复的影响

针对石油烃植物修复过程中的主要影响因素,研究了不同植物种类、不同土壤调理剂和菌剂使用等不同条件对土壤中石油烃植物修复效果的影响.结果表明,不同种类的植物修复可使总石油烃的年降解率达到37.8％ ～ 73.98％,其中大豆和碱蓬具有较好的修复效果;3种不同土壤调理剂对石油烃污染土壤修复的效果为商业添加剂＞牛粪＞蛭石;先微生物修复后种植植物的处理要优于单独的微生物修复及微生物、植物修复同步进行的处理.     

3种石油烃降解菌对石油烃的降解效果及其细胞表面疏水性

选取3种石油烃降解菌:假单胞菌(Pseudomonas sp.,DS-1)、铜绿色假单胞菌(Pseudomonas aeruginosa,DS-2)和无色杆菌(Achromobacter sp.,DS-3),研究其对石油烃的降解效果及其细胞表面疏水性。结果表明,经过6d的降解,3种石油烃降解菌对石油烃的降解率分别为99.08%、79.75%、84.34%。石油烃的黏附性测试和盐析聚集测试结果表明,3种石油烃降解菌均表现出较高的细胞表面疏水性,其规律为DS-1DS-3DS-2。其中DS-1的细胞表面疏水性最高,达65.90%。DS-1、DS-2和DS-3菌株发生盐析聚集所需最小(NH4)2SO4摩尔浓度分别为2.0、2.8、2.4 mol/L。菌株的细胞表面疏水性和降解有机物的能力有着较高的相关性。     

Analysis of the Atmosphere for Light Hydrocarbons

A procedure has been developed for the analysis of trace quantities of light hydrocarbons in air. A freezetrap filled with chromatographic packing was installed in place of the gas sample loop of a flame ionization chromatograph. An air sample 0.1–0.5 liter volume was passed through the trap which was chilled with liquid oxygen. The trap wasthen brought to ice temperature and its contents simultaneously swept into the column. The resulting chrómatogram could be used to determine about 25 hydrocarbons through n-hexane. The minimum detectable concentration was below 1 ppb for these hydrocarbons. With such sensitivity it is possible to make useful measurements even on samples of light air pollution. Air samples from the Riverside area were analyzed in this fashion starting in the summer of 1965. The relative amounts of these hydrocarbons were then compared with the distribution reported for the various known hydrocarbon sources. The attenuation of the more reactive hydrocarbons by photolysis was also observed. A system for irradiating trapped air samples was also constructed. Samples were collected in 5-gallon borosilicate bottles which were then irradiated with ultraviolet radiation and the concentration changes followed.     

Development of a High-Temperature Subtractive Analyzer for Hydrocarbons

This paper discusses the development of a high-temperature subtractive analyzer for separating the hydrocarbons present in gaseous mixtures into two categories— reactive hydrocarbons and unreactive hydrocarbons. The analyzer utilizes the ability of selected substances to absorb certain groups of hydrocarbons and their derivatives from a gas mixture and is designed for operation with a flame ion-ization detector. The body of information presented in this paper is directed to individuals concerned with the analysis of the exhaust gases of gas turbine engines or other combustion sources as stationary power plants. The analyzer grew out of an investigation of a previously reported subtractive analyzer system which operates at ambient temperature. Current state-of-the-art requirements for the accurate determination of total hydrocarbons at the concentrations present in turbine exhaust gases necessitate that sampling and measurements be conducted at elevated temperatures (325-375°F), rather than ambient temperature, to reduce or eliminate condensation and wall adsorption sampling errors. To fulfill this requirement, the sampling lines and flame ionization detector must be heated. After tests determined that the previously reported scrubber system would not remove the same hydrocarbons at elevated temperature levels as it did at ambient temperatures, an investigation of the effectiveness of various absorbents at elevated temperatures was conducted. This led to the development and test of the high-temperature subtractive analyzer concept discussed in this report. In its final form, one path of this unit contains no absorbent, the second contains a column of concentrated H₂SO₄ on Ultraport and a column containing PdSO₄ and H₂SO₄ on Ultraport. The two columns are connected in series. The absorbents remove olefins, aromatics, acetylene, and oxygenated hydrocarbons but pass paraffins. As the final step in this program, a comparison of the two subtractive analyzers was made using the exhaust from a gas turbine combustion system.     

Determination of some aliphatic and polycyclic aromatic hydrocarbons in marine sediments of the Baltic Sea

Two representative samples of surficial marine sediments have been studied, one from the northern Baltic Proper and the other from the Gulf of Finland. Aliphatic hydrocarbons were determined by gas chromatography on a fused silica capillary column, and six polyaromatic hydrocarbons were determined by gas chromatography-mass fragmentography. Hydrocarbons were extracted with a benzene-methanol mixture and ultrasonic agitation. The aliphatic hydrocarbons were tentatively identified by their retention times. The polyaromatic hydrocarbons (PAHs) were identified on the basis of their retention times and mass fragmentograms by direct comparison with those of standard compounds. The aliphatic hydrocarbon contents ranged from 0,1 to 2,6 μg/g dry matter. In both samples there was a clear maximum at n-C₁₇ and also a clear odd-carbon predominance. The PAH contents ranged from 4 to 120 ng/g dry matter. The PAH concentration was about 58 per cent higher in the sample from the Gulf of Finland than in the sample from the Baltic Proper.     

PAHs analysis of fish whole gall bladders and livers from the Natural Reserve of Camargue by GC/MS

Traces of parent polycyclic aromatic hydrocarbons (PAH) in fish whole gall bladders and livers from the Natural Reserve of Camargue were determined from three different species: cels, goldfishes and catfishes by capillary gas chromatography-mass spectrometry (GC/MS) after Soxhlet extraction and florisil column cleanup. Results have been successfully correlated with biological fish parameters in order to identify adequate biomarkers of PAHs contamination.     

Concentrations of C2–C5 hydrocarbons in atmospheric air at Deonar,Bombay, in relation to possible sources

Atmospheric C₂–C₅ hydrocarbons were determined at Deonar, an industrial suburb north of Bombay, India, during 1985. Samples were pre-concentrated on silica gel at −78°C and subsequently desorbed on to a gaschromatographic column for separation and flame ionization detection. The seasonal pattern of the monthly geometric mean hydrocarbon concentrations are used to show that refinery emissions in addition to auto exhaust are a major source of hydrocarbons at Deonar.     

Using Radiocarbon to Apportion Sources of Polycyclic Aromatic Hydrocarbons in Household Soot

To determine whether polycyclic aromatic hydrocarbons (PAHs) in household soot were derived from the combustion of scrap wood or creosote that was impregnated in the wood (or some combination of both), the molecular composition and radiocarbon ( 14 C) content of the total carbon and several PAHs in the soot was investigated. The 5730-year half-life of 14 C makes it an ideal marker for identifying creosote-derived PAHs ( 14 C-free) versus those derived from the combustion of wood (contemporary 14 C). The 14 C abundance of phenanthrene, fluoranthene, pyrene, and retene was determined by accelerator mass spectrometry after solvent extraction and purification by preparative capillary gas chromatography. The molecular analysis (presence of retene and 1,7-dimethylphenanthrene) and bulk 14 C content (contemporary) of the soot indicated that wood combustion was a strong source of carbon to the soot. The 14 C of retene in two soot samples was also contemporary, indicating that it was derived from the combustion of the scrap wood. These results are consistent with previous work that has suggested that retene is an excellent marker of wood combustion. However, the 14 C content of phenanthrene, fluoranthene, and pyrene in one soot sample was much lower and revealed that these compounds had a mixed creosote and wood source. Using an isotopic mass balance approach, we estimate that 40 to 70% of phenanthrene, fluoranthene, and pyrene were derived from the combustion of the scrap wood. The results of this study show that molecular marker and bulk 14 C analysis can be potentially misleading in apportioning sources of every PAH, and that molecular-level 14 C analysis of PAHs can be a powerful tool for environmental forensics.     

Continuous Monitoring of Methane and Other Hydrocarbons In Urban Atmospheres

Continuous measurements of total hydrocarbons (and other organic substances) and of methane were made in Cincinnati and Los Angeles for three-month periods. Some of the measurements were made during episodes of photochemical air pollution. Two instruments, one for measurement of total hydrocarbons and the other for methane, were operated in parallel. Both incorporated flame ionization detectors having greater sensitivity than commercial flame ionization instruments. The flame ionization analysis for methane was made specific by use of an adsorbent carbon column preceding the analyzer to retain all organic substances except methane. Subtracting the methane concentration values from those for total hydrocarbons gave nonmethane hydrocarbon concentrations. The data showed diurnal patterns of concentrations of methane and nonmethane hydrocarbons in the atmosphere. Average hourly values for methane were strikingly similar in Los Angeles and in Cincinnati (2.6 and 2.4 ppm, respectively); those for nonmethane hydrocarbons were four times as high in Los Angeles (3.0 and 0.8 ppm, respectively). A bimodal frequency distribution pattern of the concentrations suggested that atmospheric ventilation was either good or poor, with less than a random amount of time in intermediate stages. The width of the methane frequency distribution peak was about half the width of that for nonmethane hydrocarbons, indicating a different and more constant source for the former.     

Polynuclear Aromatic Hydrocarbons Associated with Particulates in Pittsburgh Air

Pittsburgh air was sampled continuously at one site for 886 hrs./sample at 45 cfm with a high volume sampler equipped with a horizontal elutriator as a first stage of separation, and an MSA 1106B glass fiber filter as a final particulate collection stage. The horizontal elutriator was designed to simulate the particulate deposition characteristics of the human respiratory tract. Samples were collected during the period June 1964 to February 1965. Respirable and non-respirable particulate samples were analyzed for polynuclear aromatic hydrocarbon content by a new technique which utilized dual column, flame ionization gas chromatography. It was possible to quantitatively analyze a concentrated benzene extract of the particulate sample for the following individual components: 1, 2 benzanthracene; chrysene; pyrene; 3,4 benzofloranthene; 1, 12 benzoperylene. It was not possible to distinguish between 3,4 benzopyrene, 1,2 benzopyrene and perylene; only the total quantity of these compounds present was detected. This analytical technique is comparable in sensitivity to formerly reported, more time-consuming methods and is very rapid, requiring less than one hour to perform after benzene extraction. Amounts of the above compounds associated with the two particulate fractions collected are reported and discussed.     

The Detection and Estimation of Part Per Billion Concentrations of Hydrocarbons

The addition of a freeze-out step in liquid nitrogen prior to analysis by gas chromatography with flame ionization detection permits the accurate determination of C₂ and higher hydrocarbons in the part per billion (ppb) range. Concentrations of C₂ and higher hydrocarbons have been measured in commercial cylinders of nitrogen, helium and hydrogen. Using a 150 ml sample of gas, recovery of ppb concentrations is 95 to 100 percent.     

Oil residues in Baltic sediment,mussel and fish. I. Development of the analysis methods

Sediment, sediment trap, Mytilus, Macoma and flounder samples from Northern Baltic (Finnish archipelago) have been analyzed for their contents of aliphatic and aromatic hydrocarbons. Androstane and hexaethylbenzene were used as internal standards. The analysis procedure consisted of alkaline degradation of fat, column fractionation of the two residue groups and final determination by glass capillary gas chromatography with FID for aliphatic hydrocarbon group and with mass spectrometry for non-polar aromatic residue group. The latter group was also determined by high pressure liquid chromatography. The residues due to oil pollution were distinguished from compounds of pure natural origin on the basis of statistical treatment of the determination results.