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水生沉积物中天然、人为和石油类碳氢化合物的识别

Identification of natural, anthropogenic and petroleum hydrocarbons in aquatic sediments.

作者信息

Volkman J K, Holdsworth D G, Neill G P, Bavor H J

机构信息

CSIRO Division of Oceanography, Hobart, Tasmania, Australia.

出版信息

Sci Total Environ. 1992 Mar;112(2-3):203-19. doi: 10.1016/0048-9697(92)90188-x.

Abstract

Complex distributions of hydrocarbons occur in most aquatic sediments. Total concentrations can range from a few parts per million in non-polluted intertidal and oceanic areas to parts per thousand in heavily contaminated estuarine, lake and near-shore environments. Iatroscan TLC-FID provides a quick assessment of the total hydrocarbon load, but capillary GC, HPLC and GC-MS are essential for obtaining detailed composition data from which information on possible sources can be derived. Alkenes from microalgae, such as n-C21:6, n-C17:1 and unusual C25 and C30 isoprenoid alkenes, are often the most abundant single components in sedimentary hydrocarbon distributions. Some hydrocarbons are also produced from diagenetic transformation of functionalised lipids present in the sediment. Long-chain alkanes typical of plant waxes can be important constituents, even in marine sediments far from the coast. These distributions display a strong predominance of odd chain lengths, whereas n-alkane distributions in oils usually show little or no predominance of either odd or even chain lengths. However, the presence of this type of distribution in a sediment may not indicate petroleum contamination since biological sources for similar distributions are now recognised. Petroleum-derived residues are common in coastal and estuarine areas, particularly those near urban or industrial centers. This contamination is readily seen in capillary gas chromatograms of the alkanes as an unresolved complex mixture (UCM). The source of the oil can often be deduced from characteristic distributions of biomarker steranes, rearranged steranes, hopanes and methyl hopanes determined by capillary gas chromatography-mass spectrometry. Methyl hopanes are major polycyclic alkanes in oils from carbonate source rocks, such as those from the Middle East, but are uncommon in Australian oils. GC-MS fingerprinting techniques show that lubricating oils are a major source of hydrocarbon pollution in many estuaries and coastal areas around Australia. It has been estimated that natural oil seeps may also contribute as much as 10% of the hydrocarbons in the global marine environment. Examples of this include major oil seepage in the Gulf of California and the widespread occurrence of bitumen strandings on South Australian beaches. Examples from marine and estuarine environments around Australia are presented to illustrate the use of modern analytical techniques to identify, quantify and determine the origins of hydrocarbons in aquatic sediments.

摘要

大多数水生沉积物中都存在复杂的碳氢化合物分布。总浓度范围从无污染的潮间带和海洋区域中的百万分之几到重度污染的河口、湖泊和近岸环境中的千分之几。薄层色谱-氢火焰离子化检测器(Iatroscan TLC-FID)可快速评估总碳氢化合物含量,但毛细管气相色谱法(GC)、高效液相色谱法(HPLC)和气相色谱-质谱联用仪(GC-MS)对于获取详细的成分数据至关重要,从中可以得出有关可能来源的信息。来自微藻的烯烃,如n-C21:6、n-C17:1以及不常见的C25和C30类异戊二烯烯烃,通常是沉积碳氢化合物分布中最丰富的单一成分。沉积物中存在的官能化脂质经成岩转化也会产生一些碳氢化合物。即使在远离海岸的海洋沉积物中,典型的植物蜡长链烷烃也可能是重要成分。这些分布显示出奇数链长度占主导地位,而油中的正构烷烃分布通常很少或没有奇数或偶数链长度的优势。然而,沉积物中这种类型的分布并不一定表明受到石油污染,因为现在已经认识到类似分布存在生物来源。石油衍生的残留物在沿海和河口地区很常见,特别是那些靠近城市或工业中心的地区。在正构烷烃的毛细管气相色谱图中,这种污染很容易表现为未解析的复杂混合物(UCM)。通常可以从通过毛细管气相色谱-质谱法测定的生物标志物甾烷、重排甾烷、藿烷和甲基藿烷的特征分布推断出油的来源。甲基藿烷是碳酸盐源岩油中的主要多环烷烃,如中东的油,但在澳大利亚的油中并不常见。气相色谱-质谱联用指纹技术表明,润滑油是澳大利亚许多河口和沿海地区碳氢化合物污染的主要来源。据估计,天然油渗漏对全球海洋环境中碳氢化合物的贡献可能高达10%。这方面的例子包括加利福尼亚湾的大量油渗漏以及南澳大利亚海滩上广泛出现的沥青搁浅。本文列举了澳大利亚周围海洋和河口环境的例子,以说明使用现代分析技术来识别、量化和确定水生沉积物中碳氢化合物的来源。

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