ICP-MS及其联用技术在海洋地质研究中的应用前景

电感耦合等离子体质谱(ICP—MS)具有灵敏度高、检出限低、选择性好、线性范围宽、能进行多元素和同位素比测定等优点,广泛应用于环境、地质、医药、食品和高纯物质等领域。ICP—MS与其他进样及分析技术的联用,大大地扩展了其应用范围。重点介绍了ICP—MS与激光烧蚀(LA)、高效液相色谱(HPLC)及气相色谱(GC)的联用技术,探讨了它们在海洋地质研究中的应用前景。     

气相色谱指纹法在海上油污染源鉴别中的应用

通过一个具体案例,探讨了气相色谱指纹法在海上油污染源鉴别中的应用。该鉴别方法基于样品的正构烷烃气相色谱指纹分析,选择既能表征油种固有特性,又受风化影响较小的正十七烷(n-C17)、正十八烷(n-C18)、姥鲛烷(phy)、植烷(phy)和正二十烷(n-C20)等特征烷烃作为判据,可信度大,而且整个操作流程短(一般不超过半天),较简便易行。     

沉积有机质激光热裂解色谱质谱探针分析技术的尝试及其前景探讨

激光热裂解－色谱－质谱分析方法具有从技术层面上融合分子地球化学方法和有机岩石学方法的潜能。通过抚顺煤镜质组分和树脂体的研究实例，介绍了激光热裂解－色谱－质谱探针分析的基本原理及测试方法。抚顺煤显微组分的微区热裂解产物特征中，镜质组和树脂体热解产物的正烷烃、烷基萘和四氢化萘的总体面貌相似，但树脂体中正烷烃含量较低，而烷基四氢化萘明显较高，这可能反映显微组分形成过程中发生过低分子烃类在各显微组分之间的混合作用。除此之外，还把激光热裂解－色谱－质谱探针技术与传统的分子地球化学方法、有机岩石学方法进行比较。探讨了激光热裂解－色谱－质谱探针技术的应用前景以及尚待解决的技术问题。落射到样品表面的激光束能量（温度）和控制和激光辐射时间的，激光束斑大小、热解产物量、色谱－质谱检验灵敏度极限三者关系等，都是限制新技术应用的技术问题。     

华北平原冬麦田土壤CH4的吸收特征研究

利用静态箱/气相色谱(GC)法,对华北平原冬小麦拔节—成熟期间麦田土壤CH4气体通量进行了测定,得出华北平原典型冬麦田土壤是大气CH4的弱吸收汇。试验期间土壤CH4通量存在明显的季节变化和日变化,麦田拔节—成熟期间土壤CH4通量日平均值为-18.3μg.m-2.h-1,波动范围为-4.3~-24.4μg.m-2.h-1;在土壤CH4通量的日变化中,观测到麦田土壤在午间和夜间都有一个吸收峰,峰值出现的时间因生育期不同而有所不同。试验期间CH4通量日平均值与土壤温度关系不明显,而与土壤水分呈负相关(α=0.01);日变化中土壤CH4通量与地表温度的相关性较差,而与5 cm地温相关密切。麦田拔节—成熟期间土壤CH4通量日平均值随NH4 -N施用量的增加呈递减规律,农田秸秆还田后不利于土壤对CH4的吸收。     

华北平原冬麦田土壤CH4的吸收特征研究

利用静态箱/气相色谱(GC)法,对华北平原冬小麦拔节-成熟期间麦田土壤CH₄气体通量进行了测定,得出华北平原典型冬麦田土壤是大气CH₄的弱吸收汇。试验期间土壤CH₄通量存在明显的季节变化和日变化,麦田拔节-成熟期间土壤CH₄通量日平均值为-18.3μg·m^-2·h^-1,波动范围为-4.3-24.4μg·m^-2·h^-1;在土壤CH₄通量的日变化中,观测到麦田土壤在午间和夜间都有一个吸收峰,峰值出现的时间因生育期不同而有所不同。试验期间CH₄通量日平均值与土壤温度关系不明显,而与土壤水分呈负相关(α=0.01);日变化中土壤CH₄通量与地表温度的相关性较差,而与5cm地温相关密切。麦田拔节-成熟期间土壤CH₄通量日平均值随NH4+-N施用量的增加呈递减规律,农田秸秆还田后不利于土壤对CH₄的吸收。     

Biodegradation and environmental behavior of biodiesel mixtures in the sea: An initial study

Biodiesel, a mixture of fatty acid methyl esters (FAMEs) derived from animal fats or vegetable oils, is rapidly moving towards the mainstream as an alternative source of energy. However, the behavior of biodiesel, or blends of biodiesel with fossil diesel, in the marine environment have yet to be fully understood. Hence, we performed a series of initial laboratory experiments and simple calculations to evaluate the microbial and environmental fate of FAMEs. Aerobic seawater microcosms spiked with biodiesel or mixtures of biodiesel and fossil diesel revealed that the FAMEs were degraded at roughly the same rate as n-alkanes, and more rapidly than other hydrocarbon components. The residues extracted from these different microcosms became indistinguishable within weeks. Preliminary results from physical-chemical calculations suggest that FAMEs in biodiesel mixtures will not affect the evaporation rates of spilled petroleum hydrocarbons but may stabilize oil droplets in the water column and thereby facilitate transport.     

Changes in the Chemical Components of Light Crude Off During Simulated Short Term Weathering

To unambiguously identify spilled oils and to link them to the known sources are extremely important in settling questions of environmental impact and legal liability. The fate and behavior of spilled oils in the environment depend on a number of physicochemical and biological factors. This paper presents the results regarding changes in chemical composition of light crude oil during simulated short-term weathering based on natural environmental conditions. The results show that the saturated hydrocarbons of the light crude oil mainly distribute between n-C8 and n-C23 and the most abundant n-alkanes are found in the n-C10 to n-C16. The main chemical components of the light crude oil are n-alkanes and isoprenoids. The aromatic compounds are subordinate chemical components. Under the conditions of the weathering simulation experiment,n-alkanes less than n-C12,toluene and 1,3-dimethyl benzene are lost after 1 d weathering,the n-C13,n-C14,naphthalene and 2-methyl-naphthalene are lost on the fifth day of weathering,and n-C15 alkane components show certain weatherproof capability. The ratios n-C17/pristane and n-C18/phytane are unaltered and can be used to identify the source of the light crude oil during the first 8 d of weathering. After 21 d,the ratio pristine/phytane can not provide much information on the source of the spilled light crude oil. Triterpanes（m/z 191） as biomarker compounds of light crude oil are more valuable.     

Occurrence and transport of Irgarol 1051 and its major metabolite in coastal waters from South Florida

Irgarol 1051, a boosting antifouling agent often used to supplement copper based paints was found in surface waters from South Florida at stations collected from the Miami River, Biscayne Bay and selected areas of the Florida Keys. Concentrations of the herbicide ranged from below the method detection limit (1 ng/L) to as high as 182 ng/L in a canal system in Key Largo. The herbicide was present at 93% of the stations and often found in conjunction with its descyclopropyl metabolite (M1) previously reported to be the major degradation product of Irgarol under natural environmental conditions. The 90th percentile concentration calculated for all South Florida samples was 57.6 ng/L. Based on available data on the toxicity of Irgarol to algae and coral, only two stations (approximately 3%) ranked above the LC50 of 136 ng/L reported for the marine algae Naviculla pelliculosa and above the 100 ng/L level reported to reversibly inhibit photosynthesis of intact corals. However, a basic dissipation model for Irgarol using the Key Largo Harbor station as a point source indicated that concentrations of the herbicide decreased rapidly and concentrations below the MDL are observed within 2000 m of the source. No major coral based benthic habitats are documented for all the stations surveyed at distances that Irgarol may pose a substantial risk. However, other types of submerged vegetation like seagrasses are common around the marinas and the effects of Irgarol to such endpoints should be investigated further.     

低浓度磷酸一酯的膜富集和气相色谱测定

磷酸一酯（ＲＯ）Ｐ（Ｏ）（ＯＨ）２是一种强极性的有机磷化合物。研究了水体中磷酸一（１－萘）酯的富集和上色谱分析,建立了一个简便快速、高灵敏度、实用的分析方法。富集是采用固相萃取方法,选用载有十八烷基硅烷的尼龙滤膜吸附,甲醇洗脱,回收率达７２％￣７％。它的气相色谱分析选用ＢＳＴＦＡ为衍生剂,反应条件为温度６５℃,反应时间３０ｍｉｎ,获得了满意的结果。方法的最低检测限为０。０６ｎｇ。