饱和烃经5分子筛络合前后单体烃碳同位素分析对比研究

通过对自配标准样品(正构烷烃)进行5分子筛吸附试验,测定了用5分子筛吸附法分离前后正构烷烃、异构烷烃和环烷烃碳同位素值,探讨试验前后碳同位素值的变化。尽管实验过程中样品经过85℃长时间加热回流及吸附样品的5分子筛用氢氟酸酸化处理,但实验结果经仪器检测,证明该方法对正构烷烃碳同位素值影响因素不大。本文还介绍了原油和煤可溶有机质中饱和烃络合前后的单体烃碳同位素分析方法。并在前人工作的基础上,改进采用微型索氏抽提加热回流实验装置,既提高了样品的回收率,也减少了样品中轻组分的损失。     

5A分子筛吸附混合溶剂洗脱-气相色谱-同位素质谱分析土壤中正构烷烃单体碳同位素

利用5A分子筛吸附,环己烷-正戊烷混合溶剂洗脱分离富集正构烷烃,用气相色谱法测定正构烷烃含量,气相色谱-气体同位素质谱(GC-C-IRMS)测定土壤样品中正构烷烃单体碳同位素。实验优化了5A分子筛用量和洗脱剂的比例,需要络合的正构烷烃的量与分子筛加入量呈线性关系,络合x mg的正构烷烃,需加入2.75x g分子筛,络合环己烷-正戊烷最佳比例为9∶91。探讨了络合过程中5A分子筛对不同链长正构烷烃的络合规律,短链正构烷烃被5A分子筛优先吸附,长链正构烷烃的络合相对滞后。正构烷烃的络合洗脱回收率为44%～72%,精密度(RSD,n=6)为4%～8%;正构烷烃单体碳同位素分析精度为0.04‰～0.38‰(1σ)。采用5A分子筛净化混合溶剂洗脱方法,分析加油站附近的实际土壤样品,未分峰基本消除,获得良好的净化效果,满足正构烷烃单体碳同位素分析的要求。     

柱色谱分离-分子筛络合洗脱过程中正构烷烃单体碳同位素分馏研究

应用气相色谱-气体同位素质谱(GC-C-IRMS)分析正构烷烃单体碳同位素之前,需要对饱和烃样品中正构烷烃和异构烷烃进行预分离、富集,在预分离和富集过程中正构烷烃单体碳同位素是否发生分馏是高精度分析正构烷烃单体碳同位素比值(δ~(13)C)的关键。本文以正构烷烃混合溶液为对象,利用柱色谱、5■分子筛络合、环己烷-正戊烷混合溶剂两次洗脱,GC-C-IRMS分析正构烷烃单体碳同位素,研究前处理过程中正构烷烃单体碳同位素是否发生分馏。结果表明:使用柱色谱分离前后,多数正构烷烃单体碳同位素比值相差-0.2‰～0.2‰;当5■分子筛不完全络合时,未络合的正构烷烃单体碳同位素比值偏重约0.7‰,可能发生了微弱的碳同位素分馏,但并未影响洗脱后的正构烷烃单体碳同位素比值;使用环己烷-正戊烷混合溶剂洗脱前后,碳同位素比值相差-0.2‰～0.5‰,以同样方式洗脱第二次,获得的正构烷烃单体碳同位素比值与模拟样品相差-0.3‰～0.2‰。分析不同回收率(20%)正构烷烃的单体碳同位素比值,处理前后的差值基本在0.3‰以内,可见当正构烷烃回收率低至20%左右时,其单体碳同位素仍未发生明显分馏。柱色谱分离-5■分子筛络合-混合溶剂洗脱方法适用于回收率大于20%的正构烷烃单体碳同位素分析。     

单分子烃碳同位素分析方法及影响因素探讨

本文介绍了原油和岩石可溶有机质的单分子烃C同位素分析方法。通过饱和烃样品预处理与未处理、标准样品及其加入异构烷烃后的对比试验以及常见的3种基线模式数据处理方法的讨论。分析了单分子烃C同位素测定的误差来源,阐明了正构烷烃与异构烷烃预分离处理、色谱升温程序和数据处理是影响单分子烃C同位素测定结果的重要因素。指出采用尿素络合法或5A分子筛吸附法进行样品预分离处理,选择单一升温速率或在待测化合物溢出的时间范围内保持较平缓的升温梯度,对多拐点基线模式进行分段数据处理等方法可提高分析结果的精度和准确度。     

生排烃过程中正构烷烃单体碳同位素组成的变化特征及其研究意义

通过对生排烃模拟实验产物 (残留油和排出油 )中正构烷烃单体碳同位素组成的测定,揭示出生排烃过程中正构烷烃碳同位素组成的变化特征。研究表明,生烃初期,液态正构烷烃主要来自干酪根的初次裂解,它们的碳同位素组成不论是在排出油中还是在残留油中,随温度的变化都不明显,呈现较相似的分布特征;在生烃高峰期,早期形成的沥青质和非烃等组分的二次裂解以及高碳数正构烷烃可能存在的裂解,使得正构烷烃单体碳同位素组成明显富集13 C,尤其在高碳数部分呈现出较大的差异。另外,实验结果显示排烃作用对液态正烷烃单体碳同位素组成的影响不太显著。     

用于单体氢同位素分析的混合溶剂洗脱5分子筛吸附正构烷烃的方法

混合溶剂萃取洗脱5分子筛吸附正构烷烃的方法在单体碳同位素分析研究中已得到了应用。由于5分子筛在长时间加热条件下可能对有机分子的氢交换反应具有一定的催化作用,因此对于该方法能否用于正构烷烃的单体氢同位素分析需要做进一步研究。本文以两种不同类型原油的饱和烃和正构烷烃混合标准样品为对象,采用环己烷-正戊烷溶剂和氢氟酸溶解-正戊烷溶剂洗脱5分子筛吸附的正构烷烃,对比分析两种萃取方式的分离效果,并分别测定了正构烷烃的单体氢同位素比值。结果表明:两种萃取方式都得到了纯化效果良好的正构烷烃组分,氢同位素测定结果的差值总体上小于4‰,在仪器分析误差范围内。经过三次环己烷-正戊烷洗脱方式获得正构烷烃回收率平均值为58%,氢氟酸溶解-正戊烷洗脱方式经过多次萃取操作获得正构烷烃回收率平均值为68%。尽管环己烷-正戊烷洗脱方式提取正构烷烃的效率较低,并且涉及在分子筛条件下多次较长时间的加热过程,但这两个因素没有导致氢同位素发生明显的分馏或交换过程,适合用于正构烷烃分离、纯化以及单体氢同位素测定。     

尿素络合法分离-气相色谱/同位素质谱法分析土壤和植物中低含量(ppm级)正构烷烃的碳同位素

尿素络合法和5A分子筛法是常用的分离富集环境样品中正构烷烃的方法,但由于复杂的处理流程对于低含量正构烷烃的回收率普遍较低。本文通过优化尿素络合法分离富集正构烷烃的实验条件,建立了尿素络合法分离-气相色谱/同位素质谱分析土壤和植物中低含量正构烷烃单体碳同位素的方法。即采用正己烷-丙酮溶解样品,在4℃冰箱中与2 m L尿素-甲醇饱和溶液反应48 h;用去离子水溶解尿素络合物,加入正己烷后分离出有机相和水相,分别用正己烷、丙酮-正己烷萃取有机相和水相中的正构烷烃。中长链正构烷烃的回收率达79%~104%,高于5A分子筛法和已有尿素络合法的富集效果;单体碳同位素的分析精度为0.09‰~0.63‰(1σ)。利用改进的方法分析实际样品,大幅降低了未分峰和共流出物的干扰,提高了实际样品中ppm级中长链正构烷烃的回收率。     

准噶尔盆地液态烃分子碳同位素组成特征及其应用

文章报导了准噶尔盆地不同地区、不同产层原油和烃源岩样品中正构烷烃和类异成二烯烃碳同位素组成特征。在ｎＣ₁₁－ｎＣ₃₄之间，保罗系湖沼相成因的原油，正构烷烃δ13Ｃ值大部分分布在－２７．０‰──３２．４‰之间，比海相地层的原油重，具有富集13Ｃ的特征。ⅡＡ型烃源岩产出原油的单烃δ13Ｃ值比ⅡＢ型的轻，相对富集12Ｃ。碳源组成相同的原油在正构烷烃和类异成二烯烃碳同位素组成上，有相似的分布范围和较为一致的总体变化趋势，因此单烃碳同位素组成可用于油－油对比和油－源对比中。     

吐哈盆地正构烷烃具中低碳数偶碳优势煤系烃源岩地球化学特征

<正>对吐哈盆地煤系烃源岩中具偶数碳优势样品的生物标志化合物及正构烷烃单体烃碳同位素分布特征进行了分析。1)样品选取:台北凹陷中、下侏罗统正构烷烃具偶碳优势的煤系烃源岩样品:草南1井J1q,疙13井J2x4,小草1井J2x,勒2井J2x,亚1井J1s;台南凹陷正构烷烃具偶碳优势的煤系烃源岩样品:鲁南1井C,艾参1井C。2)实验方法:氯仿沥青"A"多粒子检测定量色谱/质谱;正构烷烃单体烃碳同位     

金湖凹陷阜宁组低熟烃源岩饱和烃组成及其生源探讨

本文应用气相色谱，色谱－质谱和线性同位素质谱分析技术对盆地金湖凹陷下第三系阜宁组阜二段低熟烃源岩和烃组分及单体烃稳定碳同位素组成进行了深入地研究，发现甾烷类－Ｃ２９在饱和烃中含量很高，正构烷烃呈三峰型分布，以ｎＣ２２或ｎＣ２０为主峰。最后根据烃源岩有机显微组分和单体烃碳同位素组成特征认为正构烷烃中低碳数和中等碳数正构烷烃可能主要来源于菌藻类，高碳数大部分可能主要由藻类贡献。     

Accurate Isotopic and Concentration Analyses of Small Amounts of Pb Using Isotope Dilution Coupled with the Double Spike Technique

A new method has been developed for the simultaneous determination of Pb abundance and Pb isotopic composition with high precision and accuracy for small test portion masses by thermal ionisation mass spectrometry. In this method, a ²⁰⁵pb-²⁰⁴pb double spike is added to samples prior to the chemical separation of Pb, and the isotopic composition of the spike-sample mixture is determined rigorously by the double spike technique using a ²⁰⁷Pb-²⁰⁴Pb spike. The isotopic composition and concentration of Pb in the sample are then obtained by utilising the principle of isotope dilution. Using this technique, replicate determinations of Pb from NIST SRM 981 and GSJ JP-1 (peridotite; 0.07 μg g⁻¹ Pb) were performed. The measured concentration and isotopic data were identical, within uncertainty, to published data or to data that were determined independently in this study. The application of this method to U-Pb dating and the determination of the "initial" Pb isotopic composition was also tested. Lead isotopic compositions and the concentrations of Pb, Th and U were determined for a single batch of samples, through the addition of ²⁰⁵pb-²⁰⁴pb, ²³⁰Th and ²³⁵U spikes to samples prior to chemical separation. Also in these experiments, we confirmed that this routine gives accurate data for Pb, Th and U concentrations and Pb isotopic compositions.     

碳还原法分析硫酸盐的氧同位素组成

硫酸盐矿物是自然界最常见矿物,也是自然界少数具有氧同位素非质量分馏效应的矿物之一.硫酸盐矿物的氧同位素组成可以为研究其形成过程和生成条件提供大量信息.目前,在国内外分析硫酸盐氧同位素的3种方法中,碳还原方法乃是分析硫酸盐中氧同位素组成的最精准方法.本次研究建立了分析硫酸盐中氧同位素组成的碳还原方法,介绍了硫酸钡的分析流...     

Ion microprobe analysis of O/O in authigenic and detrital quartz in the St. Peter Sandstone, Michigan Basin and Wisconsin Arch, USA: Contrasting diagenetic histories

The oxygen isotopic compositions of authigenic quartz cements in sandstones provide a monitor of the temperatures, compositions, and origins of pore-occluding fluids during diagenesis, but quartz overgrowths are too fine-grained to be amenable to conventional isotopic analysis. We have used a Cameca ims-4f ion microprobe to determine oxygen isotopic variations in authigenic and detrital quartz in four samples of the Ordovician St. Peter Sandstone from the Michigan Basin and Wisconsin Arch, midwestern USA. Ion microprobe isotopic analyses have been successfully accomplished with an internal precision of ±1‰ (1 σ) and a spatial resolution of 20–30 μm at low mass resolution using a high voltage offset technique. Repeated analyses of the quartz standard demonstrate a reproducibility of close to ±1‰ (1 sd) in good agreement with that expected from counting statistics. The four ion probe samples were chosen as representative of thirteen samples that were mechanically and chemically disaggregated, sieved, and analysed as a function of sieve size by conventional bulk-mineral techniques. Conventional and ion microprobe analyses are mutually consistent, supporting the accuracy of the ion microprobe analyses. Within-sample isotopic variations of up to 13%. and micro-scale isotopic variations of at least 4‰ over a distance of 100 μm have been measured within quartz overgrowths in a sandstone from the Wisconsin Arch. Overgrowths are uniformly higher in δ¹⁸O than detrital grains, and gradients of up to 25% exist across a few microns.

¹⁸O-enriched quartz overgrowths in sandstones from the Wisconsin Arch show complex CL zonation and reflect one of two possible processes: (1) low-temperature quartz precipitation during mixing of meteoric waters with upwelling basinal fluids; (2) higher temperature quartz precipitation during episodic gravity-driven upwelling of warm basinal fluids (of comparable isotopic composition to Michigan Basin fluids) from the Illinois Basin, related to evolution of Mississippi Valley type Pb---Zn ore-forming fluids. Quartz overgrowths in Michigan Basin sandstones, which derived their silica locally by pressure solution, are thought to have precipitated continuously over a range of temperatures from hot basinal fluids of restricted isotopic composition and circulation. Detrital quartz shows significant intea-grain and intergrain isotopic variation (5–13‰) but no significant inter-sample variation, consistent with a uniform source of granitoid and metamorphic quartz in space and time.     

Methodology and Application of Hafnium Isotopes in Ilmenite and Rutile by MC‐ICP‐MS

The high abundances of the high field‐strength elements in ilmenite and rutile make these minerals particularly suitable for hafnium isotopic investigations. We present a technique for separating Hf by ion exchange chemistry from high‐TiO₂ (> 40% m/m) minerals to achieve precise Hf isotopic composition analyses by MC (multiple collector)‐ICP‐MS. Following digestion and conversion to chlorides, the first elution column is used to separate iron and the rare earth elements, the second column is designed to separate most of the titanium from Hf, an evaporation step using HClO₄ is then performed to remove any trace of HF in preparation for the third column, which is needed to eliminate any remaining trace of titanium. The modified chemistry helped to improve the yields from < 10 to > 78% as well as the analytical precision of the processed samples (e.g., sample 2033‐A1, ¹⁷⁶Hf/¹⁷⁷Hf = 0.282251 ± 25 before vs. 0.282225 ± 6 after). The technique was tested on a case study in which the Hf isotopic ratios of ilmenite and rutile (analysed prior to the chemistry improvement) were determined and permitted to evaluate that the origin of rutile‐bearing ilmenite deposits is from the same or similar magma than their, respectively, associated Proterozoic anorthosite massifs (Saint‐Urbain and Lac Allard) of the Grenville Province in Québec, Canada.     

Isotopes of hydrogen and oxygen in nitrogen hot springs of Baikal Rift Zone in terms of interaction in the water-rock system

The negative correlation between values δD and δ¹⁸O and concentrations of dissolved silicon in nitrogen hot springs is ascertained, which attests to the directed alteration of their hydroisotopic composition towards being depleted in heavy isotopes during interaction in the water-rock system. This fact can be allowed for the cases of the lighter isotopic composition of the hot springs of meteogenic origin relative to that of local atmospheric precipitation. The shifts in points of isotopic composition of hot springs from the global meteoric water line can be caused by alterations in either oxygen or hydrogen composition.     

江西省横迳温泉区地热气体地球化学

从赣南横迳温泉区采集10个水样并分析了温泉及冷泉的水化学成分,认为热水起源于大气降水补给。在此基础上,还在温泉区采集了4个气样,测定了气体组分的含量及氦同位素．以及CO₂和CH₄的碳同位素。研究结果表明：横迳地区温泉气中CO₂的含量很高(>96％),δC_CO2较重(-4.43‰～-5.50‰),属幔源CO₂;He同位素特征值(R/Ra)变化于1.36～2.11之问．均大于1,有幔源He的加入;本区温泉气的的组合类型为二氧化碳幔源温泉气,从整体上来说属于幔源无机成因气,是地幔脱气的产物。     

天青石中锶同位素组成测定——酸溶和碱熔样品分解方法的对比

利用酸溶法和碱熔法分解天青石样品，经过离子交换分离得到纯净的Sr，测定^87Sr／^86Sr同位素比值，实验结果表明两种样品分解方法得到的^87Sr／^86Sr同位素比值的偏差〈0.0001，证明在天青石锶同位素组成测定中，酸溶法和碱熔法都是可行的；但与碱熔法相比，酸溶法更简易并且利于本底值的控制。     

Do lunar and meteoritic archives record temporal variations in the composition of solar wind noble gases and nitrogen? A reassessment in the light of Genesis data

Since about half a century samples from the lunar and asteroidal regoliths been used to derive information about elemental and isotopic composition and other properties of the present and past solar wind, predominantly for the noble gases and nitrogen. Secular changes of several important compositional parameters in the solar wind were proposed, as was a likely secular decrease of the solar wind flux. In 2004 NASA’s Genesis mission returned samples which had been exposed to the solar wind for almost 2.5 years. Their analyses resulted in an unprecendented accuracy for the isotopic and elemental composition of several elements in the solar wind, including noble gases, O and N. The Genesis data therefore also allow to re-evaluate the lunar and meteorite data, which is done here. In particular, claims for long-term changes of solar wind composition are reviewed.Outermost grain layers from relatively recently irradiated lunar regolith samples conserve the true isotopic ratios of implanted solar wind species. This conclusion had been made before Genesis based on the agreement of He and Ne isotopic data measured in the aluminum foils exposed to the solar wind on the Moon during the Apollo missions with data obtained in the first gas release fractions of stepwise in-vacuo etch experiments. Genesis data allowed to strengthen this conclusion and to extend it to all five noble gases. Minor variations in the isotopic compositions of implanted solar noble gases between relatively recently irradiated samples (<100 Ma) and samples irradiated billions of years ago are very likely the result of isotopic fractionation processes that happened after trapping of the gases rather than indicative of true secular changes in the solar wind composition. This is particularly important for the ³He/⁴He ratio, whose constancy over billions of years indicates that hardly any ³He produced as transient product of the pp-chains has been mixed from the solar interior into its outer convective zone. The He isotopic composition measured in the present-day solar wind therefore is identical to the (D + ³He)/⁴He ratio at the start of the suns’s main sequence phase and hence can be used to determine the protosolar D/H ratio.Genesis settled the long-standing controversy on the isotopic composition of nitrogen in lunar regolith samples. The ¹⁵N/¹⁴N ratio in the solar wind as measured by Genesis is lower than in any lunar sample. This proves that nitrogen in regolith samples is dominated by non-solar sources. A postulated secular increase of ¹⁵N/¹⁴N by some 30% over the past few Ga is not tenable any longer. Genesis also provided accurate data on the isotopic composition of oxygen in the solar wind, invaluable for cosmochemisty. These data superseded but essentially confirmed one value – and disproved a second one – derived from lunar regolith samples shortly prior to Genesis.Genesis also confirmed prior conclusions that lunar regolith samples essentially conserve the true elemental ratios of the heavy noble gases in the solar wind (Ar/Kr, Kr/Xe). Several secular changes of elemental abundances of noble gases in the solar wind had been proposed based on lunar and meteoritic data. I argue here that lunar data – in concert with Genesis – provide convincing evidence only for a long-term decrease of the Kr/Xe ratio by almost a factor of two over the past several Ga. It appears that the enhancement of abundances of elements with a low first ionisation potential in the solar wind (FIP effect) changed with time.Finally, Genesis allows a somewhat improved comparison of the present-day flux of solar wind Kr and Xe with the total amount of heavy solar wind noble gases in the lunar regolith. It remains unclear whether the past solar wind flux has been several times higher on average than it is today.     

微量水δ(~(17)O)和δ(~(18)O)CoF_3法线外同时测试新技术

三氧同位素(16O、17O、18O)组成特征可有效示踪天然水循环及其环境效应,微量水δ(17O)和δ(18O)CoF3法同时测试新技术的建立,可为三氧同位素定量研究提供有效的分析手段,特别是能够捕捉到像光合作用、呼吸作用等生物过程中发生的同位素分馏现象。在国内首次建立了微量水δ(17O)和δ(18O)CoF3法线外同时测试新技术,样品量仅需2μL,整个制样时间约40min。采用在质谱测试前对待测样品在100℃下预热10 min,待O2完全解吸后再进行质谱测试的方法,避免了制样和测试过程中的记忆效应及分馏效应,δ(17O)和δ(18O)的分析精度分别达到±0.07‰和±0.14‰。该法使用固体试剂CoF3替代了剧毒的气态氟化物BrF5,使得制样流程更加安全可靠且样品量少,适用性强,具有很大的推广应用价值。     

Natural Cadmium Isotopic Variations in Eight Geological Reference Materials (NIST SRM 2711, BCR 176, GSS-1, GXR-1, GXR-2, GSD-12, Nod-P-1, Nod-A-1) and Anthropogenic Samples, Measured by MC-ICP-MS

In this study, the Cd isotopic composition of various geological reference materials and anthropogenic samples was investigated. The measurements were made by multicollector ICP-MS and instrumental mass fractionation was controlled using a "sample-standard bracketing" technique. Cadmium isotopic data are reported relative to an internal Cd solution (Cd Spex) and expressed as the ¹¹⁴ Cd/¹¹⁰Cd delta value. Two other Cd solutions (Prolabo and JMC) were analysed and yielded the same 0% delta value. A fractionated Cd metal sample (Münster Cd) was used as a secondary reference material for Cd isotopic measurements and we obtained a ¹¹⁴ Cd/¹¹⁰ Cd delta value of 4.48% relative to Cd Spex solution. As opposed to multi-stage Cd purification previously published in the literature, a new one step anionic exchange purification using dilute HCl for the analysis of Cd isotopes in geological samples was developed. This method enabled a high recovery (> 95%) and effective separation of the sample matrix to be achieved. The long-term external reproducibility was evaluated at 0.12% (2 standard deviations) for the ¹¹⁴ Cd/¹¹⁰Cd ratio, based on reference solutions and replicated measurements of samples over one year. The variation of Cd isotopic composition of natural terrestrial samples is restricted to a small range of 0.4%, which is similar to previously reported results. In contrast, large variations of Cd isotopic composition were found for anthropogenic samples with values as low as −0.64% for a dust sample issued from a lead smelter and values as high as +0.50% for NIST SRM 2711 (metal-rich soil). These variations are 10 times larger than the reproducibility and suggest that Cd isotopes can be useful as tracers of anthropogenic sources of Cd in the environment.