Department of Earth Science and Engineering, Imperial College London, London, UK.
Rapid Commun Mass Spectrom. 2020 Jul 30;34(14):e8802. doi: 10.1002/rcm.8802. Epub 2020 May 23.
For clumped isotope analysis (Δ ), hydrocarbon and organic molecules present an important contaminant that cannot always be removed by CO purification through a Porapak-Q trap. Low-temperature oxygen plasma ashing (OPA) is a quick and easy approach for treatment; however, the impact of this treatment on the original carbonate clumped isotope values has never been fully studied.
We tested the isotopic impact of OPA using three natural samples with a large range of initial Δ values. Crushed and sieved (125 μm mesh) samples were placed into a Henniker Plasma HPT-100 plasma system and treated at a flow rate of 46 mL/min and a power of 100 W at a vacuum of 0.2 mbar for 10, 20, 30 and 60 min before clumped isotope analysis using two MAT 253 isotope ratio mass spectrometers modified to measure masses 44-49.
OPA treatment for 30 min or more on calcite powder samples has the potential to alter the clumped isotopic composition of the samples beyond analytical error. A systematic positive offset is observed in all samples. The magnitude of this alteration translates to a temperature offset from known values ranging from 4°C to 13°C. We postulate that the observed positive offset in Δ occurs because the bonds within lighter isotopologues are preferentially broken by plasma treatment, leading to an artificial increase in the 'clumping' value of the sample.
We recommend that any laboratory performing OPA treatments should reduce the runs to 10-20 min or carry out successive runs of 10 min followed by sample stirring, as this procedure showed no alteration in the initial Δ values. Our results validate the use of OPA for clumped isotope applications and will allow future research to use clumped isotopes for challenging samples such as oil-stained carbonates, bituminous shales or host rocks with very high organic carbon content.
对于团簇同位素分析(Δ),烃类和有机分子是一种重要的污染物,通过 Porapak-Q 阱的 CO 净化通常无法完全去除。低温氧等离子体灰化(OPA)是一种快速简便的处理方法;然而,这种处理方法对原始碳酸盐团簇同位素值的影响从未被充分研究过。
我们使用三个具有较大初始Δ值范围的天然样品来测试 OPA 的同位素影响。将粉碎和筛分(125 μm 筛网)的样品放入 Henniker Plasma HPT-100 等离子体系统中,在真空度为 0.2 mbar 下以 46 mL/min 的流速和 100 W 的功率处理 10、20、30 和 60 min,然后使用两台经过修改以测量质量 44-49 的 MAT 253 同位素比质谱仪进行团簇同位素分析。
在方解石粉末样品上进行 30 分钟或更长时间的 OPA 处理有可能使样品的团簇同位素组成发生变化,超出分析误差。在所有样品中都观察到系统的正偏移。这种变化的幅度相当于从已知值偏移 4°C 至 13°C 的温度。我们推测,观察到的 Δ 正偏移是因为等离子体处理优先破坏较轻同位素的键,导致样品的“团簇”值人为增加。
我们建议任何进行 OPA 处理的实验室都应将运行时间减少到 10-20 分钟,或者进行 10 分钟的连续运行,然后搅拌样品,因为这种程序不会改变初始Δ值。我们的结果验证了 OPA 在团簇同位素应用中的使用,并将允许未来的研究使用团簇同位素来处理具有挑战性的样品,例如油污染的碳酸盐、沥青页岩或有机碳含量非常高的母岩。