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Combined High-Resolution Solid-State ~1H~(13)C NMR Spectroscopy and ~1H NMR Relaxometry for the Characterization of Kerogen Thermal Maturation

机译:结合高分辨率固态〜1H〜(13)C NMR光谱和〜1H NMR弛豫仪,用于表征Kerogen热成熟

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摘要

A key factor for the petroleum potential of source rock is the degree of chemical and physical structure evolution of its kerogen fraction through a range of maturation processes. In this study, various high-field, solid-state NMR methods have been applied to a series of kerogen isolates (type I) over a defined maturity range (vitrinite reflectance iR _(0) from 0.98 to 1.86%). Results obtained from ~(13)C MAS NMR show that the sp~(2)/sp~(3)-hybridized carbon ratio of kerogen, here defined as the aromatic/aliphatic ratio, increases with increasing maturity. ~(1)H MAS NMR spectra contain partly overlapping aliphatic and aromatic resonances with distinct transverse relaxation behavior. In Hahn-echo experiments, the aromatic signal decays more slowly than the aliphatic signal, indicating that for these systems, transverse ~(1)H relaxation is rather controlled by local distances between hydrogen atoms than by molecular mobility. Similar relaxation differences are also found in static (nonspinning) ~(1)H Hahn-echo NMR experiments, here used to discriminate between phases with different proton mobilities and/or densities in the kerogen samples and, ultimately, between aromatic and aliphatic fractions. The distributions of the static transverse relaxation time (iT _(2)), extracted from the Hahn-echo decays, are characterized by a short-iT _(2) peak (∼10 μs) and a long-iT _(2) peak (∼100 μs). The ratio between these two peaks correlates well with the aliphatic-to-aromatic signal intensity ratios in MAS NMR spectra of the corresponding kerogen samples, suggesting that a net decrease in kerogen proton density—occurring during maturation—is also reflected by ~(1)H NMR relaxation. For the investigated kerogen isolates, the long-iT _(2) peak in the iT _(2) distribution can be considered an indicator of aromatic content, which can be directly detected by measuring ~(1)H iT _(2) relaxation.
机译:为源岩的石油潜在的关键因素是它的干酪根分数的化学和物理结构演变通过一系列成熟过程的程度。在这项研究中,各种高场,固态NMR方法已经在限定期限范围应用于一系列干酪根分离物(I型)的(镜质组反射的 [R _(0)从0.98到1.86%)。从〜获得的结果(13)C MAS NMR表明,SP〜(2)/ SP〜(3)杂化碳干酪根比,此处定义为芳族/脂肪族比,随成熟而增加。 〜(1)H MAS NMR光谱包含具有不同横向弛豫行为部分重叠的脂族和芳族共振。在哈恩回波实验中,芳族信号衰减比更慢的脂肪族的信号,这表明对于这些系统,横向〜(1)H松弛而被氢原子之间的局部距离大于由分子运动性的控制。类似松弛差异在静态的(不自旋)〜(1)H哈恩回波NMR实验中,这里用于区分相之间具有不同的质子迁移率和/或密度的干酪根样品中,并最终,芳族和脂族馏分之间也有发现。的静态横向弛豫时间分布(Ť_(2)),从哈恩回波衰减,通过短期的Ť_(2)峰(〜10微秒),其特征提取和长 - Ť_(2)峰(〜100微秒)。很好地在相应的干酪根样品的MAS NMR光谱的脂族 - 对 - 芳族信号强度比这两个峰值相关因素之间的比率,这表明在这段中的干酪根质子净减少密度存在的成熟-也由〜(1)反射1 H NMR放松。对于所研究的干酪根分离株中,长的Ť_(2)峰在Ť_(2)分布可以被认为是芳族化合物含量的指标,其可通过测量〜直接检测(1)H Ť_(2)松弛。

著录项

  • 来源
    《Energy & fuels》 |2021年第2期|1070-1079|共10页
  • 作者单位

    Department of Chemistry University of Cambridge;

    Schlumberger Cambridge Research High Cross;

    Schlumberger Cambridge Research High Cross;

    Schlumberger-Doll Research;

    Department of Chemistry University of Cambridge;

    Department of Chemistry University of Cambridge;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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