2013
DOI: 10.1016/j.orggeochem.2013.04.007
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Rapid column chromatography separation of alkylnaphthalenes from aromatic components in sedimentary organic matter for compound specific stable isotope analysis

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Cited by 18 publications
(6 citation statements)
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“…To further reduce the complexity of the aromatic hydrocarbon fraction in order to conduct CSIA, aliquots were subject to sub-fractionation using alumina (fully activated) column chromatography based on procedures described by Jiang et al (2013) to produce subfractions of mainly monodi, tri and ≥ tetra-cyclic aromatic hydrocarbons and heterocyclic structures.…”
Section: Isolation Of Maltene and Asphaltene Fractionsmentioning
confidence: 99%
“…To further reduce the complexity of the aromatic hydrocarbon fraction in order to conduct CSIA, aliquots were subject to sub-fractionation using alumina (fully activated) column chromatography based on procedures described by Jiang et al (2013) to produce subfractions of mainly monodi, tri and ≥ tetra-cyclic aromatic hydrocarbons and heterocyclic structures.…”
Section: Isolation Of Maltene and Asphaltene Fractionsmentioning
confidence: 99%
“…Separation of Aliphatic Hopanes, Benzohopanes, Secohopanes, and Sulfidic Hopanes. The details of the separation methods of aliphatic hopanes, benzohopanes, secohopanes, and sulfidic hopanes were described by Cheng et al, 74 Jiang et al, 75 Wang et al, 76 and Wu et al, 77 respectively. The methods were introduced briefly in the following.…”
Section: Samples and Methodsmentioning
confidence: 99%
“…Column chromatography of the bitumen fraction on silica gel yielded aliphatic, aromatic and polar fractions. To further con- centrate OSCs, aromatic fractions were fractionated over aluminium oxide (Type 507C neutral; Fluka); using solutions of nhexane:DCM (99:01 v/v), n-hexane:DCM (90:10 v/v) and DCM in a refined procedure outlined by Jiang et al (2013) -the OSCs exclusively eluted in the third sub-fraction. Remnant carbonates were removed from the kerogen fraction by treatment with concentrated HCl at $60°C (24 h).…”
Section: Methodsmentioning
confidence: 99%