Gas Chromatographic Determination of C6, C7, and C8 Olefins According to Their Carbon Structures

Nelson, Kurt H.; Hines, W. J. W.; Grimes, M.; Smith, Donald E.

doi:10.1021/ac60165a018

Cited by 16 publications

(2 citation statements)

References 9 publications

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“…These results support the extension of the methylene insertion synthesis to olefins for the purpose of a direct component analysis of olefinic mixtures. Also, the carbon-skeleton distribution of such mixtures can be inferred by hydrogenation of the olefins and subsequent analysis of the resulting saturated hydrocarbons (15). To the extent that the present investigation extends the possibilities of component analysis of alkanes and cycloalkanes, it correspondingly extends the carbon-skeleton analysis of olefinic systems after hydrogenation.…”

mentioning

confidence: 79%

Applications of the Methylene Insertion Reaction to Component Analysis of Hydrocarbons.

Dvoretzky¹,

Richardson²,

Durrett³

1963

Anal. Chem.

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Table IV. Total Lead in Gasolines by Gas Chromatography and X-Ray Grams of lead per gallon Gas chroma-X-ray tography fluorescence Gasoline A 2.98 3.12 Gasoline B 0.45 0.50 Gasoline C 2.21 2.09 Gasoline D 2.91 2.76 isomers were not available. The isomer distribution specified by the manufacturer was assumed correct. Greater reliability in the accuracy of the results would be obtained by calibrating with the pure isomers.

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mentioning

confidence: 79%

Applications of the Methylene Insertion Reaction to Component Analysis of Hydrocarbons.

Dvoretzky¹,

Richardson²,

Durrett³

1963

Anal. Chem.

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“…A similar prechromatographic treatment was used by Nelson et al (7) in detecting olefins in a mixture with paraffins by hydrogenation of the original sample.…”

Section: Methods Of Analysis For Individualmentioning

confidence: 99%

New Technique for Functional Group Analysis in Gas Chromatography. Syringe Reactions.

Hoff¹,

Feit²

1964

Anal. Chem.

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Gaschromatographische Untersuchungen an C₆‐Kohlenwasserstoffen

Döring

Hauthal

1963

J. Prakt. Chem.

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Zur Analyse von Mono‐, Di‐ und Cycloolefinen, wie sie in technischen C6‐Kohlenwasserstoff‐Fraktionen vorliegen, wurde eine Kombination von Feindestillation und Gaschromatographie benutzt. Als wesentliches Hilfsmittel erwies sich die Hydrierung der Proben unter gaschromatographischen Bedingungen. Eine Anzahl von Flüssigphasen unterschiedlicher Polarität wurde hinsichtlich ihrer Trenneigenschaften untersucht. Die Retentionsvolumina der interessierenden Kohlenwasserstoffe sind angegeben.

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Gas Chromatographic Determination of C₆, C₇, and C₈ Olefins According to Their Carbon Structures

Cited by 16 publications

References 9 publications

Applications of the Methylene Insertion Reaction to Component Analysis of Hydrocarbons.

Applications of the Methylene Insertion Reaction to Component Analysis of Hydrocarbons.

New Technique for Functional Group Analysis in Gas Chromatography. Syringe Reactions.

Gaschromatographische Untersuchungen an C₆‐Kohlenwasserstoffen

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Gas Chromatographic Determination of C6, C7, and C8 Olefins According to Their Carbon Structures

Cited by 16 publications

References 9 publications

Applications of the Methylene Insertion Reaction to Component Analysis of Hydrocarbons.

Applications of the Methylene Insertion Reaction to Component Analysis of Hydrocarbons.

New Technique for Functional Group Analysis in Gas Chromatography. Syringe Reactions.

Gaschromatographische Untersuchungen an C6‐Kohlenwasserstoffen

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Gas Chromatographic Determination of C₆, C₇, and C₈ Olefins According to Their Carbon Structures

Gaschromatographische Untersuchungen an C₆‐Kohlenwasserstoffen