1959
DOI: 10.1063/1.1730641
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Negative Ion Mass Spectra of Hydrocarbons and Alcohols

Abstract: The complete negative ion mass spectra and relative sensitivity for positive and negative ion formation in various organic compounds are herein reported for the first time. These compounds include methane, the C2— hydrocarbons, n-butane, and all of the alkyl alcohols through the butyls. A limited comparison of the observed ionic patterns with molecular structure and chemical properties manifests a correlation. Relative sensitivities for positive and negative ion formation in these compounds show that formation… Show more

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Cited by 41 publications
(21 citation statements)
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“…The most pronounced peak appeared at 270.24 amu, which corresponds to the hexadecanol fragment C16D31O -(hexadecanol missing one hydrogen and two deuteriums, M-H-2D). This agrees with the assumption of the alkoxide anions being prone to splitting-off two hydrogen atoms from the carbon next to the oxygen [27]. The recombination of such radical anions on the surface was assumed to cause the formation of double and triple bonds in the alkyl chain [28] or even cross-linking of the alkyl chains, i.e., polymerization of the adsorbed layer [29].…”
Section: Contact Anglesupporting
confidence: 84%
“…The most pronounced peak appeared at 270.24 amu, which corresponds to the hexadecanol fragment C16D31O -(hexadecanol missing one hydrogen and two deuteriums, M-H-2D). This agrees with the assumption of the alkoxide anions being prone to splitting-off two hydrogen atoms from the carbon next to the oxygen [27]. The recombination of such radical anions on the surface was assumed to cause the formation of double and triple bonds in the alkyl chain [28] or even cross-linking of the alkyl chains, i.e., polymerization of the adsorbed layer [29].…”
Section: Contact Anglesupporting
confidence: 84%
“…For estimating the Debye lengths (and functions f and g) of the organic solvents used here, we propose the use of mass spectrometry data to identify likely solvated ions and thereby establish the relation between (measurable) conductivity and ion density (required to predict f and g). Mass spectrometry data are available for numerous organic solvents [31][32][33], and can be classified into two types: for cations and anions. Typically, mass spectrometry data present the abundance of each ion relative to the most abundant ion which is assigned an abundance of 100% [34].…”
Section: Estimating Eo Pumping Performance Of Pure Solventsmentioning
confidence: 99%
“…Gas phase neutralization is prevented, of course, when the electrons reach the wall, even though the positive ions stay much longer in the gas phase. This conclusion is not unexpected, as it is known that saturated hydrocarbons do not readily form negative ions (7).…”
Section: Methodsmentioning
confidence: 59%