1938
DOI: 10.6028/jres.020.033
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Quantitative analysis, with respect to the component structural groups, of the infrared (1 to 2 mu) molal absorptive indices of 55 hydrocarbons

Abstract: Data from previous studies on the infrared absorption spectra between 1.2 and 1.8 JL (5 400 to 8900 cm

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Cited by 51 publications
(17 citation statements)
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“…In polymers, methylene bands were observed at 1,214 nm in polyethene and 1,206 nm in nylon (Glatt and Ellis 1951). The first and second overtones of aromatic CH group are at 1,685 and 1,143 nm (Wheeler 1959), second overtone lie in the region 1,136-1,149 nm (Liddel and Kasper 1933) and first and second overtone at 1,695 and 1,143 nm (Rose 1938). The relative absorptivities of the first, second and third CH stretch overtones in case of chloroform are in the ratio of 484:22:1 (Lauer and Rosenbaum 1952).…”
Section: (I) Carbon-hydrogen (Ch) Overtone Bandsmentioning
confidence: 96%
See 1 more Smart Citation
“…In polymers, methylene bands were observed at 1,214 nm in polyethene and 1,206 nm in nylon (Glatt and Ellis 1951). The first and second overtones of aromatic CH group are at 1,685 and 1,143 nm (Wheeler 1959), second overtone lie in the region 1,136-1,149 nm (Liddel and Kasper 1933) and first and second overtone at 1,695 and 1,143 nm (Rose 1938). The relative absorptivities of the first, second and third CH stretch overtones in case of chloroform are in the ratio of 484:22:1 (Lauer and Rosenbaum 1952).…”
Section: (I) Carbon-hydrogen (Ch) Overtone Bandsmentioning
confidence: 96%
“…The first overtone bands in alkanes would therefore be expected to be found around 2ν cm -1 or 10 7 /2ν nm =1,700 nm. Rose (1938) reported methylene bands at 1,730 and 1,764 nm and methyl bands at 1,703, 1,707, 1,724 nm. 6.24) ν = nν 0 (1 − nx) (6.24) whereν is the wavenumber of the overtone band, x is anharmonicity constant (0.01 as first approximation) and n is an integer which has the same value as υ, i.e.…”
Section: (I) Carbon-hydrogen (Ch) Overtone Bandsmentioning
confidence: 99%
“…Die bevorzugte Stellung der 2 . Oberschwingung wird dadurch unterstrichen, da5 in der Literatur sowohl zwischen 5000 und 6000 em-l als auch zwischen 8000 und 9000 cm-l die Spektren gesattigter und aromatischcr Kohlenwasserstoffe analysiert werden [ 6 -181, aber Anwendungsbeispiele fur quantitative Analysen liegen, mit wenigen Ausiiahmen [15][16][17], nur fur den Bereich der 2 . Oberschwingung vor [4, 10, ll, 15, 241. Die Literatur zeigt weiterhin deutlich, da5 nur das nalie I R die Voraussetzungen bietet, CH-Gruppen in gesattigteiz Strukturen sowie den Gesamtmethylengruppengehalt in paraffinischen und naphthenischen Strukturen auf direktem Wege qusntitat i , zu bestimmen.…”
Section: Einleitiingunclassified
“…In [15] ist kein Beispiel fur die Bestimmung gesattigter CH-Gruppen im NIR bekannt. Aufbauend auf den hier vorgelegten Ergebnissen sollte aber aus der CH-Absorption eine direkte Bestimmung des Gehaltes dieser Strukturgruppe moglich sein.…”
Section: Einleitiingunclassified
“…Both absorption bands each consist of several overlapping peaks as a result of C–H bond vibrations within the different structural groups (—CH 3 , >CH 2 , CH and >CH (aromatic)) of the lipid molecules [19–21] . The position and relative height of the peaks vary with the number and location of these different structural groups within the molecules and therefore provide chemical specificity.…”
Section: Introductionmentioning
confidence: 99%