Pyrolysis-Field Ionization Mass Spectrometry of Rubber Vulcanizates

1989 ◽  
Vol 62 (4) ◽  
pp. 698-708 ◽  
Author(s):  
Hans-Rolf Schulten ◽  
Bernd Plage ◽  
Robert P. Lattimer

Abstract Time-/temperature-resolved Py-FIMS allows for the identification of rubber components in compounds containing normal organic additives. Signals due to polymer pyrolyzates, which may be masked by processing oil in nontemperature resolved spectra, are easily obtained. Py-FI spectra from cured BR and NR differ from the corresponding uncured samples in that signals from sulfur-containing oligomers are observed. For SBR, the signals from sulfur-containing pyrolyzates were not distinguishable in the complex mixture of hydrocarbon fragments that was produced. Therefore, unambiguous distinction between cured and uncured SBR was difficult. Since Py-FI mass spectra for rubber blends appear similar to the sum of the corresponding single component spectra, secondary reactions of chain fragments from the two blend components are minimal. These results are consistent with Curie-point Py-MS studies which also showed little interaction between components in blends. Since the Py-FI mass spectrum of the styrene-butadiene block copolymer is similar to the sum of single component spectra, it is obvious that styrene-butadiene sequences are not very abundant. In contrast, mixed oligomers containing both styrene and butadiene units are found for SBR copolymers. The absence of styrene dimer and trimer, as well as high-mass oligomers of butadiene, indicates that the amount of block styrene is very low. Furthermore, the large numbers of mixed oligomers indicates a random sequence distribution. In summary, Py-FIMS is a very effective technique for direct rubber compound analysis. The sample can be examined directly, without pretreatment, and both organic additives and the rubber components can be identified in the same experiment. With programmed heating of the rubber, one can obtain separate (time-/temperature-resolved) FI mass spectra for the organic additives and the rubber pyrolyzates. The results are interesting in that much higher mass oligomers can be observed by Py-FIMS than are detected by other methods of Py-MS. For example, while the low voltage Py-EIMS typically shows no higher oligomers than trimer or tetramer for diene rubbers, Py-FIMS shows sequences containing perhaps 15–20 monomer units. This improved performance is due mainly to (a) the close proximity of the pyrolysis chamber to the field emitter (which minimizes secondary reactions) and (b) the very soft ionization provided by the FI technique. In favorable cases, Py-FIMS can be used to study long sequences in homopolymers, copolymers, and blends. As we have noted, pendent groups (e.g., mercaptobenzothiazyl) and crosslinks may be detected among the pyrolysis products. While some rubbers (e.g., polyisoprene) thermally degrade to give high abundances of oligomers, others degrade in a more random fashion (e.g., SBR) to give very complex mixtures of pyrolyzates. Polystyrene is an interesting case in which thermal degradation by retropolymerization (unzipping) is so prevalent that the monomer is by far the dominant pyrolyzate, and long oligomeric sequences are precluded. Thus, while Py-FIMS can easily be used for qualitative identification of rubber components, more detailed information may or may not be discernible in analysis of a particular rubber sample.

1987 ◽  
Vol 42 (3) ◽  
pp. 178-190 ◽  
Author(s):  
H .-R . Schulten ◽  
K. E. Murray ◽  
N. Simmleit

Field ionization (FI) and field desorption (FD) mass spectra of 35 aliphatic long-chain and branched long-chain compounds, representing the major six classes of constituents of natural waxes, are examined. In the FI mode the molecular ions are usually formed at comparatively low levels, while in FD such species are almost exclusively generated. In addition, some fast atom bombardment mass spectra, in the positive and negative ion mode, of selected lipids are recorded for comparison. In general, field ionization and field desorption techniques are found to be superior for mass spectrometric studies of low-polarity compounds. Examination of several natural waxes, such as Jojoba wax, preen gland wax of goose, beeswax and epicuticular wax of Norway spruce, shows that field desorption mass spectrometry has a most promising role in the characterization of wax components. The intense molecular ions allow the identification of the constituents of complex lipid mixtures without the need for derivatization. Thus, for the first time, the carbon number distribution, especially of the high-mass wax con­stituents can be established for the natural waxes investigated. For identification of high-mass wax constituents the present results suggest that field desorption mass spectra could be best employed in conjunction with class and individual separation of constituents by chromatographic proce­dures. The analysis of natural waxes is nowadays of major concern because of its importance in the problem of forest damage.


1997 ◽  
Vol 13 (2) ◽  
pp. 151-161 ◽  
Author(s):  
Kevin B. Thurbide ◽  
C. M. Elson ◽  
P. G. Sim

The negative‒ion chemical ionization mass spectra of a group of structural isomers of amphetamine have been studied using carbon dioxide as the reagent gas. Characteristic and reproducible differences are observed for each member of the set implying that this technique offers a means of distinguishing among groups of amphetamine isomers. Characteristic adducts to the molecular ion are observed in the form (M–[H]+[O]) and (M–[H]+[CO2]). Descriptions of some fragments are given based on the mass spectral behaviour of a set of analogue compounds and the results of oxygen-18 labelled carbon dioxide reagent gas experiments. Contents of the carbon dioxide plasma and their impact on various analytes is also discussed.


1984 ◽  
Vol 106 (23) ◽  
pp. 6877-6883 ◽  
Author(s):  
Seymour Meyerson ◽  
Donald J. Harvan ◽  
J. Ronald Hass ◽  
Fausto Ramirez ◽  
James F. Marecek

1972 ◽  
Vol 6 (11) ◽  
pp. 1171-1181 ◽  
Author(s):  
Ralph C. Dougherty ◽  
John Dalton ◽  
Francis J. Biros

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