Influence of electric field strength and emitter temperature on dehydrogenation and C-C cleavage in field desorption mass spectrometry of polyethylene oligomers

被引:17
作者
Gross, JH
Weidner, SM
机构
[1] Heidelberg Univ, Inst Organ Chem, D-69120 Heidelberg, Germany
[2] Bundesanstalt Mat Forsch & Prufung, D-12205 Berlin, Germany
关键词
field desorption; field ionization; polyethylene; oligomer; electric field strength; emitter potential; emitter temperature; dehydrogenation; C-C cleavage; metastable ion;
D O I
10.1255/ejms.300
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The influence of electric field strength and emitter temperature on dehydrogenation and C-C cleavage in field desorption (FD) mass spectrometry of polyethylene (PE) oligomers of average molecular weights ranging from 500 to 2000 is examined. Low mass oligomers yield molecular weight (MW) distributions that are basically in accordance with results from gel-permeation chromatography. For these materials, dehydrogenation can be greatly reduced by reduction of the emitter potential. Furthermore, the influence of emitter potential on MW distributions indicates the occurrence of field-induced C-C cleavages. Reliable MW distributions are more difficult to obtain from higher mass oligomers by FD-MS because of the need for higher field strength and higher emitter temperatures to effect their desorption/ionization. Experiments reveal that the application of FD-MS to PE oligomers is limited not only by field-induced but also by thermally-induced fragmentations. Even then, FD mass spectra contain valuable information on mass range and homogeneity of PE samples up to about m/z 3600.
引用
收藏
页码:11 / 17
页数:7
相关论文
共 41 条
  • [1] MATRIX-ASSISTED ULTRAVIOLET-LASER DESORPTION - EVOLUTION AND PRINCIPLES
    BEAVIS, RC
    [J]. ORGANIC MASS SPECTROMETRY, 1992, 27 (06): : 653 - 659
  • [2] Beckey H. D., 1975, ANGEW CHEM, V87, P425
  • [3] Beckey H. D., 1977, PRINCIPLES FIELD ION
  • [4] FELDIONEN-MASSENSPEKTREN ORGANISCHER MOLEKULE .3. N-PARAFFINE BIS ZUM C16 UND VERZWEIGTE PARAFFINE
    BECKEY, HD
    SCHULZE, P
    [J]. ZEITSCHRIFT FUR NATURFORSCHUNG PART A-ASTROPHYSIK PHYSIK UND PHYSIKALISCHE CHEMIE, 1965, A 20 (10): : 1329 - &
  • [5] BECKEY HD, 1965, Z NATURFORSCH PT A, VA 20, P1335
  • [6] BECKEY HD, 1962, Z NATURFORSCH PT A, VA 17, P1103
  • [7] Carr RH, 1998, RAPID COMMUN MASS SP, V12, P2047, DOI 10.1002/(SICI)1097-0231(19981230)12:24<2047::AID-RCM428>3.0.CO
  • [8] 2-9
  • [9] The characterization of synthetic polymers by matrix-assisted laser desorption/ionization mass spectrometry
    Cottrell, JS
    Koerner, M
    Gerhards, R
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1995, 9 (15) : 1562 - 1564
  • [10] THE ANALYSIS OF WATER-SOLUBLE POLYMERS BY MATRIX-ASSISTED LASER DESORPTION TIME-OF-FLIGHT MASS-SPECTROMETRY
    DANIS, PO
    KARR, DE
    MAYER, F
    HOLLE, A
    WATSON, CH
    [J]. ORGANIC MASS SPECTROMETRY, 1992, 27 (07): : 843 - 846