F. Behar et al., CLOSED PYROLYSES OF THE ISOPRENOID ALGAENAN OF BOTRYOCOCCUS-BRAUNII, L RACE - GEOCHEMICAL IMPLICATIONS FOR DERIVED KEROGENS, Geochimica et cosmochimica acta, 59(14), 1995, pp. 2983-2997
Algaenans, i.e., highly aliphatic, nonhydrolysable, insoluble macromol
ecular constituents, have been identified in a number of microalga cel
l walls and their selective preservation shown to play a major role in
the formation of numerous kerogens. All the algaenans so far examined
comprise a network of long polymethylenic chains, except for the L ra
ce of Botryococcus braunii. The resistant macromolecular material isol
ated from the latter, termed PRE L, is based on C-40 isoprenoid chains
with a lycopane-type skeleton. Recent comparative studies of PRE L an
d of Botryvococcus-derived sediments provided the first example of ker
ogen formation via the selective preservation of an ''isoprenoid'' alg
aenan. The present study is concerned with PRE L pyrolyses in sealed g
old tubes under various temperature/time conditions (260-350 degrees C
, 0.5-69 h). For the conversion rates thus obtained, ranging from 30 t
o 100%, a complete mass balance of the different families of pyrolysis
products was established; most of the C-1 to C-40 pyrolysate constitu
ents were identified and the abundances of the above compounds and the
ir variations with conversion progress were determined. This study thu
s allowed us (1) to derive further information about PRE L chemical st
ructure (location of the ether bridges, contribution of linear chains
and their relationships with the C-40 isoprenoid ones), (2) to determi
ne the behaviour of this isoprenoid algaenan to thermal stress (timing
of the formation of the different groups of products then released, n
ature of the primary cleavages, origin and mode of formation of the se
condary products, and further degradations), and (3) to show, in conne
ction with previous studies, that PRE L-derived kerogens should exhibi
t pronounced differences relative to standard type I kerogens, the lat
ter being based on polymethylenic chains, regarding not only the struc
ture of the generated products but also the timing of oil generation (
upward shift of the catagenesis zone).