The formation of cyclic diamides of polyamides 4,6 and 6,6 by thermal
catalytic depolymerization of the corresponding polyamides was investi
gated. This method was optimized by changing external factors, like: c
oncentration of catalyst; depolymerization temperature; - time; workin
g under nitrogen flow and under a high vacuum (10(-5) mbar). The catal
yst sodium-2-ethylhexanoate was used to accelerate the reaction. The d
ifferent multi-component depolymerization products were analyzed by re
versed phase HPLC. The formation of cyclic diamides of polyamides 4,6
and 6,6 was 10, respectively 20 wt.-%, under optimum conditions, which
is not sufficient to be used as feed stock for new (co)polyamides.