The extraction behavior of heptavalent technetium with cyclic amides in n-d
odecane from nitric acid solution was studied. The amides investigated are
N-(2-ethyl)hexylbutyrolactam(EHBLA), N-(2-ethyl)hexylvalerolactam(EHVLA), N
-(2-ethyl)hexyl-caprolactam (EHCLA), N-octylcaprolactam(OCLA), a mixture of
3-octyt-N-(2-ethyl)hexyl valerolactam and 4-octyl-N-(2-ethyl)hexylvalerola
ctam (3,4,OEHVLA), 2-octyl-N(2-ethyl)hexylcaprolactam(2OEHCLA), a mixture o
f 3-octyl-N-(2-ethyl)hexylcaprolactam and 5-octyl-N-(2-ethyl)hexylcaprolact
am(3,5,OEHCLA) and that of 3-octyl-N-octylcaprolactam and 5-octyl-N-octylca
prolactam(3,5,OOCLA). From the results of the distribution ratio of Tc(VII)
as a function of acid concentration, cyclic amides concentration and HTcO4
concentration, the effects of both the ring size of cyclic amide and struc
ture of the substituents attached to different positions of the cyclic ring
on the extraction behavior of Tc(VII) were discussed. A clear steric hindr
ance was observed. For applications, 3,4,OEHVLA is proposed as the best ext
ractant for Tc from acidic solution.