Element 105 / Chemical properties / Halide complex formation / Extraction into a secondary alcohol
SummaryStudies of the extraction of element 105 into diisobutylcarbinol (DIBC) from aqueous HBr and HCl solutions wcre performed on "^Ha and "^Ha produced in the "'Bk("0,5n) and reactions at a beam energy of 99 MeV. The Ha isotopes were detected by measuring the fission and a activities associated with their decay and the a-decays of their daughters, 4-s and 6-s ^''Lr. Complete extraction-elution cycles were performed on a one-minute time scale by the computer-controlled liquid chromatography apparatus, ARCA II, using reversed-phase micro-chromatographic columns incorporating DIBC on an inert support. Stimulated by the previously observed similarity of the aqueous-phase chemistry of element 105 to that of niobium and protactinium, the extraction, from concentrated HBr, was followed by the elution of a Nb fraction in 6 M HCl/ 0.0002 M HF, and a Pa fraction in 0.5 M HCl. The number of 262,263j^^ dccays observed in the Nb fraction indicated that less than 45% of the Ha was extracted into DIBC from concentrated HBr. This was confirmed in a series of experiments in which, after the extraction, the DIBC along with all extracted species was stripped from the columns with acetone. It is concluded that, in the present chemical system, the extraction behaviour of element 105 is closer to that of niobium than to that of protactinium. The decreasing extractability from HBr (Pa > Nb > Ha) is likely to be due to an increasing tendency of these Clements to form non-extractable polynegative complex species in concentrated HBr in the sequence Pa < Nb < Ha.