摘要
研究了不同浓碱皂化的D2EHPA-正庚烷体系萃取一系列稀土离子(La ̄(3+)→Lu ̄(3+),放射性的Pm 除外)过程中有机相的FTIR光谱变化规律.结果表明:D2EHPA萃取稀土离子后,P=O基团的红外吸收频率降低,吸收强度升高,说明P=O基团与稀土离子发生配位;红外光谱研究结果还表明:不同稀土离子与P=O配位能力有差别,从La ̄(3+)→Sm ̄(3+)配位能力依次增大,从Sm ̄(3+)→Lu ̄(3+)则呈下降趋势,对同一个稀土离子来说,随着有机相中稀土离子含量的增加,有机相微乳液中H_2O的含量减小,萃取过程伴随有破乳发生.
FTIR spectroscopy was used to investigate the coordination interaction of D2EHPA [di(2-ethylhexyl) phosphoric acid] with lathanide(Ⅲ)series(La(3+)→Lu(3+), except radioactive promethium ). P=O band shifts to the lower frequency when D2EHPA is saponified with concentrated basic solutions (NaOH,KOH or NH3· H2O).The coordination sequence of Na+,K+ and NH with P=O group is NH+ >Na+ >K+. The frequency of P=Oband in the extracted organic phase containing RE-D2EHPA complexes shifts to the lower wavenumbers as the lanthanide(Ⅲ)loading increases in organic phase,and the intensity of P=O band increases. FTIR spectra results show that the coordination ability of lanthanide(Ⅲ)series with P=O group is as follows:La3+<Ce3+<Pr3+<Nd3+<Sm3+>Eu3+>…>Lu3+, namely,the complexation intreaction of Sm3+ with P=O is the strongest.In addition,the w/o microemulsion was gradually destructed with the entrance RE3+into the organic phase.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
1995年第11期1664-1668,共5页
Chemical Journal of Chinese Universities
基金
国家攀登计划资助课题