Abstract
AbstractMacroreticular chelating resins (RNH) containing amidoxime groups with various degrees of crosslinking were synthesized by using various amounts of ethyleneglycol dimethacrylate (1G), dimethyleneglycol dimethacrylate (2G), triethyleneglycol dimethacrylate (3G), tetraethyleneglycol dimethacrylate (4G), and nanoethyleneglycol dimethacrylate (9G) as crosslinking reagent. The effect of crosslinking reagents on the pore structure, ion exchange capacity, swelling ratio, and adsorption ability for uranium of RNH was investigated. RNH (RNH–1G) prepared by using 1G were showed to have macroreticular structures by the measure of specific surface area. RNH–1G had the high adsorption ability and physical stability. Though RNH (RNH–4G) obtained by using 4G have little macroreticular structure (macropore), these resins showed the high adsorption ability for uranium by the treatment with 0.1 mol dm−3 NaOH at 30°C for 15 h (alkali treatment). These results suggest that the formation of not only the favorable macropore but also the micropore is important for the effective recovery of uranium in sea water, whereas RNH–4G was defined to be low physical and chemical stability. For the preparation of RNH which have effective pore structure for the recovery of uranium, chemical, and physical stability, the simultaneous use of divinylbenzene (DVB) and 1G or 4G as crosslinking reagent was examined (abbreviated as RNH–DVB–1G and RNH–DVB–4G). The specific surface area of RNH–DVB–1G increased with an increase of 1G used. These RNH–DVB–1G have been shown the high adsorption ability for uranium. On the other hand, the specific surface area and adsorption ability for uranium of RNH–DVB–4G decreased with an increase of 4G used. Repeated use did not cause the deterioration of both RNH–DVB–1G and RNH–DVB–4G. This result suggests that the simultaneous use of DVB and 1G or 4G contributed the improvement of chemical and physical stability. In particular, RNH–DVB–1G has the effective macropore and micropore for the recovery of uranium.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.