81
Views
0
CrossRef citations to date
0
Altmetric
Extraction

Synthesis of DCAP and its effects on extraction separation of light rare earth ions

, , , &
Pages 1351-1359 | Received 05 Mar 2019, Accepted 01 Jun 2020, Published online: 22 Jun 2020
 

ABSTRACT

A de-tert-butyl calix arene phosphate (DCAP) with a complete elimination of the upper edge and a complete substitution of the lower edge was synthesized by dealkylation and substitution reactions. The chemical structure of DCAP was further characterized by FTIR, mass MS and 1 H NMR. The ability of DCAP to extract light rare earth ions was studied as a function of concentration, aqueous phase pH, phase ratio, and extraction time. The results showed that DCAP had a 4% higher extraction rate of Pr3+ compared to Nd3+ under the same conditions. Preliminary extraction mechanism was also investigated.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This work was supported by the National Natural Science Foundation of China (No.21471053), the Natural Science Foundation of Hunan Province (2018JJ3211) and Scientific Research Fund of Hunan Provincial Education Department (19C0868);National Natural Science Foundation of China [21471053];Scientific Research Fund of Hunan Provincial Education Department [19C0868];Natural Science Foundation of Hunan Province [2018JJ3211];

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.