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Received September 27, 2021
Accepted November 19, 2021
- This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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A non-aqueous phase extraction system using tributyl phosphate for H3PO4 separation from wet-process superphosphoric acid: Extraction equilibrium and mechanism
School of Chemical Engineering, Sichuan University, Chengdu 610065, China
18980632893@163.com
Korean Journal of Chemical Engineering, July 2022, 39(7), 1659-1672(14), 10.1007/s11814-021-1021-z
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Abstract
Conventional wet-process phosphoric acid (WPA) extraction route encounters unsatisfactory extraction efficiency, phosphorus yield, and raffinate utilization. Herein, a new extraction route for H3PO4 separation from wetprocess superphosphoric acid (WSPA) is proposed to improve these dilemmas. We focus on the equilibrium of H3PO4 extraction by tributyl phosphate (TBP) from WSPA and the extraction mechanism of TBP under high H3PO4 loading conditions. Several critical factors affecting the extraction equilibrium were investigated to optimize the extraction process, including the initial phase ratio (R0), the volume fraction of TBP in extractant (ΦTBP), temperature (T), and the crosscurrent extraction stages. The results show that the single-stage extraction rate of H3PO4 reaches 70% at R0=6, ΦTBP=80% and T=80℃ with separation factors βP/Fe, βP/Al, βP/Mg, and βP/Ca of 12.48, 21.66, 47.57, and 8.89, respectively. In addition, Fourier transform infrared spectroscopy and Raman spectroscopy enlighten the extraction mechanism at high loading conditions. The characteristic peak positions of P=O, P=O…H2O, and P=O…H3PO4 in the infrared spectra are determined to be centered at 1,283, 1,267, and 1,233 cm-1, respectively. The semi-quantitative analysis implies that the self-polymerization behavior of the extraction complex TBP·H3PO4 and the mutual attraction of reverse micelles (RMs) through their polar cores is the trigger for the formation of a third phase. Furthermore, the red shift of P-(OH)3 asymmetrical stretching vibration in the Raman spectrum indicates the formation of hydrogen bonds among H3PO4 molecules in the organic phase, which corroborates the formation of RMs. Conclusions can be obtained that H3PO4 enters the organic phase under high loading capacity by reversed micellar extraction. The feasibility of this extraction process is further tested by scrubbing, stripping, and cycling performance experiments. The results are promising for the design of a new efficient route for separating H3PO4 from WPA.
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Assuncao MC, Cote G, Andre M, Halleux H, Chagnes A, RSC Adv., 7, 6922 (2017)
Feki M, Chem. Eng. J., 88, 71 (2002)
Zhang SJ, Chen YX, Zhang T, Lv L, Zheng DY, Zhong BH, Tang SW, Sep. Purif. Technol., 249, 117 (2020)
Chen H, Sun Z, Song X, Yu J, J. Chem. Eng. Data, 61, 438 (2015)
Chen M, Li J, Jin Y, Luo JH, Zhu XH, Yu DF, J. Chem. Technol. Biotechnol., 93, 467 (2018)
Liu D, Jiang S, Luo H, Zhang Y, Phosphate Compd. Fert, 20, 6 (2005)
Yang L, Tang C, Zhang ZY, Wang XL, Chinese Patent, CN106145075A (2016).
Yang JX, Kong XJ, Xu DH, Xie WJ, Wang XL, Chem. Eng. J., 359, 1453 (2019)
Mcgill KE, Kerns OS, Nutr. Cycl. Agroecosyst., 25, 179 (1990)
Breed CE, Mcgill KE, Holt MT, J. Environ. Sci. Health Part A-Toxic/Hazard. Subst. Environ. Eng., 21, 609 (1986)
Huang MY, Yang K, Li J, Zhong BH, Phosphate. Compd. Fert., 19, 9 (2004)
Zhong BH, Li J, Chen L, Hsien Tai Hua Kung, 25, 48 (2005)
Jin Y, Zou D, Wu S, Cao Y, Li J, Ind. Eng. Chem. Res., 54, 108 (2014)
Wei C, Hu B, Li Y, Wang S, Wuf H, Pu J, Phosphate. Compd. Fert., 33, 28 (2018)
Luo Z, Zeng B, Luo K, Wang B, Ind. Miner. Process., 43, 60 (2014)
Yang L, Phosphate. Compd. Fert., 35, 19 (2020)
Dhouib-Sahnoun R, Fekif M, Ayedi HF, J. Chem. Eng. Data, 47, 861 (2002)
Jin Y, Li J, Luo J, Zheng DS, Liu L, J. Chem. Eng. Data, 55, 3196 (2010)
Liu C, Cao J, Shen W, Ren Y, Mu W, Ding X, Fluid Phase Equilib., 408, 190 (2016)
Ziat K, Mesnaoui B, Bounahmidi T, Boussen R, Guardia M, Garrigues S, Fluid Phase Equilib., 201, 259 (2002)
Liu CQ, Ren Y, Wang YN, J. Chem. Eng. Data, 59, 70 (2013)
Ren Y, Liu CQ, Cao J, Mu W, Ding X, J. Chem. Eng. Data, 61, 1735 (2016)
Ziat K, Messnaoui B, Bounahmidi T, Guardia M, Fluid Phase Equilib., 224, 39 (2004)
Zheng DS, Li J, Zhou K, Luof JH, Jin Y, J. Chem. Eng. Data, 55, 58 (2010)
Kouzbour S, Gourich B, Gros F, Vial C, Allam F, Stiriba Y, Hydrometallurgy, 188, 222 (2019)
Xun F, Yan Z, Zheng HS, Solvent Extr. Ion Exch., 20, 241 (2002)
Tedesco PH, Rumi VB, Polyhedron, 42, 1033 (1980)
Higgins CE, Baldwin WH, Polyhedron, 24, 415 (1962)
Nave S, Mandin C, Martinet L, Berthon L, Testard F, Madic C, Zemb T, ACS Phys. Chem. Au., 6, 799 (2004)
Yi XT, Huo GS, Tang W, Hydrometallurgy, 192, 105265 (2020)
Zhou XK, Zhang ZF, Kuang ST, Li YL, Ma YQ, Li YH, Liao WP, Hydrometallurgy, 185, 76 (2019)
Mishra RK, Rout PC, Sarangi K, Nathsarma KC, Hydrometallurgy, 104, 298 (2010)
Cui L, Wang L, Feng M, Fang L, Guo Y, Cheng F, Green Energy Environ., 6, 607 (2020)
Zhao Y, Xing C, Shao C, Chen G, Sun S, Chen G, Zhang L, Pei J, Qiu P, Guo S, Fuel, 278, 118229 (2020)
Rudolph WW, Dalton Trans, 39, 9642 (2010)