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电喷雾质谱法示踪钨回收过程离子的转化路径

  • 蔺淑洁 温嘉玮 曹宏斌 宁朋歌 张懿
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  • 1. 北京市过程污染控制工程技术研究中心,中国科学院过程工程研究所湿法冶金清洁生产技术国家工程实验室,北京 100190 2. 中国科学院大学化学工程学院,北京 100049

收稿日期: 2019-03-18

  修回日期: 2019-04-07

  网络出版日期: 2019-12-22

基金资助

杰出青年基金;青促会基金

Tracking transformation pathway of tungsten recovery process by electrospray ionization time-of-flight mass spectrometry

  • Shujie LIN Jiawei WEN Hongbin CAO Pengge NING Yi ZHANG
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  • 1. Beijing Engineering Research Center of Process Pollution Control, National Engineering Laboratory for Hydrometallurgical Cleaner Production & Technology, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China 2. School of Chemical Engineering, University of Chinese Academy of Sciences, Beijing 100049, China

Received date: 2019-03-18

  Revised date: 2019-04-07

  Online published: 2019-12-22

摘要

将环隙式离心萃取器(ACCs)与电喷雾飞行时间质谱(ESI-TOF-MS)相结合,在线监测了回收过程中的钨萃取行为(宏观)和钨形态的转化路径(微观),发现宏观萃取反应和微观离子形态转化同时发生并相互补充。伯胺N1923萃取钨在144 s内即可达到萃取平衡,萃取率高达98%以上,同时,酸钨比n(H)/n(W)是一个关键变量,当酸钨比n(H)/n(W)=2.4时,全流程钨回收率超过93%。最后,得到了基于钨形态监测的萃取机理,同时,减少原料液中W1含量,增加W10含量,可有效提高钨回收效率。

本文引用格式

蔺淑洁 温嘉玮 曹宏斌 宁朋歌 张懿 . 电喷雾质谱法示踪钨回收过程离子的转化路径[J]. 过程工程学报, 2019 , 19(6) : 1135 -1142 . DOI: 10.12034/j.issn.1009-606X.219158

Abstract

Tungsten is an important rare metal, which is widely used in the fields of national defense, chemical industry, electronics and metallurgy. Solvent extraction has been widely used for tungsten recovery because of its simple operation, good continuity and high recovery rate. Previous researches have always focused on the development of new extractants while ignoring the role of tungsten ion morphology in the extraction process. In fact, ion morphology will affect the way of combining with the extractant and the extraction process. Therefore, in-depth study of ion morphology in the extraction process can better understand the extraction mechanism of tungsten, and thus provide a basis for the separation of tungsten and molybdenum. In this study, annular centrifugal contactors (ACCs) were combined with electrospray ionization time-of-flight mass spectrometry (ESI-TOF-MS) to study the transformation pathway of tungsten species in the recovery process by online monitoring method. It was found that the extraction of tungsten by primary amine N1923 was very fast and effective. Within 144 s, more than 98% of the tungsten could be extracted into the organic phase. At the same time, n(H)/n(W) was a key variable. When the acid ratio was 2.4, the whole tungsten recovery rate exceeded 93%. Finally, the extraction mechanism based on tungsten morphology monitoring was obtained. The macroscopic extraction reaction and the micro-ion exchange reaction occurred simultaneously and complemented each other. As the initial pH decreased, W2, W6 and W10 became active forms in sequence and were preferentially extracted into the organic phase, respectively. In addition, W10 was more active than any other species during the whole process. W1 was an inactive substance that only participated in the tungsten ion balance reaction to adjust the tungsten form and pH. As a result, reducing W1 and increasing W10 as much as possible would be conducive to improve tungsten extraction efficiency in solution.

参考文献

[1] Nguyen T H, Lee M S. A review on the separation of molybdenum, tungsten, and vanadium from leach liquors of diverse resources by solvent extraction [J]. Geosystem Engineering, 2016, 19(5): 247-259.
[2] Zhao Z W, Cao C F, Chen X Y. Separation of macro amounts of tungsten and molybdenum by precipitation with ferrous salt [J]. Transactions of Nonferrous Metals Society of China, 2011, 21(12): 2758-2763.
[3] Pagnanelli F, Ferella F, De Michelis I, et al. Adsorption onto activated carbon for molybdenum recovery from leach liquors of exhausted hydrotreating catalysts [J]. Hydrometallurgy, 2011, 110(1-4): 67-72.
[4] Nguyen T H, Lee M S. Separation of molybdenum (VI) and tungsten (VI) from sulfuric acid solution by ion exchange with TEVA resin [J]. Separation Science and Technology, 2015, 50(13): 2060-2065.
[5] Zhao Z W, Zhang J L, Chen X Y, et al. Separation of tungsten and molybdenum using macroporous resin: Equilibrium adsorption for single and binary systems [J]. Hydrometallurgy, 2013, 140: 120-127.
[6] Wang L P, Zhang G Q, Guan W J, et al. Complete removal of trace vanadium from ammonium tungstate solutions by solvent extraction [J]. Hydrometallurgy, 2018, 179: 268-273.
[7] Liao Y L, Zhao Z W. Comparison of 2-Octanol and tributyl phosphate in recovery of tungsten from sulfuric–phosphoric acid leach solution of scheelite [J]. Jom, 2018, 70(4): 581-586.
[8] Ning P G, Cao H B, Zhang Y. Selective extraction and deep removal of tungsten from sodium molybdate solution by primary amine N1923 [J]. Separation and Purification Technology, 2009, 70(1): 27-33.
[9] Redkin A F, Bondarenko G V. Raman spectra of tungsten-bearing solutions [J]. Journal of Solution Chemistry, 2010, 39(10): 1549-1561.
[10] Himeno S, Kitazumi I. Capillary electrophoretic study on the formation and transformation of isopolyoxotungstates in aqueous and aqueous-CH3CN media [J]. Inorganica Chimica Acta, 2003, 355: 81-86.
[11] Hastings J J, Howarth O W. A 183W, 1H and 17O nuclear magnetic resonance study of aqueous isopolytungstates [J]. Journal of the Chemical Society-Dalton Transactions, 1992, (2): 209-215.
[12] Fedotov M A, Maksimovskaya R I. NMR structural aspects of the chemistry of V, Mo, W polyoxometalates [J]. Journal of Structural Chemistry, 2006, 47(5): 952-978.
[13] Xu W, Ning P G, Cao H B,et al. Thermodynamic model for tungstic acid extraction from sodium tungstate in sulfuric acid medium by primary amine N1923 diluted in toluene [J]. Hydrometallurgy, 2014, 147-148: 170-177.
[14] Zhang J J, Zhao Z W, Chen X Y, et al. Thermodynamic analysis for separation of tungsten and molybdenum in W-Mo-H2O system [J]. The Chinese Journal of Nonferrous Metals, 2013, 23(5): 1463-1470.
[15] Zhang C, Howell R C, Scotland K B, et al. Aqueous speciation studies of europium(III) phosphotungstate [J]. Inorganic Chemistry, 2004, 43: 7691-7701.
[16] Aureliano M, Ohlin C A, Vieira M O, et al. Characterization of decavanadate and decaniobate solutions by raman spectroscopy [J]. Dalton Trans, 2016, 45(17): 7391-7399.
[17] Scancar J, Berlinger B, Thomassen Y, et al. Simultaneous speciation analysis of chromate, molybdate, tungstate and vanadate in welding fume alkaline extracts by HPLC-ICP-MS [J]. Talanta, 2015, 142: 164-169.
[18] Schramel P, Wendler I, Angerer J. The determination of metals (antimony, bismuth, lead, cadmium, mercury, palladium, platinum, tellurium, thallium, tin and tungsten) in urine samples by inductively coupled plasma-mass spectrometry [J]. Int Arch Occup Environ Health, 1997, 69(3): 219-223.
[19] Mohajerin T J, Helz G R, White C D, et al. Tungsten speciation in sulfidic waters: determination of thiotungstate formation constants and modeling their distribution in natural waters [J]. Geochimica et Cosmochimica Acta, 2014, 144: 157-172.
[20] Long D L, Streb C, Song Y F, et al. Unravelling the complexities of polyoxometalates in solution using mass spectrometry: Protonation versus heteroatom inclusion [J]. Journal of the American Chemical Society, 2008, 130(6): 1830-1832.
[21] Jia Q D, Cao J, Duan Y P, et al. The solution chemistry and reactivity of lacunary Keggin silicotungstates monitored in real-time by a combination of mass spectrometry and electrochemistry [J]. Dalton Transactions, 2015, 44 (2): 553-559.
[22] Jing X H, Ning P G, Cao H B, et al. Separation of V(V) and Cr(VI) in leaching solution using annular centrifugal contactors [J]. Chemical Engineering Journal, 2017, 315: 373-381.
[23] Wen J W, Ning P G, Cao H B, et al. Recovery of high-purity vanadium from aqueous solutions by reusable primary amines N1923 associated with semiquantitative understanding of vanadium species [J]. ACS Sustainable Chemistry & Engineering, 2018, 6(6): 7619-7626.
[24] Zhao H, Liu H J, Qu J H. Aluminum speciation of coagulants with low concentration: Analysis by electrospray ionization mass spectrometry [J]. Colloids and Surfaces A-Physicochemical and Engineering Aspects, 2011, 379 (1-3), 43-50.
[25] Truebenbach C S, Houalla M, Hercules D M. Characterization of isopoly metal oxyanions using electrospray time-of-flight mass spectrometry [J]. Journal of the Mass Spectrom, 2000, 35(9): 1121-1127.
[26] Walanda D A, Burns R C, Lawrance G A, et al. Electrospray mass spectrometry of aqueous solutions of Isopolyoxotungstates [J]. Journal of Cluster Science, 2000, 11: 5-28.
[27] Deery M J, Howarth O W, Jennings K R. Application of electrospray ionisation mass spectrometry to the study of dilute aqueous oligomeric anions and their reactions [J]. Journal of the Chemical Society-Dalton Trans, 1997, 4783-4788.
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