scholarly journals Extraction Factor Of Pure Ammonium Paratungstate From Tungsten Scraps

2015 ◽  
Vol 60 (2) ◽  
pp. 1403-1405
Author(s):  
J.-H. Pee ◽  
G.H. Kim ◽  
H.Y. Lee ◽  
Y.J. Kim

Abstract Typical oxidation process of tungsten scraps was modified by the rotary kiln with oxygen burner to increase the oxidation rate of tungsten scraps. Also to accelerate the solubility of solid oxidized products, the hydrothermal reflux method was adapted. By heating tungsten scraps in rotary kiln with oxygen burner at around 900° for 2hrs, the scraps was oxidized completely. Then oxidized products (WO3 and CoWO4) was fully dissolved in the solution of NaOH by hydrothermal reflux method at 150° for 2hrs. The dissolution rate of oxidized products was increased with increasing the reaction temperature and concentration of NaOH. And then CaWO4 and H2WO4 could be generated from the aqueous sodium tungstate solution. Ammonium paratungstate (APT) also could be produced from tungstic acid using by aqueous ammonium solution. The morphologies (cubic and plate types) of APT was controlled by the stirring process of purified solution of ammonium paratungstate.

2011 ◽  
Vol 402 ◽  
pp. 261-265
Author(s):  
Lin Sheng Wan ◽  
Dan Dan Gong ◽  
Zan Hui Fu ◽  
Hong Chao Li ◽  
Li Sun

We realize the goal of removing ammonia nitrogen in ammonium paratungstate crystal parent by using strong sodium tungstate liquid to transform-magnesium salt to take off ammonium thoroughly. The results show that removal rate of ammonia can up to 98.88%, ammonia nitrogen contented in the liquid can down to 0.042g/l. Diluting sodium tungstate solution which has been disposed through the above way can be used to confect liquid before the ion exchange,the liquid with the ion exchange can reach the national effluent standard..


Author(s):  
Yulya V. Matveichuk

For citation:Matveichuk Yu.V. FTIR-spectroscopic investigation of sodium tungstate and sodium molybdate solutions in wide range of рH. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2017. V. 60. N 1. P. 56-63. A FTIR spectroscopic study of aqueous solutions of sodium tungstate and molybdate (solution concentration was 0.1 mol/l) over a wide pH range (factor (level) of acidity Z, Z = C (H+)/C (WO42-) or Z = C (H+)/C(MoO42-)) was carried out. In solutions of sodium tungstate complex frequency band at 885-865 cm-1 correspoding to the stretching vibrations ν(W-O-W) was fixed. The frequency bands of 1720-1700 cm-1, 990, 985 and 1025 cm-1 corresponding to bending vibrations δ(W-OH) were fixed that indicates a significant change in composition of the solution as a result of hydrolytic and polycondensation processes. The sodium molybdate solution has not bands corresponding to the stretching vibrations v(Mo-O-Mo). Only the characteristic bands of the deformation vibrations δ(Mo-OH) were recorded. The low intensity complex band in the area of 885-865 cm-1 corresponding to the stretching vibrations ν(W-O-W) even for freshly prepared 0.1 mol/l sodium tungstate solution was appeared as well as the band at 1720-1700 cm-1 attributed to deformation vibrations δ(W-OH) that indicates a fast change in the solution composition. For solutions of sodium molybdate bands of stretching vibrations v(Mo-O-Mo) are fixed at a pH less than 6 after standing for several days. With Hydra/Medusa program diagrams of distribution of molybdate and tungsten particle depending on the pH were calculated. In relatively dilute solutions, the diagrams received with Hydra/Medusa program showed the only protonated (monomeric) form of molybdate ions, where as in the sodium tungstate solution until pH of 9 W6O216- and HW6O215- particles exist that agrees with the results of IR spectroscopy. The results of IR spectroscopy and modeling with Hydra/Medusa program will be used to support the pH operating range for molybdate and tungstate-selective electrodes, since they are an important feature of any analytical ion-selective electrodes. For tungstate-selective electrode it is necessary to maintain the pH less than 9, for molybdate-selective electrode - less than 8 (with dilute ammonia). Considering the changes in the composition of sodium molybdate and tungstate solutions, for the design of molybdate and tungstate-selective electrodes the freshly prepared solutions have to be only used, rather than stored for more than two days.


NANO ◽  
2008 ◽  
Vol 03 (04) ◽  
pp. 223-227 ◽  
Author(s):  
KATARÍNA SEDLÁCKOVÁ ◽  
RADU IONESCU ◽  
CSABA BALÁZSI

In this work, nanocrystalline hexagonal tungsten oxide was prepared by acidic precipitation from sodium tungstate solution. TEM studies of nanopowders showed that the average size of the hexagonal nanoparticles is 30–50 nm. Novel nanocomposites were prepared by embedding a low amount of gold-decorated carbon nanotubes into the hex- WO 3 matrix. The addition of MWCNTs lowered the temperature range of sensitivity of hex- WO 3 nanocomposites to NO 2 hazardous gas. The sensitivity of hex- WO 3 with Au -decorated MWCNTs to NO 2 is at the temperature range between 25°C and 250°C.


2014 ◽  
Vol 88 ◽  
pp. 9-14
Author(s):  
Irina V. Nikolaenko ◽  
Nikolay Kedin ◽  
Gennadii Shveikin

In this work a new method of nanoand ultrafine powder of tungsten oxide and carbide synthesis by means of combinating carbon carrier supported classic liquid-phase precipitation and low-temperature microwave treatment was offered. The full range of intermediate substances obtained during thermolysis, reduction and carbidization precursors to final products were presented. The thermolysis of tungstic acid with the formation of tungsten oxide and carbide ultrafine particles of different modifications were studied. It was shown, that cooling ammonium tungstate solution to 4 °C, and use of carbon carrier on the precipitation stage can increase specific surface area from 20 to 100 m2g-1. With the use of SEM precursors particles size were examined (∼200 nm) and the morphology of initial, intermediate and final products was shown.


1979 ◽  
Vol 34 (3) ◽  
pp. 412-422 ◽  
Author(s):  
Joachim Fuchs ◽  
Ernst-Peter Flindt

Abstract Polytungstates are obtained by the reaction of hydrated tungsten (VI) oxide with bases or salts after occasional addition of organic solvents. With liquid ammonia the as yet unknown ditungstate, (NH4)2W2O7, is produced. Its IR spectrum has few absorption bands suggesting a very simple constitution. Piperidine yields 5 compounds according to varied experimental conditions, which all exhibit approximately paratungstate compositions but different crystal habits, lattice parameters, solubility and IR spectra. Structure determinations indicate that two of these compounds are heptatungstates, the anion of which, W7O246-, has the same structure as the heptamolybdate ion, Mo7O246-. From a comparison of their Raman spectra with the spectrum of a freshly acidified sodium tungstate solution (designated as Paratungstate A) it may be concluded that the heptatungstate ion is the predominant species in such a solution. The anion structure of the previously described tributylammonium(5:24):tungstate [(C4H9)3NH]5H3W12O40 was elucidated by X-ray methods. Here the tungsten atoms show the same arrangement as in the α-dodecatungstatophosphate ion (Keggin structure).


2015 ◽  
Vol 154 ◽  
pp. 17-19 ◽  
Author(s):  
Linsheng Wan ◽  
Xiaojing Huang ◽  
Dengfei Deng ◽  
Hongchao Li ◽  
Yongming Chen

2017 ◽  
Vol 264 ◽  
pp. 87-90 ◽  
Author(s):  
Yuet Lee Ying ◽  
Swee Yong Pung ◽  
Ming Thong Ong ◽  
Yuk Fen Pung

This work studied the photocatalytic performance of ZnO nanorods and WO3/ZnO nanorods in bromocresol green (BCG). The ZnO nanorods were pre-synthesized via solution precipitation method. Subsequently, the nanorods were kept in sodium tungstate solution for the deposition of WO3. The present of WO3 was confirmed by XRD and EDX analysis. ZnO nanorods (64.34%) showed a higher photodegradation efficiency of BCG removal than WO3/ZnO nanorods (60.03%) under 75 minutes of UV irradiation. This could be attributed to the formation of WO3/ZnO shell-core nanostructure which limited the generation of holes and hydroxyl free radicals that needed for the photodegradation of BCG dyes.


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