Abstract

Phosphate tungsten bronzes, obtained by thermal treatment, are insufficiently investigated bronzes and there is scarce literature data on their chemical behavior and structure. Due to high-sensitivity of the Briggs-Rauscher (BR) reaction to addition of different analytes, this oscillatory reaction presents a potentially important chemical system for investigation and characterization of phosphate-tungsten bronzes, doped and undoped. The reaction mixture for the oscillatory BR reaction typically consists of H2O2, HClO4, KIO3, Mn(II) (catalyst), and CH2(COOH)2 (malonic acid, as an organic substrate). This paper deals with phosphate tungsten bronzes (PWB) and lithium doped phosphate tungsten bronzes (LiPWB) and their effects on the Briggs-Rauscher reaction dynamics. It is shown that the addition of phosphate tungsten bronzes decreases the oscillatory period length in this reaction. Furthermore, the obtained results show that PWB has a stronger influence on the BR reaction dynamics then LiPWB. In both cases, the oscillatory period is a linear function of the added bronze mass. The obtained linear functions can be successfully used for determination of the unknown bronze mass. Furthermore, due to different slopes of these functions, the Briggs-Rauscher reaction can be used as a system-detector for lithium doped and undoped phosphate tungsten bronzes. In order to elucidate the mechanism of bronze action, the inductively coupled plasma optical emission spectrometry (ICP-OES) was used to measure the total contents of K, Mn, W, Li. The aliquots of the above solution (i.e. CH2(COOH)2, MnSO4, HClO4, KIO3 but without H2O2) with the identical masses of PWB and LiPWB were examined. For the sake of comparison, contents of the metals in the solution without the bronze addition were measured, as well. Results obtained by the ICP-OES analysis show that the bronze structure is disturbed in the strong oxidizing environment (iodate in acidic solution) so that both, tungsten and lithium, leach into the BR solution. Accordingly, the proposed mechanism of the bronze action is probably by the reaction of tungsten ion with hydrogen-peroxide resulting in formation of a tungsten-peroxo complex. This complex is a stronger oxidizing agent then hydrogen peroxide itself. Thus, formation of the tungsten-peroxo complex potentially affects the kinetics of the Briggs-Rauscher reaction.

Highlights

  • The reaction mixture for the oscillatory BR reaction typically consists of H2O2, HClO4, KIO3, Mn(II), and CH2(COOH)2

  • The oscillatory period is a linear function of the added bronze mass

  • Due to different slopes of these functions, the Briggs-Rauscher reaction can be used as a system-detector for lithium doped and undoped phosphate tungsten bronzes

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Summary

EKSPERIMENTALNI DEO

Za sintezu 12-volframfosforne heteropoli kiseline korišćene su supstance p.a. čistoće: Na2MoO4 x 2H2O, Na2WO4 x 2H2O, H3PO4, HCl i etar (Merck, Germany) i Drekselova (Drechsel) metoda, postupak za dobijanje 12-volframfosforne heteropoli kiseline detaljno opisan je u referenci [40]. Fosfat-volframove bronze dobijene su termičkim tretmanom 12-volframfosforne heteropoli kiseline i litijumove soli 12-volframfosforne heteropoli kiseline, pri brzini odgrevanja od 10 oC u minuti, do temperature na kojoj dolazi do transformisanja (rušenja) Keginovog anjona. Sve korišćene hemikalije (CH2(COOH) je Acrōs Organics (Belgium), MnSO4 Fluka (Switzerland), dok su HClO4, KIO3 i H2O2 Merck (Germany) proizvodnje) su p.a. čistoće i korišćene su za pravljenje rastvora bez dodatnog prečišćavanja. Uzorci su pripremljeni na isti način kao i za analizu bronzi u Brigs-Raušer reakciji, sa bitnom razlikom da reakcija nije inicirana dodatkom vodonik-peroksida. Sniman je sadržaj metala: kalijuma (K), mangana (Mn), litujuma (Li) i volframa (W) u rastvoru (CH2(COOH), MnSO4, HClO4, KIO3 bez dodatka H2O2) iznad fosfat-volframove (PWB) i litijumom dopirane fosfat-volframove bronze (LiPWB), pojedinačno. Radi poređenja sadržaja metala snimljen je i rastvor (CH2(COOH), MnSO4, HClO4, KIO3) bez dodatka bronzi.

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